Direct immunosensor assay

• US 20030180814A1
• Filed: 03/21/2002
• Published: 09/25/2003
• Est. Priority Date: 03/21/2002
• Status: Abandoned Application

• Current Assignee: Universal Biosensors Pty Ltd. (Universal Biosensors, Inc.)
• Original Assignee: Universal Biosensors Pty Ltd. (Universal Biosensors, Inc.)
• Inventors: Hodges, Alastair, Chatelier, Ronald
• Application Number:
  US10/105,050
• Publication Number:
  US 20030180814A1
• Time in Patent Office: Days
• US Class Current: 435/7.9
• CPC Class Codes: C12Q 1/001 Enzyme electrodes
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

This invention describes a quantitative, inexpensive, disposable immunosensor that requires no wash steps and thus generates no liquid waste. Moreover, in preferred embodiments of the sensor no timing steps are required of the user, and the sensor can be readily adapted to antigen-antibody interactions over a wide kinetic range.

Claims

1. A disposable device for use in detecting a target antigen in a fluid sample, the device comprising a reaction chamber;

an immobilized antibody fixed within the reaction chamber;

a reporter complex comprising a probe and a reporter complex antigen, wherein the probe is linked to the reporter complex antigen, wherein the reporter complex antigen is bound to the immobilized antibody, and wherein the reporter complex antigen binds less strongly than the target antigen to the immobilized antibody;

a detection chamber;

a sample ingress to the reaction chamber; and

a sample passageway between the reaction chamber and the detection chamber.

2. The device of claim 1, wherein the reporter complex antigen is selected from the group consisting of the target antigen, a pseudo-antigen, and a modified-antigen.

3. The device of claim 1, wherein the probe is selected from the group consisting of radioisotopes, chromophores, and fluorophores.

4. The device of claim 1, wherein the probe comprises an enzyme.

5. The device of claim 4, wherein the enzyme comprises a glucose dehydrogenase.

6. The device of claim 4, further comprising an enzyme substrate.

7. The device of claim 6, wherein the enzyme substrate is an oxidizable substrate.

8. The device of claim 7, wherein the enzyme substrate comprises glucose.

9. The device of claim 6, further comprising a mediator.

10. The device of claim 9, wherein the mediator is selected from the group consisting of dichlorophenolindophenol and complexes between transition metals and nitrogen-containing heteroatomic species.

11. The device of claim 10, wherein the mediator comprises ferricyanide.

12. The device of claim 4, wherein the sample has a pH, and wherein the device further comprises a buffer that adjusts the pH of the sample.

13. The device of claim 12, wherein the buffer comprises a phosphate.

14. The device of claim 12, wherein the buffer comprises a mellitate.

15. The device of claim 4, further comprising a stabilizer, wherein the stabilizer stabilizes at least one component selected from the group consisting of the target antigen, the reporter complex antigen, the enzyme, and the immobilized antibody.

16. The device of claim 6, wherein the enzyme substrate is supported on a detection chamber interior surface.

17. The device of claim 1, wherein the immobilized antibody is supported on a reaction chamber interior surface.

18. The device of claim 1, further comprising a support material.

19. The device of claim 18, wherein the support material is contained within the detection chamber, and wherein a first substance selected from the group consisting of an enzyme substrate, a mediator, and a buffer is supported on or contained within the support material.

20. The device of claim 18, wherein the support material is contained within the reaction chamber, and wherein a second substance selected from the group consisting of the immobilized antibody, the reporter complex, and an agent that prevents non-specific binding of proteins to a reaction chamber internal surface is supported on or contained within the support material.

21. The device of claim 18, wherein the support material comprises a mesh material.

22. The device of claim 21, wherein the mesh material comprises a polymer selected from the group consisting of polyolefin, polyester, nylon, cellulose, polystyrene, polycarbonate, polysulfone, and mixtures thereof.

23. The device of claim 18, wherein the support material comprises a fibrous filling material.

24. The device of claim 23, wherein the fibrous filling material comprises a polymer selected from the group consisting of polyolefin, polyester, nylon, cellulose, polystyrene, polycarbonate, polysulfone, and mixtures thereof.

25. The device of claim 18, wherein the support material comprises a porous material.

26. The device of claim 25, wherein the porous material comprises a sintered powder.

27. The device of claim 25, wherein the porous material comprises a macroporous membrane.

28. The device of claim 27, wherein the macroporous membrane comprises a polymeric material selected from the group consisting of polysulfone, polyvinylidene difluoride, nylon, cellulose acetate, polymethacrylate, polyacrylate, and mixtures thereof.

