首页> 外文期刊>Food analytical methods >Reversed electrode polarity stacking sample preconcentration combined with micellar electrokinetic chromatography for the analysis of carbamate insecticide residues in fruit juices.
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Reversed electrode polarity stacking sample preconcentration combined with micellar electrokinetic chromatography for the analysis of carbamate insecticide residues in fruit juices.

机译:反向电极极性叠加样品预浓缩与胶束电动色谱联用,用于分析果汁中的氨基甲酸酯杀虫剂残留。

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摘要

Reversed electrode polarity stacking mode (REPSM) coupled to micellar electrokinetic chromatography (MEKC) was employed for the simultaneous determination of carbamate insecticide residues in fruit juice samples. A mixture of the studied insecticides (i.e., methomyl, propoxur, carbofuran, carbaryl, isoprocarb, and promecarb) in 10 mmol L--1 phosphate buffer (pH 7.0) was introduced into the capillary tube by hydrodynamic injection at 0.5 psi for 30 s followed by removal of the sample matrix at --15 kV for 0.5 min. The analytes were successfully separated within 8 min using 10 mmol L--1 borate buffer containing 60 mmol L--1 sodium dodecyl sulfate at pH 9.5, and photodiode array detection at 205, 214, and 225 nm. The REPSM-MEKC gave stacking enhancement factors of about 4-13, compared to that without stacking. The limits of detection were in the range 0.01-0.10 mg L--1, which is acceptable with respect to the maximum residue limits. Good precisions were obtained with relative standard deviation lower than 1.8% (for migration time) and 10% (for peak area). The recoveries for most fruit juice samples were acceptable (>80%). No contamination of the studied carbamates was observed in any sample. The proposed method is simple and effective for preconcentration and removal of matrix interferences in a single step for the determination of the studied carbamate insecticides. copyright Springer Science+Business Media, LLC 2011.
机译:反向电极极性叠加模式(REPSM)结合胶束电动色谱(MEKC)用于同时测定果汁样品中的氨基甲酸酯类农药残留。通过流体力学将在10 mmol L -1 磷酸盐缓冲液(pH 7.0)中混合的已研究杀虫剂(灭多威,丙草胺,呋喃呋喃,西维因,异丙草威和丙草威)的混合物引入毛细管中。在0.5 psi下注入30 s,然后在-15 kV下去除样品基质0.5 min。使用含有60 mmol L -1 十二烷基硫酸钠的10 mmol L -1 硼酸盐缓冲液(pH 9.5)在8分钟内成功分离出分析物205、214和225 nm。与没有堆叠相比,REPSM-MEKC的堆叠增强因子约为4-13。检测限在0.01-0.10 mg L -1 范围内,相对于最大残留限量而言是可以接受的。相对标准偏差低于1.8%(对于迁移时间)和10%(对于峰面积),可以获得良好的精度。大多数果汁样品的回收率是可以接受的(> 80%)。在任何样品中均未观察到所研究的氨基甲酸酯的污染。所提出的方法简单,有效,可在单个步骤中预富集和消除基质干扰物,从而确定所研究的氨基甲酸酯类杀虫剂。版权所有Springer Science + Business Media,LLC 2011。

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