Gas Sensor With a Microporous Electrolyte Layer

• US 20110079523A1
• Filed: 07/16/2010
• Published: 04/07/2011
• Est. Priority Date: 01/18/2008
• Status: Active Grant

• Current Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Original Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Inventors: Muresanu, Claudia-Gemma, Offenbacher, Helmut, Steiner, Gregor
• Granted Patent: US 8,163,165 B2
• Time in Patent Office: Days
• US Class Current: 205/793
• CPC Class Codes: G01N 33/4925 measuring blood gas content, e.g. O2, CO2 , HCO3

Abstract

The present invention relates to electrochemical sensors for determining gaseous analytes in an aqueous measuring medium, to a process for producing such sensors, and to a process for determining gaseous analytes dissolved in an aqueous measuring medium using the electrochemical sensors. The electrolyte layer of the sensors comprises at least one particulate material and at least one binder which together form a porous, non-swellable framework structure, wherein the pores in this framework structure are configured to absorb a liquid electrolyte or contain the liquid electrolyte.

Claims

1. An electrochemical sensor for determining a gaseous analyte dissolved in an aqueous measuring medium, comprising:

(a) a working electrode and a counter electrode,

(b) an electrolyte layer located between the working electrode and the counter electrode, and

(c) a gas-permeable cover layer configured to spatially separate the working electrode, the counter electrode and the electrolyte layer from the aqueous measuring medium, wherein the electrolyte layer comprises at least one particulate material and at least one binder which together form a porous, non-swellable framework structure, the pores of the non-swellable framework structure configured to absorb a liquid electrolyte or contain the liquid electrolyte.

2. The electrochemical sensor according to claim 1, wherein the particulate material is an inorganic particulate material selected from the group consisting of controlled porous glass (CPG), silica gels, silicates and alumosilicates.

3. The electrochemical sensor according to claim 1, wherein the particulate material is a naturally occurring or synthetic alumosilicate.

4. The electrochemical sensor according to claim 1, wherein the particulate material has channels, said channels having a diameter of between about 0.1 nm and about 10 nm.

5. The electrochemical sensor according to claim 4, wherein said channels further comprise ion exchanger groups.

6. The electrochemical sensor according to claim 1, wherein the particulate material is zeolite.

7. The electrochemical sensor according to claim 1, wherein the particulate material is faujasite.

8. The electrochemical sensor according to claim 1, wherein the particles of the particulate material have an average particle diameter of from about 0.1 μ

m to about 10 μ

m.

9. The electrochemical sensor according to claim 1, wherein the particles of the particulate materials have an average particle diameter of from about 1.0 μ

m to about 5.0 μ

m.

10. The electrochemical sensor according to claim 1, wherein the binder is an organic binder.

11. The electrochemical sensor according to claim 10, wherein the organic binder comprises a crosslinked or uncrosslinked synthetic polymer.

12. The electrochemical sensor according to claim 11, wherein the crosslinked or uncrosslinked synthetic polymer is a compound selected from the group consisting of a phenolic resin, an epoxy resin, a vinyl resin, a PVC copolymer, a two-component epoxy resin, a polyurethane resin system and a UV-curable polyacrylate monomer mixture.

13. The electrochemical sensor according to claim 12, wherein the UV-curable polyacrylate monomer mixture is a phenolic resin.

14. The electrochemical sensor according to claim 1, wherein the pores of the non-swellable framework structure have a diameter of from about 500 nm to about 5 μ

m.

15. The electrochemical sensor according to claim 1, wherein the pores of the non-swellable framework structure have a diameter of from about 1 μ

m to about 3 μ

m.

16. The electrochemical sensor according to claim 1, wherein the porous, non-swellable framework structure causes a relative absorption of liquid of from about 20% by weight to about 50% by weight based on the dry weight of the porous, non-swellable framework structure.

17. The electrochemical sensor according to claim 1, wherein the porous, non-swellable framework structure causes a relative absorption of liquid of from about 26% by weight to about 44% by weight based on the dry weight of the porous, non-swellable framework structure.

