Latex agglutination immunoassay in the presence of hemoglobin

• US 4,847,209 A
• Filed: 11/09/1987
• Issued: 07/11/1989
• Est. Priority Date: 11/09/1987
• Status: Expired due to Term

• Current Assignee: Miles, Inc. (Bayer AG)
• Original Assignee: Miles, Inc. (Bayer AG)
• Inventors: Yip, Kin F., Lewis, Lynette A., Messenger, Lowry, Yeager, Frances M.
• Primary Examiner(s): Nucker, Christine M.
• Application Number:
  US07/118,469
• Time in Patent Office: 610 Days
• Field of Search: 436/533, 436/534, 436/825, 436/67, 436/826, 436/808, 422/61
• US Class Current: 436/533
• CPC Class Codes: G01N 33/5306 Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/723 Glycosylated haemoglobin
• CPC Class Codes: Y10S 436/808 Automated or kit
• CPC Class Codes: Y10S 436/825 Pretreatment for removal of interfering factors from sample
• CPC Class Codes: Y10S 436/826 Additives, e.g. buffers, diluents, preservatives

Abstract

A latex agglutination immunoassay method for determining an analyte in a blood sample in which the pH of the reaction mixture is maintained at about 8.5 or greater in order to overcome nonspecific agglutination of latex particles by hemoglobin present in the sample. The method is particularly applicable to the determination of glycated hemoglobin, e.g., Hb Alc. In another embodiment, native hemoglobin (Ao) can be determined based on its ability to cause agglutination of latex particles suspended in an aqueous solution having a pH of about 8 or below.

Claims

1. In an analytical method for determining an analyte in a lysed blood sample by latex agglutination immunoassay, wherein (a) an aqueous reaction mixture is formed by combining the lysed blood sample with a multivalent latex antibody reagent comprising an anti-analyte antibody, or a fragment thereof, bound to a water suspensible latex particle, and additionally when the analyte is monovalent, with an agglutinator reagent comprising a plurality of epitopic binding sites for the anti-analyte antibody or fragment thereof, and (b) the resulting agglutination in the aqueous reaction mixture is measured as a function of analyte in the blood sample,

the improvement which comprises forming the aqueous reaction mixture to have a pH of about 8.5 or greater, whereby nonspecific agglutination of the latex reagent due to the presence of hemoglobin in the blood sample is substantially overcome.

2. The method of claim 1 wherein said latex particle has an effective net negative surface charge when suspended in an aqueous solution having a pH of about 7 or below.

3. The method of claim 1 wherein said latex particle is polystyrene.

4. The method of claim 1 wherein the aqueous reaction mixture is formed to have a pH of from about 8.5 up to the pH at which the immunoreactivity between the analyte and the latex reagent is substantially diminished.

5. The method of claim 1 wherein the aqueous reaction mixture is formed to have a pH of between about 8.75 and about 10.

6. The method of claim 1 wherein the aqueous reaction mixture is formed to have a pH of about 9.

7. An analytical method for determining hemoglobin Alc in a test sample comprising blood lysate by particle agglutination inhibition immunoassay, which method comprises the steps of:

(a) forming an aqueous reaction mixture comprising the blood sample and assay reagents comprising (1) a multivalent antibody reagent comprising an antibody, or a fragment thereof, to hemoglobin Alc bound to a water suspensible polystyrene latex particle, and (2) an agglutinator reagent comprising a plurality of glycated peptides corresponding to the glycated peptide sequence of hemoglobin Alc, said reaction mixture formed to have a pH of about 8.5 or greater, and

(b) measuring the resulting agglutination as a function of hemoglobin Alc in the blood sample.

8. The method of claim 7 wherein the pH of the reaction mixture is less than about 10.

9. The method of claim 7 wherein the pH of the reaction mixture is between about 8.75 and about 9.5.

10. The method of claim 7 wherein the pH of the reaction mixture is about 9.

11. The method of claim 7 wherein the blood sample has been pretreated with a hemoglobin denaturant and the antibody reagent comprises a monoclonal antibody, or a fragment thereof, that binds specifically to denatured hemoglobin Alc.

12. A test system for determining an analyte in a blood sample by latex agglutination immunoassay, comprising:

(1) a multivalent latex antibody reagent comprising an anti-analyte antibody, or a fragment thereof, bound to a water suspensible latex particle,

(2) when the analyte is monovalent, an agglutinator reagent comprising a plurality of epitopic binding sites for the anti-analyte antibody or fragment thereof, and

(3) a buffer capable of maintaining the pH of the reaction mixture formed by combination of the test system components with the blood sample at about 8.5 or above.

13. The test system of claim 12 wherein said latex particle has an effective net negative surface charge when suspended in an aqueous solution having a pH of about 7 or below.

14. The test system of claim 12 wherein said latex particle is polystyrene.

15. The test system of claim 12 wherein the aqueous reaction mixture is formed to have a pH of from about 8.5 up to the pH at which the immunoreactivity between the analyte and the latex reagent is substantially diminished.

16. The test system of claim 12 wherein the aqueous reaction mixture is formed to have a pH of between about 8.75 and about 10.

17. The test system of claim 12 wherein the aqueous reaction mixture is formed to have a pH of about 9.

18. The test system of claim 12 wherein the analyte is hemoglobin Alc and the agglutinator reagent comprises a plurality of glycated peptide residues corresponding to the glycated peptide sequence of hemoglobin Alc.

19. The test system of claim 18 wherein the latex particle is polystyrene.

20. The test system of claim 19 wherein the buffer is capable of maintaining the pH of the reaction mixture at between about 8.75 and about 10.

21. The test system of claim 19 wherein the buffer is capable of maintaining the pH of the reaction mixture at about 9.

22. The test system of claim 19 which additionally comprises a hemoglobin denaturant and wherein the antibody reagent comprises a monoclonal antibody, or a fragment thereof, that binds specifically to denatured hemoglobin Alc.

23. An analytical method for determining hemoglobin Ao in a lysed blood sample, comprising the steps of:

(a) forming an aqueous reaction mixture comprising the lysed blood sample and suspended latex particles and maintaining the pH of the reaction mixture at about 8 or below, and

(b) measuring the agglutination of said latex particles as a function of hemoglobin Ao in the blood sample.

24. The method of claim 23 wherein said latex particles have an effective net negative surface charge when suspended in an aqueous solution having a pH of about 7 or below.

25. The method of claim 24 wherein said latex particles are made of polystyrene.

26. The method of claim 23 wherein the pH of the reaction mixture is maintained from about 8 down to the pH at which the ability of hemoglobin Ao to agglutinate the polystyrene latex particles is substantially diminished.

27. The method of claim 23 wherein the pH of the reaction mixture is maintained between about 8 and about 4.

28. A test system for determining hemoglobin Ao in a blood sample, comprising:

(1) latex particles, and

(2) a buffer capable of maintaining the pH of an aqueous reaction mixture comprising the latex particles and the blood sample at about 8 or below.

29. The test system of claim 28 wherein said latex particles have an effective net negative surface charge when suspended in an aqueous solution having a pH of about 7 or below.

30. The test system of claim 29 wherein said latex particles are made of polystyrene.

31. The test system of claim 28 wherein the buffer is capable of maintaining the pH of the reaction mixture at between about 8 and about 4.