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Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles

dc.contributor.authorCarvalho, Suzana Gonçalves [UNESP]
dc.contributor.authorHaddad, Felipe Falcão [UNESP]
dc.contributor.authordos Santos, Aline Martins [UNESP]
dc.contributor.authorScarim, Cauê Benito [UNESP]
dc.contributor.authorFerreira, Leonardo Miziara Barboza [UNESP]
dc.contributor.authorMeneguin, Andréia Bagliotti [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorGremião, Maria Palmira Daflon [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:42:36Z
dc.date.issued2024-04-01
dc.description.abstractBevacizumab (BVZ) was the first monoclonal antibody approved by the FDA and has shown an essential advance in the antitumor therapy of colorectal cancer (CRC), however, the systemic action of BVZ administered intravenously can trigger several adverse effects. The working hypothesis of the study was to promote the modulation of the mucoadhesion properties and permeability of the BVZ through the formation of nanoparticles (NPs) with gellan gum (GG) with subsequent surface modification with chitosan (CS). NPs comprising BVZ and GG were synthesized through polyelectrolyte complexation, yielding spherical nanosized particles with an average diameter of 264.0 ± 2.75 nm and 314.0 ± 0.01 nm, polydispersity index of 0.182 ± 0.01 e 0.288 ± 0.01, and encapsulation efficiency of 29.36 ± 0.67 e 60.35 ± 0.27 mV, for NPs without (NP_BVZ) and with surface modification (NP_BVZ + CS). The results showed a good ability of nanoparticles with surface modification to modulate the NPs biological properties.en
dc.description.affiliationDepartment of Drugs and Pharmaceutics School of Pharmaceutical Sciences São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Drugs and Pharmaceutics School of Pharmaceutical Sciences São Paulo State University (UNESP), SP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipUniversidade Estadual Paulista
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2014/50928-2
dc.description.sponsorshipIdFAPESP: 2019/10761-5
dc.description.sponsorshipIdFAPESP: 2022/14075-1
dc.description.sponsorshipIdCNPq: 465687/2014-8
dc.identifierhttp://dx.doi.org/10.1016/j.ijbiomac.2024.130272
dc.identifier.citationInternational Journal of Biological Macromolecules, v. 263.
dc.identifier.doi10.1016/j.ijbiomac.2024.130272
dc.identifier.issn1879-0003
dc.identifier.issn0141-8130
dc.identifier.scopus2-s2.0-85185409841
dc.identifier.urihttps://hdl.handle.net/11449/299514
dc.language.isoeng
dc.relation.ispartofInternational Journal of Biological Macromolecules
dc.sourceScopus
dc.subjectAngiogenesis
dc.subjectAntibody
dc.subjectBevacizumab
dc.subjectChitosan
dc.subjectGellan gum
dc.subjectPolymeric nanoparticle
dc.titleChitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticlesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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