自愈水凝胶
伤口愈合
药物输送
药品
化学
再生(生物学)
糖尿病
多细胞生物
细胞生物学
细胞外
药理学
细胞
组织工程
炎症
药物开发
作者
Manxuan Liu,Zhongcheng Li,Qian Ren,Ziqian Lu,Yubing Zhang,Yili Guo,Ruomeng Li,Die Hu,Linglin Zhang
标识
DOI:10.1002/advs.202517028
摘要
ABSTRACT The chronic and refractory infected wounds of diabetes are primarily attributed to the persistent bacterial infection and the inhibition of wound healing caused by hypoxia. Hydrogel with intelligent drug delivery systems hold significant potential in the treatment of diabetic wounds. Herein, we have developed an glucose‐responsive intelligent hydrogel named as CF‐CPGaMPN, which incorporates polyvinylpyrrolidone‐coated calcium peroxide (PVP@CaO 2 ) nanoparticles, catalase, and gallium‐polyphenol (GaMPN) nanoparticles. The borate ester bonds in the CF‐CPGaMPN hydrogel break under high glucose conditions, releasing GaMPN nanoparticles, thereby achieving glucose‐triggered on‐demand drug release. The CF‐CPGaMPN hydrogel not only inhibits various microorganisms but also continuously releases oxygen, thereby promoting the healing of diabetic infection wounds. Furthermore, the multicellular ecosystem surrounding the CF‐CPGaMPN hydrogel is also explored, and the diverse cellular heterogeneity is analyzed by single‐cell RNA sequencing, highlighting the critical roles of Neutrophils, Fibroblasts, and Epidermal cells in diabetic infected wound. In addition, CF‐CPGaMPN hydrogel inhibits the Neutrophil extracellular trap (NET) formation and alleviates the cellular hypoxic environment to improve diabetic wound healing. In conclusion, the CF‐CPGaMPN hydrogel not only provides a promising drug release strategy for the healing of diabetic infected wounds, but also contributes to the rational design of customized hydrogels for biomedical use targeting different cellular functions.
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