| Literature DB >> 7120073 |
V P Shah, P Knight, V K Prasad, B E Cabana.
Abstract
Based on the initial dissolution rate profiles in water, a slow-dissolving, an intermediate-dissolving, and a fast-dissolving chlorothiazide 250-mg tablet were selected for the bioavailability and bioequivalence study. In addition, two marketed 500-mg chlorothiazide tablets were studied. The three 250-mg tablets were bioequivalent, as were the two 500-mg tablets. Therefore, the dissolution test conditions were modified to associate in vitro dissolution with in vivo performance of the product. Based on these results, it was concluded that a dissolution of 75% in 60 min by paddle method at 75 rpm in pH 7.4 phosphate buffer can be used as a quality assurance test for 250- and 500-mg chlorothiazide tablets.Entities:
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Year: 1982 PMID: 7120073 DOI: 10.1002/jps.2600710727
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534