Microfluidic devices and methods for assaying a fluid sample using the same

Patent metadata

Field	Value
Publication number	US-9841417-B2
Application number	US-201213630240-A
Country	US
Kind code	B2
Filing date	Sep 28, 2012
Priority date	Sep 30, 2011
Publication date	Dec 12, 2017
Grant date	Dec 12, 2017

Abstract

Multi-directional microfluidic devices and methods for using the same are provided. Aspects of the present disclosure include microfluidic devices that include a chamber having a separation medium, a first binding medium, and a second binding medium. In addition, the devices include a flow field element configured to subject the chamber to two or more directionally distinct flow fields. Methods of using the devices, as well as systems and kits that include the devices are also provided. The devices, systems and methods find use in a variety of different applications, including diagnostic, research and validation assays.

First claim

That which is claimed is:

1. A microfluidic device for detecting two or more analytes in a fluid sample, wherein the microfluidic device comprises:
a chamber containing a contiguous monolith comprising:
a loading medium;
a separation medium, wherein the loading medium and the separation medium have a first flow field along a first directional axis and are arranged in series along the first directional axis;
two distinct binding regions comprising:
a first binding region comprising a first binding medium including a first binding member; and
a second binding region comprising a second distinct binding medium including a second distinct binding member, and
wherein the first binding region and the second binding region have a directionally distinct second flow field along a second directional axis and are arranged in series along the second directional axis; and

a flow field element configured to subject the chamber to the directionally distinct first and second flow fields.

2. The microfluidic device according to claim 1 , wherein the directionally distinct flow fields comprise directionally distinct electric fields.

3. The microfluidic device according to claim 2 , wherein the directionally distinct electric fields are orthogonal electric fields.

4. The microfluidic device according to claim 1 , wherein the separation medium comprises a polymeric gel.

5. The microfluidic device according to claim 1 , wherein the chamber further comprises a stacking medium in contact with the separation medium.

6. The microfluidic device according to claim 1 , wherein the first binding medium is positioned between the separation medium and the second binding medium.

7. The microfluidic device according to claim 1 , wherein the first and second binding members are stably associated with a polymeric gel.

8. The microfluidic device according to claim 7 , wherein the binding member comprises a protein or a binding fragment thereof.

9. The microfluidic device according to claim 8 , wherein the protein is an antibody.

10. The microfluidic device according to claim 1 , wherein the two or more analytes are not labeled.

11. A method of assaying a fluid sample for two or more analytes, the method comprising:
(a) introducing the fluid sample into a microfluidic device comprising:
(i) a chamber containing a contiguous monolith comprising:
a loading medium;
a separation medium, wherein the loading medium and the separation medium have a first flow field along a first directional axis and are arranged in series along the first directional axis;
two distinct binding regions comprising:
a first binding region comprising a first binding medium including a first binding member; and
a second binding region comprising a second distinct binding medium including a second distinct binding member, and
wherein the first binding region and the second binding region have a directionally distinct second flow field along a second directional axis and are arranged in series along the second directional axis; and

(ii) a flow field element configured to subject the chamber to the directionally distinct first and second flow fields;

(b) directing the sample through the separation medium to produce a separated sample;
(c) directing the separated sample through the first and second binding mediums; and
(d) evaluating the first and second binding mediums for the presence of the two or more analytes.

12. The method according to claim 11 , wherein the directionally distinct flow fields comprise directionally distinct electric fields.

13. The method according to claim 12 , wherein the chamber further comprises a stacking medium and the method further comprises concentrating the sample prior to directing the sample through the separation medium.

14. The method according to claim 13 , wherein the method further comprises flowing first and second labeling agents through the first and second binding mediums prior to evaluating the first and second binding mediums for the presence of the two or more analytes.

15. The method according to claim 12 , wherein the method is a diagnostic method.

16. A system for assaying a fluid sample for the presence of two or more analytes, the system comprising:
(a) a microfluidic device comprising:
(i) a chamber containing a contiguous monolith comprising:
a loading medium;
a separation medium, wherein the loading medium and the separation medium have a first flow field along a first directional axis and are arranged in series along the first directional axis;
two distinct binding regions comprising:
a first binding region comprising a first binding medium including a first binding member; and
a second binding region comprising a second distinct binding medium including a second distinct binding member, and
wherein the first binding region and the second binding region have a directionally distinct second flow field along a second directional axis and are arranged in series along the second directional axis; and

(ii) a flow field element configured to subject the chamber to the directionally distinct first and second flow fields; and

(b) a detector.

17. The system according to claim 16 , wherein the detector is a photomultiplier tube, a charge-coupled device, an intensified charge-coupled device, a complementary metal-oxide-semiconductor sensor, visual colorimetric readout, or a photodiode.

18. The system according to claim 16 , further comprising microfluidic components configured to direct a fluid through the microfluidic device.

19. A kit comprising:
(a) a microfluidic device comprising:
(i) a chamber containing a contiguous monolith comprising:
a loading medium;
a separation medium, wherein the loading medium and the separation medium have a first flow field along a first directional axis and are arranged in series along the first directional axis;
two distinct binding regions comprising:
a first binding region comprising a first binding medium including a first binding member; and
a second binding region comprising a second distinct binding medium including a second distinct binding member, wherein the first binding region and the second binding region have a directionally distinct second flow field along a second directional axis and are arranged in series along the second directional axis; and

(ii) a flow field element configured to subject the chamber to the directionally distinct first and second flow fields; and

(b) a buffer.

20. The kit according to claim 19 , wherein the kit further comprises first and second labeling reagents that respectively specifically bind to first and second analytes.

21. The microfluidic device according to claim 1 , wherein the loading medium is in contact with the separation medium.

22. The microfluidic device according to claim 1 , wherein the first binding medium and second binding medium are positioned such that the fluid sample flows from the first binding medium to the second binding medium along the second directional axis.

23. The microfluidic device according to claim 1 , wherein the second binding medium is not in direct fluid communication with the separation medium.

24. The microfluidic device according to claim 1 , wherein the contiguous monolith comprises a contiguous polymeric gel monolith.

25. The microfluidic device according to claim 1 , wherein the separation medium and the first binding medium are in direct physical contact wit

Assignees

• Univ California

Inventors

• Tia Samuel
• Herr Amy E
• He Mei
• Kim Dohyun

Classifications

• G01N21/6428 Primary

  Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title

• G01N2021/0346

  Capillary cells; Microcells · CPC title

• G01N21/05

  Flow-through cuvettes (G01N21/09 takes precedence; handling fluid samples G01N1/10) · CPC title

• G01N2021/058

  Flat flow cell · CPC title

• G01N33/54366

  Apparatus specially adapted for solid-phase testing · CPC title