Material extrusion additive manufacturing of graphene oxide reinforced 13-93B1 bioactive glass scaffolds for bone tissue engineering applications

被引:1
|
作者
Dixit, Kartikeya [1 ,2 ]
Vishwakarma, Ashok [2 ]
Kumar, Hitendra [1 ,3 ]
Kim, Keekyoung [1 ,4 ]
Sinha, Niraj [2 ]
机构
[1] Univ Calgary, Dept Mech & Mfg Engn, Calgary, AB T2N 1N4, Canada
[2] Indian Inst Technol, Dept Mech Engn, Biomed Res Lab, Kanpur 208016, India
[3] Indian Inst Technol Indore, Dept Biosci & Biomed Engn, Indore 453552, India
[4] Univ Calgary, Dept Biomed Engn, Calgary, AB T2N 1N4, Canada
关键词
Bioactive Glass; Graphene Oxide; Scaffolds; Material Extrusion Additive Manufacturing; Bone Tissue Engineering; WALL SHEAR-STRESS; 3D DIRECT INK; CARBON NANOTUBE; CONTROLLABLE DEGRADATION; FINITE-ELEMENT; PERMEABILITY; CERAMICS; REGENERATION; BOROSILICATE; CONSTRUCTS;
D O I
10.1016/j.addma.2024.104481
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Graphene-reinforced bioactive glass scaffolds have gained significant attention in the field of bone tissue engineering due to their unique combination of mechanical strength, bioactivity, and electrical conductivity. Additive manufacturing techniques, such as 3D printing, provide a versatile platform for fabricating these scaffolds with precise control over their architecture and composition. Consequently, in this work, we have fabricated graphene oxide (GO)-reinforced 13-93B1 bioactive glass scaffold using the material extrusion-based additive manufacturing. A Pluronic F-127-based ink was prepared for scaffold fabrication, and its rheological properties were assessed for shear thinning behaviour, structural support, and recovery. Further, the fabricated scaffolds were characterized using micro-computed tomography, scanning electron microscopy, and energy dispersive xray spectroscopy. Additionally, computational fluid dynamics simulations with Dulbecco's modified eagle medium and blood were performed to evaluate the perfusion kinetics of the scaffolds. The inclusion of GO enhanced the compressive strength of the fabricated scaffolds by similar to 202 %. The morphological characterization based on micro-computed tomography showed that additively manufactured scaffolds have appropriate porosity, pore size, pore throat size, and interconnectivity for bone tissue engineering. The synergy with surrounding muscle tissue is also crucial for scaffold-guided bone regeneration. A scaffold supporting the muscle growth around the bone will be able to promote bone-muscle crosstalk and, in turn, bone regeneration. The live-dead assay results showed no cytotoxicity towards C2C12 mouse myoblast cells. Also, cell adhesion and cell viability results show better cell growth on the nanocomposite scaffolds. Overall, the fabricated scaffolds are found suitable for bone tissue engineering applications.
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页数:17
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