MICROFLUIDIC CHIP FOR MULTI-ANALYTE DETECTION

• US 20150233907A1
• Filed: 09/27/2013
• Published: 08/20/2015
• Est. Priority Date: 09/27/2012
• Status: Abandoned Application

• Current Assignee: Nanospeed Diagnostics Incorporated
• Original Assignee: Nanospeed Diagnostics Incorporated
• Inventors: Gupta, Rajan, Gupta, Seema
• Application Number:
  US14/425,522
• Publication Number:
  US 20150233907A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 2021/6482 Sample cells, cuvettes
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/645 Specially adapted constructive features of fluorimeters
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/582 with fluorescent label

Abstract

A microfluidic chip and compatible bio-sensor are provided to detect and/or quantify an analyte in a sample fluid, and preferably to simultaneously quantify multiple analyte(s) in a sample fluid volume. A fluid volume containing microbeads is flowed through an elongate planar sample chamber of the microfluidic chip. Microbead traps or barriers in the sample chamber retain the microbeads. The sample fluid volume is Excitation flowed through the sample chamber. A conjugate specific to the analyte is and labeled with a fluorophore is introduced into the sample chamber. In the biosensor, an excitation wavelength is directed parallel to the plane of the sample chamber. Any fluorescent emissions from the sample chamber are detected in a direction substantially orthogonal to the plane of the sample chamber by a photodetector, and correlated to an amount or concentration length of sample chamber of analyte in the sample fluid volume.

Claims

1. A microfluidic chip for use with an assay using a plurality of microbeads, the microfluidic chip comprising:

(a) two opposed planar sides defining therebetween an elongate planar sample chamber in fluid communication with an inlet and an outlet, wherein the direction from the inlet to the outlet defines a downstream longitudinal direction and a lateral direction perpendicular to the longitudinal direction in the plane of the sample chamber; and

(b) at least one microbead trap within the sample chamber between the inlet and the outlet.

2. The microfluidic chip of claim 1 wherein the volume of the sample chamber is about 10 μ

L or less.

3. The microfluidic chip of claim 1 wherein at least a portion of one of at least one of the planar sides of the sample chamber is transparent to fluorescent excitation and emission wavelengths.

4. The microfluidic chip of claim 3 wherein at least a portion of both planar sides are transparent to fluorescent excitation and emission wavelengths.

5. The microfluidic chip of claim 3 wherein the chip defines an internal reflection waveguide to guide light along the length of the sample chamber.

6. The microfluidic chip of claim 1 comprising a plurality of microbead traps which comprise at least two micropillars spaced apart by an intra-trap gap smaller than the microbeads to be retained.

7. The microfluidic chip of claim 6 wherein the micropillars of each microbead trap comprise upstream-facing surfaces that converge laterally toward their respective intra-pair gaps, at an acute angle in the downstream longitudinal direction.

8. The microfluidic chip of claim 6 wherein each microbead trap comprises three micropillars laterally spaced apart to define gaps smaller than the microbeads to be retained.

10. The microfluidic chip of claim 1 wherein the at least one microbead trap is formed by a plurality of elongate microwalls in side-by-side relation to define or approximate a plurality of microchannels therebetween, wherein the microchannels have widths smaller than the microbeads to be retained.

11. The microfluidic chip of claim 1 wherein the at least one microbead trap comprises a boundary formed by a plurality of elongate microwalls in end-to-end relation with each other to define gaps between the ends, wherein the gaps are smaller than the microbeads to be retained.

12. The microfluidic chip of claim 11 wherein the at least one microbead trap boundary comprises a curved barrier forming a bulb-shaped receptacle for the microbeads.

13. The microfluidic chip of claim 1 comprising a plurality of microbead traps, divided into at least two physically separated groups of microbead traps.

14. The microfluidic chip of claim 13 comprising a first set of microbead traps located in a first region of the sample chamber, and a second set of microbead traps located in a second region of the sample chamber spatially separated from the first region, and wherein the first set and second set of microbead traps are sized and arranged to selectively retain different sizes of microbeads.

15. The microfluidic chip of claim 14 wherein the second region is located downstream longitudinally of the first region, the first set of microbead traps or barriers are sized and arranged to selectively retain larger microbeads, and the second set of microbead traps or barriers are sized and arranged to selectively retain smaller microbeads.

16. The microfluidic chip of claim 14 further comprising a shield or filter that opaquely masks at least one of the planar sides in either the first region or the second region to a selected emission wavelength.

9. (canceled)

17. A method of detecting and/or quantifying at least one analyte in a fluid sample, the method comprising the steps of:

(a) providing a microfluidic chip defining an elongate planar sample chamber in fluid communication with an inlet and an outlet, and comprising at least one microbead trap within the sample chamber between the inlet and the outlet;

(b) causing microbeads to be retained by the at least one microbead trap by flowing a fluid containing a plurality of microbeads through the sample chamber, wherein the microbeads each comprise a binding conjugate specific to the at least one analyte;

(c) introducing the sample into the inlet and allowing the sample to flow through the sample chamber to the outlet such that any analyte present in the sample binds to the binding conjugates;

(d) introducing a fluorophore into the sample chamber, wherein the fluorophore is bound to a labelling conjugate specific to the at least one analyte, or is bound to a control analyte which competes with the at least one sample analyte for binding to the binding conjugates;

(e) directing an excitation wavelength into the sample chamber in a direction substantially parallel to the plane of the sample chamber; and

(f) detecting any fluorescent emissions or absence thereof emitted from the sample chamber in a direction substantially orthogonal to the plane of the sample chamber.

18. The method of claim 17 further comprising the step of measuring an intensity of the emission wavelength and correlating the intensity to an amount or concentration of the analyte in the sample fluid volume.

19. The method of claim 17 adapted to detect a first analyte and a second analyte, comprising the steps of retaining microbeads specific to both the first analyte and the second analyte in the sample chamber;

using a first labelled conjugate specific to the first analyte and a second labelled conjugate specific to the second analyte; and

detecting the presence or absence of the first and second labels.

20. The method of claim 17 adapted to detect a first analyte and a second analyte, comprising the steps of retaining microbeads specific to both the first analyte and the second analyte in the sample chamber;

using a first labelled analyte to compete with a sample first analyte for microbead binding sites, and a second labelled analyte to compete with a second sample analyte for microbead binding sites, and detecting the presence, absence or intensity of any fluorescent emissions.

21-25. -25. (canceled)

26. A biosensor for detecting a fluorophore in an elongate sample chamber defining a longitudinal direction, the biosensor comprising:

(a) an excitation/emission chamber for retaining the sample chamber;

(b) an excitation light source directed at the sample chamber along the longitudinal direction; and

(c) at least one photodetector positioned to detect light emissions from the sample chamber in a direction substantially orthogonally to the longitudinal direction.

27-32. -32. (canceled)