Pharmaceutical Dosage Forms - Disperse Systems

Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this three-volume reference provides detailed information on specialized products, such as emulsions, liposomes, polymers, and polymeric pharmaceutical excipients. Written by over twenty-five international experts, it explains the requirements for conducting clinical research and obtaining approval for new drug products-furnishing a current, comprehensive review of U.S. drug regulations.

List 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.

About the author

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

Product details

• Authors: Herbert Lieberman, Herbert (Livingston Lieberman
• Assisted by: Herbert Lieberman (Editor), Lieberman Herbert (Editor)
• Publisher: Taylor & Francis Ltd.
• Languages: English
• Product format: Paperback / Softback
• Released: 31.08.2019
• EAN: 9780367400606
• ISBN: 978-0-367-40060-6
• No. of pages: 584
• Subjects: Natural sciences, medicine, IT, technology > Medicine > Non-clinical medicine; SCIENCE / Chemistry / General, MEDICAL / Pharmacology, Biology, life sciences, Pharmaceutical technology, Pharmaceutical chemistry and technology