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可注射水凝胶支架,内含载钴生物活性玻璃微球,用于骨愈合。

Injectable hydrogel scaffold incorporating microspheres containing cobalt-doped bioactive glass for bone healing.

机构信息

Department of Medical Biotechnology, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.

Department of Mechanical Engineering, K. N. Toosi University of Technology, Tehran, Iran.

出版信息

J Biomed Mater Res A. 2024 Dec;112(12):2225-2242. doi: 10.1002/jbm.a.37773. Epub 2024 Jul 10.

DOI:10.1002/jbm.a.37773
PMID:38984402
Abstract

Injectable in situ-forming scaffolds that induce both angiogenesis and osteogenesis have been proven to be promising for bone healing applications. Here, we report the synthesis of an injectable hydrogel containing cobalt-doped bioactive glass (BG)-loaded microspheres. Silk fibroin (SF)/gelatin microspheres containing BG particles were fabricated through microfluidics. The microspheres were mixed in an injectable alginate solution, which formed an in situ hydrogel by adding CaCl. The hydrogel was evaluated for its physicochemical properties, in vitro interactions with osteoblast-like and endothelial cells, and bone healing potential in a rat model of calvarial defect. The microspheres were well-dispersed in the hydrogel and formed pores of >100 μm. The hydrogel displayed shear-thinning behavior and modulated the cobalt release so that the optimal cobalt concentration for angiogenic stimulation, cell proliferation, and deposition of mineralized matrix was only achieved by the scaffold that contained BG doped with 5% wt/wt cobalt (A-S-G5Co). In the scaffold containing higher cobalt content, a reduced biomimetic mineralization on the surface was observed. The gene expression study indicated an upregulation of the osteogenic genes of COL1A1, ALPL, OCN, and RUNX2 and angiogenic genes of HIF1A and VEGF at different time points in the cells cultured with the A-S-G5Co. Finally, the in vivo study demonstrated that A-S-G5Co significantly promoted both angiogenesis and osteogenesis and improved bone healing after 12 weeks of follow-up. These results show that incorporation of SF/gelatin microspheres containing cobalt-doped BG in an injectable in situ-forming scaffold can effectively enhance its bone healing potential through promotion of angiogenesis and osteogenesis.

摘要

可注射原位形成支架,可诱导血管生成和成骨,已被证明在骨愈合应用中具有广阔的前景。在此,我们报告了一种含有钴掺杂生物活性玻璃(BG)负载微球的可注射水凝胶的合成。通过微流控技术制备了载有 BG 颗粒的丝素蛋白(SF)/明胶微球。将微球混入可注射的藻酸盐溶液中,通过添加 CaCl 形成原位水凝胶。通过评估其物理化学性质、与成骨细胞样细胞和内皮细胞的体外相互作用以及在大鼠颅骨缺损模型中的骨愈合潜力来评估水凝胶。微球在水凝胶中分散良好,形成>100μm的孔。水凝胶表现出剪切稀化行为,并调节钴的释放,只有含有 5wt%wt 钴掺杂 BG 的支架(A-S-G5Co)才能实现对血管生成刺激、细胞增殖和矿化基质沉积的最佳钴浓度。在含有更高钴含量的支架中,观察到表面仿生矿化减少。基因表达研究表明,在细胞培养过程中,A-S-G5Co 可上调 COL1A1、ALPL、OCN 和 RUNX2 等成骨基因以及 HIF1A 和 VEGF 等血管生成基因。最后,体内研究表明,A-S-G5Co 可显著促进血管生成和成骨,并在 12 周的随访后改善骨愈合。这些结果表明,将含有钴掺杂 BG 的 SF/明胶微球掺入可注射原位形成支架中,可通过促进血管生成和成骨有效增强其骨愈合潜力。

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