Blocking support frame and preparation method thereof
A technology of metal stents and bacteria strains, which is applied in the fields of medical formula, medical science, surgery, etc., and can solve the problems of expensive products
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[0033] Aiming at the characteristics of the barrier stent in the prior art, the present application provides a preparation method of the barrier stent. The barrier stent is essentially a barrier stent based on bacterial fermentation to produce a bacterial cellulose film and filled with a metal stent. The barrier stent has good Its barrier function can block bacteria and cells while permeating growth factors, and has good biocompatibility. It is an ideal clinical barrier scaffold. Specifically, the preparation method of the barrier stent of the present invention comprises the following steps:
[0034] A) microbial strains are inoculated onto a solid substrate, and a solid substrate having a bacterial cellulose film on the surface is obtained after fermentation; the microbial strains are bacterial strains that can produce bacterial cellulose;
[0035] B) placing the solid substrate obtained in step A) in an aerosol containing nutrient solution, and fermenting;
[0036] C) placi...
Embodiment 1
[0050] Prepare 500mL aqueous solution containing 10wt% glucose, 1wt% yeast powder, 2wt% calcium carbonate, and 1.5wt% agar, stir to dissolve and boil, divide into five 250mL beakers, seal the beakers with tissue culture film, and autoclave Sterilize the pot, cool and stand to obtain a solid substrate; prepare an aqueous solution containing 5wt% glucose and 1wt% yeast powder as a nutrient solution; prepare a metal titanium mesh and sterilize it for use;
[0051] Inoculate the strain of Gluconacetobacter xylinum on the above solid substrate, put it into a constant temperature incubator, and cultivate it at 28°C for 24h;
[0052] The solid substrate obtained above is transferred from the constant temperature incubator to the aerosol spray formed by the nutrient solution, and the spray speed of the nutrient solution is adjusted to 2mL / hour;
[0053] After the above-mentioned process was fermented for 2 days, a sterilized titanium mesh was placed on the surface of the formed bacter...
Embodiment 2
[0058] Prepare 500mL aqueous solution containing 10wt% glucose, 1wt% yeast powder, 2wt% calcium carbonate, and 1.5wt% agar, stir to dissolve and boil, sterilize in an autoclave, pour into a square shallow dish with a side length of 40cm, cool and stand Obtain a solid substrate; prepare an aqueous solution containing 5wt% glucose and 1wt% yeast powder as a nutrient solution; prepare a 3 mg / mL nano-hydroxyapatite solution with sterile water; prepare a metal titanium mesh and sterilize it for use;
[0059] Inoculate the strain of Gluconacetobacter xylinum on the above solid substrate, put it into a constant temperature incubator, and cultivate it at 28°C for 24h;
[0060] The solid substrate obtained above is transferred from the constant temperature incubator to the aerosol spray formed by the nutrient solution and the nano-hydroxyapatite solution, and the spray speed of the two solutions is adjusted to 2mL / hour;
[0061] After the above-mentioned process was fermented for 3 day...
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