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Topical nitric oxide releasing nanoparticles are effective in a murine model of dermal Trichophyton rubrum dermatophytosis

dc.contributor.authorMordorski, Breanne
dc.contributor.authorCosta-Orlandi, Caroline Barcelos [UNESP]
dc.contributor.authorBaltazar, Ludmila M.
dc.contributor.authorCarreño, Leandro J.
dc.contributor.authorLandriscina, Angelo
dc.contributor.authorRosen, Jamie
dc.contributor.authorNavati, Mahantesh
dc.contributor.authorMendes-Giannini, Maria Jose Soares [UNESP]
dc.contributor.authorFriedman, Joel M.
dc.contributor.authorNosanchuk, Joshua D.
dc.contributor.authorFriedman, Adam J.
dc.contributor.institutionAlbert Einstein College of Medicine
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidad de Chile
dc.contributor.institutionGeorge Washington School of Medicine and Health Sciences
dc.date.accessioned2018-12-11T17:13:42Z
dc.date.available2018-12-11T17:13:42Z
dc.date.issued2017-10-01
dc.description.abstractSystemic therapies are preferred for treating dermal dermatophytosis due to inadequate penetration of topical agents. However, systemic antifungals are associated with off-target effects and limited tissue penetration, and antimicrobial resistance is a growing concern. To address this, we investigated topical nitric oxide-releasing nanoparticles (NO-np), which have been used against superficial fungal infections and bacterial abscesses. In addition to enhanced penetration and permeation conferred by nanoparticles, nitric oxide, a broad-spectrum multi-mechanistic antimicrobial agent, offers decreased likelihood of resistance development. In the current study, NO-np inhibited Trichophyton rubrum in vitro, as well as in a murine model of dermal dermatophytosis. In mice, NO-np reduced fungal burden after three days, with complete clearance after seven. Furthermore, NO-np decreased tissue IL-2, 6, 10 and TNFα, indicating earlier attenuation of the host inflammatory response and decreased tissue morbidity. Thus, topical NO-np represent an attractive alternative to systemic therapy against dermal T. rubrum infection.en
dc.description.affiliationDepartment of Medicine (Division of Dermatology) Albert Einstein College of Medicine
dc.description.affiliationDepartment of Medicine (Division of Infectious Diseases) Albert Einstein College of Medicine
dc.description.affiliationDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista (UNESP)
dc.description.affiliationDepartment of Microbiology & Immunology Albert Einstein College of Medicine
dc.description.affiliationMillennium Institute on Immunology and Immunotherapy Programa de Inmunología Instituto de Ciencias Biomédicas Facultad de Medicina Universidad de Chile
dc.description.affiliationDepartment of Physiology & Biophysics Albert Einstein College of Medicine
dc.description.affiliationDepartment of Dermatology George Washington School of Medicine and Health Sciences
dc.description.affiliationUnespDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista (UNESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdCNPq: 150261/2016-0
dc.description.sponsorshipIdCAPES: 99999.007910/2014-02
dc.format.extent2267-2270
dc.identifierhttp://dx.doi.org/10.1016/j.nano.2017.06.018
dc.identifier.citationNanomedicine: Nanotechnology, Biology, and Medicine, v. 13, n. 7, p. 2267-2270, 2017.
dc.identifier.doi10.1016/j.nano.2017.06.018
dc.identifier.file2-s2.0-85026456792.pdf
dc.identifier.issn1549-9642
dc.identifier.issn1549-9634
dc.identifier.scopus2-s2.0-85026456792
dc.identifier.urihttp://hdl.handle.net/11449/174977
dc.language.isoeng
dc.relation.ispartofNanomedicine: Nanotechnology, Biology, and Medicine
dc.relation.ispartofsjr1,743
dc.relation.ispartofsjr1,743
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.titleTopical nitric oxide releasing nanoparticles are effective in a murine model of dermal Trichophyton rubrum dermatophytosisen
dc.typeArtigo
unesp.departmentAnálises Clínicas - FCFpt

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