Method and device for detecting analytes in fluids

• US 6,551,842 B1
• Filed: 03/14/2000
• Issued: 04/22/2003
• Est. Priority Date: 03/26/1999
• Status: Expired due to Term

• Current Assignee: IDEXX Laboratories Incorporated
• Original Assignee: IDEXX Laboratories Incorporated
• Inventors: Carpenter, Charles R.
• Primary Examiner(s): Le, Long V.
• Assistant Examiner(s): Do, Pensee T.
• Application Number:
  US09/525,151
• Time in Patent Office: 1,134 Days
• Field of Search: 435/7.1, 435/7.9, 435/287.1, 435/287.2, 435/287.7, 435/286.5, 435/810, 435/970, 436/518, 436/528, 436/530, 436/541, 422/68.1, 422/70, 422/99
• US Class Current: 436/518
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 435/91 Xanthomonas

Abstract

A disposable, dry chemistry analytical system is disclosed which is broadly useful for the detection of a variety of analytes present in biological fluids such as whole blood, serum, plasma, urine and cerebral spinal fluid. The invention discloses the use of the reaction interface that forms between two liquids converging from opposite directions within a bibulous material. The discovery comprises a significant improvement over prior art disposable, analytical reagent systems in that the detectable reactant zone is visually distinct and separate from the unreacted reagents allowing for the use of reaction indicators exhibiting only minor changes as well as extremely high concentrations of reactants. In addition, staged, multiple reagents can be incorporated. Whole blood can be used as a sample without the need for separate cell separating materials. Finally, the invention is useful for the detection of analytes in a broad variety of materials such as milk, environmental samples, and other samples containing target analytes.

Claims

1. A device for detecting and quantifying at least one analyte in a fluid sample suspected of containing the analyte by employing a reagent that binds to the analyte and forms a detectable reaction product from a substrate, comprising,

a fluid transport material that absorbs a liquid and supports capillary flow of the liquid, the fluid transport material having a first zone for the application of the fluid sample containing the reagent to a first pad in the first zone containing the analyte bound substantially irreversibly to the first pad, and a second zone for the application of a liquid to a second pad in the second zone that contains a reconstitutable substrate, wherein when the fluid sample containing the reagent is added to the first pad, and the liquid is added to the second pad, the fluid sample containing reagent not bound by the analyte bound substantially irreversibly to the first pad flows in a first direction from a fluid sample edge toward the second zone, and the substrate is reconstituted by the liquid to form a liquid reactant that reacts with the reagent, and the liquid reactant flows in a second direction opposite to that of the first direction and toward the first zone from a liquid reactant edge;

whereby when the flowing fluid sample containing the reagent not bound by the analyte bound substantially irreversibly to the first pad and the flowing liquid reactant meet, flow stops and the detectable reaction product is formed by a reaction between the liquid reactant and the reagent, and a stable reaction interface is formed at a juncture between and visually distinct from the fluid sample and the liquid reactant.

2. The device of claim 1, wherein said fluid transport material is a material that separates red blood cells from blood and is selected from the group consisting of:

nitrocellulose membranes, cellulose sheets, porous polyethylene, and polyethersulfone.

3. The device of claim 1, wherein said fluid transport material is a nitrocellulose material cast on a backing material.

4. The device of claim 3, wherein the backing material is polyvinylchloride or a polyester film.

5. The device of claim 1, further comprising a means for detecting and optionally measuring an amount of said detectable reaction product.

6. The device of claim 1, further comprising a means for calibrating a concentration of said liquid reagent, said means comprising a calibration zone for application of an amount of said reagent, said calibration zone being located between said first zone and said reaction interface, whereby when said amount of said reagent is added to said calibration zone, said reagent flows in a first direction toward said second zone, and said liquid reactant flows in a second direction opposite to that of said first direction and toward said first zone from a liquid reactant edge;

whereby when said flowing reagent and said flowing liquid reactant meet, flow stops and a detectable calibration product is formed by a reaction between said reagent and said liquid reactant, and a stable calibration reaction interface is formed at a juncture between and visually distinct from said reagent in said amount of said reagent and said liquid reactant.

7. The device of claim 6, wherein said amount of said reagent added to said calibration zone is in excess of said amount of said reagent in said fluid sample, such that said amount of said reagent added to said calibration zone is sufficient to form an amount of said detectable calibration product that enables determination of an amount of said liquid reactant.

