Method of electrochemical analysis of an analyte

• US 8,163,163 B2
• Filed: 11/10/2005
• Issued: 04/24/2012
• Est. Priority Date: 11/11/2004
• Status: Expired due to Fees

• Current Assignee: Vantix Holdings Limited
• Original Assignee: Sensortec Limited
• Inventors: Purvis, Duncan Ross
• Primary Examiner(s): Olsen, Kaj K
• Assistant Examiner(s): Thai, Susan
• Application Number:
  US11/718,746
• Publication Number:
  US 20080164154A1
• Time in Patent Office: 2,357 Days
• Field of Search: 205/81, 205/777.5, 205/779, 205/792, 204/229.8, 204/403.11, 204/403.1
• US Class Current: 205/792
• CPC Class Codes: C12Q 1/004 mediator-assisted
• CPC Class Codes: G01N 2458/30 Electrochemically active labels
• CPC Class Codes: G01N 27/3273 Devices therefor, e.g. test element readers, circuitry details not specific to biochemical electrodes G01N33/4875

Abstract

A method of electrochemical analysis using a sensor electrode specific for an analyte under test. The method comprises immersing the sensor electrode in a sample solution suspected of containing the analyte; forming an electrochemically active complex by exposure to solutions containing secondary receptors or competing molecules labelled with a charged or enzyme label; and subsequently exposing the sensor to an electrochemically active solution. The measurement step comprises driving the sensor electrode potential to a predetermined fixed potential by applying a current or activation waveform then monitoring the potential difference between the sensor electrode and a reference electrode following removal of the holding current. Current, rate and potential can all be measured and used to determine analyte concentration or sensor state.

Claims

1. A method of electrochemical detection of an analyte in a sample consisting of:

(a) providing a sensor electrode comprising an electrically conductive electrode coated with a layer of electroconductive polymer;

(b) contacting the sensor electrode with a solution comprising the sample to be tested for the presence of the analyte under conditions which permit formation of an electrochemically active analyte complex comprising the analyte and an electrochemically active label component on the electroconductive polymer layer;

(c) contacting the sensor electrode plus electrochemically active analyte complex with an electrochemically active measuring solution which promotes electrochemical activity of the electrochemically active analyte complex;

(d) applying a current to induce a pre-determined holding potential on the sensor electrode;

(e) removing the current thereby allowing the sensor electrode to return to an open circuit resting potential; and

(f) measuring one or more of the following parameters as an indicator of the amount of analyte present in the sample;

(i) the difference between the pre-determined holding potential and the open circuit resting potential,

(ii) the initial rate at which the sensor electrode returns from the pre-determined holding potential to the open circuit resting potential; and

(iii) the open circuit resting potential;

wherein optionally the sensor electrode plus electrochemically active anaylyte complex is washed prior to step (c).

2. The method according to claim 1 wherein in step (d) a constant current is applied such that the sensor electrode is held at a single pre-determined holding potential.

3. The method according to claim 1 wherein in step (d) the current is varied such that the sensor electrode is held at one or more different electrically induced potentials and/or open circuit potentials prior to the pre-determined holding potential.

4. The method according to claim 1,wherein step (c) is carried out by transferring the sensor electrode from the solution comprising the sample of step (b) to the measuring solution of step (c).

5. The method according to claim 1, wherein step (c) is carried out by adding an excess of the measuring solution of step (c) to the solution comprising the sample of step (b).

6. The method according to claim 1, wherein the electrochemically active label component of the electrochemically active analyte complex comprises an enzyme capable of converting a substrate to a product, the action of which directly affects the redox composition of the electroconductive polymer coating of the sensor electrode.

7. The method according to claim 6 wherein the enzyme is horseradish peroxidase, alkaline phosphatase, urease, catalase, or glucose oxidase.

8. The method according to claim 6 wherein the enzyme is capable of converting a substrate which has no detectable effect on the redox composition of the electroconductive polymer layer of the sensor electrode to a product which directly or indirectly affects the redox composition of the electroconductive polymer layer.

9. The method according to claim 6 wherein the enzyme is capable of converting a substrate which directly or indirectly affects the redox composition of the electroconductive polymer layer of the sensor electrode to a product which has no detectable effect on the redox composition of the electroconductive polymer layer.

10. The method according to claim 6 wherein the enzyme is capable of converting a substrate which has no detectable effect on the redox composition of the electroconductive polymer coating of the sensor electrode to a product which is a substrate for a second enzyme, the action of the second enzyme generating a second product the production of which directly or indirectly affects the redox composition of the electroconductive polymer coating of the sensor electrode.

11. The method according to claim 1, wherein the electrochemically active label component of the electrochemically active analyte complex comprises a charged label having the following properties:

a) it carries a net charge at the pH of the electrochemically active measuring solution of claim 1; and

b) the magnitude of this charge changes when a predetermined holding potential is induced at the sensor electrode, thereby charging the particle positively or negatively with respect to its preferred charge state.

12. The method according to claim 11 wherein the charged label is gold, ferrocene or latex microspheres.

13. The method according to claim 1 wherein the electroconductive polymer layer of the sensor electrode has immobilized therein or adsorbed thereto capture receptors which are capable of binding quantitatively to the desired analyte to be detected in the sample.

14. The method according to claim 13 wherein formation of the electrochemically active analyte complex in step (b) is carried out by:

(b1) contacting the sensor electrode with a solution comprising the sample so that the analyte binds to the immobilized or adsorbed capture receptors;

(b2) contacting the sensor electrode with a solution comprising secondary receptors capable of binding to the analyte at a site spatially distinct from the site of binding to the capture receptors, said secondary receptors being conjugated with the label component.

15. The method according to claim 13 wherein formation of the electrochemically active analyte complex in step (b) is carried out by:

(b1) contacting the sensor electrode with a solution comprising the sample so that the analyte binds to the immobilized or adsorbed capture receptors;

(b2) contacting the sensor electrode with a solution comprising competing molecules capable of binding to the capture receptors, said competing molecules being conjugated with the label component.

16. The method according to claim 14 wherein steps (b1) and (b2) are performed simultaneously by contacting the sensor electrode with a solution comprising the sample to which has been added secondary receptors or competing molecules conjugated with the label component.

17. The method according to claim 1, wherein the sample is milk, a food homogenate or a soil extract.

18. The method according to claim 1, wherein the sample is a biological fluid.

19. The method according to claim 18 wherein the biological fluid is whole blood, serum, lymph, urine, saliva, ascites, pleural effusion, cerebrospinal fluid or semen.