Enhanced biologically based chronotropic biosensing

• US 6,650,919 B2
• Filed: 05/03/2001
• Issued: 11/18/2003
• Est. Priority Date: 05/03/2000
• Status: Expired due to Fees

• Current Assignee: Cornell Research Foundation Incorporated (Cornell University)
• Original Assignee: Cornell Research Foundation Incorporated (Cornell University)
• Inventors: Christini, David J., Edelberg, Jay M.
• Primary Examiner(s): Nasser, Robert L.
• Assistant Examiner(s): Mallari, Patricia C.
• Application Number:
  US09/848,064
• Publication Number:
  US 20020062072A1
• Time in Patent Office: 929 Days
• Field of Search: 204/403-1-4, 436/63, 436/149, 436/806, 435/176, 422/82.01, 422/82.02, 600/345-361, 600/365, 600/372-381, 600/300
• US Class Current: 600/345
• CPC Class Codes: A61L 27/3604 characterised by the human or animal origin of the biological material, e.g. hair, fascia, fish scales, silk, shellac, pericardium, pleura, renal tissue, amniotic membrane, parenchymal tissue, fetal tissue, muscle tissue, fat tissue, enamel
• CPC Class Codes: A61L 27/3826 Muscle cells, e.g. smooth muscle cells
• CPC Class Codes: A61L 27/383 Nerve cells, e.g. dendritic cells, Schwann cells
• CPC Class Codes: Y10S 977/853 Biological sample

Abstract

The present invention provides implantable physiological or pathophysiological biosensors. The subject biosensors comprise tissue or cells capable of carrying out a physiological or pathophysiological function, which can be used to monitor a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function. In one embodiment, the tissue or cells are coupled via an electrical interface to an electronic measuring device or an electronic amplifying device. In another embodiment, the tissue or cells are coupled via an electrical interface to endogenous tissue or cells, including the blood. Preferably, the tissue or cells are excitable tissue or cells such as cardiac tissue or cells and neuronal tissue or cells. The subject biosensors may be placed, inserted or implanted in any animal including but not limited to a mouse, rat, rabbit, pig, cat, dog, cattle, horse, sheep or human. The present invention also provides various methods which employ a biosensor of the present invention. Such methods include a method of monitoring physiological or pathophysiological function, a method of regulating output of a signal to a subject, and a method for controlling heart function.

Claims

1. An implantable physiological or pathophysiological biosensor comprising:

tissue or cells capable of carrying out a physiological or pathophysiological function, wherein the tissue or cells can be coupled via an electrical interface to an electronic measuring device or an electronic amplifying device, and wherein the biosensor monitors a chemical, physiological or pathophysiological variable associated with an endogenous physiological or pathophysiological function in a mammalian subject.

3. The biosensor according to claim 1 or 2, wherein the tissue or cells are excitable tissue or cells.

4. The biosensor according to claim 3, wherein the excitable tissue or cells are cardiac tissue or cells.

5. The biosensor according to claim 3, wherein the tissue or cells are neuronal tissue or cells.

6. The biosensor according to claim 1 or 2, wherein the tissue or cells are molecularly, genetically, or cellularly engineered.

7. The biosensor according to claim 1 or 2, wherein the physiological or pathophysiological variable is heart rate regulation or heart rate dynamics.

8. The biosensor according to claim 1 or 2, wherein the physiological or pathophysiological variable is a level or activity of at least one of blood glucose, insulin, thyroid hormone, clotting factors or components, endocrine hormone, paracrine hormone, autocrine hormone, antibodies, receptor antagonists, ligands, antigens, antagonists, signal pathway cofactors, signal pathway components, pathogens, drugs, metabolites, or toxins.

9. The biosensor according to claim 1 or 2, wherein the biosensor is implanted or inserted in an animal.

10. The biosensor according to claim 9 wherein the animal is a mammal.

11. The biosensor according to claim 10, wherein the mammal is selected from the group consisting of a mouse, rat, rabbit, pig, cat, dog, cattle, horse, and sheep.

