LC-MS/MS检测溶磷脂酰乙醇作为潜在的酒精消耗量新标志物。

IF 1.1 4区 化学 Q4 PHYSICS, ATOMIC, MOLECULAR & CHEMICAL
European Journal of Mass Spectrometry Pub Date : 2023-10-01 Epub Date: 2023-09-14 DOI:10.1177/14690667231200143
Matthias Bantle, Lanya van Tieghem, Wolfgang Weinmann, Marc Luginbühl
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引用次数: 0

摘要

酒精生物标志物能够反映最近或长期饮酒的程度,涵盖不同的检测窗口。磷脂酰乙醇(PEths)是一类新兴的直接醇类生物标志物,广泛应用于临床和法医领域。它们的量化可以让我们深入了解一个人的饮酒行为。在这里,我们提出了一个未知的PEth物种的新亚类,LysoPEths,它在结构上与PEth相关,但缺少一个脂肪酰基链。溶血碱既可以是PEth的降解产物,也可以是溶血磷脂酰胆碱(LysoPC)与乙醇酯交换的产物。以PC 16:0/18:1为原料合成LysoPEth 16:0,采用液相色谱-质谱联用(LC-MS/MS)对其进行表征,酶法为磷脂酶D (PLD) -磷脂酶A2 (PLA2)。然后,在MRM模式下建立了LysoPEth 16:0的LC-MS/MS方法,并添加了LysoPEth 18:1, LysoPEth 18:2和LysoPEth 20:4和PEth 16:0/20:4。用不同浓度的乙醇孵育新鲜取样的禁酒者静脉血,研究了与PEth平行的LysoPEth的形成。随着乙醇浓度的增加,除了已知的PEth物种(PEth 16:0/18:1, PEth 16:0/18:2)外,LysoPEth 16:0可形成长达72 h, LysoPEth浓度约为PEth浓度的三分之一。在37°C下保存酒精消费者的无乙醇PEth阳性血液表明,冷冻/解冻血液在前24小时内LysoPEth 16:0浓度升高,而PEth 16:0/18:1浓度降低,而新鲜采集的血液则没有。此外,在临床和法医病例工作的静脉和冻干血液中检测到LysoPEth 16:0,以及PEth 16:0/18:1, 16:0/18:2,以及其他PEth和LysoPEth物种(PEth 16:0/20:4, LysoPEth 18:1, LysoPEth 18:2和LysoPEth 20:4)。LysoPEth 16:0浓度与PEth 16:0/18:1呈线性相关(r2 = 0.75)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lyso-phosphatidylethanol detected by LC-MS/MS as a potential new marker for alcohol consumption.

Alcohol biomarkers are able to reflect the degree of recent or long-term alcohol consumption, covering different windows of detection. Phosphatidylethanols (PEths) are an emerging group of direct alcohol biomarkers that are widely applied in clinical and forensic applications. Their quantification can provide insight into an individual's drinking behaviour. Here, we present a new sub-class of yet unknown PEth species, LysoPEths, which are structurally related to PEth, but miss one fatty acyl chain. LysoPEths can be either a degradation product of PEth or a product of transesterification of lyso-phosphatidylcholine (LysoPC) with ethanol. To set up an analytical method, LysoPEth 16:0 was synthesised from PC 16:0/18:1 and characterised by LC-MS/MS, using an enzymatic method: phospholipase D (PLD), followed by phospholipase A2 (PLA2). Then, an LC-MS/MS method in MRM mode for LysoPEth 16:0 with additional LysoPEth species (LysoPEth 18:1, LysoPEth 18:2, and LysoPEth 20:4) and PEth 16:0/20:4 was developed. By incubation of freshly sampled venous blood of a teetotaller with ethanol at different concentrations, the formation of LysoPEth in parallel to PEth was investigated. With increasing ethanol concentrations, LysoPEth 16:0 was formed besides the known PEth species (PEth 16:0/18:1, PEth 16:0/18:2) for up to 72 h with LysoPEth concentrations being about three times lower than PEth concentrations. Storage of ethanol-free PEth-positive blood of an alcohol consumer at 37 °C showed that LysoPEth 16:0 concentrations increased, while PEth 16:0/18:1 concentrations decreased in the first 24 h for frozen/thawed blood, however not for freshly collected blood. Furthermore, LysoPEth 16:0 was detected in venous as well as lyophilised blood from clinical and forensic case work alongside with PEth 16:0/18:1, 16:0/18:2, and other PEth and LysoPEth species (PEth 16:0/20:4, LysoPEth 18:1, LysoPEth 18:2, and LysoPEth 20:4). LysoPEth 16:0 concentrations were found to be in linear correlation with PEth 16:0/18:1 (r2 = 0.75).

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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
16
审稿时长
>12 weeks
期刊介绍: JMS - European Journal of Mass Spectrometry, is a peer-reviewed journal, devoted to the publication of innovative research in mass spectrometry. Articles in the journal come from proteomics, metabolomics, petroleomics and other areas developing under the umbrella of the “omic revolution”.
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