Department of Forensic Pharmacology and Toxicology, Zurich Institute of Forensic Medicine, University of Zurich, Zurich, Switzerland.
Drug Test Anal. 2023 Aug;15(8):840-852. doi: 10.1002/dta.3480. Epub 2023 Apr 18.
Being able to attest when a bloodstain was deposited at a crime scene can be invaluable to a prosecution process, and methods to provide that information have long been desired. Determining the Time since Deposition (TsD) of a trace would allow placing a subject both in space and time to the crime scene-or prove that a trace left by that person was unrelated to it because it was deposited before or after the time the crime had occurred. To this day, no method for TsD determination has made its way into routine forensic casework, mainly because of the numerous challenges that await when trying to understand and account for all the influencing and confounding factors that affect the aging process (such as, e.g., temperature, UV-light exposure, or humidity). Here, we present an untargeted metabolomics-based study using liquid chromatography high-resolution mass spectrometry (LC-HR-MS) and data-dependent acquisition to analyze blood samples aged under two distinctly different storage conditions over 48 weeks. Global differences in age- and storage-dependent changes in blood metabolomes were described, and TsD-classification strategies based on qualitative and quantitative assessment of molecular features (MFs) have been proposed. Based on the selected criteria to best predict the TsD, the dipeptide Phenylalanylalanine (PheAla) can be considered as a promising candidate for TsD prediction. In essence, changes in the blood metabolome dynamics showed a strong association with increasing TsD, but significant differences depending on storage conditioning were observed, facilitating the need to study further the influence of individual influencing factors on TsD determination.
能够证明血迹是在犯罪现场沉积的,这对于起诉过程来说是非常有价值的,因此人们长期以来一直希望有一种方法可以提供这种信息。确定微量血迹的沉积时间(TsD)可以将主体在时间和空间上定位到犯罪现场,或者证明该人留下的痕迹与犯罪无关,因为它是在犯罪发生之前或之后沉积的。迄今为止,没有一种 TsD 测定方法能够应用于常规法医工作中,主要是因为在试图理解和解释所有影响老化过程的因素(例如温度、紫外线暴露或湿度)并考虑到这些因素时,会遇到许多挑战。在这里,我们使用基于非靶向代谢组学的研究方法,使用液相色谱高分辨率质谱(LC-HR-MS)和数据依赖采集,分析了在两种截然不同的储存条件下老化的血液样本,时间跨度为 48 周。描述了血液代谢组随时间和储存条件变化的全局差异,并提出了基于定性和定量评估分子特征(MF)的 TsD 分类策略。根据最佳预测 TsD 的选择标准,二肽苯丙氨酸-丙氨酸(PheAla)可以被认为是预测 TsD 的有前途的候选物。本质上,血液代谢组动力学的变化与 TsD 的增加密切相关,但观察到储存条件的显著差异,这使得有必要进一步研究个别影响因素对 TsD 测定的影响。