Hollow-Tube-Whisker-Modified Biphasic Calcium Phosphate Ceramics Loaded with SDF-1α and EPCs for Steroid-Induced Osteonecrosis of Femoral Head

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2025-02-05 DOI:10.1002/adfm.202415041
Yi Zhou, Jiang Yu, Yuyi Wang, Cong Feng, Xiaolong Yang, Xiangfeng Li, Weili Fu, Xiangdong Zhu, Jian Li, Xingdong Zhang
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Abstract

Steroid-induced osteonecrosis of the femoral head (SONFH) remains a significant challenge in orthopedic clinical treatment. In this study, a novel 3D hollow-tube-whisker-modified biphasic calcium phosphate ceramic (H-BCP) is successfully fabricated using an in-situ growth technique. Compared to conventional BCP ceramics, H-BCP exhibited increased specific surface area, enhanced mechanical strength, and improved biocompatibility. Utilizing the hollow-tube whisker structure, H-BCP is functionalized with stromal cell-derived factor-1α (SDF-1α) to construct the H-BCP@SDF-1α sustained-release system. In vitro studies demonstrated that H-BCP@SDF-1α effectively recruited bone marrow stromal cells (BMSCs), promoted their osteogenic differentiation, and supported the angiogenic differentiation of endothelial progenitor cells (EPCs). Furthermore, EPC-loaded H-BCP@SDF-1α (H-BCP@SDF-1α/EPC) is used to construct vascularized tissue-engineered bone and implanted into a SONFH rabbit model following core decompression surgery. At 12 weeks post-surgery, animals implanted with H-BCP@SDF-1α/EPC exhibited significant new bone formation, bone integration, and in situ revascularization. Additionally, it is found that H-BCP@SDF-1α/EPC activated the PI3K/AKT signaling pathway in BMSCs, upregulating osteogenic gene expression. This study explores a novel material system integrating mechanical support, bioactivity, and drug delivery, offering a promising approach for SONFH treatment.

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载SDF-1α和EPCs的空心管晶须修饰双相磷酸钙陶瓷用于类固醇性股骨头坏死
类固醇性股骨头坏死(SONFH)仍然是骨科临床治疗中的一个重大挑战。在本研究中,利用原位生长技术成功制备了一种新型的三维空心管晶须修饰的双相磷酸钙陶瓷(H-BCP)。与传统的BCP陶瓷相比,H-BCP陶瓷具有更高的比表面积、更高的机械强度和更好的生物相容性。利用空心管晶须结构,H-BCP与基质细胞衍生因子-1α (SDF-1α)功能化,构建H-BCP@SDF-1α缓释体系。体外研究表明,H-BCP@SDF-1α能有效募集骨髓基质细胞(BMSCs),促进其成骨分化,并支持内皮祖细胞(EPCs)的血管生成分化。此外,利用内皮细胞负载H-BCP@SDF-1α (H-BCP@SDF-1α/EPC)构建带血管的组织工程骨,并在核心减压手术后植入SONFH兔模型。术后12周,植入H-BCP@SDF-1α/EPC的动物表现出明显的新骨形成、骨整合和原位血运重建。此外,研究发现H-BCP@SDF-1α/EPC激活骨髓间充质干细胞中PI3K/AKT信号通路,上调成骨基因的表达。本研究探索了一种集机械支持、生物活性和药物传递于一体的新型材料系统,为SONFH的治疗提供了一种有前景的方法。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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