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关于盐酸瓦多卡因安全性和镇咳活性的首次人体研究。

First human studies on the safety and antitussive activity of vadocaine hydrochloride.

作者信息

Karttunen P, Tukiainen H, Uusitupa M, Männistö P T

机构信息

Orion Corporation Ltd., Orion Pharmaceutica, Medical Department, Kuopio, Finland.

出版信息

Arzneimittelforschung. 1988 Apr;38(4A):631-4.

PMID:3395401
Abstract

Vadocaine hydrochloride (2',4'-dimethyl-6'-methoxy-3-(2-methylpiperidyl)propionanilide+ ++ hydrochloride, OR K-242-HCl; INN: vadocaine) is a new anilide derivative which resembles lidocaine in chemical structure. The safety and antitussive effects of this new compound were studied in 6 healthy male volunteers in the first Phase I clinical trial. Vadocaine was administered in single doses of 5, 10, 15, 20, 30 and 50 mg. At these dose levels vadocaine had no effects on the cardiovascular system, the haematological variables, blood biochemistry or urinary sediment examined as safety evaluation. The antitussive properties of the compound were studied using inhaled citric acid for induction of the cough response. The antitussive properties of vadocaine were most effective at a dose of 15 mg, although no statistical significance was found. Neither was any dose-response relationship noted. However, at this dose level vadocaine is apparently safe and its antitussive properties seem promising enough for further evaluation.

摘要

盐酸瓦多卡因(2',4'-二甲基-6'-甲氧基-3-(2-甲基哌啶基)丙酰苯胺盐酸盐,即K-242-HCl;国际非专利药品名称:瓦多卡因)是一种新的酰苯胺衍生物,其化学结构与利多卡因相似。在第一项I期临床试验中,对6名健康男性志愿者研究了这种新化合物的安全性和镇咳作用。瓦多卡因的给药剂量分别为5、10、15、20、30和50毫克。作为安全性评估,在这些剂量水平下,瓦多卡因对心血管系统、血液学指标、血液生化或尿沉渣均无影响。使用吸入柠檬酸诱导咳嗽反应来研究该化合物的镇咳特性。瓦多卡因在15毫克剂量时镇咳效果最为显著,尽管未发现统计学意义。也未观察到任何剂量反应关系。然而,在此剂量水平下,瓦多卡因显然是安全的,其镇咳特性似乎有足够的前景进行进一步评估。

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