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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Magnetic-, Acoustic-, and Optical-Triple-Responsive Microbubbles for Magnetic Hyperthermia and Pothotothermal Combination Cancer Therapy
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Synergistic ROS Generation via Core-Shell Nanostructures with Increased Lattice Microstrain Combined with Single-Atom

Liu-Chun Wang1,2, Li-Chan Chang3, Hsiang-Lin Huang1

  • 1Department of Chemistry, National Cheng Kung University, Tainan 701, Taiwan.

ACS Applied Materials & Interfaces
|August 15, 2024
PubMed
Summary
This summary is machine-generated.

This study introduces novel FePt@Cu core-shell nanostructures with gold single-atom catalysis for enhanced hydroxyl radical (•OH) generation. This breakthrough offers a potent and biodegradable strategy for effective cancer therapy.

Keywords:
Fenton-like reactionchemodynamic therapycore−shell effectsingle-atom catalyststrain effect

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Area of Science:

  • Nanomaterials Science
  • Catalysis
  • Biomedical Engineering

Background:

  • Reactive oxygen species (ROS) generation is crucial for cancer therapy.
  • Developing efficient catalysts for ROS production remains a challenge.
  • Core-shell nanostructures offer tunable properties for catalytic applications.

Purpose of the Study:

  • To investigate the synergistic effect of FePt@Cu core-shell nanostructures and Au single-atom catalysis on hydroxyl radical (•OH) generation.
  • To evaluate the efficacy of these nanostructures in catalytic tumor therapy.
  • To explore the underlying mechanisms of enhanced •OH production.

Main Methods:

  • Synthesis of FePt@Cu core-shell nanostructures.
  • Incorporation of Au single atoms onto the nanostructures.
  • Characterization of lattice microstrain and catalytic activity.
  • Density Functional Theory (DFT) calculations to elucidate reaction mechanisms.
  • In vitro and in vivo evaluation of tumor suppression efficacy and biodegradability.

Main Results:

  • FePt@Cu core-shell nanostructures with increased lattice microstrain significantly enhanced •OH generation.
  • Synergistic effects observed in FePt@Cu, further boosted by Au single atoms (FePt@Cu/Au).
  • Enhanced O2 → H2O2 → •OH pathway and Fenton-like reactions were confirmed.
  • DFT calculations revealed reduced O2 adsorption energy and energy barriers due to lattice mismatch and Au catalysis.
  • FePt@Cu/Au demonstrated remarkable tumor suppression and rapid biodegradability.

Conclusions:

  • FePt@Cu core-shell nanostructures with Au single-atom catalysis represent a novel and effective strategy for enhancing •OH generation in cancer therapy.
  • The synergistic effects and optimized catalytic pathways contribute to superior tumor suppression.
  • The biodegradable nature of FePt@Cu/Au highlights its potential as a safe and efficient therapeutic agent.