Antifungal nanofibers made by controlled release of sea animal derived peptide.
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , , , , , , |
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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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) instacron:EMBRAPA |
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Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
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EMBRAPA |
institution |
EMBRAPA |
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Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
collection |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
repository.name.fl_str_mv |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
repository.mail.fl_str_mv |
cg-riaa@embrapa.br |
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1794503459092824064 |