Chamomile

Industrial Profiles

Edited by Rolf Franke and Heinz Schilcher

Medicinal and Aromatic Plants Industrial Profiles

Boca Raton London New York Singapore

A CRC title, part of the Taylor & Francis imprint, a member of the
Taylor & Francis Group, the academic division of T&F Informa plc.

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Published in 2005 by
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Chamomile : industrial proles / edited by Rolf Franke and Heinz Schilcher
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Includes bibliographical references and index.
ISBN 0-415-33463-2 (alk. paper)
1. German chamomile--Therapeutic use. I. Franke, Rolf. II. Series.
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Preface to the Series

There is increasing interest in industry, academia, and the health sciences in medicinal and aromatic
plants. In passing from plant production to the eventual product used by the public, many sciences
are involved. This series brings together information that is currently scattered through an everincreasing number of journals. Each volume gives an in-depth look at one plant genus, about which
an area specialist has assembled information ranging from the production of the plant to market
trends and quality control.
Many industries are involved, such as forestry, agriculture, chemicals, food, flavor, beverage,
pharmaceutical, cosmetics, and fragrance. The plant raw materials are roots, rhizomes, bulbs, leaves,
stems, barks, wood, flowers, fruits, and seeds. These yield gums, resins, essential (volatile) oils,
fixed oils, waxes, juices, extracts, and spices for medicinal and aromatic purposes. All these
commodities are traded worldwide. A dealers market report for an item may say drought in the
country of origin has forced up prices.
Natural products do not mean safe products, and account of this has to be taken by the above
industries, which are subject to regulation. For example, a number of plants that are approved for
use in medicine must not be used in cosmetic products.
The assessment of safe to use starts with the harvested plant material, which has to comply
with an official monograph. This may require absence of, or prescribed limits of, radioactive
material, heavy metals, aflatoxin, pesticide residue, as well as the required level of active principle.
This analytical control is costly and tends to exclude small batches of plant material. Large-scale,
contracted, mechanized cultivation with designated seed or plantlets is now preferable.
Today, plant selection is not only for the yield of active principle, but for the plants ability to
overcome disease, climatic stress, and the hazards caused by mankind. Such methods as in vitro
fertilization, meristem cultures, and somatic embryogenesis are used. The transfer of sections of
DNA is giving rise to controversy in the case of some end uses of the plant material.
Some suppliers of plant raw material are now able to certify that they are supplying organically
farmed medicinal plants, herbs, and spices. The Economic Union directive CVO/EU No. 2092/91
details the specifications for the obligatory quality controls to be carried out at all stages of
production and processing of organic products.
Fascinating plant folklore and ethnopharmacology lead to medicinal potential. Examples are the
muscle relaxants based on the arrow poison, curare, from species of Chondrodendron, and the
antimalarials derived from species of Cinchona and Artemisia. The methods of detection of pharmacological activity have become increasingly reliable and specific, frequently involving enzymes
in bioassays and avoiding the use of laboratory animals. By using bioassay-linked fractionation of
crude plant juices or extracts, compounds can be specifically targeted which, for example, inhibit
blood platelet aggregation, or have antitumor, or antiviral, or any other required activity. With the
assistance of robotic devices, all the members of a genus may be readily screened. However, the
plant material must be fully authenticated by a specialist.
The medicinal traditions of ancient civilizations such as those of China and India have a large
armamentarium of plants in their pharmacopoeias that are used throughout Southeast Asia. A similar
situation exists in Africa and South America. Thus, a very high percentage of the worlds population
relies on medicinal and aromatic plants for their medicine. Western medicine is also responding.
Already in Germany all medical practitioners have to pass an examination in phytotherapy before
being allowed to practice. It is noticeable that medical, pharmacy, and health-related schools
throughout Europe and the United States are increasingly offering training in phytotherapy.

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Multinational pharmaceutical companies have become less enamored of the single compound,
magic-bullet cure. The high costs of such ventures and the endless competition from me-too
compounds from rival companies often discourage the attempt. Independent phytomedicine companies have been very strong in Germany. However, by the end of 1995, 11 (almost all) had been
acquired by the multinational pharmaceutical firms, acknowledging the lay publics growing
demand for phytomedicines in the Western world.
The business of dietary supplements in the Western world has expanded from the health store to
the pharmacy. Alternative medicine includes plant-based products. Appropriate measures to ensure
their quality, safety, and efficacy either already exist or are being answered by greater legislative
control by such bodies as the U.S. Food and Drug Administration and the recently created European
Agency for the Evaluation of Medicinal Products based in London.
In the United States, the Dietary Supplement and Health Education Act of 1994 recognized the
class of phytotherapeutic agents derived from medicinal and aromatic plants. Furthermore, under
public pressure, the U.S. Congress set up an Office of Alternative Medicine, which in 1994 assisted
the filing of several Investigational New Drug (IND) applications, required for clinical trials of
some Chinese herbal preparations. The significance of these applications was that each Chinese
preparation involved several plants and yet was handled as a single IND. A demonstration of the
contribution to efficacy of each ingredient of each plant was not required. This was a major step
toward more sensible regulations in regard to phytomedicines.
My thanks are due to the staff of CRC Press who have made this series possible and especially
to the volume editors and their chapter contributors for the authoritative information.
Dr. Roland Hardman

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Preface
For more than 2000 years, preparations of chamomile flowers count among the medicinal treasures
of various cultural groups. Since ancient times, the chamomile has survived the storms of time as
well as different trends in the art of healing throughout the world.
It is certainly one of the most fascinating medicinal plants of our globe, although the True
chamomile, often called German chamomile, is native only to Europe and the Near East, but
naturalized in many other regions too. There are only a few medicinal plants with a millennium-lasting
successful therapeutic use that can claim to be part of a wide interdisciplinary scientific research.
Over 100 years ago, the first attempts in cultivation and breeding were made and these are still
up to date. In 1921, Chemiewerke Homburg received the patent for the first chamomile extract.
Today, university and industrial research groups work on the optimal extraction and optimal stability
of the ingredients that have an influence on the efficacy in different galenic preparations. The
relatively good findings on hydrophilic and lipophilic ingredients are not finalized yet, as the recent
analytic results show.
As other modern pharmacopoeae, the European Pharmacopoeia in its 5th edition (published
in February 2004) determines minimum and maximum values for three ingredients that have an
influence on the efficacy of the essential chamomile oil and require a test for the so-called
chromatographic profile by gas chromatography (GCP).
Chamomile flowers are also interesting objects for the research of the biosynthesis of monoand sesquiterpenes.
Of great interest are naturally the numerous tests on efficacy and safety studies of chamomile
flower preparations. They shall serve as scientifically well-founded confirmations of therapeutic
reports from prescientific times and also for precision of application fields and correct dosage.
Here, too, chamomile flower preparations and essential chamomile flower oil have a special position.
In the 1930s, pharmacological studies with chamazulen and chamomile flower extracts were
realized and were confirmed later on with modified testing methods of a more recent date. Only very
few medicinal plants exist, of which a similarly high number of qualified pharmacological or experimental studies are available. There are also a surprising number of clinical studies; most of which,
however, do not correspond to the GCP test design, as they were conducted before the GCP test
design was developed in 1994. Whether these clinical studies, realized between 1960 and 1992, are
less meaningful is questionable because they are of high scientific level. A similar case is the reported
allergenic potential of chamomile flowers, particularly if the myriad uses of chamomile flower
preparations are taken into account.
When Roland Hardman suggested that we edit a book for his series Medicinal and Aromatic
Plants Industrial Profiles, we accepted with pleasure, although we are aware that chamomile
has many faces. Therefore, it was our aim to involve various competent persons from different
specialized fields and countries.
The present compendium, Chamomile: Industrial Profiles, provides an interdisciplinary inventory of the scientific level of knowledge about True chamomile as well as Roman chamomile
and shall discuss controversial questions too.
We would like to thank the co-authors for their factual, well-founded articles, the project
coordinators for their friendly support, and CRC Press for the printing of this compendium. Finally,
we would like to thank all the people who contributed to the success of the cultivation and use of
this fascinating plant.
Rolf Franke and Heinz Schilcher
Munich, April 2005

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Contributors
Dr. sc. Rolf Franke, Salus Haus Dr. med. Otto Greither Nachf. GmbH & Co. KG, Bahnhofstrae
24, D-83052 Bruckmhl/Obb., Germany
e-mail: [email protected]
Prof. Dr. rer. nat. Dr. med h.c. Heinz Schilcher, Zaumberg 25, D-87509 Immenstadt/Allgu,
Germany
e-mail: [email protected]
Prof. Dr. Jeno Bernth, Corvinus University, Faculty of Horticultural Sciences, Department of
Medicinal and Aromatic Plants, Villnyi str., 29, H-1118 Budapest, Hungary
e-mail: [email protected]
Prof. Dr. Horst Bttcher, Institut fr Ernhrungswissenschaften der Martin-Luther-Universitt
Halle-Wittenberg, EmilAbderhaldenStr. 25 b, D-06108 Halle (Saale), Germany
e-mail: [email protected]
Prof. Dr. Reinhold Carle, Hohenheim University, Institute of Food Technology, Department
of Plant Foodstuff Technology, Garbenstrae 25, D-70599 Stuttgart, Germany
e-mail: [email protected]
Tamer Fahmi, 32 Abdallah Ben Taher St., Nasr City, Cairo, Egypt
e-mail: [email protected]
Norberto R. Fogola, Av. Gral. Chenaut 1757 Piso 9 B, RA-1426 Buenos Aires, Argentina
e-mail: [email protected]
Dr. Susanne Goeters, c/o Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Strae
65, D-88397 Biberach/Ri, Germany
e-mail: [email protected]
Prof. Dr. Peter Imming, Institut fr Pharmazeutische Chemie, Martin-Luther-Universitt, HalleWittenberg, Wolfgang-Langenbeck-Str. 4, D-06120 Halle (Saale), Germany
e-mail: [email protected]
Dusan Jednak, Mierova 20, SK-06401 Star Lubovna, Slovakia
Ingeborg Gnther, Institut fr Ernhrungswissenschaften der Martin-Luther-Universitt HalleWittenberg, Emil-Abderhalden-Str. 25 b, D-06108 Halle (Saale), Germany
e-mail: [email protected]
Dr. Hans-Jrgen Hannig, Martin Bauer GmbH & Co. KG, Dutendorfer Strae 5-7, D-91487
Vestenbergsgreuth, Germany
e-mail: [email protected]
Dr.-Ing. Albert Heindl, Marktplatz 5, D-84048 Mainburg, Germany
e-mail: [email protected]
Jozef Holubr, stredn kontroln a zkusebn stav zemedelsky, Hroznova 3, CZ-65606
Brno, Czech Republic

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Prof. Dr. va Nmeth, Corvinus University, Department of Medicinal and Aromatic Plants;
Villnyi str., 29, H-1118 Budapest, Hungary
e-mail: [email protected]
Dr. Viliam Oravec, 17. Novembra 32, SK-064 01 Star Lubovna, Slovakia
e-mail: [email protected]
Viliam Oravec, Jr., Helsinska 5, SK-04000 Kosice, Slovakia
e-mail: [email protected]
Dr. Andreas Plescher, Pharmaplant GmbH, Strae am Westbahnhof, D-06556 Artern, Germany
e-mail: [email protected]
Asst. Prof. Dr. Miroslav Repck, Department of Experimental Botany and Genetics, Prrodovedeck fakulta, Universitat P.J. Safarik, Mnesova 23, SK-04154 Kosice, Slovakia
e-mail: [email protected]
Lubomr S ebo, 17. Novembra 7, SK-06401 Star Lubovna, Slovakia
Ivan Varga, Veterna 11, SK-92027 Hlohovec, Slovakia
Eduardo Weldt S., Puelche S.A., P.O. Box 902, Los Angeles, Chile
e-mail: [email protected]

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Table of Contents
Chapter 1
Introduction
Rolf Franke
Chapter 2
Legal Situation of German Chamomile: Monographs
Heinz Schilcher
Chapter 3
Plant Sources
Rolf Franke
Chapter 4
Active Chemical Constituents of Matricaria chamomilla L. syn. Chamomilla recutita
(L.) Rauschert
Heinz Schilcher, Peter Imming, and Susanne Goeters
Chapter 5
Cultivation
Rolf Franke with cooperation of Jen Bernath, Tamer Fahmi, Norberto R. Fogola,
Dusan Jedinak, Hans-Jrgen Hannig, Josef Holubr, va Nmeth, Viliam Oravec,
Viliam Oravec, Jr., Miroslav Repck, Lubomir Sebo, Ivan Varga, and
Eduardo Weldt S.
Chapter 6
Abiotic and Biotic Stress Affecting the Common Chamomile (Matricaria recutita L.)
and the Roman Chamomile (Chamaemelum nobile L. syn. Anthemis nobilis L.)
Andreas Plescher
Chapter 7
Raw Plant Material and Postharvest Technology
Horst Bttcher and Ingeborg Gnther
Chapter 8
Processing of Raw Material
Horst Bttcher and Ingeborg Gnther with cooperation of Reinhold Carle and Albert Heindl
Chapter 9
Storage of the Dry Drug
Horst Bttcher and Ingeborg Gnther

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Chapter 10
Chemical Analysis of the Active Principles of Chamomile
Heinz Schilcher, Peter Imming, and Susanne Goeters
Chapter 11
Pharmacology and Toxicology
Heinz Schilcher, Peter Imming, and Susanne Goeters
Chapter 12
Traditional Use and Therapeutic Indications
Heinz Schilcher

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1 Introduction
Rolf Franke
The medicinal plant of chamomile and the species related to it are of manifold interest as both the
drug Matricariae flos (Ph. Eur. 4.6, 2004) [1] and the native plants. Cultivated and wild plants
offer a number of subjects that belong to the range of basic and applied research; on the other
hand, they are of great economic interest as well.
Considering the fact that the traded chamomile flowers show a very heterogeneous spectrum
of content [2, 3], a drug bound to a pharmacopoeia can if it is to be recognized by the medical
sciences in the rational sense only reach a high standard relating to natural science provided
there is a comprehensive knowledge about the biology of the medicinal plant and the species related
to it, as well as the drug obtained from it.
Chamomile flowers belong to those drugs that experienced a wide medical application in ancient
times [2, 3]. The curative effect of chamomile has been known by physicians for about 2500 years.
Hippocrates gives a description of the drug in the 5th century B.C., and chamomile appears as a
medicinal plant in the work De Materia Medica written by Dioscorides (1st century A.D.). Galen
and Asclepios describe the application of a chamomile infusion at some length. In Palladius
writings dating back to the 4th or 5th century, notes about chamomile are to be found as well.
Medical applications continued in the Middle Ages. Bock, for example, gives the following report
about chamomile in his Kreutterbuch of 1539 (described as gantz gemein Chamill: quite
ordinary/common chamomile): Es ist bei allen menschen kein breuchlicher kraut in der artznei
als eben Chamillenblumen/dann sie werden beinahe zu allen presten gebraucht. (In Old High
German, There is no herb in medicine for people being more usual than chamomile flowers because
they are used against nearly all kinds of ailments.)
From the New Kreuterbuch written by Mathiolus (1626) it may be gathered that das
Kamillenl dienet sonderlich wol wider den krampf (chamomile oil serves as a remedy against
convulsion). Tabernaemontanus mentions chamomile in 1664 [4]: zu mancherley gebrauch in
der Artzeney/als in Pflaster/Salben/Behung/Scklein/Bder und dergleichen ntzlich gebraucht
wird/und vielerley Artzeneyen darau bereiten (for manifold use in medicine such as in plasters/ointments/pouches, [medicinal] baths and for other useful purposes, many different medicines
can be prepared out of it). In his Medizinisches Lexikon (Medical Encyclopaedia, 1755) von Haller
makes honorable mention of the pain-relieving and spasmolytic effect of chamomile flowers, and
in his Praktische Arzneimittellehre (1814, Vol. 1) (Practical Pharmacology), Hecker as well as
Hufeland and colleague Collenbuch report the successful use of chamomile preparations in cases
of ulcerations (in Hufelands Journal) [5]. Saladin von Asculum mentioned the blue volatile oil of
chamomile in 1488 and Hieronimus Brunschwig described the distillation of the volatile chamomile
oil in 1500. High appreciation is also given to chamomile preparations in the various works written
by Sebastian Kneipp (18211897) [6]. In the first edition of the Lehrbuch der Phytotherapie
(Textbook of Phytotherapy) (1942) Weiss refers to chamomile as being one of the most significant
medicinal plants, giving wider space to it in the review [7].
The summary of a choice of internationally known pharmacopoeias (see Chapter 2, Table 2.1)
shows that since the publication of the German Pharmacopoeia in 1882, chamomile flowers and
preparations from chamomile flowers have been included in a number of pharmacopoeias. In the

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current pharmacopoeia for the Federal Republic of Germany, the drug called Matricariae flos is to
be found in the European Pharmacopoeia 4.6, edition 2004 [1].
Roman chamomile has also been significant as a drug from ancient times. Tabernaemontanus
had already known filled and unfilled forms in 1664 [4]. This Roman chamomile is included in a
number of pharmacopoeias and also in the European Pharmacopoeia, Suppl. 4.3 2003 (see Chapter
2, Table 2.2).
In 1956 Heeger [8] reported that true chamomile has been worked on to a small extent [only]
and that it is on its way to becoming a culture plant. In the past 40 years chamomile has developed
into a real culture plant that is cultivated on a wide scale.

FIGURE 1.1 True chamomile (Matricaria recutita L.). (Fuchs, L. [1543] New Kreterbuch. Basel. With
permission of Botanical Garden and Botanical Museum, Berlin-Dahlem.)

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FIGURE 1.2 The capitulum of the True chamomile has a cone-shaped, hollow bottom. (Khler [1987]
Medizinal-Pflanzen in naturgetreuen Abbildungen mit kurz erluterndem Text. Gera. Vol. With permission of
Botanical Garden and Botanical Museum, Berlin-Dahlem.)

FIGURE 1.3 True chamomile (Matricaria recutita L.). (Hayne, F.G. [1805] Getreue Darstellung und
Beschreibung der in der Arzneykunde gebruchlichen Gewchse. Berlin. Vol. 1. With permission of Botanical
Garden and Botanical Museum, Berlin-Dahlem.)

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FIGURE 1.4 True chamomile (Matricaria recutita L.) [4].

FIGURE 1.5 Roman chamomile (Chamaemelum nobile [L.] All.). (Chaumeton, F.P. [1815] Flore mdicinale.
Paris. Vol. 2. With permission of Botanical Garden and Botanical Museum, Berlin-Dahlem.)

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FIGURE 1.6 Roman chamomile (Chamaemelum nobile [L.] All.) (Tabernaemontanus, 1664 p. 58) [4].

FIGURE 1.7 Roman chamomile (Chamaemelum nobile [L.] All.) (Tabernaemontanus, 1664 p. 59) [4].

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REFERENCES
1. European Pharmacopoeia 4.6 (edition 2004) Deutscher Apotheker Verlag, Stuttgart, Germany.
2. Isaac, O., Schimpke, H. (1965) Mitt. Dtsch. Pharmazeut. Ges., 35, 133.
3. Schilcher, H. (1973) Neuere Erkenntnisse bei der Qualittsbeurteilung von Kamillenblten bzw. Kamillenl Einteilung der Handelskamille in vier chemische Typen. Planta Medica, 23, 132.
4. Tabernaemontanus, J.T. (1664) New vollkommenlich Kruter-Buch, Jacob Werenfels, Basel, 1529 pp.
5. Hufelands Journal, ref. in Madaus, G. (1979) Lehrbuch der biologischen Heilmittel. Band I.G. Olms,
Hildesheim, New York.
6. Kneipp, S. (1882) ffentliche Vortrge, p. 232 and (1985) p. 46; (1866) Meine Wasserkur, p. 137; (1893)
Kneippbltter, p. 52; (1889) Ratgeber fr Gesunde und Kranke, p. 283; (1894) Mein Testament, p. 122.
7. Weiss, R.F. (1942) Lehrbuch der Phytotherapie, Hippokrates, Stuttgart, Germany.
8. Heeger, E.F. (1956) Handbuch des Arznei- und Gewrzpflanzenanbaus. Drogengewinnung. Deutscher
Bauernverlag, Berlin, pp. 186, 494495.

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Situation of German
2 Legal
Chamomile: Monographs
Heinz Schilcher
CONTENTS
2.1
2.2
2.3
2.4

2.5

Overview of the Pharmacopoeias: Monographs

Overview of the Test Regulations in Pharmacopoeias
Overview of the Quantitative Determination of Essential Oil in Pharmacopoeias
Monographs of the European Pharmacopoeia
2.4.1 Matricaria Flower Matricariae flos
2.4.1.1 Definition
2.4.1.2 Content
2.4.1.3 Characteristics
2.4.1.4 Identification
2.4.1.5 Tests
2.4.1.6 Assay
2.4.1.7 Test Solution
2.4.1.8 Reference Solution
2.4.1.9 Precolumn
2.4.1.10 Column
2.4.1.11 Mobile Phase
2.4.2 Matricaria Oil Matricariae aetheroleum
2.4.2.1 Definition
2.4.2.2 Characteristics
2.4.2.3 Identification
2.4.2.4 Tests
2.4.2.5 Storage
2.4.2.6 Labeling
2.4.3 Matricaria Liquid Extract Matricariae extractum fluidum
2.4.3.1 Definition
2.4.3.2 Production
2.4.3.3 Characteristics
2.4.3.4 Identification
2.4.3.5 Tests
2.4.3.6 Assay
ESCOP: Matricariae flos Matricaria flower
2.5.1 ESCOP Monograph Matricariae Flos Matricaria Flower
2.5.1.1 Definition
2.5.1.2 Constituents
2.5.1.3 Clinical Particulars

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2.5.2

Pharmacological Properties
2.5.2.1 Pharmacodynamic Properties
2.5.2.2 Anti-Inflammatory Effects
2.5.2.3 Antispasmodic Effects
2.5.2.4 Antiulcerogenic Effects
2.5.2.5 Wound Healing Effect
2.5.2.6 Sedative Effects
2.5.2.7 Antimicrobial Effects
2.5.2.8 Clinical Studies
2.5.2.9 Pharmacokinetic Properties
2.5.2.10 Preclinical Safety Data
2.6 Commission E Monograph Matricariae flos (Chamomile Flowers)
2.6.1 Matricariae flos (Chamomile flowers)
2.6.1.1 Official Name
2.6.1.2 Description
2.6.1.3 Indications
2.6.1.4 Contraindications
2.6.1.5 Side Effects
2.6.1.6 Dosage
2.6.1.7 Method of Application
2.6.1.8 Medicinal Actions
2.7 WHO: Flos Chamomillae
2.7.1 WHO: Monographs on Selected Medicinal Plants
2.7.1.1 Definition
2.7.1.2 Synonyms
2.7.1.3 Selected Vernacular Names
2.7.1.4 Description
2.7.1.5 Plant Material of Interest: Flower Heads
2.7.1.6 Geographical Distribution
2.7.1.7 General Identity Tests
2.7.1.8 Purity Tests
2.7.1.9 Chemical Assays
2.7.1.10 Major Chemical Constituents
2.7.1.11 Dosage Forms
2.7.1.12 Medicinal Uses
2.7.1.13 Internal Use
2.7.1.14 External Use
2.7.1.15 Inhalation
2.7.1.16 Pharmacology
2.7.1.17 Clinical Pharmacology
2.7.1.18 Contraindications
2.7.1.19 Warnings
2.7.1.20 Precautions
2.7.1.21 Adverse Reactions
2.7.1.22 Posology
2.8 Legal Classification of the Use of German Chamomile in Germany and
in the European Community
2.8.1 Foodstuff
2.8.2 Drug
References

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2.1 OVERVIEW OF THE PHARMACOPOEIAS: MONOGRAPHS

TABLE 2.1
Pharmacopoeias Containing Monographs on Chamomile Flowers, Chamomile Oil, or
Chamomile Preparations (e.g., Extracts)
Year

Pharmacopoeia

Part of the Plant

1882
1893
1894
1897
1900
1901
1905
1905
1905

DAB 2 German Pharmacopoeia 2nd edition

Pharmacopoeia Helvetica 3rd edition
DAB 3 German Pharmacopoeia 3rd edition
Supplement for DAB 3, drugs not being included in
DAB 3, 2nd edition
DAB 4 German Pharmacopoeia 4th edition
Svenska Farmakopen 8
Pharmacopoeia of the USA, 1900 edition
Pharmacopoea Nederlandica 4 (Dutch Ph)
Farmacopea Espaola 7

1906

3rd supplementary volume for DAB 4

1906

Pharmacope Belgicae 3

1906
1907
1908

Pharmacopoea Austria 8
Pharmacopoeia of Japan, English edition
Pharmacope Franaise

1910
1916

DAB 5 German Pharmacopoeia 5th edition

DAB 5 4th supplementary volume

1925
1926
1934
1939
1940
1941

Svenska Farmacopen X
DAB 6 German Pharmacopoeia 6th edition
HAB Dr. Willmar Schwabe
Den Norske Farmakopo V (Norwegian PhP)
Pharmacopoea Nederlandica 5 (2nd print)
DAB 6 Supplementary volume

1941
1941
1946
1946
1948
1953

Pharmacopoea Helvetica 5
Farmacopea Chilena
Svenska Farmakopen XI (Sweden)
Farmacopea Portuguesa 46
Pharmacopoea Danica
Pharmacope Belge V

1953
1954
1958
1959
1960

Indian Pharmaceutical Codex

Farmacopea oficial Espaola IX
Nederlandse Pharmacopee 6
Farmacopeia dos Estados Unidos do Brasil
sterreichisches Arzneibuch 9 Austrian
Pharmacopoeia 9
Pharmacope Belge VI
Farmakopea Polska IV (Polish Ph.)

Flowers
Flowers and volatile oil
Flowers
Volatile oil, extract with fatty oil, volatile oil
combined with lemon oil, spissum extract
Flowers
Flowers and spissum extract
Flowers under the name Matricaria
Flowers
Flowers under the name Manzanilla and extract
with fatty oil
Volatile oil, extract with fatty oil, volatile oil
combined with lemon oil, spissum extract
Flowers under Flores Chamomillae that originate
from Anthemis nobilis (!)
Flowers
Flowers
Flowers of Arthemis nobilis (!) extract from fatty
oil, extract with camphor oil from A. nobilis
Flowers
Volatile oil, extract with fatty oil, volatile oil
combined with lemon oil, spissum extract
Flowers
Flowers with a volatile oil content of 0.4%
Fresh plant collected at flowering time
Flowers
Flowers
Volatile oil, extract with fatty oil, fluid extract,
chamomile tincture, chamomile syrup, chamomile
water
Flowers and volatile oil
Flowers
Flowers
Flowers
Flowers
Flowers, volatile oil, chamomile water and (ethyl)
alcohol
Flowers
Flowers with an volatile oil content of 0.4%
Flowers with an volatile oil content of 0.6%
Flowers
Flowers with an volatile oil content of 0.4%

1962
1965

Copyright 2005 CRC Press, LLC

Flowers
Flowers

TF4015_book.fm Page 10 Wednesday, April 6, 2005 12:17 PM

TABLE 2.1
Pharmacopoeias Containing Monographs on Chamomile Flowers, Chamomile Oil, or
Chamomile Preparations (e.g., Extracts) (continued)
Year

Pharmacopoeia

1966
1967
1967
1968

Farmacopea Argenina 6
Pharmacopoea Hungarica VI
Martindale 25 (The Extra Pharmacopoeia, London)
DAB 7 BRD German Pharmacopoeia of the FRG,
7th edition
Pharmacopoea Helvetica 6

1971
1971
1972
1973
1974
1975
1975
1976
1976
1978
1978
1980
1981
1982
1982
1983
1984
1984
1985
1986
1986
1987

Nederlandse Pharmacopee 8
Farmacopea ufficiale della Repubblica Italiana VIII
Pharmacope Franaise 9
Estra farmakope Indonesia
DAB 7 DDR German Pharmacopoeia of the GDR,
7th edition (2nd issue)
Europ. Pharmacopoeia, 1st edition, volume III
Pharmacopoea Bohemeslovenica III (addendum)
(Czechoslovakia)
Farmacopea Romana IX (Rumania)
DAB 8 BRD German Pharmacopoeia of the FRG,
8th edition
1st official edition of the Homeopathic
Pharmacopoeia with 4th addendum of 1985
British Pharmacopoeia
sterreichisches Arzneibuch 1981 Austrian
Pharmacopoeia 1981
Standard Admission 36 AMG 76
Martindale 28
British Herbal Pharmacopoeia
Egyptian Pharmacopoeia
Farmacopea Jugoslavica IV
African Pharmacopoeia 1st ed.
DAB 9 BRD German Pharmacopoeia of the FRG,
9th edition
Pharmacopea Hungarica VII
Pharmacopea Helvetica VII

1988
1989
1990

Pharmacope Franaise X
Martindale (London)
sterreichisches Arzneibuch Austrian
Pharmacopoeia

1990

Commission E Monograph (revised version)

(Germany)
British Herbal Pharmacopoeia, (Volume 1)
DAB 10 German Pharmacopoeia, 10th edition, 1st
addendum

1990
1992

Copyright 2005 CRC Press, LLC

Part of the Plant

Flowers
Flowers with a volatile oil content of 0.4%
Flowers with a volatile oil content of 0.4%
Flowers with a volatile oil content of 0.4%
Flowers with a volatile oil content of 0.5% and fluid
extract
Flowers
Flowers
Flowers with a volatile oil content of 0.5%
Flowers
Flowers and fluid extract
Flowers with a volatile oil content of 0.4%
Flowers
Flowers
Flowers with a volatile oil content of 0.4%
Fresh whole plants of Chamomilla recutita (L.)
Rauschert collected at flowering time
Flowers of Arthemis nobilis (!) under Chamomile
Flowers with a volatile oil content of 0.7%
Flowers, volatile oil, chamomile fluid extract, and
tincture
Flowers with a volatile oil content of 0.4%
Flowers with a volatile oil content of 0.4%
Flowers
Flowers
Flowers
Flowers
Flowers with a volatile oil content of 0.4%
Flowers and volatile oil
Flowers with a volatile oil content of 0.4%,
standardized chamomile fluid extract with a
volatile oil content of 0.120.18%
Fresh flowers for homeopathic preparation
Flowers and volatile oil
Flowers with a volatile oil content of 0.4%, volatile
oil, chamomile fluid extract (with a volatile oil
content of 0.3%), and tincture
Flowers
Flowers
Chamaemelum nobile (L.) All. with not less than
0.7% of volatile oil

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TABLE 2.1
Pharmacopoeias Containing Monographs on Chamomile Flowers, Chamomile Oil, or
Chamomile Preparations (e.g., Extracts) (continued)
Year

Pharmacopoeia

Part of the Plant

1992
1993
1993
1993
1993
1994
1995
1996
1996
1996
1997

British Herbal Compendium (Volume 1)

DAB 10 German Pharmacopoeia, 10th edition, 2nd
addendum
Martindale (London)
Pharmacope Franaise
Pharmacopoeia Helvetica VII (Addendum)
Austrian Pharmacopoeia
Polish Pharmacopoeia
British Herbal Pharmacopoeia 1996
Pharmacope Franaise
Martindale (London), 31st edition
European Pharmacopoeia, 3rd edition

1997

DAB 1997 German Pharmacopoeia 1997

1997

Real Farmacopea Espaola, 1st edition

1997
1999
1999
1999
1999
1999
2000

European Pharmacopoeia (valid until 2001)

ESCOP Monograph
WHO Monograph
Martindale (London), 32nd edition
DAB 1999 German Pharmacopeia
USP 24/NF 19
British Pharmacopoeia

2001
2001
2002
2003
2003
2004

European Pharmacopoeia (Addendum 2001)

USP 24/NF 19 (Addendum 3)
European Pharmacopeia
USP 26/NF 21
European Pharmacopoeia 4.5
European Pharmacopoeia 4.6 (since 01/2004)

Flowers
Flowers with a minimum volatile oil content of
0.4%
Flowers
Flowers
Flowers
Fluid extract/tincture
Flowers
Flowers
Flowers
Flowers and volatile oil
Flowers with a minimum volatile oil content of
0.4%
Volatile oil, chamomile liquid extract (with a
volatile oil content of min. 0.3%)
Flowers with a minimum volatile oil content of
4 ml/kg
Flowers
Flowers
Flowers
Flowers and volatile oil
Liquid extract/volatile oil
Flowers
Flowers of Chamaemelum nobile (L.) All. with not
less than 7 ml/kg of volatile oil
Liquid extract with 0.3% blue volatile oil
Flowers (changes to read)
Flowers/liquid extract
Flowers
Liquid extract/volatile oil
Flowers

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TABLE 2.2
Some Pharmacopoeias Containing Monographs on Roman Chamomile Flowers, Roman
Chamomile Oil, or Roman Chamomile Preparations (e.g., Extracts)
Year

Pharmacopoeia

1906

Pharmacope Belgicae 3

1908
1934
1940
1941
1953

Pharmacope Franaise
HAB Dr. Willmar Schwabe
Nederlandsche Pharmacopee, 5th edition
Pharmacopoeia Helvetica, 5th edition
Pharmacope Belge V

1954

British Pharmaceutical Codex

1954
1954
1959
1960

Farmacopea oficial Espaola IX (Hisp IX)

Farmakopea Polska III (Polish Ph.)
Farmacopeia dos Estados Unidos do Brasil
sterreichisches Arzneibuch (AB 9) Austrian
Pharmacopoeia
Farmacopea ufficiale della Repubblica Italiana VIII
British Herbal Pharmacopoeia
Pharmacope Franaise IX
Pharmacopoeia Helvetica VI
British Pharmacopoeia

1972
1976
1976
1979
1980

1981
1983
07/87
01/93
1987
1988

sterreichisches Arzneibuch 1981 Austrian

Pharmacopoeia 1981
British Herbal Pharmacopoeia
Pharmacope Franaise X
Pharmacopea Helvetica VII
British Pharmacopoeia

1992
1993
1993

DAB 10 German Pharmacopoeia, 10th edition

Pharmacopoeia Helvetica VII
British Pharmacopoeia

1997

European Pharmacopoeia, 3rd edition

1999

British Pharmacopoeia

2003

European Pharmacopoeia 4.3 (German version)

Copyright 2005 CRC Press, LLC

Part of the plant

Monograph title: Flores Chamomillae originating
from Anthemis nobilis
Flowers of Arthemis nobilis
Fresh total plant from Anthemis nobilis
Flowers
Flowers
Flowers under Chamomillae flos that originate from
Anthemis nobilis
Flowers of Anthemis nobilis L. under the name
Chamomile, content of volatile oil not less than
0.4% (v/w)
Flowers
Flowers as Anthodium anthemidis
Flowers
Flowers with a content of volatile oil not less than
0.7% (v/w)
Flowers under Camomilla romana (Anthemidis flos)
Flowers
Flowers
Flowers
Flowers of Anthemis nobilis L. under the name
Chamomile flowers, content of volatile oil not less
than 0.7% (v/w)
Flowers
Flowers
Flowers
Flowers
Flowers of Anthemis nobilis L. under the title
Chamomile flowers, content of volatile oil not less
than 0.7% (v/w)
Flowers
Flowers
Flowers of Anthemis nobilis L. under the title
Chamomile flowers, content of volatile oil not less
than 0.7% (v/w)
Flowers with a content of volatile oil not less than
0.7% (v/w)
Flowers of Chamaemelum nobile (L.) All. under the
title Chamomile flowers, content of essential oil
not less than 7 mg/kg
Flowers

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2.2 OVERVIEW OF THE TEST REGULATIONS IN

PHARMACOPOEIAS
An overview of the test regulations for chamomile flowers and chamomile preparations in pharmacopoeias since 1882 and on some pharmacopoeias containing monographs on Roman chamomile
flowers, Roman chamomile oil, or Roman chamomile preparations (e.g., extracts) is given in Chapter
10, Chemical Analysis of the Active Principles of Chamomile (see Tables 10.1 and 10.2).

2.3 OVERVIEW OF THE QUANTITATIVE DETERMINATION OF

ESSENTIAL OIL IN PHARMACOPOEIAS
An overview of the quantitative determination of the essential oil in Chamomile flowers by means
of steam distillation is given in Chapter 10, Chemical Analysis of the Active Principles of
Chamomile (see Table 10.3).

2.4 MONOGRAPHS OF THE EUROPEAN PHARMACOPOEIA

2.4.1

MATRICARIA FLOWER MATRICARIAE

FLOS

European Pharmacopoeia 4.6 [16]

Matricaria flower
Matricariae flos
2.4.1.1 Definition
Dried capitula of Matricaria recutita L. (Chamomilla recutita [L.] Rauschert)
2.4.1.2 Content

Blue essential oil: minimum 4 ml/kg (dried drug)

Total apigenin-7-glucoside (C21H20O10): minimum 0.25% (dried drug)

2.4.1.3 Characteristics
Macroscopic and microscopic characters described under identification tests A and B
2.4.1.4 Identification
A. Capitula, when spread out, consists of an involucre made up of many bracts arranged in
one to three rows; an elongated-conical receptacle, occasionally hemispherical (young
capitula); 12 to 20 marginal ligulate florets with a white ligule; several dozen yellow
central tubular florets. The involucre bracts are ovate to lanceolate, with a brownish-grey
scarious margin. The receptacle is hollow, without paleae. The corolla of the ligulate
florets has a brownish-yellow tube at the base extending to form a white, elongated-oval
ligule. The inferior ovary is dark brown, ovoid to spherical, and has a long style and
bifid stigma. The tubular florets are yellow and have a five-toothed corolla tube; five
syngenesious, epipetalous stamens; and a gynoecium similar to that of the ligulate florets.
B. Separate the capitulum into its different parts. Examine under a microscope using chloral
hydrate solution R. The bracts have thin-walled cells and a central region composed of
elongated sclereids with occasional stomata. The inner epidermis of the corolla of the
ligulate florets, in surface view, consists of thin-walled, polygonal cells, slightly papillose;
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those of the outer epidermis are markedly sinuous and strongly striated; corolla of the
tubular florets with longitudinally elongated epidermal cells; and with small groups of
papillae near the apex of the lobes. Glandular trichomes each consists of a short stalk and
a head of two to three tiers of two cells each occur on the outer surfaces of the bracts and
on the corollas of both types of florets. The ovaries have a sclerous ring at the base and
the wall is composed of vertical bands of thin-walled, longitudinally elongated cells with
numerous glandular trichomes, alternating with fusiform groups of small, radially elongated
cells containing mucilage. The cells at the apex of the stigmas are extended to form rounded
papillae. Numerous small, cluster crystals of calcium oxalate occur in the inner tissues of
the ovaries and the anther lobes. Pollen grains are spherical to triangular, about 30 m in
diameter with three pores and a spiny exine.
C. Thin-layer chromatography (TLC) (2.2.27)
Test solution: Dilute 50 l of essential oil obtained in the assay of essential oil in 1 ml of xylene R.
Reference solution: Dissolve 2 l of chamazulene R, 5 l of levomenol R, and 10 mg of bornyl
acetate R in 5 ml of toluene R.
Plate: TLC silica gel plate R
Mobile phase: Ethyl acetate R, toluene R (5:95 V/V)
Application: 10 l, as bands
Development: Over a path of 10 cm
Drying: In air
Detection: Spray with anisaldehyde solution R and heat at 100105C for 510 min. Examine
immediately in daylight.
Results: See below the sequence of the zones present in the chromatograms obtained with the
reference solution and the test solution. Furthermore, other zones are present in the chromatogram
obtained with the test solution.
Top of the TLC Plate
One or two blue to bluish-violet zones
Chamazulene: a red to
reddish-violet zone
_______
Bornyl acetate: a yellowishbrown zone

A red to reddish-violet zone

(chamazulene)
_______

A brown zone (en-yne

dicycloether)
_______
Levomenol: a reddish-violet to
bluish-violet zone
Reference solution

_______
A reddish-violet to bluish-violet
zone (levomenol)
Test solution

2.4.1.5 Tests
Broken drug: Maximum 25%, determined on 20.0 g, passes through a sieve (710).
Foreign matter (2.8.2): Maximum 2% m/m
Loss on drying (2.2.32): Maximum 12.0% is determined on 1000 g of the powdered drug (355)
by drying in an oven at 100105C for 2 h.
Total ash (2.4.16): Maximum 13.0%

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2.4.1.6 Assay
Essential oil (2.8.12): Use 30 g of whole drug, a 1000-ml flask, 300 ml of water R as distillation
liquid, and 0.50 ml of xylene R in the graduated tube. Distill at a rate of 34 ml/min for 4 h.
Toward the end of this period, stop the flow of water to the condenser assembly but continue
distilling until the blue, steam-volatile components have reached the lower end of the condenser.
Immediately restart the flow of water to the condenser assembly to avoid warming the separation
space. Stop the distillation after a further 10 min.
Total apigenin-7-glucoside: Liquid chromatography (2.2.29)
2.4.1.7 Test Solution
Reduce 40 g of the drug to a powder (sieve 500). Place 2.00 g of the powdered drug in a 500-ml
round-bottomed flask. Add 200 ml of alcohol R. Heat the mixture under a reflux condenser on a
water bath for 15 min. Cool and filter. Rinse the filter and the residue with a few milliliters of
alcohol R. To the filtrate add 10 ml of freshly prepared dilute sodium hydroxide solution R and
heat the mixture under a reflux condenser on a water bath for about 1 h. Cool. Dilute to 250.0 ml
with alcohol R. To 50.0 ml of the solution add 0.5 g of citric acid R. Shake for 5 min and filter.
Dilute 5.010.0 ml with the mobile phase (initial mixture).
2.4.1.8 Reference Solution
A. Dissolve 10.0 mg of apigenin 7-glucoside R in 100.0 ml of methanol R. Dilute 25.0 ml
of this solution to 200 ml with the mobile phase (initial mixture).
B. Dissolve 10.0 mg of 5,7-dihydroxy-4-methylcoumarin R in 100.0 ml of methanol R.
Dilute 25.0 ml of this solution to 100 ml of the mobile phase (initial mixture). To 4.0
ml of this solution add 4.0 ml of reference solution (a) and dilute to 10.0 ml with the
mobile phase (initial mixture).
The following chromatogram is published for information.

100
1

m Au

80
60
40
20

0
0

1. apigenin-7-glucoside

10

15
Minutes

20

2. 5,7-dihydroxy-4-methylcoumarin

FIGURE 2.1 Chromatogram for the assay of total apigenin-glucoside in matricaria flower.

Copyright 2005 CRC Press, LLC

25

TF4015_book.fm Page 16 Wednesday, April 6, 2005 12:17 PM

2.4.1.9

Precolumn

Size: l = 8 mm, = 4.6 mm

Stationary phase: octadecylsilyl silica gel for chromatography R (5 m)

2.4.1.10 Column

Size: l = 0.25 m, = 4.6 mm

Stationary phase: octadecylsilyl silica gel for chromatography R (5 m)

2.4.1.11 Mobile Phase

Mobile phase A: phosphoric acid R, water R (0.5:99.5 V/V)

Mobile phase B: phosphoric acid R, acetonitrile R (0.5:99.5 V/V)
Time
(min)

Mobile Phase A
(% V/V)

Mobile Phase B
(% V/V)

09
919
1924
2429
2930

75
75 25
25
25 75
75 90

25
25 75
75
75 25
25 10

Flow rate: 1 ml/min

Detection: Spectrophotometer at 340 nm
Injection: 20 l
System suitability: Reference solution (b):
Resolution: minimum 1.8 between the peaks due to apigenin-7-glucoside and 5,7-dihydroxy-4-methylcoumarin
Calculate the percentage content of total apigenin-7-glucoside from the expression:
A1 m2
------------------- P 0, 625
A2 m1

A1

= Area of the peak due to apigenin-7-glucoside in the chromatogram obtained with

the test solution

A2

= Area of the peak due to apigenin-7-glucoside in the chromatogram obtained with

the reference solution

m1

= Mass of the drug in the test solution, in grams

m2

= Mass of apigenin-7-glucoside R in reference solution (a), in grams

= Percentage content of apigenin-7-glucoside in the reagent

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2.4.2 MATRICARIA OIL MATRICARIAE

AETHEROLEUM

European Pharmacopoeia 4.5 [15]

Matricaria oil
Matricariae aetheroleum
2.4.2.1 Definition
Blue essential oil is obtained by steam distillation from the fresh or dried flower heads or flowering
tops of Matricaria recutita L. (Chamomilla recutita L. Rauschert). There are two types of matricaria
oil that are characterized as rich in bisabolol oxides, or rich in levomenol.
2.4.2.2 Characteristics
Appearance: Clear, intensely blue, viscous liquid. It has an intense characteristic odor.
2.4.2.3 Identification
First identification: B
Second identification: A
A. Thin-layer chromatography (2.2.27)
Test solution: Dissolve 20 l of the substance to be examined in 1.0 ml of toluene R.
Reference solution: Dissolve 2 mg of guaiazulene R, 5 l of levomenol R, and 10 mg of bornyl
acetate R in 5.0 ml of toluene R.
Plate: TLC silica gel plate R
Mobile phase: Ethyl acetate R, toluene R (5:95 V/V)
Application: 10 l, as bands
Development: Over a path of 10 cm
Drying: In air
Detection A: Examine in daylight.
Results A: See below for the sequence of the zones present in the chromatograms obtained with
the reference solution and the test solution.

Top of the TLC Plate

Guaiazulene: a blue zone
_______
_______
Reference solution

A blue zone (chamazulene)

_______
_______
Test solution

Detection B: Spray with anisaldehyde solution R and heat at 100105C for 510 min. Examine
immediately in daylight.

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Results B: See below for the sequence of the zones present in the chromatograms obtained with
the reference solution and the test solution. Furthermore, yellowish-brown to greenish-yellow zones
(lower third), violet zones (lower third), and further weak zones may be present in the chromatogram
obtained with the test solution.
Top of the TLC Plate
One or two blue to bluish-violet
zones
Guaiazulene: a red to
reddish-violet zone
_______
Bornyl acetate: a
yellowish-brown to grayish-green
zone
_______
Levomenol: a reddish-violet to
bluish-violet zone

Reference solution

A red to reddish-violet zone

(chamazulene)
_______
A brown zone (en-ynedicycloether)
_______
A reddish-violet to bluish-violet
zone (levomenol)
A brownish zone
Test solution

B. Examine the chromatograms obtained in the test for chromatographic profile.

Results: The characteristic peaks corresponding to levomenol and to chamazulene in the chromatogram obtained with the test solution are similar in retention time to those in the chromatogram
obtained with the reference solution.
2.4.2.4

Tests

Chromatographic profile: Gas chromatography (2.2.28): use the normalization procedure.

Test solution: Dissolve 20 l of the oil to be examined in cyclohexane R and dilute to 5.0 ml with
the same solvent.
Reference solution: Dissolve 20 l of levomenol R, 5 mg of chamazulene R, and 6 mg of guaiazulene
R in cyclohexane R and dilute to 5.0 ml with the same solvent.
Column:

Material: Fused silica

Size: l = 30 m (a film thickness of 1 m may be used) to 60 m (a film thickness of 0.2
m may be used), = 0.250.53 mm; when using a column longer than 30 m, an
adjustment of the temperature program may be necessary.
Stationary phase: Macrogol 20,000 R

Carrier gas: Helium for chromatography R

Flow rate: 12 ml/min
Split ratio: 1:100

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Temperature:

Column

Time (min)

Temperature (C)

040

70 230

4050

230

Injection port

250

Detector

250

Detection: Flame ionization

Injection: 1.0 l
Elution order: Order indicated in the composition of the reference solution. Record the
retention times of these substances.
Relative retention: With reference to chamazulene (retention time = about 34.4 min): -farnesene
= about 0.5; bisabolol oxide B = about 0.8; bisabolone = about 0.87; levomenol = about 0.9;
bisabolol oxide A = about 1.02.
System suitability: Reference solution:
Resolution: Minimum of 1.5 between the peaks due to chamazulene and to guaiazulene.
Using the retention times determined from the chromatogram obtained with the reference
solution, locate levomenol and chamazulene in the chromatogram obtained with the test solution;
locate bisabolol oxides (bisabolol oxide B, bisabolone, and bisabolol oxide A) using Figures
1836.-1 and 1836.-2 (disregard the peak due to cyclohexane). The chromatogram obtained with
the test solution does not show a peak with the retention time of guaiazulene.
Determine the percentage content of the components. The limits are within the following ranges:

Matricaria Oil Rich in

Bisabolol Oxides (%)
Bisabolol oxides

2981

Levomenol
Chamazulene
Total of bisabolol oxides and
levomenol

Matricaria Oil Rich in

Levomenol (%)

1065
1.0

1.0
20

2.4.2.5 Storage
Store in a well-filled, airtight container, protected from light at a temperature not exceeding 25C.
2.4.2.6 Labeling
The label states the type of matricaria oil (rich in bisabolol oxides or rich in levomenol).

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50.00
48.00
46.00
44.00
42.00
40.00
38.00
36.00
34.00
32.00
30.00
28.00
26.00
24.00
22.00
20.00
18.00
16.00
14.00
12.00
10.00
8.00
6.00
4.00
2.00
0.00
0.00

3
2
5

5.00

10.00

1. -farnesene
2. bisabolol oxide B

15.00

20.00

25.00

30.00

35.00

3. bisabolone
4. levomenol

40.00

45.00

50.00

5. chamazulene
6. bisabolol oxide A

FIGURE 2.2 1836.-1 Chromatogram of matricaria oil rich in bisabolol oxides.

50.00
48.00
46.00
44.00
42.00
40.00
38.00
36.00
34.00
32.00
30.00
28.00
26.00
24.00
22.00
20.00
18.00
16.00
14.00
12.00
10.00
8.00
6.00
4.00
2.00
0.00
0.00

6
3

5.00

1. -farnesene
2. bisabolol oxide B

10.00

15.00

20.00

25.00

3. bisabolone A
4. levomenol

30.00

35.00

40.00

5. chamazulene
6. bisabolol oxide

FIGURE 2.3 1836.-2 Chromatogram of matricaria oil rich in levomenol.

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45.00

50.00

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2.4.3 MATRICARIA LIQUID EXTRACT MATRICARIAE

EXTRACTUM FLUIDUM

European Pharmacopoeia 4.5 [14]

Matricaria liquid extract
Matricariae extractum fluidum
2.4.3.1 Definition
Matricaria liquid extract is produced from Matricaria flower (0404). It contains not less than 0.30%
of blue residual oil.
2.4.3.2 Production
The extract is produced from the drug and a mixture of 2.5 parts of a 10% m/m solution of
ammonia (NH3), 47.5 parts of water, and 50 parts of alcohol with an appropriate procedure for
liquid extracts.
2.4.3.3 Characteristics
The extract is a brownish, clear liquid with an intense characteristic odor and characteristic bitter
taste; miscible with water and with alcohol with development of turbidity; soluble in alcohol (50%
V/V).
2.4.3.4 Identification
A. Examine by thin-layer chromatography (2.2.27), using a TLC silica gel F254 plate R.
Test solution: Place 10 ml of the extract in a separating funnel and shake with two quantities,
each of 10 ml, of pentane R. Combine the pentane layers, dry over 2 g of anhydrous
sodium sulphate R, and filter. Evaporate the filtrate to dryness on a water bath and dissolve
the residue in 0.5 ml of toluene R.
Reference solution: Dissolve 4 mg of guaiazulene R, 20 mg of levomenol R, and 20 mg of
bornyl acetate R in 10 ml of toluene R.
Apply 10 l of each solution to the plate as bands. Develop over a path of 10 cm using a
mixture of 5 volumes of ethyl acetate R and 95 volumes of toluene R. Allow the plate to dry in
air and examine in ultraviolet light at 254 nm. The chromatogram obtained with the test solution
shows several quenching zones, of which two main zones are in the middle third (en-yne-dicycloether). Examine in ultraviolet light at 365 nm. The chromatogram obtained with the test solution
shows an intense blue fluorescent zone (herniarin) in the middle part. Spray the plate with anisaldehyde solution R. Examine in daylight while heating at 100105C for 510 min. The chromatogram obtained with the reference solution shows a reddish-violet to bluish-violet zone (levomenol)
in the lower third, a yellowish-brown to grayish-green zone (bornyl acetate) in the middle third,
and a red to reddish-violet zone (guaiazulene) in the upper third. The chromatogram obtained with
the test solution shows in the lower third yellowish-brown to greenish-yellow and violet zones and
a reddish-violet to bluish-violet zone, corresponding to levomenol in the chromatogram obtained
with the reference solution; a brownish zone (en-yne-dicycloether) similar in position to bornyl
acetate in the chromatogram obtained with the reference solution; a red or reddish-violet zone
(chamazulene) corresponding to guaiazulene in the chromatogram obtained with the reference
solution and immediately above it one or two blue to bluish-violet zones; further weak zones may
be present in the chromatogram obtained with the test solution.

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B. Examine by thin-layer chromatography (2.2.27), using a TLC silica gel plate R.

Test solution: Use the extract.
Reference solution: Dissolve 1.0 mg of chlorogenic acid R, 2.5 mg of hyperoside R, and
2.5 mg of rutin R in 10 ml of methanol R.
Apply to the plate as bands 10 l of each solution. Develop over a path of 15 cm using a
mixture of 7.5 volumes of anhydrous formic acid R, 7.5 volumes of glacial acetic acid R, 18
volumes of water R, and 67 volumes of ethyl acetate R. Dry the plate at 100105C and spray the
warm plate with a 10-g/l solution of diphenylboric acid aminoethyl ester R in methanol R. Subsequently spray the plate with a 50-g/l solution of macrogol 400 R in methanol R. Allow the plate
to dry in air for about 30 min and examine in ultraviolet light at 365 nm. The chromatogram
obtained with the reference solution shows in the middle part a light blue fluorescent zone (chlorogenic acid), below it a yellowish-brown fluorescent zone (rutin), and above it a yellowish-brown
fluorescent zone (hyperoside). The chromatogram obtained with the test solution shows a yellowishbrown fluorescent zone corresponding to the zone of rutin in the chromatogram obtained with the
reference solution, a light blue fluorescent zone corresponding to the zone of chlorogenic acid in
the chromatogram obtained with the reference solution, a yellowish-brown fluorescent zone similar
in position to the zone of hyperoside in the chromatogram obtained with the reference solution; it
also shows above the yellowish-brown fluorescent zone a green fluorescent zone, then several bluish
or greenish fluorescent zones and near the solvent front a yellowish fluorescent zone.
2.4.3.5 Tests
Ethanol (2.9.10): 3853% V/V; dry residue (2.8.16): minimum 12.0%
2.4.3.6 Assay
Place 20.0 g in a 1000-ml round-bottomed flask, add 300 ml of water R, and distill until 200 ml
has been collected in a flask. Transfer the distillate into a separating funnel. Dissolve 65 g of sodium
chloride R in the distillate and shake with three quantities, each of 30 ml, of pentane R previously
used to rinse the reflux condenser and the flask. Combine the pentane layers, dry over 2 g of
anhydrous sodium sulphate R, and filter into a tared 100-ml round-bottomed flask that has been
dried in a desiccator for 3 h. Rinse the anhydrous sodium sulphate and the filter with two quantities,
each 20 ml, of pentane R. Evaporate the pentane in a water bath at 45C. The residue of pentane
is eliminated in a current of air for 3 min. Dry the flask in a desiccator for 3 h and weigh. The
residual oil is blue (chamazulene).

2.5 ESCOP: MATRICARIAE FLOS MATRICARIA FLOWER

2.5.1 ESCOP* MONOGRAPH MATRICARIAE FLOS MATRICARIA FLOWER ([12];
SEE ALSO CHAPTERS 11 AND 12)
Matricariae flos
Matricaria Flower

2.5.1.1 Definition
Matricaria flower consists of the dried flower heads of Matricaria recutita L. (Chamomilla recutita
[L.] Rauschert). It contains not less than 4 ml/kg of blue essential oil.
*

European Scientific Cooperative on Phytotherapy.

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The material complies with the European Pharmacopoeia [12].

Fresh material may also be used provided that when dried it complies with the European Pharmacopoeia.
2.5.1.2 Constituents
The main characteristic constituents of matricaria flower are the essential oil and flavone derivatives
[21, 32, 60, 98, 116] such as apigenin-7-glucoside (approximately 0.5%) [32].
The essential oil contains approximately 50% of the sesquiterpenes ()--bisabolol and its oxides
A and B [98], bisabolonoxide, up to 25% of cis- and trans-en-yn-dicycloethers (or spiroethers) [32],
and matricin, which is converted to chamazulene on distillation (up to 15%) [32].
Other constituents of matricaria flower include coumarins (herniarin and umbelliferone) [21,
32, 98, 116], phenolic acids [21, 32, 98], and polysaccharides (up to 10%) [21, 32, 52, 98].
2.5.1.3

Clinical Particulars

2.5.1.3.1 Therapeutic indications

2.5.1.3.2 Internal use
Symptomatic treatment of gastrointestinal complaints such as minor spasms, epigastric distension,
flatulence, and belching [24, 27, 32, 45, 60, 65, 83, 93, 112]
2.5.1.3.3 External use
Minor inflammation and irritations of skin and mucosa, including the oral cavity and the gums
(mouthwashes), the respiratory tract (inhalations), and the anal and genital areas (baths, ointments)
[24, 27, 28, 35, 50, 54, 69, 74, 78, 83, 85, 86, 94, 96, 99, 105, 111, 112]
2.5.1.3.4 Posology and method of administration
2.5.1.3.5 Dosage
2.5.1.3.6 Internal use
Adults: As a tea infusion: 3 g of the drug to 150 ml of hot water, three to four times daily
Fluid extract (ethanol 4560%): Single dose 14 ml [4, 32]
Dry extract: 50300 mg three times daily [64]
Elderly: Dose as for adults
Children: Proportion of adult dose according to age or body weight
2.5.1.3.7 External use
For compresses, rinses, or gargles: 310% m/V infusion or l% V/V fluid extract or 5% V/V tincture
[32, 64]
For baths: 5 g of the drug, or 0.8 g of alcoholic extract, per liter of water [32]
For solid and semisolid preparations: Hydroalcoholic extracts corresponding to 310% m/m of the
drug [60, 116]
For vapor inhalation: 1020 ml of alcoholic extract per liter of hot water [96]
2.5.1.3.8 Method of administration
For oral administration, local application, and inhalation
Duration of administration
No restriction
2.5.1.3.9 Contraindications
Sensitivity to Matricaria or other Compositae

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2.5.1.3.10 Special warnings and special precautions for use

None required
2.5.1.3.11 Interaction with other medicaments and other forms of interaction
None reported
2.5.1.3.12 Pregnancy and lactation
No harmful effects reported
2.5.1.3.13 Effects on ability to drive and use machines
None known
2.5.1.3.14 Undesirable effects
Rare cases of contact allergy have been reported in persons with known allergy to Artemisia species
[98]. Matricaria flower of the bisabolol oxide B-type can contain traces of the contact allergen
anthecotulide [27, 62, 98]. Matricaria recutita L. possesses a much lower allergenic potential than
other chamomile species, and therefore allergic reactions to Matricaria must be considered as
extremely rare. Most of the described allergic reactions to Matricaria were due to contamination
with Anthemis cotula or related Anthemis species, which contain high amounts of anthecotulide.
However, in cases where Matricaria contact allergy has been acquired, cross-reactions to other
sesquiterpene lactone-containing plants are common [62].
2.5.1.3.15 Overdose
No toxic effects reported

2.5.2 PHARMACOLOGICAL PROPERTIES

2.5.2.1 Pharmacodynamic Properties
2.5.2.2 Anti-Inflammatory Effects
2.5.2.1.1 In vitro studies
Ethanolic (48% V/V) and isopropanolic (48% V/V) extracts of matricaria flower inhibited 5lipoxygenase, cyclooxygenase, and the oxidation of arachidonic acid with IC50 values of 0.050.3%,
while a supercritical carbon dioxide extract had an IC50 of 625 g/ml for these activities [22].
Investigation of individual constituents revealed that apigenin inhibited 5- and 12-lipoxygenase
(IC50: 8 and 90 M, respectively); chamazulene and ()--bisabolol inhibited only 5-lipoxygenase
(IC50: 13 and 40 M, respectively); apigenin, cis-en-yn-spiroether and ()--bisabolol inhibited
cyclooxygenase (IC50: 7080 M); only chamazulene had antioxidative activity (IC50: 2 M) [22].
2.5.2.1.2 In vitro studies
The anti-inflammatory effects of orally administered ()--bisabolol have been demonstrated in
carrageenan-induced rat paw edema, adjuvant arthritis of the rat, ultraviolet-induced erythema of
the guinea pig, and yeast-induced fever of the rat [72]. In the carrageenan-induced rat paw edema
test the following ED50 values (mmol/kg) were obtained after oral administration: ()--bisabolol
2.69, chamazulene 4.48, guaiazulene 4.59, matricin 2.69, and salicylamide 1.53 [71].
An extract prepared from infusion of 20 g of matricaria flower in 100 ml of ethanol 42%,
topically applied at a dose of 750 g dry extract per ear, inhibited croton oil-induced edema of
mouse ear by 23.4% compared to controls; benzydamine at 450 g/ear showed comparable inhibition of 26.6% [66]. In the same test system, two polysaccharides from matricaria flower at a dose
of 300 g/ear inhibited edema by 14 and 22%, respectively [53].

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2.5.2.3 Antispasmodic Effects

2.5.2.3.1 In vitro studies
A hydroethanolic extract of matricaria flower showed antispasmodic activity on isolated guinea pig
ileum stimulated by various spasmogens. The ED50 (mg/ml) and the strength of activity relative to
papaverine (= 1.0), respectively, were 1.22 and 0.0011 with barium chloride, 1.15 and 0.0019 with
histamine dihydrochloride, 2.24 and 0.00074 with bradykinin, and 2.54 and ca. 0.00062 with
serotonin. Pure constituents were also investigated: with barium chloride, ()-bisabolol (ED50 =
136 g/ml) showed activity comparable to papaverine, while apigenin (ED50 = 0.8 g/ml) was more
than three times as active [17].
2.5.2.4 Antiulcerogenic Effects
2.5.2.4.1 In vivo studies
The development of ulcers induced in rats by indomethacin stress or ethanol was inhibited by an
orally administered extract of matricaria flower with an ED50 of 1 ml per rat and by ()--bisabolol
with an ED50 of 3.4 mg/kg body weight. These substances also reduced healing times for ulcers
induced in rats by chemical stress (acetic acid) or heat coagulation [103].
2.5.2.5 Wound Healing Effect
2.5.2.5.1 In vivo studies
The wound healing activity of azulene has been demonstrated in studies on the thermally damaged
rat tail [40] and of matricaria flower constituents in accelerated healing of experimental injuries
[115].
2.5.2.6 Sedative Effects
2.5.2.6.1 In vitro studies
Apigenin competitively inhibited the binding of flunitrazepam to the central benzodiazepine receptor (Ki = 4 M) but had no effect on muscarinic receptors, 1-adreno-receptors, or the binding of
muscimol to GABAA receptors [109].
HPLC fractions of a methanolic extract of matricaria flower were able to displace flunitrazepam
from its receptors in rat cerebellar membranes, the ligand RO 5-4864 from peripheral benzodiazepine receptors in rat adrenal gland membranes, and muscimol from GABA receptors in rat
cortical membranes. This last activity is mainly due to GABA present in the fractions [23].
2.5.2.6.2 In vitro studies
A sedative effect of matricaria flower was demonstrated through prolongation of hexobarbital-induced
sleep, reduction of spontaneous mobility, and reduction of explorative activity in mice [43, 44].
Restricted stress-induced increases in plasma ACTH levels in normal and ovariectomized rats
were decreased by administration of diazepam and inhalation of matricaria flower oil vapor. Inhaling
the vapor induced greater decreases in plasma ACTH levels in ovariectomized rats than treatment
with diazepam; this difference was not observed in normal rats. Furthermore, the inhalation of
matricaria flower oil vapor induced a decrease in plasma ACTH level that was blocked by pretreatment with flumazenil, a potent and specific benzodiazepine receptor antagonist [113].
2.5.2.7 Antimicrobial Effects
Matricaria flower essential oil exerted a bactericidal effect against Gram-positive bacteria and a
fungicidal effect against Candida albicans at a concentration of 0.7% V/V [98]. The essential oil
was not active against Gram-negative bacteria, even in concentrations as high as 8% V/V [19].

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An infusion of matricaria flower, a hydroethanolic extract, and pure herniarin showed antimicrobial activity against various bacteria and fungi in the presence of near UV light [37, 82].
2.5.2.8 Clinical Studies
2.5.2.8.1 Anti-inflammatory effects
In a bilateral comparative study, 161 patients with inflammatory dermatoses, who had been treated
initially with 0.1% diflucortolone valerate, were treated during maintenance therapy with a cream
containing matricara flower extract or one of three alternatives: 0.25% hydrocortisone, 0.75%
fluocortin butyl ester, or 5% bufexamac. The therapeutic results with the extract were equivalent
to those of hydrocortisone and superior to those of fluocortin butyl ester and bufexamac [18].
In a comparative study on 20 healthy volunteers with chemically induced toxic dermatitis, the
smoothing effect on the skin of an ointment containing matricara flower extract was significantly
superior (p < 0.01) to that of 0.1% hydrocortisone acetate or the ointment base [87].
In a study on 12 healthy subjects, a cream containing matricaria flower extract (20 mg/g) did
not suppress UV-induced erythema but it reduced visual scores of skin redness in the adhesive tape
stripping test (p = 0.0625) [76]. In an analogous study, the cream produced 69% of the effect of a
hydrocortisone-27-acetate ointment [20].
In a randomized, double-blind study, 25 healthy volunteers with UVB light-induced erythema
were treated with various matricara flower preparations, hydrocortisone cream, or the respective
vehicle. Ranking the preparations according to visual assessment scores and mean values from
chromametry, a cream containing a hydroalcoholic extract of matricaria flower gave the best result
[75].
In an open study on 98 cancer patients, a matricaria flower extract preparation containing 50
mg of -bisabolol and 150300 mg of apigenin-7-glucoside per 100 g, applied three times daily,
reduced oral mucositis caused by localized irradiation or systemic chemotherapy [30].
In a phase III double-blind, placebo-controlled clinical trial involving 164 patients, a mouthwash
containing matricaria flower extract did not decrease 5-fluorouracil-induced stomatitis [49].
2.5.2.8.2 Anti-inflammatory and antispasmodic effects
In an open multicentric study, 104 patients with gastrointestinal complaints such as gastritis,
flatulence, or minor spasms of the stomach were treated orally for 6 weeks with a matricaria flower
extract preparation (standardized to 50 mg -bisabolol and 150300 mg apigenin-7-glucoside per
100 g) at a daily dose of 5 ml. Subjectively evaluated symptoms improved in all patients and
disappeared in 44.2% of patients [98, 100].
2.5.2.8.3 Wound healing effects
In an open study, 147 female patients episiotomized during childbirth were treated for 6 days with
either an ointment containing matricaria flower extract or a 5% dexpanthenol cream. The healing
effect of the two preparations was comparable [73].
In a double-blind study on 14 patients, weeping dermatoses following dermabrasion of tattoos
were treated with a matricaria flower extract preparation (standardized to 50 mg of -bisabolol and
3 mg of chamazulene per l00 g). The decrease in the weeping wound area and the improvement
in drying tendency were statistically significant (p < 0.05) [54].
In a randomized, open, placebo-controlled study, 120 patients with second-degree hemorrhoids
were treated with rubber band ligature alone, rubber band ligature with anal dilator and vaseline,
or rubber band ligature with anal dilator and an ointment containing matricaria flower extract. The
last group showed the best results in amelioration of hemorrhage, itching, burning, and oozing [50].

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2.5.2.9 Pharmacokinetic Properties

After cutaneous administration of [14C]()--bisabolol on mice, 82% of the radioactivity was found
in the urine [59, 66].
Apigenin and luteolin were also readily absorbed by the skin. In vivo skin penetration studies
of hydroethanolic solutions of apigenin and luteolin with nine healthy female volunteers gave a
steady-state flux of 10.31 and 6.11 ng/min.cm2, respectively [84].
After oral administration of apigenin-7-glucoside to rats free apigenin was detected in the urine
[57].
After oral administration of 40 ml of a hydroethanolic matricaria flower extract (containing
225.52 mg% apigenin-7-glucoside, 22.51 mg% apigenin, 15.14 mg% herniarin) to a female volunteer, no flavones could be detected in blood plasma nor in 24-h urine, while herniarin was found
in both (max. plasma concentration: 35 mg/ml and 0.324 mg in 24-h urine) [106].
In germ-free rats no hydrolysis of flavone glycosides could be observed; obviously, intestinal
microflora can affect the cleavage of the glycosidic bonds [56, 57]. Furthermore, orally administered
apigenin was detected in the blood serum of animals [91].
2.5.2.10 Preclinical Safety Data
The acute oral LD50 of matricaria flower essential oil in rats and the acute dermal LD50 in rabbits
exceeded 5 g/kg. No irritant effects of the oil were observed after application to the skin of nude
mice [88].
In a 48-h patch test in volunteers, matricaria oil neither caused skin irritation nor were there
any discernible sensitization reactions or phototoxic effects. Matricaria oil was granted generally
recognized as safe (GRAS) status by FEMA and has been approved by the FDA for use in food
and cosmetics [88].
The acute oral toxicity of ()--bisabolol in mice and rats was very low with an LD50 of about
15 ml/kg. A 6-week subacute toxicity study showed that the lowest toxic oral dose of ()--bisabolol
in rats and dogs was between 1 and 2 ml/kg. Oral doses up to 1 ml/kg of ()--bisabolol produced
no discernible effects on the prenatal development of rats or rabbits. No malformations were found
at any of the tested dose levels [58].
The acute intraperitoneal LD50 of cis- and trans-en yn-dicycloether is 670 mg/kg [17]. In the
Ames test, apigenin and an aqueous matricaria flower extract showed no mutagenic or toxic activity
[26, 95].
2.5.2.10.1 Allergenicity
Based on the fact that German-matricaria flower generally contains no, or only traces of, the
sesquiterpene lactone anthecotulide and that millions of people come into contact with matricaria
flower daily, allergic reactions due to matricaria flower can be considered to be extremely rare [64].
However, cross-reactions with other sesquiterpene lactone-containing plants are common [64]: a
patient allergic to Artemisia vulgaris underwent severe anaphylactic reactions following ingestion
of matricaria flower infusions and after eye washing with similar infusions [97]; 18 of 24 patients
with Compositae allergy were also allergic to an ether extract of matricaria flower [89]; 96 patients
of 4800 showed contact hypersensitivity to an ethanolic matricaria flower extract [39].
In a study on contact allergy performed with 540 type IV allergic patients, some of whom gave
positive reactions to standard phytogenic allergens, an anthecotulide-free matricaria flower extract
gave a positive reaction in none. This demonstrates the importance of using anthecotulide-free
matricaria flower [70, 98].

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2.6 COMMISSION E MONOGRAPH MATRICARIAE FLOS

(CHAMOMILE FLOWERS)
Commission E is an expert committee on herbal remedies of the German Federal Health Agency,
composed of physicians, pharmacists, pharmacologists, toxicologists, and statisticians.

2.6.1 MATRICARIAE FLOS (CHAMOMILE

FLOWERS)

2.6.1.1 Official Name

Matricariae flos, chamomile flowers
2.6.1.2 Description
Chamomile flowers consist of fresh or dried heads of Matricaria recutita L. (syn. Chamomillla
recutita [L.] Rauschert) and preparations of these in effective doses. The flowers contain not less
than 0.4% (v/w) of volatile oil. The main constituents of the oil are ()--bisabolol or bisabolol
oxides A and B.
2.6.1.3 Indications
External use: Skin and mucosal inflammation, bacterial skin conditions including oral cavity
and parodontium
Inflammatory conditions and irritation of respiratory tract (inhalation)
Conditions affecting anal region and genitalia (bath and irrigation)
Internal use: Gastrointestinal spasms and inflammatory diseases of the gastrointestinal tract
2.6.1.4 Contraindications
None reported
2.6.1.5 Side Effects
None reported
2.6.1.6 Dosage
Pour hot water (c. 150 ml) onto 1 heaping tablespoonful of chamomile flowers (= c. 3 g), cover,
and put through a tea strainer after 510 min.
Unless otherwise prescribed, gastrointestinal conditions are treated by taking a cup of the freshly
made tea three or four times daily between meals. For inflammation of oral and pharygeal mucosa,
rinse or gargle several times daily with the freshly made tea.
External use: 310% infusions for compresses and lavage; for baths, 50 g of the drug to 10 l
of water; semisolid formulations equivalent to 310% of the plant drug
2.6.1.7 Method of Application
Liquid and solid formulations are for external and internal use.
2.6.1.8 Medicinal Actions
Inflammatory and antipyretic, musculotropic spasmolytic, vulnerary, deodorant, antibacterial and
bacterial toxin inhibitor, stimulates skin metabolism.
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2.7 WHO*: FLOS CHAMOMILLAE

2.7.1 WHO: MONOGRAPHS

ON

SELECTED MEDICINAL PLANTS [13]

Flos Chamomillae
2.7.1.1 Definition
Flos Chamomillae consists of the dried flowering heads of Chamomilla recutita (L.) Rauschert
(Asteraceae) [2, 3, 8, 9].
2.7.1.2 Synonyms
Matricaria chamomilla L., M. recutita L., M. suaveolens L. [3, 98]
In most formularies and reference books, Matricaria chamomilla L. is regarded as the correct
species name. However, according to the International Rules of Botanical Nomenclature, Chamomilla recutita (L.) Rauschert is the legitimate name for this species [90]. Asteraceae are also known
as Compositae.
2.7.1.3 Selected Vernacular Names
Baboonig, babuna, babunah camornile, babunj, bunga kamil, camamilla, camomile, chamomile,
camomilla, chamomille allemande, campomilla, chamomille commune, camomille sauvage, fleurs
de petite camomille, flos chamomillae, German chamomile, Hungarian chamomile, Kamille,
Kamillen, kamitsure, kamiture, manzanilla, manzanilla chiquita, manzanilla comun, manzanilla
dulce, matricaire, matricaria flowers, pin heads, sweet false chamomille, sweet feverfew, wild
chamomile [1, 3, 48, 80, 114]
2.7.1.4 Description
Herbaceous annual; 1030 cm in height, with erect, branching stems and alternate, tripinnately
divided leaves below and bipinnately divided leaves above, both types having almost filiform lobes;
the capitulum (to 1.5 cm in diameter) comprises 1220 white ligulate florets surrounding a conical
hollow receptacle on which numerous yellow tubular (disk) florets are inserted; the inflorescence
is surrounded by a flattened imbricated involucre; fruit small, smooth, yellowish [3, 29, 114].
2.7.1.5 Plant Material of Interest: Flower Heads
2.7.1.5.1 General appearance
Flos Chamomillae consists of conical flower heads, each bearing a few white ligulate florets and
numerous yellowish orange to pale yellow tubular or disk florets on conical, narrow hollow
receptacles with a short pedunde; disk florets are perfect and without a pappus; ray florets are
pistillate, white, 3-toothed and 4-veined; involucre hemispherical, composed of 2030 imbricate,
oblanceolate, and pubescent scales; peduncles are weak brown to dusky greenish yellow, longitudinally furrowed, more or less twisted, and up to 2.5 cm long; achenes are more or less obovoid
and faintly 3- to 5-ribbed; pappus none, or slightly membranous crown [5, 114].
2.7.1.5.2 Organoleptic properties
Odor is pleasant and aromatic; taste is aromatic and slightly bitter [3, 8, 9].
2.7.1.5.3 Microscopic characteristics
Receptacle and bracteoles have schizogenous secretory ducts; vascular bundles have phloem fibers;
spiral, annular, and reticulate but pitted vessels; lignified cells at the bases of the ovaries are absent;
*

World Health Organization.

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nearly all parts of florets bear composite-type glandular hairs with short, biseriate stalk and enlarged
head, formed of several tiers, each of two cells; ovary with longitudinal bands of small mucilage
cells; stigma with elongated papillae at the apex; pollen grains, spherical or triangular, have
numerous short spines [3].
2.7.1.5.4 Powdered plant material
Powdered Flos Chamomillae is greenish-yellow to yellowish-brown; spiny pollen grains numerous,
1825 m in diameter; fragments of yellow or white corolla, with polygonal, small epidermal cells
having straight or slightly wavy walls, sometimes papillosed, and sometimes bearing glandular
hairs of composite type; fragments of the fibrous layer of anther; fragments from ovary, with
glandular hairs and rows of small mucilage cells; green fragments of parenchyma of involucre;
stigma with papillae; cells of the achenes with sclariform perforations in walls; fragments of
fibrovascular bundles with spiral, annular, and reticulate vessels and sclerenchyma fibers; fragments
of involucral bracts with epidermis having elliptical stomata up to 30 m in length; also vessels
and fibers; occasional fiber from the stems; minute cluster crystals of calcium oxalate, up to 10
m in diameter; fragments of lignified parenchyma of the filaments and occasional fragments of
vessels [3, 29, 114].
2.7.1.6 Geographical Distribution
The plant is indigenous to northern Europe and grows wild in central European countries; it is
especially abundant in eastern Europe and is also found in western Asia, the Mediterranean region
of northern Africa, and the United States. lt is cultivated in many countries [1, 3, 5, 6, 29, 80, 98,
108, 114].
2.7.1.7 General Identity Tests
The drug is identified by its macroscopic and microscopic characteristics, and by thin-layer chromatography [3, 8, 9].
2.7.1.8 Purity Tests
2.7.1.8.1 Microbiology
The test for Salmonella spp. in Flos Chamomillae products should be negative. The maximum
acceptable limits of other microorganisms are as follows [7, 8, 11]: for preparation of decoction:
aerobic bacteria, not more than 107/g; fungi, not more than 105/g; Escherichia coli, not more than
102/g. Preparations for internal use: aerobic bacteria, not more than 105/g or ml; fungi, not more
than 104/g or ml; enterobacteria and certain Gram-negative bacteria, not more than 103/g or ml; E.
coli, 0/g or ml. Preparations for external use: aerobic bacteria, not more than 102/g or ml; fungi,
not more than 102/g or ml; enterobacteria and certain Gram-negative bacteria, not more than 101/g
or ml.
2.7.1.8.2 Foreign organic matter
Not more than 10% stems and not more than 2% foreign organic matter [3]; no flowering heads
of Anthemis cotula L. or A. nobilis L. [114]
2.7.1.8.3 Total ash
Not more than 13% [9]
2.7.1.8.4 Acid-insoluble ash
Not more than 4% [5]
2.7.1.8.5 Moisture
Not more than 12% [6]
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2.7.1.8.6 Pesticide residues

To be established in accordance with national requirements. Normally, the maximum residue limit
of aldrin and dieldrin for Flos Chamomillae is not more than 0.05 mg/kg [8]. For other pesticides,
see WHO guidelines on quality control methods for medicinal plants [11] and guidelines for
predicting dietary intake of pesticide residues [10].
2.7.1.8.7 Heavy metals
Recommended lead and cadmium levels are no more than 10 and 0.3 mg/kg, respectively, in the
final dosage form of the plant material [11].
2.7.1.8.8 Radioactive residues
For analysis of strontium-90, iodine-131, caesium-134, caesium-137, and plutonium-239, see WHO
guidelines on quality control methods for medicinal plants [11].
2.7.1.8.9 Other tests
Chemical, dilute ethanol-soluble extractive, and water-soluble extractive tests are to be established
in accordance with national requirements.
2.7.1.9 Chemical Assays
Contain not less than 0.4% v/w of essential oil [3, 8, 9]. Total volatile oil content is determined
by pharmacopoeial methods [3, 8, 9].
Thin-layer [8, 9] and gas-liquid [33] chromatography is for volatile oil constituents, and highperformance liquid chromatography is for flavonoids [46, 92].
2.7.1.10 Major Chemical Constituents
Flos Chamomillae contains an essential oil (0.41.5%), which has an intense blue color owing to
its chamazulene content (115%). Other major constituents include -bisabolol and related sesquiterpenes (up to 50% of the oil). Apigenin and related flavonoid glycosides constitute up to 8%
(dry weight) of the drug [29, 46].
CH3
H3C

H 3C

OH
H

CH3

CH3
CH3

H 3C

chamazulene

()--bisabolol
OH

HO

OH

apigenin

2.7.1.11

Dosage Forms

Dried flower heads, liquid extract (1:1 in 45% alcohol), tinctures, and other galenicals [5]. Store
in well-closed containers, protected from light [3, 8, 9].

