Issue 101, 2014

Cyclodextrin mediated polymer coupling via thiol–maleimide conjugation: facile access to functionalizable hydrogels

Abstract

Fabrication of well-defined chemically cross-linked poly(ethylene glycol) (PEG)-based hydrogels using the thiol–maleimide addition reaction is reported. Maleimide containing homobifunctional PEGs with different molecular weights were synthesized and reacted with thiol functionalized β-cyclodextrin (β-CD(SH)7) to yield hydrogels with high efficiency under mild conditions. The resulting hydrogels were characterized by their water uptake properties, surface morphologies and rheological behaviours. In order to introduce reactive functional groups into the hydrogels, the stoichiometry of the thiol and maleimide groups was varied to obtain either thiol or maleimide functionalized hydrogels. Efficient functionalization of these reactive hydrogels in a tailored fashion was demonstrated through conjugation of appropriately functionalized fluorescent dye molecules.

Graphical abstract: Cyclodextrin mediated polymer coupling via thiol–maleimide conjugation: facile access to functionalizable hydrogels

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2014
Accepted
28 Oct 2014
First published
28 Oct 2014

RSC Adv., 2014,4, 57834-57841

Author version available

Cyclodextrin mediated polymer coupling via thiol–maleimide conjugation: facile access to functionalizable hydrogels

M. Arslan, T. N. Gevrek, A. Sanyal and R. Sanyal, RSC Adv., 2014, 4, 57834 DOI: 10.1039/C4RA12408A

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