GB2107548A - Method of analyzing particles in a dilute fluid sample - Google Patents

Abstract

The method, particularly for analyzing sediments of urine, is accomplished by flowing the sample over an extended area 18. A plurality of optical still images are taken of the sample using a stroboscopic lamp 32, microscope 30 and camera 34 with each image representing a different portion of the area. Each optical image is converted into an electronic image. The plurality of electronic images are superimposed to form one resultant electronic image, displayed on a monitor 38. <IMAGE>

Description

SPECIFICATION Method of analyzing particles in a dilute fluid sample The present invention relates to a method of analyzing particles in a fluid sample and more particularly to a method of analyzing biological fluid samples, such as urine, that are dilute, but without the necessity of physically creating a concentrated sample for analysis.

Heretofore the method for urine sediment examination requires the following steps: (i) urine must be poured into a tube and spun down in a centrifuge to separate the sediment from its suspending fluid; (ii) most of the cleared suspending fluid must be poured out; (iii) the sediment must be resuspended in the remaining fluid; (iv) the suspension must be transferred to and spread on a microscope slide; (v) a coverslip must be placed over the suspension on the slide; (vi) the slide must be focused under a microscope; and (vii) a number of fields of view must be searched and examined for the presence of abnormal numbers of red and white blood cells, epithelial cells, casts, bacteria, yeast, parasites, mucoid threads, crystals, etc., which compose urine sediment in various proportions depending upon the presence of disease.The steps of centrifugation (i), decantation (ii) and resuspension (iii) are used because the fluid sample is dilute. All these steps are currently performed manually. The manipulations involved frequently make the method messy and unpleasant. Spreading of the sediment suspension on the microscope slide often is uneven.

When numerous sediments are viewed, prolonged peering into the eyepieces of a microscope becomes tiring. All these factors contribute to imprecision.

Other apparatus for handling biological specimens include the so-called Coulter counter.

In this counter blood cells are passed in single file through an orifice and detected and counted by the manner in which they change the electric properties at the orifice. However, information from the Coulter counter is limited to the analysis of a single type of measurement. Where multiple parameter information is desired, the standard commercial way of obtaining it is by preparing a microscope slide with the cells fixed on an image plane and having a human operator or pattern recognition machine count statistically significant numbers of the cells as the cells are observed one-at-a-time on the slide through a microscope.

Other attempts have been made in recent years to provide optical analysis of particles flowing in a flow stream. For instance, Kay, et al., Journal of Histochemistry and Cytochemistry, Volume 27, page 329 (1979) shows a Coulter type orifice for moving cells in single file with the cells magnified on a vidicon.

Additionally, Kachel, et al., Journal of Histochemistry and Cytochemistry, Volume 27, page 335, shows a device for moving cells in single file through a microscope area where they are photographed. See also for instance Flow Cytometry and Sorting, Melaned et al., John Wiley a Sons 1 979, Chapter 1.

U.S. patent application no. 146064 filed on May 2 1980 discloses an apparatus and a method for quantitative analysis of particle information.

However, none of the references cited heretofore teach or suggest a solution to the problem of analysis of particles in a dilute fluid sample, without the necessity of initially creating a concentrated sample through centrifugation, decantation and resuspension.

The method according to the invention is defined in claims 1 and 9 below.

The present invention will be described in more detail, by way of example, with reference to the accompanying drawings: Figure 1 is a perspective view of an apparatus which can be used with the method of this invention.

Figure 2 is a plan view of the flow chamber in Fig. 1.

Figure 3 is a cross-sectional view of the apparatus of Fig. 2 taken on the plane indicated at 3-3.

Figure 4 is a schematic diagram of the electronic processor employed by the apparatus of Fig. 1.

The method of the present invention comprises distributing a fluid sample, such as urine, over a extended area, such as smearing the sample over a microscope slide. A plurality of optical still images of the sample are taken, with each image representing a different portion of the slide. Thus, for example, the slide with the sample thereon may be mounted in a microscope and moved about such that a portion of the slide is in the imaging area. Each image will be of a different portion of the slide. Each of the optical images is converted to an electronic image.

The plurality of electronic images are electronically composited to form one resultant electronic image. The one resultant electronic image may be further processed.

