Hollow fiber-liquid-phase microextraction of fungicides from orange juices

被引:68
作者
Barahona, Francisco [1 ]
Gjelstad, Astrid [2 ]
Pedersen-Bjergaard, Stig [2 ]
Rasmussen, Knut Einar [2 ]
机构
[1] Inst Nacl Invest Tecnol & Agr & Alimentaria, Dept Med Ambiente, Madrid 28040, Spain
[2] Univ Oslo, Sch Pharm, N-0316 Oslo, Norway
关键词
Liquid-phase microextraction; Supported liquid membrane; Fungicides; Orange juice; Thiabendazole; Carbendazim; Imazalil; CHROMATOGRAPHY-MASS SPECTROMETRY; MEMBRANE SOLVENT MICROEXTRACTION; CARRIER-MEDIATED TRANSPORT; CAPILLARY-ELECTROPHORESIS; PESTICIDE-RESIDUES; GAS-CHROMATOGRAPHY; SAMPLE PREPARATION; KINETIC CALIBRATION; BIOLOGICAL MATRICES; SCREENING METHOD;
D O I
10.1016/j.chroma.2010.01.077
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liquid-phase microextraction (LPME) based on polypropylene hollow fibers was evaluated for the extraction of the post-harvest fungicides thiabendazole (TBZ), carbendazim (CBZ) and imazalil (IMZ) from orange juices. Direct LPME was performed without any sample pretreatment prior to the extraction, using a simple home-built equipment. A volume of 500 mu L of 840 mM NaOH was added to 3 mL of orange juice in order to compensate the acidity of the samples and to adjust pH into the alkaline region. Analytes were extracted in their neutral state through a supported liquid membrane (SLM) of 2-octanone into 20 wL of a stagnant aqueous solution of 10mM HCl inside the lumen of the hollow fiber. Subsequently, the acceptor solution was directly subjected to analysis. Capillary electrophoresis (CE) was used during the optimization of the extraction procedure. Working under the optimized extraction conditions, LPME effectively extracted the analytes from different orange juices, regardless of different pH or solid material (pulp) present in the sample, with recoveries that ranged between 17.0 and 33.7%. The analytical performance of the method was evaluated by liquid chromatography coupled with mass spectrometry (LC/MS). This technique provided better sensitivity than CE and permitted the detection below the mu g L(-1) level. The relative standard deviations of the recoveries (RSDs) ranged between 3.4 and 10.6%, which are acceptable values for a manual microextraction technique without any previous sample treatment, using a home-built equipment and working under non-equilibrium conditions (30 min extraction). Linearity was obtained in the range 0.1-10.0 mu g L(-1), with r=0.999 and 0.998 for TBZ and IMZ, respectively. Limits of detection were below 0.1 mu g L(-1) and are consistent with the maximum residue levels permitted for pesticides in drinking water, which is the most restrictive regulation applicable for these kinds of samples. It has been demonstrated the suitability of three-phase LPME for the extraction of pesticides from citrus juices, suppressing any pretreatment step such as filtration or removal of the solid material from the sample, that may potentially involve a loss of analyte. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1989 / 1994
页数:6
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