Thermoresponsive Injectable Hydrogel To Mimic the Heat- and Strain-Stiffening Behavior of Biopolymers toward Muscle Cell Proliferation.
Debasish NathJahanvi RalhanJojo P JosephChirag MiglaniAsish PalPublished in: Biomacromolecules (2024)
Injectable hydrogels with nonlinear mechanical attributes to emulate natural biopolymers hold paramount significance in tissue engineering, offering the potential to create scaffolds that seamlessly mimic the biomechanical intricacies of living tissues. Herein, we unveil a synthetic design strategy employing Schiff base chemistry to furnish a peptide-polymer hierarchical contractile injectable hydrogel network. This innovative design demonstrates cross-linking of supramolecular peptide nanostructures such as nanofibers, 1 NF , and twisted bundles, 1 TB , with a thermosensitive aldehyde-functionalized polymer, P CHO . These networks exhibit interesting nonlinear mechanical stiffening responses to temperature and external stress. Furthermore, the hydrogels transform into a gel state at physiological temperature to exhibit injectable behavior and demonstrate compression load-bearing capabilities. Finally, the hydrogel network exhibits excellent biocompatibility and cell proliferation toward fibroblast, L929, and myoblast, C2C12, to validate their use as potential extracellular matrix mimetic injectable scaffolds.
Keyphrases
- tissue engineering
- cell proliferation
- extracellular matrix
- skeletal muscle
- cell cycle
- signaling pathway
- gene expression
- wound healing
- risk assessment
- human health
- quantum dots
- oxidative stress
- inflammatory response
- mass spectrometry
- nuclear factor
- network analysis
- simultaneous determination
- finite element
- liquid chromatography
- finite element analysis