๐งช Inorganic Chemistry Unit 1 Notes (B.Pharm) Lacture -1 Impurities in Pharmaceutical substances explained with examples
๐งช Inorganic Chemistry Unit 1 Notes (B.Pharm)
๐ Introduction
Inorganic chemistry is a fundamental subject in pharmaceutical sciences. It focuses on drug purity, detection of impurities, and maintaining quality standards.
๐งฉ What are Impurities?
Impurities are unwanted substances present in pharmaceutical products that may affect their safety and efficacy.
Types of Impurities:
- Organic impurities
- Inorganic impurities
- Residual solvents
⚠️ Sources of Impurities
Impurities can originate from:
- Raw materials
- Manufacturing process
- Storage conditions
- Containers
๐ฌ Limit Test
Limit tests are semi-quantitative tests used to detect impurities within acceptable limits.
Common Limit Tests:
- Chloride
- Sulphate
- Iron
- Arsenic
- Heavy metals
๐งช Example: Limit Test for Chloride
Principle:
Chloride ions react with silver nitrate to form a white precipitate of silver chloride.
Reaction:
NaCl + AgNO₃ → AgCl ↓
Interpretation:
The turbidity of the test solution is compared with a standard solution.
- Within limit → Acceptable
- Above limit → Rejected
๐ Pharmacopoeia
Pharmacopoeia is an official reference book that sets standards for drugs.
Types:
- Indian Pharmacopoeia (IP)
- British Pharmacopoeia (BP)
- United States Pharmacopoeia (USP)
๐ฏ Conclusion
Understanding impurities and limit tests is essential for ensuring drug safety, quality, and effectiveness.
๐ฅ Watch this video to understand “Impurities in Pharmaceutical Substances” in the easiest way using daily life examples like salt, water, rice, and tea.
“Impurities in Pharmaceutical Substances explained with examples | B.Pharm Notes | PharmaEasyNotes”
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