Unitized solid phase immunoassay kit and method

• US 4,017,597 A
• Filed: 10/30/1974
• Issued: 04/12/1977
• Est. Priority Date: 10/30/1974
• Status: Expired due to Term

• Current Assignee: Monsanto Company (Bayer AG)
• Original Assignee: Monsanto Company (Bayer AG)
• Inventors: Reynolds, John H.
• Primary Examiner(s): Padgett, Benjamin R.
• Assistant Examiner(s): Nucker, Christine M.
• Application Number:
  US05/519,317
• Time in Patent Office: 895 Days
• Field of Search: 424/1.5, 424/12, 23/230 B, 23/259, 23/253 R
• US Class Current: 435/7.92
• CPC Class Codes: G01N 33/545 Synthetic resin
• CPC Class Codes: Y10S 435/962 Prevention or removal of interfering materials or reactants or other treatment to enhance results, e.g. determining or preventing nonspecific binding
• CPC Class Codes: Y10S 436/804 Radioisotope, e.g. radioimmunoassay
• CPC Class Codes: Y10S 436/808 Automated or kit
• CPC Class Codes: Y10S 436/81 Tube, bottle, or dipstick
• CPC Class Codes: Y10S 436/815 Test for named compound or class of compounds
• CPC Class Codes: Y10S 436/817 Steroids or hormones

Abstract

A unitized solid phase kit for radioimmunoassay is disclosed. All of the necessary assay reagents are incorporated in a single tube wherein all phases of the assay procedure are performed, requiring only the addition of the patient'"'"'s sample. Antibody is bound to the tube surface, while labelled antigen is also present but unbound. Storage in the absence of air and water results in the stabilization of the reagents such that the system can be stored for long periods.

Claims

1. A means for use in the immunoassay of a component of the antigen-antibody reaction comprising a surface within a receptacle to at least a part of which one of the components in solid form is bound and in proximity to which the other component is present in labelled and in solid form but not bound, said components being present within said receptacle under conditions substantially impervious to the ambient atmosphere.

2. The means of claim 1 in which an antibody is bound to the surface and antigen is labelled and unbound.

8. The means of claim 2 in which antibody is adsorbed on a plastic polymeric surface.

9. The means of claim 8 in which a relatively impermeable smooth polyolefinic surface is employed.

10. The means of claim 9 in which a polystyrene surface is employed.

11. The means of claim 2 in which the antigen is digoxin and the antibody is antibody to digoxin.

12. The means of claim 2 in which the antigen is human growth hormone and the antibody is antibody to human growth hormone.

13. The means of claim 2 in which the antigen is cyclic adenosine monophosphate and the antibody is antibody to cyclic adenosine monophosphate.

31. The means of claim 1 in which the unbound component is labelled with a radioactive atom.

32. The means of claim 1 in which the unbound component is labelled with an enzyme.

33. The means of claim 1 in which the unbound component is labelled with a fluorescent group.

3. A means for use in radioimmunoassay comprising a surface within a receptacle having an antibody in solid form bound to at least a part thereof and radioactively labelled antigen in solid form dispersed over a portion thereof but not bound thereto, said antigen and antibody being present within said receptacle under conditions substantially impervious to the ambient atmosphere.

7. The means of claim 3 stored under a mositure-free nitrogen atmosphere.

4. A means for radioimmunoassay comprising a plastic assay tube having a relatively impermeable smooth surface and having antibody in solid state bound to a part of its interior surface and containing radioactively-labelled antigen in proximity thereto in solid state but not bound to the surface, said antigen and antibody being present within said tube under conditions substantially impervious to the ambient atmosphere.

5. The means of claim 4 in which the antibody is present in amount sufficient to bind 40 to 60% of the labelled antigen.

6. The means of claim 4 in which the tube contains an inert, moisture-free atmosphere and is hermetically sealed.

14. A method of preparing an immunoassay means which comprises coating and binding one of the components of an antigen-antibody reaction to at least part of a surface within a receptacle, and contacting the surface with the other component in labelled form in a manner to cause a dispersion of such component in solid form over at least part of the surface but not bound thereto nor to the other component, said components being present within said receptacle under conditions substantially impervious to the ambient atmosphere.

