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在致命和非致命阿片类药物过量后采集的生物样本中右美托咪定的定量及对映体鉴别

Medetomidine Quantitation and Enantiomer Differentiation in Biological Specimens Collected After Fatal and Non-Fatal Opioid Overdoses.

作者信息

Walton Sara E, Stang Brianna N, Kacinko Sherri, Papsun Donna M, Logan Barry K, Krotulski Alex J

机构信息

Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Horsham, PA.

College of Science and Technology, Temple University, Philadelphia, PA.

出版信息

J Anal Toxicol. 2025 May 8. doi: 10.1093/jat/bkaf040.

Abstract

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.

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毒品供应中,会因心脏效应和镇静作用对使用者健康构成重大风险。美托咪定有两种对映体形式:右美托咪定和左美托咪定。右美托咪定用于医疗环境中的人类,而单独的右美托咪定以及右美托咪定和左美托咪定的外消旋混合物用于兽医环境中的动物。在涉及合成阿片类药物(如芬太尼)和其他镇静剂(如赛拉嗪、苯二氮䓬类药物)的情况下,关于美托咪定或其对映体在人体中的循环血液浓度知之甚少。开发并验证了一种使用液相色谱串联四极杆质谱(LC-QQQ-MS)的新毒理学工作流程,用于定量美托咪定以及对右美托咪定和左美托咪定进行对映体定性分离。该分析方法应用于一系列100个真实样本,这些样本来自急诊科入院患者和法医尸检调查,其中含有美托咪定、芬太尼、赛拉嗪及其代谢物等物质。非致命过量中毒中美托咪定的血液浓度范围为0.1 - 16 ng/mL(中位数:1.5 ng/mL),致命过量中毒中为0.1 - 32 ng/mL(中位数:0.31 ng/mL)。76%的病例中同时检测到赛拉嗪,其浓度中位数较高:8.3 ng/mL(非致命)和15 ng/mL(致命)。93%的病例中同时检测到芬太尼,其浓度中位数为5.2 ng/mL(非致命)和21 ng/mL(致命)。90%的病例中鉴定出了右美托咪定和左美托咪定;其余病例经确认或怀疑是在医疗环境中使用了右美托咪定。这些发现表明美托咪定源自兽医或非法渠道,我们推测是后者。滥用美托咪定会导致诸如严重心动过缓和深度镇静等不良反应,尤其是与芬太尼和赛拉嗪合用时。法医实验室必须时刻警惕传统阿片类产品(如芬太尼、海洛因)中出现的掺杂物,如美托咪定,及时更新检测方法以实时捕捉这些新出现的掺杂物。

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