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Switchable-hydrophilicity solvent liquid-liquid microextraction prior to magnetic nanoparticle-based dispersive solid-phase microextraction for spectrophotometric determination of erythrosine in food and other samples

机译:可切换 - 亲水性溶剂液 - 液体微萃取,以磁性纳米粒子的分散性固相微萃取,用于分光光度法测定食品和其他样品中的赤藓胺

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A combination of switchable-hydrophilicity liquid-liquid microextraction prior to magnetic nanoparticle-based dispersive solid-phase microextraction is proposed for the determination of erythrosine using UV/Vis spectrophotometry at 520 nm. Under optimum conditions (i.e., 1.0 mL octylamine as the extraction solvent, 1.5 mL of 10.0 M sodium hydroxide as the phase separation trigger, pH 4.0, 750 mu L of acetone as the eluent, 10.0 mg of Fe3O4@XAD-16 as the adsorbent, and 15.0 mL of the sample solution), the method showed a superior analytical performance with limits of detection less than 25.9 ng mL(-1), limits of quantitation less than 86.3 ng mL(-1) and linear dynamic ranges ranging between 86.3 and 1000 ng mL(-1). Percentage relative standard deviations were less than 4.1 and 7.2% for intra-day and inter-day, respectively. The method was successfully applied for the extraction and determination of erythrosine in food samples and other consumer products with recoveries in the range of 94.6-103.9% and within extraction time of 7.8 min per sample.
机译:提出了在磁性纳米颗粒基分散体微萃取之前的可切换 - 亲水性液液微萃取的组合,用于使用520nm处的UV / Vis分光光度法测定赤藓胺。在最佳条件下(即1.0ml辛酸为萃取溶剂,1.5ml 10.0M氢氧化钠作为相分离触发,pH4.0,750μl丙酮作为洗脱液,10.0mg Fe3O4 @ XAD-16作为吸附剂和15.0ml样品溶液),该方法显示出优异的分析性能,检测限值小于25.9 ng ml(-1),量限制小于86.3 ng ml(-1),线性动态范围在86.3之间。和1000 ng ml(-1)。百分比相对标准偏差分别为日期和日内的日期和日期小于4.1%和7.2%。该方法已成功地应用于食品样品中赤藓胺和其他消费产品的射出和测定,其恢复在94.6-103.9%的恢复范围内,并且在每种样品的提取时间为7.8分钟。

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