Extraction and Matrix Cleanup Method for Analyzing Novel Per- and Polyfluoroalkyl Ether Acids and Other Per- and Polyfluoroalkyl Substances in Fruits and Vegetables

被引:22
|
作者
Meng, Pingping [1 ]
DeStefano, Noelle J. [1 ]
Knappe, Detlef R. U. [1 ]
机构
[1] North Carolina State Univ, Dept Civil Construct & Environm Engn, Raleigh, NC 27695 USA
基金
美国国家环境保护局;
关键词
PFEAs; PFAS; method quantification limits; extraction and matrix cleanup method; fruits and vegetables; PERFLUOROALKANE SULFONIC-ACIDS; DRINKING-WATER CONTAMINANTS; PERFLUORINATED ALKYL ACIDS; CAPE FEAR RIVER; CARBOXYLIC-ACIDS; FLUORINATED COMPOUNDS; FLUOROTELOMER ACIDS; MASS-SPECTROMETRY; TEMPORAL TRENDS; SOUTH CHINA;
D O I
10.1021/acs.jafc.1c07665
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Per- and polyfluoroalkyl ether acids (PFEAs) are a subclass of per- and polyfluoroalkyl substances (PFAS) that are detected with increasing frequency in environmental matrices. Diet can be an important route of PFEA exposure, but the presence of PFEAs in food is poorly understood. Extraction methods for food samples exist for traditionally studied PFAS, but their suitability for PFEAs and other novel PFAS remains unknown. In this study, an extraction and matrix cleanup method was developed to quantify 45 PFAS, including 13 PFEAs, 3 perfluoroalkane sulfonamides, and 6 fluorotelomer carboxylic acids in 10 types of fruits and vegetables. Homogenized samples were extracted with basic methanol, and resulting extracts were diluted with water and cleaned up using solid-phase extraction with weak anion-exchange cartridges. The method was validated by performing spike-recovery experiments at spike levels of 1 ng/g in all 10 matrices and 0.1 ng/g in 2 matrices. For PFAS without a corresponding isotopically labeled internal standard (IS), adopting an IS with a similar chromatographic retention time generated the most accurate recoveries. Dependent upon the matrix, recoveries of 38-44 PFAS (including 10-13 PFEAs) fell within 50-150% for samples spiked at 1 ng/g. Recoveries of 40 and 38 PFAS in blueberries and corn, respectively, fell within 50-150% for samples spiked at 0.1 ng/g. Method quantification limits (MQLs) of PFAS in pure solvents were determined as the lowest calibration level with an accuracy between 70 and 130%. To compensate for matrix effects, a matrix factor was applied on the basis of the analyte response in different matrices relative to the pure solvent. The MQLs of 45 PFAS (including 13 PFEAs) in 10 matrices ranged from 0.025 to 0.25 ng/g. Overall, this method is capable of sensitively quantifying 45 PFAS in many fruits and vegetables.
引用
收藏
页码:4792 / 4804
页数:13
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