Unitary multiple electrode sensor

• US 5,066,372 A
• Filed: 06/21/1990
• Issued: 11/19/1991
• Est. Priority Date: 05/02/1986
• Status: Expired due to Fees

• Current Assignee: CIBA Vision Corporation (Novartis Ag)
• Original Assignee: CIBA Vision Corporation (Novartis Ag)
• Inventors: Weetall, Howard H.
• Primary Examiner(s): TUNG, TA HSUNG
• Application Number:
  US07/541,566
• Time in Patent Office: 516 Days
• Field of Search: 204/153.1, 204/153.12, 204/412, 204/415, 204/403, 204/416-419, 435/7, 435/14, 435/25, 435/817, 436/518, 436/532, 436/535, 436/806
• US Class Current: 506/4
• CPC Class Codes: G01N 27/3271 Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood amperometry per se G01N27/49; aspects concerning the enzyme reagent C12Q1/001
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property

Abstract

A unitary multiple electrode sensor for detecting analytes in test samples and devices for using them. The unitary multiple electrode sensor includes a sensor support member and at least one electrode array being deposited on the sensor support member, the electrode array having sensor-activating chemical(s) attached to an embodient thereof. A test sample is applied to the electrode array to begin the test; and a sensor apparatus measures the test reaction which is occurring on the electrode array.

Claims

1. A method for detection of an analyte in test sample on a unitary electrochemical sensor, the method comprising:

(a) applying a test sample onto a unitary electrochemical sensor, said sensor comprising;

(i) a sensor support member including an electrically non-conductive surface; and

(ii) at least one well deposited on the support member, wherein within each well is deposited an electrode array, the array defining an area on the support member for applying a test sample, the array consisting of a working electrode, a counter electrode and a reference electrode; and

wherein the electrodes of the array are spaced from one another horizontally and vertically in said well, and wherein sensor activating chemicals are located on or attached to the working electrode of the array, the sensor activating chemicals comprising an electron transfer mediator, a first conjugate including a specific binding partner for the analyte to be measured, and a second conjugate including a known amount of the said analyte attached to an oxidizing catalyst or oxidizing substrate;

(b) applying an electron source onto the array on which said test sample was applied;

(c) applying a preselected potential between the working electrode and the counter electrode of the array;

(d) measuring the current between the working electrode and the counter electrode of the array; and

(e) determining the amount of the analyte in the test sample from the measurement of the current in step d) relative to the preselected potential of step c).

2. The method of claim 1, wherein said first conjugate and said second conjugate are attached to distinct magnetic particles.

3. The method of claim 2, wherein said magnetic particles are drawn to a magnet during the performance of said method;

and wherein said magnet is located adjacent to the working electrode or the array.

4. The method of claim 3, wherein said magnetic is a component of an apparatus, said apparatus being adapted to receive the unitary electrochemical sensor.

5. The method of claim 1, wherein said electron source is a hormone;

and wherein said oxidizing catalyst is a hormone-glucose oxidase conjugate of the same hormone as said electron-source.

6. The method of claim 5, wherein said hormone is free thyroid hormone thyroxine.

7. The method of claim 1, wherein said electron source is an immunoglobulin and;

wherein said oxidizing catalyst is an immunoglobulin-glucose oxidase conjugate of the same immunoglobulin as said electron source.

8. The method of claim 7, wherein said immunoglobulin is IgE.

9. The method of claim 1, wherein said electron source is glucose or nicotinamide adenine dinucleotide.

10. The method of claim 1, wherein said oxidizing catalyst is glucose oxidase.

11. The method of claim 1, wherein said electron transfer mediator is ferrocene or benzoquinone.

12. The method of claim 1, wherein said electron source is a clinical chemistry analyte and wherein said oxidizing catalyst or oxidizing substrate is an enzyme in a conjugate.