IMPEDANCE SPECTROSCOPY OF BIOMOLECULES USING FUNCTIONALIZED NANOPARTICLES

• US 20090117571A1
• Filed: 08/15/2008
• Published: 05/07/2009
• Est. Priority Date: 08/15/2007
• Status: Abandoned Application

• Current Assignee: Oregon State University (Oregon University System)
• Original Assignee: Oregon State University (Oregon University System)
• Inventors: King, Jeffrey S., Singh, Kanwar Vikas, Solanki, Rajendra
• Application Number:
  US12/192,822
• Publication Number:
  US 20090117571A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

A biosensor system includes a functionalized interdigitated electrode, functionalized nanoparticles, a current/voltage signal generator, and a circuit analyzer. The interdigitated electrode can be functionalized by coating an exposed surface with first biomolecular probes. The nanoparticles are functionalized by coating an outer surface with second biomolecular probes. A signal generator provides a signal (e.g., an alternating current or voltage) having a selected range of frequencies. A circuit analyzer analyzes electrical parameters of the circuit as the signal is applied. Sensitivity is increased by the presence of functionalized nanoparticles in the system. An analytic method includes measuring changes in electrical parameters of the circuit over the range of frequencies. Using these measurements, the biosensor system can determine whether a target biomolecule is bound. The biosensor system can also identify a biomolecule by comparing the detected signal or “electro-fingerprint” with a reference set of signals over the frequency range.

Claims

1. A method of detecting and analyzing biomolecules in a sample analyte, the method comprising:

functionalizing a plurality of metallic nanoparticles;

providing a plurality of electrodes, each electrode having an exposed surface;

applying the plurality of functionalized metallic nanoparticles and the sample analyte to the plurality of electrodes; and

using impedance spectroscopy to detect a sample signal profile for a group of sample electrical parameters across a selected frequency range.

2. The method of claim 1, wherein the plurality of electrodes are functionalized by coating the exposed surfaces with a plurality of first biomolecular probes.

3. The method of claim 2, wherein the first biomolecular probe includes at least one of a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.

4. The method of claim 2, wherein the first biomolecular probe is specific for a disease marker.

5. The method of claim 2, wherein functionalizing the plurality of metallic electrodes includes first coating the exposed surface with a layer comprising a polymer or a silicon oxide.

6. The method of claim 1, wherein the plurality of metallic nanoparticles is functionalized by coating an outer surface of the metallic nanoparticles with a plurality of second biomolecular probes.

7. The method of claim 6, wherein the second biomolecular probe includes at least one of a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.

8. The method of claim 6, wherein the second biomolecular probe is specific for a disease marker.

9. The method of claim 6, wherein functionalizing the plurality of metallic nanoparticles includes first coating the outer surface with a layer comprising a polymer, a silicon oxide, or a surfactant.

10. The method of claim 1, wherein the plurality of electrodes is formed in an interdigitated relationship, the electrodes having multiple fingers with opposed side walls at a spacing of about an order of magnitude greater than a dimension of the metallic nanoparticles.

11. The method of claim 1, wherein each electrode has an exposed surface formed of a metal such as chromium, gold, iron, platinum, or palladium.

12. The method of claim 1, wherein the plurality of functionalized metallic nanoparticles is applied to the plurality of electrodes separately from the sample analyte.

13. The method of claim 1, wherein the plurality of functionalized metallic nanoparticles are combined with the sample analyte to form a mixture that is then applied to the plurality of electrodes.

14. The method of claim 1, wherein the plurality of metallic nanoparticles comprise gold nanoparticles, silver nanoparticles, iron nanoparticles, iron oxide nanoparticles, platinum nanoparticles, or palladium nanoparticles.

15. The method of claim 1, wherein the group of sample electrical parameters comprises one or more of an impedance, a capacitance, a dissipation factor, and a phase.

16. The method of claim 1, wherein the selected frequency range includes 25 Hz to 50 kHz.

17. The method of claim 1, further comprising comparing the sample signal profile with a reference sample signal profile across the selected frequency range.

18. A biosensor system for detecting or identifying biomolecules in a sample analyte, the biosensor system comprising:

a substrate;

an electrode formed on the substrate, the electrode including one or more pairs of opposed fingers, each finger having an exposed upper surface and exposed side walls;

a stimulator electrically coupled to the electrode and structured to provide a plurality of input frequencies over a selected frequency range;

a detector operative to detect a signal of the sample analyte over the selected frequency range and generate a sample signal profile for a group of sample electrical parameters;

means for comparing the sample signal profile with a reference signal profile across the selected frequency range; and

a plurality of functionalized nanoparticles.

19. The biosensor system of claim 18, further comprising a sample channel structured to contain the functionalized electrode such that a flow of the sample analyte can be introduced to the system.

20. The biosensor system of claim 18, wherein the electrode is functionalized with a plurality of first biomolecular probes selected from a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.

21. The biosensor system of claim 18, wherein the exposed upper surface and the exposed side walls are formed of a metal such as chromium, gold, iron, platinum, or palladium.

22. The biosensor system of claim 18, wherein the fingers of the electrode are spaced with a gap of a size greater than both a length and a width of the functionalized nanoparticles.

23. The biosensor system of claim 18, wherein the stimulator is operative to provide a selected frequency range which includes 25 Hz to 50 kHz.

24. The biosensor system of claim 18, wherein the detector is operative to detect a group of sample electrical parameters which includes one or more of an impedance, a capacitance, a dissipation factor, and a phase.

25. The biosensor system of claim 18, wherein the functionalized nanoparticles are functionalized with a plurality of second biomolecular probes selected from a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.

26. The biosensor system of claim 18, wherein the functionalized nanoparticles comprise at least one of a metal such as gold, silver, iron, iron oxide, platinum, or palladium.

27. The biosensor system of claim 18, wherein the functionalized nanoparticles further comprise functionalized nanowires or functionalized nanotubes.

28. A method of detecting and analyzing biomolecules in a reference sample analyte, the method comprising:

functionalizing a plurality of metallic nanoparticles;

providing a plurality of electrodes, each electrode having an exposed surface;

applying the plurality of functionalized metallic nanoparticles and the reference sample analyte to the plurality of electrodes; and

using impedance spectroscopy to detect a reference sample signal profile for a group of sample electrical parameters across a selected frequency range.

29. The method of claim 28, wherein the reference sample signal profile is stored in a database for future comparison to a detected sample signal profile of a sample analyte.

30. The method of claim 28, further comprising subtracting a signal of a buffer solution from a reference sample signal to obtain the reference sample signal profile.

31. The method of claim 30, wherein the plurality of electrodes are functionalized by coating the exposed surfaces with a plurality of first biomolecular probes, the first biomolecular probes including at least one of a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.

32. The method of claim 30, wherein plurality of metallic nanoparticles is functionalized by coating an outer surface of the metallic nanoparticles with a plurality of second biomolecular probes, the second biomolecular probes including at least one of a group of proteins consisting of an antigen, an antibody, a secondary antibody, an isotype, an enzyme, a nucleic acid, a cytokine, and a peptide.