Sandwich immunoassay utilizing a separation specific binding substance

Claim 2

An immunoassay method for determining the amount of a polyvalent ligand in a liquid test sample, said ligand being an antibody or a substance capable of specific binding to an antibody, said method comprising the steps of: (a) providing an insoluble phase to which is bound a separation specific binding substance which does not bind said ligand, wherein said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) incubating said insoluble phase with (1) said liquid test sample; (2) a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to said hapten comprising said carborane moiety which is specifically bound by said separation specific binding substance; and (3) a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, said probe specific binding substance being not substantially bound by said separation specific binding substance, and being detectable by at least one direction procedure; (c) separating said insoluble phase, after said incubation, from resultant liquid phase containing unbound reagents and components of said test sample; and (d) determining, by means of said detection procedure, the amount of said detectable probe which is bound to said separated insoluble phase, or the amount of said detectable probe remaining in said resultant liquid phase, said determination being related to the amount of said ligand in said test sample.

Claim 3

The method of claim 1, wherein said ligand is an antibody, and said capture specific binding substance comprises a specific binding complement to said antibody.

Claim 4

The method of claim 1, wherein said probe specific binding substance is labeled with an enzyme, a radioisotope or a fluorescent marker.

Claim 5

The method of claim 1, wherein each of said probe specific binding substance and said capture specific binding substance comprises an antibody, and said ligand is a specific binding complement to both of said antibodies.

Claim 6

The method of claim 4, wherein said ligand is a tumor-associated marker.

Claim 7

The method of claim 5, wherein said marker is carcinoembryonic antigen, colon-specific antigen-p, human chorionic gonadotrophin or its beta-subunit, alpha-fetoprotein, meconium antigen or prostatic acid phosphatase.

Claim 8

The method of claim 4, wherein said ligand is an infectious organism.

Claim 9

The method of claim 7, wherein said infectious organism is a virus, bacterium, fungus or protozoan.

Claim 10

An immunoassay method for determining the amount of each of a plurality of polyvalent ligands in a liquid test sample, each of said ligands being an antibody or a substance capable of specific binding to an antibody, said method comprising the steps of; (a) providing an insoluble phase to which is bound at least one separation specific binding substance which does not bind any of said ligands, wherein each said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) incubating said insoluble phase with (1) said liquid test sample; (2) for each said ligand, a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to a hapten comprising a carborane moiety which is specifically bound by at least one of said separation specific binding substances; and (3) for each said ligand, a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, each said probe specific binding substance being not substantially bound by said separation specific binding substance, and each being separately detectable by at least one detection procedure; (c) separating said insoluble phase, after said incubation, from resultant liquid phase containing unbound reagents and components of said test sample; and (d) determining, by means of said detection procedure, the amount of each said detectable probe which is bound to said separated insoluble phase, or the amount of each said detectable probe remaining in said resultant liquid phase, said determination being related to the amount of said ligand in said test sample.

Claim 11

An immunoassay method for determining the amount of each of a plurality of polyvalent ligands in a liquid test sample, each of said ligands being an antibody or a substance capable of specific binding to an antibody, said method comprising the steps of; (a) providing an insoluble phase to which is bound at least one separation specific binding substance which does not bind any of said ligands, wherein each said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) incubating said insoluble phase with (1) said liquid test sample; (2) for each said ligand, a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to a hapten comprising a carborane moiety which is specifically bound by at least one of said separation specific binding substances; and (3) for each said ligand, a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, each said probe specific binding substance being not substantially bound by said separation specific binding substance, and each being separately detectable by at least one detection procedure; (c) separating said insoluble phase, after said incubation, from resultant liquid phase containing unbound reagents and components of said test sample; and (d) determining, by means of said detection procedure, the amount of each said detectable probe which is bound to said separated insoluble phase, or the amount of each said detectable probe remaining in said resultant liquid phase, said determination being related to the amount of said ligand in said test sample.

