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作 者:卢挺 Edward P C Lai Jorn C C Yu 胡风祖[3]
机构地区:[1]青海省产品质量监督检验所,青海西宁810008 [2]卡尔顿大学化学系 [3]中国科学院西北高原生物研究所,青海西宁810001
出 处:《食品科学》2006年第12期582-587,共6页Food Science
基 金:青海省重点科技攻关项目(2002-N-119);科技部农业科技成果转化资金项目(02EFN216301200)
摘 要:使用毛细管电泳法(CE)检测了健康食品中常见的六种黄酮类化合物:橙皮甙、海棠甙、异鼠李素、山奈酚、槲皮素、芦丁。研究了一系列的试验参数,如:pH、缓冲溶液浓度、分离电压以及UV检测器波长等,以确定出最佳条件。使用H3BO3-Na2B4O7缓冲液(pH9.2),各分析物可在8min内分出。相对标准偏差(RSD):8次进样的迁移时间为0.77%~0.93%;峰面积为3.8%~8.6%;各检测限(S/N=3)范围为0.34μg/ml~2.9μg/ml,回收率为80.4%~113.9%。方法简单、灵敏,重现性高,线性好,无须固相萃取前处理,用于蜂花粉分析结果准确。A capillary electrophoresis (CE) method has been developed for the determination of six bioactive flavonoids that are commonly found in health foods: hesperidin, hyperin, isorhamnetin, kaempferol, quercetin and turin. The effects of several parameters, such as pH, buffer concentration, separation voltage and UV detector wavelength, were investigated to find the optimal conditions. Using a H3BO3-Nad3407 buffer (pH 9.2), the analytes can be separated within 8 min. The relative standard deviations of migration times in eight injections were between 0.77% and 0.93%, and those of the peak areas ranged from 3.8% to 8.6%. A high reproducibility and excellent linearity was observed over two orders of magnitude, with detection limits (S/N = 3) ranging from 0.34μg ml to 2.9μg ml for all the six analytes. Recoveries ranged from 80.4 % to 113.9 %. The new method is simple, reproducible and sensitive. No solid phase extraction for sample pretreatment is necessary. Analysis results are accurate in application to bee pollens.
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