Department of Legal Medicine, Teikyo University School of Medicine, 2-11-1, Kaga, Itabashi-ku, Tokyo 173-8605, Japan.
Department of Legal Medicine, Teikyo University School of Medicine, 2-11-1, Kaga, Itabashi-ku, Tokyo 173-8605, Japan.
J Pharm Biomed Anal. 2022 Jan 5;207:114429. doi: 10.1016/j.jpba.2021.114429. Epub 2021 Oct 16.
In this research, we have developed a novel and simple liquid chromatography coupled with electrospray ionization-tandem mass spectrometry (LC/ESI-MS/MS) method for quantification of 2-aminothiazoline-4-carboxylic acid (ATCA), which is produced by the direct reaction of cyanide (CN) with endogenous cystine. In forensic science, detection of CN is important because CN is a poison that is often used for murder or suicide, in addition to being produced by the thermal decomposition of natural or synthetic materials. However, because CN disappears rapidly from body tissue, ATCA is thought to be a more reliable indicator of CN exposure. For the method reported herein, human blood samples (20 μL) were subjected to protein precipitation followed by derivatization with 4-bromoethyl-7-methoxycoumarin. Blood spiked with ATCA at concentrations ranging from 50 to 1500 ng/mL was used to prepare a calibration curve (lower limit of quantification; 50 ng/mL, lower limit of detection; 25 ng/mL). Our method uses chemical derivatization, so unlike previously reported methods, it does not require tedious pretreatment procedures, hydrophilic interaction liquid chromatography columns, or specialized equipment. In addition, our method allows for repeatable and accurate quantification of ATCA, with intra- and inter-assay coefficients of variation of below 5.0% and below 6.0%, respectively. We used the method to analyze ATCA in postmortem human blood samples, including samples from people who had intentionally ingested CN or were fire victims. Blood ATCA concentrations were higher among people who had ingested CN or were fire victims than among people in a control group (P < 0.0001). The data reported herein demonstrate that our LC/ESI-MS/MS method can be used to detect and quantify ATCA in postmortem blood samples and that CN exposure strongly affects ATCA concentration, providing a useful tool for detection of CN poisoning.
在这项研究中,我们开发了一种新颖而简单的液相色谱-电喷雾串联质谱(LC/ESI-MS/MS)方法,用于定量检测 2-氨基噻唑-4-羧酸(ATCA)。ATCA 是由氰化物(CN)与内源性胱氨酸直接反应生成的。在法医学中,检测 CN 很重要,因为 CN 是一种毒药,常被用于谋杀或自杀,此外,它还会由天然或合成材料的热分解产生。然而,由于 CN 会从组织中迅速消失,因此 ATCA 被认为是更可靠的 CN 暴露指标。本文报道的方法中,用人血(20 μL)进行蛋白沉淀,然后用 4-溴乙基-7-甲氧基香豆素衍生化。使用 ATCA 浓度为 50 至 1500 ng/mL 的血样制备校准曲线(定量下限为 50 ng/mL,检测下限为 25 ng/mL)。我们的方法使用化学衍生化,因此与以前报道的方法不同,它不需要繁琐的预处理程序、亲水作用色谱柱或专用设备。此外,我们的方法可以对 ATCA 进行可重复和准确的定量,其日内和日间变异系数分别低于 5.0%和 6.0%。我们使用该方法分析了死后人体血液样本中的 ATCA,包括故意摄入 CN 或火灾受害者的样本。摄入 CN 或火灾受害者的血液 ATCA 浓度明显高于对照组(P < 0.0001)。本文报告的数据表明,我们的 LC/ESI-MS/MS 方法可用于检测和定量死后血液样本中的 ATCA,且 CN 暴露强烈影响 ATCA 浓度,为检测 CN 中毒提供了有用的工具。