Claim 12

The method of claim 9, suitable for the simultaneous determination of CEA and CSAp, wherein one of said capture specific binding substances and one of said probe specific binding substances are each a monoclonal antibody which specifically binds CEA, and a different one of said capture specific binding substances and a different one of said probe specific binding substances are each a monoclonal antibody which specifically binds CSAp.

Claim 13

An immunoassay kit, suitable for determining the amount of a polyvalent ligand in a liquid test sample, comprising: (a) an insoluble phase to which is bound a separation specific binding substance which does not bind said ligand, wherein said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to said hapten comprising said carborane moiety which is specifically bound by said separation specific binding substance; and (c) a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, said probe specific binding substance being not substantially bound by said separation specific binding substance, and being detectable by at least one detection procedure.

Claim 14

An immunoassay kit, suitable for determining the amount of a polyvalent ligand in a liquid test sample, comprising: (a) an insoluble phase to which is bound a separation specific binding substance which does not bind said ligand, wherein said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to said hapten comprising said carborane moiety which is specifically bound by said separation specific binding substance; and (c) a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, said probe specific binding substance being not substantially bound by said separation specific binding substance, and being detectable by at least one detection procedure.

Claim 15

The kit of claim 11, suitable for use wherein said ligand is an antibody, wherein said capture specific binding substance comprises an antigen which is a specific binding complement to said antibody.

Claim 16

The kit of claim 11, wherein said probe specific binding substance is labeled with an enzyme, a radioisotope or a fluorescent marker.

Claim 17

The kit of claim 11, wherein each of said probe specific binding substance and said capture specific binding substance comprises an antibody which specifically binds the ligand to be assayed.

Claim 18

The kit of claim 14 suitable for use for immunoassay of a ligand which is a tumor-associated marker, wherein said capture specific binding substance and said probe specific binding substance each comprise an antibody which specifically binds the tumor-associated marker to be assayed.

Claim 19

The kit of claim 15 wherein said marker is carcinoembryonic antigen, colon-specific antigen-p, human chorionic gonadotrophin or its beta-subunit, alpha-fetoprotein, meconium antigen or prostatic acid phosphatase.

Claim 20

The kit of claim 14, wherein said capture and probe antibodies each specifically bind an infectious organism.

Claim 21

The kit of claim 17, wherein said infectious organism is a virus, bacterium, fungus or protozoan.

Claim 22

An immunoassay kit, suitable for determining the amount of each of a plurality of polyvalent ligands in a liquid test sample, each of said ligands being an antibody or a substance capable of specific binding to an antibody, said kit comprising; (a) an insoluble phase to which is bound at least one separation specific binding substance which does not bind any of said ligands, wherein each said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) for each said ligand, a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to a hapten comprising a carborane moiety which is specifically bound by at least one of said separation specific binding substances; and (c) for each said ligand, a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, each said probe specific binding substance being not substantially bound by said separation specific binding substance, and each being separately detectable by at least one detection procedure.

Claim 23

An immunoassay kit, suitable for determining the amount of each of a plurality of polyvalent ligands in a liquid test sample, each of said ligands being an antibody or a substance capable of specific binding to an antibody, said kit comprising; (a) an insoluble phase to which is bound at least one separation specific binding substance which does not bind any of said ligands, wherein each said separation specific binding substance is an antibody which specifically binds the carborane moiety of a hapten comprising a carborane moiety, said hapten being conjugated to a capture specific binding substance; (b) for each said ligand, a capture specific binding substance which specifically binds said ligand, and which is itself conjugated to a hapten comprising a carborane moiety which is specifically bound by at least one of said separation specific binding substances; and (c) for each said ligand, a probe specific binding substance which specifically binds said ligand at a site which is accessible when said ligand is bound to said capture specific binding substance, each said probe specific binding substance being not substantially bound by said separation specific binding substance, and each being separately detectable by at least one detection procedure.

Claim 24

The kit of claim 19, suitable for the simultaneous determination of CEA and CSAp, wherein one of said capture specific binding substances and one of said probe specific binding substances are each a monoclonal antibody which specifically binds CEA, and a different one of said capture specific binding substances and a different one of said probe specific binding substances are each a monoclonal antibody which specifically binds CSAp.