The Role of Microstructure in Topical Drug Product Development

2019

ISBN: 9783030173548
Код товара 145332

20 962 ₽

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Автор
Nigel Langley; Bozena Michniak-Kohn; David W. Osbo
Издатель
Springer
Тип обложки
Hardcover
Размеры
164 x 244 x 16
Год издания
2019
Вес (г)
464
ISBN
9783030173548
Язык
ENG
Кол-во страниц
199

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Following the Semi-solid Microstructure Workshop sponsored by BASF and hosted by the Rutgers Center for Dermal Research, a pharmaceutical product development working group was formed. The group, known as the Q3 Working Group, selected the following five areas of focus: Particle/Globule Size and Distribution, Viscosity/Rheology/Spreadability, In Vitro Testing, State of API, State of Excipients. A committee was appointed for each of these five areas. The committees were tasked to review the literature, identify best practices, list experimental details required for an independent lab to duplicate the test, and propose scientific studies that may meaningfully advance this specific area of focus. Each committee has a chair (or co-chairs) that are the lead author(s) of the chapter. The Q3 Working Group members serve as the critical reviewers of each chapter, making suggestions that improve the quality of the document and that make each of the five chapters uniform in scope and content.

Pharmaceutical development scientists that formulate topical products (creams, lotions, gels suspensions, foams, etc) and all the allied raw material suppliers, packaging suppliers, contract laboratories including CROs, CMOs and regulators need access to this book. Overall, the topic of semisolid microstructure is of equal importance to the generic pharmaceutical companies (filing Abbreviated New Drug Applications or ANDAs) and pharmaceutical companies filing New Drug Applications (NDAs). In addition to products applied to the skin, hair, and nails, The Role of Microstructure in Topical Drug Product Development’ crosses over and is essential reading to developers of oral suspensions, ophthalmic ointments and gels, otic suspension, vaginal semisolids and retention enemas.

Part I - Critical Quality Attributes: 1. Rheological Characterization in the Development of Topical Drug Products.- 2. In Vitro Release & Permeation Tests as Critical Quality Attributes in Topical Product Development.- 3. Determination of Particle Size an

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