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通过具有晶格微应变增强的核壳纳米结构与单原子催化协同产生 ROS 以增强肿瘤抑制作用。

Synergistic ROS Generation via Core-Shell Nanostructures with Increased Lattice Microstrain Combined with Single-Atom Catalysis for Enhanced Tumor Suppression.

机构信息

Department of Chemistry, National Cheng Kung University, Tainan 701, Taiwan.

Center of Applied Nanomedicine, National Cheng Kung University, Tainan 701, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45356-45370. doi: 10.1021/acsami.4c10392. Epub 2024 Aug 14.

Abstract

This study emphasizes the innovative application of FePt and Cu core-shell nanostructures with increased lattice microstrain, coupled with Au single-atom catalysis, in significantly enhancing OH generation for catalytic tumor therapy. The combination of core-shell with increased lattice microstrain and single-atom structures introduces an unexpected boost in hydroxyl radical (OH) production, representing a pivotal advancement in strategies for enhancing reactive oxygen species. The creation of a core-shell structure, FePt@Cu, showcases a synergistic effect in OH generation that surpasses the combined effects of FePt and Cu individually. Incorporating atomic Au with FePt@Cu/Au further enhances OH production. Both FePt@Cu and FePt@Cu/Au structures boost the O → HO → OH reaction pathway and catalyze Fenton-like reactions. This enhancement is underpinned by DFT theoretical calculations revealing a reduced O adsorption energy and energy barrier, facilitated by lattice mismatch and the unique catalytic activity of single-atom Au. Notably, the FePt@Cu/Au structure demonstrates remarkable efficacy in tumor suppression and exhibits biodegradable properties, allowing for rapid excretion from the body. This dual attribute underscores its potential as a highly effective and safe cancer therapeutic agent.

摘要

本研究强调了具有增大晶格微应变的 FePt 和 Cu 核壳纳米结构与 Au 单原子催化的创新应用,可显著增强用于催化肿瘤治疗的 OH 生成。核壳结构与增大晶格微应变和单原子结构的结合引入了羟基自由基(OH)生成的意外提升,这是增强活性氧物种策略的重要进展。FePt@Cu 的核壳结构的创建展示了 OH 生成中的协同效应,超过了 FePt 和 Cu 各自的组合效果。将原子 Au 与 FePt@Cu/Au 结合进一步提高了 OH 的生成。FePt@Cu 和 FePt@Cu/Au 结构都促进了 O → HO → OH 反应途径,并催化芬顿样反应。这种增强是由 DFT 理论计算揭示的,其中晶格失配和单原子 Au 的独特催化活性降低了 O 的吸附能和能量势垒。值得注意的是,FePt@Cu/Au 结构在抑制肿瘤方面表现出显著的功效,并具有可生物降解的特性,可迅速从体内排出。这种双重特性突出了其作为高效、安全的癌症治疗剂的潜力。

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