Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/118191
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dc.creatorBarros, D-
dc.creatorLima, S-
dc.creatorCordeiro-da-Silva, A-
dc.date.accessioned2019-01-08T09:55:05Z-
dc.date.available2019-01-08T09:55:05Z-
dc.date.issued2015-
dc.identifier.issn1743-5889-
dc.identifier.urihttps://repositorio-aberto.up.pt/handle/10216/118191-
dc.description.abstractTo characterize the production and application of carbohydrate functionalized poly(d,l-lactide-co-glycolide) (PLGA) nanospheres as immune-modulatory mediators in the treatment of visceral leishmaniasis (VL). Materials & methods: PLGA nanospheres were prepared by nanoprecipitation and surface functionalized with mannose, mannan or mannosamine moieties using a carbodiimide reaction. Flow cytometry and fluorescence microscopy revealed the interaction of these nanospheres with macrophages. Results: The nanocarriers were taken up by murine primary macrophages using clathrin-mediated endocytosis. Co-culture of macrophages with carbohydrate-functionalized nanospheres led to their activation and production of pro-inflammatory cytokines. One dose of amphotericin B-loaded on mannan-functionalized nanospheres resulted in an efficacy VL therapy. Conclusion: This approach provides a promising therapy for VL and a new therapeutic nanoplatform for obligate intracellular pathogens.-
dc.description.sponsorshipThis work was supported by Fundo Europeu de Desen­volvimento Regional (FEDER) funds through the Opera­tional Competitiveness Program–COMPETE and by national funds through Fundação para a Ciência e a Tecnologia un­der projects FCOMP-01-0124-FEDER-015718 (PTDC/SAU-ENB/113151/2009). D Barros was supported by FCOMP-01- 0124-FEDER-015718 (PTDC/SAU-ENB/113151/2009) project. SA Costa Lima was supported by SFRH/BPD/37880/2007 and by QREN under contract NORTE-07-0124-FEDER-000067. The authors have no other relevant affiliations or financial involve­ment with any organization or entity with a financial inter­est in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.-
dc.language.isoeng-
dc.publisherFuture Medicine-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/113151/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/113151/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F37880%2F2007/PT-
dc.relation.ispartofNanomedicine, vol.10(3), p. 387-403-
dc.rightsopenAccess-
dc.subject.meshAmphotericin B/administration & dosage-
dc.subject.meshAnimals-
dc.subject.meshAntiprotozoal Agents/chemistry-
dc.subject.meshCells, Cultured-
dc.subject.meshCytokines/immunology-
dc.subject.meshDrug Carriers/chemistry-
dc.subject.meshLactic Acid/chemistry-
dc.subject.meshLactic Acid/immunology-
dc.subject.meshLeishmaniasis/drug therapy-
dc.subject.meshLeishmaniasis/immunology-
dc.subject.meshMacrophage Activation/drug effects-
dc.subject.meshMacrophages/drug effects-
dc.subject.meshMacrophages/immunology-
dc.subject.meshMale-
dc.subject.meshMannans/chemistry-
dc.subject.meshMannans/immunology-
dc.subject.meshMannose/chemistry-
dc.subject.meshMannose/immunology-
dc.subject.meshMice-
dc.subject.meshMice, Inbred BALB C-
dc.subject.meshNanospheres/chemistry-
dc.subject.meshPolyglycolic Acid/chemistry-
dc.subject.meshPolymers/chemistry-
dc.titleSurface functionalization of polymeric nanospheres modulates macrophage activation: Relevance in Leishmaniasis therapy-
dc.typeArtigo em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.2217/nnm.14.116-
dc.relation.publisherversionhttps://www.futuremedicine.com/doi/abs/10.2217/nnm.14.116?rfr_dat=cr_pub%3Dpubmed&url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&journalCode=nnm-
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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