Ma Cheng-Jun, Li Gui-sheng, Zhang Da-lei, Liu Ke, Fan Xiao
Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, PR China.
J Chromatogr A. 2005 Jun 17;1078(1-2):188-92. doi: 10.1016/j.chroma.2005.01.053.
High-speed counter-current chromatography (HSCCC) technique in semi-preparative scale has been successfully applied to the separation of bioactive flavonoid compounds, liquiritigenin and isoliquiritigenin in one step from the crude extract of Glycyrrhiza uralensis Risch. The HSCCC was performed using a two-phase solvent system composed of n-hexane-ethyl acetate-methanol-acetonitrile-water (2:2:1:0.6:2, v/v). Yields of liquiritigenin (98.9% purity) and isoliquiritigenin (98.3% purity) obtained were 0.52% and 0.32%. Chemical structures of the purified liquiritigenin and isoliquiritigenin were identified by electrospray ionization-MS (ESI-MS) and NMR analysis.
半制备规模的高速逆流色谱(HSCCC)技术已成功应用于从甘草粗提物中一步分离生物活性黄酮类化合物甘草素和异甘草素。HSCCC使用由正己烷 - 乙酸乙酯 - 甲醇 - 乙腈 - 水(2:2:1:0.6:2,v/v)组成的两相溶剂系统进行。获得的甘草素(纯度98.9%)和异甘草素(纯度98.3%)的产率分别为0.52%和0.32%。通过电喷雾电离质谱(ESI-MS)和核磁共振分析鉴定了纯化的甘草素和异甘草素的化学结构。