15. Method of claim 14 in which a test tube of water insoluble impervious polymeric material is coated with antibody from aqueous solution followed by removal of excess solution and washing, and then an aqueous solution of antigen is introduced and contacts the surface at a low temperature, followed by lyophilization to remove water, and the test tube contents are then protected by providing an inert atmosphere and sealing against external atmosphere.

16. A method for the immunochemical determination of a component of the antigen-antibody reaction which comprises:

a. coating by adsorption at least a small portion of the internal surface of a test tube of water insoluble polymeric material with the component not to be determined, said water insoluble polymeric material being capable of sorbing said component;

b. contacting the internal surface of said test tube with a buffered aqueous solution of protein to reduce the non-specific binding of the other component;

c. contacting the internal surface of said test tube, cooled to a temperature between about -10°

C and about 5°

C, with the buffered sample containing the other component in labelled form capable of emitting radiation;

d. freezing immediately the contents of said test tube;

e. lyophilizing the contents of said test tube; and

f. storing said test tube in the absence of air and water until required for use.

17. A method of determining a component of an antigen-antibody reaction in a sample solution which comprises coating and binding one of the components to at least part of a surface within a receptacle capable of binding said component and contacting the surface with the other component in labelled form in a manner to disperse it over the surface but not bound thereto, said components being retained within said receptacle under conditions substantially impervious to the ambient atmosphere, thereafter contacting the surface with a sample solution containing one of the components thereby producing a two-phase system and permitting interaction between the components causing some of the labelled component to be indirectly bonded to the surface, separating the two phases, and measuring the labelled content of one of the phases which is a function of the concentration of the component in the sample solution.

18. The method of claim 17 in which the labelled component in solution is quick-frozen upon contacting the surface followed by lyophilization to leave the labelled component as a solid residue on the surface.

19. The method of claim 17 in which part of the internal surface of a test tube of water-insoluble impervious polymeric material is coated with antibody from aqueous solution to bind antibody to its surface, followed by aspiration and washing, and an aqueous solution of labelled antigen is then introduced and contacts the surface at a low temperature no higher than about freezing temperature, followed by lyophilization to remove water, and storage under inert atmosphere prior to use.

20. The method of claim 19 in which the test tube is coated with protein prior to introduction of labelled antigen.

21. The method of claim 19 in which the test tube is composed of polyolefinic polymer and the antibody is adsorbed thereon.

22. The method of claim 19 in which a polystyrene tube is employed.

23. The method of claim 19 in which a sample solution of antigen is assayed and the quantity of bound antibody is insufficient to react with all of the labelled antigen and antigen in the sample solution.

24. A method for the immunochemical determination of a component of the antigen-antibody reaction which comprises:

a. coating by adsorption at least a small portion of the internal surface of a test tube of water insoluble polymeric material with the component not to be determined, said water insoluble polymeric material being capable of sorbing said component;

b. contacting the internal surface of said test tube with a buffered aqueous solution protein to reduce the non-specific binding of the other component;

c. contacting the internal surface of said test tube, cooled to a temperature between about -10°

C and about 5°

C, with the buffered sample containing the other component in labelled form capable of emitting radiation;

d. freezing immediately the contents of said test tube;

e. lyophilizing the contents of said test tube;

f. adding a sample containing the component to be determined to said test tube.

g. allowing the immunochemical reaction to take place to produce a two-phase system, comprising a solid phase and a liquid phase, wherein said solid phase includes the bound part of the labelled and unlabelled component to be determined and the liquid phase includes the unbound labelled and unlabelled component to be determined;

h. separating the solid phase from the liquid phase; and

i. determining the activity of the solid phase, said activity being a function of the concentration of said component to be determined in said sample.

25. The method of claim 24 wherein the antibody is antidigoxin and the method is used to determine digoxin.

26. The method of claim 24 wherein the antibody is anticyclic adenosine monophosphate and the method is used to determine cyclic adenosine monophosphate.

27. The method of claim 24 wherein the antibody is antihuman growth hormone and the method is used to determine human growth hormone.

28. The method of claim 24 wherein the protein bound to the internal surface of the container is serum albumin.

29. The method of claim 24 wherein the component to be determined in labelled form is labelled with a radioactive isotope of iodine.

30. The method of claim 24 wherein the radioactive isotope is I¹²⁵.