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dc.contributor.authorClemente-Napimoga, Juliana T.-
dc.contributor.authorMoreira, Juscelaine A.-
dc.contributor.authorGrillo, Renato-
dc.contributor.authorde Melo, Nathalie F. S.-
dc.contributor.authorFraceto, Leonardo F.-
dc.contributor.authorNapimoga, Marcelo H.-
dc.date.accessioned2014-05-20T15:34:47Z-
dc.date.accessioned2016-10-25T18:11:08Z-
dc.date.available2014-05-20T15:34:47Z-
dc.date.available2016-10-25T18:11:08Z-
dc.date.issued2012-06-14-
dc.identifierhttp://dx.doi.org/10.1016/j.lfs.2012.04.035-
dc.identifier.citationLife Sciences. Oxford: Pergamon-Elsevier B.V. Ltd, v. 90, n. 23-24, p. 944-949, 2012.-
dc.identifier.issn0024-3205-
dc.identifier.urihttp://hdl.handle.net/11449/42646-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/42646-
dc.description.abstractAims: To verify whether the nanoencapsulation of 15d-PGJ(2) in poly(D,L-lactide-co-glycolide) (PLGA) nanocapsules (15d-PGJ(2)-NC) might potentialize its antinociceptive activity into rats' temporomandibular joint (TMJ).Main methods: Transmission electron microscopy (TEM) and atomic force microscopy (AFM) were used to evaluate the morphology and suspension of the PLGA nanocapsules. Rats were pretreated (15 min) with an intra-TMJ injection of unloaded 15d-PGJ(2) or 15d-PGJ(2)-NC at concentrations of 10, 100 or 1000 pg followed by an ipsilateral intra-TMJ injection of 1.5% formalin. The nociceptive behavioral response was observed during 45 min: animals were then sacrificed and the periarticular tissue was removed for IL-1 beta measurements.Key finding: TEM and AFM analyses showed that 15d-PGJ(2)-NC is spherical without any aggregates or adhesion confirming that this formulation is a good drug carrier system for 15d-PGJ(2). Pretreatment with 15d-PGJ(2)-NC (100 and 1000 pg/TMJ), but not unloaded 15d-PGJ(2), was found to significantly decrease the release of IL-1 beta cytokine and the animals' nociceptive behavioral response induced by intra-TMJ injection of formalin.Significance: The compound 15d-PGJ(2)-NC might be used as a potential antinociceptive and anti-inflammatory agent to treat temporomandibular disorders in clinical practice. (c) 2012 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent944-949-
dc.language.isoeng-
dc.publisherPergamon-Elsevier B.V. Ltd-
dc.sourceWeb of Science-
dc.subject15d-PGJ2en
dc.subjectPPAR-gammaen
dc.subjectNociceptionen
dc.subjectTemporomandibular jointen
dc.subjectInflammationen
dc.title15d-PGJ2-loaded in nanocapsules enhance the antinociceptive properties into rat temporomandibular hypernociceptionen
dc.typeoutro-
dc.contributor.institutionSao Leopoldo Mand Inst & Res Ctr-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniv Uberaba-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSao Leopoldo Mand Inst & Res Ctr, Lab Immunol & Mol Biol, BR-13045755 Campinas, SP, Brazil-
dc.description.affiliationUniv Estadual Campinas, Piracicaba Dent Sch, Dept Physiol, Lab Orofacial Pain, Campinas, SP, Brazil-
dc.description.affiliationUniv Uberaba, Lab Biopathol & Mol Biol, Uberaba, MG, Brazil-
dc.description.affiliationUniv Estadual Campinas, Dept Biochem, Campinas, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Environm Engn, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Environm Engn, São Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 10/15014-9-
dc.description.sponsorshipIdCNPq: 303080/2010-8-
dc.identifier.doi10.1016/j.lfs.2012.04.035-
dc.identifier.wosWOS:000305546800010-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000305546800010.pdf-
dc.relation.ispartofLife Sciences-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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