Method and apparatus for processing electrochemical signals

• US 7,090,764 B2
• Filed: 01/15/2003
• Issued: 08/15/2006
• Est. Priority Date: 01/15/2002
• Status: Active Grant

• Current Assignee: Agamatrix Incorporated (AgaMatrix Holdings LLC d/b/a WaveForm Diabetes)
• Original Assignee: Agamatrix Incorporated (AgaMatrix Holdings LLC d/b/a WaveForm Diabetes)
• Inventors: Iyengar, Sridhar G., Haas, Daniel, Bolon, Craig
• Primary Examiner(s): Noguerola, Alex
• Application Number:
  US10/342,794
• Publication Number:
  US 20030178322A1
• Time in Patent Office: 1,308 Days
• Field of Search: 2044034-40315, 204416-419, 204/433, 204/431, 205/775, 205/777.5, 205/778, 205/778.5, 205/779, 205/787, 205/787.5, 205/789, 205/789.5, 205/790.5, 205/791, 205/792, 205/793.5, 205/794, 702/19, 702/22, 702/23
• US Class Current: 205/775
• CPC Class Codes: G01N 27/3274 Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration coding of calibration information G01N33/48771

Abstract

Systems and methods are provided herein for improving the selectivity and productivity of sensors via digital signal processing techniques. According to one illustrative embodiment, in an electrochemical method for monitoring of a select analyte in a mixed sample with an interfering analyte, an improvement is provided that includes applying a large amplitude potential stimulus waveform to the sample to generate a nonlinear current signal; and resolving a signal contribution from the select analyte in the generated signal by a vector projection method with an analyte vector comprising a plurality of real and imaginary parts of one or more Fourier coefficients at one or more frequencies of a reference current signal for the select analyte.

Claims

1. In an electrochemical method for monitoring of a select analyte in a mixed sample with an interfering analyte, the improvement comprising:

applying a large amplitude potential stimulus waveform to the sample to generate a nonlinear current signal; and

resolving a signal contribution from the select analyte in the generated signal by a vector projection method with an analyte vector comprising a plurality of real and imaginary parts of one or more Fourier coefficients at one or more frequencies of a reference current signal for the select analyte.

2. An electrochemical method of determining concentration of a select analyte in a mixed sample with an interfering analyte, comprising:

applying a large amplitude potential stimulus waveform to the sample to generate a nonlinear current signal;

measuring the generated signal;

computing at least one parameter of all or some portion of the generated signal; and

determining a concentration of the select analyte in the mixed sample by resolving an estimation equation based on analyte vectors for each of the select and interfering analytes and the at least one parameter.

3. The method of claim 2, wherein the estimation equation is based on analyte vectors at one frequency.

4. The method of claim 2, wherein the estimation equation is based on analyte vectors at multiple frequencies.

5. The method of claim 2, wherein one or both of the analyte vectors and the at least one parameter are weighted.

6. The method of claim 2, wherein the analyte vectors are comprised of the at least one parameter and relate to different portions of the stimulus waveform and/or generated signal.

7. The method of claim 2, wherein the analyte vectors are comprised of the at least one parameter and relate to at least one of a non-periodic portion and a DC portion of the stimulus waveform and/or generated signal.

8. The method of claim 2, wherein the estimation equation is based on a plurality of the at least one parameter selected from the group consisting of:

one or more real or imaginary parts of a Fourier coefficient at one or more frequencies;

one or more weighted real or imaginary parts of a Fourier coefficient at one or more frequencies;

one or more portions of the stimulus waveform and/or generated signal;

one or more periodic portions of the stimulus waveform and/or generated signal;

one or more non-periodic portions of the stimulus waveform and/or generated signal; and

one or more DC portions of the stimulus waveform and/or generated signal.

9. The method of claim 2, wherein the estimation equation is based on a select number of the at least one parameter to balance performance and robustness.

10. The method of claim 2, wherein the select analyte is glucose.

11. The method of claim 10, wherein the interfering analyte is ascorbic acid.

12. An apparatus comprising:

a potentiostat circuit for applying a voltage waveform to and detecting a resulting current from an electrode system;

at least one memory having program instructions and a processor configured to execute the program instructions to perform the operations of;

applying a large amplitude potential stimulus waveform to the sample to generate a nonlinear current signal;

measuring the generated signal;

computing at least one Fourier coefficient of a desired frequency component of all or some portion of the generated signal; and

determining a concentration of the select analyte in the mixed sample by use of the at least one Fourier coefficient to resolve an estimation equation based on analyte vectors for each of the select and interfering analytes.

