A Highly Efficient and Biocompatible Cupper-Based Single-Atom Nanocatalyst with Unsaturated Coordination Structure for Efficient Diabetic Wound Healing

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-06-04 DOI:10.1002/smll.202502896
Shiyu Xu, Yin Yuan, Yukun Pan, Huihui Zhang, Siyuan Yin, Xinya Zhang, Yayun Zhang, Sheng Dai, Huawei Shen, Yongsheng Li, Dechao Niu
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Abstract

The unsaturated coordination alters the electronic structure of metal atoms, exposing more active sites, and thereby demonstrating high catalytic activity. It is extremely difficult to precisely regulate the unsaturated coordination environment of single-atom catalysts due to the thermodynamically unstable structure. Herein, a facile “micelle-confined oxidative crosslinking and coupled coordination” strategy is proposed to construct a copper single-atom catalyst with an unsaturated Cu-N2 coordination structure in a confined silica-carbon framework (Cu SA@MCSN), which demonstrate unique pH-dependent multiple-enzymatic activity (peroxidase (POD)-like activity in an acidic environment with a low Km of 6.9 mM and Vmax of 6.3 × 10−8 M s−1 and superoxide dismutase (SOD)- and catalase (CAT)-like activity under neutral conditions). Density functional theory calculations also further confirm that the asymmetric Cu-N2 sites with edge configurations exhibit a strong adsorption capacity for oxygen-containing intermediates showing a faster reaction rate compared to their saturated coordination structure. More importantly, the metformin (MET)-loaded Cu SA@MCSN demonstrates multi-pathway antibacterial ability in acidic microenvironments and long-term anti-inflammatory effects in neutral microenvironments through the downregulation of pro-inflammatory factors and the up-regulation of anti-inflammatory and tissue regeneration factors on a rat model of methicillin-resistant Staphylococcus aureus (MRSA)-infected diabetic wounds.

Abstract Image

具有不饱和配位结构的高效生物相容性铜基单原子纳米催化剂用于糖尿病伤口的高效愈合
不饱和配位改变了金属原子的电子结构,暴露出更多的活性位点,从而表现出较高的催化活性。单原子催化剂的不饱和配位环境由于其热力学结构不稳定而难以精确调控。本文提出了一种简单的“胶束限制氧化交联和偶联配位”策略,以构建具有不饱和Cu- n2配位结构的铜单原子催化剂(Cu SA@MCSN)。它们表现出独特的ph依赖性多酶活性(酸性环境下过氧化物酶(POD)样活性,低Km为6.9 mM, Vmax为6.3 × 10−8 M s−1,中性条件下超氧化物歧化酶(SOD)和过氧化氢酶(CAT)样活性)。密度泛函理论计算也进一步证实了具有边缘构型的不对称Cu-N2位点对含氧中间体具有较强的吸附能力,其反应速率比饱和配位结构更快。更重要的是,在耐甲氧西林金黄色葡萄球菌(MRSA)感染的糖尿病伤口大鼠模型上,二甲双胍(MET)负载Cu SA@MCSN通过下调促炎因子和上调抗炎因子和组织再生因子,在酸性微环境中表现出多途径的抗菌能力,在中性微环境中表现出长期的抗炎作用。
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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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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