Pharmaceutical Dosage Forms: Disperse Systems / Edition 2

by Herbert Lieberman

Overview

This third volume of the second edition offers information on specialized products such as emulsions, liposomes, polymers and polymeric pharmaceutical excipients. It explains the requirements for conducting clinical research and obtaining marketing approval for new drug products

Product Details

ISBN-13:	9780367400606
Publisher:	Taylor & Francis
Publication date:	09/23/2019
Series:	Pharmaceutical Dosage Forms Disperse System
Edition description:	2nd ed.
Pages:	584
Product dimensions:	7.00(w) x 10.00(h) x (d)

About the Author

Herbert A. Lieberman, Martin M. Rieger , Gilbert S. Banker

Table of Contents

Part 1 Specialized dispersed system: specialized pharmaceutical emulsions liposomes; polymeric dispersions as drug carriers; aqueous polymer dispersions as film formers; biodegradable nanoparticles of poly(lactic acid) and poly(lactic-co-glycolic acid) for parenteral administration; aqueous polymeric dispersions; polymeric pharmaceutical excipients. Part 2 Equipment, processing, quality assurance, validation, regulation: a practical guide to equipment selection and operating techniques; set-up to manufacturing; scale-up of dispersed parenteral dosage form; quality assurance; validation of disperse systems; drug regulatory affairs.

Editorial Reviews

"Praise for previous volumes. . . . . .serve[s] as a text book for advanced students and as a reference for all pharmacists (and other professionals) who are engaged in this area. . .recommended to all formulators, as well as scientists and teachers, seeking for a source of quick and comprehensive information about general aspects of disperse system dosage forms. "
—-European Journal of Pharmaceutics and Biopharmaceutics
". . .a valuable resource with plenty of useful tips and insights. "
—-Journal of the American Chemical Society
". . .these books are indispensable for those pharmaceutical scientists involved in the development of disperse dosage forms. . .[they] will also be very helpful in teaching. . .there is no doubt that these books will serve as valuable reference books for the years to come. "
—-Pharmaceutical Research
". . .recommend[ed]. . .for inclusion into a department reference library, or its use in an academic course because of its broad approach in some areas, such as polymeric coating and nanoparticle development, as well as its specific focus on certain areas such as scale-up and liposomes."
—-Journal of Controlled Release

From the Publisher

Praise for previous volumes... ...serve[s] as a text book for advanced students and as a reference for all pharmacists (and other professionals who are engaged in this area...recommended to all formulators, as well as scientists and teachers, seeking for a source of quick and comprehensive information about general aspects of disperse system dosage forms.

European Journal of Pharmaceutics and Biopharmaceutics

...a valuable resource with plenty of useful tips and insights.

Journal of the American Chemical Society

...these books are indispensable for those pharmaceutical scientists involved in the development of disperse dosage forms...[they] will also be very helpful in teaching...there is no doubt that these books will serve as valuable reference books for the years to come.

Pharmaceutical Research

...recommend[ed]...for inclusion into a department reference library, or its use in an academic course because of its broad approach in some areas, such as polymeric coating and nanoparticle development, as well as its specific focus on certain areas such as scale-up and liposomes.

Journal of Controlled Release

The third and final volume on disperse systems contains contributions from both the academic and business sides of the pharmaceutical industry. Part A details several specialized products such as certain types of emulsions, liposomes, polymers used in dispersions as either drug or film carriers, biodegradable and new polymeric dispersions, and the characteristics of polymeric pharmaceutical excipents currently used in drug formulations. Part B describes equipment selection and processing, scale-up manufacturing, quality assurance, validation, and drug regulatory affairs related to disperse system pharmaceutical products and dosage forms. Annotation c. by Book News, Inc., Portland, Or.

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