Dual Functionalized Injectable Hybrid Extracellular Matrix Hydrogel for Burn Wounds.
Kamakshi BankotiArun Prabhu RameshbabuSayanti DattaPiyali GoswamiMadhurima RoyDipankar DasSudip Kumar GhoshAmit Kumar DasAnalava MitraSagar PalDhrubajyoti MaulikBo SuPaulomi GhoshBikramajit BasuSantanu DharaPublished in: Biomacromolecules (2020)
Low strength and rapid biodegradability of acellular dermal matrix (ADM) restrict its wider clinical application as a rapid cell delivery platform in situ for management of burn wounds. Herein, the extracted ADM was modified by a dual cross-linking approach with ionic crosslinking using chitosan and covalent cross-linking using an iodine-modified 2,5-dihydro-2,5-dimethoxy-furan cross-linker, termed as CsADM-Cl. In addition, inherent growth factors and cytokines were found to be preserved in CsADM-Cl, irrespective of ionic/covalent crosslinking. CsADM-Cl demonstrated improvement in post crosslinking stiffness with a decreased biodegradation rate. This hybrid crosslinked hydrogel supported adhesion, proliferation, and migration of human foreskin-derived fibroblasts and keratinocytes. Also, the angiogenic potential of CsADM-Cl was manifested by chick chorioallantoic membrane assay. CsADM-Cl showed excellent antibacterial activity against Escherichia coli and Staphylococcus aureus. Moreover, CsADM-Cl treated full thickness burn wounds and demonstrated rapid healing marked with superior angiogenesis, well-defined dermal-epidermal junctions, mature basket weave collagen deposition, and development of more pronounced secondary appendages. Altogether, the bioactive CsADM-Cl hydrogel established significant clinical potential to support wound healing as an apt injectable antibacterial matrix to encounter unmet challenges concerning critical burn wounds.
Keyphrases
- wound healing
- extracellular matrix
- escherichia coli
- staphylococcus aureus
- hyaluronic acid
- endothelial cells
- high throughput
- loop mediated isothermal amplification
- ionic liquid
- optical coherence tomography
- magnetic resonance imaging
- mesenchymal stem cells
- cell therapy
- tissue engineering
- climate change
- molecularly imprinted