Apparatus and method for volumetric capillary cytometry

• US 5,547,849 A
• Filed: 05/02/1994
• Issued: 08/20/1996
• Est. Priority Date: 02/17/1993
• Status: Expired due to Term

• Current Assignee: Biometric Imaging, Inc. (Becton, Dickinson & Co)
• Original Assignee: Biometric Imaging, Inc. (Becton, Dickinson & Co)
• Inventors: Hodges, Michael, Baer, Thomas M., Dubrow, Robert S., Hayter, Paul G., Dietz, Louis J., Manian, Bala S., Shartle, Robert J.
• Primary Examiner(s): Housel, James C.
• Assistant Examiner(s): Tanigawa, Gary
• Application Number:
  US08/236,342
• Time in Patent Office: 841 Days
• Field of Search: 356/244, 356/246, 356/427, 382/128, 382/133, 382/134, 250/432 R, 250/459.1, 250/458.1, 250/461.1, 250/461.2, 435/7.2, 435/7.21, 435/7.1, 435/7.22, 435/7.23, 435/7.24, 435/7.25, 435/287.2, 435/288.7, 422/50, 422/55, 422/57-59, 422/68.1, 422/73, 422/82.05
• US Class Current: 435/7.24
• CPC Class Codes: G01N 15/1468 with spatial resolution of the texture or inner structure of the particle
• CPC Class Codes: G06V 20/69 Microscopic objects, e.g. biological cells or cellular parts

Abstract

The apparatus and method of the present invention disclose a scanning imaging cytometer wherein an unprocessed biological fluid sample is reacted with a fluorescently-labeled binding agent. The reacted sample undergoes minimal processing before it is placed into a capillary tube. The sample is optically scanned and fluorescence excitation is recorded from a plurality of columnar regions of the capillary tube, each columnar region generally defined by the spot size of the excitation beam and the depth dimension of the capillary tube. A spatial filter of a sufficient pinhole diameter is selected to allow simultaneous volumetric detection of all fluorescent targets in each columnar region.

Claims

1. A method of identifying and enumerating cellular components of biological fluids via fluorescence, the method comprising:

obtaining a sample of biological fluid having cellular components;

incubating the sample with an excess amount of a fluorescently-labeled binding agent directed to binding sites present on the cellular components to form fluorescent complexes;

placing the sample into a capillary tube, the capillary tube having specified dimensions and a longitudinal axis;

optically scanning the sample with an incident beam of light having a wavelength selected to excite the fluorescent complexes, so as to sequentially intersect the capillary tube in a plurality of beam spots of specified diameter to illuminate a plurality of columnar regions;

sequentially detecting emitted fluorescence confined to an interior depth dimension of each columnar region;

recording the emitted fluorescence from each columnar region of heightened fluorescence intensity; and

enumerating the cellular component of the sample from the emitted fluorescence.

2. A method as in claim 1, further comprising diluting the sample after said incubating step and prior to said placing the sample into a capillary tube step.

3. A method as in claim 1 wherein optically scanning the sample comprises intersecting a horizontally positioned capillary tube with an incident beam positioned directly above the capillary tube.

4. A method as in claim 1 wherein optically scanning the sample comprises scanning with an incident beam of a wavelength of 600 to 1000 nanometers.

5. A method as in claim 1 wherein reacting the sample with a fluorescently-labeled binding agent comprises using a binding agent labeled with a fluorophore that is activated at an excitation wavelength in the range of 600 to 1000 nanometers.

6. A method as in claim 1 wherein optically scanning the sample comprises scanning with an incident beam that is 5 to 15 microns in diameter at an intersection of the incident beam and the capillary tube.

7. A method as in claim 1 wherein placing the sample in a capillary tube comprises placing the sample in a capillary tube of rectangular cross-section with a shorter dimension of the cross-section defining a depth of the capillary tube and a longer dimension of the cross-section defining a width of the capillary tube.

8. A method as in claim 1 wherein placing the sample in a capillary tube comprises placing the sample in a capillary tube having a depth dimension of 25 to 225 microns.

9. A method as in claim 1 wherein optically scanning the sample comprises traversing a path in a first direction transverse to the longitudinal axis of the capillary tube and a second direction along the longitudinal axis of the capillary tube.

10. A method as in claim 9 wherein optically scanning the sample in a first direction transverse to the longitudinal axis of the capillary tube comprises traversing a scan path that originates and terminates at points beyond respective outer boundaries of the capillary tube.

11. A method as in claim 1 wherein optically scanning the sample comprises scanning a capillary tube that is in a fixed position.

12. A method as in claim 1 further comprising

determining a concentration of a cellular component of the sample by calculating an amount of enumerated component per specified volume of the capillary tube, the volume being determined by origination and termination points of a scan in a direction along the longitudinal axis of the capillary tube and a cross-sectional area of the capillary tube.

13. A method as in claim 1 further comprising

determining ratios of different cellular components of the sample by calculating an amount of each enumerated component and comparing relative amounts of each enumerated component.

