Dissolution Technologies

Papers
(The median citation count of Dissolution Technologies is 0. 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 2022-05-01 to 2026-05-01.)
ArticleCitations
In Vitro Product Performance Testing of Oral Drug Products: View of the USP Expert Panel10
Book Review: The Handbook of Dissolution Testing, 4th Edition9
Validation of Spectrophotometric Method for Quantification of Folic Acid in Capsules6
Evaluation of Critical Quality Attributes of Dapsone Gel6
Evaluation of a pH-Gradient Biphasic Dissolution Test for Predicting In Vivo Performance of Weakly Basic Drugs6
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 Panel5
Questions and Answers May 20234
In Vitro Characterization of Multi-Source Omeprazole Capsule Dissolution Performance Under Biorelevant Conditions4
Highlights from 2022 AAPS 360-In Vitro Release and Dissolution Testing Community Annual Meeting4
Parametric Tolerance Interval Test for Dissolution Testing of Immediate-Release Solid Oral Dosage Forms4
Comparative Study of Metformin Hydrochloride Tablets in Argentina3
Rapid Development of an Accelerated In Vitro Release Method for a Novel Antibiotic-Eluting Biologic Envelope3
Questions and Answers February 20253
Comparative Study of Metformin Hydrochloride Tablets in Argentina2
Questions and Answers May 20252
Evaluation of NanoDis as an Automated Sampling Technology for In Vitro Release Testing of Nanomedicines2
Factors Influencing the Selection of Medium for Evaluating Drug Solubility and Dissolution in Bovine Milk2
Dissolution Specifications for Ibuprofen Soft Gelatin Capsules: A Proposal2
Evaluation of Pharmaco-Equivalence Properties of Lisinopril Dihydrate Tablets in Saudi Arabia: A Local Comparative Study2
Dissolution Performance of Verapamil-HCl Tablets Using USP Apparatus 2 and 4: Prediction of In Vivo Plasma Profiles2
Using a Laser Monitoring Technique for Dissolution and Thermodynamic Study of Celecoxib in 2-Propanol and Propylene Glycol Mixtures1
Report on the Virtual Workshop: A Quest for Biowaiver, Including Next Generation Dissolution Characterization and Modeling1
Comparison of Rosuvastatin Calcium Tablets Marketed in Saudi Arabia Under Biowaiver Conditions: In Vitro Quality Control Dissolution Study1
Comparative Dissolution Study of Various Brands of Valsartan Tablets Marketed in Pakistan1
In Vitro Pharmaceutical Quality Evaluation of Loratadine Tablets in Saudi Arabia1
RKinetDS: A Flexible Open-Source Software for Modeling Dissolution Profiles1
Testing the In Vitro Product Performance of Inhalation and Nasal Drug Products: Views of the USP Expert Panel1
Release Profile of Branded Atorvastatin Calcium Tablet Relative to Commercially Available Counterpart Generics1
Questions and Answers November 20231
Comparative Study of Metronidazole Tablets Marketed in Saudi Arabia1
Highlights from the 2023 AAPS 360 Annual Meeting - In Vitro Release and Dissolution1
Dissolution Test of Patent and Generic Drugs of Metformin Hydrochloride0
Questions and Answers August 20240
Comparative Dissolution Study of Enzalutamide Capsules in India0
Quality Control Parameters of Antihypertensive Medications Marketed in Eastern Ethiopia: Amlodipine Besylate and Enalapril Maleate Tablets0
Comparative Assessment of 1% Luliconazole Cream Release Profile Through Franz Diffusion Cells - A Way Towards Qualification and Validation of Critical In Vitro Parameters0
Investigating the Influence of HPMC K4M and Eudragit L 100-55 on Guanfacine-Loaded Extended-Release Tablets0
Comparative Dissolution of Budesonide from Four Commercially Available Products for Oral Administration: Implications for Interchangeablity0
Characterization of Apex Vessel Geometries and Irregularities0
Establishing In Vitro-In Vivo Correlation (IVIVC) for Formulations of Vitamin C and Iron in Daily Plus Tablets0
Quality Evaluation of Azithromycin Oral Solid Dosage Forms in Nigeria: In Vivo-In Vitro Correlation Study0
Evaluation of Different Methods for Dissolution Profile Similarity Comparison of Montelukast Tablets in Türkiye0
Improved Melatonin Dissolution Properties: A Way Forward for Treating Children with Sleep Disorders0
Influence of Storage Conditions on the Pantoprazole Dissolution Profile for Gastro-Resistant Tablet Formulations0
Dissolution Method Development for Regulatory Approval: A Comprehensive Review and Case Study0
Hypothetical Plasma Concentration-Time Profiles of Amiodarone-HCl From In Vitro Release Data0
Questions and Answers November 20240
In Vitro Evaluation of the Bioequivalence of Different Brands of Doxycycline Marketed in Burkina Faso, Africa0
New USP Dissolution Performance Verification Standard: What, Where, and When0
