Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/154618
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dc.contributor.authorViveiros, Raquel-
dc.contributor.authorPinto, José J.-
dc.contributor.authorCosta, Nuno-
dc.contributor.authorHeggie, William-
dc.contributor.authorCasimiro, Teresa-
dc.date.accessioned2023-06-29T22:16:58Z-
dc.date.available2023-06-29T22:16:58Z-
dc.date.issued2023-03-
dc.identifier.issn0896-8446-
dc.identifier.otherPURE: 64820451-
dc.identifier.otherPURE UUID: 0b4482d2-5c0f-4eb5-b796-720b5edc3dae-
dc.identifier.otherScopus: 85146686812-
dc.identifier.otherWOS: 000926460700001-
dc.identifier.otherORCID: /0000-0002-0449-2343/work/151431393-
dc.identifier.urihttp://hdl.handle.net/10362/154618-
dc.descriptionFunding Information: The Associate Laboratory for Green Chemistry for Green Chemistry - Clean Technologies and Processes - LAQV is financed by national funds from FCT/MCTES and co-financed by the ERDF under the PT2020 Partnership Agreement ( POCI-01–0145-FEDER – 007265 ). Publisher Copyright: © 2023-
dc.description.abstractPolymeric particles with affinity for 4-dimethylaminipyridine (DMAP) were developed by molecular imprinting using supercritical carbon dioxide (scCO2) technology, for cleanup of this potentially genotoxic impurity from crude mixtures of Active Pharmaceutical Ingredients (APIs). DMAP-molecularly imprinted polymer (DMAP-MIP) and the respective control, the non-molecularly imprinted polymer (NIP) were produced by free radical polymerization using methacrylic acid as monomer, ethylene glycol dimethacrylate as crosslinker and AIBN as free-radical initiator in scCO2. The materials were obtained in high yield and were characterized chemically, physically and morphologically. Their extraction efficiency was evaluated by dynamic binding experiments using two solutions: i) a solution containing 104 ppm DMAP solution; ii) model pharmaceutical mixture containing 104 ppm of DMAP and 1018 ppm of Mometasone furoate (API). Particles were able to remove 18.3 µmol DMAP/g polymer from a 104 ppm DMAP solution (i) and 1004.6 µmol DMAP/g API (ii). In addition, high recoveries of both DMAP and API were obtained, above 99%.en
dc.format.extent6-
dc.language.isoeng-
dc.relationinfo:eu-repo/grantAgreement/FCT/Projetos de Investigação Científica e Desenvolvimento Tecnológico - 2012/PTDC%2FQEQ-PRS%2F2757%2F2012/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FEQU-EQU%2F32473%2F2017/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/OE/SFRH%2FBDE%2F51907%2F2012/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 3ed/2020.00377.CEECIND%2FCP1586%2FCT0033/PT-
dc.rightsopenAccess-
dc.subjectAffinity purification-
dc.subjectGenotoxin removal-
dc.subjectMolecularly imprinted polymer-
dc.subjectSolid-phase extraction-
dc.subjectSupercritical carbon dioxide-
dc.subjectChemical Engineering(all)-
dc.subjectCondensed Matter Physics-
dc.subjectPhysical and Theoretical Chemistry-
dc.titleDevelopment of affinity polymeric particles for the removal of 4-dimethylaminopyridine (DMAP) from active pharmaceutical ingredient crude streams using a green technology-
dc.typearticle-
degois.publication.titleJournal of Supercritical Fluids-
degois.publication.volume194-
dc.peerreviewedyes-
dc.identifier.doihttps://doi.org/10.1016/j.supflu.2023.105853-
dc.description.versionpublishersversion-
dc.description.versionpublished-
dc.contributor.institutionLAQV@REQUIMTE-
dc.contributor.institutionDQ - Departamento de Química-
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