Enantioresolution of pharmaceutical compounds by capillary electrophoresis. Use of cyclodextrins and antibiotics

Citation
S. Fanali et al., Enantioresolution of pharmaceutical compounds by capillary electrophoresis. Use of cyclodextrins and antibiotics, ENANTIOMER, 4(3-4), 1999, pp. 229-241
Citations number
110
Categorie Soggetti
Chemistry
Journal title
ENANTIOMER
ISSN journal
10242430 → ACNP
Volume
4
Issue
3-4
Year of publication
1999
Pages
229 - 241
Database
ISI
SICI code
1024-2430(1999)4:3-4<229:EOPCBC>2.0.ZU;2-T
Abstract
Capillary electroyhoresis (CE) is a powerful tool for the analysis of chira l compounds of pharmaceutical interest. The separation of enantiomers can b e achieved using a chiral environment responsible for the diastereoisomers formation (stable or labile in the indirect or direct separation method, re spectively). A wide number of chiral selectors have been employed in CE and among them cyclodextrins or their derivatives and antibiotics are the most used stereoselective agents. The review surveys the chiral separation of d rugs using the above mentioned chiral selectors by CE. The main parameters influencing the enantioresolution, e.g., chiral selector type and concentra tion, buffer type, concentration, pH, organic modifier as well as the capil lary temperature are discussed. Finally some selected applications to real samples such as pharmaceutical formulations, serum, urine are also discusse d.