Evaluation of bioequivalence of two tablet forms of lisinopril in healthy volunteers

Under cross, single, open, randomized trial with 1 week washout period, with two sequences of 18 volunteers studied bioequivalence coated tablets, two manufacturers of lisinopril (20 mg dose). The concentration of lisinopril in the plasma samples was determined using HPLC with fluorimetric detection...

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Auteurs principaux:	S. A. Altynbekov, G. A. Dzholdygulov, V. N. Seryakov, Y. M. Budach, O. E. Kurilo, N. I. Kuznetsova
Format:	Artigo
Langue:	Russo
Publié:	LLC “Publisher OKI” 2013-09-01
Collection:	Фармакокинетика и Фармакодинамика
Sujets:	лизиноприл вэжх флуорометрическое детектирование биоэквивалентность lisinopril hplc fluorometric detection bioequivalence
Accès en ligne:	https://www.pharmacokinetica.ru/jour/article/view/133
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