首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Data-independent acquisition with ion mobility mass spectrometry for suspect screening of per- and polyfluoroalkyl substances in environmental water samples
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Data-independent acquisition with ion mobility mass spectrometry for suspect screening of per- and polyfluoroalkyl substances in environmental water samples

机译:具有离子迁移率质谱的数据无关,可疑筛选环境水样中的筛选和多氟烷基物质

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Per- and polyfluoroalkyl substances (PFASs) have environmentally persistent, and the various types of PFASs have been detected in water environments. Many previous studies have performed data-dependent acquisition (DDA) of mass spectra from an environmental sample by high-resolution mass spectrometry to identify PFAS suspects individually. In comparison, the data-independent acquisition (DIA) of comprehensive mass spectra of the sample is a technology which enables to know the occurrences of suspects and non-targets simultaneously. However, it is difficult to associate the fragment ions of targeted precursor ions by retention time only, because of the existence of co-eluting ions derived from environmental samples. Since the separation of ions is not enough with only the conventional DIA method, here, we attempted to support it using ion mobility mass spectrometry (IMS) to distinguish the relevant ions from co-eluting ions by drift time. Firstly, suspect screening of PFASs with eternal database resulted in determining 32-96 PFAS suspects in firefighting foam impacted groundwater samples (n = 8) by suspect screening. Among all the pairs of respective precursor ions and fragment ions of the PFAS suspects, 5%-19% (4-9 PFASs) of them were associated without considering the drift time of IMS, while 37%-49% (15-43 PFASs) of them were associated with considering the drift time. The consideration of the drift time increased the association ratios in all samples. In a sample, most precursor ions could be associated with their fragment ions (41 of 43 PFASs) because at least one probable fragment ion was observed among three of maximum intensity fragment ions. Thus, the method improved the identification by excluding the unrelated co-eluting ions by IMS. Moreover, the method can acquire a certain reliable MS/MS spectra of suspects in environmental samples in one analysis. It is not essential to conduct instrumental analyses again for samples stored for a long time even when the data sets and/or methodologies of data analyses are modified (e.g., the original database, screening list, or statistical filtering/data cleaning approach). It will be particularly useful for studies that must analyze a large number of environmental samples. (C) 2021 Elsevier B.V. All rights reserved.
机译:Per-和聚氟烷基物质(PFASs)具有环境持久性,并且在水环境中检测到各种类型的PFASs。以前的许多研究都通过高分辨率质谱仪对环境样品的质谱进行了数据相关采集(DDA),以单独识别PFAS嫌疑人。相比之下,样品综合质谱的数据独立采集(DIA)是一种能够同时知道可疑物和非目标物出现情况的技术。然而,由于存在来自环境样品的共洗脱离子,仅通过保留时间很难关联目标前体离子的碎片离子。由于仅用传统的DIA方法分离离子是不够的,在这里,我们尝试使用离子迁移率质谱(IMS)来支持它,以通过漂移时间区分相关离子和共洗脱离子。首先,通过eternal数据库对PFAS进行可疑筛查,通过可疑筛查,在受消防泡沫影响的地下水样本(n=8)中确定了32-96个PFAS可疑。在PFAS嫌疑人的所有前体离子和碎片离子对中,5%-19%(4-9 PFASs)与IMS的漂移时间无关,而37%-49%(15-43 PFASs)与漂移时间有关。考虑漂移时间会增加所有样本中的关联比率。在样品中,大多数前体离子可能与其碎片离子(43个PFASs中的41个)相关,因为在三个最大强度碎片离子中至少观察到一个可能的碎片离子。因此,通过IMS排除不相关的共洗脱离子,该方法改进了鉴定。此外,该方法可以在一次分析中获得环境样品中可疑物的一定可靠MS/MS光谱。即使修改了数据集和/或数据分析方法(例如,原始数据库、筛选列表或统计过滤/数据清理方法),也无需对长期存储的样本再次进行仪器分析。它对于必须分析大量环境样本的研究特别有用。(c)2021爱思唯尔B.V.保留所有权利。

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