SAMPLE CHARACTERIZATION BASED ON AC MEASUREMENT METHODS

• US 20110168575A1
• Filed: 01/08/2010
• Published: 07/14/2011
• Est. Priority Date: 01/08/2010
• Status: Abandoned Application

• Current Assignee: Roche Diabetes Care Inc. (Roche Holding AG)
• Original Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Inventors: Buck, Harvey B., Groll, Henning, Lica, Georgeta
• Application Number:
  US12/684,277
• Publication Number:
  US 20110168575A1
• Time in Patent Office: Days
• US Class Current: 205/782
• 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

One aspect concerns a technique for detecting analyte concentrations, such as glucose concentrations, in blood or other bodily fluids. This technique utilizes an electrochemical test strip that includes a mediator system that generates a linear faradic response at relatively low applied potential differences. An alternating current excitation signal is applied to blood in the test strip. The alternating current excitation signal includes a low frequency signal and a high frequency signal that has a higher frequency than the low frequency signal. The glucose concentration is determined by measuring a low frequency response to the low frequency signal, measuring a high frequency response to the high frequency signal, estimating the glucose concentration based on the low frequency response, and correcting the glucose concentration for one or more error-causing variables based on the high frequency response.

Claims

1. A method, comprising:

providing an electrochemical test strip with a mediator system that generates a linear faradic response at a low applied potential difference;

introducing blood to the mediator system and in contact with electrodes of the test strip;

applying an alternating current excitation signal as a potential difference between electrodes of the test strip and across the blood, wherein the alternating current excitation signal includes a low frequency signal and a high frequency signal that has a higher frequency than the low frequency signal; and

determining glucose concentration of the blood, wherein said determining glucose concentration includes

measuring a low frequency response to the low frequency signal,

measuring a high frequency response to the high frequency signal,

estimating the glucose concentration based on the low frequency response, and

correcting the glucose concentration for one or more error causing variables based on the high frequency response.

2. The method of claim 1, further comprising:

wherein the one or more error causing variables include hematocrit; and

wherein said correcting the glucose concentration includes correcting for the hematocrit based on the high frequency response.

3. The method of claim 2, further comprising:

wherein the one or more error causing variables include temperature; and

wherein said correcting the glucose concentration includes correcting for the temperature based on the high frequency response.

4. The method of claim 1, further comprising:

wherein the one or more error causing variables include temperature; and

wherein said correcting the glucose concentration includes correcting for the temperature based on the high frequency response.

5. The method of claim 1, wherein the high frequency signal and the low frequency signal have the same amplitude.

6. The method of claim 1, wherein the low frequency signal and the high frequency signal are applied at the same time.

7. The method of claim 1, further comprising superimposing the low frequency signal and the high frequency signal to create the alternating current excitation signal.

8. The method of claim 1, wherein the low frequency signal and the high frequency signal are applied sequentially.

9. The method of claim 1, wherein the alternating current excitation signal in one variation includes a waveform comprising at least six frequencies

10. The method of claim 1, wherein said determining the glucose concentration includes measuring cell impedance at multiple frequencies by sweeping from the high frequency signal to the low frequency signal.

11. The method of claim 1, wherein said determining the glucose concentration includes measuring cell impedance at multiple frequencies by sweeping from the low frequency signal to the high frequency signal.

12. The method of claim 1, wherein said determining the glucose concentration includes

applying the high frequency signal until no significant change in impedance is observed in the high frequency response;

observing no significant change in the impedance of the high frequency response; and

applying the low frequency signal after said observing no significant change in the impedance of the high frequency response.

13. The method of claim 1, wherein the alternating current excitation signal is selected from a range of 1 Hz to 20,000 Hz.

14. The method of claim 1, wherein the alternating current excitation signal has a potential of at most 12 mV RMS.

15. The method of claim 1, wherein the low frequency signal is at most 2000 Hz

16. The method of claim 1, wherein the low frequency signal is selected from a range of 1000 Hz to 2000 Hz.

17. The method of claim 1, wherein the low frequency signal is selected from a range of 100 Hz to 1000 Hz.

18. The method of claim 1, wherein the high frequency signal is at least 2000 Hz.

19. The method of claim 1, wherein said measuring the low frequency response includes measuring phase angle, magnitude, resistance, capacitance, and/or impedance.

20. The method of claim 1, wherein said measuring the high frequency response includes measuring phase angle, magnitude, resistance, capacitance, and/or impedance.

21. The method of claim 1, wherein said determining the glucose concentration includes fitting the low frequency response and the high frequency response to an equivalent circuit.

22. The method of claim 1, wherein the mediator includes a single mediator type system.

23. The method of claim 1, wherein the mediator includes a dual mediator type system.

24. The method of claim 1, further comprising:

wherein a blood glucose meter performs said determining the glucose concentration; and

displaying the glucose concentration on the blood glucose meter.