Jochemsen R, van Boxtel C J, Hermans J, Breimer D D
Clin Pharmacol Ther. 1983 Jul;34(1):42-7. doi: 10.1038/clpt.1983.126.
Kinetics of five benzodiazepine hypnotics (15 mg flurazepam, 1 mg flunitrazepam, 5 mg nitrazepam, 10 mg temazepam, and 0.5 mg triazolam) were compared in the same group of 12 healthy subjects. Plasma concentrations of parent drugs were determined by capillary gas chromatography with electron-capture detection. For flurazepam, the N-desalkyl metabolite (DAF) was measured. Flunitrazepam, nitrazepam, temazepam, and triazolam were rapidly absorbed, although there was considerable variability; mean peak times (ranges) were: 1.3 (0.3 to 3) hr, 1.8 (0.7 to 6) hr, 1.2 (0.3 to 4) hr, and 1.1 (0.7 to 2) hr. Plasma concentrations of DAF increased rather slowly and reached their maximum between 3 and 48 hr after flurazepam. There were considerable differences in elimination t1/2s, with means of 35 (15 to 66) hr for flunitrazepam, 28 (22 to 33) hr for nitrazepam, 12 (8 to 22) hr for temazepam, 2.4 (1.4 to 3.9) hr for triazolam, and 84 (40 to 114) hr for DAF. Sex differences in elimination t1/2 were only observed for DAF: 99 hr in women and 69 hr in men. Our results show that there are considerable differences in the kinetics of the diazepines.
在同一组12名健康受试者中比较了五种苯二氮䓬类催眠药(15毫克氟西泮、1毫克氟硝西泮、5毫克硝西泮、10毫克替马西泮和0.5毫克三唑仑)的药代动力学。采用带电子捕获检测的毛细管气相色谱法测定母体药物的血浆浓度。对于氟西泮,测定了N-去烷基代谢物(DAF)。氟硝西泮、硝西泮、替马西泮和三唑仑吸收迅速,尽管存在相当大的变异性;平均达峰时间(范围)分别为:1.3(0.3至3)小时、1.8(0.7至6)小时、1.2(0.3至4)小时和1.1(0.7至2)小时。氟西泮给药后,DAF的血浆浓度升高相当缓慢,在3至48小时之间达到最大值。消除半衰期存在相当大的差异,氟硝西泮的平均值为35(15至66)小时,硝西泮为28(22至33)小时,替马西泮为12(8至22)小时,三唑仑为2.4(1.4至3.9)小时,DAF为84(40至114)小时。仅在DAF的消除半衰期观察到性别差异:女性为99小时,男性为69小时。我们的结果表明,苯二氮䓬类药物的药代动力学存在相当大的差异。