Immunoassay with antigen or antibody labelled microcapsules containing fluorescent substance

Claim 2

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding complement to the mixture to initiate lysis of the microcapsules wherein the number of microcapsules lysed is dependent upon the antigen concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 3

The immunoassay method of claim 1, wherein said microcapsules contain a viscosity modifier in sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 4

The immunoassay method of claim 1, wherein the mixture outside said microcapsules contains a viscosity modifier in a sufficient concentration to make the viscosity of the fluid inside said microcapsules lower than the viscosity of the mixture outside said microcapsules.

Claim 5

The immunoassay method of claim 2, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 6

The immunoassay method of claim 3, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 7

The immunoassay method of claim 4, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin and sucrose.

Claim 8

The immunoassay method of claim 5, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin and sucrose.

Claim 9

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding complement to the mixture to initiate lysis of the microcapsules wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥ of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 10

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding complement to the mixture to initiate lysis of the microcapsules wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥ of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 11

The immunoassay method of claim 8, wherein said microcapsules contain a viscosity modifier in sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 12

The immunoassay method of claim 8, wherein the mixture outside said microcapsules contains a viscosity modifier in a sufficient concentration to make the viscosity of the fluid inside said microcapsules lower than the viscosity of the mixture outside said microcapsules.

Claim 13

The immunoassay method of claim 9, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 14

The immunoassay method of claim 10, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 15

The immunoassay method of claim 11, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin, and sucrose.

Claim 16

The immunoassay method of claim 12, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin, and sucrose.

Claim 17

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysising upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed are dependent upon the antigen concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; and, (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 18

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysising upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed are dependent upon the antigen concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; and, (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 19

The immunoassay method of claim 15, wherein said microcapsules contain a viscosity modifier in sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 20

The immunoassay method of claim 15, wherein the mixture outside said microcapsules contains a viscosity modifier in a sufficient concentration to make the viscosity of the fluid inside said microcapsules lower than the viscosity of the mixture outside said microcapsules.

Claim 21

The immunoassay method of claim 16, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 22

The immunoassay method of claim 17, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 23

The immunoassay method of claim 18, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin and sucrose.

Claim 24

The immunoassay method of claim 19, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin, and sucrose.

Claim 25

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 26

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid having a viscosity different from that of the mixture outside the microcapsules; (ii) contain a fluorescent substance; and, are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (c) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (d) irradiating the reaction mixture with excited light and detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (e) comparing the detection results of the vertical-polarization component of I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture with the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (f) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 27

The immunoassay method of claim 22, wherein said microcapsules contain a viscosity modifier in sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 28

The immunoassay method of claim 22, wherein the mixture outside said microcapsules contains a viscosity modifier in a sufficient concentration to make the viscosity of the fluid inside said microcapsules lower than the viscosity of the mixture outside said microcapsules.

Claim 29

The immunoassay method of claim 23, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 30

The immunoassay method of claim 24, wherein said viscosity modifier is a water-soluble organic compound having a viscosity higher than that of water.

Claim 31

The immunoassay method of claim 25, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin and sucrose.

Claim 32

The immunoassay method of claim 26, wherein said viscosity modifier is selected from the group consisting of polyvinyl alcohol, glycerin and sucrose.

Claim 33

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU3## (e) adding complement to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antigen concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU4## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence P B of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentration of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 34

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU3## (e) adding complement to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antigen concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU4## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence P B of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentration of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 35

The immunoassay method of claim 29, wherein said viscosity modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 36

The immunoassay method of claim 30, wherein said modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules greater than 0.01, in terms of degree of polarization fluorescence, the viscosity of the mixture outside said microcapsules.

Claim 37

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU5## (e) adding complement to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU6## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence P B of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 38

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with a sample to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU5## (e) adding complement to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU6## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence P B of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 39

The immunoassay method of claim 32, wherein said viscosity modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 40

The immunoassay method of claim 32, wherein said modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules greater than 0.01, in terms of degree of polarization fluorescence, the viscosity of the mixture outside said microcapsules.

