@prefix prodottidellaricerca: . @prefix istituto: . @prefix prodotto: . istituto:CDS053 prodottidellaricerca:prodotto prodotto:ID32987 . @prefix pubblicazioni: . @prefix unitaDiPersonaleInterno: . unitaDiPersonaleInterno:MATRICOLA6038 pubblicazioni:autoreCNRDi prodotto:ID32987 . @prefix rdf: . @prefix retescientifica: . prodotto:ID32987 rdf:type retescientifica:ProdottoDellaRicerca , prodotto:TIPO1101 . @prefix rdfs: . prodotto:ID32987 rdfs:label "Enantiomeric separation of acidic compounds of pharmaceutical interest by capillary electrochromatography employing glycopeptide antibiotic stationary phases. (Articolo in rivista)"@en . @prefix xsd: . prodotto:ID32987 pubblicazioni:anno "2003-01-01T00:00:00+01:00"^^xsd:gYear . @prefix skos: . prodotto:ID32987 skos:altLabel "
Fanali S. , Catarcini P. , Presutti C. (2003)
Enantiomeric separation of acidic compounds of pharmaceutical interest by capillary electrochromatography employing glycopeptide antibiotic stationary phases.
in Journal of chromatography (Print)
"^^rdf:HTML ; pubblicazioni:autori "Fanali S. , Catarcini P. , Presutti C."^^xsd:string ; pubblicazioni:paginaInizio "227"^^xsd:string ; pubblicazioni:paginaFine "232"^^xsd:string ; pubblicazioni:numeroVolume "994"^^xsd:string . @prefix ns10: . prodotto:ID32987 pubblicazioni:rivista ns10:ID294073 ; skos:note "ISI Web of Science (WOS)"^^xsd:string ; pubblicazioni:titolo "Enantiomeric separation of acidic compounds of pharmaceutical interest by capillary electrochromatography employing glycopeptide antibiotic stationary phases."^^xsd:string ; prodottidellaricerca:abstract "Enantiomeric separation of some selected acidic compounds of pharmaceutical interest belonging to the group of non-steroidal anti-inflammatory drugs were separated by capillary electrochromatography employing silica based glycopeptide antibiotic stationary phases, namely vancomycin or a teicoplanin derivatives (Hepta-Tyr). The vancomycin stationary phase allowed to achieve the chiral resolution of some racemic studied compounds only using mobile phases containing ammonium formate at a relatively low pH 2.5\u00963.5 and acetonitrile. Employing the teicoplanin derivative stationary phase, good enantiomeric resolution was achieved eluting with mobile phases containing sodium phosphate pH 6\u0096acetonitrile. Enantiomers were moved to the detector because a relatively high reversed electroosmotic flow (due to the positive charge of the stationary phase) and to the electrophoretic mobility of analytes." ; prodottidellaricerca:prodottoDi istituto:CDS053 ; pubblicazioni:autoreCNR unitaDiPersonaleInterno:MATRICOLA6038 . ns10:ID294073 pubblicazioni:rivistaDi prodotto:ID32987 .