Ti-6Al-4V最小表面骨类似物的不对称力学行为和前成骨细胞分化:孔隙拓扑结构的作用。

IF 9.6
Bijay Kumar Karali, Suresh Suthar, Sushant Banerji, Bikramjit Basu
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引用次数: 0

摘要

基于细胞结构的材料的可制造性代表了医疗植入物和设备增材制造中最新兴的主题之一。因为天然骨具有独特的多孔结构,这在传统制造中是无法模仿的。尽管最近取得了一些进展,但在将支架拓扑结构和可制造性与不对称三维孔隙结构控制的机械生物学反应联系起来方面,仍然存在一个关键的知识缺口。从这个角度来看,本研究的重点是Ti6Al4V中Schwarz金刚石基三周期最小表面(TPMS)结构的选择性激光熔化,同时改变单位晶胞尺寸从2.5到3.0 mm。使用定制设计评估协议对三维孔隙拓扑进行了广泛的微观计算机断层扫描分析,确定了基于slm的优化工艺参数对TPMS结构的尺寸公差和可制造性的有效性。有趣的是,压缩弹性模量(14-20 GPa)、拉伸弹性模量(38 - 55 GPa)、抗压强度(413-547 MPa)和拉伸强度(325-475MPa)的非对称力学响应,以及独特的3D孔隙结构,与人类皮质骨的特性非常相似。当使用Gibson-Ashby模型拟合强度/模量与相对密度数据时,弯曲主导的不对称微观结构响应显示为压缩指数为~ 1.5,拉伸指数为~ 2.0。此外,体外研究表明MC3T3-E1前成骨细胞的粘附、增殖和成熟与早期成骨标志物和骨矿化的调节有关,无论是定量的还是定性的。共聚焦显微镜观察显示细胞桥接、迁移和定植,表明细胞相容性。目前的研究最终确定了SDW-TPMS结构提供了一个令人信服的皮质骨模拟力学性能和有利的生物反应的组合。它强调了它们在承重关节重建手术中的潜力。意义声明:传统的高模量金属种植体可以通过应力屏蔽诱导假体周围骨吸收。虽然增材制造的多孔生物材料解决了这个问题,但一个强大的结构-性能-功能范式仍然难以捉摸。本研究提出了一种Ti-6Al-4V最小表面支架,在提供适合前成骨细胞分化的微环境的同时,实现了承载应用的生物力学保真度。核心创新是我们使用定量孔隙网络建模,在制造的孔隙拓扑结构、支架明显的拉伸-压缩不对称及其促成骨生物反应之间建立预测联系。这项工作为下一代生物集成骨科植入物的合理设计提供了一个有效的框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asymmetric Mechanical Behavior and pre-osteoblast differentiation in Ti-6Al-4V Minimal-Surface Bone-Analogues: The Role of Pore Topology.

The manufacturability of the cellular structure-based materials represents one of the most emerging themes in the additive manufacturing of medical implants and devices. This has been more relevant as natural bone possesses a unique porous architecture, which cannot be mimicked in conventional manufacturing. Despite recent advances, a critical knowledge gap persists in connecting scaffold topology and manufacturability with the mechano-biological responses, governed by asymmetric 3D pore structures. In this perspective, the present study focuses on selective laser melting of Schwarz diamond-based triply periodic minimal surface (TPMS) structures in Ti6Al4V, while varying unit cell size from 2.5 to 3.0 mm. The extensive micro-computed tomography analysis of 3D pore topology using customised design evaluation protocols established the efficacy of SLM-based optimised process parameters on dimensional tolerance and manufacturability of the TPMS structures. Intriguingly, an asymmetric mechanical response with a clinically relevant combination of the compressive elastic modulus (14-20 GPa), tensile elastic modulus (38 - 55 GPa), compressive strength (413-547 MPa), and tensile strength (325-475MPa), together with unique 3D pore architecture, closely resembled the properties of human cortical bone. While fitting the strength/modulus to relative density data using the Gibson-Ashby model, the bending-dominated asymmetric microstructural response was revealed with exponents of ∼1.5 in compression and ∼2.0 in tension. Furthermore, in vitro studies demonstrate MC3T3-E1 pre-osteoblasts' adhesion, proliferation, and maturation with modulation of early osteogenic markers and bone mineralisation, both quantitatively and qualitatively. The confocal microscopy observations revealed the cellular bridging, migration, and colonisation, indicating cytocompatibility. The present study conclusively establishes that SDW-TPMS structures offer a compelling combination of cortical bone-mimicking mechanical properties and a favourable biological response. It highlights their potential for reconstructive surgeries of load-bearing joints. STATEMENT OF SIGNIFICANCE: Conventional high-modulus metallic implants can induce periprosthetic bone resorption via stress shielding. While additively manufactured porous biomaterials address this, a robust structure-property-function paradigm has remained elusive. This study presents a Ti-6Al-4V minimal-surface scaffold that achieves the biomechanical fidelity for load-bearing applications while providing a microenvironment suitable for differentiataion of pre-osteoblasts. The central innovation is our use of quantitative pore network modeling to establish a predictive link between the as-manufactured pore topology, the scaffold's pronounced tension-compression asymmetry, and its pro-osteogenic biological response. This work provides a validated framework for the rational design of next-generation bio-integrated orthopedic implants.

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