You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/129763
Full metadata record
DC FieldValueLanguage
dc.contributor.authorOkuma, Cindy Hana-
dc.contributor.authorAndrade, Thiago Antônio Moretti de-
dc.contributor.authorCaetano, Guilherme Ferreira-
dc.contributor.authorFinci, Lorenzo I.-
dc.contributor.authorMaciel, Naira Rezende-
dc.contributor.authorTopan, José Fernando-
dc.contributor.authorCefali, Letícia Caramori-
dc.contributor.authorPolizello, Ana Cristina Morseli-
dc.contributor.authorCarlo, T.-
dc.contributor.authorRogerio, A. P.-
dc.contributor.authorSpadaro, Augusto Cesar Cropanese-
dc.contributor.authorIsaac, Vera Lucia Borges-
dc.contributor.authorFrade, Marco Andrey Cipriani-
dc.contributor.authorRocha-Filho, Pedro Alves da-
dc.date.accessioned2015-10-22T06:45:31Z-
dc.date.accessioned2016-10-25T21:16:17Z-
dc.date.available2015-10-22T06:45:31Z-
dc.date.available2016-10-25T21:16:17Z-
dc.date.issued2015-04-25-
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/25684193-
dc.identifier.citationEuropean Journal Of Pharmaceutical Sciences. Amsterdam: Elsevier Science Bv, v. 71, p. 62-72, 2015.-
dc.identifier.issn0928-0987-
dc.identifier.urihttp://hdl.handle.net/11449/129763-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/129763-
dc.description.abstractAppropriate therapeutics for wound treatments can be achieved by studying the pathophysiology of tissue repair. Here we develop formulations of lamellar gel phase (LGP) emulsions containing marigold (Calendula officinalis) oil, evaluating their stability and activity on experimental wound healing in rats. LGP emulsions were developed and evaluated based on a phase ternary diagram to select the best LGP emulsion, having a good amount of anisotropic structure and stability. The selected LGP formulation was analyzed according to the intrinsic and accelerated physical stability at different temperatures. In addition, in vitro and in vivo studies were carried out on wound healing rats as a model. The LGP emulsion (15.0% marigold oil; 10.0% of blend surfactants and 75.0% of purified water [w/w/w]) demonstrated good stability and high viscosity, suggesting longer contact of the formulation with the wound. No cytotoxic activity (50-1000 mu g/mL) was observed in marigold oil. In the wound healing rat model, the LGP (15 mg/mL) showed an increase in the leukocyte recruitment to the wound at least on days 2 and 7, but reduced leukocyte recruitment after 14 and 21 days, as compared to the control. Additionally, collagen production was reduced in the LGP emulsion on days 2 and 7 and further accelerated the process of re-epithelialization of the wound itself. The methodology utilized in the present study has produced a potentially useful formulation for a stable LGP emulsion-containing marigold, which was able to improve the wound healing process. (C) 2015 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent62-72-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectCalendula officinalis oilen
dc.subjectLamellar gel phase emulsionen
dc.subjectLiquid crystalen
dc.subjectStability testsen
dc.subjectWound healingen
dc.titleDevelopment of lamellar gel phase emulsion containing marigold oil (Calendula officinalis) as a potential modern wound dressingen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionPeking University-
dc.contributor.institutionHarvard Medical School-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Triângulo Mineiro (UFTM)-
dc.description.affiliationDepartment of Pharmaceutical Sciences, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Brazil-
dc.description.affiliationDivision of Dermatology, Department of Internal Medicine, School of Medicine of Ribeirao Preto, University of Sao Paulo, Brazil-
dc.description.affiliationState Key Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing, China-
dc.description.affiliationDana-Farber Cancer Institute, Harvard Medical School, Boston, USA-
dc.description.affiliationDepartment of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Brazil-
dc.description.affiliationPulmonary and Critical Care Medicine Division, Department of Internal Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA-
dc.description.affiliationFederal University of Triangulo Mineiro, Uberaba, Brazil.-
dc.description.affiliationUnespSchool of Pharmaceutical Sciences of Araraquara, Sao Paulo State University (UNESP), Brazil-
dc.identifier.doihttp://dx.doi.org/10.1016/j.ejps.2015.01.016-
dc.identifier.wosWOS:000351807400007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofEuropean Journal Of Pharmaceutical Sciences-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.