Pharmaceutical Chemistry (ER20-12T) covers the chemical properties, purity, and analysis of drugs and pharmaceutical substances.
Core Topics
1. Inorganic Pharmaceutical Chemistry
Gastrointestinal agents (Antacids)
- Sodium Bicarbonate, Aluminium Hydroxide, Magnesium Hydroxide, Calcium Carbonate
- Mechanism: neutralise gastric acid (HA + Base → Salt + H2O)
Electrolytes
- Sodium Chloride, Potassium Chloride
- Fluid and electrolyte balance
- Normal saline = 0.9% NaCl
Haematinics
- Ferrous Sulfate, Ferrous Gluconate — iron-deficiency anaemia
- Folic Acid — pregnancy anaemia prevention
2. Organic Pharmaceutical Chemistry
| Class | Representative | Key Feature |
|---|
| Sulfonamides | Sulfadiazine | Para-amino group |
| Antitubercular | Isoniazid (INH) | Isonicotinic acid hydrazide |
| Antimalarials | Chloroquine | Quinoline ring |
| Local anaesthetics | Lignocaine | Amide linkage |
| Barbiturates | Phenobarbitone | Barbituric acid ring |
3. Medicinal Chemistry Basics
Structure-Activity Relationship (SAR) — how chemical structure affects pharmacological activity. Example: para-position substitution in sulfonamides increases antibacterial activity.
Drug stability
- Hydrolysis — most common degradation
- Oxidation — Ascorbic acid, catecholamines
- Light degradation — Nifedipine, Tetracycline
4. Analytical Methods (Indian Pharmacopoeia)
Physical tests — melting point (identity / purity), solubility, colour and odour.
Chemical tests — acid-base titration, redox titration, precipitation reactions.
Common limit tests in IP — Arsenic, Chloride, Sulfate, Heavy metals.
Official Pharmacopoeias
- Indian Pharmacopoeia (IP) — official Indian standard
- British Pharmacopoeia (BP) — UK standard
- United States Pharmacopeia (USP) — US standard
- Extra Pharmacopoeia (Martindale) — drug information reference
FAQ
What is the Indian Pharmacopoeia?+
Official book that specifies standards for drugs, excipients, and medical devices in India. Published by IPC.
What is SAR?+
Structure-Activity Relationship — how molecular changes affect drug activity.
What is a limit test?+
Test confirming specific impurities are within acceptable limits.
Most common drug degradation?+
Hydrolysis — especially esters and amides in aqueous formulations.
Why is melting point important?+
Pure substances have sharp melting points. Impurities lower and broaden the range.