Enantioseparation by ligand-exchange using particle-loaded monoliths:: Capillary-LC versus capillary electrochromatography

被引:35
|
作者
Schmid, Martin G. [1 ]
Koidl, Julia [1 ]
Wank, Pamela [1 ]
Kargl, Gabriele [1 ]
Zoehrer, Helga [1 ]
Guebitz, Gerald [1 ]
机构
[1] Karl Franzens Univ Graz, Inst Pharmaceut Sci, Dept Pharmaceut Chem, A-8010 Graz, Austria
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2007年 / 70卷 / 01期
关键词
amino acids; continuous beds; capillary HPLC; capillary electrochromatography; ligand-exchange; monolithic column; particle-loaded monoliths;
D O I
10.1016/j.jbbm.2006.06.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Particle-loaded monoliths containing a polymethacrylamide backbone were prepared by suspending a silica-based chiral phase in the mixture of the monomers followed by in-situ polymerization in the capillary. As chiral selector L-4-hydroxyproline chemically bonded to 3 mu m silica particles was used following the separation principle of ligand-exchange. Electrolytes containing Cu(II) ions were used. Amino acid enantiomers were separated by capillary-LC and CEC, whereby the latter showed the better resolution properties. For the chiral separation of alpha-hydroxy acids the EOF was reversed by copolymerizing diallyldimethylammonium chloride instead of vinylsulfonic acid as charge providing agent. Short columns of 6 cm were found to be sufficient in the case of CEC for baseline separations of amino acids with alpha values up to 5. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 85
页数:9
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