Literature DB >> 12833387

Direct enantiomeric resolution of (+/-)-atenolol, (+/-)-metoprolol, and (+/-)-propranolol by impregnated TLC using L-aspartic acid as chiral selector.

R Bhushan1, Meenakshi Arora.   

Abstract

Resolution of three commonly used beta-blockers, (+/-)-atenolol, (+/-)-metoprolol and (+/-)-propranolol, into their enantiomers has been achieved using normal-phase TLC on silica gel plates impregnated with L-aspartic acid as the chiral selector. Different combinations of acetonitrile-methanol-water as mobile phase were found to be successful in resolving the enantiomers. The spots were detected with iodine and the detection limits were found to be 0.26 microg for atenolol and 0.23 microg for each of metoprolol and propranolol as racemate. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 12833387     DOI: 10.1002/bmc.216

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


  1 in total

1.  Development of a New Method Based on Chiral Ligand-Exchange Chromatography for the Enantioseparation of Propranolol.

Authors:  Taher Alizadeh
Journal:  Iran J Pharm Res       Date:  2017       Impact factor: 1.696

  1 in total

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