...
首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Urinary Excretion Kinetics of 3,4-Methylenedioxymethamphetamine (MDMA, Ecstasy) and Its Phase I and Phase II Metabolites in Humans following Controlled MDMA Administration
【24h】

Urinary Excretion Kinetics of 3,4-Methylenedioxymethamphetamine (MDMA, Ecstasy) and Its Phase I and Phase II Metabolites in Humans following Controlled MDMA Administration

机译:受控MDMA给药后人体内3,4-亚甲二氧基甲基苯丙胺(MDMA,摇头丸)及其I和II期代谢产物的尿排泄动力学

获取原文
   

获取外文期刊封面封底 >>

       

摘要

BACKGROUND: 3,4-Methylendioxymethamphetamine (MDMA) is excreted in human urine as unchanged drug and phase I and II metabolites. Previous urinary excretion studies after controlled oral MDMA administration have been performed only after conjugate cleavage. Therefore, we investigated intact MDMA glucuronide and sulfate metabolite excretion.METHODS: We used LC–high-resolution MS and GC-MS to reanalyze blind urine samples from 10 participants receiving 1.0 or 1.6 mg/kg MDMA orally. We determined median C max, t max, first and last detection times, and total urinary recovery; calculated ratios of sulfates and glucuronides; and performed in vitro–in vivo correlations.RESULTS: Phase II metabolites of 3,4-dihydroxymethamphetamine (DHMA), 4-hydroxy-3-methoxymethamphetamine (HMMA), 3,4-dihydroxyamphetamine (DHA), and 4-hydroxy-3-methoxyamphetamine were identified, although only DHMA sulfates, HMMA sulfate, and HMMA glucuronide had substantial abundance. Good correlation was observed for HMMA measured after acid hydrolysis and the sum of unconjugated HMMA, HMMA glucuronide, and HMMA sulfate ( R 2 = 0.87). More than 90% of total DHMA and HMMA were excreted as conjugates. The analyte with the longest detection time was HMMA sulfate. Median HMMA sulfate/glucuronide and DHMA 3-sulfate/4-sulfate ratios for the first 24 h were 2.0 and 5.3, respectively, in accordance with previous in vitro calculations from human liver microsomes and cytosol experiments.CONCLUSIONS: Human MDMA urinary metabolites are primarily sulfates and glucuronides, with sulfates present in higher concentrations than glucuronides. This new knowledge may lead to improvements in urine MDMA and metabolite analysis in clinical and forensic toxicology, particularly for the performance of direct urine analysis.
机译:背景:3,4-甲基二乙氧基甲基苯丙胺(MDMA)作为不变的药物以及I和II期代谢产物在人尿中排出。仅在偶联物裂解后才进行受控口服MDMA给药后的先前尿排泄研究。因此,我们研究了完整的MDMA葡萄糖醛酸苷和硫酸盐代谢产物的排泄。方法:我们使用LC-高分辨率MS和GC-MS重新分析了10名口服1.0或1.6 mg / kg MDMA的参与者的盲尿样品。我们确定了中值C max,t max,第一个和最后一个检测时间以及总尿液恢复;计算的硫酸盐和葡萄糖醛酸的比率;结果:3,4-二羟基甲基苯丙胺(DHMA),4-羟基-3-甲氧基甲基苯丙胺(HMMA),3,4-二羟基苯丙胺(DHA)和4-羟基-3的II期代谢产物尽管仅DHMA硫酸盐,HMMA硫酸盐和HMMA葡糖醛酸具有大量丰度,但仍可识别出-甲氧基苯丙胺。观察到酸水解后测得的HMMA与未结合的HMMA,HMMA葡糖醛酸苷和HMMA硫酸盐的总和具有良好的相关性(R 2 = 0.87)。 DHMA和HMMA总量的90%以上作为结合物排泄。检测时间最长的分析物是硫酸HMMA。根据先前从人肝微粒体和细胞质液实验得出的体外计算结果,前24小时HMMA硫酸盐/葡萄糖醛酸和DHMA 3-硫酸盐/ 4-硫酸盐的比率分别为2.0和5.3。硫酸盐和葡萄糖醛酸,其中硫酸盐的浓度高于葡萄糖醛酸。这种新知识可能会改善尿液中的MDMA和代谢物分析的临床和法医毒理学,尤其是直接尿液分析的性能。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号