Dissolution Technologies is a peer reviewed quarterlypublication reporting ongoing, useful information ondissolution testing of pharmaceuticals. It provides aninternational forum for dissolution analysts to receiveand exchange information on various dissolution topics.Dissolution Technologies welcomes submissions relatedto dissolution, in vitro release, and disintegration testing.These topics should be the major focus of the article.Do not submit articles where the focus is formulationdevelopment with dissolution testing as one of manytests.
溶出度技术是一份同行评审的季度出版物,报告了有关药物溶出度测试的持续、有用的信息。它为溶出度分析人员提供了一个国际论坛,以接收和交流各种溶出度主题的信息。溶出度技术公司欢迎提交与溶出度、体外释放度和崩解度测试相关的文章。这些主题应该是文章的主要重点。如果文章的重点是将溶出度测试作为众多测试之一的配方开发,请不要提交文章。
Stability of Biorelevant Media Under Various Storage Conditions
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260219P6
Physiologically Based Pharmacokinetic (PBPK) Modelling for In Vitro-In Vivo Extrapolation: Emphasis on the Use of Dissolution Data
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260319p18
Discriminatory dissolution testing for liquisolid compacts containing a poorly water-soluble drug (Hydrochlorothiazide)
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P46
Dissolution Universal Strategy Tool (DUST): A Tool to Guide Dissolution Method Development Strategy
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260319p6
Pharmaceutical Equivalence and Stability of Furosemide Tablets in Argentina
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p30
The Critical Role of the USP Performance Verification Test in Dissolution Testing and Qualification of the Paddle Apparatus
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P6
In Vitro Dissolution Testing to Assess Pharmaceutical Equivalence of Selected Amoxicillin Products Available in Sri Lanka: A Post-Marketing Study
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P56
Development of Analytical Method for In Vitro Release Testing of Dexamethasone Nanosuspensions
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260219p40
In Vitro Performance Testing of Nanoparticulate Drug Products for Parenteral Administration
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260319p28
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
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p6
Real-Time Monitoring of Nicotine Release Behavior from Smokeless Tobacco (Snus) Based on Fiber Optic Sensing Technology
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p24
Primer on the Science of In Vitro Dissolution Testing of Oral Dosage Forms and Factors Influencing its Biological Relevance
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P14
Effect of Thyme Oil on the Transdermal Permeation of Pseudoephedrine HCl from Topical Gel
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p18
Highlights from the 2018 pharm sci AAPS annual meeting in Washington DC
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p38
Dissolution-Controlled Salt of Pramipexole for Parenteral Administration: In Vitro Assessment and Mathematical Modeling
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P28
In vitro Characterization and Evaluation of Commercialized Paracetamol Products in Jordan
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260119P36
Workshop Report: USP Workshop on Exploring the Science of Drug Absorption
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260319p38
Accelerated Dissolution Method to Facilitate In Vitro Evaluation of Risperidone-Containing Microspheres
来源期刊:Dissolution TechnologiesDOI:10.14227/DT260219P48
Comparison of In Vitro Release Rates of Diclofenac Topical Formulations Using an In-Line Cell Automated Diffusion System
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260419p10
Technical Note: Comparison of USP Apparatus 5 and 7 for In Vitro Drug Release from Nicotine Transdermal Systems
来源期刊:Dissolution TechnologiesDOI:10.14227/dt260319p68