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Multicolumn based liquid chromatography processes for the separation of nadolol racemates

dc.contributor.authorRibeiro, António E.
dc.contributor.authorArafah, Rami
dc.contributor.authorRodrigues, Alírio
dc.contributor.authorPais, Luís S.
dc.date.accessioned2020-02-27T10:05:17Z
dc.date.available2020-02-27T10:05:17Z
dc.date.issued2017
dc.description.abstractA few decades passed since the pharmaceutical industry realized the need to produce chiral drugs with reduced severe side-effects. To overcome this issue, the international agencies for drug safety become a real driving force, pushing more and more the industry towards the commercialization of drugs based on pure enantiomers. Traditionally, enantiomerically pure drugs are still produced in large-scale by organic asymmetric synthesis. However, it is also accepted that, in several cases, it is a too much time consuming production path. The direct resolution of racemic compounds, using multicolumn or fixed-bed liquid chromatography technologies, are nowadays, recognized at an industrial scale has a true alternative. The use of such technologies, like simulated moving bed (SMB) chromatography allows both high yields and purities of both enantiomers present in the racemic chiral compound. Also, these techniques can be applied to a wide range of racemic mixtures, since different stationary phases for enantiomer separation are now available. Nadolol is a pharmaceutical drug marketed as a mixture of four stereoisomers, used to treat cardiovascular diseases. This drug is a mixture of two pairs of racemates, therefore, its complete separation represents a challenging task. Recently, our research group reported the pseudo-binary separation of nadolol by SMB chromatography using both coated Chiralpak AD and Chiralpak IA immobilized chiral stationary phases [1,2]. 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]. 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. 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 is a result of project “AIProcMat@N2020 - Advanced Industrial Processes and Materials for a Sustainable Northern Region of Portugal 2020”, with the reference NORTE-01-0145-FEDER-000006, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) and of Project POCI-01-0145-FEDER-006984 – Associate Laboratory LSRE-LCM funded by ERDF through COMPETE2020 - Programa Operacional Competitividade e Internacionalização (POCI) – and by national funds through FCT - Fundação para a Ciência e a Tecnologia.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRibeiro, António E.; Arafah, Rami; Rodrigues, A.E.; Pais, L.S. (2017). Multicolumn based liquid chromatography processes for the separation of nadolol racemates. In 10º Encontro Nacional de Cromatografia: livro de resumos. Bragança: Instituto Politécnico. ISBN 978-972-745-234-7pt_PT
dc.identifier.isbn978-972-745-234-7
dc.identifier.urihttp://hdl.handle.net/10198/20707
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relation.publisherversionhttp://hdl.handle.net/10198/8896pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectMulticolumn processespt_PT
dc.subjectNadolol racematespt_PT
dc.subjectpreparative separationpt_PT
dc.titleMulticolumn based liquid chromatography processes for the separation of nadolol racematespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBragança, Portugalpt_PT
oaire.citation.title10º Encontro Nacional de Cromatografiapt_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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