Pharmacognosy

Professor in Pharmacy

Tuesday, June 17, 2025

Introduction History scope & development to Pharmacognosy

 Introduction to Pharmacognosy:


Pharmacognosy: is a branch of science that deals with crude drugs. Crude drugs are those substances that are obtained from Plants, Animals, and Mineral Sources.

History of Pharmacognosy:

Pharmacognosy is the study of medicinal drugs derived from plants, animals, and other natural sources. It is one of the oldest branches of pharmaceutical sciences, having evolved significantly over time.

🔹 Ancient Period

·         Earliest Records:

o  Pharmacognosy has roots in ancient civilizations like Mesopotamia, Egypt, India, and China.

o  Around 3000 BC, the Sumerians listed medicinal plants on clay tablets.

o  Ebers Papyrus (c. 1550 BC, Egypt) documented about 700 drugs, mostly of plant origin.

·      Indian System (Ayurveda):

o  Described in texts like Charaka Samhita and Sushruta Samhita.

o  Used herbs like Ashwagandha, Tulsi, Turmeric, and Neem.

·      Traditional Chinese Medicine (TCM):

o  Shennong Bencao Jing (~100 AD) documented hundreds of herbal medicines.


🔹 Greek and Roman Period

  • Hippocrates (460–370 BC): Considered the "Father of Medicine", emphasized natural remedies.
  • Dioscorides (1st century AD): Authored "De Materia Medica", a foundational text listing ~600 medicinal plants.
  • Galen (131–200 AD): Developed formulations called “Galenicals”, which are still referenced today.

🔹 Medieval Period

  • Arab scholars like Avicenna (Ibn Sina) compiled knowledge of Greek and Indian medicine.
  • His book "The Canon of Medicine" included numerous herbal remedies.
  • Monasteries in Europe preserved herbal knowledge through herb gardens and manuscripts.

🔹 Renaissance and Early Modern Period

  • The printing press (15th century) allowed the wide distribution of herbals (books describing plants).
  • Explorers brought new plants (e.g., cinchona bark for malaria) from the Americas, Africa, and Asia.

🔹 18th–19th Century (Scientific Era)

  • The term “Pharmacognosy” was first used in 1811 by C.A. Seydler in his thesis "Analecta Pharmacognostica".
  • Focus shifted from whole herbs to active constituents:
    • 1805: Morphine was isolated from opium by Friedrich Sertürner.
    • Followed by the isolation of quinine, caffeine, cocaine, etc.

🔹 20th–21st Century (Modern Era)

  • Advancement in analytical techniques: chromatography, spectroscopy, etc.
  • Emphasis on:
    • Phytochemistry
    • Standardization of herbal products
    • Pharmacological testing
    • Ethnobotany and ethnopharmacology
  • Interest revived in herbal medicine due to side effects of synthetic drugs and increasing antibiotic resistance.

🔸 Summary

Era

Key Highlights

Ancient

Use of herbs in Egypt, India, and China

Greek-Roman

Dioscorides’ De Materia Medica, Galen’s preparations

Medieval

Islamic and European herbals

Renaissance

Global plant exchange, early scientific study

18th–19th Century

Coining of “Pharmacognosy”, isolation of alkaloids

Modern

Analytical techniques, integration with biotechnology

 


Scope of Pharmacognosy

Pharmacognosy plays a vital role in the discovery, development, and quality control of drugs derived from natural sources. Its scope extends across multiple scientific and healthcare domains.


🔹 1. Drug Discovery & Development

  • Natural Products as Drug Sources: Many modern drugs (e.g., morphine, quinine, artemisinin) are derived from natural sources.
  • Lead Compound Identification: Plant, microbial, and marine extracts provide templates for synthetic drugs.
  • Bioprospecting: Searching ecosystems for novel bioactive compounds.

🔹 2. Herbal Drug Industry

  • Formulation of Herbal Medicines: Based on traditional systems (Ayurveda, TCM, etc.).
  • Standardization: Ensures safety, efficacy, and consistency of herbal products.
  • Regulation & Quality Control: Pharmacognosy supports authentication and purity testing of raw materials.

🔹 3. Pharmacognostic Evaluation

  • Identification of Crude Drugs: Using morphological, microscopic, and chemical methods.
  • Adulteration Detection: Ensures drug authenticity and prevents substitution or contamination.

