Sequential interpenetrating poly(ethylene glycol) hydrogels prepared by UV-initiated thiol–ene coupling chemistry

Authors

  • Ting Yang,

    1. Department of Fiber and Polymer Technology, KTH Royal Institute of Technology, School of Chemical Science and Engineering, SE 100 44 Stockholm, Sweden
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  • Michael Malkoch,

    1. Department of Fiber and Polymer Technology, KTH Royal Institute of Technology, School of Chemical Science and Engineering, SE 100 44 Stockholm, Sweden
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  • Anders Hult

    Corresponding author
    1. Department of Fiber and Polymer Technology, KTH Royal Institute of Technology, School of Chemical Science and Engineering, SE 100 44 Stockholm, Sweden
    • Department of Fiber and Polymer Technology, KTH Royal Institute of Technology, School of Chemical Science and Engineering, SE 100 44 Stockholm, Sweden
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Abstract

Poly(ethylene glycol) (PEG)-diallyls, ranging from 2 to 8 kDa, were successfully reacted with a trifunctional thiol crosslinker via thiol–ene coupling reaction to construct four different primary PEG hydrogels. These systems were used as scaffolds for the preparation of a library of sequential interpenetrating networks (SeqIPNs). The solid content of the secondary networks varied between 21 and 34% and was dependent on the length of the absorbing PEGs. The gel fractions for the IPNs were above 85%. Additionally, the lowest degree of swelling was found for the IPN based on 2-kDa PEG (315%), whereas the 8-kDa PEG IPN exhibited a value of 810%. The SeqIPN strategy facilitated hydrogel systems that cover a larger domain of tensile modulus (192–889 kPa) when compared with single hydrogel networks (175–555 kPa). © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

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