Diagnostic assay for a sample of biological fluid

• US 6,312,888 B1
• Filed: 10/16/2000
• Issued: 11/06/2001
• Est. Priority Date: 06/10/1998
• Status: Expired due to Fees

• Current Assignee: Abbott Laboratories Incorporated
• Original Assignee: Abbott Laboratories Incorporated
• Inventors: Hiltibran, Robert G., Calfin, Brenda B., Shain, Eric B., Schapira, Thomas G., Young, Douglas F., Pope, Mark R., Huang, Tung-Ming, Wong, Sie Ting
• Primary Examiner(s): Leary, Louise N.
• Application Number:
  US09/688,636
• Time in Patent Office: 386 Days
• Field of Search: 435/4, 435/283.1
• US Class Current: 435/4
• CPC Class Codes: G01N 33/525 Multi-layer analytical elements
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/66 involving blood sugars, e.g. galactose

Abstract

An article and a method for monitoring the concentration of an analyte, e. g., glucose, in blood. In one aspect, the invention involves an article comprising a multiple-layer element. In one embodiment, the article comprises:

a multiple-layer element comprising:

(a) a base layer

(b) a cover layer, the cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a biological sample; and

(c) a core layer having a first major surface and a second major surface, the core layer disposed between the base layer and the cover layer, the core layer comprising a sample introduction chamber and a optical reading chamber, the first major surface of the core layer in face-to-face contact with the base layer, the second major surface of the core layer in face-to-face contact with the cover layer.

The multiple-layer element of this invention allows the use of samples of blood or other biological fluids, such as interstitial fluid, to provide extremely sensitive assay results. The device has been shown to provide accurate and reproducible results with samples having volumes ranging from about 5 μL to about 20 μL. In another aspect, the invention involves a method for using the aforementioned article.

Claims

1. An article suitable for use in determining the concentration of an analyte in a biological sample comprising:

a multiple-layer element comprising

(a) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a sample of biological fluid; and

(b) a base layer having a major surface in contact with said cover layer, said base layer or said cover layer or said base layer and said cover layer comprising a sample introduction chamber and an optical reading chamber, wherein said optical reading chamber contains a reagent capable of reacting with glucose, wherein said reagent comprises β

-nicotinamide adenine dinucleotide.

2. An article suitable for use in determining the concentration of an analyte in a biological sample comprising:

a multiple-layer element comprising

(a) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a sample of biological fluid; and

(b) a base layer having a major surface in contact with said cover layer, said base layer or said cover layer or said base layer and said cover layer comprising a sample introduction chamber and an optical reading chamber, wherein said optical reading chamber contains a reagent capable of reacting with, wherein said reagent comprises 3-[4,5-dimethylthiazol-2-yl]-2, 5-diphenyltetrazolium bromide.

3. An article suitable for use in determining the concentration of an analyte in a biological sample comprising:

a multiple-layer element comprising

(a) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a sample of biological fluid; and

(b) a base layer having a major surface in contact with said cover layer, said base layer or said cover layer or said base layer and said cover layer comprising a sample introduction chamber and an optical reading chamber, further including a colorant for indicating when said optical reading chamber contains an amount of sample sufficient for determining the concentration of an analyte in a biological sample.

4. The article of claim 3, wherein said colorant comprises a dye.

5. The article of claim 4, wherein said dye is selected from the group consisting of Acid Black 2, Acid Black 48, Acid Green 41, Indocyanine Green, Copper Phthalocyaninetetrasulfonic acid, Eriochrome Black T, Gallocyanine, and Janus Green B.

6. The article of claim 3, wherein said colorant is located in said sample introduction chamber.

7. The article of claim 3, wherein said colorant is located in a fluid-transporting layer overlying said sample introduction chamber.

8. The article of claim 3, wherein said colorant is capable of absorbing light at a wavelength of from about 350 nm to about 1400 nm.

9. The article of claim 3, wherein said colorant comprises a pigment.

10. An article suitable for use in determining the concentration of an analyte in a biological simple comprising:

a multiple-layer element comprising

(a) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a sample of biological fluid; and

(b) a base layer having a major surface in contact with said cover layer, said base layer or said cover layer or said base layer and said cover layer comprising a sample introduction chamber and an optical reading chamber, wherein said optical reading chamber contains a reagent capable of reacting with the sample, wherein a layer of highly reflective material is located on said cover layer in register with the optical path of said optical reading chamber.

11. The article of claim 10, wherein said layer of highly reflective material becomes less reflective upon being wetted by a liquid sample.

12. The article of claim 10, wherein said layer of highly reflective material is capable of being removed from said optical path by a liquid sample.

13. An article suitable for determining the concentration of an analyte in a biological sample, comprising:

a multiple-layer element comprising;

(a) a base layer

(b) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a biological sample; and

(c) a core layer having a first major surface and a second major surface, said core layer disposed between said base layer and said cover layer, said core layer comprising a sample introduction chamber and a optical reading chamber, said first major surface of said core layer in face-to-face contact with said base layer, said second major surface of said core layer in face-to-face contact with said cover layer, wherein said optical reading chamber contains a reagent capable of reacting with glucose, wherein said reagent comprises β

-nicotinamide adenine dinucleotide.

