Electrochemical sensor and method for continuous analyte monitoring

• US 7,731,835 B2
• Filed: 01/19/2005
• Issued: 06/08/2010
• Est. Priority Date: 09/20/1999
• Status: Expired due to Fees

• Current Assignee: Roche Diabetes Care Inc. (Roche Holding AG)
• Original Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Inventors: Essenpreis, Matthias, Buck, Harvey B.
• Primary Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US11/038,970
• Publication Number:
  US 20050211572A1
• Time in Patent Office: 1,966 Days
• Field of Search: 20440301-40315, 205/777.5, 205/778, 205/792
• US Class Current: 205/792
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1486 using enzyme electrodes, e.g. with immobilised oxidase
• CPC Class Codes: C12Q 1/001 Enzyme electrodes
• CPC Class Codes: C12Q 1/004 mediator-assisted
• CPC Class Codes: C12Q 1/006 for glucose

Abstract

Sensors and a method for detecting an analyte are described. Sensors each have a volume of a hydrophilic medium that retains an amount of analyte proportionate to the concentration of analyte in a biological fluid, electrodes and a redox enzyme in contact with medium, and an electron transfer mediator. The fluid contacts sensors and at initially predetermined intervals intermittently applies a potential to electrode sufficient to oxidize the mediator and sensing current through electrode as a function of the duration of the applied potential. The applied mediator oxidizing applied potential is maintained for a period of time sufficient to determine the rate of change of current with time through electrode. The current flow is correlated with the current flow for known concentrations of the analyte in medium.

Claims

1. A method for monitoring analyte concentration in a biological fluid by use of a sensor, the method comprising the steps of:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte proportionate to the concentration of analyte in a biological fluid in contact with the sensor, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and a covalently bound electron transfer mediator that shifts between oxidized and reduced states for facilitating transfer of electrons between the enzyme and the electrode, the enzyme substantially not capable of transferring electrons to or from components of the biological fluid other than said analyte,

contacting the biological fluid with the sensor and at initially predetermined intervals intermittently applying a potential to the electrode sufficient to oxidize the electron mediator and sensing current through said electrode during the application of the mediator oxidizing potential,

maintaining the applied mediator oxidizing potential at least for a period of time sufficient to determine the rate of change of current with time through the electrode,

correlating the current flow resulting from the applied mediator oxidizing potential with the current flow for known concentrations of said analyte in the retention medium, and

between the intermittent applications of the mediator oxidizing potential, removing the applied mediator oxidizing potential from the electrode to stop oxidation of the mediator.

2. The method of claim 1 wherein the intervals between the intermittent applied mediator oxidizing potentials are less than the time necessary for the concentration of the analyte in the retention volume to equilibrate with that in the biological fluids in contact with the enclosure.

3. The method of claim 1 further comprising the step of applying a reducing potential to the electrode sufficient to reduce the oxidized form of the electron mediator.

4. The method of claim 1, further comprising retaining the redox enzyme and the mediator in the analyte retention volume by covalently bonding the redox enzyme to a polymer component of a hydrophilic medium.

5. The method of claim 1, further comprising retaining the redox enzyme and the mediator in the analyte retention volume by forming a diffusion-limiting analyte permeable membrane over the electrode.

6. The method of claim 1, wherein the predetermined intervals of intermittently applying a potential to the electrode sufficient to oxidize the electron mediator are of varying duration.

7. A method for monitoring analyte concentration in a biological fluid by use of a sensor, the method comprising the steps of:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte proportionate to the concentration of analyte in a biological fluid in contact with the sensor, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and an electron transfer mediator for facilitating transfer of electrons between the enzyme and the electrode, the enzyme substantially not capable of transferring electrons to or from components of the biological fluid other than said analyte,

contacting the biological fluid with the sensor and at initially predetermined intervals intermittently applying a potential to the electrode sufficient to oxidize the electron mediator and sensing current through said electrode as a function of the duration of the applied potential,

maintaining the applied mediator oxidizing applied potential at least for a period of time sufficient to determine the rate of change of current with time through the electrode, and

correlating the current flow with the current flow for known concentrations of said analyte in the retention medium,

wherein the sensor additionally comprises at least a reference electrode and an auxiliary electrode and the method further comprises the steps of;

intermittently establishing predetermined level of current to flow between said working electrode and said auxiliary electrode at initially predetermined intervals, and measuring the potential difference between said working electrode and the reference electrode to establish said level of current flow,

maintaining said level of current flow at least for a period of time sufficient to determine the rate of change of potential necessary to maintain said current through said electrode with time, and

correlating said potential with the potential for known concentrations of said analyte in the biological fluid.

8. The method of claim 7 wherein the intervals between the intermittent potential measurements are less than the time necessary for the concentration of the analyte in the retention volume to equilibrate with that in the biological fluids in contact with the enclosure.

9. The method of claim 8 wherein the intervals are increased incrementally and the concentration of the analyte in the biological fluid is determined as a function of the rate of increase in analyte concentration in the retention volume.

