Methods and devices for sample analysis

Patent metadata

Field	Value
Publication number	US-10466178-B2
Application number	US-201815984075-A
Country	US
Kind code	B2
Filing date	May 18, 2018
Priority date	Jun 19, 2013
Publication date	Nov 5, 2019
Grant date	Nov 5, 2019

Abstract

Methods and devices for cytometric analysis are provided. A cytometry apparatus is provided which may be used with a stationary sample cuvette for analysis of a stationary sample or with a flow sample cuvette for analysis of a flowing sample. The methods and devices provided herein may be used to perform cytometric analysis of samples under a wide range of experimental and environmental conditions.

First claim

We claim:

1. A cytometry apparatus comprising:
a stage, wherein the stage is configured to receive and support a cytometry cuvette, wherein the cytometry cuvette is configured to receive and support a biological sample, and wherein the cytometry cuvette comprises a sample plane on which the biological sample is supported;
an objective, wherein the objective comprises an entrance pupil and an exit pupil, and wherein the objective is optically coupled to the stage such that light from the biological sample supported by the cytometry cuvette supported by the stage may enter the entrance pupil and exit the exit pupil;
a sample coplanar light source disposed in substantially the same plane as the sample plane, wherein light from said sample coplanar light source is not in optical communication with said objective;
a sample coplanar optical sensor disposed substantially the same plane as the sample plane, wherein said sample coplanar optical sensor is not in optical communication with the objective;
an actuatable structure for directing light, wherein the actuatable structure is configured to direct light from the exit pupil of the objective to a first detection train or a second detection train; and
an illumination train, wherein the illumination train comprises a light source, wherein the illumination train is configured to provide at least a first illumination output and a second illumination output, and wherein for the first illumination output the illumination train is configured to focus light of a first range of wavelengths from the light source on a first location on the sample plane of the cytometry cuvette and the illumination train is configured to focus light of a second range of wavelengths from the light source on a second location on the sample plane of the cytometry cuvette.

2. The apparatus of claim 1 , wherein the first location and second location each have a diameter between 10 and 200 microns.

3. The apparatus of claim 1 , wherein the biological sample comprises multiple cells.

4. The apparatus of claim 1 , wherein light from the light source travels through the objective before reaching the sample plane of the cuvette.

5. The apparatus of claim 1 , wherein the cytometry cuvette is configured to support a stationary biological sample on the sample plane.

6. The apparatus of claim 1 , wherein the cytometry cuvette is configured to support a flowing biological sample on the sample plane.

7. The apparatus of claim 1 , wherein the cytometry cuvette comprises a sample introduction port, a flow channel, and a sample collection area, wherein the flow channel comprises the sample plane, wherein the sample introduction port, the flow channel, and the sample collection area are fluidically linked, and wherein the biological sample may be introduced in the introduction port, flow the through flow channel, and collect in the sample collection area.

8. The apparatus of claim 1 , wherein the first detection train comprises at least 3 image sensors.

9. The apparatus of claim 1 , wherein the second detection train comprises at least a first light detector, a second light detector, and a third light detector, wherein the detection train is configured such that the first light detector is configured to receive light of a first range of wavelengths, the second light detector is configured to receive light of a second range of wavelengths, and the third light detector is configured to receive light of a third range of wavelengths.

10. The apparatus of claim 9 , wherein the second detection train comprises a first emission filter before the first light detector, a second emission filter before second light detector, and a third emission filter before the third light detector.

11. The apparatus of claim 1 , wherein for the first illumination output the illumination train is further configured to focus light of a third range of wavelengths from the light source on a third location on the sample plane of the cytometry cuvette.

12. The apparatus of claim 1 , wherein for the first illumination output the illumination train is configured to illuminate an imaging area of the sample plane with light of the same range of wavelengths across the imaging area.

13. The cytometry apparatus of claim 1 , wherein the apparatus is configured to receive at least two different types of cuvettes.

14. The cytometry apparatus of claim 13 , wherein the apparatus is configured to receive a stationary sample cuvette and a flow sample cuvette.

15. The cytometry apparatus of claim 14 , wherein the apparatus is configured to obtain data from stationary samples and moving samples.

16. The cytometry apparatus of claim 15 , wherein light from stationary samples is directed to a first optical pathway, and wherein light from moving samples is directed to a second optical pathway.

17. A method of analyzing a biological sample, the method comprising:
moving a flow sample cuvette onto a stage of a cytometry apparatus, wherein the flow sample cuvette is configured to receive and support a biological sample, wherein the flow sample cuvette contains a flow channel through which a biological sample may flow, and wherein the flow channel comprises a bottom surface, wherein the bottom surface comprises a sample plane over which the biological sample and objects therein may flow, and wherein the cytometry apparatus comprises:
an objective, wherein the objective comprises an entrance pupil and an exit pupil, and wherein the objective is optically coupled to said stage such that light from the biological sample supported by the flow sample cuvette supported by the stage may enter the entrance pupil and exit the exit pupil;
a sample coplanar light source disposed in substantially the same plane as the sample plane of a flow sample cuvette supported by said stage, wherein light from said sample coplanar light source is not in optical communication with said objective;
an illumination train, wherein the illumination train comprises a light source, wherein the illumination train is configured to provide at least a first illumination output and a second illumination output, and wherein for the first illumination output the illumination train is configured to focus light of a first range of wavelengths from the light source onto a first location on the sample plane of the flow cytometry cuvette and the illumination train is configured to focus light of a second range of wavelengths from the light source on a second location on the sample plane of the flow cytometry cuvette;

loading a biological sample comprising multiple cells into the flow sample cuvette;
flowing the biological sample through the flow channel of the flow sample cuvette, wherein during the flowing, light of a first range of wavelengths from the light source is focused on a first location in the flow channel and light of a second range of wavelengths from the light source is focused on a second location in the flow channel; and
detecting light emitted from a cell in the first location in the flow channel and light emitted from another cell in the second location in the flow channel.

18. The method of claim 17 , wherein the cells are white blood cells.

19. The method of claim 17 , wherein the first location and second location each have a diameter between 10 and 200 microns.

20. The method of claim 18 wherein said detecting light from cells in the first location and in the second location in the flow channel comprises detecting light with at least two image sensors.

21. The method of cl

Assignees

• Theranos Ip Co Llc

Inventors

• Pangarkar Chinmay
• Mohan Karan

Classifications

• G01N21/47

  Scattering, i.e. diffuse reflection (G01N21/25, G01N21/41 take precedence {G01N21/55 takes precedence}) · CPC title

• G01N21/6486 Primary

  Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence) · CPC title

• G01N15/1434

  Optical arrangements · CPC title

• G01N15/1459 Primary

  the analysis being performed on a sample stream · CPC title

• G01N2201/08

  Optical fibres; light guides · CPC title