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Preparative separation of ketoprofen enantiomers: choice of mobile phase composition and measurement of competitive adsorption isotherms

dc.contributor.authorRibeiro, António E.
dc.contributor.authorGraça, Nuno S.
dc.contributor.authorPais, Luís S.
dc.contributor.authorRodrigues, Alírio
dc.date.accessioned2009-04-17T16:43:05Z
dc.date.available2009-04-17T16:43:05Z
dc.date.issued2008
dc.date.submitted2008
dc.description.abstractThe present work intends to investigate how mobile phase composition influences the adsorption behavior of ketoprofen enantiomers (a nonsteroidal anti-inflammatory drug) on an amylose-based chiral stationary phase (Chiralpak AD). Three mobile phase compositions were studied: the usual 20% ethanol/80% n-hexane mixture and two pure mobile phases; methanol and ethanol. Pulse and breakthrough experiments under preparative conditions were carried out in order to measure and test adsorption isotherms. The results obtained show that, for preparative separations, pure ethanol is a better mobile phase than the usual 20% ethanol/80% n-hexane mixture: it allows higher solubility of the racemate, lower retention times, and also a higher selectivity at high enantiomer concentrations. These are aspects of crucial importance when the final goal is to achieve high productivity preparative separations, as it is shown for the simulated moving bed (SMB) operation.en
dc.identifier.citationRibeiro, A.E.; Graça, N.S.; Pais, L.S.; Rodrigues, A.E. (2008). Preparative separation of ketoprofen enantiomers: choice of mobile phase composition and measurement of competitive adsorption isotherms. Separation and Purification Technology. ISSN 1383-5866. 61:3, p.375-383en
dc.identifier.issn1383-5866en
dc.identifier.slugSeparation and Purification Technologyen
dc.identifier.urihttp://hdl.handle.net/10198/1156
dc.language.isoengen
dc.language.rfc3066engen
dc.number3en
dc.pagination375-383en
dc.peerreviewedyesen
dc.publisherElsevieren
dc.relationMeasurement of Competitive Adsorption Isotherms for Preparative Chromatographic Chiral Separations
dc.subjectKetoprofenen
dc.subjectEnantiomer separationen
dc.subjectMobile phase compositionen
dc.subjectPreparative chromatographyen
dc.subjectSimulated moving beden
dc.titlePreparative separation of ketoprofen enantiomers: choice of mobile phase composition and measurement of competitive adsorption isothermsen
dc.typejournal article
dc.volume61en
dspace.entity.typePublication
oaire.awardTitleMeasurement of Competitive Adsorption Isotherms for Preparative Chromatographic Chiral Separations
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCTI%2FEQU%2F38811%2F2001/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCI%2FEQU%2F59738%2F2004/PT
oaire.fundingStreamPOCI
oaire.fundingStreamPOCI
person.familyNameRibeiro
person.familyNamePais
person.givenNameAntónio E.
person.givenNameLuís S.
person.identifier.ciencia-id3211-D5B0-870D
person.identifier.ciencia-id421E-0CCD-A84F
person.identifier.orcid0000-0003-4569-7887
person.identifier.orcid0000-0002-3000-2862
person.identifier.scopus-author-id23390701300
person.identifier.scopus-author-id6603930478
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccessen
rcaap.typearticleen
relation.isAuthorOfPublication52666376-f100-4407-87ef-dc5df3613761
relation.isAuthorOfPublicationc6d25534-8487-45b1-90af-d350f4e3ac55
relation.isAuthorOfPublication.latestForDiscovery52666376-f100-4407-87ef-dc5df3613761
relation.isProjectOfPublication5249c996-c97d-4232-9d5f-386e74100da3
relation.isProjectOfPublicationc1579565-f41c-4825-a596-1aa3d09bc04b
relation.isProjectOfPublication.latestForDiscovery5249c996-c97d-4232-9d5f-386e74100da3

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