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Types of Reaction Orders

Physical and Chemical Factors Influencing Chemical Degradation

Stabilization of medicinal agents against common reactions


Physical Pharmaceutics II

Other Subjects of B Pharmacy 4th Semester

Topic wise notes of:

Medicinal Chemistry I


Topic wise notes of:

Pharmacognosy & Phytochemistry I

  • Pharmacognosy: Sources, Classification, and Quality Control
  • Conservation and Cultivation of Medicinal Plants
  • Plant tissue culture
  • Role of Pharmacognosy and Secondary Metabolites
  • Drugs of Natural Origin: Plant, Marine, and Primary Metabolites

Topic wise notes of:

Pharmacology I

  • Introduction to Pharmacology & Pharmacokinetics
  • Pharmacodynamics & Drug Interaction
  • Pharmacology of drugs acting on peripheral nervous system
  • Pharmacology of drugs acting on central nervous system-1
  • Pharmacology of drugs acting on central nervous system-2

Topic wise notes of:

Pharmaceutical Organic Chemistry III

  • Stereo isomerism
  • Geometrical isomerism
  • Heterocyclic compounds
  • Heterocycles: Synthesis, Reactions & Uses
  • Reactions of synthetic importance

Drug Stability and Reaction Kinetics – Summary

Unit V focuses on the stability of pharmaceutical drugs and the reaction kinetics involved in their degradation. It begins with an explanation of various reaction orders, including zero-order, pseudo-zero-order, first-order, and second-order kinetics, along with the units of rate constants and methods used to determine reaction order. Understanding these principles is essential for predicting the shelf-life and efficacy of pharmaceutical products.

The unit also explores physical and chemical factors that influence drug stability. These include temperature, solvent type, ionic strength, dielectric constant, and the roles of specific and general acid-base catalysis, all of which can accelerate chemical degradation.

Moreover, it discusses the stabilization of medicinal agents against common degradation reactions such as hydrolysis and oxidation. Various formulation strategies and the use of stabilizers are highlighted to enhance the stability and longevity of pharmaceutical products.

The unit also introduces accelerated stability testing, a crucial method used in determining the expiration dating of dosage forms under elevated stress conditions to predict long-term stability. Additionally, it covers photolytic degradation—light-induced decomposition—and outlines strategies for its prevention, such as using light-resistant packaging. This unit provides essential knowledge for ensuring the safety and efficacy of drug formulations over time.

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