Biochips including ion transport detecting structures and methods of use

• US 7,723,029 B2
• Filed: 06/15/2005
• Issued: 05/25/2010
• Est. Priority Date: 01/24/2002
• Status: Expired due to Fees

• Current Assignee: AVIVA Biosciences Corporation
• Original Assignee: AVIVA Biosciences Corporation
• Inventors: Guia, Antonio, Huang, Mingxian, Rothwarf, David, Wang, Xiaobo, Wu, Lei, Xu, Jia
• Primary Examiner(s): Kim; Young J
• Application Number:
  US11/153,825
• Publication Number:
  US 20050266478A1
• Time in Patent Office: 1,805 Days
• Field of Search: None
• US Class Current: 435/6.11
• CPC Class Codes: B01L 2200/027 for microfluidic devices
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2300/0627 Sensor or part of a sensor is integrated
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0819 Microarrays; Biochips
• CPC Class Codes: B01L 2300/089 Virtual walls for guiding liquids
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0418 electro-osmotic flow [EOF]
• CPC Class Codes: B01L 2400/0421 electrophoretic flow
• CPC Class Codes: B01L 2400/043 magnetic forces
• CPC Class Codes: B01L 2400/0436 acoustic forces, e.g. surface acoustic waves [SAW]
• CPC Class Codes: B01L 2400/0457 passive flow or gravitation
• CPC Class Codes: B01L 2400/049 vacuum
• CPC Class Codes: B01L 3/50273 characterised by the means or forces applied to move the fluids micropumps F04B19/006, of the membrane type F04B43/043
• CPC Class Codes: B01L 3/502761 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules investigating characteristics of particles G01N15/00
• CPC Class Codes: B01L 3/502792 for moving individual droplets on a plate, e.g. by locally altering surface tension
• CPC Class Codes: B01L 3/5088 confining liquids at a location by surface tension, e.g. virtual wells on plates, wires B01L3/50857 takes precedence
• CPC Class Codes: G01N 33/48728 Investigating individual cells, e.g. by patch clamp, voltage clamp investigating individual particles in general G01N15/10

Abstract

The present invention recognizes that the determination of an ion transport function or property using direct detection methods, such as patch-clamps, whole cell recording or single channel recording, are preferable to methods that utilize indirect detection methods, such as FRET based detection system. The present invention provides biochips and methods of use that allow for the direct analysis of ion transport functions or properties using microfabricated structures that can allow for automated detection of one or more ion transport functions or properties. These biochips and methods of use thereof are particularly appropriate for automating the detection of ion transport functions or properties, particularly for screening purposes.

Claims

1. A biochip, comprising:

one or more holes that extends through said biochip,

wherein when said biochip is in contact with a measurement solution, said holes have negatively charged surfaces and are capable of engaging particles or membranes with high resistance electric seals, wherein said resistance is between 1 mega ohm and 100 giga ohms,

wherein said biochip comprises one or more materials selected from the group consisting of glass, quartz, silicon dioxide, silicon, plastics, polymers, polydimethylsiloxane (PDMS), oxygen plasma treated PDMS, and combinations thereof, and

wherein said surfaces of said one or more holes comprise one or more SiOM groups or oxidized SiOM groups (SiO⁻

), where M is hydrogen or a metal, and the surface density of said SiOM groups and SiO⁻

groups is more than about 10%.

2. The biochip of claim 1, wherein said surfaces of said one or more holes possess surface charge density approximately that or substantially equivalent to that of a capillary that has an electro-osmotic mobility between about 10⁻

9 cm²/(V sec) and about 10<sup>−

4</sup> cm²/(V sec) in an aqueous solution that has an ionic concentration equivalent to that of a one in ten dilution of PBS in water, and a pH between about 7 and about 8.

3. The biochip of claim 1, wherein said surfaces of said one or more holes possess surface charge density approximately that or substantially equivalent to that of a capillary that has an electro-osmotic mobility between about 10⁻

4 cm²/(V sec) and about 3×

10<sup>−

4</sup> cm²/(V sec) in an aqueous solution that has an ionic concentration equivalent to that of a one in ten dilution of PBS in water, and a pH between about 7 and about 8.

4. The biochip of claim 1, wherein said surfaces of said one or more holes possess surface charge density approximately that or substantially equivalent to that of a capillary that has an electroosmotic mobility between about 3×

10<sup>−

4</sup> cm²/(V sec) and about 6×

10<sup>−

4</sup> cm²/(V sec) in an aqueous solution that has an ionic concentration equivalent to that of a one in ten dilution of PBS in water, and a pH between about 7 and about 8.

