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[头孢曲松胆汁排泄及其肝脏处置的实验评估]

[Experimental evaluation of the biliary tract passage of ceftriaxone and its hepatic disposition].

作者信息

Brogard J M, Blickle J F, Jehl F, Dorner M, Monteil H

出版信息

Pathol Biol (Paris). 1987 May;35(5):441-7.

PMID:3302844
Abstract

The biliary elimination of ceftriaxone was studied by an isolated perfused rabbit liver model (n = 5). After adding of 10 mg of this antibiotic to the circulating blood of this preparation, a mean biliary peak level reaching 120.5 +/- 24.6 micrograms/ml was obtained between the 30th and 60th minutes. The total amount of ceftriaxone eliminated unchanged in the bile collected during a 3h period represents 8.8 +/- 2.6% of the administered dose. At the end of this study period, 32.7 +/- 3.3% of the initial dose remained in the circulating blood. The hepatic tissue concentrated 3.7% of the whole dose. At last, control experiments proved that 36.4% of the added antibiotic has been degraded by the experimental system itself. Thus the remaining 18.4% can be attributed to a hepatic biotransformation of ceftriaxone.

摘要

采用离体灌注兔肝模型(n = 5)研究了头孢曲松的胆汁排泄情况。在该制剂的循环血液中加入10 mg这种抗生素后,在第30至60分钟之间获得了平均胆汁峰值水平,达到120.5±24.6微克/毫升。在3小时内收集的胆汁中未变化消除的头孢曲松总量占给药剂量的8.8±2.6%。在本研究期结束时,初始剂量的32.7±3.3%仍留在循环血液中。肝组织浓缩了全剂量的3.7%。最后,对照实验证明,添加的抗生素中有36.4%已被实验系统自身降解。因此,其余的18.4%可归因于头孢曲松的肝脏生物转化。

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