Comparison of enantioseparation of amino acid derivatives in aqueous and mixed aqueous-organic media by capillary zone electrophoresis |
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Authors: | Lili Yang Zhuobin Yuan |
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Affiliation: | Department of Chemistry, Hebei University, Baoding 071002, P.?R.?China e-mail: yangll@excite.com, CN Department of Chemistry, Graduate School, USTC, Chinese Academy of Science, Beijing 100039, P.?R.?China, CN
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Abstract: | The chiral separation of dansyl-amino acids has been performed by capillary zone electrophoresis using ¶β-cyclodextrin as a chiral selector, urea as an additive and 2-propanol and methanol as organic modifiers. The enantiomeric separations of dansyl-amino acids were investigated in aqueous medium and compared with the separation in mixed aqueous-organic medium as background electrolytes. The separation conditions, (concentration of buffer, β-cyclodextrin, methanol, urea and the pH value of buffer) were optimized. In the absence of organic modifier, only five pairs of 8 separated dansyl-amino acids were resolved when run separately. A mixture of up to eight chiral amino acids can be baseline resolved in less than 19 min by β-cyclodextrin-modified capillary zone electrophoresis with a buffer of 60 mmol L–1 H3BO3-KCl/40 mmol L–1 NaOH (pH 9.0), 4 mol L–1 urea, 100 mmol L–1β-cyclodextrin and 10% (v/v) methanol. |
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