血管生成
氧化应激
医学
糖尿病足
再生(生物学)
炎症
巨噬细胞
新生血管
活性氧
癌症研究
糖尿病
药物输送
微阵列
药理学
伤口愈合
细胞凋亡
细胞
表型
微阵列分析技术
药品
体内
内皮干细胞
细胞生长
生物信息学
作者
Yuxu Wu,Kan Jiang,Xiao Wen,Chihao Jin,Kai Zhang,Jiakai Zhang,Jiale Jin,Jiaqian Wang,Huiyu Hu,Zonghan Xu,Xianzhu Zhang,Yihe Hu
出处
期刊:Exploration
[Wiley]
日期:2026-05-28
卷期号:6 (4): 20250129-20250129
被引量:2
摘要
Diabetic foot ulcers (DFUs) present a persistent clinical challenge, posing a significant and ongoing threat to patient health. Current treatment strategies are failing to concurrently address the excessive oxidative stress and impaired angiogenesis during whole-course management of diabetic wounds. To overcome these limitations, this study developed an innovative microneedle (MN)-based drug delivery system incorporating cerium-based metal‒organic frameworks (MOFs) loaded with dihydrocapsaicin (DHC). Fabricated from a Gelatin Methacryloyl (GelMA) hydrogel, the resulting MN-MOF@DHC system exhibited a sustained release profile of DHC that nearly covered the whole-course management of diabetic wounds. Our results revealed that the MN-MOF@DHC system effectively reduced the levels of reactive oxygen species (ROS), promoted the transformation of macrophage phenotypes from the pro-inflammatory M1 subtype to the anti-inflammatory M2 subtype, and significantly enhanced endothelial cell angiogenesis. These combined actions markedly accelerated wound closure. Collectively, the advanced MN platform offers a highly promising strategy for the treatment of DFUs.
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