Fused silica-packed capillary columns containing vancomycin immobilized by reductive amination on an aldehyde-silica were used to separate enantiomers of some non-steroidal anti-inflammatory drugs. Attempts have been made to qualitatively explain the influence of various mobile phase compositions on
Evaluation of a vancomycin chiral stationary phase in packed capillary supercritical fluid chromatography
✍ Scribed by Jürgen Dönnecke; Lars A. Svensson; Olle Gyllenhaal; Karl-Erik Karlsson; Anders Karlsson; Jörgen Vessman
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 273 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1040-7685
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✦ Synopsis
Vancomycin immobilized on an aldehyde functionalized silica support in packed capillary columns has been used as a chiral stationary phase in supercritical fluid chromatography under subcritical conditions. The use of carbon dioxide with methanol as the mobile phase modifier is shown to offer an extended scope of chiral separations compared with reversed-phase liquid chromatography, especially for basic analytes. It could be demonstrated that the chiral recognition of vancomycin for different analytes is based on several kinds of interactions. Large differences in enantioselectivity in a homologous series of local anesthetic compounds indicate that the fit of a host᎐guest interaction between an analyte and vancomycin could be very precise. Nonlinear van't Hoff plots implied that the enantiomers of metoprolol and the modifiers evaporated from their adsorption sites at different temperatures.
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Chiral separation of basic compounds was achieved by using 75 or 100 microm ID fused-silica capillaries packed with a vanoomycin-modified diol silica stationary phase. The capillary was firstly packed for about 12 cm with a slurry mixture composed of diolsilica (3:1) then with the vancomycin modifie
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