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具有光热电活性的相工程化 CuS-AgS 用于增强多酶活性和动态治疗。

Phase Engineered CuS-AgS with Photothermoelectric Activity for Enhanced Multienzyme Activity and Dynamic Therapy.

机构信息

Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Material Science and Chemical Engineering, Harbin Engineering University, Harbin, 150001, P. R. China.

State Key Laboratory of Rare Earth Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.

出版信息

Adv Mater. 2024 Jun;36(24):e2400416. doi: 10.1002/adma.202400416. Epub 2024 Mar 6.

Abstract

The insufficient exposure sites and active site competition of multienzyme are the two main factors to hinder its therapeutic effect. Here, a phase-junction nanomaterial (amorphous-crystalline CuS-AgS) is designed and prepared through a simple room temperature ion-exchange process. A small amount of Ag is added into CuS nanocrystals, which transforms CuS into amorphous phased CuS and produces crystalline AgS simultaneously. In this structure, the overhanging bonds on the amorphous CuS surface provide abundant active sites for optimizing the therapeutic activity. Meanwhile, the amorphous state enhances the photothermal effect through non-radiative relaxation, and due to its low thermal resistance, phase-junction CuS-AgS forms a significant temperature gradient to unlock the optimized thermo-electrodynamic therapy. Furthermore, benefiting from the high asymmetry of the amorphous state, the material forms a spin-polarized state that can effectively inhibit electron-hole recombination. In this way, the thermoelectric effect can facilitate the enzyme-catalyzed cycle by providing electrons and holes, enabling an enhanced coupling of thermoelectric therapy with multienzyme activity, which induces excellent anti-tumor performance. More importantly, the catalytic process simulated by density-functional theory proves that Ag alleviates the burden on the Cu sites through favorable adsorption of O and prevents active site competition.

摘要

多酶的暴露位点不足和活性位点竞争是阻碍其治疗效果的两个主要因素。在这里,通过简单的室温离子交换过程设计并制备了一种相结纳米材料(非晶-晶态 CuS-AgS)。在 CuS 纳米晶中少量添加 Ag,可将 CuS 转变为非晶相的 CuS 并同时生成晶态的 AgS。在这种结构中,非晶 CuS 表面的悬键为优化治疗活性提供了丰富的活性位点。同时,非晶态通过非辐射弛豫增强了光热效应,并且由于其低热阻,相结 CuS-AgS 形成了显著的温度梯度,从而解锁了优化的热电动力学治疗。此外,得益于非晶态的高不对称性,该材料形成了一种自旋极化态,可有效抑制电子-空穴复合。通过这种方式,热电器件可以通过提供电子和空穴来促进酶催化循环,增强热电治疗与多酶活性的耦合,从而诱导出优异的抗肿瘤性能。更重要的是,通过密度泛函理论模拟的催化过程证明,Ag 通过对 O 的有利吸附减轻了 Cu 位点的负担,并防止了活性位点竞争。

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