Immunoassay utilizing formazan-prelabeled reactants

• US 4,786,589 A
• Filed: 08/18/1986
• Issued: 11/22/1988
• Est. Priority Date: 08/18/1986
• Status: Expired due to Fees

• Current Assignee: Huntington Medical Research Institutes
• Original Assignee: Huntington Medical Research Institutes
• Inventors: Rounds, Donald E.
• Primary Examiner(s): Nucker, Christine M.
• Application Number:
  US06/897,601
• Time in Patent Office: 827 Days
• Field of Search: 436/528, 436/530, 436/536, 436/537, 436/541, 436/805, 436/807, 436/810, 435/7, 435/26,5, 435/805, 435/810
• US Class Current: 435/5
• CPC Class Codes: G01N 33/538 by sorbent column, particles or resin strip , i.e. sorbent materials
• CPC Class Codes: G01N 33/54386 Analytical elements
• CPC Class Codes: G01N 33/583 with non-fluorescent dye label
• CPC Class Codes: Y10S 435/805 Test papers
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/807 Apparatus included in process claim, e.g. physical support structures
• CPC Class Codes: Y10S 436/81 Tube, bottle, or dipstick

Abstract

An immunoassay procedure utilizing a formazan-labeled primary antibody to detect the presence of an antigen is disclosed. The formazan-labeled antibody is dissolved in a test fluid suspected to containing the antigen. A dipstick having a first section on which primary antibodies are bonded and a second section free of primary antibodies and antigens and blocked to prevent bonding of primary antibodies and antigens is immersed in the test fluid and removed after a select period of time. A difference in color between the first and second sections indicate the presence of the antigen.

Claims

1. A method for detecting the presence of target proteins in a test fluid comprising:

mixing a sample of the test fluid with a solution free of target proteins and containing a primary protein having a specific affinity for the target protein which has been prelabeled with formazan for a time sufficient to form a colored reaction product between the prelabeled primary proteins and any target proteins in the test fluid;

separating any formed reaction product from unreacted prelabeled primary proteins; and

visually detecting the presence of any formed reaction product.

2. A method as claimed in claim 1 wherein the formed reaction product is separated from unreacted prelabeled primary proteins remaining in the mixture by immersing into the mixture a solid substrate having said primary proteins not labeled with formazan bonded to the surface of the solid substrate for a time sufficient for the formed reaction product to bind to the nonlabeled primary proteins bound to the solid substrate and then withdrawing the solid substrate from the mixture.

3. A method as claimed in claim 2 wherein the solid substrate comprises a first section on which said nonlabeled primary proteins are bonded and a second section free of said primary proteins and which is blocked to prevent bonding of said primary proteins.

4. A method as claimed in claim 3 wherein the solid substrate further comprises a third section on which said target proteins are bonded.

5. A method as claimed in claim 1 wherein said target protein is a antigen and the primary protein is an antibody having a specific affinity for that antigen.

6. A method as claimed in claim 1 wherein the target protein is selected from the group consisting of beta-human chorionic gonadotropin hormone, HTLV III virus, herpes simplex type II virus, streptococcus A, feline leukemia virus, psittacosis, nuclear antigens, thyroidal antigens, mitochondrial antigens, smooth muscle antigens, treponema pallidum, cytomegalo virus, and tumor cell markers.

7. A dipstick immunodot procedure for detecting the presence of a target protein in a test fluid comprising:

mixing the test fluid with a solution containing primary proteins having a specific affinity for the target protein, said primary proteins being prelabeled with formazan;

immersing into the mixture a dipstick on which is mounted a membrane having a first section on which said primary proteins not prelabeled with formazan are bonded and a second section free of said primary proteins and which is blocked to prevent bonding of said primary proteins;

removing the dipstick from the mixture after a select period of time; and

visually comparing the intensity of color on the first section of the dipstick membrane with the intensity of color on the second section of the dipstick membrane.

8. A procedure as claimed in claim 7 wherein the dipstick further comprises a third section on which said target proteins are bonded.

9. A procedure as claimed in claim 7 wherein said target protein is an antigen and the primary protein is an antibody having a specific affinity for the antigen.

10. A prelabeled immunological reactant for use in detecting the presence of a select target protein in a test sample comprising a primary protein having a specific affinity for the select target protein and formazan bound to the primary protein.

11. A reactant as claimed in claim 10 wherein formazan is bound directly to the primary protein.

12. A reactant as claimed in claim 10 wherein formazan is bound to a secondary protein which is conjugated to the primary protein.

13. A reactant as claimed in claim 12 wherein the secondary protein is protein A.

14. A reactant as defined in claim 12 wherein the secondary protein is avidin and the primary protein is first conjugated with biotin and then conjugated with the formazan-labeled avidin.

15. A prelabeled immunological reactant for use in detecting the presence of a specific target protein in a test sample comprising a formazan-labeled primary protein wherein formazan is bound directly or indirectly to the primary protein prepared by mixing a solution of the primary protein and a water soluble tetrazolium salt and then reducing the tetrazolium salt in the presence of the primary protein.

16. A reactant as defined in claim 15 wherein the formazan is bound directly to the primary protein and the tetrazolium salt is reduced enzymatically by an enzyme conjugated to the primary protein.

17. A reactant as claimed in claim 15 wherein the formazan is bound to a secondary protein which is conjugated to the primary protein and the tetrazolium salt is reduced enzymatically by an enzyme conjugated to the secondary protein.

18. A reactant as claimed in claim 17 wherein the secondary protein is selected from the group consisting of avidin, protein A, secondary antibodies having a specific affinity for the primary antibody, and mixtures thereof.