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采用纳升液相色谱-纳升电喷雾-轨道阱质谱联用技术,考虑到最近制定的可耐受每周摄入量(TWI)限值,痕量测定食品中四种优先全氟烷基物质。

Application of nano-LC - nano-ESI - Orbitrap-MS for trace determination of four priority PFAS in food products considering recently established tolerable weekly intake (TWI) limits.

机构信息

Institute of Food Safety, Animal Health and Environment "BIOR", Lejupes Iela 3, Riga, LV-1076, Latvia.

Institute of Food Safety, Animal Health and Environment "BIOR", Lejupes Iela 3, Riga, LV-1076, Latvia.

出版信息

Anal Chim Acta. 2023 Apr 22;1251:341027. doi: 10.1016/j.aca.2023.341027. Epub 2023 Mar 2.

Abstract

An analytical method was developed and validated for the analysis of four priority perfluoroalkyl substances (PFAS), namely, perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorohexanesulfonic acid (PFHxS), and perfluorooctanesulfonate (PFOS) in food products using nanoscale liquid chromatography (nano-LC) coupled with nanoscale electrospray ionization (nano-ESI) and Orbitrap mass spectrometry (Orbitrap-MS) detection. The efficiency of two different nano-LC setups for chromatographic separation of selected PFAS was evaluated. The optimal LC separation of analytes was achieved using a reversed phase C18 (RP-C18) nano bore column with an integrated emitter. The effect of matrix concentration factor on signal suppression/enhancement was evaluated for different matrices. The method validation indicated analyte recoveries in the range 83-118% and within-laboratory reproducibility from 7 to 18%, while reanalysis of the materials from proficiency tests (PTs) showed that the accuracy of the obtained concentrations ranged from 85 to 124% of the provided consensus values. The method limits of quantification (m-LOQs) were set as first validation levels ranging from 0.001 to 0.3 ng g sample depending on the type of the food group. The observed method performance characteristics met the criteria stated in Commission Regulation (EU) 2022/1428, Commission Recommendation (EU) 2022/1431, as well as Guidance Document on Analytical Parameters for the Determination of Per- and Polyfluoroalkyl Substances (PFAS) in Food and Feed with regards to the compliance testing of PFAS maximum levels (MLs) and monitoring purposes. The elaborated method was applied for the analysis of selected priority PFAS in different food groups collected from the Latvian retail market.

摘要

建立并验证了一种分析方法,用于使用纳升级液相色谱(nano-LC)与纳升级电喷雾电离(nano-ESI)和轨道阱质谱(Orbitrap-MS)联用,分析食品中四种优先全氟烷基物质(PFAS),即全氟辛酸(PFOA)、全氟壬酸(PFNA)、全氟己烷磺酸(PFHxS)和全氟辛烷磺酸(PFOS)。评估了两种不同的 nano-LC 装置对所选 PFAS 色谱分离效率的影响。采用带有集成喷针的反相 C18(RP-C18)纳孔柱,实现了分析物的最佳 LC 分离。评估了不同基质中基质浓度因子对信号抑制/增强的影响。方法验证表明,分析物回收率在 83-118%范围内,实验室内部重现性在 7-18%范围内,而对能力验证(PT)材料的重新分析表明,获得的浓度准确性在提供的共识值的 85-124%范围内。方法定量限(m-LOQs)设定为首次验证水平,根据食品组的类型,范围为 0.001-0.3 ng g 样品。观察到的方法性能特征符合欧盟委员会法规(EU)2022/1428、欧盟委员会建议(EU)2022/1431 以及关于全氟和多氟烷基物质(PFAS)在食品和饲料中测定的分析参数指南中规定的标准,用于 PFAS 最大限量(MLs)的合规性测试和监测目的。所开发的方法用于分析从拉脱维亚零售市场采集的不同食品组中选定的优先 PFAS。

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