微泡
伤口愈合
外体
明胶
血管生成
细胞生物学
炎症
自愈水凝胶
化学
缺氧(环境)
细胞内
小RNA
癌症研究
免疫学
医学
生物
氧气
生物化学
有机化学
基因
作者
Xiaoxue Han,Chaimongkol Saengow,Leah Ju,Wen Ren,Randy H. Ewoldt,Joseph Irudayaraj
标识
DOI:10.1038/s41467-024-47696-5
摘要
Abstract Wound healing is an obvious clinical concern that can be hindered by inadequate angiogenesis, inflammation, and chronic hypoxia. While exosomes derived from adipose tissue-derived stem cells have shown promise in accelerating healing by carrying therapeutic growth factors and microRNAs, intracellular cargo delivery is compromised in hypoxic tissues due to activated hypoxia-induced endocytic recycling. To address this challenge, we have developed a strategy to coat oxygen nanobubbles with exosomes and incorporate them into a polyvinyl alcohol/gelatin hybrid hydrogel. This approach not only alleviates wound hypoxia but also offers an efficient means of delivering exosome-coated nanoparticles in hypoxic conditions. The self-healing properties of the hydrogel, along with its component, gelatin, aids in hemostasis, while its crosslinking bonds facilitate hydrogen peroxide decomposition, to ameliorate wound inflammation. Here, we show the potential of this multifunctional hydrogel for enhanced healing, promoting angiogenesis, facilitating exosome delivery, mitigating hypoxia, and inhibiting inflammation in a male rat full-thickness wound model.
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