The method of the present invention may be practised by using an apparatus 5, shown in Fig. 1. The apparatus 5 includes a body 10 containing a flow chamber having an inlet 1 2 for for a fluid sample, such as urine, and an outlet 14 with a passageway 1 6 extending between them past an imaging area 1 8. The passageway 1 6 has an inlet with a conduit 20 adapted to be connected to a volume of saline solution 22. As illustrated in Figs. 2 and 3, the inlet 1 2 for the urine sample has a needle 24 in the passageway 1 6 downstream from the conduit 20 with the needle 24 connected to a container 26 adapted to hold the urine sample to be analyzed.The urine sample flows in a direction from the inlet 1 2 to the outlet 14.

The cross-sectional area of the passageway 1 6 becomes progressively smaller as the passageway extends from the inlet 1 2 to the outlet 14 while at the same time the passageway 1 6 becomes much shallower and much wider.

Thus, as illustrated in Figs. 2 and 3 the passageway 1 6 has a width and depth of about 5,000 microns at the inlet 1 2 and a width and depth of about 500 microns at midpoint 28, and a depth of 100 microns with a width exceeding 5,000 microns at the examination area 18.

It will be appreciated that the fluid sample flowing through the examination area 1 8 is many times deeper than the largest cells which have a maximum dimension of about 20 microns, but with the flow passageway shaped in this way the fluid sample entering through the opening 1 2 is confined to a stable flow path of minimum shear in the examination area 18, and the particles in the fluid sample are oriented in that area with their maximum cross-sectional area visible in the plane of Fig. 2. The flow characteristics in the passageway 1 6 may be controlled by adjusting the fluid pressure in containers 22 and 26 either automatically or by adjusting the static heights thereof.

Preferably the fluid sample flowing in the examination area 1 8 has a cross-sectional area of minimum shear which is not substantially larger than the minimum cross-sectional area of the particles. Hence the particles are aligned in the fluid sample flowing in the examination area 1 8 with their minimum cross-sectional area extended transverse to the direction of flow. The term "minimum shear" is used herein to means "minimum velocity gradient" so that a particle moving in the stream tends to align itself with the direction of the stream much as a log floating down a river will align itself with the direction of flow where there is a flow gradient.

A microscope 30 is focused on the examination area 18 and the examination area 18 is illuminated from below by a strobe light 32 which is preferably a U.S. Scientific Instrument Corporation Model 3018 containing a 2UP1.5 lamp. The light 32 is directed at the microscope 30 in a direction substantially parallel to the thickness of the body 10. The stroble light 32 operates, preferably, at onesixtieth or one-fiftieth of a second, thereby forming a series of still optical images at the microscope 30. The output of the microscope 30 is focused on a CCD camera 34 which is preferably a CCD camera model number TCl 1 60BD manufactured by RCA. The CCD camera 34 converts each optical image into an electonic image.The CCD Camera 34 also segments each of the electronic image into a plurality of pixels, with each pixel corresponding to a defined portion of each image. The plurality of electronic images (each optical image is converted into an electronic image) are then composited to create one resultant electronic image. This may be done, for example, by summing all the pixels that correspond to the same defined portion of each image.

The one resultant electronic image is an image of an apparent concentrated fluid sample, but without the necessity of physically creating a concentrated fluid sample. Moreover, the degree of apparent concentration is controlled by the number of images that are composited. Thus, an image of an apparent ten-fold concentration is accomplished by compositing ten images to form one resultant image. Since the degree of apparent concentration is controlled electronically, it should be obvious that with the method of the present invention, the image of the apparent concentration of the fluid sample may be varied with considerable ease.

The one resultant electronic image may be further processed, electronically, and displayed. Alternatively, each electronic image may be processed, electronically, prior to being composited to form the one resultant electronic image. One processor which may be employed, to process electronically either each electronic image or the one resultant electronic image, is the processor marketed as Image Analysis System Model C-1285 by Hamamatsu Systems, Inc., Waltham, Massachusetts. Preferably, however, the output of the CCD camera 34 is connected to an electronic processor 36 which is illustrated in greater detail in Fig. 4 and includes a black and white television monitor 38 and a frame grabber 40 which stores still electronic images of the subject viewed by the CCD camera 34.

The frame grabber 40 is preferably a Model FG08 frame grabber made by the Matrox Corporation of Montreal, the output of which is supplied to a videc refresh memory 42 model RGB 256 made by Matrox Corporation which are both coupled to the multibus 44 of the central processing unit 46 which is preferably an Intel 80/20 computer. The multibus 44 is also coupled to a 48K random access memory 48 of Electronic Solutions, Inc., and a 1 6K dual port random access memory 50 model RM 11 7 of Data Cube Corporation.

