Tissue-engineered blood vessel cultured in vitro
A technology of blood vessels and tissue cells, which can be applied to the devices of blood vessels and human tubular structures, etc., can solve the problems of unsatisfactory effects, source and strength limitations, etc.
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Embodiment 1
[0012] Take 0.1 g of commercially available type I collagen and soak it in 100 ml of 0.2 mol / L acetic acid solution. Stir well to fully dissolve, then place in the glass tube of a tumble mixer and roll the coating. Pour off excess collagen solution after forming a uniform collagen film. Pour 0.1 g of commercially available polyethylene glycol into 100 ml of sterilized physiological saline and stir evenly, take an appropriate amount of polyethylene glycol liquid and drop it on the collagen film, and roll the coating with a drum agitator. Press 1.25×10 5 Add the recipient's own bone marrow-differentiated smooth muscle cells at a concentration of 1 / ml, plant continuously for 2 days, and then simultaneously press 1.25×10 5 Individual / ml concentration planted recipient's own bone marrow differentiated fibroblasts. Planted continuously for 3 days respectively. Next, the recipient's own bone marrow vascular endothelial progenitor cells and vascular endothelial growth factor were ...
Embodiment 2
[0014] Take 0.2 g of commercially available type I collagen and soak it in 100 ml of 0.5 mol / L acetic acid solution. Stir well to fully dissolve, then place in the glass tube of a tumble mixer and roll the coating. Pour off excess collagen solution after forming a uniform collagen film. Pour 0.5 g of commercially available polyethylene glycol into 100 ml of sterilized physiological saline and stir evenly, take an appropriate amount of polyethylene glycol liquid and drop it on the collagen film, and roll the coating with a drum agitator. Press 1.25×10 5 Add the recipient's own bone marrow-differentiated smooth muscle cells at a concentration of 1 / ml, plant continuously for 2 days, and then simultaneously press 1.25×10 5 Individual / ml concentration planted recipient's own bone marrow differentiated fibroblasts. Planted continuously for 3 days respectively. Next, the recipient's own bone marrow vascular endothelial progenitor cells and vascular endothelial growth factor were ...
Embodiment 3
[0016] Take 1.0 g of commercially available type I collagen and soak it in 100 ml of 0.01 mol / L acetic acid solution. Stir well to fully dissolve, then place in the glass tube of a tumble mixer and roll the coating. Pour off excess collagen solution after forming a uniform collagen film. Pour 0.1 g of commercially available polyethylene glycol into 100 ml of sterilized physiological saline and stir evenly, take an appropriate amount of polyethylene glycol liquid and drop it on the collagen film, and roll the coating with a drum agitator. Press 1.25×10 5 Add the recipient's own bone marrow-differentiated smooth muscle cells at a concentration of 1 / ml, plant continuously for 2 days, and then simultaneously press 1.25×10 5 Individual / ml concentration planted recipient's own bone marrow differentiated fibroblasts. Planted continuously for 3 days respectively. Next, the recipient's own bone marrow vascular endothelial progenitor cells and vascular endothelial growth factor were...
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