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丙氧芬与地西泮、阿普唑仑及劳拉西泮的相互作用。

Interaction of propoxyphene with diazepam, alprazolam and lorazepam.

作者信息

Abernethy D R, Greenblatt D J, Morse D S, Shader R I

出版信息

Br J Clin Pharmacol. 1985 Jan;19(1):51-7. doi: 10.1111/j.1365-2125.1985.tb02612.x.

Abstract

Healthy volunteers received single doses of three benzodiazepines (diazepam, 10 mg i.v.; alprazolam, 1.0 mg orally; lorazepam, 2 mg i.v.) on two occasions in random sequence. One trial was a control; for the other, subjects ingested propoxyphene, 65 mg every 6 h, for the duration of the benzodiazepine study. The kinetics of each benzodiazepine were determined from multiple plasma concentrations measured following each dose. For diazepam, propoxyphene produced a small and statistically insignificant prolongation of elimination half-life (43 vs 38 h) and reduction of total clearance (0.41 vs 0.47 ml min-1 kg-1). Propoxyphene significantly prolonged alprazolam half-life (18 vs 12 h, P less than 0.005) and reduced total clearance (0.8 vs 1.3 ml min-1 kg-1, P less than 0.005). Propoxyphene had no apparent influence on lorazepam half-life (13.4 vs 13.5 h) or clearance (1.5 vs 1.4 ml min-1 kg-1). Thus propoxyphene significantly impairs the clearance of alprazolam, biotransformed mainly by the oxidative reaction of aliphatic hydroxylation. Propoxyphene has far less effect on the oxidation of diazepam by N-demethylation, and has no apparent influence on lorazepam conjugation.

摘要

健康志愿者分两次随机接受三种苯二氮䓬类药物的单剂量给药(地西泮,静脉注射10毫克;阿普唑仑,口服1.0毫克;劳拉西泮,静脉注射2毫克)。一次试验为对照;另一次试验中,在苯二氮䓬类药物研究期间,受试者每6小时服用65毫克丙氧芬。每种苯二氮䓬类药物的动力学由每次给药后多次测量的血浆浓度确定。对于地西泮,丙氧芬使消除半衰期略有延长(43小时对38小时),但在统计学上无显著意义,总清除率降低(0.41毫升·分钟⁻¹·千克⁻¹对0.47毫升·分钟⁻¹·千克⁻¹)。丙氧芬显著延长了阿普唑仑的半衰期(18小时对12小时,P<0.005),并降低了总清除率(0.8毫升·分钟⁻¹·千克⁻¹对1.3毫升·分钟⁻¹·千克⁻¹,P<0.005)。丙氧芬对劳拉西泮的半衰期(13.4小时对13.5小时)或清除率(1.5毫升·分钟⁻¹·千克⁻¹对1.4毫升·分钟⁻¹·千克⁻¹)没有明显影响。因此,丙氧芬显著损害了主要通过脂肪族羟基化氧化反应进行生物转化的阿普唑仑的清除。丙氧芬对通过N-去甲基化进行的地西泮氧化影响小得多,对劳拉西泮的结合没有明显影响。

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