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    ACS applied bio materials. 2022 Dec 20. doi: 10.1021/acsabm.2c00856
    Highly Stretchable, Swelling-Resistant, Self-Healed, and Biocompatible Dual-Reinforced Double Polymer Network Hydrogels.
    Fan W1,  Jensen LR2,  Dong Y3,  Deloria AJ4,  Xing B5,  Yu D6,  Smedskjaer MM7
    Author information
    1Department of Chemistry and Bioscience, Aalborg University, 9220Aalborg, Denmark.
    2Department of Materials and Production, Aalborg University, 9220Aalborg, Denmark.
    3School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore637459, Singapore.
    4Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, 1090Vienna, Austria.
    5Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore637371, Singapore.
    6Department of Chemistry and Bioscience, Aalborg University, 9220Aalborg, Denmark.
    7Department of Chemistry and Bioscience, Aalborg University, 9220Aalborg, Denmark.
    Abstract

    Superior flexibility and toughness can be achieved in bioactive hydrogels by the use of a double polymer network with complementary properties. Inspired by this design principle, we here combine polyacrylic acid (PAA) and sodium alginate (SA) to obtain a dual-reinforced double interpenetrating network (d-DIPN) hydrogel. The dual reinforcement involves ionic cross-linking and introduction of SiO nanoparticles, which leads to extraordinary improvements in strength and toughness. Compared with the standard PAA hydrogel that offers an elongation of 240% and a breakage stress of 0.03 MPa, the prepared SA(Ca)-PAA-SiO hydrogel shows an elongation above 1000% and a breakage stress of 1.62 MPa. Moreover, the combination of strong covalent cross-links and weak reversible interactions provides the d-DIPN hydrogel with swelling resistance and self-healing behavior, adhesive abilities, and shape memory performance. Furthermore, we show that the biocompatibility and bone cell proliferation ability of the hydrogels can be improved through a mineralization process despite an observed reduction in breakage strain and stress. Taken as a whole, our work paves the way for the design of strong and tough hydrogels, with potential applications within biomedicine and particularly tissue engineering.


    KEYWORDS: bioactive hydrogel, double network, dual reinforcement, highly stretchable, multifunctional

    Publikations ID: 36537710
    Quelle: öffnen
     
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