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2.7.1.12 Medicinal Uses

2.7.1.12.1 Uses supported by clinical data
2.7.1.13 Internal Use
Use for symptomatic treatment of digestive ailments such as dyspepsia, epigastric bloating, impaired
digestion, and flatulence [1, 3, 5, 29, 34, 35, 114]. Infusions of camomile flowers have been used
in the treatment of restlessness and in mild cases of insomnia due to nervous disorders [34, 55].
2.7.1.14 External Use
Use for inflammation and irritations of the skin and mucosa (skin cracks, bruises, frostbite, and
insect bites) [29, 67], including irritations and infections of the mouth and gums, and hemorrhoids
[5, 29, 34, 35, 67].
2.7.1.15 Inhalation
Symptomatic relief of irritations of the respiratory tract due to the common cold [112].
2.7.1.15.1 Uses described in pharmacopoeias and in traditional systems of
medicine
Adjuvant in the treatment of minor inflammatory conditions of the gastrointestinal tract [112].
2.7.1.15.2 Uses described in folk medicine, not supported by experimental
or clinical data
As an antibacterial and antiviral agent, an emetic, and an emmenagogue. It is also used to relieve
eye strain, and to treat urinary infections and diarrhea [108].
2.7.1.16 Pharmacology
2.7.1.16.1 Experimental pharmacology
Both camomile extract and ()--bisabolol demonstrated antipeptic activity in vitro [68, 98, 104].
A hydroalcoholic extract of camomile inhibited the growth of Staphylococcus aureus, Streptococcus
mutans, group B Streptococcus, and Streptococcus salivarius, and it had a bactericidal effect in
vitro on Bacillus megatherium and Leptospira icterohaemorrhagiae [38]. In vitro, the volatile oil
of camomile also inhibited Staphylococcus aureus and Bacillus subtilis [19]. In vitro, camomile
extracts inhibited both cyclooxygenase and lipoxygenase [110], and thus the production of prostaglandins and leukotrienes, known inducers of inflammation. Both bisabolol and bisabolol oxide
have been shown to inhibit 5-lipoxygenase, but bisabolol was the more active of the two compounds
[21]. Numerous in vivo studies have demonstrated the anti-inflammatory effects of the drug. The
anti-inflammatory effects of camomile extract, the essential oil, and the isolated constituents have
been evaluated in yeast-induced fever in rats and against ultraviolet radiation-induced erythema in
guinea-pig models [72]. The principal anti-inflammatory and antispasmodic constituents of camomile appear to be the terpene compounds matricin, chamazulene, ()- -bisabololoxides A and B,
and ()- -bisabolol [20, 41, 42, 51, 71, 77, 81, 107]. While matricin and ()- -bisabolol have
been isolated from the plant, chamazulene is actually an artefact formed during the heating of the
flowers when an infusion or the essential oil is prepared [29]. The anti-inflammatory effects of
these compounds in various animal models, such as inhibition of carrageenin-induced rat paw
edema, have been demonstrated [21], although their activity was somewhat less than that of
salicylamide [20]. In the mouse model for croton oil-induced dermatitis, topical application of

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either the total camomile extract, or the flavonoid fraction only, was very effective in reducing
inflammation [41]. Apigenin and luteolin were more active than indometacin and phenylbutazone
[41]. Activity decreased in the following order: apigenin > luteolin > quercetin > myricetin >
apigenin-7-glucoside > rutin [41]. The spasmolytic activity of camomile has been attributed to
apigenin, apigenin-7-O-glucoside [29, 77], and ()--bisabolol, which have activity similar to
papaverine [29, 42].
Intradermal application of liposomal apigenin-7-glucoside inhibited, in a dose-dependent manner, skin inflammations induced in rats by xanthine oxidase and cumene hydroperoxide [51].
Intraperitoneal administration to mice of a lyophilized infusion of camomile decreased basal
motility, exploratory and motor activities, and potentiated hexobarbital-induced sleep [43]. These
results demonstrated that in mice camomile depresses the central nervous system [43].
2.7.1.17 Clinical Pharmacology
A double-blind study of the therapeutic effects of a camomile extract on re-epithelialization and
drying of wound weeping after dermabrasion demonstrated a statistically significant decrease in
the wound size and drying tendency [54].
In clinical trials, topical application of a camomile extract in a cream base was found to be
superior to hydrocortisone 0.25% for reducing skin inflammation [18]. In an international multicenter trial camomile cream was compared with hydrocortisone 0.25%, fluocortin butyl ester 0.75%,
and bufexamac 5% in the treatment of eczema of the extremities [18]. The camomile cream was
shown to be as effective as hydrocortisone and superior to the other two treatments, but no statistical
analysis was performed. Camomile preparations have also been found to be beneficial in the
treatment of radiation mucositis owing to head and neck radiation and systemic chemotherapy [31].
2.7.1.18 Contraindications
Camomile is contraindicated in patients with a known sensitivity or allergy to plants of the
Asteraceae (Compositae) such as ragweed, asters, and chrysanthemums [34].
2.7.1.19 Warnings
No information available.
2.7.1.20 Precautions
2.7.1.20.1 Carcinogenesis, mutagenesis, impairment of fertility
No mutagenic effects were found in Salmonella typhimurium strains TA 97a, TA 98, TA 100, and
TA 104, with or without metabolic activation [95].
2.7.1.20.2 Pregnancy: teratogenic effects
No adverse effects reported in vivo [79].
2.7.1.20.3 Other precautions
No information available concerning general precautions, drug interactions, drug and laboratory
test interactions, nonteratogenic effects on pregnancy, nursing mothers, or pediatric use.
2.7.1.21 Adverse Reactions
The presence of lactones in Flos Chamomillae-based preparations may cause allergic reactions in
sensitive individuals, and there have been reports of contact dermatitis due to camomile preparations
[47, 89, 102]. It should be noted that very few cases of allergy were specifically attributed to

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German camomile [63]. A few cases of anaphylactic reactions to the ingestion of Flos Chamomillae
have also been reported [25, 36, 101].
2.7.1.22 Posology
2.7.1.22.1 Internal use
Adult dose of flower head: average daily dose 28 g, three times a day [1, 5, 114]; of fluid extract
1:1 in 45% ethanol: dose 14 ml, three times a day [5, 48]. Childs dose of flower head: 2 g, three
times daily; of fluid extract (ethanol 4560%): single dose 0.62 ml [5]. Should not be used by
children under 3 years old.
2.7.1.22.2 External use
For compresses, rinses, or gargles: 310% (30100 g/1) infusion or 1% fluid extract or 5%
tincture [5]. For baths: 5 g/l of water or 0.8 g/l of alcoholic extract. For semisolid preparations:
hydroalcoholic extracts corresponding to 310% (30100 g/kg) of the drug. For vapor inhalation:
6 g of the drug or 0.8 g of alcoholic extract per liter of hot water [5].

2.8 LEGAL CLASSIFICATION OF THE USE OF GERMAN CHAMOMILE

IN GERMANY AND IN THE EUROPEAN COMMUNITY
Chamomile flowers and chamomile herb with flowers can be distributed both as a foodstuff as well
as a drug with different fields of application.

2.8.1 FOODSTUFF
There are two substantial differences between chamomile tea as a foodstuff and as medicinal
chamomile:
1. Chamomile teas of the food category are not allowed to carry any indications but they
can only be sold as so-called domestic teas.
2. The quality of chamomile tea as a foodstuff does not have to correspond to the regulations
of the national pharmacopoeias, especially the European one; a minimum content of
essential oil is, for instance, not required and it is also permitted to use chamomile herb
with a certain percentage of chamomile flowers (510% only). About 23 weeks after
the last harvest of chamomile flowers chamomile herb is, as a rule, obtained from those
aerial parts of the plants still carrying flowers of the afterbloom, and mainly after crushing
it is packed into teabags. In the Federal Republic of Germany the main quality points
are laid down in 8 of the Food Regulations (prohibitions for health protection) and in
10 of the Food Regulations (authorization for hygienic regulations).

2.8.2 DRUG
1. Chamomile flowers as a drug have to correspond to the different pharmacopoeias (see
Table 1.1) and normally they must have a minimum essential oil content.
2. Depending on the indications chamomile flowers for medicinal purposes as such can
be traded on their own or as preparations obtained thereof either as freely saleable drugs
(i.e., outside the pharmacy) or as drugs being subject to sale by pharmacists only.
Chamomile flowers according to 44.2 of AMG 76 (Second Drug Law of the Federal Republic
of Germany) may with the exception of certain limitations by the so-called list of diseases
also be prescribed outside the pharmacy to cure and alleviate diseases. A limitation by the list of
diseases would, for example, be an application in case of hemorrhoids or phlebitis.
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The AMG 76 of the FRG provides another possibility of free sale; viz., as a so-called traditionally applied drug according to 109 a. In this case the range of application comprises: For
[health] improvement with gastric complaints and assistance for the function of the stomach. The
ranges of application according to the monography of Commission E are not allowed to be used
with drugs of 109 a, because these drugs need only a minimum of about 10% of the Commission
E dosage.
Chamomile preparations (e.g., tinctures, fluid extracts, dry extracts, etc.) being subject to sale
by pharmacists only may carry all indications of the monography of Commission E; they are
available by prescription and as a rule until April 2004 they were also reimbursed by the health
insurance companies. Chamomile flower extracts, especially the pure essential chamomile oil, are
parts of medical prescriptions, particularly of preparations used in dermatology.

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86. Nasemann, T. (1975) in L. Demling, T. Nasemann, W. Rsch (Eds.) Erfahrungstherapie spte

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87. Nissen, H.P., Biltz, H., Kreysel, H.W. (1988) Z. Hautkr., 63, 184190.
88. Opdyke, D.L.J. (1974) Fd. Cosmet. Toxicol., 12, 851.
89. Paulsen, E., Andersen, K.E., Hausen, B.M. (1993) Compositae dermatitis in a Danish dermatology
department in one year. Contact Dermatitis, 29, 610.
90. Rauschert, S. (1990) Nomenklatorische Probleme in der Gattung Matricaria L., Folia geobotanica
phytotaxonomica, 9, 249260.
91. Redaelli, C., Formentini, L., Santaniello, E. (1980) HPLC-determination of apigenin in natural
samples, chamomile extracts and blood serum. Poster Int. Res. Congress on Natural Products and
Medicinal Agents, Strasbourg, France.
92. Redaelli, C., Formentini, L., Santaniello, E. (1981) Reversed-phase high-performance liquid chromatography analysis of apigenin and its glucosides in flowers of Matricaria chamomilla and chamomille
extracts. Planta Med., 42, 288292.
93. Reicher, K. (1925) Mnch. Med. Wschr., 7, 261262.
94. Riepelmeier, F. (1933) Monatsschr. Ohrenheilkunde Laryngo-Rhinol., 67, 483487.
95. Rivera, I.G., Martins, M.T., Sanchez, P.S., Sato, M.I.Z., Coelho, M.C.L., Akisue, M., Akisue, G.
(1994) Genotoxicity assessment through the Ames test of medicinal plants commonly used in Brazil.
Environ. Toxicol. Water Quality, 9, 8793.
96. Saller, R., Beschorner, M., Hellenbrecht, D., Bhring, M. (1990) Eur. J. Pharmacol., 183, 728729.
97. Snchez Palacios, A. (1992) Rev. Esp. Alergol. Immunol. Clin., 7, 3739.
98. Schilcher, H. (1987) Die Kamille Handbuch fr rzte, Apotheker und andere Naturwissenschaftler,
Stuttgart, Germany: Wissenschaftliche Verlagsgesellschaft, 152 pp.
99. Schmid, F. (1975) in L. Demling, T. Nasemann, W. Rsch (Eds.) Erfahrungstherapie spte
Rechtfertigung, Karlsruhe, Germany: G. Braun, 4346.
100. Stiegelmeyer, H. (1978) Kassenarzt, 18, 3605366.
101. Subiza, J. et al. (1989) Anaphylactic reaction after the ingestion of chamomile tea: a study of crossreactivity with other composite pollens. J. Allergy and Clin. Immunol., 84, 353358.
102. Subiza, J. et al. (1990) Allergic conjunctivitis to chamomile tea. Ann. Allergy, 65, 127132.
103. Szelenyi, I., Isaac, 0., Thiemer, K. (1979) Planta Med., 35, 218227.
104. Thiemer, V.K., Stadler, R., Isaac, 0. (1972) Biochemische Untersuchungen von Kamilleninhaltsstoffen.
Arzneimittel-Forschung/Drug Res., 22, 10861087.
105. Tissot, H.C. (1929) Schweiz. Med. Wschr., 39, 992993.
106. Tschiersch, K., Hlzl, J. (1993) Pharmazie, 48, 554555.
107. Tubaro, A., Zilli, C., Redaelli, C., Della Loggia, R. (1984) Evaluation of anti-inflammatory activity
of chamomile extract after topical application. Planta Med., 51, 359.
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109. Viola, H., Wasowski, C., Levi de Stein, M., Wolfman, C., Silveira, R., Dajas, F. (1995) Planta Med.,
61, 213216.
110. Wagner, H., Wierer, M., Bauer, R. (1986) In vitro inhibition of prostaglandin biosynthesis by essential
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112. Wei, R.F. (1987) Kamille Heilpflanze 1987. Kneipp-Bltter, 1, 48.
113. Yamada, K., Miura, T., Mimaki, Y., Sashida, Y. (1996) Biol. Pharm. Bull., 19, 12441246.
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116. Zwaving, J.H. (1982) Pharm. Weekbl., 117, 157165.

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3 Plant Sources
Rolf Franke
CONTENTS
3.1
3.2

Systematics
Latin Botanical Names, Synonyms
3.2.1 Matricaria recutita L
3.2.2 Chamaemelum fuscatum (Brot.) Vasc
3.2.3 Chamaemelum nobile (L.) All
3.2.4 Anthemis arvensis L
3.2.5 Anthemis cotula L
3.2.6 Anthemis tinctoria L
3.3 Common Names, Synonyms
3.3.1 Matricaria recutita L
3.3.2 Chamaemelum nobile (L.) All
3.3.3 Anthemis arvensis L
3.3.4 Anthemis cotula L
3.3.5 Anthemis tinctoria L
3.3.6 Tripleurospermum inodorum (L.) Schultz-Bip
3.4 Description of the Plant
3.4.1 Botany
3.4.2 Chromosome Numbers
3.5 Drug Names
3.5.1 Matricaria recutita L
3.5.2 Chamaemelum fuscatum (Brot.) Vasc
3.5.3 Chamaemelum nobile (L.) All
3.5.4 Chamomilla suaveolens (Pursh) Rydb
3.5.5 Anthemis arvensis L
3.5.6 Anthemis cotula L
3.5.7 Anthemis tinctoria L
3.6 Parts Used
3.6.1 Chamomile Flowers, Matricariae flos
3.6.2 Chamomile Fines
3.6.3 Chamomile Herb with Flowers
3.6.4 Chamomile Herb
3.6.5 Chamomile for Extraction, Industrial Chamomile
3.6.6 Chamomile Root
3.6.7 Chamomile Oil, Matricaria aetheroleum
3.6.8 Chamomile Fluid Extract
3.6.9 Chamomile Tincture
References

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3.1 SYSTEMATICS
In 1664, Tabernaemontanus [19] distinguished six different varieties of chamomile (contrary to
Dioscorides, who distinguished three):
1. Unsere gemeine Chamillenblum (our common chamomile flower) is identified as
the plant named Anthemis or Leucanthemum by Dioscoride and Galeno. Dann wann
wir die Beschreibung DIOSKORIDIS mit flei bersehen/und das Capitel von dem
wolriechenden Krutlein Anthemidis oder Leucanthemi vorhanden nehmen/die liebliche
Gestalt und Abconterfeyung dieser wolriechenden Chamillenblumen dagegenhalten/darneben auch ihre Krafft und Wirckung beyderseits erwegen/so beyde diesem
Krutlein oder Blumen von DIOSCORIDE und GALENO zugeschrieben/und auch durch
langwrige tgliche Erfahrung gewi erfunden worden/knnen wir mit der Warheit nicht
anders urtheilen/dann da unser wolriechend gemeine Feld- Chamillen/das recht Anthemis und Leucanthemum der Alten seye. (Old High German: If we duly disregard
Dioscorides description/and go through the chapter about the sweet-scented herb Anthemidis or Leucanthemi/comparing it with the lovely appearance of these fragrant chamomile flowers/considering also their power as well as their effect/both ascribed to this
herb by Dioscoride and Galeno/and also found by long daily experience/we can only
say that the sweet-scented ordinary/common field chamomile/is the true Anthemis and
Leucanthemum of the ancients.)
2. Rmisch Chamillen (Roman chamomile). Das andere Geschlecht der Chamillen
Leucanthemi ist den Alten unbekannt gewesen/und nicht von ihnen beschrieben worden:
Das ist erstlich au Hispanien/Engelland und andern frembden Orten zu uns gebracht
worden und ist heutigen Tags in Teutschland sehr gemein . (The other variety of
Chamomile Leucanthemi was unknown to the ancients/and it was not described by them.
It was first brought to us from Spain/England and other foreign places, nowadays it is
very common in Germany )
In this case the modern variety of Chamaemelum nobile (L.) All. is obviously meant.
3. Gefllt Rmisch Chamillen (Filled Roman chamomile). Here the modern variety of
Chamaemelum nobile (L.) All. is meant as well.
4. Gefllt Rmisch Chamillen anderer Gattung (Filled Roman chamomile of another
genus). In this case the determination is not clear. Among others, the designation
indicated by Tabernaemontanus (1664) [19] is Chamaemelum Anglicum flore multiplici
dieweil solche au Engelland erstlich zu uns in Teutschland gebracht worden seynd
( because they were brought from England to Germany for the first time).
5. Geel Chamillen (yellow chamomile), probably meaning Anthemis tinctoria L.
6. Rothe Chamillen (red chamomile). This is probably Adonis aestivalis L. or Adonis
flammea Jacq. being indicated by the following description: Gegen dem Brachmonat
bringt es an den Gipffeln der Stengel und Nebenstlein ber die ma schne/rothe/Mennigfarbe/oder feuerrothe Blmlein/inwendig mit einem schwarzen Btzlin/hat ein jede
Blum sieben Blttlein/die seynd am end ein wenig hintersich zurck gebogen. Nach der
Blth folgewn kleine stachlichte Klblein/darinnen der Saamen verschlossen ist
(towards June most beautiful/miniaceous/or small fire red flowers/are produced at the
end of the stems and their small side branches/inside with a black center/every flower
has seven small leaves/which are somewhat bent down at the end. After flowering small
thorny spadices are following/where the seeds are to be found). The name also points
to this classification: Oculus daemonis. Teutsch/roth Chamillen/und in Thringen/Teufels Aug/von wegen der rothen Fewerfarben Blumen (Oculus daemonis. German/red chamomile/and in Thuringia/devils eye/because of the fire red flowers).

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Although the systematic status is quite clear nowadays, there are a number of inaccuracies
concerning the names. Apart from misdeterminations and confusion, the synonymous use of the
names of Anthemis, Chamomilla, and Matricaria leads to uncertainty with regard to the botanical
identification, particularly in the area of English speech. So, in the BelgV Anthemis nobilis L. is
called Chamomillae flos. Marokkanische Kamille (Moroccan chamomile) often consists of
Ormenis multicaulis Braun-Blanq. et Maire [4].
Moreover, the nomenclatural situation is complicated by the fact that Linneaus made mistakes
in the first edition of his Species Plantarum that he corrected later on. According to this description
Matricaria chamomilla L. 1753 is definitely not the name for True chamomile medically used
but for Scentless chamomile. The name applicable to True chamomile is the one of the species
published at the same time, i.e., Matricaria recutita L. [12,18].
The name of the genus of Matricaria used by Linneaus is derived from matrix (womb). The
popular name of Mutterkraut (Mothers Herb) also points to the application for various female
complaints, being surely derived from this range of applications. As, however, the Parthenion
mentioned by Dioscoride does not stand for True chamomile but for Tanacetum parthenium, the
popular German name of Mutterkraut ( Mothers Herb) also used by Zander [21] should not
be used for chamomile.
The genus of Matricaria in a wider sense is often divided into: Tripleurospermum Schultz-Bip.
among others with Matricaria maritima and Matricaria perforata (syn. M. inodora) and Matricaria
sensu stricto among others with Matricaria recutita L. (syn. Matricaria chamomilla L.) and
Matricaria suaveolens (syn. M. matricarioides).
This division needs a revision. Linneaus does not seem to have separated Matricaria chamomilla
and Matricaria maritima, including M. inodora. In 1974 Rauschert pointed out that Linneaus used
M. chamomilla rather than M. maritima for M. chamomilla in a modern sense [12].
It seems to be quite obvious that Linn used the name of Matricaria recutita for our medically
applied chamomile (Matricariae flos, Ph. Eur. 4.6). Later Linn named this tribe called Matricaria
suaveolens suavius olens.
In his systematic reinvestigation Rauschert [12] also mentions that when dividing the genus
Linn called Matricaria, the separated part with our medically used chamomile should bear the
name of Chamomilla S.F. Gray, and that furthermore the name of Matricaria L. sensu stricto would
be correct for the genus of Tripleurospermum Schultz-Bip. In volume IV (pp. 5860) of Flora
Europea the medically used chamomile was called Chamomilla recutita (L.) Rauschert, whereas
the scentless chamomile was given the names Matricaria maritima L. and Matricaria perforata
Mrat (syn. M. inodora L.).
Considering a new botanical classification there is a mere nomenclatural problem on the one
hand (viz., whether the name of Chamomilla, Matricaria, or Tripleurospermum should be
used), and on the other hand there is a systematic problem (viz., whether the genus fixed by Linn
is to be segregated).
When segregating Linns genus of Matricaria L. into the genera of Chamomilla S.F. Gray
and Matricaria L. sensu stricto another difficulty arises because Matricaria chamomilla was chosen
as a species type of the genus of Matricaria [9]; so according to Rauschert [12] True
chamomile would be added to the genus of Chamomilla. What speaks against it is the fact that
Matricaria chamomilla 1753 does not correspond to the diagnosis of the genus, as the achenes
have a coronule. Thus, the choice of the species type was made by mistake, and Matricaria recutita
has to be regarded as a type of the genus [18]. The differences to be found in botanical literature
still continue today. In connection with the aim of this book the name of Matricaria recutita L.
(syn. M. chamomilla L., Chamomilla recutita L. Rauschert) should, however, be used; this is
particularly recommended as even in the latest literature with exception of Flora Europea
and in all pharmacopoeias at present the name of Matricaria recutita L. is used.
For a considerable length of time it was not quite clear as to whether chemical races exist
within the species of Matricaria recutita L. Personal investigations as well as tests of other teams

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point to the existence of genetically conditioned chemical variations in local populations. Instead
of using the word race, the more neutral term of dem should be applied with Matricaria recutita
L. [8,14]; even more precise are the terms chemodem, ecodem, and topodem. Considering
the fact that chamomile is a widely common plant the existence of chemodems, topodems, and
ecodems is not only very likely but the research results of several working groups confirm that
such dems exist. The following chamomile varieties still traded a few years ago could be called
topodems, because their names give knowledge of the regions from which they originate: Holsteiner
Marschkamille (Holstein Marsh chamomile), Ostfriesische Kamille (East Frisian chamomile),
Frnkische Kamille (Franconian chamomile), Niederbayrische Kamille (Lower Bavarian chamomile), Quedlinburger grobltige Kamille (Quedlinburg large-flowered chamomile), Erfurter kleinbltige Kamille (Erfurt small-flowered chamomile), Bhmische Kamille (Bohemian chamomile).
However, a number of goods still handled today, coming from wild collections and not from selective
cultivation of breeding lines, may also be put into this category (for example, Egyptian chamomile,
Hungarian Puszta chamomile, Argentinian chamomile, Spanish chamomile).
Moreover, there are chamomile chemocultivars (cultivar = cv), thus chemical races produced
by breeding and maintained constant by maintenance breeding. Depending on the spectrum of
active principles, the culture varieties could, for example, be specified as Matricaria recutita L. cv.
rich in bisabolol or as Matricaria recutita L. cv. rich in bisabololoxide (see Section 5.3).
Nonradial chamomile, Scentless chamomile, Roman chamomile, as well as the species of
Anthemis have to be distinguished from True chamomile.
Different species can appear as confusion or falsification of the collected drug. Here are some
distinctive features of some of these other Anthemis and Matricaria species and how they can be
used [6]:
1. Without scale-like palets between the flowers of the capitulum
Capitulum bottom cone-shaped long, hollow
Plant with white ligulate flowers, smells pleasantly of chamomile (typical chamomile smell), annual True chamomile (Matricaria recutita L.)
Plant without white ligulate flowers, smells like chamomile (typical chamomile
scent), annual Rayless chamomile (Matricaria matricarioides [Less.] Porter,
syn. Matricaria discoidea DC.)
Capitulum bottom-arched or only short cone-shaped, marrowy. Plant without typical
chamomile scent, but smells not unpleasant. Flower capitulum big (diameter approx.
3 cm), annual, biennial (or perennial) Odorless, false chamomile (Matricaria
maritima L.)
2. With, at least in the middle part of the flower capitulum, small setiform paleae between
the flowers of the flower heads
Palets longish acuminate or with pointed stings
Plant with revolting smell, annual Stinking chamomile (Anthemis cotula L.)
Plant without revolting smell, mostly annual Field chamomile (Anthemis arvensis L.)
Palets blunt, with dry tips. Plant smells pleasantly, perennial, many-headed rootstock Roman
chamomile (Chamaemelum nobile [L.] All. syn. Anthemis nobilis L.)

3.2 LATIN BOTANICAL NAMES, SYNONYMS

In the various florae and books for the identification of plants the names used differ considerably.
The synonyms already mentioned by Tabernaemontanus (1664) [19] are most interesting where
they are specified in many different languages. This currently shows an amazing constancy as far
as the use of the popular names in central Europe, but also in the Mediterranean area, in the Balkans,
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and in Arabia. Considerable revisions of the Latin nomenclature have been made in recent years.
Nevertheless, it is difficult to make clear statements in this respect. The most detailed explanation
for the correct nomenclature existing at present was surely indicated by Schultze-Motel in 1986
[18]. The name of the genus of Matricaria L. dates back to the year 1753. Later Chamomilla S.F.
Gray (1841), Lepidotheca Nutt. (1841), Tripleurospermum Schultz-Bip. (1844), Sphaeroclinium
Schultz-Bip. (1844), Gastrosulum Schultz-Bip. (1844), Gastrostylum Schultz-Bip. (1844), Rhytidospermum Schultz-Bip. (1844), Courrantia Schultz-Bip. (1844), Dibothrospermum Knaf (1846),
Chamaemelum Vis. (1847) non Adans. (1753), Trallesia Zumag. (1949), Akylopsis Lehm. (1850),
Otospermum Willk. (1864), Heteromera Pomel (1874) were names used more recently. Matricaria
recutita L. is to be considered as a type.
In the older statement by Bolkhovskikh et al. [3] the following species are united in the genus
of Matricaria L.: M. ambigua (Lebed.) Kryl., M. chamomilla L., M. discoidea DC., M. grandiflora,
M. inodora L., M. maritima L., M. matricarioides (Less.) Porter, M. pubescens (Desf.) SchultzBip., M. suaveolens Buch., M. tchichatchewii Boiss.
The genus of Anthemis L. includes the species of A. alpina L., A. altissima L., A. arvensis L.,
A. austriaca Jacq., A. carpatica Waldst. et Kit., A. cotula L., A. cupaniana, A. iberica Bieb., A.
jailensis Zefir., A. kelwayi, A. maritima L., A. monantha Willd., A. montana Willd., A. nobilis (L.)
J. Gray, A. orientalis (L.) Deg., A. peregrina L., A. rigescens Willd., A. rudolphiana Adams, A.
ruthenica Bieb., A. santi-johannis, A. sosnovskyana Fed., A. tigreensis J. Gray ex A. Rich., A.
tinctoria L., A. trotzkiana Claus ex Bunge, A. woronowii Sosn., A. zyghia Woronow.
The genus of Chamomilla is not indicated.
In the meantime nomenclatural knowledge could be actualized. Today the genus of Anthemis
L. comprises about 210 species, thus representing one of the greatest genera of the chamomile
relatives [3]. In Europe these include (among others):

Anthemis altissima L. emend. Spreng. (syn. Anthemis cota L. emend. Vis.), being common in Europe, the Mediterranean area, Portugal, the Near East, and Central Asia
Anthemis arvensis L., Field chamomile, spread over Europe, North Africa, Asia Minor,
established in the eastern part of North America
Anthemis austriaca Jacq., Austrian Field chamomile, being common in the eastern part
of central Europe, southeast Europe, Anatolia, Armenia, the Caucasus Mountains, North
Africa
Anthemis carpatica Waldst. et Kit. ex Willd., spread over northern Spain, the Pyrenees,
the Austrian Alps up to the eastern Carpathian Mountains and northern Greece
Anthemis cinerea Panc., being common in the Balkans
Anthemis cotula L., Stinking chamomile, being common in Europe, the Near East, North
Africa, Canary Islands, established in North and South America, Australia
Anthemis cretica L., spread over south Europe and the western part of the Czech Republic
Anthemis haussknechtii Boiss. et Reut., being common in Syria, Iraq, Iran, Southern
Anatolia
Anthemis marschalliana Willd. (syn. A. biebersteiniana (Adams) K. Koch, Chrysanthemum biebersteinianum Adams), spread over the Caucasus Mountains and in the mountainous regions of Asia Minor
Anthemis plutonia Meikle, being common in Cyprus as an endemic variety
Anthemis ruthenica M. Bieb., Ruthenic Field chamomile, spread over Germany and
Austria
Anthemis sancti-johannis Turrill, being common in the southwestern part of Bulgaria
Anthemis tinctoria L., Yellow chamomile, spread nearly all over Europe, western Asia,
established in North America
Anthemis tricolor Boiss., being common in Cyprus as an endemic variety
Anthemis triumfettii (L.) DC., spread over Switzerland and southern Europe.

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Zander [21] puts both True chamomile as Chamomilla recutita (L.) Rauschert (syn. Matricaria
recutita L., M. chamomilla L. pro parte) and nonradial chamomile as Chamomilla suaveolens
(Pursh) Rydb. (syn. Matricaria matricarioides (Less.) Porter pro parte, M. discoidea DC., M.
suaveolens (Pursh) Buchenau non L., Santolina suaveolens Pursh) in a genus of its own: Chamomilla S.F. Gray. This classification was also used by Schubert and Vent [17]. But in Zander [22]
this nomenclature is revised back to Matricaria recutita L.
According to Zander [21, 22] the genus of Matricaria L. (syn. Tripleurospermum Schultz-Bip.)
comprises the following species:

M. capensis hort. non L. now Tanacetum parthenium (L.) Sch. Bip.

M. caucasica (Willd.) Poir. now Tripleurospermum caucasicum (Willd.) Hayek, spread
over Bulgaria, Albania, the Caucasus Mountains, Asia Minor
M. inodorum L. now Tripleurospermum perforatum (Mrat) Lanz, spread over Asia
Minor, Caucasus, Siberia, Amur, Sachalin, Kamchatka
M. maritima L. now Tripleurospermum maritimum (L.) W.D.J. Koch, spread over
Iberic peninsula, France, central Europe, Poland
M. oreades Boiss. (syn. Chrysanthemum oreades (Boiss.) Wehrh.) now Tripleurospermum oreades (Boiss.) Rech., being common in Asia Minor and Syria
M. parthenioides (Desf.) hort. now Tanacetum parthenium (L.) Sch. Bip.
M. perforata Mrat (syn. M inodora L., M. maritima L. ssp. inodora (K. Koch) Soo,
Chrysanthemum maritimum (L.) Pers. ssp. inodorum (K. Koch) Vaar., Chamaemelum
inodorum (L.) Vis.) now Tripleurospermum inodorum (L.) Schultz-Bip., spread nearly
all over Europe, the Caucasus Mountains, western Asia. With Schubert and Vent [17]
this species is among others classified as Scentless chamomile, carrying the name
of M. maritima L. (syn. T. maritimum (L.) Koch, M. inodora L.) and subdivided into the
ssp. maritima and ssp. inodora (L.) Dostal. (see also Reference 2)
M. recutita L. (see Section 3.2.1)
M. tchihatchewii (Boiss.) Voss (syn. Chamaemelum tchihatchewii Boiss.) now Tripleurospermum tchihatchewii (Boiss.) Bornm., being common along the coasts of Asia
Minor

In the genus of Chamaemelum Mill. Zander [21] is only specifying the species of Ch. nobile
(L.) All. (syn. Anthemis nobilis L. is an older name often still used in drug trade, Ormenis nobilis
(L.) J. Gray ex Coss. et Germ.) spread over western Europe (up to Northern Ireland), established
in south Europe and in the southern part of central Europe as well as in North Africa. A more
detailed subdivision into the following species is made by Hnsel et al. [5]: Chamaemelum eriolepis
(Cosson ex Maire) Benedi, Ch. flahaultii (Emberger) Benedi, Ch. fuscatum (Brot.) Vasc. (syn.
Anthemis fuscata Brot., A. praecox Link in Schrader., Chamomilla fuscata (Brot.) Gren et Godr.,
Maruta fuscata Brot., Ormensis fuscata (Brot.) Schultz-Bip., Ormensis praecox (Link in Schrader)
Briq. et Cavill., Perideraea fuscata (Brot.) Webb.), Ch. mixtum (L.) All. with var. glabrescens
(Maire) Benedi, var. aureum Durieu in Bory et Durieu) Benedi, Ch. nobile (L.) All.

3.2.1 MATRICARIA

RECUTITA

L.

The best-known botanical name for True chamomile, also used in the pharmacopoeias, is Matricaria recutita (syn. Matricaria chamomilla L., Chamomilla recutita (L.) Rauschert). The Latin
name of recutitus refers to the petals, meaning truncated, trimmed. The name of chamomilla
may well originate from Dioscoride and Plinius the Elder who due to the pomaceous odor
called the plant chamaimelon. Chamaimelon means, more or less, low growing apple tree
(Greek: chamai = low, melon = apple). Plinius the Elder wrote about Chamaimelon quoniam
odorem mali habet. Tabernaemontanus [19] also noted this applelike odor: Die Chamillen-

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blum/die bey uns in Teutschland vor sich selbst in Fruchtfeldern huffig wchst/ist die rechte
Chamillen oder Chamaemelum der Alten/die den Namen daher empfangen hat/dieweil sie
reucht/wie ein lieblicher wolriechender Apffel. (The chamomile flower frequently growing on
fruit fields with us in Germany/is the true chamomile or chamaemelum of the ancients/which
has got its name because it smells like a delicious apple.)
With Bolkhovskikh et al. [3] chamomile is classified as Matricaria chamomilla L. Zander [21],
Schubert and Vent [17], and others call the True chamomile Chamomilla recutita (L.) Rauschert;
Aichele and Schwegler [1] call it Matricaria chamomilla L.; with Hnsel et al. [5] the name of
Chamomilla recutita (L.) Rauschert is preferred (syn. Chamomilla meridionalis C. Koch, Ch.
vulgaris S.F. Gray, Matricaria chamomilla L. pro parte, M. coronata Gay ex Koch, M. pusilla
Willd., M. recutita L., M. suaveolens L.).
In Schultze-Motel [18] a detailed compilation of the available nomenclatural literature is to be
found. Here the name of Matricaria recutita L. is given primacy (1753). The following names may
be regarded as derived: Matricaria suaveolens L. (1755), M. chamomilla L. (1755 and 1763), M.
chamaemilla Hill (1761), Leucanthemum chamaemelum Lam. (1779), Matricaria patens Gilib.
(1782), Chamomilla patens Gilib. (1782), Matricaria tenuifolia Salisb. (1796), Chrysanthemum
chamomilla Bernh. (1800), Ch. suaveolens (L.) Cav. (1803), non (Pursh) Aschers. (1864), Matricaria pusilla Willd. (1807), Chamomilla vulgaris S.F. Gray (1821), Matricaria courrantiana DC.
(1837), M. pyrethroides DC. (1837), Chamomilla officinalis C. Koch (1843), Ch. meridionalis C.
Koch (1843), Matricaria coronata Gay ex Koch (1843), M. kochianum Schultz-Bip. (1844), Courrantia chamomilloides Schultz-Bip. (1844), Chamomilla courrantiana C. Koch (1851), Matricaria
bayeri Kanitz (1862), M. obliqua Dulac (1867), Chamomilla recutita (L.) Rauschert (1974).
The habit of Matricaria recutita L. is relatively stable. In Hegi [7], four differing forms are
distinguished:
1. f. nana Custer (= monocephala Junge = f. gracilis Chenvard): The plant is a dwarf plant
and remains small (10 to 15 cm), not ramified, small leafed. Stem approx. 1 mm thick,
capitulums small (8 to 15 mm in diameter).
2. f. paleata Abromeit: Capitulums with fine palets.
3. f. eradiata Rupr. (f. subdiscoidea A. Peter): The ligulate flowers are missing completely
or are very short.
4. f. coronata (J. Gay) Coss. et Germ.: Widespread above all in southern Europe, with
clearly developed pappus.

3.2.2 CHAMAEMELUM

FUSCATUM

(BROT.) VASC.

Syn. Anthemis fuscata Brot., A. praecox Link in Schrader., Chamomilla fuscata (Brot.) Gren et
Godr., Maruta fuscata Brot., Ormensis fuscata (Brot.) Schultz-Bip., Ormensis praecox (Link in
Schrader) Briq. et Cavill., Perideraea fuscata (Brot.) Webb.

3.2.3 CHAMAEMELUM

NOBILE

(L.) ALL.

Syn. Anthemis nobilis L., Ormenis nobilis (L.) J. Gray ex Coss. et Germ., Anthemis chamomillaromana Crantz, Anthemis nobilis L., A. odorata Lam., Chamaemelum odoratum Dod., Chamomilla
nobilis God., Leucanthemum odoratum Eid Ap., Lyonnetia abrotanifolia Webb., Matricaria nobilis
Baill., Ormensis aurea R. Loewe, Ormensis nobilis J. Gay.

3.2.4 ANTHEMIS

ARVENSIS

L.

Syn. Anthemis agrestis Wallr., Chamaemelum arvensis (L.) All.

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3.2.5 ANTHEMIS

COTULA

L.

Syn. Anthemis foetida Lam., A. psorosperma Ten, A. ramosa Link, A. heterophylla Wallr., A.
abyssinica J. Gay, Chamaemelum cotula (L.) All., Ch. foetidum Baumg., Maruta cotula (L.) DC.,
M. foetida (Lam.) S.F. Gray, M. vulgaris Bluff et Fingerh.

3.2.6 ANTHEMIS

TINCTORIA

L.

Syn. Chamaemelum tinctorium (L.) All., Cota tinctoria J. Gay ex Guss.

3.3 COMMON NAMES, SYNONYMS

3.3.1 MATRICARIA

RECUTITA

L.

German: Echte Kamille, Deutsche Kamille, Feldkamille, Gemeine Kamille, Hermel,

Kamille, Kleine Kamille, Mgdeblume, Apfelkraut, Kummerblume, Mutterkraut, Kindbettblume, Hermnnle, Helmchen, Lungenblume, Ramerian, Remey, Stomeienblume
English: True chamomile, common camomile, German chamomile, Hungarian chamomile,
small camomile, horse gowan, wild camomile, camomile flowers, pin heads
French: Camomille, matricaire, camomille vraie, camomille allemande, camomilla commune, camomille ordinaire, camomille vulgaire, chamomille dAllemagne, matricaire
camomille
Dutch: Kamille
Italian: Camomilla, camomilla comune, capomilla
Portuguese: Camomila, camomilla des Alemes, camomilla vulgar, mananilha, margaa
das boticas
Spanish: Manzanilla, camomilla, manzanilla alemana, manzanilla comn, manzanilla de
Aragn, manzanilla dulce, manzanilla ordinaria, camamilda
Danish: Kamille
Swedish: Kamomill
Czech: Hermnek pravy, kamilka, rumancek kamilkovy
Slovakian: Rumancek pravy
Hungarian: Orvosi szkf, kamilla, szkf
Polish: Rumaniek pospolity
Russian: Romaska aptecnaja, romaska obodrannaja
Turkish: Papatya
Indian: Babunphul
Persian: Babunah

3.3.2 CHAMAEMELUM

NOBILE

(L.) ALL.

German:Rmische Kamille, Rmische Hundskamille, Edel-Kamille, Gartenkamille, Doppelte Kamille, Groe Kamille, Dickkpfe, Welsche Kamille, Dicke Gramille, Gaadekamille, Krampf-Kamille, Gartenchamille, Gemeine Chamille, Hemdknpkes, Hemmerknebche, Kragenknebcher, Hrmelchen, Johannisgnebel, Kathreinenblume,
Kragengebcher, Khmelle, Mandl, Mnetli, Rmischer Romey, Tfelschrut, Wlschi
pfelblmli, Zandelkraut
English: Roman chamomile, Noble chamomile, small camomile, ground apple, low camomile, whig plant, English camomile, Scotch camomile, May-then, sweet chamomile,
double chamomile, white or low camomile
French: Camomille romaine
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Dutch: Roomse kamille

Italian: Camomilla romana, camomilla odorosa, camomilla de Boemia, camomilla di Germania, camomilla inglese, camomilla nobile, camomilla ortense
Portuguese: Camomilla verdadeira, camomilla nobre, camomilla odorante, macela dourada,
macela galega, camomila romana
Spanish: Manzanilla romana, manzanilla noble, manzanilla inglesa, manzanilla de Paris,
manzanilla officinal
Catalonian: Camamilla romana
Basque: Bitxilora, lilibitxi, enbasabedarr, larranbillo
Danish: Romerske cameelblomster, Rmerske Kamille
Czech: Rmen slicny , Hermnek rmsky, paruman spanily
Slovakian: Ruman rmsky (spanily ), paruman spanily
Hungarian: Rmikamilla, rmai kamilla, nemes pipitr, rmai szkf
Polish: Koszyszek rumianku rzymskiego, Rumianek rzymski, Rumian szlachetny
Russian: Rimskaja romas ka
Swedish: ngsrllika
Turkish: Rumi papatya, Alman papatyasi
Arab: Babunj, Babunaj, Shajrat-ol-kafur
Indian: Babunike-phul, Shimedapu, Shimaichamantipu
Persian: Babunah

3.3.3 ANTHEMIS

ARVENSIS

L.

German: Acker-Hundskamille, Feld-Hundskamille, Ackerkamille, Afterkamille, Chrotechrut, Dreckkamille, Gensstck, Hundsblume, Hundsdille, Korngckala, Kretengosch,
Krtendill, Pferdskamille, Renblaume, Schafkamille, Stinkpotsch, Taube Kamille, Wilde
Kamille
English: Wild chamomile, corn chamomile, field camomile
French: Oeil-de-vache, camomille sauvage, fausse camomille
Dutch: Valse kamille
Italian: Camomilla senza odore, camomilla bastarda
Spanish: Manzanilla bastarda, manzanilla borde, manzanilla de los campos, manzanilla
silvestre
Swedish: kerkulla

3.3.4 ANTHEMIS

COTULA

L.

German: Hundskamille, Stinkende Hundskamille, Kuhdille

English: Dog fennel, wild camomile, stinking chamomile, dog chamomile, stinking mayweed
French: Camomille des chiens
Italian: Camomilla mezzana
Portuguese: Macela fetida
Spanish: Magarza, manzanilla hedionda, manzanilla malagata

3.3.5 ANTHEMIS

TINCTORIA

L.

German: Frber-Hundskamille, Frberkamille, Rindsauge, Ochsenauge

English: Dyers camomile, golden marguerite, ox-eye chamomile, yellow chamomile
French: Camomille de teintures
Russian: Pupavka krasilnaja

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3.3.6 TRIPLEUROSPERMUM

INODORUM

(L.) SCHULTZ- BIP.

German: Bitterstock, Brautschleier, Falsche Kamille, Feinblttrichte Johannisblume, Feinblttrige Wucherblume, Geruchlose Bertramwurz, Geruchlose Wucherblume, Hemdeknppchen,
Hummel, Hundskamille, Krtenstock, Pferdekamille, Wilde Kamille
English: Bachelors button, barnyard daisy, corn feverfew, corn mayweed, false chamomile,
false mayweed, scentless camomile, wild chamomile
French: Matricaire inodore
Danish: Falsk kamelblomst, hundeblomst
Swedish: Baldersbr, knoppsrrt
Hungarian: Pupa
Romanian: Musetel-prost, romanita-neadevarata

3.4 DESCRIPTION OF THE PLANT

3.4.1 BOTANY
True chamomile is an annual plant, grows 10 to 80 cm high, prefers sandy to loamy, mostly sour
fields and fresh ruderal places. Salty soils like in the Puszta or in Argentina are duly tolerated. The
plant has thin spindle-shaped roots that only penetrate flatly into the soil. The stem is in an upright
position, mostly heavily ramified, bare, round, and filled with marrow. The leaves are alternate,
double to triple pinnatipartite, with narrow-linear prickly pointed sections being hardly 0.5 mm
wide. The flower heads are placed separately, they have a diameter of 10 to 30 mm, and they are
pedunculate and heterogamous. The involucre is semispherical. The 26 to 48 involucral leaves are
arranged in one to three rows, they are ovoid to lanceolate upside down, green with a narrow
brownish membranous rim. The golden yellow tubular florets with five teeth are 1.5 to 2.5 mm
long, ending always in a glandulous tube. The plant flowers concentrically from the bottom to the
top. The 11 to 27 white ligulate flowers are 6 to 11 mm long and 3.5 mm wide, longer than the
involucre and bent back. The filamentous style shows two stigmata. The pollen has short prickles
and three hila. The receptacle is 6 to 8 mm wide, flat in the beginning and conical, cone-shaped
later, hollow (being a very important distinctive character) and without paleae. The fruit is a
yellowish brown to brown achene, 0.8 to 1.3 mm long, about 0.3 mm wide, slightly pressed together
and bent horn-like, attenuated at the base, truncated at an angle at the top, with four to five ribs
on the concave lower side. On the ribs small mucous glands are to be found, rounded on the back,
ribless, poorly punctured with glands on the outside, humid, mucous. Pappus is missing or can be
traced as a rim being hardly developed. The thousand kernel weight is 0.02 to 0.06 grams with
diploid forms and 0.04 to 0.12 grams with tetraploids (see Figure 3.1).
True chamomile is very often confused with plants of the genera Anthemis and Matricaria.
Special attention has to be paid to confusions with Anthemis cotula L. For the differentiation from
A. cotula the following characters may particularly be taken into account: A. cotula has setiform
paleae, a receptacle with marrow, and a revolting smell. A. arvensis L. and A. austriaca Jacq. also
have prickly pointed paleae and a filled receptacle. Both species are, however, nearly odorless.
Matricaria maritima L. and M. perforata Mrat are odorless as well. These species have a filled
receptacle but no paleae. Chamomilla suaveolens (Pursh) Rydb. (syn. Matricaria discoidea DC,
M. matricarioides [Less.] Porter) has a typical chamomile scent, too, but has no ligulate flowers
and a compact growth can be noticed.
After exclusion of the genus of Chamaemelum Mill. (syn. Ormenis Cass.) Anthemis L. is well
separable as a genus. Contrary to True chamomile the following generic characteristics may be
noted: the leaves are alternate, mono or double pinnatipartite with mostly linear-lanceolate to linear
sections. The laciniae are comb-shaped pinnatifid. The involucre is bowl-shaped to semispherical

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5
e

8
g

9
a. Scheme of a plant
b. Form of flowering horizon
c. Petal, ligulate floret
d. Tubular floret

10

11

e. Flower head with the cavity

f. 111: different stages of flower development and ripeness
g. Fragments of epidermis
h. Seeds

FIGURE 3.1 True chamomile (Matricaria recutita L.) in schemes [14].

or funnel-shaped. The involucral leaves are multiserial and blunt and have a dry membranous seam.
The receptacle is flat or curved semispherically to conically, filled and mostly provided with leathery
to membranous paleae. The white or yellow uniserial ligulate flowers are female or sterile, and
sometimes they are missing. The numerous hermaphroditic yellow tubular florets often have a
somewhat applanate and thickened tube with no pouchlike enlargement at the base. The achenes
are oblong conical upside down to cylindrical and applanate from the front to the back, tetragonal
with numerous (10 to 20) more or less distinct ribs. The pappus is a membranous collar or it is
missing altogether.
Matricaria recutita L., Chamaemelum nobile (L.) All., and some Cotula species are morphologically closely related, so there is a danger of adulteration. The major palynological characteristics that
proved useful to distinguish all three taxa were equatorial and polar diameters, colpi length, spine
length, number of spine rows between colpi, and foraminate and non-foraminate sculpturing [20].
The independence of the genus of Chamaemelum Mill. in comparison with the genus of
Anthemis L. is nowadays accepted on account of the following characteristics: Chamaemelum
plants reach a height of 6 to 40 cm. The plants have many stems and are hairy. The long pedunculate
flower heads have a diameter of 20 to 25 mm. The multiserial involucre is hairy with a dry
membranous rim. The bottom of the inflorescence is conical. The paleae are broadly spatulate,
curved, thin-skinned, the central nerve is often hairy. The marginal white ligulate flowers are female

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or sterile, the tongue has three laciniae. The yellow hermaphroditic tubular florets with five laciniae
have a ring-shaped enlargement at the base. The brownish achenes are 1 to 1.6 mm long, roundish
in the cross section, little applanate, smooth, without distinct ribs, but on the lower side they have
three thin longitudinal stripes. The pappus is missing.

3.4.2

CHROMOSOME NUMBERS

Considering a basic chromosome number of n = 9 the diploid chromosome number 2n = 18 is

predominant in nearly all species. An exception may well be Anthemis tchichatchewii with 2n =
4x = 36, and A. carpatica with both 2n = 4x = 36 and 2n = 6x = 54. Only a few species like
Anthemis maritima and Matricaria perforata exhibit diploid and polyploid forms. Furthermore, Bchromosomes were found on the diploid stage [10] with M. perforata. In breeding forms of
Chamaemelum nobile and Matricaria recutita polyploidizations were carried out so that now
tetraploid breeding forms/varieties are available (see Chapter 5, Table 5.3.1).

3.5

DRUG NAMES

In numerous names of the medical literature the plural is used and the constituent parts of the
plants are put in front (e.g., Flos or Flores Chamomillae). Linguistically this is not correct.
In the following the singular of the constituent part of the plant is therefore always used and
the name of the constituent part of the plants drug name is placed behind (Matricariae flos), as it
is also done in the European Pharmacopoeia (1997), even if that was not always the case in the
primary literature.

3.5.1 MATRICARIA

RECUTITA

Chamomillae flos officinalis, Chamomillae flos courant I or II variety, Chamomillae vulgaris

flos, Chamomillae vulgaris flos fines, Chamomillae vulgaris flos pro balneo (bath chamomile), Chamomilla, Matricariae flos, Chamomillae anthodium, Chamomillae cribratum,
Chamomillae stramentum, Chamomillae herba, Chamomillae cum floribus herba
Chamomillae aethereum oleum, Chamomillae aetheroleum, Chamomillae oleum, Matricariae aetheroleum
Chamomillae tinctura

3.5.2 CHAMAEMELUM

L.

FUSCATUM

(BROT.) VASC.

Chamaemelum fuscatum flowers

The drug is not traded in Europe.

3.5.3 CHAMAEMELUM

(L.) ALL.

Chamomillae romanae flos, Chamomillae hortensis flos, Chamomillae majoris flos, Chamomillae nobilis flos, Chamomillae odorati flos, Anthemidis flos, Leucanthemi (romani)
flos, Chamomilla romana, Chamaemelum nobile hom., Anthemidis nobilis hom.
Chamomillae romanae aethereum oleum, Chamomillae romanae aetheroleum, Chamomillae romanae oleum, Anthemidis aethereum oleum, Anthemidis oleum

3.5.4 CHAMOMILLA

NOBILE

SUAVEOLENS

(PURSH) RYDB.

Matricariae discoideae herba, Matricariae suaveolens herba

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TABLE 3.1
Chromosome numbers in the genera Anthemis, Chamaemelum,
Matricaria (according to [3], modified)
Chromosome
number

Genus

Species

Anthemis

alpina L.
altissima L.
arvensis L.
austriaca Jacq.
carpatica Waldst. et Kit.
cotula L.
cupaniana
iberica Bieb.
jailensis Zefir.
kelwayi
maritima L.
monantha Willd.
montana Willd.
orientalis (L.) Deg.
peregrina L.
rigescens Willd.
rudolphiana Adams
ruthenica Bieb.
santi-johannis Turill
sosnovskyana Fed.
tigreensis J. Gray ex A. Rich.
tinctoria L.
trotzkiana Claus ex Bunge
woronowii Sosn.
zyghia Woronow

18
18
18
18
36, 54
18
18
18
18
18
18, 36, 54
18
18
18
18
18
16, 18
18
18
18
18
18
18
18
18

Chamaemelum

nobile (L.) All.

18

Matricaria

ambigua (Lebed.) Kryl.

recutita L.
discoidea DC.
grandiflora
perforata L.
pubescens (Desf.) Schultz-Bip.
suaveolens (Pursh) Rydb.
tchichatchewii Boiss.

18
18
18
18
18, 36
18
18
36

3.5.5 ANTHEMIS

ARVENSIS

L.

As a drug, the name Buphthalmi herba is often used. Anthemis arvensis has no medicinal value.

3.5.6 ANTHEMIS

COTULA

L.

Anthemis cotula is without any medicinal value. Sometimes the powder is used against insects.
The drug is not traded in Europe. From time to time the flowers and the herb are traded in the
Southwest United States as a substitute for chamomile, and in Russia they are used against worms.

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3.5.7 ANTHEMIS

TINCTORIA

L.

Anthemidis tinctoriae flos is without any medicinal value. Due to the xanthophyl content, there
has been an increased use as a natural yellow dye for textiles, particularly for wool [16].

3.6 PARTS USED

Chamomile is known and highly appreciated as a medicinal plant. However, chamomile is also of
great importance as a foodstuff and as raw material for the cosmetic industry. Extracts, mono-drug,
as well as tea mixtures are used both for pharmaceuticals and in the foodstuff sector. In the cosmetic
sector extracts and essential oil are preferred. Depending on the use in the foodstuff, cosmetic, or
pharmaceutical sector, different demands are made on the original drug, and according to the field
of application very different trade qualities are offered worldwide.
Chamomile
Pharmaceutical products
Extract
Special extract Fluid extract

Food

Drug
Monodrug

Extract

Tea mixtures

Cosmetics
Tea

Monotea

Extract

Essential oil

Tea mixtures

3.6.1 CHAMOMILE FLOWERS, MATRICARIAE FLOS

This drug is (mostly) used medicinally. The quality requirements are fixed by the pharmacopoeias
of the different countries, and they can vary in wide ranges.
Almost complete flowers, flowers not fallen apart, or those fallen apart to a very small extent
only with a small amount of fines are mostly called pharmaceutical chamomile. This quality is
packed and delivered in cartons. Sometimes this drug is still harvested by hand. With mechanically
harvested material a cost-effective sorting is necessary before or after drying. Mechanically harvested leaves and stems in addition to the flowers have to be sorted out. If the demands made on
intact flower heads are not very high, they may be packed in pressed bales to save space.

3.6.2 CHAMOMILE FINES

Chamomile fines in Hungary they are also handled under the name of Chamomillae cribratum
contain the tubular flowers of the chamomile flowers separated during the mechanical cleaning
process, seeds and wing-petals. Depending on the content of essential oil, this material is either
used for pharmaceutical purposes or as a foodstuff.

3.6.3 CHAMOMILE HERB

WITH

FLOWERS

This material comprises mechanically harvested chamomile flowers with a higher percentage of
stems due to technological reasons. The quality requirements of the pharmacopoeias are usually
not reached, but the material can easily be used as food teas.

3.6.4 CHAMOMILE HERB

Contrary to all other chamomile qualities this material is not produced by harvesting the flowers,
but the flowering herb as such is cut and dried in one working operation and processed without
any further cleaning or separation.

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3.6.5 CHAMOMILE

FOR

EXTRACTION, INDUSTRIAL CHAMOMILE

This material comprises chamomile flowers, the evaluating properties of which are in accordance
with the pharmacopoeia. Because of the mechanical harvest and its preparation, however, its external
structure is in such a condition that this material is not suitable as pharmaceutical chamomile. From
this quality medicinally used extracts are produced. Because of their high oil content flower heads
fallen apart should not be regarded as worthless. If used in tea mixtures/blends a limitation of the
fines is, however, justified due to the tendency of showing inhomogeneities.

3.6.6 CHAMOMILE ROOT

Roots of Matricaria recutita are used for pharmaceuticals of the anthroposophical therapy trend.
Their active principles, especially the essential oil, differ considerably from the aerial parts [13].

3.6.7 CHAMOMILE OIL, MATRICARIA AETHEROLEUM

Chamomile oil is produced by distillation from fresh and dried flower heads and stems of the
chamomile flowers. The essential oil of fresh flowers results in a higher yield, and the quality is
said to be better.

3.6.8 CHAMOMILE FLUID EXTRACT

This product originated from flowers and has a content of 3% blue essential oil.

3.6.9 CHAMOMILE TINCTURE

Tinctures are mainly produced from fresh material for homoeopathic purposes.

REFERENCES
1. Aichele, D., Schwegler, H.-W. (1995) Die Bltenpflanzen Mitteleuropas, Vol. 4, Franck-Kosmos,
Stuttgart, Germany, 528 pp.
2. Br, B. (1995) Analytik und Mikrobiologie des therischen ls verschiedener Kamillenarten. Dissertation, Univ. Berlin.
3. Bolkhovskikh, Z., Grif, V., Matvejeva T., Zakharyeva O. (1969) Chromosome Numbers of Flowering
Plants, Nauka, Leningrad, Russia, 926 pp.
4. Carle, R., Fleischhauer, I., Fehr, D. (1987) Dtsch. Apoth. Ztg., 127, 2, 451457.
5. Hnsel, R., Keller, K., Rimpler, H., Schneider, G. (Eds.) 1992 Hagers Handbuch der pharmazeutischen
Praxis, 5th Ed., Vol. 4, Springer, Berlin, Heidelberg, New York, 1209 pp.
6. Heeger, E. F., Brckner, K. (1952) Heil-und Gewrzpflanzen/Arten-und Sortenkunde. 2nd ed., Berlin,
7780.
7. Hegi, G. (1987) in Conert, H. J., Hamann, U., Schultze-Motel, W., Wagenitz, G. (eds.) Illustrierte
Flora von Mitteleuropa. Spermatophyta IV, Angiospermae Dicotyledones 4, Part 4, 2nd ed., Parey
Verlag, Berlin, Hamburg, p. 582.
8. Hegnauer, R. (1978) Dragoco Report, 24, 10, 203.
9. Hitchcock, A. S., Green, M. L. (1935) Species lectotypicae generum Linnaei. International Rules of
Botanical Nomenclature, Jena, pp. 139143.
10. Mulligan, G. A. (1959) Chromosome number of Canadian weeds II. Canadian J. Bot., 37, 1, 8192.
11. Oberprieler, C. (1997) Untersuchungen zur morphologischen und phytochemischen Variabilitt zweier
Hundskamillen-Arten (Anthemis tricolor Boiss. & A. plutonia Meikle Compositae, Anthemideae) aus
Zypern. Drogenreport, 10, 17, 74.
12. Rauschert, S. (1974) Folia Geobot. Phytotax., 9, 249260.
13. Reichling, J., Bisson, W., Becker, H. (1984) Planta Medica, 4, 334.

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14. Ruminska, A. (1983) Rosliny lecznize. Podstawy biologii i agrotechniki (Heilpflanzen. Grundlagen
der Biologie und Anbau). 3rd Ed. Panstwaowe Wydw. Naukowe, Warszawa, p. 444.
15. Schilcher, H. (1987) Die Kamille. Handbuch fr rzte, Apotheker und andere Naturwissenschaftler,
Wiss. Verlagsgesell., Stuttgart, Germany, 152 pp.
16. Schweppe, H. (1992) Handbuch der Naturfarbstoffe. Vorkommen, Verwendung, Nachweis, ecomed,
Landsberg/Lech, Germany, 800 pp.
17. Schubert, R., Vent, W. (Eds.) (1988) Exkursionsflora, kritischer Band, 7th ed., Volk und Wissen Verlag,
Berlin, 811 pp.
18. Schultze-Motel, J. (Ed.) (1986) Rudolf Mansfelds Verzeichnis landwirtschaftlicher und grtnerischer
Kulturpflanzen (ohne Zierpflanzen), 2nd Ed., Akademie Verlag, Berlin, 1998 pp.
19. Tabernaemontanus, J. T. (1664) New vollkommenlich Kruter-Buch, Jacob Werenfels, Basel, 1529 pp.
20. Uzma Nasreen, Khan, M. A. (1998) Palynological studies of Matricaria chamomilla L. (Babuna) and
its related genera. Hamdard Medicus, 41, 4, 9497.
21. Zander, R. (1994) Handwrterbuch der Pflanzennamen, 15th Ed., Ulmer, Stuttgart, Germany, 810 pp.
22. Zander, R. (2002) Handwrterbuch der Pflanzennamen, 17th Ed., Ulmer, Stuttgart, Germany, 990 pp.

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Chemical Constituents
4 Active
of Matricaria chamomilla L. syn.
Chamomilla recutita (L.)
Rauschert
Heinz Schilcher, Peter Imming, and Susanne Goeters
CONTENTS
4.1

Main Active Constituents

4.1.1 The Essential Oil and Its Constituents
4.1.1.1 Matricin/Chamazulene
4.1.1.2 Bisabolols
4.1.1.3 Bisaboloids
4.1.1.4 Other Terpenes
4.1.1.5 Spiroether (Syn. Enyne Dicycloether)
4.1.1.6 Quantitative Composition of the Essential Oil
4.1.2 Flavonoids
4.1.2.1 Comparative Quantitative Tests of the Flavonoids
4.1.3 Chamomile Polysaccharides, Mucilaginous Substances
4.2 Other Constituents
4.2.1 Other Lipophilic Constituents
4.2.1.1 Coumarins
4.2.1.2 Ceraceous Substances
4.2.2 Other Hydrophilic Constituents
4.2.2.1 Phenyl Carboxylic Acids (Phenyl Substituted Carboxylic Acids)
4.2.2.2 Other Constituents
References
Chamomile contains a large number of therapeutically interesting and active compound classes.
The most important ones are the components of the essential oil and the flavonoid fraction.
Apart from them, the following compound classes were detected and characterized: mucins,
coumarins, phenol carboxylic acids (phenyl substituted carboxylic acids), amino acids, phytosterols,
choline, and mineral substances.
The chamomile constituents are best categorized according to their lipophilicity [103]. The
lipophilic fraction includes individual components of the essential oil, coumarins, methoxylated
flavone aglyca, phytosterols, and lipidic and waxy substances [119]. The hydrophilic fraction
consists of flavonoids, mucilage, phenyl carboxylic acids, amino acids, and choline.

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4.1 MAIN ACTIVE CONSTITUENTS

4.1.1 THE ESSENTIAL OIL

AND ITS

CONSTITUENTS

The essential oil is present in all organs of the chamomile plant, with only the roots containing
small quantities. The flowers and flower heads are the main organs of the production of essential
oil. The composition of the essential oil in roots differs from that in flowers. The oil content changes
during ontogenesis, reaching a maximum of 0.31.5% in flowers just before full bloom [103].
It is remarkable that chamomile flower oil mainly consists of sesquiterpene derivatives
(7590%) but only traces of monoterpenes [72]. The oil contains up to 20% of polyynes.
A recent study with two different chamomile cultivars reported the following rather typical
values for capitula (flowers), shoot, and root as determined by gas chromatography (GC) and
GC/mass spectrometry (MS): The major constituents of the oils of the capitula of the two cultivars
were (E)--farnesene (4.98.1%), -bisabolol oxide B (12.230.9%), -bisabolol (4.811.3%),
chamazulene (2.310.9%), -bisabolol oxide A (25.528.7%), and cis-enyne dicycloether
(4.87.6%). The shoot oil contained (Z)-3-hexenol (1.13.1%), (E)--farnesene (5.737.7%), germacrene D (0.514.6%), (E)-nerolidol (0.43.5%), spathulenol (0.5-3.5%), hexadec-11-yn-11, 13diene (3.19.7%), and cis-en-yn-dicycloether (6.615.0%). The main constituents of the root oils
were linalool (0.54.4%), nerol (3.516.6%), geraniol (1.29.0%), -elemene (1.02.7%), (E)-farnesene (2.718.4%), spathulenol (11.99.4%), chamomillol (1.54.4%), -cadinol, -muurolol
(0.56.4%), hexadec-11-yn-13,15-diene (0.36.2%), and cis-enyne dicycloether (4.75.3%). The
shoot and root oils were found to be devoid of chamazulene. The presence of -bisabolol and its
oxides A and B as minor constituents in the shoot and root oils was established. -Humulene,
hexadec-11-yn-13,15-diene, phytol, isophytol, and methyl palmitate were detected for the first time
in Chamomilla recutita [60].
The individual components are described in the following sections.
4.1.1.1 Matricin/Chamazulene
In 1863, the French chemist Piesse isolated a blue substance from the essential oil of chamomile.
He characterized the compound as a hydrocarbon and called it azulene cause de sa couleur
franchement bleue [83].
The antiphlogistic effect of chamazulene had been known long before its constitution was found
to be 1,4-dimethyl-7-ethyl-azulene in 1953 [68, 112]. It had first been assumed to be 1,4-dimethyl7-isopropyl azulene [117]. The structure elucidation was actually done on chamazulene isolated
from Artemisia arborescens L. [68]. The presence of chamazulene precursors had been reported
for quite a long time until Cekan and co-workers finally isolated a substance. The structure of the
compound that they called matricin was assigned as (3S,3aR,4S,9R,9aS,9bS)-4-acetyloxy3a,4,5,9,9a,9b-hexahydro-9-hydroxy-3,6,9-trimethylazuleno[4,5-b]furan-2(3H)-one in 1956 [16,
17, 18]. Matricin is present in ligulate florets and tubular florets of chamomile only, but not in the
bottom of the flower heads. In 1982, the constitution of matricin (see Figure 4.1) was confirmed
by Flaskamp et al. using modern spectrometric methods [27].
The cycloheptene ring adopts a chair conformation, as was shown by 1H nuclear magnetic
resonance (NMR) data. The stereochemical assignment of matricin rests on these NMR data and
a normal x-ray analysis of 4-epimatricin and of the adduct of 4-epimatricin with 3-hydroxydihydrocostunolide, both isolated from Artemisia arborescens L. [1]. The absolute configuration was
assigned on the basis of the assumption that 7-H always has -orientation in guaianolides [2, 12,
20]. This assumption was shown to be true for matricin when Goeters et al. determined the absolute
configuration of chamazulene carboxylic acid ([34, 47], v.i.). They also published a detailed analysis
of the 1H and 13C NMR spectra of matricin and matricin epimers [34, 47].

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FIGURE 4.1 Matricin [()-(3S*.3aR*.4S*.9R*.9aS*.9bS*4-acetoxi-2.3.3a.4.5.9.9a.9b-octahydro-9-hydroxy3-6-9-trimethylaculeno [4.5-b] furan-2-one]. (Formula and picture of 1.5 g pale yellow crystals isolated from
chamomile by Mai Ramadan and Peter Imming, Marburg University, Germany [48].)
H
H3C
6

6a

5 4
H
H
9b
9a
O
1

H
HO

OAc

H
CH3

3a
H
2

H
3
CH3

Matricin is very unstable and decomposes visibly by turning blue after a short time, particularly
in aqueous solution [108, 109]. This color reaction also occurs during steam distillation of chamomile oil [103]. It is caused by decomposition to chamazulene. The transition of matricin to
chamazulene can easily be demonstrated by treating a thin-layer chromatography (TLC) spot with
steam [103]. The matricin content of chamomile varies considerably between cultivars.
Mabamille, a proazulene and ()--bisabolol-rich cultivar of Martin Bauer GmbH and Robugen
GmbH (both in Germany), contains up to 0.05% in dried flowers [39]. Of all chamomile preparations, the extract made with supercritical carbon dioxide has the highest matricin content (approx.
0.2%) [39]. Schmidt et al. published a procedure for the isolation of very pure matricin [105] and
on the development of a matricin-rich chamomile preparation [80, 106, 107]. They also isolated
and identified 8-desacetylmatricin, the product of the first degradation step of matricin [79].
The immediate precursor of chamazulene is chamazulene carboxylic acid (CCA). It is formed
from matricin by the elimination of water and acetic acid and decarboxylates to chamazulene,
probably through an electrocyclic reaction (see Figure 4.2).
Chamazulene carboxylic acid was first isolated by E. Stahl from chamomile and yarrow
(Achillea millefolium s.l.) in 1954 [116]. Its constitution was confirmed by Cuong et al. using mass
spectrometry and NMR. Apart from that, the compound was almost forgotten until in 2000, Imming
recognized it to be a natural profen, constitutionally similar to synthetic antiphlogistic compounds

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14
10 9

2
3
HO
15

1
4
CH3

O
5
H

16

H 8

9
8

6 7
11
O 12
O

Matricin

10

17

O
13
CH3
H

HOAc
2H2O

4
15

7
11
12
HO
6

CO2

CH3
13

O
Chamazulene carboxylic acid

Chamazulene

FIGURE 4.2 Hydrolytic degradation of matricin to chamazulene carboxylic acid and further decarboxylation
to chamazulene.

like ibuprofen and naproxen. It was again isolated from a chamomile cultivar with a high proazulene
content (Mabamille), extensively characterized (physico)chemically and shown to be more stable
than originally reported, especially in neutral and weakly basic aqueous solutions [33]. In aqueous
acid and in aprotic organic solvents, however, it rapidly loses carbon dioxide. Assuming first-order
kinetics, the rate constant of decarboxylation k1 was determined by 1H NMR to be 1.70 10-3 in
pure D2O, 1.78 10-3 in pH 7.4 buffer, but 1.19 10-2 in pH 2.0 buffer. Its absolute configuration
was found to be S by circular dichroism comparing with S- and R-naproxen [34, 47]. Its pKa value
(4.84) and log D (0.79 at pH 7.4) [33] are almost identical to ibuprofen, so CCA will be taken up
equally well after oral application. The R-enantiomer was isolated from the Central American Stevia
serrata [48].
An early paper claimed the presence of guaiazulene in chamomile [114], but this was never
found again.
4.1.1.2 Bisabolols
In 1951, Sorm et al. isolated another essential constituent of chamomile oil, the monocyclic tertiary
sesquiterpene alcohol ()--bisabolol (INN: Levomenol) [114]. The constitution of bisabolol from
chamomile was confirmed [40, 42] by comparing spectroscopic data with synthetic bisabolol already
described by Ruzicka et al. [95, 96]. The isopropylidene structure of natural ()--bisabolol was
proved through infrared (IR) and nuclear magnetic resonance spectra [50].
This seems to be contradictory to S orm et al., who determined bisabolol in chamomile oil to
be a mixture of 85% and 15% of isopropylidene and isopropenyl isomers. As the two isomers were
identified by ozonolysis, the isopropenyl isomer could have been formed during the ozonolysis.
This is very likely in view of Naves observation [77, 78] that a terminal isopropylidene group is
found exclusively in aliphatic terpenes in plant metabolism, whereas the isopropenyl isomer is
always an artifact.
As synthetic bisabolol has two intensive signals at 6.07 and 11.25 m [42], the isopropenyl
isomer is a by-product of the synthesis [50]. A 1:2 ratio of isopropylidene:isopropenyl determined
for a commercially available synthetic mixture could not be confirmed in a later study [26].
Four optical isomers of -bisabolol are possible. Three of them were isolated from different
plants and distinguished because of their different optical rotation [49].
In 1977, Kergomard and Veschambre [57] determined the absolute configuration of ()--bisabolol isolated from chamomile by stereoselective synthesis of the corresponding diastereoisomers and
comparison of the NMR spectra. ()--bisabolol has 5R,6S configuration (atom numbering as in bisabolol, isolated from cotton buds [69]). This result was confirmed by Knll and Tamm [58].
The stereochemistry of the bisaboloids has been fully elucidated with the exception of bisabolol
oxide C. In contrast to earlier assumptions, all steric centers of bisabolol oxides A and B, ()-bisabolol and bisabolone oxide A have an S-configuration. The identical stereochemistry of all
bisaboloids is also shown by the fact that some bisaboloids are interconvertible [26].

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TABLE 4.1
Stereoisomers of -bisabolol [15]
Configuration

())D20

Source

(+)-epi--bisabolol

1'R,2S

+ 67.4

()-epi--bisabolol

1'S,2R

68.9

(+)--bisabolol

1'R,2R

()--bisabolol

1'S,2S

+ 54.9
+ 52.6
57.7
55.4

Salvia stenophylla
(purity 99.9%)
Myoporum crassifolium
(purity 99.9%)
Populus balsamifera
(purity approx. 97.6%)
Vanillosmopsis erythropappa (purity 99.9%)
Matricaria chamomilla

Isomer

()--Bisabolol from Vanillosmopsis erythropappa is identical with that from chamomile,

showing the same stereochemistry (1'S,2S) [26]. The essential oil obtained from buds of the
European Populus balsamifera [113] and the North American Populus tacamahaca [21] mainly
consist of (+)--bisabolol. Both species are presumably identical. (+)--Bisabolol from Populus
balsamifera is 1'R,2R configured and thus the optical antipode of bisabolol from chamomile.
Levogyrate -bisabolol was also detected in the essential oil of Myoporum crassifolium [23,
81], making up more than 80% of the oil [23]. It had been found previously in small quantities in
the essential oil of ylang-ylang (Canaga odorata) [58], neroli (Citrus bigaradia) [75], cabreuva
(Myrocarpus fastigiatus and M. frondosus [76]), and lavender (Lavandula spica) [111] (quoted
according to Reference 50).
Table 4.1 summarizes properties and origins of the four stereoisomers of -bisabolol.
4.1.1.3 Bisaboloids
In 1951, ()--bisabolol oxide A was isolated by Sorm et al. Many years later, Sampath et al.
determined its structure [97] and isolated the isomeric bisabolol oxide B from chamomile [98]:
()--bisabolol oxide A (C15H26O2): molecular mass 238, syrupy []D = 42.2
()--bisabolol oxide B (C15H26O2): molecular mass 238, []D = 46.95
Two isomeric oxides of -bisabolol, and consequently four cyclic structures, are possible
(Figure 4.3): two containing a tertiary hydroxyl group and two with a secondary hydroxyl group.
They differ stereochemically at C-5 when numbered according to Reference 26 (previously C2). The third chiral center in bisabolol oxide A and B has S-configuration [26].
During the isolation of the two liquid ()--bisabolol oxides A and B, a small quantity of a
crystalline substance was obtained and identified as ()--bisabolol oxide C by Schilcher et al. (Figure
4.3) [104].
While testing chamomile material collected in Turkey, Hlzl and Demuth found a bisaboloid
unknown so far [43]. Its constitution was determined by IR and NMR spectroscopy and through
the products of oxidation and reduction found to be an -bisabolone oxide (Figure 4.4) [44].
Bisabolol oxide A either can be transformed to it or can be obtained from it by reduction. The
bisabolone oxide isolated from plant material displayed a different optical rotation compared to
material prepared from ()--bisabolol oxide A:
[]D = 6,2 [97]
[]D = +3,5 [44]
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1
2
3

OH

1 2

6 5

4
6

7
Bisabolol

OH
O

O
OH

O
O

OH
OH

Bisabolole oxide A

Bisabolole oxide B

Bisabolole oxide C Theoretically possible,

but not yet isolated

FIGURE 4.3 Products of the oxidation of bisabolol.

O
O

FIGURE 4.4 ()--Bisabolone oxide A.

The nomenclature of the chamomile bisaboloids was reviewed according to the IUPAC guidelines and should be used as follows:
()--bisabolol:
()-(1'S, 2S)-6-methyl-2-(4-methyl-3-cyclohexene-1-yl)-hepten(e)-2-ol
()-bisabolol oxide A:
()-(1'S,3S,6S)-tetrahydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen(e)-1-yl)-2H-pyran(e)3-ol
()-bisabolol oxide B:
()-(1"S,2'S, 5S)-1-methyl-I-[tetrahydro-5-methyl-5-(4-methyl-3-cyclohexen(e)-1-yl)furan(e)-2-yl]-ethanol
(+)-bisabolone oxide A:
(+)-(1'S,6S)-tetrahydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen(e)-1-yl)-2H-pyran(e)-3on.
Bisabolol oxide A, B, and sometimes bisabolone oxide A are the main constituents of the
essential oil. Schilcher [101] established a classification in chemotypes based on the composition
of the essential oil (see Chapter 3, Plant Sources). In chamomile flowers, bisabolol oxide C is found
in small quantities only or is chemically available from ()--bisabolol by oxidation. Table 4.2
summarizes the results of different oxidation experiments, which led to varying quantities of
bisabolol oxides A, B, and C [102, 104].
The photochemical tests were carried out in a quartz glass apparatus [102]. The rotation of the
bisabolols was determined using long-wave UV light (mercury high-pressure lamp TQ 150 Hanau).

