WO1993007471A1 - Detecting a radiation signal - Google Patents

Detecting a radiation signal Download PDF

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Publication number
WO1993007471A1
WO1993007471A1 PCT/US1992/008274 US9208274W WO9307471A1 WO 1993007471 A1 WO1993007471 A1 WO 1993007471A1 US 9208274 W US9208274 W US 9208274W WO 9307471 A1 WO9307471 A1 WO 9307471A1
Authority
WO
WIPO (PCT)
Prior art keywords
signal
radiation
detector
sample
focal point
Prior art date
Application number
PCT/US1992/008274
Other languages
French (fr)
Inventor
Wilbur I. Kaye
Original Assignee
Beckman Instruments, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US07/938,818 external-priority patent/US5292483A/en
Application filed by Beckman Instruments, Inc. filed Critical Beckman Instruments, Inc.
Publication of WO1993007471A1 publication Critical patent/WO1993007471A1/en

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J3/00Spectrometry; Spectrophotometry; Monochromators; Measuring colours
    • G01J3/02Details
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J1/00Photometry, e.g. photographic exposure meter
    • G01J1/02Details
    • G01J1/04Optical or mechanical part supplementary adjustable parts
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J1/00Photometry, e.g. photographic exposure meter
    • G01J1/02Details
    • G01J1/04Optical or mechanical part supplementary adjustable parts
    • G01J1/0407Optical elements not provided otherwise, e.g. manifolds, windows, holograms, gratings
    • G01J1/0422Optical elements not provided otherwise, e.g. manifolds, windows, holograms, gratings using light concentrators, collectors or condensers
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J3/00Spectrometry; Spectrophotometry; Monochromators; Measuring colours
    • G01J3/02Details
    • G01J3/0205Optical elements not provided otherwise, e.g. optical manifolds, diffusers, windows
    • G01J3/0216Optical elements not provided otherwise, e.g. optical manifolds, diffusers, windows using light concentrators or collectors or condensers
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/447Systems using electrophoresis
    • G01N27/44704Details; Accessories
    • G01N27/44717Arrangements for investigating the separated zones, e.g. localising zones
    • G01N27/44721Arrangements for investigating the separated zones, e.g. localising zones by optical means
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N2021/1738Optionally different kinds of measurements; Method being valid for different kinds of measurement
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/47Scattering, i.e. diffuse reflection
    • G01N2021/4702Global scatter; Total scatter, excluding reflections
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/65Raman scattering
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/76Chemiluminescence; Bioluminescence
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/84Systems specially adapted for particular applications
    • G01N21/85Investigating moving fluids or granular solids

Definitions

  • This invention relates to the efficient collection and detection of low levels of radiation arising within microliter volumes of sample.
  • the radiation may be in the form of luminescence from a chemical reaction or result from the interaction of an intense light source and the sample.
  • the processes of light scattering, Raman scattering, fluorescence and- phosphorescence may be used.
  • the technique of light scattering is particularly useful in the detection of particle ⁇ , and two broad cla ⁇ sifications of in ⁇ truments can be identified.
  • Particles of diameters significantly smaller than the wavelength of probe light scatter isotropically, i.e. equally in all directions. This type of scattering is usually called Rayleigh scattering.
  • This type of scattering is usually called Mie scattering.
  • the intensity of forward scattered light varies as the sixth power of the particle diameter; hence, special precautions must be taken when attempting to measure the light scattered from very small particles.
  • the present invention permits for the determi ⁇ nation of relative particle size and/or concentration of very small particles, particularly in a flowing system.
  • Intense light sources such as lasers are used for studying small particles.
  • the use of such sources introduces problems associated with discrimination of light scattered by instrumental components from that scattered by the sample.
  • the intensity of light scattered from small particles may be less than one millionth the intensity of laser radiation.
  • To measure such low intensities it is necessary to collect as much of the light scattered by the sample as possible, yet reject that scattered by the instrument.
  • Raman scattering is used for the chemical characterization of the samples rather than particle size. Like Rayleigh scattering, the signal intensities are very low and it is important to capture as large a solid angle of Raman scattered light as possible while also u ⁇ ing very intense sources of incident radiation.
  • the Raman scattered signals are of different wavelength from the incident light.
  • Chemical characterization of the sample is determined by the difference between the frequency of the Raman signal and the frequency of the exciting radiation. It is customary to use a blocking filter to reject the incident radiation followed by a monochromator to determine the frequency of the Raman signal. While this frequency difference helps in the discrimination between exciting and Raman signals, the Raman bands are often narrow; hence, the signals are very weak. It is important to use whatever geometric means are available to minimize the detection of the incident radiation and maximize the detection of the weak Raman radiation from the sample.
  • Fluorescence techniques are used when the sample or some component(s) of the sample can be tagged with a fluorescing dye.
  • the sample is then excited by an intense beam of exciting radiation, usually from a laser.
  • the wavelength of the exciting radiation is chosen to correspond to the wavelength of maximum sample excitation.
  • the wavelength of the fluorescing radiation will usually be greater than the exciting wavelength, and a filter or monochromator will be chosen to pass only that radiation corresponding to the wavelength of maximum fluorescence emission.
  • a filter or monochromator will be chosen to pass only that radiation corresponding to the wavelength of maximum fluorescence emission.
