High-throughput quantification of emerging "nitazene" benzimidazole opioid analogs by microextraction and UHPLC-MS-MS.

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL Journal of analytical toxicology Pub Date : 2023-12-12 DOI:10.1093/jat/bkad071
Maria Schüller, Ivana Lucic, Åse Marit Leere Øiestad, Stig Pedersen-Bjergaard, Elisabeth Leere Øiestad
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Abstract

Benzimidazole opioids, often referred to as nitazenes, represent a subgroup of new psychoactive substances with a recent increase in fatal overdoses in the USA and Europe. With a variety of analogs emerging on the illicit drug market, forensic laboratories are challenged to identify these potent drugs. We here present a simple quantitative approach for the determination of nine nitazene analogs, namely, clonitazene, etodesnitazene, etonitazene, etonitazepyne, flunitazene, isotonitazene, metodesnitazene, metonitazene and protonitazene in whole blood using liquid-phase microextraction and electromembrane extraction in a 96-well format and liquid chromatography-tandem mass spectrometry. Green and efficient sample preparation was accomplished by liquid-phase microextraction in a 96-well format and resulted in high extraction yields for all analytes (>81%). Here, blood diluted with buffer (1:1, %v) was extracted from a donor compartment across a thin organic liquid membrane and into an aqueous acceptor solution. The acceptor solution was collected and directly injected into the analysis platform. Chromatographic separation was accomplished with a biphenyl column, allowing for a baseline separation of the structural isomers isotonitazene and protonitazene before detection by multiple reaction monitoring. Validation was performed according to Scientific Working Group of Forensic Toxicology guidelines. The calibration range was from 0.5 to 50 nM (except for protonitazene and clonitazene from 0.1 nM) with good linearity and limits of detection down to 0.01 nM. An AGREEprep assessment was performed to evaluate sample preparation greenness, with a final score of 0.71. Nitazenes represent a current threat to public health, and analytical methods that cover a wide range of these analogs are limited. Here, the described method may assist in the detection of nitazenes in whole blood and prevent these substances from being missed in postmortem investigations.

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通过微萃取和超高效液相色谱-质谱-质谱联用技术高通量定量新出现的 "硝基苯 "苯并咪唑类阿片类似物。
苯并咪唑类阿片通常被称为硝氮烯类,是一类新型精神活性物质,最近在美国和欧洲因过量使用而致死的人数有所增加。由于非法药物市场上出现了各种类似物,法医实验室在识别这些强效药物方面面临挑战。我们在此介绍一种简单的定量方法,采用 96 孔液相微萃取、电膜萃取和液相色谱-串联质谱法测定全血中的九种硝氮类似物,即氯硝哒嗪、依托尼哒嗪、依托尼哒嗪、依托尼哒哌嗪、氟硝哒嗪、异托尼哒嗪、甲氧硝哒嗪、甲硝哒嗪和质子哒嗪。96 孔液相微萃取技术实现了绿色、高效的样品制备,所有分析物的萃取率都很高(大于 81%)。在这里,用缓冲液(1:1,%v)稀释的血液从供体室穿过薄薄的有机液体膜,被萃取到水性受体溶液中。收集受体溶液后直接注入分析平台。使用联苯色谱柱进行色谱分离,在通过多反应监测进行检测之前,可对结构异构体异烟肼和质子异烟肼进行基线分离。根据法医毒理学科学工作组指南进行了验证。校准范围为 0.5 至 50 nM(质子他嗪和氯硝他嗪的校准范围为 0.1 nM 除外),线性关系良好,检测限低至 0.01 nM。对样品制备的绿色性进行了 AGREEprep 评估,最终得分为 0.71。目前,硝氮类化合物对公众健康构成威胁,而涵盖这些类似物的多种分析方法却十分有限。在此,所述方法可帮助检测全血中的硝氮类物质,并防止在尸检中漏检这类物质。
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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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