3D-printed biodegradable magnesium alloy scaffolds with zoledronic acid-loaded ceramic composite coating promote osteoporotic bone defect repair

唑来膦酸 骨愈合 骨质疏松症 骨吸收 生物医学工程 材料科学 脚手架 间充质干细胞 镁合金 牙科 合金 医学 复合材料 外科 内科学 病理
作者
Zhaoyang Ran,Yan‐Feng Wang,Jiaxin Li,Wenyu Xu,Tan Jia,Bojun Cao,Dinghao Luo,Yiwen Ding,Junxiang Wu,Lei Wang,Kai Xie,Liang Deng,Penghuai Fu,Xiaoying Sun,Liyi Shi,Yongqiang Hao
出处
期刊:International Journal of bioprinting [Whioce Publishing Pte Ltd.]
卷期号:9 (5): 769-769 被引量:10
标识
DOI:10.18063/ijb.769
摘要

Osteoporotic fracture is one of the most serious complications of osteoporosis. Most fracture sites have bone defects, and restoring the balance between local osteogenesis and bone destruction is difficult during the repair of osteoporotic bone defects. In this study, we successfully fabricated three-dimensional (3D)-printed biodegradable magnesium alloy (Mg-Nd-Zn-Zr) scaffolds and prepared a zoledronic acid-loaded ceramic composite coating on the surface of the scaffolds. The osteogenic effect of Mg and the osteoclast inhibition effect of zoledronic acid were combined to promote osteoporotic bone defect repair. In vitro degradation and drug release experiments showed that the coating significantly reduced the degradation rate of 3D-printed Mg alloy scaffolds and achieved a slow release of loaded drugs. The degradation products of drug-loaded coating scaffolds can promote osteogenic differentiation of bone marrow mesenchymal stem cells as well as inhibit the formation of osteoclasts and the bone resorption by regulating the expression of related genes. Compared with the uncoated scaffolds, the drug-coated scaffolds degraded at a slower rate, and more new bone grew into these scaffolds. The healing rate and quality of the osteoporotic bone defects significantly improved in the drug-coated scaffold group. This study provides a new method for theoretical research and clinical treatment using functional materials for repairing osteoporotic bone defects.
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