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碘海醇在大鼠体内的药代动力学

Pharmacokinetics of iopentol in the rat.

作者信息

Michelet A A, Skinnemoen K

机构信息

Department of Pharmacology and Toxicology Nycomed AS, Oslo, Norway.

出版信息

Acta Radiol Suppl. 1987;370:101-4.

PMID:2980301
Abstract

The pharmacokinetic properties and potential metabolism of iopentol have been investigated after intravenous injection in rats. The elimination was rapid, with more than 95 per cent of the injected dose recovered in urine and faeces within the first 24 h. The biologic half-life of iopentol in rat blood was 24 min. There was no significant biotransformation and only trace amounts were detected in tissues 24 hr after the injection of 200 mg I/kg or 7 days after the injection of 1 or 10 g I/kg.

摘要

在大鼠静脉注射后,已对碘海醇的药代动力学特性和潜在代谢进行了研究。消除迅速,在最初24小时内,超过95%的注射剂量在尿液和粪便中回收。碘海醇在大鼠血液中的生物半衰期为24分钟。没有明显的生物转化,在注射200毫克碘/千克后24小时或注射1或10克碘/千克后7天,组织中仅检测到痕量。

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