PLGA公司
血管生成
脚手架
材料科学
脐静脉
壳聚糖
血管内皮生长因子
京尼平
乙醇酸
人脐静脉内皮细胞
体外
生物医学工程
生物物理学
纳米技术
化学
血管内皮生长因子受体
生物化学
生物
癌症研究
乳酸
医学
纳米颗粒
遗传学
细菌
作者
Yuanman Yu,Jie Chen,Rui Chen,Lingyan Cao,Wei Tang,Dan Lin,Jing Wang,Changsheng Liu
标识
DOI:10.1021/acsami.5b02324
摘要
Rapid and controlled vascularization within scaffolds remains one of the key limitations in tissue engineering applications. This study describes the fabrication and characterization of 2-N,6-O-sulfated chitosan (26SCS)-coated hierarchical scaffold composed of poly(lactic-co-glycolic acid) (PLGA) microspheres, as a desirable vehicle for vascular endothelial growth factor (VEGF) delivery and consequent angiogenic boosting in vitro. Owing to the hierarchical porous structure and high affinity between VEGF and 26SCS, the 26SCS-modified PLGA (S-PLGA) scaffold possesses excellent entrapment and sustained release of VEGF. Using human umbilical vein endothelial cells (HUVECs) as a cell model, the VEGF-loaded S-PLGA scaffold shows desirable cell viability and attachment. The bioactivity of released VEGF is validated by intracellular nitric oxide secretion and capillary tube formation, demonstrating the improved capacity of VEGF-mediated pro-angiogenesis ascribed to 26SCS incorporation. Such a strategy will afford an effective method to prepare a scaffold with promoted angiogenesis.
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