14. An assay for identifying and enumerating leukocyte subclasses in whole blood via fluorescence, the assay comprising;

obtaining a sample of whole uncoagulated blood;

incubating the sample with an excess amount of a fluorescently-labeled antibody directed to specific cell surface markers of a leukocyte subclass within the sample to form fluorescent complexes;

placing the sample into a capillary tube having specified dimensions;

optically scanning the sample with an incident beam of light having a wavelength selected to excite the fluorescent complexes and to minimize interference from red blood cells present in the sample, the incident beam sequentially intersecting the capillary tube in a plurality of beam spots of specified diameter to illuminate a plurality of columnar regions;

sequentially detecting emitted fluorescence confined to an interior depth dimension of each columnar region;

recording the emitted fluorescence from each columnar region of heightened fluorescence intensity; and

enumerating a subclass of leukocytes by determining a presence of the subclass in the sample from the emitted fluorescence.

15. An assay as in claim 14, further comprising diluting the sample after said incubating step and prior to said placing the sample into a capillary tube step.

16. An assay as in claim 14 wherein incubating the sample with a fluorescently-labeled antibody comprises incubating with a plurality of fluorescently-labeled antibodies, each antibody directed to a different specific cell surface marker of a leukocyte subclass, and each antibody labeled with a different fluorophore having different optical characteristics.

17. A scanning imaging cytometer for non-flowing fluids in a capillary tube, the cytometer comprising:

a transparent capillary tube containing a non-flowing fluid having complexes of cells and fluorescently-labeled binding agent in suspension with free fluorescently-labeled binding agent, said capillary tube having outer and inner walls;

a beam of light impinging upon the outer wall of said capillary tube transverse to a longitudinal axis of said capillary tube in a beam spot having a first diameter illuminating a columnar region of the fluid, said beam of light having an excitation wavelength for stimulating fluorescent emission from the complexes and the free binding agent;

a light detector spaced apart from said capillary tube and responsive to the fluorescent emission;

a wide angle light collector positioned proximate said capillary tube, said light collector configured to gather fluorescent emission from the illuminated columnar region and to transmit the fluorescent emission towards said light detector in a retrobeam;

a spatial filter having a pinhole aperture, said spatial filter positioned between said light collector and said detector, the pinhole aperture disposed to intercept the retrobeam and having a second diameter admitting only a portion of the retrobeam to said detector, the second diameter of the pinhole aperture substantially exceeding the first diameter of the beam spot, so as to confine a depth of detection to an interior depth dimension of said capillary tube; and

means for providing motion of said beam of light relative to said capillary tube to cause said beam of light to sequentially impinge upon said capillary tube in a plurality of beam spots, so as to illuminate within the capillary tube a plurality of columnar regions whose total volume can be determined.

18. A scanning imaging cytometer as in claim 17 wherein the fluorescently-labeled binding agent contains a fluorophore that is activated at an excitation wavelength in the range of 600 to 1000 nanometers.

19. A scanning imaging cytometer as in claim 17 wherein the binding agent is an antibody.

20. A scanning imaging cytometer as in claim 17 wherein the binding agent is specific to cell surface markers.

21. A scanning imaging cytometer as in claim 17 wherein the binding agent is an intercalating dye.

22. A scanning imaging cytometer as in claim 17 wherein the binding agent is a nucleic acid probe.

23. A scanning imaging cytometer as in claim 17 wherein the binding agent reacts with specific receptors.

24. A scanning imaging cytometer as in claim 17 wherein the beam of light impinging upon the outer wall of the capillary tube passes through a central portion of the wide angle light collector and then impinges on the outer wall of the capillary tube and is focused into an interior depth of the capillary tube.

25. A scanning imaging cytometer as in claim 17 further comprising particle counting means associated with the detector for distinguishing background fluorescence associated with free binding agent from fluorescence associated with complexes.

26. A scanning imaging cytometer as in claim 17 wherein the means for providing motion causes the plurality of spots to partially overlap each other.

27. A scanning imaging cytometer as in claim 17 wherein the means for providing motion causes the said beam of light to overscan lateral edges of the capillary tube.

28. A scanning imaging cytometer as in claim 17 wherein the means for providing motion causes the said beam of light to sequentially impinge upon the capillary tube in a two-dimensional array of spots, illuminating a two-dimensional array of columnar regions whose total volume can be determined.

29. A scanning image cytometer as in claim 17, wherein said light detector comprises a spectral dispersion device positioned between said spatial filter and first and second light sensitive members, the spectral dispersion device configured for separating a plurality of fluorescent emission wavelengths and directing the separated wavelengths to the first and second light sensitive members.

30. A scanning imaging cytometer as in claim 17 wherein the volume probed is determined by a known cross-sectional area of the capillary tube and a distance that has been scanned along the capillary tube.

31. A scanning imaging cytometer as in claim 17 wherein the volume is determined by a known cross-sectional area of the capillary tube and by providing specific identification marks on the capillary tube to define distance.

32. A scanning imaging cytometer as in claim 17 wherein the beam is focused to a location within the capillary tube.

33. A scanning imaging cytometer as in claim 17 wherein the beam of light has a wavelength in the range of 600 to 1000 nanometers.

