Enantiomeric separation of citalopram analogues by HPLC using macrocyclic glycopeptide and cyclodextrin based chiral stationary phases |
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| Authors: | Maressa D. Dolzan Yang Shu Jonathan P. Smuts Hans Petersen Peter Ellegaard Gustavo A. Micke |
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| Affiliation: | 1. Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas, USA;2. Department of Chemistry, Federal University of Santa Catarina, Florianopolis, Santa Catarina, Brazil;3. College of Life and Health Sciences, Northeastern University, Shenyang, China;4. H. Lundbeck A/S, Valby, Denmark;5. Department of Chemistry, Federal University of Santa Catarina, Florianopolis, Santa Catarina, Brazil |
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| Abstract: | The enantiomeric separation of a novel series of twenty-eight racemic mixtures of citalopram analogues was performed by high performance liquid chromatography (HPLC). Due to the effectiveness of citalopram as an antidepressant drug, the development of new compounds based on its chemical structure is interesting, and their enantiomeric separation is needed to allow further pharmacokinetic studies. Several bonded cyclodextrin (both native and derivatized) and macrocyclic glycopeptide based chiral stationary phases (CSPs) were evaluated for their ability to separate this set of compounds via HPLC. Polar ionic, polar organic, and reversed phase modes were tested. Twenty-five of the racemic mixtures were separated with resolutions and enantiomeric selectivities up to 2.9 and 1.33, respectively. A total of eighteen baseline separations were achieved, while seven compounds were partially separated. Vancomycin based columns operated in the polar ionic mode resulted in the greatest number of separations. Lastly, the chromatographic behaviors of similar compounds were compared based on their chemical structure and also on the chiral selectors used. |
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| Keywords: | Chiral separation citalopram cyclodextrin enantiomeric separation HPLC macrocyclic glycopeptide |
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