Adipose tissue preserving fluid in vitro and preparation method thereof
A technology of in vitro preservation and adipose tissue, applied in the field of cell engineering, can solve the problem of insufficient contact of preservation solution, and achieve the effect of preventing damage
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Embodiment 1
[0038] An adipose tissue in vitro preservation solution, which contains 1 mL of autologous platelet lysate, 2 g of sodium hyaluronate, 3 mL of human albumin, 1 g of Vc, 0.2 g of trehalose, 12 mL of temperature-sensitive hydrogel, and 0.5 g of penicillin per 100 mL. , Streptomycin 0.3g, Amphotericin B 0.02g, and the rest of the solute medium is a phosphate buffer with a pH of 7.4.
[0039] Among them, the preparation method of the temperature-sensitive hydrogel is: mixing polyacrylamide, methacrylic acid, acrylic acid and chitosan, then adding ammonium persulfate, stirring uniformly, after standing for 15 hours for reaction, washing the reaction product three times to obtain a temperature-sensitive hydrogel Glue; wherein the weight ratio of polyacrylamide, methacrylic acid, acrylic acid, chitosan and ammonium persulfate is 8:1:0.6:0.15:1.
[0040] The preparation method of the preservation solution is:
[0041] Under aseptic conditions, the above-mentioned components are evenly mixed...
Embodiment 2
[0045] An adipose tissue in vitro preservation solution, which contains 0.5 mL of autologous platelet lysate, 1 mL of human albumin, 0.5 g of Vc, 0.3 g of trehalose, 20 mL of temperature-sensitive hydrogel, 0.6 g of penicillin, and streptomycin per 100 mL. 0.5g, 0.05g amphotericin B, and the rest of the solute medium is a phosphate buffer with a pH of 7.6.
[0046] Among them, the preparation method of the temperature-sensitive hydrogel is: mixing polyacrylamide, methacrylic acid, acrylic acid and chitosan, then adding sodium persulfate, stirring uniformly, after standing for 15 hours, and washing the reaction product 3 times to obtain a temperature-sensitive hydrogel Glue; wherein the weight ratio of polyacrylamide, methacrylic acid, acrylic acid, chitosan and sodium persulfate is 10:0.5:0.8:0.2:0.6.
[0047] The preparation method of the preservation solution is:
[0048] Under aseptic conditions, the above-mentioned components are evenly mixed to prepare a fat tissue in vitro pre...
Embodiment 3
[0052] An adipose tissue in vitro preservation solution, which contains 1.5 mL of autologous platelet lysate, 5 g of sodium hyaluronate, 5 mL of human albumin, 0.1 g of trehalose, 10 mL of temperature-sensitive hydrogel, 0.2 g of penicillin, and chain 0.1g amphotericin, 0.01g amphotericin B, and the rest of the solute medium is a phosphate buffer with a pH of 7.2.
[0053] Among them, the preparation method of the temperature-sensitive hydrogel is: mixing polyacrylamide, methacrylic acid, acrylic acid and chitosan, then adding lauroyl peroxide, stirring evenly, after standing for 15 hours, washing the reaction product 3 times to obtain temperature-sensitive water Gel; wherein the weight ratio of polyacrylamide, methacrylic acid, acrylic acid, chitosan and lauroyl peroxide is 6:0.8:1:0.3:1.
[0054] The preparation method of the preservation solution is:
[0055] Under aseptic conditions, the above-mentioned components are evenly mixed to prepare a fat tissue in vitro preservation so...
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