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Heparin-chitosan nanoparticle functionalization of porous poly(ethylene glycol) hydrogels for localized lentivirus delivery of angiogenic factors

机译:肝素-壳聚糖纳米颗粒功能化的多孔聚乙二醇水凝胶的局部慢病毒传递血管生成因子。

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摘要

Hydrogels have been extensively used for regenerative medicine strategies given their tailorable mechanical and chemical properties. Gene delivery represents a promising strategy by which to enhance the bioactivity of the hydrogels, though the efficiency and localization of gene transfer have been challenging. Here, we functionalized porous poly(ethylene glycol) hydrogels with heparin-chitosan nanoparticles to retain the vectors locally and enhance lentivirus delivery while minimizing changes to hydrogel architecture and mechanical properties. The immobilization of nanoparticles, as compared to homogeneous heparin and/or chitosan, is essential to lentivirus immobilization and retention of activity. Using this gene-delivering platform, we over-expressed the angiogenic factors sonic hedgehog (Shh) and vascular endothelial growth factor (Vegf) to promote blood vessel recruitment to the implant site. Shh enhanced endothelial recruitment and blood vessel formation around the hydrogel compared to both Vegf-delivering and control hydrogels. The nanoparticle-modified porous hydrogels for delivering gene therapy vectors can provide a platform for numerous regenerative medicine applications.
机译:鉴于其可调节的机械和化学特性,水凝胶已广泛用于再生医学策略。尽管基因转移的效率和定位具有挑战性,但是基因传递代表了一种有前途的策略,通过该策略可以增强水凝胶的生物活性。在这里,我们用肝素-壳聚糖纳米粒子功能化了多孔聚乙二醇水凝胶,以局部保留载体并增强慢病毒的传递,同时最大程度地减少了水凝胶结构和机械性能的变化。与均质肝素和/或壳聚糖相比,纳米粒子的固定化对于慢病毒固定化和保持活性至关重要。使用此基因传递平台,我们过表达了血管生成因子声波刺猬(Shh)和血管内皮生长因子(Vegf),以促进血管募集到植入部位。与递送Vegf的水凝胶和对照水凝胶相比,Shh增强了水凝胶周围的内皮募集和血管形成。用于递送基因治疗载体的纳米粒子修饰的多孔水凝胶可为众多再生医学应用提供平台。

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