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Design and 3D Printing of Personalized Hybrid and Gradient Structures for Critical Size Bone Defects.
Altunbek, Mine; Afghah, Seyedeh Ferdows; Fallah, Ali; Acar, Anil Ahmet; Koc, Bahattin.
Afiliación
  • Altunbek M; Nanotechnology Research and Application Center, Sabanci University, Istanbul 34956, Turkey.
  • Afghah SF; University of Massachusetts Lowell, Lowell, Massachusetts 01854, United States.
  • Fallah A; Nanotechnology Research and Application Center, Sabanci University, Istanbul 34956, Turkey.
  • Acar AA; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
  • Koc B; Nanotechnology Research and Application Center, Sabanci University, Istanbul 34956, Turkey.
ACS Appl Bio Mater ; 6(5): 1873-1885, 2023 05 15.
Article en En | MEDLINE | ID: mdl-37071829
ABSTRACT
Treating critical-size bone defects with autografts, allografts, or standardized implants is challenging since the healing of the defect area necessitates patient-specific grafts with mechanically and physiologically relevant structures. Three-dimensional (3D) printing using computer-aided design (CAD) is a promising approach for bone tissue engineering applications by producing constructs with customized designs and biomechanical compositions. In this study, we propose 3D printing of personalized and implantable hybrid active scaffolds with a unique architecture and biomaterial composition for critical-size bone defects. The proposed 3D hybrid construct was designed to have a gradient cell-laden poly(ethylene glycol) (PEG) hydrogel, which was surrounded by a porous polycaprolactone (PCL) cage structure to recapitulate the anatomical structure of the defective area. The optimized PCL cage design not only provides improved mechanical properties but also allows the diffusion of nutrients and medium through the scaffold. Three different designs including zigzag, zigzag/spiral, and zigzag/spiral with shifting the zigzag layers were evaluated to find an optimal architecture from a mechanical point of view and permeability that can provide the necessary mechanical strength and oxygen/nutrient diffusion, respectively. Mechanical properties were investigated experimentally and analytically using finite element analysis (FEA), and computational fluid dynamics (CFD) simulation was used to determine the permeability of the structures. A hybrid scaffold was fabricated via 3D printing of the PCL cage structure and a PEG-based bioink comprising a varying number of human bone marrow mesenchymal stem cells (hBMSCs). The gradient bioink was deposited inside the PCL cage through a microcapillary extrusion to generate a mineralized gradient structure. The zigzag/spiral design for the PCL cage was found to be mechanically strong with sufficient and optimum nutrient/gas axial and radial diffusion while the PEG-based hydrogel provided a biocompatible environment for hBMSC viability, differentiation, and mineralization. This study promises the production of personalized constructs for critical-size bone defects by printing different biomaterials and gradient cells with a hybrid design depending on the need for a donor site for implantation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Materiales Biocompatibles / Andamios del Tejido Límite: Humans Idioma: En Revista: ACS Appl Bio Mater Año: 2023 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Materiales Biocompatibles / Andamios del Tejido Límite: Humans Idioma: En Revista: ACS Appl Bio Mater Año: 2023 Tipo del documento: Article País de afiliación: Turquía
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