TABLE 1.
The fabrication and application of hydrogels for wound healing.
| Type of application | Cargo | Polymer scaffold | Crosslinking | Stimuli effect | Fabrication | Property | Outcome | References |
|---|---|---|---|---|---|---|---|---|
| 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) |