Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.ijbiomac.2024.130272 https://hdl.handle.net/11449/299514 |
Resumo: | Bevacizumab (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. |
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Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticlesAngiogenesisAntibodyBevacizumabChitosanGellan gumPolymeric nanoparticleBevacizumab (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.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Estadual PaulistaFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Drugs and Pharmaceutics School of Pharmaceutical Sciences São Paulo State University (UNESP), SPDepartment of Drugs and Pharmaceutics School of Pharmaceutical Sciences São Paulo State University (UNESP), SPFAPESP: 2014/50928-2FAPESP: 2019/10761-5FAPESP: 2022/14075-1CNPq: 465687/2014-8Universidade Estadual Paulista (UNESP)Carvalho, Suzana Gonçalves [UNESP]Haddad, Felipe Falcão [UNESP]dos Santos, Aline Martins [UNESP]Scarim, Cauê Benito [UNESP]Ferreira, Leonardo Miziara Barboza [UNESP]Meneguin, Andréia Bagliotti [UNESP]Chorilli, Marlus [UNESP]Gremião, Maria Palmira Daflon [UNESP]2025-04-29T18:42:36Z2024-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.ijbiomac.2024.130272International Journal of Biological Macromolecules, v. 263.1879-00030141-8130https://hdl.handle.net/11449/29951410.1016/j.ijbiomac.2024.1302722-s2.0-85185409841Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Biological Macromoleculesinfo:eu-repo/semantics/openAccess2025-05-01T05:15:36Zoai:repositorio.unesp.br:11449/299514Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-01T05:15:36Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
title |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
spellingShingle |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles Carvalho, Suzana Gonçalves [UNESP] Angiogenesis Antibody Bevacizumab Chitosan Gellan gum Polymeric nanoparticle |
title_short |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
title_full |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
title_fullStr |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
title_full_unstemmed |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
title_sort |
Chitosan surface modification modulates the mucoadhesive, permeation and anti-angiogenic properties of gellan gum/bevacizumab nanoparticles |
author |
Carvalho, Suzana Gonçalves [UNESP] |
author_facet |
Carvalho, Suzana Gonçalves [UNESP] Haddad, Felipe Falcão [UNESP] dos Santos, Aline Martins [UNESP] Scarim, Cauê Benito [UNESP] Ferreira, Leonardo Miziara Barboza [UNESP] Meneguin, Andréia Bagliotti [UNESP] Chorilli, Marlus [UNESP] Gremião, Maria Palmira Daflon [UNESP] |
author_role |
author |
author2 |
Haddad, Felipe Falcão [UNESP] dos Santos, Aline Martins [UNESP] Scarim, Cauê Benito [UNESP] Ferreira, Leonardo Miziara Barboza [UNESP] Meneguin, Andréia Bagliotti [UNESP] Chorilli, Marlus [UNESP] Gremião, Maria Palmira Daflon [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Carvalho, Suzana Gonçalves [UNESP] Haddad, Felipe Falcão [UNESP] dos Santos, Aline Martins [UNESP] Scarim, Cauê Benito [UNESP] Ferreira, Leonardo Miziara Barboza [UNESP] Meneguin, Andréia Bagliotti [UNESP] Chorilli, Marlus [UNESP] Gremião, Maria Palmira Daflon [UNESP] |
dc.subject.por.fl_str_mv |
Angiogenesis Antibody Bevacizumab Chitosan Gellan gum Polymeric nanoparticle |
topic |
Angiogenesis Antibody Bevacizumab Chitosan Gellan gum Polymeric nanoparticle |
description |
Bevacizumab (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. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-04-01 2025-04-29T18:42:36Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.ijbiomac.2024.130272 International Journal of Biological Macromolecules, v. 263. 1879-0003 0141-8130 https://hdl.handle.net/11449/299514 10.1016/j.ijbiomac.2024.130272 2-s2.0-85185409841 |
url |
http://dx.doi.org/10.1016/j.ijbiomac.2024.130272 https://hdl.handle.net/11449/299514 |
identifier_str_mv |
International Journal of Biological Macromolecules, v. 263. 1879-0003 0141-8130 10.1016/j.ijbiomac.2024.130272 2-s2.0-85185409841 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
International Journal of Biological Macromolecules |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834482767321104384 |