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病例报告:以U-47700为例说明代谢物鉴定在检测新型合成阿片类药物中毒中的相关性。

Case report: relevance of metabolite identification to detect new synthetic opioid intoxications illustrated by U-47700.

作者信息

Richeval Camille, Gaulier Jean-Michel, Romeuf Ludovic, Allorge Delphine, Gaillard Yvan

机构信息

Unité Fonctionnelle de Toxicologie, CHU Lille, 59000, Lille, France.

EA 4483 - IMPECS - IMPact de l'Environnement Chimique sur la Santé humaine, University of Lille, 59000, Lille, France.

出版信息

Int J Legal Med. 2019 Jan;133(1):133-142. doi: 10.1007/s00414-018-1969-3. Epub 2018 Nov 15.

Abstract

Today, new psychoactive substances (NPS) producers increasingly appear to be targeting new synthetic opioids (NSOs), and the recent emergence of NSOs is causing considerable concern in North America and in Europe. For toxicologists, NSO detection in a forensic context presents three additional difficulties to the general NPS analytical detection challenge: (i) high frequency of new products, (ii) low concentrations (in μg/L range and under) in biological samples related to their high opioid potency, and (iii) extensive metabolism. In this context, the present work aims to highlight the relevance of NSO metabolite detection in potential intoxication cases. Illustration is given with U-47700, an emerging NSO, (i) that was identified in a powder recently collected in France and in a fatality case, (ii) whose metabolites were in vitro produced using human liver microsomes and their mass spectra (MS) added in our MS/MS and HRMS libraries, and (iii) for which metabolism data were compared to those of the literature: U-47700 was identified in the powder and at 3040 μg/L in peripheral blood in the fatality case. In addition, high amounts of several U-47700 metabolites, especially N-desmethyl-U-47700, were observed in urine. Even if metabolite formation may largely depend on the enzymatic activity as well as on the length of the survival time, confrontation of these results to data found in the literature strongly suggests that this metabolite is regularly a better blood and (mainly) urine biomarker of U-47700 intake than U-47700 itself. Indeed, in this fatality and in other previous reports, N-desmethyl-U-47700 produced the main observed chromatographic signal (i) systematically in vitro and (ii) commonly in vivo, especially in urines. N,N-Didesmethyl-U-47700 is also sometimes a better biomarker of U-47700 intake than U-47700 itself. Accordingly, we suggest adding N-desmethyl-U-47700 (and N,N-didesmethyl-U-47700) in mass spectrum databases used for toxicological screening in order to reduce the risk of false-negative results in intoxication cases involving U-47700.

摘要

如今,新型精神活性物质(NPS)生产者似乎越来越多地将目标对准新型合成阿片类物质(NSO),而NSO的近期出现引起了北美和欧洲的相当大关注。对于毒理学家而言,在法医背景下检测NSO给一般NPS分析检测带来了三个额外难题:(i)新产品出现频率高,(ii)由于其高阿片类效力,生物样本中浓度低(在μg/L及以下范围),以及(iii)广泛的代谢。在此背景下,本研究旨在强调在潜在中毒案例中检测NSO代谢物的相关性。以新兴的NSO U - 47700为例进行说明:(i)在法国近期收集的一份粉末以及一起死亡案例中被鉴定出来,(ii)其代谢物利用人肝微粒体在体外产生,并将其质谱(MS)添加到我们的MS/MS和高分辨质谱(HRMS)库中,(iii)将其代谢数据与文献数据进行比较:在粉末中鉴定出了U - 47700,在死亡案例的外周血中浓度为3040μg/L。此外,在尿液中观察到了大量的几种U - 47700代谢物,尤其是去甲基 - U - 47700。即使代谢物的形成可能在很大程度上取决于酶活性以及存活时间的长短,但将这些结果与文献中的数据对比强烈表明,这种代谢物通常是比U - 47700本身更好的U - 47700摄入的血液和(主要是)尿液生物标志物。确实,在该死亡案例以及其他先前报告中,去甲基 - U - 47700(i)在体外系统地产生了主要观察到的色谱信号,(ii)在体内通常也如此,尤其是在尿液中。去二甲基 - U - 47700有时也是比U - 47700本身更好的U - 47700摄入生物标志物。因此,我们建议在用于毒理学筛查的质谱数据库中添加去甲基 - U - 47700(和去二甲基 - U - 47700),以降低在涉及U - 47700的中毒案例中出现假阴性结果的风险。

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