10. A method for monitoring analyte concentration in a biological fluid by use of a sensor, the method comprising the steps of:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte proportionate to the concentration of analyte in a biological fluid in contact with the sensor, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and an electron transfer mediator for facilitating transfer of electrons between the enzyme and the electrode, the enzyme substantially not capable of transferring electrons to or from components of the biological fluid other than said analyte,

contacting the biological fluid with the sensor and at initially predetermined intervals intermittently applying a potential to the electrode sufficient to oxidize the electron mediator and sensing current through said electrode as a function of the duration of the applied potential,

retaining the redox enzyme and the mediator in the analyte retention volume by covalently bonding the mediator and the redox enzyme to the enclosure,

maintaining the applied mediator oxidizing potential at least for a period of time sufficient to determine the rate of change of current with time through the electrode, and

correlating the current flow with the current flow for known concentrations of said analyte in the retention medium.

11. A method for monitoring analyte concentration in a biological fluid, comprising:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte in a biological fluid, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and an electron transfer mediator for facilitating transfer of electrons between the enzyme and the electrode, the enzyme substantially not capable of transferring electrons to or from components of the biological fluid other than said analyte;

contacting the biological fluid with the sensor and allowing an analyte of the biological fluid to diffuse into the analyte retention volume;

varying the potential of the electrode over time from a mediator oxidizing potential sufficient to oxidize the electron mediator, to a potential at which no oxidation of the mediator occurs, to a reduction potential at which reduction of the mediator takes place;

maintaining the mediator oxidizing applied potential at least for a period of time sufficient to determine the rate of change of current with time through the electrode; and

sensing current through said electrode during application of the mediator oxidizing potential and correlating the sensed current with concentration of said analyte in the retention volume.

12. The method of claim 11, wherein at least one of the mediator oxidizing potential and the reduction potential is applied in pulses of varying pulse width.

13. The method of claim 11, wherein at least one of the mediator oxidizing potential and the reduction potential is applied in pulses and the intervals between pulses have varying durations.

14. A method for monitoring analyte concentration in a biological fluid, comprising:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte in a biological fluid, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and a covalently bound electron transfer mediator that shifts between oxidized and reduced states for facilitating transfer of electrons between the enzyme and the electrode, the enzyme substantially not capable of transferring electrons to or from components of the biological fluid other than said analyte;

contacting the biological fluid with the sensor and allowing an analyte of the biological fluid to diffuse into the analyte retention volume;

applying in pulses of varying width a mediator oxidizing potential sufficient to oxidize the electron mediator to a potential at which no oxidation of the mediator occurs;

maintaining the duration of the pulses of applied mediator oxidizing potential for a period of time sufficient to determine the rate of change of current with time through the electrode; and

sensing current through said electrode during application of the mediator oxidizing potential and correlating the sensed current with concentration of said analyte in the retention volume.

15. The method of claim 14, further comprising applying a reduction potential to the electrode sufficient to reduce the oxidized form of the electron mediator.

16. The method of claim 14, further comprising varying the duration of the intervals between the pulses of mediator oxidizing potential.

17. A method for monitoring analyte concentration in a biological fluid, comprising:

providing a sensor comprising a volume of a hydrophilic medium for retaining an amount of analyte in a biological fluid, an enclosure for said analyte retention volume, an electrode in contact with the hydrophilic medium, a redox enzyme in contact with the medium, and a covalently bound electron transfer mediator that shifts between oxidized and reduced states for facilitating transfer of electrons between the enzyme and the electrode;

contacting the biological fluid with the sensor and allowing an analyte of the biological fluid to diffuse into the analyte retention volume;

intermittently varying the potential of the electrode over time from a first potential at which no oxidation of the mediator takes place, to a second potential at which oxidation of the electron mediator takes place, to a third potential at which no oxidation of the mediator takes place;

maintaining the second potential at least for a period of time sufficient to determine the rate of change of current with time through the electrode; and

sensing current through said electrode during application of the second potential and correlating the sensed current with concentration of said analyte in the retention volume.

18. The method of claim 17, wherein the first and third potentials are different.

19. The method claim 17, wherein at least one of the first, second and third potentials is applied in pulses of varying pulse width.

20. The method of claim 17, wherein at least one of the first, second and third potentials is applied in pulses and the intervals between pulses have varying durations.

21. The method of claim 17, wherein one of the first and third potentials is zero.

22. The method of claim 17, wherein the first and third potentials are the same.

23. The method claim 17, wherein one of the first and third potentials is sufficient to reduce the oxidized form of the electron mediator.

24. The method of claim 17, further comprising retaining the redox enzyme and the mediator in the analyte retention volume by entrapping the redox enzyme and mediator in a hydrophilic matrix on the electrode.

25. The method of claim 17, further comprising retaining the redox enzyme and mediator in the analyte retention volume.

26. The method of claim 25, further comprising covalently bonding the redox enzyme to a polymer component of a hydrophilic medium.

27. The method of claim 17, further comprising retaining the redox enzyme and the mediator in the analyte retention volume by forming a diffusion-limiting analyte permeable membrane over the electrode.