Method and system for imaging a blood sample

1. A method comprising:

forming a cell suspension by diluting a blood sample comprising red blood cells;

using capillary forces to introduce the cell suspension comprising the red blood cells into a carrier that is a closed cavity that includes a base surface and a closed top, via an inlet defined by the carrier;

allowing the cells in the cell suspension to settle on the base surface of the carrier to form a monolayer of cells on the base surface of the carrier, such that after the cell suspension settles on the base surface (a) a density of the cells of the cell suspension is between about 10,000 and about 30,000 cells per mm2, and (b) the cell suspension forms the monolayer having an average base surface coverage of between 40 percent and 90 percent; and

acquiring at least one microscope image of at least a portion of the monolayer of cells.

2. The method according to claim 1 , wherein allowing the cells in the cell suspension to settle on the base surface of the carrier to form the monolayer of cells on the base surface of the carrier comprises allowing a period of time of less than 5 minutes for the cells to settle as a monolayer on the base surface.

3. The method according to claim 1 , wherein a vertical height of the carrier is between 20 micrometers and 300 micrometers.

4. The method according to claim 1 , wherein acquiring the at least one microscope image comprises acquiring a plurality of microscope images, at least two of which are provided under different conditions, the different conditions being selected from the group consisting of:

different portions of the base surface being imaged, and different illumination conditions being used.

5. The method according to claim 1 , wherein the cell suspension has a concentration that is such that when substantially all of the cells in the cell suspension are allowed to settle on the base surface of the carrier to form the monolayer of cells, a monolayer is formed on the surface with substantially no overlap between the cells.

6. The method according to claim 1 , wherein diluting the blood sample comprises diluting the cells by a dilution factor to obtain the cell suspension.

7. The method according to claim 6 , wherein the dilution factor is between 50 and 300.

8. The method according to claim 1 , wherein a vertical height of the cell suspension when settled on the base surface is between 20 micrometers and 1000 micrometers.

9. The method according to claim 8 , wherein the at least one microscope image is obtained by a microscope set to a Depth of Field that is between 0.5 micrometers and 10 micrometers.

10. The method according to claim 1 , wherein acquiring the at least one microscope image of the portion of the monolayer of cells comprises acquiring the at least one microscope image using a microscope set to a Depth of Field that is not more than 20 percent of a vertical height of the cell suspension when settled on the base surface.

11. The method according to claim 10 , wherein the at least one microscope image is obtained using a microscope set to a Depth of Field that is not more than 15 percent of the vertical height of the cell suspension when settled on the base surface.

12. A method comprising:

using capillary forces to introduce a cell suspension comprising red blood cells into a carrier that is a closed cavity that includes a base surface and a closed top, via an inlet defined by the carrier;

allowing the cells in the cell suspension to settle on the base surface of the carrier to form a monolayer of cells on the base surface of the carrier;

acquiring at least one microscope image of at least a portion of the monolayer of cells; and

analyzing the at least one image to determine based thereon presence or absence of a pathogen in the cell suspension;

wherein analyzing the at least one image to determine based thereon presence or absence of a pathogen in the cell suspension comprises analyzing the at least one image to determine based thereon presence or absence of a blood infecting protozoa in the cell suspension; and

wherein the blood infecting protozoa is selected from the genus consisting of Trypanosoma, Plasmodium; Toxoplasma and Babesia , and wherein analyzing the at least one image to determine based thereon presence or absence of the pathogen in the cell suspension comprises analyzing the at least one image to determine based thereon presence or absence of the blood infecting protozoa from the selected genus in the cell suspension.

13. A method comprising:

using capillary forces to introduce a cell suspension comprising red blood cells into a carrier that is a closed cavity that includes a base surface and a closed top, via an inlet defined by the carrier;

allowing the cells in the cell suspension to settle on the base surface of the carrier to form a monolayer of cells on the base surface of the carrier; and

acquiring at least one microscope image of at least a portion of the monolayer of cells, using a microscope set to a Depth of Field that is not more than 20 percent of a vertical height of the cell suspension when settled on the base surface; and

selecting a microscope objective lens that provides the Depth of Field, wherein the lens permits acquiring an image of at least one object being no more than 3 micrometers long at any dimension thereof.

14. The method according to claim 13 , wherein selecting the microscope objective lens comprises selecting a lens that permits acquiring an image of at least one object having a height with respect to the base surface of no more than 3 micrometers.

15. A system for imaging a blood sample, the system comprising:

a carrier that defines a closed cavity having a base surface and a closed top, and an inlet into the closed cavity;

a blood sample preparing unit configured:

to receive a blood sample comprising red blood cells and at least one blood cell diluting agent, and

to form therefrom a blood cell suspension, that is such that the cell suspension forms a monolayer of the cells when introduced, via the inlet, into the closed cavity defined by the carrier, and allowed to settle on the base surface such that after the cell suspension settles on the base surface (a) a density of the cells of the cell suspension is between about 10,000 and about 30,000 cells per mm2, and (b) the cell suspension forms the monolayer having an average base surface coverage of between 40 percent and 90 percent;

a microscope image acquisition unit for acquiring at least one image of the blood cell suspension when on the base surface of the carrier, the microscope acquisition unit comprising a microscope; and

a controller being configured to acquire at least one microscope image of the cell suspension using the microscope.

16. The system according to claim 15 , wherein the controller is configured to drive the microscope to acquire a plurality of microscope images of the monolayer, at least two of which are provided under different conditions, the different conditions being selected from the group consisting of: different portions of the monolayer being imaged, and different illumination conditions being used.

17. The system according to claim 15 , wherein the blood sample preparing unit is configured to facilitate forming a blood cell suspension, that is such that that when substantially all of the cells in the cell suspension are allowed to settle on the base surface of the carrier to form the monolayer of cells, a monolayer is formed on the base surface with substantially no overlap between the cells.

18. The system according to claim 15 , wherein the controller is configured to acquire the at least one microscope image of the cell suspension using the microscope, the microscope being set to a Depth of Field that is not more than 20 percent of a vertical height of the cell suspension when settled on the base surface.

19. The system according to claim 15 , wherein the carrier is configured such that when the cell suspension is introduced into closed cavity via the inlet, the closed cavity fills with the cell suspension, via capillary forces.