Antifungal nanofibers made by controlled release of sea animal derived peptide.

Detalhes bibliográficos
Autor(a) principal: VIANA, J. F. C.
Data de Publicação: 2015
Outros Autores: CARRIJO, J., FREITAS, C. G., PAUL, A., ALCARAZ, J., LACORTE, C. C., MIGLIOLO, L., ANDRADE, C. A., FALCAO, R., SANTOS, N. C., GONÇALVES, S., OTERO-GONZÁLES, A. J., KHADEMHOSSEINI, A., DIAS, S. C., FRANCO, O. L.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1026638
Resumo: Candida albicans is a common human-pathogenic fungal species with the ability to cause several diseases including surface infections. Despite the clear difficulties of Candida control, antimicrobial peptides (AMPs) have emerged as an alternative strategy for fungal control. In this report, different concentrations of antifungal Cm-p1 (Cencritchis muricatus peptide 1) were electrospun into nanofibers for drug delivery. The nanofibers were characterized by mass spectrometry confirming the presence of the peptide on the scaffold. Atomic force microscopy and scanning electronic microscopy were used to measure the diameters, showing that Cm-p1 affects fiber morphology as well as the diameter and scaffold thickness. The Cm-p1 release behavior from the nanofibers demonstrated peptide release from 30 min to three days, leading to effective yeast control in the first 24 hours. Moreover, the biocompatibility of the fibers were evaluated through a MTS assay as well as ROS production by using a HUVEC model, showing that the fibers do not affect cell viability and only nanofibers containing 10% Cm-p1?PVA improved ROS generation. In addition, the secretion of pro-inflammatory cytokines IL-6 and TNF-? by the HUVECs was also slightly modified by the 10% Cm-p1?PVA nanofibers. In conclusion, the electrospinning technique applied here allowed for the manufacture of biodegradable biomimetic nanofibrous extracellular membranes with the ability to control fungal infection.
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spelling Antifungal nanofibers made by controlled release of sea animal derived peptide.FungosControle de fungosNanofibrasCândida AlbicansCandida albicans is a common human-pathogenic fungal species with the ability to cause several diseases including surface infections. Despite the clear difficulties of Candida control, antimicrobial peptides (AMPs) have emerged as an alternative strategy for fungal control. In this report, different concentrations of antifungal Cm-p1 (Cencritchis muricatus peptide 1) were electrospun into nanofibers for drug delivery. The nanofibers were characterized by mass spectrometry confirming the presence of the peptide on the scaffold. Atomic force microscopy and scanning electronic microscopy were used to measure the diameters, showing that Cm-p1 affects fiber morphology as well as the diameter and scaffold thickness. The Cm-p1 release behavior from the nanofibers demonstrated peptide release from 30 min to three days, leading to effective yeast control in the first 24 hours. Moreover, the biocompatibility of the fibers were evaluated through a MTS assay as well as ROS production by using a HUVEC model, showing that the fibers do not affect cell viability and only nanofibers containing 10% Cm-p1?PVA improved ROS generation. In addition, the secretion of pro-inflammatory cytokines IL-6 and TNF-? by the HUVECs was also slightly modified by the 10% Cm-p1?PVA nanofibers. In conclusion, the electrospinning technique applied here allowed for the manufacture of biodegradable biomimetic nanofibrous extracellular membranes with the ability to control fungal infection.Juliane F. C. Viana, UnB; Jéssica Carrijo, UCB; Camila G. Freitas, UCB; Arghya Paul, Massachusetts Institute of Technology, Cambridge, USA; Jarib Alcaraz, Universidade Federal de Pernambuco; CRISTIANO CASTRO LACORTE, CENARGEN; Ludovico Migliolo, UCB; César A. Andrade, Universidade Federal de Pernambuco; ROSANA FALCAO, CENARGEN; Nuno C. Santos, Universidade de Lisboa; Sónia Gonçalves, Universidade de Lisboa; Anselmo J. Otero-González, Universidad de La Habana; Ali Khademhosseini, Massachusetts Institute of Technology, Cambridge, USA; Simoni C. Dias, UCB; Octávio L. Franco, UnB.VIANA, J. F. C.CARRIJO, J.FREITAS, C. G.PAUL, A.ALCARAZ, J.LACORTE, C. C.MIGLIOLO, L.ANDRADE, C. A.FALCAO, R.SANTOS, N. C.GONÇALVES, S.OTERO-GONZÁLES, A. J.KHADEMHOSSEINI, A.DIAS, S. C.FRANCO, O. L.2018-07-19T01:02:56Z2018-07-19T01:02:56Z2015-10-1620152018-07-19T01:02:56Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleNanoscale, v. 7, p. 6238-6246, 2015.http://www.alice.cnptia.embrapa.br/alice/handle/doc/1026638porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2018-07-19T01:03:03Zoai:www.alice.cnptia.embrapa.br:doc/1026638Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542018-07-19T01:03:03falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542018-07-19T01:03:03Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv Antifungal nanofibers made by controlled release of sea animal derived peptide.
title Antifungal nanofibers made by controlled release of sea animal derived peptide.
spellingShingle Antifungal nanofibers made by controlled release of sea animal derived peptide.