12. The biosensor according to claim 10, wherein the mammal is a human.

13. The biosensor according to claim 1 or claim 2 wherein the tissue or cells are incorporated within a device.

14. The biosensor of claim 13 wherein the device is at least one of a tube, tubing, catheter, wire, wire leads, or an electronic pacemaker.

54. The biosensor according to claim 1 or 2, wherein the tissue or cells receive blood-borne signals from the mammalian subject.

2. An implantable physiological or pathophysiological biosensor comprising:

tissue or cells capable of carrying out a physiological or pathophysiological function, wherein the tissue or cells can be coupled via an electrical interface to endogenous tissue or cells, and wherein the biosensor may be used to monitor a chemical, physiological or pathophysiological variable associated with an endogenous physiological or pathophysiological function in a mammalian subject.

15. A method for monitoring a physiological or pathophysiological function of a subject, said method comprising:

placing into a site within a subject isolated tissue or cells wherein the site can be distant from an endogenous site of the physiological or pathophysiological function within the subject, and wherein the tissue or cells may be used to monitor a chemical, physiological or pathophysiological variable associated with the endogenous site of the physiological or pathophysiological function of the subject, and;

monitoring the physiological or pathophysiological function of the exogenous tissue or cells placed therein.

16. The method according to claim 15, wherein the tissue or cells are excitable tissue or cells.

17. The method according to claim 16 wherein the excitable tissue or cells are cardiac tissue or cells.

18. The method according to claim 16, wherein the excitable tissue or cells are neuronal tissue or cells.

19. The method according to claim 15, wherein the tissue or cells are coupled via an electrical interface to endogenous tissue or cells.

20. The method according to claim 15, wherein the tissue or cells are coupled via an electrical interface to an electronic measuring device or an electric amplifying device.

21. The method according to claim 15, wherein the tissue or cells are molecularly, genetically, or cellularly engineered.

22. The method according to claim 15, wherein the physiological or pathophysiological variable is heart rate regulation or heart rate dynamics.

23. The method according to claim 15, wherein the chemical, physiological or pathophysiological variable is a level or activity of at least one of blood glucose, insulin, thyroid hormone, clotting factors and components, endocrine hormone, paracrine hormone, autocrine hormone, antibodies, receptor antagonists, ligands, antigens, antagonists, signal pathway cofactors, signal pathway components, pathogens, drugs, metabolites, or toxins.

24. The method according to claim 15, wherein the tissue or cells can be incorporated into a device that is placed inside an animal.

25. The method of claim 24 wherein the device is at least one of a tube, tubing, catheter, wire, wire leads, or an electronic pacemaker.

26. The method according to claim 24, wherein the animal is a mammal.

27. The method according to claim 26, wherein the mammal is selected from the group consisting of a mouse, rat, rabbit, pig, cat, dog, cattle, horse, and sheep.

28. The method according to claim 26, wherein the mammal is a human.

29. A method of regulating output of a signal, substance, or action in a subject, said method comprising:

placing within the subject, exogenous tissue or cells capable of carrying out a physiological or pathophysiological function, wherein the exogenous tissue or cells can be used to monitor a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function;

coupling the exogenous tissue or cells to an interventional device or a delivery device; and

regulating the output of a signal, substance, or action from the interventional device or delivery device in response to the physiological or pathophysiological function of the exogenous tissue or cells.

30. The method according to claim 29, wherein the signal is an electrical signal.

31. The method according to claim 29, wherein the signal is a chemical signal.

32. The method according to claim 29, wherein the tissue or cells are excitable tissue or cells.

33. The method according to claim 32, wherein the excitable tissue or cells are cardiac tissue or cells.

34. The method according to claim 32, wherein the excitable tissue or cells are neuronal tissue or cells.

35. The method according to claim 29, wherein the tissue or cells are molecularly, genetically, or cellularly engineered.

36. The method according to claim 29, wherein the physiological or pathophysiological variable is heart rate regulation or heart rate dynamics.

