Dosimeters including lensless imaging systems

Patent metadata

Field	Value
Publication number	US-10107997-B2
Application number	US-201815943595-A
Country	US
Kind code	B2
Filing date	Apr 2, 2018
Priority date	Dec 17, 2013
Publication date	Oct 23, 2018
Grant date	Oct 23, 2018

Abstract

Among other things, a method comprises imaging a sample displaced between a sensor surface and a surface of a microscopy sample chamber to produce an image of at least a part of the sample. The image is produced using lensless optical microscopy, and the sample contains at least blood from a subject. The method also comprises automatically differentiating cells of different types in the image, generating a count of one or more cell types based on the automatic differentiation, and deriving a radiation dose the subject has absorbed based on the count.

First claim

What is claimed is:

1. A method comprising:
incorporating beads into a blood sample from a subject,
producing an image of the blood sample using lensless optical microscopy;
automatically differentiating cells of one or more different types in the image;
generating a count of cells of one or more of the different types; and
based on the count, deriving a radiation dose the subject has absorbed.

2. The method of claim 1 in which the beads are configured to provide a precise spacing between two opposing surfaces enclosing a space in which the blood sample is held when the images produced.

3. The method of claim 2 in which the beads are of a uniform size.

4. The method of claim 3 in which the uniform size is between 1 μm and 5 μm.

5. The method of claim two in which the beads are of a uniform size within a specified precision.

6. The method of claim 1 in which the beads are spherical.

7. The method of claim 1 in which the beads are non-spherical.

8. The method of claim 1 in which the blood sample comprises sample units suspended in a liquid matrix.

9. The method of claim 8 in which the sample units are smaller than the beads.

10. The method of claim 2 in which the beads are of a uniform size, the method comprising reducing the distance between the two opposing surfaces to be the same as the uniform size.

11. The method of claim 10 in which the beads are sufficiently distributed within the sample so that the reduced distance between the two opposing surfaces is uniformly the same as the uniform size of the beads.

12. The method of claim 11 in which the concentration of beads within the sample is in a range of 10,000 to 500,000 beads per microliter.

13. The method of claim 11 in which the beads have approximately neutral buoyancy in the sample and the beads are distributed within the sample by mechanical agitation.

14. The method of claim 1 in which incorporating beads into the blood sample comprises incorporating beads of two different sizes.

15. The method of claim 1 in which the beads of the larger of the two different sizes and the method comprises reducing the distance between the two opposing surfaces to be the same as the size of the larger beads.

16. The method of claim 14 in which the number of the smaller size beads per unit volume of the sample is known and the smaller beads are distributed reasonably uniformly in the sample, the method comprising determining a volume of a space between two opposing surfaces within which the sample lies by counting the number of the smaller size beads within the space.

17. The method of claim 1 in which the beads are transparent.

18. The method of claim 1 in which the beads are colored, or fluorescent, or opaque, or a combination of two or more of those characteristics.

19. The method of claim 1 in which the beads label antibodies.

20. The method of claim 1 in which generating a count of cells of one or more of the different types comprises generating a count of lymphocytes.

21. The method of claim 20 comprising estimating lymphocyte depletion based on the count of lymphocytes.

22. The method of claim 20 in which the blood sample comprises a first sample taken at a first time from the subject and the count of lymphocytes comprises a first count of lymphocytes, and the method comprises
imaging a second blood sample taken at a second, different time from the subject,
generating a second count of lymphocytes based on the second blood sample, and
estimating lymphocyte depletion based on the first and second counts of lymphocytes.

23. The method of claim 1 in which cells of the different types are differentiated based on one or more of color, size of cell, nuclear shape, and nuclear size.

24. The method of claim 1 in which the count of cells of the one or more differentiated types is generated taking account of a volume of the imaged blood sample.

25. The method of claim 1 in which the blood sample contains diluted blood from the subject, and the count of cells of the one or more different types is generated taking account of dilution of the blood.

26. The method of claim 1 in which the blood sample contains one or more of anticoagulant, diluent, stain, antibody, erythrocyte lysing solution, and other reagents.

27. The method of claim 1 in which generating a count of cells of the one or more different types comprises generating the count based on detection of one or more surface antigens associated with the one or more cell types.

28. The method of claim 1 in which producing the image comprises producing the image at a resolution of 1 megapixels or higher.

29. The method of claim 1 in which producing the image comprises remixing and resampling of the blood sample by raising and lowering a surface of a microscopy sample chamber.

30. The method of claim 29 in which the remixing and resampling comprises moving a mixing element relative to a sensor surface.

31. The method of claim 30 in which moving of the mixing element comprises moving the mixing element toward or away from the sensor surface or both.

32. The method of claim 31 in which the moving of the mixing element comprises moving the mixing element toward and away from the sensor surface more than one time.

Assignees

• Alentic Microscience Inc

Inventors

• Fine Alan Marc

Classifications

• G06T2207/10056

  Microscopic image · CPC title

• G01N2015/1006

  for cytology · CPC title

• Y10S435/808

  Optical sensing apparatus · CPC title

• G01N15/1429

  Signal processing · CPC title

• G01N2015/1486

  Counting the particles · CPC title