新生血管
血管生成
PLGA公司
材料科学
治疗性血管生成
先天免疫系统
生物医学工程
灌注
血管
血管内皮生长因子
可生物降解聚合物
微球
体内
免疫系统
纳米技术
医学
免疫学
癌症研究
生物
血管内皮生长因子受体
聚合物
内科学
化学工程
工程类
生物技术
复合材料
纳米颗粒
作者
Eseelle K. Hendow,Francesco Iacoviello,Mar Casajuana Ester,Caroline Pellet‐Many,Richard M. Day
标识
DOI:10.1002/adhm.202401832
摘要
Abstract Promoting neovascularization is a prerequisite for many tissue engineering applications and the treatment of cardiovascular disease. Delivery of a pro‐angiogenic stimulus via acellular materials offers several benefits over biological therapies but has been hampered by interaction of the implanted material with the innate immune response. However, macrophages, a key component of the innate immune response, release a plurality of soluble factors that can be harnessed to stimulate neovascularization and restore blood flow to damaged tissue. This study investigates the ability of biodegradable poly(D,L‐lactic‐co‐glycolic acid) (PLGA) microspheres to restore tissue perfusion in a hind limb model of ischaemia. Microspheres exhibiting a hierarchical porous structure are associated with an increase in blood flow at day 21 post‐implantation compared with solid microspheres composed of the same polymer. This corresponds with an increase in blood vessel density in the surrounding tissue. In vitro simulation of the foreign body response observed demonstrates M2‐like macrophages incubated with the porous microspheres secreted increased amounts of vascular endothelial growth factor (VEGF) compared with M1‐like macrophages providing a potential mechanism for the increased neovascularization. The results from this study demonstrate implantable biodegradable porous microspheres provide a novel approach for increasing neovascularization that could be exploited for therapeutic applications.
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