29. The device of claim 18, wherein the support material comprises a bead.

30. The device of claim 1, wherein the detection chamber comprises a first electrode and a second electrode.

31. The device of claim 30, wherein at least one of the first electrode and the second electrode comprises a material selected from the group consisting of aluminum, copper, nickel, chromium, steel, stainless steel, palladium, platinum, gold, iridium, carbon, carbon mixed with binder, indium oxide, tin oxide, a conducting polymer, and mixtures thereof.

32. The device of claim 1, wherein a detection chamber wall is transparent to a radiation emitted or absorbed by the probe, wherein the radiation is indicative of a presence or absence of the reporter complex in the detection chamber.

33. The device of claim 1, further comprising a detector that detects a condition wherein the reaction chamber is substantially filled.

34. The device of claim 1, further comprising a piercing means that forms a detection chamber vent in a distal end of the detection chamber.

35. The device of claim 1, further comprising a reaction chamber vent at a distal end of the reaction chamber.

36. The device of claim 1, wherein the target antigen comprises a human C-reactive protein.

37. The device of claim 36, wherein the reporter complex antigen comprises a monomeric C-reactive protein.

38. The device of claim 36, wherein the reporter complex antigen comprises a C-reactive protein derived from a non-human species.

39. The device of claim 36, wherein the reporter complex antigen comprises a chemically-modified C-reactive protein, wherein an affinity of the chemically-modified C-reactive protein to the antibody is less than an affinity of the human C-reactive protein to the antibody

40. The device of claim 1, wherein a wall of the detection chamber or a wall of the reaction chamber comprises a material selected from the group consisting of polyester, polystyrene, polycarbonate, polyolefin, polyethylene terephthalate, and mixtures thereof.

41. The device of claim 40, wherein the wall of the detection chamber or the wall of the reaction chamber further comprises a filler.

42. The device of claim 41, wherein the filler is a filler material selected from the group consisting of titanium dioxide, carbon, silica, glass, and mixtures thereof.

43. The device of claim 1, wherein the probe comprises an enzyme co-factor.

44. The device of claim 43, wherein the enzyme co-factor is selected from the group consisting of flavin mononucleotide, flavin adenine dinucleotide, nicotinamide adenine dinucleotide, and pyrroloquinoline quinone.

45. The device of claim 43, wherein the enzyme co-factor is linked to the reporter complex antigen through a flexible spacer.

46. The device of claim 43, further comprising an enzyme substrate.

47. The device of claim 43, further comprising an apoenzyme.

48. The device of claim 1, wherein the probe comprises an enzyme activity regulator.

49. The device of claim 48, wherein the enzyme activity regulator comprises a kinase or phosphorylase.

50. The device of claim 48, further comprising an enzyme substrate.

51. The device of claim 48, further comprising an enzyme.

52. The device of claim 1, wherein the probe comprises a protein subunit of a multi-subunit enzyme.

53. A method for determining an amount of a target antigen in a fluid sample, the method comprising the steps of:

placing the fluid sample in a reaction chamber containing an immobilized antibody and a reporter complex comprising a probe linked to a reporter complex antigen, wherein the antibody is fixed within the reaction chamber, wherein the reporter complex antigen is bound to the immobilized antibody, and wherein the reporter complex antigen binds less strongly than the target antigen to the immobilized antibody;

dissociating a portion of the reporter complex antigen from the immobilized antibody into the fluid sample;

binding a portion of the target antigen to the immobilized antibody;

transferring the fluid sample to a detection chamber; and

determining an amount of reporter complex in the fluid sample, wherein the amount of reporter complex is indicative of the amount of target antigen initially in the fluid sample.

54. The method of claim 53, wherein the step of transferring the fluid sample to a detection chamber comprises transferring the fluid sample to an electrochemical cell, the electrochemical cell comprising a first electrode and a second electrode.

55. The method of claim 54, wherein the step of determining an amount of reporter complex in the fluid sample comprises:

applying a potential between the first electrode and the second electrode; and

measuring a current, wherein the current is indicative of an amount of reporter complex present in the fluid sample, and wherein the amount of reporter complex is indicative of the amount of target antigen initially in the fluid sample.

56. The method of claim 53, wherein the step of transferring the fluid sample to a detection chamber comprises transferring the fluid sample to a detection chamber comprising an electromagnetic radiation transmissive portion.

57. The method of claim 56, wherein the step of determining an amount of reporter complex in the fluid sample comprises the steps of:

exposing the electromagnetic radiation transmissive portion to electromagnetic radiation, whereby the electromagnetic radiation passes through the fluid sample or reflects from the fluid sample; and

monitoring a property of the electromagnetic radiation after it passes through the fluid sample or reflects from the fluid sample, wherein the property is indicative of an amount of reporter complex present in the fluid sample, and wherein the amount of reporter complex is indicative of the amount of target antigen initially in the fluid sample.