Methods for rejuvenating red blood cells
US-2015290247-A1 · Oct 15, 2015 · US
US2025161542A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025161542-A1 |
| Application number | US-202418955258-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 21, 2024 |
| Priority date | Nov 22, 2023 |
| Publication date | May 22, 2025 |
| Grant date | — |
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Blood processing systems, devices, and methods including a durable hardware component, a single use fluid flow circuit, and a controller configured to estimate the concentration of platelets in a donor's circulating blood.
Opening claim text (preview).
1 . A system for collecting platelets comprising: a reusable hardware unit, wherein the reusable hardware unit comprises a separator; a disposable fluid circuit configured to be associated with the reusable hardware unit; and a controller configured to estimate a platelet concentration of a donor's circulating blood (C donor ). 2 . The system of claim 1 , wherein C donor is based on a concentration of platelets in collected whole blood entering the separator (C wbcent ) and a percentage of collected whole blood in a separator inlet line (WB %). 3 . The system of claim 2 , wherein C donor is obtained by determining a product of the concentration of platelets in collected whole blood entering the separator (C wbcent ) and the percentage of collected whole blood in a separator inlet line (WB %), such that: C d o n o r = C wbcent W B % . 4 . The system of claim 2 , wherein the WB % is obtained by dividing an amount of collected whole blood in the separator inlet line with a total amount of collected whole blood and other fluid in the separator inlet line. 5 . (canceled) 6 . The system of claim 4 , wherein the WB % is obtained by dividing parts of collected whole blood with a sum of the parts of collected whole blood (Parts WB) and parts of anticoagulant, such that: W B % = Parts W B / ( Parts W B + Parts Anticoagulant ) . 7 . The system of claim 2 , wherein C wbcent is based on a platelet concentration of separated platelet rich plasma (C prp ) and a hematocrit of collected whole blood entering the separator (H wbcent ). 8 . (canceled) 9 . The system of claim 7 , wherein C wbcent is determined by an equation: C wbcent = C prp * ( 1 - H w b c e n t ) . 10 . The system of claim 7 , wherein H wbcent is based on a flow rate of separated packed red blood cells exiting the separator (Q rbc ), a flow rate of collected whole blood flowing into the separator (Q wbcent ), and a hematocrit of the separated packed red blood cells exiting the separator (H rbc ). 11 . The system of claim 10 , wherein H wbcent is determined by dividing a product of H rbc and Q rbc with Q wbcent , such that: H wbcent = ( H rbc * Q rbc ) / Q wbcent . 12 . The system of claim 10 , wherein Q rbc is based on the flow rate of collected whole blood flowing into the separator (Q wbcent ) and a flow rate of separated platelet rich plasma flowing out of the separator (Q prp ), wherein Q rbc is determined by subtracting Q prp from Q wbcent such that: Q rbc =Q wbcent −Q prp . 13 . The system of claim 12 , wherein Q wbcent is based on a pump rate of a separator pump and Q prp is based on a pump rate of a platelet rich plasma pump. 14 . (canceled) 15 . (canceled) 16 . The system of claim 10 , wherein H rbc is a predetermined value. 17 . The system of claim 10 , wherein H rbc is determined by an optical sensor or based on separator flow rates and separator q-force. 18 . (canceled) 19 . The system of claim 11 , wherein the controller is configured to determine C wbcent , WB %, C prp , H wbcent , H rbc , and Q rbc . 20 . The system of claim 2 , wherein the controller is configured to estimate the platelet concentration of a donor's circulating blood (C donor ) with an equation: C donor = ( C prp * W B % ) * ( 1 - ( H
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