Neilson Andrew P, Green Rodney J, Wood Karl V, Ferruzzi Mario G
Department of Food Science, Purdue University, 745 Agriculture Mall Dr. West Lafayette, IN 47907, United States.
J Chromatogr A. 2006 Nov 3;1132(1-2):132-40. doi: 10.1016/j.chroma.2006.07.059. Epub 2006 Aug 17.
Increased interest in potential health-protective activities of flavonoid-rich tea has created the need to take advantage of HPLC column and system advances in order to optimize methodologies for flavonoid analysis. Two new RP-C18 methods for HPLC-DAD analysis of tea flavonoids were developed to facilitate separation of catechins within 5 min and separation of catechins and theaflavins within 10 min total analysis time. Calibration results indicate that these methods have on-column limits of detection on the order of 1-10 pmol for most tea catechins, and method replication generally resulted in intraday and interday peak area variation of <5% for catechins and <9% for theaflavins in green and black tea infusions. These new methods are therefore sensitive, reproducible, and represent a 2-4-fold reduction in HPLC analysis time from existing analytical methods. These improvements are readily achievable with commonly used HPLC equipment, thus facilitating increased sample throughput and efficiency across a broad range of experimental applications.
对富含黄酮类化合物的茶潜在健康保护活性的兴趣增加,使得有必要利用高效液相色谱(HPLC)柱和系统的进展来优化黄酮类化合物分析方法。开发了两种用于茶黄酮类化合物HPLC-二极管阵列检测(DAD)分析的新型反相C18方法,以便在5分钟内实现儿茶素的分离,并在10分钟的总分析时间内实现儿茶素和茶黄素的分离。校准结果表明,这些方法对大多数茶儿茶素的柱上检测限约为1-10皮摩尔,方法重复性通常导致绿茶和红茶浸出液中儿茶素的日内和日间峰面积变化<5%,茶黄素的变化<9%。因此,这些新方法灵敏、可重复,并且与现有分析方法相比,HPLC分析时间减少了2-4倍。使用常用的HPLC设备很容易实现这些改进,从而有助于在广泛的实验应用中提高样品通量和效率。