材料科学
骨形态发生蛋白2
骨愈合
复合数
牛血清白蛋白
壳聚糖
血管内皮生长因子
骨形态发生蛋白
生物医学工程
脚手架
纳米颗粒
再生(生物学)
生长因子
骨形态发生蛋白7
纳米技术
血管内皮生长因子受体
细胞生物学
复合材料
化学
癌症研究
解剖
生物化学
生物
受体
医学
体外
基因
作者
Mingcong Chen,Yang Chen,Cheng Wei
摘要
Abstract Bone healing is a complex cascade involving precisely coordinated spatiotemporal presentation of multiple growth factors (GFs), including osteogenic and angiogenic GFs, and each stage of bone healing requires varying types and content of GFs. In this study, we fabricated a composite nanocoating with tunable vascular endothelial growth factor (VEGF) and bone morphogenetic protein‐2 (BMP‐2) that was coated on the surface of a polydopamine (PDA)‐decorated tertiary calcium phosphate (TCP) scaffold using VEGF‐loaded chitosan/bovine serum albumin nanoparticles (CS/BSA‐NPs) and BMP‐2‐loaded poly‐L‐lysine/oxidized alginate nanoparticles (PLL/OALG‐NPs). It was found that VEGF could be efficiently released to promote vascularization in early bone repair stages due to the rapid biodegradation of CS/BSA‐NPs, while bone formation can be promoted by a sustained release of BMP‐2 from the slowly degrading PLL/OALG‐NPs. The composite coating and TCP scaffold can be conjugated due to the excellent adhesive property of PDA. The composite coating can achieve the rapid release of VEGF and sustained release of BMP‐2, which can activate GFs for accelerating bone healing.
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