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Gelation and adhesion behavior of mussel adhesive protein mimetic polymer

Authors

  • Jin Nishida,

    1. JST, ERATO, Takahara Soft Interfaces Project, CE80, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
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  • Motoyasu Kobayashi,

    1. JST, ERATO, Takahara Soft Interfaces Project, CE80, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
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  • Atsushi Takahara

    Corresponding author
    1. JST, ERATO, Takahara Soft Interfaces Project, CE80, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
    2. Institute for Materials Chemistry and Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
    3. International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University, Fukuoka, Japan
    • JST, ERATO, Takahara Soft Interfaces Project, CE80, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
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Abstract

An acrylamide-type copolymer containing catechol, amino, and hydroxyl groups was synthesized as a mimetic of the natural mussel adhesive protein (MAP). The obtained copolymer in a phosphate buffer solution (pH = 8.0) formed a hydrogel within 2 h under air, whereas gelation did not proceed under argon atmosphere. We confirmed that the cross-linking reaction of the synthesized MAP mimetic copolymer was triggered by aerobic oxidation of catechol moieties to form an adhesive hydrogel. Two aluminum plates were adhered by the gelation of the MAP mimetic copolymer solution under humid air at room temperature. The interfacial region between the two aluminum plates failed at a lap shear strength of 0.46 MPa due to cohesive failure of the hydrogel. The adhesion strength was dominated by mechanical strength of the hydrogel as well as the interface interaction of catechol groups with substrate surface. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

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