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. 2022 Dec 19;10:rbac105. doi: 10.1093/rb/rbac105

Table 3.

Application of in situ bioprinting in skin regeneration and wound repair

Printing strategy Scanning approach Bioink Laden cells Models Ref.
Automatic
 Extrusion-based bioprinting NA Fibrinogen + collagen AFSCs, BMSCs Murine full-thickness skin wound model [118]
NA Thiolated HA + thiolated gelatin + PEGDA AFSCs Murine full-thickness skin wound model [119]
  (For soft tissue repair) droplet-based bioprinting 3D laser scanner (For soft tissue repair) fibrinogen + collagen + KGF (For soft tissue repair) dermal fibroblasts Murine composite skin and calvarial bone defect [114]
 Inkjet-based bioprinting 3D laser scanner Fibrinogen + collagen Dermal fibroblasts, epidermal keratinocytes Murine and porcine full-thickness skin wounds [91]
 Two-photon bioprinting NA HCC-PEG Muscular fibroblasts Printing inside murine normal dermis [111]
Handheld
 Extrusion-based bioprinting Not required GelMA + VEGF NA Porcine full-thickness skin wound model [109]
Fibrinogen + HA UMSCs Porcine full-thickness skin burn injury model [116]
Alginate + collagen; fibrinogen + HA + collagen (For in vitro experiments)
dermal fibroblasts, epidermal keratinocytes
Murine and porcine full-thickness skin wounds [117]
Alginate + gelatin + PRP Dermal fibroblasts, epidermal stem cells Murine full-thickness skin wound model [66]

AFSCs, amniotic fluid-derived stem cells; BMSCs, bone marrow-derived mesenchymal stem cells; GelMA, gelatin methacryloyl; HA, hyaluronic acid; HCC, 7-hydroxycoumarin-3-carboxylate; KGF, keratinocyte growth factor; NA, not applicable; PEG, polyethylene glycol; PRP, platelet-rich plasma; UMSCs, umbilical cord-derived mesenchymal stromal cells; VEGF, vascular endothelial growth factor.