Retarded release of small-molecule drugs from phase-separated dextran hydrogels through host-guest complexation

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Retarded release of small-molecule drugs from phase-separated dextran hydrogels through host-guest complexation
Title:
Retarded release of small-molecule drugs from phase-separated dextran hydrogels through host-guest complexation
Journal Title:
Biofunctional Materials
Keywords:
Publication Date:
15 March 2023
Citation:
Bae, K. H., Ng, S., Li, L., & Kurisawa, M. (2023). Retarded release of small-molecule drugs from phase-separated dextran hydrogels through host-guest complexation. Biofunctional Materials. https://doi.org/10.55092/bm20230002
Abstract:
Hydrogels have emerged as promising materials for diverse applications in biomedicine and biotechnology, but their use as a drug carrier has been limited by the difficulty of achieving controlled drug release. Herein we report the development of phaseseparated dextran hydrogels with 4-arm poly(ethylene glycol)-β-cyclodextrin (4-arm PEG- βCD) microdomains for prolonged release of small-molecule drugs. These hydrogels are designed to enhance the partition of drug molecules in the PEG microdomains through host-guest complexation, leading to delayed drug diffusion through the dextran gel matrix. Three different drugs (β-lapachone, imiquimod and oxaliplatin) were used to investigate the effect of 4-arm PEG-βCD on their partitioning behavior. The mechanical property and microdomain structure of the hydrogels were characterized by oscillatory rheology measurements and confocal laser scanning microscopy, respectively. Interestingly, we observed non-Fickian diffusion phenomena of β-lapachone and imiquimod from the phaseseparated hydrogels, suggesting the potential applicability of host-guest interactions for the design of sustained drug release systems.
License type:
Attribution 4.0 International (CC BY 4.0)
Funding Info:
This research is supported by core funding from: Biomedical Research Council
Grant Reference no. : NIL
Description:
ISSN:
2959-0574
2959-0582
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