Use of nitric oxide gas in an extracorporeal circuitry to treat blood plasma

• US 7,531,133 B2
• Filed: 06/01/2006
• Issued: 05/12/2009
• Est. Priority Date: 09/10/2002
• Status: Active Grant

• Current Assignee: Advanced Inhalation Therapies (AIT) Ltd
• Original Assignee: Pulmonox Technologies Corp.
• Inventors: Hole, Douglas, Miller, Christopher C.
• Primary Examiner(s): Deak; Leslie R
• Application Number:
  US11/445,965
• Publication Number:
  US 20070014688A1
• Time in Patent Office: 1,076 Days
• Field of Search: 604/4.01, 604/5.01, 604/5.02, 604/5.04, 604/6.09, 604/6.11, 604/6.13, 604/6.14, 604/6.08, 604/23, 604/25, 424/140.1, 424/158.1, 424/134.1, 422 44- 46, 422/48, 210/645
• US Class Current: 422/44
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 33/00 Medicinal preparations containing inorganic active ingredients
• CPC Class Codes: A61M 1/1698 Blood oxygenators with or without heat-exchangers intracorporal A61M1/1678; manufacturing of membranes therefor B01D67/00; semi-permeable membranes for separation processes characterised by their properties B01D69/00; semi-permeable membranes characterised by their material B01D71/00
• CPC Class Codes: A61M 1/3472 with treatment of the filtrate
• CPC Class Codes: A61M 1/3486 Biological, chemical treatment, e.g. chemical precipitation; treatment by absorbents
• CPC Class Codes: A61M 1/3496 Plasmapheresis; Leucopheresis; Lymphopheresis A61M1/3472 takes precedence
• CPC Class Codes: A61M 1/3687 Chemical treatment A61M1/3675 takes precedence
• CPC Class Codes: A61M 2202/0275 Nitric oxide [NO]
• CPC Class Codes: A61M 2202/0456 Lipoprotein

Abstract

A method of reducing pathogens in blood by exposure to a nitric oxide containing gas in an extracorporeal circuitry is provided. The method includes: obtaining blood from a mammal or a blood source, separating the blood into plasma and blood cells, exposing the plasma to nitric oxide containing gas, combining the exposed plasma with the blood cells, reducing nitric oxide content in the recombined blood, and returning the blood to the mammal or blood source.

Claims

1. A method of reducing pathogens in blood, the method comprising:

obtaining blood from a mammal or a blood source;

separating the blood into plasma and blood cells;

exposing the plasma to nitric oxide containing gas;

combining the exposed plasma with the blood cells;

reducing nitric oxide gas content in the recombined blood by contacting the recombined blood with a gaseous source having a nitric oxide content that is less than the recombined blood; and

returning the recombined blood to the mammal or blood source.

2. The method of claim 1, wherein the gaseous source is ambient air.

3. The method of claim 1, further comprising exposing the blood to oxygen, wherein the exposing to oxygen step occurs before the separation step or after the recombining step.

4. The method of claim 1, wherein the separating is through one or more of a filter, a centrifuge, or dialysis.

5. The method of claim 1, wherein the plasma is exposed to a concentration of nitric oxide over a period of time sufficient to reduce pathogen concentration in the blood.

6. The method of claim 1, wherein the pathogens are selected from viruses, bacteria, mycobateria, parasites, and fungi.

7. The method of claim 1, wherein the nitric oxide containing gas is controllably introduced in relation to an amount of plasma separated from the blood.

8. The method of claim 1, wherein the exposing step comprises:

providing a semipermeable membrane selectively permeable to nitric oxide gas and impermeable to nitrogen gas adapted to allow contact of an outside of the membrane with the plasma; and

delivering nitric oxide containing gas to an inside of the membrane under pressure sufficient to drive the nitric oxide across the membrane for contact with the plasma on the outside of the membrane within a desired concentration range sufficient to reduce pathogen concentration in the plasma.

9. The method of claim 1, wherein the concentration of nitric oxide in the nitric oxide containing gas is about 120 ppm to about 400 ppm.

10. The method of claim 9, wherein the concentration is about 160 ppm to about 220 ppm.

11. The method of claim 1, wherein the concentration of nitric oxide in the nitric oxide containing gas is less than about 120 ppm and more than 0.

12. The method of claim 1, wherein before the combining the exposed plasma with the blood cells step, the exposed plasma is treated by a bacterial particulate filter to reduce levels of lipopolysaccharide (LPS) in the plasma.

13. An extracorporeal blood circuit comprising:

an inlet line adapted to obtain blood from a mammal or a blood source;

an outlet line adapted to return blood to the mammal or blood source;

a fluid circuit for fluid communication between the inlet and the outlet line, wherein the fluid circuit comprises;

at least one pump acting on the fluid circuit to circulate the blood therethrough;

a separation unit in fluid communication with the inlet line, wherein the separation unit is adapted to separate the blood received from the mammal or source into plasma and blood cells;

a nitric oxide unit that exposes the plasma with a nitric oxide containing gas;

a mixer for combining the exposed plasma with the blood cells; and

a reduction unit for reducing the nitric oxide content in the recombined blood, wherein the reduction unit is in fluid communication with the outlet line and contacts the recombined blood with a gaseous source having a nitric oxide content that is less than the recombined blood.

14. The extracorporeal blood circuit of claim 13, further comprising one or more of a reservoir to collect the blood from the mammal or source, an oxygenator, a dialysis component, an organ perfusion component, a heat exchange component, and an oxygenation component.

15. The extracorporeal blood circuit of claim 13, wherein the gaseous source is ambient air.

16. The extracorporeal blood circuit of claim 13, wherein the separation unit comprises one or more of a filter, a centrifuge, and dialysis.

