中毒死亡涉及各种新的精神活性物质,包括溴唑仑

IF 1.8 Q4 TOXICOLOGY
Maxime Alexandre , Romain Pelletier , Brendan Le Dare , Isabelle Morel , Renaud Bouvet , Thomas Gicquel
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引用次数: 0

摘要

苯并二氮卓类药物经常与具有毒理学成分的死亡有关。近年来,合成设计苯二氮卓类药物(DBZD)的出现,导致了新的消费模式。在毒理学诱发的死亡病例中,识别这些记录不佳的分子至关重要。我们在这里报告一个42岁的白人妇女死于NPS多元消费的情况下。在尸体附近发现了十包标有“研究用化学品”的包裹。三包被鉴定为含有溴唑仑和2-MMC的包裹是空的。另外七个被标记为含有4F-MPH, 4-FMA, 2-MMC和O-DSMT的药片有各种形状和颜色。为了采集血液样本,对尸体进行了法医检查。我们采集了右锁骨下动脉的血样。收集并分析了片剂和死后血液样本。该研究的目的是报告涉及各种新型精神活性物质(NPS)的死亡浓度水平,包括溴唑仑和2-MMC。方法用300 μL 0.1 M硫酸锌溶液提取血样(200 μL),外加500 μL含内标品的甲醇。蒸发上清液,将残留物溶于200 μL流动相中。采用定性液相色谱-串联质谱(LC-MS/MS) (Xevo TQ-XS, Waters)对血液和片剂中的NPS进行鉴定。血液样品采用液相色谱-高分辨率质谱(LC-HRMS)全扫描分析(Q-Exactive®,Thermo Scientific),标准溶液为2-MMC、溴唑仑、4-FMA、o -去甲基曲马多,并进行质量控制。结果死后外周血分析显示:溴唑仑308 ng/mL, 2-MMC 12616 ng/mL, o -去甲基曲马多1410 ng/mL, 4-FMA 3176 ng/mL。片剂的标识与包装标签一致。结论2-MMC、4-FMA、o -去甲基曲马多、溴唑仑等多种NPS中毒导致死亡,其中溴唑仑在法国首次报道。该浓度高于科学文献中报道的“致命”浓度。NPS的可及性导致高风险的多重消费。结合来自不同化学家族的多种物质,如DBZD,在文献中相对常见,并可能导致毒理学死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Death by intoxication involving various new psychoactive substances including bromazolam

Aim

Benzodiazepines are frequently involved in deaths with toxicological components. In recent years, synthetic designer benzodiazepines (DBZD) have emerged, leading to new consumption patterns. Identifying these poorly documented molecules is essential in toxicologically induced death cases. We report here the case of a Caucasian 42-year-old woman who died in a context of NPS poly-consumption. Ten packets labeled as Research Chemicals were found near the body. Three packets, identified as containing Bromazolam and 2-MMC, were empty. Seven others, labeled as containing 4F-MPH, 4-FMA, 2-MMC, and O-DSMT, held tablets of various shapes and colors. A forensic body examination was conducted in order to collect blood sample. We performed a blood sample collection from the right subclavian artery. The tablets and post-mortem blood samples were collected and analyzed. The aim of the study is to report concentration levels in a fatality involving various new psychoactive substances (NPS), including Bromazolam and 2-MMC.

Method

Blood sample (200 μL) was extracted with 300 μL of zinc sulfate solution at 0.1 M and additional 500 μL of methanol containing the internal standards were supplemented. Supernatants were evaporated and residues were dissolved in 200 μL of mobile phase. NPS identification in blood and tablets were performed using a qualitative liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) (Xevo TQ-XS, Waters).
Quantification was conducted on blood sample using a full scan analysis by liquid chromatography-high-resolution mass spectrometry (LC-HRMS) (Q-Exactive®, Thermo Scientific) with standard solution of 2-MMC, bromazolam, 4-FMA, O-desmethyltramadol and quality controls.

Results

The post-mortem peripheral blood analysis revealed the following concentrations: bromazolam 308 ng/mL, 2-MMC 12616 ng/mL, O-desmethyltramadol 1410 ng/mL, and 4-FMA 3176 ng/mL. The identification of the tablets was consistent with the packaging label.

Conclusion

The death resulted from intoxication involving multiple NPS: 2-MMC, 4-FMA, O-desmethyltramadol, and bromazolam, with the latter being reported for the first time in France. The concentrations were higher than “lethal” concentrations reported in the scientific literature.
The accessibility of NPS leads to high-risk poly-consumption. Combining multiple substances from different chemical families, such as DBZD, is relatively common in the literature and can result in toxicological fatalities.
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来源期刊
CiteScore
0.90
自引率
33.30%
发文量
393
审稿时长
47 days
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