  • Phosphorescence techniques are employed where the sample, itself, or the tagged sample continues to emit radiation a significant time after excitation. Time as well as wavelength can then be used to discriminate between exciting and emitting radiation.
  • Luminescence techniques are u ⁇ ed when the sample or some component of the sample emits radiation as a re ⁇ ult of a chemical reaction of the sample with a reagent. No external exciting radiation is needed; hence, all of the radiated light may be detected without recourse to filtering.
  • the luminescence signals are usually very weak and depend on the number of reacting molecules within the detected sample volume. A compromise must usually be made between detected sample volume and concentration of reacting molecules. The efficient collection and detection of the radiation emitted within the detected sample volume is of great importance.
  • a generated radiation signal from an excited sample is collected over a large solid angle by means of a reflecting curvilinear surface of revolution and is directed to a detector.
  • the angle should preferably be between about 35° and 145°.
  • the sample enters a detection volume in a flowing stream and the axis of sample flow is collinear with the axis of revolution of the reflecting curvilinear surface of revolution.
  • the scattering volume which is part of the detection volume, is retained relatively small.
  • the radiation signal after the above interaction has the same wavelength as the radiation signal incident on the sample.
  • This type of interaction is called "light scattering."
  • the incident radiation is of high intensity and is usually produced by a laser. There are means for directing this laser beam along an axis of the curvilinear reflection means.
  • sample flow past the point of interaction.
  • the axis of sample flow is coaxial with the axis of a reflective light collector.
  • the scattered light ray output is the generated signal at the focus of the reflecting means.
  • the output reflection signal from the reflective means can be a collimated beam which is directed to a detector directly.
  • the reflecting curvilinear surface of revolution producing a collimated beam is selectively a paraboloid.
  • the collimated beam may also be focused onto a detector by a focusing lens.
  • the curvilinear means can reflect the generated signal directly to a remote focal point.
  • the curvilinear means for doing this is preferably an ellipsoid.
  • the generated radiation signal may arise selectively from light scattering, Raman scattering, fluore ⁇ cence, phosphorescence or luminescence.
  • Figure 1 shows the invention used to monitor some property of a sample as it changes in time as a result of pas ⁇ age through a ⁇ eparation means.
  • the sample may be mixed with a reagent, and the geometric axes in the vicinity of the point of radiation generation are illustrated.
  • Figures 2A and 2B are respectively a side diagrammatic view and end diagrammatic view of the sy ⁇ tem for detection of scattered light.
  • Figure 3 shows the details of the containment ves ⁇ el in ⁇ ert fitting into the curvilinear reflecting surface.
  • Figure 4 shows an alternate design of the insert in a configuration optimized for the detection of sample luminescence.
  • Figure 5 is a diagrammatic view of an embodiment wherein an annular aperture determines the detected scattering angle of a scattering signal.
  • Figure 6 is a diagrammatic view of a monochromator suitable for addition to any of the above light collection systems.
  • a Fery prism is used to disperse the radiation onto one or more detectors.
  • An aperture plate in the focal surface and in front of the detector( ⁇ ) determines the portion of the spectrum detected.
  • an array detector may be located at the focal surface of the prism and the spectrum measured.
  • Figure 7 is an embodiment illustrating an ellipsoidal version of the reflective surface, and is similar to Figures 2A and 2B.
  • Figure 1 identifies the major components of the system.
  • a sample processed by some type of separation system such as a chromatograph column, mixes with a reagent from a delivery ⁇ y ⁇ tem 2 at point 3. The mixture enter ⁇ a ⁇ ample containment ve ⁇ sel 4.
  • An intense light source 5 such as a laser produces a beam 102 which is filtered by a filter 6 and focu ⁇ ed by a len ⁇ 7 onto a point of radiation generation 8.
  • Thi ⁇ generation point 8 corresponds to a focal point of a curvilinear surface of revolution 9 milled into a block 10.
  • the curvilinear surface 9 is a paraboloid.
  • the surface 9 of this paraboloid is reflecting and collimates the radiation generated at the point 8. From the point 8, there is generated a beam 111 of incident radiation which is directed through a large solid angle to reflective surface 9.
  • the collimated beam 100 of reflected radiation is filtered by a filter 11 and focused by a lens 12 onto an aperture 13 in a plate 14. Radiation passing through the aperture 13 is detected by a detector 15.
  • An imaginary straight line 101 from the intense light source 5 to the aperture 13 defines the axis of the curvilinear surface 9 and also the axis of sample flow in the vicinity of the point of generation 8. Where pertinent, this imaginary line 101 defines the axis of the exciting light beam 102 in the vicinity of the point 8 of radiation generation.
  • Figure 2A shows an embodiment of the invention specifically for the detection of scattered light.
  • the light beam 102 from a laser 5 is focused by the lens 7 and directed by means of a two-axis adjusting device 16 down the axis of a channel 17 in the sample containment vessel 4 which screws into the block 10 of the para- boloid.
  • the sample from point 3 enters the containment vessel 4 at 18 and exits at 19.
  • the laser beam 102 must not strike the walls of the channel 17 in the sample containment vessel 4. Alignment is accomplished by viewing the generation point 8 by means of viewing lens 20 and a hole 21 in block 10 into which the curvilinear surface 9 is formed.
