Extension of the QuEChERS Method for Pesticide Residues in Cereals to Flaxseeds, Peanuts, and Doughs

被引:196
作者
Koesukwiwat, Urairat [1 ,2 ]
Lehotay, Steven J. [1 ]
Mastovska, Katerina [1 ]
Dorweiler, Kelly J. [3 ]
Leepipatpiboon, Natchanun [2 ]
机构
[1] ARS, Eastern Reg Res Ctr, USDA, Wyndmoor, PA 19038 USA
[2] Chulalongkorn Univ, Fac Sci, Dept Chem, Chromatog & Separat Res Unit, Bangkok 10330, Thailand
[3] James Ford Bell Tech Ctr, Golden Valley, MN 55427 USA
关键词
Pesticide residues; analysis; QuEChERS; gas chromatography time-of-flight mass spectrometry (GC-TOF); flaxseed; peanut; dough; SOLID-PHASE EXTRACTION; CHROMATOGRAPHY-MASS SPECTROMETRY; LOW-TEMPERATURE CLEANUP; GAS-CHROMATOGRAPHY; LIQUID-CHROMATOGRAPHY; MULTIRESIDUE METHOD; OLIVE OIL; FOOD; MATRICES; ENHANCEMENT;
D O I
10.1021/jf902988b
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
A simple method was evaluated for the determination of pesticide residues in flaxseeds, doughs, and peanuts using gas chromatography time-of-flight mass spectrometry (GC-TOF) for analysis. A modified QuEChERS (quick, easy, cheap, effective, rugged, and safe) method, which was previously optimized for cereal grain samples, was evaluated in these fatty matrices. This extraction method involves first mixing the sample with 1:1 water/acetonitrile for an hour to swell the matrix and permit the salt-out liquid liquid partitioning step using anhydrous MgSO4 and NaCl. After shaking and centrifugation, cleanup is done by dispersive solid-phase extraction (d-SPE) using 150 mg of anhydrous MgSO4, 150 mg of PSA, and 50 mg of C-18 per milliliter of extract. This method gave efficient separation of pesticides from fat and removal of coextracted substances better than gel permeation chromatography or use of a freeze-out step, which involved excessive use of solvent and/or time. The optimized analytical conditions were evaluated in terms of recoveries, reproducibilities, limits of detection, and matrix effects for 34 representative pesticides using different types of flaxseeds, peanuts, and doughs. Use of matrix-matched standards provided acceptable results for most pesticides with overall average recoveries between 70 and 120% and consistent RSDs <20% for semipolar pesticides and <26% for lipophilic pesticides. The recoveries of these latter types of pesticides depended on the fat content in the matrices and partitioning factor between the lipids and acetonitrile. We believe that the consistency of the pesticide recoveries for different samples in multiple experiments and the physicochemical partitioning explanation for <70% recoveries of lipophilic pesticides justify compensation of results for the empirically determined recovery values. In any case, this method still meets 10 ng/g detection limit needs for lipophilic pesticides and may be used for qualitative screening applications, in which any identified pesticides can be quantified and confirmed by a more intensive method that achieves >70% recoveries for lipophilic pesticides.
引用
收藏
页码:5950 / 5958
页数:9
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