Integrating ultrashort-chain compounds into the comprehensive analysis of per- and polyfluorinated substances in ready-to-feed liquid milk samples

IF 3.2
Shun-Hsin Liang, Justin A. Steimling
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引用次数: 0

Abstract

Ultrashort-chain (USC) per- and polyfluoroalkyl substances (PFAS) are highly polar compounds with carbon chains shorter than C4. Their widespread occurrence in aquatic environments has raised growing concerns about potential contamination in food products, particularly ready-to-feed liquid milk. To fully assess and mitigate PFAS contamination, it is essential to include USC compounds in PFAS analysis of milk samples. The high polarity of USC PFAS poses a significant challenge for standard chromatographic practices in PFAS analysis, primarily due to insufficient chromatographic retention. This study introduces a simple and reliable workflow for the simultaneous analysis of C1 to C14 perfluoroalkyl carboxylic and sulfonic acids, along with other PFAS classes, in various liquid milk matrices. The chromatographic analysis was performed using an inert-coated polar-embedded alkyl phase LC column. Method verification was conducted using three different milk types—dairy milk, almond milk, and infant formula—to demonstrate the workflow’s applicability for measuring 41 PFAS in diverse milk samples. A sample preparation procedure involving protein precipitation, extractant drying, and reconstitution was optimized for the effective extraction and quantification of all analytes. This streamlined procedure was evaluated by accuracy and precision analysis at five fortification levels, ranging from 0.01 to 0.25 µg/kg, equivalent to 10 to 250 ng/L in the final sample solution for LC-MS/MS analysis. Eighteen isotopes, serving as quantitative internal standards, were added to the sample before extraction to ensure accurate quantification by correcting variations in sample preparation, matrix effects, and instrument response. Calibration ranges varied among different analytes, spanning from 4 – 2500 ng/L. All analytes exhibited recovery values within 30 % of the nominal concentration across all fortification levels. Satisfactory method precision was demonstrated with %RSD values below 15 %. The established workflow was then applied to the analysis of additional milk samples collected from various grocery stores, providing a comprehensive profile of PFAS contamination across a diverse range of milk matrices.

Abstract Image

将超短链化合物整合到对即食液态奶样品中全氟和多氟物质的综合分析中
超短链(USC)全氟烷基和多氟烷基物质(PFAS)是碳链短于C4的高极性化合物。它们在水生环境中的广泛存在引起了人们对食品,特别是即食液态奶中潜在污染的日益关注。为了充分评估和减轻PFAS污染,必须在牛奶样品的PFAS分析中包括USC化合物。USC PFAS的高极性对PFAS分析中的标准色谱实践提出了重大挑战,主要是由于色谱保留不足。本研究介绍了一种简单可靠的工作流程,用于同时分析各种液体牛奶基质中的C1至C14全氟烷基羧酸和磺酸,以及其他PFAS类别。色谱分析采用惰性包被极性包埋的烷基相色谱柱。方法验证使用三种不同的牛奶类型-牛奶,杏仁牛奶和婴儿配方奶粉-来证明该工作流程适用于测量不同牛奶样品中的41种PFAS。样品制备过程包括蛋白质沉淀、萃取剂干燥和重构,优化了所有分析物的有效提取和定量。在5个强化水平(范围为0.01至0.25µg/kg,相当于LC-MS/MS最终样品溶液中的10至250 ng/L)下,通过准确度和精密度分析评估了该简化程序。在提取前,将18种同位素作为定量内标添加到样品中,通过纠正样品制备、基质效应和仪器响应的变化来确保准确的定量。校准范围因不同的分析物而异,范围从4 - 2500 ng/L。在所有强化水平下,所有分析物的回收率均在标称浓度的30%以内。方法精密度满意,RSD值小于15%。然后将建立的工作流程应用于分析从各个杂货店收集的其他牛奶样品,从而提供跨各种牛奶基质的PFAS污染的全面概况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of chromatography open
Journal of chromatography open Analytical Chemistry
CiteScore
2.50
自引率
0.00%
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0
审稿时长
50 days
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