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用于食品中扩展全氟和多氟烷基物质监测的高分辨率质谱法:结合可疑物和非靶向方法

High-resolution mass spectrometry for extended PFAS surveillance in food: combining suspect and non-targeted approaches.

作者信息

Jeannot Cassandre, Macorps Nicolas, Amziane Ahmed, Le Bizec Bruno, Parinet Julien, Dervilly Gaud

机构信息

Oniris, INRAE, LABERCA, 44300 Nantes, France.

ANSES, Laboratory for Food Safety, Pesticides and Marine Biotoxins Unit, 14 rue Pierre et Marie Curie, F-94701 Maisons-Alfort, France.

出版信息

Food Chem X. 2025 Jul 29;29:102843. doi: 10.1016/j.fochx.2025.102843. eCollection 2025 Jul.

Abstract
  • and polyfluoroalkyl substances (PFAS) are persistent, potentially harmful synthetic chemicals. While they can accumulate in foodstuffs, current monitoring often targets only a few compounds, likely underestimating dietary exposure. In this study, 58 food samples from Europe and North Africa-including commercial products and items from known European contamination hotspots-were analyzed using a validated high-resolution mass spectrometry workflow combining suspect screening (SS) and non-targeted screening (NTS). Seventeen PFAS were confirmed through SS, with up to 15 different PFAS in fish samples from hotspots. While NTS revealed four additional fluorinated substances: Perfluoropropanoic acid (PFPrA) detected in 48 % of samples, 6:2 Fluorotelomer sulfonic acid (6:2 FTS), Fipronil, and Fipronil sulfone. These results highlight the geographical variability of PFAS contamination in food and demonstrate the value of combined SS/NTS approaches in identifying both known and emerging PFAS, supporting more comprehensive, regulation-aligned risk assessments.
摘要

多氟烷基物质(PFAS)是持久性的、潜在有害的合成化学物质。虽然它们会在食品中蓄积,但目前的监测通常仅针对少数几种化合物,这可能低估了膳食暴露量。在本研究中,使用经过验证的高分辨率质谱工作流程,结合可疑物筛查(SS)和非靶向筛查(NTS),对来自欧洲和北非的58份食品样本进行了分析,这些样本包括商业产品以及来自欧洲已知污染热点地区的物品。通过SS确认了17种PFAS,在来自热点地区的鱼类样本中发现了多达15种不同的PFAS。而NTS还发现了另外四种含氟物质:全氟丙酸(PFPrA)在48%的样本中被检测到、6:2氟调聚物磺酸(6:2 FTS)、氟虫腈和氟虫腈砜。这些结果突出了食品中PFAS污染的地理变异性,并证明了SS/NTS联合方法在识别已知和新出现的PFAS方面的价值,有助于进行更全面的、符合监管要求的风险评估。

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