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1.
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
2.
Chemistry ; 24(6): 1231-1240, 2018 Jan 26.
Article in English | MEDLINE | ID: mdl-28804933

ABSTRACT

Hydrogels have emerged as a highly interdisciplinary topic as they play a significant role for a vast number of applications. They have been studied extensively as materials for contact lenses, wound dressing and as filler material in soft-tissue augmentation, in which classical polymer backbones such as hydroxyethylmethacrylate (HEMA) are typically employed. More recently, polysaccharides have received attention, particularly in the fields of regenerative medicine and tissue engineering, as ideal candidate materials for artificial extracellular matrices (ECM). The polysaccharides of choice are dextran, alginate, chitosan, hyaluronic acid and pullulan and in order to obtain suitable hydrogels from these polysaccharides, controlled chemical functionalization is of critical importance. This short review summarizes recent developments in the chemical derivatization of polysaccharides to pave the way for crosslinking and to decorate individual polysaccharide chains with bioactive ligands. The report covers convergent and divergent protocols for crosslinking, as well strategies for bisfunctionalization of polysaccharides. Additionally, information on biological properties and biomedical applications are covered.


Subject(s)
Biocompatible Materials/chemistry , Hydrogels/chemical synthesis , Polysaccharides/chemistry , Contact Lenses , Cross-Linking Reagents/chemistry , Drug Delivery Systems/methods , Humans , Tissue Engineering/methods , Wound Healing
3.
Chemistry ; 22(52): 18777-18786, 2016 Dec 23.
Article in English | MEDLINE | ID: mdl-27864999

ABSTRACT

A synthetic toolbox for the introduction of aldehydo and hydrazido groups into the polysaccharides hyaluronic acid, alginate, dextran, pullulan, glycogen, and carboxymethyl cellulose and their use for hydrogel formation is reported. Upon mixing differently functionalized polysaccharides derived from the same natural precursor, hydrazone cross-linking takes place, which results in formation of a hydrogel composed of one type of polysaccharide backbone. Likewise, hydrogels based on two different polysaccharide strands can be formed after mixing the corresponding aldehydo- and hydrazido-modified polysaccharides. A second line of these studies paves the way to introduce a biomedically relevant ligand, namely, the adhesion factor cyclic RGD pentapeptide, by using an orthogonal click reaction. This set of modified polysaccharides served to create a library of hydrogels that differ in the combination of polysaccharide strands and the degree of cross-linking. The different hydrogels were evaluated with respect to their rheological properties, their ability to absorb water, and their cytotoxicity towards human fibroblast cell cultures. None of the hydrogels studied were cytotoxic, and, hence, they are in principal biocompatible for applications in tissue engineering.


Subject(s)
Alginates/chemistry , Dextrans/chemistry , Fibroblasts/chemistry , Glucans/chemistry , Hyaluronic Acid/chemistry , Hydrogels/chemical synthesis , Polysaccharides/chemical synthesis , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Hydrogels/chemistry , Polysaccharides/chemistry , Tissue Engineering
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