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Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study
Published on: August 15, 2016
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Embedding Well-Defined Responsive Hydrogels with Nanocontainers: Tunable Materials from Telechelic Polymers and
Mehmet Arslan1, Duygu Aydin1, Aysun Degirmenci1
1Department of Chemistry, Bogazici University, Bebek, Istanbul 34342, Turkey.
ACS Omega
|August 29, 2019
Summary
Researchers created thermoresponsive hydrogels using cyclodextrin (CD) and thiol-reactive polymers. These biocompatible hydrogels control drug release, showing slower release at physiological temperatures due to network collapse.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Thermoresponsive hydrogels offer tunable properties for controlled release applications.
- Cyclodextrins (CDs) can be incorporated into hydrogel networks to enhance drug loading and release modulation.
- Thiol-ene click chemistry provides an efficient method for hydrogel network formation.
Purpose of the Study:
- To design and synthesize novel thermoresponsive hydrogels incorporating cyclodextrin (CD) crosslinkers.
- To investigate the fabrication of these hydrogels using thiol-reactive telechelic polymers and thiol-ene conjugation.
- To evaluate the physicochemical properties, cytocompatibility, and drug release behavior of the synthesized CD-containing hydrogels.
Main Methods:
- Synthesis of hydrophilic telechelic polymers with thiol-reactive end groups.
- Fabrication of hydrogels via thiol-ene click reaction with multivalent thiol-containing CDs.
- Characterization of hydrogel properties: morphology, water uptake, rheology, and residual thiol content.
- Assessment of cytocompatibility using fibroblast cell viability assays.
- Evaluation of puerarin loading and controlled release kinetics at different temperatures.
Main Results:
- Clear, transparent hydrogels were formed with good conversion rates (79-89%) using thiol-ene click reactions.
- Hydrogels exhibited moderately well-defined network structures and tunable physical properties.
- The hydrogels demonstrated excellent cytocompatibility with low toxicity to fibroblast cells.
- Drug release studies showed a slower, sustained release of puerarin at physiological temperatures compared to ambient conditions.
- Rheological analysis confirmed network structure collapse near physiological temperatures, influencing drug release.
Conclusions:
- A versatile strategy for fabricating thermoresponsive, CD-containing hydrogels with controlled network structures was developed.
- The hydrogels exhibit promising potential for controlled drug delivery, particularly for antiglaucoma medications like puerarin.
- Temperature serves as an effective stimulus to modulate drug release kinetics by altering hydrogel network compactness.
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