Electronic Detection Immunoassays that Utilize a Binder Support Medium

• US 20070202561A1
• Filed: 08/11/2006
• Published: 08/30/2007
• Est. Priority Date: 02/10/2006
• Status: Abandoned Application

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Rosenstein, Robert
• Application Number:
  US11/463,909
• Publication Number:
  US 20070202561A1
• Time in Patent Office: Days
• US Class Current: 435/14
• CPC Class Codes: C12Q 1/004 mediator-assisted
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

A binder support medium-based immunoassay device and method is provided, utilizing the catalyzed formation of dopants and their subsequent effects on electroconductive polymers to detect an analyte of interest.

Claims

1. A device comprising:

a) a binder support medium comprising at least one detection zone for the detection of an analyte in a liquid sample;

b) at least one label moiety, wherein the label is capable of participating in the generation of a dopant;

c) a conducting polymer in fluid communication with the binder support medium, the conducting polymer capable of having its electrical conductivity changed after being doped with the dopant;

d) a circuit that comprises a voltage source, wherein an electric potential may be maintained across at least one portion of one dimension of the conducting polymer by means of the circuit.

2. The device of claim 1, wherein the electrical conductivity of the conducting polymer increases after being doped with the dopant.

3. The device of claim 1, wherein the circuit further comprises a readout mechanism capable of registering an indication of the magnitude of a measured electrical property in response to an electrical current that is conducted through the conducting polymer.

4. The device according to claim 1, wherein the label moiety comprises a first reduction-oxidation enzyme.

5. The device according to claim 4, wherein the device further comprises at least one reducing agent.

6. The device according to claim 5, wherein the device further comprises at least one precursor molecule capable of conversion to the dopant upon interaction with the reduction-oxidation enzyme and the reducing agent.

7. The device according to claim 5, wherein the device further comprises a second reduction-oxidation enzyme.

8. The device according to claim 6, wherein the precursor molecule is located within the detection zone of the binder support medium.

9. The device according to claim 4, wherein the reduction-oxidation enzyme is selected from the group consisting of lactose peroxidase and glucose oxidase.

10. The device according to claim 1, wherein the dopant is selected from the group consisting of iodine and iodide.

11. The device according to claim 1, wherein the binder support medium is in fluid communication with one or more elements selected from the group consisting of a sample pad, a tracer pad, a reagent pad, and a sump.

12. A device comprising:

a) a binder support medium comprising at least one detection zone for the detection of an analyte in a liquid sample;

b) at least one chemical compound that is in fluid communication with the binder support medium, and which is capable of being transformed into a dopant or a dopant precursor compound by a reduction-oxidation enzyme;

c) at least one label moiety, wherein the label moiety is a reduction-oxidation enzyme capable of participating in the generation of the dopant;

d) a conducting polymer component in fluid communication with the binder support medium, the conducting polymer component capable of having its electrical conductivity changed after being doped with the dopant; and

,

e) a circuit that comprises a voltage source, wherein an electric potential may be maintained across at least one portion of one dimension of the conducting polymer by means of the circuit.

13. The device of claim 12, wherein the electrical conductivity of the conducting polymer increases after being doped with the dopant.

14. The device of claim 12, wherein the circuit further comprises a readout mechanism capable of registering an indication of the magnitude of a measured electrical property in response to an electrical current.

15. The device according to claim 12, wherein the label moiety is selected from the group consisting of glucose oxidase and lactose peroxidase.

16. The device according to claim 12, wherein the device further comprises additional reagents selected from the group consisting of reducing agents and dopant precursor compounds, or combinations thereof.

17. The device according to claim 12, wherein the device further comprises a second reduction-oxidation enzyme.

18. The device according to claim 12, wherein the binder support medium is in fluid communication with one or more elements selected from the group consisting of a sample pad, a tracer pad, a reagent pad, and a sump.

19. A method for detecting the presence or amount of an analyte in a liquid sample comprising:

a) applying a liquid sample suspected of containing an analyte to a device;

b) contacting the analyte, if present, with a labeled receptor molecule, wherein the label is a reduction-oxidation enzyme, to form an analyte-labeled receptor complex;

c) transporting the analyte-labeled receptor complex through a binder support medium by means of liquid flow to a detection zone portion of the binder support medium;

d) immobilizing the analyte-labeled receptor complex in the detection zone portion of the binder support medium;

e) removing by liquid flow any reduction-oxidation enzyme that is not immobilized in the detection zone portion of the binder support medium, wherein the removal by liquid flow may occur prior to or concurrent with any of the events below;

f) transforming at least one chemical compound by the reduction-oxidation enzyme portion of the immobilized analyte-labeled receptor complex to form a dopant;

g) diffusing the dopant into or onto the surface of a conducting polymer that is in fluid communication with the detection zone portion, to form a doped conducting polymer; and

,

h) detecting the degree of doping of the conducting polymer by applying an electrical potential across the conducting polymer, to determine the presence, the amount, or the presence and amount of the analyte.

