Selective adsorption devices and systems

• US 20020197252A1
• Filed: 12/21/2001
• Published: 12/26/2002
• Est. Priority Date: 04/10/2001
• Status: Abandoned Application

• Current Assignee: Donald Brodie, RenalTech International LLC, Stefan Brodie
• Original Assignee: RenalTech International LLC
• Inventors: Winchester, James F., Davankov, Vadim, Pavlova, Ludmila, Salsberg, Jamie A., Brady, James A., Norris, Frank M., Tsyurupa, Maria, Quartararo, Peter J. Jr.
• Application Number:
  US10/038,053
• Publication Number:
  US 20020197252A1
• Time in Patent Office: Days
• US Class Current: 424/140.1
• CPC Class Codes: A01N 1/0247 for perfusion, i.e. for circulating fluid through organs, blood vessels or other living parts
• CPC Class Codes: A61L 29/085 Macromolecular materials
• CPC Class Codes: A61M 1/1678 intracorporal peritoneal dialysis A61M1/28
• CPC Class Codes: A61M 1/1696 with dialysate regeneration
• 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 1/28 Peritoneal dialysis ; Other peritoneal treatment, e.g. oxygenation
• CPC Class Codes: A61M 1/281 Instillation other than by gravity
• CPC Class Codes: A61M 1/284 Continuous flow peritoneal dialysis [CFPD]
• CPC Class Codes: A61M 1/34 Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
• CPC Class Codes: A61M 1/3403 Regulation parameters
• CPC Class Codes: A61M 1/3486 Biological, chemical treatment, e.g. chemical precipitation; treatment by absorbents
• CPC Class Codes: A61M 1/3679 by absorption A61M1/3675 takes precedence
• CPC Class Codes: A61M 1/3681 by irradiation
• CPC Class Codes: A61M 2205/3331 Pressure; Flow
• CPC Class Codes: A61M 2205/50 with microprocessors or computers
• CPC Class Codes: B01D 39/04 Organic material, e.g. cellulose, cotton
• CPC Class Codes: B01J 20/321 consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds
• CPC Class Codes: B01J 20/327 Polymers obtained by reactions involving only carbon to carbon unsaturated bonds
• CPC Class Codes: B01J 20/3272 Polymers obtained by reactions otherwise than involving only carbon to carbon unsaturated bonds
• CPC Class Codes: B01J 20/3293 Coatings on a core, the core being particle or fiber shaped, e.g. encapsulated particles, coated fibers

Abstract

Intravenous, or indwelling, or integrated multi-functional devices and systems reduce levels of a targeted compound in blood by selective adsorption. The devices and systems can be used, e.g., to reduce levels of pro-inflammatory or anti-inflammatory stimulators or mediators in blood by selective adsorption. The devices and systems are useful in situations where abnormal levels of or unregulated or excessive interaction among pro-inflammatory or anti-inflammatory stimulators or mediators occur, or during events that do induce or have the potential for inducing abnormal production of pro-inflammatory or anti-inflammatory stimulators or mediators. The devices and systems serve to prevent, control, reduce, or alleviate the severity of the inflammatory response and disease states that are associated with abnormal levels of or unregulated or excessive interaction among pro-inflammatory or anti-inflammatory stimulators or mediators.

Claims

1. An intravenous catheter comprising an in-line housing, and a material within the housing that removes a targeted compound from the blood by selective adsorption.

7. A catheter according to claim 1 or 2 or 3 or 4 or 5 or 6

wherein the material comprises polymeric particles.

8. A catheter according to claim 7

wherein the polymeric particles include a coating to impart biocompatibilty.

9. A catheter according to claim 7

wherein the polymeric particles comprise particles prepared by polymerization or copolymerization of a monomer selected from a group consisting of styrene, ethylstyrene, α

-methylstyrene, divinylbenzene, di isopropenyl benzene, trivinylbenzene, and alkyl methacrylate.

10. A catheter according to claim 7

wherein the polymeric particles comprise particles formed from crosslinked polystyrene-type resins having a surface modified to minimize activation of blood complement system.

11. A catheter according to claim 7

wherein the polymeric particles comprise particles formed from a porous hydrophobic divinylbenzene copolymer having a surface modified to include surface exposed functional groups selected from the group of polymers of 2-hydroxyethyl methacrylate, N-vinylpyrrolidine, N-vinylcaprolactame and N-acrylamide.

12. A catheter according to claim 7

wherein the polymeric material comprise particles formed by polymerization of aromatic divinyl compounds or their copolymerization with aromatic monovinyl compounds in the presence of porogens or mixtures of porogens with properties close to those of e-solvents.

13. A catheter according to claim 1 or 2 or 3 or 4 or 5 or 6

wherein the material is characterized by a Biocompatibility Index of not greater than 14.

14. A catheter according to claim 13

wherein the Biocompatibility Index is not greater than 7.

15. A catheter according to claim 1 or 2 or 3 or 4 or 5 or 6

wherein the targeted compound includes cytokines or other species of pro-inflammatory or anti-inflammatory stimulators or mediators.

