Fan Lan-Lan, Tu Peng-Fei, Chen Hu-Biao, Cai Shao-Qing
School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China.
Biomed Chromatogr. 2009 Nov;23(11):1191-200. doi: 10.1002/bmc.1242.
A high-performance liquid chromatographic (HPLC) method was developed for the simultaneous quantification of five major bioactive constituents in the stems of resiniferous Dracaena plants from China and Vietnam, as well as those in the related traditional Chinese medicinal preparations. A diode array detector with the wavelength of 330 nm was used to monitor resveratrol, 7,4'-dihydroxyflavone and pterostilbene, while loureirin A and loureirin B were monitored at 280 nm. The five constituents were separated on an Agela SB C(18) column by gradient elution using 0.008% (v/v) formic acid solution (A) and acetonitrile (B) as the mobile phase. The validation of the method included recovery, linearity, accuracy and precision (intra- and inter-day variation). The range of recoveries of this method was 98.1-104.9%, with all the constituents showing good linearity (r(2) > 0.9999). The accuracy and precision were satisfactory, with the overall intra- and inter-day variation being less than 4%. The present method has been successfully applied for the determination of all five constituents in 21 related herbal samples including 10 D. cochinchinensis stem samples, seven D. cambodiana stem samples and four purchased medicinal preparations. The contents of these constituents were analyzed using principal component analysis, which can efficiently identify raw herb of Dracaena from different sources. The study may be considered helpful to the quality control of Dracena plants and its medicinal preparations.
建立了一种高效液相色谱(HPLC)法,用于同时定量分析中国和越南产含树脂龙血树属植物茎中的五种主要生物活性成分以及相关的传统中药制剂中的这些成分。使用波长为330 nm的二极管阵列检测器监测白藜芦醇、7,4'-二羟基黄酮和紫檀芪,而龙血素A和龙血素B则在280 nm处进行监测。以0.008%(v/v)甲酸溶液(A)和乙腈(B)作为流动相,通过梯度洗脱在Agela SB C(18)柱上分离这五种成分。该方法的验证包括回收率、线性、准确度和精密度(日内和日间变化)。该方法的回收率范围为98.1-104.9%,所有成分均显示出良好的线性(r(2)>0.9999)。准确度和精密度令人满意,总体日内和日间变化小于4%。本方法已成功应用于21个相关草药样品中所有五种成分的测定,包括10个柬埔寨龙血树茎样品、7个海南龙血树茎样品和4个购买的药用制剂。使用主成分分析对这些成分的含量进行分析,该分析可以有效地鉴别不同来源的龙血树生药。该研究可能有助于龙血树属植物及其药用制剂的质量控制。