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TABLE 4.2
-Bisabolol [65, 102104]
Oxidation Stability of (-)-
Reaction Conditions

Main Components, Determined by GC

1. Bisabolol in hexane or heptane solution in brown glass

containers with glass stopper

After 12 months: unchanged

2. ()--bisabolol in ethanol 50% in white glass containers

that were opened for 10 min once a week

After 12 months: ca. 70% ()--bisabolol

ca. 18% bisaboloids (mainly bisabolole oxide B) and
unidentified other peaks (artifacts)
After 18 months
ca. 51% ()--bisabolol
ca. 25% bisabolole oxide B
Remainder: not identified
After 24 months:
ca. 37% ()--bisabolol
ca. 31% bisabolole oxide B
Remainder: not identified

3. ()--bisabolol in Miglyol 812 (Nobel Co.) (see

Schilcher, H. German Offenlegungsschrift Nr. 2331853, 22,
6, 1973) in brown glass containers with glass stopper
4. Passage of purified air for 3 h without UV irradiation

After 24 months:
ca. 98.5% ()--bisabolol
Remainder: not identified
ca. 85% ()--bisabolol
ca. 10% bisabolole oxide B
Remainder: not identified

5. Passage of pure oxygen for 3 h without UV irradiation

ca. 68% ()--bisabolol

ca. 14% bisabolole oxide B
Remainder: not identified

6. Irradiation of a bisabolol solution with visible light under

exclusion of air for 6 h

Unchanged

7. Passage of pure oxygen for 5 h with UV irradiation

ca. 32% ()--bisabolol

ca. 42% bisabolole oxide B
ca. 15% bisabolole oxide C, crystallized on wall of reaction
chamber
ca. 2% bisabolole oxide A
Remainder: not identified

8. Passage of pure oxygen for 8 h with UV irradiation

Only traces of ()--bisabolol and oxides B, C, and A left

Reaction products had lower polarity and shorter GC
retention times; mass spectra showed C8 and C7 fragments
of mass 236

The increase of bisabolol oxide during the drying process was the object of further experiments.
The plant material in this study consisted of flower heads of a chamomile variety being rich in
bisabolol. The drying procedures were as follows [102, 103]:
1. Drying at room temperature in a dark and dry room (the relative atmospheric moisture
was 35%)
2. Drying at 40C
3. Drying at 50C

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TABLE 4.3
Relative Content of Constituents (GC) after Different Drying Procedure
-Bisabolol
()-
1
2
3
4
5

~34%
~34%
~24%
~17%
~7%

Bisabolole oxide A
~
~
~
~
~

4%
4%
5%
8%
26%

Bisabolole oxide B
~
~
~
~
~

20%
20%
28%
33%
19%

Chamazulene
~
~
~
~
~

12%
12%
10%
7%
1%

4. Drying at 60C
5. Drying under conditions being similar to those of fermentation (e.g., layers of 10 cm
height in a damp atmosphere)
Quantitative analysis of important constituents of the essential oil was done by gas chromatography. The results are summarized in Table 4.3.
Conditions similar to fermentation or high temperatures led to oxidation of bisabolol by
atmospheric oxygen to the bisabolol oxides [102, 103]. The reactions during the drying process
[102, 103] and the results of the oxidation experiments were evidence for the dependence of the
content of bisaboloids on not only genetic or ecologic factors, but also on conditions of drying and
storage of the plant material. Many analytical results found in the literature should be reinterpreted
in the light of these findings [102, 103].
4.1.1.4 Other Terpenes
Motl et al. isolated the azulenogenic sesquiterpene alcohol, spathulenol [71]. Its constitution was
determined by 1H and 13C NMR and by IR [55]. Its constitution was corroborated by regio- and
stereoselective synthesis from (+)-aromadendrene [124]. In 1979, Lemberovics identified two
farnesene isomers, viz., trans-- and trans--farnesene [63]. According to her findings, -farnesene appeared to be the main component, whereas -farnesene was present in traces. Reichling
et al. were not able to detect -farnesene in the essential oil of chamomile flowers [89]. Further
monoterpene hydrocarbons such as -terpinene, 3-carene, and the sesquiterpene hydrocarbons
-cubebene, -muurolene, and calamemene were detected by GC/MS [72].
Applying the same analytical procedure for a petroleum ether extract made from Czech chamomile flowers, Motl found a crimson fragrant azulene [72]. Its constitution was determined later
[73] and found to be the aldehyde chamavioline (Figure 4.5). It had been synthesized previously
as an intermediate of a chamazulene synthesis [74].
The constitution of matricarin was elucidated in 1978 [70] (Figure 4.5) and was corroborated
by NMR data [67] and finally by a single-crystal x-ray analysis in 2002 [82]. The absolute
configuration was not determined.
Motl et al. claimed [70] that not all active constituents of the petroleum ether extract have been
identified yet. According to Stransky [118], the hydrocarbons found in chamomile flowers can be
subdivided into n-alkanes, branched-chain alkanes, monoalkenes, terpenoid hydrocarbons, alkadienes, and aromatic hydrocarbons (see Figure 4.6).
In the essential oil of the root the sesquiterpene alcohol muurol-4-en-7-ol, also called chamomillol, was detected by Reichling et al. [90] (Figure 4.5). The authors also identified -caryophyllene, cis-caryophyllene, and caryophyllene epoxide in this oil.

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H3C
O

HO

CH2CH3

O
O

Spathulenol

Chamaviolin

Matricarin

CH3
H
8

2
4

H3 C
H3C

OH

O
2
O1
5

CH3
Chamomillol (Muurol-4-en-7-ol)

Anthecotulid

FIGURE 4.5 Sesquiterpenes in chamomile flowers and roots. Anthecotulid is from Anthemis cotula (see text).

Farnesen

Myrcen

CH2OH

Cadinen

Gerianol

FIGURE 4.6 Monoterpenes in chamomile flowers.

Yamazaki et al. reported the isolation of anthecotulide, a sesquiterpene lactone with an exocyclic
methylene group (Figure 4.5), from chamomile collected in Argentina [130]. They claim to have
isolated it in 7.3% (!) yield from aerial parts of Matricaria chamomilla L. (This number is sometimes
wrongly quoted for the anthecotulide content of Anthemis cotula, but actually stems from the
Yamazaki paper.) One of the authors of this chapter (P.I.) asked the curator of the Herbarium of
the University of Texas, Austin, to redetermine the voucher specimen of Yamazaki et al. As
suspected, it was actually Anthemis cotula L. [129]. Anthecotulide was originally isolated from
Anthemis cotula L. (stinking mayweed, dog chamomile), where it is present in relatively high
quantities [3, 9]. It is a very potent contact allergen [38]. Hausen et al. claim that it is present in
variable but low levels in strains of the bisabolol oxide B chamomile type [38]. Bisabolol oxide B
is the main constituent in the essential oil of this chemodem (chemical type), according to Schilcher
[101, 103]. In all likelihood, the occasional presence of anthecotulide results from contamination
of chamomile collections with A. cotula flowers and plants.

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4.1.1.5 Spiroether (Syn. Enyne Dicycloether)

Two spirocyclic polyynes, the isomeric cis and trans enyne dicycloether, were found in the petroleum
ether extract of chamomile flowers by Bohlmann et al. in 1961 [7] and reinvestigated in 1982,
including a discussion of NMR data [8]. The cis spiroether (according to [114], cis-2-[hexadiyne)(2,4)-ylidene]-1,6-dioxaspiro-[4,4]-nonene) is the major component in most plant specimens [102].
The trans spiroether was predominant only in certain commercially available chamomile flowers
[102]. Both compounds were found in petroleum ether extracts and in freshly distilled essential oil
[11].
The enyne dicycloethers were frequently accompanied by an aromatic compound with the
molecular formula of C10H12O4. Motl et al. [72] identified it as 2-hydroxy-4,6-dimethoxy-acetophenone by means of NMR spectroscopy. In the literature, this compound is also called xanthoxylin, brevifolin, or 6-methoxypaeonal. Motl et al. state that xanthoxylin is not separated from
the spiroethers by thin-layer chromatography using usual solvent systems. Quantitative TLC
(densitometry) may thus give too high quantities of spiroethers [72]. Unlike the enyne dicycloethers, xanthoxylin has no antiphlogistic effect.
H
H 3C

Z-Enyne dicycloether
[(2Z)-2-(2,4-Hexadiynylidene)1,6-dioxaspiro[4.4]non-3-ene]

H3 C
H
E-Enyne dicycloether
[(2E)-2-(2,4-Hexadiynylidene)1,6-dioxaspiro[4.4]non-3-ene]

4.1.1.6 Quantitative Composition of the Essential Oil

The approximate ratio of the main components in the essential oil is as follows [29, 102, 103]:

Up
Up
Up
Up

to
to
to
to

15%
33%
45%
25%

chamazulene and its precursor matricin [116]

bisabolols and bisabolol oxides [50, 102]
trans--farnesene [14, 102]
cis- and trans-isomers of the spiroethers [28, 102]

4.1.2 FLAVONOIDS
Flavonoid glycosides represent the major fraction of water-soluble components in chamomile. Apart
from the glycosides, flavonoid aglyca were found in great variety among the lipophilic constituents.
Chamomile flavonoids were recognized to be spasmolytic and antiphlogistic and are therefore of
great interest.
Apigenin was the first flavone to be isolated from chamomile [85] in 1914. Its constitution,
however, was elucidated as late as 1952 [115].
Lang and Schwand successfully isolated and identified apigenin-7-glucoside from ligulate
florets and quercimeritin from tubular florets of chamomile [62].
Apiin (apigenin-7-[6"-O-apiosyl]-glucoside) had previously been found in white ligulate florets
of some Chrysanthemum species and was again isolated from Matricaria chamomilla. Its constitution was elucidated by Wagner and Kirmayer in 1957 [125]. Six compounds separated by paper
chromatography [123] were identified as apigenin glycosides through hydrolysis to apigenin.

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Further constituents (e.g., luteolin-7-glucoside and patulitrin) were detected by Hrhammer et

al., who also confirmed the presence of quercetin-7-glucoside and apigenin-7-glucoside [46]. The
separation of 11 different flavonoid derivatives was successfully performed on polyamide plates.
Less than six of them were apigenin glycosides [cf. 123].
Egyptian chamomile flowers were the subject of a qualitative analysis in 1963. They contained
the flavonoids quercetin-3-rutinoside and quercetin-3-galactoside, but no luteolin-7-glucoside [22].
In 1965, the chromatographic separation of six to nine different apigenin glycosides was
reported [99].
The first lipophilic chamomile flavone to be isolated and identified by Hnsel et al. in 1966
was chrysosplenitin (= 3,6,7,3'-tetramethyl-quercetagetin) [37].
Several papers were concerned with the analysis of the distribution of the flavonoids in different
plant organs. Apart from chrysosplenitin and apigenin, three further apigenin glycosides were
detected in ligulate florets, one of them apigenin-7-glucoside [128]. The tubular florets contained
luteolin, luteolin-7-glucoside, and quercetin as well as numerous other flavonoids that were not
identified yet. Surprisingly, apigenin and apigenin-7-glucoside were also observed in tubular florets,
whereas luteolin glucoside could not be detected in ligulate florets (cf. [6]). Patulitrin, quercimeritrin, luteolin-7-glycoside, and apigenin-7-glucoside were detected in tubular florets of a new
cultivar. In ligulate florets, only apigenin-7-glucoside was found [84].
In another report published in 1979, apigenin and apigenin-7-glucoside were again detected in
ligulate florets. Two further glycosides were found and the presence of an isoflavone assumed.
According to a study published in 1979, the hydrolysis of flavonoids for the first time yielded
the aglyca of isorhamnetin and chrysoeriol [88], apart from quercetin, patuletin, apigenin, and
chrysosplenetin that had previously been found. In 1979 Kunde and Isaac, independently also
Redaelli et al. [86], reported the isolation and identification of a new chamomile flavone, apigenin7-(6"-O-acetyl-)-glucoside [61]. The aglyca apigenin, luteolin, patuletin, quercetin, and isorhamnetin were detected and the glycosides apigenin-7-glucoside, luteolin-7-glucoside, patulitrin, and
quercimeritrin. They further reported the presence of flavonoid mono-glycosides and postulated a
diacetylated apigenin-7-glucoside.
Kunde and Isaac classified chamomile flavonoids according to their polarity (Figure 4.7) [61]:

Lipophilic flavone aglyca (e.g., methoxylated compounds)

Hydroxylated flavone aglyca
Acetylated flavone monoglycosides
Flavone diglycosides

Systematic screening of a chloroform extract of Egyptian chamomile flowers [24] yielded

further methylated flavones [37]. Apart from known compounds such as apigenin, patuletin, chrysoeriol, chrysosplenetin, and isorhamnetin, a number of thus far unknown methylated flavone aglyca
such as jaceidin, chrysosplenol, eupatoletin, spinacetin, axillarin, eupaletin, and a 6-methoxykaempferol were discovered in chamomile. Especially noteworthy is the isolation of two methyl
ethers of 6-hydroxy-kaempferol, eupaletin and 6-methoxy-kaempferol, since no kaempferol or
kaempferol derivatives had been isolated from chamomile before [24] (Figure 4.8).
Again, the distribution of flavonoids in individual plant organs was studied and included organs
studied earlier (ligulate florets and tubular florets, foliage, and roots) and additional organs such
as involucral leaves, the receptacle, and the stems [6].
Comparing the glycoside pattern of tubular florets and ligulate florets as obtained from ethyl
acetate extractions, the following conclusions can be drawn: on TLC plates, the ligulate florets
showed uniformly dark violet spots that turned a greenish yellow color after spraying with natural
product reagent. A total of five to seven substances were detectable. The spots obtained from the
tubular florets showed yellow, green, and orange colors after spraying.

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OMe
OH

e.g., Jaceidin

HO
MeO

OMe
OH

OH

Increasing polarity

OH

HO
HO

OH

OH
O

e.g., Apigenin-7-O-D-(6-O-acetylglucoside)
O

OH
e.g., Apigenin-7-O-glucoside
(= Cosmetin, Apigetrin)

OH
OH

OH
HO
HO
O
H3C
O
HO
HO

Acetylated monoglycosides
of flavones

OH
OH

HO
HO

Hydroxylated aglycones of flavones

e.g., Apigenin

HO

OAc
O

Methoxylated aglycones of flavones

(lipophilic flavones)

Diglycosides of flavones

OH
O

e.g., Apigenin-7-O--Drutinoside

OH
OH

FIGURE 4.7 Classification of flavones from chamomile according to polarity [61].

In ligulate florets, the following flavonoids were found:

Lipophilic chamomile flavones (for details see above, plus eupatoletin and spinacetin)
Luteolin-7-glucoside
Apigenin
Apigenin-7--glucoside, apigenin-7-(6-O-acetyl)-glucoside, apigenin-(6-O-apiosylglucoside, apigenin-7-rutinoside)

After hydrolysis, the ligulate florets and tubular florets showed almost the same aglyca pattern
except that patuletin and quercitin were missing in the ligulate florets, whereas apigenin was missing
in the tubular florets.
According to the same report, receptacles, involucral leaves, foliage, and caulome contain
mainly the same aglyca. Interestingly, oligomethylated aglyca are missing completely. The only
aglyca to be found in all parts of the plant are isorhamnetin and luteolin with the exception of the
root, which does not contain flavonoids at all [6, 128].

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OMe

Chrysoeriol

OMe

Isohamnetin

HO

HO

OH

Quercetin
OH

OH
O

OH
HO

OH
OH O

OH
OH

Patuletin
HO

MeO

Apigenin
HO

OH O
OH

OH
OH O

Jaceidin
HO

O
OMe

OH O
Spinacetin
HO

OMe
OH O

OMe

OH
OH

6-Methoxykmpferol

OH

Eupalitin
O

MeO
OMe

OH

MeO
OH O

OH
OH

Luteolin
HO

OH O
OH

OH O

OH

OH

MeO

MeO

OH

OH

Eupatoletin
MeO
O

OH

Axillarin
HO

OH O

OH

OMe
OH O

OH
OH

MeO
OH

MeO

Chrysosplenol
MeO

OMe

Chrysosplenetin
O
MeO
MeO

OH O

OMe
OH

MeO

HO

OH
OH O

OH

MeO
OH O

OH O

FIGURE 4.8 Flavone aglyca from chamomile flowers (according to Carle and Isaac [15]).

The following flavonoid glycosides were found in leaves by chromatographic methods:

Quercetin-7-glucoside, isorhamnetin-7-glucoside, luteolin-7-glucoside, chrysoeriol-7-glucoside, 6-hydroxyluteolin-7-glucoside, luteolin-7-rhamnoglucoside, and chrysoeriol-7-rhamnoglucoside [36]. No apigenin glycosides were observed; however, in another study [6] apigenin could be
detected after hydrolysis.
Figure 4.8 shows a summary of flavonoid aglyca found in chamomile flowers. Apigenin is the
most important therapeutically of them.
The presence of apigenin had not been proved unequivocally. Hlzl [41, 45, 122] radiolabeled
apigenin and apigenin-7-glucoside through incorporation of 14CO2 during biosynthesis in the ligulate
florets. They measured the specific activity after selective ultrasound-assisted extractions with
methanol and dichlormethane and proved that apigenin is in fact present in ligulate florets of
chamomile. They isolated another acetylated glucoside, apigenin-7--D-(4-O-acetyl) glucoside
[122].
Carle et al. [13, 110] compared extracts from freshly collected wild plants with those from
greenhouse plants. They assumed that apigenin is originally not present in fresh chamomile, but is
the result of secondary enzymatic processes. This explains the great differences in the ratio of
apigenin and apigenin-7-glycoside in the literature, which may also be due to different harvest
conditions [110]. In the course of their work, they isolated flavone-glucoside-cleaving -glucosidase
from the protein fraction of flower heads, and in particular from freeze-dried ligulate florets, by
means of fractionated ammonium sulfate precipitation and subsequent fast protein liquid chromatography (FPLC) on a Superose column. The enzyme has a relative molecular mass of 500,000 kD
[6466]. At its optimum temperature (37C) and pH (5.6), this glycosidase showed a specificity
for flavone-7-O-glucosides but did not hydrolyze -glycosides or disaccharides. Agents carrying

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TABLE 4.4
Flavonoid Glycosides and Aglyca in Chamomile Flowers
5`
4`

6`

R1

8
7

1`
2`

R2

4
5

OH

R4

3`

R5

R3

Luteolin
Luteolin-7-glucoside
Luteolin-4'-glucoside
Luteolin-7-rutinoside
6-Hydroxy-luteolin-7-glucoside
Chrysoeriol
Chrysoeriol-7-glucoside
Apigenin
Apigenin-7-glucoside (Apigetrin)
Apigenin-7-(6"-O-acetyl)-glucoside
Apigenin-7-(6"-O-apiosyl)-glucoside (Apiin)
Apigenin-7-rutinoside

R1

R2

R3

R4

H
OG1u
H
OGlu-Rham
OGlu
OH
OGlu
OH
OGlu
OGlu-ac
OGlu-Apio
OGlu-Rham

H
H
H
H
OH
H
H
H
H
H
H
H

OH
OH
OGlu
OH
OH
OH
OH
OH
OH
OH
OH
OH

OH
OH
OH
OH
OH
OCH3
OCH3
H
H
H
H
H

sulfhydryl groups strongly inhibited the enzyme. They found that free apigenin is produced only
after destruction of the cell compartments (e.g., after harvest), by enzymatic decomposition of
glucosides [66]. During ontogenesis, an increase of the enzymatic activity and simultaneously the
accumulation of flavonoids in flowers could be observed [66].
By HPLC with photodiode array detection and by thermospray liquid chromatography/mass
spectrometry (TSP LC/MS), the isomeric 2-, 3-, and 4-monoacetates and the 2-, 3-, and 3-,
4-diacetates of apigenin-7-glucoside could be separated and isolated from an O-acetyl-glycoside
mixture [13].
Tables 4.4 and 4.5 summarize the flavonoid glycosides and corresponding aglyca identified so far.
4.1.2.1 Comparative Quantitative Tests of the Flavonoids
The quantities of (Z)- and (E)-2--D-glucopyranosyloxy-4-methoxycinnamic acids (GMCA) and
apigenin glucosides of Chamomilla recutita were studied in progenies of selected tetraploid mother
plants with significantly high and low contents of GMCA [94]. The relations between GMCA and
apigenin aglycon content suggested that among the plants studied, groups of individuals with a
high content of GMCA (6.49.2 mg/g dry weight) and high (4.15.1 mg/g dry weight) and medium
(2.53.6 mg/g) contents of apigenin, as well as a group with a lower content of both compounds,
could be distinguished.
Apigenin was also analyzed at two ploidy levels during a 3-year period. Higher percentages
of apigenin were found in the ligulate florets of a diploid cultivar, in comparison with tetraploid
plants. However, when the total apigenin in the anthodium was evaluated, tetraploid individuals
accumulated significantly more flavonoid. Apigenin percentage in the ligulate florets was constant
and not influenced by environmental conditions. Apigenin content was also found to change during
inflorescence ontogeny. It represented the highest percentage of dry mass in young developing
florets and anthodia of both cultivars. The total apigenin content of the anthodium, however,

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TABLE 4.5
Flavonoid Glycosides and Aglyka, Especially Methoxylated Derivatives, in Chamomile
Flowers
5`
4`

6`

R1

8
7

1`
2`

R2

4
5

OH

R4

3`

R5

R3

Quercetin
Isorhamnetin
Quercetin-7-glucoside (Quercimeritrin)
Quercetin-3-rutinoside (Rutin)
Quercetin-3-galaktoside (Hyperoside)
Isorhamnetin-7-glucoside
6-Methoxy-kaempferol
Eupaletin
Patuletin
Patuletin-7-glucoside
Axillarin
Spinacetin
Eupatoletin
Chrysoplenol
Chrysoplenetin
Jaceidin

R1
OH
OH
OGlu
OH
OH
OGlu
OH
OCH3
OH
OGlu
OH
OH
OCH3
OCH3
OCH3
OH

R2
H
H
H
H
H
H
OCH3
OCH3
OCH3
OCH3
OCH3
OCH3
OCH3
OCH3
OCH3
OCH3

R3
OH
OH
OH
OGlu-Rham
OGal
OH
OH
OH
OH
OH
OCH3
OH
OH
OCH3
OCH3
OCH3

R4
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH
OH

R5
OH
OCH3
OH
OH
OH
OCH3
H
H
OH
OH
OH
OCH3
OH
OH
OCH3
OCH3

increased during flowering, although at later stages apigenin forms only a minor part of ligulate
floret and anthodium dry mass [120].
While there are no qualitative differences between samples of individual chamomile types
according to Reichling et al. [88], there are in fact considerable quantitative differences [102, 103].
They were established both in respect to the quantitative distribution of the aglyca and the total
flavonoid content. Reichling et al. reported that a Bohemian chamomile variety, assigned as K,
and an Egyptian variety, assigned as ART, contained much more quercetin than all other samples
analyzed. Another Bohemian chamomile variety, assigned C, had by far the highest apigenin
content.
Repcak and Martonfi observed that the content of apigenin aglyca in ligulate florets and flower
heads increases by polyploidization. In di- and tetraploid samples the amount of apigenin aglyca
increased by about 15% [93].
Tests of about 100 samples performed by Schilcher [102] as well as the analysis of material
obtained from 12 different origins, raised from seeds and cultivated under the same conditions,
clearly showed that the total flavonoid content considerably differed, too. The flavonoid content of
the samples tested ranged from 1.02.57%. Table 4.6 summarizes the results of these experiments.
The total flavonoid content was determined photometrically [19]. This method is not suitable to
obtain absolute values, but is sufficient for comparative analysis.
The results of Reichling and Schilcher demonstrate that it is important to determine the content
of flavonoids in order to examine the quality of the plant material or preparation, especially with
respect to the therapeutic significance of the flavonoids.

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TABLE 4.6
Total Flavonoid Content of Chamomile from Different Locations [102, 103],
Determined According to Reference 19
Origin of Cultivar

Location

Harvest Date

Total Flavonoids (%)

Wroclaw (Poland)
Sample No. 1

Kempten
Kempten
Herrenberg
Herrenberg
Kempten
Herrenberg
Marburg
Marburg
Marburg
Marburg
Marburg
Marburg
Kempten
Kempten
Kempten
Kempten
Marburg
Kempten
Marburg
Marburg
Marburg
Kempten
Kempten
Marburg
Marburg
Kempten
Kempten
Marburg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg
Herrenberg

1.
2.
1.
2.
1.
1.
1.
2.
3.
1.
2.
3.
1.
2.
3.
4.
1.
1.
1.
2.
3.
1.
2.
1.
2.
1.
2.
1.
3.
3.
1.
3.
1.
2.
3.
4.
1.
2.
3.
1.
2.

2.17
2.96
2.33
2.52
0.27
2.33
2.13
2.71
2.17
2.88
2.96
2.80
2.5
1.42
1.82
0.17
2.21
1.98
2.17
1.21
1.30
2.5
1,0
2.29
2.31
2.17
1.38
2.13
2.97
1.83
2.8
2,7
2.82
2.75
2.73
2.29
2.06
2.28
2.5
2.71
2.75

Niederrhein/Krefeld (Germany)
Sample No. 4
Bukarest (Romania)
Sample No. 2
Aachen (Germany)
Sample No. 11

Oldenburg (Germany)
Sample No. 12
Modena (Italy)
Sample No. 28

Halle (Germany)
Sample No. 39

Bremen (Germany)
Sample No. 33
Oberstedten (Germany)
Argentina
Spain

Bratislava (Slovakia)
Tripleurospermum sp.
Nijmegen (the Netherlands)
Tripleurospermum sp.

harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest
harvest

22. 6. 1977
30. 6. 1977
2. 8. 1978
14. 8. 1978
23. 6. 1977
24. 8. 1978
27. 6. 1977
5. 7. 1977
13. 7. 1977
22. 6. 1977
27. 6. 1977
5. 7. 1977
23. 6. 1977
28. 6. 1977
12. 7. 1977
2. 9. 1977
22. 6. 1977
23. 6. 1977
22. 6. 1977
27. 7. 1977
5. 8. 1977
23. 6. 1977
29. 7. 1977
22. 6. 1977
27. 6. 1977
23. 6. 1977
29. 6. 1977
22. 6. 1977
24. 8. 1978
24. 8. 1978
25. 6. 1980
28. 7. 1980
22. 7. 1980
6. 8. 1980
12. 9. 1980
16. 9. 1980
1980
1980
1980
1980
1980

4.1.3 CHAMOMILE POLYSACCHARIDES, MUCILAGINOUS SUBSTANCES

In recent years, there has been an increased interest in chamomile polysaccharides, formerly called
mucilaginous substances. In the literature, the content of this class of compounds varies considerably
from 17% [56] to 10% [15] and even 35% [30, 31]. Polysaccharides are localized in the so-called

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slime ribs of chamomile flowers. The main chain of the polysaccharide consists of -1->4
connected D-galacturone acid [15]. Other components of polysaccharides are as follows: xylose
(about 21%), arabinose (about 10%), galactose (about 15%), glucose (about 7%), and rhamnnose
(about 2%). In addition to these findings of Janecke and Weisser [53, 54], Schilcher identified
fucose [102, 103].
Wagner et al. [126] characterized the crude mucilage of chamomile. They found it to be of
high molecular mass (>500,000) and heavily branched with (1->4)--connected xylose moieties
and a large amount of 4-O-methyl-glucuronic acid. In an in vitro test system, a significant stimulation of phagocytose was observed in the presence of chamomile polysaccharide [127]. The
detection was done by means of phagocytose-chemoluminescence (CL). The test of the granulocytes
was modified according to Brandt [10].
Recently Franz [31] could confirm the structure of the polysaccharide as a 4-O-methyl-glucurone
oxylane, but not its activity toward phagocytose. He also identified a neutral fructane of medium
molecular mass (3600) containing 74.3% fructose and 3.4% glucose (similar to inulin), and a strongly
branched rhamnogalacturonane of medium molecular mass (93,000) consisting of 28% uronic acid,
3.2% protein (similar to pectin). They were found to have arabino-3,6-galactane glycoproteins as side
chains. In an aqueous alcoholic chamomile extract preparation [31], only fructanes could be found.
All three isolated chamomile polysaccharides showed remarkable antiphlogistic activity against mouse
ear edema induced by crotone oil [29]. Further pharmacological tests are necessary. Nevertheless, a
total extract is obviously superior to extracts containing the essential oil only because of the therapeutical relevance of the polysaccharides.
According to Janecke and Kehr [51, 52], the crude mucilage of chamomile has an exceptionally
high mineral content. 100 g of dry mucilage extracted with hot-water extraction contained 18 to
29 g of ash. In measurements of the viscosity (see Chapter 10), the high mineral content has to be
taken into consideration.

4.2 OTHER CONSTITUENTS

4.2.1 OTHER LIPOPHILIC CONSTITUENTS
4.2.1.1 Coumarins
Both the 7-methoxy-coumarin herniarin and the 7-hydroxy-coumarin umbelliferone (Figure 4.9)
are of analytical and pharmacological interest. Herniarin is mainly present.
Analysis of material of different origins resulted in a range of 37.498.5 mg of herniarin [102]
and 617.8 mg of umbelliferone both per 100 g of chamomile flowers. Both were detected in
ligulate and tubular florets. The average content in ligulate florets was significantly higher [102,
103].
In herbal chamomile preparations sold in Italy, the preparations containing ligulate florets
showed a higher content of coumarin when compared to other parts of the anthodia (flower heads).
The ratio of umbelliferone:herniarin was <1:5 [121].
The content of herniarin decreased during anthodia ontogenesis in both diploid and tetraploid
varieties, the tetraploid cultivar showing a higher concentration [91].
Umbelliferone was identified as a stress metabolite of the plant [92].
A Ukranian group claimed the isolation of another four coumarins: viz., coumarin itself,
isoscopoletin, esculetin, and scopoletin from chamomile flowers [59].

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RO

R = CH3
R=H

Herniarin
Umbelliferon

FIGURE 4.9 Coumarins in chamomile flowers.

4.2.1.2 Ceraceous Substances

Streibel [118, 119] reported lipidic and ceraceous substances in a petrol ether extract of chamomile flowers. The composition was as follows:
Approximately
Approximately
esters
Approximately
Approximately
Approximately

13.0% hydrocarbons
16.0% simple aliphatic esters, sterol esters (phytosterols), and triterpenol
3.0% triglycerides
0.5% keto-esters
6.0% esters containing acetylene

Schilcher isolated a white ceraceous substance from steam distillate (using a glycerol bath for
6 h) by chromatography on silica gel [102, 103]. 1% of the compound was present in the dried
drug. According to the 13C spectrum, it was a straight-chain fatty acid with 30 carbon atoms.

4.2.2 OTHER HYDROPHILIC CONSTITUENTS

4.2.2.1 Phenyl Carboxylic Acids (Phenyl Substituted Carboxylic Acids)
Reichling et al. detected the following phenyl carboxylic acids chromatographically [88]: anisic
acid, caffeic acid, syringic acid, and vanillic acid (Figure 4.10).
COOH
HO
OH
R2
R1

R3

COOH

FIGURE 4.10 Arylcarboxylic acid derivatives.

Above: Caffeic acid
Below:

R1

R2

R3

Syringic acid
Vanillic acid
Anisic acid

OCH3
H
H

OH
OH
OCH3

OCH3
OCH3
H

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Table 4.7 summarizes different contents of phenyl carboxylic acids observed [88]. In most of
the tests anisic acid was used as reference.

TABLE 4.7
Phenylcarboxylic Acid Derivatives and Coumarins in Chamomile Flowers
Coumarins
Chamomile Sample
Bulgarian chamomile
Bulgarian chamomile
Mexican chamomile
I, chamomile
II, chamomile
Bohemian chamomile, C
Bohemian chamomile, K
Egyptian chamomile, type Art
Egyptian chamomile, type HH
Egyptian chamomile, type M 77
Egyptian chamomile

Herniarin

Umbelliferon

++
+
++
+
+
+
+
+
+
++
+

+
+
++
+
+
+
+
+
(+)
+
+

Phenylcarboxylic
Acids
Anis
Vanillic
Acid
Acid
++
++
+
++
++
++
++
++
+
++
+

+
+
+
++
++
+
+
+
+
+
+

Syringic
Acid

Caffeic
Acid

(+)
(+)
(+)
+
+
(+)
+
+
(+)
(+)
(+)

+
+
(+)
+
+
(+)
+
+
+
(+)
+

Note: ++ = high concentration; + = low concentration; (+) = only trace detectable.

4.2.2.2 Other Constituents

Bayer et al. observed up to 0.3% choline [4, 5]. Choline is very likely to participate in the
antiphlogistic activity of total extracts and aqueous preparations (infusions, etc.).
Graner found 6 amino acids in chamomile herb [35]. In 1970, Schilcher succeeded in detecting
13 different amino acids in fresh chamomile herb by paper chromatography. It is likely that L-leucine,
DL-methionine, DL--alanine, glycine, L-histidine, and L-(+)-lysine are present, possibly also DLthreonine, DL-serine, and L-glutaminic acid [100]. Redaelli et al. found a nitrogenous component
without reporting a further characterization.

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5 Cultivation
Rolf Franke with cooperation of Jen Bernath, Tamer Fahmi,
Norberto R. Fogola, Dusan Jedinak, Hans-Jrgen Hannig,
Josef Holubr, va Nmeth, Viliam Oravec, Viliam Oravec,
Jr., Miroslav Repck, Lubomir Sebo, Ivan Varga, and
Eduardo Weldt S.
CONTENTS
5.1

Ecological Requirements
5.1.1 Origin and Areas
5.1.2 Soil
5.1.3 Flowering
5.2 Methods of Cultivation
5.2.1 Cultivation Procedure
5.2.1.1 Autumn Sowing
5.2.1.2 Spring Sowing
5.2.1.3 Cultivation of Several Years Duration by Self-Sowing
5.2.2 Nutrient Supply
5.2.3 Harvest
5.2.4 Cultivation in Specic Countries
5.3 Plant Selection and Breeding
5.3.1 Breeding Targets and Techniques
5.4 Other Species
References
5.5 Production of Chamomile (Matricaria recutita L.) in East and
South European Countries Jen Bernth and va Nmeth
5.5.1 Introduction
5.5.2 Production of Chamomile from Indigenous Populations
5.5.2.1 Distribution of Chamomile
5.5.2.2 Chemical Diversity of Wild Populations
5.5.2.3 Harvest of Wild Populations
5.5.3 Cultivation of Chamomile
5.5.3.1 Selection of Land
5.5.3.2 Cultivation Methods
5.5.3.3 Postharvest Processing
5.5.3.4 Cultivars
References
5.6 Cultivation Experiences in Slovakia Viliam Oravec, Viliam Oravec, Jr., Miroslav
Repck, Lubomir Sebo, Dusan Jedinak, and Ivan Varga
5.6.1 Introduction
5.6.2 Research, Breeding, Seed Growing, and Varieties
5.6.2.1 Research

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5.6.3
5.6.4

5.6.5

5.6.6

5.6.2.2 Breeding and Seed Growing

5.6.2.3 Varieties
Principles of Quality: Drug Description
Mechanization: Picking Technique and Picking Machines
5.6.4.1 Technique of Picking
5.6.4.2 Picking Machines
5.6.4.2.1 Technical Data
Plant Raw Material and Processing in Slovakia
5.6.5.1 Picking Conditions and Picking Methods
5.6.5.2 Postharvest Processing
Processing in Slovakia
5.6.6.1 Essential Oils
5.6.6.2 Extracts

References
5.7 Growing Varieties of Chamomile in the Czech Republic Josef Holubr
References
5.8 Experiences with the Cultivation of Chamomile in Argentina Norberto Fogola
5.8.1 Cultivation
5.8.1.1 Date of Sowing
5.8.1.2 Seed Amount
5.8.1.3 Row Distance
5.8.1.4 Germination Factors
5.8.1.5 Growth Factors
5.8.1.6 Soil Properties
5.8.1.7 Climate
5.8.1.8 Fertilizing
5.8.2 Weed and Pathogen Control
5.8.2.1 Herbicides
5.8.2.2 Insecticides
5.8.3 Yield Formation
5.8.3.1 Stage of Development and Content of Nutrients
5.8.3.2 Distribution of the Active Substances
5.8.4 Harvest and Processing
5.8.4.1 Time of Harvest
5.8.4.2 Yield
5.8.4.3 Harvest Methods
5.8.4.4 Seed Harvest
References
5.9 Chamomile in Chile: Cultivation and Industrialization Eduardo Weldt S
5.9.1 Botanical Considerations
5.9.2 Use
5.9.3 Cultivation
5.9.3.1 Sowing
5.9.3.2 Weed Control
5.9.3.3 Harvest
5.9.4 Final Products
References
5.10 Cultivation Experiences in Egypt Tamer Fahmi
5.10.1 Cultivation Regions
5.10.2 Cultivation Areas

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5.10.3
5.10.4
5.10.5
5.10.6

Cultivation Procedure
Insects that Infect the Plant and the Methods of Fighting Them
Cultivated Varieties/Types
Harvesting, Drying, and Preparation
5.10.6.1 Harvest Date
5.10.6.2 Harvest
5.10.6.3 Treatment after Harvest
5.10.6.4 Packaging, Storage, and Shipping
5.10.6.5 Production Quantity, Export Quantity, and Usage
5.11 Cultivation in Germany Rolf Franke and Hans-Jrgen Hannig
5.11.1 Introduction
5.11.2 Cultivation
5.11.3 Seed Production
References

5.1 ECOLOGICAL REQUIREMENTS

5.1.1 ORIGIN

AND

AREAS

The actual origin of Matricaria recutita L. is the Near East and south and east Europe. The species
is to be found almost all over Europe, in western Siberia, Asia Minor, the Caucasus Mountains,
Iran, Afghanistan, and India. After its introduction it also became common in North America, South
America, New Zealand, and Australia [83]. It even appears in the coat of arms of Pehuaj (a
provincial town in the Pampas about 500 km southwest of Buenos Aires), although chamomile is
not found in a botanical statement containing the medicinal plants of Argentina found.
Good proof of the existence of chemodems has meanwhile been given. With regard to the
sesquiterpene alcohols, original forms mostly show bisabololoxides. A form rich in ()-bisabolol
could be found in Spain. Nowadays the origin of chamomile owers from wild collections can
easily be determined by means of the chemical composition [26, 77, 80, Table 5.1.1].
Types rich in bisabolol are to be found endemically in Catalonia/Spain [14]:

Bisabolol oxide A types originate from Egypt and central Europe (e.g., Hungary, Czech
Republic, Slovakian Republic).
Bisabolol oxide B types are from South American collections.
Bisabolone oxide A types originate from southeast Europe and Turkey.
Types poor in or free of matricine are to be found in Egypt, the Balkans (Romania and
parts of Bulgaria), and Turkey; the types growing there are mostly those with yellowishgreen oil [77].
The composition of essential oil is obviously to a higher degree genetically determined
than oil content. The oil content is more strongly inuenced by environmental factors
and shows considerable variation, even within a relatively small area (see Reference 89).

As a very high percentage of the material comes from cultivation, the required types are
cultivated in various regions of the world, depending on what is needed.

5.1.2 SOIL
As far as the location is concerned, True chamomile is extremely tolerant and modest. It grows
equally well in light and heavy soils of different scopes of reaction (from sour to neutral-alkaline).
Wild locations are often sandy to loamy, mostly sour elds and fresh ruderal places. Salty soils

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Identity
number

Origin or type

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

Density

Optical
rotation

Chemical
type or
comment

Ref.

Bulgaria

Bulgaria

82.0
77.6

81.9
77.5

0.1
0.1

13.6
13.1

1.5
1.3

66.8
63.1

0.1
0.1

11.2
12.2

7.5
12.0

0.59
0.60

[70]
[70]

Mexico

84.9

81.4

3.5

68.0

5.8

7.6

2.0

4.2

9.1

0.99

[70]

I-chamomile

86.5

84.4

2.1

73.4

6.0

5.0

1.0

3.4

9.1

0.91

[70]

II-chamomile

86.8

84.8

2.0

74.4

5.2

5.2

1.0

3.0

9.2

0.98

[70]

76.0

73.5

2.5

60.4

5.8

7.3

9.7

5.1

9.5

0.76

[70]

77.7

75.5

2.2

64.0

5.8

5.7

9.8

3.1

10.1

0.94

[70]

Bohemian
chamomile c
Bohemian
chamomile K
Egypt Type Art

81.9

79.6

2.3

65.5

8.6

5.5

3.5

3.4

11.5

0.90

[70]

Egypt Type HH

82.0

77.6

4.4

61.5

8.5

7.6

3.4

4.3

10.4

0.80

[70]

10

Egypt Type M77

81.6

78.8

2.8

64.6

7.4

6.8

2.1

5.5

10.2

0.88

[70]

11

Egypt

81.4

76.3

5.1

64.6

5.9

5.8

2.8

4.2

12.0

0.94

12

gypten

13

gypten

14

Egypt

15

Africa

16

Yemen

17

India

18

Japan

19

Frankonia

20

Self-cultivation

21

Czechoslovakia

22

Czechoslovakia

23

Bohemia

24

Hungary Variety I

60.0
63.3
63.3
48.9
71.5
67.7
61.6
42.9
58.3
48.1
56.0
78.4
58.9

50.5
55.8
56.0
41.2
64.4
51.7
57.2
30.9
50.5
40.6
48.1
66.7
50.6

9.5
7.5
7.3
7.6
7.1
16.0
4.4
12.1
7.8
7.5
7.9
11.8
8.3

44.2
49.5
50.2
36.5
58.9
36.0
52.0
22.4
40.9
35.9
35.7
53.9
40.7

6.3
6.3
5.8
4.8
5.6
15.7
5.2
8.5
9.6
4.7
12.3
12.8
9.9

6.6
4.2
10.3
8.0
2.6
11.3
5.9
6.7
7.6
8.8
6.0
10.5
7.5

0.85
0.80
0.80
0.65
0.95
0.65
0.40
0.75
1.00
0.80
0.70
0.80
1.00

Copyright 2005 CRC Press, LLC

2.7
3.3
6.3
2.4
2.6
8.9
0.0
11.3
2.7
11.1
8.6
8.7
15.2

2.4
5.5
5.0
2.8
4.7
6.6
0.3
10.7
4.1
7.5
6.1
6.4
14.8

[70]
A
A
A
A
A
A
A
A
A
A
A
A
A

[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]

TF4015_C005.fm Page 80 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23])

39.2
47.4
39.2
48.4
39.7
34.8
32.1
39.6
61.0
37.7
46.4
42.3
41.9
20.1
33.1
41.3
81.5

5.8
15.4
13.1
8.1
7.2
6.4
7.7
8.8
12.9
9.8
11.4
14.0
16.2
8.5
19.6
15.0
4.0

30.8
32.
25.2
39.1
31.7
26.2
23.8
5.3
8.8
6.6
7.2
24.2
16.1
10.4
23.1
23.4
67.5

8.3
15.0
14.1
9.3
8.0
8.6
8.3
34.3
52.3
31.1
39.1
18.1
25.8
9.6
10.0
18.0
7.5

6.5

17.7
5.4
9.5
6.7
13.4
10.7
8.6
6.5
5.4
8.0
6.7
3.7
1.9
3.0
7.1
7.9
5.0

Argentina

84.5

81.0

3.5

66.0

10.0

5.0

5.0

0.75

[80]

43

Bulgaria

85.1

85.0

0.1

13.5

1.5

70.0

0.1

0.60

[80]

44

Germany

81.5

71.5

10.0

54.0

15.0

2.5

16.5

0.80

[80]

45

Yugoslavia

76.8

64.8

12.0

25.8

31.5

7.5

19.0

0.90

[80]

46

Mexico

86.1

86.0

0.1

75.0

6.0

5.0

0.1

0.95

[80]

47

Czechoslovakia

82.5

79.5

3.0

65.0

7.0

7.5

12.5

0.80

[80]

48

Turkey

92.0

92.0

0.0

23.5

3.5

65.0

0.0

0.75

[80]

49

Hungary

84.5

77.0

7.5

63.5

8.0

5.5

10.0

0.85

[80]

50

Czechoslovakia

71.0

70.0

1.0

56.0

10.5

3.5

25.0

1.00

[80]

51

GDR

79.5

78.5

1.0

35.5

40.0

3.0

16.5

0.90

[80]

52

Poland

68.5

67.5

1.0

40.0

20.0

7.5

25.0

1.10

[80]

53

Hungary

67.5

65.0

2.5

52.0

8.0

5.0

27.5

1,00

[80]

54

Germany, Marburg
1974/1975

54.9

53.1

1.8

33.5

13.4

6.2

16.6

0.80

[80]

Hungary Variety II

26

Poland

27

Frankonia

28

Bohemia

29

Hungary Variety B1

30

Hungary Variety B2

31

Poland

32

Argentina

33

Argentina

34

Argentina

35

Buenos Aires

36

Yugoslavia A

37

Brazil

38

Yugoslavia B

39

Yugoslavia E

40

Poland

41
42

Copyright 2005 CRC Press, LLC

17.1
5.9
10.3
7.5
13.5
10.4
0.0
8.1
7.7
4.1
0.0
2.1
2.3
3.2
2.9
6.8

9.2
9.3
4.8
5.7
5.2
4.4
5.0
4.8
4.1
9.9
9.8
10.7
9.2
10.3
5.5
9.5

14.1

11.0

1.00
0.42
0.36
0.52
0.78
0.66
0.40
0.80
0.70
0.45
0.38
0.35
0.60
0.32
0.23
0.60
0.85

A
A
A
A
A
A
A
B
B
B
B
D
D
D
D
D

[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]
[80]

TF4015_C005.fm Page 81 Friday, April 8, 2005 2:23 PM

Egypt

44.9
62.8
52.3
56.5
46.9
41.2
39.8
48.4
74.0
47.5
57.7
56.2
58.1
28.5
52.7
56.3
85.5

25

Identity
number

Origin or type

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

Density

Optical
rotation

Chemical
type or
comment

Ref.

70.6

69.8

0.8

59.8

3.1

6.9

8.1

11.5

8.1

0.80

[80]

74.1

65.9

8.2

54.3

4.6

7.0

4.3

6.5

14.0

0.90

[80]

62.6

60.1

2.5

49.2

9.3

1.6

2.9

12.2

20.7

0.75

[80]

74.6

71.2

3.4

65.4

4.9

0.9

1.8

7.7

15.2

0.90

[80]

67.7

65.8

1.9

20.3

44.7

0.8

6.1

8.3

16.2

1.00

[80]

60

Germany,
Rauischholzhausen
1975
Germany, KrefeldNiederrhein 1975
Germany, Oldenburg
1975
Germany, Berlin
1974/1975
Italy, Modena
1974/1975
Argentina 1975/1976

66.6

56.9

9.7

3.3

53.2

0.4

9.4

14.1

7.2

0.90

[80]

61

Argentina 1980

58.8

24.4

34.4

3.4

20.6

0.4

12.5

7.1

17.0

0.90

[80]

62

60.3

57.2

3.1

48.6

6.2

2.4

5.9

6.7

25.8

1.10

[80]

63

Germany,
Herrenberg
1979/1980
Chile 1974

25.0

22.6

2.4

5.3

12.4

4.9

7.3

2.1

45.1

0.60

[80]

64

Bohemia CSSR 1975

66.1

63.8

2.3

48.4

9.7

5.7

9.5

6.5

17.5

0.70

[80]

65

Turkey 1975

81.3

81.3

0.0

23.2

3.8

54.3

0.0

5.9

12.0

0.90

[80]

66

Hungary 1975

61.8

53.1

8.7

39.3

11.4

2.4

10.4

16.4

11.0

1.20

[80]

67

Bulgaria 1974

32.7

16.6

16.1

9.2

5.6

1.8

2.9

46.0

9.4

1.00

[80]

68

Argentina 1974

71.0

62.4

8.6

7.7

53.5

1.2

6.3

9.9

7.4

1.10

[80]

69

Argentina 1975

61.8

53.6

8.2

6.7

45.8

1.1

6.5

14.1

11.5

0.80

[80]

70

Argentina 1979

63.2

54.6

8.6

5.6

47.7

1.3

7.0

10.5

7.0

0.80

[80]

71

Bodegold 1975

72.9

71.6

1.3

32.2

34.6

4.8

11.3

4.2

11.3

1.00

72

Egypt

73

Egypt

39.1
43.3

36.7
40.8

2.4
2.5

27.0
29.0

4.2
5.8

5.5
6.0

2.8
1.5

20.0

2.7
6.0

55

56
57
58
59

Copyright 2005 CRC Press, LLC

[80]
A
A

[12]
[12]

TF4015_C005.fm Page 82 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23]) (continued)

Egypt

75

44.0
42.9
37.6

40.5
40.7
22.3

3.5
2.2
15.3

30.4
30.5
19.8

4.7
4.5
2.5

5.4
5.7

2.2
2.4
4.3

15.8
16.3
0.0

2.5
4.0

76

A
A
A/V

[12]
[12]
[12]

77

26.5

25.9

0.6

3.9

2.9

19.1

1.7

31.2

3.1

[12]

78

31.0

14.8

16.2

5.5

6.1

3.2

2.9

0.0

2.8

[12]

23.7

22.7

1.0

7.4

6.6

8.7

7.0

17.3

5.2

Bisabolono
xid-type
Bisabololtype
V

80

17.9

10.9

7.0

5.2

3.3

2.4

3.2

39.2

1.8

[12]

81

15.8

10.0

5.8

5.2

2.9

1.9

3.6

39.6

2.0

[12]

82

18.0

16.9

1.1

3.6

5.8

7.5

4.8

28.6

2.2

[12]

83

14.3

5.4

8.9

3.2

2.2

2.8

22.0

1.2

[12]

84

15.2

13.9

1.3

10.0

3.9

8.2

35.0

3.8

[12]

85

3.0

0.3

2.7

0.3

0.0

0.0

[12]

86

10.5

6.4

4.1

5.7

0.7

90

Degumille

20.5

2.1

18.4

0.6

1.3

0.2

3.6

0.7

91

Degumille

43.2

10.7

32.5

4.1

5.4

1.2

14.2

2.8

92

Degumille

25.1

5.2

19.9

1.7

2.8

0.7

5.9

36.6

1.6

93

Degumille

32.8

6.8

26.0

3.0

3.5

0.3

11.3

16.7

8.5

94

Fresh owers

41.0

7.7

33.3

2.7

5.0

7.8

19.8

[13]

95

Drug

37.3

9.4

27.9

2.8

6.6

2.1

36.4

[13]

96

Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)

0.0

0.0

0.9096

0.0

0.0

0.9171

1.5031

[3]

0.0

0.0

0.9152

1.5032

[3]

10.4

2.8

79

97
98
99

Balkan

Copyright 2005 CRC Press, LLC

7.6

2.8

0.2

4.7

45.4

0.898

[12]

[12]

Bisabololtype
Bisabololtype
Bisabololtype
Bisabololtype

[12]
[12]
[12]
[12]

[3]

[3]

TF4015_C005.fm Page 83 Friday, April 8, 2005 2:23 PM

74

Identity
number
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114

Origin or type
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Bulgarie (Adrian)
Chamomile Bleue
Egypte
Chamomile Bleue
Egypte
Chamomile Bleue
Egypte
Chamomile Bleue
Bulgarie
Chamomile Bleue
Bulgarie
Chamomile Bleue
Bulgarie
Chamomile Bleue
Bulgarie
Chamomile Bleue
Bulgarie
Chamomile Bleue
Bulgarie
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

Density

Optical
rotation

Chemical
type or
comment

Ref.

8.2

6.2

2.0

6.2

4.1

45.8

0.898

[3]

8.4

6.5

1.9

6.5

4.0

41.2

0.901

[3]

8.4

3.6

4.8

3.6

5.8

45.6

[3]

7.1

3.3

3.8

3.3

5.9

48.0

[3]

31.5

29.0

2.5

29.0

1.5

20.0

[3]

33.9

30.4

3.5

30.4

2.2

15.8

[3]

32.7

30.5

2.2

30.5

2.4

16.3

[3]

8.4

7.4

1.0

7.4

7.0

17.3

[3]

12.2

5.2

7.0

5.2

3.2

39.2

[3]

11.0

5.2

5.8

5.2

3.6

39.6

[3]

4.7

3.6

1.1

3.6

4.8

28.6

[3]

12.1

3.2

8.9

3.2

2.8

22.0

[3]

11.3

10.0

1.3

10.0

8.2

35.0

[3]

38.2

36.2

2.0

36.2

4.3

23.6

0.952

[3]

45.2

43.1

2.1

43.1

3.0

20.8

0.954

[3]

Copyright 2005 CRC Press, LLC

TF4015_C005.fm Page 84 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23]) (continued)

116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133

Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)
Chamomile Bleue
Egypte (Adrian)

Copyright 2005 CRC Press, LLC

44.8

42.7

2.1

42.7

3.9

20.3

0.9631

1.5068

[3]

44.5

42.4

2.1

42.4

3.9

19.4

0.962

1.5093

[3]

43.9

41.9

2.0

41.9

2.8

23.3

0.958

43.2

41.6

1.6

41.6

2.7

25.4

0.954

46.3

44.7

1.6

44.7

3.6

19.0

0.963

[3]

45.9

44.1

1.8

44.1

2.8

19.7

0.961

[3]

43.3

41.7

1.6

41.7

2.9

19.5

0.961

[3]

45.9

43.6

2.3

43.6

2.6

19.6

0.961

[3]

34.4

32.2

2.2

32.2

3.2

26.0

0.946

1.5063

[3]

41.2

39.2

2.0

39.2

3.1

24.2

0.950

1.5050

[3]

35.7

33.6

2.1

33.6

2.4

24.7

0.948

1.5030

[3]

40.2

38.1

2.1

38.1

3.0

20.8

0.957

1.5050

[3]

40.3

38.2

2.1

38.2

2.8

22.1

0.956

1.5050

[3]

35.5

33.4

2.1

33.4

2.8

26.8

0.946

1.5050

[3]

38.3

36.0

2.3

36.0

3.0

23.3

0.955

1.5064

[3]

46.2

44.0

2.2

44.0

4.1

19.2

0.963

1.5068

[3]

42.0

40.0

2.0

40.0

2.8

19.3

0.959

1.5062

[3]

47.1

45.0

2.1

45.0

4.3

20.3

0.958

1.5062

[3]

46.3

44.2

2.1

44.2

4.2

20.1

0.962

1.5084

[3]

[3]
1.5050

[3]

TF4015_C005.fm Page 85 Friday, April 8, 2005 2:23 PM

115

Identity
number
134

135

136
137
138
139
140
141
142
143
144
145
146

Origin or type
Chamomile oil,
Germany 304093
March 1994
Chamomile oil,
Germany 324509
July 1994
Dragoco, 1996, lab
sample
Dragoco, 1984, prod.
Batch
Dragoco, 1984,
Argentina I
Dragoco, 1984,
Argentina II
Dragoco, 1984,
Egypt, Kato
Dragoco, 1984, prod.
Batch
Dragoco, 1980, prod.
Batch
Dragoco, 1978, prod.
Batch I
Dragoco, 1978, prod.
Batch II
Dragoco, 1975, prod.
Batch
KMI-R99-1

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

Density

Optical
rotation

Chemical
type or
comment

Ref.

39.5

34.7

4.8

8.8

24.2

1.7

4.7

25.8

2.9

[36]

39.9

34.9

5.0

9.4

24.0

1.5

4.2

25.1

3.2

[36]

66.6

66.1

0.5

23.4

2.9

0.0

[36]

37.3

32.3

5.0

6.1

21.3

5.4

[36]

40.2

35.5

4.7

5.6

22.9

0.0

[36]

38.3

33.9

4.4

7.7

25.2

0.0

[36]

53.4

51.3

2.1

3.1

22.7

0.0

[36]

43.0

15.7

27.3

15.7

18.9

0.0

[36]

46.3

40.0

6.3

6.8

22.6

0.0

[36]

49.0

42.5

6.5

11.5

7.5

0.0

[36]

41.5

35.0

6.5

10.0

8.0

0.0

[36]

35.0

29.0

6.0

5.0

24.0

4.0

[36]

62.0

61.6

0.3

13.0

2.3

19.7

Copyright 2005 CRC Press, LLC

52.4

4.4

4.8

0.66

Distilled
from the
drug

[11]

TF4015_C005.fm Page 86 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23]) (continued)

KMI-R99-2

50.5

1.5

49.0

0.3

1.1

0.0

14.4

3.2

26.0

0.55

148

KMI-R99-3

55.2

54.7

0.5

17.4

25.0

12.3

12.7

1.7

22.6

0.43

149

KMI-R99-4

49.6

5.6

44.0

0.6

5.0

0.0

19.6

2.2

22.6

0.25

150

KMI-R99-5

59.0

0.9

58.1

0.9

0.0

0.0

17.3

3.8

14.4

0.38

151

KMI-R99-6

59.8

59.8

0.0

42.3

12.9

4.6

10.6

2.9

16.3

0.53

152

KMI-R99-7

52.5

13.9

38.6

5.7

7.8

0.5

19.3

2.9

20.0

0.40

153

KMI-R99-8

53.6

53.3

0.4

29.8

11.9

11.7

13.2

2.1

24.3

0.51

154

KMI-R99-9

49.6

8.1

41.5

3.8

4.3

0.0

14.0

3.6

27.8

0.62

155

KMI-R99-10

49.9

9.3

40.5

1.8

7.5

0.0

18.1

4.7

23.3

0.49

156

KMI-R99-11

48.5

11.6

36.9

7.8

3.5

0.4

17.6

4.4

23.2

0.54

157

KMI-R99-12

60.4

56.6

3.8

46.3

6.8

3.5

11.2

3.2

21.2

0.27

158

KMI-R99-13

56.9

3.8

53.1

2.1

1.7

0.0

10.4

2.7

24.5

0.47

Copyright 2005 CRC Press, LLC

Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

TF4015_C005.fm Page 87 Friday, April 8, 2005 2:23 PM

147

Identity
number

Origin or type

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

159

KMI-R99-14

56.0

55.4

0.5

33.0

11.9

10.6

15.2

2.6

21.4

0.53

160

KMI-R99-15

47.6

3.9

43.7

0.3

3.6

0.0

14.7

4.9

27.7

0.46

161

KMI-R99-16

51.9

3.4

48.5

0.0

3.4

0.0

15.8

3.1

24.9

0.40

162

KMI-R99-17

48.2

0.0

48.2

0.0

0.0

0.0

20.9

2.7

20.4

0.30

163

KMI-R99-18

54.6

54.2

0.4

25.7

18.6

9.9

12.0

1.9

24.1

0.60

164

KMI-R99-19

50.6

48.4

2.1

16.2

20.9

11.4

13.9

1.8

27.0

0.50

165

KMI-R99-20

64.1

63.0

1.2

48.8

9.9

4.3

10.2

2.7

19.6

0.49

166

KMI-R99-21

55.2

45.7

9.6

25.5

18.1

2.1

8.2

5.4

25.6

0.43

167

RP KMI 2000-1

65.8

63.0

2.7

42.7

15.7

4.6

11.3

2.3

13.5

0.36

Copyright 2005 CRC Press, LLC

Density

Optical
rotation

Chemical
type or
comment
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug

Ref.
[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

TF4015_C005.fm Page 88 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23]) (continued)

RP KMI 2000-2

46.6

1.4

45.2

0.0

1.4

0.0

21.3

2.2

25.0

0.27

169

RP KMI 2000-3

52.8

12.3

40.5

0.0

12.3

0.0

15.5

2.9

24.1

0.47

170

RP KMI 2000-4

66.0

57.6

8.4

41.9

12.1

3.6

10.7

3.1

17.9

0.50

171

RP KMI 2000-5

60.0

59.4

0.5

47.9

3.4

8.2

12.8

2.4

20.7

0.44

172

RP KMI 2000-6

55.2

1.4

53.7

0.0

1.4

0.0

18.4

2.4

19.4

0.27

173

RP KMI 2000-7

61.1

1.5

59.6

0.0

1.5

0.0

19.1

2.4

14.0

0.30

174

RP KMI 2000-8

59.1

45.0

14.1

23.2

19.9

2.0

10.1

6.3

21.5

0.25

175

RP KMI 2000-9

48.3

13.9

34.4

8.9

4.4

0.6

17.3

4.6

25.0

0.33

176

RP chamomile
2001-1

72.5

70.6

1.9

51.3

14.1

5.2

10.7

1.7

11.8

0.81

177

RP chamomile
2001-2

51.3

1.1

50.2

0.0

1.1

0.0

21.6

3.9

20.7

0.52

178

RP chamomile
2001-3

51.8

1.0

50.7

0.0

1.0

0.0

23.5

4.2

18.4

0.63

179

RP chamomile
2001-4

66.7

63.0

3.7

51.4

5.6

6.0

12.8

3.3

15.0

0.55

Copyright 2005 CRC Press, LLC

Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

[11]

TF4015_C005.fm Page 89 Friday, April 8, 2005 2:23 PM

168

Identity
number

Origin or type

BisaBisaBisaLevomenol bololbolol- bolonAmount Bisabolol (Bisabolol) oxide A oxide B oxide A

bisabolane -oxide
%
%
%
%

Chamazulene
%

Chamazulen%
spectralphotom.

-Farnesene
%

Spiroether
%

Total
amount
essential
oil%

180

RP chamomile
2001-5

62.1

0.6

61.5

0.0

0.6

0.0

21.2

3.0

12.0

0.43

181

RP chamomile
2001-6

56.8

56.8

0.0

51.7

5.1

0.0

15.9

2.5

16.8

0.68

182

RP chamomile
2001-7

69.9

63.7

6.2

38.1

22.4

3.2

9.6

4.9

14.8

0.58

183

RP chamomile
2001-8

57.1

15.5

41.6

9.9

5.0

0.5

20.6

3.4

17.3

0.58

184

RP chamomile
2001-9

56.1

11.1

45.0

4.7

6.4

0.0

18.0

3.3

20.4

0.63

Traces are given with 0.1% to be able to grade them.

n.d. or not detectable are given with 0.0.

Copyright 2005 CRC Press, LLC

Density

Optical
rotation

Chemical
type or
comment
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug
Distilled
from the
drug

Ref.
[11]

[11]

[11]

[11]

[11]

TF4015_C005.fm Page 90 Friday, April 8, 2005 2:23 PM

TABLE 5.1.1
Composition of Chamomile Oil (According to Frank, Data from Different References and Laboratories [23]) (continued)

TF4015_C005.fm Page 91 Friday, April 8, 2005 2:23 PM

like in the Hungarian Puzsta or in Argentina are duly tolerated. As a matter of fact, however,
chamomile has to be sown on a smooth and solidied eld to make sure that the ne seeds (thousand
kernel weight 0.02 to 0.06 g with diploid forms and 0.04 to 0.12 g with tetraploids) are not washed
in the soils due to rainfall. The soil should therefore be prepared on a at working level only; it
should duly settle before sowing is done and it should be solidied by means of a roller. The seeds
require a lot of humidity for germination and for a quick juvenile development.

5.1.3 FLOWERING
True chamomile owers over a longer period and produces new owers. For the cultivation this
is taken into consideration by a multiple harvest of owers. The owering time can last about
50 to 65 days. It takes about 20 to 35 days before a ower is fully developed. The relatively
short vegetation period of 150 to 180 days also allows a cultivation at higher altitudes up to 500 m.

5.2 METHODS OF CULTIVATION

Cultivation measures such as sowing time, fertilization, weed control, and harvest have to be
arranged in such a way that the yield properties and those of quality xed in the genotype ensure
an optimum development.

5.2.1 CULTIVATION PROCEDURE

In 1956 Heeger still reported that with respect to cultivation chamomile had been worked on to a
small extent only [40]. Over the past 40 years rapid development could be observed. Preference is
given to chamomile being cultivated. In most countries extensive eld cultivation with mechanized
sowing, nursing, harvest, and processing has gained acceptance [13, 28, 38, 75, 84]. In nearly all
companies specializing in cultivation, technological innovations have been tested and introduced
repeatedly. Often technological solutions are quite specic to the companies and having been
adapted to the locations and varieties were developed for the individual sections of production [62,
68]. Therefore, a compilation of a generally applicable sample technology does not seem to be
recommended. Some experiences from various countries of cultivation are shown in the paragraphs
to follow.
Presently three basic variants being mostly complementary to each other are applied:
autumn sowing, spring sowing, and cultivation of several years duration with self-sowing.
5.2.1.1 Autumn Sowing
In the Northern Hemisphere graduated autumn sowing is done at the end of the summer at an
interval of about 8 to 14 days, from the beginning to the end of September. A precondition is,
however, that the anticipated fruit is removed as quickly as possible. If sowing is done too early,
this leads to premature formation of shoots [16]. Both plants developed too far as well as those
that are too small die in winter. Chamomile should start the winter months at a stage of six to eight
leaves. At this stage it is denitely cold resistant. Autumn sowing means that the best yields are
achieved with the possibility of a long vegetative developmental and tillering phase within the
physiological short day. Being largely independent from the sowing time, the owering period
starts with an achieved day length of about 17 hours (in central Europe at the end of May/beginning
of June). Due to the fact that owering generally starts at the same time, the possible cultivation
area is strongly determined by the harvest and drying capacity. Even if chamomile is owering
over a longer period, producing new owers again and again temporarily, the rst harvest process
has to take place according to exact timing. Thoroughly ripening ower heads favor plant aging.
Overripe owers strongly tend to fall apart during the drying and preparation process after the

Copyright 2005 CRC Press, LLC

TF4015_C005.fm Page 92 Friday, April 8, 2005 2:23 PM

harvest [50]. Seeds dropping out mean a burden to the location in the years to follow, changing
the spectrum of active principles [18, 24, 30, 81].
5.2.1.2 Spring Sowing
The advantage of spring sowing is the possibility of graduated steps of cultivation in order to be
able to utilize the harvesting and drying technique to the maximum by temporally graduated harvest
dates. In central Europe it is a usual practice to start sowing in March at an interval of about 14
days. It is, however, a fact that the yield and the homogeneity of the populations decrease the later
sowing is done. The pressure of contamination by diseases and infestation by parasitic insects in
the course of the summer months increases just as well [21].
5.2.1.3 Cultivation of Several Years Duration by Self-Sowing
With extensive production, a cultivation of several years duration is possible on the same eld
considering that the population is being formed by the chamomile seeds that dropped out. Additional
seeds may also be sown. After the last economically justiable harvesting passage, the population
remains on the eld for a few more days and the plants are mulched. The next step is a non-turning
supercial soil preparation. From September onward the self-sown seeds germinate, which may be
compared with a thick carpet. This procedure is similar to broadcast sowing without a drilling
machine. The strong competitive capability of chamomile against weed, the possibility of utilizing
a harrow and a chain harrow or curry-comb for weed control, and thinning out make the procedure
a cheap alternative. Companies particularly in Germany, Argentina, Hungary, and in the Czech
Republic have practiced this procedure on the same eld for nearly ten years. In the total remaining
area the weed is reduced by taking the autumn chamomile from the crop rotation. The yields to
be expected and the other peculiarities of this procedure may be compared with those of the sowings
done in autumn. This form of cultivation is not recommended for the ower production of breeding
lines, especially with the cultivation of dened chemotypes, because of the uncontrolled procedure
of the pollination as a germination of wild (i.e., nonbred) chamomile or a segregation with hybrid
seeds may occur in the following year.
Especially with autumn sowing slightly humid locations are more favorable than regions
with plenty of summer rains where chamomile tends to have a luxurious growth of herb and
leaves; consequently it is less suitable for being harvested and shows a lower content of active
principles. The development of chamazulene substantially depends on the duration of sunshine
and the day temperatures from the time of the formation of ower buds.
It is reported repeatedly that chamomile is self-compatible [16, 19]. Experiences regarding
cultivation of several years duration and self-sowing point in the same direction. Precise indications concerning the value of different fruit rotations are missing but it is a fact that chamomile
grows particularly well in elds free from weed; viz., after root crops such as potatoes and sugarbeet, maize, winter cereals, and leguminosae. Using elds for the production of chamomile for
several years has also proved to be a success. Chamomile should generally be cultivated as nal
crop in the rotation without any N-fertilization. A high content of Nmin in the soil leads to strong
vegetative growth, makes the harvest more difcult, and can nally also lead to a lower content
of active principles. Weeds cause problems for the cultures to follow. First of all a nonturning
supercial soil preparation should in any case take place after the chamomile cultivation to
stimulate the germination of chamomile seeds dropped out, to be followed by mechanical weed
control in autumn. In course of the following year a culture is started after refertilization, being
tolerant against herbicides combating chamomile.
Chamomile particularly absorbs the heavy metal cadmium from the soil [78], at least it
concentrates due to the mobility in the owers like with other ower drugs, e.g., St. Johns wort

Copyright 2005 CRC Press, LLC

TF4015_C005.fm Page 93 Friday, April 8, 2005 2:23 PM

TABLE 5.2.1
Maximum Tolerable Content of Cadmium for Soils Planned for the
Production of Chamomile in Central Europe (According to Plescher
[66], Cd Maximum Value for Matricariae flos 0.2 mg/kg)
pH Value of the Soil

Max. Cd Content of the Soil in mg Cd/kg Soil, Dry Matter

Spring Sowing

Autumn Sowing

0.13
0.16
0.20
0.27
0.42

0.20
0.24
0.29
0.36
0.49

5.5
6.0
6.5
7.0
7.5

and owering yarrow herb [67, 72]. As long as the maximum value of 0.2 mg Cd/kg of drug
a recommendation of the German Federal Ministry of Health since 1991 is applicable, the
maximum soil values indicated in Table 5.2.1 may be used for the choice of the location,
depending on the individual pH value and on the method of cultivation [66]. If there are critical
soil values a trial cultivation should always be used to determine whether the location is suitable.

5.2.2 NUTRIENT SUPPLY

Although chamomile is a nitrogen-loving plant species, it is, in view of the harvest mechanization,
seen that when cultivating it the soil only contains small amounts of Nmin and mostly it is done without
any N-fertilization whatsoever [87]. Otherwise moist and leafy populations with a delayed ower
maturity or endless owering develop and with the application of harvest technique the speciestypical appearance of foreign matter (percentage of leaves and stems) increases. Table 5.2.2 gives a
general idea of recommendations for fertilization with respect to the cultivation of chamomile.
For the development of active principles, a good owering, and sufcient rmness of stems, a
good potassium supply is necessary [29]. On the other hand chamomile is delicate with regard to
excessive quantities of P2O5. According to Franz and Kirsch [32] the nutrient ratio of nitrogen:potassium oxide should be 1:2. Fertilization by using potassium and if necessary also nitrogen takes
place during the tillering phase, i.e., in October (at the Northern Hemisphere) or April (at the

TABLE 5.2.2
Recommendations for Fertilization Concerning the
Cultivation of Chamomile in kg/ha

Heeger [39] 1956

Schrder [82] 1965
Fink [22] 1978
Ebert [19] 1982
Ruminska [74] 1983
Traxl [88] 1986
Dachler, Pelzmann [16] 1989
Bomme, Nasta [8] 1998
Bernath [7] 1993
a

Nutrient uptake.

Copyright 2005 CRC Press, LLC

P205

K 2O

3040
4080
6080
2050
4050
30
40
17a
4060

4060
3645
2030
3050
5060
50
50
8a
4060

120140
80120
70100
100150
6080
80
100
22a
5070

TF4015_C005.fm Page 94 Friday, April 8, 2005 2:23 PM

Southern Hemisphere) when sowing in autumn; if sowing is done in spring it takes place at a
correspondingly later date. Organic fertilizers should by no means be used for chamomile, as the
limits of microbial contamination could easily be exceeded. Organic fertilizers may only be used
for the anticipated fruit.
With extensive cultivation the recommendations for fertilization based on Nmin values ascertained are the basis for the determination of fertilizer requirements pertaining to the elds. The
deprivation of nutrients has become the basis of fertilization to an increasing extent [65, 72]. (See
Table 5.2.3.)

5.2.3 HARVEST
Even though chamomile is cultivated throughout the world, the collection from wild populations,
particularly in central, eastern, and southern Europe, Greece, and Turkey has not lost its importance.
There is a difference between pure wild collection as in Greece and Turkey and the organized
harvest of wild populations, as is the case in Hungary for about 95% of the whole harvested quantity.
From such wild collections or small cultivations and in gardens, chamomile is harvested at the
period of full owering, i.e., when most owers are already open. Today, cultivation areas are
mainly harvested automatically, although partly manual harvesting is still being practiced as well.
The harvest schedule plays an important role with regard to the quality of the product. Harvest
of cultivated chamomile should be realized in the same way as for wild populations, i.e., when the
major part of the owering heads has already opened. The essential oil content of inorescence

TABLE 5.2.3
Deprivation of Nutrients by Chamomile Flowers and Flowering Herb as well as Nutrient
Content of the Herb Residues (According to References 48, 66, 72) (The deprivation
of nutrients pertaining to the area is based on an average drug yield of 500 kg flower
drug/ha.)
Plant nutrients
N
Chamomile flowers, fresh
Nutrient content kg/t fresh
kg nutrient in 3 t fresh material (kg
nutrient/ha)

P2O5

K2O

Mg

MgO

4.2
12.6

0.9
2.7

2.1
6.3

4.5
13.5

5.4
16.2

0.4
1.2

0.6
1.8

21.829.3

4.54.9

12.6

23.429.8

32.4

2.22.4

3.6

10.914.6

2.22.4

6.3

11.714.9

16.2

1.11.2

1.8

Flowering chamomile herb, fresh

Nutrient content kg/t fresh

3.0

0.4

0.9

4.1

5.0

0,4

0.7

Flowering chamomile herb, dry

Nutrient content kg/t drug

9.118.6

1.92.6

5.9

24.725.8

31.1

1.22.7

4.5

Herb without flowers, fresh

Nutrient content in kg/t fresh

2.6

0.4

0.9

4.4

5.3

0.4

0.7

Herb without flowers, dry

Nutrient content in kg/t drug

16.3

2.5

5.7

27.6

33.3

2.7

4.5

Chamomile flowers, dry

Nutrient content
kg/t drug
kg nutrient in 500 kg drug
(kg nutrient/ha)

Copyright 2005 CRC Press, LLC

TF4015_C005.fm Page 95 Friday, April 8, 2005 2:23 PM

increases continuously starting from the creation of owers and achieves its maximum when the
ligulate owers are in a horizontal position (see Section 5.5). As per Rhricht et al. [72] harvest
is realized from the starting of the owering period up to the period of full owering, whereas two
or three pickings are effected. As per Dachler and Pelzmann [17] the optimal time for harvest of
the owers is when a circle of tubular orets has already opened in the second third of the vaulted
owering receptacle.
In order to create an objective base for the determination of the optimal harvest time and not
leaving this matter to the cultivators intuition, the German Working Committee for Cultivation of
Medicinal Plants proposed the following owering index formula in the years 1971, 1972, 1973,
1977, and 1979. It is a compromise between an increasing yield of owers, a decreasing content
of essential oil, and changes in the composition of the essential oil [4, 30].
flowering index =

V Kn
Kn + eB + V

Kn = ower buds not yet ourished

eB = owers ready to be harvested (ourished tubular owers + ligulate owers)
V = withering owers
With this formula the point of time for harvest of the owers is calculated from the relation of
the number of withering owers minus ower buds to the total amount of owers (ower buds +
owers ready to be harvested + withering owers). The rst picking should take place when the
owering index reaches a value of 0.3 to 0.2. As the owering period depends on the location,
climatic conditions, and the variety of the ower and therefore ranges between several weeks up
to 3 months (according to [19] eight to ten manual picking cycles are possible), this formula is a
good way to determine the corresponding optimal time for harvest. In practical applications harvest
takes place two or in rare cases three times.
In 1985 Franz [27] proposed the following owering index formula:
IK =
IK
I
II
III
IV

=
=
=
=
=

IV I
= 1 < IK < +1
I + II + III + IV

Indexchamomile
ower buds
owers ready to be harvested with a 50% open tubular owers
owers ready to be harvested with more than 50% open tubular owers
withered, decomposed owering heads

The realization of the harvest of the owering heads can take place in different ways, whereas
the most labor-intensive method is manual picking. This manual picking is carried out in most
countries only for small cultivation areas; in Egypt, however, it is still very popular and is applied
almost exclusively (Figure 5.2.1).
Picking yield of freshly harvested short-stemmed chamomile owers is about 3 to 5 kg/h.
Slightly higher picking amounts can be obtained already with so-called chamomile picking combs.
Today they are used (e.g., in Hungary) above all for organized harvest in wild populations, and
have a capacity of about 50 to 150 kg fresh per day (see also Section 5.5).
Such a harvest with chamomile picking combs has already been carried out in Hungary well
into the 1970s, as well for harvest on cultivated elds. Due to the higher plant and ower density,
the picking yield was about 100 to 180 kg per day. Other procedures were the use of special forks

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FIGURE 5.2.1 Handpicking in Egypt.

or comb shovels, applied in Hungary, similar to a scythe for harvesting the chamomile crop (Figures
5.2.2 and 5.2.3).
Finally, such manual methods are not practicable above all due to the labor time requirement
of about 25 to 30 working days per ha for the production of larger quantities. This problem had

FIGURE 5.2.2 Comb shovel.

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FIGURE 5.2.3 Harvest with comb shovels in Hungary.

FIGURE 5.2.4 Manually pushed picking cart.

to be solved through construction of mechanized harvesting machines. A rst step in this direction
was the use of manually pushed picking carts with two wheels (Figures 5.2.4 and 5.2.5).
Later on these picking carts were drawn by horses or tractors, which above all were applied
in Argentina and again increased the yield per area.
Today the large-area industrial cultivation of chamomile worldwide uses automatic harvesting
techniques with a picking yield of 200 to 300 kg/h and a capacity of about 3.5 ha per day, whereby
(dependent on climate and crop-specic conditions) about 65 to 90% of all owers are harvested.
Since 1962 in Germany [19, 20] and since approximately 1975 as well abroad (e.g., in Argentina
and Hungary), chamomile picking machines were used that pick the owering heads on the eld
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FIGURE 5.2.5 Manually pushed picking carts in Argentina.

automatically and are self-propelling, as a cutter mounted in the front part of a tractor (see also
Oravec et al., Chapter 5.6) or as combined harvesters (Figures 5.2.6 and 5.9.3).
For a competitive production of ower drugs a decrease of the high labor time requirement for
the harvest is essential, whereby particular importance has to be attached to the outer quality of
the harvested owers. The demands on the harvest quality are high. The adherent stalk rests have
to be as short as possible and the impurities of herb and other constituents the lowest possible.
This can be achieved safely by manual picking. Such important countries of production as Italy
[1, 5, 6], Argentina, Hungary [9], Russia [2], former Yugoslavia [9, 52], former Czechoslovakia
[45], and former GDR [42, 71, 73] have developed and applied high-capacity harvesting machines
with different picking systems.

