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Published on: January 24, 2025
pH-Responsive Nanoscale Coordination Polymer for Efficient Drug Delivery and Real-Time Release Monitoring
Kai Han1, Wei-Yun Zhang1, Jin Zhang1
1State Key Laboratory of Agricultural Microbiology, College of Science, Huazhong Agricultural University, Wuhan, 430070, China.
This study introduces a novel iron-gallic acid nanoplatform for effective tumor treatment. It enables real-time monitoring of doxorubicin (DOX) release, enhancing efficacy and reducing cardiotoxicity in cancer therapy.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Cancer Therapy
Background:
- Drug delivery systems are crucial for effective tumor therapy, but challenges remain regarding dosage control and side effects.
- Uncontrolled drug release and carrier toxicity can lead to severe adverse events and treatment failure.
- Developing intelligent nanocarriers for real-time drug release monitoring is essential for improving cancer treatment outcomes.
Purpose of the Study:
- To design and evaluate an Fe3+-gallic acid based nanoscale coordination polymer for efficient drug delivery and real-time monitoring of doxorubicin (DOX) release in tumors.
- To assess the antitumor efficacy and safety profile of this novel nanoplatform.
- To investigate the potential of this system as a promising nanoplatform for advanced tumor treatment.
Main Methods:
- Formation of nanoscale coordination polymers from Fe3+ and gallic acid in aqueous solution.
- High-efficiency loading of doxorubicin (DOX) onto the coordination polymer, achieving up to 48.3% loading efficacy.
- In vitro studies to assess DOX loading, fluorescence quenching, and release triggered by lysosomal acidity.
- In vivo studies to evaluate tumor growth inhibition and cardiotoxicity of the drug delivery system.
Main Results:
- The Fe3+-gallic acid coordination polymer demonstrated high doxorubicin loading capacity.
- DOX fluorescence was quenched upon loading and recovered in acidic lysosomal environments, enabling real-time release monitoring.
- In vitro and in vivo studies showed significant tumor growth inhibition.
- The nanoplatform exhibited negligible cardiotoxicity, a common side effect of doxorubicin.
Conclusions:
- The Fe3+-gallic acid nanoplatform is an effective system for high-efficiency doxorubicin loading and controlled release.
- Real-time monitoring of drug release is achievable through fluorescence changes, aiding therapeutic assessment.
- This polyphenol-rich drug delivery system shows significant promise for enhanced tumor treatment with reduced side effects.
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