Metabolite sensor including a chemical concentration sensitive flow controller for a drug delivery system

• US 4,705,503 A
• Filed: 02/03/1986
• Issued: 11/10/1987
• Est. Priority Date: 02/03/1986
• Status: Expired due to Term

• Current Assignee: Regents of The University of Minnesota Morrill Hall 100 Church St SE Minneapolis MN
• Original Assignee: Regents of The University of Minnesota (University of Minnesota)
• Inventors: Wigness, Bruce D., Dorman, Frank D.
• Primary Examiner(s): Truluck, Dalton L.
• Application Number:
  US06/825,211
• Time in Patent Office: 645 Days
• Field of Search: 128/632-637, 604/28, 604/53, 604/265, 604/50, 604/66
• US Class Current: 604/504
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1486 using enzyme electrodes, e.g. with immobilised oxidase
• CPC Class Codes: A61M 2025/0057 Catheters delivering medicament other than through a conventional lumen, e.g. porous walls or hydrogel coatings
• CPC Class Codes: A61M 37/00 Other apparatus for introducing media into the body for reproduction or fertilisation A61B17/425; apparatus for iontophoresis or cataphoresis A61N1/30; Percutany, i.e. introducing medicines into the body by diffusion through the skin salt baths A61H33/04
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00

Abstract

A system for the measurement of a metabolite in a physiological fluid is disclosed which comprises a catheter which includes an internal metabolite sensor downstream from a semipermeable region where dynamic equilibrium is attained between the external metabolite and a higher concentration of the same metabolite contained in an infusate which is flowed through the catheter. The changing metabolite concentration also can open and close a chemical valve to control the codelivery of a drug through the catheter.

Claims

1. A method for the measurement of the concentration of a metabolite present in a physiological fluid such as blood, comprising the steps of:

(a) inserting a catheter into a stream of said blood containing the metabolite;

(b) flowing an aqueous infusate into said catheter at a pressure above that of the blood stream, wherein said infusate contains a concentration of said blood metabolite which is higher than the concentration of the metabolite in the blood;

(c) contacting said flowing infusate with a microporous segment of the wall of said catheter for a period of time effective to bring the concentration of the metabolite within the infusate and the concentration of the metabolite in the blood into equilibrium;

(d) measuring the concentration of the metabolite in the flowing infusate by means of a sensor positioned within the catheter downstream from the microporous segment; and

(e) passing said flowing infusate out the catheter and into the blood.

2. The method of claim 1 wherein the catheter is implanted in a blood vessel of a human.

3. The method of claim 2 wherein the infusate is flowed through the catheter by means of a pump which is implanted in the body of a human.

4. The method of claim 3 wherein the pump provides a uniform flow rate of infusate.

5. The method of claim 1 wherein said microporous segment comprises a sheet or tube of a polymeric material.

6. The method of claim 1 wherein the sensor is an enzyme electrode sensor, a fuel cell sensor or an optical affinity sensor.

7. The method of claim 1 wherein the metabolite is glucose.

8. The method of claim 7 wherein the glucose concentration in the infusate is about 100-1000 mg/dl.

9. The method of claim 1 wherein the infusate includes an amount of an anticoagulant effective to inhibit thrombus formation on said microporous wall segment.

10. A system for the measurement of a metabolite in the blood, comprising:

a catheter having a fluid input port, a fluid output port, a lumen interconnecting the ports, and a microporous wall segment located between the ports which is permeable to water and to said metabolite but which is substantially impermeable to blood components of higher molecular weight;

a sensor for said metabolite positioned within the lumen of said catheter at or downstream from the microporous wall segment; and

means for flowing an aqueous infusate through said catheter with a pressure and metabolite concentration relatively higher than that of the blood so that the concentrations of metabolites equilibrate, whereby the amount of metabolite in the infusate measured by said sensor corresponds to the amount of metabolite in the blood.