  • the lens 12 and the aperture in plate 14 serve as a spatial filter and allow only the radiation generated at 8 from passing to the detector 15. In some applications, this spatial filter is unnecessary, but the photosensitive area of the detector 15 must then be as large as the mouth of the paraboloid.
  • Figure 2B is an end view of the apparatus looking down the axis 101 of the curvilinear surface 9. Looking into the open end of the paraboloid, one "sees" the end of the end cap 27 of the containment vessel. The inner edge 103 and outer edge 104 of the paraboloid mouth as well as the outer edge of the lens 12 are visible.
  • Figure 3 shows the details of the sample containment vessel 4 and the end cap 27.
  • the .parts are made of a material such as black "Delrin.”
  • the containment vessel 4 is threaded at 105 to fit into the paraboloid block 10 which has mating threads and position the generation point 8 at the focal point of the paraboloid surface 9.
  • the sample enters at 18 through a stainless steel tube 22 tightly inserted in a hole 23 drilled into the black plastic.
  • a second hole 24, at 90° to the first hole 23, is drilled into the black plastic and conveys the sample mixture to channel 107 running down the axis of the containment ves ⁇ el.
  • the second hole 24 is closed by plug 25 to keep the sample mixture from escaping from the de ⁇ ired channel 24.
  • a glas ⁇ tube 26 fit ⁇ tightly into bore 107 in the sample containment vessel 4 and extends into the second black pla ⁇ tic end cap 27.
  • a gla ⁇ s plate 28 ⁇ erves as a window to allow laser radiation 102 to pass into the containment vessel while keeping the sample in its channel 24.
  • the glass plate 28 is held against an "O ring" 29 by means of retainer 30.
  • the glas ⁇ tube 26 does not come in optical contact with the glass plate 28. Thereby, the light scattered at the surface of the glass plate 28 does not channel into the glass tube 26. Were a significant fraction of the light scattered by glass plate 28 to enter tube 25, some unwanted radiation could escape from tube 26 in the vicinity of the generation point 8.
  • the end cap 27 allows the sample to exit the sy ⁇ tem through hole 108 and al ⁇ o act ⁇ a ⁇ a light trap for * the exce ⁇ incident radiation from la ⁇ er beam 102.
  • the black glas ⁇ plate fits against the wall of the black plastic by means of a threaded plug 32.
  • Another "O-ring” 33 seals against escape of the sample stream.
  • a 10 second plug 25 again confines the sample to the desired stream.
  • a short piece of stainless steel tubing 34 fitted into a hole 110 conveys the sample stream to a
  • Teflon tubing 35 which mates with still another piece 36 of stainless steel tubing by which the sample stream exits the containment vessel at 19.
  • the plastic tubing 35 blocks only a negligible portion of the scattered rays from falling on the paraboloid.
  • the end cap 27 is dimensioned to slip through the hole in the paraboloid block 10 at its ba ⁇ e.
  • the solid angle 112 of incident radiation is 25 between about 45° and 135° relative to the axis 101.
  • the end face 113 of the vessel 4 defines one limit of the angle 112.
  • the end face 114 of the end cap 27 can define a second limit of the angle 112.
  • the limit 103 of the parabaloid surface 9 30 can limit the extent of the angle, as illustrated in Figure ⁇ l and 2.
  • Figure 4 how ⁇ another embodiment of the containment vessel 4 and its end cap 27.
  • 35 the sample mixture is introduced to the generation point by means of a capillary tubing 41.
  • a chemiluminescence reagent is introduced through entry 18.
  • This embodiment is primarily intended for use with chemiluminescent samples. Exciting light source is not necessary in this application. It is presumed that the luminescence resulting from the chemical reaction is of short lifetime, hence, has a maximum intensity at the point of reaction which in this case occurs at the generation point.
  • Plate 43 with an annular aperture 42 is inserted into the apparatus where the beam from the sample is collimated.
  • the inner and outer diameters of this annular aperture determine the solid angle 112 of detected scattered light.
  • Figure 6 is an extension of Figure 2A and shows the focused radiation 106 passing through the aperture 13 in plate 14 and on to a Fery prism 44 which disperse ⁇ the radiation 116 and focu ⁇ e ⁇ a ⁇ pectrum on a curved plate 45.
  • the location and size of the aperture 47 in plate 45 determine ⁇ the wavelength and wavelength interval of radiation detected by detector 46.
  • a multiplicity of apertures and detectors may be used when it is desired to monitor different spectral intervals simultaneously.
  • means other than a Fery prism may be used to disperse radiation 106.
  • an array detector may be positioned in place of the aperture plate.
  • the signal from the array of detectors 46 may be processed in the usual manner to provide the dynamic changing spectra as samples flow through the system. It should be apparent that any type of dispersing system may be employed in Figure 6. However, the Fery prism 44 affords a high efficiency along with low stray light.
  • surface 9 of block 10 may be in the shape of an ellipsoid. As shown in Figure 7, the beam 106 is then focused directly onto aperture plate 14 and lens 12 is not needed.
  • the apparatus in its light scattering configuration is useful in the study of antigen-antibody reactions.
  • the antigen specific to an antibody mixes with a solution containing the antibody, there is a reaction producing aggregates of rapidly increasing size. If the concentration of antibody and antigens is sufficiently high, the aggregates may become large enough to see with the naked eye. However, at low concentration, the limiting aggregate size may be submicroscopic and detectable only by very sensitive light scattering techniques.
