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非离子表面活性剂萃取-高效液相色谱法测定枇杷叶中的绿原酸、槲皮素和山奈酚
引用本文:张丽贤,周光明,姜兰芳,许丽.非离子表面活性剂萃取-高效液相色谱法测定枇杷叶中的绿原酸、槲皮素和山奈酚[J].食品科学,2012,33(6):150-153.
作者姓名:张丽贤  周光明  姜兰芳  许丽
作者单位:发光与实时分析教育部重点实验室,西南大学化学化工学院
基金项目:国家科技重大专项(2008ZX07315);重庆市自然科学基金项目(CSTC,2007BB5370)
摘    要:目的:以5g/100mL非离子表面活性剂Triton X-100为萃取剂,建立一种简单快速的采用超声提取,高效液相色谱法测定枇杷叶中的绿原酸、槲皮素和山奈酚的方法。方法:采用Phenomenex C18色谱柱(250mm×4.6mm,5.0μm),以甲醇-0.25%乙酸溶液为流动相梯度洗脱,流速1.0mL/min,紫外检测波长350nm。结果:绿原酸、槲皮素和山奈酚分别在0.011~220μg/mL(r=0.9997)、0.065~130μg/mL(r=0.9999)、0.068~136μg/mL(r=0.9999)线性关系良好,检出限(RSN=3)依次是1.94、0.22、0.27ng/mL;样品的加标回收率为90.40%~96.82%。结论:该方法具有样品前处理简单、绿色环保、灵敏快速等优点,可为枇杷叶中一些黄酮类物质和绿原酸的检测提供一个有效的方法。

关 键 词:枇杷叶  Triton  X-100表面活性剂  HPLC  绿原酸  槲皮素  山奈酚  

Simultaneous Determination of Chlorogenic Acid,Quercetin and Kaempferol in Loquat Leaves by Non-ionic Surfactant Extraction Solvent Followed by High Performance Liquid Chromatography
ZHANG Li-xian,ZHOU Guang-ming,JIANG Lan-fang,XU Li.Simultaneous Determination of Chlorogenic Acid,Quercetin and Kaempferol in Loquat Leaves by Non-ionic Surfactant Extraction Solvent Followed by High Performance Liquid Chromatography[J].Food Science,2012,33(6):150-153.
Authors:ZHANG Li-xian  ZHOU Guang-ming  JIANG Lan-fang  XU Li
Affiliation:(Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China)
Abstract:Objective:An HPLC method for the simultaneous determination of chlorogenic acid,quercetin and kaempferol in loquat leaves was proposed based on rapid ultrasonic-assisted extraction using the non-ionic surfactant Triton X-100 as the extractant.Methods:The chromatographic separation was achieved on a Phenomenex C18 column using a mobile phase made up of methanol and 0.25% acetic acid at a flow rate of 1.0 mL/min,and the analytes were detected with a UV detector at 350 nm.Results:The calibration curves for chlorogenic acid,quercetin and kaempferol were linear in the range of 0.011-220μg/mL(r=0.9997),0.065-130μg/mL(r=0.9999),0.068-136μg/mL(r=0.9999),respectively.The limit of detection(LOD) was 1.94,0.22,0.27 ng/mL(RSN=3),respectively.The average recoveries across three spike levels ranged from 90.71% to 94.88%(n=3).Conclusion:The method is simple,rapid,convenient,sensitive,and environment-friendly,and thus can provide a new and scientific means for assaying the contents of flavonoids and chlorogenic acid in loquat leaves.
Keywords:folium eriobotryae  Triton X-100 surfactant  high performance liquid chromatography(HPLC)  chlorogenic acid  quercetin  kaempferol
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