Modulated physical and chemical sensors

• US 8,697,029 B2
• Filed: 06/29/2005
• Issued: 04/15/2014
• Est. Priority Date: 04/18/2002
• 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: Anker, Jeffrey, Behrend, Caleb, Kopelman, Raoul, McNaughton, Brandon
• Primary Examiner(s): Hartley, Michael G
• Assistant Examiner(s): PERREIRA, MELISSA JEAN
• Application Number:
  US11/169,977
• Publication Number:
  US 20060008924A1
• Time in Patent Office: 3,212 Days
• Field of Search: 424/1.65
• US Class Current: 424/1.11
• CPC Class Codes: G01N 33/58 involving labelled substances G01N33/53 takes precedence
• CPC Class Codes: G01N 33/587 Nanoparticles

Abstract

The present invention relates to modulated (e.g., magnetically modulated) chemical sensors. In particular, the present invention relates to particles comprising fluorescent indicator dyes and methods of using such particles. Magnetic fields and/or Brownian motion modulate an optical property of the particle to distinguish it from background signals. The present invention thus provides improved methods of detecting a wide variety of analytes in fluids, fluid samples, cells and tissues.

Claims

1. A method of detecting an analyte, the method comprising:

a) providing

i) a plurality of magnetic probes; and

ii) a device configured for the detection of different fluxes of light from said magnetic probes as they rotate;

b) contacting a sample with said magnetic probes under conditions such that analyte objects comprising non-adherent prokaryotic cells or non-adherent eukaryotic cells in the sample are able to bind to said magnetic probes;

(c) applying a rotating magnetic field at a driving rotation rate to rotate the magnetic probes so that the non-adherent prokaryotic cells or non-adherent eukaryotic cells bound to the magnetic probes have a net rotation rate that is slower than the driving rotation rate, the magnetic probes and the bound non-adherent prokaryotic cells or the bound non-adherent eukaryotic cells are directionally free to rotate in response to the rotating magnetic field; and

(d) while applying the rotating magnetic field, detecting said different fluxes of light with said device to generate a modulated probe signal over time, as non-adherent prokaryotic cells or non-adherent eukaryotic cells bind or swell on the magnetic probes.

2. The method of claim 1, wherein said magnetic probes further comprise a labeling particle, said labeling particle attached to said magnetic probes.

3. The method of claim 2, wherein said labeling particle is an indicator dye.

4. The method of claim 1, further comprising identifying said analyte object based on changes in said modulated probe signal.

5. The method of claim 1, wherein said sample is selected from the group consisting of a bodily fluid and a cellular homogenate.

6. The method of claim 1, wherein the magnetic probes comprise a plurality of probes each having a matrix coated with a metal half-shell.

7. The method of claim 1, further comprising detecting an increase in drag on the magnetic probe from the modulated probe signal.

8. The method of claim 1, wherein the modulated probe signal corresponds to changes in the rate of rotation of the non-adherent prokaryotic cells or non-adherent eukaryotic cells bound to the magnetic probes and represents changes in the hydrodynamic radius of the non-adherent prokaryotic cells or non-adherent eukaryotic cells bound to the magnetic probes.

9. A method of detecting analytes in a sample, the method comprising:

contacting a sample with a plurality of magnetic probes to permit binding analyte objects within the sample to the magnetic probes, wherein the magnetic probes and bound analyte are directionally free to rotate in response to a rotating magnetic field;

applying the rotating magnetic field at a driving rotation rate to rotate the magnetic probes so that the magnetic probes and the bound analytes have a net rotation rate that is slower than the driving rotation rate;

optically monitoring the rotation rate of the magnetic probes and the bound analytes over time while applying the rotating magnetic field; and

detecting an increase in drag of the magnetic probes based on a change in their rotation rate as the analyte objects bind or swell while applying the rotating magnetic field.

10. The method of claim 9, wherein contacting the sample comprises contacting the sample with the plurality of magnetic probes to permit binding of analyte objects comprising prokaryotic cells or eukaryotic cells to the magnetic probes.

11. The method of claim 9, wherein optically monitoring the rotation rate comprises measuring changes in light intensity.

12. The method of claim 9, wherein detecting an increase in drag comprises detecting a phase delay between the rotation rate of the magnetic probes compared to a driving rate of the applied rotating magnetic field.

13. A method of detecting analytes in a sample, the method comprising:

contacting a sample with a plurality of magnetic probes to permit binding of analyte objects in the sample to the magnetic probes;

applying a rotating magnetic field at a driving rate to rotate the analyte objects bound to the magnetic probes so that the analyte probes bound to the magnetic probes have a net rotation rate that is slower than the driving rotation rate, wherein the magnetic probes and the bound analyte objects are directionally free to rotate in response to the rotating magnetic field;

optically monitoring the rotation rate of the analyte objects bound to the magnetic probes over time while applying the rotating magnetic field; and

detecting different fluxes of light from said probes as they rotate while applying the rotating magnetic field.

14. The method of claim 13, wherein contacting the sample comprises contacting the sample with the plurality of magnetic probes to permit binding of an analyte comprising non-adherent prokaryotic cells or non-adherent eukaryotic cells to the magnetic probes.

15. The method of claim 13, wherein detecting different fluxes of light comprises detecting the different probe orientations as the probes rotate.