Table 1.
Collagen-based scaffolds for skin regeneration application.
Biomaterial | Fabrication method | Cell(s) | Performance | Ref. |
---|---|---|---|---|
Collagen | Freeze-drying + DHTa) crosslinking | Acellular | Wound contraction is disrupted in the favor of skin regeneration | [69] |
Collagen | Electrospinning + GA vapor crosslinking | NHOK, NHEK | Cell attachment is not sufficient unless ECM proteins added to the scaffold | [94] |
Collagen | Freeze-drying vs electrospinning (DHT + EDC crosslinking) | HDF, HEK | Electrospun scaffold led to less wound contraction | [58] |
Matriderm (collagen + elastin) | LaBP (Laser-assisted bioprinting) | NIH-3T3 and HaCaT keratinocytes | Multilayered epidermis formation with angiogenesis from wound bed and edges | [59] |
Collagen–C6S | Freeze-drying + DHT crosslinking | HDF, HEK | Formation of a mature epidermis and a nearly physiological dermis without hair follicles with delayed wound contraction compared with acellular scaffold | [23] |
Collagen–C6S | Freeze-drying + DHT crosslinking + a laminated layer | HEK | HEK were restricted to the outer layer of the substitute | [70] |
Collagen–C6S | Freeze-drying + chemical crosslinking | HDF, HEK | Improved degradation and wound contraction | [73] |
Collagen–HA | freeze-drying + EDC crosslinking | HDF | Improved HDF attachment in vitro with no effect on wound contraction in vivo | [74] |
Collagen–gelatin | SCPL + Freeze-drying | DF | Improved DF infiltration and reduced inflammatory response | [103] |
Collagen–elastin | elastin hydrolysate-coated collagen scaffold | Autologous dermal fibroblasts | Lower degradation rate and reduced migration and/or proliferation of subcutaneous fibroblasts in the wound tissue compared with acellular scaffold | [78] |
Collagen–elastin | Commercial collagen–elastin membrane | Keratinocyte | Promoted dermal vascularization and basement membrane formation | [79] |
Collagen–chitosan | Freeze-drying | HDF, HEK | Promoted rapid remodeling of ECM nearly similar to normal dermis as well as organization of elastin deposits in thin fibrils after 90 d | [85,80] |
Collagen–chitosan | Freeze-drying | HDF, HEK, HUVEC | Capillary-like structures were formed without addition of external angiogenesis promoting agents | [90] |
Collagen–chitosan | Freeze-drying | HDF, HEK | Nerve fibers were observed four months after transplantation | [91] |
Collagen–chitosan-laminin | Freeze-drying | HDF, HEK | Enhanced sensory perception recovery | [92] |
Collagen–chitosan | Freeze-drying + GA crosslinking | HDF | Chitosan reduced biodegradation of the scaffold | [93] |
Chitosan–collagen | Freeze-drying | HDF | Improved HDF proliferation and decreased contraction | [89] |
DHT crosslinking: dehydrothermal crosslinking, C6S: chondroitin 6-sulfate, HDF: human dermal fibroblast, HEK: human epidermal keratinocyte, SCPL: solvent casting-particulate leaching, DF: dermal fibroblast, GA: glutaraldehyde, HA: Hyaluronic acid, BM-MSCs: bone marrow mesenchymal stem cells, NHOK: Normal human oral keratinocytes, NHEK: Normal human epidermal keratinocytes, LaBP: Laser-assisted bioprinting, HaCaT cells: human keratinocyte cell line.