Apheresis apparatus and method

• US 5,494,592 A
• Filed: 01/13/1995
• Issued: 02/27/1996
• Est. Priority Date: 04/27/1993
• Status: Expired due to Term

• Current Assignee: Haemonetics Corporation
• Original Assignee: Haemonetics Corporation
• Inventors: Knapp, Tracey E., Jorgensen, Glen E., Plante, Joseph R., Sibinga, Theodoor H. S., Latham, Allen Jr.
• Primary Examiner(s): KIM, SUN U
• Application Number:
  US08/372,890
• Time in Patent Office: 410 Days
• Field of Search: 210/782, 210/789, 210/805, 604/4, 604/5, 604/6, 494/37
• US Class Current: 210/805
• CPC Class Codes: A61M 1/30 Single needle dialysis ; Reciprocating systems, alternately withdrawing blood from and returning it to the patient, e.g. single-lumen-needle dialysis or single needle systems for hemofiltration or pheresis
• CPC Class Codes: A61M 1/304 Treatment chamber used as reservoir, e.g. centrifuge bowl or filter with movable membrane
• CPC Class Codes: A61M 1/3603 in the same direction
• CPC Class Codes: A61M 1/3693 using separation based on different densities of components, e.g. centrifuging
• CPC Class Codes: A61M 1/3696 with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
• CPC Class Codes: A61M 2205/331 used as turbidity change detectors, e.g. for priming-blood or plasma-hemoglubine-interface detection
• CPC Class Codes: B04B 2005/0464 with hollow or massive core in centrifuge bowl
• CPC Class Codes: B04B 2005/0471 with additional elutriation separation of different particles

Abstract

An apheresis apparatus and method is disclosed for increasing the purity and yield of platelets separated from donated whole blood in a centrifuge. The whole blood in the centrifuge is diluted by recirculating fluid, such as plasma or saline, at a first flow rate, to mix with further withdrawn whole blood prior to entering the centrifuge. As plasma is collected, it is recirculated through the centrifuge at a second flow rate to further improve the separation between the intermediate density components, i.e., platelets and white blood cells in the "buffy coat." The plasma is then recirculated through the centrifuge at a third flow rate and platelets are displaced out of the centrifuge while the plasma is recirculating through the centrifuge at the third flow rate.

Claims

1. A method of increasing intermediate density blood component yield from donated whole blood in a centrifugation fractionation volume, the intermediate density component consisting primarily of at least one of a platelet constituent and a white blood cell constituent, the method comprising the steps of:

(i) diluting whole blood, by mixing fluid with the whole blood at a first flow rate as the blood is introduced into the volume;

(ii) separating lower density component in the volume from higher density components in the volume including said intermediate density component, and displacing said lower density component to a first container;

(iii) recirculating the lower density component to the volume at a second, substantially constant flow rate to further dilute the components remaining in the volume and widen the region occupied by said intermediate density component without causing said intermediate density component to exit the fractionation volume;

(iv) recirculating the lower density component through the volume at a third, accelerating flow rate; and

(v) displacing said intermediate density component from the volume while the lower density component is recirculating through the volume at the third flow rate.

2. The method of claim 1 wherein the components remaining in the bowl after (v) are reinfused.

3. The method of claim 1 wherein the second flow rate is greater than the first flow rate.

4. The method of claim 1 wherein the third flow rate is greater than the second flow rate.

5. The method of claim 1 further comprising collecting the intermediate density component in a second container.

6. The method of claim 5 further comprising anticoagulating the whole blood with anticoagulant stored in a third container.

7. The method of claim 6 wherein said intermediate density component consists primarily of platelets and wherein the method further comprises displacing white blood cells from the volume and collecting the white blood cells in a fourth container.

8. The method of claim 1 in which said intermediate density component consists primarily of platelets.

9. The method of claim 1 wherein said intermediate density component consists primarily of white blood cells.

10. The method of claim 1 wherein said intermediate density component consists primarily of platelets and white blood cells.

11. A method of increasing intermediate density component yield from donated whole blood in a centrifuge having an enclosed fractionation volume, the intermediate density component consisting primarily of at least one of a platelet constituent and a white blood cell constituent, the method comprising:

(i) pumping whole blood into the volume along a first flow route;

(ii) separating lower density component in the volume from higher density components in the volume including said intermediate density component, and displacing the lower density component to a first container;

(iii) closing the first flow route and opening a second flow route, and returning the lower density component to the volume at a first, substantially constant flow rate to widen the region occupied by said intermediate density component without causing said intermediate density component to exit the fractionation volume;

(iv) recirculating the lower density component through the volume at a second, accelerating flow rate; and

(v) displacing said intermediate density component from the volume while the lower density component is recirculating though the volume at the second flow rate.

12. The method of claim 11 wherein the components remaining in the bowl after (v) are reinfused.

13. The method of claim 11 wherein the second flow rate is greater than the first flow rate over an entire range of acceleration of the second flow rate.

14. The method of claim 11 further comprising collecting the intermediate density component in a second container.

15. The method of claim 14 further comprising anticoagulating the whole blood with anticoagulant stored in a third container.

16. The method of claim 15 wherein the intermediate density component comprises primarily platelets and the method further comprises displacing white blood cells from the volume and collecting the white blood cells in a fourth container.

17. The method of claim 11 in which said intermediate density component consists primarily of platelets.

18. The method of claim 11 wherein the lower density component initially returns to the volume at a flow rate which exceeds the first flow rate before slowing to the first flow rate.

19. The method of claim 11 wherein said intermediate density component consists primarily of white blood cells.

20. The method of claim 11 wherein said intermediate density component consists primarily of platelets and white blood cells.

21. A method of increasing component yield from donated whole blood in a centrifuge having an enclosed fractionation volume, the method comprising:

(i) pumping into the volume anticoagulated whole blood having components of varying density including an intermediate density component which consists primarily of at least one of a platelet constituent and a white blood cell constituent;

(ii) separating lower density component in the volume from higher density components including said intermediate density component in the volume and displacing the lower density component to a first container;

(iii) returning the lower density component to the volume at a first, substantially constant flow rate to dilute components remaining in the volume and widen the region occupied by said intermediate density component without causing said intermediate density component to exit the fractionation volume;

(iv) recirculating the lower density component through the volume at a second, accelerating flow rate; and

(v) displacing said intermediate density component from the volume while the lower density component is recirculating through the volume at the second flow rate.

22. The method of claim 21 wherein the components remaining in the bowl after (v) are reinfused.

23. The method of claim 21 further comprising collecting said intermediate density component in a second container.

24. The method of claim 23 further comprising anticoagulating the whole blood with anticoagulant stored in a third container.

25. The method of claim 24 wherein said intermediate density component consists primarily of platelets and the method further comprises displacing white blood cells from the volume and collecting the white blood cells in a fourth container.

26. The method of claim 24 wherein said intermediate density component consists primarily of platelets.

27. The method of claim 24 wherein the lower density component initially returns to the volume at a flow rate which exceeds the first flow rate before slowing to the first flow rate.

28. The method of claim 24 wherein the whole blood is diluted with lower density component recirculating at a low flow rate before reaching the volume, the low rate being less than the first flow rate.

29. The method of claim 21 wherein said intermediate density component consists primarily of white blood cells.

30. The method of claim 21 wherein said intermediate density component consists primarily of platelets and white blood cells. hite blood cells.