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Multiresidue Method For High-performance Liquid Chromatography Determination Of Carbamate Pesticides Residues In Tea Samples

机译:高效液相色谱多残留法测定茶叶样品中的氨基甲酸酯类农药残留

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摘要

A multiresidue method was developed to determine 19 carbamate pesticides in tea samples. Optimizations of different parameters, such as the type of extraction solvents, clean-up cartridges, and elution solvents were carried out. The developed method used acetonitrile as extraction solvent, amino cartridge for adsorbents and acetone-n-hexane as the eluting solution. Nineteen carbamate residues were then analyzed by high-pressure liquid chromatography (HPLC) with fluorescence detector. The present results showed good linearity by correlation coefficients of more than 0.9999 for all analyses. Limits of detection and quantification varied from 0.0005-0.023 mg L~(-1), 0.008-0.077 mg L~(-1), respectively. Recoveries of sixteen carbamate pesticides ranged from 65% to 135% at the spiked level of 0.5, 1.0 and 2.0 mg L~(-1). The relative standard deviations were lower than 20% and coefficient of variations were lower than 15%. The results indicate that the proposed method provides an effective multi and trace level screening determination of carbamate pesticides residues for tea samples.
机译:开发了一种多残留方法来测定茶叶样品中的19种氨基甲酸酯农药。进行了不同参数的优化,例如萃取溶剂的类型,净化柱和洗脱溶剂。所开发的方法以乙腈为萃取溶剂,氨基滤芯为吸附剂,丙酮-正己烷为洗脱液。然后通过带有荧光检测器的高压液相色谱(HPLC)分析19个氨基甲酸酯残留物。对于所有分析,本研究结果均显示相关系数均大于0.9999,具有良好的线性度。检出限和定量限分别为0.0005-0.023 mg L〜(-1),0.008-0.077 mg L〜(-1)。在浓度为0.5、1.0和2.0 mg L〜(-1)时,十六种氨基甲酸酯类农药的回收率在65%至135%之间。相对标准偏差小于20%,变异系数小于15%。结果表明,该方法为茶叶样品中氨基甲酸酯类农药的残留提供了有效的多重和痕量筛选方法。

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