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Article Dans Anglais | IMSEAR | ID: sea-87212

Résumé

OBJECTIVE: To assess the bioavailability of clonazepam from two brands of 2 mg tablet formulations--Epitril and reference brand. METHODS: A two-way randomised cross-over bioavailability study was carried out in 12 healthy male volunteers. Coded plasma samples were analysed for levels of clonazepam by high performance liquid chromatography (HPLC) method. RESULTS: The mean Cmax, Tmax t1/2 beta and AUC (0-48) for Epitril were: 16.31 +/- 3.07 ng/mL, 1.63 +/- 0.48 h, 46.97 +/- 12.26 h and 207.70 +/- 57.07 ng/ml.h; for reference brand were 19.75 +/- 5.95 ng/mL, 1.42 +/- 0.29 h, 46.88 +/- 11.29 h and 215.70 +/- 50.89 ng/ml.h respectively. These were comparable and the differences were not statistically significant. CONCLUSION: Based on above pharmacokinetic parameters, Epitril was bioequivalent to reference brand.


Sujets)
Administration par voie orale , Adulte , Analyse de variance , Biodisponibilité , Chimie pharmaceutique , Chromatographie en phase liquide à haute performance , Clonazépam/administration et posologie , Études croisées , Humains , Mâle , Adulte d'âge moyen , Valeurs de référence , Sensibilité et spécificité , Comprimés
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