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Multiresidue analysis of pesticides in peanuts using modified QuEChERS sample preparation and liquid chromatography-mass spectrometry detection

机译:改进的QuEChERS样品制备和液相色谱-质谱法检测花生中的农药多残留

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A multiclass method has been optimized and validated for the simultaneous determination of 113 pesticide residues belonging to several classes in peanuts. It has been based on the QuEChERS methodology (quick, easy, cheap, effective, rugged and safe) and ultra high performance liquid chromatography coupled to triple quadrupole tandem mass spectrometry (UHPLC-MS/MS). Several extraction solutions were tested and the composition that showed the best results consisted of a mixture of ethyl acetate and acetonitrile. A cleanup step using the dispersive phases C18 (octadecyl) and PSA (Primary and Secondary Amine) was necessary due to the high amount of oil present in the matrix. The method was validated and the parameters of validation were satisfactory. The accuracy was assessed by calculating the recovery of spiked blank samples in four concentration levels (0.010; 0.025; 0.050 and 0.100 mg kga?’1). The results showed satisfactory recoveries (between 70 and 120%), except for oxamyl and tricyclazol at the 0.010 mg kga?’1 level that did not show acceptable parameters for the recovery assays. Repeatability and intermediate precision showed coefficients of variation 20%, except for buprofezin, etione and picolinafen at the 0.100 mg kga?’1 level. Limits of detection and quantification of the method were 0.005 and 0.010 mg kga?’1, respectively, except for oxamyl and tricyclazol.
机译:一种多类方法已经过优化和验证,可以同时测定花生中几类的113种农药残留。它基于QuEChERS方法(快速,简便,便宜,有效,坚固和安全)和超高效液相色谱结合三重四极杆串联质谱(UHPLC-MS / MS)。测试了几种萃取溶液,显示出最佳结果的组合物由乙酸乙酯和乙腈的混合物组成。由于基质中存在大量油,因此需要使用分散相C18(十八烷基)和PSA(伯胺和仲胺)进行净化。对该方法进行了验证,验证参数令人满意。通过计算四种浓度水平(0.010、0.025、0.050和0.100 mg kga?-1)的加标空白样品的回收率来评估准确性。结果表明,回收率令人满意(在70%至120%之间),但草酰胺和三环唑的含量为0.010 mg kga?1时,回收率未显示可接受的参数。重复性和中间精度显示变异系数<20%,除了布洛芬锌,依替丁和皮考那芬的浓度为0.100 mg kga?-1时。该方法的检出限和定量限分别为0.005和0.010 mg kga?1,除草酰胺和三环唑外。

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