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      Proangiogenic alginate-g-pyrrole hydrogel with decoupled control of mechanical rigidity and electrically conductivity

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          Abstract

          Background

          An electrically conductive hydrogel has emerged to regulate cellular secretion activities with electrical stimulation. However, the electrical conductivity of typical hydrogel systems decreases with increasing elastic modulus of the hydrogels because of decreased transport of ions through a polymeric cross-linked mesh.

          Method

          This study hypothesized that the inverse dependency between electrical conductivity and elastic modulus would be made through the cross-linking of conductive monomer-units conjugated to a hydrophilic polymeric backbone. This hypothesis was examined through the cross-linking of pyrrole groups that were conjugated to an alginate backbone, termed alginate-g-pyrrole.

          Results

          Hydrogels with increased degrees of pyrrole substitution exhibited a simultaneous increase in the gels mechanical rigidity and electrical conductivity. The resulting hydrogel could control the adhesion and vascular endothelial growth factor secretion of cells via applied electrical stimulation.

          Conclusions

          This material design principle will be broadly useful to fabricating materials used for various actuation, cell culture, and biomedical applications.

          Electronic supplementary material

          The online version of this article (10.1186/s40824-017-0110-x) contains supplementary material, which is available to authorized users.

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          Most cited references19

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          Conducting polymers in biomedical engineering

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            Electroconductive hydrogels: synthesis, characterization and biomedical applications.

            Electroconductive hydrogels (ECHs) are composite biomaterials that bring together the redox switching and electrical properties of inherently conductive electroactive polymers (CEPs) with the facile small molecule transport, high hydration levels and biocompatibility of cross-linked hydrogels. General methods for the synthesis of electroconductive hydrogels as polymer blends and as polymer co-networks via chemical oxidative, electrochemical and/or a combination of chemical oxidation followed by electrochemical polymerization techniques are reviewed. Specific examples are introduced to illustrate the preparation of electroconductive hydrogels that were synthesized from poly(HEMA)-based hydrogels with polyaniline and from poly(HEMA)-based hydrogels with polypyrrole. The key applications of electroconductive hydrogels; as biorecognition membranes for implantable biosensors, as electro-stimulated drug release devices for programmed delivery, and as the low interfacial impedance layers on neuronal prostheses are highlighted. These applications provide great new horizons for these stimuli responsive, biomimetic polymeric materials. 2009 Elsevier Ltd. All rights reserved.
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              Controlling alginate gel degradation utilizing partial oxidation and bimodal molecular weight distribution.

              Degradability is often a critical property of materials utilized in tissue engineering. Although alginate, a naturally derived polysaccharide, is an attractive material due to its biocompatibility and ability to form hydrogels, its slow and uncontrollable degradation can be an undesirable feature. In this study, we characterized gels formed using a combination of partial oxidation of polymer chains and a bimodal molecular weight distribution of polymer. Specifically, alginates were partially oxidized to a theoretical extent of 1% with sodium periodate, which created acetal groups susceptible to hydrolysis. The ratio of low MW to high MW alginates used to form gels was also varied, while maintaining the gel forming ability of the polymer. The rate of degradation was found to be controlled by both the oxidation and the ratio of high to low MW alginates, as monitored by the reduction of mechanical properties and corresponding number of crosslinks, dry weight loss, and molecular weight decrease. It was subsequently examined whether these modifications would lead to reduced biocompatibility by culturing C2C12 myoblast on these gels. Myoblasts adhered, proliferated, and differentiated on the modified gels at a comparable rate as those cultured on the unmodified gels. Altogether, this data indicates these hydrogels exhibit tunable degradation rates and provide a powerful material system for tissue engineering.
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                Author and article information

                Contributors
                devolde1@illinois.edu
                wdt1013@illinois.edu
                hjkong06@illinois.edu
                Journal
                Biomater Res
                Biomater Res
                Biomaterials Research
                BioMed Central (London )
                1226-4601
                2055-7124
                7 November 2017
                7 November 2017
                2017
                : 21
                : 24
                Affiliations
                [1 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Chemical and Biomolecular Engineering, , University of Illinois at Urbana-Champaign, ; Urbana, IL 61801 USA
                [2 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Bioengineering, , University of Illinois at Urbana-Champaign, ; Urbana, IL 61801 USA
                [3 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Pathobiology, , University of Illinois at Urbana-Champaign, ; Urbana, IL 61801 USA
                Article
                110
                10.1186/s40824-017-0110-x
                5678582
                a559d840-fad4-4ccc-80d9-ad82fefc04a6
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 July 2017
                : 31 October 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: STC-EBICS Grant CBET-0939511
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: 1R21HL131469-01A1
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                alginate hydrogel,pyrrole,electrical stimulation,vascular endothelial growth factor,elastic modulus

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