The output of the video refresh memory 42 is also coupled to a color monitor 52 which may be used to provide digitally enhanced video images of individual still frames for human examination.

The second output of the dual port ram 50 is connected to a multibus 54 which is connected to an Applied Micro Devices central processing unit 56, a 48K random access memory of Electronic Solutions, Inc. 58 and removable storage in the form of a floppy disc controller 60, such as an Advanced Micro Devices Model 8/8 and two units of Shugart floppy disc storage 62.

With the apparatus shown in Fig. 4, a number of specific methods, for the creation of the one resultant electronic image, is possible.

In the first alternative, fluid sample such as urine is entered into the inlet 1 2. The fluid is illuminated by the strobe light 32 and a plurality of optical still images of the sample are taken by the microscope 30. Because the fluid is translucent and the illumination is from below, the optical image will be of dark particles on a light background. The optical images are converted into electronic images which are then digitized and stored in memory 48. The one resultant electronic image, the composition of the plurality of electronic images, is formed by summing the digitized data of each electronic image with that data stored in memory 48.

In a variation of the above described method, prior to the data of the digitized image being stored in memory 48, the background data of each image is first removed, electronically. The pertinent information from each image may be collected and stored in one resultant electronic image.

In yet another alternative, urine is injected into the inlet 1 2 as before. The urine is illuminated by the strobe light 32. However, using the well known technique of dark field illumination or phase contrast illumination, the optical image produced at the microscope 30 will be of light particles on a dark background. Each optical image is converted into an electronic image by the CCD camera 34.

Due to the nature of the CCD camera 34, it retains the electronic image in the camera, if the electronic image is not read out. Thus, a subsequent electronic image (converted from an optical image) will be composited to the previous electronic image. The one resultant electronic image may therefore be formed at the CCD camera 34.

A wide variety of programming may be employed for further processing the one resultant electronic image with the apparatus of Fig. 4 depending upon the particular task which user wishes to perform.

For example with urine, in the method of the prior art, if chemical particles, such as phosphates are in the imaging area and obscure the view of the biological particles, the phosphate particles are removed chemically through the addition of hydrochloric acid.

With the method of the present invention, however, the chemical particles may be removed electronically, i.e. through image processing techniques. If it is desired to remove particles of particular size, colour or shape from view, this may be done electronically without repairing the sample each time. Moreover, with the method of the present invention, biological particles which heretofore may not be removed chemically, may be similarly electronically removed from the image. Thus a greater degree of flexibility is possible with the present invention.

It should be appreciated that there are many advantages ot the method of the present invention. The first and foremost is that the analysis of particles of a dilute sample may be made without first physically creating a concentrated sample, with its attending problems of centrifugation, decantation and resuspension. The method of resuspension of the prior art results in overlap of the various particles or results in a biased image. With the method of the present invention, the fluid is more statistically representative of the particles with less likelihood of overlap of the particles, and there is no bias of the image.

Next, it should be appreciated that the degree of apparent condcentration may be varied electronically. In addition, the elimination of manual handling steps saves time, potential sources of error and offers biological safeguards (potentially infectious samples are analyzed with a minimum of human handling).

Then too, consumable items, such as tubes, pipettes and microscope slides, are not used resulting in economic savings. Finally, with the image in electronic form, a number of imaging techniques may be used to further process the image, including the electronic removal of chemical and biological particles.

Claims (14)

