透明质酸
材料科学
明胶
血管生成
再生(生物学)
血管内皮生长因子
伤口愈合
活性氧
纳米颗粒
药物输送
生物膜
纳米技术
生物物理学
化学
血管内皮生长因子受体
细菌
癌症研究
生物化学
免疫学
生物
细胞生物学
遗传学
作者
Weihang Peng,Jinze Li,Jiale Cheng,Jinlong Yang,Lingzhi Yang,Haifeng Dong,Xueji Zhang
标识
DOI:10.1021/acsami.5c07830
摘要
Infected wounds are difficult to treat due to biofilm formation, drug-resistant bacteria, and inefficient localized therapy. To address these challenges, we developed a core-shell microneedle (MN) patch that enables sequential delivery of copper peroxide (CuO2) nanoparticles and vascular endothelial growth factor (VEGF) for synergistic healing. CuO2 was encapsulated in zeolitic imidazolate framework-8 (CuO2@ZIF-8) to improve the aqueous stability and regulate reactive oxygen species (ROS) generation. The antibacterial nanocomposite was loaded into a pH-sensitive hyaluronic acid (HA) core layer for rapid release under a weakly acidic wound microenvironment, while VEGF was incorporated into a gelatin methacryloyl (GelMA) shell for sustained delivery. Upon application, the core dissolves to release Cu2+, Zn2+, and ROS, disrupting biofilms and killing bacteria. Subsequently, the shell swells and degrades to release VEGF, promoting angiogenesis and tissue regeneration. In a Staphylococcus aureus-infected wound model, the MN patch demonstrated potent antibacterial activity, enhanced neovascularization, and accelerated healing. This programmable, dual-functional MN platform offers an effective strategy for treating infected wounds by integrating infection control with tissue regeneration in a temporally coordinated manner.
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