Cationic disulfide-functionalized worm gels

L. P.D. Ratcliffe, K. J. Bentley, R. Wehr, N. J. Warren, B. R. Saunders, S. P. Armes

    Research output: Contribution to journalArticlepeer-review

    42 Downloads (Pure)

    Abstract

    The recent development of polymerization-induced self-assembly (PISA) has facilitated the rational synthesis of a range of diblock copolymer worms, which hitherto could only be prepared via traditional post-polymerization processing in dilute solution. Herein we explore a new synthetic route to aqueous dispersions of cationic disulfide-functionalized worm gels. This is achieved via the PISA synthesis of poly[(glycerol monomethacrylate-stat-glycidyl methacrylate)]-block-poly(2-hydroxypropyl methacrylate) (P(GMA-stat-GlyMA)-PHPMA) block copolymer worms via reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization of HPMA. A water-soluble reagent, cystamine, is then reacted with the pendent epoxy groups located within the P(GMA-stat-GlyMA) stabilizer chains to introduce disulfide functionality, while simultaneously conferring cationic character via formation of secondary amine groups. Moreover, systematic variation of the cystamine/epoxy molar ratio enables either chemically cross-linked worm gels or physical (linear) primary amine-functionalized disulfide-based worm gels to be obtained. These new worm gels were characterized using gel permeation chromatography, 1H NMR spectroscopy, transmission electron microscopy, dynamic light scattering, aqueous electrophoresis and rheology. In principle, such hydrogels may offer enhanced mucoadhesive properties.

    Original languageEnglish
    Pages (from-to)5962-5971
    Number of pages10
    JournalPolymer Chemistry
    Volume8
    Issue number38
    Early online date6 Sept 2017
    DOIs
    Publication statusPublished - 14 Oct 2017

    Fingerprint

    Dive into the research topics of 'Cationic disulfide-functionalized worm gels'. Together they form a unique fingerprint.

    Cite this