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Comparison of methods for bifenthrin residues determination in fermented wheat samples

机译:发酵小麦样品中联苯菊酯残留量测定方法的比较

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Efficiency of three different sample preparation methods for GC/MS determination of bifenthrin residues in wheat (Triticum spelta) samples fermented by Lactobacillus plantarum was tested. The first method was based on a methanol:acetone=1:1 extraction folowed by a purification on columns containing mixture of aluminium oxide and activated charcoal slurry-packed and eluted with dichlormethane, the second was based on methanol:acetone=1:1 extraction folowed by the purification on florisil column and elution by ethil acetate:acetone=4:1, while the third tested method was based on a combination of the first two mentioned methods, thus methanol:acetone=1:1 extraction and clean-up throught columns filled with a mixture of aluminum oxide and activated charcoal slurrypacked and eluted with ethil acetate:acetone=4:1. The second method was the most effective for obtaining satisfactory recoveries for bifenthrin in a range of 79-83% for four fortification levels, with good reproducibility i.e. RSD% in a range of 2.2-7.4%. The chosen method was further optimized by assessing the optimum volume of elution solvent used during the clean-up procedures. The highest recovery of 82.1% was obtained after elution with 25 ml of solvent. Overall, two-step extraction with 25 ml of methanol:acetone=1:1 solvent mix for 30 min, followed by clean-up procedure through a glass column with florisil coupled with elution with 25 ml of ethyl acetate: acetone=4:1, allows simple, efficient and reliable GC/MS detection of bifenthrin residues from wheat grain fermented by L. plantarum.
机译:测试了三种不同样品制备方法的GC / MS测定植物乳杆菌发酵小麦样品中联苯菊酯残留的效率。第一种方法是基于甲醇:丙酮= 1:1萃取,然后在装有氧化铝和活性炭浆料混合物的色谱柱中进行纯化,然后用二氯甲烷填充,第二种方法基于甲醇:丙酮= 1:1萃取。随后在弗洛里西尔柱上纯化,然后用乙酸:丙酮= 4:1洗脱,而第三种测试方法是基于前两种方法的结合,因此以甲醇:丙酮= 1:1萃取并进行纯化填充有氧化铝和活性炭浆液混合物的色谱柱,用醋酸乙酯:丙酮= 4:1填充并洗脱。第二种方法最有效地获得了四个强化水平在79-83%范围内的联苯菊酯的满意回收率,并且具有良好的重现性,即RSD%在2.2-7.4%的范围内。通过评估清理程序中使用的最佳洗脱溶剂体积,进一步优化了所选方法。用25 ml溶剂洗脱后,最高回收率为82.1%。总体而言,用25 ml甲醇:丙酮= 1:1的溶剂混合物分两步萃取30分钟,然后通过带有硅酸镁的玻璃柱进行纯化,并用25 ml乙酸乙酯:丙酮= 4:1洗脱,可通过简单,高效和可靠的GC / MS检测植物乳杆菌发酵的小麦籽粒中联苯菊酯残留。

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