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Development of lamellar gel phase emulsion containing marigold oil (Calendula officinalis) as a potential modern wound dressing

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 [UNESP]
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 [UNESP]
dc.contributor.authorFrade, Marco Andrey Cipriani
dc.contributor.authorRocha-Filho, Pedro Alves da
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.date.accessioned2015-10-22T06:45:31Z
dc.date.available2015-10-22T06:45:31Z
dc.date.issued2015-04-25
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.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.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.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.doi10.1016/j.ejps.2015.01.016
dc.identifier.issn0928-0987
dc.identifier.lattes4842462513285606
dc.identifier.urihttp://hdl.handle.net/11449/129763
dc.identifier.wosWOS:000351807400007
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofEuropean Journal Of Pharmaceutical Sciences
dc.relation.ispartofjcr3.466
dc.relation.ispartofsjr1,016
dc.rights.accessRightsAcesso restritopt
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.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes4842462513285606
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt

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