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托拉塞米及其代谢产物在健康对照者和慢性肾衰竭患者中的药代动力学

Pharmacokinetics of torasemide and its metabolites in healthy controls and in chronic renal failure.

作者信息

Spahn H, Knauf H, Mutschler E

机构信息

Pharmakologisches Institut für Naturwissenschaftler der Johann Wolfgang Goethe-Universität Frankfurt/Main, FRG.

出版信息

Eur J Clin Pharmacol. 1990;39(4):345-8. doi: 10.1007/BF00315407.

Abstract

The pharmacokinetics of 20 mg torasemide i.v. has been studied in 7 healthy controls and 9 patients with varying degrees of renal impairment. Torasemide had a t1/2 of about 4h which was independent of kidney function, as the nonrenal clearance of torasemide was 3-times greater than its renal clearance. The active metabolite M 1 and the main metabolite M 5 were accumulated in chronic renal failure. In contrast to liver function, therefore, kidney failure does not have an important effect on the pharmacokinetics of torasemide.

摘要

已在7名健康对照者和9名不同程度肾功能损害患者中研究了静脉注射20毫克托拉塞米的药代动力学。托拉塞米的半衰期约为4小时,这与肾功能无关,因为托拉塞米的非肾清除率是其肾清除率的3倍。活性代谢物M1和主要代谢物M5在慢性肾衰竭中会蓄积。因此,与肝功能不同,肾衰竭对托拉塞米的药代动力学没有重要影响。

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