11. The system of claim 10 wherein the microporous wall segment comprises a sheet or tube of a polymeric material.

12. The system of claim 10 wherein the sensor is an enzyme electrode sensor, a fuel cell sensor or an optical affinity sensor.

13. The system of claim 10 wherein the catheter comprises a second lumen.

14. The system of claim 10 which further comprises a pump in connection with said input port of said catheter to establish a flow of a drug inan amount effective to regulate the level of said metabolite in the blood.

15. A method for the controlled delivery of a drug which is effective to reduce the concentration of a metabolite present in the blood, comprising the steps of:

(a) inserting a catheter into a stream of said blood containing the metabolite;

(b) flowing an aqueous infusate into said catheter at a pressure above that of the blood stream, wherein said infusate contains;

(i) an amount of said drug effective to reduce the concentration of said metabolite;

(ii) a concentration of said metabolite which is higher than the concentration of the metabolite in blood; and

(iii) a biopolymer comprising a moiety derived from said metabolite;

(c) contacting said flowing infusate with a microporous segment of the wall of said catheter for a period of time effective to bring the concentration of the metabolite within the infusate and the concentration of the infusate in the blood into equilibrium, wherein said microporous segment is permeable with respect to the metabolite, but is substantially impermeable to the drug and to the biopolymer;

(d) passing the infusate through a porous matrix positioned within the catheter, wherein said matrix comprises a binding substance in an amount effective to decrease the porosity of the matrix as the concentration of the metabolite in the infusate decreases by competitively complexing both the metabolite and the biopolymer; and

(e) passing the flowing infusate out the catheter and into the blood.

16. The method of claim 15 wherein the catheter is implanted in a blood vessel of a human.

17. The method of claim 15 wherein the catheter is inserted into an extracorporeal blood stream.

18. The method of claim 15 wherein the infusate is flowed at a constant pressure by a pump which is implanted in a human body.

19. The method of claim 15 wherein the infusate comprises an anticoagulant in an amount effective to inhibit thrombus formation on the microporous wall segment.

20. The method of claim 15 wherein the metabolite is glucose.

21. The method of claim 20 wherein the biopolymer is a polysaccharide comprising glucose sub-units.

22. The method of claim 21 wherein the polysaccharide is dextran.

23. The method of claim 15 wherein the binding substance is a lectin.

24. The method of claim 23 wherein the binding substance is conconavalin A.

25. The method of claim 15 wherein the drug is insulin.

26. The method of claim 20 wherein the infusate comprises about 100-1000 mg/dl of glucose.

27. The method of claim 25 wherein the infusate comprises about 2-1000 units/ml of insulin.

28. The method of claim 22 wherein the infusate comprises about 0.1-0.5 μ

M dextran.

29. The method of claim 15 wherein the pH of the infusate is buffered to about 6-8.

30. A system for the controlled delivery of a drug which is effective to reduce the concentration of a metabolite present in the blood, comprising:

a catheter having a fluid input port, a fluid output port, a microporous polymeric wall segment downstream from the input port which is permeable to water and to the metabolite but which is substantially impermeable to blood components of higher molecular weight, and a flow controller comprising a porous matrix positioned within catheter at or downstream from said microporous wall segment;

wherein said matrix comprises a binding substance in an amount effective to decrease the porosity of the matrix as the concentration of the metabolite within the catheter decreases by competitively complexing both the metabolite and a biopolymer which comprises a moiety derived from said metabolite.

31. The system of claim 30 which further comprises a constant-pressure drug infusion pump in connection with said input port of said catheter, wherein said pump comprises a recycling chemical vapor-liquid constant pressure energy source.

32. The system of claim 30 wherein the metabolite is glucose.

33. The system of claim 30 wherein the binding substance comprises conconavalin A.

34. The system of claim 30 wherein the biopolymer comprises dextran.

35. The system of claim 30 wherein the porous matrix comprises polytetrafluoroethylene fibers.

36. The system of claim 30 wherein the matrix pores have an effective diameter of about 0.01-1 microns.