FIGURE 5.2.6 Harvester.

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Automatic harvest is to be carried out successfully in the case of a large-owered chamomile

variety, having their owering heads almost at one level. The major part of the commercial drug
originates from this automatic ower harvest, which entails Pharmacopoeias monographs of chamomile owers, describing chamomile to only sometimes have stem rests of 10 to 20 mm [79], are
not applicable. If the harvested material is not processed after automatic harvesting, it is impossible
to avoid stem rests with a length of 20 to 30 mm. With a corresponding postprocessing however, it
is possible to produce chamomile of pharmaceutical quality. These not sometimes but almost always
existing stem rests of 20 to 30 mm in length in no way disturb the medical benet, insofar as the
owering head disposes of the required content of ingredients. Consequently this should appear in
the Pharmacopoeias monographs as reality and therefore should be allowed [80].
Flourishing herb for production of Chamomillae herba cum floribus, that can be used for the
production of tea in lter bags, mostly is harvested by the help of rotary mowers, forage harvesters,
chaff cutters with blower, or combined harvesters [17, 19]. To obtain extraction quality for pharmaceutical use, the whole owering heads are preferably harvested automatically. In this case, a
posterior separation of stem rests is not necessary.
Another harvesting principle represent the machine developed in Argentina. Drums equipped
with blades are used here. They run top down against a comb and shear the chamomile owers.
Here as well, industrial chamomile is preferably harvested due to the long ower stems. This
principle of the rotating blades primarily has been developed for trailer machines that are drawn
sideways behind the tractor. Later on these machines were developed further to self-propelling
combined harvesting machines.
A third principle of mechanized harvesting is the picking procedure with picking combs. Here,
machine widths of 2 to 6 meters of the width of the cutting unit are achieved. The picking drum
is equipped with shifted comb strips, whereby long round tines in a wide distance or shorter sharpedged tines with a lower interspace are used. The picking drum rotates against the driving direction,
whereas the combs pass through the crop from the bottom up and separate the owers from the
plants. Adherent stalk rests are cut off with a cutting machine. For further cutting of the stalk parts
the harvest is transported onto a swinging sieve with conveyor belts and then is collected in a silo.
This is the basic principle of the machine of Ebert-Schubert [20], the Hungarian machines type
Szilasmenti (see as well Section 5.5), the Slovakian machines type VZR (see as well Section
5.6), the Russian machines [2] and the machine Linz III, developed in the years 1972 to 1978
in the GDR [71, 73] and built until 1988 [56]; the Linz proved itself in various countries (including
Egypt), the quality and performance of which has not been achieved by other constructions so far.
This is due to contra blades operated by cam discs behind the comb strips, that in contrast to other
machines with picking combs lead mainly to an exact cutting of the owering heads and clearly
reduce the common tearing effect (Figure 5.2.7).
A fourth principle is the rotation of the picking drum in the driving direction, as realized with
the Yugoslavian machine [9, 52]. The chamomile herb is grasped by the tines and then drawn into
the machine. There, on the vaulted bafe plate a plant pad is formed that is repeatedly combed due
to the high-revolution speed of the threshing drum. The combing effect results from a shifted
arrangement of consecutive comb strips. The distance between the tines of the comb strips is wider
than the diameter of the owers and consequently inhibits a clogging of the picking drum.
The principle of immobile combs with appropriate separation of the owers from the plant,
e.g., by means of a modied scraper chain on top of the comb, similar to marigold harvesters [46]
has been realized in the Italian Chamaemelum harvester [5, 6].
Summarizing, it can be noted the best principle is a picking drum with comb strips rotating
against the driving direction. Unfortunately, at present there is no new, well-priced, and similarly
effective machine on the market (see also [38, 57, 58, 59, 60]).
For after-harvest treatment there are two possibilities. In countries with high availability of
manual work, e.g., Egypt, primarily drying is effected and afterward processing and sorting take
place. In this way, drying often is realized in racks, e.g., from palm fronds (in Egypt) or on frames

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FIGURE 5.2.7 Comb strips of the chamomile picking machine Linz III.

covered with gauze (as was used formerly on a large scale in Argentina). During daytime these
racks or frames are placed in the open air; at night they are piled (mostly) under the roof, in order
not to take up humidity. In Argentina after 1970, in the mornings workers brought daily 35,000
racks outside for sun drying and back to the stockrooms in the evenings. Temporarily during season
more than 5000 persons were occupied with harvesting and processing.
A further increase in production was only possible by use of modern picking machines. In
1974 the Argentine production amounted to 2000 tons. With such a high grade of mechanization
of harvesting and processing as in Argentina and Germany, sorting and sieving is effected automatically before drying. If need be, after drying short stem rests are separated in a further step.
That way, pure ower material is obtained. During season 60 to 80 tons of fresh plant material are
processed per day, running continuously through the sorting machines to the belt dryers or discontinuous atbed dryers and after drying are sorted by the help of transport conveyors and are freed
from weeds.
In Poland, which has become an important country for the production of chamomile drug in
recent years, such harvesting procedures are applied that by cutting the ower horizon after drying
by threshing, and separation by sieving and sifting, lead to a production of chamomile pollen and
industrial pollen.

5.2.4 CULTIVATION

IN

SPECIFIC COUNTRIES

Cultivation areas in the different countries vary greatly. In France approximately 100 ha of Roman
chamomile are cultivated, mostly used for perfumery. In Italy cultivation of Roman chamomile is
about 25 ha, of which 7 ha is organic, and 170 ha Matricaria recutita, of which about 100 ha is

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organic. From Sweden cultivation of 10 ha, from Austria cultivation of 15 ha, from BosniaHerzegovina 40 ha [47], Bulgaria 100 ha [47] of True chamomile, whereas in the United Kingdom
80 ha Roman chamomile and 120 ha Matricaria recutita are cultivated. In Spain plants are collected
rather than cultivated. This is the origin of the diploid bisabolol-rich form Degumill. In Brazil
the main production is concentrated in the southern region Mandirituba (Parana state).
Cultivation experiences in some counties are shown in the following sections:
Section 5.5: Production of chamomile (Matricaria recutita L.) in east and south European
countries
Section 5.6: Cultivation experiences in Slovakia
Section 5.7: Growing varieties of chamomile in the Czech Republic
Section 5.8: Experiences with the cultivation of chamomile in Argentina
Section 5.9: Chamomile in Chile: Cultivation and industrialization
Section 5.10: Cultivation experiences in Egypt
Section 5.11: Cultivation in Germany

5.3 PLANT SELECTION AND BREEDING

5.3.1 BREEDING TARGETS

AND

TECHNIQUES

The composition of the essential oil with varying percentages of bisabolol, bisabololoxide, bisabolone, and matricine is xed genetically [25]. Schick and Reimann-Philipp [76] remarked in 1957:
As far as breeding is concerned Matricaria Chamomilla has not yet been worked on. In 1950
only the two group varieties Quedlinburger Grobltige Kamille (Quedlinburg large-owered
chamomile) and Erfurter Kleinbltige Kamille (Erfurt small-owered chamomile) were mentioned [41]. Often the stability, the resistance against diseases, the germinability, the ower yield,
the fact that the individual ower heads are ripe at the same time, the homogeneous owering
horizon, the stability of the ower head, and consequently the suitability for a mechanical harvest
are not sufcient [42, 85]. Since then a rapid development has been experienced. A number of
chemotypes [80] with a varying content of matricine/chamazulene, ()--bisabolol, spiroethers,
and the bisabolol oxides A and B as well as bisabolone oxide A were selected. Varieties with very
different breeding targets were bred. The content, especially the composition of the active principles,
was worked on by precise selections [16, 32, 49, 80]. For nondestructive characterization of valuable
substances in chamomile single plants, a near-infrared (NIR) spectroscopical rapid method is
available [55].
Some of the present breeding targets are (sequence does not mean order of priority):

High yield
Large owers
Compact ower heads
Stability of the owers for a mechanical harvest with a low percentage of stems
Regular growth with basilar ramication and many owers (close proportion of
herb:owers)
Narrow homogeneous owering horizon
Uniform owering time, especially simultaneous ripening
Good shooting capacity for a high yield with the harvest to follow
Firm ower head with little inclination of disintegration and formation of nes
High content of chamazulene (blue oil) >25% within the oil
High content of ()--bisabolol >3050% within the oil
Low or much bisabololoxide

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High content of total avonoids >3%

High content of essential oil (0.7>1%)
Desirable composition of the essential oil
High germinability
Resistance against powdery mildew and other diseases
Stable stand

Particularly the working group led by Franz has made intense genetical investigations ([44, 53,
54] and others). By this research it was proved that medicinally relevant ()--bisabolol is inherited
recessively. The formation of the ()--bisabolol oxides A and B is dominant over ()--bisabolol,
whereas ()--bisabolone oxide A dominates ()--bisabolol as well as the ()--bisabolol oxide
A and B [33, 34]. This is veried by using PCR-based marker techniques like Random Amplied
Polymorphic DNAs (RAPDs) and Amplied Fragment Length Polymorphisms (AFLPs) as useful
tools for the acceleration and improvement of the breeding process [88].
Nowadays quite different forms are available to cover various demands. It should be taken into
consideration that not all results of these breeding works are admitted as varieties or not all of
them can be purchased but often individual rms use them for their internal cultivation to produce
special products. A short (incomplete) survey of released varieties and used breeding material is
given in Table 5.3.1, in Table 5.3.2 some of this breeding material is classied according to its
characteristics.
Most of these are realized in tetraploid varieties [10, 51]. When choosing the breeding place
as well as the company for seed multiplication and maintenance breeding, this should be done with
care. In case of a contamination of the soil by chamomile seeds (wild growing or cultivated
populations some years ago) a crossing of tetraploid and diploid chamomile takes place. A clear
separation by mere sifting of the (mostly) bigger tetraploid seeds is not possible. As a large amount
of chamomile seeds is found in the soil of the cultivation areas and as there is no reproductive
isolation in respect of wild chamomile, it is impossible to cover the next years seed requirements
from normal material of cultivation being mostly still the case with traded material from Egypt.
The multiplication of seeds has to be regulated by taking suitable steps of organization and
agrotechnical measures. For this purpose the basic material has to be produced from individual
plants by partly taking in vitro multiplication steps. The seeds on hand are more or less treated as
a hoe culture to make sure that no unwanted chamomile can contaminate the seeds. If the multiplication of seeds is done properly there is little danger of hybridization even with diploid chamomile, so that this supposed advantage of tetraploid chamomile does not seem to be relevant in the
main cultivation areas.
With the breeding at a diploid stage of valence, in Germany for instance, the rst step was a
selection on an early owering time on relatively shortened long-day terms. In the breeding pattern
individual plant selection from more than 10,000 plants of an Argentinean population in connection
with diallel crossings, backcrossings, and in vitro cloning was applied. By means of thin-layer
chromatography a preselection of plants of suitable qualitative composition was made. After the
in vitro phase the clones (adapted to substrate culture and recultivated) were planted on plots of
comparison at two places in four repetitions, then they were tested on susceptibility to diseases
and nally the oil content and the oil composition was determined. So the material could be
restricted to a great extent.
After the calculation of suitability for combination according to method II, model II, on the
basis of the parents and F1- descendants kept in tissue culture further seven diallel crossings of the
suitable clones were carried out, which were multiplied again by a tissue culture before. The
crossing partners ceased owering isolated from the other crossings. From each crossing about
15,000 plants could be cultivated, which were planted into elds of 500 m2 each with a distance
of normally several kilometers from each other. A hybridization of wild material was prevented by
protective sowings such as by a broad belt of maize or cereals and by control of the surrounding

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TABLE 5.3.1
Varieties and Breeding Material in Chamomile (Matricaria recutita L.)
Country

Variety/line

Austria

Manzana (4x)

Bulgaria

Lazur (4x)
Bisabolol
Sregez (17% chamazulene)

Brazil

Mandirituba

Chile

Manzanilla Primavera Puelche

Czech Republic

Bohemia (2x)
Bona (2x)
Goral (=Kosice II, 4x, high content oil, chamazulene, bisabolol)
Lutea (4x)
Novbona (2x)
Pohorelicky Velkosvety

France

MA.VS.1 (ca. 1% oil, 25% chamazulene, 45% bisaboloxid A/B)

Germany

(Leipzig)
Bodegold (4x)
Camoora (2x)
Chamextrakt (2x)
Degumill (2x)
Euromille
Mabamille (4x)
Manzana (4x)
Robumille (4x)

Hungary

Budakalszi 2 (=BK2,4x, high content oil, chamazulene)

Soroksari 40 (2x)

Italy

Minardi (2x)
Olanda (matricin)

Poland

Zloty Lan (4x, high content of oil, chamazulene, low bisabolol)

Tonia
Promyk (2x)

Rumania

Margaritar (4x)
Flora (4x)

Slovak Republic

Bona (2x)
Goral (=Kosice II, 4x, high content oil, chamazulene, bisabolol)
Lutea (4x)
Novbona (2x)

Slovenia

Tetra

Spain

Adzet (2x, bisabolol)

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TABLE 5.3.2
Characteristics of Varieties and Breeding Material in Chamomile
(Matricaria recutita L.)
Characteristics

Variety/line/origin

High matricin-/chamazulene

Olanda
Sregez
Turkey

Low matricin-/chamazulene

Egypt
Turkey

High matricin-/chamazulene and bisabolol

Adzet
Bona
Camextrakt
Degumill
Goral
Lutea
Mabamille
Manzana
Novbona
Robumille

High matricin-/chamazulene and bisabololoxid

Bodegold
Bohemia
Budakalaszi 2 [BK 2]
Camoora
Flora
MA.VS.1
Pohorelicky Velkosvety
Promyk
Soroksari 40
Tetra
Tonia
Zloty Lan
Egypt
Argentina (usually bisaboloxid B)
Mexico

High matricin-/chamazulene and bisabolon

Lazur
Turkey
Bulgaria

elds on wild chamomile. Any unsuitable plants were removed by negative mass selection. With
the crossing descendants from bisabolol-azulene parent plants, the bisabololoxide A-azulene parent
plants and the bisabolol oxide B-azulene parent plants backcrossings were carried out with the
maternal parent from the in vitro depot.

5.4 OTHER SPECIES

With regard to the propagation of Chamaemelum nobile (L.) All. and some species of Anthemis
and Matricaria short notations are made in Chapter 3, Plant Sources. The main area of Anthemis

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L. ranges from the Mediterranean area to central Asia. The genus is particularly rich in species and
forms in the Balkans, Transcaucasia, Anatolia, and the Near East. The genus of Chamaemelum
Mill. is mainly spread over the Mediterranean area, west Europe, the British Isles, France, the
Iberian Peninsula, and North Africa, whereas the main distribution area of the genus of Matricaria
L. is to be found nearly all over Europe (including Scandinavia) and northern Asia.
The chief countries of origin of traded material of Chamaemelum nobile (L.) All. were Germany,
Belgium, England, France, Spain, and Italy, but also the United States and Argentina [43]. Nowadays
the lled owering form is almost exclusively cultivated for drug production. At present the main
supplier countries are France, Belgium, England, Belorussia, Ukraina, Transcaucasia, Czech Republic, and Poland. More rarely the drugs originate from India, North America, Brazil, Argentina,
Chile, Mexico, Germany, and Austria. Regarding Chamaemelum nobile (L.) All. the lled owering
form is the one almost exclusively cultivated in sunny altitudes for drug production. Sometimes
the cultivars weikpg (white headed), gelbkpg (yellow headed) [55], doppia, stradoppia [69], and ore pleno [19, 40] are traded. With the pollination of the completely lled forms
consisting of female ligulate owers only, the descendants are segregating into all intermediate
forms from lled to unlled due to the high grade of heterozygosis. That is why in most cases the
multiplication is done vegetatively by division of the root-stock [35, 40]. The culture can be utilized
for about 3 to 4 years.

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18. Drangend, S., Paulsen, B. S., Wold, J. K. et al. (1994) Experiments on chamomile in South East
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36. Hammerschmidt, P. (2002) Personal communication, February 13, 2002.
37. Hannig, H.-J. (1991) Qualittsanforderungen der EG und der Arzneimittelprfrichtlinie Zchtung
von Arzneipanzen, in Mitt. APV Pflanzliche Arzneimittel Aktuelles zu Qualitt, Wirksamkeit,
Unbedenklichkeit, Knigswinter, October 2830, 1991.
38. Hecht, H., Mohr, T., Lembrecht, S. (1992) Mechanisierung der Bltendrogenernte. Landtechnik 47,
276281.
39. Heeger, E. F. (1946) Die Kamille. Pharmazie, 1, 211.
40. Heeger, E. F. (1956) Handbuch des Arznei- und Gewrzpflanzenanbaus. Drogengewinnung. Deutscher
Bauernverlag, Berlin, 775 pp.
41. Heeger, E. F., Brckner, K. (1950) Arten-und Sortenkunde der deutschen Heil-und Gewrzpflanzen.
Vol. 1, Berlin.
42. Herold, M., Pank, F., Menzel, E., Kaltofen, H., Loogk, E., Rust, H. (1989) Verfahrenstechnische
Entwicklungen zum Anbau von Chamomille recutita (L.) Rauschert und Calendula officinalis L. fr
die Gewinnung von Bltendrogen. Drogenreport, 2, 2, 4362.
43. Hoppe, H. A. (1958) Drogenkunde. 7. Ed. Cram, de Gruyter & Co., Hamburg, 1229 pp.
44. Horn, W., Franz, C., Wickel, I. (1988) Zur Genetik der Bisaboloide bei der Kamille. Plant Breed.,
101, 307312.
45. Isaac, O. (1992) Die Ringelblume. Handbuch fr rzte, Apotheker und andere Naturwissenschaftler,
Wiss. Verlagsgesell., Stuttgart, Germany.
46. Kaltofen, H. (2002) Personal communication.
47. Kathe, W., Honnef, S., Heym, A. (2003) Medicinal and Aromatic Plants in Albania, Bosnia-Herzegovina, Bulgaria, Croatia and Romania. Bundesamt fr Naturschutz/Federal Agency for Nature
Conservation, Bonn, 200 pp.
48. Kerschberger, M. et al. (1997) in Anleitung und Richtwerte fr Nhrstoffvergleiche nach Dngeverordnung, Jena.
49. Kirsch, C., Franke, R. (1993) Neue Ergebnisse der Kamillenzchtung. Herba Germanica, 3, 97.
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50. Letschamo, W. (1991) Vergleichende Untersuchungen ber die nacherntetechnisch bedingten Einsse
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128134.
51. Letschamo, W. (1992) kologische, genetische und ontogenetische Einflsse auf Wachstum, Ertrag
und Wirkstoffgehalt von diploiden und tetraploiden Kamillen, Chamomilla recutita (L.) Rauschert.
Dissertation, University of Giessen, Germany, 171 pp.
52. Martinov, M., Tesic, M., Mller, J. (1992) Erntemaschine fr Kamille. Landtechnik, 47, 10, 505507.
53. Massoud, H., Franz, C. (1990a) Quantitative genetical aspects of Chamomilla recutita (L.) Rauschert.
J. Ess. Oil Res., 2, 1520.
54. Massoud, H., Franz, C. (1990b) Quantitative genetical aspects of Chamomilla recutita (L.) Rauschert.
II. Genotype: environment interactions and proposed breeding methods. J. Ess. Oil Res., 2, 299305.
55. Melegari, M., Albasini, A., Pecorari, P., Vampa, G., Rinaldi, M., Rossi, T., Bianchi, A. (1988)
Fitoterapia, 59, 449455.
56. Menzel, W. (2002) Personal communication.
57. Mohr, T. (2002) Untersuchung und Weiterentwicklung einer Erntemaschine fr Heilpanzenblten.
Z. Arznei. Gewrzpflanzen, 7, Sonderausgabe, 196202.
58. Mohr, T., Hecht, H. (1996) Entwicklung einer Pckmaschine. Ernte von Echter Kamille, (Chamomilla recutita (L.) Rauschert), Ringelblume (Calendula officinalis L.) und Johanniskraut (Hypericum
perforatum L.). Z. Arznei. Gewrzpflanzen, (Sonderheft) 6877.
59. Mohr, T., Hecht, H., Eichhorn, H. (1996) Vergleichende Untersuchungen einer verbesserten Pckmaschine zur Gewinnung von Bltendrogen der Echten Kamille (Chamomilla recutita (L.) Rauschert),
Ringelblume (Calendula officinalis L.) und Johanniskraut (Hypericum perforatum L.). Drogenreport,
9, 14, 1523.
60. Mohr, T., Hecht, H., Eichhorn, H. (1996) Vergleichende Untersuchungen einer verbesserten Pckmaschine zur Gewinnung von Bltendrogen (Teil 2). Drogenreport, 9, 15, 59.
61. Mller, J. (2003) Stand und Forschungsbedarf bei der Erntetechnik von Arznei-und Gewrzpanzen.
Z. Arznei. Gewrzpflanzen, 8, 2, 5660.
62. Mller, J., Kll-Weber, M., Kraus, W., Mhlbauer, W. (1996) Trocknungsverhalten von Kamille
(Chamomilla recutita (L.) RAUSCHERT), Z. Arznei. Gewrzpflanzen, 1, 104110.
63. Pank, F., Wettrich, K., Rust, H. (1997) Rationalisierung von Produktionsverfahren der Arznei- und
Gewrzpanzen. konomische Effekte am Beispiel von Fenchel (Foeniculum vulgare MILL.) und
Kamille (Chamomilla recutita (L.) Rauschert). Z. Arznei. Gewrzpflanzen (Sonderheft), 2530.
64. Pfeffer, S., Krger, H., Schtze, W., Schulz, H. (2002) Schnelle Erfassung von Qualittsparametern
in Kamillenblten mit Hilfe der Nah-Infrarotspektroskopie. Drogenreport, 15, 28, 2932.
65. Plescher, A. (1997) Akkumulation von Cadmium in Echter Kamille (Chamomilla recutita (L.)
Rauschert) und Johanniskraut (Hypericum perforatum L.). Drogenreport, 10, 17.
66. Plescher, A. (1997) Verfahrenstechnische Entwicklungen zum Anbau von Kamille (Chamomilla
recutita Rauschert). Z. Arznei. Gewrzpflanzen, 4, 193201.
67. Plescher, A., Pohl, H., Vetter, A., Frtsch, U. (1995) bergang von Schwermetallen aus dem Boden
in Arznei-und Gewrzpanzen. Herba Germanica, 3, 116125.
68. Plescher, A., Stodollik, A. (1995) Tendenzen im Panzenschutz bei nachwachsenden pharmazeutisch
genutzten Rohstoffen. Mitt. Biol. Bundesanstalt Landw., 310, 109118.
69. Pomini, L. (1972) Riv. Ital. EPPOS, 54, 627630.
70. Reichling, J. et al. (1979) Vergleichende Untersuchung verschiedener Handelsmuster von Matricariae
os. Pharm. Ztg., 124, 41.
71. Rimpler, R. (1972) Gutachten Nr. 121: Kamillenbltenerntemaschine. Potsdam-Bornim, Zentrale
Prfstelle fr Landtechnik Potsdam-Bornim des Staatlichen Komitees fr Landtechnik und MTV.
72. Rhricht, C., Mnicke, S., Grunert, M. (1997) Der Anbau von Kamille (Chamomilla recutita [L.]
Rauschert) in Sachsen. Z. Arznei. Gewrzpflanzen, 2, 135146.
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Prfstelle fr Landtechnik Potsdam-Bornim des Ministeriums fr Land-, Forst-und Nahrungsgterwirtschaft.
74. Ruminska, A. (1983) Rosliny lecznize. Podstawy biologii i agrotechniki (Heilpflanzen. Grundlagen
der Biologie und Anbau). 3rd ed. Panstwaowe Wydw. Naukowe, Warsaw, 550 pp.
75. Salomon, I. (1992) Chamomille: a medicinal plant. Herb, Spice and Med. Plant Digest, 10, 14.
76. Schick, E. R. and Reimann-Philipp, R. (1957) Die Zchtung von Heilpanzen. Zchter, 27, 7, 337.
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77. Schilcher, H. (1973) Planta Medica, 23, 132.

78. Schilcher, H. (1978) Inuence of herbicides and some heavy metals on growth of Matricaria chamomilla L. and the biosynthesis of essential oil. Acta Horticulturae Spices and Medicinal Plants,
73, 339.
79. Schilcher, H. (1981) Pharm. Ztg., 126, 2119.
80. Schilcher, H. (1987) Die Kamille. Handbuch fr rzte, Apotheker und andere Naturwissenschaftler,
Wiss. Verlagsgesell., Stuttgart, Germany, 152 pp.
81. Schreiber, A., Carle, R., Reinhard, E. (1990) On the Accumulation of Apigenin in Chamomile Flowers.
Planta Medica, 56, 179181.
82. Schrder, H. (1965) Die Dngung von Sonderkulturen, in Linser, H. (Ed.) Pflanzenernhrung und
Dngung, III/2 Springer, Vienna.
83. Schultze-Motel, J. (Ed.) (1986) Rudolf Mansfelds Verzeichnis landwirtschaftlicher und grtnerischer
Kulturpflanzen (ohne Zierpflanzen), 2. Ed. Akademie Verlag, Berlin, 1998 pp.
84. Seitz, P. (1987) Arznei-und Gewrzpanzen in der DDR. Deutsch. Gartenbau, 51, 30403046.
85. Svab, J. (1969) Untersuchungen ber den Einu der kologischen Faktoren auf den l-und Chamazulengehalt von Kamilledrogen. Herba Hungarica, 8, 9196.
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Bratislava, 142 pp.
87. Vrany, J. (1968) (Can you cultivate Chamomile?) (Slovak.) Nase liecive rastliny, 5, 170.
88. Wagner, C., Marquard, R., Friedt, W., Ordon, F. (2001) Untersuchungen zur genetischen Diversitt
der Echten Kamille (Chamomilla recutita (L.) Rausch.) mittels PCR-basierter Markertechniken. Z.
Arznei. Gewrzpflanzen, 6, 216221.
89. Wogiatzki, E., Marquard, R. (2002) Gehalte und Zusammensetzung des therischen ls von Wildkamillen von 25 Standorten in Griechenland. Drogenreport, 15, 27, 4953.

5.5 PRODUCTION OF CHAMOMILE (MATRICARIA RECUTITA L.)

IN EAST AND SOUTH EUROPEAN COUNTRIES
JEN BERNTH AND VA NMETH

5.5.1 INTRODUCTION
Medicinal and aromatic plants, especially for self consumption, have been produced in the territory
of Hungary and other east and south European countries for many centuries. However, until the
end of the 19th century the cultivation of medicinal and aromatic plants was carried out on the
garden scale in a limited area [1]. The intensication of the production only started in the early
years of the 20th century, when the processing of the raw plant including industrial oil distillation
was started as well.
The shortage of medicines, teas, and spices at the time of World War I and afterward drew
much more attention to the production and utilization of medicinal and aromatic plants. Both the
collection of the wild populations and the cultivation of some selected species started at that special
period, due to the enlarging local and export demand. This specialization took place spontaneously,
effected by different biological, economical, and social factors.
Natural occurrence of Matricaria recutita in Hungary is an example of how the regional
specialization could have happened for the utilization of actual species of indigenous ora [2]. As
a result of the increasing west European demand (especially that of Germany) the Great Plain of
Hungary became an important indigenous region of chamomile production. The Chamomillae flos
became a well-known Hungarian product sold on the world market with high success. From a
socio-economical point of view the formation of this special region was promoted by the abundance
of labor. According to the data of trade companies, during the harvest of chamomile owers as
much as 15,000 to 20,000 people are involved in the collection today [2].
As a result of the modern scientic and industrial achievements the demand for raw chamomile
changed from both a qualitative and a quantitative point of view [3, 18, 29]. However, the traditional
wild collection of plant material is practiced even today; many efforts were made in the past four
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decades to establish economical cultivation [5, 12, 14, 27, 32]. At present, collection and largescale cultivation methods are practiced in east and south European countries in parallel, having
biological and economical advantages or disadvantages. This section discusses the utilization of
indigenous ora and the effective methods of cultivation.

5.5.2 PRODUCTION

OF

CHAMOMILE

FROM INDIGENOUS

POPULATIONS

5.5.2.1 Distribution of Chamomile

5.5.2.1.1 Distribution in East and South European Countries
Chamomile is a species of east Mediterranean origin, occurring naturally in all the above-mentioned
regions of Europe [21, 23, 30]. However, it is proved by botanical investigations that its distribution
may vary from region to region depending on the ecological conditions of the actual habitats. Based
on the Hungarian analysis different types of growing areas have to be distinguished. In the western
part of Hungary (Transdanubia) as well as in the Hungarian Central Chain located in the north, the
chamomile grows in sporadic populations being a constituent of the ruderal plant communities.
The individuals show robust habit, forming a large number of branches, many relatively large
owers. In contrast, the dwarf type, with a limited number of owers, is very frequent in the great
Plain of Hungary where the plants grow on the ruderal places as well, occupying sodic elds, lay
lands, and sowings in abundance. These morphological features are reected in the differentiation
of the chemical characteristics of the populations, which will be discussed later.
5.5.2.1.2 Soil Conditions
Analyzing the natural occurrence of the populations of chamomile, it is obvious that it is present
in the poor sodic elds, lay lands, and sowings in great abundance. In spite of physiological optimum
measured at pH 7 the plant grows well up to pH 9. However, the statement that chamomile should
prefer the poor sodic eld must be a false one, which was refuted even by the rst cultivation
experiences. Based on the results of Kerekes [13] the high tolerance of certain species can be
explained by the outstanding salt accumulation ability of the root. The plant can accumulate sodium
salts in the root cells in amounts up to 10 mg/g. The high salt concentration helps the plant in
water uptake when its level in the soil is under the limit, which is not available for other members
of the plant community [11]. The interspecic competition ability of the plants under extreme
condition is supported by this physiological feature.
5.5.2.1.3 Coenological Aspects
It is obvious from Section 5.5.2.1.2 that chamomile shows good interspecic competition under
extreme conditions. However, this advantage due to the salt accumulation is lost in other plant
communities. To clear up the competition regularities of chamomile, more detailed coenological
investigations are required. It would have both practical and theoretical importance. From a practical
point of view, the presence of related species (Matricaria matricarioides, M. inodora, Anthemis
austriaca, A. cotula, etc.) spoils the quality of the collected drug, as was proved by Romanian experts.
The investigation carried out by Math [21] can be considered as an outstanding one in this
respect. Analyzing the coenological aspects of chamomile at ten different regions of Hungary, the
most frequent associated plant species were pointed out. The result is summarized in Table 5.5.1.
It is obvious that the related species Matricaria matricarioides and M. inodora, which may decrease
the drug quality, can be present in the majority of habitats used for wild collection.
5.5.2.2 Chemical Diversity of Wild Populations
The chemical diversity of wild-growing chamomile populations had been studied by numerous
scientic groups worldwide. In Hungary the rst investigations were carried out by Rom [26] at the
beginning of the large-scale commercial utilization of Hungarian chamomile populations. The high

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TABLE 5.5.1
The Most Frequent Plant Species Associated with Indigenous Chamomile Plant
Communities at Ten Different Districts of Hungary [20]
Accompanying Plant
Species
1

Frequency of the Distribution in Different Communities (%)

3
4
5
6
7
8
9

10

Polygonum aviculare
Capsella bursa-pastoris
Malva neglecta
Lepidium ruderale
Matricaria matricarioides
Lepidium draba
Taraxacum ofcinale
Matricaria inodora
Chenopodium album
Festuca pseudovina
Plantago media
Lolium perenne
Sisymbrium sophia
Ranunculus arvensis
Achillea millefolium
Bromus mollis
Poa angustifolia
Plantago major
Plantago lanceolata
Erigeron canadensis
Arctium lappa
Potentilla anserina
Agropyron repens
Ballota nigra
Vicia sepium
Consolida regalis
Artemisia monogyna
Poa bulbosa
Adonis aestivalis
Hordeum hystrix
Cerastium anomalum
Puccinellia distans
Rorippa kerneri
Lepidium perfoliatum
Camphorosma annua
Apera spica-venti
Poa annua
Xanthium stumarium
Rorippa silvestris
Rumex crispus
Urtica urens
Centaurea cyanus

2040%

4060%

6080%

80100%

2040%

4060%

1. Plain in Northwestern Hungary, 2. Danubian basin, 3. Territory east of the River Tisza, 4. District of Rivers Krs-Tisza,
5. District of Rivers Krs-Maros, 6. Nyirsg, 7. Bodrog River district, 8. Plain of Bereg, 9. Hungarian Central Chain, 10.
Transdanubia

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chemical diversity of the species was proved even by the rst data. To fulll the requirement for
collecting equalized and standardized drug, more detailed analysis were needed on the chemical
diversity of indigenous populations. In the period 19591961 500 wild chamomile plants were sampled
by Math [21]. However, the accumulation of essential oil and its chamazulene content were affected
by conditions of the year, and also regional differences were established. The frequency of populations
of low pro-chamazulene content is very high in the regions, located to the east from the River Tisza
(region 3 in Table 5.5.1). In this region about one third of populations accumulate chamazulene in a
range as low as 029 mg%, and the presence of the pro-chamazulene-free individuals is very common,
too. In contrast, in the region of the Bodrog River (northeast Hungary) and Transdanubia, 2527%
of populations accumulate 100 mg% or higher amount of pro-chamazulene.
According to recent investigations [36] at 12 collection areas of Hungary, populations accumulating typically chamazulene (1020%), -bisabolol (3050%) or bisabolol-oxid (3050%)
could be completely distinguished (Table 5.5.2). Samples collected in Danube-Tisza Mid Region
could be characterized by highest accumulation of chamazulene (up to 20% of oil). According to
Math [21] the compositional characteristics of the populations may be affected by the climatic
conditions and the soil properties, too.
In the same experiment, the avonoid concentrations had also been checked. The quantity of
apigenin-7-glucoside proved to be outstanding in the populations originating from the Great Hungarian Plain (1.82.8 mg/g), while samples collected in Transdanubia could be characterized by
lower levels (2 mg/g).
The chemical diversity of the chamomile populations was justied in the Bulgarian ora as
well. It was proved by the investigations of Peneva et al. [23], analyzing populations for presence
of essential oil, chamazulene content, and avonoids during the period 19821983. Some of their
data are presented in Table 5.5.3.
In the experimental eld, chamazulene was found even in the populations that had been
characterized as chamazulene-free local races. In fact, the avonoid content did not change in the
course of the introduction. However, by the opinion of the authors the local populations of
chamomile show low productivity of essential oil, which makes them unsuitable as a starting
material for enlarging production. By the more detailed investigations of Stanev et al. [30], four
different chemotypes of chamomile were identied in Bulgaria. Analyzing the samples collected
from 29 regions of Bulgaria, two main groupswere separated: populations accumulating chama-

TABLE 5.5.2
Main Components of the Wild Growing Chamomile Populations in Different Regions in
Hungary [36]
Number of Habitats
Essential oil content
Farnesene-a
Farnesene-b
Bisabolol-oxid-II
-Bisabolol
Chamazulene
Bisabolol-oxid-I
En-in-dicycloether
Others

10

11

12

0.7
3.4
0.0
10.7
13.0
8.7
41.3
17.6
5.2

0.8
4.5
0.0
11.9
16.9
5.1
34.8
21.6
5.2

0.7
2.4
0.0
8.2
13.3
7.0
50.1
14.8
4.3

0.6
3.2
3.2
13.8
46.3
6.8
3.5
15.8
7.4

0.6
3.1
0.7
11.5
44.5
9.7
5.9
16.1
8.3

0.5
2.5
2.7
18.4
30.9
11.0
7.3
17.7
9.5

1.0
1.8
0.2
15.4
29.2
16.3
24.0
10.1
3.0

1.3
3.0
0.0
7.6
19.3
20.1
35.2
13.8
1.0

0.6
2.8
0.0
9.7
10.5
11.0
44.9
18.0
3.1

0,5
2,6
1,8
10,1
17,5
13,0
38,9
13,3
2,8

0,9
3,6
0,0
12,2
22,3
10,0
22,8
25,3
3,7

1,3
2,6
0,0
13,0
9,3
12,5
41,4
18,2
3,0

Habitats: 1. Jszberny, 2. Csincse, 3. Poroszlo, 4. Hortobgy, 5. Pspkladany, 6. Bakonyszeg, 7. Felskerek, 8. Akaszto,

9. Szabadszallas, 10. Apajpuszta, 11. Nikla, 12. Somogytarnoca

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TABLE 5.5.3
Essential Oil and Flavonoid Content of Bulgarian Chamomile Populations of Different
Origin under Natural and Field Conditions [23]
Essential Oil (%)

Origin of Population

Original

Introduced

0.533
0.850
0.675
0.566
0.680
0.800
0.400

0.320
0.360
0.240
0.320
0560
0.720
0.271

Razgrad
Mezdra
Roman
Karlovo
Stara Zagora
Dbenye
Kazanlik

Flavonoids (%)

0,318
0.195
0.239
0.250
0.298
0.345
0.309

+
+
+
+
+
+
+

+
+
+
+
+
+
+

+
+
+
+
+

+
+
+
+
+
+
+

tr
+
+

+
+
+
+
+

tr

+
+
+
+
+

Flavonoids: 1. quercetagenin, 2. ferulic acid, 3. apigenin-7-O-glycoside, 4. luteoline-7-O-glycoside, 5. hyperosid,

6. rutin, 7. apigenin

zulene and populations characterized by the presence of bisabolol. In the chamazulene type the
chamazulene content ranges between 4.0 and 10.3% of the oil. Populations with cultivar Lazur,
especially in southeastern Bulgaria, accumulated threefold higher amounts of -bisabolol (73.7%).
At the same time a great variation in the bisabololoxide A and bisabololoxide B content was found
in the natural populations. It is conrmed by the data that Bulgarian chamomile populations are
rich in bisabololoxide A, and its amount varies slightly (the variation coefcient calculated to the
presence of bisabololoxide A is 21%). From the practical point of view the southeastern Bulgarian
population could have a special importance in selecting plant material producing high amounts
of -bisabolol.
5.5.2.3 Harvest of Wild Populations
The cultivation of chamomile is practiced all over the world; however, the collection of the wild
population did not lose its importance, especially in the east and south European countries. In
Hungary about 95 percent of 500 to 700 t of Chamomillae flos produced yearly comes from the
wild population. For collection the regions are chosen where the chamomile plant forms a compact
stand on relatively large elds. These territories in Hungary are as follows: territories east to the
River Tisza, district of Rivers Krs-Tisza, and districts of Rivers Krs-Maros, Nyirsg, and the
Bodrog River. In Figure 5.5.1 the distribution of the main collection regions of chamomile are
shown from the data of a Hungarian merchant company.
The collection area is much smaller compared to natural distribution of the plant, which can
be explained by practical consideration to make economical production.
In Hungary the blossom of wild chamomile starts in the second half of April and continues till
the beginning of June. However, large yearly variability can be found in the time of owering,
which is affected by the weather and ecological conditions. The earliest owering usually occurs
in poor sodic elds, which is followed by the populations distributed in showings. The owering
of plants shows 5 to 8 days delay in heavy clay soils comparing to the sandy ones.
The wild populations of chamomile should be harvested when most of the owers are already
opened (at the time of the full blossom). If collection is done before the optimal time the yield will
be small and large amount of unripe ower heads will depreciate the quality. As a result of the late
harvest, the ower heads fall into pieces in the course of postharvest processing, which depreciates
the quality, too. For choosing the proper time of harvest the essential oil content of the drug has
to be taken into consideration. It is supported by both practical and scientic observations; the
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Populations of high productivity

Population of low productivity

FIGURE 5.5.1 Distribution of the main collection regions of chamomile in Hungary from the point of view
of economic production [15].

essential oil content of the inorescence increases continuously from the time of budding and
reaches its maximum when the ligulate owers stand in a horizontal position. In the course of the
ripening afterward, the essential oil content and the amount of chamazulene decreases again.
However, the essential oil content may depend on the weather conditions. For collection warm and
sunny days are recommended by the agencies responsible for purchasing.
In the wild populations the inorescences are collected exclusively with a chamomile comb
(Figure 5.5.2).

FIGURE 5.5.2 Harvest of inorescences of indigenous chamomile populations in Hungary with the aid of a
special chamomile comb.

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An experienced worker can gather 50150 kg fresh ower in a ten-hour shift. At the time of
combing, the stems and large leaf segments should be removed, which will avoid quality problems.
According to the data of purchasing rms 20,000 to 25,000 people can participate in the collection
of Hungarian chamomile during the harvest period.
After the collection, the chamomile ower has to be dried immediately. The traditional methods,
drying on balks and sheds etc., are only used for making drug for home consumption. The collected
raw material is transported to the processing centers of the purchasing rms, which are usually
equipped with up-to-date drying machines. The drying procedure is the same as for the cultivated
crop and is discussed later.

5.5.3 CULTIVATION

OF

CHAMOMILE

5.5.3.1 Selection of Land

Chamomile is a characteristic plant of poor sodic elds, ruderal places, lay lands, and sowings.
However, the statement that chamomile should prefer poor soil conditions is a false one. The selection
of the land depends on many factors and changes country by country. In Hungary, because of
economical reasons, the poor sandy soils are recommended, which are unsuitable for cultivation of
other agricultural crops [10]. Based on the Rumanian experiences, the plant can be grown on the light
neutral sandy soils, sodic elds, and other soils of low fertility [25]. Yugoslavia's poor or fertile soil
conditions are utilized [14]. In Slovenia the production method of chamomile has been developed for
the farms, which are specialized for hop cultivation [37]. Hop grows there in the form of monoculture
on large and small elds. The monoculture of hop has an adverse effect on the soil fertility. Between
the two plantations of the hop, cultivating other plant species including chamomile is recommended.
In accordance with this situation the production of chamomile has developed on heavy clay and also
on light sandy soils, where the hop gardens are spread. However, as an effect of heavy clay soil the
plant stand may become an inhomogenous one, showing vegetative habit.
There have been some efforts to cultivate chamomile under extreme conditions. It was reported
by Yugoslavian scientists [31] that chamomile grows well on waste lands, especially on recultivated
elds around the Pljevlja coal mine.
5.5.3.2 Cultivation Methods
5.5.3.2.1 Soil Preparation
It is agreed by different authors that chamomile can be cultivated in monoculture. This type of culture
suits the biological characteristics of the species, being a self-sowing plant under natural conditions
in sodic and ruderal places. According to recent experiences in Hungary [33], it can be cultivated for
4 to 5 years, or even longer, with proper agronomic techniques (not only with self-sowing), in the
same eld. The eld should be changed when the presence of the resistant plant species in the weed
ora becomes dominant. The advantage of not changing chamomile elds frequently is to avoid the
appearance of chamomile plants in the following culture for years.
One of the preconditions of the effectual cultivation of chamomile is the proper preparation of
the seedbed. As a rst step of the cultivation, the stable of the predecessor plant should be turned
over immediately, with disc. Ploughs are not recommended, except when the stable cannot be turned
over by disc because of the weather conditions. The eld should be worked over with disc tillers and
rushing rollers until the soil is smooth, free of lumps, well compacted, and hard. If the plant is
cultivated in monoculture, after the harvest of chamomile the stem residues should be removed by
mobile chafng machines. This action is followed by stubble stripping and rolling.
5.5.3.2.2 Sowing
The optimum time for sowing chamomile in this region is the end of August or the rst half of
September. This statement has been supported by Slovenian [37], Hungarian [33], and Yugoslavian
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TABLE 5.5.4
The Effect of Sowing Time on the Yield of Dry Inflorescences of
Chamomile [12]
Time of Sowing

Yield of Inflorescences (kg/ha)

1958

1959

1960

284
366
362
322
214
110
274.6

400
462
576
593
646
580
542.8

532
378
364
390
198
342
367.3

256
181
13
40
60
11
93.5

188
68
91
107
103
93
108.3

346
308
196
202
79
0
205.2

Autumn sowing
1316 July
36 August
2427 August
1417 September
58 October
Average of autumn sowing
Spring sowing
29 February15 March
14 March1 April
28 March15 April
11 April29 April
25 April12 May
9 May27 May
Average of spring sowing

[14] experiences. The advantage of the autumn sowing was rst proved by Kerekes [12]. The results
of his investigations, which were carried out for three years, are summarized in Table 5.5.4.
It is supported by the data that the optimum time for sowing is the rst half of September. The
spring sowing could be suggested only exceptionally, and the success of spring sowing depends
on weather conditions and the type and state of soil. In the case of spring sowing the earliest time
possible should be proposed (second half of February or rst half of March); however, the yield
is less compared to any of the autumn variation. There is only a single contradictory result, achieved
by Gasic et al. [8], in the evaluation of time of sowing. Investigating 17 chamomile cultivars in
Yugoslavia the essential oil content was signicantly higher if the plants were grown by spring
sowing. It is in contrast to the majority of the experiences as well as to the result of Franz [7], who
found that plants sown in the autumn reached a higher oil content due to slower development at
the time of blossom. However, in spite of the observation of Gasic et al. [8], in this region the
optimum time for sowing is autumn. Autumn sowing avoids the adverse effects of the dry springs,
which are very common in that region.
For sowing chamomile seed pulvis is used in the majority of cases. The pulvis consists of
2030% of seeds, and about 7080% of parts of the inorescence, which help to make a homogenous
sowing. About 50 kg/ha of pulvis is used. In the cases of monoculture good results were attained
with ploughing of chamomile elds after harvest and sowing only 25 kg/ha pulvis in Reference
37. According to Hungarian experiences in the case of monoculture no sowing is necessary at all.
The seeds germinate well after suitable turning and rolling. Because the seed of chamomile prefers
light for germination, the pulvis should be spread on the soil surface in 1215-cm rows. Depending
on the local technology and ecological conditions other row distances are recommended; for
instance, 1236 cm in Yugoslavia [14], or up to 40 cm in Romania if the eld is weedy and a path
is required for mechanized weed killing [25]. In order to facilitate uniform sowing on the surface,
the coulter of the sowing machine should be adjusted according to the usual row distance of cereals,

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and should be locked in the raised position. After sowing, a Cambridge roller should be used; it
helps to prevent the blowing away of small seeds and presses them to the soil surface, helping the
water uptake. A seed-covering harrow must not be used after sowing chamomile.
5.5.3.2.3 Nutrient Supply
Chamomile grows in the sodic soils or in poor ruderal habitats under natural conditions. According
to the former studies [11] chamomile takes 53 kg of N, 85 kg K2O, and 21 kg P2O5 from the soil
for production of 1.0 t of inorescence. According to Hungarian cultivation experiences, the
chamomile gives good yield on the medium quality soils without any fertilization, because of the
limited nutrient requirement of species. In Slovenia chamomile production is located to the hop
production areas, where the plant is alternated with maize and wheat, which are fertilized with 50
kg nitrogen, 100 kg phosphorous, and 150 kg potassium per ha. For this reason only 13 kg/ha
nitrogen is proposed to spread over at the time of vegetation [37]. There are experiences with the
adverse effect of high amounts of fertilizers, too, causing intensive vegetative growth of plants,
which results in decreasing yield as an effect of the plant leaning to the ground.
However, in the loose sandy soils or on eroded sands fertilization is required for a good yield.
In exceptionally poor soils, application of 2030 kg/ha N and 2030 kg/ha P2O5 is recommended.
On eroded sands, with neutral pH, the dosage of P2O5 can be raised up to the 40- to 60-kg level
and nitrogen top-dressing in a dosage of 3040 kg may be effectual.
The cultivation of chamomile in monoculture cannot be economical without regular application of fertilizers. In monoculture the nutrient reserve of soil decreases to the critical level by
the third year; in consequence, chamomile starts to disappear from the eld. To manage successful
monoculture both basic fertilization (in autumn) and top-dressing in spring is necessary. From
the second year 1012 kg/ha N, 6070 kg/ha P2O5, and 5070 kg/ha K2O must be applied before
wintering and 4060 kg/ha N in top-dressing form.
There is a special case when top-dressing with N fertilizers should be suggested. In east and
south European countries chamomile may be damaged by late frosts. As a result of low temperature
the development of plants stops, and the leaves become yellow. In this situation the nitrogen topdressing in a dosage of 3040 kg/ha will help the plants through the critical period.
5.5.3.2.4 Care of Plants
In the cultivation of chamomile chemical weed control is solved [32]. The former manual mechanical methods have no importance and are practiced on small parcels only. Maloran (chlor-bromuron),
the most effective herbicide, should be applied in April with 34 kg/ha dosage. The optimum time
for application is when the plants are in the two- or three-leaf stage and the weeds are just starting
to sprout. Chamomile tolerates Afalon (linuron) in 34 kg/ha dosage. This herbicide is suggested
for Yugoslavian [14] and Slovenian [37] farmers, too, but in a much lower (12 kg/ha) dosage. The
effectiveness of such a low amount could be uncertain; however, it may contribute to avoid damaging
owers, which could happen under disadvantageous weather conditions. In monoculture the amount
of tolerant weeds increases continuously. In that case special herbicide treatments are required. For
instance in Hungary the most dangerous monocotyledonous weed is Bromus tectorum. It can be
controlled by spraying Kerb (propizamid) in a dosage of 2 kg/ha in the late autumn. Against the
tolerant dicotyledonous weeds, the application of Sys 67 Prop (2,4-D) has to be considered.
5.5.3.2.5 Harvest
Chamomile in the indigenous populations should be harvested when the majority of the owers
have already opened. The essential oil content of the inorescence increases continuously from
budding, and reaches its maximum when the ligulate owers take the horizontal position.
The harvesting process of chamomile depends on the purpose: whether plain owers or a mixed
product (owers with 1020% leaf and stem material) are to be gathered. The latter serves chiey
as raw material for oil distillation.

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The owers should be gathered when they are in full blossom. Up to the 1970s gathering was
done mainly by hand, with the help of a long-handled ower comb. By this method a very good
quality drug can be produced, both from the wild-growing plants, and also from the cultivated ones.
From 100 to 150 kg of owers were collected by experienced workers from the cultivated stand
in 10-hour shifts. In the case of the cultivated plants, which can be characterized by more robust
habit, the stem parts should be removed more frequently from the ower comb, as the amount of
green parts torn by the tool is much more than in the case of plants growing under sodic conditions.
However, turning to large-scale cultivation, manual harvesting (because of manpower input of
2530 workdays per ha) became simply unfeasible. This problem had to be solved by the construction of mechanized harvesters.
One of the possibilities was the application of the well-known Ebert-Schubert chamomile
harvester. This type of machine produced excellent quality drug, but its output was low. In the
1980s, the majority of countries belonging to this region of Europe started to develop their own
type of harvester [14, 19, 32, 37]. For instance, in Hungary a new and effective combine-harvester
system was invented by the team of Cooperative Szilasmenti. It was a complementary, highcapacity system, eliminating manual labor. The equipment consisted of a ower picker and a
sifter for gathering 810 t of raw material per day. By this harvester raw material both for flos
production, consisting of 5060% of plain ower, and for essential oil distillation, coming from
the sifter-top, were made simultaneously. The expected yield in Hungary is 0.52.0 t/ha of fresh
ower, from which 0.10.5 t/ha dry drug can be produced. Much higher dry yield is reported
from Romania, Slovenia, and Yugoslavia, which are 0.61.0 t, 0.5 t, and 0.40.5 t on average,
respectively.
A different type of harvesting method was developed for collection of chamomile biomass used
for isolating active agent complexes either by distillation or chemical extraction. The silo harvester
(E 280) proved to be the most suitable for this purpose. The cutting level of the machines should
be adjusted below the average height of the owers, avoiding high amount of stem in the harvested
material. The green stem parts impose an extra load on the essential oil distillation. The mixture
of owers and stems, especially that was gathered with mobile ensilage machines, should be
immediately taken to the distillation vessel. By this mechanized harvesting method 4.08.0 t/ha of
ower-stem mixture can be harvested. The yield varies widely because a second harvest of the crop
becomes possible under suitable weather and edaphic conditions.
Further, remarkable progress was achieved recently by the elaboration of distilling containers,
considerably reducing manpower input and operating at a higher output level.
5.5.3.2.6 Drying
The drying is one of the most important postharvest processes of chamomile. Its importance had
been recognized even at the beginning of the large-scale cultivation of the plant [35]. There is no
doubt that the ower collected either by ower comb or mechanized harvester should be
transported to the drying location at once. The continuous transportation of the collected chamomile
is a basic organizational task. If the delivered owers cannot be put into the drier immediately,
they should be spread in the shade for temporary storage for several hours.
For reducing the cost of drying, the collected ower should be screened before drying. A
motorized chamomile screen of 712 mm mesh size can be used for this procedure.
For drying chamomile, either natural or articial methods can be applied. In the case of largescale cultivation, articial drying is the only reliable method; it results in more aesthetic and highquality drug, which is not easily disintegrated to dust. Different types of driers can be used for
dehydration of chamomile. The most frequent type is counterow driers (belt conveyor and tunnel
types) managed at 4070C. However, different kind of driers can be used successfully as well, as
it is proved by the Slovenian example [37]. There the harvested chamomile ower is transported
to hop drying-house and put on drying meshes. The thickness of stratum is 8 cm, and the drying
lasts from 810 hours at 40C.

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FLOWERING STAND OF CAMOMILE

COMBINE-HARVESTER
(CP)

Sifting

SILO-HARVESTER
(E 280)

CONTAINER

Sifter-top
DISTILLATOR

ESSENTIAL OIL
Distillation waste

DRYER

Fresh flower

DRUG OF III. CLASS QUALITY

"BINDER" DRYER

TSZP-DRYER

EXTRACTION

Dried flower

COMPOST

FODDER
EXTRACT

SEED FOR PROPAGATION

For extraction

Waste processing

Stem separation

DRUG OF I. (II.) CLASS QUALITY

FIGURE 5.5.3 Complex processing system employed for the large-scale production of chamomile in Hungary
[34].

5.5.3.3 Postharvest Processing

To make an economic large-scale production of chamomile, a complex processing system has to
be employed. Such a system was worked out by Svb [34] for the Hungarian conditions. It is
demonstrated by the scheme in Figure 5.5.3.
5.5.3.4 Cultivars
The importance of growing high-quality chamomile cultivars has been emphasized by many authors.
However, the productivity of the chosen material and its chemical composition are affected by the
local ecological conditions and the cultivation method, as well. That is the reason that the majority
of the countries in the above-mentioned regions have their own cultivars.
The selection of chamomile was started in the early 1960s in Hungary [28]. As a result of this
breeding work two cultivars were registered and used for large-scale cultivation. The main characteristics of these cultivars are as follows:
Budakalszi 2 (BK 2): It is a well-known Hungarian cultivar, used as a control population
in different parts of the world, even proposed for commercial production [4, 6, 16, 17]. The cultivar
is a tetraploid form and has large owers [28]. It has a relatively long vegetation period, producing
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TABLE 5.5.5
Changes of the Chemical Characters of Selected Cultivars during Three Vegetation Cycles
(19801982) in the Experiment Carried out in Backi Petrovac, Yugoslavia [9]
Cultivar or
Population

ZA-2
min./max.
Ljubljana
min./max.
Banat
min./max.

Essential Oil Content

(%)

Ratio of Main Components in %

1st harvest

2nd harvest

()-bisabolol

Chamazulene

Bisabololoxide A

Bisabololoxide B

Farnesene

0.710.74

0.510.59

510

1015

4050

1015

510

0.650.89

0.480.66

510

1020

4050

1015

510

0.360.48

0.340.46

2030

1020

1020

3540

515

a high yield of rst-quality ower. Its essential oil content is 0.70.9% on average, and it contains
1220% of chamazulene and about 10% of ()--bisabolol.
Soroksri 40: The cultivar Soroksri 40 is a diploid form selected from local populations
[13]. Its vegetation period is considered to be moderately long, producing high ower yield.
Its essential oil content is about 0.81.1%. The ratio of chamazulene is 1619% and that of the
()--bisabolol 610%.
The Romanian cultivars were selected from Polish polyploid variety Zloty Lan [22].
Margaritar: This is a polyploid cultivar [24] selected from Polish variety Zloty Lan. The
essential oil content is about 0.7% with 14% of azulene.
Flora: The cultivar was created by repeated individual selection combined with self-pollination of the valuable elite of the Polish polyploid variety Zloty Lan. It has higher ower production
capacity compared to Margaritar and the essential oil content is higher, too, up to 0.8%. The
ratio of azulene is about 15%. Another advantage of this cultivar is its higher tolerance against the
infection of Peronospora leptosperma and Erysiphe cichoracearum.
The chamomile production in Bulgaria is based on a single cultivar, Lazur. It was selected
from the local wild growing chamomile populations [38].
Lazur: Lazur is a tetraploid form, selected from local Bulgarian ora. Its essential oil
content is about 0.7%. From the components of the essential oil the presence of chamazulene
(24.37%), bisabolol oxide (19.42%), and bisabolol (12.38%) has to be mentioned as a characteristic
feature of the cultivar.
In Yugoslavia different types of chamomile cultivars and populations were tested for getting
starting material of high productivity for the large-scale cultivation [9]. Some of their results are
shown in Table 5.5.5.
It is obvious from the data that the essential oil content of cultivars depends on both the time
and the year of the harvest. It can also be concluded that external factors could induce quantitative
modications in the composition of essential oil; however, the basic chemical characteristics of the
populations did not change.

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3. Carle, R. and Isaac, O. (1987) Die Kamille Wirkung und Wirksamkeit. Z. Phytotherapie, 8, 6777.
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4. Carle, R., Seidel, F., and Franz, C. (1991) Investigation into seed germination of Chamomilla recutita
(L.) Rauschert. Angewandte Botanik., 65 (12), 18.
5. Correa, C. Jr. (1995) Mandirituba: new Brazilian chamomile cultivar. Horticultura Brasileira, 13 (1),
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6. Falistocco, E., Menghini, A., and Veronesi,F. (1996) Osservazioni cariologiche in Chamomilla recutita
(L.) Rauschert. Atti del convegno internazionale: Coltivazione e miglioramento di piante officinali,
Trento, Italy (23 June), Proceedings, 459463.
7. Franz, Ch. (1980) Content and composition of the essential oil in ower heads of Matricaria chamomilla L. during its ontogenetical development. Acta Horticulturae, 96, 317321.
8. Gasic, O., Lukic, V., and Adamovic, D. (1991) The inuence of sowing and harvesting time on the
essential oils of Chamomilla recutita (L.) Rausch. J. Ess. Oil Res., 3, 295302.
9. Gasic, O., Lukic, V., Adamovic, R., and Durkovic, R. (1989) Variability of content and composition
of essential oil in various camomile cultivars (Matricaria chamomila L.). Herba Hung., 28 (12),
2128.
10. Hornok, L. (1978) Gygynvnyek termesztse s feldolgozsa (Cultivation and Processing of Medicinal Plants). Mezgazdasgi Kiad, Budapest, 356 pp.
11. Hornok, L. (1992) Cultivation and Processing of Medicinal Plants. Akadmiai Kiad, Budapest, 338
pp.
12. Kerekes, J. (1966) Kamillatermesztsi ksrletek (Experiments for the production of chamomile).
Herba Hung., 5 (23), 141147.
13. Kerekes, J. (1969) Gygynvnytermeszts (Production of Medicinal Plants). Mezgazdasgi Kiad,
Budapest.
14. Kisgeci, J. and Adamovic, D. (1994) Gajenje lekovitog bilja. Nolit, Beograd. 185 pp.
15. Lenchs, O. (1993) Matricaria recutita L., in Bernth, J. (Ed.) Wild Rowing and Cultivated Medicinal
Plants. Mezgazda Kiad, Budapest, 566 pp.
16. Letchamo, W. (1996) Developmental and seasonal variations in avonoids of diploid and tetraploid
camomile ligulate orets. J. Plant Physiol., 148, 6, 645651.
17. Letchamo, W. and Gosselin, A. (1996) High quality camomile for North American commercial
processing. Acta Horticulturae, 426, 593600.
18. Mann, C. and Staba, J. (1986) The chemistry, pharmacology and commercial formulations of chamomile, in Craker, L. and Simon, J. (Eds.) Herbs, Species and Medicinal Plants. Oryx Press, Phoenix,
AZ, pp. 239.
19. Martinov, M., Tesic, M., and Mller, J. (1992) Erntemaschine fr Kamille. Landtechnik, 47 (10),
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20. Math, I. (1963) A kamilla (Matricaria chamomilla L.) magyarorszgi termhelyei s hatanyagvizsglata (Hungarian growing areas of chamomile and examination on active agents). Ksrletgyi
Kzlemnyek, Kertszet, 56/C, 1126.
21. Math, I. (1979) A kamilla (Matricaria chamomilla L.) (The chamomile). Magyarorszg kulturflrja.
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22. Paun, E., Verzea, M., Dumitrescu, A, Barbu, C., and Ungureanu, N. (1996) Breeding research on
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the wild camomile (Matricaria recutita). Rastheviedni Nauki, 26 (6), 2533.
24. Plugaru, V. (1996) Cercetari privind metodologia obtinerii de seminte la specia musetel (Matricaria
chamomilla L.). Herba Rom., 13, 2533.
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Plants). Ceres Knyvkiad, Bucharest.
26. Rom, P. (1930) Adatok a chamomilla sszehasonlto vizsglathoz (Data on comparison experiments
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e miglioramento di piante officinali, Trento Italy, Proceedings, 413416.
28. Srkny, S. (1965) A kamilla (Matricaria chamomilla L.) nemestse (Breeding of chamomile). Herba
Hung., 4, 125168.

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29. Schilcher, H. (1987) Die Kamille. Wissenschaftliche Verlagsgesell., Stuttgart, Germany, pp. 99.
30. Stanev, S., Zheljazkov, V., and Janculoff, Y. (1996) Variation of chemical compounds in the essential
oil from some native forms of chamomile (Chamomilla recutita L.). Int. Symposium, Breeding
Research on Medicinal and Aromatic Plants (June 30July 4, 1996), Quedlinburg, Proceedings,
214217.
31. Stepanovic, B., Jovanovic, M., and Knezevic, D. (1989) Ispitivanje mogucnosti gajemja lekovitog I
aromaticnog bilja na jalovistu rudnika uglja Pljevlja. Zemljiste Biljka, 38 (1), 5762.
32. Svb, J. (1983) Results of chamomile cultivation in large-scale production. Acta Horticulturae, 132,
4347.
33. Svb, J. (1992) German camomile, in Hornok, L. (Ed.) Cultivation and Processing of Medicinal
Plants. Akadmiai Kiad, Budapest, 246254.
34. Svb, J. (1997) Personal communication.
35. Svb, J., Tyihk, E., and Rpoti, J. (1966) A magyar kereskedelmi kamillval vgzett szrtsi kirlet
(Drying experiment with Hungarian chamomile). Herba Hung., 5 (1), 3135.
36. Sztefanov A., Szab K., and Bernth J. (2003). Comparative analysis of Hungarian Matricaria recutita
(L.) Rausch. populations. J. Horticult. Sci., in press.
37. Wagner, T. (1993) Camomile production in Slovenia. Acta Horticulturae, 244, 476478.
38. Zheljazkov, V., Yankuloff, Y., Raev, R.Tc., Stanev, S., Margina, A., and Kovatcheva, N. (1996)
Achievements in breeding on medicinal and aromatic plants in Bulgaria. Int. Symposium, Breeding
Research on Medicinal and Aromatic Plants (June 30July 4, 1996), Quedlinburg, Proceedings,
142146.

5.6 CULTIVATION EXPERIENCES IN SLOVAKIA

VILIAM ORAVEC, VILIAM ORAVEC, JR., MIROSLAV REPCK, LUBOMR SEBO,
DUSAN JEDINAK, AND IVAN VARGA

5.6.1 INTRODUCTION
Chamomile has long been one of the most important medicinal plants cultivated in Slovakia. Its
cultivation started in the beginning of the 1950s in the former Czechoslovak Republic. Diploid
variety Bohmia with a high content of chamazulene and -bisaboloxide A and B was sown. In
1957 the tetraploid variety Pohoelicky Velkokvety with similar characteristics, as far as efcacious
compounds are concerned, was bred, but this variety was restricted because of the high degree of
disintegration.
Chamomile is a plant with a wide growing range and can be grown in the Slovak Republic
almost everywhere. It grows best in warmer areas protected from wind with plentiful sunshine and
mean yearly precipitation ranging from 550 to 800 mm. Soils rich in nutrients and humus, heavy
to mild, mold to luvisol character are the most suitable. After almost 40 years of experience, the
crops reached the required level of market production; the cultivation of chamomile in beet and
potato regions was proved to be the most suitable.
With regard to the initial slow growth of chamomile, it is necessary to choose the foregoing
agricultural plant that leaves the land weed-free and in a good state. From this point of view root
crops, peas, beans, and mustard are the most suitable; corn is also good. Clover, clover and grass
mixtures, dill, coriander, and caraway are not suitable at all. It is also possible to grow chamomile
in monoculture until the weed ora resistant to the herbicides permitted is formed.
The second precondition of successful chamomile cultivation is a high-quality soil preparation.
In one-year chamomile cultivation, the stubble is ploughed over by medium-deep ploughing
(180220 mm) immediately after the foregoing agricultural plant harvest. Soil surface is adjusted
by cold-crusher and harrow so that it was smooth enough, clod-free, and hardened. In monocultural
growing, after the harvest of chamomile, it is necessary to remove the rest of the herb by a
postharvest cutting machine and then a break-up and rolling follows [7].

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Simultaneously with the medium-deep ploughing, fertilizers are applied. To produce 1 ton of
drug from 1 ha the following average doses of pure nutrients are recommended in the ratio
1N:0.14P:2.05K for 1 ha: 60 kg N, 10 kg P, 142 kg K. Only one third of nitrogenous fertilizers
is applied before sowing, the remaining two thirds are applied in two doses after overwintering
and the second weeding [4].
Chamomile can be sown at any time of year on the soil surface, because the germination
requires the presence of light. However, in order to reach a high crop and to be able to dry the
harvested biomass, the sowing is limited to two periods.
Autumn sowing from August 15th to September 15th is recommended for the regions with
regular autumn rainfall and frosts coming after October 20th. Chamomile sown in this period
germinates quickly, takes roots well, and grows in the period of humid and warm-enough weather.
Spring sowing is suitable for all regions with the exception of dry and warm ones, where total
rainfall for April and May does not reach 50 mm and day temperatures exceed 15C. Spring sowing
is applied to approximately 30% of production area in order to ensure continuous harvest up to August
15th. The sowing takes place from March to the end of April, and ve to six harvests are reached.
The quantity of the seeds sown depends on the seed quality and varies from 1.5 to 2.5 kg/ha.
In monoculture a self-seeding occurs, thus the quantity of seeds for sowing applied is lower.
Chamomile is sown, dependent on the subsequent mechanization, to rows 3045 mm apart.
From the point of view of mechanized harvest and drug quality, overriding attention should
be paid to the purity and the state of health of the stand. Herbicides are effective in the struggle
against weeds; however, they must be applied correctly. The most important damage to chamomile is caused by sucking insects, above all by Erophyes convolvens and representatives of
Thysanoptera, Heteroptera, and Homoptera [3].
Cultivation areas of chamomile in Slovakia have varied from 150 to 400 ha in the last ten years,
according to market demands. These demands are much inuenced by the amount of chamomile
collected from natural resources, which reached 30 to 50%. Up to 1990 only one rm was a
monopoly bulk buyer and processor of chamomile. Export is recorded directly by producers for
west European countries (Table 5.6.1).
The present need of chamomile drug is insufcient for the inland market in Slovakia. Chamomile ower is imported by processing pharmaceutical rms. On the other hand, producers export
their product directly, or by means of commercial rms to west European markets under relatively
advantageous conditions. In order to intensify producers activities in the eld of medicinal plants,

TABLE 5.6.1
Purchase of Chamomile by Liec iv Rastliny (Medicinal
Plants) Malacky Division, Export in Tons and Prices
Year

Wild

Cultivated

Export

Price, 1st class

()

1986
1987
1988
1989
1990
1991
1992
1993
1994
1995

46
46
28
62
34
20
26
34
18
19

5
15
15
14
15
7

5
16

14
34
39
45
27

2.13
2.13
2.25
2.25
2.50
2.75
3.00
3.00
3.25
3.50

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TABLE 5.6.2
Economy of Model Firm of Agricultural Company ROZKVET Nov Lubovna at the
Complex Exploitation of Chamomile
Euro ()
Year

Overall
Takings

Overall
Expenses

1983
1984
1985
1986
1987
1988
1989
1990
1991
1992

4,150
13,250
11,478
32,673
33,425
36,250
55,200
51,625
42,500
59,325

2,312
8,950
8,626
23,323
25,600
24,350
18,550
25,750
34,750
47,200

Area [ha]]
5
13
15
22
30
31
43
60
82
94

Profit
1,538
4,300
2,852
9,350
7,826
11,900
36,650
25,875
7,750
12,125

Takings
per 1 ha

Expenses
per 1 ha

830
1,019
765
1,485
1,114
1,169
1,284
860
518
631

522
688
575
1,060
853
785
431
429
424
502

Profit
per 1 ha
308
331
190
425
261
384
852
431
95
129

the interest group Rumancek (Chamomile) was found in 1996. It is a nonprot association of both
trade and juristic persons that represents the interests of improvers, cultivators, and processors of
medicinal, aromatic, and tonic plants. The objective of the association is the enlargement of area
and the rise of efciency of breeding, cultivation, and processing of medicinal, aromatic, and tonic
plants both for inland market and export, which should reach 20% of domestic production. The
next goal of the association is to ensure the coordination in the eld of breeding, cultivation,
research, and production of nal products from medicinal, aromatic, and tonic plants and to reach
2500 ha of cultivation area in the Slovak Republic, including the area for chamomile up to 500 ha.
The overall picture of chamomile cultivation gives us its economic evaluation. It was applied
to a model rm in the Agricultural Farm Rozkvet in Nov Lubovna village in the years 19831992.
This agricultural rm completely exploited the chamomile biomass for drug, seeds, essential oils,
and extracts. Adequate prices and state appropriation for the years 19911992, when there was a
disproportion caused by the growth of outlays and fall of prices and a substantial reduction of
appropriations, had a favorable inuence on economic results. The negative inuence of prices and
appropriation inputs changed the orientation of the market with respect to the export of chamomile
drug above. The conditions for prospective quick growth of chamomile cultivation also within the
criteria of alternative cultivation are given by long-term absence of pesticides in soil, fertilizers
being applied only in minimum doses, and mechanical cultivation (Table 5.6.2).

5.6.2 RESEARCH, BREEDING, SEED GROWING,

AND

VARIETIES

5.6.2.1 Research
State research of medicinal plants in the former Czechoslovakia was a dominant task mostly of the
institutions situated in Slovakia. From the beginning of complex research, Slovakofarma Hlohovec
was a co-ordinator. Ing. Ivan Varga, present director for science and research of Slovakofarma, was
the responsible coordinator of these activities in the years 19801997.
Chamomile research started in 1976 at the Department of Experimental Botany and Genetics
of the Faculty of Science of P. .J S afrik University in Kosice (FS PJSU) by a partial task force
on the research of chamomile cultivation in soils with high salt content. The goal of the research
was to nd the most suitable complex chamomile farming technology aimed at the obtaining the
maximum crop of high-quality drug [5].

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The research continued from 1980 to 1990 and was expanded by another research workplace:
Agricultural Farm in Nov Lubovn a. It was aimed at the solution of problems of large-scale
cultivation of this medicinal plant, harvest, the development of a wide-space chamomile harvester,
postharvest arrangement by presorting of plant biomass, and also the sorting and stalk removing of
the dry drug. It also built up a shop for scientic and technological development and piece production
of machines for harvest, postharvest arrangement, and technological processing of chamomile.
5.6.2.2 Breeding and Seed Growing
Simultaneously with cultivation research, the research collectives dealt with breeding and preparing
the material for registration for a variety tests.
In the course of 20 years the collective of breeders of the Department of Experimental Botany
and Genetics of FS PJSU in Kosice, Agricultural Farm Rozkvet, and the rm Vilora bred up to
four varieties of chamomile. Breeding work consisted principally of breeding of indigenous Spanish
chemotypes with local varieties and was aimed at maintenance of chamazulene content on the
original level, but reaching high content of -bisabolol to the detriment of -bisaboloxide A and
B. This was reached in the period evaluated. Prospective work in this eld is aimed at coumarine
and avonoid compounds [11].
In order to maintain or improve the qualitative characters of chamomile essential oil, maintenance breeding and seed growing on the principles of production process are carried out [12].
5.6.2.2.1 Production Process Scheme
Seed plot: maintenance breeding
Area 5 acres: founded by the sowing of seeds from plants
with verified essential oil content and composition

Analyses of essential oil content and composition

for individual plants (the number of plants
dependent on needs of seeds for sowing) by thin
layer chromatography and gas chromatography

Area of propagation: production of seeds for

sowing elite, original, trade seed

5.6.2.2.2 Methods
Chamomile is grown on seed plots with a 5-acre area. Seed plots are founded by sowing the seeds
of plants in which essential oil contents and composition fullls the standards of the drug quality.
With this objective individual plants are analyzed by thin-layer chromatography, essential oil
composition is studied, and plants with detectable amounts of -bisaboloxides A and B are eliminated. The propagation areas are founded from the seeds produced on seed plots.

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FIGURE 5.6.1 Crop of chamomile.

Chamomile anthodia disintegrate during the manipulation after harvest and drying. The mass
is sieved; receptacles, ligulate orets and disc orets, dust, and ower and seed fragments are
removed. Sorted seeds are dispatched packaged.
5.6.2.3 Varieties
At the present four varieties of chamomile are permitted in Slovakia.
Bona (National Variety Book CSFR 1495/1984)
Reproduction concerned the rise of content in ()--bisabolol essential oil at the expense of
bisaboloxides, keeping a high level of chamazulene. Reproduction started in 1975 through the
cross-breeding of wild-growing material from Spain with the variety Bohemia and following
selections on the screening basis for individuals with high content of ()--bisabolol in dichlormethan extracts by reduction with thin-layer chromatography and gas chromatography. The variety
testing was executed from 1980 up to 1983.
The early diploid variety was of a smaller size with middle-green leaves and middle-sized
reductions. The content of volatile oil equals 0.9%, chamazulene content in essential oil 16.1% and
()--bisabolol 35%. During maintaining breeding ()--bisabolol increased in essential oil by 42.9%.
Novbona (National Variety Book CR reg. No 3052 and SR ev. No 3332)
The variety Bona served as the basic material. The breeding took place in Nov Lubovna
from 1983 to 1990. By the selection through evaluation of the chemotype, inside the variety
population, the part of plants with a high content of ()--bisabolol and chamazulene increased.
The early diploid variety consisted of up to small plants, bright green ne leaves, small up to
middle size of ower level, middle average of reduction, without tongue-shaped owers, and
including tongue-shaped owers. In the variety population the ()--bisabolol chemotype is represented by 94%. The content of essential oil in the drug equals 0.9%. The essential oil contains
18.0% chamazulene and 46.1% bisabolol.
Goral (National Variety Book CSFR 1888/1990)
As basic material for the polyploid induction through colchicining in 1978, this was used in
newbreeding and later registered as Bona. In the following years the population was selected on

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the basis of analysis for chromosome numbers and through chemotype screening individuals with
appropriate characteristics. On the basis of the variety examined from 1986 to 1988, the variety
was agreed on in 1989.
In comparison with diploid varieties, the variety distinguishes itself by increased breakdown.
The mesh oversize up to 2 mm is 26% in comparison with 10% in the case of the variety Bona.
The variety population represents itself as a mixture of chemotypes (35% ()--bisabolol and 65%
bisabololoxide). The content of essential oil is 1.1% and chamazulene in essential oil is 24.5% but
the content of ()--bisabolol 24% does not exceed the sum of other materials of the bisabolol
type. Goral is favored by the farmers because of good harvest characteristics.
R reg. No 3051 and SR reg. No 3333)
Lutea (National Variety Book C
The basic material for breeding the variety of the bisabolol type is the variety Goral. In 1987
and 1988 under laboratory conditions and in strong isolation, selected individuals were cultivated
on the basis of chemotype screening. In 1989 and 1990 the breeding was implemented under eld
conditions in Nov Lubovna.
Middle early tetraploid variety consisted of middle high plants, middle green central leaves,
middle height of ower level, high detracted average without tongue-shaped leafs and with
tongue-shaped leaves. The variety has a stable chemotype composition of the population (over
92% of ()--bisabolol). The content of essential oil in the drug equals 1.2%, chamazulene in
essential oil is represented by 21.2%, and ()--bisabolol 43.3%. The breakdown is on the level
of diploid varieties [9].
Values of secondary metabolites in the period 19911995 can be studied in Figure 5.6.2 (the
varieties Bona and Novbona) and Figure 5.6.3 (varieties Goral and Lutea) [9].

r
B

a-

et

bi

sa

bo

Sp

lo

lo

iro

xi

A
d
xi
lo
lo
bo
sa

bi

BONA
NOVBONA

Al

ph

aph
Al

he

l
lo
bo
bi
a-

ph
Al

ha

of

sa

az

Es

ul

.O

en

il

Diploid Type
50
45
40
35
30
25
20
15
10
5
0

FIGURE 5.6.2 Values of secondary metabolites in diploid varieties (19911995).

he

bi

et
ro
Sp
i

sa

bo

lo

lo

xi

A
aph
Al

Al

ph

a-

Al

bi

ph

sa

a-

bo

bi

lo

sa

lo

xi

bo

lo

en
az
m
ha

of

Es

ul

.O
il

Tetraploid Type
50
45
40
35
30
25
20
15
10
5
0

GORAL
LUTEA

FIGURE 5.6.3 Values of secondary metabolites in tetraploid varieties (19911995).

