Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/51460
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degois.publication.firstPage1543pt_PT
degois.publication.issue12pt_PT
degois.publication.lastPage1556pt_PT
degois.publication.titleParasitologypt_PT
dc.relation.publisherversionhttps://www.cambridge.org/core/journals/parasitology#pt_PT
dc.contributor.authorMacedo, Taís S.-
dc.contributor.authorColina-Vegas, Legna-
dc.contributor.authorda Paixão, Marcelo-
dc.contributor.authorNavarro, Maribel-
dc.contributor.authorBarreto, Breno C.-
dc.contributor.authorOliveira, Poliana C. M.-
dc.contributor.authorMacabira, Simone G.-
dc.contributor.authorMachado, Marta-
dc.contributor.authorPrudêncio, Miguel-
dc.contributor.authorD'Alessandro, Sarah-
dc.contributor.authorBasilico, Nicoletta-
dc.contributor.authorMoreira, Diogo R. M.-
dc.contributor.authorBatista, Alzir A.-
dc.contributor.authorSoares, Milena B. P.-
dc.date.accessioned2022-02-22T17:33:01Z-
dc.date.available2022-02-22T17:33:01Z-
dc.date.issued2016-
dc.identifier.citationParasitology (2016), 143, 1543-1556pt_PT
dc.identifier.issn0031-1820-
dc.identifier.urihttp://hdl.handle.net/10451/51460-
dc.description© Cambridge University Press 2016pt_PT
dc.description.abstractWe report the pharmacological activity of organoruthenium complexes containing chloroquine (CQ) as a chelating ligand. The complexes displayed intraerythrocytic activity against CQ-sensitive 3D7 and CQ-resistant W2 strains of Plasmodium falciparum, with potency and selectivity indexes similar to those of CQ. Complexes displayed activity against all intraerythrocytic stages, but moderate activity against Plasmodium berghei liver stages. However, unlike CQ, organoruthenium complexes impaired gametocyte viability and exhibited fast parasiticidal activity against trophozoites for P. falciparum. This functional property results from the ability of complexes to quickly induce oxidative stress. The parasitaemia of P. berghei-infected mice was reduced by treatment with the complex. Our findings demonstrated that using chloroquine for the synthesis of organoruthenium complexes retains potency and selectivity while leading to an increase in the spectrum of action and parasite killing rate relative to CQ.pt_PT
dc.description.sponsorshipThis research was funded by FAPESB (grant PET0042/2013, Brazil) to M.B.P.S, FAPESP (grant 14/10516-7, Brazil) to A.A.B. and Fundação para a Ciência e Tecnologia (grant PTDC/SAU-MIC/117060/2010 Portugal) to M.P. A.A.B. and M.B.P.S. are recipients of senior fellowships by CNPq (Brazil)pt_PT
dc.language.isoengpt_PT
dc.publisherCambridge University Presspt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FSAU-MIC%2F117060%2F2010/PTpt_PT
dc.rightsrestrictedAccesspt_PT
dc.subjectMalariapt_PT
dc.subjectPlasmodium bergheipt_PT
dc.subjectPlasmodium falciparumpt_PT
dc.subjectChloroquinept_PT
dc.subjectOrganoruthenium complexespt_PT
dc.subjectOxidative stresspt_PT
dc.titleChloroquine-containing organoruthenium complexes are fast-acting multistage antimalarial agentspt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume143pt_PT
dc.identifier.doi10.1017/S0031182016001153pt_PT
dc.identifier.eissn1469-8161-
Aparece nas colecções:IMM - Artigos em Revistas Internacionais
FM - Artigos em Revistas Internacionais

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