Allibe Nathalie, Richeval Camille, Phanithavong Mélodie, Faure Amandine, Allorge Delphine, Paysant François, Stanke-Labesque Françoise, Eysseric-Guerin Hélène, Gaulier Jean-Michel
Forensic Laboratory, Grenoble Alpes University, F-38041, Grenoble, France.
CHU Lille, Unité Fonctionnelle de Toxicologie, F-59000, Lille, France.
Drug Test Anal. 2018 Jun;10(6):995-1000. doi: 10.1002/dta.2326. Epub 2017 Nov 23.
The use of new psychoactive substances (NPS) has rapidly increased over the last decade. In the last 4 years, producers increasingly appear to be targeting non-controlled synthetic opioids, involving fentanyl derivatives such as ocfentanil (OcF). Identification of metabolites is of major importance in the context of NPS use, as it could improve the detection window in biological matrices in clinical and forensic intoxication cases. Hence, this work aims to report a fatality involving OcF documented by the identification of metabolites. A 30-year-old woman was found dead at home: an unidentified powder was found near her body and some injection sites were found at the autopsy. Toxicological analyses allowed to determine the presence of OcF in the powder, blood (3.7/3.9 μg/L, peripheral/cardiac) and in other post-mortem samples. The most relevant potential CYP- and UGT-dependent metabolites of OcF were investigated in vitro using human liver microsome incubation and liquid chromatography coupled with high resolution mass spectrometry, and subsequently confirmed in post-mortem samples. Four OcF metabolites were produced in vitro (a mono-hydroxylated OcF, O-desmethylOcF, a hydroxylated desmethylOcF and a glucuronidated form of the O-desmethylOcF), and all except the glucuronide were observed in blood and bile post-mortem samples. Considering the relative intensity of the chromatographic peak areas, O-desmethylOcF can be suggested to be an abundant metabolite of OcF. Nevertheless, the relevance of O-desmethylOcF as being a complementary analytical target of OcF for OcF use detection needs further in vivo confirmation, especially through analysis of urines from users.
在过去十年中,新型精神活性物质(NPS)的使用迅速增加。在过去4年里,生产商似乎越来越多地将目标对准非管制合成阿片类药物,其中包括芬太尼衍生物,如奥芬太尼(OcF)。在使用NPS的背景下,代谢物的鉴定至关重要,因为它可以延长临床和法医中毒案例中生物基质的检测窗口期。因此,这项工作旨在报告一例通过代谢物鉴定记录的涉及OcF的死亡案例。一名30岁女性被发现死于家中:在她尸体附近发现了一种不明粉末,尸检时发现了一些注射部位。毒理学分析确定了粉末、血液(外周血/心脏血中为3.7/3.9μg/L)和其他死后样本中存在OcF。利用人肝微粒体孵育和液相色谱-高分辨率质谱联用技术在体外研究了OcF最相关的潜在细胞色素P450(CYP)和尿苷二磷酸葡萄糖醛酸转移酶(UGT)依赖性代谢物,随后在死后样本中得到证实。体外产生了四种OcF代谢物(一种单羟基化的OcF、O-去甲基OcF、一种羟基化的去甲基OcF和O-去甲基OcF的葡萄糖醛酸苷形式),除了葡萄糖醛酸苷外,所有代谢物均在死后血液和胆汁样本中被观察到。考虑到色谱峰面积的相对强度,O-去甲基OcF可被认为是OcF的一种丰富代谢物。然而,O-去甲基OcF作为OcF使用检测的补充分析靶点的相关性需要进一步的体内证实,尤其是通过对使用者尿液的分析。