Ratiometric immunoassay method and blood testing device

• US 9,795,962 B2
• Filed: 05/01/2015
• Issued: 10/24/2017
• Est. Priority Date: 12/03/2010
• 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
• Primary Examiner(s): Brown, Melanie Yu
• Application Number:
  US14/702,501
• Publication Number:
  US 20150233951A1
• Time in Patent Office: 907 Days
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 3/50273 characterised by the means or forces applied to move the fluids micropumps F04B19/006, of the membrane type F04B43/043
• CPC Class Codes: G01N 2333/4737 C-reactive protein
• CPC Class Codes: G01N 2333/805 Haemoglobins; Myoglobins
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/76 Human chorionic gonadotropin including luteinising hormone, follicle stimulating hormone, thyroid stimulating hormone or their receptors

Abstract

The invention is to devices and methods for rapid determination of analytes in liquid samples. The devices and methods incorporate a sample dilution feature and multiple immunosensors for performing a ratiometric immunoassay on a first analyte and a second analyte, for example, hemoglobin and hemoglobin A1c or albumin and glycosylated albumin. The devices are preferably capable of being used in the point-of-care diagnostic field.

Claims

1. A cartridge for performing a ratiometric assay in a sample, comprising:

a sample holding chamber oriented between a sample entry port and a sample extraction unit, wherein a portion of said sample extraction unit is configured to define a metered volume of a sample;

an analysis conduit in fluid communication with the sample extraction unit, the analysis conduit including a sensing region comprising a first sensor comprising an immunosensor for a first analyte, and a second sensor comprising an immunosensor for a second analyte;

a diluent conduit in fluid communication with the sample extraction unit, wherein said diluent conduit is oriented between a diluent entry port and a diluent introduction port, the diluent conduit includes an air introduction port disposed between the diluent entry port and the diluent introduction port, a volume within the diluent conduit between the air introduction port and the diluent introduction port defines a metered volume of a diluent, and the diluent introduction port is configured to dispel the metered volume of the diluent over and/or through the sample extraction unit to create a diluted sample;

a diluent chamber in fluid communication with the diluent conduit and containing the diluent; and

a pump configured to transfer at least a portion of the diluent through said diluent conduit, over and/or through said sample extraction unit, and into said analysis conduit.

2. The cartridge of claim 1, wherein the first sensor comprises an immobilized first antibody to the first analyte, and wherein the second sensor comprises an immobilized second antibody to the second analyte.

3. The cartridge of claim 1, further comprising a reagent coating comprises a mobile labeled antibody for binding to the first analyte and the second analyte.

4. The cartridge of claim 1, wherein the diluent that is introduced into the sample holding chamber comprises a metered volume of diluent.

5. The cartridge of claim 1, wherein the first analyte comprises hemoglobin and the second analyte comprises hemoglobin A1c.

6. The cartridge of claim 1, wherein the cartridge comprises a lysing agent capable of dissolving in the sample, the diluent, or the diluted sample.

7. The cartridge of claim 6, wherein said lysing agent comprises sodium deoxycholate.

8. The cartridge of claim 6, wherein said lysing agent comprises saponin.

9. The cartridge of claim 1, wherein the first analyte comprises albumin and the second analyte comprises glycosylated albumin.

10. The cartridge of claim 1, wherein said extraction unit comprises a porous hydrophilic material.

11. The cartridge of claim 1, wherein said extraction unit comprises a cellulose material.

12. The cartridge of claim 1, wherein said extraction unit comprises nitrocellulose.

13. The cartridge of claim 1, wherein said extraction unit comprises cotton fiber.

14. The cartridge of claim 1, wherein said extraction unit comprises paper.

15. The cartridge of claim 1, wherein said extraction unit comprises glass-filled paper.

16. The cartridge of claim 1, wherein said extraction unit comprises a transverse filter material.

17. The cartridge of claim 1, wherein said extraction unit comprises a porous outer coating.

18. The cartridge of claim 1, wherein said sample extraction unit is configured to become saturated with the metered volume of the sample from the sample entry port.

19. The cartridge of claim 1, wherein said sample extraction unit comprises a hydrophilic porous material.