Wang Yuan-Chuen, Yang Yi-Shan
Department of Food Science and Biotechnology, National Chung Hsing University, 250 Kuokuang Road, Taichung 402, Taiwan, ROC.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 May 1;850(1-2):392-9. doi: 10.1016/j.jchromb.2006.12.032. Epub 2007 Jan 16.
Numerous bioactive compounds are present in licorice (Glycyrrhizae Radix), including flavonoids and triterpenoids. In this study, a reversed-phase high-performance liquid chromatography (HPLC) method for simultaneous quantification of three flavonoids (liquiritin, liquiritigenin and isoliquiritigenin) and four triterpenoids (glycyrrhizin, 18alpha-glycyrrhetinic acid, 18beta-glycyrrhetinic acid and 18beta-glycyrrhetinic acid methyl ester) from licorice was developed, and further, to quantify these 7 compounds from 20 different licorice samples. Specifically, the reverse-phase HPLC was performed with a gradient mobile phase composed of 25 mM phosphate buffer (pH 2.5)-acetonitrile featuring gradient elution steps as follows: 0 min, 100:0; 10 min, 80:20; 50 min, 70:30; 73 min, 50:50; 110 min, 50:50; 125 min, 20:80; 140 min, 20:80, and peaks were detected at 254 nm. By using our technique, a rather good specificity was obtained regarding to the separation of these seven compounds. The regression coefficient for the linear equations for the seven compounds lay between 0.9978 and 0.9992. The limits of detection and quantification lay in the range of 0.044-0.084 and 0.13-0.25 microg/ml, respectively. The relative recovery rates for the seven compounds lay between 96.63+/-2.43 and 103.55+/-2.77%. Coefficient variation for intra-day and inter-day precisions lay in the range of 0.20-1.84 and 0.28-1.86%, respectively. Based upon our validation results, this analytical technique is a convenient method to simultaneous quantify numerous bioactive compounds derived from licorice, featuring good quantification parameters, accuracy and precision.
甘草(甘草根)中存在多种生物活性化合物,包括黄酮类和三萜类化合物。在本研究中,开发了一种反相高效液相色谱(HPLC)方法,用于同时定量甘草中的三种黄酮类化合物(甘草苷、甘草素和异甘草素)和四种三萜类化合物(甘草酸、18α-甘草次酸、18β-甘草次酸和18β-甘草次酸甲酯),并进一步对20种不同甘草样品中的这7种化合物进行定量。具体而言,采用由25 mM磷酸盐缓冲液(pH 2.5)-乙腈组成的梯度流动相进行反相HPLC,梯度洗脱步骤如下:0分钟,100:0;10分钟,80:20;50分钟,70:30;73分钟,50:50;110分钟,50:50;125分钟,20:80;140分钟,20:80,在254 nm处检测峰。通过使用我们的技术,在分离这七种化合物方面获得了相当好的特异性。这七种化合物线性方程的回归系数在0.9978至0.9992之间。检测限和定量限分别在0.044 - 0.084和0.13 - 0.25 μg/ml范围内。这七种化合物的相对回收率在96.63±2.43和103.55±2.77%之间。日内和日间精密度的变异系数分别在0.20 - 1.84和0.28 - 1.86%范围内。基于我们的验证结果,这种分析技术是一种方便的方法,可同时定量源自甘草的多种生物活性化合物,具有良好的定量参数、准确性和精密度。