Integrated planar microfluidic bioanalytical systems

• US 20060171654A1
• Filed: 01/20/2006
• Published: 08/03/2006
• Est. Priority Date: 06/15/2004
• Status: Abandoned Application

• Current Assignee: Brigham Young University (The Church of Jesus Christ of Latter-Day Saints)
• Original Assignee: Brigham Young University (The Church of Jesus Christ of Latter-Day Saints)
• Inventors: Barber, John, Peeni, Bridget, Schmidt, Holger, Woolley, Adam T., Lee, Milton L., Hawkins, Aaron R.
• Application Number:
  US11/336,646
• Publication Number:
  US 20060171654A1
• Time in Patent Office: Days
• US Class Current: 385/147
• CPC Class Codes: G01N 2021/0346 Capillary cells; Microcells
• CPC Class Codes: G01N 21/05 Flow-through cuvettes G01N21/09 takes precedence; handling fluid samples G01N1/10
• CPC Class Codes: G01N 21/6428 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 Class Codes: G02B 2006/12138 Sensor
• CPC Class Codes: G02B 6/032 with non solid core or cladding G02B6/02295 takes precedence
• CPC Class Codes: G02B 6/12 of the integrated circuit kind electric integrated circuits H01L27/00
• CPC Class Codes: G02B 6/122 Basic optical elements, e.g. light-guiding paths

Abstract

A system and method for performing rapid, automated and high peak capacity separations of complex protein mixtures through the combination of fluidic and electrical elements on an integrated circuit, utilizing planar thin-film micromachining for both fluidic and electrical components.

Claims

1. A method for designing a microfluidic circuit, said method comprising the steps of:

(1) identifying design rules for spacing and width of hollow fluid channels;

(2) designing a microfluidic circuit using the hollow fluid channels; and

(3) disposing the microfluidic circuit design on a planar substrate using thin film microfabrication techniques of attachment.

2. The method as defined in claim 1 wherein the method is further comprised of the step of identifying robust designs for active microfluidic components to be used in the construction of the microfluidic circuit.

3. The method as defined in claim 2 wherein the method is further comprised of the step of selecting the active microfluidic components from the group of active microfluidic components comprising fluid pumps, separation devices, reaction systems, purification modules, concentration systems, and detectors.

4. The method as defined in claim 1 wherein the method is further comprised of the step of programming design rules for the hollow fluid channels in a microfluidic circuit computer aided drafting (CAD) program to thereby use the microfluidic circuit CAD program to design microfluidic circuits.

5. The method as defined in claim 1 wherein the method further comprises the step of providing the planar substrate that is also suitable for disposing microelectronic circuits thereon.

6. The method as defined in claim 5 wherein the method further comprises the step of disposing microelectronic circuits on the substrate, wherein the microelectronic circuits are comprised of active devices including logic, switching, communication, filtering, power circuitry, and electrical routing circuitry.

7. The method as defined in claim 6 wherein the method further comprises the step of disposing microfluidic circuits over but separate from the microelectronic circuits.

8. The method as defined in claim 7 wherein the method further comprises the step of providing electrical interconnection points between the microelectronic circuits and the microfluidic circuits.

9. The method as defined in claim 1 wherein the method further comprises the steps of:

(1) removing abundant proteins from a sample;

(2) concentrating less abundant proteins; and

(3) desorbing the concentrated proteins for separation.

10. The method as defined in claim 1 wherein the method further comprises the step of integrating an isoelectric focusing channel with a plurality of capillary gel electrophoresis channels disposed along the isolectric focusing channel to thereby generate two-dimensional separation of proteins.

11. The method as defined in claim 1 wherein the method further comprises the step of integrating a capillary gel electrophoresis channel with a monolithic enzyme digestion channel segment and a capillary electrophoresis channel to thereby obtain peptide digest profiles for identifying proteins.

12. The method as defined in claim 1 wherein the method further comprises the step of integrating on-channel detection with the capillary electrophoresis channel for the identification of analytes.

13. The method as defined in claim 12 wherein the method further comprises the step of utilizing electric impedance measurements to identify analytes.

14. The method as defined in claim 12 wherein the method further comprises the step of utilizing fluorescence emission to identify analytes.

15. The method as defined in claim 14 wherein the step of utilizing fluorescence emission further comprises the step of incorporating anti-resonant reflecting waveguide technology to transmit optical data.

16. The method as defined in claim 1 wherein the step of creating a plurality of hollow fluid channels is further comprised of the steps of:

(1) disposing a sacrificial material on the substrate in a desired layout;

(2) disposing an overcoat layer over the sacrificial material; and

(3) exposing the sacrificial material to an etchant to thereby enable the sacrificial material to be removed and thereby form the plurality of hollow channels.

17. The method as defined in claim 16 wherein the method further comprises the step of utilizing photolithography and etching techniques to thereby dispose the sacrificial material on the substrate in the desired layout.

18. The method as defined in claim 17 wherein the step of disposing an overcoat layer over the sacrificial material further comprises the step of selecting the method from the group of methods comprised of chemical vapor deposition (CVD), plasma enhanced CVD (PECVD), physical vapor deposition, sputtering, spin-on, dip-coating, electroplating, and spray coating.

19. The method as defined in claim 16 wherein the step of disposing the sacrificial material on the substrate further comprises the step of using any material having properties sufficiently different from the substrate such that the sacrificial material can be etched away leaving the substrate undamaged.

20. The method as defined in claim 19 wherein the step of disposing the sacrificial material on the substrate further comprises the step of selecting the sacrificial material from the group of sacrificial material comprising polymers, photosensitive polymers, semiconductors, silica-based dielectrics, and metals.

21. The method as defined in claim 20 wherein the method further comprises the step of selecting the sacrificial material to obtain at least one of the properties selected from the group of properties comprised of a desired cross-section for the hollow fluid channel, faster etch times, desired dimensions for the hollow fluid channel, conformality of the overcoat layer, texture of the hollow fluid channel, reduced pressure generation during etching, and using different temperatures for the overcoat process.

22. The method as defined in claim 16 wherein the step of disposing an overcoat layer over the sacrificial material further comprises the step of selecting the overcoat layer from the group of overcoat layers comprising semiconductors, insulators, ceramics, and polymers.

23. The method as defined in claim 16 wherein the step of disposing an overcoat layer over the sacrificial material further comprises the step of selecting the overcoat layer from the group of overcoat layers comprising CVD oxide and nitride, PECVD oxide and nitride, silicon nitride, silica, alumina, photosensitive resist, photosensitive epoxy and polyimide.

24. The method as defined in claim 16 wherein the method further comprises the step of selecting the substrate from the group of substrates comprised of semiconductors, insulators, polymers, ceramics, metals and glasses.

25. The method as defined in claim 1 wherein the step of designing a microfluidic circuit using the hollow fluid channels further comprises the step of forming branching structures from the hollow fluid channels.

26. The method as defined in claim 1 wherein the step of designing a microfluidic circuit using the hollow fluid channels further comprises the step of forming a first hollow channel so that it crosses over a second hollow channel.

27. The method as defined in claim 26 wherein the step of forming a first hollow channel so that it crosses over a second hollow channel further comprises the step of creating a via between the first hollow channel and the second hollow channel.