BP106T

Pharmaceutical Inorganic and Analytical Chemistry (Theory)

L-T-P3-0-0 Credits3 Session2026-27 TypeTheory
Appears in 1 semester

B.Pharm · Sem 1 (Core)

Syllabus

5 units · 45 lecture hours
Unit1

Unit 1

7 hrs

Introduction to pharmaceutical analysis Different techniques of analysis, Methods of expressing strength of solutions, Primary and secondary standards with examples. Errors Sources of errors, types of errors, methods of minimizing errors, accuracy, precision and significant figures. Impurities Definition, types, contents and regulatory importance. Sources and types of impurities in Pharmaceuticals, limit tests for chloride, sulphate, iron, arsenic, lead, heavy metals, and modified limit test for chloride and sulphate.

Unit2

Unit 2

8 hrs

Acid-Base Chemistry and Buffer Systems in Pharmacy Definition of acids, bases, buffers, pH Scale and its significance, Buffer equation, calculation of pH for Buffer solution. Isotonicity and its application in IV Fluids and Ophthalmic Solutions. Major extra and intracellular electrolytes Functions of major physiological ions, Electrolytes used in the replacement therapy: Sodium chloride*, Potassium chloride, Calcium chloride and Oral Rehydration Salt (ORS), Physiological acid base balance.

Unit3

Unit 3

14 hrs

Acid base titrations Theories of acid base indicators, classification of acid base titrations. Preparation and standardization of titrants viz. hydrochloric acid and sodium hydroxide. Theory involved in titrations of strong, weak, and very weak acids and bases, neutralization curves. Assay of Ammonium hydroxide. Non-aqueous titrations Types of solvents used, acidimetric and alkalimetric titration using non-aqueous solvents. Preparation and standardization of acidic and basic titrants. Estimation of weakly acidic and basic substances using non-aqueous titrants, estimation of Sodium benzoate. Precipitation titrations and gravimetry sulphate by gravimetry. Complexometric titrations Classification, metal ion indicators, masking and demasking reagents, preparation and standardization of disodium EDTA. Estimation of Magnesium sulphate and Calcium gluconate*. Redox titrations Concepts of oxidation and reduction, Types of redox titrations viz. Permanganometry, Cerimetry, Iodimetry, Iodometry and titrations with potassium iodate.

Unit4

Unit 4

10 hrs

Gastrointestinal agents Acidifiers: Sodium acid phosphate and Dilute Hydrochloric acid. Antacids: Ideal properties of antacids, combinations of antacids, Sodium bicarbonate*, Aluminium hydroxide gel*. Agents promote bowel movements: Magnesium hydroxide, Sodium orthophosphate, Sodium Potassium tartrate and magnesium trisilicate. Antimicrobials: Mechanism, classification, Potassium permanganate, Boric acid, Hydrogen peroxide*, Chlorinated lime*, Iodine and its preparations. Radiopharmaceuticals Basics of radioactivity, applications of radioisotopes of Sodium Iodide I-131, Technetium-99m, Cobalt-60, Phosphorus-32 including safe handling, storage, and disposal of radiopharmaceuticals, adhering to regulatory guidelines for safety.

Unit5

Unit 5

6 hrs

Miscellaneous Compounds Expectorants: Potassium iodide, Ammonium chloride*. Emetics: Copper sulphate*, Sodium potassium tartrate. Haematinics: Ferrous sulphate*, Ferrous gluconate. Poison and Antidote: Definition, classification of antidotes, Sodium thiosulphate

Course Objectives6 points
  • The objectives of this course are to:
  • Understand the importance of errors, impurities in pharmaceuticals.
  • Comprehend the principles of buffer systems.
  • Develop skills in performing and interpreting limit tests and titrimetric analysis.
  • Emphasize the importance of inorganic compounds and radiopharmaceuticals in Pharmacy
  • Explain synthesis and analysis of inorganic compounds/products of pharmaceutical importance
Course Outcomes (COs)5 outcomes

After completion of the course student will be able to:

  1. CO1Identify sources and types of errors in pharmaceutical analysis, and impurities products
  2. CO2Apply concepts of acid-base chemistry, buffer systems with importance of electrolytes
  3. CO3Describe and differentiate various analytical techniques used in pharmaceutical analysis, including titrimetric methods, and their specific applications in quality assessment.
  4. CO4Analyze the properties, mechanisms, and therapeutic uses of gastrointestinal agents, radiopharmaceuticals, expectorants, antidotes, and other pharmaceutical compounds, illustrating their roles in therapy and safety considerations.
  5. CO5Describe the drugs used in expectorants, emetics, haemintics, poison and antidote and astringents.
Recommended References (Preferably latest editions):5 books
  1. Bentley, R. and Driver, J., Bentley and Driver's Textbook of Pharmaceutical Chemistry. Oxford: Oxford University Press.
  2. Vogel, A.I., . Essex: Pearson Education Limited.
  3. Beckett, A.H. and Stenlake, J.B., Practical Pharmaceutical Chemistry. Part I & II. London: The Athlone Press, University of London.
  4. Schroff, M.L., Inorganic Pharmaceutical Chemistry. New Delhi: Oxford Book Company.
  5. Indian Pharmacopoeia Commission, Indian Pharmacopoeia. Ghaziabad, India. Course Title Course Type

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Official AKTU syllabus

This subject is on page 21, 22, 23, 24 of the original AKTU PDF.

Official AKTU syllabus PDF ↗