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新型非镇静性H1抗组胺药咪唑斯汀(SL 85.0324)的药效学与药代动力学

Pharmacodynamics and pharmacokinetics of mizolastine (SL 85.0324), a new nonsedative H1 antihistamine.

作者信息

Rosenzweig P, Thebault J J, Caplain H, Dubruc C, Bianchetti G, Fuseau E, Morselli P L

机构信息

Synthélabo Recherche, Bagneux, France.

出版信息

Ann Allergy. 1992 Aug;69(2):135-9.

PMID:1354949
Abstract

The antihistaminic activity, clinical safety, and pharmacokinetics of mizolastine (SL 85.0324) were studied in a 5-way, double-blind crossover study of ten healthy volunteers with doses of 1 to 75 mg. Inhibition of the histamine-induced wheal and flare showed clear dose-dependent antihistaminic activity beginning from the 2-mg dose with a maximum attained between 10 and 20 mg. The onset of action was rapid (one hour) and the effect persisted for more than 24 hours after a 10-mg dose or more. Mizolastine was well tolerated at doses up to 75 mg; subjective and objective signs of transient sedative activity were not observed at doses below 30 mg. The pharmacokinetic profile (rapid absorption with Tmax congruent to 1 h and elimination T1/2 of about eight hours) parallels the pharmacodynamic activity. Within the considered dose range, the pharmacokinetics was linear with no saturation phenomena.

摘要

在一项针对10名健康志愿者的五组双盲交叉研究中,研究了咪唑斯汀(SL 85.0324)的抗组胺活性、临床安全性和药代动力学,剂量为1至75毫克。组胺诱导的风团和潮红抑制试验显示,从2毫克剂量开始即呈现明显的剂量依赖性抗组胺活性,在10至20毫克之间达到最大活性。起效迅速(1小时),10毫克或更高剂量给药后,效果持续超过24小时。高达75毫克的剂量下,咪唑斯汀耐受性良好;30毫克以下剂量未观察到短暂镇静活性的主观和客观体征。药代动力学特征(快速吸收,Tmax约为1小时,消除半衰期约为8小时)与药效学活性相似。在所考虑的剂量范围内,药代动力学呈线性,无饱和现象。

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