IP Library Granted Patent US 8,647,487
Granted Patent B2
US 8,647,487 · App. 13/025,203 · Granted Feb 11, 2014

System and methods for automatically recognizing a control solution

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Quick Facts
Patent No.
US 8,647,487
App. No.
13/025,203
Granted
Feb 11, 2014
Kind
B2
Abstract

Methods and devices for automatically distinguishing between a control solution and an actual patient/user sample in a biosensor are provided. The solution is introduced into an electrochemical cell having a working and counter electrode. Electric pulses are applied to the cell and resultant signals are measured. Based on a comparison of the measured signals, a meter can determine whether the sample is a control solution or an actual patient/user sample.

Claims (22)

1. A system for automatically distinguishing between a control solution having a known, predetermined concentration of an analyte and an actual patient/user sample in a biosensor comprising:

a sample reception region;

a reaction reagent system in said sample reception region comprising:

an oxidation-reduction enzyme specific for the analyte;

a first electron mediator capable of being reversibly reduced and oxidized; and

a second electron mediator, capable of being reversibly reduced and oxidized, wherein the second electron mediator has a redox potential different from that of the first mediator; and

a distinction system configured to detect the electro-chemical response signal produced by the reduction of the second electron mediator in order to identify a control solution.

2. The system of claim 1 , wherein the control solution comprises the second electron mediator.

3. The system of claim 1 , wherein the analyte is glucose.

4. The system of claim 1 , wherein the second electron mediator does not interfere with the measurement of the analyte.

5. The system of claim 1 , wherein the first electron mediator is a ruthenium containing material.

6. The system of claim 5 , wherein the ruthenium containing material comprises hexaamine (III) trichloride.

7. The system of claim 1 , wherein the second mediator is Ferrocene Dicarboxylic Acid.

8. The system of claim 1 , wherein the second mediator is Ferrocenecarboxylic Acid.

9. The system of claim 1 , wherein the second mediator is gentisic acid (2,5-dihydroxybenzoic acid).

10. The system of claim 1 , wherein the second mediator is 2,3,4-trihydroxybenzoic acid.

11. The system of claim 1 , wherein the second mediator is reduced in a potential range distinguishable from that of the first mediator.

12. The system of claim 1 , wherein the second electron mediator is reduced at a potential having a magnitude at least 0.2 volts greater or less than that used to oxidize or reduce the first electron mediator.

13. The system of claim 1 , wherein the distinction system comprises a meter configured to apply at least a first and a second electric pulse to the biosensor.

14. The system of claim 13 , wherein the distinction system is configured to measure at least a first and a second current signal generated in response to at least the first and the second applied electric pulses.

15. The system of claim 13 , wherein electric potentials of at least the first and the second applied electric pulses are of different magnitudes.

16. The system of claim 1 , wherein the distinction system is configured to measure a hematocrit level of the control solution or the actual patient/user sample.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Aug 29, 2025
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: TRIVIDIA HEALTH, INC.
Reel/Frame 072743/0697 →
CHANGE OF NAME Recorded Mar 4, 2016
From: NIPRO DIAGNOSTICS, INC.
To: TRIVIDIA HEALTH, INC.
Reel/Frame 038002/0867 →
SECURITY AGREEMENT Recorded Nov 5, 2013
From: NIPRO DIAGNOSTICS, INC.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 031580/0094 →