14. An article suitable for determining the concentration of an analyte in a biological sample, comprising:

a multiple-layer element comprising;

(a) a base layer

(b) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a biological sample; and

(c) a core layer having a first major surface and a second major surface, said core layer disposed between said base layer and said cover layer, said core layer comprising a sample introduction chamber and a optical reading chamber, said first major surface of said core layer in face-to-face contact with said base layer, said second major surface of said core layer in face-to-face contact with said cover layer, wherein said optical reading chamber contains a reagent capable of reacting with glucose, wherein said reagent comprises 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide.

15. An article suitable for determining the concentration of an analyte in a biological sample, comprising:

a multiple-layer element comprising;

(a) a base layer

(b) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a biological sample; and

(c) a core layer having a first major surface and a second major surface, said core layer disposed between said base layer and said cover layer, said core layer comprising a sample introduction chamber and a optical reading chamber, said first major surface of said core layer in face-to-face contact with said base layer, said second major surface of said core layer in face-to-face contact with said cover layer, further including a colorant for indicating when said optical reading chamber contains an amount of sample sufficient for in determining the concentration of an analyte in a biological sample.

16. The article of claim 15, wherein said colorant comprises a dye.

17. The article of claim 16, wherein said dye is selected from the group consisting of Acid Black 2, Acid Black 48, Acid Green 41, Indocyanine Green, Copper Phthalocyaninetetrasulfonic acid, Eriochrome Black T, Gallocyanine, and Janus Green B.

18. The article of claim 15, wherein said colorant is located in said sample introduction chamber.

19. The article of claim 15, wherein said colorant is located in a fluid-transporting layer overlying said sample introduction chamber.

20. The article of claim 15, wherein said colorant is capable of absorbing light at a wavelength of from about 350 nm to about 1400 nm.

21. The article of claim 15, wherein said colorant comprises a pigment.

22. An article suitable for determining the concentration of an analyte in a biological sample, comprising:

a multiple-layer element comprising;

(a) a base layer

(b) a cover layer, said cover layer having a first opening for venting the multiple-layer element and a second opening for receiving a biological sample; and

(c) a core layer having a first major surface and a second major surface, said core layer disposed between said base layer and said cover layer, said core layer comprising a sample introduction chamber and a optical reading chamber, said first major surface of said core layer in face-to-face contact with said base layer, said second major surface of said core layer in face-to-face contact with said cover layer, wherein a layer of highly reflective material is located on said cover layer in register with the optical path of said optical reading chamber.

23. The article of claim 22, wherein said layer of highly reflective material becomes less reflective upon being wetted by a liquid sample.

24. The article of claim 22, wherein said layer of highly reflective material is capable of being removed from said optical path by a liquid sample.

25. A method for determining the concentration of an analyte in a biological sample, said method comprising the steps of:

(a) introducing a sample of biological fluid obtained from the body of a patient to an article comprising a multiple-layer element having a sample introduction chamber and an optical reading chamber;

(b) allowing a reagent to react with the analyte of interest in the sample; and

(c) measuring the concentration of analyte in the sample by means of an optical instrument, wherein said reagent comprises β

-nicotinamide adenine dinucleotide.

26. A method for determining the concentration of an analyte in a biological sample, said method comprising the steps of:

(a) introducing a sample of biological fluid obtained from the body of a patient to an article comprising a multiple-layer element having a sample introduction chamber and an optical reading chamber;

(b) allowing a reagent to react with the analyte of interest in the sample; and

(c) measuring the concentration of analyte in the sample by means of an optical instrument, wherein said reagent comprises 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide.

27. A method for determining the concentration of an analyte in a biological sample, said method comprising the steps of:

(a) introducing a sample of biological fluid obtained from the body of a patient to an article comprising a multiple-layer element having a sample introduction chamber and an optical reading chamber;

(b) allowing a reagent to react with the analyte of interest in the sample; and

(c) measuring the concentration of analyte in the sample by means of an optical instrument, further including a colorant for indicating when said optical reading chamber contains an amount of sample sufficient for determining the concentration of an analyte in a biological sample.

28. The method of claim 27, wherein said colorant comprises a dye.

29. The method of claim 28, wherein said dye is selected from the group consisting of Acid Black 2, Acid Black 48, Acid Green 41, Indocyanine Green, Copper Phthalocyaninetetrasulfonic acid, Eriochrome Black T, Gallocyanine, and Janus Green B.

30. The method of claim 27, wherein said colorant is located in said sample introduction chamber.

31. The method of claim 27, wherein said colorant is located in a fluid-transporting layer overlying said sample introduction chamber.

32. The method of claim 27, wherein said colorant is capable of absorbing light at a wavelength of from about 350 nm to about 1400 nm.

33. The method of claim 27, wherein said colorant comprises a pigment.

34. A method for determining the concentration of an analyte in a biological sample, said method comprising the steps of:

(a) introducing a sample of biological fluid obtained from the body of a patient to an article comprising a multiple-layer element having a sample introduction chamber and an optical reading chamber;

(b) allowing a reagent to react with the analyte of interest in the sample; and

(c) measuring the concentration of analyte in the sample by means of an optical instrument, wherein a layer of highly reflective material is located on said cover layer in register with the optical path of said optical reading chamber.

35. The method of claim 34, wherein said layer of highly reflective material becomes less reflective upon being wetted by a liquid sample.

36. The method of claim 34, wherein said layer of highly reflective material is removed from said optical path by a liquid sample.

37. The method of claim 34, wherein a change in reflectance in the optical reading chamber indicates that the optical reading chamber contains a sufficient amount of sample to allow an accurate determination of concentration of glucose.