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Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I

dc.contributor.authorMazia, Renata Sespede
dc.contributor.authorAraujo Pereira, Raphaela Regina de [UNESP]
dc.contributor.authorBelloto de Francisco, Lizziane Maria
dc.contributor.authorMarcal Natali, Maria Raquel
dc.contributor.authorDias Filho, Benedito Prado
dc.contributor.authorNakamura, Celso Vataru
dc.contributor.authorBruschi, Marcos Luciano
dc.contributor.authorUeda-Nakamura, Tania
dc.contributor.institutionUniversidade Estadual de Maringá (UEM)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-26T15:31:03Z
dc.date.available2018-11-26T15:31:03Z
dc.date.issued2016-01-01
dc.description.abstractThe aim of the present work was to develop a topical delivery system that contains Brazilian green propolis extract (PE-8) to increase efficiency and convenience when applied to herpetic lesions. The cytotoxicity and antiherpetic activity was determined in vitro and in vivo. The PE-8 was added to a system that contained poloxamer 407 and carbopol 934P. The in vitro characterization of the system included rheological studies, texture profile analysis, and mucoadhesion analysis. The PE-8 inhibited the virus during the phase of viral infection, induced virion damage, and exhibited an ability to protect cells from viral infection. The system had advantageous mucoadhesive properties, including a suitable gelation temperature of approximately 25 degrees C for topical delivery, a desirable textural profile, and pseudoplastic behavior. The in vitro release study showed a rapid initial release of the PE-8 in the first 3 h, and the rate of drug release remained constant for up to 24 h. The system appeared to be macroscopically and microscopically innocuous to skin tissue. Therefore, the mucoadhesive thermoresponsive system that contained the PE-8 appears to be promising for increasing bioavailability and achieving prolonged release of the PE-8 when applied to skin lesions caused by herpes simplex virus type 1. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.en
dc.description.affiliationUniv Estadual Maringa, Programa Posgrad Ciencias Farmaceut, Maringa, Parana, Brazil
dc.description.affiliationUniv Estadual Paulista, Programa Posgrad Ciencias Farmaceut, Fac Ciencias Farmaceut Araraquara, Sao Paulo, Brazil
dc.description.affiliationUniv Estadual Maringa, Dept Ciencias Morfol, Maringa, Parana, Brazil
dc.description.affiliationUniv Estadual Maringa, Dept Ciencias Basicas Saude, Maringa, Parana, Brazil
dc.description.affiliationUniv Estadual Maringa, Dept Farm, Maringa, Parana, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Programa Posgrad Ciencias Farmaceut, Fac Ciencias Farmaceut Araraquara, Sao Paulo, Brazil
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundacao Araucaria
dc.description.sponsorshipFINEP
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent113-121
dc.identifierhttp://dx.doi.org/10.1016/j.xphs.2015.11.016
dc.identifier.citationJournal Of Pharmaceutical Sciences. Hoboken: Wiley-blackwell, v. 105, n. 1, p. 113-121, 2016.
dc.identifier.doi10.1016/j.xphs.2015.11.016
dc.identifier.issn0022-3549
dc.identifier.urihttp://hdl.handle.net/11449/159040
dc.identifier.wosWOS:000381768000016
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofJournal Of Pharmaceutical Sciences
dc.relation.ispartofsjr0,984
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectherpes simplex type I
dc.subjectBrazilian green propolis
dc.subjectmucoadhesive
dc.subjectviscoelastic
dc.subjectrheology
dc.titleFormulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type Ien
dc.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0001-5057-3518[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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