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5.6.3 PRINCIPLES

OF

QUALITY: DRUG DESCRIPTION

The criteria for quality classes of chamomile owers are governed by the Branch Standard 86 62 11.
Quality, max. %
Criteria

Overripe, crushed ower heads passing through the sieve III (2 mm)
Flower heads with stem longer than 20 mm and with leaves
Flower heads with stems longer than 40 mm
Bare receptacles and undeveloped ower heads
Inorganic impurities
Loss by drying
Ash
Ash insoluble in HCl solution
Content of oil min.%

8
7
1
Unique
0.5
14
13
4
0.4

16
10
2
8
1
14
14
5
0.4

30
15
3
12
1.5
14
15
6
0.3

40
20
4
16
2
14
16
7
0.3

In special cases of the use of chamomile owers, Flos chamomillae, for pharmaceutical needs,
the evaluation was performed according to the Czechoslovak Pharmacopoeia IV 1984 and 1987
[2, 3].
Synonym: Flos chamomillae vulgaris is the dried ower head of Matricaria recutita L. species
chamomile. It must contain min. 0.4% oil and min. 0.035% chamazulene calculated to guayzulene
(1,4-dimethyl-7-isopropylezulene-C15H18-Mr198.31).
Identity Tests
Microscopy: methodical procedure as with DAB10 standard.
CHAMOMILE FLOWER (Matricariae Flos)
The chamomile ower consists of ower sets Matricaria recutita with the min. content of 0.4%
(V/m) blue volatile oil.
Properties
The drug has an aromatic agreeable aroma. The opened ower heads consist of a single covering,
which has the shape of one to three rows of leaves, conical lengthwise, eventually half-round bed
(young ower heads), 12 to 20 edge-placed tongue-shaped owers with white tongues, as well as
several dozen central yellow tubular owers.
Identity Test
A. The covering leaves are egg-formed or spear-formed having bright brown-gray edges.
The ower bed is mostly conical and hollow without chaffs. The crown of tongue-shaped
owers consists of a single basal bright yellow or bright brownish and yellow tubular
part coming over to white wide egg-shaped tongue. The crown of the tubular owers is
yellow, increasing in height, where it becomes ve-pointed having on the base bright
brownish to brown colors.
B. The ower heads will be separated into proper parts. Follows test with microscope using
chlorhydrate R solution. The outer epidermis of bed owers has a skin edge composed
of one layer of radial prolonged cells and a central zone of chlorophyll-containing
structure. Over the structure can be found the epidermis with lengthwise-shaped cells

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with lateral wavy walls and crack openings as well as glandular hairs. On the edges of
guiding beams can be found multiple pointed basic cells with big diameter.
C. The test follows the chromatography method on the small layer (V.6.20.2) using a layer
of silicate gel GF 34 R.
D. The identity test. Into reagent ask is placed 0.1 ml of reagent solution with a 2.5-ml
solution containing 0.25 g dimethylaminobenzaldehyde in the solution of 5 ml 25%
phosphoric acid, 30% acetic acid, and 40 ml water. The solution is heated for 2 min in
water bath. After adding 5 ml petroleum ether, the solution is stirred up and the water
phase is distinctly green-blue to blue in color.
Purity Test
External state means no more than 25% particles separated by mesh 710.
Foreign matters : (V.4.2). The drug has to correspond to the ash test (V.3.2.16), upper limit 13.0%.
Content Determination
The determination follows the determination of volatile oil content in the drug (V.4.5.8) using 30.0
g drug, a 1000-ml ask, 300 ml water as distillation liquid, and 0.5 ml xylol R as receiver during
4 h distillation with the distillation velocity of 34 ml/min.
Storage: Protect against light!
Tests of Purity
Crushed and overripe ower heads (undersized on the sieve IV): max. 20%
Flower heads with the stem longer than 20 mm on other parts of the mother plant (relics of
stems, leaves, etc.): max. 8%
Flower heads with the stem longer than 40 mm: max. 1.0%
Undeveloped ower heads: max. 5.0%
Bare receptacles: max. 5%
Foreign organic impurities: max. 2%
Inorganic impurities: max. 5%
Loss due to drying: max. 14.0%
Ash: max. 11.0%
Ash insoluble in HCl: max. 3%

5.6.4 MECHANIZATION: PICKING TECHNIQUE

AND

PICKING MACHINES

5.6.4.1 Picking Technique

5.6.4.1.1 Manual Picking
This method of picking is sufcient for smaller areas in gardens. It is carried out by cutting,
trimming, or combing using combs, which are similar to those used for picking of bilberries. This
method of picking is very extensive and labor consuming, but it cannot be replaced by a mechanized
method for picking areas determined for production of seed.
5.6.4.1.2 Mechanized Picking
Great attention has been paid to the mechanized picking of chamomile during the last 20 years.
The question arises about the direct picking in several rows with the width of span from 200 cm
to 610 cm according to the type of picking machine. The adapter is equipped with a comb dresser
and cutting roller. The proper combing machine is represented by the nger comb with uniform
radius of curvature along the entire length of the bar and with constant distances between individual
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ngers. Flower heads are released by the rotary brush. Flower heads are transported by worm
conveyers or by inclined scraper conveyers, or pneumatically using underpressure [5].
5.6.4.2 Picking Machines
At the present time, the farms in Slovakia have various types of picking machines.

SKM-2 R. Attached to the RS-09 implement carrier is a single-row picking machine

with low capacity of 0.03 ha.h-1, with a great ability to comb the crop without losses.
SH 2 R: Attached to the RS-09 implement carrier, with the capacity of 0.4 ha per shift.
ST-1-003 NESET: Has a higher capacity, it is designed for multirow picking with the
working span of 2 m and capacity of 0.85 ha per shift. It is also mounted on the chassis
of the RS-09 implement carrier, or it is suspended on the tractor of the Zetor type, the
Horal system [14] (Figure 5.6.4).

The concentration of the chamomile-producing area depends directly on the technique of its
picking and on the efciency of the picking machine. Nowadays, the most specialized farms are
of a large-scale nature as to the production and processing of chamomile. The VZR 4 large-area
chamomile picking machine meets this standard (Figure 5.6.5).
7
2

FIGURE 5.6.4 Frontally attached picking machine for chamomile. 1. cutter roller, 2. comb, 3. comb dresser,
4. conveyer, 5. implement carrier, 6. container for chamomile owers, 7. rotary brush.

FIGURE 5.6.5 VZR machine for picking chamomile.

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4 7

12

13

16

14

FIGURE 5.6.6 Ground plan pf the VZR 4 picking machine for chamomile. 1. lifting cylinders, 2. relieving
springs, 3. lifting arms, 4. suspensions of bodyadapter, 5. pins, 6. pneumatic exible hoses, 7. collecting
mouth, 8. distribution system for the drive of picking machine adapter, 9. countershaft, 10. pivot of the upper
arm, 11. adapter for picking of chamomile, 12. modied chassis of E-307, 13. bin, 14. wheel spacing for drive
of fans, 16. modied chain transmission for travel.

The VZR 4 represents an adaptor for chamomile harvesting performed by an adapted unit of
the harvesting windrower Fortschritt E-303. The whole unit is designed as E-307 and is a selfpropelled chamomile collector. The undercarriage E-303 is composed of the following main parts:
frame with wheels, motor, hydraulics, and plateform with cabin.
The picker has front-wheel drive and the back wheels have hydraulic control. They can be
adapted to the spacing of the front wheels, which means an enlargement on both sides by 120 mm.
This modication was implemented with the aim of allowing the back wheels to follow in the same
path as the front wheels. It is designed for direct picking of chamomile ower heads. The separated
ower heads are pneumatically transported to the sectional storage bin. After it lls, they are
mechanically ploughed out to the vehicle body, or to the container, which is transported for further
processing. The VZR 4 is a self-propelled chamomile picking machine that consists of the following
main functional parts (Figure 5.6.6):
1.
2.
3.
4.

Adapter for picking of chamomile (11)

Modied chassis of the E-303 (12)
Two underpressure pneumatic conveyers (6)
Storage bin (13)

The adapter for picking of chamomile consists of the following main parts: frame (17), sectional
combing dresser (18), sectional trimmer (20), sectional wipe roller (21), both left-hand and righthand worm conveyer (22), distribution systems (23), and protective guards (25) (Figure 5.6.7).
The frame is made of a tube-welded structure, to which the sides are attached, and of the wall
of gears for installation of shaft-bearing boxes for picking chamomile. The sectional comb dresser
(18) is mounted in the front part of the frame. It consists of ten combs with oblique teeth. The
sectional trimmer (20) is mounted in front of the comb dresser. It partially cuts and partially tears
the chamomile stems protruding from combs, using the ve cutters attached along the periphery
of the drum. The cutter can be easily moved toward the comb dresser, so that the gap between the

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23

17

25
18
20

18

22 21

FIGURE 5.6.7 Scheme of the adapter for the chamomile picking machine. 17. frame, 18. comb dresser, 19.
scraper, 20. stemming machine, 21. wiper, 22. right-hand and left-hand worm conveyer, 23. distribution
systems, 24. divider, 25. guards.

cutter and the combs is as small as possible. The sectional wipe roller (21) is mounted in the upper
rear section of the frame. It wipes the caught chamomile ower heads into the left-hand and righthand worm conveyer (22). The wipe roller consists of plastic hairs, to avoid damaging owers. The
countershaft (9) is mounted in the rear section of the frame. It is driven by the chain transmission
(8) from the engine. The distribution system (23) of the functional parts is located in the center of
the adapter in its longitudinal axis. Three dividers (24) divide chamomile stems during operation
of the adapter. Two dividers are near the edges, and one in the middle. The central divider is
available only for design purposes, to divide the functional mechanisms of the picking machine
into two parts due to a wide span. The protective guards (25) serve as protection for workers against
the touch of rotating functional parts.
The storage bin (13) catches chamomile ower heads. It forms an independent part of the
picking machine and is attached to the rear part of the E-303 chassis. Underpressure fans (15) for
underpressure transport of the material are attached to the bin. The lower edge of the bin is 900
mm above the ground. The bin is symmetrical to the longitudinal axis of the machine symmetry
plane. Two discharging holes are in the rear part of the bin, which must be airtight after their
closing, so the fans do not suck air from outside.
5.6.4.2.1 Technical Data
Adapter for chamomile picking of the VZR type:

Length: 4230 mm
Width: 2100 mm
Height: 1180 mm
Weight: 1943.8 kg
Number of revolutions of:
Comb dresser: 0.58 s-1
Stemming machine: 12.25 s-1
Wipe roller: 10.50 s-1
Worm conveyer: 2.07 s-1
Countershaft: 10.50 s-1
Capacity:1.4 m2/s

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Engine: D-50 type:

Type: four-stroke, compression ignition

Number of cylinders: 4
Volume of cylinders: 4750 cm3
Power output: 41.25 kW
Engine speed: 1700 RPM
Alternator: 12 V, 500 W

Modied chassis: E-303 type:

Length: 3960 mm
Width: 3200 mm
Driving wheel track: 2770 mm
Control wheel track: 2400 mm
Wheel base: 2400 mm
Radius of curvature: 4200 mm
Weight with the cabin: 3565 kg
Brakes: service brake: hydraulic Duo-Duplex
Hand brake: mechanical
Clutch of travel mechanism: single-plate, dry
Fuel tank: 100 l
Battery: 12 V, 180 Ah
Tires: driving wheel: 1620 PR A 19; p = 0.17 MPa
Rear wheel: 1015 AM A 13; p = 0.20 MPa

Working speeds:
1st gear: 1.74.3 km/h
2nd gear: 4.210.7 km/h
Driving speeds: 3.48.6 km/h
Underpressure pneumatic conveyer:

Diameter of piping: 160 mm

Number of pipings: 2
Fan speed: 2900 RPM
Volume of sucked air: 0.7 m3/s

Storage bin:

Length: 1920 mm
Width: 1800 mm
Height: 2050 mm
Capacity: 3 m3

VZR 4 self-propelled chamomile picking machine:

Length: 6280 mm
Width: 4230 mm

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Height: 3900 mm
Total weight: 5300 kg

The new machine for picking chamomile owers is now in the prototype stage and there is a
question about a single-purpose machine for picking chamomile owers. It is designed to pick
chamomile owers of very high quality with maximum efciency. The picked chamomile substance
contains up to 80% chamomile owers with maximum length of stem up to 20 mm.
The new picking machine can be installed on any carrier with the front three-point suspension
and the front power take-off driving shaft. The transport of chamomile owers from the adapter to
the bin is pneumatic, which is simple and does not require any changes in the carrier design. The
bin can be solved as a common tractor trailer, or in the form of an attached tilting container in the
rear part of the carrier.
The technical data are:

Total width of adapter: 3000 mm

Working width: 2600 mm
Weight: 660 kg
Capacity: 0.32 ha/h

5.6.5 PLANT RAW MATERIAL

AND

PROCESSING

IN

SLOVAKIA

5.6.5.1 Picking Conditions and Picking Methods

The most suitable time for picking chamomile occurs when the peripheral white petals are fully
opened in the horizontal plane, when the plane of the ower forms a right angle with the axis of
the receptacle and of the stem. The rst picking shall be made when one third of ower heads
ower, by which the uniform crop with richer owering and a greater number of pickings will be
obtained. Further, it is important to pay attention to the intermediate period between individual
pickings to prevent overripening, which could result in premature disintegration of ower heads
and deterioration of drug quality.
a

b
A.A

c
1

A
A

FIGURE 5.6.8 Shape of a comb and of a nger. a: comb; b: shape of nger; c: cross sections of ngers: 1.
circular, 2. semicircular with a groove, 3. rectangular, 4. triangular with a groove.

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The number of pickings depends on the date of sowing, cultivation, fertilization, and prevailing
weather. On average, two to three pickings can be obtained from spring sowing, and ve to eight
maximum pickings can be obtained from autumn sowing. Time between individual pickings
depends on weather, and is in the range of 10 to 20 days.
Due to a better regeneration ability of plants, it is necessary to carry out the picking earlier.
Two methods or techniques can be used in picking:

Machines for picking of chamomile by combing, e.g., based on the VZR 4 principle
(Figure 5.6.8).
By beating, using the steel ngers of a rotating drum. A disadvantage of this method of
picking is later renewal of owering, because the cutting surfaces are irregular and more
stem damage takes place [7].

The sectional comb dresser is mounted on the front part of the frame. It consists of ten combs
with oblique ngers. The ngers are arranged next to each other in the single plane. The distance
between ngers should be from 4 to 6 mm. During later pickings (the second one up to the last
one), the ower heads have smaller diameters; therefore, the distance between ngers must be
smaller, so that the ower heads do not slip between the ngers. The shape and cross section are
different. The circular cross section is the most abundant. Not only is its quality of work the best,
but this nger is easy to manufacture at a bargain price. The nger with the rectangular crosssection works better than that of circular. However, it is more demanding to manufacture and is
costly. The nger with semicircular cross section with a groove combs very well, but its penetration
into the crop is worse. The nger with a triangular cross section with a groove is also demanding
to manufacture, but it combs very well and penetrates into the crop. The edges of the combing
nger function partially as cutters; therefore, it is suitable for the nger to be made of high-quality
material and to have sharp edges [5].
The sectional sweeper is mounted in front of the comb dresser. It allows better catching of
chamomile owers to the comb dresser. The sectional stemming machine is mounted in front of
the comb dresser. It partially cuts and partially tears chamomile stems protruding from combs,
using eight cutters attached along the periphery of the drum. The cutters can be moved toward the
comb dresser, so the gap between the cutter is as small as possible. The cutters can be attached
alternatively to the combs, which helps regular cutting of ower heads.
5.6.5.2 Postharvest Processing
5.6.5.2.1 Sorting
Two types of sorting lines are used in Slovakia:

Sorting line of the ST-1-005 type with a minimum capacity of 120 kg/h
Presorter of the AST-034 type with a capacity of 10001200 kg/h (Figure 5.6.9)

After picking, the chamomile is sorted on sieves, or on the chamomile sorting line of the
ST-1-005 type. The sorting line consists of the proper sorting machine and the presorter (Figure
5.6.10).
This equipment is stationary and is designed for the sorting of chamomile owers into four
qualitative classes [5].
The machine consists of the following parts: the frame, discharging conveyer (7), upper roller
separator (9), lower collecting conveyer (11), lower sorting conveyer (12), and accessories. The
preseparator consists of the frame, separating drum (2), lifting mechanism (3), drive (5), and hopper
(6).

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FIGURE 5.6.9 AST-034 presorter of chamomile.

During cleaning, the material is manually fed into the hopper, and from there, it moves to the
separating drum (2). Small material, which is suitable for sorting, falls through openings in the
separating drum into the hopper of the discharging conveyer (7). The long and coarse material falls
out of the separating drum outside the machine.
The machine is driven by an electrical motor, and its daily capacity is minimum 1000 kg.
During picking of chamomile using the VZR 4 picking machine, undesired organic impurities,
such as stalks, can get into the bin. In order to remove them, the chamomile presorter is used. The
raw material gets rid of undesired organic impurities, stalks, and parts of chamomile, which
corresponds to the third-quality class of classication (Figure 5.6.11).
Chamomile substance is transported manually or by the conveyer to the internal sieve. Both
the internal sieve (1) and external sieve (2) are mounted on the wheels with the rubber rim, which
are seated in the wheel holders with milled grooves. Using these grooves, it is possible to adjust
the inclination of these sieves from 0 to 3. The raw material thrown in the internal sieve is entrained
along the periphery in the shape of helix. The undesired organic impurities and stalks are moved
toward the end of the sieve. Chamomile substance, which has fallen through the apertures of the
internal sieve, is sorted again on the external sieve in the same manner. Falling substance is on the
roller conveyer. The preliminary sorted substance gets rid of oversizes. Chamomile substance is
transported on rotating rollers for further processing.
The driving wheel of the internal sieve is guided in the groove, in order to be secured in the
axial direction. The outer sieve is secured on one side by the locking roller, and by the semigroove
on the opposite side, in which the wheel with the rubber rim travels.
5.6.5.2.2 Drying
Chamomile must be dried immediately after sorting. All qualitative classes are dried separately so
the homogeneity of the dried material is ensured. Various types of driers are used, from simple
ones as for drying hazels (heated by hot air in chambers, box driers, and continuous driers [3].

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10

11 16

12 13 14 15

17

FIGURE 5.6.10 ST-1-005 sorting line for chamomile. 1. frame of the preseparator, 2. separating drum, 3.
lifting device, 4. drive of the drum, 5. chain of the drive, 7. conveyer, 8. frame of the sorting line, 9. sorting
rollers, 10. feeding conveyer, 11. collecting conveyer, 12. sorting conveyers, 13. chain for the drive, 11, 14.
chain for the drive 12, 15. electric motor, 16. six bins, 17. side guards.

FIGURE 5.6.11 Internal and external sieves of the preseparator.

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FIGURE 5.6.12 Stemming machine for chamomile.

The operating temperature must not exceed 40C. At the higher temperature, a large escape of
essential oil takes place, and drug is of brown color, which does not meet the criteria of the
Czechoslovak Pharmacopoeia IV. After drying, chamomile drug must be left for 10 to 15 days in
open packages to breathe.
The chamomile stemming machine is used for removing long stems. The chamomile stemming
machine of the TR-6-002 type is a one-purpose stationary unit, which processes lower-quality
classes of chamomile drug, by which a higher percentage of the rst-quality class will be obtained
(Figure 5.6.12).
5.6.5.2.3 Storage
Chamomile drug is stored in cartons or in paper bags with a net weight of 711 kg (paper bag)
and 1520 kg (carton box). [6].

5.6.6 PROCESSING

IN

SLOVAKIA

5.6.6.1 Essential Oils

Chamomile is most frequently used for production of essential oil, which takes place during its
distillation with water steam. At the same time sterilization and assurance of microbiological safety
takes place, with subsequent extraction of the obtained extract. The generally known method used
for isolation of essential oil is distillation with water steam. This method is demanding for technological equipment. The quantity of essential oil obtained depends on a large number of factors,
such as pH, drug homogeneity, and quality [16]. The technological equipment, which is used in
Slovakia, is protected by the author's certicate of invention No. 245316 (Figure 5.6.13).
The distillation kettle of the apparatus for production of essential oils from medical plants
consists of a closed conical vessel (1), with the discharging mechanism on its lower base (2). The
steam supply is connected above them (3). The lling neck (4) and the outlet (5) are located on
the upper base. The homogenizing rotor (6) driven by the driving mechanism (7) is inside of the
closed vessel.

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15

11
17

5
15
9

10

6
19
7

3
8
2

FIGURE 5.6.13 Distillation kettle of the apparatus for production of etheric oils from medical plants. 1.
vessel of the kettle, 2. discharging mechanism, 3. steam supply, 4. lling neck, 5. discharging neck, 6.
homogenizing rotor, 7. helix, 8. joint bearings, 10. eccentric, 11. drive, 15. transmission, 17. quick-closing
device, 18. glass piping of the cooler, 19. thermal insulation; 12, 13, 14, 16: discharging mechanism.

The distillation kettle has the homogenizing rotor (6) consisting of the eccentric (10), transmission (15), and helix (7) located parallel with the wall of the closed vessel (1) in such a vat that
its driven end is seated in the bearing (9) of the eccentric (10) and its free end is seated in the joint
bearing (8), which is situated in the axis of the closed vessel (1).
The distillation kettle has the discharging mechanism (2) consisting of one xed plate (12) and
one rotary plate (13), which have at least two overlapping cutouts (14).
5.6.6.2 Extracts
Processing chamomile substance using the wet method has been performed since 1976. From 1995
it was calculated with essential changes in the production program via the introduction of new
technologies for chamomile processing into the form of extracts, which can be used in cosmetics
using the alcohol method and water-alcohol method and their granulation into instant tea. It was
veried in the pilot plant in 1985 [15].
The preparation of extracts according to the developed technological procedures has the following three stages:
1. Separation of solid phase: the proper extraction
2. Fine ltration and concentration
3. Dehydration
The obtained water extract was concentrated in the classical manner in the vacuum circulation
evaporators to the desired content of dry substance. Water-alcoholic extracts were prepared according to the required qualitative parameters by extraction and percolation of chamomile drug.

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REFERENCES
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.

12.
13.
14.
15.
16.
17.

C ern, K. (1988) Systm pestovania liecivych rastln, VS Hurbanovo.

C eskoslovensky lkopis IV (1984) Avicenum Praha.
C eskoslovensky liekopis IV (1987) Avicenum Praha.
Dovjak, V. (1984) Vplyv minerlnej vyzivy na dynamiku prijmu zivn, na rodu drogy a na tvorbu
obsahovych ltok u rumanceka kamilkovho. Dizertacn prca, pp. 1126. Nitra.
Honcariv, R. (1979) Vyskum pestovania rumanc
eka kamilkovho na slanych pdach. Ciastkov
loha SPTR, Kosice.
Jech, J. (1984) Stroje pre RV II.; Prroda, Bratislava, pp. 354359.
Oravec, V., (1985) Stdium biologickych a agrotechnickych vlastnost vybranych liecivych rastln,
Nitra.
Oravec, V. (1986) Nov poznatky velkoplosnho pestovanie v podmienkach JRD "Rozkvet. I.
Celosttna konferencia liecivych rastln, Piestany, pp. 2530.
Oravec, V., Varga, I., Repck, M., Hulikov, A. (1988) Author's certicate of the invention, Praha.
Oravec, V., Repck, M., C ernaj, P. (1993) Production technology of Chamomilla recutita. Acta
Horticulturae 331, 8587.
Oravec, V., Seidler-Lozikovsk, K., Holubar , J. (1996) Genza odrd rumanceka kamilkovho
Chamomilla recutita (L.) Rauschert) v Stredoeurpskom priestore. III. Medzinrodn konferencia o
liecivych rastlinch, Piestany, pp. 4344.
Repck, M. (1991) Slachtenie rumanceka a avonoidy. Pestovanie, zber a spracovanie liecivych
rastln, Medzinrodn konferencia o liecivych rastlinch, Vysok Tatry 1991, pp. 1112.
Repck, M., Halsov. J., Honcariv, R., Podhradsky, D. (1980) Biologick Plantarum 22, 183191.
Tyl, M. (1984) Nov poznatky pri petovn, sklizni a posklizn ov prave hermnku. Zbornk:

Celosttn seminr o petovn hermnku pravho. JZD sovsko, Ceskoslovensko.

Tyl, M. (1986) Metodika petovan her mnku lkar skho., MZVz, pp. 510.
Varga, I. (1985) Sc asn roven spracovania liec ivych rastln na Slovensku. Zbornk refertov z
vedeckho kolokvia, Vyzn Ruzbachy, pp. 2730.
Varga, I. (1990) Final report, Vyskum lieciv na bze liecivych rastln a prrodnych ltok II,
Hlohovec, pp. 3940.

5.7 GROWING VARIETIES OF CHAMOMILE IN THE

CZECH REPUBLIC
JOZEF HOLUBR

Cultivation of chamomile (Matricaria recutita L.) started in the former Czechoslovakia about 1955
and the majority of the production up to this date came from the plucking of the wild-growing
chamomile. Growing in the greater areas began in the 1960s. This happened thanks to the changing
structure of agricultural production and the decrease of chamomile growth under natural conditions.
The whole production was coming from increased growing from the 1970s up to the mid-1980s.
The increase was more important in the Czech Republic than in Slovakia. The share of the total
production in the Czech Republic was 40%; in Slovakia even in 1983 this share was not even 10%.
At this time the total cultivated area in the Czech Republic was approximately 200 ha and the
production 90 t, and in Slovakia about 80 ha and 10 t [24]. From the beginning of the 1990s the
total crop area decreased rapidly and in the middle of the 1990s decreased about 50 ha. The
development of the areas and chamomile production from the mid-1980s up to the mid-1990s is
presented in Table 5.7.1.
The chamomile ower can be grown in the Czech Republic in all regions except the mountain
regions. It tolerates lighter and heavier soils. Optimal annual rainfall is about 450 to 650 mm. It
is classied just after unweeded winter crops or spring cereals; olipherous plants and medicinal
plants are cultivated because of their tops. Fertilized root crops are appropriate preceding plants as
for nutritive elements in poorer soils.

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TABLE 5.7.1
Development of Areas and Production in the Czech
Republic from 1985 to 1995
Year

Area
(ha)

1985
1986
1987
1988
1989
1990
1991
1992
1993
1994
1995

240.9
247.0
251.0
235.0
277.0
279.0
137.0
21.0
3.5
56.6a
50.0b

Production
(tons)
142.1
130.9
145.6
110.4
152.4
150.1
65.8
10.7
2.0
22.8
C

Source: Leros Ltd Praha Zbraslav

a

Investigation of MZLV Brno.

Evaluation UKZUZ Brno.
c Production not found.
b

TABLE 5.7.2
Registered Chamomile Varieties in the Czech Republic
Variety
Bohemia
Bona
Goral
Lutea
Novbona

Country
of Holding

License
Year

Registration
Prolongation

R
SR
SR
SR
SR

1952
1984
1990
1995
1995

1997
1997
1997
1997
1997

Optimal nutritive rates per 1 ha are recommended as 1.0 N/0.5 up to 0.7 P/5 up to 3.3 K, which
means 20 up to 40 kg N/15 up to 20 kg P/66 up to 100 kg K [1]. The manure will be worked in
during the middle-deep tillage and the lot will be prepared as usual. The chamomile seed needs
light and stemmed soil to grow. Because of this it is seeded during calm weather on the soil surface
and is then rolled down the whole area or in rows 10 to 12 cm wide. The sowing is 2 kg per 1 ha,
and the distance between rows is 40 to 50 cm. The experience shows that about 50% of the
programmed chamomile surface should be prepared during the autumn and 50% during the spring.
The autumn sowing is done from the middle of August to the end of September. In the following
year the growth will bloom about 3 weeks earlier than the growth coming from the spring sowing.
The spring sowing should be done in the early spring. On smaller areas and with manual harvesting
ve to eight harvests can be achieved. Mechanical harvesting means three to four harvests.
In the Czech Republic ve varieties of chamomile are actually registered; of those one is
domestic and four are foreign varieties (see Table 5.7.2).

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TABLE 5.7.3
Containing Substances of the Chamomile Varieties from SOZ
Determined during 1993 and 1994

Variety
Bohemia
Bona
Goral
Lutea
Novbona
a

Essential Oil
Content
(%)

Content of
Chamazulene
(%)

Content of
Bisabolol

1.2
1.0
1.2
1.2
0.9

21.0
18.9
21.4
21.2
18.0

a
46.1
23.0
43.3
46.1

Content was not determined by technical means.

Bill No. 92/1996, in effect since July 1, 1996, determines that a variety registered in the National
Variety Book before the above-mentioned bill was in effect can be considered as registered if the
applicant applies within 1 year for the prolongation of the registration.
During 1993 and 1994 evaluations concerning the difference, uniformity, and steadiness (DUS)
on the above-mentioned varieties were realized. One part of the evaluation was the determination
of substances contained within a variety. See the average values for all harvestings in Table 5.7.3.

REFERENCES
1. Drozen, J., Kocourkov, B. et al. (1995) Lciv, aromatick a kor eninov rostliny. Situacn a
vyhledov zprva. Mze CR, 89.
2. Tyl, M. (1984) Nov poznatky pri pestovn, sklizni a poskliznov pravy hermnku. Zbornk:
Celosttn seminar o pestovn he r mnku pravho. JZD sovsko, C eskoslovensko.
3. Tyl, M. (1986) Agrotechnika velkovyrobn produkce hermnku lkarskho, Lciv rostliny, Zbraslav
nad Vltavou.
4. Tyl, M. (1986) Metodika pestovan hermnku lkarskho., MZVz, 510.

5.8 EXPERIENCES WITH THE CULTIVATION OF CHAMOMILE

IN ARGENTINA
NORBERTO FOGOLA

5.8.1 CULTIVATION
5.8.1.1 Date of Sowing
In Argentina chamomile sowing is usually carried out in autumn, from March until June. In this
way, time remains for the chamomile to establish well and to form good roots.
The advantages of the summer-autumn sowing over the spring sowing is not based on a higher
azulene and essential oil content. The autumn sowing generates above all higher harvests, sometimes
paralleling with a higher azulene content. Between the sowing in autumn and in spring there are
great differences, not only the earlier owering of the autumn chamomile. The autumn sowing
offers the advantage of a more regular germination of the seeds.
The disadvantage is, however, that the chamomile sowed in autumn frequently becomes very
weedy in spring. The autumn sowing requires more attention than the spring sowing. If the snow

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cover is missing, the chamomile plants could be killed by hoar. Deciding the date for sowing is
frequently based on local climatic circumstances. Sometimes it is practical to carry out sowing at
different dates in order to be able to harvest at different times. So it is sowed semiannually (in
spring and summer), which results in two harvests (summer and autumn chamomile). Even an
autumn sowing at two and a spring sowing at three (different) dates is recommended. According
to the size of the elds, the sowing must occur in short intervals of 814 days. Sowing is accomplished in slightly raised lines. In order to reach a regular sowing, putting on the lines during calm
weather is recommended. If the ground circumstances make it possible, it is reasonable to roll the
soil surface. An old proverb tells us that where the chamomile is trod, it grows better.
5.8.1.2 Seed Amount
Seed material is mainly used, which is classied as Argentinas bisabolol oxide B-type. On a larger
scale seeds from Germany were used, and a company-owned type that is derived from Spanish
seeds has been used. Only recently has it been changed over to modern cultivation types.
The ne seed can be sowed without mixing with sand or semolina. For that a machine
appropriate for the sowing into lines with lifted ploughshares or a modied seeding machine for
ne seeds can be used. As chamomile seeds are plants that germinate in light, they must not be
covered with earth. In any case the seeds are slightly pressed on the soil surface. The amount
depends on the purity and the germination capacity of the seeds. The very small seeds (thousand
kernel weigh 0.0350.050 g) often are mixed with other parts of the blossoms, that can be separated
by sieving due to their different specic weight.
The germination capacity is often insufcient; after 1 year of storage it is reduced by 7 to 49%
and after 3 to 5 years after harvesting it is completely gone. Depending on the sowing machines
available, one calculates 1 to 3 kg seeds/ha. If the germination capacity of the seeds is insufcient
or the seeds are contaminated, a higher quantity has to be taken into consideration, i.e., up to 4 to
6 kg/ha. With a uctuation range of 1.5 to 3.0 kg seeds/ha, no differences were found.
5.8.1.3 Row Distance
Carrying out broadcast sowing is not recommended, as it complicates the care and harvest. Concerning the optimal row distance, opinions diverge greatly. A maximal row distance of 70 cm is
recommended, corresponding to a plant distance of 30 cm. The slightly lower yield per hectare is
compensated for by better harvest conditions. The ower yield per hectare increases the degree by
which the row distance gets smaller; the yield per plant, however, increases with the enlargement
of the distance. An enlargement of the distance would reduce the harvest amount, whereas azulene
and essential oil content are independent from the date of sowing, the row distance, and the quantity
of seeds used.
It seems to be a fact that the plants have to stand so far each from another, so that a further
harvest can be effected in the same year. The ower heads are always located at the end of the
side shoots. The more shoots a plant has, the higher the quantity of owers. Lack of light, a distance
too close, and a soil too at prevent the formation of side shoots, so that the plants grow with only
one shoot.
Optionally an optimal row distance of 40, 45, 50, or 60 cm can be determined in the case of
an automatically effected harvest. Finally, the optimal row distance is related to the frequency of
rainfall. The drier the crop eld is, the closer the row distance of the chamomile has to be; i.e., in
dry zones a distance of 45 cm is recommended; in most other zones the distance should be 60 cm.
5.8.1.4 Germination Factors
The success with the sowing of the chamomile on the eld depends to a great extent on the climatic
conditions. In years with dry spring and autumn, the chamomile yield remains very small. Cham-

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omile is a plant that germinates in light. Chamomile seeds depend on the humidity in the upper
layer of earth in order to come to germination. If this is available, germination can take place.
Sometimes, however, one single day of intensive sunlight can cause the seeds to die, as the humidity
in the upper layer of earth evaporates. Under normal circumstances, germination takes place 14
days after sowing. With dry weather, it can be delayed.
5.8.1.5 Growth Factors
The overground parts of the chamomile can develop in very different forms according to their living
conditions. The wild plants that grow unhindered develop a robust, straight, 55- to 60-cm-high
stalk, while the plants that are found at unfavorable sites grow only up to 10 cm high. If the
chamomile plants are planted not too closely, they can reach a height of 80 to 90 cm. The more
the plant branches, the more capitulums it generates, which under favorable conditions can develop.
If growth is constricted even if the plants grow between other specimens slightly constricted
the development is hindered. In extreme cases, only plants with one shoot are produced or those
that form only the nal capitulum of the primary axis and the rst upper offshoot.
5.8.1.6 Soil Properties
Generally the chamomile does not make demands; it grows on light and heavy ground, but favors
sandy and loamy soil. It adapts itself to the ground conditions very well and grows with pleasure
(as weed) in the areas that surround the crop elds. Nevertheless, the yield increases on black earth
and meadow ground and decreases on brown, sandy earth without humus. Obviously the chamomile
grows very well at a pH value between 7.3 and 8.1. So for example the alkaline and sodium
monoxide grounds of the salt steppes of Hungary (SZIK grounds) are favorable. Chamomile can
be grown successfully on grounds that due to their alkaline state (pH value 8.5 to 11) are not
suitable for cereals any more.
Chamomile that is growing on saline grounds produces a more attractive appearance and greater
purity; however, it does not contain high amounts of essential oils and azulene.
Although the drug yield is inuenced by the ground quality, there is no relation between the
basic factors of ground quality and active substance content of the chamomile.
5.8.1.7 Climate
The oil content is highly inuenced by factors such as air temperature, rainfall, and solar radiation.
The optimal temperature for the formation of essential oil during the owering period would be
20 to 25C. In an experiment with accentuated ecological differences it could be stated that the
weather conditions do not have any inuence on the amount and the composition of the essential
oil of the chamomile. The increase of the content of essential oil and chamazulene depends mainly
on genetic factors. There is no relation between the height of the plant and the content of ingredients,
either.
5.8.1.8 Fertilizing
The fertilizing depends on the composition of the ground. For big sowing areas an analysis is
recommended to consider the nutrient content and the pH value. The chamomile reacts positively
to potash. However, it is very sensitive to excessive phosphoric acid. The fertilizing with N and P
has a great inuence on the growth, the ower size, and amount as well as the content of
prochamazulene. When the N- and P- amounts are different, the result decreases. The best result
is achieved with N + P in relation 1:1. The uptake of the active substances of the chamomile per
hectare is as follows: 16 kg N, 4 kg P, 20 kg K, 4 kg Ca, 1 kg Mg < 1 g Na. The ground must
contain sufcient phosphoric acid so that the stalk becomes strong enough and owers with short

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stems can be cut. The same is valid for potash. In spite of that, the nitrogen gifts should be small.
If the nitrogen gifts are too big, the plants are overgrown with weeds and have the tendency to
burst. The ower number decreases. On the other hand, the unique fertilizing with nitrogen increases
the ower number, as in the case of simultaneous fertilizing with phosphate and potash.
Fertilization with phosphate, potash, and calcium alone or combined does not bring any
increase. A mineral fertilizing with a great amount of potash supports the ower formation. The
chamomile should not be fertilized with stable manure. Because of its ability to release nitrogen
slowly, it supports the vegetative development of the plants, which comes along with a drop of the
ower number. Before sowing, a complete fertilizing (N, P, Ca, K, etc.) is necessary. After every
harvest the ground is fertilized again, whereas the P amount has to be higher than during the rst
fertilizing. The usual fertilizer doses are as follows:
4060 kg N: 200300 kg ammonia and calcium-containing nitrate/ha.
3645 kg P2O5: 200250 kg super-phosphate/ha
80120 kg K2O: 200300 kg potash (40%)/ha.

5.8.2 WEED

AND

PATHOGEN CONTROL

5.8.2.1 Herbicides
One must distinguish between the elimination of the chamomile in other cultures and the elimination
of the weed within the chamomile elds. The elimination of the chamomile, for example, in cereal
elds, is not very easy. Chamomile is resistant against almost all herbicides that are applied for
cereals. Therefore, chamomile is often a weed in the following cultures.
In Argentina Trian (commercial denotation) is used as herbicide before sowing; chemical
nomenclature: alpha, alpha, alpha-triuor-2,6-dinitro-N,N-di-propyl-p-toluidine. The chemical classication reads: Dinitroanilin; active substance: Triuoralin. After this the chamomile plant is
processed if it begins to sprout with the herbicide 2,4-D.
A weed-free chamomile eld is the vital precondition for an impeccable quality of the drug.
Particularly the application of the local harvest equipment is only possible in weed-free chamomile
elds. It is advisable to plant chamomile on a maximally weed-free ground. The best precrops are
sugar beet as well as potato, which create a good ground structure and a favorable ground state.
Because of their high N-content, legumes (peas) are less suitable.
The chamomile tolerates also different cereals as precrop. Cornelds weed-free or preprocessed with herbicides are especially suitable.
The herbicides have to be applied at the appropriate time. If they come into direct contact with
the seeds during germination, in most cases annihilation of the chamomile crop will result.
5.8.2.2 Insecticides
In Argentina the use of insecticides is not necessary.

5.8.3 YIELD FORMATION

5.8.3.1 Stage of Development and Content of Nutrients
The owering heads pass through different development stages until they open completely.
The step-by-step owering of the tubular orets from the lower to the upper edge lasts approximately 3 to 4 weeks. When the ligulate orets bloom, they unfold themselves. While the ligulate
oret continues growing, it lifts and lowers itself daily. The bigger the owers are, the weaker the

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daily periodic movement of the ligulate orets. They do not move anymore when the last tubular
orets have opened.
The dry matter per capitulum increases during the development on an average of 1.23 mg to
39.24 mg.
The capitulums of the closed ower have the highest oil content. The second highest level is
reached with full blossom. While the weight increases during the owering process, the oil content
in the fully developed owering heads drops below the content of the half-ourished ones. The
content in a eld reaches a maximum if 50% of the tubular orets of a owering head are opened.
The increase of the essential oil content and the content of chamazulene entails an increase of
the dry weight up to the full ower. Here, the increase of the essential oil content is a little smaller
than the increase of the dry weight. Therefore the essential oil content decreases in relation to the
dry weight. The azulene content of the oil increases during the expansion period of the ower.
After the capitulums have reached their maximum size, both the oil and the azulene content decrease
as they wilt. Thus, the production of essential oil and azulene seems to be ended when the owering
heads have fully sprouted.
The chamomile variety Bodegold reaches a maximum essential oil content when the owering
head has almost ourished and the lower parts of the owering head are already hollow; a daily
periodic growth movement, however, is still notable.
5.8.3.2 Distribution of the Active Substances
In the variety Bodegold the following distribution of the essential oil content (g/100 ml/ drug)
was measured:
Flowering head:

0.95

Tubular orets:

0.82

Ligulate orets:

0.22

Lower part of the owering head:

5.8.4 HARVEST

With top:

1.18

Small fragments:

0.52

AND

PROCESSING

5.8.4.1 Time of Harvest

The chamomile harvest takes place in several gathering processes in the period October 10 to
approximately November 30.
The chamomile harvest has to be started as quickly as possible so that the plants can form new
owering heads. The harvest starts when the capitulum of the main bud on the main shoot has
ourished fully. Then it blooms for two weeks, and in this time many capitulums of the side shoots
develop in the same way; in general they develop up to half and more. A suitable time for harvest
is considered to be appropriate when the rst three rows of the tubular orets are open; otherwise,
the capitulums fall apart before they dry.
In Argentina, up to two harvests of the same plants can be achieved per annum at intervals of
10 to 14 days.
In contrast to the wild chamomile, the owering of the frequently harvested chamomile stops
with the appearance of frost.

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TABLE 5.8.1
Chamomile Exports from Argentina in the Years 1987 to 2002
Year

Tons Dry Matter

1987
1988
1989
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
2002

1800
2321
3281
2413
2843
2900
2800
2000
1800
1500
1500
1300
1200
1100
800
600

Source: Ofce of the Authority for Agriculture, Stock Breeding and Fishing of the
Republic of Argentina).

The time of day the harvest is carried out is not exact. Because of the sun inuence, in Argentina
as a rule it is carried out from sunset until 10:00 the next morning, although about noon a maximum
pro-azulene content is found.
Optimal harvest conditions are to be found when clouded sky, dry weather, and temperatures
around 20C prevail.
5.8.4.2 Yield
The ower yield strongly depends on the number of harvests. Argentina usually produces approximately 2000 to 3000 kg/ha fresh product (400 to 500 kg not-cleaned dry product). In the former
Soviet Union a yield of approximately 300 to 500 kg/ha at four harvests per year was achieved.
In Egypt approximately 3152 kg/ha (fresh) were harvested, in Germany up to 800 kg drug/ha, and
in India approximately 600 kg/ha.
The drying relation is approximately 1:5 to 6.5. According to Heeger [1] the yield of dry owers
is 500 to 2000 kg/ha, in general 500 to 1200 kg/ha, and the yield of the whole dry plant is 2000
to 5000 kg/ha, in general from 2000 to 3000 kg/ha.
In the years 1987 to 1996, the total harvest in Argentina amounted to more than 2000 tons of
drug per year with a drop during the last years of the period. The greater part of the drug crop is
exported, above all to Europe (Table 5.8.1).
5.8.4.3 Harvest Methods
The collection or the harvest of the owers is carried out as follows:
1. Manually: the ower head is torn off by shifting the stalk between the ngers and pressing
the ngers briey, as is still the case in Egypt today.
2. With a rake similar to the one that is used for blueberry and cranberry harvests. The
following systems exist:
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FIGURE 5.8.1 Manually pushed picking cart.

a. Meyer: Tubes with a multipronged fork with a mobile cutting device (scissors) on
top. No stalk-free product is produced.
b. Sartorius: Sheet steel appliance with led-off teeth. Long stalks are obtained.
c. Central Germany: Rake with 20 prongs, 14 cm width, thorn body 65 mm in length
at intervals of 6 mm.
d. Heeger [1]: Rake with 20 peaked thorns with 110 mm length each at intervals of 5
mm, 10 cm width. The device is completely open at the top.
e. Checo: Quadratic sheet box that has a grip at the upper part. Below the aperture lie
peaked teeth at intervals of 5 mm.
3. With toothed shovels.
In the salt steppes of Hungary a device is used in the form of a toothed shovel is used,
similar to a potato harrow, that must be operated with both hands because of its size (see
Figures 5.2.2 and 5.2.3 in Section 5.2).
4. With special rakes, that are pushed by humans (Figure 5.8.1) or the next larger size
pulled by horses.
5. With mechanized harvesters.
At rst, with simple devices 50 to 100 tons of chamomile drug were harvested per year. After
1950 the hand combs, common until then, were replaced by pushcarts (Figures 5.8.2 and 5.8.3).
As of 1950 the rst cultivation attempts were started. The quantities could then be increased rapidly.
The functional pushcarts were pulled by horses or motor (Figure 5.8.4).
For the formerly common solar drying, approximately 35,000 racks were brought outside in
the mornings and back to the storage area in the evenings. Temporarily more than 5,000 persons
were working the harvest and processing during a season. A further increase of production, however,
was only possible through the use of harvesters (Figure 5.8.5); the rst prototype of modern
harvesters was used starting in 1971 (Figure 5.8.6). This Argentina harvester was working effectively. By 1974 production already amounted to 2000 tons.

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FIGURE 5.8.2 Manually pushed picking cart.

FIGURE 5.8.3 Manually pushed picking carts.

For this large-scale production, hand picking is not suitable, a mechanization of the chamomile
harvest was established for economic reasons. The Linz harvester (variants I to III) developed in
the former GDR proved workable on larger cultivation areas, but it is no longer manufactured. In
Slovakia chamomile harvesters are used with good success, too.
Furthermore, it should be considered that the chamomile harvest lasts only a few weeks so that
improvements can only be tested during the following season. The cultivation of chamomile is
relatively specic in comparison to other agricultural crops. Therefore, the machine manufacturers
do not show great interest because of low demand.
Depending on the collecting method, the yield varies. With a manual harvest it amounts to 0.75
kg fresh drug (0.15 kg dry drug) per hour, 4 to 5 kg fresh drug in 6 to 8 hours. With the Heeger
device the yield can be increased to 2.0 kg fresh drug per hour (0.4 kg dry drug). The Slovakian
machine was constructed to collect 800 kg fresh drug per day.
5.8.4.4 Seed Harvest
As the owering period lasts for some months, the seeds as well mature at different times. If the
seeds begin to fall from a plant of medium size, the main maturity has started and harvest can
begin in the early mornings, when dew still lies on the plants. Harvesting is stopped when the
plants are dry and the seeds fall out.
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FIGURE 5.8.4 Mechanized picking cart.

FIGURE 5.8.5 Harvester for chamomile herb.

Large cloths are most suitable for the transport of the chamomile cut for seed extraction. The
seed yield varies between 30 and 300 kg/ha; in general it amounts to 100 to 200 kg/ha.
5.8.4.5
Extraction of the Drug, Drying
The harvested owers must not be pressed and should be transported in baskets (narrow on top,
wide at the bottom) or in at cartons. Then they should be spread out for immediate drying in the
shade (an airy place at best) in a thin layer on drying racks or on the ground covered with paper.
The water loss is 75 to 85%. If possible, the owers should not be turned nor touched nor moved
during the drying process. Fast drying is also guaranteed through natural air drying if the chamomile
is distributed in thin layers and is well ventilated.
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FIGURE 5.8.6 Argentinian chamomile harvester

Often drying in the shade at a normal temperature (under 35C) is preferred because a speededup drying process results in a loss of active substance. The loss of azulene with solar drying amounts
to more than 30%. The drug dried in the shade contains 20% more essential oil and bisabolol than
the product dried in the sun.
Nevertheless, the natural drying requires a period of 3 to 4 days (with unfavorable climatic
conditions up to 14 days), while the articial drying at 30C needs only 8 to 12 hours. Natural
drying in the shadow cannot be used if the product is cultivated in big scale, particularly if the
very lower loss of active substance is taken into consideration.
Today, during a season, 60 to more than 100 tons of fresh drug is processed per day. It
continuously passes through the sorting machines to the belt drying machines and is sorted with
the help of conveyor belts after drying and freed from weeds.

REFERENCES
1. Heeger, E.F. (1956) Handbuch des Arznei-und Gewrzpflanzenanbaus. Drogengewinnung [Handbook
of the cultivation of medicinal and spice plants]. Deutscher Bauernverlag, Berlin, 775 pp.

5.9 CHAMOMILE IN CHILE: CULTIVATION AND INDUSTRIALIZATION

EDUARDO WELDT S.

5.9.1 BOTANICAL CONSIDERATIONS

Chamomile is a foreign species in the Chilean ora [9], rst introduced in the Catalog of the
Cultivated Species in Santiagos Botanical Garden [12].
The name chamomile in Chile is applied to several species of the Asteraceae family [10], but
Common chamomile is the most commonly used [15]. Several authors have referred to this plant
using a Latin term [4], widely accepted in Europe as Matricaria recutita L. (Chamomilla recutita
L. [Rauschert]) [2, 3], also in America in the taxonomy of commercial species [7] as well as in
Chile [5]. In Europe, it is well known as Common chamomile in England, Echte Kamille and

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Gemeine Kamille in Germany, Camomille vulgaire in France, Camomilla in Italy, and Manzanilla
comn in Spain [13]. The synonym Matricaria chamomilla L. is accepted [10, 14]. Some authors
in Chile have called it Chamomilla recutita L. (Rauschert), according to the denomination for Chile
in the catalogs of R.A. Philippi [12] and F. Philippi [11].

5.9.2 USE
In Chile, the chamomile shows the highest consumption among the medical herbs, in folk medicine
as well as for use in the herbal tea and infusions industry.
The common chamomile was rst mentioned in Chile in 1881. There is a great deal of
information about its use since the arrival of the Spaniards in South America [5, 6]. Later, during
the German colonization in southern Chile, from the year 1854, the common chamomile is mentioned as being used for medicinal purposes in the chronicles of that time.
The rst industrial crops were harvested in 1977, and they were developed by Puelche S.A. to
export owers [1]. These are the rst records of this activity in the country, using German seed.
Later, in 1980, some rural rustic crops for obtaining dry owers used in the popular pharmacopoeia
were found in villages near the town of Traigun. This material was used in comparison trials with
the material from the experimental crops using German and Argentinean seeds.
The results of these trials showed that the naturally selected and acclimatized seeds in Chile
produce a sweet ower, whose quality can be compared to the German product, and proved much
better than the Argentinean product, which presents a more bitter taste. This Argentinean chamomile
represent mostly a bisabolol oxide B-type.
Puelche S.A. started working on selecting the seeds, isolating individuals of special owering
precocity and homogeneity. From this, Puelche S.A. was able to develop a high-purity line, which
has been cultivated until today. Since 1984, this variety of sweet chamomile has been grown to be
packed for herbal tea infusions and commercialized as Matricaria recutita L., type Manzanilla
Primavera Puelche.
According the analysis, the Manzanilla Primavera Puelche represents a bisabolol oxide A-type
and its composition is as follows:
Essential oil:

761.81 mg/100 g

Chamazulene:

12.47 mg/100 g

Bisabolol oxide A:

105.97 mg/100 g

Bisabolol oxide B:

26.75 mg/100 g

-Bisabolol:

8.81 mg/100 g

cis-Dicicloether:

56.36 mg/100 g

trans-Dicicloether:

4.01 mg/100 g

The industrial use of the chamomile for infusion in individual teabags started increasing in
1980 in Chile. Before this happened, the offer was provided by rural suppliers, which were quickly
replaced by a consistent offer. This allowed an interesting development of the infusion industry in
Chile, though there were sporadic imports from Argentina. The offer of an excellent quality product
allowed a sustained development of the Chilean Packing Companies until the present day.

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5.9.3 CULTIVATION
According to Lpez [8], chamomiles habitat is found in Mediterranean climate, between 0 and
1000 meters above sea level (m.a.s.l.). It is easily adaptable to different types of soils, preferably
the silica-clayish type, deep and fresh, avoiding excess moisture.
Selecting clean and fresh soils, and using articial irrigation, helps achieve an optimum phytosanitary condition.
The Puelche chamomile cultivation program considers handling 100% tech-irrigation surfaces,
using Side-Roll.
The seed time goes from May to August every year, depending on the seed land, type of
irrigation, and crop rotation periods.
The irrigation is performed using the Side-Roll system, using clean weed-free water, which
helps to obtain weed-freer soils year after year in the yearly rotation of crops. Roll sprinkling
irrigation is also used in new soils being added to the cultivation area. Other growers prefer organic
cultivation.
5.9.3.1 Sowing
Cover sowing is performed using selected seed of Manzanilla Primavera Puelche or seeds from
Europe. The dose is normally 68 kg/ha. Before sowing, the seeds are mixed with the fertilizer,
the dose varying, depending on the soil analysis.
Average of soil characteristics:
pH:

7.1

Organic matter:

4.2%

N:

6.3 ppm

P:

11.0 ppm

K:

190 ppm

Average fertilization per hectare

5080 kg:

Nitrogen

100120 kg:

Phosphorus

5070 kg:

Potassium

1520 kg:

Sulphur

1015 kg:

Magnesium

3040 kg:

Calcium

5.9.3.2 Weed Control

In Puelche a weed control plan was developed, determined by the rotation of chamomile crops.

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FIGURE 5.9.1 Handpicking with a special comb.

The rotation considers an intermediate cleaning crop once a year, using oats sown in DecemberJanuary every year. These seed are sown over the stubble formed by the chamomile that has
been immediately incorporated after the harvest.
This rotation of crops allows a weed control; the main species are:
Convolvulus arvensis L.
Polygonum persicaria L.
Veronica persica Poiret
Raphanus raphanistrum L.
Capsella bursa-pastoris (L.) Medikus
Galega officinalis L.
Spergula arvensis L.
Plantago lanceolata L.
Echium vulgare L.
Silene galica L.
Leucanthemum vulgare Lam.
Anthemis cotula L.
Chenopodium album L.
Taraxacum officinale G. Weber ex Wigg.
5.9.3.3 Harvest
The chamomile harvest starts in November using machines that cut and select the oral capitulums
(Figures 5.9.1., 5.9.2, 5.9.3).
The drying process is performed in tunnels at a controlled temperature of 45C.
Associated with harvest we can nd insects that naturally live in the farm under chamomile
crops, showing healthy living conditions for the crops.

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FIGURE 5.9.2 Tractor-drawn picking cart.

FIGURE 5.9.3 Chamomile harvester (Argentine type).

These insects are1:

Schistocerca sp. (Orthoptera, Acridiidae)
Megalometis cacicus Kuschel (Coleoptera, Curculionidae)
Naupactus xanthographus (Germar) (Coleoptera, Curculionidae)
Chrysolina gemellata (Rossi) (Coleoptera, Chrysomelidae)
Pycnosiphorus costatus Beuesh (Coleoptera, Lucanidae)
Astylus gayi Solier (Coleoptera, Dasytidae)
Hylamorpha elegans (Burmeister) (Coleoptera, Scarabaeidae)
1

We thank Professor Dr. Andrs O. Angulo (Biologist/Entomologist, University of Concepcin) for the exact determination
of insects.

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Praocis curta Solier (Coleoptera, Tenebrionidae)

Colletes cognatus Smith (Hymenoptera, Colletidae)
Apis mellifera L. (Hymenoptera, Apidae)
Synhgrapha gammoides (Blanchard) (Lepidoptera, Noctidae)

5.9.4 FINAL PRODUCTS

The harvest process, drying process, and industrial processing are destined to obtain capitulums as
the main product, which is obtained by threshing the pollen (the tubular owers of the capitulum),
which measures 0.251.25 mm. Of the remnant, an industrial-quality product is made.
Yields averages:
Dry owers:

200250 kg/ha

Pollen:

300350 kg/ha

Industrial:

600800 kg/ha

Seeds:

80100 kg/ha

REFERENCES
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.

15.

Banco Central de Chile (1978) Registros de Exportacin. Santiago, Chile.

European Pharmacopoeia 3rd Edition (1997) Council of Europe, Strasbourg, France.
Font Quer, P. (1982) Plantas Medicinales. El Dioscrides Renovado. Barcelona, Spain.
Foster, S. (1999) Chamomile, Matricaria recutita and Chamaemelum nobile. Botanical Series No.
307. American Botanical Council.
Hoffmann, A. (1992) Plantas Medicinales de uso comn en Chile. Ed. Fundacin Claudio Gay.
Santiago, Chile.
Laval, E. (1953) Botica de los Jesuitas de Santiago (1767). Biblioteca de la Historia de la Medicina
en Chile, Tomo II. Santiago, Chile.
Liberty Hyde Bailey Hortorium (1976) Hortus 3rd Edition. New York: Macmillan.
Lpez, C. (1988) Plantas Medicinales: Cultivo y Perspectivas. El Campesino, Santiago, Chile,
August/September.
Matthei, O. (1995) Manual de las Malezas que crecen en Chile. Santiago, Chile. Alfabeta Impresores.
Muoz, O. M., Montes, M., Wilkomirsky, T. (2001) Plantas medicinales de uso en Chile, Qumica y
farmacologa. Andros Imp. Ltda., Santiago, Chile.
Philippi, F. (1884) Memoria y Catlogo de las plantas cultivadas en el Jardin Botnico hasta el 1
de Mayo de 1884. Imprenta Nacional. Santiago, Chile.
Philippi, R. A. (1881) Catlogo de las plantas cultivadas para el Jardn Botnico de Santiago hasta
el 1 de Mayo de 1881. Imprenta Nacional, Santiago, Chile.
Steinmetz, E. F. (1957) Codex Vegetabilis. Amsterdam, Netherlands.
Tucker, A. O. (1986) Botanical Nomenclature of Culinary Herbs and Potherb. In Craker, L. E., Simon,
J. E. (Eds.), Herbs, Spices and Medicinal Plants: Recent Advances in Botany, Horticulture and
Pharmacology. Vol. 1. Phoenix, AZ: Oryx Press.
Zin, J., Weiss, C. (1980) La salud por medio de las Plantas Medicinales. Santiago, Chile, Ed.
Salesiano-Chile.

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5.10 CULTIVATION EXPERIENCES IN EGYPT

TAMER FAHMI

5.10.1 CULTIVATION REGIONS

Chamomile (Matricaria recutita / Asteraceae) has been cultivated in Egypt since 1960 in two
areas:
a. Oasis Fayoum, approximately 80 km southwest of Cairo, where approximately 2000
feddan (1 feddan = 0.42 ha) are cultivated (900 ha). Because of its quality, this product
is mostly used for industrial purposes.
b. Beni Suef, approximately 130 km south of Cairo, where approximately 1000 feddan of
the fertile Nile soil are used for cultivation (450 ha).
c. Small amounts of chamomile are cultivated in Belbes (northeast of Cairo), in the Nile
Delta, and also in Assiut (375 km south of Cairo).
Chamomile is densely cultivated in Beni Suef, Fayoum, and Sharqya Governorates. The best
is cultivated in Al-Menya and Assiut.
The entire cultivation area in Egypt adds up to approximately 1500 ha, depending on the market
situation.

5.10.2 CULTIVATION AREAS

In former times in Egypt, the land was one big plot of land cultivated with one crop. Then it was
divided between many woneers in the course of the agriculture reform, and this affected the actual
growing method and the cultivation and the harvesting.
Due to the agricultural reform in Egypt only small areas are cultivated (approximately 0.5 to
15 feddan = 0.225 to 6.75 ha). This results in advantages but also disadvantages:

Due to the small surfaces, mechanical harvest is rather impractical.

On the other hand, this results in individual families harvesting from their own surfaces.
Some of these families are specialized in box material with good quality.

During the last years the surface of ecologically grown chamomile has increased. For the time
being ecological cultivation proceeds mainly in the Oasis Fayoum, partially also in the Nile Delta
and in Beni Suef: approximately 850 feddan (approximately 350 ha). The Egyptian organization
ECOA maintains quality control in tight cooperation with internationally active control institutions.
Evaluations of accommodating the entire Oasis Fayoum into ecological cultivation are made.

5.10.3 CULTIVATION PROCEDURE

Cultivation in Egypt is mostly done by growing the plants in nurseries followed by planting in
prepared soils.

Soil
The plants can bear severe cold but not hot weather. Chamomile is better cultivated
in yellow soil and light alluvial soil with good drainage and airing, as well as in new
and reclaimed sandy soil where a drop-irrigation system is used, and in fertile soil.
The plants bear a proportion of salinity (12,000 parts per million), and are better
cultivated in light neutralized alkaline and in somewhat acidic soil.

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Mediterranean Sea
Damietta
Port Sald
Alexandria
Sharqlya
Seuz
EI Giza
Fayoum CAIRO Sinai
Sani Suway
Al minya
Sham
ash
Shaykh

Ni

Asyut

le

Luxor

Red
Sea

Aswan
0
0

100 200 km
100

Lake
Nasser

200 nm

FIGURE 5.10.1 Map of Egypt.

Growing of plants
During August 15 until September 15 plants are prepared in nurseries. 1 Irate (176
m2) of land is prepared with 2 m3 compost followed by full irrigation until the water
covers the compost. After dryness it should be well plowed, softened, and divided
into equal 1.5 3 m2 area basins, so we can control the sowing operation of plant
nursery seeds in the plant nursery. The plant nursery should be in a dark place and
during growing not be directly exposed to the sun so that buds do not y away. Then
the land should be plowed and the seeds must be covered.
Then 1 kg of good seed should be mixed with 3 kg of sand (3 times as much sand
as seeds) to facilitate the distribution of seeds. The land then must be plowed and
seeds must be covered one and one half times their weight with soil or sand, then
water sprayed to x the seeds, then slowly and densely irrigated so that seeds do not
compile. The plant nursery should be continuously irrigated and cleaned of weeds so
that water does not remain.
Preparing the land for cultivation
20 m3 of compost + 200 kg of rocky phosphates + 2 m3 furnace dust are distributed
with vibration. Then the land must be arranged in lines with a range of 12 lines per
2 Egyptian poles or divided into a 1-m-wide (mastaba) bench, then to segments and
basins to control irrigation water.
Planting
At the end of September/start of October the soils are prepared and the young plants
are planted into the soil. The soil is divided into rows (distance between is 0.75 m)
and fertilized with superphosphate. The soil is watered immediately before planting.
Manual watering is done as furrow irrigation.
Per
feddan
approximately
20,00025,000
seedlings
are
planted
(45,00055,000/ha). This constitutes into a seeding amount of 200250 g/feddan (ca.
500600 g/ha).
The plant nursery should not be irrigated 10 days before uprooting, which is done
with an axe from beneath the roots.
The nursery plant should be planted in the upper 1/3 portion of the line and must
be well covered with mud. Flowers should be picked if found. The distance between

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one plant and the next must be from 30 to 40 cm, and cultivation must be at the side
facing the sun. During cultivation, the soil is usually sprayed with Kroon 500 fertilizer
at a rate of 200 g for each 20 liters of water, then stirred in both directions. It is better
to cultivate the nursery plant on the same day.
Water supply
The land is irrigated 35 days after the cultivation irrigation, then resown. The land
is irrigated 1012 days after that, or according to a ower gathering program. Intervals
between irrigation must be less in sandy land and drop-irrigation land. Thirst decreases
the blossoms crop and generally it needs to be irrigated approximately 14 times
during the growing season. Irrigation is accomplished mostly as furrow irrigation in
intervals of 20 days.
Care and weed control
A light rst hoeing is done to ll up chinks and to clean up weeds after success with
the nursery plant, leaving only one or two plants in the hole. Then a second hoeing
is done. After that supporting plants are done and they are left without irrigation until
roots get deeper. Flowers must be picked if found. A third hoeing is done, adding 4
m2 compost and covering it by hoeing, and irrigation is done after 1 month at least.
Fertilization
After approximately 3 weeks the small plants are fertilized. Fertilization is repeated
after 1 month. The same fertilizer is used during the preparation of land for cultivation.
With the third hoeing 4 m3 compost is added, and at owering, quartz fertilizer is
sprayed before sunrise at a rate of 2 g for each 20 liters of water and stirred in both
directions.

5.10.4 INSECTS

THAT INFECT THE

PLANT

AND THE

METHODS

OF

FIGHTING THEM

1. White y (Bemisia tabasi GENNADIUS):

This insect feeds on plant juice, causes plant weakness, transfers leaf-wrinkling disease,
and transfers a virus that decreases owering.
Resistance: Use Bioy compound at a rate of 100 cm per 100 liters of water.
2. Honey-dew (Aphis gossypii GLOVER):
An insect that sucks the plants juices with avidity. This insect reproduces in great
numbers and secretes a sweet material called Honey Dew, which attracts Black Rot
fungus that leads to the deterioration of the crop.
Resistance:
A. Eradication and burning of the plants carrying the virus.
B. Spraying of Potash soap at a rate of 1.5 liters for each 100 liters of water.
3. Cotton worm (Spodoptera litoralis BOISDUVAL):
Infects the plants in the plant nursery and damages it.
Resistance:
A. Setting traps at a rate of four traps per feddan (=10 traps per ha)
B. Stop irrigation of trefoil after 10 days
C. Spray Bio-Ibcotic compound of a rate of 200 g per 400 liters of water for each
acre (500 g per 1000 liters per ha)
D. Bacillus thuringiensis bt*2 (double) at a rate of 200 g per 400 liters of water for
each acre (feddan)
4. Rodent worm and the digger (Pectinophora BUSCK ssp.):
Rodent worm infects the plants in the plant nursery and in the permanent land. It causes
weakness of the crop and feeds on the area that connects the root and the stem, so the
root separates from the stem. The buds die while the worm and the digger are under the
surface of the soil.
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Resistance:
Using poisoned bait that consists of 15 kg bran (in the case of rodent worm) or crushed
corn (in the case of digger) + 2 kg molasses + 100 g of leavened bread + 150 g of
crushed alum + 3 kg green material, left for 3 hours then thrown (in the lines in the
case of rodent worm) and thrown after irrigation and before sunset (in the case of
digger).
5. Tiny whiteness (Empoasca WALSH ssp.):
Infects the plants severely. It is resisted with the Bentonite mixture (powder of rocks
from Sinai Mountain) (1 kg bentonite + 1 kg miconic sulfur + 1 kg slaked lime). This
must be well mixed and sprayed at a rate of 2 kg in the early morning or from 3 to 5
kg for each 600 liters of water. The best spraying condition occurs when the weather is
sunny and a high pressure machine is used.
6. Red spider (Tetranychus ssp.):
This is a dangerous pest that causes the leaves to fade, dry, and fall. The pest is under the
surface of the leaves so it looks dull; its color turns brown, with dust stuck to spider webs.
Resistance:
Eradication of weeds, close irrigation to the plant, and use of micronic sulfur at a rate
of 250 g per 100 liters of water.
7. Strips (Sitophilus granarius L.)
It appears as a silver stain on the surface of the leaves that become black, dry, and die
in cases of severe infection.
Resistance:
A. Agricultural sulfur is added as spray at a rate of 20 kg per feddan (50 kg per ha).
B. Spraying of potash soap at a rate of 1.5 liters per 100 liters of water.

5.10.5 CULTIVATED VARIETIES/TYPES

Specic sorts are not cultivated. The Egyptian chamomile belongs to the low matricin/chamazulene
type.
For the time being, there are no breeding activities in Egypt. Seeds are harvested from existing
chamomile cultivations, cleaned, and afterward used for new cultivation areas.
For the future it is important to use selected seeds that yield owers with a high percentage of
azulene.

5.10.6 HARVESTING, DRYING,

AND

PREPARATION

Harvesting starts in mid-December. Plants are picked every 18 to 20 days, ve times until the end
of April. Immediately after picking the soil is watered again. When chamomile is cultivated there
must be assurance that there is enough manpower trained to collect, because only one picking
machine is used in Egypt (Linz III).
5.10.6.1 Harvest Date
Starting in the middle of December, owering begins; then collecting takes place, when radial
owers or white petals are in a horizontal position or parallel to the ground. This is the suitable
phase for crop ripeness.
Flower collecting occurs in December/January, performed by a workforce trained to gather
owers with horizontal, parallel-to-the-ground radial petals, because this is the suitable phase for
collecting. If the petals are leaning upward then they are not ripe, and if they are leaning downward
they are in the late phase when the owers scatter, as shown in Figure 5.10.2.

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Early: gets black

when dried

Suitable: good
for gathering

FIGURE 5.10.2 Positioning of owers/petals in relation to harvest dates.

FIGURE 5.10.3 Handpicking harvest.

FIGURE 5.10.4 Drying in palm leaf hurdles and cleaning.

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Late: gets
scattered

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5.10.6.2 Harvest
The ower neck, especially the remaining part of the stem, must not exceed 0.5 cm. Collecting is
done in baskets that are categorized immediately after collection to discard owers with long stems,
fallen petals, and small owers, while good owers are sent to the drying shelf. Collecting is done
every 1015 days at maximum according to the nature of the land and the owers; irrigation is
done after collecting ends in April and the beginning of May. The good feddan gives up to about
2000 kg of good fresh owers with a ratio of fresh to dry 5 to 1 or 400 to 500 kg of dry owers
(ca. 9001200 kg/ha).
5.10.6.3 Treatment after Harvest
Flowers are sent to the drying shelf. They are stored on clean drying shelves that are made of wood
or palm leaves lined with snack cloth; 11.5 kg of good owers are put in each cage after they are
riddled while being fresh. The layer of the owers on the drying shelf must not exceed 2 cm, so
they can dry quickly.
The drying shelf must be in the shade with good airing and away from the stables and compost
piles. The drying shelves can be put over each other in opposite directions to let in air. They should
be left in the sun on the rst day and covered with an upside-down drying shelf so they will not
be directly exposed to the sun; this helps in the drying process. At the end of the day drying shelves
must be put onto the big shelf covered with a ceiling so that they are not exposed to the dew.
Material must not be stirred on the drying shelves. Drying should be in the shade, except for
the rst day when the shelves are exposed to sunlight in order to lose humidity. The drying process
takes from 6 to 7 days, oil percentage 0.45 or 0.91.1% relative to dry weight.
Depending on the weather conditions, air drying takes from 1 to 4 weeks.
Cleaning and sorting of the dried products is done manually. There are only a few existing
machine units.
5.10.6.4 Packaging, Storage, and Shipping
Blossoms are packed in 12.5- or 25-kg boxes; pollen and industrial quality are packed in 20-kg
plastic sacks.
Export is mainly handled through shipping from Alexandria, Damietta, or Port Said to Europe
(Italy, Germany, France) as well as the United States and North and South America.
5.10.6.5 Production Quantity, Export Quantity, and Usage
Annual production is estimated to be approximately 1600 to 1800 tons. This results in a crop yield
of approximately 420 kg/feddan (1000 kg/ha). Production quantity of ecological goods is approximately 300 tons. These amounts are exported. Domestic use within Egypt is very rare.
Packaging in lter bags is done only to a small extent. These lter bags are mainly exported
to Arab countries. For the time being, evaluations for establishing oil distillations are done.

Boiled owers are used as a drink for stomach pains. It also activates digestion.
Used in most medications to decrease fever, and in creams to cure eyelid swelling.
Oil is used as a hair tincture as it contains azulene. It is used as well to activate blood
circulation, especially in children; it is also used as a u preventative.

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5.11 CULTIVATION IN GERMANY

ROLF FRANKE AND HANS-JRGEN HANNIG

5.11.1 INTRODUCTION
In Germany between 1930 and 1945, though chamomile owers were collected, only about 6 ha
were cultivated; the drug requirement was about 1000 tons [5]. In 1955 the main regions of origin
of the drug Chamomillae flos for Germany were Germany (mainly Saxony and Franconia), Hungary,
the Balkan countries, the USSR, the CSR, Yugoslavia, Belgium, France, and Spain [2, 3]. Varieties
or origins used up to the 1980s were Holsteiner Marschenkamille (Holstein Marsh Chamomile),
Quedlinburger Grobltige Kamille (Quedlinburg large-owered chamomile), and Erfurter
Kleinbltige Kamille (Erfurt small-owered chamomile) [1]. Only the tetraploid variety Bodegold brought the breakthrough for the use of cultivated forms in Germany in 1962.
In the meantime a clear shift took place in the main cultivation areas. Today, the main suppliers
are Argentina, Egypt, Hungary, Poland, and the Balkan countries; the major quantity comes from
Argentina (with decreasing quantities since 1995) (Table 5.11.1). Meanwhile, a big part is imported
from Egypt as well.

TABLE 5.11.1
Chamomile Import to Germany in the Years 19801987 (in tons) [6]

Argentina
Egypt
Others

1980

1981

1982

1983

1984

1985

1986

1987

2162
605
369

1730
594
424

1849
723
522

2334
741
850

1673
773
924

1807
760
623

962*
1537
447

2020
989
1045

* Decrease in production in 1986 was due to climatic inuences.

FIGURE 5.11.1 Chamomile harvest in Thuringia.

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In Germany as well, cultivation was extended after 1975. Today exclusively cultivated varieties
are grown. The biggest part of these are tetraploid varieties with high ()-bisabolol content.
Meanwhile, the main culture of the medicinal plants and spices cultivated in Germany is True
chamomile. The annual cultivation area amounts to more than 800 ha, more than 700 ha thereof
are to be found in Thuringia. Other German cultivation areas are Saxony (about 40 ha organically
grown chamomile) and Hesse (approximately 100 ha). The total area of organically grown chamomile has increased continuously during recent years and comprises about 100 ha at present. A
comprehensive investigation as well as an evaluation of procedures and equipment of the production
of chamomile in Saxony and Thuringia is discussed by Herold et al. [4] and Seitz [7].
The cultivation of chamomile in Germany is still increasing slightly and is limited in principle
by the availability of harvesting equipment (in 2003 and 2004, over 800 ha alone in Thuringia).
There are two reasons for the increasing cultivation of chamomile in Germany:

Cultivation of high-quality, protected chamomile varieties with a special prole of ingredients for the production of pharmaceutical products
The increasing requirement of product safety concerning undesired residues of pesticides
and heavy metals

5.11.2 CULTIVATION
Chamomile cultivation in Germany and similar climatic regions is normally effected through direct
seeding in late summer (September) and spring (March/April). The splitting of the seeding time
in autumn and spring reduces the risk of emergence that is inevitable due to the low thousand seed
mass of the chamomile seeds and the characteristic properties of a plant that germinates in light.
Furthermore, the splitting of the seeding time leads to different maturity dates, so that existing
picking techniques and drying capacity can be used reasonably over a longer period of time.
The seeding is effected with special drilling machines for ne seeds on a weed-free recompacted
and well-rolled soil.
Dependent on the available soil humidity and temperature, germination takes places within 12
weeks. In general, row distances of about 25 cm are preferred, and the seed density is approximately
2.02.5 kg per ha.
The nutrient need of chamomile is not very high and it also ourishes on moderately supplied
soils.
Increased quantities of nitrogen fertilizer lead to undesired additional herb growth and a delayed
formation of owers. For the fertilizer need, 40 kg N, 50 kg P205, and 100 kg K2O can be considered
as reference points.
In case of well-supplied soils, an additional fertilizing can be completely set aside.
Weed regulation is effected by soil herbicides that on the one hand are worked into the soil
during preparation of the seed bed, and on the other hand via machine hoeing after emergence.

TABLE 5.11.2
Cultivation of Chamomile in Germany 19922003 (in ha)
1992

1993

1994

Total
260
445
Among them in Thuringia

1995

1996

1997

1998

1999

2000

2001

2002

2003

590

650
600

703
653

796
673

761
620

723
633

824*
674

882*
723

936*
815

*Among them approx. 100 ha organic.

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FIGURE 5.11.2 Chamomile harvest with the Linz III picking machine.

FIGURE 5.11.3 Complete picking of the owering horizon with the Linz III harvester.

Post-emergence herbicides are available only on a very limited scale and are legally regulated in
the individual cultivating countries.
Chamomile has a slow development at the beginning and forms an opulently dense population
in a late stadium, that is capable of effectively suppressing weeds.
Besides downy mildew (Plasmopara leptosperma [de Bary] Skalicky), in central European
cultivation areas there are almost no other diseases or parasites that could cause economically
relevant damage.
Harvest is mostly effected with special picking machines.
Harvest time is indicated by the beginning of full blossom. In the upper ower horizon, at least
80% of the owers should have fully blossomed out, i.e., the white ligulate owers should stand
horizontally or bend slightly downward.

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The harvested material is highly endangered by fermentation. Therefore, the period of time
between harvest and the beginning of drying should be limited to a maximum of 2 to 3 hours. Any
rising pressure due to high storage levels is to be prevented.
Immediately before drying, a sorting of herb parts that have entered the product due to the
mechanical picking often takes place. This is frequently achieved by double-sided countercurrent
drum sieves.
Drying is realized with belt-drying plants or grating dryers at a maximum product temperature
of 40C.
Depending on the number of possible picking procedures, a harvest of 350600 kg drug per
ha is obtained.

5.11.3 SEED PRODUCTION

Special varieties with a high content in ()-bisabolol are used, especially in the German chamomile
cultivation. These varieties in many cases are company property and the corresponding seeds cannot
be bought commercially. Therefore, seed production is mainly realized by the companies themselves.
For this separate propagation, special seed-propagation areas are sown and cultivated until full
ripeness of the owers. The distance between the individual plants is often very wide and the
cultivation is treated analogously to a root crop in order to assure that seeds are only obtained from
one special plant.
With the selection of the propagation areas it is important to observe that natural weed pressure
of wild chamomile can be excluded.
The fully ourishing chamomile herb is mostly harvested by cutting and drying on grating
driers with cold air. This leads to an after ripening of immature seeds, and a good yield of chamomile
seed can be obtained through posterior threshing.
Cleaning is effected through the classical methods of seed preparation. The results are seed
qualities with a germinating power of 8085% with a yield of 100200 kg seeds per ha.

REFERENCES
1. Ebert, K. (1982) Arznei-und Gewrzpflanzen. Ein Leitfaden fr Anbau und Sammlung. 2nd ed., Wiss.
Verlagsgesell., Stuttgart, Germany, 221 pp.
2. Freudenberg, G. and Caesar, R. (1954) Arzneipflanzen. Anbau und Verwertung. Parey, Berlin, Hamburg, 204 pp.
3. Heeger, E.F. (1956) Handbuch des Arznei-und Gewrzpflanzenanbaus. Drogengewinnung. Deutscher
Bauernverlag, Berlin, 775 pp.
4. Herold, M., Pank, F., Menzel, E., Kaltofen, H., Loogk, E., Rust, H. (1989) Verfahrens technische
Entwicklungen zum Anbau von Chamomille recutita (L.) Rauschert und Calendula officinalis L. fr
die Gewinnung von Bltendrogen. Drogenreport, 2, 2, 4362.
5. Jaretzky, R. (1948) Taschenbuch fr den Heilpflanzenanbau. Verlag Dr. Roland Schmiedel, Stuttgart,
Germany, 33 pp.
6. Kirsch, C. (1990) Kamillenanbau in Argentinien. Dragoco Report, 2, 6775.
7. Seitz, P. (1987) Arznei-und Gewrzpanzen in der DDR. Deutsch. Gartenbau 51, 30403046.

