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A sensitive method for the determination of per- and polyfluoroalkyl substances in food and food contact material using high-performance liquid chromatography coupled with tandem mass spectrometry.
Aßhoff, Norina; Bernsmann, Thorsten; Esselen, Melanie; Stahl, Thorsten.
Afiliação
  • Aßhoff N; Chemical and Veterinary Analytical Institute Münsterland-Emscher-Lippe, Joseph-König-Str. 40, 48147 Münster, Germany; Institute of Food Chemistry, University of Münster, Corrensstr. 45, 48149 Münster, Germany. Electronic address: norina.asshoff@cvua-mel.de.
  • Bernsmann T; Chemical and Veterinary Analytical Institute Münsterland-Emscher-Lippe, Joseph-König-Str. 40, 48147 Münster, Germany.
  • Esselen M; Institute of Food Chemistry, University of Münster, Corrensstr. 45, 48149 Münster, Germany.
  • Stahl T; Chemical and Veterinary Analytical Institute Münsterland-Emscher-Lippe, Joseph-König-Str. 40, 48147 Münster, Germany.
J Chromatogr A ; 1730: 465041, 2024 Aug 16.
Article em En | MEDLINE | ID: mdl-38878743
ABSTRACT
Dietary intake is the major pathway of human exposure to per- and polyfluoroalkyl substances (PFAS). Due to their generally very low concentrations in food, especially for foods of plant origin, and their toxicological relevance, demand is growing for improved selective and sensitive analytical methods for the determination of PFAS in the lower ng/kg range. The relevance is pointed out due to the fact that the European Commission has published limits of quantification (LOQs) in the lower ng/kg range for different food matrices in Recommendation (EU) 2022/1431 on the monitoring of perfluoroalkyl substances in food. For example, LOQs of 2 ng/kg for perfluorooctanesulfonic acid (PFOS), 1 ng/kg for perfluorooctanoic acid (PFOA), 1 ng/kg for perfluorononanoic acid (PFNA) and 4 ng/kg for perfluorohexanesulfonic acid (PFHxS) in fruit, vegetables and baby foods are required. A new, very sensitive method is presented here for the determination of 22 PFAS in food and food contact materials. The method is based on liquid-solid extraction and automated clean-up using two solid phase extraction techniques. The analytes are separated and detected by HPLC-MS/MS. A limit of detection (LOD) of 0.33 ng/kg and an LOQ of 1.0 ng/kg are attained for plant foods such as fruits and vegetables as well as for milk and baby food. For foods of animal origin such as egg, meat, fish and paper-based food contact materials an LOD of 1.6 ng/kg as well as an LOQ of 5.0 ng/kg are attained. PFOS and PFOA were the most abundant compounds in the food samples with concentration as high as 1,051 ng/kg of PFOA in sea weed samples and 772 ng/kg of PFOS in eggs samples. In food contact material samples, higher levels were found with a maximum of 310,000 ng/kg PFHxA. In sum the presented method firstly allows determination of PFAS in a wide variety of foodstuffs and paper-based food contact materials at EU-required concentration ranges.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Contaminação de Alimentos / Ácidos Alcanossulfônicos / Espectrometria de Massas em Tandem / Limite de Detecção / Fluorocarbonos Limite: Animals Idioma: En Revista: J Chromatogr A Ano de publicação: 2024 Tipo de documento: Article País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Contaminação de Alimentos / Ácidos Alcanossulfônicos / Espectrometria de Massas em Tandem / Limite de Detecção / Fluorocarbonos Limite: Animals Idioma: En Revista: J Chromatogr A Ano de publicação: 2024 Tipo de documento: Article País de publicação: Holanda