Enantioseparation of semisynthetic ergot alkaloids on vancomycin and teicoplanin stationary phases

Citation
E. Tesarova et al., Enantioseparation of semisynthetic ergot alkaloids on vancomycin and teicoplanin stationary phases, J CHROMAT A, 844(1-2), 1999, pp. 137-147
Citations number
26
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
844
Issue
1-2
Year of publication
1999
Pages
137 - 147
Database
ISI
SICI code
Abstract
The macrocyclic antibiotics, vancomycin and teicoplanin, were used as chira l stationary phase selectors for the enantioselective separation of semisyn thetic ergot alkaloids in reversed-phase high-performance liquid chromatogr aphy (RP-HPLC). The chromatographic behavior of the ergot preparations was investigated in order to obtain a deeper insight into the enantiodiscrimina tive process. A variety of factors, including mobile phase parameters such as the nature and concentration of the organic modifier, buffer concentrati on and pH, were examined. Conditions for the enantioseparation of real phar maceutical preparations, i.e. Lisuride, terguride and nicergoline, were fou nd. Differences in the chiral stationary phases are presented and the inter action mechanism is discussed. (C) 1999 Elsevier Science B.V. All rights re served.