  • the above invention is applicable to the screening of antibody-antigen reactions wherein a separation technique isolates fractions of either antibodies or antigens. A ⁇ the components elute from the separations means 1 and mix with a potential conjugate steadily flowing from 2, the sample generates an elevated scattered light signal, indicative of an aggregating pair.
  • the detector means 15 can be set up to respond to a spatial or temporal signal from the generating point 8.
  • Raman spectra often characterize particular classes of molecular structure.
  • a detector can sense when sample fractions having that particular class of structure elute from a chromatograph column 11.
  • Fluorescence and phosphorescence techniques provide for extremely sensitive detection of classes of samples eluting from a separation system when certain classes of effluent can be tagged with a fluorescent dye or set of dyes. For example, DNA fragments of different size may be chromatographed to separate fragments by molecular weight. At the same time, there are only four possible end groups and these can be dyed with fluorophores specific to the end groups. The above apparatus can identify the end group of the eluting fractions.
  • Certain oxidation-reduction reactions can be sensitively detected by chemiluminescence.
  • the above apparatus can provide a good detector when an eluting sample triggers a chemiluminescence reaction.

Abstract

Focusing a generated radiation signal on a detector is effected by a curvilinear surface. The radiation beam signal from the reflected surface is collimated or focused on the detector. Light scattered, Raman scattered, fluorescence, chemiluminescence, phosphorescence radiation signals from particles as a result of a chemical procedure or reaction is enhanced through this focusing technique. The enhanced signal which is detected is subsequently measured through different detection techniques.

Description

DETECTING A RADIATION SIGNAL
RELATED APPLICATION
This application is a continuation-in-part of Serial No. 07/772,823 filed October 8, 1991 and entitled "Enhanced Fluorescence Detection of Samples in Capillary Column." The contents thereof are incorporated by reference.
BACKGROUND
This invention relates to the efficient collection and detection of low levels of radiation arising within microliter volumes of sample.
The radiation may be in the form of luminescence from a chemical reaction or result from the interaction of an intense light source and the sample. Alternatively, the processes of light scattering, Raman scattering, fluorescence and- phosphorescence may be used.
The technique of light scattering is particularly useful in the detection of particleε, and two broad claεsifications of inεtruments can be identified. Particles of diameters significantly smaller than the wavelength of probe light scatter isotropically, i.e. equally in all directions. This type of scattering is usually called Rayleigh scattering. Particles of diameters significantly larger than the wavelength of probe light scatter primarily in the forward direction and, often, the intensity of scatter is a complicated function of scattering angle. This type of scattering is usually called Mie scattering. The intensity of forward scattered light varies as the sixth power of the particle diameter; hence, special precautions must be taken when attempting to measure the light scattered from very small particles.
The present invention permits for the determi¬ nation of relative particle size and/or concentration of very small particles, particularly in a flowing system.
Intense light sources such as lasers are used for studying small particles. The use of such sources introduces problems associated with discrimination of light scattered by instrumental components from that scattered by the sample. The intensity of light scattered from small particles may be less than one millionth the intensity of laser radiation. To measure such low intensities, it is necessary to collect as much of the light scattered by the sample as possible, yet reject that scattered by the instrument. In general, it becomes increasingly difficult to eliminate instrumental light scattering as the angle of detected scattering decreaseε. Consequently, when measuring the light scattered by particles significantly smaller than the wavelength of probe light, it is best to avoid detection of the small angle scattering, while collecting as large a solid angle of scattered light as possible.
When measuring the light scattered by small particles, considerable attention must be paid to the overwhelming level of light scattered from unwanted foreign particles of large size. For this reason, it is advantageous to keep the size of the scattering volume (volume of sample simultaneously illuminated and detected) as small as possible. In a flowing sample, these particles will be evidenced as signal "spikes" abruptly rising from a base signal. The base signal represents the signal from the more numerous small particles.
Large angle scattered light instruments described in the prior art have used large scattering volumes and require extensive sample treatment to minimize the detection of large foreign particles. Furthermore, sample volume has to be large to avoid detection of light scattered from the instrument. These prior art instruments have usually used lenses and apertures to define the scattering angle and, of necessity, capture a εmall εolid angle of scattered light.
Moreover, most of the prior art has addressed the detection of relative large biological cells (cytometry) . The signalε from these large particles are much greater than those provided by the small particles of particular interest in the present invention.
Raman scattering is used for the chemical characterization of the samples rather than particle size. Like Rayleigh scattering, the signal intensities are very low and it is important to capture as large a solid angle of Raman scattered light as possible while also uεing very intense sources of incident radiation. The Raman scattered signals are of different wavelength from the incident light. Chemical characterization of the sample is determined by the difference between the frequency of the Raman signal and the frequency of the exciting radiation. It is customary to use a blocking filter to reject the incident radiation followed by a monochromator to determine the frequency of the Raman signal. While this frequency difference helps in the discrimination between exciting and Raman signals, the Raman bands are often narrow; hence, the signals are very weak. It is important to use whatever geometric means are available to minimize the detection of the incident radiation and maximize the detection of the weak Raman radiation from the sample.