16. A catheter according to claim 1 or 2 or 3 or 4 or 5 or 6

wherein the targeted compound includes middle molecular weight proteins.

18. An assembly according to claim 17

wherein the coupling means locates the first unit in an upstream flow direction relative to the second unit.

19. An assembly according to claim 17

wherein the coupling means locates the second unit in an upstream flow direction relative to the first unit.

20. An assembly according to claim 17

wherein the element of the first unit is configured to receive the blood drawn from the individual and to conduct separation of the blood into plasma and at least one cellular blood component.

21. An assembly according to claim 17

wherein the element of the first unit is configured to receive the blood drawn from the individual and to oxygenate the blood.

22. An assembly according to claim 17

wherein the element of the first unit is configured to remove waste from the blood drawn from the individual and convey waste-depleted blood to the second unit.

23. An assembly according to claim 17

wherein the material of the second unit comprises polymeric particles.

24. An assembly according to claim 23

wherein the polymeric particles include a coating to impart biocompatibilty.

25. An assembly according to claim 23

wherein the polymeric particles comprise particles prepared by polymerization or copolymerization of a monomer selected from a group consisting of styrene, ethylstyrene, α

-methylstyrene, divinylbenzene, di isopropenyl benzene, trivinylbenzene, and alkyl methacrylate.

26. An assembly according to claim 23

wherein the polymeric particles comprise particles formed from crosslinked polystyrene-type resins having a surface modified to minimize activation of blood complement system.

27. An assembly according to claim 23

wherein the polymeric particles comprise particles formed from a porous hydrophobic divinylbenzene copolymer having a surface modified to include surface exposed functional groups selected from the group of polymers of 2-hydroxyethyl methacrylate, N-vinylpyrrolidine, N-vinylcaprolactame and N-acrylamide.

28. An assembly according to claim 23

wherein the polymeric material comprise particles formed by polymerization of aromatic divinyl compounds or their copolymerization with aromatic monovinyl compounds in the presence of porogens or mixtures of porogens with properties close to those of e-solvents.

29. An assembly according to claim 17

wherein the material of the second unit is characterized by a Biocompatibility Index of not greater than 14.

30. An assembly according to claim 29

wherein the Biocompatibility Index is not greater than 7.

31. An assembly according to claim 17

wherein the targeted compound includes cytokines or other species of pro-inflammatory or anti-inflammatory stimulators or mediators.

32. An assembly according to claim 17

wherein the targeted compound includes a middle molecular weight protein.

2. An indwelling catheter comprising an in-line housing, and a material within the housing that removes a targeted compound from the blood by selective adsorption.

3. An intravenous catheter comprising an in-line exchangeable housing, and a material within the housing that removes a targeted compound from the blood by selective adsorption.

4. An indwelling catheter comprising an in-line exchangeable housing, and a material within the housing that removes a target compound from the blood by selective adsorption.

5. An intravenous catheter comprising a catheter tube having a wall, and a material impregnated in the wall, the material serving to remove a targeted compound from the blood by selective adsorption.

6. An indwelling catheter comprising a catheter tube having a wall, and a material impregnated in the wall, the material serving to remove a targeted compound from the blood by selective adsorption.

17. A blood treatment assembly comprising

a first unit comprising an element for processing the blood drawn from an individual,

a second unit comprising a material that removes a targeted compound from the blood by selective adsorption, and

coupling means for integrally coupling the first and second units together to form a blood treatment assembly that is supplied to a user as a single, integrated unit.

33. A blood treatment assembly comprising

a first unit comprising a first material that removes a first targeted compound from the blood,

a second unit comprising a second material, different than the first material, that removes a second targeted compound, different than the first targeted compound, from the blood, and

coupling means for coupling the first and second units together in a series flow relationship.

34. An assembly according to claim 33

wherein the first material comprises an adsorption medium that removes the first targeted compound by selective adsorption.

35. An assembly according to claim 34

wherein the second material comprises an adsorption medium that removes the second targeted compound by selective adsorption.

36. An assembly according to claim 34

wherein the second material comprises an ionic exchange medium that removes the second targeted compound.

37. An assembly according to claim 33

wherein the coupling means locates the first unit in an upstream flow direction relative to the second unit.

38. An assembly according to claim 33

wherein the coupling means locates the second unit in an upstream flow direction relative to the first unit.

39. An assembly according to claim 33

wherein one of the first and second targeted compounds includes cytokines or other species of pro-inflammatory or anti-inflammatory stimulators or mediators.

40. An assembly according to claim 33

wherein one of the first and second targeted compounds includes a middle molecular weight protein.

41. An assembly according to claim 33

wherein one of the first and second targeted compounds includes an endotoxin.

42. An assembly according to claim 33

wherein the first targeted compound includes cytokines or other species of pro-inflammatory or anti-inflammatory stimulators or mediators, and

wherein the second targeted compound includes another compound released into the blood as a result of trauma or injury.

43. An assembly according to claim 42

wherein the other compound includes a protein.

44. An assembly according to claim 42

wherein the other compound includes a toxin.

45. An assembly according to claim 42

wherein the other compound includes a chemical moiety.