基于细胞扩散、生长因子释放和组织再生的骨支架一体化设计初步研究

M. Şahin, A. Tabak, Gullu Kiziltas Sendur
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引用次数: 1

摘要

结合生物活性分子和细胞的三维多孔组织支架为骨修复机制提供了关键优势。一个功能性的骨组织支架应该提供机械支持,并具有足够的孔隙度和渗透性,以供营养、供氧、清除废物、释放生长因子以及控制降解。尽管存在大量的工作来解决这些挑战,但据我们所知,在时域内同时考虑组织分化、扩散和生长因子(GF)释放的设计框架尚不存在。在本文中,我们通过为COMSOL Multiphysics®软件中的有限元分析(FEA)模型中包含这些效果的仿真框架奠定基础,提供了解决此类需求的初步努力。通过模拟三维多孔弹性骨支架的初步力学生物学分析,证明了数值模型的有效性。初始的时间相关结果证明了该模型对于优化框架的适用性。更具体地说,研究表明,扩散、GF释放和分化的耦合多物理场方程可以为未来有效骨修复任务的理想骨支架系统提供有价值的输入。
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Initial Study Towards the Integrated Design of Bone Scaffolds Based on Cell Diffusion, Growth Factor Release and Tissue Regeneration
Three-dimensional (3D) porous tissue scaffolds combined with bioactive molecules and cells offer key advantages for bone repair mechanisms. A functional bone tissue scaffold should provide mechanical support with an adequate combination of porosity and permeability for nutrients, oxygen supply, waste removal, and growth factors release as well as controlled degradation. Although a vast amount of work exist to address these challenges, to the best of our knowledge, a design framework taking tissue differentiation, diffusion, and growth factor (GF) release into account in time-domain simultaneously does not exist. In this paper, we provide an initial effort to address such a need by laying down the foundations for a simulation framework incorporating these effects within a Finite Element Analysis (FEA) model in COMSOL Multiphysics® software. The effectiveness of the numerical model is demonstrated via preliminary mechano-biology analyses on a simulated 3D poroelastic bone scaffold. Initial time-dependent results demonstrate the suitability of this model for an optimization framework. More specifically, it is demonstrated that coupled Multiphysics equations of diffusion, GF release, and differentiation could provide valuable inputs for ideal bone scaffold systems for effective bone repair tasks in the future.
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