Pharmaceutical dissolution testing / edited by Jennifer Dressman, Johannes Krämer.
Material type:
TextLanguage: English Publication details: Boca Raton : Taylor & Francis, c2005. Description: xv, 429 p. : ill. ; 24 cmISBN: 9780824754679 (alk. paper); 0824754670 (alk. paper)Subject(s): Drugs -- Solubility -- Testing | Dosage Forms -- standards | Drug CompoundingDDC classification: 615.19 LOC classification: RS189 | .P446 2005NLM classification: QV 778Online resources: WorldCat details | Ebook Fulltext | Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds |
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E-Book
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EWU Library E-book | Non-fiction | 615.19 PHA 2005 (Browse shelf(Opens below)) | Not for loan | ||||
Text
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EWU Library Reserve Section | Non-fiction | 615.19 PHA 2005 (Browse shelf(Opens below)) | C-1 | Not For Loan | 18426 |
Includes bibliographical references and index.
TOC Historical Development of Dissolution Testing. Compendial Testing Equipment: Calibration, Qualification, and Sources of Error. Compendial Requirements of Dissolution Testing. The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective. Physiological Parameters Relevant to Dissolution Testing: Composition of Fluids in the GI Tract. Physiological Parameters Relevant to Dissolution Testing: Hydrodynamic Considerations. Physiological Parameters Relevant to Dissolution Testing: Behavior of Solid Pharmaceuticals in the GI Tract. Dissolution Data Analysis with a View to IVIVC. Analysis and Interpretation of Time Profiles In Vitro and In Vivo. Pharmacokinetic Study Design with a View to Quality Control. Dissolution Method Development: An Industrial Perspective. Design and Qualification of Automated Dissolution Systems
Pharmaceutical Dissolution Testing
Pharmacy
Saifun Momota
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