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Determination of parabens in human milk and other food samples by capillary electrophoresis after dispersive liquid-liquid microextraction with back-extraction

机译:分散液-液微萃取-反萃取后毛细管电泳测定人乳和其他食品样品中的对羟基苯甲酸酯

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Dispersive liquid-liquid microextraction (DLLME) with back-extraction was used prior to capillary electrophoresis (CE) for the extraction of four parabens. Optimum extraction conditions were: 200 pi chloroform (extraction solvent), 1.0 mL acetonitrile (disperser solvent) and 1 min extraction time. Back-extraction of parabens from chloroform into a 50 mM sodium hydroxide solution within 10 s facilitated their direct injection into CE. The analytes were separated at 12 degrees C and 25 kV with a background electrolyte of 25 mM borate buffer containing 5.0% (v/v) acetonitrile. Enrichment factors were in the range of 4.3-10.7 and limits of detection ranged from 0.1 to 0.2 mu g mL(-1). Calibration graphs showed good linearity with coefficients of determination (R-2) higher than 0.9957 and relative standard deviations (%RSDs) lower than 3.5%. DLLME-CE was demonstrated to be a simple and rapid method for the determination of parabens in human milk and food with relative recoveries in the range of 86.7-103.3%. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在毛细管电泳(CE)之前使用具有反萃取功能的分散液-液微萃取(DLLME)萃取四种对羟基苯甲酸酯。最佳萃取条件为:200 pi氯仿(萃取溶剂),1.0 mL乙腈(分散剂溶剂)和1分钟萃取时间。在10 s内将对羟基苯甲酸酯从氯仿中反萃取到50 mM氢氧化钠溶液中,有助于将其直接注射到CE中。使用含有5.0%(v / v)乙腈的25 mM硼酸盐缓冲液的背景电解质在12摄氏度和25 kV下分离分析物。富集因子在4.3-10.7范围内,检出限在0.1至0.2μg mL(-1)之间。校正图显示出良好的线性,测定系数(R-2)高于0.9957,相对标准偏差(%RSDs)低于3.5%。 DLLME-CE被证明是测定人乳和食品中对羟基苯甲酸酯的简单,快速的方法,相对回收率在86.7-103.3%之间。 (C)2015 Elsevier Ltd.保留所有权利。

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