Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/95769
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dc.contributor.authorGomes, Ana T. P. C.-
dc.contributor.authorNeves, M. Graça P. M. S.-
dc.contributor.authorFernandes, Rosa-
dc.contributor.authorRibeiro, Carlos F. M.-
dc.contributor.authorCavaleiro, José A. S.-
dc.contributor.authorMoura, Nuno M. M.-
dc.date.accessioned2021-09-16T15:49:04Z-
dc.date.available2021-09-16T15:49:04Z-
dc.date.issued2021-09-01-
dc.identifier.issn1420-3049pt
dc.identifier.urihttps://hdl.handle.net/10316/95769-
dc.description.abstractIn this study, we report the preparation of new mono-charged benzoporphyrin complexes by reaction of the appropriate neutral benzoporphyrin with (2,2'-bipyridine)dichloroplatinum(II) and of the analogs' derivatives synthesized through alkylation of the neutral scaffold with iodomethane. All derivatives were incorporated into polyvinylpyrrolidone (PVP) micelles. The ability of the resultant formulations to generate reactive oxygen species was evaluated, mainly the singlet oxygen formation. Then, the capability of the PVP formulations to act as photosensitizers against bladder cancer cells was assessed. Some of the studied formulations were the most active photosensitizers causing a decrease in HT-1376 cells' viability. This creates an avenue to further studies related to bladder cancer cells.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUIDB/04539/2020pt
dc.relationUIDB/50006/2020pt
dc.relationUIDP/04539/2020pt
dc.relationUID/NEU/04539/2019pt
dc.relationCDL-CTTRI-048-88-ARH/2018pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectBenzoporphyrinpt
dc.subjectCancerpt
dc.subjectPhotodynamic therapypt
dc.subjectPhotosensitizerpt
dc.subjectPlatinum complexespt
dc.titleUnraveling the Photodynamic Activity of Cationic Benzoporphyrin-Based Photosensitizers against Bladder Cancer Cellspt
dc.typearticle-
degois.publication.firstPage5312pt
degois.publication.issue17pt
degois.publication.titleMoleculespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/molecules26175312pt
degois.publication.volume26pt
dc.date.embargo2021-09-01*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.project.grantnoCenter for Innovative Biomedicine and Biotechnology - CIBB-
crisitem.project.grantnoAssociated Laboratory for Green Chemistry - Clean Technologies and Processes- REQUIMTE-
crisitem.project.grantnoCenter for Innovative Biomedicine and Biotechnology-
Appears in Collections:I&D CIBB - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
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