Antimicrobial photodynamic therapy against pathogenic bacterial suspensions and biofilms using chloro-aluminum phthalocyanine encapsulated in nanoemulsions

dc.contributor.authorRibeiro, Ana Paula Dias
dc.contributor.authorAndrade, Mariana Carvalho [UNESP]
dc.contributor.authorBagnato, Vanderlei Salvador
dc.contributor.authorVergani, Carlos Eduardo [UNESP]
dc.contributor.authorPrimo, Fernando Lucas
dc.contributor.authorTedesco, Antônio Cláudio
dc.contributor.authorPavarina, Ana Claudia [UNESP]
dc.contributor.institutionUniversidade de Brasília (UnB)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2015-08-06T16:13:08Z
dc.date.available2015-08-06T16:13:08Z
dc.date.issued2013
dc.description.abstractAntimicrobial photodynamic therapy represents an alternative method of killing resistant pathogens. Efforts have been made to develop delivery systems for hydrophobic drugs to improve the photokilling. This study evaluated the photodynamic effect of chloro-aluminum phthalocyanine (ClAlPc) encapsulated in nanoemulsions (NE) on methicillin-susceptible and methicillin-resistant Staphylococcus aureus suspensions and biofilms. Suspensions and biofilms were treated with different delivery systems containing ClAlPc. After the pre-incubation period, the drug was washed-out and irradiation was performed with LED source (660 ± 3 nm). Negative control samples were not exposed to ClAlPc or light. For the suspensions, colonies were counted (colony-forming units per milliliter (CFU/mL)). The metabolic activity of S. aureus suspensions and biofilms were evaluated by the XTT assay. The efficiency was dependent on the delivery system, superficial load and light dose. Cationic NE-ClAlPc and free-ClAlPc caused photokilling of the both strains of S. aureus. For biofilms, cationic NE-ClAlPc reduced cell metabolism by 80 and 73 % of susceptible and resistant strains, respectively. Although anionic NE-ClAlPc caused a significant CFU/ml reduction for MSSA and MRSA, it was not capable of reducing MRSA biofilm metabolism. This therapy may represent an alternative treatment for eradicating resistant strains.en
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Materiais Odontológicos e Prótese, Faculdade de Odontologia de Araraquara, Araraquara, Rua Humaitá, 1680, Centro, CEP 14801903, SP, Brasil
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Materiais Odontológicos e Prótese, Faculdade de Odontologia de Araraquara, Araraquara, Rua Humaitá, 1680, Centro, CEP 14801903, SP, Brasil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2009/17975-9
dc.description.sponsorshipIdFAPESP: 2010/05425-1
dc.format.extent549-559
dc.identifierhttp://link.springer.com/article/10.1007%2Fs10103-013-1354-x
dc.identifier.citationLasers in Medical Science, v. 30, n. 2, p. 549-559, 2013.
dc.identifier.doi10.1007/s10103-013-1354-x
dc.identifier.issn0268-8921
dc.identifier.lattes8867670539105403
dc.identifier.lattes1531215699841687
dc.identifier.lattes5809961609784365
dc.identifier.lattes3003130522427820
dc.identifier.lattes4947860249518663
dc.identifier.orcid0000-0002-7375-4714
dc.identifier.urihttp://hdl.handle.net/11449/125797
dc.language.isoeng
dc.relation.ispartofLasers in Medical Science
dc.relation.ispartofjcr1.949
dc.relation.ispartofsjr0,713
dc.rights.accessRightsAcesso restrito
dc.sourceCurrículo Lattes
dc.subjectAntimicrobial photodynamic therapyen
dc.subjectDrug delivery systemsen
dc.subjectPhthalocyanineen
dc.subjectMRSAen
dc.titleAntimicrobial photodynamic therapy against pathogenic bacterial suspensions and biofilms using chloro-aluminum phthalocyanine encapsulated in nanoemulsionsen
dc.typeArtigo
unesp.author.lattes8867670539105403[7]
unesp.author.lattes1531215699841687
unesp.author.lattes5809961609784365
unesp.author.lattes3003130522427820[4]
unesp.author.lattes4947860249518663
unesp.author.orcid0000-0002-7375-4714[4]
unesp.author.orcid0000-0002-9231-1994[7]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Odontologia, Araraquarapt
unesp.departmentMateriais Odontológicos e Prótese - FOARpt

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