VIANA, J. F. C.
Fungos
Controle de fungos
Nanofibras
Cândida Albicans
title_short Antifungal nanofibers made by controlled release of sea animal derived peptide.
title_full Antifungal nanofibers made by controlled release of sea animal derived peptide.
title_fullStr Antifungal nanofibers made by controlled release of sea animal derived peptide.
title_full_unstemmed Antifungal nanofibers made by controlled release of sea animal derived peptide.
title_sort Antifungal nanofibers made by controlled release of sea animal derived peptide.
author VIANA, J. F. C.
author_facet VIANA, J. F. C.
CARRIJO, J.
FREITAS, C. G.
PAUL, A.
ALCARAZ, J.
LACORTE, C. C.
MIGLIOLO, L.
ANDRADE, C. A.
FALCAO, R.
SANTOS, N. C.
GONÇALVES, S.
OTERO-GONZÁLES, A. J.
KHADEMHOSSEINI, A.
DIAS, S. C.
FRANCO, O. L.
author_role author
author2 CARRIJO, J.
FREITAS, C. G.
PAUL, A.
ALCARAZ, J.
LACORTE, C. C.
MIGLIOLO, L.
ANDRADE, C. A.
FALCAO, R.
SANTOS, N. C.
GONÇALVES, S.
OTERO-GONZÁLES, A. J.
KHADEMHOSSEINI, A.
DIAS, S. C.
FRANCO, O. L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Juliane F. C. Viana, UnB; Jéssica Carrijo, UCB; Camila G. Freitas, UCB; Arghya Paul, Massachusetts Institute of Technology, Cambridge, USA; Jarib Alcaraz, Universidade Federal de Pernambuco; CRISTIANO CASTRO LACORTE, CENARGEN; Ludovico Migliolo, UCB; César A. Andrade, Universidade Federal de Pernambuco; ROSANA FALCAO, CENARGEN; Nuno C. Santos, Universidade de Lisboa; Sónia Gonçalves, Universidade de Lisboa; Anselmo J. Otero-González, Universidad de La Habana; Ali Khademhosseini, Massachusetts Institute of Technology, Cambridge, USA; Simoni C. Dias, UCB; Octávio L. Franco, UnB.
dc.contributor.author.fl_str_mv VIANA, J. F. C.
CARRIJO, J.
FREITAS, C. G.
PAUL, A.
ALCARAZ, J.
LACORTE, C. C.
MIGLIOLO, L.
ANDRADE, C. A.
FALCAO, R.
SANTOS, N. C.
GONÇALVES, S.
OTERO-GONZÁLES, A. J.
KHADEMHOSSEINI, A.
DIAS, S. C.
FRANCO, O. L.
dc.subject.por.fl_str_mv Fungos
Controle de fungos
Nanofibras
Cândida Albicans
topic Fungos
Controle de fungos
Nanofibras
Cândida Albicans
description Candida albicans is a common human-pathogenic fungal species with the ability to cause several diseases including surface infections. Despite the clear difficulties of Candida control, antimicrobial peptides (AMPs) have emerged as an alternative strategy for fungal control. In this report, different concentrations of antifungal Cm-p1 (Cencritchis muricatus peptide 1) were electrospun into nanofibers for drug delivery. The nanofibers were characterized by mass spectrometry confirming the presence of the peptide on the scaffold. Atomic force microscopy and scanning electronic microscopy were used to measure the diameters, showing that Cm-p1 affects fiber morphology as well as the diameter and scaffold thickness. The Cm-p1 release behavior from the nanofibers demonstrated peptide release from 30 min to three days, leading to effective yeast control in the first 24 hours. Moreover, the biocompatibility of the fibers were evaluated through a MTS assay as well as ROS production by using a HUVEC model, showing that the fibers do not affect cell viability and only nanofibers containing 10% Cm-p1?PVA improved ROS generation. In addition, the secretion of pro-inflammatory cytokines IL-6 and TNF-? by the HUVECs was also slightly modified by the 10% Cm-p1?PVA nanofibers. In conclusion, the electrospinning technique applied here allowed for the manufacture of biodegradable biomimetic nanofibrous extracellular membranes with the ability to control fungal infection.
publishDate 2015
dc.date.none.fl_str_mv 2015-10-16
2015
2018-07-19T01:02:56Z
2018-07-19T01:02:56Z
2018-07-19T01:02:56Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Nanoscale, v. 7, p. 6238-6246, 2015.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/1026638
identifier_str_mv Nanoscale, v. 7, p. 6238-6246, 2015.
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1026638
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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reponame_str Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
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repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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