微载波
自愈水凝胶
伤口愈合
透明质酸
化学
活性氧
再生(生物学)
氧化应激
药理学
细胞生物学
生物化学
细胞
医学
免疫学
生物
高分子化学
解剖
作者
Junyi Che,Danqing Huang,Yang Wang,Guangtao Gao,Yuanjin Zhao
标识
DOI:10.1186/s12951-025-03666-7
摘要
Bioactive substance-integrated hydrogels have demonstrated efficacy in diabetic wound treatment. However, challenges remain in identifying naturally derived, multifunctional active substances capable of addressing the complex pathophysiology of wounds, as well as in tailoring hydrogels to enhance their suitability for wound applications. Here, we present a novel biological hydrogel microcarrier system by integrating Bletilla striata-derived nanoparticles (PdNPs) and polydopamine nanozymes (PDAs) into a hyaluronic acid-methacrylate (HAMA) hydrogel. PdNPs can polarize over-activated macrophages to an anti-inflammatory phenotype and restore fibroblast functionality. Meanwhile, PDAs act as potent reactive oxygen species (ROS) scavengers and protect fibroblasts from oxidative stress-induced apoptosis. When encapsulated into HAMA microcarriers, the PdNP + PDA@HAMA microcarriers significantly accelerate wound healing in a diabetic rat model. These outcomes demonstrate the therapeutic potential of our natural, multifunctional hydrogel microcarriers as a promising wound dressing platform for the treatment of chronic diabetic wounds.
科研通智能强力驱动
Strongly Powered by AbleSci AI