Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation

Bibliographic Details
Main Author: Caetano, Liliana Aranha
Publication Date: 2013
Other Authors: Figueiredo, Lara, Amaral, Rita, Almeida, António José, Gonçalves, Lídia Maria Diogo
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.21/2701
Summary: Attenuated Mycobacterium bovis bacillus Calmette-Guérin (BCG) is the only currently available vaccine against tuberculosis. It is highly effective in pre-exposure immunisation against TB in children when administered by subcutaneous route to newborns. However, it does not provide permanent protection in adults. In this work, polymeric chitosan-alginate microparticles have been evaluated as potential nasal delivery systems and mucosal adjuvants for live attenuated BCG. Chitosan (CS) has been employed as adjuvant and mucosal permeation-enhancer, and, together with alginate (ALG), as additive to enhance BCG-loaded microparticles (MPs) cellular uptake in a human monocyte cell line, by particle surface modification. The most suitable particles were used for vaccine formulation and evaluation of immune response following intranasal immunisation of BALB/c mice.
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spelling Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisationBCGBacillus Calmette-GuérinTuberculosisPolymeric chitosan-alginate microparticlesChitosanMucosal immunisationAttenuated Mycobacterium bovis bacillus Calmette-Guérin (BCG) is the only currently available vaccine against tuberculosis. It is highly effective in pre-exposure immunisation against TB in children when administered by subcutaneous route to newborns. However, it does not provide permanent protection in adults. In this work, polymeric chitosan-alginate microparticles have been evaluated as potential nasal delivery systems and mucosal adjuvants for live attenuated BCG. Chitosan (CS) has been employed as adjuvant and mucosal permeation-enhancer, and, together with alginate (ALG), as additive to enhance BCG-loaded microparticles (MPs) cellular uptake in a human monocyte cell line, by particle surface modification. The most suitable particles were used for vaccine formulation and evaluation of immune response following intranasal immunisation of BALB/c mice.RCIPLCaetano, Liliana AranhaFigueiredo, LaraAmaral, RitaAlmeida, António JoséGonçalves, Lídia Maria Diogo2013-09-24T14:35:49Z2013-042013-04-01T00:00:00Zconference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10400.21/2701enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-12T08:40:29Zoai:repositorio.ipl.pt:10400.21/2701Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:56:59.749540Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
title Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
spellingShingle Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
Caetano, Liliana Aranha
BCG
Bacillus Calmette-Guérin
Tuberculosis
Polymeric chitosan-alginate microparticles
Chitosan
Mucosal immunisation
title_short Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
title_full Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
title_fullStr Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
title_full_unstemmed Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
title_sort Cellular uptake of BCG-loaded chitosan microparticles and in vivo evaluation of immune response following intranasal immunisation
author Caetano, Liliana Aranha
author_facet Caetano, Liliana Aranha
Figueiredo, Lara
Amaral, Rita
Almeida, António José
Gonçalves, Lídia Maria Diogo
author_role author
author2 Figueiredo, Lara
Amaral, Rita
Almeida, António José
Gonçalves, Lídia Maria Diogo
author2_role author
author
author
author
dc.contributor.none.fl_str_mv RCIPL
dc.contributor.author.fl_str_mv Caetano, Liliana Aranha
Figueiredo, Lara
Amaral, Rita
Almeida, António José
Gonçalves, Lídia Maria Diogo
dc.subject.por.fl_str_mv BCG
Bacillus Calmette-Guérin
Tuberculosis
Polymeric chitosan-alginate microparticles
Chitosan
Mucosal immunisation
topic BCG
Bacillus Calmette-Guérin
Tuberculosis
Polymeric chitosan-alginate microparticles
Chitosan
Mucosal immunisation
description Attenuated Mycobacterium bovis bacillus Calmette-Guérin (BCG) is the only currently available vaccine against tuberculosis. It is highly effective in pre-exposure immunisation against TB in children when administered by subcutaneous route to newborns. However, it does not provide permanent protection in adults. In this work, polymeric chitosan-alginate microparticles have been evaluated as potential nasal delivery systems and mucosal adjuvants for live attenuated BCG. Chitosan (CS) has been employed as adjuvant and mucosal permeation-enhancer, and, together with alginate (ALG), as additive to enhance BCG-loaded microparticles (MPs) cellular uptake in a human monocyte cell line, by particle surface modification. The most suitable particles were used for vaccine formulation and evaluation of immune response following intranasal immunisation of BALB/c mice.
publishDate 2013
dc.date.none.fl_str_mv 2013-09-24T14:35:49Z
2013-04
2013-04-01T00:00:00Z
dc.type.driver.fl_str_mv conference object
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url http://hdl.handle.net/10400.21/2701
dc.language.iso.fl_str_mv eng
language eng
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repository.mail.fl_str_mv info@rcaap.pt
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