Method and apparatus for assay of electrochemical properties

• US 20100078335A1
• Filed: 10/09/2009
• Published: 04/01/2010
• Est. Priority Date: 02/10/2002
• 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: Harding, Ian S., Iyengar, Sridhar G.
• Granted Patent: US 8,293,094 B2
• Time in Patent Office: Days
• US Class Current: 205/782
• CPC Class Codes: A61B 2562/04 Arrangements of multiple sensors of the same type
• CPC Class Codes: A61B 5/1468 using chemical or electrochemical methods, e.g. by polarographic means A61B5/1486 takes precedence
• CPC Class Codes: A61B 5/1473 invasive, e.g. introduced into the body by a catheter A61B5/1482 takes precedence
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes
• CPC Class Codes: A61B 5/7203 for noise prevention, reduction or removal
• CPC Class Codes: G01N 17/02 Electrochemical measuring systems for weathering, corrosion or corrosion-protection measurement
• CPC Class Codes: G01N 27/26 by investigating electrochemical variables; by using electrolysis or electrophoresis
• CPC Class Codes: G01N 27/3273 Devices therefor, e.g. test element readers, circuitry details not specific to biochemical electrodes G01N33/4875
• 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

A method for monitoring a select analyte in a sample in an electrochemical system. The method includes applying to the electrochemical system a time-varying potential superimposed on a DC potential to generate a signal; and discerning from the signal a contribution from the select analyte by resolving an estimation equation based on a Faradaic signal component and a nonfaradaic signal component.

Claims

1-45. -45. (canceled)

46. A method for determining effective electrode area in an electrochemical test cell containing a liquid sample, wherein the electrochemical test cell comprises two electrodes and the effective electrode area is the area of the electrodes that is in contact with the liquid sample, said method comprising the steps of:

(a) applying a potential stimulus to the electrodes to generate a current signal, wherein the potential stimulus comprises a time-varying potential component superimposed on a constant potential component;

(b) isolating from the current signal a time-varying current component;

(c) determining the phase angle of the time-varying current component relative to the to time-varying potential component,

(d) using the phase angle to separate the time-varying current component into a real part and an imaginary part, the magnitude of the imaginary part being related to the effective electrode area; and

(e) determining electrode area from the determined magnitude of the imaginary part of the time-varying current component.

47. The method of claim 46, wherein the time-varying potential has a sinusoidal waveform.

48. The method of claim 47, wherein the time-varying waveform has a peak-to-peak amplitude of less than 50 mV.

49. A method for estimating an analyte concentration in a liquid sample comprising the steps of:

(a) introducing the liquid sample to an electrochemical test cell, wherein the electrochemical test cell comprises two electrodes, each having a surface that makes contact with the liquid sample, said electrodes surfaces having a surface area, A_{e, expected}, that is in contact with the liquid sample when the test cell is full,

(b) determining an initial value for the amount of analyte in the sample,

(c) determining the area of the electrodes that is actually in contact with the liquid sample by;

(i) applying a potential stimulus to the electrodes to generate a current signal, wherein the potential stimulus comprises a time-varying potential component superimposed on a constant potential component;

(ii) isolating from the current signal a time-varying current component;

(iii) determining the phase angle of the time-varying current component relative to the to time-varying potential component,

(iv) using the phase angle to separate the time-varying current component into a real part and an imaginary part, the magnitude of the imaginary part being related to the effective electrode area; and

(v) determining an actual electrode area, A_{e, actual}, from the determined magnitude of the imaginary part of the time-varying current component; and

(d) correcting the initial value to take into the difference between A_e,expected and A_{e, actual} to arrive at an estimate of analyte concentration in the sample.

50. The method of claim 49, wherein in the correction step, the initial value is multiplied by (A_{e, expected}/A_{e, actual}).

51. The method of claim 49, wherein the initial value is determined by coulometry.

52. The method of claim 49, wherein the initial value is determined by amperometry.

53. The method of claim 49, wherein the electrochemical test cell contains a mediator species.

54. The method of claim 53, wherein the mediator species is a ferrocene/ferrocenium couple.

55. The method of claim 53, wherein the mediator species is a ferrocyanide/ferricyanide couple.

56. The method of claim 53, wherein the analyte is glucose.

57. The method of claim 56, wherein the mediator species is a ferrocene/ferrocenium couple.

58. The method of claim 56, wherein the mediator species is a ferrocyanide/ferricyanide couple.