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Updated: Jun 11, 2026

Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
Published on: October 29, 2013
β-Cyclodextrin Modified Hydrogels of Kappa-Carrageenan for Methotrexate Delivery
Maria Nikitina1, Nataliya Kochkina1, Marianna Arinina2
1G.A. Krestov Institute of Solution Chemistry of RAS, 153045 Ivanovo, Russia.
This study developed kappa-carrageenan gels with higher methotrexate content using beta-cyclodextrin for enhanced topical drug delivery. The gels showed improved properties for drug release and application.
Area of Science:
- Materials Science
- Polymer Chemistry
- Pharmaceutics
Background:
- Methotrexate (MTX) is a crucial drug with limited topical delivery options.
- Carrageenan hydrogels offer potential for topical drug delivery but require optimization for drug loading and release.
- Beta-cyclodextrin (βCD) can form inclusion complexes, enhancing drug solubility and stability.
Purpose of the Study:
- To develop kappa-carrageenan (kCR) hydrogels with enhanced methotrexate (MTX) loading and controlled release.
- To investigate the impact of beta-cyclodextrin (βCD) on the rheological properties and drug release kinetics of kCR gels.
- To compare the MTX-loading and release characteristics of kappa-carrageenan versus iota-carrageenan gels.
Main Methods:
- Formulation of kCR hydrogels incorporating MTX and varying concentrations of βCD.
- Rheological measurements to assess viscoelastic properties (e.g., storage modulus, loss modulus).
- In vitro drug release studies to quantify MTX release rates over time.
- Comparison of MTX binding affinities with kappa- and iota-carrageenan.
Main Results:
- The incorporation of βCD successfully increased MTX concentration within the kCR hydrogel matrix.
- Rheological studies indicated that MTX and βCD influenced the viscoelastic properties of kCR gels, maintaining suitability for topical application.
- βCD concentration significantly affected the MTX release rate, enabling modulation of drug delivery.
- Kappa-carrageenan gels exhibited different MTX binding affinities compared to iota-carrageenan gels, influencing release profiles.
Conclusions:
- The developed kCR-βCD-MTX hydrogels demonstrate enhanced drug loading and controlled release capabilities for topical applications.
- The rheological properties are suitable for topical formulation, with βCD playing a key role in modulating drug release.
- Understanding the polymer-drug interactions is crucial for optimizing hydrogel-based drug delivery systems.
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