Container for immunochemical and enzymatical determinations or procedures

• US 4,210,418 A
• Filed: 01/10/1977
• Issued: 07/01/1980
• Est. Priority Date: 08/30/1976
• Status: Expired due to Term

• Current Assignee: Mallinckrodt Incorporated (Mallinckrodt plc)
• Original Assignee: Mallinckrodt Incorporated (Mallinckrodt plc)
• Inventors: Woods, James W., Lin, Wayne H. T., Brown, James L.
• Primary Examiner(s): Serwin, R. E.
• Application Number:
  US05/758,364
• Time in Patent Office: 1,268 Days
• Field of Search: 23/230 B, 23/259, 23/292, 23/230.6, 23/230.3, 195/103.5 A, 195/127, 424/1, 424/1.5, 424/12, 427/2
• US Class Current: 436/532
• CPC Class Codes: B01L 3/5082 Test tubes per se
• CPC Class Codes: G01N 33/545 Synthetic resin
• CPC Class Codes: Y02P 80/15 On-site combined power, heat or cool generation or distribution, e.g. combined heat and power [CHP] supply
• 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 435/963 Methods of stopping an enzyme reaction or stabilizing the test materials
• CPC Class Codes: Y10S 436/81 Tube, bottle, or dipstick
• CPC Class Codes: Y10S 436/826 Additives, e.g. buffers, diluents, preservatives

Abstract

A container useful in immunochemical and enzymatical determinations or procedures.

Claims

1. An elongated, hollow container suitable for use in an immunochemical or enzymatical procedure comprising

(a) a lower reactive part composed of a polymeric material, said part being closed at one end and having on at least a portion of its inner surface a coating of an inert protein to which a biologically active substance is attached;

and

(b) a separable inert upper part connected to and in communication with said lower part.

2. In an immunochemical or enzymatical method for determining the concentration of a member selected from the group consisting of an antigen and hapten in a measured amount of an aqueous sample wherein said aqueous solution is contacted with (1) an insoluble carrier to which has been attached a biologically active substance capable of reacting with said member and (2) a measured amount of tracer labelled member to form after substantial equilibration a 2-phase system containing a solid phase having a portion of the labelled member and unlabelled member bound to said biologically active substance and a liquid phase containing the balance of the unbound labelled member and unlabelled member, the two phases separated and the concentrated determined, the improvement comprising using as the insoluble carrier the container of claim 1.

3. In a radioimmunoassay method for determining the concentration of a member selected from the group consisting of an antigen and hapten in a measured amount of an aqueous sample wherein said aqueous sample is contacted with (1) an insoluble carrier to which has been attached a biologically active substance capable of reacting with said member and (2) a measured amount of radioactively labelled member to form after substantial equilibration a 2-phase system containing a solid phase having a portion of the labelled member and unlabelled member bound to said biologically active substance and a liquid phase containing the balance of the unbound labelled member and unlabelled member, the 2-phases separated and the radioactivity of at least one of the phases being measured, the value of radioactivity being a function of the concentration of said member in the aqueous sample, the improvement comprising using as the insoluble carrier the container of claim 1.

4. A method according to claim 3 wherein said biologically active substance is an antibody.

5. A method according to claim 4 wherein said reactive part has said coating on a portion of its inner surface and a portion of its outer surface.

6. A method according to claim 5 wherein said antibody is covalently bound to said inert protein through a coupling agent which contains α

,β

unsaturation, carbonyl groups, azo groups, sulfonic acid groups, fluoro groups activated by nitro groups, azide groups, imine groups or reactive chloro groups connected to ring structures.

7. A method according to claim 6 wherein the container is in the form of a tube.

8. A method according to claim 7 wherein said inert protein is gelatin of bovine gamma globulin.

9. A method according to claim 8 wherein said reactive part is composed of a copolymer of polyethylene and acrylic acid.

10. A method according to claim 9 wherein said biologically active substance is covalently bound with an aldehyde coupler.

11. A method according to claim 10 wherein said antibody is an antibody to triiodothyronine, thyroxine or digoxin.

12. A method according to claim 11 wherein said inert protein is bovine gamma globulin said coupler is glutaraldehyde and said lower part is composed of a copolymer of polyethylene and acrylic acid and said upper part is polypropylene.

13. A process for preparing the lower reactive part of claim 1 which comprises

(a) coating by adsorption the surface of a lower reactive part composed of a polymeric material, said part being closed at one end with an inert protein under adsorbing conditions

(b) attaching a biologically active substance to the inert protein coating on the lower reactive part of (a) under attaching conditions

(c) treating the lower reactive part of (b) having the biologically active substance attached to the inert protein coating with a stabilizing agent to stabilize such biologically active substance against denaturization and

(d) drying the reactive part under drying conditions that will not substantially denature the biologically active substance.

14. A process according to claim 13 wherein the biologically active substance is attached to the inert protein coating by covalent binding through a coupling agent which contains α

,β

unsaturation, carbonyl groups, azo groups, sulfonic acid groups, fluoro groups activated by nitro groups, azide groups, imine groups or reactive chloro groups connected to ring structures.

15. A process according to claim 14 wherein said biologically active substance is an antibody.

16. A process according to claim 15, wherein the inert protein is contained in a phosphate buffer solution, the antibody is contained in a phosphate buffer solution, the coupling agent to covalently bind the antibody is contained in a phosphate buffer solution, and the stabilizing agent is contained in a phosphate buffer solution.

