Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/64413 |
Resumo: | The most effective medicines available for the treatment of leishmaniasis, a life-threatening disease, exhibit serious toxicological issues. To achieve better therapeutic efficiency while decreasing toxicity associated with amphotericin B (AmB), water-soluble dextrin-AmB (Dex-AmB) formulations were developed. Self-assembled nanocomplexes were formed by dissolving Dex and AmB in alkaline borate buffer, followed by dialysis and either freeze-drying (FD) or nano spray-drying (SD), yielding water dispersible particles with a diameter of 214nm and 347nm, respectively. The very simple production process allowed the formation of amorphous inclusion complexes containing 14% of AmB in the form of monomers and water-soluble aggregates. Nanocomplexes were effective against parasites in axenic culture (IC50 of 0.056 and 0.096M for L. amazonensis and 0.030 and 0.044M for L. infantum, respectively for Dex-AmB FD and Dex-AmB SD) and in decreasing the intramacrophagic infection with L. infantum (IC50 of 0.017 and 0.023M, respectively for Dex-AmB FD and Dex-AmB SD). Also, the formulations were able to significantly reduce the cytotoxicity of AmB. Overall, this study demonstrates the suitability of dextrin as an AmB carrier and the facile and inexpensive development of a delivery system for the treatment of leishmaniasis. |
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Development of dextrin-amphotericin B formulations for the treatment of LeishmaniasisDextrinAmphotericin BLeishmaniasisScience & TechnologyThe most effective medicines available for the treatment of leishmaniasis, a life-threatening disease, exhibit serious toxicological issues. To achieve better therapeutic efficiency while decreasing toxicity associated with amphotericin B (AmB), water-soluble dextrin-AmB (Dex-AmB) formulations were developed. Self-assembled nanocomplexes were formed by dissolving Dex and AmB in alkaline borate buffer, followed by dialysis and either freeze-drying (FD) or nano spray-drying (SD), yielding water dispersible particles with a diameter of 214nm and 347nm, respectively. The very simple production process allowed the formation of amorphous inclusion complexes containing 14% of AmB in the form of monomers and water-soluble aggregates. Nanocomplexes were effective against parasites in axenic culture (IC50 of 0.056 and 0.096M for L. amazonensis and 0.030 and 0.044M for L. infantum, respectively for Dex-AmB FD and Dex-AmB SD) and in decreasing the intramacrophagic infection with L. infantum (IC50 of 0.017 and 0.023M, respectively for Dex-AmB FD and Dex-AmB SD). Also, the formulations were able to significantly reduce the cytotoxicity of AmB. Overall, this study demonstrates the suitability of dextrin as an AmB carrier and the facile and inexpensive development of a delivery system for the treatment of leishmaniasis.This work was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/ BIO/04469/2019 and BioTecNorte operation (NORTE-01-0145-FEDER000004 - Underpinning Biotechnology to foster the north of Portugal bioeconomy and NORTE-01-0145-FEDER-000012 - Structured program on bioengineered therapies for Infectious diseases and tissue regeneration) funded by the European Regional Development Fund under the scope of Norte2020 - Programa Operacional Regional do Norte. Ricardo Silva-Carvalho gratefully acknowledge FCT for the granted scholarship (SFRH/BD/118880/2016). Karoline Rachel Melo and Moacir Fernandes Queiroz gratefully acknowledge Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brasil for the granted scholarship.info:eu-repo/semantics/publishedVersionElsevierUniversidade do MinhoCarvalho, Ricardo Emanuel SilvaFidalgo, JoaquimMelo, K. RQueiroz, M. F.Leal, Ana Salomé BarbosaRocha, H. A.Cruz, T.Parpot, PierTomás, A. M.Gama, F. M.2020-06-152020-06-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/64413engSilva-Carvalho, Ricardo; Fidalgo, J.; Melo, K. R.; Queiroz, M. F.; Leal, S.; Rocha, H. A.; Cruz, T.; Parpot, Pier; Tomás, A. M.; Gama, F. M., Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis. International Journal of Biological Macromolecules, 153, 276-288, 20200141-81301879-000310.1016/j.ijbiomac.2020.03.01932145228http://www.elsevier.com/locate/issn/01418130info: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:RCAAP2023-07-21T12:28:30Zoai:repositorium.sdum.uminho.pt:1822/64413Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:23:19.770628Repositório 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 |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
title |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
spellingShingle |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis Carvalho, Ricardo Emanuel Silva Dextrin Amphotericin B Leishmaniasis Science & Technology |
title_short |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
title_full |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
title_fullStr |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
title_full_unstemmed |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
title_sort |
Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis |
author |
Carvalho, Ricardo Emanuel Silva |
author_facet |
Carvalho, Ricardo Emanuel Silva Fidalgo, Joaquim Melo, K. R Queiroz, M. F. Leal, Ana Salomé Barbosa Rocha, H. A. Cruz, T. Parpot, Pier Tomás, A. M. Gama, F. M. |
author_role |
author |
author2 |
Fidalgo, Joaquim Melo, K. R Queiroz, M. F. Leal, Ana Salomé Barbosa Rocha, H. A. Cruz, T. Parpot, Pier Tomás, A. M. Gama, F. M. |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Carvalho, Ricardo Emanuel Silva Fidalgo, Joaquim Melo, K. R Queiroz, M. F. Leal, Ana Salomé Barbosa Rocha, H. A. Cruz, T. Parpot, Pier Tomás, A. M. Gama, F. M. |
dc.subject.por.fl_str_mv |
Dextrin Amphotericin B Leishmaniasis Science & Technology |
topic |
Dextrin Amphotericin B Leishmaniasis Science & Technology |
description |
The most effective medicines available for the treatment of leishmaniasis, a life-threatening disease, exhibit serious toxicological issues. To achieve better therapeutic efficiency while decreasing toxicity associated with amphotericin B (AmB), water-soluble dextrin-AmB (Dex-AmB) formulations were developed. Self-assembled nanocomplexes were formed by dissolving Dex and AmB in alkaline borate buffer, followed by dialysis and either freeze-drying (FD) or nano spray-drying (SD), yielding water dispersible particles with a diameter of 214nm and 347nm, respectively. The very simple production process allowed the formation of amorphous inclusion complexes containing 14% of AmB in the form of monomers and water-soluble aggregates. Nanocomplexes were effective against parasites in axenic culture (IC50 of 0.056 and 0.096M for L. amazonensis and 0.030 and 0.044M for L. infantum, respectively for Dex-AmB FD and Dex-AmB SD) and in decreasing the intramacrophagic infection with L. infantum (IC50 of 0.017 and 0.023M, respectively for Dex-AmB FD and Dex-AmB SD). Also, the formulations were able to significantly reduce the cytotoxicity of AmB. Overall, this study demonstrates the suitability of dextrin as an AmB carrier and the facile and inexpensive development of a delivery system for the treatment of leishmaniasis. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-06-15 2020-06-15T00:00:00Z |
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/1822/64413 |
url |
http://hdl.handle.net/1822/64413 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Silva-Carvalho, Ricardo; Fidalgo, J.; Melo, K. R.; Queiroz, M. F.; Leal, S.; Rocha, H. A.; Cruz, T.; Parpot, Pier; Tomás, A. M.; Gama, F. M., Development of dextrin-amphotericin B formulations for the treatment of Leishmaniasis. International Journal of Biological Macromolecules, 153, 276-288, 2020 0141-8130 1879-0003 10.1016/j.ijbiomac.2020.03.019 32145228 http://www.elsevier.com/locate/issn/01418130 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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