Injection for treating cancer and its preparation method
A technology for injections and tumors, applied in the field of medicine, can solve the problems of cumbersome preparation, difficult quality control, and inability to industrialize production, and achieve the effect of simple treatment method, simple preparation process, and good patient tolerance
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example 1
[0057] 1, the preparation of injection of the present invention:
[0058] (1) Take type A blood from a healthy person, add 4 times the concentration of 0.01mol / L PBS, centrifuge at 3000r / min for 20 minutes, discard the supernatant, white blood cell layer and platelet layer, and wash with pre-cooled PBS equivalent to 4 times the volume of red blood cells 4 times, centrifuge at 5000r / min for 15min at 4°C each time to separate red blood cells and supernatant;
[0059] (2) Take the obtained red blood cells and add 45 times the volume of pre-cooled 0.01mol / L Tril-HCl, mix, and place at 4°C for 2 hours; then centrifuge at 9000r / min for 20min, and discard the supernatant;
[0060] (3) Repeat step (2) until there are no red blood cells visible to the naked eye to obtain a precipitate;
[0061] (4) Take the precipitate obtained in step (3) and dilute it with 0.01mol / L PBS, measure the content of erythrocyte membrane protein by Lowry's method, adjust the concentration to 20mg / ml, subpa...
example 2
[0063] (1) Take blood type B from a healthy person, add 5 times the concentration of PBS at 0.01mol / L, centrifuge at 3000r / min for 20min, discard the supernatant, white blood cell layer and platelet layer, and wash with pre-cooled PBS equivalent to 5 times the volume of red blood cells 3 times, centrifuge at 5000r / min for 15min at 4°C each time to separate red blood cells and supernatant;
[0064] (2) Take the obtained red blood cells and add 50 times the volume of pre-cooled 0.01mon / L Tril-HCl, mix, and place at 4°C for 2h; then centrifuge at 9000r / min for 20min, and discard the supernatant;
[0065] (3) Repeat step (2) until there are no red blood cells visible to the naked eye to obtain a precipitate;
[0066] (4) Take the precipitate obtained in step (3) and dilute it with 0.01mol / L PBS, measure the content of erythrocyte membrane protein by Lowry's method, adjust the concentration to 30mg / ml, subpackage, and store at -20°C.
example 3
[0068] (1) Take AB blood from a healthy person, add 3 times the concentration of 0.01mol / L PBS, centrifuge at 3000r / min for 20min, discard the supernatant, white blood cell layer and platelet layer, and wash with pre-cooled PBS equivalent to 3 times the volume of red blood cells 3 times, centrifuge at 5000r / min for 15min at 4°C each time to separate red blood cells and supernatant;
[0069] (2) Take the obtained red blood cells and add 40 times the volume of pre-cooled 0.01mol / L Tril-HCl, mix, and place at 4°C for 2 hours; then centrifuge at 9000r / min for 20min, and discard the supernatant;
[0070] (3) Repeat step (2) until there are no red blood cells visible to the naked eye to obtain a precipitate;
[0071] (4) Take the precipitate obtained in step (3) and dilute it with 0.01mol / L PBS, measure the content of erythrocyte membrane protein by Lowry's method, adjust the concentration to 10mg / ml, subpackage, and store at -20°C.
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