Surface Mapping by Optical Manipulation of Particles in Relation to a Functionalized Surface

• US 20110026009A1
• Filed: 09/14/2007
• Published: 02/03/2011
• Est. Priority Date: 09/15/2006
• Status: Active Grant

• Current Assignee: Arryx, Inc. (Haemonetics Corporation)
• Original Assignee: Haemonetics Corporation
• Inventors: Bradley, Kenneth, Knutson, Christopher, Tanner, Evan, Stacey, Gary, Chakrabarty, Tania, Mueth, Dan, Duke, Crystal, Fu, Haojun, Lancelot, Robert, Akcakir, Osman
• Granted Patent: US 8,169,600 B2
• Time in Patent Office: Days
• US Class Current: 356/39
• CPC Class Codes: G01N 33/48 Biological material, e.g. blood, urine G01N33/02, G01N33/26, G01N33/44, G01N33/46 take precedence; Haemocytometers counting blood corpuscules distributed over a surface by scanning the surface G06M11/02
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/80 involving blood groups or blood types or red blood cells white blood cells G01N33/56972

Abstract

Methods and apparatus for analyzing surface properties of particles are provided. A method for analyzing the surface properties of the particle includes a associating a first particle with a first capture zone having a specific binding affinity for a first chemical species, applying an optical force to the first particle, sensing a response of the first particle to the optical force, and using the sensed response to determine the presence, absence or quantity of the first chemical species on the first particle surface. This process may be repeated in parallel to test multiple particles. In addition to directly testing the surface properties of the particles, the method can be used in direct, indirect and competitive assays to determine the presence, absence or quantity of free or immobilized analytes. A fluidic cartridge with capture zones having avidities that are tuned for the use of optical forces is provided. A software routine for performing the method is also provided.

Claims

1. A method for analyzing surface properties of one or more particles each having a surface, the method comprising:

introducing a suspension having a plurality of particles into a sample holder having at least one capture zone with a given affinity for a specified chemical species;

contacting at least a subset of the plurality of the particles with the at least one capture zone so as to allow for binding interactions to occur between the at least one capture zone and the at least a subset of particles, the binding interactions being related to the surface composition of the particles;

applying optical forces to at least two of the at least a subset of particles concurrently, the forces tending to cause a response of the particles, wherein the responses depend on the presence, absence or degree of binding interactions between the particles and the at least one capture zone;

sensing the responses of the at least two particles to the optical forces; and

using the sensed responses to determine the presence, absence, or quantity of the specified chemical species disposed between the particle surface and the capture zone.

2. A method according to claim 1, wherein the applying optical forces includes using HOT.

3. A method according to claim 1, wherein the contacting includes contacting multiple particles with a single capture zone, and the responses of the multiple particles to optical forces are sensed.

4. A method according to claim 1, further comprising:

contacting a first particle with a first capture zone having a specific binding affinity for a first chemical species so as to allow for a binding interaction to occur between the first capture zone and the first particle, the binding interaction being related to the presence of molecules of the first chemical species disposed between the surface of the first particle and the first capture zone;

contacting a second particle with a second capture zone having a specific binding affinity for a second chemical species so as to allow for a binding interaction to occur between the second capture zone and the second particle, the binding interaction being related to the presence of molecules of the second chemical species disposed between the surface of the second particle and the second capture zone;

applying an optical force to the first and second particles, the forces tending to cause responses of the particles; and

sensing the response of the first and second particles to the optical forces;

using the sensed responses to determine the presence, absence or quantity of the first chemical species disposed between the first particle surface and the first capture zone and of the second chemical species disposed between the second particle surface and the second capture zone.

5. A method according to claim 1, further comprising identifying particles prior to applying forces to the particles.

6. A method according to claim 5, further comprising selecting a first group of identified particles, applying optical forces to the first group of particles, selecting a second group of particles, and applying optical forces to the second group of particles.

7. A method according to claim 1, further comprising repeating the process to reach a data acquisition threshold.

8. A method according to claim 1, wherein the force has a component normal to and oriented away from the capture zone.

9. A method according to claim 1, wherein the force has a component parallel to a plane defined by the capture zone.

10. A method according to claim 1, wherein the force tends to displace unbound particles to a position that is spaced from the capture zone in both a first direction that is normal to and a second direction that is parallel to a plane defined by the capture zone.

11. A method according to claim 1, wherein the response includes a dislodging of the particle from the capture zone.

12. A method according to claim 1, wherein the particle is a cell.

13. A method according to claim 1, wherein the chemical species is a cell surface antigen.

14. A method according to claim 13, wherein the particle is a red blood cell and at least one capture zone includes a cell-surface antigen-specific probe.

15. A method according to claim 14, wherein the determination is used to further determine a blood type.

16. A method according to claim 15, wherein the blood type includes determinations of more than three cell-surface antigens.

17. A method according to claim 16, wherein the blood type is a minor blood group type.

18. A method according to claim 14, wherein the probe is one of an antibody, an antibody fragment, a peptide ligand and an aptamer.

19-48. -48. (canceled)

49. A method for determining the presence, absence, or quantity of multiple blood cell surface antigens in a blood sample of a patient, the method comprising:

diluting a blood sample;

contacting the diluted blood sample with first and second capture zones, the first zone functionalized to have a specific affinity for a first blood cell antigen and the second zone functionalized to have a specific affinity for a second blood cell antigen;

applying a first optical force having a dislodging component to at least one cell in the first zone, the first force being sized to be sufficient to dislodge a cell from the first zone if the first blood cell antigen is not present on the cell yet insufficient to dislodge a cell on which the first blood cell antigen is present;

applying a second optical force having a dislodging component to at least one cell in the second zone, the second force being sized to be sufficient to dislodge a cell from the second zone if the second blood cell antigen is not present on the cell yet insufficient to dislodge a cell on which the second blood cell antigen is present; and

detecting dislodgement or non-dislodgment of the cells from the zones.

50. (canceled)

51. A apparatus for the analysis of the presence, absence or quantity of target moieties on one or more particles, the apparatus comprising:

a substrate;

a first and second capture zone disposed on the substrate, each capture zone comprising a plurality of probe moieties,

wherein the avidity of the first and second capture zones are configured so that particles having a higher affinity to the capture zones will tend to be retained in the presence of a displacing optical force and particles having a lesser affinity for the capture zones will tend to be displaced in the presence of a displacing optical force, the optical force being in a specified range.

52-88. -88. (canceled)