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[头孢菌素和羧苄青霉素在无菌性炎症大鼠组织中的渗透情况]

[Cephalosporin and carbenicillin penetration into the tissues of rats with aseptic inflammation].

作者信息

Agapitova I V, Bobrov V I

出版信息

Antibiotiki. 1984 Jun;29(6):427-30.

PMID:6476804
Abstract

Two beta-lactam antibiotics with different serum protein binding were studied for penetration into the tissues of rats with aseptic inflammation. It was found that the pharmacokinetics of the drugs in the blood serum differed only in the elimination rate. The levels of the free fraction of cephaloridin were much higher than those of carbenicillin. The maximum concentrations of free cephaloridin in the inflammation exudate, intact and inflamed tissues and the areas under its pharmacokinetic curves were higher than those of carbenicillin. The elimination rate of both the drugs was the same for all the tissues studied.

摘要

研究了两种血清蛋白结合率不同的β-内酰胺类抗生素在无菌性炎症大鼠组织中的渗透情况。结果发现,这两种药物在血清中的药代动力学仅在消除速率上有所不同。头孢菌素I的游离部分水平远高于羧苄青霉素。炎症渗出液、正常组织和炎症组织中游离头孢菌素I的最高浓度及其药代动力学曲线下面积均高于羧苄青霉素。在所有研究的组织中,两种药物的消除速率相同。

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