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采用超高效液相色谱-三重四极杆质谱联用技术测定葡萄籽提取物膳食补充剂中的多类农药残留量。

Determination of multi-class pesticide residue in dietary supplements from grape seed extracts by ultra-high-performance liquid chromatography coupled to triple quadrupole mass spectrometry.

作者信息

Nieto-García Antonio José, Romero-González Roberto, Garrido Frenich Antonia

机构信息

a Research Group 'Analytical Chemistry of Contaminants', Department of Chemistry and Physics, Research Centre for Agricultural and Food Biotechnology (BITAL) , University of Almería, Agrifood Campus of International Excellence , Almería , Spain.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2014;31(9):1550-61. doi: 10.1080/19440049.2014.935489. Epub 2014 Jul 14.

DOI:10.1080/19440049.2014.935489
PMID:24945907
Abstract

A new method was developed and validated for the determination of multi-class pesticide residues in nutraceutical products obtained from grape seed extracts. The extraction procedure was based on QuEChERS methodology using ethyl acetate as solvent and a dispersive solid-phase extraction (dSPE) clean-up stage with C18 was included to minimise matrix effects. Pesticides determination was achieved using ultra-high-performance liquid chromatography coupled to triple quadrupole mass spectrometry (UHPLC-QqQ-MS/MS); total running time was 11 min. Pesticides were quantified using matrix-matched calibration. The developed method was validated in terms of matrix effect, linearity, selectivity, limits of detection and quantification, trueness, repeatability and inter-day precision at three concentration levels (10, 50, 100 µg kg(-1)). Suitable recovery values were obtained for 76% of analysed pesticides at the lowest concentration (10 µg kg(-1)). For most of the compounds, relative standard deviation values were lower than 20% and 25% for intra- and inter-day precision, respectively. Finally, 106 pesticides were determined, and the method was applied to seven dietary supplements from grape seed extract, obtaining various positive results for piperonyl butoxide, cyromazine and diniconazole at concentrations ranging from 2.0 to 13.4 µg kg(-1).

摘要

开发并验证了一种用于测定葡萄籽提取物营养产品中多类农药残留的新方法。提取程序基于QuEChERS方法,使用乙酸乙酯作为溶剂,并包括一个使用C18的分散固相萃取(dSPE)净化阶段,以尽量减少基质效应。使用超高效液相色谱-三重四极杆质谱联用仪(UHPLC-QqQ-MS/MS)进行农药测定;总运行时间为11分钟。使用基质匹配校准对农药进行定量。该方法在基质效应、线性、选择性、检测限和定量限、准确性、重复性和日间精密度方面在三个浓度水平(10、50、100 μg kg⁻¹)下进行了验证。在最低浓度(10 μg kg⁻¹)下,76%的分析农药获得了合适的回收率值。对于大多数化合物,日内和日间精密度的相对标准偏差值分别低于20%和25%。最后,测定了106种农药,并将该方法应用于7种葡萄籽提取物膳食补充剂,获得了胡椒基丁醚、灭蝇胺和烯唑醇在2.0至13.4 μg kg⁻¹浓度范围内的各种阳性结果。

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