17. A process according to claim 16 wherein said phosphate buffer solution containing the antibody additionally contains an inert protein to retard denaturization of the antibody.

18. A process according to claim 17 wherein said antibody is covalently bound with an aldehyde coupler.

19. A process according to claim 18 wherein said reactive part is composed of a copolymer of polyethylene and acrylic acid.

20. A process according to claim 19 wherein said inert protein adsorbed on the surface is bovine gamma globulin and said inert protein to retard denaturization of the antibody is bovine serum albumin.

21. A process according to claim 20 wherein said antibody is an antibody to triiodothyronine, thyroxine or digoxin.

22. A process according to claim 21 wherein said stabilizer is polyvinyl alcohol.

23. A process according to claim 22 wherein said lower reactive part is dried utilizing vacuum drying.

24. A process for preparing a lower reactive part, composed of a copolymer of polyethylene and acrylic acid, said part being closed at one end and having on at least a portion of its inner surface a coating of the inert protein bovine gamma globulin to which digoxin antibody is attached which comprises:

(a) cleaning with 0.5% by weight, based on the total volume of the solution, of an aqueous solution of sodium dodecyl sulfate the surface of a lower reactive part, composed of a copolymer of polyethylene, 92% by weight and acrylic acid, 8% by weight, said part being closed at one end and thereafter washing one or more times with water,

(b) treating the lower reactive part of (a) with a sufficient amount of an aqueous solution of potassium hydroxide to convert the carboxyl groups on the surface to the salt form, washing one or more times with water and then with a phosphate buffer solution having a pH of about 6.4,

(c) coating by adsorption the surface of the lower reactive part of (b) by immersing in a phosphate buffer solution containing the inert protein bovine gamma globulin under adsorbing conditions and thereafter washing with water one or more times and then washing with a phosphate buffer solution having a pH of about 7.4,

(d) coupling sufficient glutaraldehyde to enable attachment of antibody to digoxin to the bovine gamma globulin coating on the reactive part of (c) by immersing said reactive part in a phosphate buffer solution having a pH of about 7.4, containing about 2% by weight based on the total volume of the solution of glutaraldehyde, thereafter washing with water one or more times and then washing with a phosphate buffer solution having a pH of 7.0,

(e) coupling antibody to digoxin to the glutaraldehyde on the reactive part of (d) by immersing said reactive part in a phosphate buffer solution having a pH of 7.0, containing antibody to digoxin in a dilution of 1/325,000 to 1/335,000 and a protective agent, bovine serum albumin, to retard denaturization of said antibody under attaching conditions, washing with water one or more times and then washing with a glycine buffer solution having a pH of about 2.4 to remove any antibody not coupled to the glutaraldehyde,

(f) washing one or more times with a phosphate buffer solution having a pH of about 7.4 and thereafter treating with a phosphate buffer solution having a pH of about 7.4 containing 2% by weight, based on the total volume of the solution, polyvinyl alcohol as a stabilizing agent, and

(g) vacuum drying under conditions which will not substantially denature the antibody.

26. An elongated, hollow container suitable for use in an immunochemical or enzymatical procedure comprising

(a) a lower reactive part composed of a polymeric material containing carboxylate salt groups, said part being closed at one end and having attached on at least a portion of its inner surface a coating of an inert protein to which a biologically active substance, stabilized against denaturization, is attached by means of a chemical coupling agent through which said biologically active substance is covalently bound to said inert protein;

and

(b) a separable inert upper part connected to and in communication with said lower part.

25. A method for preparing an elongated hollow container suitable for use in an immunochemical or enzymatical procedure comprising attaching a separable inert upper part to the lower reactive part of claim 33 so that said inert upper part is in communication with said lower part.

27. A container according to claim 26 wherein said biologically active substance is an antibody.

28. A container according to claim 27 wherein said reactive part has said coating on a portion of its inner surface and a portion of its outer surface.

29. A container according to claim 28, wherein said antibody substance is covalently bound to said inert protein through a coupling agent which contains α

,β

unsaturation, carbonyl groups, azo groups, sulfonic acid groups, fluoro groups activated by nitro groups, azide groups, imine groups or reactive chloro groups connected to ring structures.

30. A container according to claim 29 in the form of a tube.

31. A container according to claim 29 wherein said inert protein is gelatin or bovine gammaglobulin.

32. A container according to claim 29 wherein said reactive part is composed of a copolymer of ethylene and acrylic acid.

33. A container according to claim 29 wherein said biologically active substance is covalently bound with an aldehyde coupler.

34. A container according to claim 29 wherein said antibody is an antibody to triiodothyronine, thyroxine or digoxin.

35. A container according to claim 29 wherein said inert protein is bovine gammaglobulin, said coupler is glutaraldehyde said lower part is composed of a coplymer of polyethylene and acrylic acid and said upper part is polypropylene.

36. A process for preparing the lower reactive part of claim 26 which comprises

(a) coating by adsorption the surface of a lower reactive part composed of a polymeric material containing carboxylate salt groups, said part being closed at one end, with an inert protein under adsorbing conditions

(b) attaching a biologically active substance to the inert protein coating on the lower reactive part of (a) under attaching conditions by means of a chemical coupling agent through which said biologically active substance is covalently bound to said inert protein

(c) treating the lower reactive part of (b) having the biologically active substance attached to the inert protein coating with a stabilizing agent to stabilize such biologically active substance against denaturization and

(d) drying the reactive part under drying conditions that will not substantially denature the biologically active substance.