Dissolution Technologies

Papers
(The TQCC of Dissolution Technologies is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-06-01 to 2025-06-01.)
ArticleCitations
In Vitro Product Performance Testing of Oral Drug Products: View of the USP Expert Panel10
Evaluation of a pH-Gradient Biphasic Dissolution Test for Predicting In Vivo Performance of Weakly Basic Drugs7
Comparative Analysis of Commercially Available Acetaminophen Tablets in Saudi Arabia6
Evaluation of Critical Quality Attributes of Dapsone Gel5
In Vitro Performance Tests for Continuous Manufacturing: The Impact on the Current Compendial Framework from the Viewpoint of the USP New Advancements in Product Performance Testing Expert Panel4
Dissolution Profile of Apixaban Tablets: Method Development and Validation Using HPLC Analysis4
Predictive Dissolution Models for Real-Time Release Testing: Development and Implementation - Workshop Summary Report4
Simulated Lymphatic Fluid for In-Vitro Assessment in Pharmaceutical Development3
Comparison of Release Rates Derived from Cutaneous Versus Film-Forming Solution Containing Terbinafine: Approach Towards Qualification and Validation of In Vitro Parameters2
Comparative Study of Metformin Hydrochloride Tablets in Argentina2
Questions and Answers May 20232
Questions and Answers February 20252
A Novel Application of an Effervescent Agent in Naproxen Liqui-Pellets for Enhanced Drug Release2
In Vitro Characterization of Multi-Source Omeprazole Capsule Dissolution Performance Under Biorelevant Conditions2
Highlights from 2022 AAPS 360-In Vitro Release and Dissolution Testing Community Annual Meeting2
Rapid Development of an Accelerated In Vitro Release Method for a Novel Antibiotic-Eluting Biologic Envelope1
Dissolution Specifications for Ibuprofen Soft Gelatin Capsules: A Proposal1
Dissolution Performance of Verapamil-HCl Tablets Using USP Apparatus 2 and 4: Prediction of In Vivo Plasma Profiles1
Questions and Answers November 20231
In Vitro Pharmaceutical Quality Evaluation of Loratadine Tablets in Saudi Arabia1
Review: Application of Bioequivalence Testing of Medicines in Peru1
Dissolution Best Practices and International Harmonization - AAPS Workshop Report1
Evaluation of NanoDis as an Automated Sampling Technology for In Vitro Release Testing of Nanomedicines1
Report on the Virtual Workshop: A Quest for Biowaiver, Including Next Generation Dissolution Characterization and Modeling1
Factors Influencing the Selection of Medium for Evaluating Drug Solubility and Dissolution in Bovine Milk1
Questions and Answers February 20221
Questions and Answers May 20251
Comparative Study of Metformin Hydrochloride Tablets in Argentina1
Comparison of Rosuvastatin Calcium Tablets Marketed in Saudi Arabia Under Biowaiver Conditions: In Vitro Quality Control Dissolution Study1
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