Fluorescence techniques are used when the sample or some component(s) of the sample can be tagged with a fluorescing dye. The sample is then excited by an intense beam of exciting radiation, usually from a laser. The wavelength of the exciting radiation is chosen to correspond to the wavelength of maximum sample excitation. The wavelength of the fluorescing radiation will usually be greater than the exciting wavelength, and a filter or monochromator will be chosen to pass only that radiation corresponding to the wavelength of maximum fluorescence emission. When the sample concentration is low, great care is needed in the choice of filters or monochroma ors in order to discriminate between exciting and fluorescing wavelengths. No filters provide a perfect discrimination, and it is desirable to use whatever geometric means are available to minimize the detection of exciting rays scattering from the instrument. Under ideal conditions, tagged molecules can be detected at extremely low concentration.
Phosphorescence techniques are employed where the sample, itself, or the tagged sample continues to emit radiation a significant time after excitation. Time as well as wavelength can then be used to discriminate between exciting and emitting radiation. Luminescence techniques are uεed when the sample or some component of the sample emits radiation as a reεult of a chemical reaction of the sample with a reagent. No external exciting radiation is needed; hence, all of the radiated light may be detected without recourse to filtering. However, the luminescence signals are usually very weak and depend on the number of reacting molecules within the detected sample volume. A compromise must usually be made between detected sample volume and concentration of reacting molecules. The efficient collection and detection of the radiation emitted within the detected sample volume is of great importance.
There is a need to provide a system for radiation collection and detection which provides significant advances over the prior art.
SUMMARY
By this invention, there is provided a system for detecting a radiation signal in a manner which minimizes disadvantages of the prior art.
According to the invention, a generated radiation signal from an excited sample is collected over a large solid angle by means of a reflecting curvilinear surface of revolution and is directed to a detector. The angle should preferably be between about 35° and 145°.
The sample enters a detection volume in a flowing stream and the axis of sample flow is collinear with the axis of revolution of the reflecting curvilinear surface of revolution. The scattering volume, which is part of the detection volume, is retained relatively small.
In one preferred form, the radiation signal after the above interaction has the same wavelength as the radiation signal incident on the sample. This type of interaction is called "light scattering." The incident radiation is of high intensity and is usually produced by a laser. There are means for directing this laser beam along an axis of the curvilinear reflection means.
In particular, small volumes of sample flow past the point of interaction. The axis of sample flow is coaxial with the axis of a reflective light collector. There are also means for directing a sample flow in a tube along an axis collinear with the laser beam in such a way that the beam impacts the sample without impacting the sample tube wall. In this manner, the three axes are collinear.
The scattered light ray output is the generated signal at the focus of the reflecting means.
The output reflection signal from the reflective means can be a collimated beam which is directed to a detector directly. The reflecting curvilinear surface of revolution producing a collimated beam is selectively a paraboloid. The collimated beam may also be focused onto a detector by a focusing lens. Alternatively, the curvilinear means can reflect the generated signal directly to a remote focal point. The curvilinear means for doing this is preferably an ellipsoid. In different forms of the invention, the generated radiation signal may arise selectively from light scattering, Raman scattering, fluoreεcence, phosphorescence or luminescence.
The invention is further described with reference to the accompanying drawings.
DRAWINGS
Figure 1 shows the invention used to monitor some property of a sample as it changes in time as a result of pasεage through a εeparation means. The sample may be mixed with a reagent, and the geometric axes in the vicinity of the point of radiation generation are illustrated.
Figures 2A and 2B are respectively a side diagrammatic view and end diagrammatic view of the syεtem for detection of scattered light.
Figure 3 shows the details of the containment vesεel inεert fitting into the curvilinear reflecting surface.
Figure 4 shows an alternate design of the insert in a configuration optimized for the detection of sample luminescence.
Figure 5 is a diagrammatic view of an embodiment wherein an annular aperture determines the detected scattering angle of a scattering signal.
Figure 6 is a diagrammatic view of a monochromator suitable for addition to any of the above light collection systems. A Fery prism is used to disperse the radiation onto one or more detectors. An aperture plate in the focal surface and in front of the detector(ε) determines the portion of the spectrum detected. Alternatively, an array detector may be located at the focal surface of the prism and the spectrum measured.
Figure 7 is an embodiment illustrating an ellipsoidal version of the reflective surface, and is similar to Figures 2A and 2B.
DESCRIPTION
Figure 1 identifies the major components of the system. A sample processed by some type of separation system 1, such as a chromatograph column, mixes with a reagent from a delivery εyεtem 2 at point 3. The mixture enterε a εample containment veεsel 4. An intense light source 5 such as a laser produces a beam 102 which is filtered by a filter 6 and focuεed by a lenε 7 onto a point of radiation generation 8. Thiε generation point 8 corresponds to a focal point of a curvilinear surface of revolution 9 milled into a block 10.
In this illustration, the curvilinear surface 9 is a paraboloid. The surface 9 of this paraboloid is reflecting and collimates the radiation generated at the point 8. From the point 8, there is generated a beam 111 of incident radiation which is directed through a large solid angle to reflective surface 9. The collimated beam 100 of reflected radiation is filtered by a filter 11 and focused by a lens 12 onto an aperture 13 in a plate 14. Radiation passing through the aperture 13 is detected by a detector 15. An imaginary straight line 101 from the intense light source 5 to the aperture 13 defines the axis of the curvilinear surface 9 and also the axis of sample flow in the vicinity of the point of generation 8. Where pertinent, this imaginary line 101 defines the axis of the exciting light beam 102 in the vicinity of the point 8 of radiation generation.
