Pretreating liquid and freeze protecting liquid for cryopreservation of erythrocyte and their application
A technology of cryoprotective liquid and pretreatment liquid, which is applied in the fields of red blood cell pretreatment liquid, red blood cell cryopreservation, and red blood cell cryoprotective liquid.
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[0034] Take 50 ml of venous blood from healthy volunteers, add heparin for anticoagulation, and centrifuge to remove white blood cells and platelets. Mix the washed concentrated erythrocytes with 150 ml of pretreatment solution consisting of basic buffer and small molecule sugar, incubate in a water bath at 4-40°C for 1-4 hours, centrifuge to remove the supernatant, and then transfer to a solution containing 10wt%-40wt After 75 milliliters of the cryoprotectant solution of the macromolecule protective component, store it at -80°C or -196°C for 1 week (or directly add the macromolecule protective component to the pretreated erythrocyte suspension and freeze it). When thawing the cells, the samples were taken out, quickly thawed in a 40°C water bath, and the hemolysis rate of red blood cells and other indicators were measured.
[0035] The pretreatment and cryoprotection process are shown in Table 1.
[0036] Table 1
[0037] Example
Basic buffer
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