18. The electrochemical sensor according to claim 1, wherein the electrolyte layer has a thickness of from about 5 μ

m to about 30 μ

m.

19. The electrochemical sensor according to claim 1, wherein the electrolyte layer has a thickness of from about 10 μ

m to about 20 μ

m.

20. The electrochemical sensor according to claim 1, wherein the liquid electrolyte comprises an alkali metal chloride and a pH buffer system.

21. The electrochemical sensor according to claim 20, wherein the liquid electrolyte further comprises a water-soluble polymer.

22. The electrochemical sensor according to claim 21, wherein the water-soluble polymer is polyethylene glycol and/or polyvinylpyrrolidone.

23. The electrochemical sensor according to claim 20, wherein the liquid electrolyte further comprises an enzyme.

24. The electrochemical sensor according to claim 23, wherein the enzyme is carbonic anhydrase.

25. The electrochemical sensor according to claim 1, wherein the electrolyte layer comprises the non-volatile constituents of the liquid electrolyte before the sensor is put into operation.

26. The electrochemical sensor according to claim 1, wherein the gas-permeable cover layer is impermeable to ions and non-volatile constituents of the aqueous measuring medium.

27. The electrochemical sensor according to claim 1, wherein the gas-permeable cover layer comprises a siloxane, a polysulphone and/or polytetrafluoroethylene.

28. The electrochemical sensor according to claim 1, wherein the gas-permeable cover layer has a thickness of from about 5.0 μ

m to about 30 μ

m.

29. The electrochemical sensor according to claim 1, wherein the gas-permeable cover layer has a thickness of from about 8.0 μ

m to about 15 μ

m.

30. The electrochemical sensor according to claim 1, wherein the working electrode is made of a gold or ruthenium oxide-based composite material.

31. The electrochemical sensor according to claim 1, wherein the counter electrode is made of a silver or silver/silver chloride-based composite material.

32. The electrochemical sensor according to claim 1, wherein the sensor is configured for a multiple determination of the gaseous analyte dissolved in the aqueous measuring medium.

33. The electrochemical sensor according to claim 1, wherein the sensor is configured for determining a gaseous analyte in a body fluid.

34. The electrochemical sensor according to claim 33, wherein the body fluid is whole blood, plasma or serum.

35. The electrochemical sensor according to claim 1, wherein the gaseous analyte is oxygen.

36. The electrochemical sensor according to claim 1, wherein the gaseous analyte is carbon dioxide.

37. A method for manufacturing an electrochemical sensor according to claim 1, comprising:

(a) providing at least one particulate material;

(b) mixing the particulate material with at least one binder;

(c) processing the mixture obtained in step (b) into a paste;

(d) applying the paste obtained in step (c) to a support;

(e) hardening the paste applied to the support to form a porous, non-swellable framework structure; and

(f) producing an electrochemical sensor containing the porous, non-swellable framework structure obtained in step (e) as an electrolyte layer, and also a working electrode, a counter electrode and a gas-permeable cover layer.

38. The method according to claim 37 further comprising introducing a liquid containing non-volatile electrolyte constituents into the porous, non-swellable framework structure and subsequently evaporating the volatile constituents of the liquid.

39. The method according to claim 37 further comprising introducing a liquid containing non-volatile electrolyte constituents into the paste obtained in step (c).

40. The method according to claim 37 further comprising activating the electrochemical sensor by contacting said sensor with a liquid.

41. The method according to claim 40, wherein said liquid is an aqueous liquid.

42. The method according to claim 40, wherein the liquid has an osmotic pressure corresponding to the osmotic pressure of the liquid electrolyte absorbed in the porous, non-swellable framework structure.

43. A method for determining a gaseous analyte dissolved in an aqueous measuring medium, comprising:

(a) contacting the aqueous measuring medium with an electrochemical sensor according to claim 1, and

(b) determining the gaseous analyte dissolved in the aqueous measuring medium by measuring a signal generated by the electrochemical sensor.