Claim 41

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU7## (e) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antigen concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU8## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 42

An immunoassay method for determining the concentration of an antigen in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antibody for the antigen being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU7## (e) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antigen concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU8## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antigen to change in polarization fluorescence measurements, thereby determining the concentration of the antigen in the test sample.

Claim 43

The immunoassay method of claim 35, wherein said viscosity modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 44

The immunoassay method of claim 35, wherein said modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules greater than 0.01, in terms of degree of polarization fluorescence, the viscosity of the mixture outside said microcapsules.

Claim 45

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU9## (e) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU10## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 46

An immunoassay method for determining the concentration of an antibody in a test sample, comprising the steps of: (a) mixing microcapsules labelled with an antigen for the antibody being tested for with complement to produce a mixture; wherein said microcapsules (i) contain a fluid, a fluorescent substance, and, a viscosity modifier which modifies the viscosity of the fluid contained inside the microcapsules to a viscosity different from that of the mixture outside of the microcapsules; and, (ii) are susceptible to lysis upon complement activated immunoreaction; (b) irradiating said mixture with excited light; (c) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the mixture; (d) calculating the degree of polarization fluorescence P B of the mixture by the equation: ##EQU9## (e) adding a sample to be tested to the mixture to initiate lysis of the microcapsules by the activated complement-antibody-antigen reaction wherein the number of microcapsules lysed is dependent upon the antibody concentration of the sample; (f) irradiating the reaction mixture with excited light; (g) detecting the vertical-polarization component I.sub.∥B and the parallel-polarization component I.sub.⊥B of fluorescence from the reaction mixture; (h) calculating the degree of polarization fluorescence P B of the reaction mixture by the equation: ##EQU10## (i) comparing the degree of polarization fluorescence P B of the mixture with the degree of polarized fluorescence of the reaction mixture to determine the change in the degree of polarization fluorescence due to the lysis of the microcapsules; and, (j) comparing the change in the degree of polarization fluorescence with a calibration curve which was previously prepared by subjecting standard samples containing known concentrations of the antibody to change in polarization fluorescence measurements, thereby determining the concentration of the antibody in the test sample.

Claim 47

The immunoassay method of claim 38, wherein said viscosity modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules higher than the viscosity of the mixture outside said microcapsules.

Claim 48

The immunoassay method of claim 38, wherein said modifier is present in the microcapsules in a sufficient concentration to make the viscosity of the fluid inside said microcapsules greater than 0.01, in terms of degree of polarization fluorescence, the viscosity of the mixture outside said microcapsules.

Claim 49

An immunoassay test kit for determining the concentration of an antigen in a test sample, said test kit comprising: a container carrying microcapsules labelled with an antibody for the antigen being tested for, and complement, wherein said microcapsules (i) contain a fluid having a viscosity different from that of the test sample; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction.

Claim 50

An immunoassay test kit for determining the concentration of an antigen in a test sample, said test kit comprising: a container carrying microcapsules labelled with an antibody for the antigen being tested for, and complement, wherein said microcapsules (i) contain a fluid having a viscosity different from that of the test sample; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction.

Claim 51

An immunoassay test kit for determining the concentration of an antibody in a test sample, said test kit comprising: a container carrying microcapsules labelled with an antigen for the antibody being tested for, and complement, wherein said microcapsules, (i) contain a fluid having a viscosity different from that of the test sample; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction.

Claim 52

An immunoassay test kit for determining the concentration of an antibody in a test sample, said test kit comprising: a container carrying microcapsules labelled with an antigen for the antibody being tested for, and complement, wherein said microcapsules, (i) contain a fluid having a viscosity different from that of the test sample; (ii) contain a fluorescent substance; and, (iii) are susceptible to lysis upon complement activated immunoreaction.