Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1016/j.xphs.2018.11.038 |
Texto Completo: | http://dx.doi.org/10.1016/j.xphs.2018.11.038 http://hdl.handle.net/11449/187268 |
Resumo: | Alginate-based polyelectrolyte complexes (PECs) and hydrogel were engineered as platforms for local bevacizumab (BVZ) therapy. This study provides deep comprehension on the microstructures of such systems, and their correlation with drug-release patterns. PECs and hydrogel were characterized using Fourier transform infrared spectroscopy, small-angle X-ray scattering, scanning electron microscopy, atomic force microscopy, and porosimetry. Structural investigations indicated that PECs are formed by supramolecular interactions, resulting in physically cross-linked polymer networks, whereas the BVZ-loaded hydrogel has a more compact and rigid structure, promoting better entrapment of BVZ. PECs and hydrogel were able to control the BVZ release for 4 and 8 days, respectively. Their release profiles correlated best with the Higuchi and Korsmeyer-Peppas models, respectively, indicating drug diffusion as the limiting step for drug release. Furthermore, BVZ remained biologically active in vitro after its incorporation into the hydrogel system. Together, these studies confirm that PECs and hydrogel exhibit different porous structures and physicochemical properties, making them promising platforms that allow the modulation of BVZ release meeting different requirements. |
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Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Propertiesalginate hydrogelbevacizumab-alginate polyelectrolyte complexessupramolecular interactionssustained releasesystem microstructureAlginate-based polyelectrolyte complexes (PECs) and hydrogel were engineered as platforms for local bevacizumab (BVZ) therapy. This study provides deep comprehension on the microstructures of such systems, and their correlation with drug-release patterns. PECs and hydrogel were characterized using Fourier transform infrared spectroscopy, small-angle X-ray scattering, scanning electron microscopy, atomic force microscopy, and porosimetry. Structural investigations indicated that PECs are formed by supramolecular interactions, resulting in physically cross-linked polymer networks, whereas the BVZ-loaded hydrogel has a more compact and rigid structure, promoting better entrapment of BVZ. PECs and hydrogel were able to control the BVZ release for 4 and 8 days, respectively. Their release profiles correlated best with the Higuchi and Korsmeyer-Peppas models, respectively, indicating drug diffusion as the limiting step for drug release. Furthermore, BVZ remained biologically active in vitro after its incorporation into the hydrogel system. Together, these studies confirm that PECs and hydrogel exhibit different porous structures and physicochemical properties, making them promising platforms that allow the modulation of BVZ release meeting different requirements.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundació Catalana de TrasplantamentEuropean Regional Development FundFaculdade de Ciências Farmacêuticas Universidade Estadual Paulista (UNESP), Araraquara, Rodovia Araraquara–Jaú km 1I3S–Instituto de Investigação e Inovação em Saúde Universidade do Porto, Rua Alfredo Allen, 208INEB–Instituto de Engenharia Biomédica Universidade do Porto, Rua Alfredo Allen, 208CESPU–Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde, Rua Central de Gandra 1317ICBAS–Instituto Ciências Biomédicas Abel Salazar Universidade do Porto, Rua de Jorge Viterbo Ferreira 228Instituto de Química Universidade Estadual Paulista (UNESP), Araraquara, Rua Professor Francisco Degni, 55Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista (UNESP), Araraquara, Rodovia Araraquara–Jaú km 1Instituto de Química Universidade Estadual Paulista (UNESP), Araraquara, Rua Professor Francisco Degni, 55Universidade Estadual Paulista (Unesp)Universidade do PortoCESPU–Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da SaúdeFerreira, Natália Noronha [UNESP]Caetano, Bruno Leonardo [UNESP]Boni, Fernanda Isadora [UNESP]Sousa, FláviaMagnani, Marina [UNESP]Sarmento, BrunoFerreira Cury, Beatriz Stringhetti [UNESP]Daflon Gremião, Maria Palmira [UNESP]2019-10-06T15:30:57Z2019-10-06T15:30:57Z2019-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1559-1568http://dx.doi.org/10.1016/j.xphs.2018.11.038Journal of Pharmaceutical Sciences, v. 108, n. 4, p. 1559-1568, 2019.1520-60170022-3549http://hdl.handle.net/11449/18726810.1016/j.xphs.2018.11.0382-s2.0-85059962231Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Pharmaceutical Sciencesinfo:eu-repo/semantics/openAccess2021-10-22T21:15:56Zoai:repositorio.unesp.br:11449/187268Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:12:47.077018Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