5. The biochip of claim 1, wherein said biochip comprises one or more materials selected from the group consisting of silicon, plastics, polymers, polydimethylsiloxane (PDMS), oxygen plasma treated PDMS, and combinations thereof.

6. The biochip of claim 1, wherein the surface of said biochip comprises at least one chemical group selected from sulfate, phosphate, and carboxyl groups.

7. The biochip of claim 1, wherein said one or more holes is fabricated using laser ablation, laser drilling, or both.

8. The biochip of claim 1, wherein said biochip has been treated with oxygen plasma, reactive compounds, or radiation, or has been baked, fire polished, flame annealed, or laser polished.

9. The biochip of claim 8, wherein the front side surface of said biochip surrounding said at least one hole has been polished using a laser.

10. The biochip of claim 8, wherein said biochip has been baked.

11. The biochip of claim 1, wherein said one or more holes of said biochip have been treated with base, or treated with acid and with base.

12. The biochip of claim 11, wherein said one or more holes of said biochip have been treated with base.

13. The biochip of claim 12, wherein said base is selected from group consisting of NaOH, KOH, LiOH, CsOH, NaOH, Ba(OH)₂, Ca(OH)₂, and NH₄(OH).

14. The biochip of claim 12, wherein the base is a solution of a concentration of about 0.1 M or greater.

15. The biochip of claim 11, wherein said biochip has been treated with acid and then with base.

16. The biochip of claim 15, wherein said acid is selected from the group consisting of HCl, HF, HBr, HCOOH, HClO₃, H₂SO₄, NaHSO₄, H₂SO₄, or HNO₃.

17. The biochip of claim 15, wherein said acid is a solution having a concentration of greater than about 1M.

18. The biochip of claim 1, wherein said one or more holes is an array of holes.

19. The biochip of claim 18, wherein the size of said holes is between 0.5 micron and 5 microns.

20. A method of measuring ion transport activity of a particle, comprising:

(a) contacting a sample comprising at least one particle with the biochip of claim 1;

(b) engaging said at least one particle at said one or more holes; and

(c) measuring ion transport activity of said at least one particle.

21. The biochip of claim 1, wherein the surface density of said SiOM groups and SiO⁻

groups is more than about 30%.

22. The biochip of claim 1, further comprising a coating localized to the hole and optionally surrounding areas.

23. The biochip of claim 22, wherein the coating comprises a polymer that expands or contracts as temperature changes.

24. The biochip of claim 1, wherein said biochip has been laser-polished, treated with acid, then treated with base.

25. The biochip of claim 1, wherein said one or more holes of said biochip have been treated with H₂SO₄ and H₂O₂ and then with base.

26. A biochip, comprising:

one or more holes that extends through said biochip,

wherein when said biochip is in contact with a measurement solution, said holes have negatively charged surfaces and are capable of engaging particles or membranes with high resistance electric seals, wherein said resistance is between 1 mega ohm and 100 giga ohms,

wherein said biochip comprises a polymer that comprises at least one negatively charged chemical group, and

wherein said surfaces of said one or more holes possess surface charge density that is substantially pH independent over a pH range from 3 to 9.

27. The biochip of claim 26, wherein said biochip is coated with a polymer material that comprises at least one negatively charged chemical group.

28. The biochip of claim 27, wherein the coating comprises a polymer selected from the group consisting of polyimide, polyethyleneimine, PDMS, paralyene, and PMMA SU8.

29. The biochip of claim 26, wherein said one or more holes is fabricated using laser ablation, laser drilling, or both.

30. The biochip of claim 26, wherein said one or more holes of said biochip have been treated with acid, treated with base, or treated with acid and with base.

31. The biochip of claim 30, wherein said biochip has been treated with acid and then with base.

32. A method of measuring ion transport activity of a particle, comprising:

(a) contacting a sample comprising at least one particle with the biochip of claim 26;

(b) engaging said at least one particle at said one or more holes; and

(c) measuring ion transport activity of said at least one particle.

33. The biochip of claim 26, wherein said biochip has been laser-polished, treated with acid, then treated with base.

34. The biochip of claim 26, wherein said biochip has been treated with H₂SO₄ and H₂O₂ and then with base.