🔹 4. Phytochemistry

  • Isolation and Characterization of Phytoconstituents: Alkaloids, flavonoids, glycosides, tannins, etc.
  • Structure–Activity Relationship (SAR) studies for drug optimization.

🔹 5. Ethnopharmacology

  • Study of Traditional Medicine: Understanding indigenous knowledge systems to find novel treatments.
  • Conservation of Medicinal Plants: Promotes sustainable use of biodiversity.

🔹 6. Biotechnology Applications

  • Tissue Culture: For mass propagation and metabolite production.
  • Genetic Engineering: Enhancing yield or quality of active ingredients.
  • Biotransformation: Using microbes or plant cells to modify compounds.

🔹 7. Cosmetics and Nutraceuticals

  • Natural extracts are used in:
    • Cosmeceuticals (e.g., anti-aging creams, hair oils)
    • Nutraceuticals (e.g., herbal supplements, antioxidants)

🔹 8. Academic and Research Opportunities

  • Ph.D. & Postdoctoral Research: In pharmacognosy, ethnobotany, phytochemistry, etc.
  • Teaching: In pharmacy, botany, and natural product chemistry programs.

🔹 9. Industrial Roles

  • Quality control analyst in herbal drug companies
  • Research scientist in pharma or biotech firms
  • Regulatory affairs expert for herbal and nutraceutical products

✅ Summary Table

Field

Role of Pharmacognosy

Drug Discovery

Source of bioactive compounds

Herbal Industry

Standardization and QC

Research

Phytochemical and ethnopharmacological studies

Education

Academic teaching and training

Industry

Product development and regulation

 


 

Development of Pharmacognosy

The development of pharmacognosy can be traced through a series of major phases that reflect the evolution of medical science, botany, chemistry, and pharmaceutical technology.


🔹 1. Traditional Phase (Ancient to Medieval Period)

  • Use of Crude Drugs: Early humans used plants and natural materials for healing.
  • Systematic Documentation:
    • Ayurveda, Traditional Chinese Medicine, and Unani were formalized.
    • Notable texts:
      • Ebers Papyrus (Egypt)
      • Charaka Samhita (India)
      • De Materia Medica by Dioscorides (Greek-Roman era)
  • Knowledge Transfer: Oral tradition evolved into written herbal manuals and pharmacopeias.

🔹 2. Empirical Phase (16th–18th Century)

  • Herbals and Botanical Classifications: Rise of scientific classification of plants.
  • Exploration & Trade: Discovery of new medicinal plants from Asia, Africa, and the Americas.
  • Pharmacy Emerges as a Profession: Herb and drug shops began to separate from general medicine.

🔹 3. Chemical Phase (19th Century)

  • Isolation of Active Principles:
    • Morphine (1805), Quinine, Caffeine, Atropine – marked a turning point.
  • Introduction of the Term "Pharmacognosy":
    • By C.A. Seydler in 1811 (Analecta Pharmacognostica).
  • Microscopic Techniques: Crude drugs began to be studied microscopically for identification and quality control.

🔹 4. Biological Phase (20th Century)

  • Standardization: Emphasis on quality control of herbal materials.
  • Bioassays: Drugs tested for pharmacological activity.
  • Formation of Regulatory Bodies: WHO, FDA, and national pharmacopeias started including herbal monographs.
  • Development of Herbal Formulations: Based on traditional and scientific data.

🔹 5. Modern Phase (21st Century)

  • Phytochemistry and Analytical Techniques:
    • Use of HPLC, GC-MS, NMR, UV spectroscopy, etc.
  • Biotechnology & Genetic Engineering:
    • Tissue culture, cloning, and transgenic plants for secondary metabolite production.
  • Global Acceptance of Herbal Medicines:
    • Increasing market for herbal drugs, nutraceuticals, and cosmeceuticals.
  • Ethnopharmacological Studies:
    • Collaboration with indigenous communities to discover new medicines.
  • Computational Tools:
    • Molecular docking, cheminformatics, and AI in natural product research.

