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25毫克苯海拉明在青年和老年志愿者体内的药代动力学和药效学

Pharmacokinetics and pharmacodynamics of diphenhydramine 25 mg in young and elderly volunteers.

作者信息

Scavone J M, Greenblatt D J, Harmatz J S, Engelhardt N, Shader R I

机构信息

Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, New England Medical Center Hospital, Boston, Massachusetts 02111, USA.

出版信息

J Clin Pharmacol. 1998 Jul;38(7):603-9. doi: 10.1002/j.1552-4604.1998.tb04466.x.

Abstract

Thirty-seven young and elderly male and female volunteers 21 to 76 years of age received a single 25-mg oral dose of diphenhydramine or matching placebo in a double-blind, randomized, two-way crossover study. Plasma diphenhydramine concentrations, self-ratings of sedation, mood, and autonomic effects, performance on the digit-symbol substitution test (DSST), and heart rate were determined for 24 hours after administration. Information acquisition and recall were tested at 2.5 and 24 hours after administration. Age and gender did not significantly influence diphenhydramine peak plasma concentration, time of peak concentration, elimination half-life, area under the plasma concentration curve, or apparent oral clearance. Effects on psychomotor performance, sedation, mood, and memory did not differ between diphenhydramine and placebo in either group. Thus, the pharmacokinetics of single 25-mg oral doses of diphenhydramine are not influenced by age or gender. This dose of diphenhydramine produces essentially undetectable pharmacodynamic effects in both the young and elderly.

摘要

在一项双盲、随机、双向交叉研究中,37名年龄在21至76岁之间的年轻及年长男女志愿者口服了25毫克苯海拉明单剂量药物或匹配的安慰剂。给药后24小时测定血浆苯海拉明浓度、镇静、情绪和自主神经效应的自我评分、数字符号替换测试(DSST)表现以及心率。在给药后2.5小时和24小时测试信息获取和回忆情况。年龄和性别对苯海拉明的血浆峰浓度、峰浓度时间、消除半衰期、血浆浓度曲线下面积或表观口服清除率均无显著影响。两组中,苯海拉明和安慰剂对精神运动表现、镇静、情绪和记忆的影响均无差异。因此,单剂量25毫克口服苯海拉明的药代动力学不受年龄或性别的影响。该剂量的苯海拉明在年轻人和老年人中产生的药效学效应基本无法检测到。

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