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

Bibliographic Details
Main Author: Carvalho, Suzana Gonçalves [UNESP]
Publication Date: 2024
Other Authors: 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]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.ijbiomac.2024.130272
https://hdl.handle.net/11449/299514
Summary: 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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spelling 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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