Multifunctional SISTP dressing integrating AI-screened hexapeptide for sustained antimicrobial release and redox homeostasis in infected wounds.

Youjia Yue, Huifeng Liu, Ying Wang
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Abstract

Infected wound healing environments present dual challenges of microbial colonization and sustained oxidative stress, critically impairing patient outcomes. Developing advanced dressings capable of concurrent broad-spectrum antimicrobial action and redox homeostasis restoration remains an urgent clinical priority. Here, we engineered a multifunctional porcine small intestinal submucosa extracellular matrix dressing (i.e., SISTP) integrated with AI-screened antimicrobial peptides (AMPs) via tea polyphenol-mediated coordination. The CRRI6 hexapeptide (Arg-Trp-Trp-Arg-Trp-Phe) demonstrated prolonged release kinetics (>6 hours) from the SISTP scaffold, achieving ≥90% eradication of Escherichia coli and Staphylococcus aureus. Radical scavenging assays confirmed SISTP's capacity to neutralize reactive oxygen species (ROS), while in vivo studies revealed accelerated wound closure in infected rat models through synergistic microbial clearance and oxidative stress mitigation. This study pioneers a bioinspired strategy leveraging AI-optimized AMPs and polyphenol nanoengineering to address the multifactorial pathophysiology of chronic wounds. .

集成ai筛选的六肽的多功能SISTP敷料,用于感染伤口的持续抗菌释放和氧化还原稳态。
感染的伤口愈合环境面临微生物定植和持续氧化应激的双重挑战,严重损害患者的预后。开发能够同时具有广谱抗菌作用和氧化还原平衡恢复的先进敷料仍然是迫切的临床优先事项。在这里,我们设计了一种多功能猪小肠粘膜下层细胞外基质敷料(即SISTP),通过茶多酚介导的协调将ai筛选的抗菌肽(amp)整合在一起。CRRI6六肽(Arg-Trp-Trp-Arg-Trp-Phe)从SISTP支架中显示出延长释放动力学(bbb6小时),实现了≥90%的大肠杆菌和金黄色葡萄球菌的根除。自由基清除实验证实了SISTP具有中和活性氧(ROS)的能力,而体内研究表明,通过协同微生物清除和氧化应激缓解,感染大鼠模型的伤口愈合速度加快。这项研究开创了一种生物启发策略,利用人工智能优化的amp和多酚纳米工程来解决慢性伤口的多因素病理生理问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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