Devices, systems, and methods for microscale isoelectric fractionation

• US 9,005,417 B1
• Filed: 10/01/2008
• Issued: 04/14/2015
• Est. Priority Date: 10/01/2008
• Status: Active Grant

• Current Assignee: National Technology & Engineering Solutions Of Sandia LLC (Honeywell International Inc.)
• Original Assignee: Sandia Corporation (Martin Marietta Corporation)
• Inventors: Sommer, Gregory J., Hatch, Anson V., Wang, Ying-Chih, Singh, Anup K.
• Primary Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US12/243,817
• Time in Patent Office: 2,386 Days
• Field of Search: 204/644, 204/548, 204/600, 204/450, 422/99, 422/100, 422/72, 422/63, 422/64, 422/681, 435/283.1, 435/287.2, 435/288.5, 435/6, 427/430
• US Class Current: 204/450
• CPC Class Codes: B29D 7/01 Films or sheets
• CPC Class Codes: G01N 27/4473 by electric means
• CPC Class Codes: G01N 27/44791 Microapparatus sample containers with integrated microfluidic structures B01L3/5027
• CPC Class Codes: G01N 27/44795 Isoelectric focusing

Abstract

Embodiments of the present invention provide devices, systems, and methods for microscale isoelectric fractionation. Analytes in a sample may be isolated according to their isoelectric point within a fractionation microchannel. A microfluidic device according to an embodiment of the invention includes a substrate at least partially defining a fractionation microchannel. The fractionation microchannel has at least one cross-sectional dimension equal to or less than 1 mm. A plurality of membranes of different pHs are disposed in the microchannel. Analytes having an isoelectric point between the pH of the membranes may be collected in a region of the fractionation channel between the first and second membranes through isoelectric fractionation.

Claims

1. A microfluidic device comprising:

a substrate at least partially defining a fractionation microchannel having at least one cross-sectional dimension equal to or less than 1 mm;

a first membrane having a first pH disposed in the fractionation microchannel;

a second membrane having a second pH different from the first pH, the second membrane disposed in the fractionation microchannel a distance from the first membrane;

an electric field generator configured to apply an electric field perpendicular to the fractionation microchannel to retain analytes within the fractionation microchannel; and

wherein the fractionation microchannel is configured such that a target analyte having a pH between the first and the second pH is collected in a region of the fractionation channel between the first and second membranes following isoelectric fractionation.

2. The microfluidic device according to claim 1 further comprising:

a first analyte collection channel in fluid communication with the fractionation microchannel between the first and second membranes, the first analyte collection channel configured to receive the target analyte following fractionation.

3. The microfluidic device according to claim 1 further comprising:

a second analyte collection channel in fluid communication with the fractionation microchannel before the first membrane, the second analyte collection channel configured to receive analytes having a pH of less than the first pH following fractionation.

4. The microfluidic device according to claim 1 wherein the substrate comprises fused silica.

5. The microfluidic device according to claim 1 wherein the first and second membranes comprise polyacrylamide gels.

6. The microfluidic device according to claim 5 wherein the polyacrylamide gels comprise acrylamide monomer, bisacrylamide crosslinker, and a photoinitiator.

7. The microfluidic device according to claim 1 wherein the first pH is 6.0 and the second pH is 5.0.

8. The microfluidic device according to claim 1 wherein the fractionation microchannel has at least one cross-sectional dimension that is equal to or less than 500 μ

m.

9. The microfluidic device according to claim 1 further comprising a first and second electrode positioned to generate an electric field across the fractionation microchannel and between the first and second electrode to perform isoelectric fractionation.

10. The microfluidic device according to claim 1 wherein the first and second membranes have a width equal to or less than 50 μ

m.

11. The microfluidic device according to claim 1 wherein the first membrane and the second membrane are adhered to a surface of the fractionation microchannel using a self-assembled monolayer.

12. The microfluidic device according to claim 1 wherein the fractionation microchannel is in fluid communication with a sample reservoir, and wherein the sample reservoir is separable from the substrate.

13. A microfluidic system comprising:

a substrate;

a preparation module including a fractionation microchannel defined in part by the substrate, wherein the fractionation microchannel has at least one cross-sectional dimension equal to or less than 1 mm, the preparation module further comprising;

a plurality of membranes disposed in the fractionation microchannel, including a first and second membrane, the first membrane having a first pH and the second membrane having a second pH different from the first pH, the second membrane positioned a distance from the first membrane;

the fractionation microchannel configured such that a target analyte having a pH between the first and the second pH is collected in a region of the fractionation channel between the first and second membranes following isoelectric fractionation; and

a first analyte collection channel in fluid communication with the fractionation microchannel between the first and second membranes, the first analyte collection channel configured to receive the target analyte following fractionation;

a transport module supported by the substrate, the transport module including a transport channel in fluid communication with the first analyte collection channel;

an analysis module supported by the substrate, the analysis module configured to receive the target analyte from the transport module and analyze the target analyte; and

an electric field generator configured to apply an electric field perpendicular to the fractionation microchannel to retain analytes within the fractionation microchannel.

14. The microfluidic system according to claim 13 wherein the fractionation microchannel has at least one cross-sectional dimension equal to or less than 500 μ

m.

15. The microfluidic system according to claim 13 further comprising a first and second electrode positioned to generate an electric field across the fractionation microchannel and between the first and second electrode to perform isoelectric fractionation.

16. The microfluidic system according to claim 15 further comprising a power supply coupled to the first and second electrodes and configured to generate the electric field across the fractionation microchannel.

17. The microfluidic system according to claim 13 wherein the analysis module comprises a separation channel in fluid communication with the transport module, the separation channel configured to separate the received analytes from the first analyte collection channel for detection of the target analyte.

18. The microfluidic system according to claim 17 wherein the analysis module further comprises a preconcentration membrane disposed in the separation channel and configured to concentrate the analytes received from the first analyte collection channel prior to separation.

19. The microfluidic system according to claim 13 wherein the first and second membranes comprise polyacrylamide gels.

20. The microfluidic system according to claim 19 wherein the polyacrylamide gels comprise acrylamide monomer, bisacrylamide crosslinker, and a photoinitiator.

21. The microfluidic system according to claim 13 further comprising a plurality of analysis modules supported by the substrate and in fluid communication with the transport module.

22. The microfluidic system according to claim 13 wherein the first and second membranes have a width equal to or less than 50 μ

m.

23. The microfluidic system according to claim 13 wherein the first membrane and the second membrane are adhered to a surface of the fractionation microchannel using a self-assembled monolayer.

24. The microfluidic system according to claim 13 wherein the fractionation microchannel is in fluid communication with a sample reservoir, and wherein the sample reservoir is separable from the substrate.