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Published on: October 29, 2013
Cyclodextrin/poly(ethylene glycol) polypseudorotaxane hydrogels as a promising sustained-release system for lysozyme
Taishi Higashi1, Anna Tajima, Keiichi Motoyama
1Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan.
Polypseudorotaxane (PPRX) hydrogels made with poly(ethylene glycol) (PEG) and cyclodextrins (CyD) effectively sustained lysozyme release. These hydrogels show promise for protein drug delivery systems.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Polymer Chemistry
Background:
- Protein-based therapeutics require advanced delivery systems for sustained release.
- Polypseudorotaxane (PPRX) hydrogels offer potential for controlled drug delivery.
- Poly(ethylene glycol) (PEG) and cyclodextrins (CyD) are key components in PPRX hydrogel formation.
Purpose of the Study:
- To evaluate the utility of cyclodextrin (CyD) polypseudorotaxane (PPRX) hydrogels for sustained protein drug release.
- To investigate the release profiles and mechanisms of lysozyme from α- and γ-CyD PPRX hydrogels.
Main Methods:
- Preparation of CyD PPRX hydrogels incorporating lysozyme.
- In vitro release studies of lysozyme from the hydrogels.
- Analysis of release kinetics using the Korsmeyer-Peppas model.
Main Results:
- Lysozyme encapsulation significantly decreased in vitro release rates.
- α- and γ-CyD formed PPRX hydrogels via physical cross-linking of PEG chains.
- Release mechanisms from both α- and γ-CyD systems were statistically similar, indicating consistent behavior.
Conclusions:
- α- and γ-CyD PPRX hydrogels demonstrate potential as effective sustained-release systems for protein drugs like lysozyme.
- The physical cross-linking mechanism provides a basis for controlled protein release.
- Further development of CyD PPRX hydrogels could advance protein drug delivery technologies.
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