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Spectrophotometric determination of cyclamate in artificial sweeteners and beverages after ultrasound-assisted emulsification microextraction

机译:超声辅助乳化微萃取分光光度法测定人造甜味剂和饮料中的甜蜜素

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A new method has been developed for the determination of cyclamate using an ultrasound-assisted emulsification microextraction (USAE-ME) procedure coupled with UV-Vis spectrophotometry. The method is based on the protonation of cyclamate ions in acidic medium and the extraction of the formed cyclamic acid into fine droplets of chloroform as an extraction solvent that contains rhodamine B (RhB) reagent. The extracted cyclamic acid can further react with RhB for the formation of a highly colored ion-pair complex of [cyclamate][RhBH+], which is used for the subsequent spectrophotometric determination of cyclamate. One variable at a time optimization and response surface methodology (RSM) based on central composite design were used to obtain optimum conditions for the microextraction procedure, and nearly the same experimental conditions were obtained using both the optimization methods. Under the optimum conditions the calibration graph was linear over the range of 50a€“900 ng mLa?’1 (R2 = 0.9994), and the limit of detection (S/N = 3) was estimated to be 10 ng mLa?’1. The relative standard deviation for 200 ng mLa?’1 of cyclamate was 2.3% (n = 5). The proposed method was successfully applied for the determination of cyclamate in beverages and sweetener tablets. The average recovery of spiked samples was 99.7%. The results demonstrated that the developed method is simple, rapid, inexpensive, accurate and remarkably free from interference effects.
机译:已经开发了一种新方法,该方法使用超声辅助乳化微萃取(USAE-ME)程序和UV-Vis分光光度法测定甜蜜素。该方法基于甜蜜酸根离子在酸性介质中的质子化,以及将形成的环己酸提取成氯仿细小滴,作为含若丹明B(RhB)试剂的提取溶剂。萃取的环己基酸可进一步与RhB反应,形成[环己酸酯] [RhBH +]的高度着色的离子对络合物,该化合物可用于随后的分光光度法测定环己酸酯。使用一次基于中央复合设计的时间优化和响应面方法(RSM)变量来获得微萃取程序的最佳条件,并且使用这两种优化方法均获得了几乎相同的实验条件。在最佳条件下,校准曲线在50a?900 ng mLa?'1(R2 = 0.9994)的范围内呈线性,检测限(S / N = 3)估计为10 ng mLa?'1 。 200 ng mLa?1的甜蜜素的相对标准偏差为2.3%(n = 5)。该方法成功地用于饮料和甜味剂片剂中甜蜜素的测定。加标样品的平均回收率为99.7%。结果表明,该方法简便,快速,廉价,准确,无干扰。

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