Kocevar Nina, Glavac Igor, Injac Rade, Kreft Samo
University of Ljubljana, Faculty of Pharmacy, Department of Pharmaceutical Biology, Askerceva 7, 1000 Ljubljana, Slovenia.
J Pharm Biomed Anal. 2008 Feb 13;46(3):609-14. doi: 10.1016/j.jpba.2007.11.016. Epub 2007 Nov 22.
Flavonoids represent an important bioactive component in Achillea millefolium. The comparison of the most commonly used analytical methods for the identification and quantification of flavonoids, capillary electrophoresis (CE) and high performance liquid chromatography (HPLC), is presented. The methods were optimized and validated. Using a 20 mM borate buffer with 30% (v/v) of methanol (pH 9.3) in the CE analysis and a gradient elution with water-acetonitrile mobile phase in the HPLC analysis, sufficient separation of the analytes was achieved. A relatively high injection volume in the CE analysis (30 mbar x 30s) enabled low limit of detection (LOD) (0.3-0.7 mg/L). Repeatability of both methods was acceptable (relative standard deviation of peak area were <6%). Additionally, the amount of flavonoids in a real sample of the dried herbal drug was determined.
黄酮类化合物是蓍草中的一种重要生物活性成分。本文介绍了最常用的黄酮类化合物鉴定和定量分析方法——毛细管电泳(CE)和高效液相色谱(HPLC)的比较。对这些方法进行了优化和验证。在CE分析中使用含30%(v/v)甲醇的20 mM硼酸盐缓冲液(pH 9.3),在HPLC分析中使用水-乙腈流动相进行梯度洗脱,实现了分析物的充分分离。CE分析中相对较高的进样量(30 mbar×30 s)使得检测限较低(LOD)(0.3 - 0.7 mg/L)。两种方法的重复性均可接受(峰面积的相对标准偏差<6%)。此外,还测定了干草药实际样品中的黄酮类化合物含量。