Characterization of 3D-printed gelatin/sodium alginate/58S bioactive glass scaffold and osteogenesis in rabbit cranial defects

脚手架 生物活性玻璃 生物医学工程 明胶 化学 PLGA公司 骨愈合 组织工程 肿胀 的 材料科学 骨形成 羟基磷灰石 骨生长 体内 植入 生物降解 多孔性 骨组织 抗压强度
作者
Rongfeng Chen,Guocong Zheng,Chen Xiaoshi,Xinran Tu,Jinyi Xu,Kehuan Hong,Qianzhou Jiang
出处
期刊:Biomedical Physics & Engineering Express [IOP Publishing]
标识
DOI:10.1088/2057-1976/ae737a
摘要

Critical-sized maxillofacial bone defects often lead to delayed healing or non-union, necessitating clinical intervention with osteoconductive biomaterials. 58S bioactive glass (BG) is a promising candidate to release osteogenic ions (Si, Ca, P). In the present study, a dualnetwork scaffold was fabricated via 3D printing using a bioink composed of gelatin (Gel), sodium alginate (SA), and 58S BG (mass ratio 10:4:7). The scaffold's physicochemical properties, biocompatibility, and osteogenic efficacy were systematically evaluated. The scaffold demonstrated favorable structural characteristics with a high porosity of 76 ± 1% and a compressive Young's modulus of 166.3 ± 1.6 kPa. It exhibited a volumetric swelling ratio of 85.7 ± 13.1% and maintained 62% of its initial mass after 14 weeks in simulated body fluid, indicating excellent stability and controlled degradation. Subcutaneous implantation in nude mice revealed no signs of inflammation or fibrous encapsulation at 4 and 8 weeks, confirming its excellent biocompatibility. In a critical-sized rabbit calvarial defect model, micro-CT analysis after 6 months showed that the scaffold group achieved a bone volume fraction (BV/TV) of 46.8 ± 1.2%. This result was comparable to the Bio-Oss (48.7 ± 3.1%), with no residual scaffold particles observed, confirming its complete biodegradation synchronized with new bone formation. In conclusion, this biodegradable Gel/SA/58S BG scaffold combines favorable printability, structural stability, high bioactivity, and well-matched degradation kinetics, presenting a highly promising and translatable platform for the personalized reconstruction of maxillofacial bone defects.

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