Methods and devices for use in analyte concentration determination assays

• US 20040219624A1
• Filed: 05/28/2004
• Published: 11/04/2004
• Est. Priority Date: 08/01/2001
• Status: Abandoned Application

• Current Assignee: Lifescan Incorporated (Duv Holding Corporation)
• Original Assignee: Lifescan Incorporated (Duv Holding Corporation)
• Inventors: Teodorcyzk, Maria, OʼHara, Timothy James, Shah, Mahesh
• Application Number:
  US10/857,795
• Publication Number:
  US 20040219624A1
• Time in Patent Office: Days
• US Class Current: 435/14
• CPC Class Codes: G01N 27/3274 Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration coding of calibration information G01N33/48771
• CPC Class Codes: G01N 33/521 Single-layer analytical elements
• CPC Class Codes: Y10T 436/144444 Glucose

Abstract

Methods and devices are provided for use in the determination of the concentration of an analyte in a sample. In the subject methods, a sample is introduced to a reagent test strip, where the sample is either a test fluid or a control fluid, where the control fluid is free of a mediator dissolution slowing component and an oxidizing agent when used with an electrochemical analyte concentration determination assay. The concentration of analyte in the sample is determined and the sample is identified as a control fluid or a test fluid. Also provided are devices for determining the concentration of an analyte in a sample, where the devices have a sample identification element for identifying whether a sample is a control or a test fluid. The subject methods and devices find use in a variety of different applications, particularly in the determination of blood glucose concentrations.

Claims

1-25. -25. (Cancelled)

26. A method for determining the concentration of an analyte in a sample, the method comprising:

providing a system comprising a reagent test strip having a sample receiving region and an electrochemical meter for detenmining the analyte concentration in a sample introduced to the sample receiving region;

introducing a sample to the sample receiving region, wherein the sample is selected from the group consisting of a control fluid and a test fluid, wherein the control fluid is free of a mediator dissolution slowing component and an oxidizing agent;

measuring a signal produced by the sample with the meter;

comparing the value of the measured signal to a reference value;

based on the comparison, identifying whether the sample is a control fluid or a test fluid, wherein the measured signal produced by the control fluid is less than the reference value and the measured signal produced by the test fluid is greater than the reference value; and

determining the concentration of analyte in the sample.

27. The method of claim 26, wherein the sample is determined to be a control fluid or a test fluid in less than about 1 second from the time of sample introduction.

28. The method of claim 26, wherein the measured signal is a current signal and the reference value is from about 1 μ

A and about 15 μ

A.

29. The method of claim 26, further comprising:

storing the determined analyte concentration measurement and the identified sample type in a memory element of the meter.

30. The method of claim 29, further comprising:

calculating an average value of the analyte concentration values of test fluids stored over a pre-determined period of time, whereby the average value of the analyte concentration values of test fluids does not include analyte concentration values of control fluids.

31. The method of claim 26, wherein said analyte is glucose.

32. The method of claim 26, wherein said test sample is whole blood.

33. The method of claim 26, wherein the reagent test strip comprises a reference electrode and a working electrode having an arrangement such that a conductive portion of the reference electrode and a conductive portion of the working electrode face each other.

34. The method of claim 33, wherein the reagent test strip further comprises a spacer positioned between the working electrode and the reference electrode.

35. The method of claim 34, wherein the spacer has a thickness which causes the reference electrode and the working electrode to be spaced apart by about 50 microns to about 125 microns.

36. The method of claim 33, wherein a redox reagent is deposed on the working electrode.

37. The method of claim 36, wherein the redox reagent comprises a redox couple.