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健康男性志愿者单次服用盐酸西替利嗪片剂制剂的相对生物利用度。

Comparative bioavailability of single doses of tablet formulations of cetirizine dihydrochloride in healthy male volunteers.

作者信息

Muscará M N, de Nucci G

机构信息

Department of Pharmacology, Faculty of Medical Sciences, UNICAMP, Campinas, Brazil.

出版信息

Int J Clin Pharmacol Ther. 1995 Jan;33(1):27-31.

PMID:7711987
Abstract

The bioavailability of two tablet formulations of cetirizine (Zetir from Abbott and Zyrtek from UCB) were compared in 14 healthy male volunteers who received a single dose of 10 mg of cetirizine dihydrochloride in an open randomized two-period crossover design with a 7-day washout period between doses. Plasma samples were obtained over a 24 h interval and cetirizine concentrations were determined by HPLC with ultraviolet detection. From the plasma cetirizine concentration vs. time curves, AUC(0-24) (area under the concentration vs. time curves from 0 to 24 h), Cmax (maximum achieved concentration), Tmax (time to achieve Cmax), Ke (terminal first order elimination constant), elimination half-life (t1/2) and AUC(0-infinity) (area under the concentration vs. time curves extrapolated to infinity) were obtained. The two cetirizine dihydrochloride tablet brands did not show statistically significant differences in bioavailability as assessed by analysis of AUC(0-24), AUC(0-infinity), Cmax, Tmax, Ke and t1/2 values. Based on these results and on the U.S. Food and Drug Administration requirements [1985, 1993], we conclude that both formulations are bioequivalent.

摘要

在14名健康男性志愿者中,采用开放随机两周期交叉设计,在两剂之间设置7天的洗脱期,比较了两种西替利嗪片剂(雅培公司的Zetir和优时比公司的Zyrtek)的生物利用度,志愿者单次服用10mg盐酸西替利嗪。在24小时间隔内采集血浆样本,采用高效液相色谱-紫外检测法测定西替利嗪浓度。根据血浆中西替利嗪浓度-时间曲线,得出AUC(0-24)(0至24小时浓度-时间曲线下的面积)、Cmax(达到的最大浓度)、Tmax(达到Cmax的时间)、Ke(终末一级消除常数)、消除半衰期(t1/2)和AUC(0-∞)(外推至无穷大的浓度-时间曲线下的面积)。通过对AUC(0-24)、AUC(0-∞)、Cmax、Tmax、Ke和t1/2值的分析评估,两种盐酸西替利嗪片剂品牌在生物利用度上未显示出统计学显著差异。基于这些结果以及美国食品药品监督管理局的要求[1985年,1993年],我们得出结论,两种制剂具有生物等效性。

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