Rodríguez-Gómez R, Jiménez-Díaz I, Zafra-Gómez A, Morales J C
Research Group of Analytical Chemistry and Life Sciences, Department of Analytical Chemistry, University of Granada, Campus of Fuentenueva, E-18071 Granada, Spain.
Research Group of Analytical Chemistry and Life Sciences, Department of Analytical Chemistry, University of Granada, Campus of Fuentenueva, E-18071 Granada, Spain; Instituto de Investigación Biosanitaria ibs., Granada E-18012, Spain.
Talanta. 2015 Nov 1;144:883-9. doi: 10.1016/j.talanta.2015.07.042. Epub 2015 Jul 15.
A simple and reliable method for the determination of the fructooligosaccharides (FOS) kestose (GF2), nystose (GF3), fructofuranosylnystose (GF4), in the presence of fructose, glucose and lactose in dairy products is proposed. The most relevant advantages of the proposed method are the simultaneous determination of the most common FOS in enriched products and a reduction of the time required for sample treatment since the method consists merely in addition of a precipitation solution for the removal of lipids and proteins. Furthermore, the method saves a substantial amount of reagents compared with other methods and sample manipulation is reduced. Two chromatographic separations are proposed. The first one is carried out on an amino phase column for liquid chromatography with refractive index detection (HPLC-RI) (concentration of analytes higher than 0.1 mg mL(-1)) and the second one on an anion-exchange Carbopac PA-1 column for high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD) (concentration of FOS lower than 0.1 mg mL(-1)). The method was validated by recovery assays with spiked samples using matrix-matched calibration. The limits of quantification of the method ranged from 1.2 to 2.0 µg mL(-1) for HPAEC-PAD and from 140 to 200 µg mL(-1) for HPLC-RI, while inter- and intra-day variability was under 3.5% in all cases. The proposed method was applied to the determination of compounds in supplemented milk, infant formulas and milk related juices with good recoveries in all cases.
本文提出了一种简单可靠的方法,用于测定乳制品中存在的果糖、葡萄糖和乳糖时的低聚果糖(FOS)、蔗果三糖(GF2)、蔗果四糖(GF3)、呋喃果糖基蔗果四糖(GF4)。该方法最显著的优点是能够同时测定强化产品中最常见的FOS,并且由于该方法仅需添加一种沉淀溶液来去除脂质和蛋白质,从而减少了样品处理所需的时间。此外,与其他方法相比,该方法节省了大量试剂,减少了样品操作。本文提出了两种色谱分离方法。第一种方法是在氨基相柱上进行液相色谱-示差折光检测(HPLC-RI)(分析物浓度高于0.1 mg mL(-1)),第二种方法是在阴离子交换Carbopac PA-1柱上进行高效阴离子交换色谱-脉冲安培检测(HPAEC-PAD)(FOS浓度低于0.1 mg mL(-1))。该方法通过使用基质匹配校准的加标样品回收率测定进行了验证。该方法的定量限对于HPAEC-PAD为1.2至2.0 µg mL(-1),对于HPLC-RI为140至200 µg mL(-1),而在所有情况下,日内和日间变异均在3.5%以下。所提出的方法应用于补充牛奶、婴儿配方奶粉和牛奶相关果汁中化合物的测定,在所有情况下回收率均良好。