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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/65722
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dc.contributor.authorLeonardo, M. R.-
dc.contributor.authorTanomaru Filho, Mario-
dc.contributor.authorSilva, L. A B-
dc.contributor.authorNelson Filho, P.-
dc.contributor.authorBonifácio, K. C.-
dc.contributor.authorIto, I. Y.-
dc.date.accessioned2014-05-27T11:19:42Z-
dc.date.accessioned2016-10-25T18:15:36Z-
dc.date.available2014-05-27T11:19:42Z-
dc.date.available2016-10-25T18:15:36Z-
dc.date.issued1999-03-01-
dc.identifierhttp://dx.doi.org/10.1016/S0099-2399(99)80135-6-
dc.identifier.citationJournal of Endodontics, v. 25, n. 3, p. 167-171, 1999.-
dc.identifier.issn0099-2399-
dc.identifier.urihttp://hdl.handle.net/11449/65722-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/65722-
dc.description.abstractThe aim of the present study was to evaluate the in vivo antimicrobial activity of 2% chlorhexidine gluconate (FCFRP-USP) used as a root canal irrigating solution in teeth with pulp necrosis and radiographically visible chronic periapical reactions. Culture techniques and measurement of the inhibition zone were used. Twenty-two root canals of incisors and molars of 12 patients were used. After accessing the canal, the first root canal sample was collected with two sterile paper points that were transferred to a tube containing reduced transport fluid. The root canal was instrumented using chlorhexidine solution. A small sterile cotton pellet was placed at the root canal entrance, and the cavity was sealed with zinc oxide-eugenol cement. The canals were maintained empty for 48 h. Three sterile paper points were then introduced to absorb the root canal fluid (second sample). One paper point was placed on an agar plate inoculated with Micrococcus luteus ATCC 9341 and incubated for 24 h at 37°C, and the other two were submitted to microbiological evaluation. Present in 10 cases at baseline, mutans streptococci was reduced by 100% at the second assessment. Treatment showed an efficiency of 77.78% for anaerobic microorganisms at the second assessment. These data suggest that chlorhexidine prevents microbial activity in vivo with residual effects in the root canal system up to 48 h. Copyright © 1999 by The American Association of Endodontists.en
dc.format.extent167-171-
dc.language.isoeng-
dc.sourceScopus-
dc.titleIn vivo antimicrobial activity of 2% chlorhexidine used as a root canal irrigating solutionen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Pediatric Dentistry Ribeirão Preto School of Dentistry USP, Ribeirão Preto-
dc.description.affiliationDepartment of Health Sciences Faculty of Pharmaceutical Sciences of Ribeirão Preto USP, Ribeirão Preto-
dc.description.affiliationDepartamento de Endodontia Faculdade de Odontologia de Araraquara UNESP, Caixa Postal 331, 14801-385, Araraquara, SP-
dc.description.affiliationUnespDepartamento de Endodontia Faculdade de Odontologia de Araraquara UNESP, Caixa Postal 331, 14801-385, Araraquara, SP-
dc.identifier.doi10.1016/S0099-2399(99)80135-6-
dc.identifier.wosWOS:000078903500005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Endodontics-
dc.identifier.scopus2-s2.0-0033093964-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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