Raman spectroscopic lateral flow test strip assays

• US 20080064120A1
• Filed: 01/26/2007
• Published: 03/13/2008
• Est. Priority Date: 02/06/2006
• Status: Abandoned Application

• Current Assignee: Prescient Medical, Inc.
• Original Assignee: Prescient Medical, Inc.
• Inventors: Clarke, Richard, Womble, M.
• Application Number:
  US11/698,083
• Publication Number:
  US 20080064120A1
• Time in Patent Office: Days
• US Class Current: 436/514
• CPC Class Codes: G01N 21/658 enhancement Raman, e.g. surface plasmons
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/585 with a particulate label, e.g. coloured latex

Abstract

The invention provides improved Raman spectroscopy-based methods and systems for the quantitative analysis of selected analytes using lateral flow binding assay test strips.

Claims

1. A method for measuring at least one selected analyte in a liquid sample, comprising the steps of:

providing a lateral flow test strip unit that includes;

a sample zone for depositing a liquid biological sample, such as a body fluid, wherein the sample zone includes, migratable SERS-active particles, coated with a first binding element, that is specific for an analyte to be measured,

a capture zone having a second binding element that specifically binds to the analyte and/or epitopes presented by the analyte and bound first binding element, but not by the first-binding element alone; and

depositing a sample on the sample zone; and

after allowing sufficient time for migration of the particles through lateral flow strip, determining the presence, absence or concentration of the analyte in the sample by;

irradiating at least part of the capture zone with monochromatic light to generate a Raman spectra from particles that may be captured in the capture zone,

measuring the intensity of at least part of the Raman spectra that is specific for the first binding element on particles that may have been captured in the capture zone,

calculating the presence/absence or concentration of the analyte in the sample based on the measured intensity.

2. The method of claim 1, wherein at least one of the first and second binding elements is an antibody.

3. The method of claim 1, wherein the SERS-active particles comprise gold.

4. The method of claim 1, wherein the SERS-active particles are colloidal gold particles.

5. The method of claim 1, wherein the step of determining the presence, absence or concentration of the analyte in the sample further comprises inserting the lateral flow test strip unit into a portable Raman analyzer unit adapted to receive said test strip unit for reading.

6. The method of claim 5, wherein the test strip unit and the Raman analyzer unit are mutually adapted to position the test strip for reading by the Raman analyzer unit.

7. The method of claim 5, wherein the portable Raman analyzer unit comprises an excitation light source, a Raman spectroscope and a processor operably linked to the Raman spectroscope to determine the presence, absence or concentration of the analyte in the sample based, at least in part, on the intensity of the Raman signal of the first binding elements associated with the particles that are captured in the capture zone.

8. The method of claim 7, wherein the analyzer unit further comprises a display that is operably linked to the processor.

9. The method of claim 7, wherein the Raman analyzer unit is a low-resolution Raman spectroscopy unit.

10. A method for measuring at least one selected analyte in a liquid sample, that includes the steps of:

providing a lateral flow test strip unit that includes,

a sample zone for depositing a liquid biological sample, such as a body fluid, wherein the sample zone includes migratable SERS-active particles coated with a first binding element, that is specific for an analyte to be measured

a capture zone having a second binding element that specifically binds to the analyte and/or epitopes presented by the analyte and bound first binding element, but not by the first binding element alone, and

a control zone having a third binding element such as an antibody that binds to the first binding element, the control zone, wherein the capture zone is located between the sample zone and the control zone;

depositing a sample on the sample zone,

after allowing sufficient time for migration of the particles through lateral flow strip, determining the presence, absence or concentration of the analyte in the sample by;

irradiating at least part of the capture zone with monochromatic light to generate a Raman spectra from particles that may be captured in the capture zone,

measuring the intensity of at least part of the Raman spectra that is specific for the first binding element on particles that may have been captured in the capture zone,

irradiating at least part of the control zone with monochromatic light to generate a Raman spectra from particles that may be captured in the control zone,

measuring the intensity of at least part of the Raman spectra that is specific for the first binding element on particles that may have been captured in the control zone.

11. The method of claim 10, further comprising the step of:

calculating the presence/absence or concentration of the analyte in the sample based on a ratio of the intensities measured for the capture zone and the control zone.

12. The method of claim 10, wherein at least one of the first, second and third binding elements is an antibody.

13. A system for performing lateral flow test strip assays using Raman spectroscopy, comprising:

a portable Raman reader unit; and

a lateral flow assay test strip unit comprising migratable SERS-active particles to which at least one analyte binding element is bound,

wherein the Raman reader unit and test strip unit are mutually adapted to allignedly position the test strip unit with respect to the Raman reader unit for the reading of at least one test or control stripe of the strip by the reader unit.

14. The system of claim 13, wherein at least one test or control stripe of the strip comprises at least one test stripe and at least one control stripe of the strip.