|
Intrinsic Dissolution as a Tool for Evaluating Drug Solubility in Accordance with the Biopharmaceutics Classification SystemMichele G. Issa and Humberto G. Ferraz Pharmacy Department, Pharmaceutical Sciences School, University of São Paulo, São Paulo, Brazil Corrigendum to "Feasibility Study on Qualification of USP Dissolution Apparatus 1 and 2 Using the Enhanced Mechanical Calibration Procedure"
Brian Yan, Xujin Lu, and Ruben Lozano
Simulated Biological Fluids with Possible Application in Dissolution Testing
Margareth R. C. Marques1, Raimar Loebenberg2, and May Almukainzi2
Drug Transport Mechanisms from Carbopol/Eudragit Verapamil Sustained-Release Tablets
Sandile M. Khamanga and Roderick B. Walker
Formulation and Optimization of Nanosuspensions for Enhancing Simvastatin Dissolution Using Central Composite Design
Vikram M. Pandya1, Jayvadan K. Patel2, and Dhaval J. Patel3
Dissolution Method for Milnacipran Hydrochloride Capsules: Development, Validation, and Study of Changes in Dissolution Rate after Storage
Carolina Lupi Dias, Rochele Cassanta Rossi, Lisiane Bajerski, and Pedro Eduardo Fröehlich
Studies in Dissolution Enhancement of Ezetimibe by Solid Dispersions in Combination with a Surface Adsorbent
Komal R. Parmar, Sunny R. Shah, and Navin R. Sheth
Dissolution Behavior and Thermodynamic Stability of Fused-Sugar Dispersions of a Poorly Water-Soluble Drug
Ghanshyam Singh, Gulshan Chhabra, and Kamla Pathak
Gastroretentive Orlistat Microspheres: Formulation, Characterization, and In Vitro Evaluation
S. B. Sateesha1, B. Prakash Rao1, A. J. Rajamma2, and L. V. G. Nargund3
Question & Answer Section
Margareth Marques and William Brown
|