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屈他维林酸酯在大鼠和人体中的命运。II. 屈他维林 -14C-酸酯的人体药代动力学。

The fate of drotaverine-acephyllinate in rat and man. II. Human pharmacokinetics of drotaverine-14C-acephyllinate.

作者信息

Vargay Z, Deutsch T, Szatmári I, Szüts T, Várkonyi P, Kerpel-Fronius S, Eckhardt S

出版信息

Eur J Drug Metab Pharmacokinet. 1984 Jan-Mar;9(1):17-29. doi: 10.1007/BF03189602.

Abstract

Pharmacokinetics of Drotaverine-Acephyllinate, Chinoin was investigated in seven male volunteers using 14C labelled drug. Drotaverine-Acephyllinate was administered at a 100 mg single oral dose. Measurements of total radioactivity showed that the drug was absorbed completely and was eliminated by renal and biliary routes. Within 72 hours 39.9 +/- 9.9% and 47.1 +/- 4.9% of the dose were recovered in the urine and faeces respectively. Experimental results were interpreted on the basis of a complex linear compartment model. The structural identifiability of the model was proved by computer analysis, and the pharmacokinetic parameters were determined.

摘要

使用14C标记药物,在7名男性志愿者中研究了屈他维林叶酸盐(Drotaverine-Acephyllinate)(奇诺因公司生产)的药代动力学。屈他维林叶酸盐以100mg单次口服剂量给药。总放射性测量表明,药物被完全吸收,并通过肾脏和胆汁途径消除。72小时内,分别在尿液和粪便中回收了剂量的39.9±9.9%和47.1±4.9%。实验结果基于复杂的线性房室模型进行解释。通过计算机分析证明了该模型的结构可识别性,并确定了药代动力学参数。

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