伤口愈合
神童素
光热治疗
血管生成
光动力疗法
体内
移植
血管内皮生长因子
一氧化氮
药理学
慢性伤口
医学
化学
癌症研究
材料科学
外科
生物
血管内皮生长因子受体
纳米技术
内科学
生物化学
有机化学
大肠杆菌
粘质沙雷氏菌
生物技术
基因
作者
Wu Zhou,Chang Li,Changling Li,Pengxiang Xu,Liuying Liu,Aidi Tong,Yilong Li,Chunyi Tong,Bin Liu
标识
DOI:10.1002/adhm.202405100
摘要
Abstract Healing of infected chronic wounds faces dual challenges: persistent inflammation and impaired angiogenesis. To address these, SN‐PB@PG nanocomplexes were prepared by hybridisation of nitroprusside (SNP) with Prussian blue (SN‐PB NPs) and loaded with prodigiosin (PG). Under near‐infrared (NIR) irradiation, SN‐PB NPs generated mild hyperthermia, facilitating the release of nitric oxide (NO) and PG to combat bacterial biofilms and multidrug‐resistant pathogens. The in vivo assay using diabetic infected wounds demonstrated that SN‐PB@PG NPs with NIR reduced the wound area to 10.6% by the 11th day, which is superior to that of control group (29.6%). In the flap transplantation experiments, the data showed SN‐PB@PG NPs with NIR group only have a necrobiosis of 3.8% of flaps on the 8th day, which is superior to 31.3% of the control group. Additionally, the release of NO promoted vascular regeneration by up‐regulating vascular endothelial growth factor (VEGF) and platelet endothelial cell adhesion molecule‐1 (CD31), and regenerated sarcomeric tissue by down‐regulating MMP‐9. The results indicated that the combination of SN‐PB@PG NPs with gas and photothermal therapy exerted a combined antibacterial and wound healing effect. Compared to traditional clinical methods such as surgical debridement and hyperbaric oxygen therapy, this new strategy efficiently addresses issues of infection and healing, which is convenient for clinical application.
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