Immune cell preparation for treating chronic atrophic gastritis and gastric precancerous lesions and preparation method and application of immune cell preparation
A technology for atrophic gastritis and gastric precancerous lesions, applied in the field of biomedicine, can solve the problems of inability to achieve mass production and industrial development, inability to facilitate patient treatment, and limited cell sources, and to achieve mass production and production. Industrialization development, remarkable curative effect, and the effect of expanding the source
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Embodiment 1
[0025] This embodiment provides an immune cell preparation for the treatment of chronic atrophic gastritis and gastric precancerous lesions, which is prepared by the following steps: use a blood bag to take the peripheral blood leukocytes of healthy people isolated from a blood bank, and use alcohol with a concentration of 75vt% Wipe the outer wall of the blood bag 2 times. Using Ficoll-hypaque lymphocyte separation medium, mononuclear cells were separated from human peripheral blood leukocytes in blood bags by density gradient centrifugation; in the operation of density gradient centrifugation, the centrifugation speed was controlled at 2000rpm / min, and the centrifugation time was 20min. After the separation, sterile physiological saline was added to the isolated mononuclear cells and washed twice by centrifugation at a speed of 2000 rpm / min for 20 minutes. After centrifugation and washing, add GT-T551 culture medium to the washed mononuclear cells to obtain a basic culture s...
Embodiment 2
[0028] This example provides an immune cell preparation for the treatment of chronic atrophic gastritis and gastric precancerous lesions, which is prepared by the following steps: take whole blood from a healthy person in a blood bag, and wipe the outer wall of the blood bag twice with 72vt% alcohol . Using Ficoll-hypaque lymphocyte separation medium, mononuclear cells were separated from human peripheral blood leukocytes in blood bags by density gradient centrifugation; in the operation of density gradient centrifugation, the centrifugation speed was controlled at 1800rpm / min, and the centrifugation time was 22min. After the separation, sterile physiological saline was added to the isolated mononuclear cells and washed twice by centrifugation at a speed of 1800 rpm / min for 22 minutes. After centrifugation and washing, add GT-T551 culture medium to the washed mononuclear cells to obtain a basic culture system, and control the cell density in the basic culture system to 3.5×10 ...
Embodiment 3
[0030] This embodiment provides an immune cell preparation for the treatment of chronic atrophic gastritis and gastric precancerous lesions, which is prepared by the following steps: use a blood bag to take whole blood from a healthy person in a blood bank and separate red blood cell suspension, plasma, platelets and other components After leaving the remaining peripheral blood leukocytes, wipe the outer wall of the blood bag 3 times with 74vt% alcohol. Using Ficoll-hypaque lymphocyte separation medium, mononuclear cells were separated from human peripheral blood leukocytes in blood bags by density gradient centrifugation; in the operation of density gradient centrifugation, the centrifugation speed was controlled at 2200rpm / min, and the centrifugation time was 18min. After the separation, sterile physiological saline was added to the isolated mononuclear cells and washed by centrifugation for 3 times at a rotational speed of 2200 rpm / min for 18 minutes. After centrifugation a...
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