IRCCS Istituto Ortopedico Rizzoli, Laboratorio di NanoBiotecnologie (NaBi), Via di Barbiano 10/2, 40136 Bologna, Italy.
IRCCS Istituto Ortopedico Rizzoli, Laboratorio di Biomeccanica e Innovazione Tecnologica, Via di Barbiano 10/2, 40136 Bologna, Italy; Department of Information Engineering, University of Brescia, Via Branze 38, 25123 Brescia, Italy.
Med Eng Phys. 2019 Jul;69:92-99. doi: 10.1016/j.medengphy.2019.04.009. Epub 2019 May 14.
In order to increase manufacturing and experimental efficiency, a certain degree of control over design performances before realization phase is recommended. In this context, this paper presents an integrated procedure to design 3D scaffolds for bone tissue engineering. The procedure required a combination of Computer Aided Design (CAD), Finite Element Analysis (FEA), and Design methodologies Of Experiments (DOE), firstly to understand the influence of the design parameters, and then to control them. Based on inputs from the literature and limitations imposed by the chosen manufacturing process (Precision Extrusion Deposition), 36 scaffold architectures have been drawn. The porosity of each scaffold has been calculated with CAD. Thereafter, a generic scaffold material was considered and its variable parameters were combined with the geometrical ones according to the Taguchi method, i.e. a DOE method. The compressive response of those principal combinations was simulated by FEA, and the influence of each design parameter on the scaffold compressive behaviour was clarified. Finally, a regression model was obtained correlating the scaffold's mechanical performances to its geometrical and material parameters. This model has been applied to a novel composite material made of polycaprolactone and innovative bioactive glass. By setting specific porosity (50%) and stiffness (0.05 GPa) suitable for trabecular bone substitutes, the model selected 4 of the 36 initial scaffold architectures. Only these 4 more promising geometries will be realized and physically tested for advanced indications on compressive strength and biocompatibility.
为了提高制造和实验效率,建议在实现阶段之前对设计性能进行一定程度的控制。在这种情况下,本文提出了一种用于骨组织工程 3D 支架设计的综合程序。该程序需要结合计算机辅助设计 (CAD)、有限元分析 (FEA) 和实验设计方法 (DOE),首先了解设计参数的影响,然后控制它们。基于文献中的输入和所选制造工艺(精密挤出沉积)的限制,绘制了 36 种支架结构。使用 CAD 计算了每个支架的孔隙率。然后,考虑了一种通用的支架材料,并根据田口方法(即 DOE 方法)将其可变参数与几何参数结合在一起。通过 FEA 模拟了这些主要组合的压缩响应,并阐明了每个设计参数对支架压缩性能的影响。最后,获得了一个将支架的机械性能与其几何和材料参数相关联的回归模型。该模型已应用于由聚己内酯和创新的生物活性玻璃制成的新型复合材料。通过设置适合小梁骨替代品的特定孔隙率(50%)和刚度(0.05 GPa),该模型选择了 36 个初始支架结构中的 4 个。只有这 4 种更有前途的几何形状将被实现并进行物理测试,以获得有关抗压强度和生物相容性的高级指示。