37. The method according to claim 29, wherein the chemical, physiological or pathophysiological variable is a level or activity of at least one of blood glucose, insulin, thyroid hormone, clotting factors and components, endocrine hormone, paracrine hormone, autocrine hormone, antibodies, receptor antagonists, ligands, antigens, antagonists, signal pathway cofactors, signal pathway components, pathogens, drugs, metabolites or toxins.

38. The method according to claim 29, wherein the tissue or cells are implanted in a mammal.

39. The method according to claim 29, wherein the tissue or cells are incorporated into a device that is placed inside the subject.

40. The method of claim 39 wherein the device is at least one of a tube, tubing, catheter, wire, wire leads, or an electronic pacemaker.

41. The method according to claim 38, wherein the mammal is selected from the group consisting of a mouse, rat, rabbit, pig, cat, dog, cattle, horse, and sheep.

42. The method according to claim 38, wherein the mammal is a human.

43. The method according to claim 29, wherein the delivery device delivers a drug or compound.

44. The method according to claim 29 wherein the interventional device is an alarm system or mechanical device.

45. The method according to claim 29 wherein the delivery device is a an electronic pacemaker, insulin pump, or drug pump.

46. The method according to claim 29, wherein the delivery device delivers electrical stimuli or mechanical stimuli.

47. A system for controlling heart function comprising:

exogenous tissue or cells that can be placed within a subject; and

an electrical connection that can be placed between the exogenous tissue or cells and a natural pacemaker region of the subject'"'"'s heart, wherein the exogenous tissue or cells are capable of carrying out a physiological or pathophysiological function and may be used to monitor a chemical, physiological or pathophysiological variable associated with a physiological or pathophysiological function of the subject'"'"'s heart.

48. The system according to claim 47 further comprising:

an amplifier to boost the signal from the exogenous tissue or cells.

49. The system according to claim 47 wherein the exogenous tissue is connected to an electronic pacemaker.

50. The system according to claim 47 wherein the exogenous tissue comprises cells which are molecularly, genetically, or cellularly engineered.

51. The system according to claim 47 wherein the exogenous tissue or cells are incorporated into a device that i-scan be placed inside the subject.

52. The system of claim 51 wherein the device is at least one of a tube, tubing, catheter, wire, or wire leads.

53. The system according to claim 47 wherein the exogenous tissue or cells are cardiac or neuronal tissue or cells.

55. An implantable physiological or pathophysiological biosensor comprising genetically modified cells that can be coupled via an electrical interface to an electronic measuring device or an electronic amplifying device, wherein the genetically modified cells can be implanted into a mammalian subject at a site distant from a natural site for a physiological or pathophysiological function of the subject, and wherein the genetically modified cells monitor a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function of the subject.

56. An implantable physiological or pathophysiological biosensor comprising:

genetically modified cells that can be coupled via an electrical interface to endogenous tissue or cells, wherein the genetically engineered cells can be implanted into a mammalian subject at a site distant from a natural site for a physiological or pathophysiological function of the subject, and wherein the genetically modified cells monitor or modulate a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function of the subject.

57. An implantable physiological or pathophysiological biosensor comprising in vitro or ex vivo modified stem cells that can be coupled via an electrical interface to an electronic measuring device or an electronic amplifying device, wherein the in vitro or ex vivo modified stem cells can be implanted into a mammalian subject at a site distant from a natural site for a physiological or pathophysiological function of the subject, and wherein the in vitro or ex vivo modified stem cells monitor a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function of the subject.

58. An implantable physiological or pathophysiological biosensor comprising:

in vitro or ex vivo modified stem cells that can be coupled via an electrical interface to endogenous tissue or cells, wherein the in vitro or ex vivo modified stem cells can be implanted into a mammalian subject at a site distant from a natural site for a physiological or pathophysiological function of the subject, and wherein the in vitro or ex vivo modified stem cells monitor or modulate a chemical, physiological or pathophysiological variable associated with the physiological or pathophysiological function of the subject.