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Updated: Oct 20, 2025

Synthesis and Evaluation of a Ruthenium-based Mitochondrial Calcium Uptake Inhibitor
Published on: October 26, 2017
Biocompatible Ruthenium Single-Atom Catalyst for Cascade Enzyme-Mimicking Therapy
Wenyu Wang1, Yang Zhu2, Xiaorong Zhu3
1Department of Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, Hefei 230026, China.
Researchers developed ruthenium single-atom enzymes (Ru SAEs) using carbon dots for enhanced tumor therapy. These Ru SAEs mimic multiple enzymes, boosting reactive oxygen species (ROS) to kill cancer cells effectively.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Materials Science
Background:
- Developing single-atom enzymes (SAEs) with high activity, stability, and biocompatibility is critical for cancer therapy.
- Existing SAEs face challenges in achieving optimal performance for therapeutic applications.
Purpose of the Study:
- To rationally construct highly active and stable ruthenium single-atom enzymes (Ru SAEs) using biocompatible carbon dots for enhanced tumor therapy.
- To investigate the multi-enzyme-like activities and mechanism of action of the developed Ru SAEs.
Main Methods:
- Synthesized Ru SAEs by loading ruthenium single atoms onto biocompatible carbon dots.
- Evaluated the oxidase, peroxidase, and glutathione oxidase-like activities of Ru SAEs.
- Assessed the efficacy of Ru SAEs in generating reactive oxygen species (ROS) and depleting glutathione.
- Utilized theoretical calculations to elucidate the mechanism of H2O2 activation by Ru SAEs.
Main Results:
- Achieved Ru SAEs with superior multi-enzyme-like activity and stability.
- Demonstrated that Ru SAEs mimic oxidase, peroxidase, and glutathione oxidase, leading to amplified ROS generation and glutathione depletion.
- Ru SAEs exhibited excellent peroxidase-like activity (7.5 U/mg), significantly outperforming Ru/C.
- Theoretical analysis confirmed efficient H2O2 activation via electron transfer in Ru SAEs, producing hydroxyl radicals (•OH).
Conclusions:
- The developed Ru SAEs show significant potential for cancer therapy due to their enhanced enzyme-like activities and mechanism of action.
- This study provides a promising strategy for designing advanced SAEs for biomedical applications, particularly in tumor treatment.
- The use of biocompatible carbon dots as carriers offers a pathway for creating stable and effective single-atom enzyme therapeutics.
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