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Multicomponent separation of nadolol stereoisomers combining different preparative technologies and chiral and achiral-chiral strategies

dc.contributor.authorArafah, Rami
dc.contributor.authorRibeiro, António E.
dc.contributor.authorRodrigues, Alírio
dc.contributor.authorPais, L.S.
dc.date.accessioned2020-03-06T11:12:17Z
dc.date.available2020-03-06T11:12:17Z
dc.date.issued2019
dc.description.abstractNadolol is a common prescribed pharmaceutical drug for the relieve of several cardiovascular diseases and represents a very interesting case-study of multicomponent chiral separation since it is composed by four stereoisomers, being two pairs of enantiomers. In this way, it introduces the possibility of alternative strategies, using different kind of preparative separation sequences and techniques, the use of different packings (chiral and achiral stationary phases), and the corresponding mobile phase optimization at both normal and reversed-phase modes. When considering preparative and multicomponent separation, the complexity deeply increases by introducing the necessity of multi-step separation sequences (or a much more complex multi-region separation process), by opening the possibility to combine chiral and achiral stationary phases (when in presence of stereoisomers instead of just one pair of enantiomers) and to combine different separation techniques (fixed-bed and simulated moving bed (SMB) related processes). The design of the complete preparative separation of nadolol stereoisomers asks for a global experimental and simulation methodology considering both the characterization and optimization of each separation step and its sequences to achieve the four nadolol components pure. New strategies using combinations of achiral and chiral stationary phases and sequences of different separation techniques will be presented. Extensive experimental and simulation results for the complete separation of all the four nadolol stereoisomers using Chiralpak IA (chiral) and different Waters C18 (achiral) stationary phases will be presented.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 Program (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 Fundação para a Ciência e a Tecnologia (FCT)pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationArafah, Rami; Ribeiro, António E.; Rodrigues, Alírio; Pais, L.S. (2019). Multicomponent separation of nadolol stereoisomers combining different preparative technologies and chiral and achiral-chiral strategies. In The 12th European Congress of Chemical Engineering: book of abstracts. Florencept_PT
dc.identifier.isbn978-88-95608-75-4
dc.identifier.urihttp://hdl.handle.net/10198/20843
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherECCEpt_PT
dc.relationNORTE‐01‐0145‐FEDER‐000006pt_PT
dc.relationPOCI‐01‐0145‐FEDER‐006984pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectNadolol stereoisomerspt_PT
dc.subjectChiral and achiralpt_PT
dc.subjectPreparative separationpt_PT
dc.titleMulticomponent separation of nadolol stereoisomers combining different preparative technologies and chiral and achiral-chiral strategiespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceFlorencept_PT
oaire.citation.endPage411pt_PT
oaire.citation.startPage411pt_PT
oaire.citation.titleThe 12th European Congress of Chemical Engineering: book of abstractspt_PT
person.familyNameArafah
person.familyNameRibeiro
person.familyNamePais
person.givenNameRami
person.givenNameAntónio E.
person.givenNameLuís S.
person.identifier.ciencia-idAB16-ECBF-B886
person.identifier.ciencia-id3211-D5B0-870D
person.identifier.ciencia-id421E-0CCD-A84F
person.identifier.orcid0000-0002-7743-4988
person.identifier.orcid0000-0003-4569-7887
person.identifier.orcid0000-0002-3000-2862
person.identifier.scopus-author-id57151342900
person.identifier.scopus-author-id23390701300
person.identifier.scopus-author-id6603930478
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication3cd4864a-8aa6-46a2-9415-767a7551ee62
relation.isAuthorOfPublication52666376-f100-4407-87ef-dc5df3613761
relation.isAuthorOfPublicationc6d25534-8487-45b1-90af-d350f4e3ac55
relation.isAuthorOfPublication.latestForDiscovery3cd4864a-8aa6-46a2-9415-767a7551ee62

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