炎症
自愈水凝胶
血管生成
伤口愈合
材料科学
巨噬细胞极化
下调和上调
药理学
免疫学
癌症研究
医学
化学
体外
巨噬细胞
生物化学
高分子化学
基因
作者
Wenguang Liu,I‐Ming Chen,Meng Luo,Ting Li,Chaoyan Hu,Chenxi Xie,Sihua Li,Tongtong Leng,Jie Tian,Ping Xu,Bo Lei
标识
DOI:10.1016/j.matdes.2023.111669
摘要
Inflammation-related infected wound and rheumatoid arthritis (RA) are still the challenge in biomedical filed. Bioactive molecules and materials are showing much interest in treating inflammation-related diseases. Herein, we report an antiinflammatory antioxidant angiogenetic bioactive ions-based scaffold based on the bioactive nanoglass for treating methicillin-resistant staphylococcus aureus (MRSA) infected wound and RA. It was found that the bioactive nanoglass ions (BNGI) with 3 × and 6 × dilution demonstrated the significant anti-inflammation ability (the inhibition of Tnf-α and IL1β), macrophage polarization function (the decrease of CD86+ cells), antioxidant and angiogenic capacities (the increased node number, branching length and CD31 expression). 1 × diluted BNGI-derived Pluronic F127 and gelatin methacryloyl hydrogels could significantly enhance the MRSA-infected wound healing and attenuate the RA progression through stimulating the secretion of antiinflammation exosomes from macrophage (3-fold upregulation compared with 3MTM dressing) and proper angiogenesis based on the important role of silicon (about 150 mg/L in vivo and 25.4 to 48.1 mg/L in vitro) in BNGI. Our findings revealed the therapeutic function and potential mechanism of BNGI in inflammatory diseases and tissue engineering.
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