摘要
目的:建立同时测定一枝黄花药材中绿原酸、芦丁和山奈素含量的高效液相色谱法。方法:采用Diamonsil C18柱(4.6 mm×200 mm,5μm),流动相乙腈-0.2%磷酸水溶液梯度洗脱,流速1.0 mL·min-1,柱温25℃,检测波长282 nm,柱温25℃。结果:绿原酸、芦丁和山奈素的回归方程分别为Y=1712.1X+11.686(r=0.9993)、Y=13584.0X+13.984(r=0.9994)、Y=5971.2X+4.6175(r=0.9998);线性范围分别为63.2-442.4μg、8.1-56.8μg、10.8-75.7μg;回收率分别为98.6%(RSD=1.4%)、99.2%(RSD=0.8%)、100.3%(RSD=1.0%)。结论:本法简便快捷,重复性好,可用于一枝黄花中绿原酸、芦丁和山奈素的定量分析。
This study was aimed to establish an HPLC method for the determination of chlorogenic acid, rutin and kaempferide in Solidago decurrens Lour. A Diamonsil C18 column (4.6 mm í 200 mm, 5 μm) was adopted with the mobile phase of acetonitrile-0.2% phosphoric acid. The flow rate was 1.0 mL·min-1. The column temperature was at 25℃. The wavelength of detection was set at 282 nm. The results showed that the calibration curve was linear over the range of 63.2-442.4 μg for chlorogenic acid (r = 0.999 3), 8.1-56.8 μg for rutin (r = 0.999 4) and 10.8-75.7μg for kaempferide (r = 0.999 8). The average recovery of chlorogenic acid was 98.6% (RSD = 1.4%), that of rutin was 99.2% (RSD = 0.8%) and that of kaempferide was 100.3% (RSD = 1.0%). It was concluded that the method was simple, economical and accurate with good reproducibility.
出处
《世界科学技术-中医药现代化》
北大核心
2014年第4期904-907,共4页
Modernization of Traditional Chinese Medicine and Materia Medica-World Science and Technology
基金
贵州省科技厅贵州省中药现代化科技产业研究开发专项(黔科合中药字[2010]5028号):酢酱草
艾纳香
土知母等贵州民族药材指纹图谱及质量标准提高研究
负责人:冯华
贵州省中医药管理局中药
民族医药科学技术研究项目(QZYY2010-93):一枝黄花药材HPLC指纹图谱研究
负责人:冯华