Mechanobiologically optimized 3D titanium-mesh scaffolds enhance bone regeneration in critical segmental defects in sheep

再生(生物学) 生物医学工程 医学 材料科学 细胞生物学 生物 冶金
作者
Anne‐Marie Pobloth,Sara Checa,Hajar Razi,Ansgar Petersen,James C. Weaver,Katharina Schmidt‐Bleek,Markus Windolf,András Áron Tatai,Claudia P. Roth,Klaus‐Dieter Schaser,Georg N. Duda,P. Schwabe
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:10 (423) 被引量:297
标识
DOI:10.1126/scitranslmed.aam8828
摘要

Three-dimensional (3D) titanium-mesh scaffolds offer many advantages over autologous bone grafting for the regeneration of challenging large segmental bone defects. Our study supports the hypothesis that endogenous bone defect regeneration can be promoted by mechanobiologically optimized Ti-mesh scaffolds. Using finite element techniques, two mechanically distinct Ti-mesh scaffolds were designed in a honeycomb-like configuration to minimize stress shielding while ensuring resistance against mechanical failure. Scaffold stiffness was altered through small changes in the strut diameter only. Honeycombs were aligned to form three differently oriented channels (axial, perpendicular, and tilted) to guide the bone regeneration process. The soft scaffold (0.84 GPa stiffness) and a 3.5-fold stiffer scaffold (2.88 GPa) were tested in a critical size bone defect model in vivo in sheep. To verify that local scaffold stiffness could enhance healing, defects were stabilized with either a common locking compression plate that allowed dynamic loading of the 4-cm defect or a rigid custom-made plate that mechanically shielded the defect. Lower stress shielding led to earlier defect bridging, increased endochondral bone formation, and advanced bony regeneration of the critical size defect. This study demonstrates that mechanobiological optimization of 3D additive manufactured Ti-mesh scaffolds can enhance bone regeneration in a translational large animal study.
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