Description
Taylor & Francis Ltd Pharmaceutical Dosage Forms And Drug Delivery by Ram I. Mahato
Integrating aspects of physical pharmacy, biopharmaceuticals, drug delivery, and biotechnology, Pharmaceutical Dosage Forms and Drug Delivery elucidates basic physicochemical principles and their application in the design of dosage forms. The author addresses the relevance of these principles to the biopharmaceutical aspects of drugs. He explores the latest developments in the application of biomaterials, including polymers and biotechnology-based agents, to the development of novel dosage forms. _x000D_The book covers physicochemical principles of dosage design, biopharmaceutical and physiological considerations, types of commonly used pharmaceutical dosage forms, introduction to polymeric biomaterials, protein and nucleic acid-based dosage forms, and novel and targeted drug delivery systems. It highlights the physicochemical parameters used for the design, development, and evaluation of biotechnological dosage forms and describes the biological barriers to drug absorption. _x000D__x000D__x000D_Containing the right blend of mathematics, equations, diagrams, pictorials, and other pertinent information, this book provides a unified perspective that creates a greater overall understanding of basic science and cutting-edge technology._x000D_ _x000D_
Drug Development and Regulatory Process _x000D_
Introduction _x000D_
Identification of New Therapeutic Molecules _x000D_
Preclinical Research _x000D_
Formulation Development _x000D_
Regulatory Issues _x000D_
Pharmaceutical and Formulation Considerations _x000D_
Introduction _x000D_
Advantages of Pharmaceutical Dosage Forms _x000D_
Influential Factors in Dosage Form Design _x000D_
Biopharmaceutical and Physiological Considerations _x000D_
Introduction _x000D_
Drug Transport across a Polymeric Barrier _x000D_
Fick's Laws of Diffusion _x000D_
Pore Diffusion _x000D_
Matrix (Monolithic)-Type Nondegradable Device _x000D_
Biological Membranes and Drug Absorption _x000D_
Dissolution Rate and Noyes-Whitney Equation of Dissolution _x000D_
Factors Influencing Dissolution Rate _x000D_
Complexation and Protein Binding _x000D_
Introduction _x000D_
Types of Complexation _x000D_
Drug Interaction with Plasma Proteins _x000D_
Binding Equilibria _x000D_
Impact of Plasma Protein Binding on Dosing Regimens Chemical Kinetics and Stability _x000D_
Introduction _x000D_
Rates and Order of Reaction _x000D_
Factors Affecting Reaction Kinetics _x000D_
Pathways and Prevention of Chemical Decomposition of Drugs Interfacial Phenomena _x000D_
Introduction _x000D_
Liquid Interfaces _x000D_
Adsorption at Solid-Gas Interfaces _x000D_
Adsorption at Solid-Liquid Interface Rheology _x000D_
Introduction _x000D_
Newtonian Flow _x000D_
Non-Newtonian Flow _x000D_
Thixotropy Disperse System Basics _x000D_
Introduction _x000D_
Types of Colloidal Systems _x000D_
Kinetic Properties of Colloids _x000D_
Electrical Properties _x000D_
Electrostatic Effect _x000D_
Electrical Double Layer _x000D_
Stability of Colloids Surfactants and Micelles _x000D_
Introduction _x000D_
Surfactants _x000D_
HLB Systems _x000D_
Micelles _x000D_
Cloud Point _x000D_
Pharmaceutical Suspensions _x000D_
Introduction _x000D_
Classification of Suspensions _x000D_
Characteristics of Pharmaceutical Suspensions _x000D_
Formulation of Suspensions _x000D_
Flocculation and Deflocculation Pharmaceutical Emulsions _x000D_
Introduction _x000D_
Advantages of Emulsion Dosage Forms _x000D_
Types of Emulsions _x000D_
Roles of Interfacial Free Energy on Emulsification _x000D_
Formulations of Emulsions _x000D_
Emulsifying Agents Pharmaceutical Solutions _x000D_
Introduction _x000D_
pH and Solubility _x000D_
Buffer and Buffer Capacity _x000D_
Vehicles _x000D_
Types of Solutions _x000D_
Dry or Lyophilized Mixtures for Solution Tablets _x000D_
Introduction _x000D_
Types of Tablets _x000D_
Tablet Formulation _x000D_
Powder Flow and Compressibility _x000D_
Manufacturing of Tablets _x000D_
Relationship among Disintegration, Dissolution, and Absorption _x000D_
Evaluation of Tablets _x000D_
Capsules _x000D_
Introduction _x000D_
Hard Gelatin Capsules _x000D_
Soft Gelatin Capsules _x000D_
Evaluation of Capsules Injectable Dosage Forms _x000D_
Introduction _x000D_
Isotonicity.. _x000D_
Parenteral Routes of Administration _x000D_
Formulation of Parenteral Products _x000D_
Sterilization of Parenteral Products _x000D_
Types of Parenteral Dosage Forms _x000D_
Evaluation of Injectable Products _x000D_
Semisolid Dosage Forms _x000D_
Introduction _x000D_
Ointments _x000D_
Creams _x000D_
Gels _x000D_
Lotions _x000D_
Pastes _x000D_
Inserts, Implants, and Devices _x000D_
Introduction _x000D_
Inserts _x000D_
Implants _x000D_
Suppositories _x000D_
Aerosol Products _x000D_
Transdermal Patches Pharmaceutical Polymers _x000D_
Introduction _x000D_
Definitions and Architectures of Polymers _x000D_
Polymer Molecular Weight and Weight Distribution _x000D_
Biodegradablity and Biocompatibility _x000D_
Polymer Solubility _x000D_
Block Copolymers _x000D_
Intelligent or Stimuli-Sensitive Polymers _x000D_
Water-Soluble Polymers _x000D_
Bioadhesive/Mucoadhesive Polymers Drug Delivery Systems _x000D_
Introduction _x000D_
Prodrugs _x000D_
Soluble Macromolecular Carriers _x000D_
Particulate Carrier Systems _x000D_
Oral Drug Delivery _x000D_
Alternative Routes of Delivery Protein-and Peptide-Based Dosage Forms _x000D_
Introduction _x000D_
Structure of Peptides and Proteins _x000D_
Hydrophobicity of Peptides and Proteins _x000D_
Solubility of Peptides and Proteins _x000D_
Instability of Peptides and Proteins _x000D_
Formulation of Proteins and Peptides _x000D_
Antibody-Based Therapy and Delivery _x000D_
Antigenicity and Immunogenicity Biotechnology-Based Dosage Forms _x000D_
Introduction _x000D_
Genes and Gene Expression _x000D_
Gene Silencing _x000D_
Classification of Gene-Silencing Technologies _x000D_
Gene Therapy _x000D_
Each chapter contains Learning Objectives, Review Questions, and a Bibliography. _x000D_
Answers to Review Questions _x000D_
Index_x000D_