Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol

Detalhes bibliográficos
Autor(a) principal: Prezotti, Fabíola Garavello [UNESP]
Data de Publicação: 2020
Outros Autores: Boni, Fernanda Isadora [UNESP], Ferreira, Natália Noronha [UNESP], Silva, Daniella Souza, Almeida, Andreia, Vasconcelos, Teófilo, Sarmento, Bruno, Gremião, Maria Palmira Daflon [UNESP], Cury, Beatriz Stringhetti Ferreira [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1080/03639045.2020.1716374
http://hdl.handle.net/11449/201495
Resumo: Nanoparticles based on gellan gum/pectin blends were designed for colon-targeted release of resveratrol (RES). Their impact on drug release rates and permeability were evaluated using Caco-2 cell model and mucus secreting triple co-culture model. Polymeric nanoparticles (PNP) were successfully prepared by nebulization/ionotropic gelation, achieving high drug loading (>80%). PNP were spherical with a low positive charge density (+5mV) and exhibited diameters of around 330 nm. Developed PNP were able to promote effective modulation of drug release rates, so that only 3% of RES was released in acidic media over 2 h, and, in pH 6.8, the drug was released in a sustained manner, reaching 85% in 30 h. The permeability of RES-loaded PNP in the Caco-2 model was 0.15%, while in the triple co-culture model, in the presence of mucus, it reached 5.5%. The everted gut sac experiment corroborated the low permeability of RES-loaded PNP in the presence or absence of mucus and highlighted their high ability to interact with the intestinal tissue. Results indicate that the novel PNP developed in this work are safe and promising carriers for controlled delivery of RES at the colon.
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spelling Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrolcaco-2 cellscolon-targeted releaseeverted gut sacin vitro permeabilityPolymeric nanoparticlestriple co-culture modelNanoparticles based on gellan gum/pectin blends were designed for colon-targeted release of resveratrol (RES). Their impact on drug release rates and permeability were evaluated using Caco-2 cell model and mucus secreting triple co-culture model. Polymeric nanoparticles (PNP) were successfully prepared by nebulization/ionotropic gelation, achieving high drug loading (>80%). PNP were spherical with a low positive charge density (+5mV) and exhibited diameters of around 330 nm. Developed PNP were able to promote effective modulation of drug release rates, so that only 3% of RES was released in acidic media over 2 h, and, in pH 6.8, the drug was released in a sustained manner, reaching 85% in 30 h. The permeability of RES-loaded PNP in the Caco-2 model was 0.15%, while in the triple co-culture model, in the presence of mucus, it reached 5.5%. The everted gut sac experiment corroborated the low permeability of RES-loaded PNP in the presence or absence of mucus and highlighted their high ability to interact with the intestinal tissue. Results indicate that the novel PNP developed in this work are safe and promising carriers for controlled delivery of RES at the colon.School of Pharmaceutical Sciences São Paulo State University (UNESP)Chemistry Institute of São Carlos São Paulo University (USP)I3S-Instituto de Investigação e Inovação em Saúde Universidade do PortoINEB-Instituto de Engenharia Biomédica Universidade do PortoCESPU-Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da SaúdeSchool of Pharmaceutical Sciences São Paulo State University (UNESP)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Universidade do PortoCESPU-Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da SaúdePrezotti, Fabíola Garavello [UNESP]Boni, Fernanda Isadora [UNESP]Ferreira, Natália Noronha [UNESP]Silva, Daniella SouzaAlmeida, AndreiaVasconcelos, TeófiloSarmento, BrunoGremião, Maria Palmira Daflon [UNESP]Cury, Beatriz Stringhetti Ferreira [UNESP]2020-12-12T02:34:00Z2020-12-12T02:34:00Z2020-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article236-245http://dx.doi.org/10.1080/03639045.2020.1716374Drug Development and Industrial Pharmacy, v. 46, n. 2, p. 236-245, 2020.1520-57620363-9045http://hdl.handle.net/11449/20149510.1080/03639045.2020.17163742-s2.0-85078402703Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDrug Development and Industrial Pharmacyinfo:eu-repo/semantics/openAccess2024-06-24T13:45:18Zoai:repositorio.unesp.br:11449/201495Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:59:08.768524Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
title Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
spellingShingle Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
Prezotti, Fabíola Garavello [UNESP]
caco-2 cells
colon-targeted release
everted gut sac
in vitro permeability
Polymeric nanoparticles
triple co-culture model
title_short Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
title_full Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
title_fullStr Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
title_full_unstemmed Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
title_sort Oral nanoparticles based on gellan gum/pectin for colon-targeted delivery of resveratrol
author Prezotti, Fabíola Garavello [UNESP]
author_facet Prezotti, Fabíola Garavello [UNESP]
Boni, Fernanda Isadora [UNESP]
Ferreira, Natália Noronha [UNESP]
Silva, Daniella Souza
Almeida, Andreia
Vasconcelos, Teófilo
Sarmento, Bruno
Gremião, Maria Palmira Daflon [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
author_role author
author2 Boni, Fernanda Isadora [UNESP]
Ferreira, Natália Noronha [UNESP]
Silva, Daniella Souza
Almeida, Andreia
Vasconcelos, Teófilo
Sarmento, Bruno
Gremião, Maria Palmira Daflon [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Universidade do Porto
CESPU-Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde
dc.contributor.author.fl_str_mv Prezotti, Fabíola Garavello [UNESP]
Boni, Fernanda Isadora [UNESP]
Ferreira, Natália Noronha [UNESP]
Silva, Daniella Souza
Almeida, Andreia
Vasconcelos, Teófilo
Sarmento, Bruno
Gremião, Maria Palmira Daflon [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
dc.subject.por.fl_str_mv caco-2 cells
colon-targeted release
everted gut sac
in vitro permeability
Polymeric nanoparticles
triple co-culture model
topic caco-2 cells
colon-targeted release
everted gut sac
in vitro permeability
Polymeric nanoparticles
triple co-culture model
description Nanoparticles based on gellan gum/pectin blends were designed for colon-targeted release of resveratrol (RES). Their impact on drug release rates and permeability were evaluated using Caco-2 cell model and mucus secreting triple co-culture model. Polymeric nanoparticles (PNP) were successfully prepared by nebulization/ionotropic gelation, achieving high drug loading (>80%). PNP were spherical with a low positive charge density (+5mV) and exhibited diameters of around 330 nm. Developed PNP were able to promote effective modulation of drug release rates, so that only 3% of RES was released in acidic media over 2 h, and, in pH 6.8, the drug was released in a sustained manner, reaching 85% in 30 h. The permeability of RES-loaded PNP in the Caco-2 model was 0.15%, while in the triple co-culture model, in the presence of mucus, it reached 5.5%. The everted gut sac experiment corroborated the low permeability of RES-loaded PNP in the presence or absence of mucus and highlighted their high ability to interact with the intestinal tissue. Results indicate that the novel PNP developed in this work are safe and promising carriers for controlled delivery of RES at the colon.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T02:34:00Z
2020-12-12T02:34:00Z
2020-02-01
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/10.1080/03639045.2020.1716374
Drug Development and Industrial Pharmacy, v. 46, n. 2, p. 236-245, 2020.
1520-5762
0363-9045
http://hdl.handle.net/11449/201495
10.1080/03639045.2020.1716374
2-s2.0-85078402703
url http://dx.doi.org/10.1080/03639045.2020.1716374
http://hdl.handle.net/11449/201495
identifier_str_mv Drug Development and Industrial Pharmacy, v. 46, n. 2, p. 236-245, 2020.
1520-5762
0363-9045
10.1080/03639045.2020.1716374
2-s2.0-85078402703
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Drug Development and Industrial Pharmacy
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 236-245
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
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