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Non-linear intestinal absorption kinetics of cefadroxil in the rat.

作者信息

Sánchez-Picó A, Peris-Ribera J E, Toledano C, Torres-Molina F, Casabó V G, Martín-Villodre A, Plá-Delfina J M

机构信息

Department of Pharmacology and Pharmacetics, Faculty of Pharmacy, University of Valencia, Spain.

出版信息

J Pharm Pharmacol. 1989 Mar;41(3):179-85. doi: 10.1111/j.2042-7158.1989.tb06425.x.

Abstract

Absorption of cefadroxil in a selective intestinal absorption area (the proximal third of the small intestine) of the anaesthetized rat, at seven initial perfusion concentrations, ranging from 0.01 to 10.0 mg mL-1, is shown to be a non-linear transport mechanism. With the aid of computer-fitting procedures based on differential and integrated forms of Michaelis-Menten equation, Vm and Km values of 36.7-37.3 mg h-1 and 12.0-13.0 mg, respectively, were found. The statistical parameters were better than those obtained both for first-order and for combined Michaelis-Menten and first-order kinetics. There is no evidence for substantial passive diffusion processes. The results reported here, together with allometric considerations and literature data analysis, may help to explain some particular non-linear features of plasma level curves associated with the administration of fairly high oral doses of cefadroxil to humans.

摘要

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