Literature DB >> 3816872

[Relative bioavailability in man of 2 pharmaceutical forms of canrenone].

F Bressolle, J Bres, A Faure, M C Pistre.   

Abstract

The relative bioavailability of 100 mg canrenone capsules and the commercial 50 mg capsules has been determined in 12 healthy male subjects. The study was conducted in a cross over design. After the absorption phase canrenone plasma concentrations followed a biexponential decay. The half lives of the three phases observed were respectively 40.7 +/- 21.7 min, 1.94 +/- 0.558 hr and 18.5 +/- 3.93 hr after administration of a 100 mg capsules; they were respectively 31.8 +/- 14 min, 1.64 +/- 0.513 hr and 16.1 +/- 3.09 hr after administration of two 50 mg capsules. These values were similar to those reported in man. Bioequivalence of the two forms tested was ascertained by a two way analysis of variance and by the Westlake symmetrical confidence interval (95%). Peak plasma levels, Cmax, time to reach the peak, tmax, and the rate constant of absorption showed great inter and intra individual variations. In vivo hydrolysis of canrenone into canrenoic acid and subsequent lactonization of the acid are pH-dependent and could give rise to these variations if occurring before absorption.

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Year:  1986        PMID: 3816872     DOI: 10.1007/BF03189843

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  11 in total

1.  Symmetrical confidence intervals for bioequivalence trials.

Authors:  W J Westlake
Journal:  Biometrics       Date:  1976-12       Impact factor: 2.571

2.  Enhancement by food of canrenone bioavailability from spironolactone.

Authors:  A Melander; K Danielson; B Scherstén; T Thulin; E Wåhlin
Journal:  Clin Pharmacol Ther       Date:  1977-07       Impact factor: 6.875

3.  Pharmacokinetics of spironolactone, canrenone and canrenoate-K in humans.

Authors:  W Sadée; M Dagcioglu; R Schröder
Journal:  J Pharmacol Exp Ther       Date:  1973-06       Impact factor: 4.030

4.  Disposition of tritium-labeled spirolactones in the dog.

Authors:  W Sadée; S Riegelman; S C Jones
Journal:  J Pharm Sci       Date:  1972-07       Impact factor: 3.534

5.  Prediction of stability in pharmaceutical preparations. XVI. Kinetics of hydrolysis of canrenone and lactonization of canrenoic acid.

Authors:  E R Garrett; C M Won
Journal:  J Pharm Sci       Date:  1971-12       Impact factor: 3.534

6.  [Bioequivalence of dosage forms. The confidence interval approach. Westlake's method (author's transl)].

Authors:  J L Steimer; J J Thebault
Journal:  Therapie       Date:  1980 Nov-Dec       Impact factor: 2.070

7.  [Intersubject comparison of the bioavailability of spironolactone in 2 pharmaceutical dosage forms].

Authors:  P D Lucchelli; A Monarca; S Del Mastro; R Sega
Journal:  Boll Chim Farm       Date:  1978-08

8.  Application of a simple fluorometric method on absorption of canrenone.

Authors:  J P Radó; L Szende; J Takó; O Nagy; C Kozma
Journal:  Int J Clin Pharmacol Biopharm       Date:  1976-03

9.  Spironolactone. II. Bioavailability.

Authors:  A Karim; J Zagarella; T C Hutsell; A Chao; B J Baltes
Journal:  Clin Pharmacol Ther       Date:  1976-02       Impact factor: 6.875

10.  A fluorimetric method for the determination of a major spironolactone (Aldactone) metabolite in human plasma.

Authors:  N GOCHMAN; C L GANTT
Journal:  J Pharmacol Exp Ther       Date:  1962-03       Impact factor: 4.030

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