Cell differentiation based on multi-directional light from a microfluidic chip

Patent metadata

Field	Value
Publication number	US-12350665-B2
Application number	US-202217696688-A
Country	US
Kind code	B2
Filing date	Mar 16, 2022
Priority date	Mar 17, 2021
Publication date	Jul 8, 2025
Grant date	Jul 8, 2025

Abstract

Disclosed is an approach to differentiating between different particle types in samples flowing through microfluidics chips. A sample may have an initial proportion of a first cell type to a second cell type. An illuminating light source may emit a coherent light at the sample, and light leaving the chip in a first direction may be detected using a first light detector, and light leaving the chip in a second direction (e.g., orthogonal to the first direction) may be detected using a second light detector. The detected light may be fluorescence. An orientational feature of a plurality of cells in the sample may be determined based on the light detected by the detectors. Based on the orientational features and the detected light, a biasing operation may be performed for each cell in the sample to obtain a modified proportion of cell types in the sample.

First claim

What is claimed is:

1. A method comprising:
providing, to a microfluidic chip having a sample channel, a sample comprising a particle population having a proportion of a first particle type to a second particle type;
emitting, from a light source, an illuminating light along a first axis such that the illuminating light coincides with particles in the sample as the sample passes through the channel;
detecting, using a first light detector, a first light emitted from the sample along a first axis;
detecting, using the first light detector or a second light detector, a second light emitted from the sample along a second axis; and
performing, based on the detected first light emitted along the first axis and on the detected second light emitted along the second axis, a biasing operation that modifies the proportion of the first particle type to the second particle type;
wherein the first light and the second light are fluorescence (i) that results from incidence of the illuminating light on particles in the sample and (ii) that travels in multiple different directions from fluorescing particles in the sample, and wherein the method further comprises:
generating, based on the light emitted from the sample along the first and second axes, an intensity map of peak fluorescence associated with each particle type;
detecting, based on the intensity map, a first population center associated with the first particle type, and a second population center associated with the second particle type;
calculating a relative intensity along a first line passing through the first population center;
calculating a slope of a second line joining the first population center and the second population center;
locating a first saddle point along a third line joining a first population associated with the first particle type, and a second population associated with a second particle type;
locating a second saddle point along a fourth line joining the first population, and the second population; and
generating a gate by bounding the first population or the second population, wherein the gate is bounded based on the first saddle point, the second saddle point, and additional bounding points.

2. A method comprising:
providing, to a microfluidic chip having a sample channel, a sample comprising a particle population having a proportion of a first particle type to a second particle type;
emitting, from a light source, an illuminating light along a first axis such that the illuminating light coincides with particles in the sample as the sample passes through the channel;
detecting, using a first light detector, a first light emitted from the sample along a first axis;
detecting, using the first light detector or a second light detector, a second light emitted from the sample along a second axis; and
performing, based on the detected first light emitted along the first axis and on the detected second light emitted along the second axis, a biasing operation that modifies the proportion of the first particle type to the second particle type;
wherein the first light and the second light are fluorescence (i) that results from incidence of the illuminating light on particles in the sample and (ii) that travels in multiple different directions from fluorescing particles in the sample, and wherein the method further comprises:
calculating a kernel within a pixel map;
adding a first instance of the kernel to the pixel map based on the light emitted from the sample along the first and second axes;
adding a second instance of the kernel to the pixel map based on the light emitted from the sample along the first and second axes;
deriving a first histogram from the pixel map;
removing data from the pixel map;
deriving a second histogram from a first row of the pixel map;
generating a first trough point from the second histogram;
deriving a third histogram from a second row of the pixel map;
generating a second trough point from the third histogram;
generating a polynomial function based on the first and second trough points; and
bounding a population based on the polynomial function and additional bounding points.

3. A method comprising:
providing, to a microfluidic chip having a sample channel, a sample comprising a particle population having a proportion of a first particle type to a second particle type;
emitting, from a light source, an illuminating light along a first axis such that the illuminating light coincides with particles in the sample as the sample passes through the channel;
detecting, using a first light detector, a first light emitted from the sample along a first axis;
detecting, using the first light detector or a second light detector, a second light emitted from the sample along a second axis; and
performing, based on the detected first light emitted along the first axis and on the detected second light emitted along the second axis, a biasing operation that modifies the proportion of the first particle type to the second particle type;
wherein the first light and the second light are fluorescence (i) that results from incidence of the illuminating light on particles in the sample and (ii) that travels in multiple different directions from fluorescing particles in the sample, and wherein the method further comprises:
calculating a kernel within a pixel map;
adding a pre-defined number of instances of the kernel to the pixel map based on the light emitted from a plurality of samples along the first and second axes;
deriving a first histogram from the pixel map along the first axis;
removing data from the pixel map, based on the first histogram;
generating a second histogram from the pixel map along the second axis;
determining an area of interest within the pixel map, based on the second histogram;
generating an additional plurality of histograms along the second axis of the area of interest of the pixel map;
determining a plurality of trough points based on the additional plurality of histograms;
generating a polynomial function based on the plurality of trough points; and
bounding a population based on the polynomial function and additional bounding points.

4. The method of claim 1 , wherein the first axis is orthogonal to the second axis.

5. The method of claim 1 , wherein no more than two detectors are used to detect light emissions from the sample.

6. The method of claim 1 , wherein the biasing operation comprises emitting, using a second light source, a third light at the sample to change states of individual particles in the sample.

7. The method of claim 6 , wherein the second light is emitted to deactivate a particle in the sample.

8. The method of claim 7 , wherein particles in the particle population are cells, and wherein deactivating the cells comprises ablating the cells.

9. The method of claim 7 , wherein the illuminating light coincides with the sample at a first location in a path of the sample flowing through the sample channel, and wherein the third light is emitted at the sample so as to coincide with the sample at a second location in the path of the sample, wherein the second location is downstream of the first location.

10. The method of claim 1 , further comprising determining an orientational feature of each particle in a set of one or more particles in the sample.

11. The method of claim 10 , wherein the orientational feature is determined based on the detected first light and on the detected second light.

12. The method of claim 1 , wherein the particle population is a cell population, wherein the first particle type is a first cell type, and wherein the second particle type is a second cell type.

1

Assignees

• Abs Global Inc

Inventors

• Appleyard David
• Mcada Daniel
• Xia Zheng
• Schiller James Maxwell
• Savage Frederick
• Rupel Ii John Walker
• Miller Timothy
• Fisher Alec

Classifications

• G01N15/1434

  Optical arrangements · CPC title

• B01L2300/0663

  Whole sensors · CPC title

• G01N15/1425

  using an analyser being characterised by its control arrangement · CPC title

• G01N2015/1402

  Data analysis by thresholding or gating operations performed on the acquired signals or stored data · CPC title

• G01N15/1484 Primary

  microstructural devices · CPC title