Tensile Strain-Mediated Bimetallene Nanozyme for Enhanced Photothermal Tumor Catalytic Therapy.

Angew Chem Int Ed Engl

Key Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, Electron Microscopy Center, China-Japan Union Hospital of Jilin University, No.126 Sendai Street, Changchun, 130033, China.

Published: June 2024

AI Article Synopsis

  • * This study introduces a new type of nanomaterial called local amorphous RhRu (la-RhRu), engineered with tensile strain to improve its catalytic abilities and photothermal effects.
  • * The research demonstrates that the strain in the bimetallene enhances multiple enzyme-like activities, leading to improved cancer treatment outcomes in lab experiments and living organisms.

Article Abstract

Nanozymes have demonstrated significant potential in combating malignant tumor proliferation through catalytic therapy. However, the therapeutic effect is often limited by insufficient catalytic performance. In this study, we propose the utilization of strain engineering in metallenes to fully expose the active regions due to their ultrathin nature. Here, we present the first report on a novel tensile strain-mediated local amorphous RhRu (la-RhRu) bimetallene with exceptional intrinsic photothermal effect and photo-enhanced multiple enzyme-like activities. Through geometric phase analysis, electron diffraction profile, and X-ray diffraction, it is revealed that crystalline-amorphous heterophase boundaries can generate approximately 2 % tensile strain in the bimetallene. The ultrathin structure and in-plane strain of the bimetallene induce an amplified strain effect. Both experimental and theoretical evidence support the notion that tensile strain promotes multiple enzyme-like activities. Functioning as a tumor microenvironment (TME)-responsive nanozyme, la-RhRu exhibits remarkable therapeutic efficacy both in vitro and in vivo. This work highlights the tremendous potential of atomic-scale tensile strain engineering strategy in enhancing tumor catalytic therapy.

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Source
http://dx.doi.org/10.1002/anie.202403203DOI Listing

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