4.5 Article

Cyclodextrin-cross-linked diaminotriazine-based hydrogen bonding strengthened hydrogels for drug and reverse gene delivery

Journal

JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
Volume 24, Issue 16, Pages 1869-1882

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09205063.2013.808150

Keywords

high-strength hydrogel; cyclodextrin; ibuprofen; drug delivery; reverse gene delivery

Funding

  1. National Natural Science Foundation of China [21274105]

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A hydrogen bonding strengthened hydrogel was prepared by radical copolymerization of poly(ethylene glycol) methacrylated -cyclodextrin (PEG--CD) and 2-vinyl-4,6-diamino-1,3,5-triazine (VDT) monomer. PEG--CD served not only as a cross-linker, but also as a built-in solubilizing agent of the hydrophobic drug in the gel. Increasing VDT content resulted in a notable enhancement in the mechanical strengths of hydrogels whose equilibrium water contents could be modulated from 75% to 85% by varying the ratio of PEG--CD cross-linker. It was shown that copolymerizing more PEG--CDs could load higher amount of ibuprofen (IBU) in the gels and contribute to a slower release rate of IBU. Plasmid DNA could be anchored onto the surface of hydrogels due to the hydrogen bonding between the base pairs and diaminotriazine, thereby mediating efficient reverse gene transfection of luciferase gene in COS-7 cells cultured on the gel surface. The cytocompatible PEG--CD-cross-linked PVDT hydrogels with multifunction of drug and gene delivery hold a potential as tissue engineering scaffold.

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