Montanari Eva, Madeo Graziella, Pichini Simona, Busardò Francesco Paolo, Carlier Jeremy
Unit of Forensic Toxicology, Section of Legal Medicine, Department of Excellence of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.
Brain&Care, Neuromodulation and Clinical Research Unit, Rimini, Italy.
Ther Drug Monit. 2022 Aug 1;44(4):494-510. doi: 10.1097/FTD.0000000000000970.
Synthetic benzimidazole opioids (BOs) are highly potent µ-opioid receptor agonists with heroin-like effects. Isotonitazene was first available in 2019 in the drug market, although new analogs have multiplied recently. The authors aimed to identify BO use trends and gather toxicological data from BO-related cases to assist in clinical and forensic investigations.
A systematic literature search was conducted according to the PRISMA guidelines. PubMed and Scopus databases were accessed in October 2021 to identify scientific reports of BO-related intoxication and fatalities. Publication dates, case descriptions, symptoms, autopsy findings, and concentrations of BOs and metabolites in biological matrices were compiled.
Data from 8 case reports with 93 fatalities involving isotonitazene ( n = 65), metonitazene ( n = 20), etonitazepyne ( N -pyrrolidino etonitazene) ( n = 8), flunitazene ( n = 4), and/or butonitazene ( n = 1), and 1 acute intoxication involving etonitazepyne were collected. Autopsy findings included pulmonary congestion/high lung weight (66%), cardiomegaly/high cardiac weight (39%), cerebral edema (22%), gastric contents in the airways (22%), and organ congestion (22%). Median peripheral blood concentrations were 1.7 ng/mL for isotonitazene (0.4-9.5 ng/mL, n = 13), 5.4 ng/mL for metonitazene (0.52-33 ng/mL, n = 17), 5.4 ng/mL for etonitazepyne (2.4-8.3 ng/mL, n = 2), 1.3 ng/mL for flunitazene (0.58-2.1 ng/mL, n = 2), and 3.2 ng/mL for butonitazene ( n = 1). Central nervous system depressants were almost always coadministered.
Isotonitazene was predominant in cases from 2019 to mid-2020 and was replaced by metonitazene after scheduling in the United States. Typical findings on opioid overdoses have been reported. Peripheral blood concentrations were consistent with a potency similar to that of fentanyl. These results must be interpreted carefully, considering the scarcity of reports on BO-related cases and drug co-exposures.
合成苯并咪唑类阿片类药物(BOs)是高效的μ-阿片受体激动剂,具有类似海洛因的作用。异噻吨酮于2019年首次进入药品市场,尽管最近新的类似物不断增加。作者旨在确定BOs的使用趋势,并收集与BOs相关病例的毒理学数据,以协助临床和法医调查。
根据PRISMA指南进行系统的文献检索。2021年10月检索了PubMed和Scopus数据库,以确定与BOs相关的中毒和死亡的科学报告。汇总了发表日期、病例描述、症状、尸检结果以及生物基质中BOs和代谢物的浓度。
收集了8篇病例报告的数据,其中93例死亡涉及异噻吨酮(n = 65)、美托酮(n = 20)、乙噻吨(N-吡咯烷基乙噻吨)(n = 8)、氟硝西泮(n = 4)和/或丁噻吨(n = 1),以及1例涉及乙噻吨的急性中毒。尸检结果包括肺充血/肺重量增加(66%)、心脏肥大/心脏重量增加(39%)、脑水肿(22%)、气道中有胃内容物(22%)和器官充血(22%)。异噻吨酮的外周血中位浓度为1.7 ng/mL(0.4 - 9.5 ng/mL,n = 13),美托酮为5.4 ng/mL(0.52 - 33 ng/mL,n = 17),乙噻吨为5.4 ng/mL(2.4 - 8.3 ng/mL,n = 2),氟硝西泮为1.3 ng/mL(0.58 - 2.1 ng/mL,n = 2),丁噻吨为3.2 ng/mL(n = 1)。几乎总是同时使用中枢神经系统抑制剂。
在2019年至2020年年中,异噻吨酮在病例中占主导地位,在美国被列入管制后被美托酮取代。报告了阿片类药物过量的典型发现。外周血浓度与芬太尼相似的效力一致。考虑到与BOs相关病例和药物共同暴露的报告较少,这些结果必须谨慎解释。