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https://doi.org/10.1016/j.jdent.2022.104163


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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Guerrero Gironés, Julia | - |
dc.contributor.author | López García, Sergio | - |
dc.contributor.author | Pecci Lloret, Miguel Ramón | - |
dc.contributor.author | Pecci Lloret, María Pilar | - |
dc.contributor.author | Rodríguez Lozano, Francisco Javier | - |
dc.contributor.author | García Bernal, David | - |
dc.date.accessioned | 2025-01-28T08:20:43Z | - |
dc.date.available | 2025-01-28T08:20:43Z | - |
dc.date.issued | 2022-05-14 | - |
dc.identifier.citation | Journal of Dentistry, 2022, Vol. 123 : 104163 | - |
dc.identifier.issn | Print: 0300-5712 | - |
dc.identifier.issn | Electronic: 1879-176X | - |
dc.identifier.uri | http://hdl.handle.net/10201/149390 | - |
dc.description | © 2022 The Author(s). This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ This document is the Published Manuscript, version of a Published Work that appeared in final form in Journal of Dentistry. To access the final edited and published work see https://doi.org/10.1016/j.jdent.2022.104163 | - |
dc.description.abstract | Objective: To assess and compare the in vitro biocompatibility of new resins (Keysplint Soft (Keystone Industries), NextDent Ortho Rigid (3D System), and Freeprint Splint (Detax)) and traditional resins (Orthocryl (Dentaurum)) used for dental splints. Methods: Standardized discs (n = 40) and 1:1, 1:2, and 1:4 extracts of the tested materials were prepared. Human gingival fibroblasts (hGFs) were isolated from gingival tissues. Different biological tests were carried out, including MTT assays to assess cell metabolic activity, cell migration assays, cell cytoskeleton staining, cell apoptosis, generation of intracellular reactive oxygen species (ROS), and scanning electron microscopy (SEM). Statistical analyses were performed using one-way ANOVA and Tukey’s post hoc test (p<0.05). Results: MTT experiments showed that Freeprint Splint significantly reduces the hGF metabolic activity (***p<0.001), whereas SEM analysis showed almost no cells adhered on its surface. Cell migration was significantly lower after exposure to undiluted extracts of Freeprint Splint at 48 and 72 h (***p<0.001). Cell cytoskeleton staining assays showed fewer attached cells in 1:1 and 1:2 dilutions of Freeprint Splint. Annexin-V and 7-AAD staining assays showed that only cells exposed to Keysplint Soft extracts displayed similar cell viability to the control group. Finally, ROS levels detected in undiluted extracts of all resins were significantly enhanced compared to the control group (***p<0.001). Conclusions: The 3D-printed resins and the conventional dental resin showed a similar biocompatibility, except for Freeprint Splint, which was the most cytotoxic on hGFs. Clinical significance: 3D printing has been on the rise in recent years and its use in daily clinical practice is expanding over time. Two of the three 3D-printed resins tested in this study performed as well in the cytotoxicity tests as the conventional one, supporting their use, but caution and further testing are required | es |
dc.format | application/pdf | es |
dc.format.extent | 9 | es |
dc.language | eng | es |
dc.publisher | Elsevier | - |
dc.relation | Spanish Net of Cell Therapy (TerCel), RETICS subprograms of the I + D + I 2013–2016 Spanish National Plan, and project “RD16/0011/0001′′ funded by the Instituto de Salud Carlos III to JMM and co-funded by the European Regional Development Fund. | es |
dc.rights | info:eu-repo/semantics/openAccess | es |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Dental resins | es |
dc.subject | 3d printing | es |
dc.subject | Bicompatibility | es |
dc.subject | Citotoxicity | es |
dc.subject | Occlusal devices | es |
dc.title | In vitro biocompatibility testing of 3D printing and conventional resins for occlusal devices | es |
dc.type | info:eu-repo/semantics/article | es |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0300571222002196 | - |
dc.identifier.doi | https://doi.org/10.1016/j.jdent.2022.104163 | - |
dc.contributor.department | Departamento de Dermatología, Estomatología, Radiología y Medicina Física | - |
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