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Separation of nadolol racemates by fixed-bed and continuous preparative liquid chromatography using C18 columns

dc.contributor.authorRibeiro, António E.
dc.contributor.authorArafah, Rami
dc.contributor.authorRodrigues, Alírio
dc.contributor.authorPais, Luís S.
dc.date.accessioned2020-02-27T10:25:01Z
dc.date.available2020-02-27T10:25:01Z
dc.date.issued2017
dc.description.abstractNadolol is a pharmaceutical drug marketed as a mixture of four stereoisomers, used to treat cardiovascular diseases. However, its prescription is also related with some severe risks such as heart failure. Its chemical structure has three stereogenic centers which allows for eight possible stereoisomers. However, the two hydroxyl substituents on the cyclohexane ring are fixed in the cis-configuration, which precludes four stereoisomers. Nadolol is presently marketed as an equal mixture of the four stereoisomers. It is well known that pure enantiomer separation is important to control chiral drugs safety. Recently, our research group reported the pseudo-binary separation of nadolol by simulated moving bed (SMB) chromatography using both coated Chiralpak AD and Chiralpak IA immobilized chiral stationary phases (CSP).1,2 This technology is generally based on the use of chiral adsorbents which must have enough recognition for all the chiral species. In this work it is proposed an alternative strategy, implementing a first achiral separation step, to be followed by two subsequent parallel chiral separation steps.3,4 In this first achiral step, C18 columns are used to perform the separation of the two pairs of nadolol enantiomers (“racemate A” from “racemate B”) under reversed-phase mode. The C18 achiral adsorbent allows the separation of the two pairs of nadolol diastereomers, i.e., the first racemate (composed by the nadolol compounds 2 and 3) co-eluting in the raffinate, and the second racemate (composed by the nadolol compounds 1 and 4) to be obtained in the extract SMB stream. After this preliminary achiral separation step, two parallel SMB runs must be carried out using a chiral stationary phase to achieve the complete separation of all the four nadolol stereoisomers. Extensive experimental and simulation results will be presented including solvent screening, measurement of equilibrium and kinetic data, and both fixed-bed and SMB preparative separations.pt_PT
dc.description.sponsorshipThis work was financially supported by Project POCI-01-0145-FEDER-006984 - Associate Laboratory LSRE-LCM - funded by FEDER funds through COMPETE2020 - Programa Operacional Competitividade e Internacionalização (POCI) – and by national funds through FCT - Fundação para a Ciência e a Tecnologia. This work was also co-financed by QREN, ON2 and FEDER through Project NORTE-07-0162-FEDER-000050.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.urihttp://hdl.handle.net/10198/20710
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectNadolol racematespt_PT
dc.subjectFixed-bedpt_PT
dc.subjectContinuous preparativept_PT
dc.subjectC18 columnspt_PT
dc.titleSeparation of nadolol racemates by fixed-bed and continuous preparative liquid chromatography using C18 columnspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.titleXXV Encontro Nacional da Sociedade Portuguesa de Químicapt_PT
person.familyNameRibeiro
person.familyNameArafah
person.familyNamePais
person.givenNameAntónio E.
person.givenNameRami
person.givenNameLuís S.
person.identifier.ciencia-id3211-D5B0-870D
person.identifier.ciencia-idAB16-ECBF-B886
person.identifier.ciencia-id421E-0CCD-A84F
person.identifier.orcid0000-0003-4569-7887
person.identifier.orcid0000-0002-7743-4988
person.identifier.orcid0000-0002-3000-2862
person.identifier.scopus-author-id23390701300
person.identifier.scopus-author-id57151342900
person.identifier.scopus-author-id6603930478
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication52666376-f100-4407-87ef-dc5df3613761
relation.isAuthorOfPublication3cd4864a-8aa6-46a2-9415-767a7551ee62
relation.isAuthorOfPublicationc6d25534-8487-45b1-90af-d350f4e3ac55
relation.isAuthorOfPublication.latestForDiscovery3cd4864a-8aa6-46a2-9415-767a7551ee62

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