角膜新生血管
生物相容性
纳米纤维
肽
体内
体外
血管生成
血管内皮生长因子
新生血管
化学
生物相容性材料
生物物理学
材料科学
药理学
血管内皮生长因子受体
癌症研究
纳米技术
角膜
生物化学
生物医学工程
医学
生物
眼科
有机化学
生物技术
作者
Zhongxing Chen,Xin-Jie Mao,Xiuhong Ye,Siheng Li,Tianlu Wu,Qing Wang,Jun Zhang,Lu Chen,Nana Tang,Huanhuan He,Zhen Wang,Colm McAlinden,Qinmei Wang,Shihao Chen,Rongrong Gao,Jinhai Huang
标识
DOI:10.1016/j.cej.2021.129081
摘要
Corneal neovascularization (CoNV) secondary to vascular endothelial growth factor (VEGF) can occur in a variety of corneal pathologies. Inhibition of VEGF or its receptor is a promising strategy to treat CoNV. The HRH peptide sequence, screened by phage display library, has a good affinity with VEGFR and inhibits abnormal vascular development. However, a high dose of peptides is usually required to obtain an ideally therapeutic effect, due to the instability and low bioactivity of peptides. In this study, we conjugated a bioactive epitope of HRH peptide to NapFF peptide to produce amphiphilic peptides which could self-assemble into nanofibers. This nanofibrous structure efficiently improved the bioactivity of the HRH peptide by prolonging the degraded time and increasing multivalency of the surface of the material. The excellent anti-angiogenic activity of NapFFHRH at lower concentrations was demonstrated both in vitro and in vivo alkali burn CoNV model. In addition, repeated subconjunctival injection of NapFFHRH did not induce acute irritative reactions or have any detrimental effect on the retina. NapFFHRH with its anti-angiogenic potency and biocompatibility could become a promising strategy for CoNV.
科研通智能强力驱动
Strongly Powered by AbleSci AI