8. The device of claim 7, wherein said detectable reaction product is formed at a rate sufficient for it to be detected within about fifteen seconds after application of said fluid sample to said fluid sample zone.

9. The device of claim 1, further comprising:

a means for simultaneously applying said fluid sample to said first zone and said liquid reactant to said second zone; and

a sensor, said sensor being effective to detect said detectable reaction product.

10. The device of claim 9, wherein said sensor is effective to detect said detectable reaction product having at least one desired wavelength of reflectance or absorption of ≧

250 nanometers.

11. The device of claim 9, wherein said sensor is effective to detect and measure an amount of said detectable reaction product that is proportional to a concentration of said analyte based on a peak intensity of reflectance or absorption of said detectable reaction product.

12. The device of claim 9, wherein said sensor is effective to detect and measure a rate of formation of said detectable reaction product that is proportional to a concentration of said analyte.

13. The device of claim 12, wherein said rate is calculated as a change over time of a peak intensity of reflectance or absorption of said detectable reaction product.

14. The device of claim 13, wherein said peak intensity of reflectance or absorption is measured across a line substantially perpendicular to said reaction interface.

15. The device of claim 13, wherein said peak intensity of reflectance or absorption is measured within a polygonal region encompassing all or a portion of said reaction interface.

16. The device of claim 9, wherein said sensor is effective to detect and measure an amount of said detectable reaction product that is greater than or equal to a predetermined threshold intensity of reflectance or absorption indicative of the presence of said analyte.

17. The device of claim 1, wherein said reagent comprises an enzyme or a portion thereof linked to a monoclonal antibody or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said monoclonal antibody or a portion thereof being capable of binding to said analyte.

18. The device of claim 17, wherein said enzyme is a member selected from the group consisting of alkaline phosphatase, β

-galactosidase, and peroxidase.

19. The device of claim 17, wherein said portion of a monoclonal antibody is selected from the group consisting of an F(ab) fragment, an F(ab′

) fragment, an F(ab′

)₂ fragment, an Fv fragment, and an scFv fragment.

20. The device of claim 1, wherein said reagent comprises an enzyme or a portion thereof linked to a receptor protein or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said receptor protein or a portion thereof being capable of binding to said analyte.

21. The device of claim 1, wherein said reagent comprises an enzyme or a portion thereof linked to an abtide or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said abtide or a portion thereof being capable of binding to said analyte.

22. A method for detecting and quantifying at least one analyte in a fluid sample suspected of containing the analyte by employing a reagent, which binds to the analyte and forms a detectable reaction product from a substrate, comprising,

providing a fluid transport material that absorbs a liquid and supports capillary flow of the liquid, the fluid transport material having a first zone for the application of the fluid sample containing the reagent to a first pad containing the analyte bound substantially irreversibly to the first pad, and a second zone for the application of a liquid to a second pad containing a reconstitutable substrate;

contacting a reagent that binds to analyte with the fluid sample suspected of containing the analyte;

adding said fluid sample containing the reagent to the first pad, and the liquid to the second pad, wherein the fluid sample thereafter flows in a first direction from a fluid sample edge toward the second zone, and the substrate is reconstituted by the liquid to form a liquid reactant that reacts with the reagent, and the liquid reactant flows in a second direction opposite to that of the first direction and toward the first zone from a liquid reactant edge;

whereby when the flowing fluid sample containing the reagent not bound by the analyte bound substantially irreversibly to the first pad and the flowing liquid reactant meet, flow stops and the detectable reaction product is formed by a reaction between the liquid reactant and the reagent, and a stable reaction interface is formed at a juncture between and visually distinct from the fluid sample and the liquid reactant.

23. The method of claim 22, wherein said fluid transport material is a material that separates red blood cells from blood and is selected from the group consisting of:

nitrocellulose membranes, cellulose sheets, porous polyethylene, and polyethersulfone.

24. The method of claim 22, wherein said fluid transport material is a nitrocellulose material cast on a backing material.

25. The method of claim 24, wherein the backing material is polyvinylchloride or a polyester film.

26. The method of claim 22, further comprising measuring an amount of said detectable reaction product.

27. The method of claim 26, wherein said amount of said detectable reaction product is proportional to a concentration of said analyte based on a peak intensity of reflectance or absorption of said detectable reaction product.

28. The method of claim 22, wherein said step of measuring an amount of said detectable reaction product includes measuring a member selected from the group consisting of absorbance, reflectance, transmission, fluorescence, luminescence, and conductance.

