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单剂量和多剂量氯贝丁酯的动力学

Clofibrate kinetics after single and multiple doses.

作者信息

Gugler R, Hartlapp J

出版信息

Clin Pharmacol Ther. 1978 Oct;24(4):432-8. doi: 10.1002/cpt1978244432.

Abstract

The kinetics of chlorphenoxyisobutyric acid (CPIB) were studied in 5 healthy subjects after single 500-mg, 1,000-mg, and 2,000-mg doses of clofibrate, and in steady-state after 8 days' treatment with 1,000 mg twice daily. Maximum plasma concentrations of CPIB were observed 4 to 6 hr after dosing. A mean plasma half-life of 16.7 hr was recorded which was independent of dose and duration of treatment. Total plasma clearance (-Cl) calculated from area under the curve with the use of the total plasma concentration was 5.6 ml/min for the 500-and the 1,000-mg doses but increased to 6.8 ml/min for the 2,000-mg dose and was even higher (8.1 ml/min) in steady-state. This change in -Cl is a consequence of progressive reduction in the plasma protein binding of clofibrate at plasma concentrations above 50 microgram/ml, since -Cl rises in association with reduced protein binding at the high plasma concentrations measured after the 2,000-mg single dose and in steady-state. -Cl and apparent volume of distribution were identical for all doses tested when calculations were based on the nonprotein-bound CPIB concentrations only. Due to the inconsistant protein binding of CPIB, total steady-state concentrations could not be predicted from the single dose kinetic data.

摘要

在5名健康受试者中,研究了氯贝丁酯单次服用500毫克、1000毫克和2000毫克剂量后氯苯氧基异丁酸(CPIB)的动力学情况,以及在每日两次服用1000毫克、持续8天治疗后的稳态情况。给药后4至6小时观察到CPIB的最大血浆浓度。记录的平均血浆半衰期为16.7小时,其与剂量和治疗持续时间无关。使用总血浆浓度根据曲线下面积计算的总血浆清除率(-Cl),500毫克和1000毫克剂量时为5.6毫升/分钟,但2000毫克剂量时增至6.8毫升/分钟,在稳态时甚至更高(8.1毫升/分钟)。-Cl的这种变化是由于血浆浓度高于50微克/毫升时氯贝丁酯的血浆蛋白结合逐渐减少所致,因为在单次服用2000毫克剂量后及稳态时所测高血浆浓度下,-Cl随蛋白结合减少而升高。当仅基于未与蛋白结合的CPIB浓度进行计算时,所有测试剂量的-Cl和表观分布容积均相同。由于CPIB的蛋白结合不一致,无法根据单剂量动力学数据预测总稳态浓度。

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