A kind of cik cell cryopreservation liquid and cryopreservation method
A cryopreservation method and cryopreservation solution technology, which is applied to the preservation and application of animal cells, human or animal bodies, etc., can solve the problems of complex cryopreservation procedures, reduced activity, and difficulty in obtaining serum autologous serum, etc., and achieve simplified cryopreservation. storage method, the effect of improving the survival rate
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Embodiment 1
[0066] Example 1: Preparation of logarithmic phase CIK cells
[0067] (1) Separate peripheral blood mononuclear cells from peripheral blood, resuspend in X-VIVO15 serum-free medium, and make the cell concentration of peripheral blood mononuclear cells 1×10 6 cells / mL, add IL-2 at the same time, so that the concentration of IL-2 is 1×10 3 U / mL, static culture for 3 days;
[0068] (2) Add X-VIVO15 serum-free medium to 100 mL in the culture medium prepared in step (1), and add IL-2 at the same time, so that the concentration of IL-2 is 1×10 3 U / mL, static culture for 1 day;
[0069] (3) Add X-VIVO15 serum-free medium to 200-240mL to the culture medium prepared in step (2), and add IL-2 at the same time, so that the concentration of IL-2 is 1×10 3 U / mL, static culture for 3 days; seed CIK cells in the logarithmic growth phase were prepared.
Embodiment 2
[0070] Embodiment 2: the preparation of CIK cell cryopreservation liquid
[0071] (1) Place human autologous plasma in a sterile centrifuge tube and centrifuge at 1800rpm for 6 minutes;
[0072] (2) Absorb the upper layer of plasma, transfer it to a new centrifuge tube, centrifuge at 3000rpm for 20 minutes, and absorb the supernatant, which is the human autologous plasma for cryopreservation;
[0073] (3) Mix dimethyl sulfoxide, the above-mentioned human autologous plasma, and medium X-VIVO15 at a volume ratio of 1:4:5 to obtain CIK cell cryopreservation solution.
Embodiment 3
[0074] Example 3: Cryopreservation of CIK cells
[0075] (1) Take the CIK cells cultured to the 7th day, centrifuge at 1800rpm for 6 minutes, discard the supernatant, add the above CIK cell freezing solution, and adjust the cell concentration to 1*10 8 Each / mL, each / 5mL was added to a 5mL sterile cryopreservation tube. Place the cryovials in a programmed cooling box pre-cooled at 4°C;
[0076] (2) Place the programmed cooling box with the cryopreservation tube in a -80°C refrigerator for 24 hours, and then store the cryopreservation tube in liquid nitrogen for long-term storage.
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