IP Library Granted Patent US 8,846,319
Granted Patent B2
US 8,846,319 · App. 12/630,777 · Granted Sep 30, 2014

Lateral flow strip assay with immobilized conjugate

Inventors: Rajesh K. Mehra (Sunnyvale, CA); Kenneth P. Aron (Burlingame, CA)
Assignee: Abaxis, Inc.
G01N33/54313
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Quick Facts
Patent No.
US 8,846,319
App. No.
12/630,777
Granted
Sep 30, 2014
Kind
B2
Abstract

The present invention discloses analyte detection devices for detecting one or more analytes present in test samples, especially biological samples. In particular, the devices of the invention are lateral flow assay devices comprising immobilized metal nanoparticle conjugates as the detection means. Methods of using the devices and kits comprising the devices are also described.

Claims (47)

1. An analyte detection device comprising

a sample pad;

an accelerant, wherein the accelerant is polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, or mixtures thereof;

a detecting complex immobilized on a first portion of a first surface, wherein the detecting complex comprises a first binding partner coupled to a metallic nanoparticle or metallic nanoshell, wherein the first binding partner is capable of forming a complex with a target analyte;

wherein the accelerant is deposited on a second portion of said first surface, said second portion being positioned upstream of said first portion and between the sample pad and said first portion,

wherein the first and the second portions do not overlap;

wherein the sample pad is in operable fluid communication with the second portion, which in turn is in fluid communication with said first portion of the first surface,

and wherein the accelerant is capable of accentuating a spectral shift of the detecting complex upon binding of a target analyte.

2. The device of claim 1 , wherein the first surface is a porous surface.

3. The device of claim 1 , wherein the first surface is of nitrocellulosic material, polyvinylidene fluoride (PVDF), polyethylene material, nylon, cellulose acetate, polyester material, polyethersulfone (PES), or polysulfone.

4. The device of claim 1 , wherein the first binding partner is an antibody, receptor, ligand, polynucleotide, polypeptide, glycopeptide, lipoprotein, or nucleoprotein.

5. The device of claim 1 , wherein the metallic nanoparticle or metallic nanoshell is selected from the group consisting of gold particles, silver particles, copper particles, platinum particles, cadmium particles, composite particles, gold hollow spheres, gold-coated silica nanoshells, and silica-coated gold shells.

6. The device of claim 1 , wherein the detecting complex is covalently bonded to the first surface.

7. The device of claim 1 , wherein the first surface comprises a blocking agent, neutralizing agent or a combination thereof.

8. The device of claim 1 , wherein the sample pad comprises a blocking agent, neutralizing agent or a combination thereof.

9. The device of claim 1 , wherein the sample pad comprises one or more dried buffers or detergents or a combination thereof.

10. The device of claim 1 , further comprising an adsorbent pad, which is in operable fluid communication with the first surface.

11. The device of claim 1 , wherein the device is positioned in an enclosed housing.

12. The device of claim 11 , wherein the housing comprises a sample port positioned over the sample pad.

13. The device of claim 11 , wherein the housing comprises a test window positioned over the first surface.

14. The device of claim 11 , wherein housing comprises one or more vents to facilitate fluid movement through the device.

15. The device of claim 1 , further comprising a reagent pad comprising a second binding partner capable of forming a complex with the target analyte, wherein the reagent pad is in operable fluid communication with the first surface and is positioned between the sample pad and the first surface.

16. The device of claim 15 , wherein the first binding partner is the same as the second binding partner.

17. The device of claim 15 , further comprising a control zone in operable fluid communication with the sample pad, reagent pad and the first surface, wherein the control zone is capable of indicating a positive control for the device.

18. The device of claim 1 , wherein the detecting complex further comprises an enzyme directly linked to the first binding partner or metallic nanoparticle or metallic nanoshell.

19. The device of claim 1 , further comprising a second detecting complex immobilized on the first portion of the first surface, separately from the first detecting complex, wherein the second detecting complex comprises a second binding partner coupled to a second detectable entity, and wherein the second binding partner is capable of forming a complex with a second target analyte.

20. An analyte detection device comprising

a sample pad comprising an accelerant, wherein the accelerant is polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, or mixtures thereof;

a first surface and a second surface, wherein the second surface is adjacent to the first surface, and wherein the sample pad is in operable fluid communication with the first and second surfaces;

a first detecting complex immobilized on the first surface, wherein the first detecting complex comprises a first binding partner coupled to a first detectable entity;

a second detecting complex immobilized on the second surface, wherein the second detecting complex comprises a second binding partner coupled to a second detectable entity;

wherein the first binding partner is capable of forming a complex with a first target analyte and the second binding partner is capable of forming a complex with a second target analyte;

wherein the first detectable entity and the second detectable entity are metallic nanoparticles or metallic nanoshells; and

wherein the accelerant is capable of accentuating a spectral shift of the first or second detecting complex upon binding of the first or second target analyte, respectively.

21. The device of claim 20 , wherein the first target analyte and the second target analyte are different analytes in a biological sample.

22. The device of claim 20 , wherein the first detectable entity and the second detectable entity are the same.

23. The device of claim 20 , wherein the first detectable entity is a different metallic nanoparticle or metallic nanoshell than the second detectable entity.

24. A kit comprising the detection device of claim 1 and instructions for using the device to detect an analyte in a test sample.

25. A method of detecting a target analyte in a test sample comprising:

contacting the test sample with the sample pad of the device of claim 1 , wherein the test sample flows through said second portion of the first surface carrying the accelerant to said first portion of the first surface on which the detecting complex is immobilized, and

detecting a signal corresponding to the binding of the target analyte to the detecting complex, wherein the presence of the signal is indicative of the presence of the target analyte.

26. The method of claim 25 , further comprising contacting the sample pad with an enhancing agent.

27. The method of claim 26 , wherein the enhancing agent is silver nitrate or osmium tetroxide.

28. The method of claim 25 , wherein the signal is a spectral shift.

29. The method of claim 25 , wherein detecting the signal comprises measuring a change in absorbance of the signal.

30. The method of claim 25 , wherein the test sample is a biological sample.

31. The method of claim 25 , wherein the target analyte is a protein, peptide, nucleic acid, hapten, or chemical.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2021
From: ABAXIS LLC
To: ZOETIS SERVICES LLC
Reel/Frame 055474/0599 →
CHANGE OF NAME Recorded Mar 3, 2021
From: ABAXIS, INC.
To: ABAXIS LLC
Reel/Frame 055474/0653 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2010
From: MEHRA, RAJESH K.; ARON, KENNETH P.
To: ABAXIS, INC.
Reel/Frame 023820/0206 →
Continuity (2)
Provisional Application 61119612 · Dec 3, 2008
Related Publication 20100136566A1 · Jun 3, 2010