Synergistic ROS Generation via Core-Shell Nanostructures with Increased Lattice Microstrain Combined with Single-Atom Catalysis for Enhanced Tumor Suppression.
Liu-Chun WangLi-Chan ChangHsiang-Lin HuangPo-Ya ChangChih-Wen PaoYin-Fen LiuKeng-Shiang HuangYi-Hsin ChienHwo-Shuenn SheuWen-Pin SuChen-Hao YehChen-Sheng YehPublished in: ACS applied materials & interfaces (2024)
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 2 → H 2 O 2 → • OH reaction pathway and catalyze Fenton-like reactions. This enhancement is underpinned by DFT theoretical calculations revealing a reduced O 2 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.
Keyphrases
- aqueous solution
- sensitive detection
- molecular dynamics
- reduced graphene oxide
- reactive oxygen species
- metal organic framework
- visible light
- density functional theory
- high resolution
- electron transfer
- dna damage
- drug delivery
- stem cells
- papillary thyroid
- cell death
- wastewater treatment
- young adults
- crystal structure
- molecular docking
- hydrogen peroxide
- squamous cell
- cell therapy
- mass spectrometry