| A New Model of a 3D-Printed Shell with Convex Drug Release Profile |
5 |
| Design of an Innovative Advanced Gastric Simulator |
4 |
| In Vitro Release Testing Methodology and Variability with the Vertical Diffusion Cell (VDC) |
4 |
| The Significance of Disintegration Testing in Pharmaceutical Development |
4 |
| Towards Standardized Dissolution Techniques for In Vitro Performance Testing of Dry Powder Inhalers |
3 |
| Stability of Biorelevant Media Under Various Storage Conditions |
2 |
| Simulated Genital Tract Fluids and Their Applicability in Drug Release/Dissolution Testing of Vaginal Dosage Forms |
2 |
| In Vitro Performance Testing of Medicated Chewing Gums |
2 |
| In Silico Simulation of Dissolution Profiles for Development of Extended-Release Doxazosin Tablets |
2 |
| In Vitro Release Test Methods for Drug Formulations for Parenteral Applications |
2 |
| Evaluation of the Discriminatory Power of USP Dissolution Method for Candesartan Cilexetil Tablets through Testing of Marketed Products in Egypt |
1 |
| 3D Printing for Fast Prototyping of Pharmaceutical Dissolution Testing Equipment for Nonstandard Applications |
1 |
| A Comparative Study of Propranolol Release by In Vitro Dissolution Profiles in Pharmaceutical Formulations |
1 |
| Formulation of Hedera helix L. in Topical Dosage Forms: In Vitro and Ex Vivo Evaluation |
1 |
| Effect of Thyme Oil on the Transdermal Permeation of Pseudoephedrine HCl from Topical Gel |
1 |
| Physiologically Based Pharmacokinetic (PBPK) Modelling for In Vitro-In Vivo Extrapolation: Emphasis on the Use of Dissolution Data |
1 |
| Dissolution Universal Strategy Tool (DUST): A Tool to Guide Dissolution Method Development Strategy |
1 |
| Dissolution Method Development and Validation for Lercanidipine Hydrochloride Tablets |
1 |
| Mebeverine HCl and Aluminium/Magnesium Antacid Interactions: A Potential Impact on Electrolyte Replacement Therapy |
1 |
| Determination of Dissolution Profile and Bioaccessibility of Ketosteril Using an Advanced Gastrointestinal In Vitro Model |
1 |
| The Critical Role of the USP Performance Verification Test in Dissolution Testing and Qualification of the Paddle Apparatus |
1 |
| In vitro Characterization and Evaluation of Commercialized Paracetamol Products in Jordan |
1 |
| In Vitro Dissolution Testing to Assess Pharmaceutical Equivalence of Selected Amoxicillin Products Available in Sri Lanka: A Post-Marketing Study |
1 |
| Discriminatory Dissolution Testing for Liquisolid Compacts Containing a Poorly Water-Soluble Drug (Hydrochlorothiazide) |
1 |
| Dissolution-Controlled Salt of Pramipexole for Parenteral Administration: In Vitro Assessment and Mathematical Modeling |
0 |
| Primer on the Science of In Vitro Dissolution Testing of Oral Dosage Forms and Factors Influencing its Biological Relevance |
0 |
| Development of Analytical Method for In Vitro Release Testing of Dexamethasone Nanosuspensions |
0 |
| Accelerated Dissolution Method to Facilitate In Vitro Evaluation of Risperidone-Containing Microspheres |
0 |
| Technical Note: Content Uniformity Measurement of an OTC Product Using a Dedicated Sample Preparation Station and a Fiber Optic UV Analysis System |
0 |
| Pharmaceutical Equivalence and Similarity Studies of Metoclopramide Tablets |
0 |
| Similar or Not? Comparison of Dissolution Profiles of Different Hydroxypropylmethyl Cellulose (HPMC) Capsules |
0 |
| Technical Note: Comparison of USP Apparatus 5 and 7 for In Vitro Drug Release from Nicotine Transdermal Systems |
0 |
| Workshop Report: USP Workshop on Exploring the Science of Drug Absorption |
0 |
| In Vitro Performance Testing of Nanoparticulate Drug Products for Parenteral Administration |
0 |
| Pharmaceutical Equivalence and Stability of Furosemide Tablets in Argentina |
0 |
| Real-Time Monitoring of Nicotine Release Behavior from Smokeless Tobacco (Snus) Based on Fiber Optic Sensing Technology |
0 |
| Highlights from the 2018 Pharm Sci AAPS Annual Meeting in Washington DC |
0 |
| Comparison of In Vitro Release Rates of Diclofenac Topical Formulations Using an In-Line Cell Automated Diffusion System |
0 |
| A Novel Kinetic Model for Dissolution of Herbal Medicine |
0 |
| Pharmaceutical Equivalence of Hydrochlorothiazide Tablets in Argentina |
0 |
| In Vitro-In Vivo Correlation (IVIVC): From Current Achievements Towards the Future |
0 |
| In Situ UV Fiber Optics for Dissolution Testing-What, Why, and Where We Are After 30 Years |
0 |
| Application of Biowaiver Methodology for a Post-Marketing Study of Generic and Brand Name Metronidazole Tablets |
0 |
| Influence of Tablet Splitting on Dissolution of Tablets with Naproxen Sodium |
0 |
| Application of a Modified Disk for Testing Orally Disintegrating Tablets by USP < 701 > |
0 |
| Film-Controlled Synchronized Release Multicomponent Preparations of Chinese Materia Medica for Oral Administration |
0 |
