Process and composition for the rapid quantitation of small levels of creative kinase-MB isoenzyme

Claim 2

A two site immunometric sandwich assay method for the assay of creatine phospho kinase-MB(CK-MB) in human serum comprising: (a) reacting a serum specimen suspected of containing CK-MB with a matrix to form a first reaction solution, said matrix including; 1. a solid-phase having an antibody to an isoenzyme selected from the group consisting of CK-MM and CK-BB bound to the surface of said solid phase; and 2. a liquid phase surrounding said solid phase including therein a substantial component of pooled human serum; (b) separating the solid phase portion of said first reaction solution from the liquid portion thereof; (c) reacting said solid-phase portion from said first reaction solution with tracer including a labeled antibody being drawn against the remaining isoenzyme not selected in step (a) hereinabove; (d) separating the solid-phase portion of the second reaction solution from the liquid portion thereof; (e) testing said solid-phase portion from said second reaction solution to detect the tracer as an indication of the presence of CK-MB.

Claim 3

A two site immunometric sandwich assay method as recited in claim 1 and further comprising repeating steps (a)-(e) several times substituting for said serum sample in each repetition of steps (a)-(e) a calibrating sample containing a differing known amount of CK-MB whereby a calibration curve is created, and comparing the test results for said serum to said calibration curve, each said calibration sample containing a quantity of pooled human serum and said liquid phase portion of said matrix also containing a quantity of human serum drawn from the same pooled human serum as utilized in said calibrating sample.

Claim 4

A two site immunometric sandwich assay method as recited in claim 1 wherein said tracer is formulated according to the following procedure: (a) tagging the antibody with a radiolabel; (b) aging the radiolabeled antibody at a temperature of 0-6 degrees C. for at least four hours; (c) filtering the aged antibody.

Claim 5

The two site immunometric sandwich assay method as recited in claim 1 wherein said liquid phase includes Bovine serum albumin, Polyoxyethylenesorbitan, Polyethylene glycol and human IgG.

Claim 6

The two site immunometric sandwich assay method as recited in claim 1 wherein said human serum includes unclarified human serum.

Claim 7

The two site immunometric sandwich assay method as recited in claim 1 wherein said solid phase comprises a particulate solid phase.

Claim 8

The two site immunometric sandwich assay method as recited in claim 1 wherein said solid phase is selected from a group consisting of latex, nylon, polyacrylamide and aragose.

Claim 9

A two site immunometric sandwich assay method for the assay of creatine phospho kinase-MB(CK-MB) in human serum comprising: (a) reacting a serum specimen suspected of containing CK-MB with a matrix to form a first reaction solution, said matrix including; 1. a particulate solid-phase having an antibody to CK-BB bound to the surface of said solid phase, said solid phase being selected from a group consisting of latex, nylon, polyacrylamide, polyvinylidene fluoride and agarose. 2. a liquid phase surrounding said solid phase including therein a substantial component of pooled human serum, bovine serum albumin, Polyoxyethylenesorbitan, Polyethylene glycol and human IgG. (b) diluting the volume of the matrix at least 10 fold with water; (c) centrifuging the mixture and removing the resultant solid pellet; (d) resolubilizing and incubating the pellet material with a volume of a reagent including 125 I labeled antiCK-MM which has been produced as follows: (1) forming 125 I labeled antibodies made against human CK-MM in a species other than human; (2) purifying the antibody; (3) diluting the result of step (2) with a phosphate buffer having a pH of about 7.5; (4) refrigerating the result of step 3 at 0-6 degrees celsius for at least eight hours; (5) filtering the refrigerated result of step 4; and (6) adding Polyoxyethylenesorbitan, Polyethylene glycol and human IgG to the product of step (5). (e) diluting the volume of the mixture at least 10 fold; (f) centrifuging and removing the resultant solid; and (g) counting the radioactivity of the resultant solid; and (h) repeating steps (a)-(g) several times substituting for said serum sample in each repetition of steps (a)-(g) a calibrating sample containing a different known amount of CK-MB whereby a calibration curve is created, and comparing the test results for said serum to said calibration curve; each said calibration sample containing a quantity of pooled human serum and said liquid phase of said matrix also containing a quantity of human serum drawn from the same pooled human serum as utilized in said calibrating sample.

