Liu Rong-Xia, Wang Qiao, Guo Hong-Zhu, Li Li, Bi Kai-Shun, Guo De-An
School of Pharmaceutical Sciences, Peking University, Beijing 100083, PR China.
J Pharm Biomed Anal. 2005 Sep 15;39(3-4):469-76. doi: 10.1016/j.jpba.2005.04.007.
A reversed-phase liquid chromatographic method was developed for the simultaneous quantification of 10 major flavonoids, namely butin, (3R)-4'-methoxy-2',3,7-trihydroxyisoflavanone, liquiritigenin, melanettin, violanone, vistitone, formononetin, dalbergin, sativanone and medicarpin in the heartwood of Dalbergia odorifera, an important traditional Chinese medicine. Samples were extracted with 60% methanol. The optimal conditions of separation and detection were achieved on an Agilent Zorbax SB-C18 column (250 mm x 4.6 mm, 5 microm) with a gradient of acetonitrile and 0.3% (v/v) aqueous acetic acid, at a flow rate of 0.8 ml/min, detected at 275 nm. The complete separation was obtained within 55 min for the 10 target compounds. All calibration curves showed good linearity (r2>0.999) within test ranges. The assay was reproducible with overall intra- and inter-day variation of less than 3%. The mean recovery of the method was 100+/-10%, with R.S.D. less than 5%. The current assay method was considered to be suitable for the quality control of D. odorifera samples and could be readily utilized for the determination of the active principles present in this medicinal herb.
建立了一种反相液相色谱法,用于同时定量测定降香檀(一种重要的传统中药)心材中的10种主要黄酮类化合物,即紫铆因、(3R)-4'-甲氧基-2',3,7-三羟基异黄酮、甘草素、黑黄檀素、紫罗酮、维斯通酮、芒柄花素、黄檀素、萨替瓦酮和苜蓿素。样品用60%甲醇提取。在Agilent Zorbax SB-C18柱(250 mm×4.6 mm,5μm)上,以乙腈和0.3%(v/v)乙酸水溶液为流动相梯度洗脱,流速为0.8 ml/min,检测波长为275 nm,实现了分离和检测的最佳条件。10种目标化合物在55 min内实现了完全分离。所有校准曲线在测试范围内均显示出良好的线性(r2>0.999)。该方法具有良好的重现性,日内和日间总体变异均小于3%。该方法的平均回收率为100±10%,相对标准偏差小于5%。目前的测定方法被认为适用于降香檀样品的质量控制,并且可以很容易地用于测定这种草药中存在的活性成分。