精心设计的三维打印支架具有微结构和可控肽释放功能,可促进骨再生。

Biomaterials Translational Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI:10.12336/biomatertransl.2024.01.007
Jin Yang, Kanwal Fatima, Xiaojun Zhou, Chuanglong He
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引用次数: 0

摘要

修复大面积承重骨缺损需要超强的机械强度,这是单一水凝胶支架无法实现的。我们的目标是无缝整合最佳微结构、机械坚固性、血管化和骨诱导生物反应,以有效解决这些关键的承重骨缺损问题。为了应对这一挑战,我们采用三维(3D)打印技术制备了一种基于聚己内酯(PCL)的集成支架。在三维打印 PCL 支架的空隙中,嵌入了甲基丙烯酸酯明胶(GelMA)/甲基丙烯酸丝纤维素(SFMA)复合水凝胶,其中含有甲状旁腺激素(PTH)肽负载介孔二氧化硅纳米颗粒(PTH@MSNs),从而形成了多孔的 PTH@MSNs/GelMA/SFMA/PCL (PM@GS/PCL)支架。通过细致的化学和物理表征,证实了制造这种具有定制分层结构的功能性支架的可行性。压缩测试显示,复合支架的强度达到了令人印象深刻的 17.81 ± 0.83 兆帕。此外,通过使用人脐静脉内皮细胞进行 Transwell 和管形成试验,对 PM@GS/PCL 支架的体外血管生成潜力进行了评估,结果表明其细胞迁移和管网形成性能优越。使用骨髓间充质干细胞进行的茜素红和碱性磷酸酶染色试验清楚地表明,这种支架具有强大的成骨分化特性。此外,还利用微计算机断层扫描和组织学检查在大鼠股骨缺损模型上研究了这种支架的骨修复潜力,结果表明它具有更强的成骨和血管生成性能。这项研究提出了一种用于骨组织工程的微环境匹配复合支架的制造策略,为有效修复骨缺损提供了一种潜在的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meticulously engineered three-dimensional-printed scaffold with microarchitecture and controlled peptide release for enhanced bone regeneration.

The repair of large load-bearing bone defects requires superior mechanical strength, a feat that a single hydrogel scaffold cannot achieve. The objective is to seamlessly integrate optimal microarchitecture, mechanical robustness, vascularisation, and osteoinductive biological responses to effectively address these critical load-bearing bone defects. To confront this challenge, three-dimensional (3D) printing technology was employed to prepare a polycaprolactone (PCL)-based integrated scaffold. Within the voids of 3D printed PCL scaffold, a methacrylate gelatin (GelMA)/methacrylated silk fibroin (SFMA) composite hydrogel incorporated with parathyroid hormone (PTH) peptide-loaded mesoporous silica nanoparticles (PTH@MSNs) was embedded, evolving into a porous PTH@MSNs/GelMA/SFMA/PCL (PM@GS/PCL) scaffold. The feasibility of fabricating this functional scaffold with a customised hierarchical structure was confirmed through meticulous chemical and physical characterisation. Compression testing unveiled an impressive strength of 17.81 ± 0.83 MPa for the composite scaffold. Additionally, in vitro angiogenesis potential of PM@GS/PCL scaffold was evaluated through Transwell and tube formation assays using human umbilical vein endothelium, revealing the superior cell migration and tube network formation. The alizarin red and alkaline phosphatase staining assays using bone marrow-derived mesenchymal stem cells clearly illustrated robust osteogenic differentiation properties within this scaffold. Furthermore, the bone repair potential of the scaffold was investigated on a rat femoral defect model using micro-computed tomography and histological examination, demonstrating enhanced osteogenic and angiogenic performance. This study presents a promising strategy for fabricating a microenvironment-matched composite scaffold for bone tissue engineering, providing a potential solution for effective bone defect repair.

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