DISSOLUTION TECHNOLOGIES

Dissolution Universal Strategy Tool (DUST): A Tool to Guide Dissolution Method Development Strategy

Pharmaceutical Equivalence and Stability of Furosemide Tablets in Argentina

The Critical Role of the USP Performance Verification Test in Dissolution Testing and Qualification of the Paddle Apparatus

In Vitro Dissolution Testing to Assess Pharmaceutical Equivalence of Selected Amoxicillin Products Available in Sri Lanka: A Post-Marketing Study

Development of Analytical Method for In Vitro Release Testing of Dexamethasone Nanosuspensions

In Vitro Performance Testing of Nanoparticulate Drug Products for Parenteral Administration

Comment on the Importance of Documenting Drug Solubility Measurement Methodology, Including Characterizing the Physical Form of the Solute, for Meaningful Understanding, Interpretation, and Reporting of Solubility Data

Real-Time Monitoring of Nicotine Release Behavior from Smokeless Tobacco (Snus) Based on Fiber Optic Sensing Technology

Primer on the Science of In Vitro Dissolution Testing of Oral Dosage Forms and Factors Influencing its Biological Relevance

Effect of Thyme Oil on the Transdermal Permeation of Pseudoephedrine HCl from Topical Gel

Highlights from the 2018 pharm sci AAPS annual meeting in Washington DC

Dissolution-Controlled Salt of Pramipexole for Parenteral Administration: In Vitro Assessment and Mathematical Modeling

In vitro Characterization and Evaluation of Commercialized Paracetamol Products in Jordan

Workshop Report: USP Workshop on Exploring the Science of Drug Absorption

Accelerated Dissolution Method to Facilitate In Vitro Evaluation of Risperidone-Containing Microspheres

Comparison of In Vitro Release Rates of Diclofenac Topical Formulations Using an In-Line Cell Automated Diffusion System

Technical Note: Comparison of USP Apparatus 5 and 7 for In Vitro Drug Release from Nicotine Transdermal Systems