29. The method of claim 22, wherein said detectable reaction product is measured by one of absorbance and reflectance.

30. The method of claim 29, wherein said one of absorbance and reflectance is measured at one or more wavelengths of >

250 nanometers.

31. The method of claim 22, wherein said detectable reaction product is formed at a rate that is proportional to a concentration of said analyte.

32. The method of claim 31, wherein said rate is calculated as a change over time of a peak intensity of reflectance or absorption of said detectable reaction product.

33. The method of claim 32, wherein said peak intensity of reflectance or absorption is measured across a line substantially perpendicular to said reaction interface.

34. The method of claim 32, wherein said peak intensity of reflectance or absorption is measured within a polygonal region encompassing all or a portion of said reaction interface.

35. The method of claim 22, wherein said detectable reaction product is formed in an amount greater than or equal to a predetermined threshold intensity of reflectance or absorption indicative of the presence of said analyte.

36. The method of claim 22, further comprising measuring a member selected from the group consisting of:

a distance between said fluid sample edge and a midpoint of said stable reaction interface, a distance between said liquid reactant edge and a midpoint of said stable reaction interface, a distance between said fluid sample edge and a midpoint of a stable liquid interface, a distance between said liquid reactant edge and a midpoint of a stable liquid interface, a distance between said midpoint of said stable reaction interface and said midpoint of a stable liquid interface, a reflectance or absorption of said detectable reaction product at a plurality of fixed time points, a reflectance or absorption of said stable liquid interface at a plurality of fixed time points, a rate of change of said reflectance or absorption of said detectable reaction product, an area of said stable reaction interface, an area of said stable liquid interface, a background level of said fluid sample, and a background level of said liquid reactant.

37. The method of claim 22, further comprising calibrating a concentration of said liquid reagent by applying an amount of said reagent to a calibration zone, said calibration zone being located between said first zone and said reaction interface, whereby when said reagent is added to said calibration zone, said reagent flows in a first direction toward said second zone, and said liquid reactant flows in a second direction opposite to that of said first direction and toward said first zone from a liquid reactant edge;

whereby said flowing reagent and said flowing liquid reactant meet, flow stops and a detectable calibration product is formed by a reaction between said reagent and said liquid reactant, and a stable calibration reaction interface is formed at a juncture between and visually distinct from said reagent in said excess amount of said reagent and said liquid reactant; and

detecting said detectable calibration product.

38. The method of claim 37, wherein said amount of said reagent added to said calibration zone is in excess of said amount of said reagent in said fluid sample, such that said amount of said reagent added to said calibration zone is sufficient to form an amount of said detectable calibration product that enables determination of an amount of said liquid reactant.

39. The method of claim 37, wherein said detectable calibration product is formed at a rate that is proportional to a concentration of said reagent.

40. The method of claim 39, wherein said rate is calculated as a change over time of a peak intensity of reflectance or absorption of said detectable calibration product.

41. The method of claim 40, wherein said peak intensity of reflectance or absorption is measured across a line substantially perpendicular to said calibration interface.

42. The method of claim 40, wherein said peak intensity of reflectance or absorption is measured within a polygonal region encompassing all or a portion of said calibration interface.

43. The method of claim 37, wherein said detectable calibration product is formed in an amount greater than or equal to a predetermined threshold intensity of reflectance or absorption indicative of the presence of said reagent.

44. The method of claim 22, wherein said reagent comprises an enzyme or a portion thereof conjugated to a monoclonal antibody or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said monoclonal antibody or a portion thereof being capable of binding to said analyte.

45. The method of claim 44, wherein said enzyme is a member selected from the group consisting of alkaline phosphatase, β

-galactosidase, and peroxidase.

46. The method of claim 44, wherein said portion of a monoclonal antibody is selected from the group consisting of an F(ab) fragment, an F(ab′

) fragment, an F(ab′

)₂ fragment, an Fv fragment, and an scFv fragment.

47. The method of claim 22, wherein said reagent comprises an enzyme or a portion thereof conjugated to a receptor protein or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said receptor protein or a portion thereof being capable of binding to said analyte.

48. The method of claim 22, wherein said reagent comprises an enzyme or a portion thereof conjugated to an abtide or a portion thereof;

said enzyme or a portion thereof being capable of forming said detectable reaction product from said substrate;

said abtide or a portion thereof being capable of binding to said analyte.