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Efficiencies of different methods for determination of organophosphate pesticide residues in fermented wheat substrate

机译:不同方法测定小麦发酵基质中有机磷酸酯农药残留的效率

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In the present work, the efficiencies of three different sample preparation methods for GC/ MS determination of pirimiphos-methyl and chlorpyrifos-methyl residues in wheat (Triticum spelta) samples fermented by Lactobacillus plantarum were compared. All three methods were based on methanol:acetone=1:1 extraction, while further purification of the obtained samples was altered. First purification was through a column containing a mixture of aluminium oxide and activated charcoal slurry-packed and eluted with dichlormethane, the second was purification on a florisil column slurry-packed and eluted with ethyl acetate:acetone=4:1, while the third was based on a combination of the former two methods, i.e. clean-up through columns filled with a mixture of aluminum oxide and activated charcoal slurry-packed and eluted with ethyl acetate:acetone=4:1. The second method was found the most effective for obtaining satisfactory recoveries at four fortification levels. For pirimiphos-methyl, recoveries were in the range of 91.3-96.0% and had good reproducibility, i.e. RSD ranging from 2.2-4.1%, while the corresponding range for chlorpyrifos-methyl was 81.6-88.2%, and the RSD range 2.5-5.4%. The chosen method was further optimized in order to establish the optimum volume of elution solvent used during the clean-up procedures. The highest recoveries of 93.7±3.5% for pirimiphos-methyl and 85.3±2.5% for chlorpyrifos-methyl were obtained after elution with 25 ml volume of solvent. Considering all, simple, efficient and reliable GC/MS detection of pirimiphosmethyl and chlorpyrifos-methyl residues in wheat grain substrate altered by fermentation with L. plantarum was achieved by the two-steps extraction with 25 ml of methanol:acetone=1:1 solvent mix for 30 min, followed by a clean-up procedure through a glass column with florisil coupled with elution by 25 ml of ethyl acetate:acetone=4:1. [Projekat Ministarstva nauke Republike Srbije, br. TR31043]
机译:在本工作中,比较了三种不同的样品前处理方法对用植物乳杆菌发酵的小麦(Tripelum spelta)样品中的丙胺磷和甲基毒死os残留量进行GC / MS测定的效率。这三种方法均基于甲醇:丙酮= 1:1萃取,同时改变了所得样品的进一步纯化。第一次纯化是通过装有氧化铝和活性炭浆液混合物的色谱柱进行填充,并用二氯甲烷洗脱,第二次纯化是在硅藻土浆液中进行色谱纯化,并用乙酸乙酯:丙酮= 4:1洗脱,而第三次是基于前两种方法的组合,即通过填充有氧化铝和活性炭浆液混合物的柱进行净化,并用乙酸乙酯:丙酮= 4:1进行填充和洗脱。发现第二种方法对于在四个设防级别获得满意的回收率最有效。甲基嘧啶磷的回收率在91.3-96.0%范围内,并且具有良好的重现性,即RSD为2.2-4.1%,而毒死rif甲基的相应范围为81.6-88.2%,RSD范围为2.5-5.4 %。为了确定在清洗程序中使用的最佳洗脱溶剂体积,对所选方法进行了进一步优化。用25 ml体积的溶剂洗脱后,对丙胺磷的甲基的最高回收率为93.7±3.5%,对毒死rif的甲基的最高回收率为85.3±2.5%。综合考虑,通过用25 ml甲醇:丙酮= 1:1溶剂分两步萃取,可实现通过用植物乳杆菌发酵而改变的小麦籽粒基质中的嘧啶二甲基和毒死rif甲基残留的简单,高效和可靠的GC / MS检测混合30分钟,然后通过具有弗洛里西尔的玻璃柱进行清洁程序,并用25ml乙酸乙酯:丙酮= 4∶1洗脱。 [Projekat Ministarstva nauke Republike Srbije,br。 TR31043]

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