Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/146199
Campo DC Valoridioma
dc.contributor.authorVega Rodríguez, Gisela Del Carmen-
dc.contributor.authorPaz Hernández, Rubén-
dc.contributor.authorMonzón Verona, Mario Domingo-
dc.contributor.authorDonate González, Ricardo-
dc.contributor.authorGleadall, Andrew-
dc.date.accessioned2025-09-04T13:30:52Z-
dc.date.available2025-09-04T13:30:52Z-
dc.date.issued2025-
dc.identifier.issn1996-1944-
dc.identifier.otherWoS-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/146199-
dc.description.abstractAdditive manufacturing technology, specifically material extrusion, offers great potential for scaffold manufacturing in tissue engineering. This study presents a novel methodology for the design and optimization of 3D printed polymeric scaffolds to enhance cell viability, thereby promoting improved cell proliferation for tissue engineering applications. Different infill patterns, including gyroid, parallel sinusoidal, and symmetric sinusoidal, were evaluated to determine their impact on cell proliferation and tissue regeneration. To overcome the limitations of existing slicer software, a novel open-source software called FullControl GCode Designer was utilized, enabling the creation of customized infill patterns without restrictions. VOLCO software was employed to generate voxelized 3D models of the scaffolds, simulating the material extrusion process. Finite element analysis was conducted using Abaqus software to evaluate the mechanical properties of the different designs. Additionally, new scripts were developed to evaluate the interconnectivity and pore size of the voxelized models. A factorial design of experiments and a genetic algorithm (combined with Kriging metamodels) were applied to identify the optimal configuration based on optimization criteria (keeping the mechanical stiffness and pore size within the recommended values for trabecular bone and maximizing the surface and interconnectivity). Biological testing was conducted on polylactic acid scaffolds to preliminarily validate the effectiveness of the modeling and optimization methodologies in this regard. The results demonstrated the agreement between the optimization methodology and the biological test since the optimum in both cases was a symmetric sinusoidal pattern design with a configuration resulting in a structure with 53.08% porosity and an equivalent pore size of 584 µm. Therefore, this outcome validates the proposed methodologies, emphasizing the role of pore surface area and interconnectivity in supporting cell proliferation. Overall, this research contributes to the advancement of AM technology in tissue engineering and paves the way for further optimization studies in scaffold design.-
dc.languagespa-
dc.relationNuevos Scaffolds Piezoeléctricos de Compuestos Nanoestructurados Para la Regeneración Ósea Mediante Fabricación Aditiva-
dc.relation.ispartofMaterials-
dc.sourceMaterials [ISSN 1996-1944], v, 18, (Agosto 2025)-
dc.subject3313 Tecnología e ingeniería mecánicas-
dc.subject3314 Tecnología médica-
dc.subject.otherOptimization-
dc.subject.otherScaffold-
dc.subject.otherTissue engineering-
dc.subject.otherAdditive manufacturing-
dc.subject.otherModeling-
dc.subject.otherFEA-
dc.titleCurve-Based Infill Pattern Optimization for 3D Printed Polymeric Scaffolds for Trabecular Bone Applications-
dc.typeinfo:eu-repo/semantics/article-
dc.typeArticle-
dc.identifier.doi10.3390/ma18174055-
dc.identifier.isi001569947100001-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.identifier.eissn1996-1944-
dc.identifier.issue17-
dc.relation.volume18-
dc.investigacionIngeniería y Arquitectura-
dc.type2Artículo-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.identifier.external190775272-
dc.description.numberofpages25-
dc.utils.revision-
dc.contributor.wosstandardWOS:Vega, G-
dc.contributor.wosstandardWOS:Paz, R-
dc.contributor.wosstandardWOS:Monzón, M-
dc.contributor.wosstandardWOS:Donate, R-
dc.contributor.wosstandardWOS:Gleadall, A-
dc.date.coverdateAgosto 2025-
dc.identifier.ulpgc-
dc.contributor.buulpgcBU-ING-
dc.description.sjr0,614-
dc.description.jcr3,2-
dc.description.sjrqQ2-
dc.description.jcrqQ2-
dc.description.scieSCIE-
dc.description.miaricds10,6-
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptDepartamento de Ingeniería Mecánica-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptDepartamento de Ingeniería Mecánica-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptDepartamento de Ingeniería de Procesos-
crisitem.author.orcid0000-0002-9141-537X-
crisitem.author.orcid0000-0003-1223-7067-
crisitem.author.orcid0000-0003-2736-7905-
crisitem.author.orcid0000-0002-4337-5991-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.fullNameVega Rodríguez, Gisela Del Carmen-
crisitem.author.fullNamePaz Hernández, Rubén-
crisitem.author.fullNameMonzón Verona, Mario Domingo-
crisitem.author.fullNameDonate González, Ricardo-
crisitem.project.principalinvestigatorMonzón Verona, Mario Domingo-
Colección:Artículos
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