Method for determining the concentration of sugar using an electrocatalytic sugar sensor

• US 4,366,033 A
• Filed: 04/11/1979
• Issued: 12/28/1982
• Est. Priority Date: 04/20/1978
• Status: Expired due to Term

• Current Assignee: Siemens AG
• Original Assignee: Siemens AG
• Inventors: Gebhardt, Ulrich, Luft, Gunter, Richter, Gerhard
• Primary Examiner(s): Kaplan, G. L.
• Application Number:
  US06/029,128
• Time in Patent Office: 1,357 Days
• Field of Search: 204/1 P, 204/1 E, 204/195 P, 204/195 B, 204/1 T, 128/635
• US Class Current: 205/782.5
• 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

A method for determining the concentration of sugar in the presence of interfering foreign substances, particularly for determining glucose in a body fluid, by means of an electrocatalytic sugar sensor which has a measuring electrode in which the measuring electrode is alternatingly set potentiostatically to a reactivation and a measuring potential and the current flowing during the measuring period is evaluated as the measurement signal. To prevent foreign substances from exerting an interfering influence and thereby permit a sensitive sugar determination which is reliable over an extended period of time, a hydrophilic diaphragm is arranged in front of the measuring electrode to impede the resupply of the interfering foreign substances to the measuring electrode so that a diffusion limit current adjusts itself during the reactivation phase in the oxidation of the foreign substances; and the current is evaluated with a time delay relative to the start of the measuring period.

Claims

1. A method for determining the concentration of sugar in the presence of interfering foreign substances, especially for determining glucose in a body fluid, by means of an electrocatalytic sugar sensor comprising a measuring electrode, the measuring electrode adapted to be alternatingly set potentiostatically to a reactivation potential and a measuring potential and the current flowing during the measuring period evaluated as the measurement signal, comprising impeding the resupply of the interfering substances to the measuring electrode by a hydrophilic diaphragm, of a thickness less than one hundred micrometers and a diffusion coefficient for glucose of less than 10^-7 cm² sec^-1, placed in front of the measuring electrode in such a manner that a diffusion limit current adjusts itself during the reactivation phase in the oxidation of the foreign substances, and performing the evaluation of the current after a time delay relative to the start of the measuring period.

2. The method according to claim 1, wherein the reaction charge is determined as the measurement signal by integrating the current in the measuring period.

3. The method according to claim 2, wherein the integration of the current is started after a delay of up to 10 sec.

4. The method according to claim 2 wherein, integration of current is started after a delay of about 2 seconds.

5. The method according to claim 1 wherein the measurement is made at a potential between 100 and 800 mV, relative to the potential of a reversible hydrogen electrode.

6. The method according to claim 5 wherein said measurement is made at a potential of about 400 mV, relative to the potential of a reversible hydrogen electrode.

7. The method according to claim 1, wherein the reactivation is performed at a potential above 800 mV, relative to the potential of a reversible hydrogen electrode.

8. The method according to claim 7 wherein said reactivation is performed at a potential equal to or above 1500 mV, relative to the potential of a reversible hydrogen electrode.

9. The method according to claim 1 wherein the measurement is made in a time of less than 1 min.

10. The method according claim 1 wherein the measuring period and the reactivation phase are chosen to be of about the same length.

11. The method according to claim 10, wherein the measurement and the reactivation are each executed in a time of about 25 sec.

12. The method according to claim 1 wherein, said hydrophilic diaphragm consists of hydrophilized polytetrafluoroethylene.

13. The method according to claim 1 wherein, said measuring electrode has an active layer which consists of activated platinum metal-iron metal alloy.