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首页> 外文期刊>Analytical and bioanalytical chemistry >Determination of pesticide residues in wine by membrane-assisted solvent extraction and high-performance liquid chromatography-tandem mass spectrometry
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Determination of pesticide residues in wine by membrane-assisted solvent extraction and high-performance liquid chromatography-tandem mass spectrometry

机译:膜辅助溶剂萃取-高效液相色谱-串联质谱法测定葡萄酒中的农药残留

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The determination of pesticides in food products is an essential issue to guarantee food safety and minimise health risks of consumers. A protocol based on membraneassisted solvent extraction and liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) that allows the determination of 18 pesticides in red wine at minimum labour effort for sample preparation was developed and validated. Ten millilitres of wine were extracted using 100 μL of toluene filled in a non-porous polyethylene membrane bag which is immersed in the wine sample. After 150 min extraction under stirring, an aliquot of the extraction solution is analysed using HPLC-MS/MS. The limits of quantification ranged from 3 ng/L for Pirimicarb to 1.33 μg/L for Imidacloprid. Quantification by matrixmatched calibration provided relative standard deviations =16 % for most of the target pesticides. The linearity of calibration was given over three to four orders of magnitude, which enables the reliable measurement of a broad range of pesticide concentrations, and for each target pesticide, the sensitivity of the protocol meets the maximum residue levels set by legislations at least for wine grapes. Good agreement of results was found when the new method was compared with a standard liquid-liquid extraction protocol. In five wine samples analysed, Carbendazim and Metalaxyl were determined at micrograms per litre concentrations, even in some of the organic wines. Tebuconazol and Cyprodinitril were determined at lower abundance and concentration, followed by Spiroxamin and Diuron.
机译:食品中农药的测定是确保食品安全并最大程度降低消费者健康风险的重要问题。制定并验证了基于膜辅助溶剂萃取和液相色谱-串联质谱(HPLC-MS / MS)的方案,该方案能够以最少的劳动量测定红酒中的18种农药。使用装在无孔聚乙烯膜袋中的100μL甲苯提取十毫升葡萄酒,并将其浸入葡萄酒样品中。在搅拌下萃取150分钟后,使用HPLC-MS / MS分析萃取溶液的等分试样。定量限的范围从吡虫威的3 ng / L到吡虫啉的1.33μg/ L。通过基质匹配校准进行定量,大多数目标农药的相对标准偏差为16%。标定的线性度超过3到4个数量级,这使得能够可靠地测量各种农药浓度,并且对于每种目标农药,该方案的灵敏度至少要达到法规规定的最大残留水平,至少针对葡萄酒葡萄。当将该新方法与标准液-液萃取方案进行比较时,发现了很好的结果一致性。在分析的五种葡萄酒样品中,甚至在某些有机葡萄酒中,多菌灵和甲霜灵的浓度也以微克/升为单位。在较低的丰度和浓度下测定戊丁唑和赛普地尼,然后测定螺旋藻胺和敌草隆。

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