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  • Chiral separation of catechin by capillary electrophoresis using mono-, di-, tri-succinyl-beta-cyclodextrin as chiral selectors.

Chiral separation of catechin by capillary electrophoresis using mono-, di-, tri-succinyl-beta-cyclodextrin as chiral selectors.

Chirality (2009-02-11)
Hyunmyung Kim, Youngjin Choi, Jun Lim, Seung-R Paik, Seunho Jung
RESUMEN

The chiral separation of (+/-)-catechin was investigated by capillary electrophoresis using characterized succinyl-beta-cyclodextrins (Suc-beta-CDs) with one to three degree of substitution values. The effects of nature and concentration of Suc-beta-CDs and running buffer pH on the migration time and resolution of (+/-)-catechin are discussed. All three kinds of Suc-beta-CDs show a clear baseline separation of (+/-)-catechin in capillary electrophoresis. Mono-Suc-beta-CD effectively separated (+/-)-catechin, and additional substituted CDs (di- and tri-Suc-beta-CD) were capable of chiral separation at a broad pH range. The optimum running conditions were found to be 100 mM borate buffer (pH 9.8) containing 5 mM mono-Suc-beta-CD with no methanol organic modifier.

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Sigma-Aldrich
Succinyl-β-cyclodextrin