Publicação:
Peptide KSL-W-loaded mucoadhesive liquid crystalline vehicle as an alternative treatment for multispecies oral biofilm

dc.contributor.authorBernegossi, Jéssica [UNESP]
dc.contributor.authorCalixto, Giovana Maria Fioramonti [UNESP]
dc.contributor.authorDa Silva Sanches, Paulo Ricardo [UNESP]
dc.contributor.authorFontana, Carla Raquel [UNESP]
dc.contributor.authorCilli, Eduardo Maffud [UNESP]
dc.contributor.authorGarrido, Saulo Santesso [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:30:23Z
dc.date.available2018-12-11T17:30:23Z
dc.date.issued2016-01-01
dc.description.abstractDecapeptide KSL-W shows antibacterial activities and can be used in the oral cavity, however, it is easily degraded in aqueous solution and eliminated. Therefore, we aimed to develop liquid crystalline systems (F1 and F2) for KSL-W buccal administration to treat multispecies oral biofilms. The systems were prepared with oleic acid, polyoxypropylene (5) polyoxyethylene (20) cetyl alcohol (PPG-5-CETETH-20), and a 1% poloxamer 407 dispersion as the oil phase (OP), surfactant (S), and aqueous phase (AP), respectively. We characterized them using polarized light microscopy (PLM), small-angle X-ray scattering (SAXS), rheology, and in vitro bioadhesion, and performed in vitro biological analysis. PLM showed isotropy (F1) or anisotropy with lamellar mesophases (F2), confirmed by peak ratio quantification using SAXS. Rheological tests demonstrated that F1 exhibited Newtonian behavior but not F2, which showed a structured AP concentration-dependent system. Bioadhesion studies revealed an AP concentration-dependent increase in the system's bioadhesiveness (F2 = 15.50 ±1.00 mN s) to bovine teeth blocks. Antimicrobial testing revealed 100% inhibition of multispecies oral biofilm growth after KSL-W administration, which was incorporated in the F2 aqueous phase at a concentration of 1 mg/mL. Our results suggest that this system could serve as a potential vehicle for buccal administration of antibiofilm peptides.en
dc.description.affiliationSchool of Pharmaceutical Sciences Sao Paulo State University UNESP, Rodovia Araraquara-Jaú Km 01
dc.description.affiliationChemistry Institute UNESP Sao Paulo State University
dc.description.affiliationUnespSchool of Pharmaceutical Sciences Sao Paulo State University UNESP, Rodovia Araraquara-Jaú Km 01
dc.description.affiliationUnespChemistry Institute UNESP Sao Paulo State University
dc.identifierhttp://dx.doi.org/10.3390/molecules21010037
dc.identifier.citationMolecules, v. 21, n. 1, 2016.
dc.identifier.doi10.3390/molecules21010037
dc.identifier.file2-s2.0-85000783346.pdf
dc.identifier.issn1420-3049
dc.identifier.lattes1427125996716282
dc.identifier.scopus2-s2.0-85000783346
dc.identifier.urihttp://hdl.handle.net/11449/178447
dc.language.isoeng
dc.relation.ispartofMolecules
dc.relation.ispartofsjr0,855
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectAntimicrobial peptide
dc.subjectBiofilm
dc.subjectKSL-W
dc.subjectLiquid crystalline systems
dc.subjectOral cavity
dc.titlePeptide KSL-W-loaded mucoadhesive liquid crystalline vehicle as an alternative treatment for multispecies oral biofilmen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes1427125996716282
unesp.author.lattes5168319315634298[4]
unesp.author.orcid0000-0002-9135-3690[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentBioquímica e Tecnologia - IQpt

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