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建立并验证了 LC-MS/MS 法分析死后检材中沃替西汀的方法。真实案例的初步数据。

Development and validation of a LC-MS/MS method for analysis of vortioxetine in postmortem specimens. First data from an authentic case.

机构信息

Laboratory of Forensic Toxicology, Department "G.F. Ingrassia", University of Catania, Catania, Italy.

出版信息

J Forensic Sci. 2023 Mar;68(2):578-585. doi: 10.1111/1556-4029.15198. Epub 2023 Jan 13.

Abstract

Vortioxetine is an antidepressant recently licensed in USA and EU for the treatment of major depressive disorder. Neither fatal case due to overdose nor data about postmortem concentrations on blood or other specimens have been reported. The aims of this study were the development and validation of a method for vortioxetine analysis by Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS) in postmortem samples and its application in an authentic case. The method was validated and applied on blood, vitreous humor, bile, brain, liver, kidney, and gastric content. After protein precipitation, the supernatant was directly injected into LC-MS/MS. Analysis was carried out by Multiple Reaction Monitoring (MRM) mode. The authentic case concerned a 38 years-old woman, affected by depression, who was found hanged at home. The method determined an acceptable sensitivity, selectivity, linearity, precision, and accuracy for all matrices. No interference was shown for all matrices. The matrices do not significantly reduce the peak intensity of vortioxetine. No carryover was shown. Toxicological analysis of the authentic case showed vortioxetine in blood (234 ng/ml), vitreous humor (10.5 ng/ml), brain (490 ng/g), lung (479 ng/g), liver (3751 ng/g), kidney (798 ng/g), bile (2267 ng/ml) and gastric content (253 ng/ml). Our case suggests that even at blood concentrations of vortioxetine equal to 234 ng/ml, the subject was able to stage and carry out the hanging. Vortioxetine concentrations found in the other cadaveric samples (biological fluids, organs, and gastric content) may be helpful to evaluate further similar comparable cases.

摘要

文拉法辛是一种抗抑郁药,最近在美国和欧盟获得许可,用于治疗重度抑郁症。尚未报道因过量服用而导致的致命病例,也没有关于血液或其他样本中死后浓度的数据。本研究的目的是开发和验证液相色谱串联质谱法(LC-MS/MS)在死后样本中分析文拉法辛的方法,并将其应用于真实案例。该方法在血液、玻璃体、胆汁、脑、肝、肾和胃内容物中进行了验证和应用。蛋白沉淀后,上清液直接注入 LC-MS/MS。分析采用多重反应监测(MRM)模式进行。真实案例涉及一名 38 岁女性,患有抑郁症,被发现在家中上吊。该方法在所有基质中均表现出可接受的灵敏度、选择性、线性、精密度和准确度。所有基质均未显示干扰。基质不会显著降低文拉法辛的峰强度。无交叉污染。真实案例的毒理学分析显示,血液(234ng/ml)、玻璃体(10.5ng/ml)、脑(490ng/g)、肺(479ng/g)、肝(3751ng/g)、肾(798ng/g)、胆汁(2267ng/ml)和胃内容物(253ng/ml)中均存在文拉法辛。我们的案例表明,即使血液中文拉法辛浓度达到 234ng/ml,受试者仍有能力策划并实施上吊。在其他尸体样本(生物体液、器官和胃内容物)中发现的文拉法辛浓度可能有助于进一步评估类似可比案例。

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