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International Journal of Bioprinting                              Blood components for tissue graft bioprinting




                                 Characterization of bioink formulation/cytocompatibility





                                      Cell viability using different mixing methods Mixing success: Homogenous mixing of highly viscous bioma- terial inks and cell suspensions Printability, rheology, cell migration Printability, bioprinting performance, biofunctionality  Versatile bioink  Tissue engineering: Bone growth, cartilage repair wound   healing  Characterization of ADA-gel-PRP bioink formulation: Print- ability, cell viability, cytotoxicity, hemolysis, histocompa



















                                 Blood-derived product  FFP (blood bank), n = 5   donors  PRP  PL (n = 12 donors), platelet   concentrate >10 6 /µL, freeze   (-196°C)/thawing (37°C)   dialysis  3D-printable PL (PLMA)-  based hydrogel, which con- sists of PL from whole blood   of humans  PRP (750 g, 5 min) HUVECs, human umbilical vein endothelial cells; MC, methylcellulose; MSCs, mesenchymal stem cells; RFP, red fluorescent protein; PCL, polycaprolactone; PL, platelet lysa










                                 Cell phenotype  Immortalized MSCs  MSCs  hASCs  Comparison of   HUink with GelMA   and with ALG  GFP-hMSCs  RFP-HUVEC  L929 mouse fibro-  blast cell line Another strategy in bioink development consists of developing formulations optimal for extrusion bioprinting but without tissue specifications. We consider both situations, such as when blood-derived biomaterial is part of the bioink formulation or is added later to the bioprinted constru






                                      30 mg/mL ALG dissolved in plasma and added   with MC (90 mg/mL)  HUink = Cellulose nanocrystals (18% wt) Mixed with PL (67–160 mg/mL) (+ thrombin   PLMA-based hydrogels Methacrylated photo-polymerization of PL PCL/PLMA (PCL frame and cells encapsulated   Covalent crosslinking in the presence of borax  * Development of mixing units developed using computer-aided design (CAD) and 3D printing.











                             Table 2. Multipurpose applications  Ink formulation Author (year);  Dani et al. (2021);   Alginate 1% Faramazi et al. (2018);   PRP 50 U/mL Adv Healthcare Mat  Mendes et al. (2020);   Biofabrication [73]  + CaCl 2 )  Min et al. (2021);   Biofabrication  [74]  in PLMA)  ALG:PLMA  Gelatin:PLMA  ADA Somasekharan et al.   Gelatin (2020); Bioengineering   PRP  methacrylated; PRP, platelet-rich plasma.

















            Volume 9 Issue 5 (2023)  Journal  Gels * [72]  287            [75]         https://doi.org/10.18063/ijb.762
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