PARTICLE STANDARDS FOR REFLECTED LIGHT SCATTER MEASUREMENTS FROM DEGENERATE PARTICLE FOCI

Abstract

A method of selecting a type of particle for use in standardisation and/or calibration of a flow cytometer. The method includes determining the location of two or more particle focal points of particles flowing through a cross section of a channel in the flow cytometer; for each type of particle, determining for each particle focal point, for a beam of light directed at a type of particle at said particle focal point from a first direction, the total intensity of light scattered along a second direction; determining the difference between the highest and lowest determined light intensities of the light intensities determined at the two or more particle focal points; and selecting a type of particle for which the difference between the highest and lowest determined light intensities at the two or more particle focal points is below a predetermined threshold.

Claims

1. A method of selecting a type of particle for use in standardization and/or calibration of a flow cytometer, the method comprising: (a) determining a location of two or more particle focal points of particles flowing through a cross section of a channel in the flow cytometer; (b) for each type of particle of two or more different types of particles: (b1) for each particle focal point of the two or more particle focal points, determining, for a beam of light directed at a particle of said type at said particle focal point from a first direction, a total intensity of light scattered along a second direction, the second direction lying within 90 degrees of the first direction; and (b2) determining, for the type of particle, the difference between the highest and lowest determined light intensities of the light intensities determined at the two or more particle focal points; and (c) selecting a type of particle for which the difference between the highest and lowest determined light intensities of the light intensities determined at the two or more particle focal points is below a predetermined threshold.

2. The method according to claim 1, wherein the two or more different types of particles have the same refractive index.

3. The method according to claim 1, wherein the two or more different types of particles each have a different diameter.

4. The method according to claim 1, wherein the first direction lies along a normal to a lower surface of the channel.

5. The method according to claim 4, wherein the second direction lies at an angle of less than about 20 degrees to the first direction.

6. The method according claim 1, wherein the light scattered along the second direction comprises light reflected from the particle, light refracted by the particle, and light reflected from a lower surface of the channel.

7. The method according to claim 1, wherein the particle focal points lie on a normal to a lower surface of the channel.

8. The method according to claim 1, wherein the flow cytometer comprises an inertial focuser upstream of the channel.

9. The method according to claim 1, wherein a lower surface of the channel is opaque.

10. The method according to claim 1, wherein the predetermined threshold is less than or equal to about 10%.

11. The method according to claim 10, wherein the predetermined threshold is less than or equal to about 5%.

12. A method of selecting a type of particle for use in standardization and/or calibration of a flow cytometer, the method comprising: (a) for each type of particle of two or more types of particles, determining, for a plurality of particles of said type flowing through a channel in the flow cytometer, for a beam of light directed at the channel along a first direction, a coefficient of variation in a total intensity of light scattered along a second direction, the second direction lying within 90 degrees of the first direction; and (b) selecting a type of particle for which the coefficient of variation is below a predetermined threshold.

13. The method according to claim 12, wherein step (a) comprises determining, for each particle of the plurality of particles, the total intensity of light scattered along the second direction.

14. The method according to claim 12, wherein the predetermined threshold is less than or equal to about 10%.

15. The method according to claim 12, wherein the predetermined threshold is less than or equal to about 5%.

16. The method according to claim 12, wherein the first direction lies along a normal to a lower surface of the channel.

17. The method according to claim 12, wherein the flow cytometer comprises an inertial focuser upstream of the channel.

18. The method according to claim 12, wherein the two or more different types of particles have the same refractive index.

19. The method according to claim 12, wherein a lower surface of the channel is opaque.

20. The method according to claim 12, wherein the second direction lies at an angle of less than about 20 degrees to the first direction.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0041] Examples will now be described, by way of example, with reference to the accompanying figures in which:

[0042] FIG. 1 shows an optical train diagram for measuring rFSC of a particle in degenerate inertial foci in a channel;

[0043] FIG. 2 shows ray tracing predictions of rFSC measurements of a lymphocyte as a function of distance from the substrate;

[0044] FIG. 3 shows ray tracing predictions of rFSC measurements of polystyrene beads of different diameters as a function of distance from the substrate; and

[0045] FIG. 4 shows experimental measurements of reflected versus transmitted forward scatter measurements from polystyrene size calibration beads of different diameters.

DETAILED DESCRIPTION

[0046] FIG. 1 shows a geometric model of reflected forward scatter, in the form of an optical train. A laser beam 101 is focused at the substrate surface 102, where the beam focus width is significantly greater than the particles to be measured. Thus, the incident light is close to a collimated beam while passing through the particle to be measured. The light passes through the particle 103 before impinging on the surface. It then passes through the same particle again, shown as a reflection image 104. The upper boundary of the channel 105 is also labelled, both before and after the reflection. Note that the channel height is defined as the distance between the substrate surface 102 and the upper boundary of the channel 105. The Gaussian waist of the laser beam is also depicted as 106. The channel width is not shown in FIG. 1.

[0047] As discussed above, inertial focusing typically leads to degenerate particle foci and the particles will therefore typically pass through one of two points in the cross section of the channel. These two positions are shown in FIG. 1 and are at a distance x and a distance h-x from the substrate surface, where h is the height of the channel and x is a distance dependent on factors such as the height of the channel, the width of the channel, the medium in which the particles are dispersed, and the speed at which the particles are flowing through the channel. The path length between the first and second scattering events will therefore be either 2x or 2(h-x), depending on which of the two foci the particle passes through.

[0048] FIGS. 2 and 3 show predictions of rFSC for particles with different diameters and refractive indices. The medium is modelled with the refractive index of water (1.33). The predicted measurements of rFSC are given as a percentage difference to the predicted measurements for FSC. The in this model were simulated using ray-tracing software (Zemax OpticStudio, Zemax LLC, Kirkland, Wash. 98033, USA).

[0049] FIG. 2 shows the prediction for lymphocytes, which have a refractive index of 1.37 and a diameter of around 6 μm. The percentage difference between the predicted measurements for rFSC as compared with the predicted measurements for FSC are shown as a function of distance of the particle from the lower surface of the channel, while the degenerate inertial foci for channels of 31 microns height are labelled. There is approximately 5% difference in rFSC between the degenerate foci, and as such the error in rFSC measurements of lymphocytes of around 5% CV is not unduly large compared with the variability between lymphocytes of around 30% CV. The example of lymphocytes is typical of most biological cells, particularly mammalian cells.

[0050] FIG. 3 shows the prediction for polystyrene beads, which have a refractive index of 1.6, of three different diameters—6 μm, 9 μm, and 15 μm. The locations of the particle foci are once again shown for a channel of 31 microns in height. For particles of 6 μm and 15 μm in diameter there is a significant difference in rFSC between the degenerate foci. However, for beads 9 μm diameter the difference in measurements of rFSC is small enough (approximately 1%) that the beads are still useful as a measurement standard. Typically, a CV of 5% or less will be low enough that the particles may still be used for standardization, set-up, calibration, and quality control of a flow cytometer, although a CV of 2% or less is more preferable.

[0051] FIG. 4 shows the measurement of polystyrene size calibration beads in an experimental system, where transmitted and reflected forward scatter have been measured simultaneously, and are plotted as a 2D histogram (commonly known in cytometry as a dot plot). Peaks in measurements for polystyrene beads of a diameter of 5.17, 7.56, 10.1, and 16.5 μm are annotated. This experimental result is approximately in agreement with the simulation, and verify that by selecting polystyrene beads with a diameter in a range of approximately 7 to 10 μm, the effects of the degeneracy in the particle foci are substantially removed, yielding a single rFSC measurement of the bead.