Figure 2A shows an embodiment of the invention specifically for the detection of scattered light. The light beam 102 from a laser 5 is focused by the lens 7 and directed by means of a two-axis adjusting device 16 down the axis of a channel 17 in the sample containment vessel 4 which screws into the block 10 of the para- boloid. The sample from point 3 enters the containment vessel 4 at 18 and exits at 19.
The laser beam 102 must not strike the walls of the channel 17 in the sample containment vessel 4. Alignment is accomplished by viewing the generation point 8 by means of viewing lens 20 and a hole 21 in block 10 into which the curvilinear surface 9 is formed.
The lens 12 and the aperture in plate 14 serve as a spatial filter and allow only the radiation generated at 8 from passing to the detector 15. In some applications, this spatial filter is unnecessary, but the photosensitive area of the detector 15 must then be as large as the mouth of the paraboloid.
Figure 2B is an end view of the apparatus looking down the axis 101 of the curvilinear surface 9. Looking into the open end of the paraboloid, one "sees" the end of the end cap 27 of the containment vessel. The inner edge 103 and outer edge 104 of the paraboloid mouth as well as the outer edge of the lens 12 are visible.
Figure 3 shows the details of the sample containment vessel 4 and the end cap 27. The .parts are made of a material such as black "Delrin." The containment vessel 4 is threaded at 105 to fit into the paraboloid block 10 which has mating threads and position the generation point 8 at the focal point of the paraboloid surface 9.
The sample enters at 18 through a stainless steel tube 22 tightly inserted in a hole 23 drilled into the black plastic. At a point below the stainless steel tube 22, a second hole 24, at 90° to the first hole 23, is drilled into the black plastic and conveys the sample mixture to channel 107 running down the axis of the containment vesεel. The second hole 24 is closed by plug 25 to keep the sample mixture from escaping from the deεired channel 24. A glasε tube 26 fitε tightly into bore 107 in the sample containment vessel 4 and extends into the second black plaεtic end cap 27.
A glaεs plate 28 εerves as a window to allow laser radiation 102 to pass into the containment vessel while keeping the sample in its channel 24. The glass plate 28 is held against an "O ring" 29 by means of retainer 30. The glasε tube 26 does not come in optical contact with the glass plate 28. Thereby, the light scattered at the surface of the glass plate 28 does not channel into the glass tube 26. Were a significant fraction of the light scattered by glass plate 28 to enter tube 25, some unwanted radiation could escape from tube 26 in the vicinity of the generation point 8. The end cap 27 allows the sample to exit the syεtem through hole 108 and alεo actε aε a light trap for * the exceεε incident radiation from laεer beam 102. A plate 31 of poliεhed black glaεε actε aε the primary 5 light trap. This plate 31 is angled to send the weak reflected beam to the end wall 109 at the end of hole 108. The black glasε plate fits against the wall of the black plastic by means of a threaded plug 32. Another "O-ring" 33 seals against escape of the sample stream. A 10 second plug 25 again confines the sample to the desired stream.
A short piece of stainless steel tubing 34 fitted into a hole 110 conveys the sample stream to a
15 piece of Teflon tubing 35 which mates with still another piece 36 of stainless steel tubing by which the sample stream exits the containment vessel at 19. The plastic tubing 35 blocks only a negligible portion of the scattered rays from falling on the paraboloid.
20
The end cap 27 is dimensioned to slip through the hole in the paraboloid block 10 at its baεe.
The solid angle 112 of incident radiation is 25 between about 45° and 135° relative to the axis 101. The end face 113 of the vessel 4 defines one limit of the angle 112. The end face 114 of the end cap 27 can define a second limit of the angle 112. Alternatively to the end face 114, the limit 103 of the parabaloid surface 9 30 can limit the extent of the angle, as illustrated in Figureε l and 2.
» Figure 4 εhowε another embodiment of the containment vessel 4 and its end cap 27. In this case, 35 the sample mixture is introduced to the generation point by means of a capillary tubing 41. A chemiluminescence reagent is introduced through entry 18. This embodiment is primarily intended for use with chemiluminescent samples. Exciting light source is not necessary in this application. It is presumed that the luminescence resulting from the chemical reaction is of short lifetime, hence, has a maximum intensity at the point of reaction which in this case occurs at the generation point.
Figure 5 iε similar to Figure 2A and is useful in certain types of light scattering measurements. Plate 43 with an annular aperture 42 is inserted into the apparatus where the beam from the sample is collimated. The inner and outer diameters of this annular aperture determine the solid angle 112 of detected scattered light.
Figure 6 is an extension of Figure 2A and shows the focused radiation 106 passing through the aperture 13 in plate 14 and on to a Fery prism 44 which disperseε the radiation 116 and focuεeε a εpectrum on a curved plate 45. The location and size of the aperture 47 in plate 45 determineε the wavelength and wavelength interval of radiation detected by detector 46. A multiplicity of apertures and detectors may be used when it is desired to monitor different spectral intervals simultaneously. Similarly, means other than a Fery prism may be used to disperse radiation 106.
