伤口愈合
基因传递
碱性成纤维细胞生长因子
遗传增强
生长因子
血小板
血管内皮生长因子
血管内皮生长因子A
药理学
医学
生物医学工程
癌症研究
外科
化学
基因
免疫学
血管内皮生长因子受体
内科学
受体
生物化学
作者
Bolin Wang,Jianle Chen,Chuwei Zhang,Qingrong Zhang,Zhihan Zhu,Ling Qiu,Jun Yan,Zihan Li,Xinghua Zhu,Yi Zhang,Yun Jiang
标识
DOI:10.1016/j.intimp.2023.111164
摘要
The treatment of burn wounds, especially deep burn wounds, remains a major clinical challenge. Growth factors such as basic fibroblast growth factor (bFGF) and vascular endothelial growth factor A (VEGFA) show great potential in promoting the healing of damaged tissues. This study explored wound healing following targeted delivery of bFGF and VEGFA genes into deep burn wounds through a novel platelet membrane-coated nanoparticle (PM@gene-NP) complex delivery system.First, bFGF and VEGFA genes were inserted into plasmid (pEGFP-N1) vectors. Subsequently, the assembled plasmids were loaded onto nanoparticles to form gene-loaded nanoparticle complexes, which were then wrapped with extracted platelet membrane, fully simulating the characteristics of platelets, in order to actively target sites of inflammatory damage. After administration of PM@gene-NP complexes through the tail vein of rats, a series of experiments were conducted to evaluate wound healing.The PM@gene-NP complexes effectively targeted the burn sites. After the administration of the PM@gene-NP complexes, the rats exhibited increased blood flow in the burn wounds, which also healed faster than control groups. Histological results showed fewer inflammatory cells in the burned skin tissue after treatment. After the wounds healed, the production of hair follicles, sebaceous glands and other skin accessories in the skin tissue increased.Our results showed that the PM@gene-NP complexes can effectively deliver gene therapy to the injured area, and this delivery system should be considered as a potential method for treating deep burns.
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