METHOD OF PERFORMING AN IMMUNOASSAY IN BLOOD

• US 20100203550A1
• Filed: 02/18/2010
• Published: 08/12/2010
• Est. Priority Date: 09/10/2003
• Status: Active Grant

• Current Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Miller, Cary James, Campbell, John Lewis Emerson
• Granted Patent: US 8,309,364 B2
• Time in Patent Office: Days
• US Class Current: 435/7.100
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: Y10S 436/807 Apparatus included in process claim, e.g. physical support structures
• CPC Class Codes: Y10T 436/25 including sample preparation

Abstract

An electrochemical immunosensor system with reduced interference, comprising: a first immunosensor that generates an electrochemical signal based on the formation of a sandwich between an immobilized antibody, a target analyte and a labeled antibody, wherein a portion of the signal arises from non-specific binding of the labeled antibody in the region of the first immunosensor, and

• • a second immunosensor that acts as an immuno-reference sensor and generates a signal that is the same as or predictably related to the degree of non-specific binding which occurs in the region of the first immunosensor, and has an immunocomplex between an immobilized antibody and an endogenous or exogenous protein that is in the sample and that is not the target analyte.

Claims

1-68. -68. (canceled)

69. A method of performing an immunoassay for an analyte in blood and correcting for the hematocrit of the sample, comprising:

(a) contacting an immunosensor with a blood sample,

(b) contacting said blood sample with a bulk conductivity sensor and measuring its resistance,

(c) contacting the immunosensor and conductivity sensor with an aqueous solution having known conductivity and containing reagents sufficient to generate a detectable product related to the amount of analyte bound to the immunosensor,

(d) measuring the signal at the immunosensor generated by said product,

(e) converting by means of an algorithm the signal from the immunosensor to an analyte concentration,

(f) calculating the hematocrit value of the blood sample from the measured resistance of the blood sample, and

(g) correcting the calculated analyte concentration for the hematocrit of the sample.

70. The method of claim 69, wherein the immunosensor is an electrochemical sensor.

71. The method of claim 69, in which the resistance of the aqueous solution in (c) is measured at the conductivity sensor.

72. The method of claim 71, in which the hematocrit value in (f) is further calculated using the measured aqueous solution resistance and the known conductivity of the aqueous solution.

73. The method of claim 69, wherein the sample contains a salt reagent added to increase the ionic strength and thereby reduce interference from leukocytes.

74. The method of claim 73, wherein the reagent comprises enough salt to increase the sodium concentration of the sample to at least 200 mM.

75. The method of claim 69, wherein the sample is used in a disposable cartridge for measuring analytes in whole blood.

76. The method of claim 75, wherein the cartridge contains a reference-immunosensor used to determine a corrected analyte concentration in the sample.