dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2018-12-11T17:06:07Z
dc.date.available2018-12-11T17:06:07Z
dc.date.created2018-12-11T17:06:07Z
dc.date.issued2016-08-18
dc.identifierBiofouling, v. 32, n. 9, p. 995-1006, 2016.
dc.identifier1029-2454
dc.identifier0892-7014
dc.identifierhttp://hdl.handle.net/11449/173532
dc.identifier10.1080/08927014.2016.1218850
dc.identifier2-s2.0-84988878589
dc.identifier2-s2.0-84988878589.pdf
dc.identifier5651874509493617
dc.identifier0000-0002-2575-279X
dc.description.abstractThis study evaluated the cytotoxicity and effect of fragments derived from three oral cationic peptides (CP): LL-37, D6-17 and D1-23 against cariogenic bacteria under planktonic and biofilm conditions. For cytotoxicity analysis, two epithelial cell lines were used. The minimum inhibitory concentration and the minimal bactericidal concentration were determined for the CP fragments and the control (chlorhexidine-CHX) against cariogenic bacteria. The fractional inhibitory concentration was obtained for the combinations of CP fragments on Streptococcus mutans. Biofilm assays were conducted with the best antimicrobial CP fragment against S. mutans. The results indicated that D6-17 was not cytotoxic. D1-23, LL-37 and CHX were not cytotoxic in low concentrations. D1-23 presented the best bactericidal activity against S. mutans, S. mitis and S. salivarius. Combinations of CP fragments did not show a synergic effect. D1-23 presented a higher activity against S. mutans biofilm than CHX. It was concluded that D1-23 showed a substantial effect against cariogenic bacteria and low cytotoxicity.
dc.languageeng
dc.relationBiofouling
dc.relation0,835
dc.relation0,835
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectBiofilms
dc.subjectCell culture
dc.subjectDental caries
dc.subjectPeptides
dc.titleCytotoxicity and the effect of cationic peptide fragments against cariogenic bacteria under planktonic and biofilm conditions
dc.typeArtículos de revistas


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