Department of Chemistry, National Cheng Kung University, Tainan 701, Taiwan.
Center of Applied Nanomedicine, National Cheng Kung University, Tainan 701, Taiwan.
ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45356-45370. doi: 10.1021/acsami.4c10392. Epub 2024 Aug 14.
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.
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。