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健康女性志愿者中苯扎贝特和氯贝丁酯的稳态动力学

Steady-state kinetics of bezafibrate and clofibrate in healthy female volunteers.

作者信息

Abshagen U, Spörl-Radun S, Marinow J

出版信息

Eur J Clin Pharmacol. 1980 Apr;17(4):305-8. doi: 10.1007/BF00625805.

Abstract

The steady-state kinetics of chlorophenoxyisobuytric acid (CPIB) and of bezafibrate were investigated in a strictly controlled, randomised cross-over study in 10 female volunteers, after the conventional oral doses of clofibrate 0.5 g and bezafibrate f0.2 g at 8-h intervals. The mean steady-state concentration of CPIB in serum was 34 times higher than that of bezafibrate, which was due to the considerable cumulation of CPIB, whereas no cumulation of bezafibrate was observed. This is supported by comparison of the AUCs, and of the maximum and mean concentrations of bezafibrate after the first and last doses. beta (0.44 and 0.49 h(-1)) and the half-lives (1.6 and 1.4h) were almost identical after the first and last doses of bezafibrate. The median total clearances of CPIB and bezafibrate amounted to 10.5 and 142.5ml/min, respectively, if complete absorption of both drugs is assumed. Since the apparent volumes of distribution were in the same range for both drugs, the amount of drug present in the organism in steady-state also differed by a factor of approximately 30 under the usual dosage regimen.

摘要

在一项严格控制的随机交叉研究中,对10名女性志愿者进行了氯苯氧基异丁酸(CPIB)和苯扎贝特的稳态动力学研究。研究中,按照常规口服剂量,每隔8小时分别给予氯贝丁酯0.5 g和苯扎贝特0.2 g。血清中CPIB的平均稳态浓度比苯扎贝特高34倍,这是由于CPIB有相当程度的蓄积,而未观察到苯扎贝特的蓄积。这一点通过比较苯扎贝特首剂和末剂后的AUC、最大浓度和平均浓度得到了证实。苯扎贝特首剂和末剂后的β(分别为0.44和0.49 h⁻¹)以及半衰期(分别为1.6和1.4 h)几乎相同。如果假定两种药物均完全吸收,CPIB和苯扎贝特的中位总清除率分别为10.5和142.5 ml/min。由于两种药物的表观分布容积处于同一范围,在通常的给药方案下,稳态时体内存在的药物量也相差约30倍。

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