Method and apparatus for assay of electrochemical properties
View Patent ↗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.
1. A method for determining the extent of electrode fouling in an implantable electrochemical sensor comprising at least two electrodes, the extent of electrode fouling being determined from effective electrode area, said method comprising:
applying a potential stimulus to the electrodes to generate a current signal having a time-varying component, the potential stimulus comprising a time-varying potential component superimposed on a constant potential component;
using the time-varying component of the generated current signal to determine capacitive signal information; and
using the capacitive signal information to correct for measurement errors arising from variations in effective electrode area.
2. The method of claim 1 , wherein the effective electrode area changes as a result of electrode fouling.
3. The method of claim 2 , wherein the measured extent of electrode fouling is used to adjust the measured current signal and correct for signal distortion caused by electrode fouling.
4. The method of claim 3 , wherein the adjustment corrects for a decrease in signal intensity due to fouling.
5. The method of claim 1 , wherein the measured effective electrode area is used to adjust the computation of concentration of an analyte and correct for signal distortion caused by changes in effective electrode area.
6. The method of claim 5 , wherein the adjustment is based on relative changes from initial analyte estimates.
7. The method of claim 5 , wherein the adjustment is based on reference to an external data source.
8. The method of claim 7 , wherein the external data source comprises calibration curves from calibration data gathered from electrodes having different electrode areas.
9. The method of claim 8 , wherein the calibration curves are constructed from samples containing multiple different concentrations of ferrocyanide.
10. The method of claim 9 , wherein the calibration curves are constructed from electrodes having different effective electrode areas.
11. The method of claim 1 , wherein the applied potential stimulus is a high frequency small amplitude sine wave superimposed on a DC potential.
12. The method of claim 11 , wherein the high frequency small amplitude sine wave has a peak-to-peak amplitude below 50 MV and a frequency above 100 Hz.
13. The method of claim 11 , wherein the high frequency small amplitude sine wave is sufficient to generate a current.
14. The method of claim 11 , wherein the frequency of the high frequency small amplitude sine wave is stepped through a range of frequencies to probe the spectral characteristics of the electrochemical system over a spectral range.
15. The method of claim 11 , wherein using capacitive signal information comprises obtaining a current signal from the high frequency small amplitude sine wave.
16. The method of claim 1 , wherein using capacitive signal information comprises taking the Fourier Transform of the resulting current signal.
17. The method of claim 1 , wherein using capacitive signal information comprises
determining an imaginary part of a time-varying current component from a resulting signal, and
computing the effective electrode area using the equation I i,AC =(818.26)(A e,actual )−14.33, where I i,AC is the imaginary component of the AC current at 1000 Hz and A e,actual is the actual effective electrode area.