Course Name: Pharmacognosy
Course code: Phar 2082
Module Name: Pharmacognosy and Alternative Medicine I
Module Code: 08
Course ECTS: 7
Totally required hours for the module: 189 hours
Assessment:
Seminar/Assignments/ quizzes: 35%
Laboratory report writing and written exam: 15%
Practical exam: 10%
Final Exam: 40%
Year/Semester Course is offered: Year II Semester II
Course prerequisite/s: Chemistry of Natural Products
Course description: The course is designed in such a way that the trainee gets well acquainted
with the study of the physical, chemical, biochemical and biological properties of drugs, drug
substances, or potential drugs or drug substances of natural origin as well as the search for new
drugs from natural sources. The course familiarizes trainees with the basic scientific knowledge
and skill needed to obtain and characterize active substances from natural sources. It also helps
trainees to understand and realize the fact that nature provides the origin and continuous supply
of drugs or drug substances, and think about the proper management and utilization of such
natural products.
Course objective:
After completion of this course students will be able to:
To familiarize themselves to general aspects of crude drugs, extraction and isolation
methods and the distribution, properties and uses of various primary and secondary
metabolites of plant, animal and mineral origin.
Course mode of delivery: Parallel
Course learning and teaching methods
Illustrated Lecture: 48 hours
Practical sessions: 48 hours
Tutorial: 12 hours
Seminars, assignments and presentation: 16 hours
Assessment (continuous & final): 10 hours
Independent study (alone or in groups): 45 h hours
Field visits (10 h)
Assessment techniques:
Seminar/Assignments: 10%
Quizzes/Continuous assessment: 25%
Laboratory written exam: 15%
Practical exam: 10%
Final Exam: 40%
Teachers’ and students’ role
Roles of Instructors
The instructor will be expected to:
Be a facilitator (introduce the subject; give guidance, moderate discussions,
etc.)
Read and comment assignments of students on time;
Prepare his/her lessons and deliver lectures;
Provide available and necessary reference materials;
Encourage active participation of students in the teaching learning process;
Assist students with learning difficulties and
Arrange and follow up practical sessions
Roles of Students
Students are expected to:
Engage in learning by doing (independent study, project work; group work,
etc.)
Be active learners (participate effectively in laboratory activities, in group
assignments, make presentations, write reports, etc.);
References:
Required readings (Text)
William C. Evans, George E. Trease, and Daphne Evans, Trease and Evans’
Pharmacognosy (16th ed.), Elsevier (2009).
Recommended readings
Dewick PM. Medicinal Natural Products: A biosynthetic Approach, 3rd edition. Jhon
Wiley and Sons, LTD, England 2009.
Sarker D, Latif Z, Gray A. Methods in Biothechnology Natural Products Isolation, 2nd edition,
Human Press, Totowa, New Jersey, 2006
Pulok K. Mukherejee. Quality control of herbal drugs; an approach to evaluation of
botanicals. Business Horizons pharmaceutical publishers 2002
Course schedule*
Week Contact
Topic/sub-topic/chapter/Assessments/Assignments
Hours
1&2 1. General Introduction
1.1. Definition, History and scope of Pharmacognosy (1 hr)
1.2. Crude drugs (6 h)
1.2.1. Pharmaceutical botany
1.2.2. Definition and Nomenclature of crude drugs
1.2.3. Classification of crude drugs
1.2.4. Evaluation of crude drugs
1.2.5. Types of preparations from plants
1.2.6. Schemes for pharmacognostic studies of crude drugs.
1.2.7. Official and Unofficial drugs
1.2.8. Factors affecting crude drug quality
1.3. Steps in the scientific analysis of drugs from natural resources
1.3.1. Selection of plant material
1.3.2. Taxonomic identification of the plant
1.3.3. Literature survey on the identified plant
1.3.4. Design of appropriate extraction and separation methods
1.3.5. Checking extracts/ fractions for pharmacological activity
1.3.6. Identification of classes of compounds found in the plant (phytochemical
screening)
1.3.7. Isolation of active compounds or fractions responsible for the pharmacological
activity of the plant
8hrs 2. General methods in studying constituents of crude drugs
2.1. Extraction (3 hrs)
2.1.1. Definition and the need for extraction
2.1.2. Preparation of plant material for solvent extraction
2.1.3. Choice of suitable solvents
3&4
2.1.4. Methods of extraction
2.2. Isolation and purification of active constituents (5hrs)
2.2.1. Classical methods of separation
2.2.2. Modern methods/chromatographic methods
2.2.2.1.
