Osseyi E S, Wehling R L, Albrecht J A
Department of Food Science and Technology, University of Nebraska, Lincoln 68583-0919, USA.
J Chromatogr A. 1998 Nov 27;826(2):235-40. doi: 10.1016/s0021-9673(98)00731-6.
Reversed-phase ion-pair high-performance liquid chromatography (HPLC) was coupled with detection by UV absorption (280 nm) for separation and quantitation of added folic acid (FA) in fortified cereal based foods. A simple and rapid liquid-solid extraction method, combined with enzymatic digestion, to recover FA from the sample matrices is also presented. The quantitation of added FA was achieved in products including corn (maize), wheat-, rice- and oat-based cereal breakfast foods fortified at 25% and 100% of the reference daily intake (RDI). The retention time for FA was ca. 15 min, and the detection limit was 2 ng/20 microliters injection for standard FA. When FA was added to unfortified samples of wheat flour at concentrations of 3.08 or 20.0 micrograms/g, recoveries were 93% and 96%, respectively. Comparison of HPLC results with those of a standard microbiological assay has shown quite good agreement (r = 0.998). A solid-phase extraction clean-up procedure has also been developed for use with samples fortified with low levels of FA, where interferences may otherwise hinder quantitation.
反相离子对高效液相色谱法(HPLC)与紫外吸收检测(280nm)联用,用于分离和定量强化谷物类食品中添加的叶酸(FA)。本文还介绍了一种简单快速的液固萃取方法,结合酶消化,从样品基质中回收FA。在以玉米、小麦、大米和燕麦为基础的谷物早餐食品中,添加量为参考每日摄入量(RDI)的25%和100%时,实现了对添加FA的定量。FA的保留时间约为15分钟,标准FA的检测限为2ng/20微升进样量。当将FA以3.08或20.0微克/克的浓度添加到未强化的小麦粉样品中时,回收率分别为93%和96%。HPLC结果与标准微生物测定结果的比较显示出相当好的一致性(r = 0.998)。还开发了一种固相萃取净化程序,用于低水平添加FA的样品,否则干扰可能会妨碍定量。