Method for rapid multi-nozzle 3D printing of tumor tissue model using supporting bath
A tumor tissue, 3D printing technology, applied in the field of biological 3D printing, can solve the problems of increasing the bioprinting time, restoring the tumor tissue structure, accuracy and time effects, avoiding the uncontrollable cell density and species space, and slowing down the activity. The effect of reducing, reducing printing time
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Embodiment 1
[0036] Preparation of Example 1 Liver Tumor Tissue Model
[0037] (1) Preparation of liver tumor cell ink
[0038] With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 2% and sodium alginate 2% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; Tumor cells (2×10 6 / mL) DMEM complete medium, pipet evenly with a pipette gun, and put it into the incubator for use.
[0039] (2) Preparation of liver tissue ink
[0040] With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 2% and sodium alginate 2% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; Tissue cells (2×10 6 / mL) into the DMEM complete medium, blow evenly with a pipette gun, and put it into the incubator for use.
[0041] (3) Preparation of hydrogel support bath
[0042] The main material of the hydrogel support ...
Embodiment 2
[0045] The preparation of embodiment 2 lung tumor tissue model
[0046] (1) Preparation of lung tumor cell ink
[0047] With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 3% and sodium alginate 2% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; add lung Tumor cells (3×10 6 / mL) DMEM complete medium, pipet evenly with a pipette gun, and put it into the incubator for use.
[0048] (2) Preparation of lung tissue cell ink
[0049]With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 3% and sodium alginate 2% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; lung normal Tissue cells (3×10 6 / mL) into the DMEM complete medium, blow evenly with a pipette gun, and put it into the incubator for use.
[0050] (3) Preparation of hydrogel support bath
[0051] The main mate...
Embodiment 3
[0054] Example 3 Preparation of Pancreatic Tumor Tissue Model
[0055] (1) Preparation of pancreatic tumor cell ink
[0056] With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 4% and sodium alginate 1% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; add pancreas containing Tumor cells (2×10 6 / mL) DMEM complete medium, pipet evenly with a pipette gun, and put it into the incubator for use.
[0057] (2) Preparation of pancreatic tissue cell ink
[0058] With 25mM HEPES buffer solution containing 10% volume FBS as solvent, configure GelMA (photocurable gelatin) 4% and sodium alginate 1% magnetically stir evenly, sterilize with ultraviolet light, add 0.1% Irgacure 2959 photoinitiator; normal pancreas Tissue cells (2×10 6 / mL) into the DMEM complete medium, blow evenly with a pipette gun, and put it into the incubator for use.
[0059] (3) Preparation of hydrogel suppo...
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