Wei Shan-Shan, Yang Min, Chen Xin, Wang Qiu-Rong, Cui Ya-Jun
School of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
National Engineering Laboratory for TCM Standardization Technology, Shanghai Research Center for TCM Modernization, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Chin J Nat Med. 2015 Mar;13(3):232-40. doi: 10.1016/S1875-5364(15)30009-1.
To determine 13 flavonoids and glycyrrhizic acid in licorice (Glycyrrhiza spp.), several samples from different areas were examined by HPLC-DAD analysis. The analysis was performed on a Zorbax Extend-C18 (250 mm × 4.6 mm, 5 μm) column connected with a Zorbax Extend guard column (20 mm × 4.6 mm, 5 μm). The mobile phase consisted of (A) acetonitrile and (B) 0.026% aqueous H3PO4 (VV) using a gradient elution of 20%-25% A at 0-20 min, 25%-33% A at 20-30 min, 33%-50% A at 30-55 min, 50%-60% A at 55-65 min, and 60% A between 65 min and 80 min, and peaks were detected at 280 nm. The fourteen compounds were assigned by HPLC-Orbitrap MS methods. The regression coefficient for the linear equations for the 14 compounds ranged between 0.9998 and 1. The limits of detection and quantification lay in the range of 0.032-2.461 and 0.154-8.202 μg·mL(1), respectively. The relative recovery rates for the 14 compounds were in the range of 93.90%-106.73% with RSDs being less than 5%. Coefficient variations for intra-day and inter-day precisions were in the range of 0.27%-2.38% and 0.31%-3.51%, respectively. In summary, the validated method was applied to the simultaneous determination of the 14 components in 29 different licorice samples and was proven to be suitable for quality evaluation of licorices and their active fractions.
为测定甘草(甘草属植物)中的13种黄酮类化合物和甘草酸,采用高效液相色谱-二极管阵列检测(HPLC-DAD)分析法对来自不同地区的多个样品进行了检测。分析在一根Zorbax Extend-C18(250 mm×4.6 mm,5μm)色谱柱上进行,该色谱柱与一根Zorbax Extend保护柱(20 mm×4.6 mm,5μm)相连。流动相由(A)乙腈和(B)0.026%的磷酸水溶液(V/V)组成,采用梯度洗脱:0 - 20分钟时A为20% - 25%,20 - 30分钟时A为25% - 33%,30 - 55分钟时A为33% - 50%,55 - 65分钟时A为50% - 60%,65分钟至80分钟时A为60%,在280 nm处检测峰。这14种化合物通过HPLC-轨道阱质谱法进行了鉴定。14种化合物线性方程的回归系数在0.9998至1之间。检测限和定量限分别在0.032 - 2.461和0.154 - 8.202μg·mL⁻¹范围内。14种化合物的相对回收率在93.90% - 106.73%范围内,相对标准偏差小于5%。日内和日间精密度的变异系数分别在0.27% - 2.38%和0.31% - 3.51%范围内。总之,该验证方法用于同时测定29个不同甘草样品中的14种成分,被证明适用于甘草及其活性成分的质量评价。