34. A scanning imaging cytometer for non-flowing fluids in a capillary tube, the cytometer comprising:

a transparent capillary tube containing a non-flowing fluid having complexes of cells and fluorescently-labeled binding agent, the capillary having outer and inner walls;

a beam of light impinging upon the outer wall of said capillary tube transverse to a longitudinal axis of said capillary tube in a beam spot having a first diameter illuminating a columnar region of the fluid, said beam of light having an excitation wavelength for stimulating fluorescent emission from the complexes;

a light detector spaced apart from said capillary tube and responsive to the fluorescent emission;

a wide angle light collector positioned proximate said capillary tube, said light collector configured to gather fluorescent emission from the illuminated columnar region and to transmit the fluorescent emission towards said light detector in a retrobeam;

a spatial filter having a pinhole aperture, said spatial filter positioned between said light collector and said detector, the pinhole aperture disposed to intercept the retrobeam and having a second diameter admitting most of the retrobeam to said detector, the second diameter of the pinhole aperture substantially exceeding the first diameter of the beam spot, so as to confine a depth of detection to an interior depth dimension of said capillary tube; and

means for providing motion of said beam of light relative to said capillary tube to cause said beam of light to sequentially impinge upon said capillary tube in a plurality of beam spots, so as to illuminate within the capillary tube a plurality of columnar regions whose total volume can be determined.

35. An apparatus for making volumetric fluorescence measurements of a cell suspension, the apparatus comprising:

a capillary tube of rectangular cross-section with a shorter dimension of the cross-section defining a depth of said capillary tube and a longer dimension of the cross-section defining a width of said capillary tube, said capillary tube containing a cell suspension therein;

optical scanning means for generating an incident beam of a wavelength selected to excite the cell suspension of the capillary tube, the incident beam sequentially intersecting the capillary tube in a plurality of beam spots of specified diameter to illuminate a plurality of columnar regions;

detection means having a light sensitive member for detection of fluorescent emission;

collection means for gathering of fluorescent emission from the columnar region and for directing the fluorescent emission to said detection means;

a spatial filter with a specified pinhole aperture for allowing detection of fluorescent light emitted from the entire columnar region, said spatial filter disposed between said collection means and said detection means, so as to confine a depth of detection to an interior depth dimension of said capillary tube; and

a data reader in communication with said detection means for recordation of fluorescent emission signals.

36. An apparatus as in claim 35 wherein the capillary tube is positioned horizontally and the incident beam of the optical scanning means intersects the capillary tube from a position directly above the capillary tube.

37. An apparatus as in claim 35 wherein the wavelength of the incident beam is 600 to 1000 nanometers.

38. An apparatus as in claim 35 wherein the diameter of the beam spot is in the range of 5 to 15 microns.

39. An apparatus as in claim 35, wherein the capillary tube has a depth in the range of 25 to 225 microns.

40. An apparatus as in claim 35 wherein the incident beam of the optical scanning means traverses a path in a first direction along the width of the capillary tube and a second direction along a longitudinal axis of the capillary tube.

41. An apparatus as in claim 35 wherein the optical scanning means traverses a path in a direction along the width of the capillary tube and the path originates and terminates at points beyond the respective outer boundaries of the capillary tube.

42. An apparatus as in claim 35, wherein said detection means comprises a spectral dispersion device positioned between said spatial filter and first and second light sensitive members, the spectral dispersion device configured for separating a plurality of fluorescent emission wavelengths and directing the separated wavelengths to the first and second light sensitive members.

43. An apparatus as in claim 35 further comprising a lens, a central portion of the lens being used by the optical scanning means for passage of the incident beam before intersection of the incident beam with the capillary tube, and the entire lens being used by the collection means for gathering of fluorescent emission from the capillary tube.

44. An apparatus for the detection of subclasses of blood cells, the apparatus comprising:

a transparent capillary having a known rectangular cross-sectional area and having a known depth, thereby providing a known volume, wherein the depth substantially exceeds ten microns;

means for generating a beam of light having an excitation wavelength of at least 600 nanometers and configured to impinge upon the upper surface of said capillary so as to provide a beam spot having a diameter of at least five microns;

means for providing motion of the beam of light relative to said capillary for causing the beam of light to impinge upon said capillary in a plurality of beam spots so as to illuminate within the capillary tube a plurality of columnar regions of known volume;

a light collector positioned proximate said capillary and configured to gather a fluorescent emission caused by said means for generating a beam of light and further configured to transmit the fluorescent emission in a retrobeam;

a light detector responsive to the fluorescent emission, said detector being positioned away from said capillary and positioned to be impinged by the retrobeam from said light collector; and

a spatial filter positioned between said light collector and said detector, the spatial filter disposed to intercept the retrobeam and configured to admit only a portion of the retrobeam to said detector so as to limit light detected to a single columnar region illuminated by a single beam spot and confined to an interior depth dimension of each columnar region.

45. The apparatus of claim 44, wherein the depth of said capillary is in the range of 25 to 225 microns.

46. The apparatus of claim 45, wherein the excitation wavelength of the beam of light from said means for generating is in the range of 600 to 1000 nanometers.

47. The apparatus of claim 46, wherein the beam spot has a diameter in the range of five to fifteen microns.