Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Susana
Data de Publicação: 2017
Outros Autores: Alves, Ana D., Cavaco, Joana S., Pontes, Jorge Filipe, Guerreiro, Filipa, Rosa Da Costa, Ana, Buttini, Francesca, Grenha, Ana
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/13031
Resumo: Despite the existence of effective oral therapy, tuberculosis remains a deadly pathology, namely because of bacterial resistance and incompliance with treatments. Establishing alternative therapeutic approaches is urgently needed and inhalable therapy has a great potential in this regard. As pathogenic bacteria are hosted by alveolar macrophages, the co-localisation of antitubercular drugs and pathogens is thus potentiated by this strategy. This work proposes inhalable therapy of pulmonary tuberculosis mediated by a single locust bean gum (LBG) formulation of microparticles associating both isoniazid and rifabutin, complying with requisites of the World Health Organisation of combined therapy. Microparticles were produced by spray-drying, at LBG/INH/RFB mass ratio of 10/1/0.5. The aerodynamic characterisation of microparticles revealed emitted doses of more than 90% and fine particle fraction of 38%, thus indicating the adequacy of the system to reach the respiratory lung area, thus partially the alveolar region. Cytotoxicity results indicate moderate toxicity (cell viability around 60%), with a concentration-dependent effect. Additionally, rat alveolar macrophages evidenced preferential capture of LBG microparticles, possibly due to chemical composition comprising mannose and galactose units that are specifically recognised by macrophage surface receptors. (C) 2017 Elsevier B.V. All rights reserved.
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spelling Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticlesAlveolar macrophagesPhysicochemical propertiesIn-vitroNanoparticlesPowderFormulationsChitosanDesignInhalationDepositionDespite the existence of effective oral therapy, tuberculosis remains a deadly pathology, namely because of bacterial resistance and incompliance with treatments. Establishing alternative therapeutic approaches is urgently needed and inhalable therapy has a great potential in this regard. As pathogenic bacteria are hosted by alveolar macrophages, the co-localisation of antitubercular drugs and pathogens is thus potentiated by this strategy. This work proposes inhalable therapy of pulmonary tuberculosis mediated by a single locust bean gum (LBG) formulation of microparticles associating both isoniazid and rifabutin, complying with requisites of the World Health Organisation of combined therapy. Microparticles were produced by spray-drying, at LBG/INH/RFB mass ratio of 10/1/0.5. The aerodynamic characterisation of microparticles revealed emitted doses of more than 90% and fine particle fraction of 38%, thus indicating the adequacy of the system to reach the respiratory lung area, thus partially the alveolar region. Cytotoxicity results indicate moderate toxicity (cell viability around 60%), with a concentration-dependent effect. Additionally, rat alveolar macrophages evidenced preferential capture of LBG microparticles, possibly due to chemical composition comprising mannose and galactose units that are specifically recognised by macrophage surface receptors. (C) 2017 Elsevier B.V. All rights reserved.National Portuguese funding through FCT - Fundacao para a Ciencia e a Tecnologia [PTDC/DTP-FTO/0094/2012, UID/BIM/04773/2013, UID/Multi/04326/2013, UID/QUI/00100/2013, PEst-OE/QUI/UI4023/2011]ElsevierSapientiaRodrigues, SusanaAlves, Ana D.Cavaco, Joana S.Pontes, Jorge FilipeGuerreiro, FilipaRosa Da Costa, AnaButtini, FrancescaGrenha, Ana2019-11-20T15:07:25Z2017-082017-08-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/13031eng0378-517310.1016/j.ijpharm.2017.06.088info: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:RCAAP2023-07-24T10:25:03Zoai:sapientia.ualg.pt:10400.1/13031Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:04:15.041624Repositório 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 Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
title Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
spellingShingle Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
Rodrigues, Susana
Alveolar macrophages
Physicochemical properties
In-vitro
Nanoparticles
Powder
Formulations
Chitosan
Design
Inhalation
Deposition
title_short Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
title_full Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
title_fullStr Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
title_full_unstemmed Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
title_sort Dual antibiotherapy of tuberculosis mediated by inhalable locust bean gum microparticles
author Rodrigues, Susana
author_facet Rodrigues, Susana
Alves, Ana D.
Cavaco, Joana S.
Pontes, Jorge Filipe
Guerreiro, Filipa
Rosa Da Costa, Ana
Buttini, Francesca
Grenha, Ana
author_role author
author2 Alves, Ana D.
Cavaco, Joana S.
Pontes, Jorge Filipe
Guerreiro, Filipa
Rosa Da Costa, Ana
Buttini, Francesca
Grenha, Ana
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Rodrigues, Susana
Alves, Ana D.
Cavaco, Joana S.
Pontes, Jorge Filipe
Guerreiro, Filipa
Rosa Da Costa, Ana
Buttini, Francesca
Grenha, Ana
dc.subject.por.fl_str_mv Alveolar macrophages
Physicochemical properties
In-vitro
Nanoparticles
Powder
Formulations
Chitosan
Design
Inhalation
Deposition
topic Alveolar macrophages
Physicochemical properties
In-vitro
Nanoparticles
Powder
Formulations
Chitosan
Design
Inhalation
Deposition
description Despite the existence of effective oral therapy, tuberculosis remains a deadly pathology, namely because of bacterial resistance and incompliance with treatments. Establishing alternative therapeutic approaches is urgently needed and inhalable therapy has a great potential in this regard. As pathogenic bacteria are hosted by alveolar macrophages, the co-localisation of antitubercular drugs and pathogens is thus potentiated by this strategy. This work proposes inhalable therapy of pulmonary tuberculosis mediated by a single locust bean gum (LBG) formulation of microparticles associating both isoniazid and rifabutin, complying with requisites of the World Health Organisation of combined therapy. Microparticles were produced by spray-drying, at LBG/INH/RFB mass ratio of 10/1/0.5. The aerodynamic characterisation of microparticles revealed emitted doses of more than 90% and fine particle fraction of 38%, thus indicating the adequacy of the system to reach the respiratory lung area, thus partially the alveolar region. Cytotoxicity results indicate moderate toxicity (cell viability around 60%), with a concentration-dependent effect. Additionally, rat alveolar macrophages evidenced preferential capture of LBG microparticles, possibly due to chemical composition comprising mannose and galactose units that are specifically recognised by macrophage surface receptors. (C) 2017 Elsevier B.V. All rights reserved.
publishDate 2017
dc.date.none.fl_str_mv 2017-08
2017-08-01T00:00:00Z
2019-11-20T15:07:25Z
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/10400.1/13031
url http://hdl.handle.net/10400.1/13031
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0378-5173
10.1016/j.ijpharm.2017.06.088
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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
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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
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