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3.22:  Theories of Dissolution: The Danckwerts’ Model and Interfacial Barrier Model

3.23:  Factors Affecting Dissolution: Particle Size and Effective Surface Area

3.24:  Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

3.25:  Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH

3.26:  Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry

3.27:  Methods for Studying Drug Absorption: In vitro

3.28:  Methods for Studying Drug Absorption: In situ

3.29:  Non-Oral Extravascular Drug Absorption Routes

4.2:  Factors Affecting Drug Distribution: Tissue Permeability

4.3:  Factors Affecting Drug Distribution: Physiological Barriers

4.4:  Factors Affecting Drug Distribution: Organ Perfusion Rate

4.5:  Factors Affecting Drug Distribution: Miscellaneous Factors

4.6:  Volume of Distribution

4.7:  Protein-Drug Binding: Mechanism and Kinetics

4.8:  Drug Binding to Blood Components

4.9:  Tissue-Drug Binding: Localization of Drugs and its Significance

4.10:  Protein-Drug Binding: Determination Methods

4.12:  Factors Affecting Protein-Drug Binding: Protein-Related Factors

5.1:  Drug Biotransformation: Overview

5.2:  Phase I Oxidative Reactions: Overview