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口服给药后血液中未检测到阿莫地喹。

Failure to detect amodiaquine in the blood after oral administration.

作者信息

Salako L A, Idowu O R

出版信息

Br J Clin Pharmacol. 1985 Oct;20(4):307-11. doi: 10.1111/j.1365-2125.1985.tb05068.x.

Abstract

Plasma and red blood cell concentrations of amodiaquine (AM) and its metabolite, desethylamodiaquine (DAM), were monitored at intervals up to 21 days after a single oral dose of 600 mg amodiaquine in five normal African subjects. Concentrations of AM and DAM were determined using a high performance liquid chromatography technique with a lower limit of sensitivity of 10 ng ml-1 for both compounds. AM was not detectable in plasma and red blood cell samples withdrawn from any of the subjects. DAM was detectable in both media. It appeared in the blood 0.5-1 h after administering AM, reached a peak in 1.5-2 h and subsequently declined slowly. We conclude that AM is rapidly converted to DAM and its blood concentration, compared with that of DAM, is very low if not negligible.

摘要

在五名正常非洲受试者单次口服600毫克阿莫地喹后,每隔一段时间监测血浆和红细胞中阿莫地喹(AM)及其代谢产物去乙基阿莫地喹(DAM)的浓度,最长监测至21天。采用高效液相色谱技术测定AM和DAM的浓度,两种化合物的最低检测限均为10纳克/毫升。在从任何受试者采集的血浆和红细胞样本中均未检测到AM。在两种介质中均检测到了DAM。它在服用AM后0.5 - 1小时出现在血液中,1.5 - 2小时达到峰值,随后缓慢下降。我们得出结论,AM迅速转化为DAM,与DAM相比,其血药浓度即使不可忽略也非常低。

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Failure to detect amodiaquine in the blood after oral administration.口服给药后血液中未检测到阿莫地喹。
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