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Updated: Jul 11, 2026

The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications
Published on: October 7, 2016
ROS-Responsive 4D Printable Acrylic Thioether-Based Hydrogels for Smart Drug Release
Maria Regato-Herbella1,2, Isabel Morhenn1, Daniele Mantione1,3
1POLYMAT University of the Basque Country UPV/EHU, Joxe Mari Korta Center. Avda. Tolosa 72, 20018 Donostia-San Sebastián, Spain.
Researchers developed novel ROS-responsive hydrogels using thioether-based monomers for targeted cancer therapy. These smart hydrogels enable controlled drug delivery and show promising in vitro efficacy against melanoma cells.
Area of Science:
- Materials Science
- Polymer Chemistry
- Biomedical Engineering
Background:
- Reactive oxygen species (ROS) are implicated in diseases like cancer, necessitating targeted therapies.
- ROS-responsive polymers offer potential for engineering smart hydrogels for localized treatment.
- Existing materials may lack specific responsiveness or optimal properties for drug delivery applications.
Purpose of the Study:
- To synthesize novel thioether-based ROS-responsive monomers (EGSA) for hydrogel development.
- To fabricate and characterize EGSA-based hydrogels for 4D printing and drug delivery.
- To evaluate the ROS-responsive drug release and in vitro efficacy of these hydrogels against cancer cells.
Main Methods:
- Synthesis of ethylene glycol/thioether acrylate (EGSA) monomers via thiol-Michael addition.
- Photopolymerization of EGSA monomers and copolymerization with 2-hydroxyethyl acrylate (HEA).
- Characterization of hydrogel properties (mechanical, swelling) and drug release kinetics (5-fluorouracil).
- In vitro evaluation of hydrogel efficacy on B16F10 melanoma cells.
Main Results:
- Successfully synthesized ROS-responsive EGSA monomers and fabricated photopolymerizable hydrogels.
- EGSA-HEA copolymer hydrogels exhibited enhanced stability and tunable swelling in response to hydrogen peroxide.
- Sustained release of 5-fluorouracil was achieved, modulated by ROS levels.
- In vitro studies demonstrated significant inhibition of B16F10 melanoma cell growth.
Conclusions:
- Developed novel ROS-responsive hydrogels with tunable properties for controlled drug delivery.
- The hydrogels show significant potential for targeted cancer therapy, particularly for localized pathologies.
- The material's responsiveness to ROS and its efficacy against melanoma cells highlight its therapeutic promise.
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