13. A method of constructing an estimation equation for monitoring a select analyte in a mixed sample with an interfering analyte, the method comprising:

selecting a large amplitude potential stimulus waveform to generate a nonlinear current signal When applied to the sample;

applying the waveform to samples containing multiple different concentrations of each of the select and interfering analytes alone, and measuring the resulting reference current signals;

computing values of real and imaginary parts of a Fourier transform for each of the reference current signals;

plotting the real and imaginary values of a Fourier coefficient of the Fourier transform at each of a multiple number of frequencies;

selecting one of the multiple frequencies at which the real and imaginary parts exhibit a relatively larger difference in phase angle;

computing analyte vectors for each of the select and interfering analytes at the selected one frequency; and

constructing the estimation equation based on the analyte vectors and calibration information that relates a concentration of the respective analyte in the sample to a length of the respective analyte vector in a complex plane.

14. The method of claim 13, wherein the waveform is selected based on theoretical and/or experimental factors.

15. The method of claim 14, wherein the factors reflect one or more of reaction kinetics, reaction mechanism and transport properties of the select and/or interfering analyte.

16. The method of claim 13, wherein the waveform is selected based on cyclic voltammetry to determine a potential at which the select and/or interfering analyte will oxidize or reduce.

17. The method of claim 13, wherein the waveform has a greater than 50 mV variation.

18. The method of claim 13, wherein the waveform or some portion of the waveform has a selected rate of variation based on one or more of a reaction kinetics, reaction mechanism and transport properties involving the select and/or interfering analyte.

19. The method of claim 13, wherein the waveform is selected to generate a Faradaic current signal arising from an electrochemical reaction of the select and/or interfering analyte.

20. An electrochemical method of determining concentration of a select analyte in a mixed sample with an interfering analyte, comprising:

applying a stimulus waveform to the sample to generate a nonlinear signal;

measuring the generated signal;

computing at least one parameter of all or some portion of the generated signal; and

determining a concentration of the select analyte in the mixed sample by resolving an estimation equation based on analyte vectors for each of the select and interfering analytes and the at least one parameter, wherein the at least one parameter is a frequency-domain parameter and/or a time-domain parameter.

21. The method of claim 20, wherein, the at least one parameter and/or analyte vectors are weighted.

22. The method of claim 20, wherein the stimulus waveform is a potential or a current waveform.

23. The method of claim 20, wherein the analyte vectors and the at least one parameter relate to different portions of the generated signal and/or stimulus waveform.

24. The method of claim 20, wherein the at least one parameter includes one or more of:

values of the generated signal and/or stimulus waveform (hereinafter “

the signal”

) at some point in time;

computed functions of all or some portion of the signal, including one or more of;

slope of the signal at a point or slope of some portion of the signal;

decay rate over some portion of the signal;

rise rate over some portion of the signal;

average value of some portion of the signal;

frequency transform of all or some portion of the signal;

logarithm of some portion of the signal;

some root of some portion of the signal;

some portion of the signal raised to some power;

time elapsed between two specified points in the signal;

combinations of the parameters, including one or more of;

decay rate of the signal during some interval of time divided by the average value of the signal during this interval;

difference in value of the signal between two specified points; and

difference in slopes of the signal between two different portions of the signal.

25. The method of claim 20, wherein the analytes are one or more of:

glucose, an enzyme, hydrogen peroxide, a mediator, ferricyanide, ferrocene, ferrocyanide, ascorbic acid, uric acid, acetaminophen, and dopamine.

26. The method of claim 20, wherein the method includes monitoring multiple analytes.

27. The method of claim 20, wherein the applied waveform and generated signal are implemented with a galvanostat circuit or a potentiostat circuit.

28. The method of claim 20, wherein the at least one parameter is selected based on one or more of:

separation of the analyte vectors;

noise in the generated signal; and

sensitivity of the generated signal at the analyte concentration.

29. The method of claim 20, wherein the estimator equation is further based on calibration information.

30. The method of claim 20, wherein the at least one parameter is selected based on one or more of:

cyclic voltammetry;

linear sweep voltammetry;

square voltammetry;

AC polarography; and

AC impedance spectroscopy.

31. The method of claim 20, wherein the stimulus waveform is a current and the generated signal is a potential.

32. The method of claim 20, wherein the estimation equation is a linear estimator.

33. The method of claim 20, wherein the estimation equation is selected based on an estimation error determined by one or more of root mean squared (RMS), adjusted RMS, variance and standard deviation.

34. The method of claim 20, wherein the interfering analyte contributes a capacitive current to the generated signal.

35. The method of claim 20, wherein the stimulus waveform is applied to one or multiple electrodes.

36. An electrochemical method of determining concentration of a select analyte in a mixed sample with an interfering analyte, comprising:

applying a stimulus waveform to the sample to generate a nonlinear signal;

measuring the generated signal;

computing at least one parameter of all or some portion of the generated signal; and

determining a concentration of the select analyte in the mixed sample by resolving an estimation equation based on analyte vectors for each of the select and interfering analytes and the at least one parameter, wherein the stimulus waveform is a current and the generated signal is a potential.