Chiral separation of naproxen and flurbiprofen by capillary electrophoresis
Zhu, X.F.; Lin, B.C.
Se Pu 18(1): 70-72
2000
ISSN/ISBN: 1000-8713 PMID: 12541462 Document Number: 517926
The acidic chiral drugs naproxen and flurbiprofen were successfully separated into two enantiomers when beta-cyclodextrins (beta-CDs) were used as chiral selectors by capillary zone electrophoresis, under the conditions of 0.1 mol/L phosphate buffer with pH 4.92. The comparison of four CDs, namely beta-CD, DM-beta-CD, HP-beta-CD and TM-beta-CD for chiral separation was made. Naproxen can be separated by either beta-CD or its derivatives, while flurbiprofen can only be separated by TM-beta-CD among the CDs. The elution order of enantiomers of naproxen in different CDs was also studied, and the R form always eluted before S form when any of the four CDs was used as chiral selectors. The method of chiral separation for weak acidic compounds was also developed. It was proved that the optimum pH value for their chiral separation was about 5, close to its pKa value.