Decoupling Pore Size and Porosity in Sheet-Based TPMS Scaffolds: Assessing Early Osteogenesis via a Capture-Then-Differentiate Framework.

IF 2.1 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Xiaochen Jia, Xiaoshuai Yang, Qihao Wei, Changwen Mi, Teng Lu, Jiabao Pan, Zhongwei Sun
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Abstract

Triply periodic minimal surface (TPMS) scaffolds possess significant application potential in bone tissue engineering owing to their smooth and continuous surface morphology and highly interconnected pore networks. However, in conventional parametric modeling of TPMS scaffolds, porosity and pore size usually vary in a coupled manner, restricting the systematic evaluation of scaffold structure-function relationships. In this study, a decoupled single-variable design strategy was adopted to construct homogeneous sheet-based TPMS scaffolds, including diamond sheet (DS), gyroid sheet (GS), and primitive sheet (PS) topologies, with independently controlled porosities (50%-90%) and pore sizes (500-900 μm). A sequential multiphysics framework integrating static compression finite element analysis (FEA), computational fluid dynamics (CFD), the discrete phase model (DPM), and mechano-regulation analysis was established to evaluate osteogenic potential during the early post-implantation hematoma stage. Results demonstrated that porosity primarily governed apparent stiffness, while permeability was highly sensitive to topological changes and pore size enlargement. The initial capture efficiency of mesenchymal stem cells (MSCs) was closely associated with the specific surface area (SSA) and dynamically regulated by flow trajectories and wall accessibility. Furthermore, mechano-regulation stimulus factor analysis, combining wall shear stress (WSS) and octahedral shear strain (OSS), revealed that WSS contributed dominantly to the local osteogenic microenvironment. Osteogenic differentiation efficiency was not maximized by any single structural parameter, but rather emerged from an optimal balance between the capacity to capture MSCs and adequate mechanical stimulation. These findings validate a "capture-then-differentiate" mechanism for early osteogenesis in sheet-based TPMS scaffolds, providing a quantitative multiphysics strategy for the topological optimization of bone scaffolds.

基于片状TPMS支架的解耦孔径和孔隙度:通过捕获-分化框架评估早期成骨。
三周期最小表面(TPMS)支架具有光滑连续的表面形态和高度互联的孔隙网络,在骨组织工程中具有重要的应用潜力。然而,在传统的TPMS支架参数化建模中,孔隙率和孔径通常是耦合变化的,这限制了对支架结构-功能关系的系统评价。本研究采用解耦单变量设计策略,构建了具有独立控制孔隙率(50% ~ 90%)和孔径(500 ~ 900 μm)的均质片基TPMS支架,包括金刚石片(DS)、陀螺仪片(GS)和原始片(PS)拓扑结构。建立了一个集静态压缩有限元分析(FEA)、计算流体动力学(CFD)、离散相模型(DPM)和力学调节分析于一体的顺序多物理场框架,以评估植入后早期血肿阶段的成骨潜能。结果表明,孔隙度主要控制表观刚度,而渗透率对拓扑变化和孔径增大高度敏感。间充质干细胞(MSCs)的初始捕获效率与比表面积(SSA)密切相关,并受流动轨迹和壁可及性的动态调节。此外,结合壁剪切应力(WSS)和八面体剪切应变(OSS)的力学调节刺激因子分析表明,壁剪切应力在局部成骨微环境中起主导作用。成骨分化效率的最大化并不取决于任何单一的结构参数,而是来自于捕获MSCs的能力和充分的机械刺激之间的最佳平衡。这些发现验证了片状TPMS支架早期成骨的“捕获-分化”机制,为骨支架的拓扑优化提供了定量的多物理场策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal for Numerical Methods in Biomedical Engineering
International Journal for Numerical Methods in Biomedical Engineering ENGINEERING, BIOMEDICAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
4.50
自引率
9.50%
发文量
103
审稿时长
3 months
期刊介绍: All differential equation based models for biomedical applications and their novel solutions (using either established numerical methods such as finite difference, finite element and finite volume methods or new numerical methods) are within the scope of this journal. Manuscripts with experimental and analytical themes are also welcome if a component of the paper deals with numerical methods. Special cases that may not involve differential equations such as image processing, meshing and artificial intelligence are within the scope. Any research that is broadly linked to the wellbeing of the human body, either directly or indirectly, is also within the scope of this journal.
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