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两起涉及3-甲氧基苯环利定的致命中毒事件。

Two Fatal Intoxications Involving 3-Methoxyphencyclidine.

作者信息

Mitchell-Mata Christie, Thomas Brittany, Peterson Brianna, Couper Fiona

机构信息

Email:

Washington State Toxicology Laboratory, 2203 Airport Way S Suite 360, Seattle, WA 98134, USA.

出版信息

J Anal Toxicol. 2017 Jul 1;41(6):503-507. doi: 10.1093/jat/bkx048.

Abstract

3- and 4-methoxyphencyclidine (3-MeO-PCP, 4-MeO-PCP), structural analogs of phencyclidine (PCP), were among the first legal PCP alternatives to show up on the novel psychoactive substances (NPS) market in Europe in the 2000s. Their structural similarities to PCP and ketamine likely contribute to their demonstrated dissociative anesthetic effects. Limited information exists in the literature about toxic and lethal concentrations of these drugs in biological samples. This case report presents the first two death cases in Washington State in which 3-MeO-PCP was identified. Alkaline drug screen analysis by gas chromatography-mass spectrometry (GC-MS) revealed a peak with a retention time similar to PCP and base peak of m/z 230. Certified reference materials for 3-and 4-MeO-PCP were obtained and the isomers were able to be distinguished based on different retention times and mass spectra. A quantitative GC-MS method was developed and validated for casework, utilizing a dynamic range of 10-1,000 ng/mL and a limit of detection of 1 ng/mL. Postmortem (peripheral/central) blood samples were analyzed using this method and the resulting concentrations were 0.63 and 3.2 mg/L of 3-MeO-PCP. Methamphetamine (0.11 mg/L) was additionally detected in the blood of one of the decedents; while the second decedent was additionally positive for ethanol (0.047 g/100 mL), bupropion (1.8 mg/L), delorazepam, paroxetine and mitragynine. The results presented in this case report are higher than previously reported concentrations in fatal cases, but the presence of polysubstance abuse is consistent with previously reported NPS intoxications. Both of these individuals were in drug rehabilitation facilities prior to their deaths; however, users continue to be drawn to 3-MeO-PCP due to its dissociative effects and its accessibility on the internet.

摘要

3-甲氧基苯环己哌啶(3-MeO-PCP)和4-甲氧基苯环己哌啶(4-MeO-PCP)是苯环己哌啶(PCP)的结构类似物,是21世纪初在欧洲新型精神活性物质(NPS)市场上最早出现的合法PCP替代物。它们与PCP和氯胺酮的结构相似性可能导致其已证实的解离麻醉作用。文献中关于这些药物在生物样本中的毒性和致死浓度的信息有限。本病例报告介绍了华盛顿州首例两例检测出3-MeO-PCP的死亡病例。通过气相色谱-质谱联用(GC-MS)进行的碱性药物筛查分析显示出一个保留时间与PCP相似且基峰为m/z 230的峰。获得了3-和4-MeO-PCP的认证参考物质,并且能够根据不同的保留时间和质谱图区分异构体。开发并验证了一种用于案件处理的定量GC-MS方法,其动态范围为10-1,000 ng/mL,检测限为1 ng/mL。使用该方法分析了死后(外周/中心)血样,所得3-MeO-PCP浓度分别为0.63和3.2 mg/L。在其中一名死者的血液中还检测出甲基苯丙胺(0.11 mg/L);而第二名死者的血液中乙醇(0.047 g/100 mL)、安非他酮(1.8 mg/L)、地洛西泮、帕罗西汀和帽柱木碱呈阳性。本病例报告中的结果高于先前报道的致命病例中的浓度,但多药滥用的情况与先前报道的NPS中毒情况一致。这两名死者在死亡前都在戒毒所;然而,由于其解离作用以及在互联网上易于获取,使用者仍然被3-MeO-PCP所吸引。

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