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Pathogenesis-Guided Engineering: pH-Responsive Imprinted Polymer Co-Delivering Folate for Inflammation-Resolving as Immunotherapy in Implant-Related Infections

dc.contributor.authorCosta, Raphael C.
dc.contributor.authorNagay, Bruna E.
dc.contributor.authorVilla, Javier E. L.
dc.contributor.authorSotomayor, Maria D. P. T. [UNESP]
dc.contributor.authorNeres, Lariel Chagas da Silva [UNESP]
dc.contributor.authorBenso, Bruna
dc.contributor.authorAguayo, Sebastian
dc.contributor.authorSacramento, Catarina M.
dc.contributor.authorRuiz, Karina G. S.
dc.contributor.authorSpada, Fernanda P.
dc.contributor.authorde Avila, Erica Dorigatti [UNESP]
dc.contributor.authorda Costa, Monique G. [UNESP]
dc.contributor.authorFaverani, Leonardo P. [UNESP]
dc.contributor.authorCintra, Luciano T. A. [UNESP]
dc.contributor.authorSouza, Joāo Gabriel S.
dc.contributor.authorBarão, Valentim A. R.
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionPontificia Universidad Católica de Chile
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionGuarulhos University
dc.date.accessioned2025-04-29T19:30:15Z
dc.date.issued2024-10-15
dc.description.abstractFolate (FT) is a suitable targeting ligand for folate receptors (FOLR) overexpressed on inflamed cells. Thus, FT-loaded polymers can be used as FOLRs-targeted immunotherapy to positively modulate the inflammatory process. A novel biodegradable imprinted polymer with a FT delivery mechanism driven by pH changes [PCL-MIP@FT] is designed with molecularly imprinted technology. The pH mechanism is validated in vitro, demonstrating that an acidic environment accelerated and increased the release of FT for a period of 7 days (∼100 µg mL−1). For the first time, FT receptors (FOLR-1 and FOLR-3) are discovered and also overexpressed on activated human gingival fibroblasts, representing a favorable target in the oral environment. Although FT itself does not have antimicrobial effects, the nanomechanical properties of biofilm are changed after topical FT administration. In vivo systemic toxicity of PCL-MIP@FT has been demonstrated to be a safe biomaterial (up to 1.3 mg kg−1). When the PCL-MIP@FT is assessed in the subcutaneous tissue, it promoted an alleviating inflammation and may be able to stimulate tissue repair. The present findings have demonstrated the reliable in vitro and in vivo anti-inflammatory actions of FT-loaded polymer and support its use as a novel drug-free therapeutic platform for modulating and mitigating inflammatory responses in dental implant-related infections.en
dc.description.affiliationDepartment of Prosthodontics and Periodontology Piracicaba Dental School Universidade Estadual de Campinas (UNICAMP), São Paulo
dc.description.affiliationInstitute of Chemistry University of Campinas (UNICAMP), São Paulo
dc.description.affiliationInstitute of Chemistry State University of São Paulo (UNESP), São Paulo
dc.description.affiliationSchool of Dentistry Faculty of Medicine Pontificia Universidad Católica de Chile
dc.description.affiliationInstitute for Biological and Medical Engineering Schools of Engineering Medicine and Biological Sciences Pontificia Universidad Católica de Chile
dc.description.affiliationDepartment of Agri-food Industry Food and Nutrition “Luiz de Queiroz” College of Agriculture University of São Paulo (USP), São Paulo
dc.description.affiliationDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), Sāo Paulo
dc.description.affiliationDepartment of Diagnosis and Surgery Division of Oral and Maxillofacial Surgery and Implantology São Paulo State University (UNESP) School of Dentistry, São Paulo
dc.description.affiliationDepartment of Preventive and Restorative Dentistry São Paulo State University (UNESP), São Paulo
dc.description.affiliationDental Research Division Guarulhos University, São Paulo
dc.description.affiliationUnespInstitute of Chemistry State University of São Paulo (UNESP), São Paulo
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), Sāo Paulo
dc.description.affiliationUnespDepartment of Diagnosis and Surgery Division of Oral and Maxillofacial Surgery and Implantology São Paulo State University (UNESP) School of Dentistry, São Paulo
dc.description.affiliationUnespDepartment of Preventive and Restorative Dentistry São Paulo State University (UNESP), São Paulo
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCNPq: #307471/2021-7
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdFAPESP: 2018/20719-3
dc.description.sponsorshipIdFAPESP: 2020/05231-4
dc.description.sponsorshipIdFAPESP: 2020/10436-4
dc.description.sponsorshipIdFAPESP: 2021/09434-0
dc.description.sponsorshipIdFAPESP: 2022/16267-5
dc.identifierhttp://dx.doi.org/10.1002/adfm.202406640
dc.identifier.citationAdvanced Functional Materials, v. 34, n. 42, 2024.
dc.identifier.doi10.1002/adfm.202406640
dc.identifier.issn1616-3028
dc.identifier.issn1616-301X
dc.identifier.scopus2-s2.0-85199141387
dc.identifier.urihttps://hdl.handle.net/11449/303638
dc.language.isoeng
dc.relation.ispartofAdvanced Functional Materials
dc.sourceScopus
dc.subjectbiomaterial
dc.subjectfolate
dc.subjectimplant infection
dc.subjectinflammation
dc.subjectmolecular imprinting
dc.titlePathogenesis-Guided Engineering: pH-Responsive Imprinted Polymer Co-Delivering Folate for Inflammation-Resolving as Immunotherapy in Implant-Related Infectionsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0002-2684-5488[1]
unesp.author.orcid0000-0002-4927-0779[2]
unesp.author.orcid0000-0001-6681-1269[11]
unesp.author.orcid0000-0001-5944-6953[15]
unesp.author.orcid0000-0002-6391-9917[16]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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