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伯氨喹的药代动力学研究。

Studies on the pharmacokinetics of primaquine.

作者信息

Fletcher K A, Evans D A, Gilles H M, Greaves J, Bunnag D, Harinasuta T

出版信息

Bull World Health Organ. 1981;59(3):407-12.

Abstract

A sensitive and specific assay for primaquine in plasma and urine using gas chromatography/mass spectrometry has been developed and used to study the plasma kinetics of primaquine. Preliminary studies on the effects of single and multiple oral doses have been carried out. In both cases the drug was completely, or almost completely, removed from the plasma in 24 h. The concentration of primaquine in the plasma usually reached a peak 1-2 hours after oral administration. The plasma elimination half-life was about 4 h. Less than 1% of the dose was detected in the urine collected over a 24-h period following drug ingestion. When Caucasian volunteers were given primaquine and chloroquine concurrently, some of them developed significant methaemoglobinaemia. Primaquine was not detectable in the plasma of any of the volunteers, 24 h after each daily dose.

摘要

已开发出一种使用气相色谱/质谱法测定血浆和尿液中伯氨喹的灵敏且特异的分析方法,并用于研究伯氨喹的血浆动力学。已对单次和多次口服剂量的效果进行了初步研究。在这两种情况下,药物在24小时内从血浆中完全或几乎完全清除。血浆中伯氨喹的浓度通常在口服给药后1 - 2小时达到峰值。血浆消除半衰期约为4小时。在药物摄入后24小时收集的尿液中检测到的剂量不到1%。当白种人志愿者同时服用伯氨喹和氯喹时,其中一些人出现了明显的高铁血红蛋白血症。在每天给药后24小时,任何志愿者的血浆中均未检测到伯氨喹。

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