Particle agglutination assay of antigens

Claim 2

In a particle agglutination assay for an antigen (Ag) in a liquid sample, which comprises the steps of forming a reaction mixture of the liquid sample and finely divided particles bearing a reagent, the reagent being such as to bind with the Ag to cause agglutination of the particles; and measuring the extent of agglutination of the particles and therefrom determining the amount of Ag present; the improvement comprising introducing in solution in the reaction mixture a predetermined sensitivity increasing amount of a substance which is univalent towards the Ag and which specifically binds therewith so that the Ag bound to the substance is unable to agglutinate the particles, the quantity of substance being insufficient to bind with all the Ag under assay, and wherein the amount of Ag is determined from the extent of agglutination and the quantity of substance used.

Claim 3

A method according to claim 1, wherein the univalent substance is derived from whole antibody which specifically binds to the Ag under assay.

Claim 4

A method according to claim 2, wherein the univalent substance is a fragment of said whole antibody which is univalent to and specifically binds to the Ag.

Claim 5

A method according to claim 2, wherein the univalent substance is a hybrid antibody which is univalent to and specifically binds to the Ag.

Claim 6

A method according to claim 1, wherein the reagent is whole antibody, or F(ab') 2 fragments of whole anitbody, and specifically binds to the Ag.

Claim 7

In a method of assaying an Ag in a sample by a particle agglutination assay, in which the sample is mixed with a suspension of unagglutinated finely divided particles bearing a reagent which binds with the Ag to cause agglutination of the particles, the amount of Ag being determined by measuring the extent of agglutination and referring to standard results obtained by measuring the extent of agglutination with a range of known amounts of Ag, the improvement whereby amounts of Ag greater than said range can be assayed, which improvement comprises

Claim 8

In a method of assaying an Ag in a sample by a particle agglutination assay, in which the sample is mixed with a suspension of unagglutinated finely divided particles bearing a reagent which binds with the Ag to cause agglutination of the particles, the amount of Ag being determined by measuring the extent of agglutination and referring to standard results obtained by measuring the extent of agglutination with a range of known amounts of Ag, the improvement whereby amounts of Ag greater than said range can be assayed, which improvement comprises

Claim 9

(a) establishing new standard results for an assay in which there is also included in the mixture a known quantity of a substance which is univalent towards the Ag and is capable of binding therewith so that Ag so bound is not able to agglutinate the particles, said quantity of substance being insufficient to bind with all the Ag under assay; and (b) conducting said assay, using said known quantity of substance, on said sample of Ag and determining from the extent of agglutination and the said new standard results, the amount of Ag in the sample.

Claim 10

(a) establishing new standard results for an assay in which there is also included in the mixture a known quantity of a substance which is univalent towards the Ag and is capable of binding therewith so that Ag so bound is not able to agglutinate the particles, said quantity of substance being insufficient to bind with all the Ag under assay; and (b) conducting said assay, using said known quantity of substance, on said sample of Ag and determining from the extent of agglutination and the said new standard results, the amount of Ag in the sample.

Claim 11

In a particle agglutination assay for an antigen (Ag) in a liquid sample, which comprises forming a reaction mixture of the liquid sample and finely divided particles bearing a reagent, the reagent being such as to bind with the Ag to cause agglutination of the particles, said Ag being of the group consisting of C-reactive protein, thyroxin binding globulin, human placental lactogen, prealbumin or pregnancy protein SP1; and measuring the extent of agglutination of the particles and therefrom determining the amount of Ag present; the improvement comprising introducing in solution in the reaction mixture a predetermined sensitivity increasing amount of a fragment of whole antibody which is univalent towards and is derived from whole antibody which specifically binds to the Ag, the antibody fragment binding to the Ag so that the Ag so bound is unable to agglutinate the particles, the quantity of substance being insufficient to bind with all the Ag under assay, and wherein the amount of Ag is determined from the extent of agglutination and the quantity of substance used.

Claim 12

In a particle agglutination assay for an antigen (Ag) in a liquid sample, which comprises forming a reaction mixture of the liquid sample and finely divided particles bearing a reagent, the reagent being such as to bind with the Ag to cause agglutination of the particles, said Ag being of the group consisting of C-reactive protein, thyroxin binding globulin, human placental lactogen, prealbumin or pregnancy protein SP1; and measuring the extent of agglutination of the particles and therefrom determining the amount of Ag present; the improvement comprising introducing in solution in the reaction mixture a predetermined sensitivity increasing amount of a fragment of whole antibody which is univalent towards and is derived from whole antibody which specifically binds to the Ag, the antibody fragment binding to the Ag so that the Ag so bound is unable to agglutinate the particles, the quantity of substance being insufficient to bind with all the Ag under assay, and wherein the amount of Ag is determined from the extent of agglutination and the quantity of substance used.