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作 者:刘小乔[1] 李忠岐[1] 高静[1] 陈蓓[1] 杨建雄[1]
机构地区:[1]陕西师范大学生命科学学院,西安市710062
出 处:《光谱实验室》2012年第5期2611-2615,共5页Chinese Journal of Spectroscopy Laboratory
基 金:国家自然科学基金资助项目(20175012)
摘 要:建立一种用高效液相色谱法(HPLC)测定茶叶中儿茶素类的方法,建立了同时分离测定了5种儿茶素组分(EGC、C、EGCG、EC、ECG)及咖啡碱(CAF)的方法,得到的最佳色谱条件为:ODS(5μm,4.6mm×250mm)色谱柱,流动相A:0.1%的磷酸甲醇溶液;流动相B:0.1%的磷酸水溶液;流速为1.0mL/min;柱温为30℃;UV检测波长278nm。儿茶素单体及咖啡碱在给定的浓度范围内线性关系良好,方法精密度和重复性的相对标准偏差在5%以内,测定样品中各标准品的平均加标回收率为98.20%—100.64%。与国标法GB/T 8313-2008相比,本方法解决了国标法中EC和EGCG难分离的问题。An analytical method for the simultaneous qualitative and quantitative analysis of 5 kind of catechins(including EGC,C,EGCG,EC and ECG) and caffeine(CAF) was established by high performance liquid chromatography(HPLC),and the optimal chromatographic conditions were as follows:ODS column(5μm,4.6mm×250mm),mobile phase A of 0.1% phosphoric acid in methanol(V/V),mobile phase B of 0.1% phosphoric acid in water(V/V),the flow rate of 1mL/min,the column temperature of 30℃ and the detection wavelength of 278nm.The linear relationship of catechins and caffeine was good in a given range of concentration,the RSDs of the method repeatability and the precision were less than 5%,and the average standard recoveries of each standard sample were in the range of 98.20%—100.64% for catechins and caffeine.Meanwhile,compared with the national standard method GB/T 8313-2008,the method can solve the difficult questions of separation of EGCG and EC in national standard method.
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