An Integrated Zn Battery‐Powered Iontophoresis Patch Enhances Healing of Radiation‐Induced Skin Injury by Inhibiting Ferroptosis

离子导入 材料科学 伤口愈合 生物医学工程 药品 药物输送 药理学 电极 血管生成 烧伤 纳米技术 电池(电) 细胞迁移 电穿孔 刺激 疤痕 哈卡特 生物物理学 细胞
作者
Tao Liu,Chen Meng,Fang Wang,Yì Wáng,Haitao Zhu,Yifan Qu,Siyu Lu,Siyu Han,Yuting Wang,Ruixuan Liu,Yì Wáng,Guilai Zuo,Wenguo Cui,Peng Jia
出处
期刊:Advanced Functional Materials [Wiley]
标识
DOI:10.1002/adfm.76191
摘要

ABSTRACT Ferroptosis induced by ionizing radiation impairs the healing of radiation‐induced skin injury (RISI). However, conventional topical drug therapies rely primarily on passive diffusion and lack an active driving force for drug delivery, making it difficult to maintain an effective local drug concentration in the wound bed to suppress ferroptosis. Here, we developed a wound exudate‐activated iontophoresis patch with a built‐in Zn battery, termed the epigallocatechin gallate (EGCG)‐loaded MXene/poly(vinyl alcohol) battery (EMPB). An integrated porous EGCG/MXene/PVA (EMP) conductive hydrogel serves as both the Zn battery cathode and the drug reservoir, reducing interfacial resistance at the junction between the electrode layer and the drug‐loaded reservoir. When placed on the wound bed, the EMPB patch uses wound exudate as the electrolyte to activate the battery and generate a stable direct‐current microelectric field that drives iontophoresis, thereby promoting efficient EGCG delivery through electroosmotic flow. In vitro, the electrical stimulation generated by the patch accelerated cell migration, while the actively delivered EGCG upregulated the NRF2/SLC7A11/GPX4 axis to suppress radiation‐induced ferroptosis. In vivo, EMPB inhibited ferroptosis and inflammation, alleviated oxidative injury, promoted angiogenesis and collagen remodeling, and accelerated wound closure to 89.3% by day 14. Collectively, EMPB represents a promising bioelectronic platform for accelerating RISI healing.
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