Alternately, an array detector may be positioned in place of the aperture plate. The signal from the array of detectors 46 may be processed in the usual manner to provide the dynamic changing spectra as samples flow through the system. It should be apparent that any type of dispersing system may be employed in Figure 6. However, the Fery prism 44 affords a high efficiency along with low stray light.
When there is no need to filter the light from the sample (by means of filter 11 shown in Figure 1) , surface 9 of block 10 may be in the shape of an ellipsoid. As shown in Figure 7, the beam 106 is then focused directly onto aperture plate 14 and lens 12 is not needed.
Applications
Description of a few applications for the above equipment may help to understand the invention.
The apparatus in its light scattering configuration is useful in the study of antigen-antibody reactions. When the antigen specific to an antibody mixes with a solution containing the antibody, there is a reaction producing aggregates of rapidly increasing size. If the concentration of antibody and antigens is sufficiently high, the aggregates may become large enough to see with the naked eye. However, at low concentration, the limiting aggregate size may be submicroscopic and detectable only by very sensitive light scattering techniques.
The above invention is applicable to the screening of antibody-antigen reactions wherein a separation technique isolates fractions of either antibodies or antigens. Aε the components elute from the separations means 1 and mix with a potential conjugate steadily flowing from 2, the sample generates an elevated scattered light signal, indicative of an aggregating pair. The detector means 15 can be set up to respond to a spatial or temporal signal from the generating point 8.
Raman spectra often characterize particular classes of molecular structure. A detector can sense when sample fractions having that particular class of structure elute from a chromatograph column 11.
Fluorescence and phosphorescence techniques provide for extremely sensitive detection of classes of samples eluting from a separation system when certain classes of effluent can be tagged with a fluorescent dye or set of dyes. For example, DNA fragments of different size may be chromatographed to separate fragments by molecular weight. At the same time, there are only four possible end groups and these can be dyed with fluorophores specific to the end groups. The above apparatus can identify the end group of the eluting fractions.
Certain oxidation-reduction reactions can be sensitively detected by chemiluminescence. The above apparatus can provide a good detector when an eluting sample triggers a chemiluminescence reaction.
Many more examples of the invention exist, each differing from the other in matters of detail only. The invention is to be determined solely by the appended claims.

Claims

1. Apparatus for directing a radiation signal to a detector comprising means for generating an incident radiation signal caused by the interaction of a flowing sample with an exciting radiation source, a reflecting surface of revolution having an axis and having a focal point, the reflecting means being means for receiving the generated incident radiation signal and for reflecting the incident signal as an output reflection signal, and means for generating the incident signal at substantially the focal point of the reflection means, the reflection signal output is directed to the detector, and wherein at least one of the directions of the flowing sample or the direction of the exciting radiation is substantially collinear with the axes of the reflecting surface at least at the focal point.
2. Apparatus as claimed in claim 1 wherein the reflection means outputs a reflected collimated signal.
3. Apparatus as claimed in claim 1 wherein the reflection means outputs a reflected signal converging at a remote focus location.
4. Apparatus as claimed in claim 1 wherein the reflection means includeε a parabolic surface.
5. Apparatus as claimed in claim 1 wherein the reflection means includes an ellipsoidal surface.
6. Apparatus as claimed in claim 1 including lens means between a reflection means and the detector.
7. Apparatus as claimed in claim 1 including filter means between the reflection means and the detector.
8. Apparatuε as claimed in claim 1 including grating monochromator means between the reflection means and the detector.
9. Apparatuε aε claimed in claim 1 including an annular aperture between the reflection eanε and the detector, the annular aperture being located in a plate spaced from the reflection means and wherein the center of the annular aperture is located on an axis of the reflection means.
10. Apparatus as claimed in claim 9 wherein the annular aperture has a selected diameter, the selected diameter being determined in accordance with a selected incident radiation signal and a reflected signal from the reflection means.
11. Apparatus as claimed in claim 1 including means at the focal point for generating the incident light permitting for a solid angle of incident light in the range between about 45° and about 135° relative to the axis of revolution.
12. Apparatus as claimed in claim 1 wherein the generated incident radiation signal is selectively at least one of a light scattered signal, Raman scattering fluorescence, phosphorescence, or luminescence signal, the incident radiation signal being generated by the impact of a laser radiation source directed on particles in the sample at the focal point.
13. Apparatus as claimed in claim 1 wherein the signal is selectively at least one of a light scattering signal, Raman scattering, fluorescence or phosphorescence and wherein the light beam laser radiation directed axially relative to the reflecting means and towards the focal point of the reflecting means, and wherein the sample flows axially substantially parallel with the laser radiation, and the axis of revolution.
14. Apparatus aε claimed in claim 1 including an elongated tube for the sample flow substantially along the axis of revolution, and wherein the tube includes a side wall, wherein the light beam is laεer radiation, and including focus means for the laser radiation such that the radiation essentially travels wholly within the tube and is free of contacting the tube side wall, and the focus means directs the radiation into contact with the sample at substantially the focal point.
15. Apparatus for directing a light scattered signal to a detector comprising a reflecting surface of revolution for receiving an incident light scattered signal, a focal point for the reflecting surface, a detector spaced from the reflecting surface, the reflecting means being for reflecting the light scattered signal to the detector, means for generating a laser radiation beam along an axis of the reflecting surface, means for directing a sample coaxially with the reflecting surface, such that the laser radiation beam and the sample impact at least at the focal point, means for directing the light scattered signal from the focus of the reflecting surface εuch that the incident light scattered signal is directed from the reflecting surface towards the detector.
