Non-linear rotation rates of remotely driven particles and uses thereof

• US 9,068,977 B2
• Filed: 03/06/2008
• Issued: 06/30/2015
• Est. Priority Date: 03/09/2007
• Status: Active Grant

• Current Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Original Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Inventors: McNaughton, Brandon H., Kopelman, Raoul, Torres-Isea, Ramon, Clarke, Roy
• Primary Examiner(s): Chin, Chris L
• Application Number:
  US12/043,481
• Publication Number:
  US 20080220411A1
• Time in Patent Office: 2,672 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/54326 Magnetic particles
• CPC Class Codes: G01N 33/569 for microorganisms, e.g. protozoa, bacteria, viruses

Abstract

The present invention relates to biological sensors. In particular, the present invention relates to the use of remotely driven nonlinear rotation of particles (e.g., magnetic particles) for detection of cells such as microorganisms (e.g., bacteria and viruses). The present invention further relates to the use of remotely driven nonlinear rotation of particles for measurement of physical properties of a solution (e.g., viscosity).

Claims

1. A method of detecting the presence of an analyte in a sample, comprising:

contacting a magnetic particle with said sample under conditions such that said particle interacts with said analyte;

rotating said magnetic particle using an external rotating magnetic field applied to the sample;

measuring the non-linear rotation rate of said magnetic particle during application of the rotating magnetic field; and

determining the presence of said analyte in said sample when said non-linear rotation rate is altered relative to a rotational rate of the magnetic particle in the absence of said sample.

2. The method of claim 1, wherein said analyte is a cell.

3. The method of claim 2, wherein said particle further comprises a ligand that specifically binds to said cell.

4. The method of claim 3, wherein said ligand is an antibody.

5. The method of claim 2, further comprising:

determining growth in cell population in said sample over a sampling time period, by measuring changes in the non-linear rotation rate of said magnetic particle over time.

6. The method of claim 2, wherein said cell is a microorganism.

7. The method of claim 6, wherein said microorganism is a bacteria.

8. The method of claim 1, further comprising the step of contacting said sample with a label that binds to said analyte, wherein the rotation rate of said particle is altered when said label is bound to said analyte.

9. The method of claim 1, wherein the magnetic particle is a ferromagnetic particle.

10. The method of claim 1, wherein the magnetic particle is a paramagnetic particle.

11. The method of claim 1, wherein rotating said magnetic particle using the external rotating magnetic field comprises maintaining the external rotating magnetic field at a single driving frequency.

12. The method of claim 1, wherein rotating said magnetic particle using the external rotating magnetic field comprises maintaining the external rotating magnetic field above a critical driving frequency.

13. The method of claim 1, further comprising:

determining a critical driving frequency for the rotating magnetic field, where the critical driving frequency depends upon particle volume, viscosity, magnetic moment, a magnetic field amplitude; and

applying the external rotating magnetic field to the sample at a driving frequency above the critical driving frequency.

14. The method of claim 1, wherein the external rotating magnetic field is supplied by pairs of Helmholtz coils producing the rotating magnetic field in a plane.

15. The method of claim 1, wherein measuring the non-linear rotation rate of said magnetic particle and determining the presence of said analyte in said sample comprises:

illuminating the magnetic particle and analyte with an light source; and

detecting a resulting optical signal from the illuminated magnetic particle, where the optical signal varies with the non-linear rotation rate.

16. The method of claim 15, wherein detecting the optical signal comprises collecting the optical signal using a photodiode apparatus.

17. The method of claim 15, wherein detecting the optical signal comprises collecting the optical signal using a charged coupled device or camera.

18. The method of claim 15, wherein detecting the optical signal comprises collecting the optical signal using a fluorescence detection apparatus.

19. The method of claim 15, wherein the magnetic particle is rotating in a plane perpendicular to a sample plane of a detection apparatus.

20. The method of claim 15, wherein the magnetic particle is rotating in a plane parallel to a sample plane of a detection apparatus.

21. The method of claim 1, wherein measuring the non-linear rotation rate of said magnetic particle and determining the presence of said analyte in said sample comprises passively monitoring the non-linear rotation rate.

22. The method of claim 1, wherein the analyte comprises a cell and a virus.

23. The method of claim 1, wherein the analyte comprises a virus.

24. The method of claim 1, wherein the analyte comprises a biological molecule.

25. A method for measuring changes in the number and/or size of cells bound to magnetic particles, the method comprising:

contacting magnetic particles with a solution comprising cells under conditions such that said magnetic particles bind to said cells;

rotating said magnetic particles using an external rotating magnetic field; and

during application of the rotating magnetic field, measuring changes in the non-linear rotation rate of said magnetic particles over time, wherein said non-linear rotation rate is altered in response to change in the number and/or size of said cells bound to said magnetic particles.

26. The method of claim 25, wherein said cells comprise microorganisms.

27. The method of claim 25, wherein the magnetic particle is a ferromagnetic particle.

28. The method of claim 25, wherein the magnetic particle is a paramagnetic particle.

29. The method of claim 25, wherein rotating said magnetic particles comprises maintaining the external rotating magnetic field at a single driving frequency.

30. The method of claim 25, wherein rotating said magnetic particles comprises maintaining the external rotating magnetic field above a critical driving frequency.

31. The method of claim 25, further comprising determining growth in the number of said cells bound to said magnetic particles.