US2014378290A1PendingUtilityA1

Blood Component Separation Device

Assignee: TERUMO CORPPriority: Mar 27, 2012Filed: Sep 9, 2014Published: Dec 25, 2014
Est. expiryMar 27, 2032(~5.7 yrs left)· nominal 20-yr term from priority
B04B 11/00A61M 1/3696B04B 11/02A61M 2202/0427A61M 1/0209A61M 1/3693A61M 1/0218B04B 5/0442A61M 1/0231A61M 2205/331A61M 2205/42A61M 1/38A61M 1/382
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Claims

Abstract

A blood component separation device includes a centrifuge bowl for separating a blood component from blood, a plasma bag for storing a plasma component, a platelet intermediate bag for storing high-concentration platelet liquid having high-concentration of platelets, and a temporary storage bag (also used as a buffy coat bag) for storing low-concentration platelet liquid having low-concentration of platelets. The blood component separation device performs control, from the second cycle onward, to mix the low-concentration platelet liquid stored in the temporary storage bag in the immediately preceding cycle with whole blood to supply the mixed liquid to the centrifuge bowl. An amount of high-concentration platelet liquid to be collected in the platelet intermediate bag in the first cycle is set to be smallest among all cycles, and an amount of high-concentration platelet liquid to be collected in a last cycle is set to be greatest among all the cycles.

Claims

exact text as granted — not AI-modified
1 . A blood component separation device comprising:
 a centrifugal separator configured to separate a predetermined blood component from blood; and   a container for containing the predetermined blood component centrifugally separated,   wherein the blood component separation device is configured to perform   (a) centrifugal separation step for introducing whole blood drawn from a donor into the centrifugal separator to separate whole blood into a plurality of blood components,   (b) circulation flow step for introducing a predetermined first blood component, among centrifugally separated blood components, separated by the centrifugal separation into the centrifugal separator together with whole blood,   (c) circulation/acceleration step, performed after a predetermined amount of the first blood component is separated in the circulation flow step, in which supply of whole blood to the centrifugal separator is stopped to introduce only the first blood component into the centrifugal separator to further circulate the first blood component for a predetermined period of time, and a circulation speed is then increased so that a second blood component is separated by the centrifugal separator and collected, and   (d) blood returning step for returning blood components remaining after collecting a predetermined amount of the second blood component in the circulation/acceleration step to the donor,   wherein the circulation/acceleration step includes a first collecting step for transferring a portion of the second blood component with low-concentration to a temporary storage container and   a second collecting step for collecting a portion of the second blood component with high-concentration,   wherein the second blood component with low-concentration transferred to the temporary storage container is introduced into the centrifugal separator together with whole blood drawn in a following cycle, where the steps (a) to (d) constitute one cycle, and   wherein, as for the second collecting step, an amount of the second blood component with high-concentration to be collected in a first cycle is set to be smallest among all cycles, and an amount of the second blood component with high-concentration to be collected in a last cycle is set to be greatest among all the cycles.   
     
     
         2 . The blood component separation device according to  claim 1 ,
 wherein an amount of the second blood component with high-concentration to be collected in the second collecting step in each cycle is varied.   
     
     
         3 . The blood component separation device according to  claim 2 ,
 wherein an amount of the second blood component with high-concentration to be collected in the second collecting step in each cycle is varied so as the amount to be collected shall not be smaller than an amount of the second blood component with high-concentration to be collected in a preceding cycle.

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