Pharmaceutical dissolution testing / edited by Jennifer Dressman, Johannes Krämer.
Contributor(s): Dressman, J. B | Krämer, JohannesMaterial type: TextLanguage: English Publisher: Boca Raton : Taylor & Francis, c2005Description: 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 2005Online resources: WorldCat details | Ebook Fulltext
|Item type||Current location||Collection||Call number||Copy number||Status||Date due||Barcode||Item holds|
|E-Book||EWU Library E-book||Non-fiction||615.19 PHA 2005 (Browse shelf)||Not for loan|
|Text||EWU Library Reserve Section||Non-fiction||615.19 PHA 2005 (Browse shelf)||C-1||Not For Loan||18426|
Includes bibliographical references and index.
Table of contents 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