Device for measuring the light scattering of biological cells in flow cytophotometers

• US 4,915,501 A
• Filed: 03/06/1987
• Issued: 04/10/1990
• Est. Priority Date: 07/16/1985
• Status: Expired due to Term

• Current Assignee: Flowtech As
• Original Assignee: Harald Steen
• Inventors: Steen, Harald
• Primary Examiner(s): Rosenberger, Richard A.
• Application Number:
  US07/043,552
• Time in Patent Office: 1,131 Days
• Field of Search: 356/73, 356/336, 356/337, 356/338, 356/339, 356/340, 356/341, 356/343
• US Class Current: 356/343
• CPC Class Codes: G01N 15/1434 Optical arrangements
• CPC Class Codes: G01N 2015/016 White blood cells
• CPC Class Codes: G01N 2015/1493 Particle size
• CPC Class Codes: G01N 2021/4711 Multiangle measurement

Abstract

A device which enables the measurement of light scattering from microscopical particles and biological cells in two different regions of scattering angle in flow cytometers where the particles/cells are illuminated through microscope optics (4) having high numerical aperture. A dark field image (2) of the particles/cells is formed on a slit (7) behind which is situated a telescope (10) which reproduces the angle distribution of the scattered light from the particles/cells. Light scattered from large angles (>15°) is separated from the light field behind this telescope by means of a mirror (13) in the central part of this light field reflecting the light into a first detector (14) while the remaining light which is dominated by small scattering angles falls on another detector (15).

Claims

1. A flow cytometer device for simultaneous measurement of two angle components of light scattering from biological cells or particles comprising:

a microscope condenser having a high numerical aperture containing a central field stop means for producing a conical dark field in an illumination field of said condenser;

a microscope objective having an aperture disposed within said dark field and having an object plane in common with an object plane of the condenser, the dark field having an axis of symmetry in common with the optical axis of the objective and the condenser, and the dark field extending at an angle of at least 15°

around said axis of symmetry, the entrance aperture of said objective as seen from the object plane of this objective extending over an angle which is 1°

-2°

smaller than the angle extended by the dark field and is thus situated entirely within said dark field;

telescope means for reproducing the dark field behind an image plane of the microscope objective;

mirror means for reflecting a central portion of said reproduced dark field;

a first light detector for receiving light reflected by said mirror means; and

a second light detector for receiving light in the peripheral portion of said dark field,

whereby, scattered light at small scattering angles produced by defraction from the cell or particle surface are separated from light scattered at larger angles from structures other than the cell surface.

2. A device according to claim 1, wherein the condenser focuses light from an intense light source toward its object plane through which biological cells or particles carried by a microscopical, laminar flow of fluid are passing.

3. A device according to claim 1, wherein an adjustable slit is disposed in the image plane of said objective, said slit being set so as to cover that part of the image produced by the objective which contains the image of the particle flow where said flow passes through the common optical axis of the objective and condenser, said slit eliminating light from those parts of the object plane which do not contain particle flow.

4. A device according to claim 1, wherein a telescope is situated behind the slit and produces an image of the aperture (pupil) of the objective at infinity behind the telescope from which extends a light beam where the angle distribution of the light intensity corresponds exactly to that which can be observed within the dark field.