Photodynamic Therapy as a Novel Therapeutic Modality Applying Quinizarin-Loaded Nanocapsules and 3D Bioprinting Skin Permeation for Inflammation Treatment
| dc.contributor.author | do Amaral, Stéphanie R. [UNESP] | |
| dc.contributor.author | Amantino, Camila F. [UNESP] | |
| dc.contributor.author | Atanasov, Aleksandar | |
| dc.contributor.author | Sousa, Stefanie Oliveira [UNESP] | |
| dc.contributor.author | Moakes, Richard | |
| dc.contributor.author | Oliani, Sonia Maria [UNESP] | |
| dc.contributor.author | Grover, Liam M. | |
| dc.contributor.author | Primo, Fernando L. [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.contributor.institution | Science and Technology (IFSP) | |
| dc.contributor.institution | University of Birmingham | |
| dc.date.accessioned | 2025-04-29T19:35:41Z | |
| dc.date.issued | 2024-09-01 | |
| dc.description.abstract | Skin inflammation associated with chronic diseases involves a direct role of keratinocytes in its immunopathogenesis, triggering a cascade of immune responses. Despite this, highly targeted treatments remain elusive, highlighting the need for more specific therapeutic strategies. In this study, nanocapsules containing quinizarin (QZ/NC) were developed and evaluated in an in vitro model of keratinocyte-mediated inflammation, incorporating the action of photodynamic therapy (PDT) and analyzing permeation in a 3D skin model. Comprehensive physicochemical, stability, cytotoxicity, and permeation analyses of the nanomaterials were conducted. The nanocapsules demonstrated desirable physicochemical properties, remained stable throughout the analysis period, and exhibited no spectroscopic alterations. Cytotoxicity tests revealed no toxicity at the lowest concentrations of QZ/NC. Permeation and cellular uptake studies confirmed QZ/NC permeation in 3D skin models, along with intracellular incorporation and internalization of the drug, thereby enhancing its efficacy in drug delivery. The developed model for inducing the inflammatory process in vitro yielded promising results, particularly when the synthesized nanomaterial was combined with PDT, showing a reduction in cytokine levels. These findings suggest a potential new therapeutic approach for treating inflammatory skin diseases. | en |
| dc.description.affiliation | Department of Bioprocess and Biotechnology Engineering School of Pharmaceutical Sciences São Paulo State University (UNESP), SP | |
| dc.description.affiliation | São Paulo Federal Institute of Education Science and Technology (IFSP), SP | |
| dc.description.affiliation | School of Chemical Engineering University of Birmingham | |
| dc.description.affiliation | Department of Biology Institute of Biosciences Humanities and Exact Sciences (IBILCE) São Paulo State University (UNESP), SP | |
| dc.description.affiliationUnesp | Department of Bioprocess and Biotechnology Engineering School of Pharmaceutical Sciences São Paulo State University (UNESP), SP | |
| dc.description.affiliationUnesp | Department of Biology Institute of Biosciences Humanities and Exact Sciences (IBILCE) São Paulo State University (UNESP), SP | |
| dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
| dc.description.sponsorshipId | CAPES: 88887.839000/2023-00 | |
| dc.identifier | http://dx.doi.org/10.3390/ph17091169 | |
| dc.identifier.citation | Pharmaceuticals, v. 17, n. 9, 2024. | |
| dc.identifier.doi | 10.3390/ph17091169 | |
| dc.identifier.issn | 1424-8247 | |
| dc.identifier.scopus | 2-s2.0-85205112997 | |
| dc.identifier.uri | https://hdl.handle.net/11449/304671 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Pharmaceuticals | |
| dc.source | Scopus | |
| dc.subject | nanomedicine | |
| dc.subject | photodynamic therapy | |
| dc.subject | skin inflammation | |
| dc.title | Photodynamic Therapy as a Novel Therapeutic Modality Applying Quinizarin-Loaded Nanocapsules and 3D Bioprinting Skin Permeation for Inflammation Treatment | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isOrgUnitOfPublication | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| unesp.author.orcid | 0000-0003-2844-2604[1] | |
| unesp.author.orcid | 0000-0001-8049-8643[4] | |
| unesp.author.orcid | 0000-0001-6613-0658[5] | |
| unesp.author.orcid | 0000-0003-0918-2130[6] | |
| unesp.author.orcid | 0000-0001-6293-4157[8] | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara | pt |
| unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Preto | pt |

