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采用分散液液微萃取与反电极极性堆积模式-胶束电动色谱法测定有机磷农药。

Determination of organophosphorus pesticides using dispersive liquid-liquid microextraction combined with reversed electrode polarity stacking mode-micellar electrokinetic chromatography.

机构信息

Materials Chemistry Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand.

出版信息

Talanta. 2012 Aug 30;98:62-8. doi: 10.1016/j.talanta.2012.06.043. Epub 2012 Jun 27.

Abstract

A rapid and sensitive method using two preconcentration techniques, dispersive liquid-liquid microextraction (DLLME) followed by reversed electrode polarity stacking mode (REPSM) was developed for the analysis of five organophosphorus pesticides (OPPs) by micellar electrokinetic chromatography (MEKC). Parameters that affect the efficiency of the extraction in DLLME and preconcentration by REPSM, such as the kind and volume of the extraction and disperser solvents, salt addition, sample matrix and injection time were investigated and optimized. Under the optimum conditions, the enrichment factors were obtained in the range from 477 to 635. The linearity of the method for parathion, azinphos and fenitrithion was in the range of 20-1000 ng mL(-1), and for malathion and diazinon in the range of 50-1000 ng mL(-1), with correlation coefficients (r(2)) ranging from 0.9931 to 0.9992. The limits of detecton (LODs) at a signal-to-noice ratio of 3 ranged from 3 to 15 ng mL(-1). The relative recoveries of five OPPs from water samples at spiking levels of 20 and 200 ng mL(-1) for parathion, azinphos and fenitrithion, and 50 and 500 ng mL(-1) for malathion and diazinon, were 69.5-103%. The proposed method provided high enrichment factors, good precision and accuracy with a short analysis time.

摘要

采用两种预浓缩技术,即分散液液微萃取(DLLME)和反电极极性堆积模式(REPSM),建立了一种快速灵敏的微胶束电动色谱(MEKC)分析五种有机磷农药(OPPs)的方法。研究并优化了影响 DLLME 萃取和 REPSM 预浓缩效率的参数,如萃取和分散溶剂的种类和体积、盐的添加、样品基质和进样时间。在最佳条件下,获得了 477 至 635 的富集因子。该方法对对硫磷、azinphos 和 fenitrithion 的线性范围为 20-1000ng mL(-1),对马拉硫磷和二嗪农的线性范围为 50-1000ng mL(-1),相关系数(r(2))范围为 0.9931 至 0.9992。信噪比为 3 时,五种 OPPs 的检出限(LODs)范围为 3 至 15ng mL(-1)。在 20 和 200ng mL(-1)对硫磷、azinphos 和 fenitrithion,以及 50 和 500ng mL(-1)马拉硫磷和二嗪农的加标水平下,五种 OPPs 从水样中的相对回收率为 69.5-103%。该方法提供了高的富集因子、良好的精密度和准确度,且分析时间短。

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