Flex Method

• US 20070224702A1
• Filed: 03/22/2007
• Published: 09/27/2007
• Est. Priority Date: 03/22/2006
• Status: Abandoned Application

• Current Assignee: Gyros Patent AB (Mesa Laboratories Inc.)
• Original Assignee: Gyros Patent AB (Mesa Laboratories Inc.)
• Inventors: Inganas, Mats, Holmquist, Mats
• Application Number:
  US11/689,702
• Publication Number:
  US 20070224702A1
• Time in Patent Office: Days
• US Class Current: 436/514
• CPC Class Codes: G01N 33/54386 Analytical elements

Abstract

A method for quantifying n different analytes that are present in one or more liquid samples by performing n different affinity assay formats, each of which is dedicated for a particular one of the analytes. The characteristic feature is that each format is performed in a separate microchannel structures of a microfluidic device that contains at least n microchannel structures, and comprises formation and measurement of an immobilized product (affinity complex) that is formed on a solid phase that is placed in a microcavity of the microchannel structure used for the format in order to quantify the analyte to which the format is dedicated.

Claims

1. A method for quantifying n different analytes that are present in one or more liquid samples by performing n different affinity assay formats, each of which is dedicated for one analyte and results in an affinity complex that is related to the amount of analyte to which the format is dedicated, said method comprises the steps of:

performing each of n different affinity assay formats in a separate microchannel structure of a microfluidic device that contains at least n microchannel structures, and

forming and measuring the affinity complex that is formed on a solid phase that has been placed in a microcavity of the microchannel structure used for the format in order to quantify the analyte to which the format is dedicated.

2. The method of claim 1, wherein each of the n formats comprises the steps of:

(i) providing in a microcavity of the microchannel structure used for the format a solid phase that exposes;

a) an immobilized affinity capturer, or

b) an immobilizing group that is capable of attaching an immobilizable affinity capturer having an immobilizing tag that is reactive with the immobilizing group,

(ii) forming an immobilized form of the affinity complex within the microcavity

a) performing the affinity reaction(s) of the format to incorporate the immobilized capturer of the solid phase provided in step (i.a) into an immobilized form of said complex, or

b) performing the affinity reaction(s) of the format to incorporate the immobilizable capturer into an immobilizable form of said complex and subsequently attaching this complex to the solid phase by reacting the immobilizing tag with the immobilizing group of the solid phase provided in step (i.b), and

(iii) determining the amount of analyte in the sample by measuring the amount of the immobilized complex formed in step (ii).

3. The method of claim 2, wherein the solid phase is in the form of a porous bed during step (ii) for at least one of said n formats.

4. The method of claim 2, wherein at least one of said n formats utilizes a detectable reactant that is an affinity counterpart to the capturer or to the analyte.

5. The method of claim 4, wherein one or more of said at least one formats comprise an inhibition format comprising:

the detectable reactant is an An-analogue, and

the capturer is a counterpart to the analyte and the An-analogue and is immobilized to the solid phase, and said complex comprises the capturer bound to the detectable reactant and/or to the analyte.

6. The method of claim 4, wherein one or more of said at least one formats comprise an inhibition format comprising:

the detectable reactant is a counterpart to the analyte, and

the capturer is an An-analogue and preferably is immobilized to the solid phase, and

said complex comprises the capturer bound to the detectable reactant.

7. The method of claim 4, wherein one or more of said at least one formats comprise a sandwich format having the capturer immobilized to the solid phase comprising:

the detectable reactant and the capturer are counterparts to the analyte,

the analyte comprises two binding sites permitting simultaneous binding of both the detectable reactant and the capturer, and

said complex comprises the analyte bound to both the capturer and the detectable reactant.

8. The method of claim 4, wherein one or more of said at least one formats comprise a sandwich format having an antigen-specific antibody assay and the capturer is immobilized to the solid phase comprising:

the detectable reactant and the capturer are counterparts to the analyte,

the analyte is bivalent with respect to a binding site for which both the detectable reactant and the capturer have specificity, and

said product comprises the analyte bound to both the detectable reactant and the capturer.

9. The method of claim 4, wherein one or more of said at least one formats comprises a sandwich format having an antigen-specific antibody assay and using the capturer immobilized to the solid phase comprising:

the detectable reactant and the capturer are counterparts to the analyte and have binding specificities to two different sites on the analyte,

the analyte comprises said two different binding sites, and

said complex comprises the analyte bound to both the detectable reactant and the capturer.

10. The method of claim 1, wherein at least one of said n formats is an immunoassay.

11. The method of claim 1, wherein at least one of said n formats is an inhibition format.

12. The method of claim 1, wherein at least one of said n formats is a non-inhibition format.

13. The method of claim 1, wherein at least one of said n formats is a sandwich format.

14. The method of claim 2, wherein step (i) comprises providing the capturer in immobilized form for at least one of said n formats.

15. The method of claim 4, wherein for at least two, or more of said n formats comprises that the capturer provided in step (i) is in immobilized form, and two-step sequential formats.

16. The method of claim 1, wherein at least one of said n formats the capturer is immobilized to the solid phase via a generic immobilizing affinity pair.

17. The method of claim 1, wherein at least one of said n formats the capturer is or has been immobilized to the solid phase via a generic immobilizing affinity pair during competition with a nonsense reactant that is capable of becoming immobilized via the same immobilizing affinity pair as the capturer.

18. The method claim 1 and at least one of said n formats is an inhibition format, and at least one of said n formats is a non-inhibition format.

19. The method of claims 1, further comprising

performing at least two of said n formats in a set of microchannel structures that have a distribution manifold in common and each microchannel structure comprises one separate volume-metering microcavity;

and

passing for each structure of the set a sub-aliquot 1 that derives from one common liquid sample into the microcavity containing the solid phase by performing the sub-steps of;

(i) providing an aliquot of said common liquid sample in the distribution manifold, and dividing the sample into sub-aliquots with one sub-aliquot per structure of the set,

(ii) processing including transporting a sub-aliquot to provide sub-aliquot 1 at the inlet end of the microcavity containing the solid phase, and

(iii) passing sub-aliquot 1 into the microcavity.

20. The method of claims 1, further comprising

performing at least one of said n formats in a microchannel structure having an inlet port which is not common with the inlet port of the microchannel structures that are used for the other ones of said at least one format, and in the downstream direction is in flow communication with the microcavity containing the solid phase, possibly with a volume-metering microcavity between the microcavity containing the solid phase and the inlet port, and

passing a sub-aliquot 2 deriving from a liquid sample into the microcavity containing the solid phase by the sub-steps of:

(i) providing an aliquot of the liquid sample at said inlet port,

(ii) processing including transporting said aliquot to provide sub-aliquot 2 at the inlet of the microcavity containing the solid phase, and

(iii) passing sub-aliquot 2 into the microcavity.