分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Synergizing macroscopic lateral anchoring with microscopic pore topology: A dual-optimization strategy for large bone defect reconstruction

Hao Chen, Xingzhen Li, Wenbo Yang, Yu Sun, Jinbo Zhang, Aobo Zhang, Meng Xu, Qian Wan, Xingchen Guo, Qing Han, Luquan Ren, Jincheng Wang

Journal:CHEMICAL ENGINEERING JOURNAL

IF:12.5

DOI:10.1016/j.cej.2026.177184

PMID:

Published:2026-05-09

research field:骨再生生物医学工程增材制造组织工程骨科植入物

Abstract

A 3D-printed Ti-6Al-4V tubular implant improved initial stability via extended intramedullary and lateral fixation. • Microporous mid-segment topology promoted stronger bone-implant interface integration. • The porous mid-segment showed compliant fixation behavior. Large tubular bone defects remain difficult to reconstruct because limited fixation length compromises initial mechanical stability, whereas suboptimal implant microarchitecture hinders long-term biological integration. To address these dual challenges, this study developed an application-oriented dual-optimization framework for Ti-6Al-4 V tubular implants by integrating established fixation principles with microscopic pore-topology regulation. At the macroscopic level, finite element analysis (FEA) showed that an unfavorable exposure-to-fixation ratio increased mid-segment stress concentration and interfacial shear, which guided the design of a tubular implant with extended intramedullary fixation and lateral cortical anchoring wings. A single proof-of-concept clinical application in an ultra-long femoral defect provided preliminary support for the early technical feasibility of this fixation concept. At the microscopic level, three representative mid-segment architectures—Porous, Truss, and Solid—were comparatively evaluated. In vitro, the Porous architecture promoted superior cell adhesion, proliferation, osteogenic activity, and angiogenic response while limiting fibroblast infiltration. In a rabbit femoral defect model, the Porous implant also achieved greater fixation stability and enhanced cortical bone integration. Overall, these findings support a mechanically and biologically integrated reconstruction strategy for large tubular bone defects. However, the current evidence remains preclinical and proof-of-concept in nature. Larger clinical cohorts, longer follow-up, and dedicated fatigue testing are still required to evaluate clinical generalizability, long-term safety, and the fatigue durabilit

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