血管内皮生长因子
血管生成
骨形态发生蛋白2
明胶
材料科学
再生(生物学)
生长因子
碱性磷酸酶
壳聚糖
生物物理学
生物医学工程
化学
体外
血管内皮生长因子受体
生物化学
细胞生物学
癌症研究
医学
生物
酶
受体
作者
Seunghun S. Lee,Jung Hun Kim,Jiwoon Jeong,Seung Hyun L. Kim,Rachel H. Koh,Inseon Kim,Sunghoon Bae,Hoyon Lee,Nathaniel S. Hwang
出处
期刊:Biomaterials
[Elsevier]
日期:2020-10-01
卷期号:257: 120223-120223
被引量:86
标识
DOI:10.1016/j.biomaterials.2020.120223
摘要
Bone regeneration is a complicated physiological process regulated by several growth factors. In particular, vascular endothelial growth factor (VEGF) and bone morphogenetic protein-4 (BMP-4) are regarded as key factors that induce bone regeneration by angiogenesis and osteogenesis. In this study, we developed a double cryogel system (DC) composed of gelatin/chitosan cryogel (GC) surrounded by gelatin/heparin cryogel (GH) for dual drug delivery with different release kinetics. VEGF was loaded in GH (outer layer of DC) for the initial release of VEGF to induce angiogenesis and provide blood supply in the defect area, while BMP-4 was loaded in GC (inner layer of DC) that leads to sustained release for continuous osteogenic induction. After analyzing characteristics of the double cryogel system such as porosity, degradation rate, swelling ratio, and mechanical properties, we evaluated release kinetics of VEGF (initial release) and BMP-4 (sustained-release) by ELISA. Then, the timely release of VEGF and BMP from DC synergistically induced in vitro osteogenic differentiation as confirmed by alkaline phosphatase staining, Alizarin Red S staining, and real-time PCR analysis. Finally, a critical-sized cranial defect model confirmed the enhanced bone regeneration as a result of dual release growth factor mechanisms.
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