Enantioselective analysis of propranolol and 4-hydroxypropranolol by CE with application to biotransformation studies employing endophytic fungi

A CE method is described for the enantioselective analysis of propranolol (Prop) and 4-hydroxypropranolol (4-OH-Prop) in liquid Czapek medium with application in the study of the enantioselective biotransformation of Prop by endophytic fungi. The electrophoretic conditions previously optimized were...

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Published inElectrophoresis Vol. 30; no. 22; pp. 3910 - 3917
Main Authors Borges, Keyller Bastos, Pupo, Mônica Tallarico, Bonato, Pierina Sueli
Format Journal Article
LanguageEnglish
Published Weinheim Wiley-VCH Verlag 01.11.2009
WILEY-VCH Verlag
WILEY‐VCH Verlag
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Summary:A CE method is described for the enantioselective analysis of propranolol (Prop) and 4-hydroxypropranolol (4-OH-Prop) in liquid Czapek medium with application in the study of the enantioselective biotransformation of Prop by endophytic fungi. The electrophoretic conditions previously optimized were as follows: an uncoated fused-silica capillary, 4% w/v carboxymethyl-β-CD in 25 mmol/L triethylamine/phosphoric acid (H₃PO₄) buffer at pH 9 as running electrolyte and 17 kV of voltage. UV detection was carried out at 208 nm. Liquid-liquid extraction using diethyl ether: ethyl acetate (1:1 v/v) as extractor solvent was employed for sample preparation. The calibration curves were linear over the concentration range of 0.25-10.0 μg/mL for each 4-OH-Prop enantiomer and 0.10-10.0 μg/mL for each Prop enantiomer (rgreater-than-or-equal0.995). Within-day and between-day relative standard deviations and relative errors for precision and accuracy were lower than 15% for all the enantiomers. Finally, the validated method was used to evaluate Prop biotransformation in its mammalian metabolite 4-OH-Prop by some selected endophytic fungi. The screening of five strains of endophytic fungi was performed and all of them could biotransform Prop to some extent. Specifically, Glomerella cingulata (VA1) biotransformed 47.8% of (-)-(S)-Prop to (-)-(S)-4-OH-Prop with no formation of (+)-(R)-4-OH-Prop in 72 h of incubation.
Bibliography:http://dx.doi.org/10.1002/elps.200900216
ark:/67375/WNG-72FKPZ5H-0
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
ArticleID:ELPS200900216
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
istex:45DB473EC428AA7A64EBA0C1AFE67EC21979F317
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0173-0835
1522-2683
DOI:10.1002/elps.200900216