Biorelevant Dissolution of Dipyridamole and Piroxicam Using an Automated UV/Vis Spectrophotometric and Potentiometric Dissolution Testing Platform0
In Vitro Performance of Commercially Available Glimepiride Tablets in Indonesia0
2024 AAPS 360 Annual Meeting: Highlights in the Area of In Vitro Release and Dissolution0
Comparative Dissolution Study of Atorvastatin Calcium Tabletsin Indonesia0
Physicochemical Quality and In Vitro Bioequivalence of Amoxicillin Capsules Marketed in Burkina Faso, Africa0
Application of Salicylic Acid Tablets in the Performance Verification Test for the Flow-Through Cell Apparatus0
An In Vitro Model for Release of Acetaminophen When an Overdose is Ingested Orally0
The Importance of Dissolution Tests to Evaluate Quality of Dietary Supplements: Case Study of Controlled Release Caffeine Capsules0
Can Biorelevant Dissolution Testing Help Elucidate Salt Formulation Effects on Plasma Levels and Onset of Action? A Study of Ibuprofen and Its Salts0
Predicting Dissolution of Entecavir Using the Noyes Whitney Equation0
Questions and Answers February 20230
Paradoxical Effects of Superdisintegrants on Dissolution Performance in Ibuprofen Orodispersible Tablets0
Preparation and Characterization of a Novel Optimum Modified Liquisolid Compact to Enhance the Dissolution Profile of Mifepristone0
Development of a Discriminative Dissolution Method for Mebendazole Suspensions0
Questions and Answers August 20250
Testing the In Vitro Product Performance of Mucosal Drug Products: View of the USP Expert Panel0
Questions and Answers February 20240
Questions and Answers August 20230
Advances in Product Quality and Performance Tests for Topical and Transdermal Products: View of the USP Expert Panel0
Mathematical Model Application for In Vitro Release Kinetics of Ranolazine Extended-Release Tablets0
Questions and Answers February 20260
Investigation of Dissolution Failures of Metformin Delayed-Release Tablets During Formulation Design0
Virtual Workshop Report: Approaches, Regulatory Challenges, and Advances in Bioequivalence, Dissolution Testing, and Biowaivers: Manila, Philippines, February 22-24, 20230
Regulatory Expectations and Challenges in Alcohol-Induced Dose Dumping Studies: A Review0
Therapeutic Equivalence of Multisource Drugs Assessed by In Vitro Dissolution Studies: Amoxicillin/Clavulanic Acid Tablets0
In Vitro Biopharmaceutical Quality Control of Risperidone (2 mg) Tablets and Their Impact on Public Health0
Biorelevant Dissolution Testing of Numerically Optimized Multiparticulate Drug Delivery Systems of Gliclazide0
Dissolution Testing Strategies for Large Sample Sizes and Applications in Continuous Manufacturing0
Life Cycle Application of AQbD for Formulation Development and Validation of a Dissolution Method for Nevirapine0
Consistency Evaluation of Dissolution of Generic and Original Preparations of Sulindac Tablets0
Dissolution Profile of Calcium Supplements in Brazil: A Critical Analysis and Formulation Proposal0
Impact of Vessel Inner Diameter in USP Dissolution Apparatus 20
Biopharmaceutical and Quality Evaluation of Immediate-Release Metformin Hydrochloride Tablets in Brazil0
Development of In Vitro Dissolution Test Method for Bilastine and Montelukast Fixed-Dose Combination Tablets0
Effect of Mannitol Particle Size on Melatonin Dissolution and Tablet Properties using a Quality by Design Framework0
Evaluation of In Vitro Dissolution Behavior of Ibuprofen Suspensions Based on the Flow-Through Cell Method0
Development of a Physiologically Relevant Simulated Nasal Fluid for In Vitro Dissolution Studies0
Effects of Formulation Composition and Manufacturing Processes on the In Vitro Dissolution Profile of Estazolam Tablets0
Comparative Study of Brand and Generics Ciprofloxacin Tablets Available in the Saudi Market0
Questions and Answers May 20240
Magnesium Stearate - Its Importance and Potential Impact on Dissolution of Oral Solid Dosage Forms0
Comparative In Vitro Release of Eletriptan Hydrobromide Formulations for Buccal Administration0
Questions and Answers November 20250
Assessment of Small Volume (250-mL) Vessels for Use in Biorelevant Dissolution0
Development of a Discriminating Dissolution Method Using Apex Vessels for Enzastaurin Tablets0
Demonstrating Discriminatory Power of a Dissolution Method Using DDDPlus: Case Study of an Extended-Release Formulation and Use in Regulatory Justifications0
Consistency Evaluation of Dissolution of Granisetron Hydrochloride Tablets in China0
Selection and Parameters Affecting Dissolution Media0
Consistency Evaluation of the Dissolution of Toremifene Citrate Tablets0
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