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低剂量口服避孕药对女性劳拉西泮和奥沙西泮药代动力学的影响

Lorazepam and oxazepam kinetics in women on low-dose oral contraceptives.

作者信息

Abernethy D R, Greenblatt D J, Ochs H R, Weyers D, Divoll M, Harmatz J S, Shader R I

出版信息

Clin Pharmacol Ther. 1983 May;33(5):628-32. doi: 10.1038/clpt.1983.85.

Abstract

Women on low-dose estrogen oral contraceptives (OC) and drug-free control women matched for age, weight, and cigarette smoking habits, received single 2-mg IV doses of lorazepam or single 30-mg oral doses of oxazepam, two benzodiazepines metabolized by glucuronide conjugation. Kinetics were determined from multiple plasma concentrations measured during 48 hr after dosing. Mean kinetic variables for lorazepam in control and OC groups (n = 15 in each group) were: volume of distribution (Vd), 1.33 and 1.45 l/kg; elimination t1/2, 13.1 and 12.2 hr; total clearance, 1.25 and 1.50 ml/min/kg; free fraction in plasma, 10.3% and 10.3% unbound. For oxazepam, kinetic variables in the two groups (n = 14 and 17) were: Vd, 1.05 and 1.19 l/kg; t1/2, 7.6 and 7.2 hr; total clearance, 1.60 and 2.03 ml/min/kg; free fraction, 4.6% and 4.9% unbound. None of these differences were significant. Thus, metabolic clearance by glucuronidation of lorazepam and oxazepam is not significantly affected by OC, in contrast with the highly significant reduction in clearance of the oxidized benzodiazepine diazepam.

摘要

服用低剂量雌激素口服避孕药(OC)的女性以及在年龄、体重和吸烟习惯方面相匹配的未服药对照女性,分别静脉注射单次2毫克劳拉西泮或口服单次30毫克奥沙西泮,这两种苯二氮䓬类药物均通过葡萄糖醛酸结合代谢。给药后48小时内多次测量血浆浓度以确定动力学。对照和OC组(每组n = 15)中劳拉西泮的平均动力学变量为:分布容积(Vd),1.33和1.45升/千克;消除半衰期,13.1和12.2小时;总清除率,1.25和1.50毫升/分钟/千克;血浆中游离分数,未结合的为10.3%和10.3%。对于奥沙西泮,两组(n = 14和17)的动力学变量为:Vd,1.05和1.19升/千克;t1/2,7.6和7.2小时;总清除率,1.60和2.03毫升/分钟/千克;游离分数,未结合的为4.6%和4.9%。这些差异均无统计学意义。因此,与氧化型苯二氮䓬地西泮清除率显著降低相反,OC对劳拉西泮和奥沙西泮通过葡萄糖醛酸化的代谢清除没有显著影响。

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