5,6,7,8, 29 hrs 3. Major plant constituents and their botanical sources
9,10, 3.1. Primary and secondary plant metabolites (1 h)
11&12 3.2. Carbohydrates (2 h)
3.2.1. Sugars and sugar containing drugs
3.2.2. Compounds related to sugars
3.2.3. Polysaccharides
3.2.4. Gums and mucillages
3.3. Glycosides (6 h)
3.3.1. General properties of glycosides
3.3.2. Classification of glycosides
3.3.3. Classes of glycosides: Anthraquinones, Saponins, Cardiac glycosides,
Simplephenolic glycosides, Flavonoid glycosides, Isothiocyanate glycosides,
Cyanogenetic glycosides, Coumarin glycosides, lignans
3.4. Tannins (2 h)
3.4.1. General properties and Chemistry
3.4.2. Classification: Hydrolysable, Nonhydrolysable (condensed), Pseudotannins
3.4.3. Significance of tannins
3.5. Lipids and waxes (2 h)
3.5.1. Lipids: Physical and chemical properties, Extraction methods
3.5.2. Official fixed oils/fats and their composition
Arachis oil, castor oil, almond oil, seasame oil, theobroma oil, codeliver oil etc
3.5.3. Waxes: Definition and general properties, Animal waxes, Vegetable waxes
3.6. Volatile oils (5 h)
3.6.1. Distribution and occurrence, Uses, Methods of preparation (Distillation,
Expression, Extraction with solvent, enzymatic hydrolysis), Physical
properties, Chemistry, Biosynthesis
3.6.2. Constituents of volatile oils: Hydrocarbons, Alcohols, Aldehydes, Ketones,
Esters, Phenols and phenolic ethers Oxides Peroxides Sulfur containing
compounds Nitrogen containing compounds
3.7. Resins and resin combinations (3 h)
3.7.1. General properties and chemistry
3.7.2. Examples of drugs containing resins: Rosin, Podophyllin, Jalap, Mastic,
Cannabis (Preparation, Constituents, Factors affecting the narcotic activity,
Legal aspects, Analysis), Oleoresins Oleo-gum resins, Balsams
3.8. Alkaloids (8 h)
3.8.1. Definition, Nomenclature, Occurrence, Physical and chemical properties,
Detection, Extraction and isolation
3.8.2. Classification
3.8.3. Classes of alkaloids
3.8.3.1. Ornithine derived alkaloids: Tropane alkaloids Solanaceae alkaloids,
Coca alkaloids, Pyrolizidine alkaloids
3.8.3.2. Lysine derived alkaloids: Lobelia alkaloids, Lupine alkaloids
3.8.3.3. Nicotinic acid derived alkaloids: Ricinine, Areca alkaloids, Tobacco
alkaloids
3.8.3.4. Tyrosine derived alkaloids: (1) Simple phenylethylamines and
tetrahydroisoquinolines: Mescaline, Ephedrine, Alkaloids of ‘Khat’; (2)
Colchicine; (3) Papaver alkaloids: Phenanthrene group,
Benzylisoquinoline group; (4) Emetine and related alkaloids; (5)
Tubocurarine
3.8.3.5. Tryptophan derived alkaloids: Simple indoles, Tricyclic alkaloids:
Pegamum alkaloids, Physostigma alkaloids, Ergot alkaloids (Historical
background, Life cycle of ergot, Commertial production, Chemistry and
occurrence, Biosynthesis and use, LSD), Rauwolfia alkaloids, Strychnos
alkaloids, Cinchona alkaloids, Perwinkle alkaloids
3.8.3.6. Histidine derived alkaloids: Pilocarpine
3.8.3.7. Polyacetate derived alkaloids: Hemlock alkaloids
3.8.3.8. Psedoalkaloids: Steroidal alkaloids: Veratrum alkaloids, Solanum
alkaloids, Holarrhena alkaloids, Buxus alkaloids, Purine alkaloids
(4 h) 4. Natural compounds and cancer
• Anticancer drugs of natural origin
13&14
• Natural compounds as carcinogens
