Table 4.
3D printed NGCs for never regeneration
Type | Fabrication method | Biomaterials and cell | In vitro/in vivo | Study period | Study result | Reference |
---|---|---|---|---|---|---|
Single lumen linear NGCs | 3D printed molds | Gelatin cryogel, NIH‐3T3 cells, small molecule substance | Transected sciatic nerve in rat | 3 months | NGCs significantly benefitted the recovery of transected peripheral nerve | [ 51 ] |
3D printed molds | EHS, GelMA | 10 ‐mm sciatic nerve gap in rat | 4 months | NGCs could promote the repair of peripheral nerve | [ 44 ] | |
Layer‐by‐layer depositing, direct soaking | dECM, PCL, PDA | Cell behaviors and neuronal differentiation were assessed in vitro | − | NGCs could promote regeneration of nerve | [ 58 ] | |
Assembling spheroids for constructing NGCs | NHDF | 10 ‐mm nerve gap in rat | 8 weeks | NGCs could enhance peripheral nerve regeneration | [ 84 ] | |
Assembling spheroids for constructing NGCs | Canine dermal fibroblasts, silicon tube | 5 ‐mm ulnar nerve gap in dog | 10 weeks | NGCs were effective for nerve regeneration | [ 50 ] | |
Stereolithography and coaxial electrospraying techniques | PC‐12 neural cells, PEG, PEGDA, Irgacure 819 | Cell behaviors and neuronal differentiation were assessed in vitro | − | 3D printed NGCs improved cell function | [ 52 ] | |
Assembling spheroids for constructing NGCs | NHDF, silicone tube | 5‐mm nerve gap in rat | 8 weeks | 3D NGCs promoted nerve regeneration | [ 119 ] | |
Assembling spheroids for constructing NGCs | G‐MSCs, type I collagen gel | 5‐mm nerve gap in rat | 12 weeks | NGCs promised potential application for repair and regeneration of peripheral nerve defects | [ 11l ] | |
Multiple lumen linear NGCs | DLP‐based rapid continuous 3D printing | PDMS, GelMA, PEGDA, LAP | 4‐mm nerve gap in rat | 11 weeks | Rats showed promising recovery of motor function and sensation | [ 62c ] |
Micro‐MRI technique, a single nozzle melt 3D printer | − | − | − | This method could provide a template for the design of downstream nerve graft model | [ 1a ] | |
Mandrel adhesion method | PCL, porous collagen‐based beads (CultiSphers) | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 63 ] | |
Bifurcated 3D printed NGCs | Layer‐by‐layer 3D printing | Polyethylene‐like material | 3 ‐mm sciatic nerve gap before trifurcation in rat | 12 weeks | 3D printed NGCs with interposed autograft could prevent neuroma formation | [ 72 ] |
An imaging‐coupled 3D printing methodology | Silicone, NGF, GDNF, gelatin methacrylate hydrogel | 10 ‐mm complex nerve gap in rat | 3 months | The platform had a significant impact on both the fundamental understanding of complex nerve injuries | [ 27a ] | |
Multichannel NGCs and bifurcating NGCs | Layer‐by‐layer fabrication procedure | Sodium hyaluronate, I2959, HAbp, HA, SCs | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 66 ] |
Single lumen NGCs, multichannel NGCs, and bifurcating NGCs | 3D printed molds | CryoGelMA gel, A‐MSC | 10 ‐mm sciatic nerve gap in rat | 16 weeks | NGCs supported the re‐innervation across 10 ‐mm sciatic nerve gaps | [ 129a ] |
Irregular 3D printed NGCs | A microfluidic approach, extrusion‐based bioprinting | Gelatin, MA, chitosan, I2959 | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 75 ] |
EHD‐jet 3D printing | PCL, PAA | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 76 ] | |
An extrusion‐based type of 3D printing | PDL, RGD, PHH | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 77 ] | |
EHD‐jetting 3D printing | PCL, glacial acetic acid | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 19 ] | |
Layer‐by‐layer fabrication procedure | SCs, alginate, HA, fibrinogen, thrombin TISSEEL VHSD kits | Cell behaviors were assessed in vitro | − | 3D printed NGCs directed the extension of dorsal root ganglion neurites | [ 78 ] | |
Extrusion‐based bioprinting | Gelatin/alginate hydrogel, SCs | Cell behaviors were assessed in vitro | 4 weeks | NGCs improved cell adhesion and related factor expression | [ 87 ] | |
Multifunctional 3D printed NGCs | A novel electrohydrodynamic jet 3D printing | PCL, PPy | Cell behaviors were assessed in vitro | − | PPy‐based conductive scaffolds had the potential for peripheral neuronal regeneration | [ 91 ] |
DLP | GelMA hydrogels, MPEG‐PCL nanoparticles, LAP, SCs, HUVECs | 5‐mm sciatic nerve gap in rat | 3 months | NGCs induced the recovery of sciatic nerve injuries in vivo | [ 93 ] | |
Fused deposition modeling 3D printing | PC fiber, PLO, DWCNTs, NSCs | Cell behaviors were assessed in vitro | − | 3D printed NGCs improved cell function | [ 96 ] | |
EHD‐jet 3D printing | rGO, PCL, PC12 cells | Cell behaviors were assessed in vitro | − | NGCs could support the differentiation of PC12 cells. | [ 101 ] | |
Layer‐by‐layer casting | Graphene, PCL, PDA, RGD | 15‐mm nerve gap in rat | 18 weeks | NGCs promoted successful axonal regrowth and remyelination | [ 28b ] | |
Stereolithography | PCL, NGF, camphorquinone, ethyl 4‐dimethyl aminobenzoate | 15 ‐mm critical size sciatic nerve defect in rat | 16 weeks | 3D printed NGCs could lead to a better functional regenerative outcome | [ 62b ] | |
DLP based continuous 3D printing process | Collagenase I, GelMA, LAP, SCs, PC12 cells | 10‐mm sciatic nerve gap in rat | 3 months | NGCs could efficiently repair the injured nerves | [ 118 ] |
Abbreviations: 3D, three‐dimensional; A‐MSC, adipose‐derived mesenchymal stem cell; CryoGelMA, cryopolymerized gelatin methacryloyl; dECM, decellularized extracellular matrix; DLP, digital light processing; DWCNT, double‐walled carbon nanotube; EHD, electrohydrodynamic; EHS, Engelbreth‐Holm‐Swarm; GDNF, glial cell line‐derived neurotrophic factor; GelMA, gelatin methacryloyl; G‐MSC, gingiva‐derived mesenchymal stem cell; HA, hyaluronic acid; HAbp, HA‐binding protein; HUVEC, human umbilical vein endothelial cell; I2959, irgacure 2959; LAP, lithium phenyl‐2,4,6‐trimethyl‐benzoylphosphinate; MA, methacrylic anhydride; micro‐MRI, micro‐magnetic resonance imaging; NGC, nerve guide conduit; NGF, nerve growth factor; NHDF, normal human dermal fibroblast; NIH‐3T3 cell, mouse embryonic cell; NSC, neural stem cell; PAA, poly(acrylic acid); PC, polycarbonate; PCL, poly(ε‐caprolactone); PDA, polydopamine; PDL, poly(D‐lysine); PDMS, polydimethylsiloxane; PEG, poly(ethylene glycol); PEGDA, poly(ethylene glycol) diacrylate; PHH, PHEMA hydrogel; PLO, poly(ʟ‐ornithine); PPy, polypyrrole; RGD, arginine‐glycine‐aspartic acid; rGO, reduced graphene oxide; SC, Schwann cell.