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and Biotic Stress

6 Abiotic
Affecting the Common
Chamomile (Matricaria recutita
L.) and the Roman Chamomile
(Chamaemelum nobile L. syn.
Anthemis nobilis L.)
Andreas Plescher
CONTENTS
6.1

6.2
6.3
6.4

6.5
6.6

Abiotic Damage
6.1.1 Hail
6.1.2 Excessive Soil Moisture, Waterlogging
6.1.3 Nutrition
6.1.4 Low Temperature
6.1.5 Drought
6.1.6 Herbicides
Viruses
Mollicutes
Fungi
6.4.1 Fusarium spp
6.4.2 Powdery Mildew (Erysiphe cichoracearum D.C. ex MERAT and
E. polyphaga HAMM.)
6.4.3 Downy Mildew (Peronospora radii de BY., Syn. Peronospora danica GUM.;
Plasmopara leptosperma [de BY.] SKAL., Syn. Peronospora leptosperma
[de BY.] GUM.)
6.4.4 Chamomile Rust (Puccinia matricariae SYD., Syn. Puccinia
tanaceti D.C. a. L.)
6.4.5 White Rust (Albugo tragopogonis [PERS.] SCHROET.)
6.4.6 Leaf Spot Disease (Stemphylium botryosum WALLR.)
Plant Parasites
Herbivory
6.6.1 Chewing Herbivores on Roots and Stem Bases
6.6.2 Gall Formation on Roots
6.6.3 Chewing Herbivores on Leaves and Shoots
6.6.4 Sap Sucking on Leaves and Shoots

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6.6.5
6.6.6
6.6.7
6.6.8
6.6.9

Leaf and Stem Mining

Herbivores Mining and Chewing on Flowers
Sap Sucking on Flowers
Other Quality Deteriorations Caused by Insects
Stock Pests

Numerous abiotic and biotic stress factors can affect plant growth and survival, and the quantity
and quality of drug yield. This chapter presents some of the most common diseases and stress
agents of chamomile plants. Additional diseases may affect the two chamomile species, and the
frequency and type of disease will vary with the local climate.

6.1 ABIOTIC DAMAGE

6.1.1 HAIL
Leaves, buds, and flower heads can get scratched or knocked off by hailstones. At first the damaged
tissue turns lighter in color. Later on, necrosis is observed. Shoot tissue above the point of damage
will start wilting. Shoot tips may collapse.

6.1.2 EXCESSIVE SOIL MOISTURE, WATERLOGGING

High soil moisture caused by intense rainfall or poor drainage may restrict chamomile growth.
Especially young plants, but also old ones, will turn yellow, wilt, collapse, and die. There is also
an increased risk of root rots (cf. Section 6.4).

6.1.3 NUTRITION
Although both chamomile species do prefer certain soils, especially those with high calcium
concentrations, stress caused by deficiencies or an excess of nutrients has not been described.

6.1.4 LOW TEMPERATURE

In general, very tiny chamomile plants are sensitive to extended periods of freezing temperatures
in the spring. Older plants of the common chamomile, at a stage of having six to eight leaves, are
already remarkably resistant to frost periods, whereas the Roman chamomile remains sensitive to
freezing temperatures in springtime or early in the autumn. Flowers may be affected and the ray
florets will turn brown.

6.1.5 DROUGHT
Periods of drought may lead to the loss of the second and the following harvests. Depending on
the soil structure-related water supply, plants are likely to get scorched after the first harvest and
may die.

6.1.6 HERBICIDES
Herbicide treatment can result in abnormal or restricted growth associated with irregular tissue
bleaching and brown necrotic patches on the leaves. Bent, crooked, or twisted shoots with increased
internodal growth are indicative of hormone-containing weed killers. However, similar symptoms
are caused by mollicute infection or bug (Heteroptera) damage.

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6.2 VIRUSES
Virus infection has so far not been reported to affect the quantity or quality of chamomile yield.
However, the common chamomile is one of the host plants for the lettuce big vein virus (LBV-V)
and the cabbage black ring virus (CBR-V), but without showing any visible symptoms. Common
chamomile thereby acts as an important reservoir for these viruses, which are transmitted by aphids.

6.3 MOLLICUTES
Infection of preflowering plants by mollicutes may cause reduced elongation of the shoot tip
internodes. Flower buds will show the same symptoms in combination with abnormal greening.
Flower malformations (double and triple flowers) and fasciations may occur. Secondary shoots
or numerous small leaves develop at these points. Similar symptoms can result from herbicide
treatment or bug (Heteroptera) feeding.

6.4 FUNGI
6.4.1 FUSARIUM

SPP.

Fusarium infection is a frequent reason for the inhibition of plant growth. Plants get stunted, become
chlorotic, lose turgidity, and turn yellow. The base of the stems turns dark brown to black in color
and sometimes appears to be girdled. In addition, longitudinal cracks may appear at the base. The
roots turn dark and decay. Chamomile wilts and basal stem rots are primarily caused by Fusarium
culmorum (W. G. SM.) SACC. Similar symptoms are observed in conditions of excessive soil
moisture and afterdamage by stem-feeding herbivores.

6.4.2 POWDERY MILDEW (ERYSIPHE

POLYPHAGA HAMM.)

CICHORACEARUM

D.C.

EX

MERAT

AND

E.

Infection is characterized by the appearance of white powdery patches of fungal growth. Very soon,
the entire plant is covered by the powdery mildew growth. Newly emerging flowers are dwarfed.
Leaves fall dry, starting from their tips. In the older areas of infection, tiny pinhead-sized yellowbrown cleistothecia become visible, which later turn into black spots.

6.4.3 DOWNY MILDEW (PERONOSPORA RADII DE BY., SYN. PERONOSPORA

DANICA GUM.; PLASMOPARA LEPTOSPERMA [DE BY.] SKAL.; SYN.
PERONOSPORA LEPTOSPERMA [DE BY.] GUM.)
Infection first results in bleached patches on the leaves, from where the fungus starts to grow as a
white lawn with pinhead-like structures on both sides of the leaves. Leaves first turn yellow, then
brown, and die.

6.4.4 CHAMOMILE RUST (PUCCINIA MATRICARIAE SYD., SYN. PUCCINIA TANACETI

D.C. A. L.)
Plants cultivated in temperate to cold climates may get infected by the chamomile rust. Pale-brown
rusty pustules (uredia) form on the leaves and stems, whereas the black powdery telia are only
found on the stems.

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6.4.5 WHITE RUST (ALBUGO

TRAGOPOGONIS

[PERS.] SCHROET.)

White rust infection occurs on leaves, shoots, and buds. It is characterized by pustules that change
their color from pale yellow into white, and burst, releasing their lime-like contents. White rust
infection has so far only been observed on Roman chamomile.

6.4.6 LEAF SPOT DISEASE (STEMPHYLIUM

BOTRYOSUM

WALLR.)

Stemphylium infection is likely to occur after long periods of wet weather and results in spherical
light brown to grey or dark brown to black spots on leaves and shoots. The midribs collapse.

6.5 PLANT PARASITES

In southern Europe, broom rape (Orobanche sp.) has been recorded to parasitize common chamomile.

6.6 HERBIVORY
6.6.1 CHEWING HERBIVORES

ON

ROOTS

AND

STEM BASES

Insects feed on the roots, the stem base, and the leaves close to the ground. Plant growth is restricted.
Plants wilt and die prematurely. Some of the plants get completely detached from their roots and
are easily pulled from the soil.
Yellowish-white beetle larvae, up to 6 cm long, with dark-colored abdominal segments (May
bug larvae, Melolontha spp.; Phyllopertha spp., Rhizotrogus sp., etc.), 34 cm long, brown-grey
legless fly larvae with fleshy abdominal segments (cranefly larvae; Pales spp., Tipula spp.), or about
2.5 cm long, thin beetle larvae having a rigid cuticle (wire worms; Agriotes spp., Athous niger L.,
Melanotus brunnipes GERM.) can be found in the vicinity of the plants that have been affected.
Mainly at night, earth-colored, grey, or greenish-grey lepidopteran larvae (Scotia [Agrotis] spp.)
feed on the tissues close to the ground. They spend the day curled up in the soil. Occasionally, the
small, yellowish white larvae of the root fly (Delia [Phorbia] spp.) may cause the plant to die. In
warmer climates, the mole cricket (Gryllotalpa vulgaris LATR. = Gryllotalpa gryllotalpa L.) and
several millipede species (Blaniulus guttulatus [BOSC.], Cylindroiulus teutonicus [POCOCK], etc.)
can seriously damage the roots. In humus-rich soil with a high proportion of decaying plant tissues
(e.g., in gardeners substrates for the propagation of Roman chamomile), the larvae of the St. Marks
fly (Bibio spp.) may attack the plants.

6.6.2 GALL FORMATION

ON

ROOTS

Chamomile plants are attacked by the northern root-knot nematode Meloidogyne hapla CHITWOOD. At the point of infection roots swell and develop spherical or spindle-shaped galls in which
the females (up to 1 mm long and 0.5 mm wide, pear-shaped) can be found. Plant growth is
inhibited, and infested plants are more sensitive to drought than healthy plants.

6.6.3 CHEWING HERBIVORES

ON

LEAVES

AND

SHOOTS

Various insects and their larvae are known to cause more or less severe damage to chamomile
plants by feeding on the leaves and shoots. Some lepidopteran larvae (such as the owlet moth;
Cucullia tanaceti SCHIFF, but also other Cucullia species) damage leaves by skeletal feeding.
Phalonia implicata WCK. larvae (10 mm long, pale-yellow bodies with brown heads and a yellow
dorsal neck plate) mainly feed on the upper plant parts and spin their webs around them.

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In areas of high humidity, snails (Helix spp., Arianta spp.) and various types of slugs (Arion
spp., Deroceras reticulatum MLL.) can cause considerable damage to the plant tissues near the
ground as evidenced by their slime tracks.

6.6.4 SAP SUCKING

ON

LEAVES

AND

SHOOTS

Various aphid species live on the leaves and shoots or at the tips of the plants. The leaf blades curl
up from the tip or the sides to their base, turn yellow, and finally brown.
Whereas attack by the green aphid Cerosipha gossypii HB. has mainly been recorded in warm
climates, the black aphid Aphis fabae SCOP. and the green aphids Myzus persicae SULZ. and
Brachycaudus spp. are found on chamomile species all over the world.
Sucking by cicadas (Cicadinae, for example, Eupteryx atropunctata GOEZE, Empoasca pteridis DAHLB., E. flavescens F., and Chlorita viridula FALL.) can initially be recognized from
white spots on the leaves. Severe attack results in leaf fading and death. Patches of tissue first turn
dark green or brown and then die. Larvae usually stay on the underside of the leaves.
Leaf and stem deformations and growth abnormalities result from sucking by various types of
bugs (Heteroptera, for example, Lygus lucorum MEY. D., L. pubescens REUT., Exolygus pratensis
L., Plagioganthus chrysanthemi WOLFF., Adelphocoris lineolatus GOEZE, and Calocoris norvegicus GMEL.). If plants are cultivated in a greenhouse, the white fly, Trialeurodes vaporariorum
WESTW., and its oval-shaped larvae, living on the underside of chamomile leaves, cause considerable damage.

6.6.5 LEAF

AND

STEM MINING

Shoot weevil Ceutorhynchus rugulosus HERBST larvae (legless with brown head capsule and
whitish-yellow body) mine the central stem pith of chamomile plants. As a consequence, the lower
stem parts first turn red and then brown, while the leaves turn yellow and wilt. Flowers are
degenerate, and flowers and stems easily collapse. The adult shoot weevil is 2.0 to 2.5 mm long
and grey to chocolate-brown in color. The tiny larvae of the shrew weevil Apion confluens KHY.
similarly mine the stem, but also feed small holes into chamomile leaves.
Hardly detectable are the mining structures of the grey-brown larvae from the leaf miner species
Phytomyza atricornis MEIG., Phytomyza matricariae HAND., Liromyza strigata MEIG., and
Typetha zoe MEIG.

6.6.6 HERBIVORES MINING

AND

CHEWING

ON

FLOWERS

Beetles of the genus Meligethes (1.5 to 2.7 mm in length, metallic green, shiny blue-grey to bluepurple, or nonshiny black in color) generally feed only on mature pollen already released by the
anthers and rarely damage single florets and their anthers.
Severely reduced drug quality is caused by different insect larvae mining within the receptacle.
Larval feeding tunnels form more or less circular horizontal patterns in the tissue. The above
growing disc florets are the first to wither. Later on the entire flower head turns brown and larvae
move further down into the receptacle.
The head and abdominal end of Olibrus aenaeus FABR. larvae are dark in color. Larvae have
their thoracic legs developed. Beetles emerge from the early summer on. They are 1.8 to 2.5 mm
long and black, sometimes with a shining metallic-green appearance. The same type of damage is
caused by the legless dark-headed larvae of the weevil Pseudostyphlus pilumnus GYLL. Adults
are brown to brown-black with grey-white scales and 2.5 to 3.3 mm in length. In rare cases, larvae
of the weevil Ceutorhynchus rugulosus HERBST (see Section 6.6.5) also mine the receptacle.
Finally, larvae of the blossom boring fly Trypanea stellata FRUNSLEY cause a very similar type
of damage to chamomile flowers. Larvae are legless with a light-colored head capsule.

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Flower mining does not significantly reduce allover yield, but affects flower color and integrity
and thereby drug quality.

6.6.7 SAP SUCKING

ON

FLOWERS

A large number of thrips species feed on chamomile flower heads. They are whitish to yellowbrown, slender insects (from 0.5 mm to a maximum length of 1.5 mm) with short legs, and
sometimes fringed wings. Different species of grass thrips suck between the tubular florets and
thereby impair flower head integrity. Single tubular flowers wither and turn brown. Thrips physapus
L. and Thrips tabaci LIND. are frequently observed on chamomile. Again, this type of damage
mainly reduces drug quality not yield.

6.6.8 OTHER QUALITY DETERIORATIONS CAUSED

BY INSECTS

Various ladybug (Coleoptera: Coccinellidae) species colonize aphid-infested chamomile plants.

Since their brightly colored wing covers are difficult to remove from the harvested plant material,
chamomile marked value can be significantly reduced.

6.6.9 STOCK PESTS

A wide range of pests feeds on the dried chamomile flowers, depending on the climate of the
country of origin and the storage conditions. In Central and South America, the tobacco beetle
Lasioderma serricorne F. (Coleoptera) has been recorded. In South America the hay or cocoa moth
Ephestia elutella HB (Microlepidoptera) infests the chamomile flowers. In central Europe the dry
fruit moth Ploida interpunctella HB (Microlepidoptera) and the carpet moth Anthrenus verbasci
L. (Coleoptera) are known to feed on the stocks.

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Plant Material
7 Raw
and Postharvest
Technology
Horst Bttcher and Ingeborg Gnther
CONTENTS
7.1

Postharvest Physiological Response

7.1.1 Respiration: The Physiological Focus
7.1.2 Influence of Senescence on Respiration Rate
7.1.3 Changes in Quality Parameters
7.1.4 Characterization of Respiratory Activity
7.2 Postharvest Technological Treatments
References

7.1 POSTHARVEST PHYSIOLOGICAL RESPONSE

Freshly harvested crops of chamomile are live plant products or parts of them. They are characterized by a water content of about 80% and also by high metabolism. Therefore, the postharvest
period is of decisive importance for the maintenance of excellent external and internal quality traits;
it is the key for ensuring a stable and reliable quality of raw and processed chamomile products
with a high standard of therapeutic and medical effects. However, our knowledge about what is
happening between harvest (i.e., mowing and gathering in the field) and subsequent drying or
further processing is still very poor. The physiological processes occurring in fresh horticultural
crops, during the postharvest period in general, were described recently by References 9, 10, and
11 and more profoundly by Reference 8, but for medicinal and aromatic plants, and for chamomile
herbs and flowers in particular, little information can be found. Recently, References 4 and 6
reported first results on the respiration activity of chamomile flowers.
The main loss factors responsible for the rapid decline of the biological quality of medicinal
herb crops are characterized in Table 7.1 by Bttcher and Gnther [4].
In the postharvest period respiration, senescence, transpiration, ripening, and changes in the
biochemical constituents caused by the secondary metabolism were found to take place in the live
product. The relationships between these processes are demonstrated in Figure 7.1.
The design of the technical lines reflects the importance of the single processes with regard to
external and medical value. The external quality, important for use as tea components or powder,
is largely influenced by transpirating, senescing, and ripening and by the development of harmful
microorganisms. Medical values, however, are marked mainly by senescence and ripening. It is
typical for medicinal crops that the loss factor respiration will not in all cases react directly, but
mainly via transpiration, wilting, and secondary metabolism responses (Figure 7.1).

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TABLE 7.1
Physiological Processes in Freshly Harvested Medicinal
Plants and Their Effects [3, 4]
Respiration
Heating of the stacked crop
Extreme heating up to spontaneous combustion
Fermentation
Senescence processes
Chlorophyll degradation
Leaf siccation
Changes in the quantity of special constituents
Transpiration
Wilting and shrivelling
Changes in quantity of constituents
Microbiological contamination and spoilage
Lesions and bruises
Partial heating
Rotting losses
Influence of special constituents
Injuries and damages
Mechanical abrasion
Disintegration of flowers and buds
Quality shifts

FIGURE 7.1

Relationship between physiological loss factors and quality of the chamomile product [3].

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The reactions of the flowers are of special interest, because they are used often and are a
valuable phytopharmaca and because they contain a high level of essential ingredients. So chamomile flowers are well known in general for quickly becoming perishable.

7.1.1 RESPIRATION: THE PHYSIOLOGICAL FOCUS

Respiration is a very stringent process in living cells of freshly harvested chamomile crops. It
mediates the release of chemically bound energy through the breakdown of carbon components
and the formation of carbon skeletons necessary for maintenance and synthetic reactions after
harvest. A secondary result of respiration is the release of energy as respiration heat expressed in
terms of energy in W t-1 [watt. ton-1]. Respiration is very important under postharvest conditions;
therefore, we have to check it and abduct the heat from the stacks of the stored product.
On the other hand, the rate of respiration is also an indicator of the total rate of metabolism in
plants, plant parts like flowers, or herbs.
Crops of freshly gathered chamomile flowers, variety Bodegold, picked in the full-flowering stage in the field using the gathering harvester LINZ 3, have at free-flow measuring conditions
of 10C an unexpected high mean value of respiration rate of 999 134 W t-1 [7]. In all trials the
plants grew under representative agrotechnical and growing conditions in the field. Their activity
was much higher than that of horticultural plants with well-known high values [2, 3]. In fresh
chamomile flowers the high mean value exceeded parsley by 4.3-fold (235 W t-1) and broccoli by
2.9-fold (350 W t-1). It is also much higher than that of other medicinal and aromatic herbs harvested
at the beginning or in the half-blooming stage: 1.6-fold for marjoram (632 W t-1), 1.4-fold for
savory (696 W t-1), or 1.6-fold for sage (615 W t-1) [5, 6].
The high activity may be explained by the fact that harvest occurs in the full-flowering stage
at the end of the generative phase of plant development, which takes place in June, when sunny
and warm weather prevails in Germany.
Although each year the crops grow under equal agrotechnical and site conditions, a definite
significant influence by the annual weather and growing situation can be observed (p = 0.00357)
(Figure 7.2): 1994: x = 1141 W t-1; 1995: x = 878 W t-1 ; 1996: x = 979 W t-1. There was
measured a difference in the rate between autumn (a) and spring (s) sown crops (a: x = 958; s: x
= 1040 W t-1). But no difference could be detected between respiration and the harvest date as well
as climatic situation at the harvest date.
With rising product temperature, the respiration rate in each test series with chamomile
increased considerably (p < 0.001) (Figure 7.2). In single cases, up to 4500 to 5000 W t-1 were
reached at the 30C level. The following mean values in the above-mentioned trials of Bttcher,
Gnther, and Franke [7] were determined for 20C 2438 289 W t-1; for 30C 4552 570 W t-1.
The extent of the temperature increase in steps of 10 K (Q10) was ascertained for:
10 to 20C: Q10 = 2.47 (mean value of 6 series)
20 to 30C: Q10 = 2.00 (mean value of 6 series).
Despite the primarily high respiration rate of chamomile flowers these parameters between 10
and 20C were in full correspondence with vant Hoffs rule and confirm in this range also its
validity for freshly harvested chamomile. A heat-caused depression at the level of 30C was
definitely obvious. [7].

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FIGURE 7.2 Influence of temperature on the respiration rate of freshly harvested chamomile flowers [7].
(Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I., Franke, R., Warnstorff, K.,
Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.), pp. 3951, Copyright
(2001), with permission from Elsevier.)

So far, no measured values are known for the respiration rate of chamomile herbs in total and
herbs with flowers.
Because of this very high respiration activity measured for chamomile flowers, it is urgent to
take this into account, especially for the postharvest technological treatments like ventilating,
cooling, or drying.

7.1.2 INFLUENCE

OF

SENESCENCE

ON

RESPIRATION RATE

The high respiration intensity of chamomile flowers during postharvest storage was unexpectedly
stable, irrespectively of the actual storage temperature, when calculated in W t-1 (Figures 7.3, 7.4,
7.5). Its decline varied in each series, but its course clearly followed the regression function:
y = 1 + 1 e-c (x- z). (c < 0)

(Figures 7.3, 7.4, 7.5)

where y = respiration rate in W t-1

x = postharvest time in hours
1 = remaining respiration rate under senescence conditions
1 = variable respiration rate during postharvest senescence
c = parameter for the intensity of degression during the postharvest period
z = time from harvest to the state of equilibrium in the respiration-measuring equipment.

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FIGURE 7.3 Influence of senescence on the respiration rate of chamomile flowers at postharvest conditions
of 10C [7]. (Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I., Franke, R.,
Warnstorff, K., Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.), pp. 3951,
Copyright (2001), with permission from Elsevier.)

Regression: a (autumn sown): y = 566.54 + 390.49 e-0.023570. (x-5) R2 = 79.6%

s (spring sown): y = 682.80 + 360.00 e-0.024707 (x- 5) R2 = 82.4%

FIGURE 7.4 Influence of senescence on the respiration rate of chamomile flowers at postharvest conditions
of 20C [7]. (Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I., Franke, R.,
Warnstorff, K., Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.), pp. 3951.
Copyright (2001), with permission from Elsevier.)

Regression: a (autumn sown): y = 1003.20 + 1391.11 e-0.019800 (x-5) R2 = 89.0%

s (spring sown): y = 857.68 + 1638.07 e-0.012814 (x-5) R2 = 89.5%
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FIGURE 7.5 Influence of senescence on the respiration rate of chamomile flowers at postharvest conditions
of 30C [7]. (Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I., Franke, R.,
Warnstorff, K., Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.), pp. 3951,
Copyright (2001), with permission from Elsevier.)

Regression: a (autumn sown) y = 1452.63 + 2973.04 e-0.033322 (x-5 ) R2 = 94.2%

s (spring sown) y = 874.04 + 3884.37. e-0.016079(x-5) R2 = 89.9%
In the chosen postharvest period of 72 to 80 hours in the trials (in practice normally not so
extended) Bttcher, Gnther, and Franke [7] recorded a mean decrease in respiration for the different
postharvest conditions:
10 0.2C, ~ 98% relative air humidity:
delayed aging (senescence) due to low temperatures
20 0.1C, ~ 95% relative air humidity:
normal process of aging (senescence)
30 0.2C ~ 98 92% relative air humidity:
accelerated aging due to increased physiological temperatures.
The extent of senescence-related decrease during the postharvest period of 80 hours amounted
in these trials:
at 10C to absolutely

313.7 W t-1 or relatively 31.4% of the initial value

at 20C to absolutely

1,043.8 W t-1 or relatively 42.7% of the initial value

at 30C to absolutely

2,725.1 W t-1 or relatively 59.3% of the initial value

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It turned out that chamomile flowers have a different response to the sowing date. At all tested
temperature levels, spring-sown crops showed a significantly higher rate at harvest than autumnsown crops: at 10C +85.8 W t-1 (+8.96%), at 20C +101.5 W t-1 (+4.24%), at 30C +332.7 W t-1
(+7.52%). This results from the fact that flowers of spring-sown chamomile were harvested 11 to
25 days later in June than autumn-sown stands. This means that they were exposed to the warm
summer conditions in June for 11 to 25 additional days during the last part of the growth and
development period in comparison to the autumn-sown stands.
This difference, which was statistically significant (p < 0.000), was also maintained during
postharvest storage. Therefore, it was necessary to make separate statistic estimations and graphics
for autumn- and spring-sown crops in Figures 7.2, 7.3, 7.4, and 7.5.
On the other hand, the sowing date had a different influence on the course of respiration,
especially the radius of curvature, characterized by factor c in the equation, also at the different
temperature levels. At conditions of 10C this factor was nearly equal (autumn sown (a) = 0.02357;
spring sown (s) = 0.024707). However, at temperature steps of 20 and 30C an increasing faster
senescence-caused respiration decline in autumn-sown crop was observed: at 20C a = 0.01980;
s = 0.012814. At 30C it dropped even twice as fast: a = 0.033322; s = 0.016079 [7]. This
proves that at the optimal harvest date autumn-sown chamomile flowers are inevitably physiologically older and react with a stronger decline of the respiration rate than spring-sown plants.
The complex relationship between storage temperature, postharvest storage time, and respiration
course is shown in Figure 7.6.

7.1.3 CHANGES

IN

QUALITY PARAMETERS

Besides an essential respiration rate, freshly gathered chamomile flowers also show a trend to high
transpiration. The same applies to marjoram and sage [5, 6]. The mean fresh matter losses amounted
to 1.83% during 24 h+ (1.2 to 1.9% in 24 h) under favorable postharvest conditions (10C,

FIGURE 7.6 Complex influence of storage temperature and storage time on the respiration rate of springand autumn-sown chamomile flowers [7].

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98%) and to 6.04%/24 h+ under normal conditions (20C, 95%). When the temperature was
increased to 30C ( 92 to 98%) the losses rose to x = 13.4%/24 h+, resulting from higher
release of transpiration energy by the ascertained high respiration rate. A depression of the product
temperature by 0.6 to 1.5 K was also recorded [5, 7].
During 80 to 90 hours of postharvest time the very high released respiration heat led to pronounced
dry matter losses in the product, dependent on the temperature, calculated on the base of dry matter
at harvest: 10C 7.5%+; 20C 12.3%+; and 30C 15.8%+ (mean values of six trials) (Figure 7.7) [7].
The external quality traits of the chamomile crops are very important for a great many purposes.
They drop clearly in dependence on the storage temperature [7] and are marked by wilting and
Dry matter
0
5
10
%
15
20
25
Essential oils
30
20
10
%

0
10
20
35
Chamazulene
10
5
0
5

% 10
15
20
25
30

b
c
10C

b
c
20C

c
d
30C

Postharvest conditions

FIGURE 7.7 Changes in dry matter, essential oil, and chamazulene of chamomile flowers during a post-harvest
period of 80 hours at different temperatures calculated of the base of balance sheets (a = 1995 autumn sown; b
= 1995 spring sown; c = 1996 autumn sown; d = 1966 spring sown) [7]. (Reprinted from Postharvest Biology
and Technology 22, Bttcher, H., Gnther, I., Franke, R., Warnstorff, K., Physiological postharvest responses of
Matricaria flowers (Matricaria recutita L.), pp. 3951, Copyright (2001), with permission from Elsevier.)
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shrivelling flowers, by losing the bright white and yellow color impression of their blossoms, by
degreening the fresh green parts of the crops (small stems, leaves, etc.). The stored crop made an
increasingly faded impression, especially at 30C, and to a smaller extent at 20C. This is correlated
with the continuing generative development of the inflorescences and can be recognized very
distinctly by rising disintegration of the blossoms and the development of seeds in the inflorescences,
particularly at 30C.
A temperature of 10C guaranteed crop material of fresh and bright quality even up to 70 hours
after harvest. Acceptable chamomile quality after gathering could be supported at 20C for 25 to
30 hours, but at 30C for 15 to 20 hours only.
The main active constituents of chamomile flowers show different changes in their contents in
the drug herb (mg/100 g) during the postharvest period, in most cases not very pronounced or
significant. But the high respiration and transpiration rates of this crop material led to distinct losses
in dry matter, so that changes of the constituents could only be discovered by calculations of balance
sheets [1]. On the other hand, the plant material responded not uniformly in all trials, so that it is
not advisable to consider the trials in total.
For some constituents, there are clear differences in the extent of the reactions in dependence
to the prevailing microclimatical conditions during the growing and storing season.
Thus, the quantity of constituents, in general, turned out to have been relatively stable during
the postharvest period, but there were some unfavorable reactions [7].
In three trials the essential oils showed at 10 and 20C on the base of balance sheets small
decreases up to 20%, and only in one trial did they rise to the same extent. At 30C decreases were
only on the level of up to 30% ( x = 17.0%) (Figure 7.7). At 20C a mean value of only 5.3%
loss was estimated. So natural samples of chamomile flowers contained after a postharvest storage
period of 80 days a quantity of +46 ml essential oils/100 g dried drug at 10C and of +40 ml/100 g
dried drug at 20C in comparison to the quantity at harvest date. However, after conditions of 30C
there was a decline by 9.75 ml/100 g dried drug [7]. Chamazulene was marked by small decreases,
rising with higher temperatures x at 10C 1.95%; at 20C -8.8%, and at 30C 10.7% (Figure 7.7).
The valuable constituent ()--bisabolol and its oxidation forms showed, on the contrary, clear
reactions; however, this only at cooler and microclimatic conditions of 10C: 6070% of the amount
of ()--bisabolol as well as bisabololoxid A and B from the 1995 grown chamomile crops got
lost (Figure 7.8).
Autumn- and spring-sown crops have the same reaction. This fact is considered not as a result
of oxidation of ()--bisabolol, but as a result of temperature-involved changes in the secondary
metabolism in dependence on the annual growing and developing conditions. In the other year and
at temperatures of 20 and 30C only small changes up to 10 to 20% in the bisabolol and -oxid
quantities occurred (Figure 7.8). The same reaction was shown by cis-EN-IN-dicyloether at temperatures of 10C and to a smaller extent at 20 C ( x at 10C = 27.5%, at 20C = 18.2%), but
at 30C the changes came only to x = 3.4% (Figure 7.9).
The flavonoid quantities of apigenin-7-glycoside on the base of balance sheets are characterized
by small decreases of 10 to 35% in the single samples, apart from the reaction in the autumn-sown
trial 1995. Altogether, the decreases were x at 10C 7.7%, at 20C 16.1%, and at 30C 19.6%
in relation to the quantity at the moment of gathering [7] (Figure 7.9).
Whether the determined changes of the single constituents may cause a shift on the therapeutic
value of the drug cannot be decided yet. Temperatures of 20C led to the smallest changes in the
crops. Best external traits were obtained at 10C.

7.1.4 CHARACTERIZATION

OF

RESPIRATORY ACTIVITY

The characteristic behavior of the respiration activity of freshly gathered chamomile flower crops
was demonstrated in a nomogram (Figure 7.10). It is recommended for calculating ventilation,
drying, and manufacturing processes where chamomile is involved or for the assessment of physiological activities.
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(-)--Bisabolol
100
80
60
40
20
%
0
20
40
60
80
100

Bisabololoxid A
10
0
10
20
% 30
40
50
60
70
Bisabololoxid B
0
10
20
30
% 40
50
60
70
80

b c
10C

b c
20C

b c
30C

Postharvest conditions

FIGURE 7.8 Changes in (-)-a-bisabolol and its oxide A and B of chamomile flowers during a postharvest
period of 80 hours at different temperatures calculated on the base of balance sheets (characterization of ad
see Figure 7.7 [7]. (Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I., Franke,
R., Warnstorff, K., Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.), pp.
3951, Copyright (2001), with permission from Elsevier.)

7.2 POSTHARVEST TECHNOLOGICAL TREATMENTS

The gathered flowers should be immediately transported from the field to a processing site in a
shaded place. At first, equipment for postharvest cleaning was used. Fresh chamomile flower crops
gathered by using high-capacity chamomile combines or by hand contain different quantities of
leaves, stem parts of the herbs as well as of weed plants, and other impurities. These worthless
contaminations should be removed very carefully as soon as possible, because they increase the
energy needed for drying or steam distillation of the crops, prolong the drying time, and raise the

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EN-IN-Dicycloether
60
40
20
%

0
20
40
60
80

Apigenin-7-glycoside
20
10
0
% 10

20
30
40
a

b c
10C

b c
20C

b c
30C

Postharvest conditions

FIGURE 7.9 Changes in EN-IN-dicycloether and apigenine-7-glycoside of chamomile flowers during a postharvest period of 80 hours at different temperatures calculated on the base of balance sheets (characterization
of ad see Figure 7.7) [7]. (Reprinted from Postharvest Biology and Technology 22, Bttcher, H., Gnther, I.,
Franke, R., Warnstorff, K., Physiological postharvest responses of Matricaria flowers (Matricaria recutita L.),
pp. 3951, Copyright (2001), with permission from Elsevier.)

temperatures in the stacks (younger parts of plants are mostly characterized by higher water content
and higher respiration rates). All these processes are managed by the actual product temperature
in the summer months, additionally. Therefore, the fresh flowers will go brown within a few hours,
especially if they are stored in sacks or box pallets with insufficient ventilation. Besides, their
microbiological contamination will rise drastically. The removal of the coarse impurities is an
important contribution toward a better and more aesthetic quality of the drug.
Large, slowly rotating drums separate the bigger waste parts that are passing the drum, while
the chamomile flowers fall through small, 5- to 12-mm mesh split openings of the cleaning drum
cylinder. The latter works like a screening system. In the second step the flowers pass highly rotating
small rubber rolls to pull all small particles like leaves and other inorganic impurities out of the
crop mass. If it is not possible to start the cleaning immediately after gathering, it is essential,
based on the above-demonstrated extremely high respiration intensity especially during high summer temperatures, to ventilate the crops with outdoor air to abduct the released respiration heat
out of the stack. It is also necessary to take away the condensed water of the intensive transpiration

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FIGURE 7.10 Respiration rate of mechanically gathered fresh chamomile flowers expected at different
product temperatures during postharvest time

from the storing crop, to limit the microbiological developments, to cut off the losses of essential
oils, and to prevent quality decreases. It is favorable to stack the crop only up to a height of 30 cm.
Chamomile herb crops do not require an exclusively intensive preparation before drying or
steam distillation.
During all technological steps good agricultural practice, as recommended by the European
Herbae Infusions Association (EHIA) in 1993, should be observed [12].

REFERENCES
1. Bttcher, H., 1986. Zur Problematik des Erfassens von Qualittsvernderungen whrend der Lagerung
von Gemse. Nahrung, 30 S, pp. 723728.
2. Bttcher, H. (Ed.), 1996. Frischhaltung und Lagerung von Gemse. Ulmer-Verlag, Stuttgart, Germany,
252 pp.
3. Bttcher, H., 1998. Freshness of vegetables a decisive precondition for sales prospect. Zahradnictvi,
Horticultural Science. Praha. 25, pp. 6773.
4. Bttcher, H., Gnther, I., 1995. Nachernteverhalten und Nacherntephysiologie von Arznei-und
Gewrzpflanzen. Herba Germanica 3, pp. 4766.
5. Bttcher, H., Gnther, I., Bauermann, U., 1999a. Physiological postharvest responses of marjoram
(Majorana hortensis Moench). Postharvest Biology and Technology. 15, pp. 4152.
6. Bttcher, H., Gnther, I., Warnstorff, K., 1999. Nicht-destruktive Bestimmung des Gasstoffwechsels
zum Erfassen des Seneszenzverlaufes whrend der Nacherntezeit von Arznei-und Gewrzpflanzen.
Deutsche Gesellschaft fr Qualittsforschung DGQ, XXXIV. Vortragstagung Zerstrungsfreie Qualittsanalyse. 2223 March 1999, Freising Weihenstephan. S, pp. 107118.
7. Bttcher, H., Gnther, I., Franke, R., Warnstorff, K., 2001. Physiological postharvest responses of
Matricaria flowers (Matricaria recutita L.). Postharvest Biology and Technology 22, pp. 3951.
8. Cantwell, M.J., Reid, M.S., 1993. Postharvest physiology and handling of fresh culinary herbs. J.
Herbs, Spices, Med. Plants. 1, pp. 83127.
9. Kays, St. J. (Ed.), 1991. Postharvest Physiology of Perishable Products. Van Nostrand-Reinhold, New
York, 532 pp.

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10. Lieberman, M. (Ed.), 1983. Postharvest Physiology and Crop Preservation. Plenum Press, New York
and London, 572 pp.
11. Wills, R.B.H., McGlasson, W.B., Graham, D., Lee, T.H., Hall, E.G. (Eds.), 1989. Postharvest 3rd
Edition. BSP Professional Books, Oxford, 174 pp.
12. Richtlinien fr die gute landwirtschaftliche Praxis von Arznei- und Gewrzpflanzen, 1997. Zeitschr.
Arznei-Gewrzpfl. 4, pp. 202206.

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8 Processing of Raw Material

Horst Bttcher and Ingeborg Gnther with cooperation of
Reinhold Carle and Albert Heindl
CONTENTS
8.1 Basic Physiological and Technological Properties of the Product
References
8.2 Drying of Chamomile Flowers (Matricaria recutita L.)
8.2.1 Processing of Harvested Product before Drying Albert Heindl
8.2.2 Basics of Drying
8.2.3 Influences of Drying Parameters on Quality and Energy Consumption
8.2.3.1 Quality
8.2.3.2 Energy Consumption and Energy Costs
8.2.4 Microwave-Assisted Warm Air Drying
8.2.5 Drying Equipment
8.2.5.1 Advantages and Disadvantages of Dryers
8.2.6 Processing of the Dried Product
8.2.7 Supplement: Recommendations for Drying
8.2.7.1 Static Dryers
8.2.7.2 Band Dryers
References
8.3 Distillation of Essential Oil Reinhold Carle
8.3.1 Introduction
8.3.2 Production of Chamomile Oil
8.3.3 Methods of Production
8.3.3.1 Batch Method
8.3.3.2 Quasi-Continuous Method
8.3.3.3 Continuous Method
8.3.4 Evaluation of the Methods
References

8.1 BASIC PHYSIOLOGICAL AND TECHNOLOGICAL PROPERTIES

OF THE PRODUCT
After harvesting, chamomile is a very perishable product during storage. This applies equally for
the harvested whole herbs and, to an even greater extent, for the flowers. The main deterioration
phenomena are:

Dropping of the external quality traits, especially the natural green color of the leaves
and stems and the light colors of the flowers
Loss of particularly valuable ingredients due to material conversions, wilting due to
transpiration, and physically induced escape

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Increased formation of grit through the decay of the flowers and separation of the leaves
from the herb, both triggered by aging (senescence) processes
A rise in the microbiological contamination of the product to be dried through warming
and heating, especially in combination with mechanical damages and pressure points
A marked shortening of the subsequent storability of the dried product

The very high respiration rate of harvested chamomile, which reaches a mean value of 999
W t-1 for flowers at 10C (Section 7.1.1), accelerates these changes and leads, without ventilation,
to an extremely fast rise in the stack temperature. On the other hand, chamomile reacts very easily
to various external factors. For this reason, chamomile flowers and herbs should be regarded as
very drying-sensitive crops.
Rapid, sufficient lowering of the water content in the harvested crops is the most important
and besides extraction most frequently used option for preservation to avoid these changes.
However, the drying conditions in question also determine the quality and stability of the dry
product to a large extent. These are characterized by:

The maximal occurring product temperature during the drying process

The dwell time of the crops in the hot air section
The saturation deficit of water vapor in the drying medium (hot air), and also by the
movement of air in the drying facility
The coverage density (pile height and density) of the harvested product

The aim of drying must be to remove both the water that is physiologically bound in the
harvested product and also the external moisture (precipitation, dew) in the shortest possible time,
in order to reduce the water content of the dry product to 810%.
This will then cut off the ongoing respiration processes, the fermentative breakdown, and
conversion reactions and the physical changes, since these can easily cause changes to the natural
plant colorants (component of the external quality traits) and lead to a considerable loss of valuable
active substances. The water content quoted of 810% for chamomile dried to a high quality is
thus below the physiological water activity aw < 0.60, which prevents the dried product from being
affected even by the most xerophilic types of harmful microorganisms, the Aspergillus and Penicillium molds, during subsequent storage.
A sufficiently high drying temperature and a fast drying process have a decisive effect on the
quality of the dry product. These factors are difficult to achieve with drying in the outdoor air
(drying sheds, drying shelves, etc.), even if the chamomile is picked primarily in the months with
the most favorable weather (June and July). It is thus necessary to improve the efficiency of air as
the drying medium. This is done in practice either by adding thermal energy to the drying air
(heated air-drying) or by lowering the moisture level in the drying medium through the use of a
chilling machine such as a dehumidifier. The latter option, however, is less commercially viable in
terms of both energy consumption and economics.
The permitted temperature of the product being dried is physically very limited, since
increased evaporation of various components in the essential oils during the drying process can
lead to an increased loss of the active substances or shifts in the spectrum of active substances.
For chamomile flowers with particular, but also for the chamomile herb, which both naturally have
a low level of resistance to transpiration with respect to water vaporization, this is a particularly
high risk, requiring particular caution. The boiling points of the main components in the essential
oils are not that low (chamazulene 160C, bisabolol 121C) [1], but in combination with the large
quantities of water present in the freshly harvested plants, a further reduction in the partial steam
pressure occurs in the resultant oil and water mixture, which thus lowers the vaporization to
temperatures below 100C, as Rinder and Bomme [4] proved for the conditions for water vapor
distillation for plants containing essential oils. In addition, the particular thermolability of the

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covering membranes of the secretion containers for the essential oils are greater for chamomile
than for other medicinal plants. This can cause considerable evaporation losses during drying, even
at lower temperatures.
Thus Schilcher [5] attributes the rising losses that may occur particularly at high drying
temperatures and a high air humidity (>60%) to a type of micro water vapor distillation of the
essential oil from the glandular scales, which primarily affects the low-boiling fractions (including
farnesene).
Constant checks must be carried out to ensure that the flower base of the chamomile is
completely dried, since it has a fairly high resistance to transpiration and thus takes longer to dry.
Basically, the aim should be to achieve short drying times in order to minimize any changes
in color, odor, and tissue structure and reduce the increasing microbiological contamination and
the loss of important active substances during drying. This applies particularly to outdoor air drying.
Smaller quantities of the harvested product can also be preserved using a well-designed outdoor
air-drying system, making use of suitable outside air conditions. A good forced-air ventilation
system through the chamomile flowers that are spread flat on hurdles is important to achieve
sufficiently fast drying within 5 to 6 days.
But the physiological characteristics of the harvested chamomile also affect drying and quality
[3]. One element that is extremely important is the crushing of the flowers (gritting, or crushing
of the flower heads, which leads to the separation of the different parts of the heads) during drying.
This crushing process is of most relevance for large flowers in which more than three quarters of
all the tubular blossoms are open [2]. For tetraploid genotypes, values between 75 and 88% were
measured, with values of 64% for diploid genotypes. If the flowers are plucked at the medium
mature stage (second circle of tubular blossoms opened), the tendency to decay for tetraploids is
only 14 to 27% and for diploids 11%. If they are picked even earlier, the small flowers (buds opened
to first ring), there is hardly any decay (< 0.8%). In addition to the favorable influence of the
ambient temperature, the tetraploid genotypes are another positive factor [2].
Harvested chamomile should be taken to drying basically without any preliminary wilting, as
fresh as possible in order to guarantee that the dried medicinal product is of the highest possible
quality. Drying has to be started within 2 hours after harvest, unless the stack is not ventilated
(Section 7.2).
The cleaning and maintenance of the drying equipment should be such that microbiological
contamination and pollution are avoided. During drying, the Guidelines for a Good Agricultural
Practice (GAP) of Medicinal and Aromatic Plants [6] should be complied with at all stages.

REFERENCES
1. Gildemeister, E., Hoffmann, F. (1960) Die therischen le. Band IIIa. Akademie-Verlag, Berlin.
2. Letchamo, W. (1991) Vergleichende Untersuchngen ber die nacherntetechnisch bedingten Einflsse
auf die Wirkstoffgehalte in der Droge bei Kamille-Genotypen. Drogenreport. Sonderausgabe zur
Fachtagung in Erfurt, pp. 129134.
3. Marquard, R., Kroth, E. (2001) Anbau und Qualittsanforderungen ausgewhlter Arzneipflanzen.
Agrimedia Verlag, Bergen/Dumme.
4. Rinder, R., Bomme, U (1998) Wasserdampfdestillation therischer le aus frischen und angewelkten
Pflanzen. Bayerische Landesanstalt fr Bodenkultur und Pflanzenbau, Freising-Mnchen, pp. 112.
5. Schilcher, H. (1987) Die Kamille Handbuch fr Arzte, Apotheker und andere Naturwissenschaftler.
Wissenschaftl. Verlagsgesellschaft, Stuttgart, Germany.
6. O.V. (1998) Guidelines for Good Agricultural Practice (GAP) of Medicinal and Aromatic Plants. Z.
Arznei-und Gewrzpflanzen, 3, S. 166174.

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8.2 DRYING OF CHAMOMILE FLOWERS (MATRICARIA RECUTITA L.)

ALBERT HEINDL

8.2.1 PROCESSING

OF

HARVESTED PRODUCT

BEFORE

DRYING

Before drying, the mixture of herbs and flowers is fed to a double-drum sieve to separate stems
and other undesired matter (like stones or weed plants) from flowers. The inner sieve drum, made
of perforated plate, has a hole diameter of 25 mm, the outer sieve drum a hole diameter of 20 mm
[15]. The flowers and small stems fall down to a roller course with clear span between rollers of
34 mm. Flowers are discharged in conveying direction, whereas small stems fall down to the
waste. Figure 8.2.1 shows a sieving machine with an input capacity of approximately 1200 kg/h [15].

8.2.2 BASICS

OF

DRYING

Chamomile flowers have an initial water content of around 80% (wet weight basis, or w.w.b.) and
are dried to a final water content of 1011% (w.w.b.). The weight relation of raw chamomile flowers
to dried can be calculated to 4.5:1. So to produce 1 kg of dried flowers approximately 3.5 kg of
water has to be evaporated from 4.5 kg of raw chamomile flowers. If a herb portion of 50% is
considered, this value will increase to 9:1 (weight relation of harvested chamomile herb and flowers
to dried flowers).
Drying time of chamomile flowers is influenced by air temperature, air velocity, height of layer,
and relative humidity of drying air. Mller [13] examined the influence of these parameters for a
thin layer of flowers (approximately 1 cm of height, drying area charged initially with 1.75 kg/m2).
Doubling drying temperature from 30 to 60C reduced drying time by 97%, dramatically showing
the influence of temperature. Increasing air velocity from 0.1 m/s to 0.4 m/s at a drying temperature
of 60C resulted in a decrease of drying time of only 30%. At an air temperature of 60C drying

FIGURE 8.2.1 Chamomile sieving machine [15].

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time was significantly increased by a relative humidity (r.H.) of air exceeding 50%. At 45C an
increase of drying time can be stated at relative humidities exceeding 20%.
During the first stage of drying it is recommended to use higher air velocities. With progressive
drying, air flow should be reduced. Thus the air flow going through the product layer is adapted
to the water quantity, which has to be evaporated out of the product layer. Figure 8.2.2 shows the
drying of chamomile flowers in a layer of 40 cm in height at an air temperature of 60C and with
a constant and a staged air velocity [2]. A higher air velocity at the beginning of drying process
leads to a quick removal of the high evaporated water quantity in the first 5 hours and to a faster
drying. Thus recondensing of water vapor in the top layer is avoided. This has a positive effect on
the essential oil content of the flowers in the top layers, and the energy consumption per kg of
dried product will be reduced. These effects underline the account of time-staged control of air
velocity for static dryers.
For low-temperature drying with dehumidified air the so-called sorption isotherm in Figure
8.2.3 is important [2]. When drying is carried out at a low temperature of 25C, the relative humidity
of the drying air has to be below 55% to reach a final water content of 11% w.w.b. For reasonable
drying times (below two days) the dehumidification unit has to remove sufficient water from the
air to get a relative humidity of below 4045%.
For chamomile flowers a drying time of 24 hours was achieved in a special drying box working
with dehumidified air at a layer height of 30 cm. Drying temperatures ranged from 18 to 29C [9].

8.2.3 INFLUENCES OF DRYING PARAMETERS

CONSUMPTION

ON

QUALITY

AND

ENERGY

8.2.3.1 Quality
Convective drying of chamomile flowers causes losses of essential oils of approximately 25% in
a wide range of drying parameters [13].
90
80

Water content in % w.w.b.

70
60
50
0,2 m/s
40
30
20
0,3 m/s (5,5 h)/0,2 m/s (4h)
10
0
0

10

12

Drying time in h

FIGURE 8.2.2 Drying of chamomile flowers in a high layer (air temperature 60C, height of layer 40 cm) [2].

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Water content in % w.w.b.

25
20
15
10

25C

45C

0
0

20

40

60

80

100

Relative humidity of air in %

FIGURE 8.2.3 Sorption isotherms of chamomile flowers [2].

8.2.3.1.1 Influence of Air Temperature

Older publications on drying of chamomile recommended a maximum drying temperature of 45C
to limit the losses of essential oils. By 1969 Buschbeck [2] assumed, due to his experiments, that
a higher air temperature of 60C could be applied without having to accept decisively higher quality
losses. Mller [13] confirmed this statement by intensive examinations. Both made their tests at
an air velocity of 0.2 m/s. Drying at temperatures above this limit causes remarkably higher losses
in essential oils according to Reference 2, as shown in Figure 8.2.4.
Mller [13] could not find a sharp increase in losses even up to 90C. No clear link between
drying temperature and the composition and losses of the four main components of the chamomile
oil (chamazulene, bisabolol, bisabololoxide A, bisabololoxide B) for this temperature range could
be discovered [13].
In Hungary quality examinations were carried out on samples from industrial drying units in
1966. In the case of a band dryer the content of essential oils decreased by 27% at temperatures
of 8090C in comparison to a sample dried on a loft [18]. There were no remarkable differences
in essential oil contents at air temperatures between 4050C and 6070C. The chamazulene
content even increased at 4050C by 6% and at 6070C by 21%. Only the high-temperature
drying with 80C resulted in a loss of 6%.
Drying of chamomile flowers in a modern five-band dryer can be carried out with a staged
temperature profile. The temperature under the top band can be adjusted to 6070C, the temperature
under the second and third band to 5055C, and the temperature for the fourth and fifth band to
4550C. Thus the drying capacity of the band dryer is increased without additional deterioration

Related content of
essential oils in %

100
80
60
40
20
0
35

45

60

70

80

Drying air temperature in C

FIGURE 8.2.4 Related content of essential oils of chamomile flowers in dependence of drying air temperature
(basis sample naturally dried in a shaded place), air velocity was 0.2 m/s for convective drying experiments [2].

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of product quality. Product temperature in the layers on bands one to three does not reach air
temperatures due to the cooling effect of the water evaporating from the surfaces.
Examinations carried out by Schmitt [17] show the influence of an uneven drying within a lot
on the product quality. Samples were taken from fast-drying spots of an industrial static dryer,
which were overdried and exposed over a longer period of time to a higher temperature nearby the
air temperature of 5560C (up to 8 hours); the samples had an essential oil content of 0.5% instead
of 0.8%. This value corresponds to a related additional loss of 35% [17]. On the other hand, the
microbial counts and the fungus contamination were lower than the values of other normally dried
spots (factor 30 for microbial counts and factor 6 for fungus contamination).
8.2.3.1.2 Influence of Relative Humidity of Air
Samples of chamomile flowers dried at 60C and 0.2 m/s showed at r.H. of drying air above 50%
higher losses in total content of essential oils. Losses increased from 25% in the region of r.H.
below 50% to 30% at a r.H. of 60% and to 50% at 70% r.H. [13].
The losses of single components of essential oil reach their maximum in the case of chamazulene
at a relative humidity of 40%, for bisabolol at 30%, for bisabololoxide A at 50%, and for bisabololoxide B at 50% (air temperature 60C, air velocity 0.2 m/s). Therefore it can be concluded that
at relative air humidities above 30% increased losses for the four main components of the essential
oil occur. It is recommended that the portion of recirculated air flow has to be limited so that the
relative humidity of the drying air does not exceed 30% at a temperature of 60C and an air velocity
of 0.2 m/s [13].
8.2.3.1.3 Influence of Air Velocity and Load of Dryer
Low air velocities and high dryer loads (in kg raw material per m2 of drying area) result in a high
air humidity of drying air and even condensing of water vapor especially in the top layers of a
drying bed. Water vapor uptake capacity of drying air is limited, and air is cooled when coming
into contact with product in cool top layers. High air humidity or even condensing of water vapor
leads to a micro water vapor distillation of essential oils out of the gland chambers [16]. This
reduces the total content of essential oils in the dried product and deteriorates the oil components
as stated in Section 8.2.3.1.2. Therefore, the air flow per drying area or air velocity through a bed
has to be coordinated with load of bed and applied air temperature. Drying chamomile flowers in
big layers and at low air velocities even limits the admissible value of the relative humidity to 10%
[14].
8.2.3.2 Energy Consumption and Energy Costs
The specific energy demand per kg of dried chamomile flowers depends on:

Maximum drying temperature and resulting drying time

Applied air flow in m3/h per m2 of drying area
Number of product turning during drying period
Initial and final water content
Height of product layer or load per drying area
Kind of raw material (sieved flowers or mixed with herbs)
Portion or recirculated air flow (e.g., relative humidity of air max. 30% at 60C and 0.2 m/s)

The energy consumption of a static dryer for chamomile drying with partial recirculation of
air flow can be estimated according to the assumptions stated below. Changing conditions will
change the energy consumption, too.
Height of layer is 30 cm, bulk density is approximately 200 kg/m3, area charging with raw
flowers is approximately 60 kg/m2, the initial water content is 80% (w.w.b.), final water content is

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11%, and drying time is approximately 20 hours. Air temperature is raised by 35C by the oil-fired
air heater with an efficiency of 90%. The air velocity and the specific air volume per hour are 0.15
m/s and 540 m3/(m2*h).
The following specific values can be calculated: The thermal energy input is approximately
7.14 kWh/(m2*h) corresponding to a fuel oil light consumption of approximately 0.71 l/(m2*h)
(fuel oil light, ASTM No. 2: 1 liter = 9.96 kWh). The specific production of dried chamomile
flowers is 0.67 kg/(m2*h) and results in a specific fuel oil consumption of approximately 1.05 liter
fuel oil per kg of dried chamomile. The electric energy consumption can be calculated to approximately 0.15 kWh/(m2*h) and to 0.14 kWh/kg dried chamomile. The costs for the energy consumption are 0.43 for oil (assumed price of 0.41/liter) and 0.02 for the electric current (assumed
price of 0.13/kWh) for 1 kg of dried chamomile flowers.
Increasing the portion of recirculated air flow raises relative humidity of the drying air and
decreases energy consumption per hour for heating the drying air. On the other hand, the drying
air has a lower capacity for water uptake, leading to a longer drying time. Thus, the energy saving
by partial recirculating exhaust air might be compensated by a longer drying time caused by a
higher humidity of drying air.
Mller stated a minimal energy consumption for a drying temperature of 45C at a r.H. of 40%,
for a drying temperature of 60C at 60% r.H. But exceeding 30% r.H. at 60C leads to a quality
deterioration of essential oils as already mentioned [13].
According to Table 8.2.1 the following related energy savings could be stated for a partial
recirculating of air operation at an air velocity of 0.2 m/s in comparison to a pure fresh air operation
(60C/10% r.H., 45C/15% r.H.) [13].
An absolute limit of relative humidity is 70% for 45 and for 60C. Aside from the quality
deterioration of the essential oil, the drying time is extremely prolonged, so that fungus growth
and a general deterioration of the chamomile flowers can be assumed.
Concerning the energy consumption per kg of evaporated moisture Mller [13] found a minimum for an air temperature of 60C and for an air velocity of 0.2 m/s.
Practical measurements of an industrial five-band dryer equipped with a cross-stream heat
exchanger for heat recovery showed a consumption of fuel oil light of 0.6 liter/kg of dried
chamomile flowers despite applied low temperatures of 46/43/41C under the first/third/fifth band
and despite a low final water content of 79% [1]. The energy consumption of a five-band dryer
with partial recirculating of air flow and without heat recovery equipment can be estimated to 0.78
liter of fuel oil light per kg of dried product for a final water content of 11% and for temperatures
of 60/55/46C under the first/third/fifth band [5].

8.2.4 MICROWAVE-ASSISTED WARM AIR DRYING

By applying microwave energy, drying of chamomile flowers can be accelerated. Hereby the energy
input per kg of dried product and the time of application are decisive. Figure 8.2.5 shows the drying

TABLE 8.2.1
Possible Energy Saving through Partial Recirculating of Air Flow [13]
Drying
temperature

Relative humidity due to

partial recirculating of
air flow

Prolongation of drying
time/reduction of dryer
capacity

Energy saving in
comparison to pure fresh
air operation

45C
45C
60C
60C

30%
40%
30%
60%

20%
35%
10%
100%

50%
47%
44%
50%

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90
80

Water content in % w.w.b.

70
60
50
40
30
K2

K3

20

K4

10

K5

K1

0
0

50

100

150

200

250

Drying time in min

FIGURE 8.2.5 Microwave-assisted warm air drying of chamomile flowers [8], influence of microwave energy
application on drying time.

curves for different microwave energy concentrations, calculated in kWh per kg of dried product
with a final water content of 10%. All experiments were carried out at an air temperature of 60C,
a relative humidity of 1014%, and an air velocity of 0.2 m/s. A high microwave energy input of
10.8 kWh/kg results in a reduction of drying time of 60% in comparison with nonmicrowave warm
air drying [8].
Focusing the interest on the results of the experiments of K4 and K5, a shorter drying time in
the case of K5, it can be stated despite equal microwave energy concentration. In K4 microwave
energy is applied in the water content range of 85 to 65% w.w.b. (5.67 kg/kg to 1.86 kg/kg bone
dry basis, or b.d.b.), whereas in the case of K5 the water content ranges from 81 to 50% w.w.b.
(4.26 kg/kg to 1.00 kg/kg b.d.b.). Obviously there is a higher efficiency in microwave energy
absorption in this lower water content range. The microwave energy input in these experiments is
rather high; further trials are necessary to optimize the quantity and the time of application of
microwave energy.
The analysis in Table 8.2.2 shows higher total contents of the essential oil for the microwavetreated samples and supports the application of microwave energy. K0 is a reference sample naturally
dried in a shaded place at ambient temperature [8].
Microwave energy application also affects the optical quality of dried chamomile flowers. A
better color preservation and bigger flower heads were stated for microwave-treated samples in
comparison with air-dried products [10].

8.2.5 DRYING EQUIPMENT

The following systems and dryers can be applied for the drying of chamomile flowers or mixtures
of herbs and flowers: drying on a covered floor, drying in trays, discontinuous static dryers with
or without solar preheating of air, half-continuous basculating tier dryers (kilns), and continuousband dryers. Table 8.2.3 gives a summary on dryers for chamomile.

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TABLE 8.2.2
Total Content of Essential Oil for Microwave-Assisted Warm Air Drying of Chamomile
Flowers [8]
Experiment

Microwave energy concentration (basis

product of 10% water content)

Total content of essential oil in

ml/100 g of dried matter (b.d.b.)

K0
K1
K2
K3
K4
K5

0 kWh/kg
5.0 kWh/kg
0 kWh/kg
5.8 kWh/kg
3.3 kWh/kg
3.3 kWh/kg

0.84
0.83
0.66
0.91
0.78
0.90

TABLE 8.2.3
Comparison of Drying of Chamomile on Static Dryers, Basculating Tier Dryers (Kilns), and
Band Dryers

Kind of Dryer

Drying
Temperature

Static solar
greenhouse
dryer
Static dryer

Up to 45C
(lower in the
evening/night)
Max. 60C, often
45C

Basculating
tier dryer
Five band
dryer

Height of
Feed Layer

Drying
Time

Max. Air Velocity

or Specific Air
Volume/h

Number of
Product
Turnings

Portion of
Recirculated
Air Flow

10 cm

70 h

0.1 m/s or 360

m3/(m2*h)

No or one
manually

Low to
medium

3040 cm

1624 h

Up to 0.2 m/s or
720 m3/(m2*h)

Low to
medium

Max. 60C

15 cm

1014 h

Up to 0.4 m/s or
1440 m3/(m*h)

6070/5055/45
50C under
1/3/5 band

1015 cm
1 band

710 h

Up to 0.8 m/s or
2900
m3/(m2*h)

No or one
manually or
with grab
Two to three
by gravity
basculating
Four

Low to
medium
Medium to
high

8.2.5.1 Advantages and Disadvantages of Dryers

8.2.5.1.1 Static Dryer (Figures 8.2.6, 8.2.7)
Advantages: flexible operation; corresponds to the structure of a working day in small, medium,
and large farms or agricultural enterprises; simple operation; low investment costs; suitable for low,
medium, and large throughputs; mainly suitable for uncut plants in large layers.
Disadvantages: higher specific energy consumption, danger of uneven drying across the height
of layer, higher labor demand for filling and discharging of dryer or high investment costs for
automation of product handling, staged drying can be carried out only with high expense in time
control of relative humidity of waste air.
8.2.5.1.2 Basculating-Tier Dryer (Kiln) (Figures 8.2.8, 8.2.9)
Advantages: flexible operation, corresponds to structure of working day in small and medium farms
and agricultural enterprises, staged drying possible by additional air conduits with low expense,
automatic product turning through gravity dumping leads to an even drying, suitable for cut material
that does not stick to the tiers, high drying area combined with low ground area demand, low labor
demand for filling and discharging.

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Section
Roller-textile woven belt

Waste air recirculating conduct

Textile woven tape

Perforated metal sheet floor

Air conduit-heated air

Ventilator

Ground plan

Air heater
Burner

Chamber 3
Air conduit

Chamber 2
Temperature probes

Chamber 1
Woven belt
Movable discharging truck for filling
Discharging conveyor band

Movable conveyor band for filling

FIGURE 8.2.6 Static dryer with filling and discharging conveyor bands and air conduit for partial recirculating
of air flow [17].

FIGURE 8.2.7 Static dryer for chamomile in Slovakian Republic.

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Fan for exhaust air

Conduit for recirculated air

Additional
heated air

Tipping tiers

Fan for fresh air

Discharge conveyor
band
Air distributor

FIGURE 8.2.8 Basculating tier dryer (kiln) [3, 4].

FIGURE 8.2.9 Basculating tier dryer (kiln) [3, 4].

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Indirect air heater

Oil/gas burner

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Disadvantages: medium investment costs; not suitable for whole, uncut plants or material
sticking to the tiers.
8.2.5.1.3 Band Dryer (Figures 8.2.10, 8.2.11)
Advantages: high throughput per drying area, suitable for a small range of different products, staged
temperatures and air velocities easy to adapt to the drying curve of all products, even drying through
several product turning by gravity dumping, lower energy consumption, corresponds to the structure
of a working day in medium and large farms and agricultural enterprises, low labor demand for
filling and discharging.
Disadvantages: no correspondence with structure of a working day in small farms and small
agricultural enterprises, as a continuous feeding and operation in three shifts per day is necessary
for an economic run with good product quality; high investment costs.
The investments for basculating-tier dryers and band dryers can only be justified if medium or
higher throughputs in the range above 100200 kg of raw material per hour will be reached and
the period of operation will last up to 6 months per year. That means that other medicinal plants
and spices and even vegetables or fruits have to be processed additionally.
In general the investment costs rise with increased degree of automation, causing lower specific
energy costs and lower specific labor costs, too.
Rotating cleaning brushes
Dosing rollers
for control of loading
Feeding
conveyor band

FIGURE 8.2.10 Five-band dryer, cross section [7].

FIGURE 8.2.11 Five-band dryer [6].

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Exhaust ventilators
Wire mesh belts

Discharge
conveyor band

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FIGURE 8.2.12 Inclined harp machine for cleaning of dried chamomile flowers [15].

8.2.6 PROCESSING

OF THE

DRIED PRODUCT

The final processing of dried plant material results in a first-class, nearly pure flower product. The
dried flowers are cleaned in a so-called inclined harp machine. Long stems are separated from the
flowers. Figure 8.2.12 shows such a machine with a throughput of up to 120 kg/h, which was
developed in the Slovak Republic [15].

8.2.7 SUPPLEMENT: RECOMMENDATIONS

FOR

DRYING

The following are recommendations for drying of chamomile flowers in static and band dryers.
8.2.7.1 Static Dryers

Quick drying after harvest, storage of harvested material not in high layers and not under
the sun, maximum storage time 2 hours, for longer periods cooling with ambient air is
necessary.
Drying temperatures up to max. 5560C.
Air velocities approximately 0.150.20 m/s for static dryers corresponding to a specific
air flow of approximately 540720 m3/(m2*h), for solar-assisted static dryers values are
approximately 0.1 m/s or 360 m3/(m2*h).
Maximum relative humidity of drying air should be below 30% at 60C for partial
recirculating of waste air, for lower air velocities or drying in deep beds, 10% r.H. should
not be exceeded, affording a pure fresh air operation without recirculating [14].
In case of limited heating capacity and a maximum drying temperature of 45C, fresh
air operation is recommended until water content of lot drops under 60% w.w.b.
Feeding height of layer max. 30 cm corresponding to a raw material charging of approximately 60 kg/m2 (air pressure drop of up to 170 Pa at air velocity of 0.2 m [11]), for
solar-assisted dryers with lower air velocity max. 15 cm corresponding to 30 kg/m2 (air
pressure drop up to 85 Pa at air velocity of 0.2 m/s) of raw material load.
Even spreading of material on dryer (bed height, density).

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Drying time at least 1620 hours at 60C, at 45C up to 30 hours, for solar-assisted
dryers up to 70 hours.
Final water content under 1011% (w.w.b.).
Even drying by careful turning of product (manually), for static dryer turning is recommended after 810 hours, thus overdrying of bottom layers and recondensing of water
vapor in the top layers is avoided and even drying throughout the lot is promoted.
Reduction of air temperature and air velocity after advanced drying time recommended
due to energetic and quality reasons (measuring of relative humidity of waste air as
guideline).

8.2.7.2 Band Dryers

Quick drying after harvest, storage of harvested material not in high layers and not under
the sun, maximum storage time 2 hours, for longer periods cooling with ambient air is
advisable.
Drying temperatures staged 6070C/5055C/4550C under 1/3/5 band in a five-band
dryer.
Max. air velocity approximately 0.700.80 m/s for five-band dryers under the top band
corresponding to a specific air flow of 2500 to 2900 m3/(m2*h).
Max. relative humidity of 30% at 60C in the case of partial recirculating of waste air,
portion of recirculated waste air max. approximately 4050%.
Feeding layer height of raw material max. approximately 10 cm for pure chamomile
flowers (15 cm for higher herb portion) corresponding to a load of raw material of
approximately 20 kg/m2 (30 kg/m2).
Drying time at least 710 hours depending on drying temperatures, initial and final water
content, and herb portion.
Final water content under 1011% (w.w.b.).
Even drying by automatic gravity product turning from one band to the following band,
additionally with product-turning device above the middle of the first band or through
dividing of first band in two bands arranged in a line with gravity turning at handing
over position of product.
Application of a heat-recovery device (e.g., cross-stream heat exchanger).

REFERENCES
1. (2001) Personal communication from practice.
2. Buschbeck, E. (1969) Forschungsbericht Arzneipflanzentrocknung. Technische Universitt Dresden.
1969.
3. Heindl, A. (1997) Brochure of Heindl GmbH, D-84048 Mainburg.
4. Heindl, A. (1998) Brochure of Heindl GmbH, D-84048 Mainburg.
5. Heindl, A. (2000) Datensammlung fr das Kuratorium fr Technik und Bauwesen in der Landwirtschaft e.V., Darmstadt.
6. Heindl, A. (2001) Brochure of Heindl GmbH, D-84048 Mainburg.
7. Heindl, A., Mller, J. (1997) Trocknung von Arznei- und Gewrzpflanzen. Z. Arzn. Gew.pfl. 2, 9097.
8. Heindl, A., Mller, J. (2001) Microwave assisted warm air drying of medicinal herbs and spices.
World Conference on Medicinal and Aromatic Plants. Budapest, Hungary, July 811, 2001.
9. Herold, M., Frster, C., Mickan, P., Rhl, W. (1991) Kleintechnischer Boxentrockner fr Arznei-und
Gewrzpflanzen auf der Grundlage der Luftentfeuchtung. Drogenreport 4, Nr. 6, 94103.
10. Kartnig, Th., Lcke, W., Lassnig, Ch. (1994) Der Einsatz von Mikrowellenenergie zur Aufbereitung
von Arzneidrogen. 1. Mitteilung. Pharmazie 49, Nr. 8, 610613.

Copyright 2005 CRC Press, LLC

TF4015_book.fm Page 202 Wednesday, April 6, 2005 12:17 PM

11. Maltry, W., Ptke, E., Schneider, B. (1975) Landwirtschaftliche Trocknungstechnik. Verlag Technik,
Berlin.
12. Marquard, R., Kroth, E. (2001) Anbau und Qualittsanforderungen ausgewhlter Arzneipflanzen.
Agrimedia Verlag, Bergen/Dumme.
13. Mller, J. (1992) Trocknung von Arzneipflanzen mit Solarenergie. Diss., University Hohenheim,
Stuttgart, Germany.
14. Mller, J., Kll-Weber, M., Kraus, W., Mhlbauer, W. (1996) Trocknungsverhalten von Kamille
(Chamomilla recutita (L.) Rauschert. Z. Arzn. Gew. pfl. 3, 104110.
15. Polnohospodarske Drustvo ROZKVET (1997) Brochures and offer 11.3.97. Slovakian Republic.
16. Schilcher, H. (1987) Die Kamille Handbuch fr rzte, Apotheker und andere Naturwissenschaftler.
Wissenschaftl. Verlagsgesellschaft, Stuttgart, Germany.
17. Schmitt, E. (2000) Einfluss der Trocknungstechnik auf die Qualitt von Arzneipflanzen am Beispiel
von Echter Kamille und Ringelblume. Dipl. Thesis, University Giessen, Germany.
18. Svab, J. (1966) Trocknungsversuche mit ungarischer Handelskamille. Herba Hungarica 5, Nr. 1,
3136.

8.3 DISTILLATION OF ESSENTIAL OIL

REINHOLD CARLE

8.3.1 INTRODUCTION
Essential oils are steam-volatile mixtures of complex natural substances of plant origin. In some
cases, over a hundred different chemical compounds can be detected in an essential oil. Presently,
a total of 3000 defined compounds are known [15, 16, 19]. The wide range of application of volatiles
is due to the existence of an extensive diversity of compounds in essential oils. A market survey
(Table 8.3.1) shows that essential oils are mainly used in the food industry and in the perfume
industry. However, some essential oils, e.g., chamomile oil, are especially important in the pharmaceutical industry.
The increase in industrially processed foods has constantly increased the demand for flavoring
agents over the last ten years. The world production of natural essential oils is estimated at around
45,000 tons per annum. The price of essential oils ranges between 1.25 Euro/kg for orange oil and
60,000 Euro/kg for genuine Melissa oil (Table 8.3.2). Therefore, genuine essential oils are often
replaced by mixtures of synthetic compounds.
Advances in the field of chemical synthesis have been such as to suggest that natural essential
oils would eventually disappear. However, in reality, these products have maintained their place on
the market in the face of competition from synthetics.
The establishment of intensive methods and the simplification of production systems in the
agriculture of developed countries with fewer crop species grown over bigger areas with
mechanization led to a nearly complete abandonment of volatile oil crops in industrialized
countries. Consequently, process engineering with respect to distillation of essential oils has been
neglected.
Whoever is engaged in food technology or pharmaceutical technology would realize that process
development in the production of essential oils has been stagnant since the 1950s. Even today, the
production of essential oils is mainly performed by the traditional method of water distillation in
rather primitive field distillation stills (Figure 8.3.1).
The plant material is put into a vessel and completely covered with an appropriate volume of
water and finally closed. Steam is produced by directly heating the vessel. Technical requirements
for the separate production of steam needed for the milder steam distillation are generally not
available. Especially disadvantageous is the decomposition of hydrolysis-sensitive components as
well as the batch processing method. The alternating feeding and emptying of the vessel is associated
with high operational and energy costs.

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TABLE 8.3.1
Market Importance of Essential Oils [14]
Aroma extract in the food industry
Odoriferous agent for perfumes/cosmetics
Raw material in the aroma industry for the isolation of substances
Active component in pharmaceuticals
So-called "natural products"

50%
20%
15%
5%
5%

TABLE 8.3.2
Important Essential Oils According to Prices [14]
Oil
Melissa
Iris root
Violet leaves (absol.)
Rose (Bulgarian)
Orange flower
Jasmine flower (absol.)
Angelica roots
Chamomile (blue)
Labdanum
Galbanum
Sandalwood (East India)
Bergamot orange
Cassia (Chinese)
Lavender 40/42%
Peppermint (Mentha piperita)
Spearmint

Price per
kg
6300
6300
4300
4000
2000
1500
1250
1250
880
400
200
125
75
60
30
25

In order to improve the efficiency of the distillation process, a continuous method was developed
as an alternative to the conventional batch and quasi-continuous distillation methods. Using the
production of chamomile oil as example, the various methods will be presented. For all investigations, chamomile of the variety Degumille, which is characterized by high contents of chamazulene and ()--bisabolol, was used [10]. The quality of the chamomile oil as influenced by the
method of distillation and pretreatment, especially drying and grinding of the plant material, will
be investigated.

8.3.2 PRODUCTION

OF

CHAMOMILE OIL

As of now, with chamomile oil, there is uncertainty with regard to the nature and quality of the
raw material to be used. While the Food Chemicals Codex (1981) [7] permits the use of flowering
tops, that is the chopped flowering tops, pharmacopoeias (e.g., Ergnzungsbuch zum Deutschen
Arzneibuch 1953 [6], sterreichisches Arzneibuch 1981 [11], and Pharmakopea Helvetica 1971
[12]) specify the use of pure flower heads, that is, the picked material with a pedicel of maximum
2 cm. Due to economic reasons, the justification of this requisition is always questionable [8]. Up
until now dried chamomile flowers have been used for the production of chamomile oil. This
practice seems inappropriate since considerable losses of volatile components of the essential oil
are incurred during drying [3, 4].

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FIGURE 8.3.1 Field distillation still [14].

On the basis of comparable investigations, dried and freshly harvested chamomile with various
stalk lengths in both ground and whole forms were used. With the aim of improving profitability,
the conventional batch process of steam distillation is compared with the newly developed quasicontinuous and continuous distillation processes.

8.3.3 METHODS

OF

PRODUCTION

8.3.3.1 Batch Method

The principle of the batch steam distillation achieved with the technical apparatus is shown in
Figure 8.3.2.
The plant material is brought and evenly distributed in a supporting basket of the still. After
tightly screwing on the cover, steam is introduced. The distillation is carried out at atmospheric
pressure. To prevent water distillation, condensed water is drained off through an outlet provided
for this purpose. The specific lighter chamomile oil is separated in a Florentine bottle. Because
of the water-soluble nature of the chamomile oil, a series of several Florentine bottles is necessary.
An almost complete separation of the oil is achieved through a coalescence filter at the end of the
series [3]. The alternating feeding and emptying of the vessel results in process interruptions, which
necessitate high operational and energy costs.
8.3.3.2 Quasi-Continuous Method
For the production of highly volatile peppermint oil, mobile distillation equipment has been
developed [9, 17]. The plant material from the field is chopped into a mobile container, which can
be directly used as a still by its connection to a stationary steam generator and a condenser with
an attached oil separator. A so-called mint cooker (Newhouse, Redmond, WA) was designed to
achieve a quasi-continuous operation through the alternating usage of two or more containers.
However, energy losses cannot be avoided during heating and cooling cycles of the still. This
technology has proven its effectiveness for the production of highly volatile monoterpene-containing
oils. It should be examined whether this method is also suitable for the production of low volatile
sesquiterpene-containing chamomile oil.

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Cooling water
Distillation
apparatus

Cooler

Florentine
bottles
Oil/Organic
solvent
Water
phase
Distillate
container
Steam
Condensed water

FIGURE 8.3.2 Batch steam distillation [1].

Rotary conical feeder
Vertical shaft
Dosage funnel
Vapor outlet
Prefeeder
Preheater
Distillation chamber
Distribution chamber
Screw conveyor
Siphon

FIGURE 8.3.3 Continuous distillation apparatus [2].

8.3.3.3 Continuous Method

A still originally developed for the production of ethanol derived from marc enables a continuous
operation (Figure 8.3.3).
The plant material is introduced into the distillation chamber through a conveyor belt. The
steam flows against the plant material through a distributor plate. The steam saturated with oil
leaves the still through the vapor outlet. To prevent the formation of canals, a stirrer is provided to
ensure a uniform throughput and distribution of steam. The distillation waste is finally ejected by

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TABLE 8.3.3
Distillation: Production Balance [2]
Oil Yield
Fresh Weight
[kg/ha]
[]
Continuous distillation
Chamomile flowers
- Picked
- Chopped
- Dried (drug)
Batch distillation
Chamomile flowers
- Picked
- Chopped

Dry Weight
[]

1.03
4.28
1.04

0.51
0.44

2.22
1.75
3.18

0.43
2.00

0.61
0.63

2.78
2.50

means of a screw conveyor. If necessary, the waste can possibly be redistilled. At the end of a
distillation cycle, part of the waste is conveyed into the dosage funnel to prevent steam leakage.
To prevent water distillation conditions, the condensate formed is drained off through a siphon.

8.3.4 EVALUATION

OF THE

METHODS

Comparing the production balance (Table 8.3.3), it becomes clear that the use of picked material
in both fresh and dried forms is not economical.
Because of the high harvest, drying, and distillation costs the use of dried material is especially
unprofitable. The best yields are provided by employing chopped flowering tops. If a complete
separation of stalks is avoided, a large amount of biomass must indeed be treated; however, a
considerably better yield is obtained. This result is in agreement with previous observations made
in Reference 8, which recommended a mixture of chopped straw or chamomile weeds to prevent
the flower heads from over baking.
With both methods, the technical yields of oil on a dry weight basis do not reach even by
redistillation the amount of 0.4% specified in the pharmacopoeia. At any rate the lower yields
of the continuous method are compensated by the higher capacity and the distinctly lower energy
consumption.
Freshly harvested chamomile flowers give better oil quality than the dried chamomile drug
(Table 8.3.4).
Because of drying losses, the resulting oil has low chamazulene and bisabolol contents. Chamomile oil from flowery sprouts is comparable to that produced from chamomile drug. Due to the
lengthy heating periods in the batch method, the oil produced contains high azulene but low
bisabolol contents. Due to their content of chamazulene, high-quality chamomile oils are dark blue
in color (Food Chemicals Codex 1981 [7], Ergnzungsbuch zum Deutschen Arzneibuch 1953 [6],
sterreichisches Arzneibuch 1981 [11], Pharmakopea Helvetica 1971 [12], Pharmacopoea Hungarica 1986 [13]). Chamazulene is of course not a genuine component of chamomile flowers. It
is formed during steam distillation from its colorless precursor matricine through dehydration,
deacylation, and decarboxylation [18]. The heat-sensitive labile spiroethers are completely decomposed.
The physical and chemical properties differentiate the chamomile oils produced with the various
methods (Table 8.3.5).
Chamomile oil produced by the batch method has a higher specific gravity and a higher
refractive index. The high wax content of such oils reflects their significantly high saponification

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TABLE 8.3.4
Influence of the Distillation Method and the Raw
Material on the Quality of Chamomile Oil [2]
Chamazulene
[%]

Bisabolol
[%]

cis-Spiroether
[%]

7.8
5.9
2.1

33.3
24.0
27.9

2.5
6.1
5.6

11.4
7.8

21.1
19.4

n.d.
n.d.

