Method for electrochemical detection

• US 6,413,398 B1
• Filed: 09/13/1999
• Issued: 07/02/2002
• Est. Priority Date: 09/13/1999
• Status: Expired due to Fees

• Current Assignee: Her Majesty The Queen In Right of Canada As Represented By The Minister of National Defence
• Original Assignee: Her Majesty The Queen In Right of Canada As Represented By The Minister of National Defence
• Inventors: Baranski, Andrzej S., Gerhardt, Geoff Charles, Cassidy, Richard Murray
• Primary Examiner(s): Tung, T.
• Assistant Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US09/394,654
• Time in Patent Office: 1,023 Days
• Field of Search: 204/450, 204/451, 204/452, 204/402, 204/603, 205/775, 205/794.5
• US Class Current: 204/452
• CPC Class Codes: G01N 27/38 Cleaning of electrodes
• CPC Class Codes: G01N 27/4473 by electric means

Abstract

A method for electrochemical detection (ECD) is disclosed. The illustrated embodiments are particularly adapted to use in detection of analytes separated by capillary electrophoresis. The method is a voltammetric ECD, including a preparatory positive potential pulse, an optional stabilizing pulse at a negative potential, an analytical pulse at extreme negative potentials (e.g., −300 mV to −1,500 mV), and a positive cleaning potential pulse. The methods have been shown to detect analytes previously considered to be electrochemically inactive using more traditional electrochemical methods. Examples of such analytes include various drugs, antibiotics, and peptides.

Claims

1. A method for electrochemical detection of an analyte in a fluid, comprising;

providing a working electrode with a diameter of about 1 μ

m to 100 μ

m in association with the fluid;

applying a first positive potential pulse to the fluid at the working electrode, at a voltage of less than about 1,000 mV.

applying a negative analytical potential pulse to the fluid at the working electrode at a voltage between about 0 mV and −

2,000 mV; and

measuring the current flow through the working electrode during the analytical potential pulse.

2. The method of claim 1, wherein the fluid flows across the working electrode during the analytical potential pulse.

3. The method of claim 1, further comprising applying a second positive potential pulse to the fluid at a voltage higher than the first positive potential pulse and between about 700 mV and 3,000 mV.

4. The method of claim 1, wherein each of the first positive potential pulse and the analytical potential pulse are conducted for between about 1 ms and 100 ms.

5. The method of claim 1, wherein the first positive potential pulse and the negative analytical potential pulse are conducted in a single cycle, and the single cycle is repeated at greater than 5 Hz.

6. The method of claim 1, further comprising applying a negative stabilizing potential pulse after the first positive potential-analytical pulse to the working electrode at a voltage of about 0 mV to −

2,000, for about 1 to 100 ms.

7. The method of claim 1, wherein the analytical potential pulse comprises a scan across a range of negative potentials.

8. The method of claim 7, wherein the analytical potential pulse comprises a square waveform superimposed on a DC ramp.

9. The method of claim 7, wherein the analytical potential pulse comprises a scan across voltages within the range of between about −

500 mV and −

1,200 mV.

10. The method of claim 1, wherein the analytical potential pulse comprises a fixed potential at a voltage between about −

200 to −

2,000 mV.

11. The method of claim 1, wherein the working electrode has a diameter of less than about 100 μ

m.

12. The method of claim 11, wherein the working electrode has a diameter of less than about 50 μ

m.

13. The method of claim 1, wherein the working electrode comprises a metal.

14. The method of claim 13, wherein the working electrode is selected from the group consisting of platinum (Pt), palladium (Pd), gold (Au), ruthenium (Ru), rhodium (Rh), osmium (Os) and iridium (Ir).

15. The method of claim 1, wherein the analyte comprises an organic species.

16. The method of claim 15, wherein the analyte comprises a polypeptide.

17. The method of claim 15, wherein the analyte comprises a therapeutic agent or diagnostic substance employed in human or veterinary medicines.

18. The method of claim 15, wherein the analyte comprises a pesticide.

19. The method of claim 1, wherein the first positive potential pulse comprises a voltage less than about 800 mV.

20. The method of claim 19, wherein the first positive potential pulse comprises a voltage between about 300 mV and 600 mV.

21. The method of claim 20, wherein the first positive pulse is at a voltage of about 400 mV.

22. The method of claim 20, further comprising applying a second positive potential pulse to the fluid at a voltage higher than the first positive potential pulse and between about 800 mV to 2,000 mV.

23. The method of claim 1, wherein the fluid flows from a capillary electrophoresis separation system.

24. The method of claim 1, wherein applying the first positive potential pulse to the fluid comprises powering an auxiliary electrode immersed in a buffer solution, and wherein the fluid flows into the buffer solution.

25. A method for electrochemical detection of organic analytes, wherein one detection cycle comprises:

separating a sample of organic analytes using capillary electrophoresis;

providing the separated analytes in a flowing stream to a surface of a working electrode;

applying at least one positive potential pulse to the analytes at the working electrode for between about 1 ms and 100 ms; and

applying a negative analytical pulse to the working electrode at voltages between about −

300 mV and −

1,500 mV versus an Ag|AgCl electrode, for between about 1 ms to 100 ms; and

measuring current through the working electrode during the negative analytical pulse.

26. The method of claim 25, wherein the at least one positive potential comprises a pre-analytical preparatory pulse at between about 300 mV and 600 mV and a post-analytical cleaning pulse at between about 700 mV and 3,000 mV, each for between about 1 ms and 100 ms.

27. The method of claim 25, wherein the negative analytical pulse comprises a voltage scan from −

600 mV to −

1,100 mV.

28. The method of claim 25, further comprising applying a negative stabilizing potential pulse after the first positive potential-analytical pulse to the working electrode at a voltage of about 0 mV to −

2,000 mV versus an Ag|AgCl electrode, for about 1 to 100 ms.

29. The method of claim 25, wherein the sample has a concentration of analytes of less than about 10⁻

5 molar.

30. The method of claim 29, wherein the sample has a concentration of analytes of less than about 10⁻

7 molar.

31. An electrochemical detector, comprising electronic hardware and software controlling voltage applied to a sample fluid, the hardware and software configured to apply a voltage in repeated cycles of pulses where each cycle includes:

a positive electrode preparation pulse of a first magnitude;

a negative analytical pulse; and

a positive cleaning pulse of a second magnitude greater than the first magnitude.

32. The electrochemical detector of claim 31, configured such that each cycle further comprises a negative stabilizing pulse between the electrode preparation pulse and the analytical pulse.