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Cross-Linked Hydrogels Formed through Diels–Alder Coupling of Furan- and Maleimide-Modified Poly(methyl vinyl ether-alt-maleic acid)
journal contributionposted on 2016-01-22, 00:00 authored by S. Alison Stewart, Matilda Backholm, Nicholas A. D. Burke, Harald D. H. Stöver
The Diels–Alder [4 + 2] cycloaddition between furan- and maleimide-functional polyanions was used to form cross-linked synthetic polymer hydrogels. Poly(methyl vinyl ether-alt-maleic anhydride) was reacted with furfurylamine or N-(2-aminoethyl)maleimide in acetonitrile to form pairs of furan- and maleimide-functionalized poly(methyl vinyl ether-alt-maleic acid)s. Mixtures of these mutually reactive polyanions in water gelled within 15 min to 18 h, depending on degree of functionalization and polymer concentrations. Solution and magic-angle spinning 1H NMR were used to confirm the formation of the Diels–Alder adduct, to analyze competing hydrolytic side reactions, and demonstrate postgelation functionalization. The effect of the degree of furan and maleimide functionalization, polymer concentration, pH, and calcium ion concentration, on gelation time, gel mechanical properties, and equilibrium swelling, are described. Release of dextran as a model drug was studied using fluorescence spectroscopy, as a function of gel composition and calcium treatment.
15 minform pairswater gelledPolyacidmaleimide functionalization1 H NMRcalcium ion concentrationcalcium treatmenthydrolytic side reactionsmodel drugDielfluorescence spectroscopypolymer hydrogelspostgelation functionalizationgel compositionpolymer concentrationsreactive polyanions18 hgelation timefuranpolymer concentration