USE OF A NAPHTHYLETHYLCARBAMOYLATED-BETA-CYCLODEXTRIN CHIRAL STATIONARY-PHASE FOR THE SEPARATION OF DRUG ENANTIOMERS AND RELATED-COMPOUNDS BY SUBCRITICAL AND SUPERCRITICAL FLUID-CHROMATOGRAPHY
Kl. Williams et al., USE OF A NAPHTHYLETHYLCARBAMOYLATED-BETA-CYCLODEXTRIN CHIRAL STATIONARY-PHASE FOR THE SEPARATION OF DRUG ENANTIOMERS AND RELATED-COMPOUNDS BY SUBCRITICAL AND SUPERCRITICAL FLUID-CHROMATOGRAPHY, Chirality, 8(4), 1996, pp. 325-331
Enantiomeric separation of a variety of drugs and related compounds wa
s achieved on an (S)-naphthylethylcarbamoylated-beta-cyclodextrin (S-N
EC-CD) chiral stationary phase (CSP) using sub- and supercritical flui
d chromatography (SFC). Compounds previously resolved on native or der
ivatized cyclodextrin CSPs in liquid chromatography (LC) using reverse
d phase or polar organic mobile phase modes could be resolved in SFC u
sing a simple carbon dioxide/methanol eluent, Resolution of cromakalim
, which is not possible on the S-NEC-CD column in LC, was readily acco
mplished in SFC. The importance of modifier, temperature, and pressure
was assessed in relation to retention, selectivity, and resolution. T
he nature of the modifier and the modifier concentration were found to
be crucial parameters. (C) 1996 Wiley-Liss, Inc.