Quantitative detection of analytes on immunochromatographic strips

Claim 1

A method for determining the concentration of one or more analyte in a fluid test sample which comprises: a) providing a test strip comprising a matrix through which the fluid test sample can flow by capillarity wherein a first region of the strip contains mobile specific binding partner for the analyte which bears a detectable label and can react with the analyte to form an analyte/labeled binding partner complex and at least one second region which contains immobilized analyte or analog thereof, b) developing the strip by applying the fluid test sample suspected of containing the analyte thereto thereby allowing the same contact the mobile, labeled specific binding partner for the analyte whereby analyte present in the fluid test sample binds to the labeled specific binding partner to form the complex leaving excess, unreacted labeled binding partner free to further react whereby the fluid test sample carries the analyte/labeled binding partner complex and unreacted labeled binding partner along the strip by capillarity to the second region containing the immobilized analyte or analog thereof in which region unreacted labeled binding partner is bound to the inmlobilized analyte in inverse relationship to the concentration of analyte in the fluid test sample, c) reading the developed strip on an instrument having a detector capable of measuring the signal from the detectable label to determine the concentration of the labeled binding partner in the second region, and d) determining the concentration of analyte in the fluid test sample by comparing the signal from the detectable label measured in step c) with the measurements of the signal made in the same manner using fluid samples containing known concentrations of analyte.

Claim 2

A method for determining the concentration of one or more analyte in a fluid test sample which comprises: a) providing a test strip comprising a matrix through which the fluid test sample can flow by capillarity wherein a first region of the strip contains mobile specific binding partner for the analyte which bears a detectable label and can react with the analyte to form an analyte/labeled binding partner complex and at least one second region which contains immobilized analyte or analog thereof, b) developing the strip by applying the fluid test sample suspected of containing the analyte thereto thereby allowing the same contact the mobile, labeled specific binding partner for the analyte whereby analyte present in the fluid test sample binds to the labeled specific binding partner to form the complex leaving excess, unreacted labeled binding partner free to further react whereby the fluid test sample carries the analyte/labeled binding partner complex and unreacted labeled binding partner along the strip by capillarity to the second region containing the immobilized analyte or analog thereof in which region unreacted labeled binding partner is bound to the inmlobilized analyte in inverse relationship to the concentration of analyte in the fluid test sample, c) reading the developed strip on an instrument having a detector capable of measuring the signal from the detectable label to determine the concentration of the labeled binding partner in the second region, and d) determining the concentration of analyte in the fluid test sample by comparing the signal from the detectable label measured in step c) with the measurements of the signal made in the same manner using fluid samples containing known concentrations of analyte.

Claim 12

A method for quantitatively determining the concentration of one or more analyte in a fluid test sample which comprises the steps of: a) providing a test strip comprising a matrix through which the fluid test sample can flow by capillarity said strip having a first region wherein the first region contains mobile specific binding partner for the analyte which binding partner bears a detectable label and can react with the analyte to form an analyte/labeled binding partner complex, at least one second region which contains an immobilized analyte or analog thereof and at least one third region which contains means for immobilizing the complex formed between the analyte and labeled binding partner; b) developing the strip by applying the fluid test sample suspected of containing the analyte thereto to allow the same to contact the mobile specific binding partner whereby analyte present in the fluid test sample binds to the labeled specific binding partner to form the complex leaving excess, unreacted labeled binding partner free to further react whereby the fluid test sample carries the analyte/labeled binding partner complex and unreacted labeled binding partner along the strip by capillarity to the second region containing the immobilized analyte or analog thereof in which region unreacted labeled binding partner is bound to the immobilized analyte in inverse relationship to the concentration of the analyte in the fluid test sample and the analyte/labeled binding partner complex is carried by capillarity to the third region where it is captured by the immobilization means; c) reading the second zone of the developed strip on an instrument having a detector capable of measuring the signal from the detectable label to determine the concentration of the labeled binding partner in the second zone and reading the third zone of the developed strip in a similar manner to determine the signal from the labeled binding partner in the third zone of the strip; d) determining the ratio of the signal from the labeled binding partner immobilized in the second region to the signal from the labeled binding partner in the third region; and e) determining the concentration of the analyte in the fluid test sample by comparing the ratio of the signals measured in step c with the measurements of the ratios of the signals measured in the same manner for fluid samples containing known concentrations of the analyte.

Claim 13

A method for quantitatively determining the concentration of one or more analyte in a fluid test sample which comprises the steps of: a) providing a test strip comprising a matrix through which the fluid test sample can flow by capillarity said strip having a first region wherein the first region contains mobile specific binding partner for the analyte which binding partner bears a detectable label and can react with the analyte to form an analyte/labeled binding partner complex, at least one second region which contains an immobilized analyte or analog thereof and at least one third region which contains means for immobilizing the complex formed between the analyte and labeled binding partner; b) developing the strip by applying the fluid test sample suspected of containing the analyte thereto to allow the same to contact the mobile specific binding partner whereby analyte present in the fluid test sample binds to the labeled specific binding partner to form the complex leaving excess, unreacted labeled binding partner free to further react whereby the fluid test sample carries the analyte/labeled binding partner complex and unreacted labeled binding partner along the strip by capillarity to the second region containing the immobilized analyte or analog thereof in which region unreacted labeled binding partner is bound to the immobilized analyte in inverse relationship to the concentration of the analyte in the fluid test sample and the analyte/labeled binding partner complex is carried by capillarity to the third region where it is captured by the immobilization means; c) reading the second zone of the developed strip on an instrument having a detector capable of measuring the signal from the detectable label to determine the concentration of the labeled binding partner in the second zone and reading the third zone of the developed strip in a similar manner to determine the signal from the labeled binding partner in the third zone of the strip; d) determining the ratio of the signal from the labeled binding partner immobilized in the second region to the signal from the labeled binding partner in the third region; and e) determining the concentration of the analyte in the fluid test sample by comparing the ratio of the signals measured in step c with the measurements of the ratios of the signals measured in the same manner for fluid samples containing known concentrations of the analyte.