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

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL Journal of biomedical materials research. Part A Pub Date : 2024-07-10 DOI:10.1002/jbm.a.37773
Parmida Ghiasi Tabari, Amirmohammad Sattari, Mohsen Mashhadi Keshtiban, Nushin Karkuki Osguei, John G. Hardy, Ali Samadikuchaksaraei
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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 CaCl2. 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.

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含有掺钴生物活性玻璃微球的可注射水凝胶支架,用于骨愈合。
事实证明,同时诱导血管生成和骨生成的可注射原位成型支架在骨愈合应用中大有可为。在此,我们报告了一种含有掺钴生物活性玻璃(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含有 BG 颗粒的蚕丝纤维素(SF)/明胶微球。微球与可注射的藻酸盐溶液混合,通过添加 CaCl2 在原位形成水凝胶。在大鼠腓骨缺损模型中对水凝胶的理化性质、与成骨细胞和内皮细胞的体外相互作用以及骨愈合潜力进行了评估。微球很好地分散在水凝胶中,并形成大于 100 μm 的孔。水凝胶显示了剪切稀化行为,并调节了钴的释放,因此只有含有掺杂了 5%重量比钴的 BG(A-S-G5Co)的支架才能达到刺激血管生成、细胞增殖和矿化基质沉积的最佳钴浓度。在钴含量较高的支架中,观察到表面的仿生矿化减少。基因表达研究表明,使用 A-S-G5Co 培养的细胞在不同时间点的成骨基因 COL1A1、ALPL、OCN 和 RUNX2 以及血管生成基因 HIF1A 和 VEGF 上调。最后,体内研究表明,A-S-G5Co 能显著促进血管生成和骨生成,并在 12 周的随访后改善骨愈合。这些结果表明,在可注射的原位成形支架中加入含有掺钴 BG 的 SF/明胶微球,可通过促进血管生成和骨生成有效提高其骨愈合潜力。
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来源期刊
Journal of biomedical materials research. Part A
Journal of biomedical materials research. Part A 工程技术-材料科学:生物材料
CiteScore
10.40
自引率
2.00%
发文量
135
审稿时长
3.6 months
期刊介绍: The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device. The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.
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