Method and assay for detection of residues

• US 9,063,137 B2
• Filed: 11/29/2010
• Issued: 06/23/2015
• Est. Priority Date: 12/08/2003
• Status: Active Grant

• Current Assignee: Charm Sciences, Inc.
• Original Assignee: Charm Sciences, Inc.
• Inventors: Saul, Steven J., Markovsky, Robert J., Douglas, David W.
• Primary Examiner(s): BROWN, MELANIE YU
• Application Number:
  US12/955,331
• Publication Number:
  US 20110070127A1
• Time in Patent Office: 1,667 Days
• Field of Search: 422/420, 422/424, 422/425, 422/430, 435/805, 436/514, 436/518, 436/524, 436/525, 436/828
• US Class Current: 1/1
• CPC Class Codes: G01N 33/54386 Analytical elements
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: Y10S 435/805 Test papers
• CPC Class Codes: Y10S 436/828 Protein A

Abstract

Embodiments described herein include methods and assays for detecting an analyte in a sample using a plurality of control zone capture agents. Some embodiments include detection of multiple analytes in a sample utilizing a plurality of analyte binders and a control zone containing multiple control zone capture agents. In some embodiments, the multiple control zone capture agents capture a plurality of binders within one control zone. Test results are determined by comparison of the control zone signal to a test zone signal.

Claims

1. In a lateral flow assay for detecting a plurality of analytes in a solution, an assay comprising:

(a) a test solution having a first set of binders and a second set of binders distinct from the first set of binders, each set of binders configured for generating a detectable signal, wherein binders from the first set combine with a beta-lactam from the solution, when present, to form a binder-beta-lactam complex and binders from the second set combine with an aflatoxin, when present, to form a binder-aflatoxin complex, and wherein a test solution contains a combination of one or more binders from each set, a binder-beta-lactam complex, and a binder-aflatoxin complex;

(b) a test strip configured to allow the test solution to flow, the test strip comprising;

(i) a first test zone having immobilized thereon a first test zone capture agent specific to the first set of binders that, when the binder has not formed a binder-beta-lactam complex, captures at least one of the binders from that set;

(ii) a second test zone having immobilized thereon a second test zone capture agent specific to the second set of binders that, when the binder has not formed a binder-aflatoxin complex, captures at least one of the binders from that set, and wherein the second test zone being adjacent to the first test zone;

(iii) a single control zone having a first and second set of control zone capture agents which are able to capture, at the control zone, at least one of a corresponding set of binders, whether or not the binder has formed a corresponding binder-beta-lactam or binder-aflatoxin complex, and

wherein capture of a binder at either of the test zones or the control zone results in a detectable signal and wherein a greater signal in the control zone as compared to any one of the test zones indicates a positive result.

2. The assay of claim 1 wherein at least one of the control zone capture agents comprises an antibody.

3. The assay of claim 1 wherein at least one of the control zone capture agents comprises an antibody binding protein.

4. The assay of claim 1 wherein the first set of binders comprises a multianalyte binder with affinity for beta-lactam antibiotics.

5. The assay of claim 4 wherein the beta-lactam binder is from Geobacillus stearothermophilus.

6. The assay of claim 1 wherein the second set of binders comprises an antibody.

7. The assay of claim 6 wherein the antibody comprises an antibody to cloxacillin.

8. The assay of claim 1 wherein at least one of the control zone binders comprises an antibody to a beta-locate binder.

9. The assay of claim 1 wherein at least one of the control zone binders comprises an antispecies antibody.

10. The assay of claim 1 further comprising at least one unlabeled binder wherein the unlabeled binder reduces test sensitivity relative to the analyte to which the unlabeled binder has affinity.

11. The assay of claim 1 wherein the solution comprises an extract from a sample.

12. the assay of claim 1 wherein one of the analytes comprises a beta-lactam and another of the analytes comprises a tetracycline.

13. The assay of claim 1 wherein one of the analytes comprises a beta-lactam and another of the analytes consists of any one sulfonamide, a macrolide and an amphenicols.

14. The assay of claim 1 wherein at least one of the binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and another of the binders comprises a binder with affinity to one or more tetracyclines.

15. The assay of claim 1 wherein at least one of the binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and another of the binders consists of a binder for any one of any one sulfonamide, a macrolide and an amphenicols.

16. The assay of claim 1 wherein at least one of the binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and another of the binders comprises a binder with affinity to less than all the beta-lactam antibiotics to which the multianalyte has sensitivity.

17. The assay of claim 16 wherein the multianalyte binder has affinity to the beta-lactam family and the other binder comprises an antibody.

18. The assay of claim 17 wherein the antibody comprises an antibody to cloxacillin.

19. The assay of claim 17 wherein the antibody comprises an antibody for ceftiofur.

20. In a lateral flow assay for detecting a plurality of analytes in a solution, an assay comprising:

(a) a test solution having a first set of binders and a second set of binders distinct from the first set of binders, each set of binders configured for generating a detectable signal, wherein binders from the first set combine with a beta-lactam from the solution, when present, to form a binder-beta-lactam complex and binders from the second set combine with an aflatoxin, when present, to form a binder-aflatoxin complex, and wherein a test solution contains a combination of one or more binders from each set, a binder-beta-lactam complex, and a binder-aflatoxin complex;

(b) a test strip configured to allow the test solution to flow, the test strip comprising;

(i) a plurality of first test zone having immobilized thereon a first test zone capture agent specific to the first set of binders that, when the binder has not formed a binder-beta-lactam complex, captures at least one of the binders from that set;

(ii) a second test zone having immobilized thereon a second test zone capture agent specific to the second set of binders that, when the binder has not formed a binder-aflatoxin complex, captures at least one of the binders from that set, and wherein the second test zone being adjacent to the first test zone;

(iii) a single control zone having a first and second set of control zone capture agents,

wherein capture of a binder at either the test zones results in a detectable signal and wherein a greater signal in the control zone as compared to any one of the test zones indicates a positive result.

21. The assay of claim 20 wherein one of the analytes comprises a beta-lactam and another of the analytes comprises a tetracycline.

22. The assay of claim 20 wherein one of the analytes comprises a beta-lactam and another of the analytes is selected from the group consisting essentially of a sulfonamide, a macrolide and an amphenicol.

23. The assay of claim 20 wherein the first set of binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and the second set of binders comprises a binder with binding affinity to one or more tetracyclines.

24. The assay of claim 20 wherein the first set of binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and the second set of binders is selected from the group consisting essentially of a binder for a sulfonamide, a binder for a macrolide, and a binder for an amphenicol.

25. The assay of claim 20 wherein the first set of binders comprises a multianalyte binder with binding affinity for beta-lactam antibiotics and the second set of binders comprises a binder with affinity to less than all the beta-lactam antibiotics to which the multianalyte binder has sensitivity.

26. The assay of claim 20 wherein the multianalyte binder has affinity to the beta-lactam and the other binder comprises an antibody.

27. The assay of claim 26 wherein the antibody comprises an antibody to cloxacillin.