Vikingsson L, Claessens B, Gómez-Tejedor J A, Gallego Ferrer G, Gómez Ribelles J L
Centre for Biomaterials and Tissue Engineering, CBIT, Universitat Politècnica de València, 46022 Valencia, Spain.
Centre for Biomaterials and Tissue Engineering, CBIT, Universitat Politècnica de València, 46022 Valencia, Spain.
J Mech Behav Biomed Mater. 2015 Aug;48:60-69. doi: 10.1016/j.jmbbm.2015.03.021. Epub 2015 Apr 2.
In tissue engineering the design and optimization of biodegradable polymeric scaffolds with a 3D-structure is an important field. The porous scaffold provide the cells with an adequate biomechanical environment that allows mechanotransduction signals for cell differentiation and the scaffolds also protect the cells from initial compressive loading. The scaffold have interconnected macro-pores that host the cells and newly formed tissue, while the pore walls should be micro-porous to transport nutrients and waste products. Polycaprolactone (PCL) scaffolds with a double micro- and macro-pore architecture have been proposed for cartilage regeneration. This work explores the influence of the micro-porosity of the pore walls on water permeability and scaffold compliance. A Poly(Vinyl Alcohol) with tailored mechanical properties has been used to simulate the growing cartilage tissue inside the scaffold pores. Unconfined and confined compression tests were performed to characterize both the water permeability and the mechanical response of scaffolds with varying size of micro-porosity while volume fraction of the macro-pores remains constant. The stress relaxation tests show that the stress response of the scaffold/hydrogel construct is a synergic effect determined by the performance of the both components. This is interesting since it suggests that the in vivo outcome of the scaffold is not only dependent upon the material architecture but also the growing tissue inside the scaffold׳s pores. On the other hand, confined compression results show that compliance of the scaffold is mainly controlled by the micro-porosity of the scaffold and less by hydrogel density in the scaffold pores. These conclusions bring together valuable information for customizing the optimal scaffold and to predict the in vivo mechanical behavior.
在组织工程中,设计和优化具有三维结构的可生物降解聚合物支架是一个重要领域。多孔支架为细胞提供了一个合适的生物力学环境,允许机械转导信号促进细胞分化,并且支架还能保护细胞免受初始压缩载荷。支架具有相互连接的大孔,用于容纳细胞和新形成的组织,而孔壁应为微孔结构,以运输营养物质和代谢产物。具有双微孔和大孔结构的聚己内酯(PCL)支架已被提出用于软骨再生。这项工作探讨了孔壁微孔率对水渗透性和支架顺应性的影响。使用具有定制机械性能的聚乙烯醇来模拟支架孔内生长的软骨组织。在大孔体积分数保持恒定的情况下,进行了无侧限和侧限压缩试验,以表征不同微孔尺寸的支架的水渗透性和力学响应。应力松弛试验表明,支架/水凝胶构建体的应力响应是由两种组分的性能共同决定的协同效应。这很有趣,因为这表明支架在体内的结果不仅取决于材料结构,还取决于支架孔内生长的组织。另一方面,侧限压缩结果表明,支架的顺应性主要由支架的微孔率控制,而较少受支架孔内水凝胶密度的影响。这些结论为定制最佳支架和预测体内力学行为提供了有价值的信息。