A novel method for the determination of synthetic cathinones and related substances in postmortem blood samples using cork-based dispersive solid-phase microextraction prior to LC-MS/MS analysis.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Letícia Birk, Bruno Pereira Dos Santos, Sarah Eller, Tiago Franco de Oliveira
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Abstract

The detection of new psychoactive substances in postmortem blood is of primary importance for the investigation of related deaths. A method using cork as a biosorbent in a solid-phase microextraction with LC-MS/MS analysis was developed and validated for the determination of synthetic cathinones and related substances in blood. The sample preparation method employed 200 µL of sample and 30 mg of cork powder, and the complete procedure was optimized using multivariate strategies. LC-MS/MS analysis was performed in gradient mode, with a total run time of 7.5 min for the determination of cathinone, ethylone, fentanyl, MDA, MDMA, mephedrone, N-ethylpentylone, and pentylone. Comprehensive validation was performed through the ASB/ANSI Standard 036. Lower limit of quantification (LLOQ) values ranged between 0.5 and 1 ng/mL, with linear ranges between LLOQ and 85 ng/mL. Accuracy and precision results were satisfactory, and significant ion suppression was found (2.9-63.4%). Applicability of the method was evaluated by the analysis of three postmortem blood samples from forensic casework, suspected to have the presence of synthetic cathinones. All samples were positive for MDMA and MDA, with concentrations between 79.2-198.1 ng/mL and 23.1-26.6 ng/mL, respectively. The greenness of the method was also evaluated by AGREEprep, with an overall score of 0.53. This study is the first to apply a cork-based extraction to blood analysis. The method has proven to be reliable and a valuable greener alternative for the determination of synthetic cathinones and related substances in postmortem blood.

建立了一种在LC-MS/MS分析前采用软木基分散固相微萃取法测定死后血液样品中合成卡西酮及其相关物质的新方法。
在死后血液中检测新的精神活性物质对相关死亡的调查至关重要。建立了以软木为生物吸附剂的固相微萃取- LC-MS/MS法测定血液中合成卡西酮及相关物质的方法,并进行了验证。样品制备方法采用200µL样品和30 mg软木粉,并采用多变量策略对整个制备过程进行优化。LC-MS/MS分析采用梯度模式,总运行时间为7.5 min,用于测定卡西酮、乙炔、芬太尼、MDA、MDMA、甲氧麻黄酮、n -乙基戊酮和戊酮。通过ASB/ANSI标准036进行全面验证。定量下限(LLOQ)范围为0.5 ~ 1 ng/mL, LLOQ ~ 85 ng/mL呈线性关系。准确度和精密度令人满意,离子抑制显著(2.9-63.4%)。该方法的适用性是通过分析法医案件中疑似含有合成卡西酮的三份死后血液样本来评估的。所有样品的MDMA和MDA均呈阳性,浓度分别在79.2 ~ 198.1 ng/mL和23.1 ~ 26.6 ng/mL之间。采用AGREEprep软件对方法的绿色度进行评价,总体得分为0.53。这项研究首次将基于软木的提取应用于血液分析。该方法已被证明是可靠的,是一种有价值的绿色替代方法,用于测定死后血液中的合成卡西酮和相关物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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