Tissue engineering artificial ligament and preparing method thereof
An artificial ligament and tissue engineering technology, applied in tissue regeneration, medical science, prosthesis, etc., can solve the problem of difficult penetration of seed cells, achieve the effect of rapid recovery of activity and avoid rejection
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Embodiment 1
[0026] Example 1: Poly(lactide-caprolactone) was dissolved in a mixed solution of tetrahydrofuran and N,N-dimethylformamide to make a 0.15 g / mL polymer solution, and the solution was filled in an electrospinning The feeding port on one side of the wire equipment. Disperse the fibroblasts in the uniformly dissolved sodium alginate gel solution, fill the gel solution containing the seed cells into the feed port on the other side of the electrospinning equipment, and adjust the feed ports on both sides of the electrospinning device respectively. Propelling speed, so that the gel solution containing seed cells is in the form of a spray, evenly spread on each layer of fibers, when the thickness of the film prepared by electrospinning accumulates to about 5mm, remove it, and cut it into strips in a sterile state , the scaffold can be placed in the culture medium and cultured for 3-7 days before use as needed.
Embodiment 2
[0027] Example 2: Poly(L-lactide) was dissolved in a mixed solution of tetrahydrofuran and N,N-dimethylformamide to make a 0.05g / mL polymer solution, and the solution was filled in an electrospinning device feed port on one side. The fibroblasts were dispersed in a uniformly dissolved sodium alginate solution, and the sodium alginate gel solution containing the seed cells was added dropwise to the rapidly stirring calcium chloride solution to prepare gel microspheres containing the seed cells, which were electrospun During the preparation of tissue engineering scaffolds from silk, microspheres containing seed cells were sprayed on the scaffolds, and when the thickness of the membrane scaffolds prepared by electrospinning reached about 7mm, the membranes were removed, cut into strips under sterile conditions, and used Before that, the scaffold can be placed in cell culture medium and cultivated for 3-7 days.
Embodiment 3
[0028] Example 3: Poly(L-lactide) was dissolved in a mixed solution of tetrahydrofuran and N,N-dimethylformamide to make a 0.3g / mL polymer solution, and the solution was filled in an electrospinning device feed port on one side. Disperse the tenocytes and fibroblasts in the uniformly dissolved extracellular matrix solution, fill the gel solution containing the seed cells in the inlet of the other side of the electrospinning equipment, and adjust the inlets on both sides of the electrospinning respectively The propulsion speed is so that the gel solution containing the seed cells is sprayed and evenly spread on each layer of fibers. When the thickness of the membrane prepared by electrospinning is about 5mm, it is removed and cut into strips under sterile conditions. If necessary, the scaffold can be placed in the culture medium and cultured for 3-7 days before use.
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