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Supramolecular Core-Shell Nanoassemblies with Tumor Microenvironment-Triggered Size and Structure Switch for Improved
Ziyao Wang1, Yanqiu Wang2, Xiaohuan Sun1
1School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225002, P. R. China.
This study presents novel core-shell nanostructures for enhanced photothermal therapy (PTT). These smart nanoparticles improve tumor targeting and penetration, boosting cancer treatment efficacy.
Area of Science:
- Biomedical Engineering
- Materials Science
- Nanotechnology
Background:
- Photothermal therapy (PTT) shows promise for cancer treatment but faces challenges like low efficiency and poor tumor penetration.
- Developing advanced nanocarriers is crucial to overcome PTT limitations for clinical applications.
Purpose of the Study:
- To construct core-shell hierarchical nanostructures using host-guest interactions for improved PTT.
- To engineer pH-responsive nanoplatforms with size-switchable properties for enhanced tumor accumulation and penetration.
- To significantly boost near-infrared-II absorption and photothermal conversion efficiency for effective cancer therapy.
Main Methods:
- Host-guest complexation between water-soluble pillar[5]arene (WP5) and polyethylene glycol-modified aniline tetramer (TAPEG) to form core-shell nanostructures.
- Exploiting pH-responsive behavior for nanoparticle size switching (200 nm at neutral pH, 60 nm at acidic pH).
- Investigating structural changes and п-conjugate extension for enhanced near-infrared-II absorption and photothermal conversion.
Main Results:
- Successfully constructed WP5⊃TAPEG core-shell nanostructures with pH-responsive size-switching capabilities.
- Achieved significantly enhanced absorption in the near-infrared-II region.
- Demonstrated a high photothermal conversion efficiency of 60.2% under acidic conditions.
- Showcased improved tumor accumulation and penetration due to size changes.
Conclusions:
- The developed intelligent nanoplatform offers a promising strategy for overcoming PTT limitations.
- The pH-responsive, size-switchable nanostructures enhance tumor targeting and penetration, leading to improved antitumor efficacy.
- This approach holds potential for advancing PTT in clinical cancer treatment.
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