Literature DB >> 24861749

Liquid chromatographic enantioseparation of (RS)-mexiletine and (RS)-fluoxetine using chiral derivatizing reagents synthesized with (S)-naproxen moiety.

Sonika Batra1, Ravi Bhushan.   

Abstract

Enantiomeric separation of racemic mexiletine and fluoxetine was achieved using three chiral derivatizing reagents (CDRs) based on (S)-naproxen. Diastereomers were synthesized by reaction of mexiletine or fluoxetine with the CDRs and were separated on a C18 column under reversed-phase conditions using a binary mixture of acetonitrile and triethylammonium phosphate/water, with UV detection at 230 and 226 nm. The results obtained for enantioseparation of the two drugs using the three CDRs were compiled and compared. The conditions for derivatization and chromatographic separation were optimized. The method was validated for linearity, repeatability, limit of detection and limit of quantification.
Copyright © 2014 John Wiley & Sons, Ltd.

Entities:  

Keywords:  (RS)-fluoxetine; (RS)-mexiletine; (S)-naproxen; chiral derivatizing agent; indirect enantioseparation; reversed-phase high-performance liquid chromatography

Mesh:

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Year:  2014        PMID: 24861749     DOI: 10.1002/bmc.3144

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  1 in total

1.  Chiral Discrimination of Mexiletine Enantiomers by Capillary Electrophoresis Using Cyclodextrins as Chiral Selectors and Experimental Design Method Optimization.

Authors:  Melania Cârcu-Dobrin; Gabriel Hancu; Lajos Attila Papp; Ibolya Fülöp
Journal:  Molecules       Date:  2022-08-31       Impact factor: 4.927

  1 in total

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