Pheresis apparatus

• US 4,416,654 A
• Filed: 09/03/1981
• Issued: 11/22/1983
• Est. Priority Date: 09/03/1981
• Status: Expired due to Term

• Current Assignee: Haemonetics Corporation
• Original Assignee: Haemonetics Corporation
• Inventors: Schoendorfer, Donald W., Hansen, Lee E.
• Primary Examiner(s): Jenkins, Robert W.
• Application Number:
  US06/299,194
• Time in Patent Office: 810 Days
• Field of Search: 494/1, 494/10, 494/35, 494/36, 494/23, 494/27, 494/29, 494/37, 604/4, 604/5, 604/6, 604/29
• US Class Current: 494/10
• CPC Class Codes: A61M 1/303 having a reservoir for treated blood to be returned
• 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: B04B 5/0442 with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation

Abstract

This invention relates to an improvement in two-port centrifuge bowls in which component yield is enhanced by utilizing the centrifuge bowl for eluttriation, as well as centrifugation. In a particular embodiment, platelet yield is improved by terminating flow of anticoagulated whole blood from the donor to the bowl and pumping low density fluid, preferably plasma, back into the bowl at a relatively high rate to elutriate centrifugally separated cells in the bowl.

Claims

1. Apparatus comprising:

(a) a centrifuge;

(b) an enclosed fractionation volume on said centrifuge;

(c) an inlet and outlet port mounted on said centrifuge, the ports being in fluid communication with said fractionation volume;

(d) receptacle means outside said centrifuge for collecting a first fractionated whole blood component from said outlet port;

(e) pump means for (i) first causing whole blood to flow into said inlet port at a predetermined rate and (ii) secondly for causing a first fractionated component of whole blood to be recirculated to the inlet port of said centrifuge to elutriate the remaining contents in the fractionation volume.

2. The apparatus of claim 1 in which the first fractionated component is plasma.

3. The apparatus of claim 1 in which the pump means is initially deenergized just prior to the point in time when substantial quantity of a blood component being harvested has exited the outlet port and thereafter the pump means is energized to cause said first fractionated component to be recirculated.

4. The apparatus of claim 3 in which the pump means is thereafter deenergized when the majority of the blood component being harvested has exited the outlet port.

5. The apparatus of claim 4 in which opto-electronic means are utilized to determine when the majority of blood component being harvested has exited the outlet port.

6. The apparatus of claim 5 in which the pump means operates at a faster flow rate during elutriation then the rate used when whole blood is caused to flow into the inlet port.

7. The apparatus of claim 5 in which the opto-electronic means responds to light scattering from blood component.

8. The apparatus of claim 1 in which fluid flow during elutriation is substantially parallel to fluid flow during centrifugation.

9. The apparatus of claim 1 in which the centrifuge is a fixed volume bowl and the flow rate during elutriation is substantially greater than during collection.

10. Apparatus for fractionating whole blood into components thereof comprising:

(a) a centrifuge;

(b) an enclosed fractionation volume on said centrifuge;

(c) an inlet and outlet port mounted on said centrifuge, the ports being in fluid communication with said fractionation volume;

(d) first pump means for causing whole blood to flow into said inlet port at a predetermined rate;

(e) receptacle means outside said centrifuge for collecting fractionated whole blood component from said outlet port;

(f) second pump means for causing a first fractionated component of said whole blood to be recirculated to the inlet port of said centrifuge to elutriate the remaining contents in the fractionation volume, thereby achieving enhanced separation of component within said centrifuge.

11. The apparatus of claim 10 in which the recirculated component is substantially cell free plasma.

12. The apparatus of claim 10 in which the first pump means is deenergized just prior to the point in time when the platelets, separated from the whole blood, exit the outlet port and the second pump means is energized thereafter.

13. The apparatus of claim 12 in which the second pump is deenergized when the majority of platelets have exited the outlet port, and opto-electronic means are utilized to determine when the majority of platelets have exited.

14. The apparatus of claim 13 in which the opto-electronic means provides an electrical signal proportional to the opacity of material.

15. The apparatus of claim 10 in which the flow rate of the second pump means is at least twice the rate of the first pump means during collection.

16. The method of increasing component yield from donated whole blood in a two-port centrifugation bowl wherein:

(i) lower density component is separated in the bowl from higher density component in the bowl and the lower density component is displaced to a separate container; and

(ii) the lower density component is returned to the bowl to elutriate the higher density components remaining in the bowl; and

(iii) component with density between lower density component and higher density component is displaced out of the bowl and harvested.

17. The method of claim 16 wherein the components remaining in the bowl after (iii) are reinfused.

18. The method of claim 16 wherein the component is returned in (ii) at a higher flow rate than the rate at which whole blood was pumped into the bowl.