Microfluidic detection of analytes

Patent metadata

Field	Value
Publication number	US-8968678-B2
Application number	US-201213536423-A
Country	US
Kind code	B2
Filing date	Jun 28, 2012
Priority date	Oct 4, 2005
Publication date	Mar 3, 2015
Grant date	Mar 3, 2015

Abstract

An apparatus and methods for concentrating samples for application to microfluidic devices are disclosed. The methods involve electrophoresing charged molecules from a high volume sample into a smaller volume. The analyte of interest can be a charged molecule or can be modified to be charged using, for example, one or more ionic moieties.

First claim

What is claimed is:

1. A method for introducing an analyte of interest in a sample to a microfluidic device, comprising:
providing an aqueous sample in a large volume reservoir comprising a first microelectrode operably attached thereto, said sample containing the analyte and having a volume of greater than or equal to 1 microliter, wherein the analyte of interest is charged or has been associated with a charged molecule;
electrophoresing the analyte via a connector from the large volume reservoir to a staging reservoir positioned in a microfluidic device, wherein the connector fluidically connects the large volume reservoir and the staging reservoir, and wherein the microfluidic device comprises an analysis area, a second microelectrode located in the staging reservoir and a third microelectrode located in or distal to at least a portion of the analysis area, said microelectrodes being configured such that an electric field may be generated between the electrodes and a charged analyte electrophoresed from the first microelectrode to the second microelectrode and from the second microelectrode to the third microelectrode; and
transporting the analyte to the analysis area for a time sufficient to result in a higher concentration of analyte in the analysis area than in the sample.

2. The method of claim 1 , wherein the aqueous sample in the large volume reservoir has a volume which is about 100 to about 1000 times greater than the volume of the staging reservoir.

3. The method of claim 1 , wherein said sample has a volume of from 1 microliter to 100 milliners.

4. The method of claim 3 , wherein said sample has a volume of from 1 microliter to 20 mililiters.

5. The method of claim 1 , wherein the aqueous sample in the large volume reservoir has a volume which is about 5 to about 1000 times greater than the volume of the staging reservoir.

6. A method for introducing an analyte of interest to a microfluidic device, comprising:
introducing a solid phase hound analyte into a large volume reservoir to provide a sample, said sample having a volume of greater than or equal to 1 microliter, wherein the analyte is charged or has been associated with a charged molecule;
exposing the solid phase-bound analyte to conditions sufficient to free the analyte from the solid phase;
electrophoresing the analyte from the large volume reservoir to a microfluidic device via a connector, wherein the microfluidic device comprises an analysis area, and the large volume reservoir and the microfluidic device are fluidically connected via the connector; and
transporting the analyte to the analysis area for a time sufficient to result in a higher concentration of analyte in the analysis area than in the sample, wherein the analyte is continuously flowed from the large volume reservoir to the analysis area during said time.

7. The method of claim 6 , wherein said sample has a volume of from 1 microliter to 100 mililiters.

8. The method of claim 7 , wherein said sample has volume of from 1 microliter to 20 mililiters.

9. The method of claim 6 , wherein the solid phase is a microparticle.

10. The method of claim 9 , wherein said microparticle is a magnetic microparticle.

11. A method for introducing an analyte of interest in a sample to a microfluidic device, comprising:
providing an aqueous sample in a large volume reservoir, said sample containing the analyte and having a volume of greater than or equal to 1 microliter, wherein the analyte is charged or has been associated with a charged molecule;
electrophoresing the analyte from the large volume reservoir to a microfluidic device via a connector, wherein the microfluidic device comprises an analyis area, and the large volume reservoir and the microfluidic device are fluidically connected via the connector; and
continuously flowing the analyte to the analysis area for a time sufficient to result in a higher concentration of the analyte in the analysis area than in the sample, wherein the large volume reservoir is a chamber that is not integral with said microfluidic device.

12. The method of claim 11 , wherein said sample has a volume of from 1 microliter to 100 milliliters.

13. The method of claim 12 , wherein said sample has a volume of from 1 microliter to 20 milliners.

14. The method of claim 11 , further comprising providing at least one other aqueous sample in a large volume reservoir fluidically connected to the microfluidic device, the microfluidic device further comprising at least one other analysis area for said one other sample.

15. The method of claim 11 , wherein said connector is a capillary tube.

16. A method for introducing an analyte of interest in a sample to a microfluidic device, comprising:
providing an aqueous sample in a large volume reservoir, said sample containing the analyte and having a volume of greater than or equal to 1 microliter, wherein the analyte is charged or has been associated with a charged molecule;
electrophoresing the analyte from the large volume reservoir to a microfluidic device via a connector, wherein the microfluidic device comprises an analyis area, and the large volume reservoir and the microfluidic device are fluidically connected via the connector; and
continuously flowing the analyte to the analysis area for a time sufficient to result in a higher concentration of the analyte in the analysis area than in the sample, wherein said large volume reservoir is a well of a microwell plate, an eppendorf tube, or a test tube.

17. The method of claim 16 , wherein said sample has a volume of from 1 microliter to 100 mililiters.

18. The method of claim 17 , wherein said sample has a volume of from 1 microliter to 20 mililiters.

19. The method of claim 16 , further comprising providing at least one other aqueous sample in a large volume reservoir fluidically connected to the microfluidic device, the microfluidic device further comprising at least one other analysis area for said one other sample.

20. The method of claim 16 , wherein said connector is a capillary tube.

21. A method for introducing an analyte of interest in a sample to a microfluidic device, comprising:
providing an aqueous sample in a large volume reservoir, said sample containing the analyte and having a volume of greater than or equal to 1 microliter, wherein said analyte is covalently bound to an ionic moiety or is associated with a charged molecule by being bound to a carrier molecule that is ionically charged or is modified to be ionically charged;
electrophoresing the analyte from the large volume reservoir to a microfluidic device via a connector, wherein the microfluidic device comprises an analyis area, and the large volume reservoir and the microfluidic device are fluidically connected via the connector; and
continuously flowing the analyte to the analysis area for a time sufficient to result in a higher concentration of the analyte in the analysis area than in the sample.

22. The method of claim 21 , wherein the carrier molecule is selected from the group consisting of an antibody, a receptor, a ligand, and an antigen.

23. The method of claim 21 , wherein said sample has a volume of from 1 microliter to 100 mililiters.

24. The method of claim 23 , wherein said sample has a volume of from 1 microliter to 20 mililiters.

25. The method of claim 21 , further comprising providing at least one other aqueous sample in a large volume reservoir fluidically connected to the microf

Assignees

• Hu Celine
• Headway Technologies Inc

Inventors

• Hu Celine

Classifications

• B33Y80/00

  Products made by additive manufacturing · CPC title

• G01N33/536

  with immune complex formed in liquid phase · CPC title

• B01L2300/0636

  Integrated biosensor, microarrays · CPC title

• G01N27/447 Primary

  using electrophoresis · CPC title

• B01L3/502715 Primary

  characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces · CPC title