17. The extracorporeal blood circuit of claim 13, wherein the nitric oxide unit comprises:

a semipermeable membrane selectively permeable to nitric oxide gas and impermeable to nitrogen gas adapted to allow contact of an outside of the membrane with the plasma; and

nitric oxide containing gas deliverable to an inside of the membrane under pressure sufficient to drive the nitric oxide across the membrane for contact with the plasma on the outside of the membrane within a desired concentration range sufficient to reduce pathogen concentration in the plasma.

18. The extracorporeal blood circuit of claim 13, wherein the concentration of nitric oxide in the nitric oxide containing gas is about 120 ppm to about 400 ppm.

19. The extracorporeal blood circuit of claim 18, wherein the concentration is about 160 ppm to about 220 ppm.

20. The extracorporeal blood circuit of claim 13, wherein the concentration of nitric oxide in the nitric oxide containing gas is less than about 120 ppm and more than 0.

21. The extracorporeal blood circuit of claim 13, further comprising a bacterial particulate filter to reduce levels of lipopolysaccharide (LPS) in the plasma.

22. A method of reducing pathogens in blood, the method comprising:

obtaining blood from a mammal or a blood source;

separating the blood into plasma and blood cells;

exposing the plasma to nitric oxide containing gas;

combining the exposed plasma with the blood cells;

reducing nitric oxide gas content in the recombined blood by providing a semipermeable membrane selectively permeable to nitric oxide gas in between the recombined blood and a gaseous source; and

returning the recombined blood to the mammal or blood source.

23. The method of claim 22, wherein the gaseous source is ambient air.

24. The method of claim 22, further comprising exposing the blood to oxygen, wherein the exposing to oxygen step occurs before the separation step or after the recombining step.

25. The method of claim 22, wherein the separating is through one or more of a filter, a centrifuge, or dialysis.

26. The method of claim 22, wherein the plasma is exposed to a concentration of nitric oxide over a period of time sufficient to reduce pathogen concentration in the blood.

27. The method of claim 22, wherein the pathogens are selected from viruses, bacteria, mycobateria, parasites, and fungi.

28. The method of claim 22, wherein the nitric oxide containing gas is controllably introduced in relation to an amount of plasma separated from the blood.

29. The method of claim 22, wherein the exposing step comprises:

providing a semipermeable membrane selectively permeable to nitric oxide gas and impermeable to nitrogen gas adapted to allow contact of an outside of the membrane with the plasma; and

delivering nitric oxide containing gas to an inside of the membrane under pressure sufficient to drive the nitric oxide across the membrane for contact with the plasma on the outside of the membrane within a desired concentration range sufficient to reduce pathogen concentration in the plasma.

30. The method of claim 22, wherein the concentration of nitric oxide in the nitric oxide containing gas is about 120 ppm to about 400 ppm.

31. The method of claim 30, wherein the concentration is about 160 ppm to about 220 ppm.

32. The method of claim 22, wherein the concentration of nitric oxide in the nitric oxide containing gas is less than about 120 ppm and more than 0.

33. The method of claim 22, wherein before the combining the exposed plasma with the blood cells step, the exposed plasma is treated by a bacterial particulate filter to reduce levels of lipopolysaccharide (LPS) in the plasma.

34. An extracorporeal blood circuit comprising:

an inlet line adapted to obtain blood from a mammal or a blood source;

an outlet line adapted to return blood to the mammal or blood source;

a fluid circuit for fluid communication between the inlet and the outlet line, wherein the fluid circuit comprises;

at least one pump acting on the fluid circuit to circulate the blood therethrough;

a separation unit in fluid communication with the inlet line, wherein the separation unit is adapted to separate the blood received from the mammal or source into plasma and blood cells;

a nitric oxide unit that exposes the plasma with a nitric oxide gas containing gas;

a mixer for combining the exposed plasma with the blood cells; and

a reduction unit for reducing the nitric oxide content in the recombined blood, wherein the reduction unit is in fluid communication with the outlet line and comprises a semipermeable membrane selectively permeable to nitric oxide gas operably fitted in between the combined blood and a gaseous source.

35. The extracorporeal blood circuit of claim 34, further comprising one or more of a reservoir to collect the blood from the mammal or source, an oxygenator, a dialysis component, an organ perfusion component, a heat exchange component, and an oxygenation component.

36. The extracorporeal blood circuit of claim 34, wherein the gaseous source is ambient air.

37. The extracorporeal blood circuit of claim 34, wherein the separation unit comprises one or more of a filter, a centrifuge, and dialysis.

38. The extracorporeal blood circuit of claim 34, wherein the nitric oxide unit comprises:

a semipermeable membrane selectively permeable to nitric oxide gas and impermeable to nitrogen gas adapted to allow contact of an outside of the membrane with the plasma; and

nitric oxide containing gas deliverable to an inside of the membrane under pressure sufficient to drive the nitric oxide across the membrane for contact with the plasma on the outside of the membrane within a desired concentration range sufficient to reduce pathogen concentration in the plasma.

39. The extracorporeal blood circuit of claim 34, wherein the concentration of nitric oxide in the nitric oxide containing gas is about 120 ppm to about 400 ppm.

40. The extracorporeal blood circuit of claim 39, wherein the concentration is about 160 ppm to about 220 ppm.

41. The extracorporeal blood circuit of claim 34, wherein the concentration of nitric oxide in the nitric oxide containing gas is less than about 120 ppm and more than 0.

42. The extracorporeal blood circuit of claim 34, further comprising a bacterial particulate filter to reduce levels of lipopolysaccharide (LPS) in the plasma.