扎莱普隆的研究进展

被引：7

作者：

胡晓敏

机构：

[1] 国家药品监督局药品审评中心!北京

来源：

关键词：

扎莱普隆;

D O I：

10.13699/j.cnki.1001-6821.2000.06.011

中图分类号：

R96 [药理学];

学科分类号：

100602 ; 100706 ;

摘要：

扎莱普隆是一种非苯二氮类镇静催眠药，具有吸收迅速，消除快，无蓄积的特点。本文从药理特点、药代动力学、安全性、临床研究方面对扎莱普隆进行介绍。

引用

页码：445 / 447

页数：3

共 6 条

[1] Zaleplon and triazolam in humans: acute behavioral effects and abuse potential[J] . C. R. Rush,J. M. Frey,R. R. Griffiths.Psychopharmacology . 1999 (1)
[2] Zaleplon pharmacokinetics and absolute bioavailability
Rosen, AS
Fournié, P
Darwish, M
Danjou, P
Troy, SM
[J]. BIOPHARMACEUTICS & DRUG DISPOSITION, 1999, 20 (03) : 171 - 175
[3] Comparison of the pharmacological profiles of the hypnotic drugs, zaleplon and zolpidem[J] . David J. Sanger,Eliane Morel,Ghislaine Perrault.European Journal of Pharmacology . 1996 (1)
[4] Pharmacokinetics and Anticonvulsant Effect of a New Hypnotic, CL 284,846, in Rats[J] . Jacques Gaudreault,France Varin,Gary M. Pollack.Pharmaceutical Research . 1995 (11)
[5] Evaluation of the discriminative stimulus effects of the novel sedative-hypnotic CL 284,846[J] . Kimberly E. Vanover,James E. Barrett.Psychopharmacology . 1994 (3)
[6] Differential generalization to pentobarbital in rats trained to discriminate lorazepam, chlordiazepoxide, diazepam, or triazolam[J] . Nancy A. Ator,Roland R. Griffiths.Psychopharmacology . 1989 (1)