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Rational design of polyelectrolyte complexes based on bevacizumab and gellan gum with a surface modified with chitosan

dc.contributor.authorCarvalho, Suzana Gonçalves [UNESP]
dc.contributor.authordos Santos, Aline Martins [UNESP]
dc.contributor.authorCardoso, Ana Júlia Rocha [UNESP]
dc.contributor.authorMeneguin, Andréia Bagliotti [UNESP]
dc.contributor.authorFerreira, Leonardo Miziara Barboza [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorGremião, Maria Palmira Daflon [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:07:07Z
dc.date.issued2024-08-01
dc.description.abstractBevacizumab (BVZ) is an anti-angiogenic monoclonal antibody used to treat diseases such as various types of cancer. However, its parenteral administration causes several side effects and oral administration is limited due to the integrity of these macromolecules in the face of the extreme conditions of the gastrointestinal tract. To overcome these limitations, the study of drug delivery systems becomes a promising strategy to increase the efficiency of BVZ therapeutic delivery. Therefore, it is important that drug delivery systems are meticulously designed and that their physicochemical properties are understood. The objective of the present study was to develop nanoparticles through polyelectrolytic complexation between polysaccharides and polyampholytes, without the use of organic solvents, and to evaluate the influence of pH and molecular weight on particle formation. Different proportions of polymers were tested to obtain the nanoparticles, exhibiting average diameters in the range of 222.6–412.1 nm, zeta potential of −16.3 to −40 mV, and polydispersity index of ∼0.16–0.53. Complexation with chitosan promoted charge inversion (> +40 mV), in addition to increasing particle diameter and association efficiency, ranging from 29 % to approximately 60 %.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.mtcomm.2024.110147
dc.identifier.citationMaterials Today Communications, v. 40.
dc.identifier.doi10.1016/j.mtcomm.2024.110147
dc.identifier.issn2352-4928
dc.identifier.scopus2-s2.0-85201781908
dc.identifier.urihttps://hdl.handle.net/11449/297586
dc.language.isoeng
dc.relation.ispartofMaterials Today Communications
dc.sourceScopus
dc.subjectAntibody
dc.subjectElectrostatic interactions
dc.subjectPolyampholytes
dc.subjectPolymeric nanoparticles
dc.subjectPolysaccharides
dc.titleRational design of polyelectrolyte complexes based on bevacizumab and gellan gum with a surface modified with chitosanen
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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