Laminated assay devices

• US 7,943,089 B2
• Filed: 12/19/2003
• Issued: 05/17/2011
• Est. Priority Date: 12/19/2003
• Status: Active Grant

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Yang, Kaiyuan, Song, Xuedong, Kaylor, Rosann
• Primary Examiner(s): Yu; Melanie J
• Application Number:
  US10/741,434
• Publication Number:
  US 20050136529A1
• Time in Patent Office: 2,706 Days
• Field of Search: 422/50, 422/61, 422/68.1, 422/82.01, 422/82.03, 435/4, 435/7.1, 435/7.9, 435/7.93, 435/7.94, 435/7.95, 435/7.4, 435/174, 435/283.1, 435/285.2, 435/287.1, 435/287.2, 436/501, 436/518, 436/524, 436/525
• US Class Current: 422/82.01
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

An electrochemical-based assay device capable of detecting the presence or quantity of an analyte of interest that is provided. The device contains two or more substrates, one containing a detection working electrode and another containing an auxiliary electrode, such as a counter/reference electrode(s). The substrates are positioned in a face-to-face relationship so that the electrodes are adjacent to each other during performance of the assay. Besides the electrodes, any of a variety of other components may also be employed in the assay device.

Claims

1. An assay device for detecting the presence or quantity of an analyte residing in a test sample, the assay device comprising:

a first substrate onto which is printed a detection working electrode capable of generating a measurable detection current and a calibration working electrode capable of generating a measurable calibration current, wherein the detection working electrode has a thickness of less than about 100 micrometers, the detection working electrode comprising an immobilized immunoreactive specific binding capture ligand for the analyte, the calibration working electrode being generally configured to not specifically bind the analyte;

a second substrate onto which is printed an auxiliary electrode selected from the group consisting of a counter electrode, a reference electrode, and combinations thereof;

a multi-channel potentiostat, the multi-channel potentiostat capable of receiving the detection current from the detection working electrode and the calibration current from the calibration working electrode; and

wherein the first and second substrates are laminated together so that the auxiliary electrode is positioned adjacent to the detection working electrode and the calibration working electrode, wherein the detection current calibrated by the calibration current is proportional to the amount of the analyte within the test sample.

2. The assay device of claim 1, wherein the first substrate, the second substrate, or combinations thereof, are formed from an insulative material.

3. The assay device of claim 1, wherein both a counter electrode and a reference electrode are disposed on the second substrate.

4. The assay device of claim 3, wherein the detection working electrode further comprises a redox mediator.

5. The assay device of claim 1, wherein the assay device contains a redox label for directly or indirectly binding to the analyte.

6. The assay device of claim 5, wherein the redox label is used in conjunction with a particle modified with a specific binding member for the analyte.

7. The assay device of claim 1, wherein a sample channel is formed on the first substrate, the second substrate, or combinations thereof.

8. The assay device of claim 1, wherein the assay device comprises a porous membrane capable of being placed in fluid communication with the test sample.

9. The assay device of claim 1, wherein the specific binding capture ligand is selected from the group consisting of antigens, haptens, aptamers, antibodies, and complexes thereof.

10. The assay device of claim 4, wherein the redox mediator is selected from the group consisting of oxygen, ferrocene derivatives, quinones, ascorbic acids, redox polymers with metal complexes, glucose, redox hydrogel polymers, and organometallic complexes.

11. The assay device of claim 5, wherein the redox label is an enzyme selected from the group consisting of alkaline phosphatase, horseradish peroxidase, glucose oxidase, beta-galactosidase, urease, and combinations thereof.

12. The assay device of claim 1, wherein the auxiliary electrode contacts the first substrate only upon lamination of the first and second substrates.

13. The assay device of claim 1, wherein the specific binding capture ligand is immobilized on a surface of the detection working electrode.

14. The assay device of claim 1, wherein the detection working electrode is formed from an ink that is printed onto the first substrate.

15. The assay device of claim 1, wherein the auxiliary electrode is formed from an ink that is printed onto the second substrate.

16. The assay device of claim 1, wherein the detection working electrode has a thickness of less than about 50 micrometers.

17. The assay device of claim 1, wherein the detection working electrode has a thickness of less than about 20 micrometers.

18. The assay device of claim 1, wherein the detection working electrode has a thickness of less than about 5 micrometers.