Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity

Detalhes bibliográficos
Autor(a) principal: Reis, Catarina Pinto
Data de Publicação: 2007
Outros Autores: Ribeiro, António J., Houng, Simone, Veiga, Francisco, Neufeld, Ronald J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5859
https://doi.org/10.1016/j.ejps.2006.12.007
Resumo: Insulin-loaded alginate-dextran nanospheres were prepared by nanoemulsion dispersion followed by triggered in situ gelation. Nanospheres were characterized for mean size and distribution by laser diffraction spectroscopy and for shape by transmission electron microscopy. Insulin encapsulation efficiency and in vitro release were determined by Bradford protein assay and bioactivity determined in vitro using a newly developed Western blot immunoassay and in vivo using Wistar diabetic rats. Nanospheres ranged from 267 nm to 2.76 [mu]m in diameter and demonstrated a unimodal size distribution. Insulin encapsulation efficiency was 82.5%. Alginate-dextran particles suppressed insulin release in acidic media and promoted a sustained release at near neutral conditions. Nanoencapsulated insulin was bioactive, demonstrated through both in vivo and in vitro bioassays
id RCAP_ee1d9590ea4f8634d4f41c428bd675e0
oai_identifier_str oai:estudogeral.uc.pt:10316/5859
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivityAlginate-dextran nanospheresNanospheresInsulin bioactivityInsulin-loaded alginate-dextran nanospheres were prepared by nanoemulsion dispersion followed by triggered in situ gelation. Nanospheres were characterized for mean size and distribution by laser diffraction spectroscopy and for shape by transmission electron microscopy. Insulin encapsulation efficiency and in vitro release were determined by Bradford protein assay and bioactivity determined in vitro using a newly developed Western blot immunoassay and in vivo using Wistar diabetic rats. Nanospheres ranged from 267 nm to 2.76 [mu]m in diameter and demonstrated a unimodal size distribution. Insulin encapsulation efficiency was 82.5%. Alginate-dextran particles suppressed insulin release in acidic media and promoted a sustained release at near neutral conditions. Nanoencapsulated insulin was bioactive, demonstrated through both in vivo and in vitro bioassayshttp://www.sciencedirect.com/science/article/B6T25-4MTC6GD-1/1/c26097e450ad242243e8df9feae8643f2007info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5859http://hdl.handle.net/10316/5859https://doi.org/10.1016/j.ejps.2006.12.007engEuropean Journal of Pharmaceutical Sciences. 30:5 (2007) 392-397Reis, Catarina PintoRibeiro, António J.Houng, SimoneVeiga, FranciscoNeufeld, Ronald J.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-11-06T16:49:01Zoai:estudogeral.uc.pt:10316/5859Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:47:19.772096Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
title Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
spellingShingle Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
Reis, Catarina Pinto
Alginate-dextran nanospheres
Nanospheres
Insulin bioactivity
title_short Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
title_full Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
title_fullStr Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
title_full_unstemmed Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
title_sort Nanoparticulate delivery system for insulin: Design, characterization and in vitro/in vivo bioactivity
author Reis, Catarina Pinto
author_facet Reis, Catarina Pinto
Ribeiro, António J.
Houng, Simone
Veiga, Francisco
Neufeld, Ronald J.
author_role author
author2 Ribeiro, António J.
Houng, Simone
Veiga, Francisco
Neufeld, Ronald J.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Reis, Catarina Pinto
Ribeiro, António J.
Houng, Simone
Veiga, Francisco
Neufeld, Ronald J.
dc.subject.por.fl_str_mv Alginate-dextran nanospheres
Nanospheres
Insulin bioactivity
topic Alginate-dextran nanospheres
Nanospheres
Insulin bioactivity
description Insulin-loaded alginate-dextran nanospheres were prepared by nanoemulsion dispersion followed by triggered in situ gelation. Nanospheres were characterized for mean size and distribution by laser diffraction spectroscopy and for shape by transmission electron microscopy. Insulin encapsulation efficiency and in vitro release were determined by Bradford protein assay and bioactivity determined in vitro using a newly developed Western blot immunoassay and in vivo using Wistar diabetic rats. Nanospheres ranged from 267 nm to 2.76 [mu]m in diameter and demonstrated a unimodal size distribution. Insulin encapsulation efficiency was 82.5%. Alginate-dextran particles suppressed insulin release in acidic media and promoted a sustained release at near neutral conditions. Nanoencapsulated insulin was bioactive, demonstrated through both in vivo and in vitro bioassays
publishDate 2007
dc.date.none.fl_str_mv 2007
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://hdl.handle.net/10316/5859
http://hdl.handle.net/10316/5859
https://doi.org/10.1016/j.ejps.2006.12.007
url http://hdl.handle.net/10316/5859
https://doi.org/10.1016/j.ejps.2006.12.007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv European Journal of Pharmaceutical Sciences. 30:5 (2007) 392-397
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv aplication/PDF
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799133750586507264