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1.
Chemistry ; 30(22): e202303843, 2024 Apr 16.
Article in English | MEDLINE | ID: mdl-38217885

ABSTRACT

The development of hydrogels based on dextrans, pullulan and lentinan to be used in biomedical applications including tissue engineering is reported. Despite the fact that selected polysaccharides such as hyaluronic acid are well established, little is known, how these polysaccharides can be chemically modified to create hydrogels under controlled conditions. In this study we present a small library of chemically modified polysaccharides which are used for a divergent approach to achieve biomedical relevant hydrogels. In this case the crosslinking is based on thio ether formation between thiol modified donor and vinylsulfone or maleimide modified acceptor components. Successful synthesis of the linker systems and coupling at the polysaccharides, hydrogel formation takes place under physiological conditions. We extended the study by coupling small molecules like adhesion factors for increasing cell compatibility as well as a dye for further studies. The different hydrogels were studied to their rheological properties, water uptake, their permeability, biodegrability and their cytotoxicity.


Subject(s)
Dextrans , Glucans , Hydrogels , Hydrogels/chemistry , Dextrans/chemistry , Lentinan , Tissue Engineering , Polysaccharides/chemistry
2.
Carbohydr Polym ; 262: 117924, 2021 Jun 15.
Article in English | MEDLINE | ID: mdl-33838803

ABSTRACT

In pursuit of a chemically-defined matrix for in vitro cardiac tissue generation, we present dextran (Dex)-derived hydrogels as matrices suitable for bioartificial cardiac tissues (BCT). The dextran hydrogels were generated in situ by using hydrazone formation as the crosslinking reaction. Material properties were flexibly adjusted, by varying the degrees of derivatization and the molecular weight of dextran used. Furthermore, to modulate dextran's bioactivity, cyclic pentapeptide RGD was coupled to its backbone. BCTs were generated by using a blend of modified dextran and human collagen (hColI) in combination with induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) and fibroblasts. These hColI + Dex blends with or without RGD supported tissue formation and functional maturation of CMs. Contraction forces (hColI + Dex-RGD: 0.27 ± 0.02 mN; hColI + Dex: 0.26 ± 0.01 mN) and frequencies were comparable to published constructs. Thus, we could demonstrate that, independent of the presence of RGD, our covalently linked dextran hydrogels are a promising matrix for building cardiac grafts.


Subject(s)
Dextrans/chemistry , Hydrogels/chemistry , Myocytes, Cardiac/metabolism , Tissue Scaffolds/chemistry , Collagen/chemistry , Cross-Linking Reagents/chemistry , Fibroblasts/metabolism , Humans , Hydrazones/chemistry , Induced Pluripotent Stem Cells/metabolism , Myocardium/metabolism , Tissue Engineering/methods
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