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首页> 外文期刊>Food analytical methods >Determination of melamine in liquid milk and milk powder by titania-based ligand-exchange hydrophilic interaction liquid chromatography.
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Determination of melamine in liquid milk and milk powder by titania-based ligand-exchange hydrophilic interaction liquid chromatography.

机译:基于二氧化钛的配体交换亲水相互作用液相色谱法测定液态奶和奶粉中的三聚氰胺。

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A simple and rapid high-performance liquid chromatography (HPLC) procedure for the analysis of melamine in liquid milk and milk powder has been developed. Decrease of acetonitrile percentage and phosphate buffer concentration in mobile phase, and lowering of buffer pH and column temperature would benefit the retention of melamine on titania. Taking advantage of the ligand-exchange and hydrophilic interaction mixed retention mode on bare titania column, neither complex pretreatment nor ion-pair reagent was required. The whole analysis for one sample including sample pretreatment and HPLC analysis could be accomplished within 30 min. The method presented good linearity (R2 = 0.9998) in a wide range of 0.02-10 mug mL--1. The limit of detection (3 sigma) and limit of quantification (10 sigma) of the method were 6 and 20 mug L--1, respectively, which were equivalent to 15 and 50 mug kg--1 melamine in liquid milk, 60 and 200 mug kg--1 melamine in milk powder, respectively. Such sensitivity could be compared with those obtained by HPLC with solid-phase extraction or HPLC coupled with tandem mass spectrometry and was adequate for the screening of melamine in tainted dairy products. The repeatability (RSDs) of the retention times and peak areas of 11 replicate detections of 1.0 mug mL--1 melamine were 0.32% and 2.5%, respectively. The intermediate precision on three consecutive days (RSDs, n = 6) of the retention times and peak areas were 1.1% and 2.3%, respectively. The recovery of spiked melamine in dairy samples ranged from 95.2% to 105%. The simplicity, sensitivity and rapidity of the proposed method make it an effective alternative detecting technique for melamine
机译:已开发出一种用于分析液态奶和奶粉中三聚氰胺的简单快速的高效液相色谱(HPLC)程序。降低流动相中乙腈的百分比和磷酸盐缓冲液的浓度,降低缓冲液的pH和柱温将有利于三聚氰胺在二氧化钛上的保留。利用在裸露的二氧化钛柱上的配体交换和亲水相互作用的混合保留模式,既不需要复杂的预处理也不需要离子对试剂。一个样品的整个分析,包括样品预处理和HPLC分析,都可以在30分钟内完成。该方法在0.02-10杯mL -1 的宽范围内具有良好的线性(R 2 = 0.9998)。该方法的检出限(3 sigma)和定量限(10 sigma)分别为6和20马克杯L -1 ,分别相当于15和50马克杯kg 液态牛奶中的--1 三聚氰胺,奶粉中的分别为60和200杯子kg -1 三聚氰胺。可以将这种灵敏度与通过固相萃取HPLC或串联质谱联用的HPLC获得的灵敏度进行比较,并且该灵敏度足以用于筛选受污染的乳制品中的三聚氰胺。 11次重复检测1.0杯mL -1 三聚氰胺的保留时间和峰面积的重复性(RSD)分别为0.32%和2.5%。连续三天的保留时间和峰面积的中间精度(RSD,n = 6)分别为1.1%和2.3%。乳制品样品中加标的三聚氰胺的回收率为95.2%至105%。该方法简便,灵敏,快速,是检测三聚氰胺的有效替代方法。

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