In Vitro–in Vivo Correlation and Dissolution Studies with Oral Theophylline Dosage Forms
- 1 February 1985
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 74 (2) , 161-164
- https://doi.org/10.1002/jps.2600740211
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Dissolution and Bioavailability Studies of Whole and Halved Sustained-Release Theophylline TabletsJournal of Pharmaceutical Sciences, 1982
- Pharmacokinetics of sustained release theophylline in low and high multidose regimens.Published by Wiley ,1981
- A new in vitro dissolution test for controlled-release theophylline tabletsInternational Journal of Pharmaceutics, 1981
- Theophylline Absorption and Disposition in Rabbits: Oral, Intravenous, and Concentration-Dependent Kinetic StudiesJournal of Pharmaceutical Sciences, 1981
- Evaluation of a new sustained release theophylline formulation by the measurements of salivary levels of the drug in humans.Journal of Pharmacobio-Dynamics, 1980
- Predictive Conversion of In Vitro Drug Dissolution Data into In Vivo Drug Response versus Time Profiles Exemplified for Plasma Levels of WarfarinJournal of Pharmaceutical Sciences, 1977
- Design and Evaluation of a Rotating Filter—Stationary Basket In Vitro Dissolution Test Apparatus I: Fixed Fluid Volume SystemJournal of Pharmaceutical Sciences, 1973
- Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to nondisintegrating dosage formsJournal of Pharmaceutical Sciences, 1967