Microfluidic affinity assays with improved performance

• US 20060246526A1
• Filed: 12/02/2005
• Published: 11/02/2006
• Est. Priority Date: 06/02/2003
• Status: Abandoned Application

• Current Assignee: Gyros Patent AB (Mesa Laboratories Inc.)
• Original Assignee: Gyros Patent AB (Mesa Laboratories Inc.)
• Inventors: Inganas, Mats, Ljungstrom, Magnus
• Application Number:
  US11/292,996
• Publication Number:
  US 20060246526A1
• Time in Patent Office: Days
• US Class Current: 435/7.930
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/581 with enzyme label (including co-enzymes, co-factors, enzyme inhibitors or substrates)

Abstract

Method for measuring the signal from a label in a labeled measuring reagent that has been specifically adsorbed to its affinity counterpart in a zone of a porous nanolitre (nl) bed that is present in a microchannel structure of a microfluidic device. The measuring is part of an assay for determining an analyte of a sample by performing one, two or more heterogeneous specific affinity reactions which comprises that said labeled measuring reagent becomes affinity bound to said zone.

Claims

1. A method for measuring the signal from a label in a labeled measuring reagent that has been specifically adsorbed to its affinity counterpart in a zone of a porous nanolitre (nl) bed that is present in a microchannel structure of a microfluidic device, said measuring being part of an assay for determining an analyte of a sample by performing one or more heterogeneous specific affinity reactions which comprises that said labeled measuring reagent becomes affinity bound to said zone, wherein a) at least one of the heterogeneous affinity reactions comprises specifically adsorbing an analyte-related reactant with an excessive amount of its counterpart immobilized and homogeneously distributed within the porous nl-bed, and b) said labeled measuring reagent comprises a label that is a component of a catalytic signal-producing system that converts a substrate to an immobilized analytically detectable product, and the measuring comprises the steps of:

i. providing the components of said catalytic signal-producing system that are necessary for the formation of said immobilized product within said zone, and

ii. producing said immobilized analytically detectable product within said zone.

2. The method of claim 1, wherein the formation of said product is taking place under static conditions and/or flow conditions.

3. The method of claim 2, wherein the formation is taking place in two or more substeps with a fresh aliquot of said components displacing the preceding aliquot.

4. The method of claim 1, wherein the catalytic signal-producing system comprises an enzyme system and the label is selected from the group consisting of enzyme, cofactor, and co-enzyme.

5. The method of claim 1, wherein said product is a precipitate.

6. The method of claim 1, wherein said product is covalently linked to said porous bed by direct covalent bonds to the matrix of the porous bed and/or to an affinity reactants.

7. The method of claim 1, wherein said product is immobilized via specific affinity adsorption to said porous bed.

8. The method of claim 1, wherein said assay has a competitive format.

9. The method of claim 8, wherein said porous bed comprises immobilized analyte analogue and one of said heterogeneous affinity reaction comprises affinity adsorption of an anti-analyte to said porous bed preferably under flow conditions.

10. The method of claim 8, wherein said labeled measuring reagent is said anti-analyte labeled with said component or an affinity reactant directed towards a binding site on said anti-analyte which is not interfering with the affinity reaction between the analyte and the anti-analyte, preferably with

a) said anti-analyte being a conjugate between a) an unconjugated anti-analyte and b) a reporter group, and

b) said labeled measuring reagent being a conjugate between a) an affinity reactant directed towards said reporter group, and b) said component.

11. The method of claim 1, wherein said assay has a non-competitive format.

12. The method of claim 11, wherein said porous bed comprises an immobilized anti-analyte, that one of said heterogeneous affinity reactions comprises affinity adsorption of said analyte to said immobilized anti-analyte, preferably under flow conditions.

13. The method of claim 11, wherein said non-competitive format is a sandwich format.

14. The method of claim 11, wherein said labeled measuring reagent is a conjugate between a) an anti-analyte that is directed to a different binding site and b) said component.

15. The method of claim 14, wherein said non-competitive format is a sandwich format comprising formation of the complex:

anti-analyte(1)—

analyte—

anti-analyte (2)

in which

a) anti-analyte(1) is directly or indirectly immobilized to said porous bed and

b) anti-analyte(2) is

i) said labeled measuring reagent, or

ii) an anti-analyte that comprises an analytically detectable group which can be detected by the use of a form of said labeled measuring reagent which is directed towards said group.

16. The method of claim 1, wherein said microfluidic device comprises a plurality of said microchannel structures and porous beds.

17. The method of claim 1, wherein said device provides for common flow control of liquid transport in said microchannel structures.

18. The method of claim 1, wherein said component is a non-substrate component of said catalytic signal-producing system.