Chronic diabetic wounds are characterized by persistent oxidative stress and microbial infections, leading to delayed healing and tissue repair. While elevated reactive oxygen species (ROS) levels can provide bactericidal effects, uncontrolled oxidative stress simultaneously impairs tissue regeneration. Thus, precise redox modulation that balances antimicrobial efficacy with tissue regeneration is critical for effective wound therapy. Herein, we developed a phytochemical nanozymes system by integrating ferulic acid (FA) with cerium oxide nanoparticles (CeO(2)), enabling precise redox modulation to balance antimicrobial efficacy with tissue regeneration. Structural analysis confirmed the uniform dispersion and pH-responsive release of FA and Ce ions, facilitating targeted redox modulation. The FA-CeO(2) nanozymes exhibited potent antioxidant activity through Ce(3+)/Ce(4+) cycling and FA-mediated radical scavenging, effectively mitigating oxidative stress while promoting bacterial clearance against S. aureus and E. coli. Furthermore, FA-CeO(2) significantly enhanced Nrf2/HO-1 pathway activation, leading to upregulated VEGF/CD31 expression, accelerated cell proliferation, and enhanced collagen deposition in vitro. In vivo, FA-CeO(2) facilitated wound closure, reduced bacterial burden, and improved tissue regeneration in acute and diabetic wound models, with minimal cytotoxicity and excellent biocompatibility. These findings highlight the critical role of precise redox modulation in balancing antibacterial and regenerative therapy, positioning phytochemical nanozymes as a dual-modality platform for effective wound therapy and advancing nanomedicine strategies targeting oxidative stress and tissue repair.
Phytochemical nanozymes reprogram redox for balanced antimicrobial and regenerative therapy in acute and chronic diabetic wounds.
植物化学纳米酶可重编程氧化还原状态,从而在急性和慢性糖尿病伤口中实现平衡的抗菌和再生治疗
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作者:Pang Yipeng, Amona Fructueux Modeste, Chen Xiaohan, You Yuxin, Sha Ziqi, Liu Zilu, Li Jiamin, Liu Yi, Fang Xingtang, Chen Xi
| 期刊: | Redox Biology | 影响因子: | 11.900 |
| 时间: | 2025 | 起止号: | 2025 Sep;85:103718 |
| doi: | 10.1016/j.redox.2025.103718 | 研究方向: | 代谢 |
| 疾病类型: | 糖尿病 | ||
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