Enantioseparation of dipeptides by capillary electrochromatography on a teicoplanin aglycone chiral stationary phase

被引:33
作者
Schmid, MG [1 ]
Grobuschek, N [1 ]
Pessenhofer, V [1 ]
Klostius, A [1 ]
Gübitz, G [1 ]
机构
[1] Karl Franzens Univ Graz, Inst Pharmaceut Chem & Pharmaceut Technol, A-8010 Graz, Austria
关键词
enantiomer separation; chiral stationary phases; electrochromatography; peptides;
D O I
10.1016/S0021-9673(02)02005-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work deals with investigations on the enantioseparation of glycyl-dipeptides by capillary electrochromatography (CEC) on a capillary packed with teicoplanin aglycone immobilized on 3.5 mum silica gel. The results were compared to those obtained with micro-HPLC using the same chiral stationary phase. Polar organic and reversed-phase mode were checked, whereby the latter showed better results. Out of 12 glycyldipetides investigated, all compounds showed baseline separation with R-s values up to 20. Plate numbers were in the range of 10 000-300 000/m. The choice of organic modifier was found to be crucial. While methanol increased retention time, acetonitrile reduced it. A ternary mixture of ethanol-acetonitrile-aqueous triethylamine acetate solution pH 4.1 was found to be a useful compromise, providing excellent resolution with retention times less than 25 min. Efficiency and resolution were generally found to be higher in CEC than with micro-HPLC. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:83 / 90
页数:8
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