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Design of fluorinated stealth poly(ε-caprolactone) nanocarriers
Beatrice Lucia Bona1, Prescillia Lagarrigue2, Cristina Chirizzi1
1SupraBioNanoLab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milano 20131, Italy.
Colloids and Surfaces. B, Biointerfaces
|January 4, 2024
Summary
Fluorinated, pegylated poly(ε-caprolactone) nanocarriers offer enhanced stability and stealth for drug delivery. These nanoparticles are detectable using (19F)-Nuclear Magnetic Resonance (NMR), even after drug encapsulation.
Area of Science:
- Polymer Chemistry
- Nanotechnology
- Biomedical Engineering
Background:
- Polymer functionalization with fluorinated groups enhances nanocarrier properties.
- Fluorination improves colloidal stability in biological settings.
- Developing multimodal nanocarriers is crucial for advanced drug delivery.
Purpose of the Study:
- To create fluorinated, pegylated, biodegradable poly(ε-caprolactone) (PCL) nanocarriers.
- To achieve high colloidal stability, stealth properties, and (19F)-NMR detectability.
- To evaluate the impact of PEGylation and fluorination on nanoparticle self-assembly and behavior.
Main Methods:
- Mixing PEG-PCL block copolymer with nonafluoro-functionalized PCL.
- Investigating self-assembly and colloidal behavior.
- Encapsulating a hydrophobic drug and evaluating (19F)-NMR properties.
Main Results:
- Optimized nanocarriers exhibited high colloidal stability and stealth.
- Nanoparticles were successfully functionalized for (19F)-NMR detection.
- Drug encapsulation did not compromise the sharp 19F NMR signal or relaxivity.
Conclusions:
- Fluorinated PEG-PCL nanocarriers are promising for multimodal drug delivery.
- The developed system offers enhanced stability and real-time monitoring via (19F)-NMR.
- These nanocarriers maintain key properties after drug loading, indicating therapeutic potential.

