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Synergistic anticancer theragnostic study of a core-shell structured galvanic cell
Bao Jiang1, Liping Wang1, Gang Wu1
1College of Chemistry and Materials Science, Jiangsu Key Laboratory of Bio-functional Materials, Jiangsu Collaborative Innovation Centre of Biomedical Functional Materials, Nanjing Normal University, Nanjing 210023, China.
This study introduces FeCNB, a novel chemodynamic therapy (CDT) drug. It overcomes neutral tumor pH limitations and protein corona effects for enhanced cancer treatment via galvanic cells.
Area of Science:
- Biomedical Engineering
- Materials Science
- Nanotechnology
Background:
- Chemodynamic therapy (CDT) efficacy is limited by neutral tumor pH and protein corona formation.
- Existing CDT catalysts suffer reduced activity in physiological environments.
Purpose of the Study:
- To develop a core-shell CDT drug (FeCNB) that functions effectively under physiological pH.
- To mitigate the impact of protein corona on catalyst activity.
- To achieve synergistic cancer therapy using multiple modalities.
Main Methods:
- Synthesis of a Fe/Fe3C core with a mesoporous graphite carbon shell, modified with biotin (FeCNB).
- Utilizing galvanic cells formed by the core-shell structure for enhanced CDT.
- Investigating FeCNB's T2-magnetic resonance imaging (MRI) and photothermal therapy (PTT) capabilities.
- Assessing FeCNB's biocompatibility and degradation profile.
Main Results:
- FeCNB demonstrates high-efficiency CDT under physiological pH by forming galvanic cells.
- The mesoporous shell prevents protein corona interference, preserving catalyst activity.
- FeCNB exhibits T2-MRI contrast and synergistic PTT/CDT effects under laser irradiation.
- FeCNB shows excellent biocompatibility due to its in-situ degradation.
Conclusions:
- FeCNB represents a novel galvanic cell-based CDT drug design.
- The core-shell structure effectively addresses pH and protein corona limitations in CDT.
- FeCNB offers a promising platform for synergistic PTT/CDT cancer treatment with enhanced safety.
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