Quantitative large area binding sensor for detecting biomarkers

Patent metadata

Field	Value
Publication number	US-11879830-B2
Application number	US-201917281221-A
Country	US
Kind code	B2
Filing date	Sep 27, 2019
Priority date	Sep 28, 2018
Publication date	Jan 23, 2024
Grant date	Jan 23, 2024

Abstract

An imaging system and method for detecting a target in a sample. The imaging system includes a lens-free holographic microscope having a light source in a first plane spaced above an image sensor. The image sensor extends in a second plane. The system also includes a microfluidic chip positioned between the light source and the image sensor. The microfluidic chip extends in a third plane, which is parallel to the second plane. There is at least one chamber in the microfluidic chip configured to receive a sample solution with a target. The system also has a plurality of functionalized beads positioned within the at least one chamber in the microfluidic chip. Any two of the plurality of functionalized beads have an affinity for binding together when exposed to the target in the sample solution.

First claim

What is claimed is:

1. An imaging system for the detection of a target, comprising:
a lens-free holographic microscope comprising a light source in a first plane spaced above an image sensor;
wherein the image sensor extends in a second plane;
a microfluidic chip positioned between the light source and the image sensor;
wherein the microfluidic chip extends in a third plane, which is parallel to the second plane;
at least one chamber in the microfluidic chip configured to receive a sample solution comprising a target; and
a plurality of functionalized beads, any two of the plurality of functionalized beads with an affinity for binding together when exposed to the target in the sample solution;
wherein the plurality of functionalized beads are positioned within the at least one chamber in the microfluidic chip.

2. The imaging system of claim 1 , wherein the at least one chamber is a plurality of wells.

3. The imaging system of claim 1 , wherein the microfluidic chip is composed of a flexible, stretchable material.

4. The imaging system of claim 1 , wherein the target is at least one of pathogens, protein molecules, DNA, or RNA.

5. The imaging system of claim 1 , wherein the light source is an LED array.

6. The imaging system of claim 1 , wherein the light source is a laser array.

7. The imaging system of claim 1 , wherein the light source is a single light source.

8. The imaging system of claim 1 , wherein the image sensor is a CCD image sensor.

9. The imaging system of claim 1 , wherein the image sensor is a CMOS image sensor.

10. The imaging system of claim 1 , wherein the functionalized beads are beads are either spherical or nonspherical.

11. The imaging system of claim 1 , wherein the functionalized beads are composed of either dielectric materials or metals.

12. The imaging system of claim 1 , wherein the functionalized beads are functionalized using one or more of the following capture agents: antibodies, protein aptamers, DNA aptamers, and RNA aptamers.

13. A method for determining the presence of a target in a sample, comprising the steps of:
providing an imaging system including a lens-free holographic microscope comprising a light source in a first plane spaced above an image sensor, wherein the image sensor extends in a second plane, a microfluidic chip positioned between the light source and the image sensor, wherein the microfluidic chip extends in a third plane, which is parallel to the second plane, at least one chamber in the microfluidic chip, and a plurality of functionalized beads, any two of the plurality of functionalized beads with an affinity for binding together when exposed to the target, wherein the plurality of functionalized beads are positioned within the at least one chamber in the microfluidic chip;
adding the sample to the at least one chamber in the microfluidic chip;
directing the light source toward the microfluidic chip and the image sensor;
capturing, via the image sensor, an interference pattern generated by light scattered by the sample;
generating a hologram image based on the interference pattern; and
reconstructing the hologram image to generate an in-focus image.

14. The method of claim 13 , wherein the step of reconstructing the hologram image to generate an in-focus image is based at least in part on the signal-to-noise ratio (SNR) of the target.

15. The method of claim 13 , wherein the step of reconstructing the hologram image to generate an in-focus image is based at least in part on pixel super-resolution (PSR).

16. The method of claim 13 , further comprising the steps of:
providing an electronic control system connected to the light source; and
illuminating the light source selectively using the electronic control system, reducing motion blur of the in-focus image.

17. The method of claim 13 , further comprising the step of measuring binding kinetics of the functionalized beads.

18. The method of claim 13 , determining, from the in-focus image, the presence of one or more clusters of functionalized beads.

19. The method of claim 18 , determining, from the in-focus image, the number of functionalized beads in each cluster in the in-focus image.

20. The method of claim 19 , determining, from the in-focus image, the concentration of the target in the sample.

Assignees

• Univ Arizona

Inventors

• Xiong Zhen
• Mcleod Euan

Classifications

• G01N15/1475 Primary

  Physics · mapped topic

• G01N15/1434

  Optical arrangements · CPC title

• G01N15/1484

  microstructural devices · CPC title

• G01N33/54313 Primary

  the carrier being characterised by its particulate form · CPC title

• G01N2015/0038

  Investigating nanoparticles · CPC title