Claim 10

A two site immunometric sandwich assay method for the assay of creatine phospho kinase-MB(CK-MB) in human serum comprising: (a) reacting a serum specimen suspected of containing CK-MB with a matrix to form a first reaction solution, said matrix including; 1. a particulate solid-phase having an antibody to CK-BB bound to the surface of said solid phase, said solid phase being selected from a group consisting of latex, nylon, polyacrylamide, polyvinylidene fluoride and agarose. 2. a liquid phase surrounding said solid phase including therein a substantial component of pooled human serum, bovine serum albumin, Polyoxyethylenesorbitan, Polyethylene glycol and human IgG. (b) diluting the volume of the matrix at least 10 fold with water; (c) centrifuging the mixture and removing the resultant solid pellet; (d) resolubilizing and incubating the pellet material with a volume of a reagent including 125 I labeled antiCK-MM which has been produced as follows: (1) forming 125 I labeled antibodies made against human CK-MM in a species other than human; (2) purifying the antibody; (3) diluting the result of step (2) with a phosphate buffer having a pH of about 7.5; (4) refrigerating the result of step 3 at 0-6 degrees celsius for at least eight hours; (5) filtering the refrigerated result of step 4; and (6) adding Polyoxyethylenesorbitan, Polyethylene glycol and human IgG to the product of step (5). (e) diluting the volume of the mixture at least 10 fold; (f) centrifuging and removing the resultant solid; and (g) counting the radioactivity of the resultant solid; and (h) repeating steps (a)-(g) several times substituting for said serum sample in each repetition of steps (a)-(g) a calibrating sample containing a different known amount of CK-MB whereby a calibration curve is created, and comparing the test results for said serum to said calibration curve; each said calibration sample containing a quantity of pooled human serum and said liquid phase of said matrix also containing a quantity of human serum drawn from the same pooled human serum as utilized in said calibrating sample.

Claim 11

The process of claim 8 wherein the animal species used to raise the antibody of step (d) is different than the species used to raise the CK antibody used in step (a).

Claim 12

A reagent matrix for sandwich immunoassay testing for CK-MB isoenzyme in a test sample comprising: (a) a solid phase having an antibody to an isoenzyme selected from the group consisting of CK-MM and CK-BB bound to the surface of the solid phase; and (b) a liquid phase surrounding said solid phase including human serum as a substantial component, and wherein said human serum does not include and is not derived from said human serum sample.

Claim 13

A reagent matrix for sandwich immunoassay testing for CK-MB isoenzyme in a test sample comprising: (a) a solid phase having an antibody to an isoenzyme selected from the group consisting of CK-MM and CK-BB bound to the surface of the solid phase; and (b) a liquid phase surrounding said solid phase including human serum as a substantial component, and wherein said human serum does not include and is not derived from said human serum sample.

Claim 14

The matrix of claim 10 wherein said liquid matrix includes bovine serum albumin, Polyoxyethylenesorbitan, Polyethylene glycol and human IgG.

Claim 15

The matrix of claim 10 wherein said human serum component of said liquid phase includes unclarified human serum.

Claim 16

The matrix of claim 10 wherein said solid phase includes a particulate solid phase.

Claim 17

The matrix of claim 11 wherein said solid phase is selected from a group consisting of latex, nylon, polyacrylamide, polyvinylidene fluoride and agarose.

Claim 18

A reagent for CK-MB immunoassay testing having a radioisotope tracer label made by the process of: (a) forming 125 I labeled antibodies made against human CK-MM in a species other that human; (b) purifying the antibody; (c) diluting the result of step (b); (d) refrigerating the result of step (c), at 0-6 degrees celsius for at least eight hours; (e) filtering the refrigerated the result of step (d), and (f) adding Polyoxyethylenesorbitan, Polyethylene glycol and human IgG to the product of step (e).

Claim 19

A reagent for CK-MB immunoassay testing having a radioisotope tracer label made by the process of: (a) forming 125 I labeled antibodies made against human CK-MM in a species other that human; (b) purifying the antibody; (c) diluting the result of step (b); (d) refrigerating the result of step (c), at 0-6 degrees celsius for at least eight hours; (e) filtering the refrigerated the result of step (d), and (f) adding Polyoxyethylenesorbitan, Polyethylene glycol and human IgG to the product of step (e).

Claim 20

A test kit for the measurement of CK-MB in human serum comprising: a first container of a reagent matrix including an antiCK-BB coated bead suspension in a liquid solution which includes pooled human serum; a plurality of containers of calibrating liquids, each liquid having a differing known amount of CK-MB in pooled human serum; the pooled human serum utilized to make the calibrating liquids also being added to the matrix; and a container of tracer having antiCK-MM antibody labeled with 125 I in a liquid solution.

Claim 21

A test kit for the measurement of CK-MB in human serum comprising: a first container of a reagent matrix including an antiCK-BB coated bead suspension in a liquid solution which includes pooled human serum; a plurality of containers of calibrating liquids, each liquid having a differing known amount of CK-MB in pooled human serum; the pooled human serum utilized to make the calibrating liquids also being added to the matrix; and a container of tracer having antiCK-MM antibody labeled with 125 I in a liquid solution.