Continuous distillation
Chamomile flowers
- Picked
- Chopped
- Dried (drug)
Batch distillation
Chamomile flowers
- Picked
- Chopped
n.d.: not detectable

TABLE 8.3.5
Physical and Chemical Properties of Chamomile Oil [2]
Batch Distillation

Specific gravity [g/ml]

Refractive value

n
20
D

Continuous Distillation

Chamomile Oil from

Drug

Chamomile Oil from

Fresh Plant

Chamomile Oil from

Drug

0.9334

0.8949

0.9077

1.5198

1.5042

1.5045

Water content [%]

0.76

0.81

0.55

Saponification number

25.6

8.3

8.0

Acid value

13.1

5.4

5.6

Ester value

12.5

2.9

2.7

Ester value after acetylation

90.5

62.0

62.7

n.d.

-3.0

-2.5

20

Optical rotation D

[*]

n.d.: not determined

numbers and acid and ester values. A comparison between chamomile oil from fresh and dried
chamomile shows that these differences are attributable to the method of production and not to the
raw material used.
According to the DAB 6 Supplementary Book (Ergnzungsbuch zum Deutschen Arzneibuch
1953 [6]), chamomile oils should congeal during cooling to a consistency similar to butter. Our
investigations reveal that only wax-rich chamomile oil meet this requisition. High-quality low-wax
chamomile oils are accordingly ruled out, so that this requisition presently seems unreasonable.
In accordance with the practice, therefore, the DAB 10 Monograph, Chamomile oil (Deutsches
Arzneibuch 1997 [5]) considered the present findings and registered chamomile oil produced from
fresh or dried flower heads or flowery sprouts through water distillation. High-quality chamomile
oils are no longer excluded from the list of key physical data.
Based on this finding, recommendations for a chamomile oil specification were established. In
Table 8.3.6 data according to the Food Chemicals Codex are compared to those recommended.

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TABLE 8.3.6
Recommendation for Chamomile Oil Specification [2]
Recommended Data
Content [mg/100 g]
Bisabolol
Chamazulene
Farnesol
Physical-chemical data
Specific gravity 25 [g/ml]
20
Optical rotation D (EtOH; c = 1,0)
Refractive value n 20
(EtOH; c = 1,0)
D
Saponification number
Acid value
Ester value
Ester value after acetylation
Heavy metals [ppm]
Water content [%]

Data According to FCC III (1981)

1530
3
45

n.m.
n.m.
n.m.

0.870.94
5 to 0
13,64015,250
40
25
15
100
2
<1

0.910.95
n.m.
n.m.
n.m.
550
40
65155
n.m.
n.m.

n.m.: not mentioned

Especially limits of saponification number, acid, and ester value (with and without acetylation)
were reduced in consideration of high-quality low-wax chamomile oils that were hitherto ruled
out, i.e., by setting minimum ester values.
With regard to production technology the continuous distillation equipment proved to be
superior to conventional techniques in yield and quality. Finally, further studies with Melissa and
Mentha distillation confirmed a broad applicability of the continuous distillation technology.

REFERENCES
1. Carle, R. (1992) Zur pharmazeutischen Qualitt biogener Wirkstoffe Untersuchungen an Kamillenl
(Chamomilla Aetheroleum). Habilitationsschrift, Regensburg.
2. Carle, R. and Fiedler, G. (1990) ber ein kontinuierliches Verfahren zur Gewinnung therischer le.
Pharm. Ind., 52, 11421146.
3. Carle, R. and Gomaa, K. (1992) Technologische Einflsse auf die Qualitt von Kamillenblten und
Kamillenl. Pharm. Ztg. Wiss., 137, 7177.
4. Carle, R., Dlle, B., and Reinhard, E. (1989) A new approach to the production of chamomile extracts.
Planta Medica, 55, 540543.
5. Deutsches Arzneibuch (1997), 10th Ed., Kamillenl, Deutscher Apotheker Verlag, Stuttgart, Germany.
6. Ergnzungsbuch zum Deutschen Arzneibuch (1953), 6th Ed., Deutscher Apotheker Verlag, Stuttgart,
Germany, p. 364.
7. Food Chemicals Codex (1981), 3rd Ed., National Academy Press, Washington, DC, pp. 8182.
8. Guenther, E. (1952) The Essential Oils, Van Nostrand, Princeton, NJ.
9. Hannig, H.J., Herold, M., and Rhl, W. (1988) Resultate der Gewinnung etherischer le nach der
Containertechnologie. Drogenreport, 1, 7387.
10. Isaac, O. (1974) German Patent Application No. 37 04 519.
11. sterreichisches Arzneibuch (1981) Verlag der sterr. Staatsdruckerei, Vienna, pp. 202203.
12. Pharmakopea Helvetica (1971), 6th Ed., Eidgen. Drucksachen- u. Materialzentrale, Bern, pp.
10311032.
13. Pharmacopoea Hungarica (1986), 7th Ed., Academia Verlag, Budapest, Hungary, pp. 1503, 1589.

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14. Protzen, K.-D. (1993) Produktion und Marktbedeutung therischer le. In Carle, R. (Ed.), therische
le Anspruch und Wirklichkeit, Wiss. Verlagsgesellschaft, Stuttgart, Germany, pp. 2332.
15. Schilcher, H. (1986) Pharmakologie und Toxikologie therischer le. Anwendungshinweise fr die
rztliche Praxis. Therapiewoche, 36, 11001112.
16. Schilcher, H. (1987) Die Kamille Handbuch fr rzte, Apotheker und andere Naturwissenschaftler,
Stuttgart: Wissenschaftliche Verlagsgesellschaft.
17. Small, B.E.J. (1982) Agfacts, Dept. Agriculture, New South Wales, Australia, pp. 14.
18. Stahl, E. (1954) ber das Chamazulen und dessen Vorstufe, 3. Mitt.: Zur Konstitution der Chamazulencarbonsure. Chem. Ber., 87, 202, 205, 16261628.
19. Verlet, N. (1993) Commercial aspects. In R.K.M. Hay and P.G. Waterman (Eds.), Volatile Oil Crops:
Their Biology, Biochemistry and Production. Longman Scientific and Technical, Harlow, pp. 137174.

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9 Storage of the Dry Drug

Horst Bttcher and Ingeborg Gnther
CONTENTS
9.1

Quality Decline in the Dried Raw Product

9.1.1 Water Absorption of the Dry Product (Moistening) in Unfavorable
Climatic Conditions
9.1.2 Effect of the Residual Water Content in the Dried Product
9.1.3 Formation of Coarse Powder in the Raw Material
9.1.4 Unfavorable Physical and Biochemical Reactions that can Lead to a Loss
of Active Ingredients
9.1.5 Attacks by Insects and Pests (Stock Pests)
9.1.6 Shrinkage Losses Caused by Changing of Constituents that are not
Essential Oils
9.2 Required Storage Conditions
9.3 Storage Room
9.4 Changes in the Essential Ingredients During Storage
9.5 Packaging
9.6 Storage Management
References

9.1 QUALITY DECLINE IN THE DRIED RAW PRODUCT

Freshly dried chamomile flowers and herbs are very storage-sensitive products, even if complete
drying of the receptacles has been achieved after a few days. The most important causes of
deterioration in quality after drying are the following conditions, which must generally also be
considered in terms of the product physiology:

9.1.1 WATER ABSORPTION OF THE DRY PRODUCT (MOISTENING)

UNFAVORABLE CLIMATIC CONDITIONS

IN

Because the dried plant chamomile organs contain a large proportion of hydrophilic constituents
(sugars, flavonoids, mucilages, phenyl carbonic acids, amino acids, choline, salts), chamomile
flowers in particular, but also the chamomile herbs are very hygroscopic products. Their moisture
content can therefore adopt the surrounding microclimatic conditions very quickly, absorbing
moisture from the air in the stack or room very fast. This means that the water content of the dry
product very soon exceeds the limit of the physiological water activity of = > 0.60, which is
responsible for microbiological deterioration. This causes a wide range of reactions: Purely biochemical transformations occur more frequently, leading to discoloration, especially of parts of the
plant that were previously damaged by pressure, heat, or a deficiency of oxygen. In the green leaves
and stems, there is a breakdown of the chlorophyll that is responsible for the green color impression
of the plants, and phaeophytin forms at the same time. In the tongue and tube blossoms, the white
and yellow colors fade, through undesirable reactions occurring with the colorings in question.

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What is particularly serious is the increase in the bacterial flora that often occur in large quantities
already at the time of harvest.
Microbiological deterioration caused by fungal agents can also occur within a short time. Thus,
at the marginal conditions of the dry product, the most xerophilic species, molds of the species
Aspergillus and Penicillium form first. The metabolism of bacteria and fungal agents releases more
and more moisture for more demanding microorganisms, such as Fusarium and Rhizopus, so that
the attack continues to develop in a kind of cascade effect. The metabolic excretions from the
microbiological agents also make the stored product smell musty or damp, which is rated very
negatively in terms of quality. In addition, there is a risk that the stored product will be contaminated
with mycotoxins, which are a health hazard.

9.1.2 EFFECT

OF THE

RESIDUAL WATER CONTENT

IN THE

DRIED PRODUCT

Even the most perfectly dried drug still contains 46% reactable water in the plant tissues, which
can lead, over longer periods of time, to the formation of undesirable flavor components and also
to increased formation of phaeophytin (loss of green color).

9.1.3 FORMATION

OF

COARSE POWDER

IN THE

RAW MATERIAL

During the time it is in storage, the chamomile flowers in the drugs will be increasingly destroyed
mechanically. This is very marked in large, fully opened flowers and at room temperatures. In cold
stores, on the other hand, this generally does not occur.

9.1.4 UNFAVORABLE PHYSICAL AND BIOCHEMICAL REACTIONS THAT CAN LEAD TO

A LOSS OF ACTIVE INGREDIENTS
These involve various reactions. For example, during storage, the steam pressure of the oil-water
vapor mixture in the drug, created through the combination of the remaining water content in the
drug with the essential oils, is lowered considerably in comparison with the essential oil, so that
at lower temperatures there is a constant evaporation of essential oils during storage, especially
if the product is not packed. Certain components of the essential oil can also lose their structure
and effect as a result of resinification. Similarly, auto-oxidations (bisabolol/bisabolol oxide) or
enzymatic splitting and rearrangement may occur, which are registered as a loss of active constituents. The role that individual value-giving components play in the processes is not yet clear in
detail. All these destructive reactions are largely dependent on the storage temperature and duration.
They run much faster at higher temperatures.
The extent of the specific quality changes in relation to the typical active ingredients in
chamomile is described in Section 7.1.
Herbs that have been finely chopped and unpacked storage goods always show higher reductions
than unprocessed crops.

9.1.5 ATTACKS

BY INSECTS AND

PESTS (STOCK PESTS)

The dried product is also a favorite habitat for certain insects. Larvae and beetles generally damage
the stored product by eating away at it and pollute it with excreta and webs. This considerably
reduces the quality and can lead to total deterioration in a short time. The evaporating essential
oils and other odor components attract the insects intensively over long distances. It is therefore
essential to ensure that they cannot penetrate the store, since the universal use of organochloric
insecticides is not possible, as it would have an adverse effect on the smell and flavor.
The main stock pests that affect drugs are (according to References 14 and 15):

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Copper-red Indian-meal moth (Plodia interpunctella Hb.)

Dark-brown thief beetle (Ptinus latro F.)
Yellow-brown thief beetle (Ptinus testaceus OLIV.)
Smooth spider beetle (Gibbium psylloides GZEMP.)

9.1.6 SHRINKAGE LOSSES CAUSED BY CHANGING OF CONSTITUENTS THAT ARE NOT

ESSENTIAL OILS
The changes during long-term storage in this important group of substances that determine quality
to a considerable extent (and are generally also directly related to the storage process) have not
yet been studied for chamomile.

9.2 REQUIRED STORAGE CONDITIONS

The safe long-term storage of chamomile flowers and herbs for several months requires the
following storage conditions:
Moisture content of stored product: 810%
Relative humidity of ambient air: <50%
Room temperature: 415C
Lighting: Largely in a darkened room
Stock pests: Free from living larvae and insects
Given these conditions, almost all the quality deteriorations described in the previous section
could be prevented or reduced. Particular efforts are required to control the occurrence of harmful
insects. Basically, the entry of such pests should be prevented by permanently covering all window,
wall, and ventilation openings with fine-mesh wire netting (12 mm mesh width). All doors and
gates should be kept automatically closed. The continuous operation of electrical UV insect traps
in the storage room is even more effective; these will have the prophylactic effect of attracting all
insects flying in and killing them with the current. Pheromone traps installed in storage rooms are
good indicators of the presence of pests. If the occurrence of pests is detected in the store,
disinfestation must be carried out immediately. All the dry crops stored in the room must be
subjected to a CO2 compressed gas disinfestation, since this is the most effective and most suitable
method. In this process (e.g., Carvex and Pex), the drugs affected are first subjected in an autoclave
to evacuation to 200 mbar (reducing the oxygen content) and then, through the addition of CO2
gas, an atmosphere of 1840 bar is created. Within a period of 150 min., complete destruction of
all development stages of the pests is achieved [8]. The process has the advantage that the drugs
can be left in their original packaging, the treatment can be carried out at normal outside temperatures, and, in contrast to chemical processes, there are no problematic residues.
Pyrethrum preparations have proved successful for the disinfestation of storage areas.
One of the basic problems with storing drugs is the considerable space requirement due to the
low bulk density of the stored product. Nonetheless, a clear, permanently accessible layout of the
individual batches in the storage room must be guaranteed so that quality can be constantly
monitored [6, 13].
The stored product must be regularly inspected to determine:

Its water content (percentage of water in the product)

Its external quality traits
Whether it is infested with stock pests
The level of value-determining active ingredients by chemical analyses

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These checks including the analyses must be carried out or repeated every 4 to 6 months. Only
in this way can the drugs minimum content requirements for the proposed usage be complied with.

9.3 STORAGE ROOM

The characteristics of the storage room also play a major part in maintaining quality and in
successful storage. These characteristics should be as follows [7, 13]:

Room cleaned and disinfected before products are taken into storage.
Airy and cool.
Dry room climate and constant curve of temperature.
Building openings sealed with wire netting to prevent entry of harmful insects, pests,
birds, and pets.
Fire prevention measures have been taken.
Avoid undesirable effects on odor caused by storing other drugs or products at the same
time.
Do not store together with toxic drugs.
Only carry out disinfestation if there is an acute occurrence of pests.
Keep dust down and prevent the transfer of the rubbed residues of other types of drug
onto the chamomile in order to exclude the possibility of cross-contamination.
Create the possibility of forced-air ventilation for dry crops that have just been taken
into storage to balance moisture levels or for cooling.
Select stack order for the sensitive chamomile drugs in such a way that the products are
not placed on the ground or subjected to mechanical pressure (avoid stacking sacks on
top of each other over 1 meter high).
Larger storage rooms should have mechanical stacking devices.

9.4 CHANGES IN THE ESSENTIAL INGREDIENTS DURING

STORAGE
Since demand for the whole year must be covered, the long-term storage of the dried drugs is
also essential. In the case of the storage-sensitive chamomile flowers, the main problem is a loss
of essential oils in the dry drug, which also contain a considerable proportion of the active
ingredients. The main reason for the losses is the low steam pressure of the oil-water vapor mixture
that forms, which encourages the evaporation of essential ingredients. The most important factors
influencing this are the storage temperature, the length of storage, the relative air humidity, and a
number of physiological-technical peculiarities of chamomile.
For loose chamomile flowers or those that are packed in simple paper bags, the representative
analytical values available [5, 7, 11] show an almost linear increase in losses with the length of
storage, which is shown in Figure 9.1.
At room temperature, it reaches 5.0%/month of storage and 2.0%/month of storage for cold
storage at 0 to +2C. This also proves the major advantage of lowering the temperature in order to
maintain quality during the postdrying period. Only after the 11th month of storage at room
temperature was a drop in the increase recorded. With extremely long periods of storage, this loss
over the total storage period becomes even clearer: 24 months: 62.5% loss at room temperature,
24% loss in cold storage [4]; 31 months: 45.1% at room temperature, 25% loss in cold storage
[11]. The greater deviation range recorded for losses at room temperature (Figure 9.1) is due to
the values for the level and fluctuations in room temperature and relative humidity, which are not
precisely known and vary considerably for this storage process.

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FIGURE 9.1 Losses of essential oil in chamomile flower drugs during storage and the prediction interval for
losses at room temperature and cold storage at 0 to +2C [4, 5, 11, 12].

The flower development stage of the chamomile at the time of harvesting also leads to major
differences in losses over a storage period of 31 months, with smaller flowers showing greater
storage stability at room temperature (16C, = 60%) [11, 12]:

Large flowers (opening of >75% of the tube blossoms): 46.1%

Medium flowers (half part of tube blossoms opened): 30.9%
Small flowers (tube blossoms opened to first ring): only 29.8% loss

In cold storage (+2C = 85%), the losses were 27.9, 16.2, and 15.6%, respectively, during
the same period.
It was also proved repeatedly that a disintegration of flowers as far as the formation of coarse
powder obviously increases the amount of evaporation, so that the loss of essential oil was 14 to
18% [3] or 5 to 19% [7] higher than in undamaged flowers. In the chamomile powder, a greater
loss in the first 4 months of storage at room temperature is typical (9.0%/month of storage), which
subsequently drops in a smaller extent (3.2%/month of storage) [7].
A strong mechanical treatment of the chamomile flowers (processing as finely chopped plants
in filter bags) does not necessarily lead to greater losses of essential oils (25.6% loss in 18 months,
with a level of 0.32% essential oil remaining in the stored drug [7]).
The active ingredient groups matricin and chamazulene in the chamomile flowers are subject
to similar losses to the essential oils, but this process shows a negatively exponentially increasing
loss as a function of storage duration (Figure 9.2), as seen in the values for representative losses
determined in experiments [7, 9].
Thus, for the first 2 months of storage, a loss of 8.0%/month of storage was determined; after
10 months, the loss was only 3.0%/month of storage, so that after 12 months at room temperature,
the losses were 48% [7] or 47.4 to 52.8% after 14 months [9]. As the mean of 33 trade samples,
Lachhammer [10] determined after 6 months a loss of chamazulene of 37.2%. In chamomile powder,
the losses of matricin are always 15% higher than in whole blossoms [7]. Blazek and Stary [2]
determined chamazulene losses of 2.5%/month of storage.

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FIGURE 9.2 Losses of matricin and chamazulene in chamomile flower drugs during storage and the prediction
interval for losses at room temperature and cold storage at 0 to +2C [4, 7, 9, 10].

The reduction in the level of chamazulene in the essential oil during long-term storage of up
to 25 months is, however, also strongly dependent on the prevailing storage temperature [5]: while,
in conditions of 20 to 23C the loss rate was 2.49%/month of storage, it was lowered at temperatures
of 0 to +2C to 1.06%/month of storage.
Chamomile flowers as finely chopped plants in filter bags also only showed a matricin loss
of 3.33%/month of storage over 18 months.
Similarly, the level of farnesene decreases during storage. As the mean of 33 trade samples,
Lachhammer [10] determined at room temperature a loss rate of 6.2%/month of storage. There are
as yet no analytical values in the literature for changes in the important ingredient bisabolol, but
there must clearly be losses, since both of its oxides A and B increase clearly in the essential oil
of the chamomile flowers during storage as a function of temperature [5]. At room temperature,
bisabolol oxide A showed an increase of 9.0%/month of storage; in cold storage it showed only
an increase of 10.0%/month of storage. With bisabolol oxide B the extent of the increases is
smaller: at room temperature 2.1%/month of storage, in cold storage 1.8%/month of storage [5].
The cis-EN-IN-dicycloethers are also not stable in storage. In cold storage conditions (0 to
+2C) in particular, the reduction rate of 1.85%/month of storage is much higher than the loss at
room temperature of 0.58%/month of storage [5].
The flavonoids, which also have a therapeutic effect, are found to be far more stable in storage
at higher temperatures than at lower temperatures [11, 12]. The apigenins, determined at the tongue
blossoms of the chamomile drug, only increased at room temperature of 20C by a mean of
5.5%/month of storage (i.e., by an absolute 28.4 mg/100 g drug a year), but at +2C they increased
by 101.6%/month of storage (i.e., by an absolute 526.8 mg/100 g drug in the course of a year).
The apigenin-7-glycoside of the same flowers, in contrast, showed clear decreases: at 20C, a
decrease of 0.60%/month of storage (an absolute 292.0 mg/100 g drug a year) and at +2C a
decrease of 0.71%/month of storage (an absolute 346.7 mg/100 g drug a year). These shifts can
be explained by a splitting of the sugar components of aglycon that occurred during storage, so
that the value for apigenin increased.

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The often very marked influence of temperature on the loss rates of some ingredients underlines
the need to cool freshly dried chamomile drugs immediately and to move them to colder storage
conditions.

9.5 PACKAGING
Dried chamomile flowers and herbs are very sensitive storage goods and so proper packaging during
storage is absolutely essential, more so than for any other drug. The packaging must meet the
following requirements:

It must provide the necessary protection against the dried products getting moist again.
It must provide sufficient protection against infestation with harmful insects of any type.
It must minimize evaporation of the value-giving essential oils.
It must prevent any mechanical stress on the dried products, which could encourage
destruction of the flowers and herbs (formation of coarse powder).
It must keep out light, since this encourages the oxidation of lipophilic constituents.
It must keep out pollutants and prevent the content of the containers from being mixed up.
It must be suitable for advertising on the outside surfaces.

The freshly produced raw material should be packed after all the parts of the plant have reached
a uniformly stable moisture level and if necessary after a further subsequent treatment with cold
outdoor air for cooling after about 2 weeks. The most suitable packing materials for whole flowers
are wooden cases, firm cardboard, metal canisters, and other containers made from plywood, board,
or metal. Mostly used are cardboards. Before filling, the dry matter must be rattle-dry right to the
bottom of the flower. These containers can also be easily stacked in the storage-room. Jute sacks
to enclose bulk deliveries, as are often used for industrial goods, are less suitable, since they do
not meet all requirements and are also difficult to stack. Paper sacks made from three layers of
paper are sometimes better, but can only be stacked ultimately using shelves or box pallets. Plastics
should not be used for packaging or directly wrapping chamomile drugs, since various plastics
may, under some circumstances, bind certain components of the essential oils from the dried drugs
or may encourage sweating of the drugs in the inside of the package water vapor (condensation)
in the event of fluctuations in temperature.
Basically, only drugs cooled to room temperature should be filled (to prevent condensation).
All packaging materials must in principle be suitable for use with foods. Before they are used, they
must be stored in clean, dry rooms.
Reused material must be cleaned and completely dried before being used again in order to
prevent contamination.
Chamomile herbs may, under some circumstances, be kept in loose piles, if the storage rooms
are very dry and largely wooden in structure.
Chamomile flowers should not be pressed or compacted. Herbs can be compacted, packed, and
delivered in bales.
During a 12-month storage of chamomile flower drugs, Schilcher [15] detected a marked
influence of the various packagings on the reduction of the quantities of essential oils, while the
storage location and temperature were of lesser importance (Table 9.1): In sealed metal cans, only
10% of the essential oils were lost; in impregnated heat-sealed paper packs and plastic bottles
(polyethylene), 12 to 18% of the essential oils were lost; while in untreated paper packs and plastic
bags (type of plastic unknown), the losses over the same period reached 26 to 44%.
In tests by Karmazin and Zadinova [9], folding cardboard cartons impregnated with crystalline
microwax also showed a slight superiority in terms of maintenance of quality, measured by the
losses of essential oil (vol.%) and chamazulene (mg%) (mean value from three locations: essential
oil 27.7%/chamazulene 47.4%). The wooden crates (28.2/48.6%) and the three-layer paper sack
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TABLE 9.1
Influence of the Mode of Packaging on the Decline of the Essential Oils during Storage
(According to Reference 14)
Mode of packaging

Temperature

Content vol%
essential oils

Relative
decline in %

Taken into storage:

Flores Chamomilleae
Removed after 12 months:
Metal cans, sealed with adhesive strips
Bags made from Diophan coated paper then heat-sealed
Plastic bottle low pressure polythene with screw top
Sealed tea packs with outside carton and inner bags in
flavor-seal, greaseproof parchment paper:
Storage place 1:
Storage place 2: dry cellar
Lacquered bags made from uncoated paper (soda kraft
paper), heat-sealed
Plastic pouch sealed with metal clip
Plastic pouch sealed with metal clip and additional
outside carton
Standard paper bags, loose product, folded over and
adhered with Selotape:
Storage place A
Storage place B

0.50

room
room
room

0.45
0.43
0.41

10
14
18

room
1015C
room

0.41
0.44
0.37

18
12
26

room
room

0.29
0.31

42
38

room
room

0.29
0.28

42
44

(28.6/52.8%) were almost the same, while the polyethylene bags (31.2/51.1%), RD glass
(33.8/54.2%), and metal cases (34.7/57.6%) were considerably worse.

9.6 STORAGE MANAGEMENT

Drugs that have just been taken into storage should be housed initially in a separate room for
quarantine until the presence of harmful agents and the quality classification have been clarified.
It is important that every individual pack unit is completely and precisely marked according
to its origin with the following information:

Drug type and form

Origin
Preparation state
Classification
Harvest year
Weight unit
Packaging date
Active ingredient content

In the store, the packed, marked product must be kept in batches, clearly laid out and with no
risk of confusion. It must be accessible at all times and it must be able to be removed according
to the development of the quality and active ingredients.
Sensory and chemical constituent analysis should be carried out every 4 to 6 months.

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Even packaged drugs should not be placed directly on the floor; they should preferably be kept
on pallets or on shelves. A distance must be kept from the walls.
Basically, the Guidelines for Good Agricultural Practice (GAP) for Medicinal and Aromatic
Plants (Chapter 5) [1] should also be followed for packing, storage, and transport.
Any disinfestation required may only be carried out by licensed personnel with approved
gasification products in accordance with European and national regulations.
The possible storage period for drugs in powder is always considerably shorter.
In determining the sequence for removal from storage and utilization, the development of the
active ingredients and the microbiological state must be taken into account.

REFERENCES
1. Anonymous (1998) Guidelines for Good Agricultural Practice (GAP) of Medicinal and Aromatic
Plants. Z. Arzn. Gew. pfl., 3, 166174.
2. Blazek, Z., Stary, F. (1961) Einflu der Aufbewahrung auf die Qualitt der Kamillenblten. Pharmazeutische Zentralhalle, 100, 366371.
3. Blazek, D., Stary, F. (1962) Einige Bemerkungen zum Siebdurchlauf der Kamillenblten. Dtsch.
Apoth. Ztg., 102, 606608.
4. Bttcher, H., Gnther, I. (2000) Unpublished.
5. Dragland, S., Aslaksen, T.H. (1996) Storing of dried chamomile flowers at different temperatures and
with different packaging. Norsk Landbruksforsking, 10, 167174.
6. Hannig, H.-J. (1993) Qualittskontrolle von Drogen vom Anbau bis zum Fertigprodukt. Herba Germanica, 1, 7177.
7. Hannig, H.-J. (1994) Lagerhaltung von Arznei-und Gewrzpflanzen. Herba Germanica, 2, 137147.
8. Kabelitz, L. (1997) Korrekturmanahmen bei Qualittsmngeln. Z. Arzn. Gew. pfl., 2, 120126.
9. Karmazin, M., Zadinova, K. (1965) Vernderungen im Gehalt des therischen ls und Chamazulens
in der Droge Flor. chamomillae unter verschiedenen Lagerungsbedingungen. Wiss. Zeitschrift der
Karl-Marx-Universitt Leipzig, Mathemat.-naturwiss. Reihe, 14, 459461.
10. Lachhammer, B. (1983) Qualitt von Kamillendrogen aus dem Handel und Qualittsvernderungen
nach Lagerung. Dipl. Thesis, Techn. University Mnchen, Dpt. Vegetables, Freising Weihenstephan.
11. Letchamo, W. (1991) Vergleichende Untersuchung ber die nacherntetechnisch bedingten Einflsse
auf die Wirkstoffgehalte in der Droge bei Kamille-Genotypen. Drogenreport. Sonderausgabe zur
Fachtagung in Erfurt, 129134.
12. Letchamo, W. (1993) Effect of storage temperatures and duration on the essential oil and flavonoids
of chamomile. J. Herbs, Spices and Med. Plants, 1 (3), 1326.
13. Pank, F., Franz, Ch., Herbst, E. (1991) Richtlinien fr den Integrierten Anbau von Arznei-.und
Gewrzpflanzen. Drogenreport Sonderausgabe 1991, 4564.
14. Schilcher, H. (1968) Lagerung von Krutertees und Einzeldrogen. Neuform-Echo, 18 (6).
15. Schilcher, H. (1987) Die Kamille - Handbuch fr Arzte, Apotheker und andere Naturwissenschaftler.
Wissenschaftl. Verlagsgesellschaft, Stuttgart, Germany.

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Analysis of
10 Chemical
the Active Principles
of Chamomile
Heinz Schilcher, Peter Imming, and Susanne Goeters
CONTENTS
10.1 Introduction
10.1.1 Test Regulations in Pharmacopoeias
10.2 Analysis of the Essential Oil
10.2.1 Methods of Extraction
10.2.2 Volumetric and Gravimetric Determination of the Total Content
10.2.3 Thin-Layer Chromatography
10.2.4 Densitometry
10.2.5 Reaction Chromatography
10.2.6 Gas Chromatography
10.2.7 Headspace Gas Chromatography
10.2.8 High-Pressure Liquid Chromatography
10.2.9 Enantioselective HPLC
10.2.10 Droplet Countercurrent Chromatography
10.2.11 HPLC/MS and GC/MS
10.2.12 Review of the Analytical Possibilities
10.3 Chemical Analysis of the Flavonoids
10.3.1 Determination of the Flavonoids
10.3.2 Paper Chromatography (PC) and Thin-Layer Chromatography
10.3.2.1 Paper Chromatography
10.3.2.2 Thin-Layer Chromatography
10.3.2.3 Two-Dimensional Thin-Layer Reaction Chromatography
10.3.3 High-Pressure Liquid Chromatography
10.4 Chemical Analysis of the Coumarins
10.5 Chemical Analysis of the Chamomile Mucilage
10.5.1 Quantitative Spectral Densitometric Determination of the Monosaccharides
and Urone Acids
10.6 Analysis of Chamomile: Summary
References

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10.1 INTRODUCTION
Analytical tests of the active principles of chamomile have the following main objectives:
1. Qualitative proof of pharmacologically relevant active principles in Matricariae flos
2. Impact of ecological and genetic factors on the qualitative and quantitative composition
of the active principles
3. Elucidation of the biosynthesis of individual active principles of chamomile
The choice of the analytical method depends on the nature of the analysis. Under all circumstances, the method chosen should provide the necessary accuracy and reproducibility. For the
development of a routine analysis, economic factors such as time and costs must be considered.

10.1.1 TEST REGULATIONS

IN

PHARMACOPOEIAS

Pharmacopoeias (Table 10.1) provide chemical, physical, and chromatographical test procedures
to detect the identity and purity of the essential oil as well as the content of matricin.

TABLE 10.1
Test Regulations for Chamomile Flowers and Chamomile Preparations in Pharmacopoeias
Since 1882
Year
1882

Pharmacopoeia

1900
1901
1905
1905
1905
1906
1906
1906

DAB (Deutsches Arzneibuch) (German Pharmacopoeia), 2nd

edition
Pharmacopoea Helvetica, 3rd edition
DAB (German Pharmacopoeia), 3rd edition
Supplement to DAB 3, i.e., those drugs not being included in DAB
3, 2nd edition
DAB (German Pharmacopoeia), 4th edition
Svenska Farmakopen 8
Pharmacopoeia of the USA, 1900 edition
Pharmacopoea Nederlandica 4
Farmacopea Espaola 7
3rd Supplement to DAB 4
Pharmacopoea Belgicae 3
Pharmacopoea Austria 8

1907
1907
1908
1910
1916
1926
1940
1941
1941
1948
1958

Pharmacopoeia of Japan, English edition

Pharmacopoea Helvetica 4
Pharmacope Franaise
DAB (German Pharmacopoeia), 5th edition
4th Supplement to DAB 5
DAB (German Pharmacopoeia), 6th edition
Pharmacopoea Nederlandica 5 (2nd printing)
Supplement for DAB 6
Pharmacopoea Helvetica 6
Pharmacopoea Danica
Pharmacopoea Nederlandica 6

1960

sterreichisches Arzneibuch (Pharmacopoea Austria) 9

1893
1894
1897

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Regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
Density, solubility
100 mercis partis ne minus quam partes 15
extracti spirituosi praebeant
No test regulations
Density, consistency on cooling
No test regulations
No test regulations
No test regulations
Determination of essential oil content
No test regulations
No additional regulation to DAB 6
Density, solubility, specific rotation
No test regulations
Determination of essential oil content results
in blauwe druppeltjes
Determination of essential oil content,
identification by reaction with
dimethylaminobenzaldehyde

TF4015_C010.fm Page 223 Friday, April 8, 2005 8:25 AM

TABLE 10.1
Test Regulations for Chamomile Flowers and Chamomile Preparations in Pharmacopoeias
Since 1882 (continued)
Year

Pharmacopoeia

1971

Pharmacopoea Helvetica 6

1968

DAB (Pharmacopoeia of the Federal Republic of Germany), 7th

edition
Pharmacopoeia of the German Democratic Republic, 7th edition

1964/
1975

1975

European Pharmacopoeia, vol. III

1976

Pharmacope Franaise 9

1980
1982

British Pharmacopoeia
Standard Registration 36 AMG 76 (Germany)

1987

DAB (Pharmacopoeia of the Federal Republic of Germany), 9th

edition

1987

Pharmacopoea Helvetica VII, supplement 1993, Flos and Extr.

Liquid

1990

Pharmacopoea Austria, Flos

1991

DAB (German Pharmacopoeia), 10th edition, supplement 1993,

Flos

1997

DAB (German Pharmacopoeia) 1997, Extr. Fluid

1997

DAB 1997 (German Pharmacopoeia) 1997, Matricariae

aetheroleum

Copyright 2005 CRC Press, LLC

Regulations
Determination of essential oil content,
swelling factor, fluid extract, color reaction,
pH-value, essential oil content
Determination of essential oil content and
comparison of the blue color
Identification by reaction with
dimethylaminobenzaldehyde, thin-layer
chromatography, absorbance of xylene
solution of steam distillate at 600 nm
(standard: guaiazulene solution)
Determination of essential oil content, test by
reaction with dimethylaminobenzaldehyde,
thin-layer chromatography
Determination of essential oil content, which
has to be of a dark blue color
Determination of essential oil content
Determination of essential oil content, test by
reaction with dimethylaminobenzaldehyde,
thin-layer chromatography
a) Determination of essential oil content
b) Identification by reaction with
dimethylaminobenzaldehyde
c) Test on purity by thin-layer
chromatography
a) Determination of essential oil content
b) Identification by reaction with
dimethylaminobenzaldehyde
c) Identification by thin-layer
chromatography, determination of essential
oil content, gravimetric
a) Determination of essential oil content
b) Identification by reaction with
dimethylaminobenzaldehyde
c) Identification by thin-layer
chromatography
a) Determination of essential oil content
b) Identification by reaction with
dimethylaminobenzaldehyde
c) Identification by thin-layer
chromatography
a) Identification by thin-layer
chromatography
b) Determination of essential oil content,
gravimetric
a) Identification by thin-layer
chromatography
b) Purity test by chromatographic profile

TF4015_C010.fm Page 224 Friday, April 8, 2005 8:25 AM

TABLE 10.1
Test Regulations for Chamomile Flowers and Chamomile Preparations in Pharmacopoeias
Since 1882 (continued)
Year

,Pharmacopoeia

1997/
2002

European Pharmacopoeia, Flos

1997/
2002

European Pharmacopoeia, Extr. Fluid

2002

European Pharmacopoeia, Flos

2002

European Pharmacopoeia, Extr. Fluid

2002

European Pharmacopoeia Draft Monograph, Matricariae

aetheroleum

Regulations
a) Determination of essential oil content
b) Identification by reaction with
dimethylaminobenzaldehyde
c) Identification by thin-layer
chromatography
a) Identification by thin-layer
chromatography
b) Determination of essential oil content,
gravimetric
a) Determination of essential oil content
b) Determination of total apigenin-7glucoside by liquid chromatography
c) Identification by thin-layer
chromatography
a) Identification by thin-layer
chromatography
b) Determination of essential oil content,
gravimetric
a) Identification by thin-layer
chromatography
b) Purity test by gas chromatographic profile

Of course there are numerous other publications on the analysis of the active principles of
chamomile [110, 1724, 2731, 33, 36, 3949, 5266, 6881, 8389, 92119, 123, 127, 130,
132139, 141143, 148157, 159, 160, 162, 163]. A summary and evaluation of the methods has
been published and continually updated by Schilcher [116121].
The most recent findings as well as established older test procedures are subject of the present
summary.

10.2 ANALYSIS OF THE ESSENTIAL OIL

10.2.1 METHODS

OF

EXTRACTION

Two different methods a steam distillation as described by Schilcher (Table 10.3) and an
extraction using methylene chloride, n-hexane, and petroleum ether (at 4060C) have been
compared. The latter resulted in a higher yield of the essential oil and significant differences in the
content of spiroethers and bisabolol oxide A as well as bisabolol oxide B, bisabolol, bisabolone
oxide, and spathulenol.
Concomitant with the higher content of the essential oil, the amount of hydrophobic compounds
such as fatty acids and carotinoids was increased. However, this will not influence the analysis by
gas chromatography (GC) or (thin-layer chromatography (TLC). Instead of quantifying chamazulene which is missing in the methylene chloride extract the amount of matricin can be
determined using TLC or GC. When extracting with methylene chloride, the amount of spiroethers
was found to be increased by 68% on average compared to steam distillation, bisabolol oxide A
by 42%, bisabolol oxide B by 20%, bisabolol by 12%, and spathulenol by 12%. Similar results

Copyright 2005 CRC Press, LLC

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TABLE 10.2
Some Pharmacopoeias Containing Monographs on Roman Chamomile Flowers, Roman
Chamomile Oil or Roman Chamomile Preparations (e.g., Extracts)
Year
1906
1908
1934
1940
1941
1954
1980
1953
1954
1959
1960
1954
1972
1976
1976
1979
1980
1981
1983
1987
1993
1987
1988
1992

Pharmacopoeia
Pharmacope Belge 3
Pharmacope Franaise
HAB Dr. Willmar Schwabe
Nederlandsche Pharmacopee, 5th edition (Dutch Ph)
Pharmacopoeia Helvetica, 5th edition
Farmacopea oficial Espaola IX (Hisp IX)
British Pharmacopoeia
Pharmacope Belge V
British Pharmaceutical Codex
Farmacopeia dos Estados Unidos do Brasil
sterreichisches Arzneibuch (AB 9), Austrian
Pharmacopoeia
Farmakopea Polska III (Polish Ph.)
Farmacopea ufficiale della Repubblica Italiana VIII
British Herbal Pharmacopoeia
Pharmacope Franaise IX
Pharmacopoeia Helvetica VI
British Pharmacopoeia
sterreichisches Arzneibuch 1981 (Austrian Pharmacopoeia
1981)
British Herbal Pharmacopoeia
Pharmacope Franaise X
Pharmacopea Helvetica VII
British Pharmacopoeia
DAB 10, German Pharmacopoeia 10th edition

1993

Pharmacopoeia Helvetica VII

1993

British Pharmacopoeia

1997

European Pharmacopoeia, 3rd edition

1999

British Pharmacopoeia

2003

European Pharmacopoeia 4.3 (German version)

Methods
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
No test regulations
Flowers, volatile oil, chamomile water
ID: macroscop., microscop.
No test regulations
ID: macroscop.
Assay: essential oil: steam distillation

ID: a. macroscop., b. microscop., c. TLC

ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: TLC
ID: a. macroscop., b. microscop., c. TLC
ID: macroscop., microscop., TLC
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: TLC
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: TLC
Assay: essential oil: steam distillation
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation
ID: a. macroscop., b. microscop., c. TLC
Assay: essential oil: steam distillation

have been published [31, 42, 91]. In order to determine the exact amount of certain components,
an extraction time of 1 hour using methylene chloride is recommended.
Formerly published data still remain useful for comparisons. Most of them were obtained by
steam distillation. For qualitative investigations, the TAS method, a thermic method developed by
E. Stahl [138], can be applied. It is very sensitive, thus a small sample (e.g., three flower heads)
is sufficient [119]. A further advantage of the TAS method is the reduction of time needed for the
analysis, allowing the processing of a series of samples within short time. Labelling experiments
are also possible using the TAS method [119]. However, the analysis is limited to the main
components of the analysis.

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TABLE 10.3
Quantitative Determination of the Essential Oil in Chamomile Flowers by Means of Steam
Distillation [112,121]

Regulation

Test portion
and degree of
crushing

Pharmacopoea
20.0 g
Austria, 9th
uncrushed
edition, 1960
Pharmacopoeia of 10.0 g
the German
uncrushed
Democratic
Republic, 7th
edition (DAB 7,
DDR), 1964 and
1975
British PharmaNo instruction
copoeia, 1968

Pharmacopoeia of
the Federal
Republic of
Germany, 7th
edition, 1968
DAB 7, BRD,
1968
Pharmacopoea
Helvetica, 6th
edition, 1971
European
Pharmacopoeia draft dated June
10, 1971
Pharmacopoeia of
CSSR, Ph.Bs. III,
vol. I
Proposal H.
Schilcher [112]

25.0 g of
coarse
powder

European
Pharmacopoeia,
vol. III, 1975

50.0 g
uncrushed

Distillation/
menstruum
400 ml of water

Solvent in
graduated
tube
Decalin

Speed of
distillation
Allow to boil

Time of
distillation

Time of
reading after
distillation

34 h

5 min

135 ml of ethylene
glycol, 15 ml of
water, 0.2 g of
silicone oil
emulsion

Not specified;
temperature at
condenser not
higher than
25C

3h

5 min

300 ml of water

Xylene

35 h

5 min

300 ml of water

Xylene

Allow to boil
so that the
lower part of
the condenser
stays cold
Allow to boil

2h

15 min

5.0 g; degree of 500 ml of water, then extract with pentane; gravimetric determination similar to DAB 6
crushing not
specified
50.0 g
500 ml of 0.5 N
Xylene
34 ml/min.
4h
10 min
uncrushed
HCI

10.0 g through
sieve 3

300 ml of water

10.0 g
300 ml of water
uncrushed
resp. passed
through sieve
Nr. 3
homogeneous
mixture

Copyright 2005 CRC Press, LLC

500 ml of 1%
NaCI solution in
a flask of 1000 ml

Decalin

Allow to boil

4 h + 30 min

Cover of
Condenser to be
Pilz stage
switched off
II, 220 volt,
after 3 h and
300 watt =
distillation to be
approx. 45
continued for
ml/min =
approx. 5 min
approx. 4045 until oil is
drops/min
removed from
condenser wall
Xylene (1.0
34 ml/min
4h
ml)

5 min

15 min

10 min

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TABLE 10.3
Quantitative Determination of the Essential Oil in Chamomile Flowers by Means of Steam
Distillation (continued)

Regulation
Pharmacopoeia of
the Federal
Republic of
Germany, 9th
edition, 1987
DAB 9, FRG,
1987
Pharmacopoea
Helvetica, 7th
edition, 1987
Pharmacopoea
Austria, 1990
German Pharmac.
= DAB 10
Ph. Eur., 1996, 3rd
edition
Ph. Eur.,
1997/2002
Ph. Eur., 2002
Draft monograph

Test portion
and degree of
crushing

Distillation/
menstruum

Solvent in
graduated
tube

Speed of
distillation

Time of
distillation

Time of
reading after
distillation

30.0 g
uncrushed

300 ml of water in Xylene

a flask of 1000 ml (0.5 ml)

34 ml/min

4h

10 min

30.0 g
uncrushed

300 ml of water in Xylene

a 1-L flask
(0.5 ml)

3-4 ml/min

4h

10 min

30.0 g
uncrushed
30.0 g
uncrushed
30.0 g
uncrushed
30.0 g
uncrushed
30.0 g
uncrushed

300 ml of water in
a 1-L flask
300 ml of water in
a 1-L flask
300 ml of water in
a 1-L flask
300 ml of water in
a 1-L flask
300 ml of water in
a 1-L flask

3-4 ml/min

4h

10 min

3-4 ml/min

4h

10 min

3-4 ml/min

4h

10 min

3-4 ml/min

4h

>10 min

3-4 ml/min

4h

>10 min;
cooling
interrupted
toward the end
of the
distillation

Xylene
(0.5 ml)
Xylene
(0.5 ml)
Xylene
(0.5 ml)
Xylene
(0.5 ml)
Xylene
(0.5 ml)

Note: Since 1987, the national European monographs on chamomile flowers were harmonized. In 1997, the monograph
Matricariae flos of the European Pharmacopoeia 3rd Edition replaced the national monographs and is officially accepted
in all member states of the European Pharmacopoeia Convention (31 states in 2003), including the 15 states of the European
Union.

10.2.2 VOLUMETRIC AND GRAVIMETRIC DETERMINATION OF THE TOTAL CONTENT

The gravimetric determination was shown to give better results than the volumetric determination
[120, 121].
The volumetric quantification was carried out according to the guidelines of the DAB (German
Pharmacopoeia) and gave the following results:
x = 0.57%
s = 7.572 x 10-2
vc% = 13.28 (vc% = relative standard deviation)

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Using the same plant material, the gravimetric determination gave the following results:
x = 0.814%
s = 1.338 x 10-2
vc = 1.64% (vc% = relative standard deviation)
With the t-value (Student test) calculated to be 10.05, a comparison of both methods is not
possible. This explains the wide range of values found in the literature. The volumetric determination
is the official method of the Ph. Eur., but the gravimetric method can be applied to small samples.

10.2.3 THIN-LAYER CHROMATOGRAPHY

In a comparison of different thin-layer chromatography conditions, the use of silica gel plates
(GF254) as stationary phase and a mobile phase of benzene/ethyl acetate (95:5, V/V) was found to
give the best results [109]. Benzene can be substituted by the less toxic toluene without loss in
separation quality. The same solvent system is used for the analysis of chamomile oil and chamomile
liquid extract according to the German Pharmacopoeia 1997. Alternatively, methylene chloride/ethyl
acetate (98:2, V/V) [101] and toluene/ethyl acetate (93:7) [158] can be used with good results. The
European Pharmacopoeia 1975, Volume III, recommended chloroform/benzene (75:25, V/V), which
does not meet present standards of Maximum Working Concentration (MWC) and Technical Standard
Concentration (TSC), but the choice of solvents of an up-to-date method should agree with these
requirements (Table 10.4). A very simple mobile phase, pure chloroform, is specified by the European
Pharmacopoeia 1997 for the identification of chamomile flowers by TLC [161].
The solvent system should be chosen according to the polarity of the compounds. For substances
usually remaining close to the starting line (e.g., matricin), a mobile phase of toluene/ethyl acetate
(80:20, V/V) gives useful retention times (e.g., matricin: RF 0.13). For the separation of the bisabolol
oxides, silanized TLC plates can be used as the stationary phase in combination with 0.1% or better
0.2% glacial acetic acid in 50% toluene [36] as the mobile phase. There are several ways to detect
the separated compounds. The best choice is a combination of an SbCl3 solution and the EP reagent
[109]; alternatively, anise aldehyde/sulfuric acid [149] or vanillin/sulfuric acid [158] as spray
reagents work well.

TABLE 10.4
x RF Values of Chamomile Constituents with Various Mobil Phases

Constituent

Benzene
(or toluene) 95
Ethyl acetate 5
(v/v)

trans--Farnesene
Chamazulene
cis-En-yne-dicycloether
trans-En-yne-dicycloether
Bisabolone oxide
Bisabolol
Spathulenol
Herniarin
Bisabolol oxide A
Bisabolol oxide B
Umbelliferon
Matricin

0.72
0.68
0.46
0.42
0.38
0.30
0.21
0.19
0.18
0.13
0.02
0.00

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Dichloromethane 98
Ethyl acetate 2
(v/v)

Chloroform 75
Benzene
or toluene 25
(v/v)

x RF after development over 12 cm

0.81
0.78
0.71
0.68
0.64
0.51
0.42
0.32
0.30
0.27
0.04
0.06

0.72
0.69
0.46
0.42
0.39
0.33
0.24
0.21
0.19
0.16
0.02
0.03

TF4015_C010.fm Page 229 Friday, April 8, 2005 8:25 AM

10.2.4 DENSITOMETRY
Chamazulene and bisabolol oxides were quantified by extracting their spots from the TLC plate
followed by photometric determination [109]. Direct measurement of the main components on TLC
has been developed using a Shimadzu CS-900 scanner system [120]. The spots were scanned in
zig-zag mode at two different wavelengths. The peak height of the transformed signal was chosen
for quantification (Figure 10.1).
After they had recognized chamazulene carboxylic acid (CCA) as a natural profen, the group
of Imming extensively studied chemical and pharmacological aspects of this compound. Goeters
[32] found the following chromatographic parameters to be suitable for both preparative and
analytical purposes: silica gel, hexane/ethyl acetate/methanol 65:30:5, RF (CCA) 0.5. She quantified
chamazulene carboxylic acid densitometrically when she looked for conditions that yielded highest
CCA content in aqueous infusions; 8-min extraction at 100C gave the best results (0.41.0 mg/ml
using 10 g of flowers of the cultivar Mabamille). Chamazulene was not detected in the infusion;
matricin was present, but was not quantified.
The content of en-yne-dicycloethers can be determined accurately by high-pressure liquid
chromatography (HPLC) or by densitometry. The values of the densitometric determination were
20 to 35% higher than those obtained by gas chromatography. Published methods using photometry
to determine bisabolol and en-yne-dicycloethers [44] and densitometry to quantify bisabolol [155,
156] have not been reproducible [44, 155, 156]. A colorimetric method to determine chamazulene
[152] showed little improvement over a previously published method [109].
GC analysis showed advantages regarding the separation of bisabolol oxides A, B, C, chamazulene, and farnesene and is therefore recommended instead of TLC.
5.0
3.5
Bisabolon

Bisabolol

FIGURE 10.1 TLC scan of bisabolol, bisabolone, and bisabolol oxides. Scanner Model: Shimadzu CS-900
Chromato-Scanner. (a) Immerse TLC plate in saturated SbCl3 solution for 5 sec; (b) dry at 110C for 5 min;
(c) immerse in EP reagent (acetic acid/phosphoric acid) for 5 sec; (d) dry in stream of cold air until odor of
acetic acid is no longer detectable; (e) heat to 110C for 10 min; (f) scan immediately. Measuring wavelength
for bisabolol and bisabolone (violet spots): 530 nm; measuring wavelength for bisabolol oxides (red spots):
520 nm; reference wavelength for all: 700 nm.
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10.2.5 REACTION CHROMATOGRAPHY

The degradation of matricin to chamazulene can be detected while running TLC. Experiments have
shown that matricin in extracts treated with steam for 510 min is gradually converted to chamazulene and three intermediates that gave three blue spots after TLC separation (see Figure 4.22 in
Reference 121).

10.2.6 GAS CHROMATOGRAPHY

The first gas chromatographic separation of the components in the essential oil was published in
1968 [49]. Since then, several GC methods have been developed [16, 29, 31, 43, 44, 47, 49, 72,
74, 112, 113, 155, 156]. Both polar and nonpolar columns were used; e.g., 510% Carbowax 20
M, 10% UCCW 982; 3% OV 17; 5% SE 30; 3% OV-1; 3% QF-1; 1,5% OV 101, and dexil 300.
Based on a comparison of the methods mentioned above [90, 120, 122], optimum results were
achieved using an OV 101 column of 50 min length and a capillary temperature of 120170C
[118]. An OV-1 column gave a similarly good separation for bisabolol oxides A, B, C, bisabolol,
and bisabolone oxide. The separation of the isomeric cis- and trans-en-yne-dicycloethers has been
achieved by the following conditions depicted in Table 10.5, using bisabolol as the an internal
standard. Its retention time was set to 100 and used as reference.
Besides calculations using an HP integrator (18850 A-GC-terminal), the absolute content
of active principles in 100 g of plant material can be determined by the internal standard
dilution method [16]. Several experiments were carried out using hexadecanol as the internal
standard [31] Schilcher proved that guaiazulene has advantages over hexadecanol in several
respects [121, 122].

TABLE 10.5
GC Retention Times of Chamomile Constituents
Compound
Hexane
Farnesene
Spathulenol
Bisabolol oxide B
Bisabolon
Bisabolol
Matricin/chamazulene
Bisabolol oxide A
Guaiazulene
cis-en-yne-dicycloether
trans-en-yne-dicycloether

Retention time/sec
225
1047
1340
1580
1647
1676
1827
1936
2076
2546
2575

Relative retention time

14
66
85
100
104
106
116
123
131
161
163

HP 5830 Chromatograph. Columns: OVI or OV 101, 50 m. Temperature program:

120170C, 5C/min. Injection temp.: 225C. FID temp.: 250C. Gas flow: Helium
at 1.2 ml/min (120C) or 1.9 ml/min (30C). Hydrogen at 1.1 bar and oxygen at
1.7 bar. Attenuation: 4 (up to 7). Paper feed: 1.5 cm/min. Integration with HP
Integrator 18850 A.

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10.2.7 HEADSPACE GAS CHROMATOGRAPHY

Headspace gas chromatography (HSGC) is an elegant method for the analysis of the components
of the essential oil with high precision, provided a multiple headspace extraction (MHE) is performed. MHE prevents the matrix from interfering with the analysis. Hiltunen et al. have shown
that HSGC is suitable for the analysis of the essential oil and individual volatile active principles
of chamomile [39, 40, 41]. Using a DANI-HSS 3850 Automatic Head Space Sampler, very precise
results were obtained. The analytes were separated by an OV-1-column with variation of the
temperature from 140 to 200C.
Stuppner and Bauer applied this method to the quantitative determination of the chamomile
preparation components in water and ethanol, using an SF 52 column and a temperature range
from 130240C [144, 145]. The results were influenced by the conditioning time and temperature,
but mainly depended on the content of ethanol in the sample. Dilution to 5% ethanol in water
guaranteed acceptable results. Compared to conventional GC, HSGC gave almost identical values
for ()--bisabolol and its derivatives, whereas values of en-yne-dicycloethers were quite low [145].

10.2.8 HIGH-PRESSURE LIQUID CHROMATOGRAPHY

10

Matricin

Chamazulen

Guajazulen

The development of an HPLC separation protocol using a Bondapak C18 column under isocratic
and gradient conditions (methanol-water mixtures) did not have advantages compared to published
TLC and GC methods [122]. Other investigations also found HPLC a less reasonable Strategy in
Chromatography [141] for the quantification of components of the essential oil. Nevertheless,
HPLC is especially suitable for the separation of isomeric compounds. Azulenes separate very well
on a Li-Chrosorb RP 8 column (reversed phase), eluting with methanol-water. This method allows
the determination of the purity of isolated azulenes as well as the separation of isomeric azulenes
(Figure 10.2) [121].

0 Min.

FIGURE 10.2 HPLC separation of azulenes. Column: RP 8 (7 m); mobile phase: methanol/water 9/1;
detection wavelength: 254 nm.

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cis

trans

t (min)

FIGURE 10.3 HPLC separation of isomeric en-yne-dicycloethers. Column: ODS sol-x; mobile phase: acetonitrile/acetic acid 2% 45/55.

For the quantification of matricin in chamomile flowers, Schmidt et al. [124, 126] recommended
the direct HPLC analysis of a methylene chloride extract using a Nucleosil 100-5 C18 column and
a gradient of acetonitrile/methanol/water (12:35:53) as solvent A and methanol as solvent B with
detection by UV (244 nm).
Isomeric en-yne-dicycloethers can be separated on an ODS sil-x column (reversed phase) with
2% acetic acid in acetonitrile (45:55, V/V) (Figure 10.3). Under these conditions, neither artifacts
nor losses are to be expected [121].
Similarly good separation results were reported by Schulz using water/methanol (70:30, V/V)
[128]. The amounts found by HPLC analysis are about 1639% higher than in GC. For the quantification of spiroethers, HPLC is best, whereas analysis by TLC is complicated and time-consuming.
Chamazulene carboxylic acid was quantitatively determined in human serum by a validated
HPLC assay. EDTA plasma was acidified with phosphoric acid, extracted with diisopropyl ether,
centrifugated, evaporated, and the residue dissolved in acetonitrile. The separation was done on an
RP-18 column, eluting with acetonitrile-buffer pH 3 (4:6) and UV detection (286 nm) [164].

10.2.9 ENANTIOSELECTIVE HPLC

After several less satisfactory attempts [12, 15, 34], Gnther et al. established an enantioselective
HPLC method to separate the four stereoisomers of -bisabolol [35]. Possible alterations of the
genuine chamomile oil can be identified by quantification of the isomers. ()--bisabolol has the
strongest antiphlogistic effect of all stereoisomers [51]. It is the main component and indicates the
quality of chamomile oil. Synthetic -bisabolol is a mixture of four isomers. Its antiphlogistic
activity is therefore weaker [51] (see also Chapter 4 on active constituents). Nevertheless, the
synthetic compound advertised to be identical to the natural one is often used as a substitute or
additive to natural chamomile oil. The preparative separation of the isomers of -bisabolol has
been achieved using tribenzoylcellulose as stationary phase (column: Superperformance, 10 mm
150 mm, 1020 m). The eluent was a mixture of ethanol/isopropanol/water (400:300:400, V/V/V;
flow rate 0.4 ml/min). The isomers were detected by a UV detector (type Soma S-3702, 208 nm),
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Absorbance

1d
1c

1b
0

Opt. Rotation

1a

30

60

90

120

150

180

210

240

Retention Time (min)

FIGURE 10.4 Analytical separation of the four -bisabolol isomers on tribenzoylcellulose: 1a = ()-bisabolol; 1d = (+)-epi--bisabolol; 1c = ()-epi--bisabolol; 1b = (+)--bisabolol. UV absorbance at 208
nm (full line), optical rotation at 546 nm (dotted line).

followed by a polarimeter (546 nm). Authentic -bisabolol isomers obtained from other natural
sources [34, 35] were used as reference substances (see Figure 10.4).
This was the first report on the separation of the four isomers without lengthy isolation and
clean-up procedures. The samples can further be analyzed using isotopic mass spectrometry (MS)
and 2H-NMR-spectroscopy [12, 15]. Columns with a wider diameter allow a semipreparative
analysis of the isomers using low pressure (LP) LC conditions. The purity of isomers obtained is
good (enantiomeric excess approximately 9598%) [34, 35].

10.2.10 DROPLET COUNTERCURRENT CHROMATOGRAPHY

Droplet countercurrent chromatography (DCCC) was successfully applied by Becker et al. to
separate both polar and apolar compounds [5]. The solvent was a mixture of hexane, ethyl acetate,
nitromethane, and methanol (9:2:2:3). However, GC gave better results regarding the chromatographic separation compared to DCCC.

10.2.11 HPLC/MS

AND

GC/MS

HPLC and GC combined with mass spectrometry allow the immediate determination of components
in chamomile extract [16, 128]. Characteristic fragmentation of the compounds can be observed
using different ionization methods: Electrospray Ionization (ESI) or Atmospheric Pressure Chemical
Ionization (APCI). The MS data can be compared with data of reference substances in experiments
or literature (see Figure 10.5).
LC/MS analysis provides quick results concerning the quality of a pure chamomile oil [16].

10.2.12 REVIEW

OF THE

ANALYTICAL POSSIBILITIES

Schilchers flow chart (Figure 4.26, page 89 in Reference 121) comprehensively shows further
methods regarding the chemical analysis of chamomile oil.

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M/z 201

6865

100

4000

201
1

90
2000

80
70

0
0

60

5 min.

50
40
30
20

202

10
0
150

160

170

180

190

200

210

FIGURE 10.5 Thermospray LC-MS chromatogram (single ion mode m/z = 201) of an aqueous/ethanolic
chamomile flower extract (concentrated) and mass spectra of the two detected peaks. 1 = cis en-yne-ether, 2
= trans en-yne-ether.

10.3 CHEMICAL ANALYSIS OF THE FLAVONOIDS

10.3.1 DETERMINATION

OF THE

FLAVONOIDS

Substances that interfere with the analysis of flavonoids (e.g., carotinoids) are usually removed by
extraction. It has to be taken into account that the majority of apolar flavonoids will also be removed
in this step, e.g., by the extraction with carbon tetrachloride [106]. Moreover, extraction by hot
water results in 3045% lower values for flavonoids compared to methanol extraction. It is therefore
not possible to avoid the co-extraction of chlorophyll and related substances by using water.
The photometric determination of flavonoids has many advantages, although the absolute values
are actually about 2030% higher. Other methods as suggested by Reichling et al. showed no
improvement [103]. The absolute content of flavonoids ranged between 1.0 and 2.5% in a study
of 102 commercially available plants and determination according to References 106 and 17. Twelve
samples of material of different origin cultivated by Schilcher showed values between 0.3 and
2.96% [121, 122].

10.3.2 PAPER CHROMATOGRAPHY (PC)

AND

THIN-LAYER CHROMATOGRAPHY

Flavonoids have musculotropic and neurotropic effects on spasmolysis. Therefore, there is a pharmacological interest in the content of flavonoids. It is known that flavonoid biosynthesis is influenced
by environmental factors. The identification and quantification of flavonoids elucidates the chemotaxonomy of the plant material.
10.3.2.1 Paper Chromatography
Paper chromatography provides quick results using isopropanol/formic acid conc./water (2:5:5,
V/V) as solvent [46]. Cyclic filter chromatography on Ederol round filters [111] is also possible.

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10.3.2.2 Thin-Layer Chromatography

The development of TLC methods has been successful for the separation of about 30 flavonoids,
among them the five main aglyca, apigenin, luteolin, quercetin, patuletin, and isorhamnetin, 20
flavonoid glycosides and so-called lipophilic methoxylated flavones [71]. This was followed by
the densitometric determination of some main constituents such as apigenin-7-glucoside, quercetin7-glucoside, quercetin-3-galactoside, and patuletin-7-glucoside.
Silica gel 60 F254 was used in combination with ethylacetate / formic acid conc. / water (10:2:3)
[38], ethylacetate / formic acid / water (100:10:15) [71] or ethylacetate / formic acid / glacial acetic
acid / water (100:11:11:26) [158] as eluent.
Aglyca were best separated on polyamide plates (Polygram DC11, MN) and a solvent system of
methanol / methylethyl ketone / acetyl acetone (10 + 5 +1) [19] or toluene / methylethyl ketone / methanol
(60 + 24 + 14) [103]. For the separation of aglyca on silica gel, toluene / ethylformiate/formic acid (50
+ 40 + 10) is suitable [158]. Nineteen flavonoids were analyzed by this method [70], not including the
methylated flavonoids (derivatives of the 6-methoxyquercetin and the 6,7-dimethoxykaempferol) [147].
The main components mentioned above can be quantified using a Shimadzu CS 900 scanner. The TLC
plates were analyzed at two wavelengths (350 nm and reference wavelength of 710 or 460 nm).
Pretreatment of the TLC plate was not necessary. The peak height of the signals was compared to
standard substances. For the TLC separation, the solvent system of ethyl acetate/formic acid/water (10
+ 2 + 3) can be used.
For qualitative analysis the TLC plate is sprayed with Natural Products (NP)-Polyethylene
Glycol (PEG) reagent. NEU-reagent consists of 1% methanolic diphenylboric acid--ethylamino
ester (NP) followed by 5% of ethanolic polyethylene glycol-4000 (PEG). The spots were detected
by UV at 356 nm (see Figure 4.27 in Reference 121).
10.3.2.3 Two-Dimensional Thin-Layer Reaction Chromatography
Flavonoid glycosides as precursors of flavonoid aglyca can be detected using the two-dimensional thinlayer reaction chromatography [37, 67]. After the first development of the TLC plate (sorbens: Silica
gel 60 F254), the sugars were hydrolyzed by hydrochloric acid applied in a microwave vapor-blast
process. Turning the TLC plate by 90 a second development was carried out (solvent system: ethyl
acetate / formic acid / water 8 + 1 + 1 for both developments). The spots were detected by NP/PEGreagent. Tschirsch and Hlzl adapted this method to acylated flavonoid glycosides, e.g., acylated
apigenin-7-glucoside-derivatives from chamomile [146] (Figure 10.6). The acyl groups were removed
by saponification, liberating the flavonoid glycoside. In this case concentrated ammonia was used after
the first development (Figure 10.7). The duration and temperature of treatment varied from 1 min at
room temperature to 1 hour at 70C depending on the stability of the acyl group (sorbens: silica gel
60 F254; solvent system: ethylacetate / formic acid water 100 + 10 + 5 for both developments, detection
by NP/PEG-reagent). The separation of apigenin-7--D-(6"-O-acetyl)- and (4"-O-acetyl)glucoside was
possible [146]. The method is particularly useful when no authentic reference substances are available.

10.3.3 HIGH-PRESSURE LIQUID CHROMATOGRAPHY

The first HPLC separation of quercetin, quercetin-7-glucoside, apigenin-7-glucoside, rutin, herniarin, umbelliferone, and two unidentified phenyl carboxylic acids was done by Schilcher [117,
118]. All compounds were separated on an RP 8 column running a gradient of methanol-water
(1580%). The method was further developed and perfected for the qualitative and quantitative
determination of chamomile flavonoids by Redaelli et al. [99, 100] in 1981 and by Dlle et al. in
1985. A comparison of three methods is shown in Table 10.6.
The method Dlle published allows reproducible determinations of the chamomile flavonoids
[18]. Method no. 3 uses the diode-array technique for detection, giving reliable results. Several
later publications used this detection method [14, 82, 124, 125, 126, 128, 146].

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Front 2

Start 2

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7
Front

6
5
4
3
2
1

Start 1

1, 3, 4, 5, 6

Front 2

Start 2

FIGURE 10.6 Two-dimensional thin-layer chromatogram without reaction of ammonia. 1 = Apigenin-7glucosid; 2 = derivative 1; 3 = derivative 2; 4 = Apigenin-7--D-(6-O-acetyl)glucoside; 5 = derivative 3; 6
= Apigenin-7--D-(4-O-acetyl)glucoside; 7 = Apigenin-7-glucosid control.

7
Front

6
5
4
3
2
1

Start 1

FIGURE 10.7 Two-dimensional thin-layer chromatogram after reaction with ammonia for 1 min. 1 = Apigenin-7-glucosid; 2 = derivative 1; 3 = derivative 2; 4 = Apigenin-7--D-(6-O-acetyl)glucoside; 5 = derivative
3; 6 = Apigenin-7--D-(4-O-acetyl)glucoside; 7 = Apigenin-7-glucosid control.

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TABLE 10.6
Comparison of Three HPLC Separation Protocols (after Dlle et al. [18])
Method
1
Mobile Phase
Eluent A

2000 ml water
40 ml glacial acetic acid

1800 ml KH2PO4 (0.005 mol/l)

175 ml methanol

2000 ml KH2PO4 (0.005 mol/l)

14 ml dil. phosphoric acid
(pH approx. 2.6)

1750 ml methanol
300 ml acetonitrile

1200 ml acetonitrile
600 ml methanol

Eluent B

110 ml acetonitrile
16 ml dil. phosphoric acid
(pH approx. 2.55)
acetonitrile

Column
Column
material
Particle size
Column size
Manufacturer

RP 18
5 m
250 4.6 I.D. (steel)
Perkin Elmer

RP 8
10 m
250 4.0 I.D. (steel)
Merck

RP 18
5 m
125 4.0 I.D. (steel)
Merck

15 l

15 l

15 l

37C
1.0 ml/min
21 l0-4 A.U./cm
335 nm
2785% B within 28 min

35C
0.75 ml/min
16 l0-4 A.U./cm
350 nm
2385% B within 40 min

37C
1.0 ml/min
64 10-4 A.U./cm
335 nm
2785% B within 22 min

Parameters
Injected
volume
Temperature
Flow rate
Sensitivity
Wavelength
Gradient
a

Modified according to Redaelli et al. [97100].

Carle et al. successfully separated the acetylated isomers of the apigenin-7-O--glucoside using
thermospray liquid chromatography/mass spectrometry (TSP LC/MS) [13]. The analysis was performed on an HPLC chromatograph HP 1090 L interfaced with an HP 5988A thermospray MS.
The mass range scanned was m/z 150800 using positive and negative ionization mode.

10.4 CHEMICAL ANALYSIS OF THE COUMARINS

The solvent system that was applied for the components in essential oil can be used to separate
umbelliferone and herniarin in the dichloromethane extract on silica gel 60/Hf 254. Table
10.4 summarizes possible mobile phase systems as well as the RF values of the two coumarins.
Both compounds show a soft blue fluorescence in short-wave UV light. Under long-wave UV,
umbelliferone has a very strong, light-blue fluorescence and herniarin, a darker blue one. The strong
fluorescence of both compounds can be used for the direct quantitative determination. It is best to
use HPTLC plates and a mobile phase system of ether/toluene (1:1, V/V) saturated with 10% acetic
acid [110]. The compounds can be determined in fluorescent light at 365 nm at a wavelength of
460 nm [147].
HPLC with UV/Vis detection rapidly and reliably allows the separation and identification of
the coumarins in purified aqueous chamomile extracts [126, 128, 129]. Good results were obtained
on an HP 1090 liquid chromatograph with microbore column. The mobile phase was a gradient of

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phosphoric acid (pH 2.8) in acetonitrile. The compounds were identified using an HP 1040 A HPLC
detection system. The diode-array technology enables the simultaneous measurement of the absorbance in a range of 190 to 600 nm. An HP 1046 A programmable fluorescence detector can also
be used [129] (see Figure 10.8).
For the isolation of both coumarins, sublimation is a suitable method [120].

10.5 CHEMICAL ANALYSIS OF THE CHAMOMILE MUCILAGE

The extraction of chamomile flowers with 96% ethanol precipitates large amounts of (natural)
mucilage. The mucilage has to be demineralized in order to determine its viscosity and identify
individual polysaccharide components. This can be done using amberlite IR-120, an acidic cation
exchanger, and amberlite IR-45, a basic anion exchanger. Comparative hydrolytic tests [120] showed
that hydrolysis with trifluoroacetic (TFE) acid (1 ml of 1% solution of chamomile mucilage + 1
ml 4N TFE, boiled for 30 min) is the most suitable method. Table 10.7 lists several solvent systems
for the TLC separation of monosaccharides and urone acids.
Good separations of the monosaccharides and urone acids are shown in Figures 4.28 and 4.29
in Reference 121, page 92.
A selection of spray reagents is summarized in Table 10.8. On heating the plates, color reactions
occur. However, for densitometric quantification, only immersed plates yield reproducible results.
Franz et al. [25, 26] extracted the polysaccharides with cold water for 7 hours, using chamomile
flowers that were pre-extracted with petrol ether and methanol, followed by precipitation with ethanol
(final ethanol concentration 80% G/G). For the fractionation of the polysaccharides, both ion exchange
and gel permeation chromatography (GPC) are recommended. Ion exchange chromatography is
performed on DEAE-Sephacel columns in phosphated form by successive elution with water/phosphate buffer (0.25/0.5/1.0 M) and water/NaOH (0.2 M). The polysaccharide fractions are detected via
an anthrone test, dialyzed (MWCO 3500 D), and lyophilized. The latter is performed by medium
6

140
120
100

mAU

80
60

8
5

12

10

11

3
40
20

B
0
5

10

15

20

25

Time (min.)

FIGURE 10.8 Reversed phase HPLC and UV/Vis spectra of an aqueous extract of fresh Matricaria chamomilla. A = flowers, B = leaves (eluent: diluted phosphoric acid, pH = 2,8/-acetonitrile; detection: 337 nm). 1
= chlorogenic acid, 2 = caffeic acid, 3 = umbelliferone, 4 = hydroxy-cinnamic acid derivate, 5 = luteolin-7glucoside, 6 = apigenin-7-glucoside, 7 = herniarin, 8 = apigeninglucoside (not specified), 9 = apigenin-7-(6O-acetyl)-glucoside, 10 = apigenin, 11 = cis En-In-Ether, 12 = trans En-In-Ether.

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pressure-GPC on HiLOAD 16/50 Superdex 75 or 200 columns. The fractions of polysaccharides were
detected with an RI detector (e.g., ERC 7512 Benthron Scientific), dialyzed, and lyophilized. The
determination of molecular weights was performed in the same GPC system [25].

10.5.1 QUANTITATIVE SPECTRAL DENSITOMETRIC DETERMINATION

MONOSACCHARIDES AND URONE ACIDS

OF THE

Spots of samples (concentration approx. 5 g) and the sugar test solutions were applied on the
TLC plate (silica gel 60 plates Merck) by microcaps. The test substances were dissolved in 10%
of isopropanol and diluted to the final concentrations of 0.25, 0.5, 0.75, 1.0, 1.25, and 1.5 g/l.
Galacturonic and glucuronic acid were used in concentrations ranging from 0.5 to 1.25 g/l [121].
The TLC plates were developed twice over a maximum length of 10 cm each. The solvent system
was ethyl acetate-isopropanol-glacial acetic acid-water (60 + 30 + 5 + 5). After thorough drying of
the TLC plates, the spots were detected by immersion in Scheffer-Kickuth reagent for 5 sec. The
plates were dried and heated for 8 min at a temperature of 120C, immediately followed by in situ
measurement. Instrument parameters were as follows:
Apparatus: Zeiss chromatogram spectral photometer KM3
Wavelength: 385 nm
Gap width: 0.5
F-stop: 6
Gap measuring head plate: 2.5
Table speed: 200 mm/min.
Recorder 120 mm/min.
Evaluation: F = h x bh/2 (h = peak height, bh/2 = peak width at half level) or by evaluation
of the peak height

10.6 ANALYSIS OF CHAMOMILE: SUMMARY

The gravimetric method gives exact quantitative determinations of the total essential oil.
In case of problems with the exact quantitative determination of individual constituents,
a 1-hour extraction with methylene chloride is recommended.
For the analysis of the individual components in the essential oil, both TLC (e.g., on silica
gel plates GF254, mobile phase methylene chloride-ethyl acetate 98 + 2) and GC (OV 101
capillary column of 50 m length) are suitable. Very exact values of the spiroethers can be
obtained by HPLC (Figure 10.3).
In the quantification of the total flavonoids, lipophilic flavonoids should also be included.
For the analysis of individual flavonoids, TLC is suitable (see Figure 4.27 in Reference
121, page 90). Quantification can be done with TLC scanners, applying the two-wavelength technique (e.g., on a Shimadzu CS 900).
For the determination of coumarins, TLC or HPLC and UV/Vis detection are best when
using the same extract as for the analysis of the essential oil. The coumarins are preferentially isolated by sublimation.
For the analysis of components of mucilage, hydrolysis with trifluoroacetic acid is
particularly suitable. The chromatographic separation of saccharides and urone acids can
be performed equally well either by thin layer, ion exchange, or gel permeation chromatography. Quantification works well after immersion of the TLC plates in SchefferKickuth reagent (see Figure 4.28 in Reference 121, page 90).

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TABLE 10.7
RF Values of Monosaccharides and Uronic Acids with Various Mobile Phases
on Commercial Silica Gel 60 TLC Plates (Merck)
RF value

Carbohydrate

Galactose
Glucose
Arabinose
Fucose
Xylose
Rhamnose
Galacturonic acid
Glucuronic acid

10

11

0.16
0.21
0.23

0.45
0.52
0.64
0.72
0.76
0.88
0
0

0.07
0.1
0.13
0.17
0.18
0.28
0
0

0.43
0.49
0.57
0.61
0.3
0.69
0.21
0.23

0.45
0.57
0.64
0.74
0.76
0.85
0
0

0.5
0.51
0.65
0.74
0.76
0.86
0
0

0.44
0.48

0.22
0.24
0.28

0.21
0.24
0.27

0.56
0.63
0.29
0.0

0.36
0.2
0.1
0.14

0.36
0.2
0.5
0

0.18
0.24
0.31
0.43
0.46
0.62
0
0

0.16
0.23
0.30
0.,7
0.44
0.57
0
0

0.31
0.39
0
0

1 : n-Propanol-Ethylacetate-Water
2 : Acetone-Water
3 : Ethylacetate-aq. 2-Propanol (65%)
4 : Acetonitrile-Water
5 : Acetone-1-Butanol-Water
6 : Acetone-1-Butanol-Acetic acid-Water
7 : 1-Butanol-Acetic acid-Water
8 : Ethylacetate-Methanol-Acetic acid-Water
9 : 2-Propanol-Ethylacetate-Water
10 : Ethylacetate-2-Propanol-Water
11 : Ethylacetate-2-Propanol-Acetic acid-Water
a

(70:20:10)
(9010)
(65:35)
(85:15)
(50:40:10)
(50:40:10:10)
(80:30:30)
(60:15:15:10)
(50:40:10)
(60:30:10)
(60:30 5:5)

(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)
(V/V)

[3]
[95]
[142]
[27]
[4]
[28]
[163]
[36]
[94]
[28]

No separation of fucose and xylose and of glucose and arabinose.

