在药物检查样本中检测到 N-去乙基依托尼他嗪:2-苄基苯并咪唑 "硝氮烯 "类新近成员的化学分析和药理特征描述

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-25 DOI:10.1016/j.jpba.2024.116453
Manuela C. Monti , Liam M. De Vrieze , Marthe M. Vandeputte , Mattias Persson , Henrik Gréen , Christophe P. Stove , Götz Schlotterbeck
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引用次数: 0

摘要

2-苄基苯并咪唑 "硝氮烯 "类阿片的出现搅动了娱乐性合成阿片市场。各种体外和体内研究表明,许多硝氮类似物是μ-阿片受体(MOR)的强效激动剂。与硝氮类似物有关的严重中毒和用药过量致死的报告越来越多。硝氮烯类阿片被列为公共健康威胁,这强调了密切监测娱乐药物市场新发展的必要性。本研究报告了 2023 年 8 月一名娱乐性毒品使用者在瑞士毒品检查服务机构上交的样本中检测出 N-去乙基依托尼他嗪。此人通过互联网渠道购买了该样品,据称样品中含有异托硝基苯。对样品进行了化学分析,以确定其特征,即核磁共振(NMR)、毛细管电泳(CE)和高分辨率质谱(HRMS)。此外,还使用两种不同的体外 MOR 活化测定法对样品进行了研究。核磁共振和与高分辨质谱联用的高效液相色谱法(HPLC)证实了 N-去乙基依托尼他嗪的高纯度存在,且不含异硝他嗪和依托尼他嗪。以前曾检测到 N-去乙基硝氮类似物是异烟肼和乙托硝胺的代谢物。不过,正如 N-去乙基异硝唑首次出现的情况一样,它们现在正逐渐成为独立的药物。应用生物测定表明,与芬太尼相比,N-去乙基依托尼他嗪的 MOR 药效更高,药力约为芬太尼的 6-9 倍。在 β-arrestin 2 招募和 Aequoscreen® 试验中,N-去乙基依托尼他嗪的 EC50 值分别为 3.35 nM 和 0.500 nM。此外,还使用生物测定法对采集样品中的阿片类活性进行了评估,结果显示与参考标准有很好的重叠,与分析纯度评估结果一致。这表明这些生物测定方法具有对真实样本进行阿片类活性快速评估的潜力。在法医和临床毒理学案例工作中,必须考虑到其他 N-去乙基硝氮类似物的出现,以避免将此类类似物的摄入误归为代谢物。最后,毒品检查服务能够密切监测市场发展和趋势,对预警和减少危害具有重要价值。
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Detection of N-desethyl etonitazene in a drug checking sample: Chemical analysis and pharmacological characterization of a recent member of the 2-benzylbenzimidazole “nitazene” class

The emergence of 2-benzylbenzimidazole “nitazene” opioids is stirring up the recreational synthetic opioid market. Many nitazene analogues act as potent agonists at the µ‑opioid receptor (MOR), as demonstrated in various in vitro and in vivo studies. Severe intoxication and overdose deaths associated with nitazene analogues are increasingly being reported. Nitazene opioids are classified as a public health threat, stressing the need for close monitoring of new developments on the recreational drug market. This study reports on the detection of N-desethyl etonitazene in a sample handed in by a recreational drug user at a Swiss drug checking service in August 2023. The person bought the sample through an internet source where it was stated to contain isotonitazene. Chemical analyses were conducted to characterize the sample, i.e. nuclear magnetic resonance (NMR), capillary electrophoresis (CE), and high-resolution mass spectrometry (HRMS). The sample was additionally investigated using two different in vitro MOR activation assays. NMR and high-performance liquid chromatography (HPLC) coupled to HRMS confirmed the presence of N-desethyl etonitazene at a high purity and in the absence of isotonitazene and etonitazene. N-Desethyl nitazene analogues have been detected before as metabolites of isotonitazene and etonitazene. However, as first seen with N-desethyl isotonitazene, they are now emerging as standalone drugs. The applied bioassays demonstrated increased efficacy and approximately 6–9-fold higher potency of N-desethyl etonitazene at MOR compared to fentanyl. N-Desethyl etonitazene showed EC50 values of 3.35 nM and 0.500 nM in the β-arrestin 2 recruitment and Aequoscreen® assays, respectively. The opioid activity present in the collected sample was additionally evaluated using the bioassays and showed good overlap with the reference standard, in line with the analytical purity assessment. This demonstrates the potential of these bioassays to provide a rapid opioid activity assessment of authentic samples. The emergence of other N-desethyl nitazene analogues must be considered during forensic and clinical toxicology casework, to avoid misclassification of intake of such analogues as metabolites. Finally, drug checking services enable the close monitoring of market developments and trends and are of great value for early warning and harm reduction purposes.

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