The Role of Microstructure in Topical Drug Product Development
David W. Osborne (Hrsg.), Bozena Michniak-Kohn (Hrsg.), Nigel Langley (Hrsg.)
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Springer International Publishing
Naturwissenschaften, Medizin, Informatik, Technik / Biochemie, Biophysik
Beschreibung
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 eachof the five chapters uniform in scope and content.
Kundenbewertungen
topical dosage forms, rheology, MDRS, particle characterization, Rheometry, suspended API, globule size, PEG, Viscometry, CPP, IVRT and IVPT, SEM, excipients, state of API, in vitro testing, particle size, semi-solid microstructure, optical microscopy of emulsions, viscosity, Thixotropy