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研究内容简介 Schematic
illustration of the fabrication and application of the ROS-responsive QCG@Exos m iR-4500 hydrogel in treating liver fibrosis. A) Preparation of the QCG@Exos miR-4500 hydrogel. B) Effective mechanisms of the QCG@Exos miR-4500 hydrogel:
reversible boronic ester bonds were dissociated under the trigger of the local
high ROS, releasing ExosmiR-4500 on demand, thus e xerting anti-oxidation,
anti-angiogenesis, and anti-fibrosis effects. 肝纤维化是慢性肝病进展至肝硬化、肝癌等终末期肝病的关键事件,其逆转需要有效的策略减少氧化应激和抑制肝星状细胞(HSC)的激活。MiR-4500 能调节病理性血管生成和胶原mRNA稳定性,具有抑制纤维化的潜力。外泌体(Exos)是miRNA的天然转运载体,具有非免疫原性和高安全性等优点。然而,Exos的临床应用必须克服稳定性差和保留率低的问题。本研究通过季铵化壳聚糖和4-羧基苯硼酸改性明胶的动态交
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