Mixed-mode retention mechanism for (-)-epigallocatechin gallate on a 12% cross-linked agarose gel media

被引:37
作者
Xu, Jun
Tan, Tianwei [1 ]
Janson, Jan-Christer
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, Dept Bioengn, Beijing 100029, Peoples R China
[2] Uppsala Univ, Uppsala Biomed Ctr, Dept Surface Biotechnol, SE-75123 Uppsala, Sweden
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
mixed-mode retention; hydrogen bond; hydrophobic interactions; epigallocatechin gallate; green tea polyphenols; agarose gel; cross-linked agarose gel;
D O I
10.1016/j.chroma.2006.10.001
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The adsorption behaviour of (-)-epigallocatechin gallate (EGCG), the major polyphenolic substance in green tea extracts, on the cross-linked agarose gel Superose 12 HR 10/30, has been studied using a variety of solvent systems and shown to be based on a mixture of hydrogen bonding and hydrophobic interaction. The hydrogen bonding was studied in acetonitrile in the presence of different co-solvents possessing varying hydrogen bond donor (HBD) and/or hydrogen bond acceptor (HBA) characteristics. The HBA-value of the co-solvent had the highest effect whereas the HBD-value played a subordinate role. Retention due to hydrophobic interaction could be demonstrated when mobile phases containing high water content were applied. The retention of EGCG, and its analogues (-)-epigallocatechin (EGC) and (-)-catechin (C) were thus shown to be dependent on the polarity of the organic modifiers added. However, the elution order of EGC and C, was inversed to that observed in reversed phase chromatography, indicating that some hydrogen bonding was still in effect. The retardation of EGCG in the presence of a wide concentration range of acetonitrile in water confirmed the interpretation that the retention mechanism is of mixed-mode character based on both hydrogen bonding and hydrophobic interaction. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 55
页数:7
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