Assay device and methods

• US 9,816,924 B2
• Filed: 08/07/2013
• Issued: 11/14/2017
• Est. Priority Date: 07/15/2008
• Status: Active Grant

• Current Assignee: L3 Technologies, Inc. (L3Harris Technologies, Inc.)
• Original Assignee: L3 Technologies, Inc. (L3Harris Technologies, Inc.)
• Inventors: Nicholls, Anthony, Garcia, Laura, Hudson, Mark, Jones, Gareth, Clarke, David
• Primary Examiner(s): White, Dennis M
• Application Number:
  US13/960,824
• Publication Number:
  US 20130344581A1
• Time in Patent Office: 1,560 Days
• CPC Class Codes: B01F 33/3021 the components to be mixed being combined in a single independent droplet, e.g. these droplets being divided by a non-miscible fluid or consisting of independent droplets
• CPC Class Codes: B01F 33/30351 using hydrophilic/hydrophobic surfaces
• CPC Class Codes: B01L 2300/161 Control and use of surface tension forces, e.g. hydrophobic, hydrophilic
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 2400/088 by specific surface properties
• CPC Class Codes: B01L 3/502769 characterised by multiphase flow arrangements
• CPC Class Codes: G01N 21/64 Fluorescence; Phosphorescence
• CPC Class Codes: G01N 33/92 involving lipids, e.g. cholesterol , lipoproteins, or their receptors steroid hormones G01N33/743
• CPC Class Codes: Y02P 20/582 Recycling of unreacted starting or intermediate materials

Abstract

The present invention relates to the use of amphipathic polymers to enhance lateral flow and reagent mixing on assay devices. More specifically, the invention relates to use of an amphipathic polymer in assay methods including a device for determining the concentration of lipids in blood serum or plasma.

Claims

1. An assay device for detecting the presence or quantity of an analyte residing in an aqueous sample, the device comprising:

a non-porous support; and

at least one flow path along which an aqueous sample can travel, wherein the at least one flow path comprises, on the non-porous support, a non-phase-separated combination of at least one amphipathic polymer and at least one hydrophobic probe, reporter or reagent, wherein, in use, the at least one amphipathic polymer dissolves in the aqueous sample and increases mixing and interaction between the at least one hydrophobic probe, reporter or reagent and the aqueous sample for any degree of water solubility of the at least one probe, reporter or reagent, including water-insolubility, and promotes and/or controls fluid flow along the at least one flow path.

2. The device of claim 1 wherein the result and/or progress of a reaction is determined by means of optical measurement.

3. The device of claim 1 wherein the amphipathic polymer is polyethylene glycol (PEG).

4. The device of claim 3 wherein the amphipathic polymer is polyethylene glycol with a molecular weight of from 1000 Da to 20,000 Da.

5. The device of claim 4 wherein the amphipathic polymer is polyethylene glycol with a molecular weight of from 1000 Da to 6000 Da.

6. The device of claim 1 wherein the amphipathic polymer is printed and/or sprayed onto a surface of the device.

7. The device of claim 6 wherein the amphipathic polymer forms one or more arrays of nano-, pico- or femto-liter droplets.

8. An assay device comprising:

(i) at least one application area suitable for application of an aqueous sample to the device;

(ii) at least one hydrophobic probe, reporter or reagent wherein, in use the at least one hydrophobic probe, reporter or reagent is able to react with an analyte residing in the aqueous sample;

(iii) at least one test area wherein, in use the result and/or progress of a reaction between the analyte and the at least one hydrophobic probe, reporter or reagent may be determined; and

(iv) at least one flow path being in fluid communication with the at least one application area and the at least one test area;

wherein the at least one flow path comprises, on a non-porous support, a non-phase-separated combination of at least one amphipathic polymer and the at least one hydrophobic probe, reporter or reagent, wherein, in use, the at least one amphipathic polymer dissolves in the aqueous sample and increases mixing and interaction between the at least one hydrophobic probe, reporter or reagent and the aqueous sample for any degree of water solubility of the at least one hydrophobic probe, reporter or reagent, including water-insolubility, and promotes and/or controls fluid flow along the at least one flow path.

9. The device of claim 8 which comprises at least three test areas and at least three flow paths wherein, a first flow path is in fluid communication with the application area and a first test area, a second flow path is in fluid communication with the application area and a second test area and a third flow path is in fluid communication with the application area and a third test area.

10. The device of claim 9 wherein a first flow path comprises Amplex Red, a second flow path comprises K37 and a third flow path comprises Nile Red.

11. The device of claim 9 wherein a first test area comprises Amplex Red, a second test area comprises K37 and a third test area comprises Nile Red.

12. The device of claim 9 wherein the first flow path further comprises cholesterol esterase, cholesterol oxidase and horse radish peroxidise.

13. The device of claim 9 wherein the first test area further comprises cholesterol esterase, cholesterol oxidase and horse radish peroxidise.

14. The device of claim 9 wherein the application area comprises the at least one probe, reporter or reagent selected from the group consisting of Amplex Red, K37, Nile Red, cholesterol esterase, cholesterol oxidase and horse radish peroxidise.

15. The device of claim 8 wherein the at least one hydrophobic probe, reporter or reagent further comprises a stabilizing agent.

16. The device of claim 15 wherein the stabilizing agent is a copolymer of vinyl pyrrolidine and dimethylaminoethyl methacrylate.

17. The device of claim 8 wherein the at least one probe, reporter or reagent is selected from the group consisting of Amplex Red, K37, Nile Red, cholesterol esterase, cholesterol oxidase and horse radish peroxidase.

18. A method of producing an assay device for detecting the presence or quantity of an analyte residing in an aqueous sample, the method comprising:

dissolving an amphipathic polymer in a solvent;

dissolving at least one hydrophobic probe, reporter or reagent in a solvent that is miscible with the amphipathic polymer;

drying the dissolved amphipathic polymer and the dissolved at least one hydrophobic probe, reporter or reagent in at least one flow path on a non-porous support, thereby forming a non-phase-separated combination;

wherein, when an aqueous sample travels along the at least one flow path, the at least one amphipathic polymer dissolves in the aqueous sample and increases mixing and interaction between the at least one hydrophobic probe, reporter or reagent and the aqueous sample for any degree of water solubility of the at least one hydrophobic probe, reporter or reagent, including water-insolubility, and promotes and/or controls fluid flow along the at least one flow path.

19. An assay device produced by the method of claim 18.