Prodolliet J, Bruelhart M
Nestec Ltd, Nestlé Research Centre, Lausanne, Switzerland.
J AOAC Int. 1993 Mar-Apr;76(2):268-74.
A liquid chromatographic method was evaluated for the determination of the intense sweetener acesulfam-K in tabletop sweetener, candy, soft drink, fruit juice, fruit nectar, yogurt, cream, custard, chocolate, and biscuit commercial preparations. Samples are extracted or simply diluted with water and filtered. Complex matrixes need a clarification step with Carrez solutions. An aliquot of the extract is analyzed on a reversed-phase mu Bondapak C18 column using 0.0125M KH2PO4 (pH 3.5)-acetonitrile (90 + 10) as mobile phase. Detection is performed by UV absorbance at 220 nm. Recoveries ranged from 95.2 to 106.8%. With one exception, all analyzed values were within +/- 15% of the declared levels. The repeatabilities and the repeatability coefficients of variation were, respectively, 0.37 mg/100 g and 0.98% for products containing less than 40 mg/100 g acesulfam-K and 2.43 mg/100 g and 1.29% for other products. The same procedure also allowed detection of many food additives or natural constituents, such as other intense sweeteners, organic acids, and alkaloids, in a single run without interfering with acesulfam-K. The method is simple, rapid, precise, and sensitive; therefore, it is suitable for routine analyses.
评价了一种液相色谱法,用于测定桌面甜味剂、糖果、软饮料、果汁、果味饮料、酸奶、奶油、蛋奶冻、巧克力和饼干等商业制剂中的强力甜味剂安赛蜜-K。样品采用水提取或简单稀释后过滤。复杂基质需要用Carrez溶液进行澄清步骤。取一份提取物,在反相μ Bondapak C18柱上进行分析,以0.0125M KH2PO4(pH 3.5)-乙腈(90 + 10)作为流动相。通过在220 nm处的紫外吸光度进行检测。回收率在95.2%至106.8%之间。除一个例外,所有分析值均在申报值的±15%范围内。对于每100克中安赛蜜-K含量低于40毫克的产品,重复性和重复性变异系数分别为0.37毫克/100克和0.98%;对于其他产品,分别为2.43毫克/100克和1.29%。相同的程序还允许在一次运行中检测许多食品添加剂或天然成分,如其他强力甜味剂、有机酸和生物碱,而不会干扰安赛蜜-K。该方法简单、快速、精确且灵敏;因此,适用于常规分析。