脚手架
PLGA公司
材料科学
生物医学工程
聚乳酸
骨愈合
再生(生物学)
体内
血管生成
纳米技术
复合材料
外科
细胞生物学
医学
癌症研究
纳米颗粒
生物技术
聚合物
生物
作者
Shihang Liu,Shuai Zhou,Tingting Zou,G. Y. Hou,Qian Xiao,Lin Li,Jianjun Yang,Wei Chen,Yingze Zhang,Hongzhi Lv
标识
DOI:10.1002/adhm.202501938
摘要
Abstract The management of long bone segmental defects represents a critical challenge in orthopedic medicine. This study focuses on developing an innovative bone repair material to overcome the inherent limitations of existing solutions. The material is synthesized by incorporating magnesium into mineralized collagen to produce Mg‐MC bone powder, which is then combined with polylactic acid‐hydroxyglycolic acid copolymer (PLGA). Using advanced 3D printing and femtosecond laser techniques, Mg‐MC/PLGA scaffolds with varying magnesium concentrations (0%, 5%, 10%, 20%) are fabricated and characterized. In vitro studies demonstrate that the 5% Mg‐MC/PLGA scaffold exhibits superior cytocompatibility, cellular proliferation, migration, angiogenesis, and osteogenic activity, supported by elevated expression of osteogenic markers. In vivo experiments in a rabbit model confirm the efficacy of the 5% Mg 2 ⁺‐doped scaffold in promoting bone regeneration, with significant improvements in bone volume, trabecular thickness, and biomechanical strength. These findings highlight the potential of the 5% Mg‐MC/PLGA scaffold as a promising solution for the clinical treatment of bone defects.
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