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阿普唑仑与三唑仑单次口服给药的药代动力学关系。

Relationship between single oral dose pharmacokinetics of alprazolam and triazolam.

作者信息

Otani K, Yasui N, Furukori H, Kaneko S, Tasaki H, Ohkubo T, Nagasaki T, Sugawara K, Hayashi K

机构信息

Department of Neuropsychiatry, Hirosaki University Hospital, Japan.

出版信息

Int Clin Psychopharmacol. 1997 May;12(3):153-7. doi: 10.1097/00004850-199705000-00006.

Abstract

The relationship between the single oral dose pharmacokinetics of alprazolam and triazolam was studied in 10 healthy male volunteers. Each subject took single oral doses of alprazolam 0.8 mg and triazolam 0.5 mg with at least a 2 week interval between each dose. Blood samplings were performed up to 48 h after alprazolam dosing and up to 12 h after triazolam dosing. Plasma concentrations of both drugs were measured by high-performance liquid chromatography. The means +/- standard deviation of the peak plasma concentration, the total area under the plasma concentration-time curve and the elimination half-life of alprazolam were 11.3 +/- 3.1 ng/ml, 232.4 +/- 59.2 ng/h/ml and 16.5 +/- 4.6 h, respectively, and those of triazolam were 3.2 +/- 1.0 ng/ml, 11.8 +/- 5.2 ng/h/ml and 2.5 +/- 1.1 h, respectively. There was no significant correlation between the two drugs in any pharmacokinetic parameters (r = 0.35, 0.25 and 0.50). The present study thus suggests that the single oral dose pharmacokinetics of alprazolam and triazolam do not correlate well in individuals.

摘要

在10名健康男性志愿者中研究了阿普唑仑和三唑仑单次口服给药的药代动力学关系。每位受试者单次口服0.8毫克阿普唑仑和0.5毫克三唑仑,每次给药间隔至少2周。在阿普唑仑给药后48小时内以及三唑仑给药后12小时内进行血样采集。两种药物的血浆浓度通过高效液相色谱法测定。阿普唑仑的血浆峰浓度、血浆浓度-时间曲线下总面积和消除半衰期的均值±标准差分别为11.3±3.1纳克/毫升、232.4±59.2纳克/小时/毫升和16.5±4.6小时,三唑仑的分别为3.2±1.0纳克/毫升、11.8±5.2纳克/小时/毫升和2.5±1.1小时。两种药物在任何药代动力学参数方面均无显著相关性(r = 0.35、0.25和0.50)。因此,本研究表明阿普唑仑和三唑仑的单次口服给药药代动力学在个体中相关性不佳。

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