致死性和非致死性阿片类药物过量后采集的生物标本中美托咪定的定量和对映体分化。

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Sara E Walton, Brianna N Stang, Sherri Kacinko, Donna M Papsun, Barry K Logan, Alex J Krotulski
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引用次数: 0

摘要

美托咪定是一种α -2激动剂和非阿片类镇静剂。它存在于非法芬太尼和海洛因药物供应中,由于心脏影响和镇静作用,对使用者的健康构成重大风险。美托咪定以两种对映体形式存在:右美托咪定和左美托咪定。右美托咪定在医疗环境中用于人类,而右美托咪定单独使用以及右美托咪定和左美托咪定的外消旋混合物在兽医环境中用于动物。在涉及合成阿片类药物(如芬太尼)和其他镇静剂(如噻嗪、苯二氮卓类药物)的情况下,人们对美托咪定或其对映异构体的血液循环浓度知之甚少。采用液相色谱串联四极杆质谱法(LC-QQQ-MS)建立了一种新的毒理学工作流程,用于美托咪定的定量分析以及右美托咪定和左美托咪定对映体的定性分离。这些分析应用于来自急诊科入院和法医尸检调查的100个真实标本的病例系列,其中含有美托咪定、芬太尼、噻嗪和代谢物等物质。美托咪定非致死性过量血药浓度范围为0.1-16 ng/mL(中位数:1.5 ng/mL),致死性过量血药浓度范围为0.1-32 ng/mL(中位数:0.31 ng/mL)。在76%的中位浓度较高的病例中共检测到Xylazine: 8.3 ng/mL(非致命)和15 ng/mL(致命)。93%的病例共检出芬太尼,中位浓度分别为5.2 ng/mL(非致死)和21 ng/mL(致死)。90%的病例中检出右美托咪定和左美托咪定;其余病例均确诊或疑似在医疗环境中使用右美托咪定。这些发现表明美托咪定来自兽医或秘密来源,我们假设是后者。娱乐性使用美托咪定会引起不良反应,如深度心动过缓和镇静作用增强,特别是与芬太尼和噻嗪联合使用时。法医实验室必须保持对传统阿片类药物(如芬太尼、海洛因)中出现的掺假物质(如美托咪定)的意识,更新检测方法以实时捕获这些新出现的掺假物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medetomidine Quantitation and Enantiomer Differentiation in Biological Specimens Collected After Fatal and Non-Fatal Opioid Overdoses.

Medetomidine is an alpha-2 agonist and non-opioid sedative. Its presence in illicit fentanyl and heroin drug supplies poses significant risks to user health caused by cardiac effects and sedation. Medetomidine exists in two enantiomeric forms: dexmedetomidine and levomedetomidine. Dexmedetomidine is used in humans in medical settings, while dexmedetomidine alone and a racemic mixture of dexmedetomidine and levomedetomidine are used in animals in veterinary settings. Little information is known about circulating blood concentrations of medetomidine or its enantiomers in humans in situations involving synthetic opioids (e.g., fentanyl) and other sedatives (e.g., xylazine, benzodiazepines). A new toxicological workflow using liquid chromatography tandem quadrupole mass spectrometry (LC-QQQ-MS) was developed and validated for the quantitation of medetomidine and the qualitative enantiomeric separation of dexmedetomidine and levomedetomidine. The assays were applied to a case series of 100 authentic specimens from emergency department admissions and forensic postmortem investigations containing medetomidine, fentanyl, xylazine, and metabolites, among other substances. Medetomidine blood concentrations in non-fatal overdoses ranged 0.1-16 ng/mL (median: 1.5 ng/mL) and in fatal overdoses ranged 0.1-32 ng/mL (median: 0.31 ng/mL). Xylazine was co-detected in 76% of cases with higher median concentrations: 8.3 ng/mL (non-fatal) and 15 ng/mL (fatal). Fentanyl was co-detected in 93% of cases with median concentrations of 5.2 ng/mL (non-fatal) and 21 ng/mL (fatal). Dexmedetomidine and levomedetomidine were identified in 90% of cases; the remaining cases were confirmed or suspected medical-setting administration of dexmedetomidine. These findings demonstrate that medetomidine is arising from veterinary or clandestine sources, and we hypothesize the latter. Recreational medetomidine use causes adverse effects such as profound bradycardia and heightened sedation, especially when combined with fentanyl and xylazine. Forensic laboratories must remain aware of adulterants, like medetomidine, appearing in traditional opioid products (e.g., fentanyl, heroin), updating testing methods to capture these emerging adulterants in real-time.

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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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