In this work, a matrix solid-phase dispersion extraction (MSPD) followed by a back-extraction method was used to determine 11 pesticides from hazelnut samples. An innovative dispersing material was prepared and a silica gel bulk was impregnated with a choline chloride:oxalic acid (molar ratio 1:1) deep eutectic solvent (DES). The material was characterized via Fourier transform infrared spectroscopy, laser diffraction analysis, and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy. Through a preliminary one-factor-at-a-time study and a final Box-Behnken Design optimization, the sample-to-dispersing material ratio, grinding time, and extraction solvent volume parameters were optimized, yielding the following values: 1:3.8 (w/w), 1.9 min, and 2.4 mL, respectively. Ultra high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) analysis was used. The method was validated according to SANTE 11,312/2021 guidelines. Recoveries were evaluated at three different spike levels (LOQ, 10LOQ, and MRL) and were all above 50 %. Precision and trueness intra- and interday were all below 20 %. Linearity was studied in the range of interest (LOQ–100 µg kg-1) with determination coefficients greater than 0.991. The limits of detection and quantification were in the range of 0.03–0.5 µg kg-1 and 0.1–1.7 µg kg-1, respectively. The sustainability of the method was evaluated using AGREEprep, BAGI and ComplexMoGAPI software.
Innovative dispersing material based on silica gel and deep eutectic solvents for the extraction of pesticides from hazelnuts followed by UHPLC-MS/MS analysis
Della Posta S;Giannitelli SM;Trombetta M;De Gara L;Fanali C
2026-01-01
Abstract
In this work, a matrix solid-phase dispersion extraction (MSPD) followed by a back-extraction method was used to determine 11 pesticides from hazelnut samples. An innovative dispersing material was prepared and a silica gel bulk was impregnated with a choline chloride:oxalic acid (molar ratio 1:1) deep eutectic solvent (DES). The material was characterized via Fourier transform infrared spectroscopy, laser diffraction analysis, and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy. Through a preliminary one-factor-at-a-time study and a final Box-Behnken Design optimization, the sample-to-dispersing material ratio, grinding time, and extraction solvent volume parameters were optimized, yielding the following values: 1:3.8 (w/w), 1.9 min, and 2.4 mL, respectively. Ultra high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) analysis was used. The method was validated according to SANTE 11,312/2021 guidelines. Recoveries were evaluated at three different spike levels (LOQ, 10LOQ, and MRL) and were all above 50 %. Precision and trueness intra- and interday were all below 20 %. Linearity was studied in the range of interest (LOQ–100 µg kg-1) with determination coefficients greater than 0.991. The limits of detection and quantification were in the range of 0.03–0.5 µg kg-1 and 0.1–1.7 µg kg-1, respectively. The sustainability of the method was evaluated using AGREEprep, BAGI and ComplexMoGAPI software.| File | Dimensione | Formato | |
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