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口服氢氯噻嗪和阿替唑胺后噻嗪类利尿剂尿液标志物的检测——与兴奋剂控制分析的相关性

Detection of urinary markers for thiazide diuretics after oral administration of hydrochlorothiazide and altizide-relevance to doping control analysis.

作者信息

Deventer K, Pozo O J, Van Eenoo P, Delbeke F T

机构信息

Department of Clinical Chemistry, DoCoLab, UGent, Zwijnaarde, Belgium.

出版信息

J Chromatogr A. 2009 Mar 20;1216(12):2466-73. doi: 10.1016/j.chroma.2009.01.032. Epub 2009 Jan 17.

DOI:10.1016/j.chroma.2009.01.032
PMID:19187939
Abstract

In sports, thiazide diuretics are used to flush out previously taken prohibited substances with forced diuresis and in sports where weight classes are involved to achieve acute weight loss. Thiazide diuretics include compounds which are very unstable and hydrolyse in aqueous media. Because information regarding the urinary detection of the hydrolysis products is limited, urinary excretion profiles for the hydrolysis product 4-amino-6-chloro-1,3-benzenedisulphonamide were established in 6 healthy volunteers after oral administration of altizide (15 mg per tablet) and hydrochlorothiazide (25mg per tablet). Additionally, the excretion profile of chlorothiazide, a metabolite of altizide and hydrochlorothiazide, was also determined. A quantitative liquid-chromatographic tandem mass spectrometric method to detect the 4 substances was developed and validated. The result of this work shows that altizide is eliminated within 48 h in urine whereas hydrochlorothiazide was detectable after 120 h. Chlorothiazide was determined to be a minor metabolite of altizide and hydrochlorothiazide and could be detected up to 120 h. The hydrolysis product, 4-amino-6-chloro-1,3-benzenedisulphonamide, was detectable 120 h after administration, with concentrations at least 10 times higher than the parent drug. Concentrations ranged between 41-239 and 60-287 ng/mL after altizide and hydrochlorothiazide administration, respectively. The study shows that 4-amino-6-chloro-1,3-benzenedisulphonamide is an important target compound for the long time detection of thiazide diuretics in urine.

摘要

在体育运动中,噻嗪类利尿剂被用于通过强制利尿排出先前摄入的违禁物质,以及在涉及体重级别的运动项目中实现快速减重。噻嗪类利尿剂包括在水性介质中非常不稳定且会水解的化合物。由于关于水解产物尿液检测的信息有限,在6名健康志愿者口服阿替利嗪(每片15毫克)和氢氯噻嗪(每片25毫克)后,建立了水解产物4-氨基-6-氯-1,3-苯二磺酰胺的尿液排泄谱。此外,还测定了阿替利嗪和氢氯噻嗪的代谢产物氯噻嗪的排泄谱。开发并验证了一种用于检测这4种物质的定量液相色谱串联质谱方法。这项工作的结果表明,阿替利嗪在48小时内从尿液中消除,而氢氯噻嗪在120小时后仍可检测到。氯噻嗪被确定为阿替利嗪和氢氯噻嗪的次要代谢产物,在120小时内均可检测到。水解产物4-氨基-6-氯-1,3-苯二磺酰胺在给药120小时后可检测到,其浓度至少比母体药物高10倍。阿替利嗪和氢氯噻嗪给药后,浓度分别在41 - 239纳克/毫升和60 - 287纳克/毫升之间。该研究表明,4-氨基-6-氯-1,3-苯二磺酰胺是尿液中噻嗪类利尿剂长时间检测的重要目标化合物。

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