Orthogonally Crosslinked Gelatin‐Norbornene Hydrogels for Biomedical Applications
Abstract
The thiol‐norbornene photo‐click reaction has exceptionally fast crosslinking efficiency compared with chain‐growth polymerization at equivalent macromer contents. The orthogonal reactivity between norbornene and thiol/tetrazine permits crosslinking of synthetic and naturally derived macromolecules with modularity, including poly(ethylene glycol) (PEG)‐norbornene (PEGNB), gelatin‐norbornene (GelNB), among others. For example, collagen‐derived gelatin contains both cell adhesive motifs (e.g., Arg‐Gly‐Asp or RGD) and protease‐labile sequences, making it an ideal macromer for forming cell‐laden hydrogels. First reported in 2014, GelNB is increasingly used in orthogonal crosslinking of biomimetic matrices in various applications. GelNB can be crosslinked into hydrogels using multi‐functional thiol linkers (e.g., dithiothreitol (DTT) or PEG‐tetra‐thiol (PEG4SH) via visible light or longwave ultraviolet (UV) light step‐growth thiol‐norbornene reaction or through an enzyme‐mediated crosslinking (i.e., horseradish peroxidase, HRP). GelNB‐based hydrogels can also be modularly crosslinked with tetrazine‐bearing macromers via inverse electron‐demand Diels‐Alder (iEDDA) click reaction. This review surveys the various methods for preparing GelNB macromers, the crosslinking mechanisms of GelNB‐based hydrogels, and their applications in cell and tissue engineering, including crosslinking of dynamic matrices, disease modeling, and tissue regeneration, delivery of therapeutics, as well as bioprinting and biofabrication.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Oct 06, 2023
- Source ID
- 10.1002/mabi.202300371
Entities
People
- Chien-Chi Lin
- Ellen Frahm
- Favour O. Afolabi
Organizations
- Indiana University
- National Institutes of Health
- United States Department of Defense