US2018243342A1PendingUtilityA1
Methods for producing and using rejuvenated red blood cells
Est. expirySep 6, 2032(~6.1 yrs left)· nominal 20-yr term from priority
Inventors:Alan Gray
A61K 2035/124A61K 35/18A01N 1/00A01N 1/0226A61K 31/19A61K 31/70C12N 5/0641C12N 2501/999A01N 1/126
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Claims
Abstract
Methods for treating blood. The methods comprise obtaining whole blood from a donor, mixing the whole blood with a red blood cell enhancement composition, and incubating the mixture of whole blood and red blood cell enhancement composition. The method can be performed at a time proximate to the time of obtaining blood from the donor, or after the blood has been stored for a period of time. The method rejuvenates red blood cells.
Claims
exact text as granted — not AI-modified1 .- 27 . (canceled)
28 . A method of processing a blood component, the method comprising:
adding a red blood cell (RBC) enhancement composition comprising inosine, adenine, pyruvate, a phosphate mixture, or a combination thereof, to a blood component comprising RBCs; incubating the blood component and the RBC enhancement composition for a period between about 30 minutes and 90 minutes to form a treated RBC composition; and measuring the pO 2 at 50% oxygen saturation (p50) of the treated RBC composition during the period.
29 . The method of claim 28 , wherein the RBC enhancement composition comprises about 25 g/L to about 30 g/L inosine, about 0.2 g/L to about 2 g/L adenine, about 5 g/L to about 15 g/L pyruvate, and about 17 g/L to about 23 g/L sodium phosphate, or a combination thereof.
30 . The method of claim 28 , wherein the RBC enhancement composition comprises about 27 g/L inosine, about 11 g/L pyruvate, about 0.7 g/L adenine, and about 21 g/L sodium phosphate.
31 . The method of claim 30 , wherein the sodium phosphate comprises about 6.2 g/L sodium phosphate, monobasic, monohydrate; and about 14.6 g/L sodium phosphate, dibasic, heptahydrate.
32 . The method of claim 28 , wherein the incubating is at a temperature between 1° C. and about 45° C.
33 . The method of claim 28 , wherein the incubating is not in a water bath.
34 . The method of claim 28 , wherein the blood component and the RBC enhancement composition are mixed during the period.
35 . The method of claim 28 , wherein the p50 of the treated RBC composition is greater than or equal to the p50 of fresh blood.
36 . A method of transfusing a blood component, the method comprising:
adding a red blood cell (RBC) enhancement composition comprising inosine, adenine, pyruvate, a phosphate mixture, or a combination thereof, to a blood component comprising RBCs; incubating the blood component and the RBC enhancement composition for a period between about 30 minutes and 90 minutes to form a treated RBC composition; measuring the pO 2 at 50% oxygen saturation (p50) of the treated RBC composition during the period; and administering the treated RBC composition to a subject if the p50 of the treated RBC composition is at least equal to the p50 of fresh blood.
37 . The method of claim 36 , further comprising testing the p50 of the blood component for before adding the RBC enhancement composition.
38 . The method of claim 36 , wherein the blood component is autologous to the subject.
39 . The method of claim 36 , the blood component is leukoreduced.
40 . The method of claim 36 , wherein the RBC enhancement composition comprises about 25 g/L to about 30 g/L inosine, about 0.2 g/L to about 2 g/L adenine, about 5 g/L to about 15 g/L pyruvate, and about 17 g/L to about 23 g/L sodium phosphate, or a combination thereof.
41 . The method of claim 36 , wherein the RBC enhancement composition comprises about 27 g/L inosine, about 11 g/L pyruvate, about 0.7 g/L adenine, and about 21 g/L sodium phosphate.
42 . The method of claim 41 , wherein the sodium phosphate comprises about 6.2 g/L sodium phosphate, monobasic, monohydrate; and about 14.6 g/L sodium phosphate, dibasic, heptahydrate.
43 . The method of claim 36 , wherein the incubating is at a temperature between 1° C. and about 45° C.
44 . The method of claim 36 , wherein the incubating is not in a water bath.
45 . The method of claim 36 , wherein the blood component and the RBC enhancement composition are mixed during the period.
46 . The method of claim 36 , wherein the p50 of the treated RBC composition is greater than the p50 of fresh blood.
47 . The method of claim 36 , wherein the treated RBC composition is stored at a temperature between −80° C. and about 6° C. before administering to the subject.Join the waitlist — get patent alerts
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