Chen X J, Guo B L, Li S P, Zhang Q W, Tu P F, Wang Y T
Institute of Chinese Medical Sciences, University of Macau, Taipa, Macao SAR, China.
J Chromatogr A. 2007 Sep 7;1163(1-2):96-104. doi: 10.1016/j.chroma.2007.06.020. Epub 2007 Jun 17.
Herba Epimedii (family Berberidaceae), Yinyanghuo in Chinese, is one of the commonly used Chinese medicines. Flavonoids are considered as its active components. In this study, a reliable pressurized liquid extraction (PLE) and HPLC method was developed for simultaneous determination of 15 flavonoids, namely hexandraside E, kaempferol-3-O-rhamnoside, hexandraside F, epimedin A, epimedin B, epimedin C, icariin, epimedoside C, baohuoside II, caohuoside C, baohuoside VII, sagittatoside A, sagittatoside B, 2''-O-rhamnosyl icariside II and baohuoside I in different species of Epimedium. The analysis was performed by using a Zorbax SB-C18 analytical column (250 mm x 4.6 mm I.D., 5 microm) at gradient elution of water and acetonitrile with diode-array detection (270 nm). All calibration curves showed good linearity (r(2)>0.9997) within test ranges. The LOD and LOQ were lower than 1.31 ng and 2.62 ng on column, respectively. The RSD for intra- and inter-day of 15 analytes was less than 3.8% at three levels, and the recoveries were 90.5-106.8%. The validated method was successfully applied for the analysis of 15 flavonoids in different species of Epimedium which had great variation on the contents of investigated flavonoids. Hierarchical clustering analysis based on the characteristics of 15 investigated compound peaks in HPLC profiles showed that 26 samples were divided into three main clusters, which were in accordance with their flavonoid contents. Four flavonoids including epimedin A, B, C and icariin were optimized as markers for quality control of the species of Epimedium used as Yinyanghuo.
淫羊藿(小檗科),中药名为淫羊藿,是常用中药之一。黄酮类化合物被认为是其活性成分。本研究建立了一种可靠的加压液体萃取(PLE)和高效液相色谱(HPLC)方法,用于同时测定不同种淫羊藿中15种黄酮类化合物,即淫羊藿苷E、山柰酚-3-O-鼠李糖苷、淫羊藿苷F、淫羊藿苷A、淫羊藿苷B、淫羊藿苷C、淫羊藿苷、朝藿定C、宝藿苷II、草藿苷C、宝藿苷VII、箭藿苷A、箭藿苷B、2''-O-鼠李糖基淫羊藿次苷II和宝藿苷I。采用Zorbax SB-C18分析柱(250 mm×4.6 mm内径,5μm),以水和乙腈为流动相进行梯度洗脱,二极管阵列检测(270 nm)。所有校准曲线在测试范围内均显示出良好的线性关系(r(2)>0.9997)。柱上检测限和定量限分别低于1.31 ng和2.62 ng。15种分析物日内和日间精密度在三个水平下的相对标准偏差均小于3.8%,回收率为90.5-106.8%。该验证方法成功应用于不同种淫羊藿中15种黄酮类化合物的分析,这些淫羊藿中所研究黄酮类化合物的含量有很大差异。基于HPLC图谱中15个所研究化合物峰的特征进行的层次聚类分析表明,26个样品分为三个主要类群,这与它们的黄酮类化合物含量一致。淫羊藿苷A、B、C和淫羊藿苷这四种黄酮类化合物被优化为淫羊藿药材质量控制的指标成分。