title |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
spellingShingle |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties Ferreira, Natália Noronha [UNESP] alginate hydrogel bevacizumab-alginate polyelectrolyte complexes supramolecular interactions sustained release system microstructure Ferreira, Natália Noronha [UNESP] alginate hydrogel bevacizumab-alginate polyelectrolyte complexes supramolecular interactions sustained release system microstructure |
title_short |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
title_full |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
title_fullStr |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
title_full_unstemmed |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
title_sort |
Alginate-Based Delivery Systems for Bevacizumab Local Therapy: In Vitro Structural Features and Release Properties |
author |
Ferreira, Natália Noronha [UNESP] |
author_facet |
Ferreira, Natália Noronha [UNESP] Ferreira, Natália Noronha [UNESP] Caetano, Bruno Leonardo [UNESP] Boni, Fernanda Isadora [UNESP] Sousa, Flávia Magnani, Marina [UNESP] Sarmento, Bruno Ferreira Cury, Beatriz Stringhetti [UNESP] Daflon Gremião, Maria Palmira [UNESP] Caetano, Bruno Leonardo [UNESP] Boni, Fernanda Isadora [UNESP] Sousa, Flávia Magnani, Marina [UNESP] Sarmento, Bruno Ferreira Cury, Beatriz Stringhetti [UNESP] Daflon Gremião, Maria Palmira [UNESP] |
author_role |
author |
author2 |
Caetano, Bruno Leonardo [UNESP] Boni, Fernanda Isadora [UNESP] Sousa, Flávia Magnani, Marina [UNESP] Sarmento, Bruno Ferreira Cury, Beatriz Stringhetti [UNESP] Daflon Gremião, Maria Palmira [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade do Porto CESPU–Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde |
dc.contributor.author.fl_str_mv |
Ferreira, Natália Noronha [UNESP] Caetano, Bruno Leonardo [UNESP] Boni, Fernanda Isadora [UNESP] Sousa, Flávia Magnani, Marina [UNESP] Sarmento, Bruno Ferreira Cury, Beatriz Stringhetti [UNESP] Daflon Gremião, Maria Palmira [UNESP] |
dc.subject.por.fl_str_mv |
alginate hydrogel bevacizumab-alginate polyelectrolyte complexes supramolecular interactions sustained release system microstructure |
topic |
alginate hydrogel bevacizumab-alginate polyelectrolyte complexes supramolecular interactions sustained release system microstructure |
description |
Alginate-based polyelectrolyte complexes (PECs) and hydrogel were engineered as platforms for local bevacizumab (BVZ) therapy. This study provides deep comprehension on the microstructures of such systems, and their correlation with drug-release patterns. PECs and hydrogel were characterized using Fourier transform infrared spectroscopy, small-angle X-ray scattering, scanning electron microscopy, atomic force microscopy, and porosimetry. Structural investigations indicated that PECs are formed by supramolecular interactions, resulting in physically cross-linked polymer networks, whereas the BVZ-loaded hydrogel has a more compact and rigid structure, promoting better entrapment of BVZ. PECs and hydrogel were able to control the BVZ release for 4 and 8 days, respectively. Their release profiles correlated best with the Higuchi and Korsmeyer-Peppas models, respectively, indicating drug diffusion as the limiting step for drug release. Furthermore, BVZ remained biologically active in vitro after its incorporation into the hydrogel system. Together, these studies confirm that PECs and hydrogel exhibit different porous structures and physicochemical properties, making them promising platforms that allow the modulation of BVZ release meeting different requirements. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-06T15:30:57Z 2019-10-06T15:30:57Z 2019-04-01 |
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.xphs.2018.11.038 Journal of Pharmaceutical Sciences, v. 108, n. 4, p. 1559-1568, 2019. 1520-6017 0022-3549 http://hdl.handle.net/11449/187268 10.1016/j.xphs.2018.11.038 2-s2.0-85059962231 |
url |
http://dx.doi.org/10.1016/j.xphs.2018.11.038 http://hdl.handle.net/11449/187268 |
identifier_str_mv |
Journal of Pharmaceutical Sciences, v. 108, n. 4, p. 1559-1568, 2019. 1520-6017 0022-3549 10.1016/j.xphs.2018.11.038 2-s2.0-85059962231 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Pharmaceutical Sciences |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1559-1568 |
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 |
|
_version_ |
1822182246857048064 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.xphs.2018.11.038 |