Effects of hydrogel scaffold |
|
QCS and Pluronic® F127 |
Schiff base bond |
pH |
Bulk hydrogel |
Self-healing, extensibility, compressibility and adhesiveness |
Antibacterial QCS improved wound healing effect |
Qu et al. (2018)
|
|
DexIEME |
Crosslinking of alkene |
|
Bulk hydrogel |
|
Restored full skin structures on both pre-existing scars and acute wounds by modulating immune |
Sun (2017)
|
|
starPEG and heparin |
Thiol-ene addition |
|
Bulk hydrogel |
|
Scavenged inflammatory chemokines for diabetic wound healing |
Lohmann et al. (2017)
|
|
|
Catechol modified PEG and UPy modified gelatin |
Catechol–Fe3+ coordination and UPy hydrogen bond |
Near-infrared and pH |
Bulk hydrogel |
Adhesiveness, shape adaptability, self-healing, antioxidant, photothermal antibacterial, degradability and removability |
Promoted full-thickness wound healing by regulating inflammation, accelerating collagen deposition, granulation tissue formation, and vascularization |
Zhao et al. (2020d)
|
Drug and biomolecule delivery |
hEGF |
PEG and heparin |
Thiol-ene addition |
|
Bulk hydrogel |
|
Accelerated wound healing by hEGF delivery |
Goh et al. (2016)
|
VEGF |
starPEG and heparin |
Amidation |
|
Bulk hydrogel |
|
Sustained release of VEGF with low anticoagulant activity and promotion of angiogenesis for diabetic wounds |
Freudenberg et al. (2015)
|
EGF and Cur |
Copolymer of lactic acid and reverse Pluronic®10R5 |
Thermo-gelling behavior |
Temperature |
In situ gelation |
|
Increased granulation tissue formation, collagen deposition, and angiogenesis |
Guo et al. (2016)
|
CeONs and AMPs |
Gelatin methacryloyl |
Crosslinking of alkene |
|
Sprayable hydrogel |
Sprayability, adhesiveness, antioxidant and antibacterial |
Enhanced wound healing speed and promoted remodeling of the healed skin |
Cheng et al. (2021)
|
BG and DFO |
Sodium alginate |
Ionic bond |
|
In situ injection |
|
Enhanced vascularization in diabetic wound by promoting HIF-1α and VEGF expression |
Kong et al. (2018)
|
Cell delivery |
hASCs |
Gelatin |
Schiff base bond |
|
Microgel injection |
|
Provided functionalized micro-niches for hASCs proliferation and growth factors secretion |
Zeng et al. (2015)
|
BMSCs |
N-isopropylacrylamide polymers |
Thermo-gelling behavior |
|
Bulk hydrogel |
|
Inhibited chronic inflammation and promoted growth factor secretion |
Chen et al. (2015)
|
ASCs |
Aloe vera hydrogel |
|
|
Injection |
|
Improved angiogenesis and re-epithelialization, subsided inflammation and scar formation |
Oryan et al. (2019)
|
HUCPVC |
Decellularized dermal matrix |
|
|
Bulk hydrogel |
|
Improved VEGFR-2 expression and vascular density |
Milan et al. (2016)
|
Dermal fibroblasts |
Gelatin |
Catechol crosslinking by HRP |
|
In situ gelation after injection |
|
Facilitated cell survival and retention, promoted mature collagen deposition and vascularization |
Lee et al. (2014)
|
Fibroblasts and insulin |
Poly(vinyl alcohol), PEG and CS |
Schiff base bond and phenylboronate ester |
pH and glucose |
In situ gelation |
|
Promoted neovascularization and collagen deposition |
Zhao et al. (2017a)
|
Cord Blood- Endothelial Colony-Forming Cells (ECFCs) |
Hyaluronic Acid Hydrogels |
Thiol-Acrylate conjugation |
MMP- sensitive |
Bulk hydrogels |
Adhesiveness, degradability |
Provided micro-niches for ECFCs to form vascular networks and integrate with the host vasculatures. Improve angiogenesis and support healthy epithelialization. |
Hanjaya-Putra et al. (2013)
|