On-line preconcentration strategies for analyzing pesticides in fruits and vegetables by micellar electrokinetic chromatography

被引:34
作者
Juan-Garcia, Ana [1 ]
Font, Guillermina [1 ]
Pico, Yolanda [1 ]
机构
[1] Univ Valencia, Fac Pharm, Lab Bromatol Toxicol, E-46100 Valencia, Spain
关键词
food analysis; SW; SRW; SRMM; reversed migration micellar electrokinetic chromatography; pesticides; solid-phase extraction;
D O I
10.1016/j.chroma.2007.01.129
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Five pesticides (fludioxonil, procymidone, pyriproxyfen, dinoseb and carbendazim) were separated in reversed migration micellar electrokinetic chromatography (RM-MEKC) using 20 mmol l(-1) phosphate buffer at pH 2.3, containing 25 mmol l(-1) sodium dodecylsulfate and 10% methanol. Three on-line concentration strategies, sweeping (SW), normal stacking with reversed migration and a water plug (SRW) and stacking with reverse migration and removal of sample matrix using polarity switching (SRMM), were compared. About 10-, 30- and 50-fold increases in detection sensitivity, compared with standard hydrodynamic injection (5 s at 0.5 psi), were observed with SW, SRW and SRMM, respectively. Limits of detection (LODs) ranged from 0.002 to 0.03 mu g ml(-1) using only the on-line preconcentration procedures without any off-line concentration of the extract. A solid-phase extraction (SPE) procedure, for previous isolation and concentration of the analytes, was used in combination with any of the proposed on-line preconcentration strategies, which achieves the determination of pesticides at limits of quantification (LOQs) lower than 0.01 mg kg(-1). The recoveries obtained by SPE in samples spiked at 0.01 mg kg(-1) were between 70 and 100%, with RSDs between 10 and 18% using SRMM. Samples of fruits and vegetables were taken from the market, extracted by the proposed procedure and analyzed with RM-MEKC with the on-line strategies. (c) 2007 Elsevier B.V. All rights reserved.
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页码:104 / 113
页数:10
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