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Microwave-assisted extraction and large-volume injection gas chromatography tandem mass spectrometry determination of multiresidue pesticides in edible seaweed

机译:微波辅助萃取-大体积进样气相色谱-串联质谱法测定食用海藻中的多残留农药

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A microwave-assisted extraction method followed by clean-up with solid-phase extraction (SPE) combined with large-volume injection gas chromatography-tandem mass spectrometry (LVI-GC-MS/MS) for the analysis of 17 pesticides in wild and aquaculture edible seaweeds has been developed. An experimental central composite design was employed to evaluate the effects of the main variables potentially affecting the extraction (temperature, time, and solvent volume) and to optimize the process. The most effective microwave extraction conditions were achieved at 125 °C and 12 min with 24 mL of hexane/ethyl acetate (80:20). SPE clean-up of the extracts with graphitized carbon and Florisil, optimized by means of the experimental design, proved to be efficient in the removal of matrix interferences. The analytical recoveries were close to 100% for all the analytes, with relative standard deviations lower than 13%. The limits of detection ranged from 0.3 to 23.1 pg∈g ~(-1) and the limits of quantification were between 2.3 and 76.9 pg∈g~(-1), far below the maximum residue levels established by the European Union for pesticides in seaweed. The results obtained prove the suitability of the microwave-assisted extraction for the routine analysis of pesticides in aquaculture and wild seaweed samples.
机译:微波辅助萃取-固相萃取(SPE)净化与大体积进样气相色谱-串联质谱(LVI-GC-MS / MS)相结合,用于分析野生和水产养殖中的17种农药已开发出可食用的海藻。采用实验性的中央复合设计来评估可能影响萃取(温度,时间和溶剂量)的主要变量的影响并优化工艺。最有效的微波萃取条件是在125°C和12分钟的条件下,使用24 mL己烷/乙酸乙酯(80:20)萃取。通过实验设计优化的用石墨化碳和弗洛里西(Florisil)对萃取物进行SPE净化,可有效去除基质干扰。所有分析物的分析回收率接近100%,相对标准偏差低于13%。检出限为0.3至23.1pg∈g〜(-1),定量限为2.3至76.9pg∈g〜(-1),远低于欧盟规定的农药最高残留量。海藻。所获得的结果证明了微波辅助萃取适合用于水产养殖和野生海藻样品中农药的常规分析。

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