Simultaneous study of the pharmacokinetics of intravenous and oral nicardipine using a stable isotope.

Abstract:

:The systemic elimination of nicardipine has been studied by an initial oral administration of nicardipine followed 1.25 h later by intravenous injection of the deuterium-labelled molecule (D3 nicardipine). To check that intravenous kinetics was not modified by the oral administration, an i.v. injection of unlabelled nicardipine (D0 nicardipine) was also given. The study was carried out in six healthy male volunteers, aged between 24 and 27 years, according to a Latin square cross-over design. Similar values were found for each kinetic parameter after i.v. administration regardless of whether it was administered alone by that route or with an oral dose. The plasma level-time curves of nicardipine were described by a three open compartment model. The total plasma clearance was about 800 ml/min, the volume of distribution was of the order of 1 l/kg and the half-life of beta-elimination ranged from 4 to 5 h. The elimination rate constant beta was independent of the route of administration.

journal_name

Eur J Clin Pharmacol

authors

Guerret M,Cheymol G,Hubert M,Julien-Larose C,Lavene D

doi

10.1007/BF00558504

subject

Has Abstract

pub_date

1989-01-01 00:00:00

pages

381-5

issue

4

eissn

0031-6970

issn

1432-1041

journal_volume

37

pub_type

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