Bimetallic-Gallic Acid Cross-Linked Hydrogels with Cascading Nanozyme Activity Promote Healing of MRSA-Infected Wounds by Modulating the Oxidative Stress Microenvironment

氧化应激 自愈水凝胶 化学 活性氧 炎症 生物物理学 材料科学 氧化磷酸化 细胞毒性 细胞生物学 伤口愈合 压力(语言学) 生物化学 纳米技术 癌症研究 氧化损伤 药理学
作者
Dong Liu,Lixin Sun,Qingyu Song,Qiujing Li,Shukun Zhang,Ning Wang,Jingdi Chen
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:18 (15): 21635-21651 被引量:1
标识
DOI:10.1021/acsami.6c00362
摘要

Chronic wounds caused by multidrug-resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) often stall during the healing process due to persistent inflammation and failed tissue repair. This pathological state primarily results from a vicious cycle formed by the interaction of oxidative stress, chronic inflammation, and impaired angiogenesis. To this end, this study employs network pharmacology to reveal that gallic acid (GA, a polyphenol with potent antioxidant and anti-inflammatory activity) promotes skin wound healing by regulating oxidative stress and apoptosis. Subsequently, based on these findings, a dynamic hydrogel dressing with cascade enzyme-like activity was developed. By synergistically modulating the oxidative stress microenvironment, eliminating bacterial infections, promoting angiogenesis, and accelerating the healing of MRSA-infected wounds, it effectively remodels the wound microenvironment. The core of this system is a metal-phenolic network particle (ZCG) self-assembled from Zn2+ (antibacterial), Cu2+ (angiogenic), and GA. These bioactive particles are embedded in a dynamic hydrogel matrix composed of oxidized fucoidan (OFD) and carboxymethyl chitosan (CMCS), which confer self-healing and injectable properties to the dressing. Simultaneously, by synergistically combining metal ions and GA, the hydrogel dressing functions as a “regenerative niche” that effectively eradicates MRSA. It further scavenges excess reactive oxygen species to alleviate inflammation and protect host cells. The system also releases pro-angiogenic copper ions to reconstruct vascular networks, effectively remodeling the wound microenvironment. This promotes collagen deposition and granulation tissue formation, accelerating wound closure. As a universal therapeutic solution for chronic nonhealing wounds, it holds significant clinical translation potential.
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