CLAIMS 1. A method of analyzing particles, from a fluid sample containing the particles, comprising the steps of distributing the fluid sample over an extended area; forming a plurality of optical still images of the sample over the said area, with each optical image representing a different portion of the area; converting each of the optical still images to an electronic image; and compositing the electronic images to form one resultant electronic image. 2. A method according to claim 1, further comprising the steps of processing the resultant image and displaying the processed image. 3. A method according to claim 1, further comprising the steps of processing each of the electronic images and displaying the resultant electronic image. 4. A method according to claim 3, comprising the steps of removing the background data from each electronic image; and collecting the pertinent information from each electronic image to form one resultant image. 5. A method to claim 2, 3 or 4, wherein the processing comprises electronically removing particles that are not desired for display. 6. A method according to any of claims 2 to 5, further comprising the steps of segmenting each of the electronic images into a plurality of pixels, with each pixel corresponding to a defined portion of each image; and summing all the pixels that correspond to the same defined portion of each image. 7. A method according to claims 1 to 6, wherein the compositing is effected by a CCD camera. 8. A method according to any of claims 1 to 7, wherein the fluid sample is urine and the particles are sediments. 9. A method of analyzing particles, from a moving fluid sample containing the particles, comprising the steps of flowing the sample and distributing the fluid sample over an extended area having a width and a thickness both measured perpendicular to the direction of flow, with the width many times the thickness; illuminating the fluid at a predetermined location in the direction of flow, with the illumination directed in a direction substantially perpendicular to the direction of flow; forming a plurality of optical still images of the fluid sample, at the said location; converting each of the optical still images to an electronic image; and compositing the plurality of electronic images to form one resultant electronic image. 10. A method according to claim 9, further comprising the steps of processing the resultant image and displaying the processed image. 11. A method according to claim 9, further comprising the steps of processing each of the electronic images and displaying the resultant electronic image. 12. A method according to claim 9, 10 or 11, wherein the fluid sample is urine and the particles are sediments. 1 3. A method according to any of claims 9 to 12, wherein the illuminating is effected by stroboscopic illumination. CLAIMS (30 Ju11982)

1. A method of analyzing particles from a fluid sample containing the particles, comprising the steps of distributing the fluid sample over an extended area; forming a plurality of optical still images of the sample over the said area; with each optical image representing a different portion of the area; converting each of the optical still images to an electronic image; compositing the electronic images to form one resultant electronic image; processing the resultant image; and displaying the processed image.

2. A method of analyzing particles from a fluid sample containing the particles, comprising the steps of distributing the fluid sample over an extended area; forming a plurality of optical images of the sample over the said area, with each optical image representing a different portion of the area; converting each of the optical still images to an electronic image; processing each of the electronic images; compositing the processed electronic images to form one resultant electronic image; and displaying the resultant electronic image.

3. A method according to claim 1 or 2, comprising the steps of removing the background data from each electronic image; and collecting the pertinent information from each electronic image to form one resultant image.

4. A method according to claim 1, 2 or 3, wherein the processing comprises electronically removing particles that are not desired for display.

5. A method according to any of claims 1 to 4, further comprising the steps of segmenting each of the electronic images into a plurality of pixels, with each pixel corresponding to a defined portion of each image; and summing all the pixels that correspond to the same defined portion of each image.

6. A method according to claims 1 to 5, wherein the compositing is effected by a CCD camera.

7. A method according to any of claims 1 to 6, wherein the fluid sample is urine and the particles are sediments.

8. A method of analyzing particles, from a moving fluid sample containing the parties, comprising the steps of flowing and the sample and distributing the fluid sample over an extended area having a width and a thickness both measured perpendicular to the direction of flow, with the width many times the thickness; illuminating the fluid at a predetermined location in the direction of flow, with the illumination directed in a direction substantially perpendicular to the direction of flow; forming a plurality of optical still images of the fluid sample, at the said location; converting each of the optical still images to an electronic image; compositing the plurality of electronic images to form one resultant electronic image; processing the resultant image; and displaying the processed image.

9. A method according to claim 8 further comprising the step of aligning the particles in the direction of flow with the minimum crosssectional area extended substantially transverse to the direction of flow and the maximum cross sectional area extended substantially parallel to the width.

10. A method of analyzing particles, from a moving fluid sample containing the particles, comprising the steps of flowing the sample and distributing the fluid sample over an extended area having a width and a thickness both measured perpendicular to the direction of flow, with the width many times the thickness; alinging the particles in the direction of flow with the minimum cross sectional area extended substantially transverse to the direction of flow and the maximum cross sectional area extended substantially parallel to the width; illuminating the fluid at a predetermined location in the direction of flow, with the illumination directed in a direction substantially perpendicular to the direction of flow; forming a plurality of optical still images of the fluid sample, at the said location; converting each of the optical still images to an electronic image; and compositing the plu rality of electronic images to form one resultant electronic image.

11. A method according to claim 10, further comprising the steps of processing the resultant image and displaying the processed image.

12. A method according to claim 8 or 10, further comprising the steps of processing each of the electronic images and displaying the resultant electronic image.

1 3. A method according to claim 8, 9 or 10, wherein the fluid sample is urine and the particles are sediments.

14. A method according to any of claims 8 to 13, wherein the illuminating is effected by stroboscopic illumination.