Hierarchical bone scaffolds with integrated trabecular topology and lacuno-canalicular connectivity modulate fluid dynamics and support osteogenic culture.

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Sara Sebastiani, Giuliana Tromba, Valentina Rafaela Herrera Millar, Laura Maria Vergani, Federica Buccino
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引用次数: 0

Abstract

The hierarchical structure of bone governs both mechanical behavior and mechanobiological signaling, yet most Bone Tissue Engineering (BTE) scaffolds reproduce only meso-scale porosity while neglecting the Lacuno-Canalicular Network (LCN), a key regulator of interstitial fluid flow. Here, we present a multi-scale bio-inspired scaffold integrating synchrotron μ-CT-derived trabecular architecture with a computationally engineered LCN-like micro-porosity. Two micro-network topologies, Regular and Canalicular-like, were fabricated via two-photon polymerization using IP-VISIO, here applied for the first time in a BTE context. Computational fluid dynamics revealed topology-dependent transport behavior: the Canalicular-like architecture exhibited >40% higher permeability and more homogeneous wall shear stress distributions within osteogenic-relevant ranges compared to the Regular design. Human bone marrow-derived mesenchymal stromal cells were cultured onto scaffolds under static conditions, showing cell attachment, osteogenic gene expression, and mineralized matrix deposition in both designs, assessed by SEM, RT-qPCR and Alizarin Red S staining. Synchrotron μ-CT showed mineral deposition throughout both trabecular regions and the engineered micro-network, with a more uniform spatial distribution in the Canalicular-like scaffold. Overall, this work proposes a multi-scale design framework and identifies LCN-inspired micro-architecture as a promising design variable for hierarchical bone scaffolds, influencing predicted fluid-dynamic behavior and supporting osteogenic culture.

具有集成小梁拓扑结构和腔隙-小管连接的分层骨支架调节流体动力学并支持成骨培养。
骨的层次结构控制着力学行为和力学生物学信号传导,然而大多数骨组织工程(BTE)支架只复制中尺度孔隙,而忽略了间质流体流动的关键调节因子——腔隙-管状网络(LCN)。在这里,我们提出了一种多尺度仿生支架,将同步加速器μ ct衍生的小梁结构与计算工程的lcn样微孔隙相结合。利用IP-VISIO通过双光子聚合制备了两个微网络拓扑,规则和管状,这是首次在BTE环境中应用。计算流体动力学揭示了拓扑依赖的输运行为:与常规设计相比,管状结构的渗透率提高了约40%,在与成骨相关的范围内,壁剪应力分布更均匀。在静态条件下将人骨髓间充质间质细胞培养到支架上,通过扫描电镜、RT-qPCR和茜素红S染色,两种设计均显示出细胞附着、成骨基因表达和矿化基质沉积。同步加速器μ-CT显示,矿物沉积遍布小梁区和工程微网络,在管状支架内的空间分布更为均匀。总的来说,这项工作提出了一个多尺度的设计框架,并确定了lcn启发的微建筑作为分层骨支架的一个有前途的设计变量,影响预测的流体动力学行为并支持成骨培养。
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
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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