Fibrin-Dextran Hydrogels with Tunable Porosity and Mechanical Properties.


Journal

Biomacromolecules
ISSN: 1526-4602
Titre abrégé: Biomacromolecules
Pays: United States
ID NLM: 100892849

Informations de publication

Date de publication:
11 09 2023
Historique:
medline: 12 9 2023
pubmed: 14 8 2023
entrez: 14 8 2023
Statut: ppublish

Résumé

Hydrogels as scaffolds in tissue engineering have gained increasing attention in recent years. Natural hydrogels, e.g., collagen or fibrin, are limited by their weak mechanical properties and fast degradation, whereas synthetic hydrogels face issues with biocompatibility and biodegradation. Therefore, combining natural and synthetic polymers to design hydrogels with tunable mechanical stability and cell affinity for biomedical applications is of interest. By using fibrin with its excellent cell compatibility and dextran with controllable mechanical properties, a novel bio-based hydrogel can be formed. Here, we synthesized fibrin and dextran-methacrylate (MA)-based hydrogels with tailorable mechanical properties, controllable degradation, variable pore sizes, and ability to support cell proliferation. The hydrogels are formed through in situ gelation of fibrinogen and dextran-MA with thrombin and dithiothreitol. Swelling and nuclear magnetic resonance diffusometry measurements showed that the water uptake and mesh sizes of fabricated hydrogels decrease with increasing dextran-MA concentrations. Cell viability tests confirm that these hydrogels exhibit no cytotoxic effect.

Identifiants

pubmed: 37574715
doi: 10.1021/acs.biomac.3c00269
doi:

Substances chimiques

Hydrogels 0
Fibrin 9001-31-4
Dextrans 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3972-3984

Auteurs

Shannon Anna Jung (SA)

DWI-Leibniz Institute for Interactive Materials, RWTH Aachen University, Forckenbeckstraße 50, Aachen 52074, Germany.
Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany.

Hanna Malyaran (H)

Helmholtz Institute for Biomedical Engineering, BioInterface Group, RWTH Aachen University, Pauwelsstrasse 20, Aachen 52074, Germany.
Interdisciplinary Centre for Clinical Research, RWTH Aachen University, Pauwelsstrasse 30, Aachen 52074, Germany.

Dan Eugen Demco (DE)

DWI-Leibniz Institute for Interactive Materials, RWTH Aachen University, Forckenbeckstraße 50, Aachen 52074, Germany.

Anna Manukanc (A)

DWI-Leibniz Institute for Interactive Materials, RWTH Aachen University, Forckenbeckstraße 50, Aachen 52074, Germany.
Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany.

Leonie Sophie Häser (LS)

DWI-Leibniz Institute for Interactive Materials, RWTH Aachen University, Forckenbeckstraße 50, Aachen 52074, Germany.
Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany.

Vytautas Kučikas (V)

Institute for Molecular Cardiovascular Research (IMCAR), RWTH Aachen University, Pauwelsstrasse 30, Aachen 52074, Germany.

Marc van Zandvoort (M)

Institute for Molecular Cardiovascular Research (IMCAR), RWTH Aachen University, Pauwelsstrasse 30, Aachen 52074, Germany.
Department of Genetics and Cell Biology, GROW, CARIM, MHeNS, Maastricht University, Maastricht 6200 MD, The Netherlands.

Sabine Neuss (S)

Helmholtz Institute for Biomedical Engineering, BioInterface Group, RWTH Aachen University, Pauwelsstrasse 20, Aachen 52074, Germany.
Institute of Pathology, RWTH Aachen University, Pauwelsstrasse 30, Aachen 52074, Germany.

Andrij Pich (A)

DWI-Leibniz Institute for Interactive Materials, RWTH Aachen University, Forckenbeckstraße 50, Aachen 52074, Germany.
Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany.

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Classifications MeSH