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抗生素蛋白结合的研究。IV. 药物与兔肝匀浆100,000 X g 上清液的结合对尿排泄的影响。

Studies on protein binding of antibiotics. IV. Effect of the binding of drug to 100,000 X g supernatant fluid of rabbit liver homogenates on urinary excretion.

作者信息

Watanabe Y, Kitayama R, Hayashi T, Nakashima Y, Noguchi M, Yasuda T, Saikawa I, Shimizu K

出版信息

J Antibiot (Tokyo). 1982 Nov;35(11):1603-9. doi: 10.7164/antibiotics.35.1603.

Abstract

The extent of the binding of beta-lactam antibiotics to 100,000 X g supernatant fluid of rabbit liver homogenates was investigated. Urinary excretion tended to decrease as the extent of the binding to 100,000 X g supernatant fluid increased. Predicting urinary excretion was achieved using the binding to 100,000 X g supernatant fluid and other physicochemical factors. A good coincidence resulted from multiple regression analysis. [14C]Benzylpenicillin binding proteins in rabbit liver were investigated and revealed that the affinity of cefoperazone was much stronger than that of cefazolin.

摘要

研究了β-内酰胺抗生素与兔肝匀浆100,000×g上清液的结合程度。随着与100,000×g上清液的结合程度增加,尿排泄量有减少趋势。利用与100,000×g上清液的结合及其他理化因素实现了对尿排泄的预测。多元回归分析得出了良好的一致性结果。对兔肝中的[14C]苄青霉素结合蛋白进行了研究,结果显示头孢哌酮的亲和力远强于头孢唑林。

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