TABLE 10.8
Color Reactions of Monosaccharides and Galacturonic Acid after Immersion of the TLC
Plates and Development at 100C
AnisaldehydeSulfuric acid
Galactose
Glucose
Arabinose
Fucose
Xylose
Rhamnose
Galacturonic acid

Dark green
Blue
Light green
Green
Light green
Green
Brown

AnilinDiphenylamin
Blue
Blue-grey
Green
Green
Grey-green
Pale green
Red-brown

-NaphtholSulfuric acid

CarbazolSulfuric acid

SchefferKickuth
Reagent

Red
Red
Dark red
Red
Dark red
Orange
Red-brown

Blue-grey
Blue-grey
Blue-green
Blue-green
Blue-green
Greyish pink
Blue-green

Yellow
Yellow
Yellow
Yellow
Yellow
Yellow
Yellow

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and
11 Pharmacology
Toxicology
Heinz Schilcher, Peter Imming, and Susanne Goeters
CONTENTS
11.1 Pharmacology Pharmacological Properties
11.1.1 Introduction
11.1.2 Antiphlogistic Effect (Subdivided According to Active Principles)
11.1.2.1 Chamazulene, Matricin, Chamazulene Carboxylic Acid,
and Guaiazulene
11.1.2.2 ()--Bisabolol and Bisabolol Oxides
11.1.2.3 Further Active Principles of the Essential Oil of Chamomile Flowers
and in Total Extracts
11.1.2.4 Flavonoids
11.1.3 Antispasmodic Effect
11.1.3.1 Flavonoids
11.1.3.2 Essential Oil
11.1.4 Antibacterial and Antimycotic Effect
11.1.5 Further Pharmacological Effects
11.2 Toxicity and Side Effects of Chamomile Preparations and Individual
Chamomile Active Principles
11.2.1 Acute and Subacute Toxicity
11.2.2 Skin Reactions (Cell-Mediated Allergy Type IV)
References

11.1 PHARMACOLOGY PHARMACOLOGICAL PROPERTIES

11.1.1 INTRODUCTION
Chamomile preparations are mainly used because of their antiphlogistic, spasmolytic, and carminative activity. However, their bacteriostatic and fungistatic properties should not be underestimated.
Application fields include dermatology, stomatology, otolaryngology, internal medicine, in
particular gastroenterology, pulmology, pediatry, and radiotherapy [11, 56, 100]. The therapeutic
effectiveness is in total due to the combined pharmacological and biochemical effects of several
chamomile constituents. For therapeutic success, it is important to use standardized total extracts
or the essential oil. The full spectrum of activity will not be reached by applying individual
chamomile substances only [100].

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11.1.2 ANTIPHLOGISTIC EFFECT (SUBDIVIDED ACCORDING TO ACTIVE PRINCIPLES)

11.1.2.1 Chamazulene, Matricin, Chamazulene Carboxylic Acid,
and Guaiazulene
Even though its constitution was not known at the time, chamazulene was identified as the antiphlogistic principle of chamomile oil in a test system of chemosis caused by mustard oil in rabbit eye
as early as 1933 [47], and again in 1942 in cavy eye [92]. Because these test systems were questioned
later [17, 89], the activity of the blue azulene was confirmed in other test models. There was a
positive effect on UV erythema of the cavy [50] and on heat-damaged mouse tail [22]. In the rat
paw test according to Selye [131, 132], an antiphlogistic activity of the azulene was proven, although
the effect of the total extract was much stronger. Guaiazulene was very helpful in the therapy of
dermatitis caused by radiation [8, 30, 74, 88, 96, 100, 131]. It displayed weak antipyretic, analgetic,
local anesthetic, and anti-histaminic activity, which contributed to the anti-inflammatory effect
clinically observed [127].
The activation of the ACTH production and the corresponding functional increase of the adrenal
cortex is one of the general effects of azulenes [86]. After applying guaiazulene to sensibilized
cavies, a prevention of the antigen-antibody reaction, even the prevention of the anaphylactic shock
[127, 131] was observed. Guaiazulene-1-sulfonic acid inhibited a serotonine-triggered shock [36].
Based on these results Stern et al. assumed that azulene prevents the liberation of histamine at the
time of antigen and antibody binding, probably via an anti-serotonine effect [104]. A comparison
of differently provoked edemas showed that the dextrane edema was inhibited strongly, whereas
the activity in hyaluronidase-, formaldehyde-, and histamine-induced edema was only moderate.
The authors assumed that the inhibition of histamine liberation, an anti-histaminic effect, an
inhibition of 5-hydroxytryptamine liberation, as well as an anti-hyaluronidase effect and a decrease
of the capillary activity [115] contributed to the total activity of the azulenes.
In the carrageenine-induced rat paw edema, chamazulene showed about double the antiphlogistic activity of guaiazulene [55]. Further investigations proved a significantly weaker antiphlogistic activity of guaiazulene compared with matricin and ()--bisabolol [60]. Guaiazulene can
be synthesized easily, but shows only half the antiphlogistic activity of the respective constituents
of chamomile (matricin, chamazulene) (see Table 11.1 [60]).
In the carrageenine-induced rat paw edema, matricin was equally active to ()--bisabolol 2
and 3 hours after peroral administration. After 4 hours, no significant activity differences were
observed between the two substances. Chamazulene and guaiazulene were significantly less effective than bisabolol and matricin. While chamazulene remained antiphlogistically active for more
than 4 hours, the effect of guaiazulene decreased. Guaiazulene thus showed a short-term effect [60].
A comprehensive investigation by Ammon with 5- and 12-lipoxygenase, cyclooxygenase, and
peroxidation assays showed that chamazulene, but not matricin, inhibited 5-lipoxygenase [3]. Both
compounds were equally ineffective regarding the formation of 12-HHT (hydroxyheptadecatriene
acid) by cyclooxygenase. Only chamazulene showed a significant anti-oxidative effect.
Chamazulene carboxylic acid (CCA) is a degradation product of sesquiterpene lactones from
Asteraceae, e.g., matricin. It was discovered not only to have a striking constitutional similarity
with profens (e.g., ibuprofen, naproxen), but also to have S-configuration, the eutomeric configuration of profens [39, 38]. It was shown to be a potent anti-inflammatory agent and the second
example of a cyclooxygenase-2 (COX-2) selective compound derived from medicinal plants [37,
95]. The inhibition of COX-2 results in anti-rheumatic therapy with greatly reduced side effects
and holds the promise of anti-neoplastic therapy. COX-2 was discovered in 1993; it therefore came
as a surprise that COX-2 inhibition seems to have been in use for thousands of years through a
chamomile and yarrow constituent.
The antiphlogistic activity of CCA was assessed in two standard animal models [37]. Locally
applied, it was approximately equipotent to S-naproxen. After oral application, its prodrug pivaloyl

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After 1 h
Molar titer
(confidence
interval)
()--Bisabolol, MR 222
Chamazulene, MR 184
Guaiazulene, MR 198
Matricin, MR 306
Salicylamide, MR 137

0.61
0.60
1.03
1.77

1
(0.380.94)
(0.390.89)
(0.621.72)
(1.252.51)

Significance

After 2 h
ED50
(mMol/kg)

a
a

ns
a

2.69
4.48
4.59
2.60
1.53

Molar titer
(confidence
interval)

0.70
0.66
1.27
2.04

Significance

1
(0.461.08)
(0.460.95)
(0.911.75)
(1.452.86)

ns
a

ns
a

After 3 h
ED50
(mMol/kg)
2.95
4.27
4.60
2.29
1.44

Molar titer
(confidence
interval)

0.49
0.33
0.92
1.99

1
(0.211.15)
(0.130.80)
(0.611.41)
(1.283.10)

Significance

ns
a

ns
a

ED50
(mMol/kg)
2.43
5.00
>7.07
2.68
1.28

Anti-inflammatory effect in terms of molar titer with confidence intervals and of ED50 (mMol/kg p.o.) in the carrageenan-induced rat paw edema 1, 2, and 3 h after edema induction, oral
application 1 h before edema induction. [60]
Calculation of molar titer:

titer rel. molecular mass

222
(222: MR of bisabolol)

Calculation of molar ED50:

Significance of the titer:

a

= significant (p = 0.05)

ns = not significant (p > 0.05)

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ED50 (mg/kg)
rel. molecular mass

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TABLE 11.1
Comparison of the Anti-Inflammatory Effect in the Carrageenan-Induced Rat Paw Edema

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ester had approximately 75% aspirin activity. As predicted by docking studies with x-ray structural
data of cyclooxygenases [28], CCA did not inhibit cyclooxygenase-1, but cyclooxygenase-2, its
selectivity and activity (43.5% inhibition at 50 M) being comparable to that of a standard COX2 inhibitor, nimesulide (Aulin, Switzerland) [37].
Because of its structural resemblance with the auxin, indolylacetic acid, it was tested for auxinbinding [54]. The positive result suggests that sesquiterpene lactones may not only function as
antifeedants, but also serve for the plant as reservoirs of auxins if they are convertible to azulenes
like CCA. Especially the systemic antiphlogistic activities of camomile (and yarrow) thus are partly
due to the conversion of guaianolides to natural naproxen CCA in vivo, especially under acidic
conditions (stomach, inflamed tissue).
In a human pharmacokinetic study with volunteers, approved by the ethics commission, three
volunteers took 500 mg matricin each orally. After 75 to 90 min, this gave rise to plasma peak
levels of 1.3 to 2.2 g of chamazulene carboxylic acid. The AUC was calculated as 14.7 g*h/ml.
So matricin indeed is a prodrug of the natural profen in man [134].
-Bisabolol and Bisabolol Oxides
11.1.2.2 ()-
Certain types of chamomile contain up to 50% ()--bisabolol in the essential oil; however, in the
majority of types the oxides are more abundant [55].
Three years after its isolation, the antiphlogistic activity of ()--bisabolol was determined in
1954. Its constitution was elucidated in 1968 [57].
After exposing cavies to UV light, ()--bisabolol decreased the skin temperature. Farnesene
and a bisabolol monoxide (not defined more specifically) showed a weaker effect [65]. ()-bisabolol reduced the time to heal burns just like chamazulene. Further, it showed an improved
blood circulation compared to chamazulene [133]. Histological experiments proved a stimulation
of epithelization and granulation by ()--bisabolol and farnesene [45]. A significant anti-inflammatory effect of ()--bisabolol occurred in the carrageenine-induced rat paw edema and cottonpellet granuloma. Guaiazulene and guaiazulene-1-sulfonic acid (azulene SN) had about the same
activity that bisabolol had [62]. A later study found only half the activity for ()--bisabolol
compared to chamazulene [63]. However, this was again revised later [60].
There is no doubt that the antiphlogistic effect of ()--bisabolol was proved in the carrageenine-induced rat paw edema and against UV erythema of the cavy, adjuvant arthritis, yeastinduced pyrexia of the rat, and in 5-lipoxygenase and cyclooxygenase tests [3, 61].
Regarding the effect on adjuvant arthritis of the rat, a dose of 500 mg/kg ()--bisabolol was
equivalent to 1.5 mg/kg of prednisolone. Even a dose of 2000 mg/kg bisabolol is far below the
toxic dose and shows strong antiphlogistic activity. Protective properties of ()--bisabolol on
skin were tested in erythemae of cavies, comparing with salicylamide. After peroral administration,
()--bisabolol weakly inhibited the development of an erythema. An increase of the dosage was
limited because 2000 mg/kg was toxic for cavies. So the toxic dose of bisabolol was smaller for
cavies than for rats.
Since percutaneous application of ()--bisabolol showed inhibition of erythemae, the substance penetrated skin well [61].
Ammon proved that ()--bisabolol was capable of inhibiting both 5-lipoxygenase and cyclooxygenase. Anti-oxidative activity was not observed, in contrast to chamazulene and ethanolic aqueous
extracts [110]. In the peroxidation assay, even a propyleneglycol extract did not have any antioxidative effect [110].
()--bisabolol had antipyretic activity against yeast-induced pyrexia of the rat. The fever was
reduced by 1.5C for 2 hours after applying 2000 mg/kg ()--bisabolol perorally [18]. The
maximum effect was delayed compared with phenacetine [61].
()--bisabolol also decreased the production of mucopolysaccharides in cell cultures. The
cells were obtained from embryonic spine tissue of mice and from fibroblast cultures.

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A report published in 1979 mentioned that -bisabolol (isomer not specified) inhibited the
incorporation of radioactive sulfate into the proteochondroitine and protokeratane sulfates in calf
cornea in vitro. At a concentration of 10-4 M, -bisabolol inhibited the incorporation by 15%. A
higher dose of 10-3 M resulted in 58% inhibition, which is comparable with well-known antiinflammatory agents [29].
Several investigations were undertaken to study if ()--bisabolol could be substituted by the
(+)-isomer found in Populus balsamifera or by the synthetic racemate [55, 60, 61]. The levogyrate
form from chamomile oil proved to be twice as antiphlogistic as the racemate and the dextrogyrate
form isolated from the oil of poplar buds. Interestingly, the racemate is weaker than expected,
taking both ()--bisabolol and (+)--bisabolol into account. The authors ascribe this to the
racemization [61]. This does not make much sense except if they meant to say that the synthetic
bisabolol they used actually was a mixture of all four stereoisomers; apart from that, they state that
it did contain 23% of the nonnatural isopropenyl isomer with unknown therapeutic efficiency.
Farnesol and bisabolol oxides A and B were also tested, as well as the commercial Dragosantol,
a mixture of racemic synthetic -bisabolol isopropylidene and isopropenyl isomers.
The test results, summarized in Table 11.2 [61], show that bisabolol oxide B (the main constituent
of Argentinian chamomile) and bisabolone oxide (the main constituent of Turkish chamomile)
had only half the activity that ()--bisabolol had. Bisabolol oxide A (the main constituent of
Egyptian chamomile) had about a third and Dragosantol a quarter of the activity of ()--bisabolol.
11.1.2.2.1 Protective and Curative Effect on Ulcers of ()--Bisabolol and
Protective Effect against Acetylsalicylic Acid
The traditional use of chamomile for gastro-intestinal diseases led to tests of ()--bisabolol
in different animal ulcer models. The substance showed activity [101] especially in the case of
ulcus ventriculi [27, 71, 102, 120].

TABLE 11.2
Comparison of the Anti-Inflammatory Effect in the Carrageenan-Induced Rat Paw Edema,
Dose-Effect Relationship [61]
Compound

ED50
(mg/kg p.o.)

Titer

Confidence interval
of the titera

No. of rats

()--Bisabolol
(+)--Bisabolol
()--Bisabolol, natural
()--Bisabolol, synthetic
Dragosantol
Bisabolol oxide A
Bisabolol oxide B
Bisabolone oxide
Olive oil

1465
>2000b)
>2000b)
>2000b)
>3000b)
3164
>2000b)
>2000s)
>2000s)

1
0.595
0.419
0.493
0.260
0.337
0.591
0.431
0.516

0.3950.898
0.1970.979
0.2770.877
0.1250.539
0.1790.635
0.3640.958
0.2230.832
0.2710.982

00
000
000
000
000
00
00
00

00
00
00
00
00
00
00
00

00
00
00
00
00
00
00
00

231
51
48
51
30
36
36
18
18

00

significant with p = 0.01

000

significant with p = 0.001

P: parallelism
L: linearity of the dose-effect lines (p = 0.01)
S: significance of the titers compared to 1
a

The confidence interval is given for the p-value the titer is significant compared to 1. Column S shows the p-value
of the confidence interval.

Largest tested dose; 50% effect (= inhibition of edema formation by 50%) not achieved.

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Preparations of chamomile flowers or individual components were not effective in inhibiting

acid secretion. Other experiments showed that ()--bisabolol was capable of inhibiting the formation of ulcers induced by indometacin, stress, or alcohol [110]. It was equally effective to
metiamide in indometacin-induced ulcus, and in the stress ulcus model it was even better. Just like
metiamide, ()--bisabolol accelerated the healing of ulcers induced mechanically (by heat coagulation) or chemically (by acetic acid). The curative and antiulcerogenous activity of a total
chamomile extract was obviously not only due to ()--bisabolol since the therapeutic effect was
stronger than expected for the amount of bisabolol present. Actually, an ED of 0.25 mg/kg for the
chamomile total extract was equivalent to 3.4 mg/kg of bisabolol. More than that, standardized
total chamomile extracts protected against ethanol-induced ulcer. This is probably because individual compounds promote the synthesis of prostaglandins, which cause an increase in the mucose
barrier that protects against ulcerogenous effects [94, 110]. In the pathogenesis of gastric and
duodenal ulcers, the balance of aggressive (e.g., gastric acid) and defensive or protective factors
(e.g., mucus of the gastric mucosa) is important, the latter being elicited by chamomile. The finding
of an antiseptic effect, first observed by Isaac and Thiemer [58], was pointed out again by Appelt
as an important reason for the traditional use of manzanilla (the Spanish name for chamomile)
[4]. The antiseptic activity of ()--bisabolol is not influenced by changes in pH [58].
Torrado et al. [113] studied the gastrotoxic influence of acetylsalicylic acid of different particle
size in rats with concomitant application of ()--bisabolol. At a dose of 200 mg/kg ASA, 0.880
mg/kg ()--bisabolol showed a significant (p < 0.05) protective effect on gastric mucosa [113].
11.1.2.3 Further Active Principles of the Essential Oil of Chamomile Flowers
and in Total Extracts
Cis- and trans-spiroether, two spirocyclic polyynes in the essential oil of chamomile flowers, have
less antiphlogistic activity as compared to matricin, chamazulene, and ()--bisabolol [16, 117].
The cis-enynedicycloether inhibited dextrane-induced edema in rats and prevented the decrease of
plasminogen caused by dextrane. However, it did not inhibit paw edema induced by injections of
serotonine, histamine, and bradykinine [16]. Verzr-Petri et al. did not find any antiphlogistic activity
of spiroethers in generalized dextrane edema of rats [117]. Chemically these compounds are
unstable; therefore, their contribution to the total activity may be low, but their participation is
obvious in certain test models.
Choline was found in concentrations of 0.3% in flowers [76] and 0.6% in the herb [10]. Mucus,
10% in flowers [114], and flavonoids [23, 25, 26] contribute to the total antiphlogistic activity of
alcoholic chamomile extracts.
In inflammation models induced by croton oil, Della Loggia proved that polysaccharides have
anti-inflammatory activity [35].
A study focusing on mitochondria in rat liver showed an increase of the oxidative phosphorylation in the presence of chamomile extract in certain degrees of dilution [112]. ATP biosynthesis
was activated simultaneously. The formation of active phosphates is only inhibited by doses that
are not achieved in vivo [112]. With mitochondria from cavy liver it was shown that the creatine
phosphate content increased time dependently and the amount of glucose-6-phosphate decreased
[112]. A positive influence of chamomile components was observed on metabolic processes,
providing energy and improving the regeneration of inflamed tissue. The use of chamomile extracts
in dermatology and cosmetics gets some scientific justification through this (see also Chapter 2).
The antiphlogistic activity of chamomile oil obtained by distillation was studied right from the
beginning. Krger-Nilsen ascribed the antiphlogistic effect to the primary development of subliminal irritations [75]. A specific activity in the leucocytic defense mechanism could indeed be proven
in 1952 [7]. The activation of the reticuloendothelial system (RES) was observed in tuberculotic
mice [68]. The effect on arthritis caused by formaldehyde was likewise assumed to be due to the
stimulation of the RES [73]. Grochulski and Borkowski demonstrated a significant decrease of

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high urea levels after applying chamomile oil to rabbits suffering from experimental glomerulonephritis [40]. Within 12 days after the commencement of the therapy, the rabbits had completely
recovered [40].
11.1.2.4 Flavonoids
While the spasmolytic effect of the chamomile flavonoids had been known for many years [42,
55], the antiphlogistic activity was proved much later [9, 20, 23, 25, 26, 126].
Della Loggia tested the flavonoids in the inflammation model induced by croton oil. He
examined apigenin, luteolin, quercetin, and also rutin and myricetin. Antiphlogistic activity
decreased in the following order: Apigenin > luteolin > quercetin > myricetin > apigenin-7-glucoside
> rutin. Apigenin even exceeded the activity of indometacin and phenylbutazone. The experiments
further showed that apigenin had both a positive influence on the vascular phase of the inflammation
(e.g., edema) and on the cellular phase (e.g., the migration of leucocytes). The processes initiated
were similar to those caused by nonsteroidal synthetic anti-inflammatory agents.
These results were confirmed by other experiments using different test systems. Apigenin and
luteolin were effective and even influenced the metabolism of arachadonic acid.
Nevertheless, the exact mechanism of action has not been understood completely. Several
possibilities are under discussion.
In summary, the traditional use of chamomile baths and infusions has been explained pharmacologically by now. The topical antiphlogistic effect of aqueous chamomile preparations which
had been questioned before seems to be true since alcoholic extracts contain both the essential
oil and flavonoids. A reasonable content of flavonoids in preparations guarantees a high antiphlogistic activity.

11.1.3 ANTISPASMODIC EFFECT

Several components found in chamomile flowers are spasmolytic. Some flavonoids and certain
components of the essential oil as well as the coumarins herniarin and umbelliferone are responsible
for this activity, apart from their fungistatic activity [82].
11.1.3.1 Flavonoids
In 1914 Power and Browning were the first to find apigenin and an apigenin glycoside in chamomile
flowers [93]. Their work was cited in numerous publications [11, 31, 53, 60, 77, 79, 98, 118] and
followed by several studies concerning the antispasmic activity of aqueous chamomile extracts as
well as of individual chamomile flavonoids [1, 45, 46, 48, 51, 52, 53, 60, 66, 67, 98].
According to Hava and Janku, apigenin inhibits the contractions of smooth muscle. The tests
were performed using rat or rabbit duodenum. The contractions were induced by barium chloride,
acetyl choline, and histamine [45, 66]. Apigenin intensified the adrenaline effect during the test.
The contractions of seminal vesicle of cavy and of rabbit uterus were inhibited by apigenin after
administering adrenaline. The spasmolytic effect of apigenin was regarded as nonspecific.
Later Hrhammer studied the effects of aqueous and methanolic chamomile extracts as well
as of pure flavonoid substances on the convulsion of rabbit ileum induced by barium chloride and
acetyl choline [51, 52, 53, 98].
The following results were observed:
1. The musculotropic effect was stronger than the neurotropic one. The chamomile flavonoids tested were mainly active on smooth muscle.
2. Alcoholic chamomile extracts seemed to have a stronger spasmolytic activity than aqueous extracts.
3. Extracts from ligulate flowers were more active than those from tubular florets.

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4. The antispasmodic effect of alcoholic extracts was not equivalent to the total effect of
flavonoids estimated; therefore, further components were assumed to contribute to the
spasmolytic effect. This was confirmed in later studies [1, 117].
5. The individual chamomile flavonoids vary in their antispasmodic activity. In general, the
flavonoid aglyca were more active compared with the flavonoid glycosides. The compounds tested can be classified in descending activity as follows: apigenin, quercetin,
luteolin, kaempferol, luteolin-7-glucoside, and apigenin-7-glucoside. 10 mg of apigenin
were equieffective to about 1 mg of papaverine as for musculotropic effect. Patuletin-7glucoside and a polyhydroxy-flavone [98] were even more effective than apigenin-7glucoside [53].
6. The flavonoid aglyca of patuletin, apigenin, quercetin, and luteolin only showed about
one fifth to one fourth the activity of papaverine in barium chloride-induced spasms.
Their glycosides were about 100 times less active [52].
About 20 years later, chamomile extracts and their components, among them also the chamomile
flavonoids already studied, were tested again for musculotropic-spasmolytic activity [1]. In gastrointestinal diseases, symptoms like pain seem to better correlate with impaired motility than with
the size of the lesion [109]. Therefore, a new test system was of great scientific interest in order
to review previously published results. The results obtained not only confirmed the spasmolytic
activity of chamomile flavonoids described by Hrhammer, they even proved a stronger spasmolytic
activity of apigenin compared with papaverine. Apigenin mono-glycosides were about equieffective
with the aglyca of luteolin, patuletin, and quercetin. Flavonoid diglycosides were about ten times
less active. The results are summarized in Tables 11.3 and 11.4 [20].
11.1.3.2 Essential Oil
Junkmann and Wiechowski [67] discussed that the carminative effect of Matricariae flos was part
of the intestinal spasmolysis. The essential oil did not show any effect on the autonomous inner-

TABLE 11.3
Antispasmodic Action of Various Fractions of the Hydrophilic Phase of the
Complete Extract of M. chamomilla on Musculotropic Spasms of Isolated
Guinea Pig Ileum (Barium Chloride 1 104 g/ml) (Data taken from Reference
20)
Substance

Fraction A
Fraction B
Fraction C
Fraction D
Fraction E
KamillosanR

ED50
(g/ml)
(p 0.05)
2.37 10-4
(1.304.31)
3.36 10-6
(2.863.95)
1.82 10-3
(1.482.24)
7.22 10-3
(5.8711.2)
6.24 10-3
(4.848.04)
1.09 10-3
(0.931.28)

Copyright 2005 CRC Press, LLC

Relative activity (Papaverine = 1)

Titer
Confidence intervals of titer
(p 0.05)

ED50
Papaverine
(g/ml)
(p 0.05)
1.64 10-6
(1.431.88)
1.81 10-6
(1.612.03)
2.05 10-6
(1.702.26)
1,42 10-6
(1.321.52)
1.33 10-6
(1.211.46)
1.37 10-6
(1.251.50)

0.07

(0.0060.008)

0.59

(0.480.73)

0.0011

(0.00080.0016)

No titer
(approx. 0.0002)
No titer
(approx. 0.0002)
0.0013

(0.00110.0015)

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TABLE 11.4
Actions of Various Flavone Aglyca and Flavone Glycosides on Musculotropic Spasms
of Isolated Guinea Pig Ileum (Barium Chloride 1 10-4 g/ml) (Data Taken from
Reference 20)
ED50
(g/ml)
(p 0.05

Substance

Flavone aglyca
Apigenin
Luteolin
Patuletin
Quercetin

Flavone glycosides
Apigenin-7-(6-Oacetyl)glucoside
Apigenin-7-glucoside
Apiin

ED50
Papaverine
(g/ml)
(p 0.05)

Relative activity (Papaverine = 1)

Titer
Confidence intervals of titer
(p 0.05)

8.02 10-7
(6.0810.6)
4.56 10-6
(3.545.87)
2.63 10-6
(2.393.02)
2.22 10-6
(1.762.79)

2.10 10-6
(1.752.52)
1.70 10-6
(1.412.04)
1.78 10-6
(1.482.14)
1.70 10-6
(1.412.04)

3.29

(2.344.62)

0.44

(0.300.64)

0.68

(0.560.81)

0.71

(0.461.09)

1.35 10-5
(1.231.48)
8.18 10-6
(6.20 10.8)
3.80 10-5
(3.164.57)

3.67 10-6
(3.503.84)
3.77 10-6
(3.144.53)

0.36
0.46

(0.270.55)
(0.390.55)

0.08

(0.060.11)

vation of rabbit intestine nor on muscarine-induced contracture. Several years later, in 1955 [48]
and 1957 [46], a spasmolytic activity of ()--bisabolol and (+)--bisabolol on rat ileum was
observed. Breinlich and Scharnagel [16] and Vezr-Petri et al. [117] reported a papaverine-like
activity of the enyne dicycloethers.
Achterrath and Tuckermann [1] reviewed the data published so far and summarized the results
as follows:
1. ()--Bisabolol, the bisabolol oxides A and B as well as the chamomile oil itself have
a papaverine-like musculotropic spasmolytic activity.
2. ()--Bisabolol with a titre of 0.91 has the same strong musculotropic antispasmodic
activity as papaverine. It is twice as active as bisabolol oxides A and B.
3. Cis-enyne dicycloethers are spasmolytic. There was no linear relationship between effect
and dose; therefore, a comparison with the other substances was not possible.
4. The essential oil showed the lowest antispasmodic activity.
5. An alcoholic extract (Kamillosan) had good spasmolytic activity.
6. The coumarin derivates umbelliferone and herniarin are antispasmodically active. It was
not possible to relate their dose to the strength of activity of papaverine, so no titers were
calculated.
7. Both hydrophilic (flavonoids) and lipophilic components (essential oil) contribute to the
musculotropic antispasmodic effect. In order to standardize chamomile preparations, it
is reasonable to include both groups of active principles. Carle and Gomaa summarized
the most important experimental data in two tables (see Tables 11.5 and 11.6 [20]).

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TABLE 11.5
Effects of Kamillosan on Various Experimental Spasms of Isolated Guinea Pig Ileum;
Papaverine Was Used as Standard, Unless Otherwise Indicated (Data Taken from
Reference 20)
Relative activity (Standard = 1)
Titer
Confidence intervals of titer
(p 0.05)

ED50
KamillosanR
(g/ml)
(p 0.05)

ED50
Standard
(g/ml)
(p 0.05)

1.22 10-3
(0.9251.61)

1.25 10-6
(1.141.37)

0.0011

(0.00080.0015)

(0.00140.0023)

0.00000116

(0.000000890.00000155)

Seratonine
(5 10-7)
Bradykinine
5 10-8

2.54 10-3
(2.372.72)
2.24 10-3
(1.782.82)

2.15 10-6
(1.752.64)
Atropine:
2.87 10-9
(2.393.45)
1.57 10-6
(1.062.32)
1.65 10-6
(1.401.94)

0.0019

Acetylcholine iodide
(5 10-8)

1.15 10-3
(1.001.32)
2.47 10-3
(2.152.84)

Spasmogen
(g/ml)

Barium chloride
(1 10-4)
Histamine dihydrochloride
(5 10-7)

(approx. 0.00062)
0.00071

(0.000520.00097)

TABLE 11.6
-Bisabolol Oxides A and B on
Antispasmodic Action of Chamomile Oil, ()-
Musculotropic Spasms of Isolated Guinea Pig Ileum (Spasmogen: Barium Chloride 1
10-4 g/ml) (from Reference 20)
ED50
KamillosanR
(g/ml)
(p 0.05)

Spasmogen
(g/ml)

Chamomile oil
()--Bisabolol
Bisabolol oxide A
Bisabolol oxide B

3.84 10-5
(3.194.62)
1.36 10-6
(1.131.63)
5.63 10-6
(5.136.17)
5.65 10-6
(5.156.19)

11.1.4 ANTIBACTERIAL

AND

ED50
Standard
(g/ml)
(p 0.05)
1.64 10-6
(1.161.84)
1.12 10-6
0.9751.28
2.60 10-6
(2.262.98)
2.80 10-6
(2.493.14)

Titer

Relative activity (Standard = 1)

Confidence interval of titer
(p 0.05)

0.04

0.030.05

0.91

(0.711.17)

0.46

(0.390.55)

0.50

(0.440.56)

ANTIMYCOTIC EFFECT

Although alcoholic chamomile preparations were used for a long time because of their antibacterial and antimycotic activity, microbiological tests of chamomile preparations of the essential
oil and of individual substances were undertaken comparatively late [2, 21, 32, 99, 100, 105109,
129]. In 1972, the first report on bacteriostatic and bactericidal activity of the essential oil was
published [2]. Both Gram-positive bacteria, such as Staphylococcus aureus and Bacillus subtilis,
and Gram-negative bacteria, such as Escherichia coli and Pseudomonas aeruginosa, were

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TABLE 11.7
Antibacterial Activity of a 42 vol.% Alcoholic Extract against Gram-Positive and Gram-Negative
Standard Microorganisms Originated in Mouth and Vagina (Data Taken from Reference 21)
Strain

B. megatherium
C. albicans
E. coli
Kl. pneumoniae
L. icterohaemorr.
Ps. aeruginosa
S. aureus
S. epidermis
St. group B
St. faecalis
St. mutans
St. salivarius
a

Concentrations (mg/ml)a

Controls

7.08 .12
5.55 .15
7.6 5 .12
8.23 .06
7.31 .15
6.87 .11
7.29 .04
7.46 .03
6.52 .07
6.78 .05
6.56 .03
7.32 .05

.31

.63

1.25

2.5

5.0

10.0

7.00 .28c)

6.48 .14c)

7.11 .10
5.84 .12
7.81 .08
8.21 .13
4.98 .12c
7.35 .16c
7.23 .06
7.99 .13c
6.75 .06
7.39 .03c
6.80 .07
7.31 .08

7.22 .10
5.77 .03
7.78 .10
8.13 .14
<2c
7.38 .08c
7.24 .05
7.42 .15
6.59 .08
7.30 .03c
5.24 .12c
7.22 .08

7.06 .06
5.29 .14
7.80 .09
7.92 .08c
<2c
7.45 .02c
6.94 .02c
7.29 .01
5.44 .15c
7.29 .03c
4.81 .08c
4.32 .07c

<2c
4.91 .03c
7.23 .19c
7.38 .07c

7.14 .05c
4.96 .02c
6.61 .02c
3.78 .11c
6.42 .09c
4.02 .06c
3.48 .14c

Inoculum
(time 0)b
5.03
3.14
5.13
5.28
5.17
4.50
4.77
4.72
4.48
5.01
4.37
3.75

.13
.13
.04
.02
.11
.21
.08
.02
.04
.05
.14
.09

Concentrations are expressed as mg of dry product c.f.u./ml of broth.

Values are logarithms of the number of the c.f.u./ml of broth recovered at the end of incubation time (means S.D. of four
determinations).

Statistically different from controls (p < 0.05).

included. A significant effect on fungi, such as Candida albicans, was also observed [2]. Later,
alcoholic chamomile extracts proved to be very effective against Bacillus subtilis, but had only
weak bacteriostatic activity against Staphylococcus aureus, Escherichia coli, and Bacillus mesentericus [129].
()--Bisabolol has the strongest antibacterial activity compared with the oxides and enyne
dicycloethers. It is active in low concentrations against Staphylococcus aureus, Bacillus subtilis,
Escherichia coli, Streptococcus faecalis, and Pseudomonas aeruginosa and inhibits the growth of
strains of Bacterium phlei that were resistant against standard anti-infectives [105, 108, 109]. ()-Bisabolol and the enyne dicycloethers were fungistatic against Candida albicans, Trichophytone
menthagrophytes, and Trichophytone rubrum at a concentration of 100 g/ml. After an incubation
of 30 minutes, a concentration of 1000 g/ml ()--bisabolol showed fungicidal effectiveness,
whereas at the same concentration, enyne dicycloethers were fungicidal after 48 hours. Chamazulene also had fungistatic activity, but at higher concentrations [106, 107].
In contrast to the aforementioned results, a study from 1968 did not find any noteworthy
bacteriostatic and fungistatic properties for the enyne dicycloethers against Staphylococcus aureus,
Streptococcus haemolyticus, Escherichia coli, or Candida albicans [16]. (+)--Bisabolol obtained
from Populus tacamahaca proved to be antibiotically active in vitro against Mycobacterium tuberculosis and other microorganisms [32].
A chamomile extract with an alcohol concentration of 42% (V/V) was antibacterial and showed
activity against trichomonads [21]. Table 11.7 summarizes the antibacterial activity against Grampositive bacteria strains (Staphylococcus aureus ATCC 12600, Staphylococcus mutans, group B
Streptococcus, and Streptococcus salivarius).
Among Gram-negative bacteria, the highest antibacterial effect was observed with Klebsiella
pneumoniae. There was little effect on the growth of Escherichia coli, and no inhibition of
Pseudomonas aeruginosa ATCC 27853. The extract showed a strong bacteriostatic effect on Bacillus megatherium ATCC 96 and Leptospira icterohaemorrhagia PB-3.
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TABLE 11.8
Comparison of Antibacterial Activity of Four Isolated Components and Defined Alcoholic
Extract [21]

Pure
S. aureus

4000

St. faecalis

500

E. coli

6000

-Bisabolol

Azulene

Bacteriaa

HEC

Pure

HEC

Bisabolol oxides
c

Pure

HEC

Dicycloethers
c

Pureb

HECc

100

300

45

1,000

80

2,000

10

50,000

90

15,000

160

100

10

300

90

50,000

160

Data are referred to the 25% inhibition of growth.

b Concentrations of the pure compounds (g/ml) inhibiting the growth of the bacteria; data from the literature (SzaboSzalontai, 1976), incubation time 24 hours.
c

Concentration of the components in the HEC dose having the same antibacterial activity; our data, incubation time 8 hours.

HEC = alcoholic chamomile extract.

Apart from this, there was a significant effect on Trichomonas vaginalis. A concentration of
2.5 mg chamomile extract per ml killed trichomonads effectively [21].
Table 11.8 names four main components of the essential oil having a considerably weaker
antibacterial effect on Staphylococcus aureus, Streptococcus faecalis, and Escherichia coli compared to the total alcoholic chamomile extract. Further investigations will have to test the assumption
that there is a contribution of hydrophilic components to the cumulative effect.
The contribution of the lipophilic components to this has been proven. As indeed various
constituents contribute to the activity, of course a complex composition of a phytopharmaceutical
is recommended. For antibacterial therapy with chamomile, standardized preparations should be
preferred to preparations containing chamazulene only. This applies accordingly to other indications.
In 1963, the influence of components of chamomile and horseradish on the activity of Streptococcus toxins was tested. It became clear that the healing effect of chamomile in inflammation
was not only due to antibacterial activity. Very small quantities of essential oil eliminated the effect
of Streptococcus and Staphylococcus toxins on the upper respiratory tract, especially of the paranasal sinus. A petroleum ether extract of chamomile flowers inactivated the toxins visibly by
preventing the hemolysis of blood cells. Allyl mustard oil from horseradish was second in this
activity; chamazulene weakest [69].
An extended screening study for mycotic and antibacterial activity included chamazulene and
()--bisabolol [99, 100]. The tests were carried out using the following organisms:
1. Arthrodermataceae (dermatophytes), Trichophytone rubrum, Trichophytone menthagrophytes, Trichophytone tonsurans, and Trichophytone quinckeanum
2. Candida albicans
3. Escherichia coli ATCC 32 902
4. Staphylococcus aureus ATCC 25 924
The minimal inhibitory concentration (MIC, g/ml) was determined directly (dilution test) and
indirectly (holed plate assay: diffusion test). The direct MIC test was carried out using four
different growing media [99]. Fulcin S (Griseofulvin) and Dermowas were chosen as reference

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antimycotic and antidermatosis agents. Antibacterial activity was compared with Actidione (cycloheximide) and chloramphenicol. Chamazulene had a MIC of 1800 g/ml, ()--bisabolol of 1000
g/ml against the tested dermatophyte strains. In the direct MIC test, a concentration of 200 g/ml
both for chamazulene and ()--bisabolol showed a slight fungistatic activity.
There was no satisfactory effect against Candida albicans compared with Dermowas and no
antibacterial effect on enterobacterial species compared with cycloheximide and chloramphenicol.
The antibacterial activity of chamazulene and bisabolol against Staphylococcus ATCC 25 294 was
about 45% of cyclohexamide and chloramphenicol. This was satisfactory [99]. These results as
well as a second study with chamomile coumarins [82] confirmed the antibacterial and fungistatic
activity of lipophilic components in chamomile, complementing other reports on antibacterial and
fungistatic activity [21, 24, 32, 100].
Infection with Helicobacter pylori is now recognized as the primary cause of peptic ulcers and
their recurrence. Compelling evidence has also been found linking H. pylori infection to gastric
cancer. Given the high rate of patient morbidity and mortality associated with gastric cancer, any
method by which one can reduce the occurrence of the disease or increase its early detection is
desirable. But antibiotics have serious side effects. Therefore, searching for new nontoxic phytopreparations with anti-Helicobacter pylori activity is urgent.
In recent studies chamomile oil extract was prepared using rotopulsed extraction of Matricaria
recutita flowers by olive oil by Shikov et al. [103]. Coumarin and flavonoid derivatives, polyynes,
bisabolol oxides, chamazulene, derivatives of humilones, and chlorophylls were found in this
extract. The propagation of H. pylori in the control experiment was typical. Chamomile oil extract
inhibited the production of urease at H. pylori. It is known that the level of activity of urease is
very important for the survival of this microorganism in the stomach. It is possible to suppose that
the mechanism of the therapeutic action of chamomile oil extract is based on inhibition of colony
activity of H. pylori and an inhibiting effect on adhesion of this microorganism of phospholipid
lecithin. Thus, chamomile oil extract is promising for application in complex therapy of stomach
ulcer and duodenal intestine, especially in patients with an allergic response to antibacterial drugs,
and also in case of a resistance of the inducer to antibiotics.

11.1.5 FURTHER PHARMACOLOGICAL EFFECTS

High doses of 1,4-dimethyl-7-isopropylazulene (guaiazulene) influenced carcinogenesis by inhibiting the development of metastases in animal experiments. Chamomile extracts and synthetic
azulene were also shown to inhibit the growth of vaccination tumors [72]. This raised the question
of how they interfered with tumor cell metabolism. Barton found [6] that guaiazulene caused
damage of the respiratory mechanism of the tumor cell, an increase of fermentation, and finally a
complete cessation of metabolism. It acted on the respiratory chain by inhibiting succinic dehydrogenase in both liver and tumor cells. Thus, one pathway of the citric acid cycle in which the
cytochrome system serves as acceptor is eliminated. Whereas the liver cell is in a position to
compensate through the other systems (di- and triphosphopyridine nucleotides), this pathway is
excluded for the tumor cell on account of its low enzymic activity. According to Emmrich et al.,
guaiazulene, structurally similar to chamazulene, as well as prednisolone, significantly reduced the
granulation tissue produced in rats [33].
Chamomile extract (Kamillosan, 34%) and 2.5 mg azulene SN (Na 1,4-dimethyl-7-isopropylazulenesulfonate) caused 24 and 94% inhibition of pepsin in vitro [111].
Della Loggia reported an activity of a freeze-dried aqueous extract (infusion) obtained from
tubular florets of Chamomilla recutita on the central nervous system [24]. The tests were carried
out with mice. The extract was applied intraperitoneally. The basal motility was reduced depending
on the dose. A dose of 360 mg/kg chamomile extract reduced the initial motility by 92% without
causing any relaxation of the muscles. The voluntary active movements (motoricity) were also
decreased significantly. In doses of 160 and 320 mg/kg chamomile extract, slight hypnotic effects

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were observed. Sleep induced by hexobarbital was extended significantly. The aqueous preparation
of chamomile flowers tested seemed to influence the state of activity of the central nervous system.
However, the effects were much weaker than those of benzodiazepines: 1 mg/kg benzodiazepine
applied perorally was already anxiolytic.
Nevertheless, it seems to be justified to apply chamomile infusion as a mild tranquilizer, a
common use in traditional medicine [24]. Wolfmann et al. even characterized apigenin as a ligand
for the benzodiazepine binding domain, causing an anxiolytic effect [122]. They write that the
results reported here demonstrate that apigenin is a ligand for the benzodiazepine receptor and
possesses anxiolytic effects without evidencing anticonvulsant or myorelaxant actions. A recent
paper [130] reported on the behavioral effects of acute administration of apigenin and chrysin in
rats. Both flavonoids were equally able to reduce locomotor activity when injected in rats at a
minimal ED of 25 mg/kg. However, while chrysin exhibited a clear anxiolytic effect when injected
at a dose of 1 mg/kg, apigenin failed to exert this activity. The sedative effect of these flavonoids
could not be ascribed to an interaction with GABA-benzodiazepine receptors, since it was not
counteracted by the benzodiazepine antagonist flumazenil. To the contrary, the anxiolytic effect of
chrysin, which was blocked by the injection of flumazenil, could be linked to an activation of the
GABAA receptor unit.

11.2 TOXICITY AND SIDE EFFECTS OF CHAMOMILE

PREPARATIONS AND INDIVIDUAL CHAMOMILE ACTIVE
PRINCIPLES
11.2.1 ACUTE

AND

SUBACUTE TOXICITY

In the United States, chamomile oil has the GRAS status (generally recognized as safe) and is
admitted for food and cosmetics by the FDA.
The LD50 of chamomile oil exceeds 5 g/kg weight for acute oral toxicity in rats and acute
dermal toxicity in rabbits [87]. Jakovlev and Schlichtegroll published values summarized in Table
11.9 [62]. Both the total chamomile oil and ()--bisabolol proved to have almost no acute toxicity,
unlike the two synthetic azulenes.
The extremely low toxicity of ()--bisabolol after oral administration was confirmed later
[41]. In dogs and Rhesus monkeys, tolerance of ()--bisabolol after oral application was good.
Undesirable effects were observed only with high doses. Doses of 12.615.9 ml/kg caused retching
and vomiting; therefore, a determination of LD50 with dogs was not possible.
A 4-week subacute test in rats and dogs resulted in a toxicity of 1.0 and 2.0 ml ()-bisabolol/kg. The prenatal development of rats and white New Zealand rabbits was not influenced

TABLE 11.9
Acute Toxicity According to Jakovlev and Schlichtegroll [62]
Substance
()--Bisabolol
Guaiazulene
Acidified sulphonic natrium of
guaiazulene
Essential chamomile oil
Phenylbutazone
Indometacin

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LD50 mouse, mg/kg, oral

administration
11,350
1,540

LD50 rat, mg/kg, oral

administration
14,850
6,380

1,300

625
24

1,550
10,00020,000
530
24

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by oral doses up to 1 ml/kg. None of the tested dosages caused any deformations. Intolerance was
only observed with doses that were toxic for the adult animal by itself (approx. 3.0 ml/kg) [41].
The LD50 of cis-enyne dicycloether was determined in mice to be 670 mg/kg [16]. A pharmacological test of an aqueous chamomile extract (freeze-dried extract from 5 g chamomile flowers
with 100 ml boiling water) did not show acute toxicity even in a dose of 1440 mg of extract/kg
applied intraperitoneally [24].

11.2.2 SKIN REACTIONS (CELL-MEDIATED ALLERGY TYPE IV)

Literature reports about irritative and allergic skin changes (contact dermatitis) as well as reactions
of the respiratory tract and the mucous membranes (rhinitis, conjunctivitis, anaphylactic shock) are
very inconsistent. A report about anaphylactic shock [13], supposedly caused by a chamomile
preparation, gave reason to include chamomile flowers in a handbook of toxic plants and plant
poisons. Hausen, University of Hamburg, re-examined this incident and stated that Chamomila
recutita plays quite an unimportant role among other environmental allergens [42, 44]. Even before
his investigations, it had been shown that hairless mice tolerated undiluted chamomile oil without
any primary skin irritations [116], whereas a moderate irritant effect on the intact and scarified
skin of rabbits was observed 24 hours after application. The same authors [116] as well as Kligman
[70] could not find any skin irritation 48 hours after applying a small cloth soaked with chamomile
oil on persons. Further reactions such as sensibilization or phototoxic effects could not be confirmed
either, whereas Beetz had provoked contact dermatitis by applying pharmaceutical and cosmetic
preparations containing chamomile [12].
According to Hausen, 46 of 51 reports on contact dermatitis by chamomile do not stand a
critical re-examination [44]. In only five of these studies, a botanical identification was carried out;
however, a determination of the origin or chemical type was never made. In at least 21 reports it
was quite obvious that the contact allergies were caused by Anthemis species (particularly Anthemis
cotula, stinking mayweed, dog chamomile). In English-speaking countries, very often there is no
linguistic differentiation between genuine chamomile (Matricaria recutita) and Roman chamomile
(Chamaemelum nobile (L.) All.). Both species contain contact allergens. The most potent in this
context is the linear sesquiterpene lactone anthecotulide from A. cotula, which has strong contact
allergenic activity in sensibilization tests. Up to 1.8% anthecotulide was found in A. cotula, which
often contaminates wild collections. Yamazaki et al. [128] claimed to have isolated 7.3% (!)
anthecotulide from Matricaria recutita L. One of the authors of this chapter (P.I.) asked the curator
of the Herbarium of the University of Texas, Austin, to redetermine the voucher specimen of
Yamazaki et al. As suspected, it was actually Anthemis cotula L. [121].
Hausen showed in Freunds complete adjuvant (FCA) test that anthecotulide was either missing
completely in cultivated chamomile or it was contained in a concentration of 0.0030.01% only,
viz. in chamomile of Argentine origin (bisabolol oxide B type). Such low concentrations are not
sufficient for irritative skin reactions. A test of 12 chamomile constituents (e.g., matricin) using
animals sensibilized with a total chamomile extract turned out to be negative [42].
Chamomile preparations as used in several studies very likely contained preservatives, ointment
bases, etc. Some additives known to be allergenic could have given falsely positive results regarding
the active principles of a chamomile preparation causing allergy after skin contact or inhalation.
Hausen [42] stated: The results [of his own experiments] are thus in good correlation to the rareness
of cases observed [in the Department of Dermatology, University of Hamburg, Germany] of a
specific hypersensitivity to genuine chamomile.
Nevertheless, pollen allergy (pollinosis) caused by chamomile pollen was found relatively often
due to multiple response to Compositae pollen (pollen of Asteraceae). This pollen allergy cannot
be excluded completely when applying chamomile pharmaceuticals, since soluble antigenes of the
pollen exines could possibly be found in extracts. Steam inhalation of chamomile flowers is most
likely to cause allergies. A publication in the American Journal of Contact Dermatitis by Bjoern

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M. Hausen summarized the results of 10 years experience and experimental testing concerning
the Compositae Allergy [43]. According to the patch test result, 3.1% of 3871 allergic patients
showed a positive reaction towards a Compositae mixture consisting of ether extracts from feverfew,
Arnica montana, German chamomile, yarrow, and tansy. In order to provoke a positive patch test,
the concentration of the German chamomile extract had to be five times higher than that of Arnica.
In individual patch tests, 70.1% responded positively to feverfew and 56.5% to German chamomile.
Hausen suggested including at least five constituents in allergy test mixtures. He considered not
only the sesquiterpene lactones but also polyynes probably to be responsible for the allergic
reactions.
Recently, Jablonski and Rudzki reported clinical observations on 540 eczema patients who
were treated with chamomile concentrate in the Dermatological Clinic in Warsaw [59]. Patients
with a positive reaction to various standard substances in the epicutaneous test responded negatively
to Kamillosan concentrate in all 540 cases. This positive result regarding Kamillosan was ascribed
to the fact that anthecotulide was absent.

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Urbach, F., Forbes, P. D. (1973) Report to RIFM 18.3.73, ref. in Habersang, S., Leuschner, F., Isaac,
O., Thiemer, K. (1979) Planta Med. 37, 115.
Verzr-Petri, G., Szegi, J., Marczal, G. (17979) Acta Pharm. Hungarica 49, 13.
Wagner, H., Kimayer, W. (1957) Naturwiss. 44, 307.

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119. Weiss, R. E. (1982) Zschr. Phytotherapie 3, 439.

120. Weiss, R. F. (1974) Lehrbuch der Phytotherapie, Hippokrates-Verlag, Stuttgart, Germany.
121. Wendt, T. (2003) Private communication (Plant Resources Center, Herbarium, University of Texas,
Austin).
122. Wolfmann, C., Viola, H., Wasowski, C., Levi de Stein, M., Silveira, R., Dajas, F., Medina, J. H.,
Paladini, A. C. (1995) Journ. Neurochem. 65, 167.
123. Wolters, B. (1969) Planta Med. 17, 42.
124. Wolters, B. (1975) Dtsch. Apoth. Ztg. 115, 213.
125. Wolters, B. (1976) Dtsch. Apoth. Ztg. 116, 667.
126. Wurm, G., Baumann, J., Geres, V. (1982) Dtsch. Apoth. Ztg. 122, 2062.
127. Yamasaki, H., Irino, S., Uda, A., Uchida, K., Onho, H., Saito, N., Kondo, K., Jinzenji, K., Yamamoto,
T. (1958) Nippon Yakurigaku Zasshi 54, 362; ref. in Chem. Abstr. 53, 10525 (1959).
128. Yamazaki, H., Miyakado, M., Mabry, T. J. (1982) J. Nat. Prod. 45, 508.
129. Zajz, K. A., Arkadjewna, H. W., Iljina, W. A. (1975) Farmatsiya (Moskva) 24, 41, ref. in Isaac, O.,
Kristen, G. (1980) Med. Welt 31, 1145.
130. Zanoli, P., Avallone, R., Baraldi, M. (2000) Fitoterapia 71 (Suppl. 1), S117-S123.
131. Zierz, P., Kiessling, W. (1953) Dtsch. Med. Wschr. 78, 1166.
132. Zierz, P., Lehmann, A., Craemer, R. (1957) Hautarzt 8, 552.
133. Zita, C. (1955) Cas. Lk. ces. 94, 203, ref. in Isaac, O. (1979) Planta Med. 35, 118.
134. Ramadan, M. (2005) Dissertation, Marburg/Lahn, Germany.

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Use and
12 Traditional
Therapeutic Indications
Heinz Schilcher
CONTENTS
12.1 Traditional Use
12.2 Clinic and Practice
12.2.1 Preliminary Remark
12.2.2 Dermatology
12.2.3 Stomatology
12.2.4 Discipline of Medicine Dealing with Ear, Nose, and Throat
(Otolaryngology)
12.2.5 Radiation Therapy
12.2.6 Pulmology
12.2.7 Pediatrics
12.2.8 Gynaecology
12.2.9 Gastroenterology
12.3 Proof of Effectiveness by Means of Fluvography, Reflex Photometry, and
Profilometric Judgment
12.4 Galenic Preparations of German Chamomile
References

12.1 TRADITIONAL USE

Chamomile has been known for centuries and is well established in therapy. In traditional folk
medicine it is found in the form of chamomile tea, which is drunk internally in cases of painful
gastric and intestinal complaints connected with convulsions such as diarrhea and flatulence, but
also with inflammatory gastric and intestinal diseases such as gastritis and enteritis.
Externally chamomile is applied in the form of hot compresses to badly healing wounds, such
as for a hip bath with abscesses, furuncles, hemorrhoids, and female diseases; as a rinse of the
mouth with inflammations of the oral cavity and the cavity of the pharynx; as chamomile steam
inhalation for the treatment of acne vulgaris and for the inhalation with nasal catarrhs and bronchitis;
and as an additive to baby baths. In Roman countries it is quite common to use chamomile tea
even in restaurants or bars and finally even in the form of a concentrated espresso. This is also a
good way of fighting against an upset stomach due to a sumptuous meal, plenty of alcohol, or
nicotine. In this case it is not easy to draw a line and find out where the limit to luxury is.

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12.2 CLINIC AND PRACTICE

12.2.1 PRELIMINARY REMARK
The suitability of the empirical application of chamomile flower has been confirmed by intense
research work over the last years. As a matter of fact, however, experience has shown that a usual
chamomile tea domestically produced with boiling hot water only contains a small portion (13%)
of the essential oil to be found in the drug [30, 34]. The important constituents of the essential oil
with an antiphlogistic effect are not water soluble and remain in the chamomile flowers. One part
of the essential oil evaporates. But the tea does contain a number of water-soluble flavonoids with
a spasmolytic and according to latest tests also an antiphlogistic effect if locally applied [14].
A systematic clinical research of chamomile preparations only started in the 1920s. In 1921 a
chamomile extract under the name Kamillosan was produced and introduced into trade. This made
available a preparation containing all essential constituents of chamomile, viz., chamazulene in the
form of the prestage of Matricin, ()--bisabolol (INN: levomenol), bisabolol oxides, cis- and transspiroether, and flavonoids. Kamillosan is produced from the chamomile varieties Degumille (DBP
24 02 802) and Manzana, being rich in azulene and bisabolol. One hundred milliliters of extract
contains at least 150 mg of apigenin-7-glucoside, at least 150 mg of essential oil from chamomile
flowers, at least 50 mg of levomenol, and at least 3 mg of prochamazulene/chamazulene (determined
and calculated as chamazulene).
The following section reports the research results of this standardized alcoholic chamomile
extract. Comparative tests with other chamomile preparations, with the exception of a few other
tests, especially with alcoholic or aqueous chamomile extracts were not available before 1998. The
most important components are chamazulene with an undisputed antiphlogistic effect [31] as well
as ()--bisabolol, a sesquiterpene alcohol with antiphlogistic, antibacterial, antimycotic, ulcusprotective, and musculotropical-spasmolytical properties. Both of them are main constituents of
the essential oil. The chamomile flavones have a musculotropical, a spasmolytical, and an antiphlogistic effect if locally applied. Further important active principles are the bisabolol oxides A and
B, cis- and trans-spiroether, coumarins, and mucilage.
The therapeutic value of chamomile preparations is not just based on one main active principle
but on the combination of many individual ones (their effects were proved both clinically and by
animal experiments and combine a total effect suitable for a wide range of indications). A chamomile
extract containing all components in an optimum concentration should be given preference to a
usual domestic infusion. When diluting such an extract with hot water the lipophile constituents
are also partly incorporated in the tea, being most suitable both for internal as well as for external
application. In addition the concentrated form of the chamomile extract makes use exceeding the
usual chamomile therapy possible.
The proven antiphlogistic effect is therapeutically used by various specialized disciplines on a
broad basis and in different ways. A particularly favorable judgment should be passed on the fact
that the corresponding preparations can be applied both internally and externally.

12.2.2 DERMATOLOGY
Prof. Born (Dermatological Clinic in Freiburg) describes the effect as soothing and antiphlogistic.
A chamomile extract is, for instance, applied for the irrigation of undermined margins of a wound,
pouches, sinus tracts, and hip baths, correspondingly diluted or in concentrated form for swabbing
inflammatory lesions of the mucosa [4]. It is duly emphasized that, as experience has shown,
chamomile preparations are willingly accepted by the patient; medically, however, there is a wellfounded understandable reserve, especially in view of allergies appearing occasionally. If an appropriate extract is applied there is no reason for such doubts. In their review article, Evidence for
the Efficacy and Safety of Topical Herbal Drugs in Dermatology: Part I: Anti-Inflammatory Agents,
Hrmann and Korting [29] came to a similar conclusion in 1994.
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This statement clearly shows that from the medical point of view preference is always given
to a standardized finished medicament compared with the usual chamomile preparations, particularly with external treatment of infected tissues.
According to Weitgasser [60], in dermatology mainly acute suppurative dermatoses of different
genesis needing an additional treatment with baths or fomentions/stupes are possible as indications.
A chamomile extract leads to good therapeutic success in the case of acute suppurative dermatoses
such as dermatitis caused by contact allergic exanthemata, intertrigo, ulcus cruris, and eczemas
as well as with diseases of the mucosae such as stomatitis, pemphigus vulgaris, and others.
After a short treatment time relief is noticed and complaints are minimized. In this connection the
cooling effect causes a particularly pleasant feeling. The antiphlogistic and slightly anaesthetizing
effect of chamomile extract makes the basic therapy considerably easier. In a controlled doubleblind study the clinical effectiveness of the medicament Kamille-Spitzner was examined [23]. The
drying and epithelizing effect on suppurative dermatoses after an abrasive tattooing was taken as
an objective study parameter. Statistically both the reduction of the discharging wound area and
the drying tendency were marked more heavily than in the placebo group.
Within 2 days the application of fomentions led to a considerable improvement of the inflammatory symptoms of dermatitis statica and dermatitis caused by contact. In a unilateral comparative
study the fomentions with the standardized chamomile medicament turned out to be superior to
those applied with salt solution. The local tolerance was very good; side effects were not observed
[15, 43]. Partial baths, rinses/irrigations, and fomentions with chamomile extracts as well as the
use of ointments also led to a quick disinfection of infected wounds and ulcers such as ulcera cruris
[7, 13, 21, 24, 28].
After a dermabrasion of the face, especially after dermashaving, a good smooth granulation
and epithelization of the skin could be observed as a positive effect with chamomile extract [22].
Decubitus ulcers, frequently found with paraplegics, are successfully treated with appropriate
chamomile bath additives. A special advantage of this form of application is that it does not cause
any pain. When judging the therapeutic success, the rapid reduction of the bad smell due to the
necrotizing inflammation also plays an important role. The chamomile bath has also proved to
be a success with the local treatment of deep second-degree burns. Apart from an accelerated
cleansing process of a wound a significant improvement of the granulation is also observed. Deep
necroses are excised; superficial ones heal without proteolytic ferments [12].
Physicians report from observational studies and case studies concerning experiences with
Kamillosan Crme under practice conditions that the effectiveness and tolerance of the preparation
are very good in more than 95% of cases. As with long-term topical application of corticosteroids,
the majority of the interviewed people had already noticed side effects such as atrophy, teleangiectasiae, etc. The product was classified as a suitable supplementary therapy and as a possibility
of eliminating corticosteroids. According to the indications the elimination ranges from 20100%,
depending on the group of patients.
A controlled clinical study with 161 patients suffering from inflammatory dermatoses on their
hands, lower arms, and lower legs (irritative-cumulative dermatitis caused by contact, neurodermitis,
allergic eczema caused by contact, lower leg eczema, dyshidrotic and seborrhoic eczema) had
already been conducted before the interview action. In a unilateral comparative study it could be
shown that an interval therapy with Kamillosan ointment and 0.25% hydrocortisone ointment is
superior to the single therapy with 0.75% fluorcortinbutylester and equieffective with 5% bufexamac
ointment [54].
Another use for applying chamomile extract refers to diseases of the anal regions. Here partial
baths have a particularly favorable influence on pruritus ani, the perianal eczema of different genesis,
and external fistulae [20]. The same good results were achieved by hip baths after anal operations,
above all after operations of fistulae. Chamomile extract is also recommended for partial hand
baths, especially for the after-treatment of hand injuries and hand operations [28]. For the preoperative cleansing of the intestine, enemas are recommended, containing chamomile as an essential

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component and protecting against irritations of the mucosa [47]. In a comparative study an irritative
dermitis caused by contact with sodium lauryl sulphate and treated with Kamillosan Creme and
0.1% of hydrocortisone acetate, incorporated into the Kamillosan ointment base, and the antiphlogistic effect of the three test substances was measured by means of profilometry in view of the
reduction of the roughness of the skin [35].

12.2.3 STOMATOLOGY
In dental and oral medicine, as well as in orthodontics, therapy with chamomile extracts is an
essential component of the medicamentous therapy for the treatment of gingivitis, stomatitis ulcerosa, and stomatitis aphtosa, i.e., for all inflammatory diseases of the gingiva and oral mucosa.
Here the treatment with oral baths is most important, whereas chamomile steam inhalation is used
after radical operations in the maxillary sinus, causing a very pleasant feeling [10, 36]. In a review
publication about the most important herbal medicinal plant products with inflammation activities
to the oral cavity and as an adjuvans for an improvement of the resistance of the oral mucosa,
Schenk [50] comes to the conclusion that two of the chamomile preparations analyzed by him
belong to the more suitable products that can be compared with sage tincture. At the same time,
however, he also criticizes the lack of clinical tests in the region of the oral cavity.
Suitable extract preparations may successfully be applied with refractory diseases of the oral
mucosa and the gingiva such as ulcers and aphtae. Decubitus ulcers caused by tartar, films (on the
teeth), or badly fitted prostheses disappear quickly. Besides the alcoholic extract, a chamomile
ointment can also be used in the region of the oral mucosa, for example, for the massage of gingiva,
which proves to be favorable for the treatment of parodontosis [18, 60].
In the Centre for Dermatology and Venerology of the University of Frankfurt/Main, 78 outand inpatients suffering from different skin diseases and diseases of the mucosa were treated with
the product base and rinses, especially irrigations produced from a chamomile extract, over a period
of 27 months.
All patients with diseases of the oral mucosa noticed a relief of their symptoms as well as a
pleasant cooling effect quickly. The durable and intense influence on existing bad breath (halitosis)
could be objectified. On top of that the pains of those patients suffering from habitual aphtae eased
remarkably, especially after eating [43]. Inflammatory diseases of the oral mucosa and the throat
region (pharynx) can be treated successfully by applying Kamillosan oral spray [10].

12.2.4 DISCIPLINE OF MEDICINE DEALING

(OTOLARYNGOLOGY)

WITH

EAR, NOSE,

AND

THROAT

Chamomile therapy is used in otolaryngology as much as in dermatology. First tonsillectomies

have to be mentioned, where badly smelling coatings are left for about 10 days. A rinse with
chamomile extract leads to an antiphlogistic effect and at the same time to a deodorant effect, so
that a local antibiotic treatment finally turns out to be completely superfluous. According to Hinz
[27], a standardized ethanolic-aqueous chamomile flower extract is suitable for the adjuvant therapy
of Angina lacunaris and for the symptomatic treatment of herpangina often occurring in (early)
childhood.
Also, after operations of the paranasal sinus [27] and in cases of inflammatory and painful
esophageal diseases, chamomile extract has a pain-alleviating effect, and moreover it was ascertained esophagoscopically that the process of healing is quick. After operations and with inflammatory changes of the oral mucosa or those changes caused by radio therapy, chamomile rinses
alleviate the complaints. With disturbances of salivary secretion due to x-ray dermatitis of mouth
and throat, chamomile extract is alternatingly added to artificial saliva. Rinses of the maxillary
sinus may also be carried out only with chamomile extract without application of antibiotics [39,
40]. In an observational report of a municipal hospital, treatment with chamomile extract of at least

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10,000 patients suffering from the symptoms mentioned above did not lead to any unpleasant side
effects [39].
With sinusitis as well as with childrens occult sinusitis, chamomile steam inhalations are
recommended [42, 53]. Rinses with chamomile extract proved to be successful with postoperative
treatment and as an adjuvant therapy with radiation treatment of the oral, nasopharyngeal, and
pharyngeal cavity [16, 19]. Saller [48] reported a significant effectiveness (p < 0.01) of chamomile
flower steam inhalations, which were produced by means of an ethanol-aqueous chamomile flower
extract [48].
Patients who have to undergo radiation treatment in the nose and throat region are frequently
suffering from pharyngitis sicca, as with this method of treatment the mucosa and submucosa are
strongly attacked. Also in this case rinses, especially irrigations with chamomile extract, mean not
only a subjective improvement that is apparent by a pleasant cooling effect in the throat and by a
reduction of bad breath, but also a pharyngoscopically and laryngoscopically noticeable decongestion of the mucosa and reduction of inflammation. This is also applicable to pharyngitis of other
etiological causes. Dryness of the mouth frequently noticed as a side effect of the radiation therapy
can be significantly reduced by chamomile extract [11].
In a more recent study at an ear, nose, and throat practice, the effectiveness of Kamillosan
inhalations, especially Kamillosan oral spray, was tested with various diseases of the oral and
pharyngeal cavity (among others, uncomplicated sinusitis, pharyngitis, tonsillitis, glossitis rhinitis,
state after tonsillectomy, etc.). The duration of the treatment was between 6 and 9 days. After the
treatment with Kamillosan 96% of all patients noticed a subjective improvement of their complaints [58].
In cases of an inflammatory nasal mucous membrane, a rapid normalization with reduced or
no crust formation can be achieved by applying chamomile ointment. The smell is not a disturbing
one but is even felt to be pleasant, so that rinses, especially irrigations, can also be carried out. In
this case a particular advantage is the fact that when swallowing no unpleasant or harmful side
effects will occur [40].
Otitis externa can be treated successfully in children as well as adults by means of chamomile
extract.

12.2.5 RADIATION THERAPY

Treatment of radiation damages in the region of the mouth, nose, and throat with chamomile extract
within the scope of an adjuvant therapy was judged distinctly favorable by the patients [19,
40] as well as were the prophylactic effects [9] on the oral mucosa with patients irradiated or treated
with chemotherapeutics ascertained by a U.S. working group. The reactions of mucosa of the rectum
resulting from a highly dosed radiation therapy, frequently felt to be unendurable, can also be
treated successfully with chamomile extract. For that purpose an enema is given three times a week;
besides antiphlogistic properties, this also has a mild cleaning effect [3].
In gynecological radiation therapy, hip baths for the alleviation of painful skin reactions are
successfully applied as well [54].
With radiation of large skin surfaces (e.g., mastocarcinoma) radiation erythemata as far as
epidermolysis can be observed. Also in these cases application of chamomile extract leads to
alleviation of pain during the time of treatment as well as to a quick regeneration of the skin after
finishing the radiation [19].
In 1952 treatment of radiation dermatitis by means of ointment containing azulene was reported.
As there was no pure chamazulene available from chamomile at that time and as the chamomile
ointments did not have enough concentration of active principles, people used an ointment preparation with synthetic azulene (1-isopropyl-5-methylazulene1).
1

Kamillen-Bad-Robugen, Producer: Robugen GmbH, Esslingen/N, Germany.

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With the radiation of tumors of still-healthy skin, the preparation proved to be the best skin
protection so that x-ray dermatitis, even with skin already damaged by radiation, could be avoided
to a large extent.
This also referred particularly to the childs skin, which tolerated higher x-ray doses without
showing any important formation of erythemata. Badly healing ulcerations disappeared rapidly
after application of ointment containing azulene, without having to interrupt the x-ray or radium
treatment [25].
At the university hospital of Helsinki the effects of Kamillosan cream in comparison with an
ointment consisting of almond oil were tested with acute reaction of radiation with patients suffering
from a mastocarcinoma [38]. With additional treatment of chamomile cream a radiation erythema
could not be avoided completely; however, no heavy reactions occurred with the chamomile cream
they could only be observed later, at the end of the radiation therapy.

12.2.6 PULMOLOGY
In pulmology chamomile extract is appreciated for use as an inhalation treatment due to its
established antiphlogistic effect. With patients suffering from chronic bronchitis with or without
obstruction, after an inhalation treatment therapeutic effects in the tracheobronchial system could
be proved in a test of longer duration. The healing process of the inflamed bronchial mucosa is
improved, and a bronchial restriction of the lumen possibly existing at the same time goes down.
Inflammable swellings of the mucosa of a nonallergic and abacterial nature caused primarily
by noxious agents (just think of the bronchial stimulus states due to chronic inhalation of tobacco
smoke) respond well to inhalation therapy by means of chamomile extract [54].

12.2.7 PEDIATRICS
In pediatrics the protective effect of chamomile preparations on skin and mucosa for babies and
infants as well as the antiphlogistic property with diseases of these tissues is most important and
well known.
Chamomile extract is outstandingly suitable for delicate skin having the tendency of being dry
and forming eczemata.
According to a pediatricians open report, very good results were achieved with using chamomile ointment for the treatment of napkin dermatitis. In this practice the effect of Kamillosan
ointment on the treatment of various kinds of dermatitis was tested with 76 babies (between 1 and
10 months) and little children: 49 children had napkin dermatitis, especially an inflammation of
the skin in the region where napkins are used; 9 of 22 cases healed up completely within a week;
another 10 improved considerably. Special emphasis is placed on easing off all complaints such as
pains and itching, which affect the general condition very much. Babies eczemas and perioral
dermatitis could also be influenced positively, although within the short time of treatment according
to expectations only partial success was achieved [56].
In pediatrics the antiphlogistic effect with inflammations of the mucosa is mainly used for the
treatment of sinusitis. Principally the exudative and festering sinusitis is, also in pediatrics, a range
of indication for chamomile steam inhalation being one of the most effective remedies. With the
inhalation of chamomile steam, produced by boiling chamomile flowers moderately in a lot of
water, allergic symptoms can very occasionally be caused by evaporating pollen allergens. Normally,
however, inhalation of chamomile steam produced from an alcoholic extract caused no allergic
reaction.
With more comprehensive defects of substance and surfaces of inflammation in the region of
skin and mucosae, chamomile baths or irrigations are not only useful for the regeneration of the
injured integument, but were also subjectively found to give a pleasant feeling. The chamomile
bath is an essential part of the treatment of sensitive skin in the anal and genital areas of young

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babies, but is also meant for cleaning wound and burn surfaces as well as for skin defects and those
of the mucosa (Lyell syndrome).
In pediatrics chamomile extract therapy is advisable in the following cases [52, 53]:

For sensitive skin care of babies and immobilized children as well as seriously ill,
chronically ill, and disabled children, mainly suffering from immobilized cerebral pareses, and wetting and defecating the bed.
For the treatment of an inflamed skin or skin defects. The main fields of indication are,
for example, dermatitis ammoniacalis, scald and burn areas and exfoliative dermatitis.
For the treatment of inflammations of the nose and the paranasal sinus by application of
a chamomile bath and inhalation.

12.2.8 GYNAECOLOGY
According to reports of various gynaecological hospitals, chamomile extract proves to be a suitable
remedy for the treatment of bartholinitis, vulvitis, and mastitis and in rare cases secondarily healing
episiotomies [10].
Hip baths and irrigations are principally indicated for the postoperative treatment of vaginal
operation wounds [32, 33] as well as for the therapy of inflammable diseases in the genital area.
Reference 44 reports about the antiphlogistic effect of Kamillosan ointment in comparison with
a nonsteroidal ointment in case of episiotomies, with colpitis senilis, and about the improvement
of the healing of wounds after surgical operations carried out by laser in gynecology after taking
a chamomile (hip) bath.

12.2.9 GASTROENTEROLOGY
The spasmolytic and antiphlogistic effects of chamomile products are taken advantage of when
treating gastrointestinal diseases of different kinds. Acute gastritis and enteritis, for example, are
regarded as empirical fields of indication for chamomile. Colitis can also be treated successfully
with chamomile, and irritations of the colon, for example, respond particularly well if such a state
has developed from chronic constipation coming along with spasms. The effect of chamomile
extract with diseases of the stomach and the duodenum was clearly proved by a number of tests.
Thus, gastro-bioptic [6, 24, 41] and cytologic [8, 37, 61] tests as well as controls of the gastric
juice were carried out [8, 41].
In a multcenter study of 104 outpatients with complex complaints of pressure on the stomach,
sensation of repletion, eructation, heartburn, loss of appetite, nausea, and sickness without any
corresponding organic findings, a 6-week therapy with Kamillosan was carried out. Further specific
medicaments were excluded. It was proved that the most frequent symptoms showed the best rate
of success, always provided the symptom in question disappeared completely. As expected, there
was the least influence on loss of appetite but 61% of the cases could still be influenced. Side
effects and incompatibilities were found in no cases [57]. This means that with mostly nonspecific
vegetatively overlapped gastric troubles, the therapy with Kamillosan only without organic findings
is most suitable.
According to Weiss [59], with different modes of gastric troubles that can be classed under the
general term of dyspepsia, the internal administration of chamomile tea or preparations from
chamomile extracts is appropriate. With gastric erosions or gastric ulcers the so-called Roll
method of treatment is recommended, in which the patient, after drinking the chamomile tea, rotates
his prone position every few minutes. Apart from the spasmolytic and thereby mainly subjectively
analgetic effect, the conducive effect of chamomile to the healing of wounds is much better, as
experience has shown. In view of the side effects turning up quite often with the application of
modern acid blockers of the cimetidine or ranitidine type (H2 antagonists) and the relatively high

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rate of relapse, the chamomile rotation method, which can also be combined well with traditional
antacida if necessary, is currently still quite justified [51, 59].
In pediatrics chamomile extract is successfully applied due to its carminative and spasmolytic
effect with diseases of the gastrointestinal tract and the effect as such is said to set in immediately
after taking the preparation [53]. A comprehensive summary of all therapeutic possibilities of
chamomile preparations with diseases of the gastrointestinal tract was published by Schilcher [51].

12.3 PROOF OF EFFECTIVENESS BY MEANS OF FLUVOGRAPHY,

REFLEX PHOTOMETRY, AND PROFILOMETRIC JUDGMENT
A publication issued in 1982 reported about successful tests to objectively prove the effectiveness
by means of fluvography according to Hensel [26] and the transcutaneous measurement of oxygen
according to Eberhardt and Mindt [17]. Chamomile extract containing the active principles of
chamomile in a standardized high concentration (according to manufacturers indications being
regarded as effective1) was applied on 10 resp. 3 volunteers. Provided the work is done accurately,
both testing methods are reliable and objective.
The fluvographical findings achieved after the chamomile extract had an effect showed a
reduction of the (blood) circulation of the skin in all 10 cases, manifesting an antiphlogistic effect.
Likewise, pO2 of the skin of the 3 testees decreased as well under the influence of the tested
chamomile extract. Although only the hemodynamic part of the antiphlogistic effect can be covered
by the reduction of blood circulation of the skin, the findings can be harmonized well by the
empirical application of chamomile [55].
The objective proof of the effectiveness of a chamomile cream in comparison with a hydrocortisone ointment was also measured precisely by means of reflex photometry [2]. The medium
AUC values for the three test substances differed significantly: 56.5 for the neutral cream foundation,
70.3 for the Kamillosan cream, and 101.4 for the hydrocortisone ointment. Thus, in this test system
the anti-inflammatory effect of Kamillosan cream reached 69% of the effectiveness of the hydrocortisone preparation [2].
As a third objective measuring system to judge the therapeutic effect of a dermatologic externum
the reconstruction of the anatomical structure of the epidermis including the corneous cellular layer
is besides the fading of an erythema also suitable to be covered objectively. For this the
dermatological university clinic in Bonn used a surface measuring instrument as it is applied in
metallurgy to judge the roughness of metal surfaces [45]. This so-called profilometric judgment
was taken as a comparing study of Kamillosan ointment, the galenic basis of the ointment, and
an ointment with 0.1% hydrocortisone acetate. Of the three ointments only the Kamillosan
ointment had a significant smoothing effect compared with the other two test preparations [45].

12.4 GALENIC PREPARATIONS OF GERMAN CHAMOMILE

The following preparations are produced from the entire plant:
1. From fresh aerial (aboveground) parts of Matricaria recutita L. a fresh press juice is
obtained, that is mainly sold in health food stores.
2. Dried, herbal parts, the so-called chamomile herb, are finely cut and packed in filter tea
bags and sold as foodstuff. Usually the herb is cut after harvesting the flower heads two
or three times. The proportion of flower heads in the mixture normally is 5 to 20%.
3. From dried or (more rarely) fresh chamomile flower heads a blue volatile oil is obtained
by various steam distillation techniques. Chamomile (essential) oil is used for cham1

Kamillen-Bad-Robugen, Producer: Robugen GmbH, Esslingen/N, Germany; new trade name is Kamillin -bath.

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TF4015_book.fm Page 273 Wednesday, April 6, 2005 12:17 PM

4.

5.
6.

7.

8.
9.
10.
11.

omile ointments, creams, and spray preparations. Additionally, it is technically used for
the standardization of ethanolic aqueous extracts (chamomile tincture).
Dried and pure chamomile flower heads (purified of stems) are used for infusions and
herbal teas. Pharmacopoeia-grade chamomile flower heads have to be proved for a
minimum content of volatile oil according to the pharmacopoeial monograph.
Sterile aqueous extracts of pharmacopoeial-quality flower heads are used for eyedrops,
mostly in single-dose quantities.
Fluid extracts and tinctures with varying ethanolwater mixtures are prepared from dried
or deep frozen flower heads, fluid extracts usually being in the ratio ethanol/water 1:1,
tinctures in the ratio 1:5 or 1:10. Extracts of high quality should be standardized on
constituents which contribute to efficacy.
Examples for a well-standardized extract read as follows:
100 g of an ethanolic-aqueous extract contain 150300 mg of blue essential chamomile oil with 50 mg ()--bisabolol and 3 mg chamazulene together with 150300
mg apigenin-7-glucoside or 100 g of an ethanolic-aqueous extract contain 170 mg
of blue essential chamomile oil with 50 mg ()--bisabolol, along with 1040 mg
free apigenin, and as a third example: 100 g of an ethanolic-aqueous extract contains
200 mg of blue essential chamomile oil, and additionally 150 mg apigenin-7-glucoside.
For the preparation of chamomile gels, ointments, and creams the ethanol-aqueous
extracts are concentrated to viscous extracts (Latin: extractum spissum) and incorporated
into the respective dermatologic vehicles.
Through further and total evaporation of the liquid of a chamomile extract a dry extract
is obtained that is used for the preparation of tablets, capsules, and coated pills.
Chamomile tablets are usually prepared of dried and purified powder of chamomile
flower heads.
For the preparation of chamomile bath oils chamomile flower heads of pharmacopoeial
quality are extracted with natural plant oils or neutral oils (e.g., Miglyol).
For anthroposophic chamomile preparations the roots of German chamomile are extracted
with ethanolic aqueous solvents.

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