🔸 Summary Table: Development Stages

Phase

Key Features

Traditional

Crude drug use, ancient systems (Ayurveda, TCM)

Empirical

Herbals, plant classifications, exploration

Chemical

Isolation of alkaloids, pharmacognosy term coined

Biological

Bioassays, standardization, regulatory inclusion

Modern

Phytochemistry, biotech, global herbal industry

 

Friday, February 7, 2025

Some Cardio tonic Crude Drugs

 

Synonym

Biological Source

Chemical constituent

Uses

Adulterants/ Allied Species

Substituent’s

Digitalis,

foxgloves

Digitalis purpurea Plantaginaceae

cardiac glycosides \ antiarrhythmic agent

atrial fibrillation\ digitoxin or digoxin

Digoxigenin (DIG) is a steroid found exclusively in the flowers and leaves of the plants Digitalis purpurea and Digitalis lanata. It is used as a molecular probe to detect DNA or RNA. It can easily be attached to nucleotides by chemical modifications. DIG molecules are often linked to uridine nucleotides; DIG labelled uridine (DIG-U) can then be incorporated into RNA probes via in vitro transcription. Once hybridisation occurs in situ, RNA probes with the incorporated DIG-U can be detected with anti-DIG antibodies that are conjugated to alkaline phosphatase. To reveal the hybridised transcripts, alkaline phosphatase can be reacted with a chromogen to produce a color precipitate.

Digitalis works by inhibiting sodium-potassium ATPase. This results in an increased intracellular concentration of sodium ion and thus a decreased concentration gradient across the cell membrane. This increase in intracellular sodium activates a sodium/calcium exchange pump that brings calcium ions into the cell while extruding sodium to restore its gradient across the membrane. The increased cytosolic calcium ion concentration results in increased calcium ion storage in the sarcoplasmic reticulum. Upon action potential (cardiac contraction) more calcium is released from the sarcoplasmic reticulum and this gives a positive inotropic effect (higher contractility).

Verbascum Thapsus contains candelabra trichomes while digitalis contain multicellular uniseriate trichomes or grandular trichomes

Digitalis canariensis

Digitalis cariensis

Digitalis ciliata

Digitalis davisiana

Digitalis dubia

Digitalis ferruginea

Digitalis grandiflora

Digitalis isabelliana

Digitalis laevigata

Digitalis lanata

Digitalis leucophaea

Digitalis lutea

Digitalis mariana

Digitalis micrantha

Digitalis obscura

Digitalis parviflora

Digitalis purpurea

Digitalis sceptrum

Digitalis thapsi

Digitalis trojana

Digitalis viridiflora

Digitalis also has a vagal effect on the parasympathetic nervous system, and as such is used in reentrant cardiac arrhythmias and to slow the ventricular rate during atrial fibrillation. The dependence on the vagal effect means that digitalis is not effective when a patient has a high sympathetic nervous system drive, which is the case with acutely ill persons, and also during  exercise.

Arjuna  bark,

arjun.

 

Terminalia arjuna

Arjuna consists of the dried stem bark of the plant known

as Terminalia arjuna Rob, belonging to family Combretaceae.

 

 

·         Tannins: A type of polyphenol that is found in the bark of the Terminalia arjuna tree 

        Flavonoids: A type of polyphenol that is found in the bark of the Terminalia arjuna tree 

       Triterpenoid saponins: A type of chemical found in the bark of the Terminalia arjuna tree 

        Gallic acid: A bioactive constituent found in the Terminalia arjuna tree 

         Ellagic acid: A bioactive constituent found in the Terminalia arjuna tree 

        Phytosterols: A bioactive constituent found in the Terminalia arjuna tree 

        Minerals: Such as calcium, magnesium, zinc, and copper 

 

Pacifies pitta and kapha

Heart tonic, angina, hypertension

         Cardiovascular disease: Terminalia arjuna is used to treat heart failure, ischemic cardiomyopathy, and atherosclerosis 

         Blood diseases: Terminalia arjuna is used to treat anemia and blood diseases 

        Skin conditions: Terminalia arjuna is used to treat wounds, skin eruptions, and leucorrhea 

        Asthma: Terminalia arjuna is used to treat asthma 

        Ulcers: Terminalia arjuna is used to treat ulcers 

        Diabetes: Terminalia arjuna is used to treat diabetes 

 

Side effects 

Constipation, Headache, Abdominal discomfort, Body ache, Mild gastritis, Hepatotoxicity, and Hypothyroidism.