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头孢唑林从蛋白结合位点的置换对血清及组织液水平的影响。

The effect of displacement from protein binding on serum and tissue fluid levels of cephazolin.

作者信息

Polacek I, Mühlbauer H

出版信息

Biopharm Drug Dispos. 1980 Jan-Mar;1(3):127-32. doi: 10.1002/bdd.2510010307.

DOI:10.1002/bdd.2510010307
PMID:7448339
Abstract

Displacement of cephazolin, a highly protein-bound beta-lactam antibiotic, by sulpha-phenazole was studied in vitro and in vivo. In vitro, the sulphonamide was effective in displacing the antibiotic from its binding sites at the concentration 100--1000 mumol 1(-1). In vivo, both the serum and the tissue fluid concentration of free cephazolin increased significantly in rats concomitantly treated with sulphaphenazole.

摘要

在体外和体内研究了磺胺苯唑对头孢唑林(一种高度蛋白结合的β-内酰胺抗生素)的置换作用。在体外,磺胺类药物在浓度为100 - 1000 μmol·L⁻¹时能有效将抗生素从其结合位点上置换下来。在体内,同时用磺胺苯唑治疗的大鼠体内游离头孢唑林的血清和组织液浓度均显著升高。

相似文献

1
The effect of displacement from protein binding on serum and tissue fluid levels of cephazolin.头孢唑林从蛋白结合位点的置换对血清及组织液水平的影响。
Biopharm Drug Dispos. 1980 Jan-Mar;1(3):127-32. doi: 10.1002/bdd.2510010307.
2
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Cefazolin serum protein binding and its inhibition by bilirubin, fatty acids and other drugs.头孢唑林的血清蛋白结合及其受胆红素、脂肪酸和其他药物的抑制作用。
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