首页 | 本学科首页   官方微博 | 高级检索  
     

反相高效液相色谱法测定刺梨中芦丁和槲皮素的含量
引用本文:王振伟,魏家红. 反相高效液相色谱法测定刺梨中芦丁和槲皮素的含量[J]. 中国酿造, 2014, 0(7): 109-112
作者姓名:王振伟  魏家红
作者单位:黄河水利职业技术学院,河南开封475000
基金项目:河南省教育厅自然科学基金项目(12B530003)
摘    要:建立反相高效液相色谱法测定刺梨中芦丁和槲皮素的含量。采用WatersSunfire ODS C18色谱柱(4.6 mm×150 mm,5μm),流动相为甲醇-0.2%磷酸缓冲溶液(60:40),流速1.0 mL/min,检测波长360nm,柱温30℃,进样量10μL。结果表明,在上述色谱条件下,芦丁和槲皮素良好分离,质量浓度分别在2~100μg/mL(R2=0.9991)和1~100μg/mL(R2=0.9992)之间线性关系良好。平均加标回收率分别为98.27%和99.15%,相对标准偏差(RSD)分别为2.98%和3.76%,重现性实验RSD分别为芦丁2.18%(n=5),槲皮素1.76%(n=5)。测得刺梨中芦丁和槲皮素的平均含量分别为7.070mg/g和1.352mg/g。RP-HPLC法简便快捷、灵敏,结果准确,可用于刺梨中黄酮成分含量的检测。

关 键 词:刺梨  黄酮  反相高效液相色谱  芦丁  槲皮素

Determination of rutin and quercetin in Rosa roxburghii by RP-HPLC
WANG Zhenwei,WEI Jiahong. Determination of rutin and quercetin in Rosa roxburghii by RP-HPLC[J]. China Brewing, 2014, 0(7): 109-112
Authors:WANG Zhenwei  WEI Jiahong
Affiliation:(Yellow River Conservancy Technical Institute, Kaifeng 475000, China)
Abstract:RP-HPLC method for quantitative determination of rutin and quercetin in Rosa roxburghii was established.Waters sunfire ODS C18 column (4.6 mm×150 mm,5μm) was used as fixed phase,and methanol-0.2% phosphate buffer solution (60:40) was used as mobile phase running with a flow rate of 1.0 ml/min.The detection wavelength was 360 nm and the column temperature was 30 ℃.The results showed that rutin and quercetin were well separated by this method.The rutin and quercetin were in good linear relationship in concentration range of 2-100 μg/ml (R2 =0.999 1) and 1-100 μg/ml (R2 =0.999 2),respectively.The standard addition recovery was 98.27% and 99.15%,relative standard deviation was 2.98% and 3.76%,and the relative standard deviation of reproducibility experiment was 2.18% (n=5) and 1.76% (n=5),respectively.The average content of rutin and quercetin in Rosa roxburghii were 7.07 mg/g and 1.352 mg/g.The RP-HPLC method was simple,quick,accurate and sensitive,which can be used in rutin and quercetin content determination.
Keywords:Rosa roxburghii  flavonoids  RP-HPLC  rutin  quercetin
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号