Qiao Xue, Song Wei, Ji Shuai, Wang Qi, Guo De-an, Ye Min
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China.
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, China.
J Chromatogr A. 2015 Jul 10;1402:36-45. doi: 10.1016/j.chroma.2015.05.006. Epub 2015 May 12.
Licorice is one of the most popular herbal medicines worldwide. It contains a big array of phenolic compounds (flavonoids, coumarins, and diphenylethanones). Due to high structural diversity, low abundance, and co-elution with licorice saponins, these phenolic compounds are difficult to be separated by conventional chromatography. In this study, a mobile phase-dependent reversed-phase×reversed phase comprehensive two-dimensional liquid chromatography (RP×RP 2DLC) method was established to separate phenolic compounds in licorice (the roots of Glycyrrhiza uralensis). Organic solvents in the mobile phase were optimized to improve orthogonality of the first and second dimensions, and a synchronized gradient mode was used to improve chromatographic resolution. Finally, licorice extracts were eluted with methanol/water/formic acid in the first dimension (Acquity CSH C18 column), and acetonitrile/water/formic acid in the second dimension (Poroshell Phenyl-Hexyl column). By using this 2DLC system, a total of 311 compounds were detected within 40min. The practical and effective peak capacity was 1329 and 524, respectively, and the orthogonality was 79.8%. The structures of 21 selected unknown compounds were tentatively characterized by mass spectrometry, and 8 of them were discovered from G. uralensis for the first time. The mobile phase-dependent 2DLC/MS system could benefit the separation and characterization of natural products in complicated herbal extracts.
甘草是全球最受欢迎的草药之一。它含有大量的酚类化合物(黄酮类、香豆素类和二苯乙烯酮类)。由于这些酚类化合物结构多样性高、丰度低且与甘草皂苷共洗脱,采用传统色谱法难以分离。本研究建立了一种基于流动相的反相×反相全二维液相色谱(RP×RP 2DLC)方法,用于分离甘草(乌拉尔甘草根)中的酚类化合物。对流动相中的有机溶剂进行了优化,以提高第一维和第二维的正交性,并采用同步梯度模式提高色谱分辨率。最后,在第一维(Acquity CSH C18柱)中用甲醇/水/甲酸洗脱甘草提取物,在第二维(Poroshell Phenyl-Hexyl柱)中用乙腈/水/甲酸洗脱。通过使用该二维液相色谱系统,在40分钟内共检测到311种化合物。实际有效峰容量分别为1329和524,正交性为79.8%。通过质谱对21种选定的未知化合物的结构进行了初步表征,其中8种是首次从乌拉尔甘草中发现的。基于流动相的二维液相色谱/质谱系统有助于复杂草药提取物中天然产物的分离和表征。