20. The method of claim 19, wherein the analyte portion of the analyte-labeled receptor complex binds to a binder by means of a ligand-receptor interaction.

21. The method of claim 19, wherein the reduction oxidation enzyme is selected from the group consisting of lactose peroxidase and glucose oxidase.

22. The method of claim 19, wherein the dopant generated is iodine or iodide, or a derivative thereof.

23. A method for detecting the presence or amount of an analyte in a liquid sample comprising:

a) applying a liquid sample suspected of containing an analyte to a device;

b) contacting the analyte, if present, with a labeled receptor molecule, wherein the label is a first reduction-oxidation enzyme, to form an analyte-labeled receptor complex;

c) transporting the analyte-labeled receptor complex through a binder support medium by means of liquid flow to a detection zone portion of the binder support medium;

d) immobilizing the analyte-labeled receptor complex in the detection zone portion of the binder support medium;

e) removing by liquid flow any first reduction-oxidation enzyme that is not immobilized in the detection zone portion of the binder support medium, wherein the removal by liquid flow may occur prior to or concurrent with any of the events below;

f) transforming at least one chemical compound with the first reduction-oxidation enzyme portion of the immobilized analyte-labeled receptor complex, to form a dopant precursor molecule;

g) transforming the dopant precursor molecule to a dopant with a second reduction-oxidation enzyme that is present within the detection zone portion;

h) diffusing the dopant into or onto the surface of a conducting polymer that is in fluid communication with the detection zone portion, to form a doped conducting polymer; and

i) detecting the degree of doping of the conducting polymer by applying an electrical potential across the conducting polymer, to determine the presence, the amount, or both the presence and amount of the analyte.

24. The method of claim 23, wherein the analyte portion of the analyte-labeled receptor complex binds to a binder by means of a ligand-receptor interaction.

25. The method according to claim 23, wherein the first reduction-oxidation enzyme is glucose oxidase.

26. The method according to claim 23, wherein the second reduction-oxidation enzyme is lactose peroxidase.

27. A method for detecting the presence or amount of an analyte in a liquid sample comprising the steps of:

a) applying a liquid sample containing or lacking an analyte to a device, wherein the device comprises a competitor bound to a label moiety forming a competitor complex, the competitor being an analyte, analogue, or derivative thereof, and the label moiety being a reduction-oxidation enzyme;

b) transporting the competitor complex and analyte contained in the liquid sample, if present, through a binder support medium by means of liquid flow to a detection zone portion of the binder support medium;

c) immobilizing the analyte in the detection zone whereby the competitor portion of the competitor complex and the analyte contained in the liquid sample compete for the binding of the binder in the detection zone by means of a ligand-receptor interaction;

d) removing by liquid flow any competitor complex that is not immobilized in the detection zone, wherein the removal by liquid flow may occur prior to or concurrent with any of the events below;

e) transforming at least one chemical compound with the reduction-oxidation enzyme portion of the immobilized competitor complex to form a dopant;

f) diffusing the dopant into or onto the surface of a conducting polymer that is in fluid communication with the detection zone portion, to form a doped conducting polymer; and

g) detecting the degree of doping of the conducting polymer by applying an electrical potential across the conducting polymer, to determine the amount, the presence or the presence and amount of the analyte.

28. The method of claim 27, wherein the reduction oxidation enzyme is selected from the group consisting of lactose peroxidase and glucose oxidase.

29. The method of claim 27, wherein the dopant generated is iodine or iodide, or a derivative thereof.

30. A method for detecting the presence or amount of an analyte in a liquid sample comprising:

a) applying a liquid sample containing or lacking an analyte to a device, wherein the device contains a competitor bound to a label forming a competitor complex, the competitor being an analyte, analogue, or derivative thereof, and the label being a reduction-oxidation enzyme;

b) transporting the competitor complex and analyte contained in the liquid sample, if present, through a binder support medium by means of liquid flow to a detection zone portion of the binder support medium;

c) immobilizing the analyte in the detection zone whereby the competitor portion of the competitor complex and the analyte contained in the liquid sample compete for the binding of the binder in the detection zone by means of a ligand-receptor interaction;

d) removing by liquid flow any competitor complex that is not immobilized in the detection zone, wherein the removal by liquid flow may occur prior to or concurrent with any of the events below;

e) transforming at least one chemical compound with the reduction-oxidation enzyme portion of the immobilized competitor complex to form a dopant precursor molecule;

f) transforming the dopant precursor molecule to a dopant with a second reduction-oxidation enzyme that is present within the detection zone portion;

g) diffusing the dopant into or onto the surface of a conducting polymer that is in fluid communication with the detection zone portion, to form a doped conducting polymer; and

h) detecting the degree of doping of the conducting polymer by applying an electrical potential across the conducting polymer component, to determine the presence, the amount or the presence and amount of the analyte.

31. The method according to claim 30, wherein the first reduction-oxidation enzyme is glucose oxidase.

32. The method according to claim 30, wherein the second reduction-oxidation enzyme is lactose peroxidase.