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静脉注射氯霉素在仔猪体内的药代动力学。

Pharmacokinetics of intravenously injected chloramphenicol in baby pigs.

作者信息

Rao V R, Clarenburg R

出版信息

Drug Metab Dispos. 1977 May-Jun;5(3):253-8.

PMID:17523
Abstract

A sensitive fluorometric assay procedure for chloramphenicol and its metabolites was used to measure distribution in tissues and elimination of the drug after injection of 22 mg/kg iv in baby pigs. Disappearance of chloramphenicol from plasma was biphasic; an initial component was rapid (half-life about 9 min) and a second component had a half-life of 55 min. The total chloramphenicol levels in tissues and body fluids had half-life periods of 1-1.5 hr and dropped below limits of detectability within 9 hr after injection. About 80% of the injected dose was recovered from urine collected over the first 6 hr, and none thereafter. Fecal elimination, if occurring, was negligible.

摘要

采用一种灵敏的氯霉素及其代谢物荧光测定法,测定了在仔猪静脉注射22mg/kg药物后,氯霉素在组织中的分布情况及其消除过程。氯霉素从血浆中的消失呈双相性;初始成分消失迅速(半衰期约9分钟),第二成分的半衰期为55分钟。组织和体液中的总氯霉素水平半衰期为1 - 1.5小时,注射后9小时内降至检测限以下。在最初6小时收集的尿液中回收了约80%的注射剂量,此后未再回收。粪便消除(若有发生)可忽略不计。

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