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Quick supramolecular solvent-based microextraction for quantification of low curcuminoid content in food

机译:基于超分子溶剂的快速微萃取技术定量分析食品中的低姜黄素含量

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There is a need to monitor the consumption of curcuminoids, an EU-permitted natural colour in food, to ensure that acceptable daily intakes are not exceeded, especially by young children. This paper describes a sensitive method able to quantify low contents of curcumin (CUR), demethoxycurcumin (DMC) and bis-demethoxycurcumin (BDMC) in foodstuffs. The method was based on a singlestep extraction by use of a supramolecular solvent (SUPRAS) made up of reverse aggregates of decanoic acid, and direct analysis of the extract by use of liquid chromatography-photodiode array (PDA) detection. The extraction involved the stirring of 200 mg foodstuff with 600 μL SUPRAS for 15 min. No cleanup or concentration of the extracts was required. Curcuminoid solubilisation occurred via dispersion and hydrogen bonding. The method was used for the determination of curcuminoids in different types of foodstuff (snack, gelatine, yoghurt, mayonnaise, butter, candy and fish products) that encompassed a wide range of protein, fat, carbohydrate, sugar and water contents (0.85-11.04, 0- 81.11, 0.06-75, 0.06-79.48, and 10.08-85.10 g, respectively, in each 100 g of food). Method quantification limits for the foodstuffs analysed were in the ranges 2.9-7.7, 2.8-11.2 and 3.3-9.0 μg kg~(-1) for CUR, DMC and BDMC, respectively. The concentrations of curcuminoids detected in the foodstuffs and the recoveries obtained from fortified samples were in the ranges ND-284, ND-201 and ND-61.3 μg kg~(-1), and 82-106, 89-106 and 90-102 %, for CUR, DMC and BDMC, respectively. The relative standard deviations were in the range 2-7 %. This method enabled quick and simple microextraction of curcuminoids with minimal solvent consumption, while delivering accurate and precise data.
机译:有必要监测类姜黄素的摄入量,这是欧盟允许的食品天然色料,以确保不超过可接受的每日摄入量,尤其是对于幼儿。本文描述了一种能够定量测定食品中低含量的姜黄素(CUR),去甲氧基姜黄素(DMC)和双去甲氧基姜黄素(BDMC)的灵敏方法。该方法基于一步法提取,方法是使用由癸酸的反向聚集体组成的超分子溶剂(SUPRAS),并通过液相色谱-光电二极管阵列(PDA)检测直接分析提取物。提取包括将200 mg食品与600μLSUPRAS搅拌15分钟。无需净化或浓缩提取物。姜黄素溶解是通过分散和氢键发生的。该方法用于测定不同类型食品(小吃,明胶,酸奶,蛋黄酱,黄油,糖果和鱼产品)中的姜黄素,这些蛋白质涵盖了广泛的蛋白质,脂肪,碳水化合物,糖和水含量(0.85-11.04)每100克食品分别添加0、81.11、0.06-75、0.06-79.48和10.08-85.10克)。对于CUR,DMC和BDMC,所分析食品的方法定量限分别在2.9-7.7、2.8-11.2和3.3-9.0μgkg〜(-1)范围内。食品中检出的姜黄素浓度以及从强化样品中回收的姜黄素的浓度范围为ND-284,ND-201和ND-61.3μgkg〜(-1)以及82-106、89-106和90-102 %,分别用于CUR,DMC和BDMC。相对标准偏差在2-7%的范围内。这种方法可以快速简单地对姜黄素进行微量萃取,同时减少了溶剂消耗,同时提供了准确而精确的数据。

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