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老年人口服普拉西泮后去甲基地西泮的动力学

Desmethyldiazepam kinetics in the elderly after oral prazepam.

作者信息

Allen M D, Greenblatt D J, Harmatz J S, Shader R I

出版信息

Clin Pharmacol Ther. 1980 Aug;28(2):196-202. doi: 10.1038/clpt.1980.150.

Abstract

Our subjects were 15 young (aged 22 to 42 yr) and 14 elderly (aged 62 to 85 yr) people who took single oral doses of 20 mg prazepam. Plasma desmethyldiazepam (DMDZ) concentrations were determined in venous blood samples drawn up to 9 days after the dose. Appearance in blood of DMDZ was slow, with peak plasma levels reached in an average of 10 to 20 hr. First-order DMDZ appearance was observed in only 17 subjects. Volume of distribution of total DMDZ (range, 1.33 to 6.30 l/kg) and of unbound DMDZ after correction for protein binding (range, 43 to 243 l/kg) was larger in women than in men of all ages, and in the elderly as opposed to the young. Elimination half-life (range, 29 to 224 hr) rose with age in men (r = 0.66, p < 0.01) but not in women (r = -0.02). Clearance of unbound DMDZ (range, 2.9 to 31.2 ml/min/kg) was greater in women than in men of all ages, and declined with age in men (r = -0.40) but not in women (r = -0.06). As in the case of diazepam, age can influence DMDZ kinetics, but changes in drug disposition with age may differ between sexes.

摘要

我们的研究对象为15名年轻人(年龄在22至42岁之间)和14名老年人(年龄在62至85岁之间),他们单次口服20毫克普拉西泮。在服药后长达9天内采集静脉血样,测定血浆去甲基地西泮(DMDZ)浓度。DMDZ在血液中的出现较为缓慢,平均在10至20小时达到血浆峰值水平。仅在17名受试者中观察到一级DMDZ出现。所有年龄段的女性中,总DMDZ的分布容积(范围为1.33至6.30升/千克)以及校正蛋白结合后的游离DMDZ分布容积(范围为43至243升/千克)均大于男性,且老年人大于年轻人。男性的消除半衰期(范围为29至224小时)随年龄增长而延长(r = 0.66,p < 0.01),而女性则不然(r = -0.02)。所有年龄段的女性中,游离DMDZ的清除率(范围为2.9至31.2毫升/分钟/千克)均大于男性,男性的清除率随年龄下降(r = -0.40),而女性则不然(r = -0.06)。与地西泮的情况一样,年龄会影响DMDZ的动力学,但药物处置随年龄的变化在性别之间可能有所不同。

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