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. 2020 Feb 13;6(1):11. doi: 10.1038/s41572-020-0145-5

Table 1.

Example commercially available skin substitutes

Name (manufacturer) Composition Advantages Disadvantages Refs
Epidermal: CEA
Epicel (Vericel Corporation, Cambridge, MA, USA) CEA from human keratinocytes embedded in fibrin mesh Autologous coverage of epidermis High cost; limited reliability; fragile; increased susceptibility to infections; complex postoperative care; tendency for blistering; poor healing 268270
Epidermal: autologous skin suspension or cell spray
ReCell (Avita Medical, Woburn, Massachusetts, USA) Autologous skin suspension produced using minimal donor skin and applied as a cell spray. Induces acceleration of re-epithelialization and wound healing; for wide meshes, most likely to improve appearance of scar High cost; no dermal substitute; limited to more superficial burns 271,272
MySkin (Regenerys, Cambridge, UK) Suspended CEA delivered as spray Promotes re-epithelialization No RCT data 273,274
SkinGun (RenovaCare, Inc., NY, USA) Epidermal cells and stem cells Expansion ratio of skin donor site to treatment surface area of ~1:20 No RCT data 275
Keraheal (MCTT, Seoul, Korea) Suspension formed of cultured epithelial cells plus fibrin glue Facilitates epithelial cell attachment No RCT data 276
Dermal
OASIS Wound Matrix (Healthpoint Ltd, Ft Worth, TX, USA) Derived from the submucosal layers of the porcine intestine; contains glycosaminoglycans and growth factors Dermal element to improve scar appearance Porcine composition; high cost 277,278
Matriderm (MedSkin Solutions Dr. Suwelack AG, Billerbeck, Germany) Made of type I collagen fibre coated with 3% α-elastin hydrosylate matrix Can be used as single-stage procedure with split-thickness skin grafts; very good outcomes in initial clinical trials Possible increased susceptibility to infections 279
NovoSorb BTM (Biodegradable Temporizing Matrix) (PolyNovo, Melbourne, Australia) Biodegradable polyurethane foam plus a temporary nonbiodegradable polyurethane seal; fully synthetic Low cost; improves appearance; good results in initial clinical trials No RCT data 280
MatriStem (ACell, Inc., Columbia, MD, USA) Composed of extracellular matrix derived from porcine urothelium Provides barrier protection No RCT data 281
Integra (Integra LifeSciences, Plainsboro, NJ, USA) Bovine collagen matrix with a silicone layer Most-studied dermal replacement matrix; improves scarring and skin appearance; used in acute and reconstructive surgery; efficacy shown in RCT High cost; possible increased susceptibility to infections 282,283
Alloderm (Allergan, Dublin, Ireland) Human cadaveric acellular matrix Improves scarring High cost 284
SUPRATHEL (Polymedics Innovations GmbH, Denkendorf, Germany) Synthetic copolymer >70% dl-lactide polymerized with ε-caprolactone and methylenecarbonate Promising results in initial clinical studies No RCT data 280
Composite
Self-Assembled Skin Substitute (SASS) (Loex, Quebec, Canada) Reconstruction of a fully autologous bilayered skin substitute No exogenous scaffold or biomaterial needed; good scar development; autologous Requires a 31-day production period; very high cost; limited clinical data 279,285,286
Epifix (MiMedx, Marietta, GA, USA) Composed of dehydrated amniotic and chorionic membrane containing collagen, connective tissue, cytokines and growth factors Improves wound healing and regeneration Not a skin substitute per se; no RCT data 287
Cultured skin substitute (prepared at Shriners Hospitals for Children, Cincinnati, OH, USA) Autologous keratinocytes and fibroblasts from patient biopsy, combined into a bilayer with bovine collagen matrix Good scaring; epithelial and dermal elements High cost; long production time; does not include melanocytes 288

CEA, cultured epithelial autograft; RCT, Randomized controlled trial.