Logotipo do repositório

Chlorin-e6 conjugated to the antimicrobial peptide LL-37 loaded nanoemulsion enhances photodynamic therapy against multi-species biofilms related to periodontitis

dc.contributor.authorGarcia de Carvalho, Gabriel [UNESP]
dc.contributor.authorMaquera-Huacho, Patricia Milagros [UNESP]
dc.contributor.authorSilva Pontes, Cristiano [UNESP]
dc.contributor.authorAnnunzio, Sarah Raquel de [UNESP]
dc.contributor.authorFontana Mendonça, Carla Raquel [UNESP]
dc.contributor.authorNara de Souza Rastelli, Alessandra [UNESP]
dc.contributor.authorde Oliveira, Kleber Thiago
dc.contributor.authorTeughels, Wim
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorLeal Zandim-Barcelos, Daniela [UNESP]
dc.contributor.authorPalomari Spolidorio, Denise Madalena [UNESP]
dc.date.accessioned2026-06-30T18:45:37Z
dc.date.issued2023-07-26
dc.description.abstractIn our previous studies, Chlorin-e6 (Ce6) demonstrated a significant reduction of microorganisms' viability against multi-species biofilm related to periodontitis while irradiated with blue light. However, the conjugation of Ce6 and antimicrobial peptides, and the incorporation of this photosensitizer in a nanocarrier, is still poorly explored. We hypothesized that chlorin-e6 conjugated to the antimicrobial peptide LL-37 loaded nanoemulsion could inhibit a multi-species biofilm related to periodontitis during photodynamic therapy (PDT), the pre-treatment with hydrogen peroxide was also tested. The nanoemulsion (NE) incorporated with Ce6 was characterized regarding the physiochemical parameters. Images were obtained by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Later, the Ce6 and LL-37 incorporated in NE was submitted to UV-Vis analysis and Reactive Oxygen Species (ROS) assay. Finally, the combined formulation (Ce6+LL-37 in nanoemulsion) was tested against multi-species biofilm related to periodontitis. The formed nanoformulation was kinetically stable, optically transparent with a relatively small droplet diameter (134.2 unloaded and 146.9 loaded), and weak light scattering. The NE system did not impact the standard UV-VIS spectra of Ce6, and the ROS production was improved while Ce6 was incorporated in the NE. The combination of Ce6 and LL-37 in NE was effective to reduce the viability of all bacteria tested. The treatment with hydrogen peroxide previous to PDT significantly impacted bacterial viability. The current aPDT regimen was the best already tested against periodontal biofilm by our research team. Our results suggest that this combined protocol must be exploited for clinical applications in localized infections such as periodontal disease. - Nanoemulsion demonstrated to be an excellent nanocarrier for photodynamic application. - Chlorin-e6 incorporated in nanoemulsion showed great physicochemical and biophotonic parameters. - The combination of chlorin-e6 and LL-37 peptide in nanoemulsion is effective to eliminate periodontal pathogenic bacteria. - The treatment with hydrogen peroxide previous to PDT significantly impacted bacterial viability.
dc.description.affiliationDepartment of Physiology and Pathology, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil. Electronic address: garcia.carvalho@unesp.br.
dc.description.affiliationDepartment of Physiology and Pathology, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.description.affiliationSão Paulo State University (Unesp), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
dc.description.affiliationDepartment of Restorative Dentistry, School of Dentistry, São Paulo State University (Unesp School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.description.affiliationDepartment of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.
dc.description.affiliationDepartment of Oral Health Sciences, University of Leuven & Dentistry University Hospitals Leuven, Leuven, Belgium.
dc.description.affiliationDepartment of Drugs and Medicines, International School of Pharmaceuticals Sciences, São Paulo State University, Araraquara, São Paulo, Brazil.
dc.description.affiliationDepartment of Oral Diagnosis and Surgery, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.description.affiliationUnespDepartment of Physiology and Pathology, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil. Electronic address: garcia.carvalho@unesp.br.
dc.description.affiliationUnespDepartment of Physiology and Pathology, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.description.affiliationUnespSão Paulo State University (Unesp), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
dc.description.affiliationUnespDepartment of Restorative Dentistry, School of Dentistry, São Paulo State University (Unesp School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.description.affiliationUnespDepartment of Drugs and Medicines, International School of Pharmaceuticals Sciences, São Paulo State University, Araraquara, São Paulo, Brazil.
dc.description.affiliationUnespDepartment of Oral Diagnosis and Surgery, São Paulo State University (Unesp), School of Dentistry at Araraquara, Araraquara, São Paulo, Brazil.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1162725036
dc.identifier.dimensionspub.1162725036
dc.identifier.doi10.1016/j.pdpdt.2023.103725
dc.identifier.issn1572-1000
dc.identifier.issn1873-1597
dc.identifier.orcid0000-0003-1202-9743
dc.identifier.orcid0000-0002-2193-9979
dc.identifier.orcid0000-0001-5477-2135
dc.identifier.orcid0000-0002-6768-2670
dc.identifier.orcid0000-0002-9131-4800
dc.identifier.orcid0000-0001-7675-5643
dc.identifier.orcid0000-0002-6698-0545
dc.identifier.orcid0000-0003-2376-1024
dc.identifier.orcid0000-0001-5442-7868
dc.identifier.pmid37500031
dc.identifier.urihttps://hdl.handle.net/11449/326967
dc.publisherElsevier
dc.relation.ispartofPhotodiagnosis and Photodynamic Therapy; v. 43; p. 103725
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleChlorin-e6 conjugated to the antimicrobial peptide LL-37 loaded nanoemulsion enhances photodynamic therapy against multi-species biofilms related to periodontitis
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

Arquivos