Methods in Molecular Biology 2013-01-01

Application of dual cyclodextrin systems in capillary electrophoresis enantioseparations.

Anne-Catherine Servais, Marianne Fillet

Index: Methods Mol. Biol. 970 , 289-95, (2013)

Full Text: HTML

Abstract

The enantioseparation of acidic and neutral compounds can be successfully achieved in capillary electrophoresis (CE) using dual cyclodextrin (CD) systems. This chapter describes how to separate the enantiomers of acidic or neutral substances using dual CD systems made up of a negatively charged CD derivative, i.e., sulfobutyl-β-CD (SB-β-CD) or carboxymethyl-β-CD (CM-β-CD), in combination with a neutral one, namely, heptakis(2,3,6-tri-O-methyl)-β-CD (TM-β-CD). An acidic compound (carprofen) and a weakly acidic drug (pentobarbital) were selected as model compounds.

Related Compounds

Structure Name/CAS No. Articles
Pentobarbital Structure Pentobarbital
CAS:76-74-4
β-cyclodextrin Structure β-cyclodextrin
CAS:7585-39-9
Carprofen Structure Carprofen
CAS:53716-49-7
Heptakis(2,3,6-tri-O-methyl)-b-cyclodextrin Structure Heptakis(2,3,6-tri-O-methyl)-b-cyclodextrin
CAS:55216-11-0