Automated dissolution testing of combination drug product using high-pressure liquid chromatography
- 1 July 1981
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 70 (7), 764-767
- https://doi.org/10.1002/jps.2600700713
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Time and Temperature Dependence of Disintegration and Correlation Between Dissolution and Disintegration Rate ConstantsJournal of Pharmaceutical Sciences, 1980
- Semiautomated System for High-Pressure Liquid Chromatographic Determination of Dissolution Rate of Fludrocortisone Acetate TabletsJournal of Pharmaceutical Sciences, 1978
- High-performance ion-pair liquid chromatographyJournal of Chromatography A, 1978
- Design and Evaluation of an Automated System for In Vitro Dissolution Testing Utilizing a High-Pressure Liquid Chromatographic Multiport Switching ValveJournal of Pharmaceutical Sciences, 1977
- Computerized Automated System for Determining Dissolution Rate Profiles for Solid Dosage FormsJournal of Pharmaceutical Sciences, 1976
- Dissolution Studies with a Multichannel Continuous-Flow ApparatusJournal of Pharmaceutical Sciences, 1975
- System for Automated Determination of Dissolution RateJournal of Pharmaceutical Sciences, 1974
- Automation of NF Method I-USP Dissolution-Rate TestJournal of Pharmaceutical Sciences, 1971
- Dissolution Rate Studies I: Design and Evaluation of a Continuous Flow ApparatusJournal of Pharmaceutical Sciences, 1970