Electrochemical affinity assay

• US 6,576,461 B2
• Filed: 06/18/2001
• Issued: 06/10/2003
• Est. Priority Date: 08/24/1998
• Status: Expired due to Term

• Current Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated), Marconi Communications Limited (Marconi Holdings Company Limited)
• Original Assignee: Therasense Incorporated (Abbott Laboratories Incorporated)
• Inventors: Campbell, Charles N., Heller, Adam
• Primary Examiner(s): Le, Long V.
• Assistant Examiner(s): Cook, Lisa V.
• Application Number:
  US09/883,591
• Publication Number:
  US 20020137193A1
• Time in Patent Office: 722 Days
• Field of Search: 435/7, 435/7.1, 435/7.5, 435/7.9, 435/14, 435/41, 435/5, 435/176, 435/403, 435/817, 435/288, 435/6, 435/91.2, 435/291, 435/7.93, 435/7.94, 435/962, 435/518, 435/25, 435/525, 436/501, 436/528, 436/531, 436/825, 436/533, 436/535, 436/806, 436/518, 204/403, 204/418, 204/291, 204/292, 204/153.12, 204/290, 204/415, 204/416, 422/82.01, 422/82.03, 205/777.5
• US Class Current: 435/287.9
• CPC Class Codes: C12Q 1/002 Electrode membranes
• CPC Class Codes: C12Q 1/005 involving specific analytes or enzymes including groups of enzymes, e.g. oxydases; C12Q1/004 takes precedence
• CPC Class Codes: G01N 33/543 with an insoluble carrier for immobilising immunochemicals
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property

Abstract

An electrochemical affinity assay system for detection of ligand—ligand receptor binding.

Claims

1. A method for detecting a second member of a ligand—

ligand receptor pair in a sample;

the method comprising;

contacting the sample with an electrode having immobilized thereon a first member of the ligand—

ligand receptor pair and with a third member that binds the second member to form a first member-second member-third member complex, wherein the first member is immobilized in a redox polymer and the third member is labeled with a detection marker;

applying a potential to the electrode, wherein the applied potential causes the detection marker-labeled first member-second member-third member complex to generate an electrical signal; and

correlating the generated electrical signal with the presence or amount of the second member in the sample.

2. The method according to claim 1, wherein the electrode further comprises an immobilized substrate generating enzyme, the substrate generating enzyme generating a detection compound.

3. The method according to claim 2, wherein the substrate generating enzyme is immobilized in the redox polymer.

4. The method according to claim 2, wherein the substrate generating enzyme comprises one or more reaction centers, and wherein the reaction centers do not exchange electrons with the electrode.

5. The method according to claim 3, wherein the substrate generating enzyme comprises one or more reaction centers, and wherein the reaction centers do not exchange electrons with the redox polymer.

6. The method according to claim 2, wherein the substrate generating enzyme comprises choline oxidase.

7. The method according to claim 3, wherein the substrate generating enzyme comprises choline oxidase.

8. The method according to claim 1, wherein the first member is immobilized in a film coating the electrode.

9. The method according to claim 8, wherein the film comprises a binding agent that binds the first member.

10. The method according to claim 1, wherein the first member is non-covalently bound to a film coating the electrode.

11. The method according to claim 9, wherein the binding agent covalently binds the first member.

12. The method according to claim 9, wherein the binding agent is avidin or streptavidin, and the first member is biotinylated.

13. The method according to claim 2, wherein the detection compound comprises hydrogen peroxide.

14. The method according to claim 1, wherein the detection marker comprises peroxidase.

15. The method according to claim 14, wherein the peroxidase is horseradish peroxidase or soybean peroxidase.

16. The method according to claim 1, wherein the potential applied to the electrode is not more reducing than −

0.0V versus the saturated calomel electrode (SCE) and not more oxidizing than +0.4V versus the saturated calomel electrode (SCE).

17. The method according to claim 1, wherein contacting further comprises the step of rotating the electrode within the sample.

18. The method according to claim 1, wherein the sample comprises blood.

19. A method for detecting a second member of a ligand—

ligand receptor pair in a sample;

the method comprising;

contacting the sample with a sensor wherein the sensor comprises;

an electrode;

a redox polymer film on the electrode;

a substrate generating enzyme on the electrode that generates a detection compound;

a first member of a ligand—

ligand receptor pair that binds the second member,

wherein the first member is immobilized in the redox polymer on the electrode;

and with a third member that binds the second member to form a first member-second member-third member complex, the third member labeled with a detection marker that reacts with the detection compound;

applying a potential to the electrode, wherein the applied potential causes the detection marker-labeled first member-second member-third member complex to generate and electrical signal; and

correlating the generated electrical signal with the presence or amount of the second member in the sample.

20. The method according to claim 19, wherein the substrate generating enzyme comprises one or more reaction centers, and wherein the reaction centers do not exchange electrons with the redox polymer.

21. The method according to claim 19, wherein the substrate generating enzyme is choline oxidase.

22. The method according to claim 19, wherein the redox polymer film on the electrode further comprises a binding agent that binds the first member.

23. The method according to claim 22, wherein the binding agent covalently binds the first member.

24. The method according to claim 22, wherein the binding agent non-covalently binds the first member.

25. The method according to claim 22, wherein the binding agent is avidin or streptavidin, and the first member is biotinylated.

26. The method according to claim 19, wherein the detection compound is hydrogen peroxide.

27. The method according to claim 26, wherein the detection marker is peroxidase.

28. The method according to claim 27, wherein the peroxidase is horseradish peroxidase or soybean peroxidase.

29. The method according to claim 19, wherein potential applied to the electrode is not more reducing than −

0.0V versus the saturated calomel electrode (SCE) and not more oxidizing than +0.4V versus the saturated calomel electrode (SCE).

30. The method according to claim 19, wherein the contacting further comprises rotating the electrode within the sample.

31. The method according to claim 19, wherein the sample comprises blood.

32. The method according to claim 19, wherein the first member of the ligand—

ligand receptor pair is an antigen and the second member of the ligand—

ligand receptor pair is an antibody.

33. The method according to claim 19 wherein the first member of the ligand—

ligand receptor pair is a growth factor receptor and the second member of the ligand—

ligand receptor pair is a growth factor.

34. The method according to claim 19, wherein the first member of the ligand—

ligand receptor pair and the second member of the ligand—

ligand receptor pair are complementary strands of nucleic acid.