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检测药物检测样本中的 N-去乙基乙他尼嗪:2-苄基苯并咪唑“硝甲西泮”类中近期成员的化学分析和药理学特征。

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.

机构信息

Institute of Forensic Medicine, Department of Biomedical Engineering, University of Basel, Basel, Switzerland; Division of Clinical Chemistry and Pharmacology, Department of Biomedical and Clinical Sciences, Faculty of Medicine and Health Sciences, Linköping University, Linköping, Sweden.

Laboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.

出版信息

J Pharm Biomed Anal. 2024 Dec 15;251:116453. doi: 10.1016/j.jpba.2024.116453. Epub 2024 Aug 25.

Abstract

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 EC 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.

摘要

2-苄基苯并咪唑类“硝甲西泮”类阿片的出现正在搅动娱乐性合成阿片市场。许多硝甲西泮类似物在各种体外和体内研究中被证明是μ-阿片受体(MOR)的有效激动剂。与硝甲西泮类似物相关的严重中毒和过量死亡的报告越来越多。硝甲西泮类阿片被归类为公共卫生威胁,强调需要密切监测娱乐性药物市场的新发展。本研究报告了 2023 年 8 月瑞士药物检测服务机构收到的一名娱乐性药物使用者提交的样本中 N-去乙基依托尼秦的检测情况。该人通过一个声称含有异硝甲西泮的网络来源购买了该样本。进行了化学分析以表征该样本,即核磁共振(NMR)、毛细管电泳(CE)和高分辨率质谱(HRMS)。该样本还使用两种不同的体外 MOR 激活测定法进行了研究。NMR 和高效液相色谱(HPLC)与 HRMS 联用证实了 N-去乙基依托尼秦的存在,其纯度高,且不存在异硝甲西泮和依托尼秦。N-去乙基硝甲西泮类似物以前曾被检测为异硝甲西泮和依托尼秦的代谢物。然而,正如首次在 N-去乙基异硝甲西泮中看到的那样,它们现在作为独立的药物出现。应用的生物测定法表明,与芬太尼相比,N-去乙基依托尼秦在 MOR 上的效力和大约 6-9 倍的效力更高。N-去乙基依托尼秦在β-arrestin 2 募集和 Aequoscreen®测定中的 EC 值分别为 3.35 nM 和 0.500 nM。使用生物测定法对收集的样本中的阿片活性进行了另外评估,结果与参考标准吻合良好,与分析纯度评估一致。这表明这些生物测定法有潜力对真实样本进行快速阿片活性评估。在法医和临床毒理学案例工作中,必须考虑到其他 N-去乙基硝甲西泮类似物的出现,以避免将此类类似物的摄入错误分类为代谢物。最后,药物检测服务使市场发展和趋势的密切监测成为可能,对于早期预警和减少伤害具有巨大价值。

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