Rey E, d'Athis P, Giraux P, de Lauture D, Turquais J M, Chavinie J, Olive G
Eur J Clin Pharmacol. 1979 Apr 17;15(3):175-80. doi: 10.1007/BF00563102.
A single dose of clorazepate 20 mg was injected i.m. in 7 pregnant and 7 non-pregnant women. Blood samples were collected for one week, and urine was collected for 24 h after the dose. The concentrations of clorazepate and its metabolite nordiazepam were determined by electron capture gas liquid chromatography. There was no difference between the two groups on physical examinations. Clorazepate was rapidly absorbed and the peak concentration was reached within 2 h. Mean pharmacokinetic parameters for clorazepate were absorption half life 0.77 h in pregnant women and 0.56 h in non-pregnant women; elimination half life 1.3 h in pregnant women and 2.0 h in non-pregnant women; volume of distribution: 0.43 1 . kg-1 in the pregnant women and 0.33 1 . kg-1 in non-pregnant women. Nordiazepam reached its peak concentration within 12 h after dosing; its mean half life of elimination was 180 h in pregnant women and 60 h in non-pregnant women. Within 24 h, 1.3% of the clorazepate was recovered in urine from pregnant women and 7% in urine from the non-pregnant women.
对7名孕妇和7名非孕妇肌肉注射单剂量20毫克氯氮䓬。采集血样一周,并在给药后24小时收集尿液。采用电子捕获气液色谱法测定氯氮䓬及其代谢产物去甲地西泮的浓度。两组的体格检查无差异。氯氮䓬吸收迅速,2小时内达到峰值浓度。氯氮䓬的平均药代动力学参数为:孕妇吸收半衰期0.77小时,非孕妇0.56小时;孕妇消除半衰期1.3小时,非孕妇2.0小时;分布容积:孕妇为0.43升/千克,非孕妇为0.33升/千克。去甲地西泮在给药后12小时内达到峰值浓度;其平均消除半衰期在孕妇中为180小时,在非孕妇中为60小时。24小时内,孕妇尿液中氯氮䓬的回收率为1.3%,非孕妇尿液中为7%。