Literature DB >> 7120073

Thiazides IV: Comparison of dissolution with bioavailability of chlorothiazide tablets.

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.

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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


  2 in total

1.  The phenomenon and cause of the dose-dependent oral absorption of chlorothiazide in rats: extrapolation to human data based on the body surface area concept.

Authors:  F H Hsu; T Prueksaritanont; M G Lee; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1987-08

2.  Influence of tablet dissolution on furosemide bioavailability: a bioequivalence study.

Authors:  P J McNamara; T S Foster; G A Digenis; R B Patel; W A Craig; P G Welling; R S Rapaka; V K Prasad; V P Shah
Journal:  Pharm Res       Date:  1987-04       Impact factor: 4.200

  2 in total

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