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      Macromolecular interactions in alginate–gelatin hydrogels regulate the behavior of human fibroblasts

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          Abstract

          Due to the presence of tripeptide arginine–glycine–aspartic acid, gelatin is considered a very promising additive material to improve the cytocompatibility of alginate-based hydrogels. Two different strategies, physical blending and chemical crosslinking with gelatin, are used in this study to modify alginate hydrogel. As the intermolecular interactions between the polysaccharide and protein in the resulting physically blended and chemically crosslinked hydrogels are different, significant differences in the properties of these hydrogel types, regarding especially their surface topography, degradation kinetics, mechanical properties, and protein release behavior, are observed. Cellular behavior on both types of alginate–gelatin hydrogels is investigated using primary human dermal fibroblasts to elucidate the effects of the different structural, mechanical, and degradation properties of the produced hydrogels on fibroblast attachment and growth. The hydrogel that is chemically crosslinked with gelatin exhibits the highest degree of cytocompatibility regarding adhesion, proliferation, metabolic activity, and morphology of growing fibroblasts.

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          Most cited references32

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          Is Open Access

          PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

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            The serial cultivation of human diploid cell strains.

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              A simplification of the protein assay method of Lowry et al. which is more generally applicable.

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                Author and article information

                Journal
                Journal of Bioactive and Compatible Polymers
                Journal of Bioactive and Compatible Polymers
                SAGE Publications
                0883-9115
                1530-8030
                May 2017
                October 16 2016
                May 2017
                : 32
                : 3
                : 309-324
                Affiliations
                [1 ]Institute of Biomaterials, Department of Materials Science and Engineering, University of Erlangen-Nuremberg, Erlangen, Germany
                [2 ]Department of Mechanical Engineering & Materials Science, Washington University in St. Louis, St. Louis, MO, USA
                [3 ]Cardiovascular Nanomedicine Unit, Section of Experimental Oncology and Nanomedicine, ENT Department, University Hospital Erlangen, Erlangen, Germany
                [4 ]Laboratory of Molecular Cardiology, Department of Cardiology and Angiology, University Hospital Erlangen, Erlangen, Germany
                Article
                10.1177/0883911516668667
                3b99b5ce-4b3e-408e-a7e0-e5fa202c812e
                © 2017

                http://journals.sagepub.com/page/policies/text-and-data-mining-license

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