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Quality Control & Standardization
Of Herbals
Guidelines For Stability Testing Of Herbal Drugs
By
Kaushal Kumar
TABLE OF CONTENTS
01 02 03 04
Introduction Need For
Stability
Preparation Reason For
Stability
Drug stability is defined as the ability of the
pharmaceutical dosage form to maintain the
Physical, chemical, therapeutic and
microbiological properties
during the time of storage and usage by the
patient.
INTRODUCTION
☺ Well being of the patient & manufacturer by
ensuring product quality.
☺ For selection od adequate formulation,
determination of shelf-life and storage conditions.
☺ Preparation and substantiation of the claimed
shelf life for the registration dossier.
☺ To provide evidence on how quality of drug
variance with time under influence of environment.
Need For Stability Studies
Herbal products are complex in nature due to high number of constituents of
different chemical classes.
Classified entirely on basis of the API.
EMEA, has subdivided herbal preparation's into three categories based on the
active constituents in the product.
Herbal Drugs & Preparations
Quantified Extract Other Extract
Standard Extract
Reason For Instability
Moisture &
Hydrolysis
Reaction with water leads to
degradation of compounds
Oxidation Geometric
Addition of oxygen, radical
formation & decomposition of
product
Trans & cis form, one form
may be more therapeutically
active
Polymerization
Combination of one or
more mol. Forming largest
molecules
Temperature
Chemical changes
increase with increase in
temperature
Light
Chemical changes due
to exposure to light auto
oxidation of volatile oil
THANKS!
Do you have any questions?
easyconceptkaushal@gmail.com
+91 9546688666

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Guidelines for stability testing of herbal drugs

  • 1. Quality Control & Standardization Of Herbals Guidelines For Stability Testing Of Herbal Drugs By Kaushal Kumar
  • 2. TABLE OF CONTENTS 01 02 03 04 Introduction Need For Stability Preparation Reason For Stability
  • 3. Drug stability is defined as the ability of the pharmaceutical dosage form to maintain the Physical, chemical, therapeutic and microbiological properties during the time of storage and usage by the patient. INTRODUCTION
  • 4. ☺ Well being of the patient & manufacturer by ensuring product quality. ☺ For selection od adequate formulation, determination of shelf-life and storage conditions. ☺ Preparation and substantiation of the claimed shelf life for the registration dossier. ☺ To provide evidence on how quality of drug variance with time under influence of environment. Need For Stability Studies
  • 5. Herbal products are complex in nature due to high number of constituents of different chemical classes. Classified entirely on basis of the API. EMEA, has subdivided herbal preparation's into three categories based on the active constituents in the product. Herbal Drugs & Preparations Quantified Extract Other Extract Standard Extract
  • 6. Reason For Instability Moisture & Hydrolysis Reaction with water leads to degradation of compounds Oxidation Geometric Addition of oxygen, radical formation & decomposition of product Trans & cis form, one form may be more therapeutically active Polymerization Combination of one or more mol. Forming largest molecules Temperature Chemical changes increase with increase in temperature Light Chemical changes due to exposure to light auto oxidation of volatile oil
  • 7. THANKS! Do you have any questions? [email protected] +91 9546688666