4.6 Article

Cationic permethylated 6-monoamino-6-monodeoxy-β-cyclodextrin as chiral selector of dansylated amino acids in capillary electrophoresis

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ELSEVIER
DOI: 10.1016/j.jpba.2014.06.028

Keywords

Cationic CD derivative; Dansylated amino acid; Enantioseparation; Isoelectric point; Lipophilicity

Funding

  1. Hungarian National Research and Development Projects [NKFP_A32008-0211, TECH-09-AI-2009-0117]

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The resolution power of permethylated 6-monoamino-6-monodeoxy-beta CD (PMMABCD) -a single isomer, cationic CD derivative - developed previously for chiral analyses in capillary electrophoresis was further studied here. Dansylated amino acids (Dns-AA) were chosen as amphoteric chiral model compounds. Changes in the resolutions of Dns-AAs by varying pH and selector concentrations were investigated and correlated with their structures and chemical properties (isoelectric point and lipophilicity). Maximal resolutions could be achieved at pH 6 or pH 4. The separations improved with increasing concentration of the selector. Baseline or substantially better resolution for 8 pairs of these Dns-AAs could be achieved. Low CD concentration was enough for the separation of the most apolar Dns-AAs. Chiral discrimination ability of PMMABCD was demonstrated by the separation of an artificial mixture of 8 Dns-AA pairs. (C) 2014 Elsevier B.V. All rights reserved.

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