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Title: Dual chiral recognition system involving cyclodextrin derivatives in capillary electrophoresis II. Enhancement of enantioselectivity. Author: Jakubetz H, Juza M, Schurig V. Journal: Electrophoresis; 1998 May; 19(5):738-44. PubMed ID: 9629908. Abstract: The enantiomer separation of hexobarbital was investigated by open tubular electrochromatography (OTEC) using the chiral stationary phase (CSP) CHIRASIL-DEX (a permethylated beta-cyclodextrin covalently linked to a dimethylpolysiloxane) and by cyclodextrin-electrokinetic chromatogaphy (CD-EKC) using anionic beta-cyclodextrin-sulfo-n-propyl ether (SPE-beta-CD) and cationic beta-cyclodextrin-2-hydroxy-3-trimethylammoniumpropyl ether chloride (HTAP-beta-CD) added to the running buffer. By employing two chiral selectors, the enantiomer separation of hexobarbital was then studied simultaneously by OTEC with CHIRASIL-DEX and by CD-EKC with either SPE-beta-CD or HTAP-beta-CD in the dual chiral recognition mode. In conjunction with CHIRASIL-DEX, anionic SPE-beta-CD decreased the chiral separation factor alpha due to compensation of enantioselectivity whereas the cationic additive HTAP-beta-CD increased the chiral separation factor alpha due to enhancement of enantioselectivity. It is concluded that CHIRASIL-DEX imparts an opposite enantioselectivity to the enantiomers of hexobarbital as compared to the charged CDs SPE-beta-CD and HTAP-beta-CD. Unusual peak broadening phenomena are observed in the dual chiral recognition system comprised of CHIRASIL-DEX and HTAP-beta-CD. The possible consequences of accidental dual chiral recognition systems caused by wall stacking effects of the mobile phase additives onto the inner surface of the capillary column are discussed.[Abstract] [Full Text] [Related] [New Search]