16. Apparatus as claimed in claim 15 including a tube axially directed relative to the reflecting surface, the tube being directed to receive the laser radiation beam axially and to permit flow of the sample axially through the tube, and means optically occluding the tube selectively around its perimeter and permitting the incident point light scattered signal to exit from the tube at the focal point.
17. Apparatus as claimed in claim 16 including a cap on a downstream end of the tube optically occluding a light scattered signal, and a window on an upstream side of the tube, the window being optically isolated from the tube.
18. Apparatus for directing a radiation signal to a detector comprising a reflecting surface of revolution having an axiε and a focal point for receiving a radiation εignal, a detector spaced from the reflecting surface, the reflecting surface being for reflecting the radiation signal to the detector, means for generating an excitation signal beam, means for directing the excitation beam to impact along the axis of radiation at the focal point for generating the incident radiation signal substantially at the focus of the reflecting surface such that the radiation signal is directed from the focal point over a solid angle in the range of about 45° to 135° relative to the axis of revolution.
19. Apparatus as claimed in claim 18 wherein an excitation beam source is located adjacent the reflecting means, and including filter means downstream the reflecting means, the reflecting means generating a reflected signal from the incident signal generated at the focal point, the filtration means being for removing an excitation εignal and for permitting pasεage of the reflected signal.
20. Apparatus as claimed in claim 19 including lens meanε downstream the filter means, the lens means focusing a reflected fluorescence signal on the detector.
21. Apparatus as claimed in claim 20 including a monochromator located between the reflecting surface and the detector, and including a diffraction mirror between the monochromator and the detector, the diffraction mirror focusing the reflected signal on the detector.
22. Apparatus for directing a radiation signal to a detector comprising a substantially curvilinear reflecting surface having a focal point and an axis of revolution, a detector, the reflecting surface reflecting an output signal to the detector, means for generating an incident radiation signal by the interaction of a sample directed along the axis of revolution with an excitation εignal at the focal point, means for directing the generated signal to the reflecting εurface and the detector and including meanε for reεponding selectively to a spatial or temporal sorted signal, selectively, a Raman scatter signal.
23. Apparatuε for directing a radiation light scattered signal to a detector comprising a curvilinear reflecting surface having a focal point and an axis of revolution, the reflecting surface being for receiving a generated incident radiation signal, means for directing a flowing sample axially relative to the axis of revolution towardε the focal point, a detector, the reflecting εurface tranεmitting a reflected signal to the detector, means for generating an incident radiation signal by the interaction of a sample with an excitation signal directed axially relative to the axis of revolution, including means for selecting the excitation radiation signal to have a wavelength greater than a particle size in the sample whereby the incident radiation reflected from the particleε iε isotropic.
24. Apparatus as claimed in claim 23 wherein the incident radiation signal disperses radiation over a solid angle range selected between about 45° and about 135° relative to the axis of the reflecting surface.
25. A method for directing a radiation signal to a detector comprising generating an incident radiation signal by the interaction of a sample with an excitation source, the sample being directed coaxially relative a curvilinear reflecting surface of revolution source, receiving the generated incident radiation signal from a focal point of reflecting surface, generating an output reflected signal from the reflecting surface, and directing the reflected signal to a detector.
26. A method as claimed in claim 25 wherein the reflected output signal is a collimated signal.
27. A method as claimed in claim 25 wherein the reflected output signal converges to a remote focus location.
28. A method as claimed in claim 25 wherein the generated radiation defines a solid angle in the range of about 45° to 135° relative to the axis of revolution.
29. A method as claimed in claim 25 wherein the curvilinear means selectively includes an ellipsoidal or parabolic surface.
30. A method as claimed in claim 25 including directing an excitation source axially relative to the reflection means.
31. A method for directing a light scattered signal to a detector comprising generating a laser radiation beam along an axis of a curvilinear reflecting surface having a focal point, directing a sample axially to the focal point whereby the laser radiation beam impacts the sample at the focal point, and directing a light scattered generated signal from an impact at the focal point to the curvilinear reflecting surface and reflecting the incident light scattered signal towards a detector.
32. A method for directing a radiation signal to a detector, the signal being selectively a light scattered εignal, Raman scattering, luminescence, phosphorescence or fluorescent signal, comprising generating an excitation signal beam and directing the excitation signal beam to a sample to generate an incident radiation signal, receiving a radiation signal on a curvilinear reflecting surface, the curvilinear means having an axis of revolution and a focal point and being for reflecting the incident radiation signal from the focal point towards a detector, the sample and the excitation signal being directed towards each other at the focal point at a selected angle relative to each other, and wherein the generated radiation signal from the impact is generated at the focal point that a generated radiation signal is directed to the curvilinear surface and in turn, towards the detector.
33. A method for directing a radiation signal to a detector comprising generating the radiation signal by the interaction of a sample with an excitation signal at a focal point of curvilinear reflecting means, directing the generated signal as an incident radiation signal to the reflecting surface, reflecting the incident signal to a detector and including having the detector responding selectively to a spatially or temporally sorted reflected signal.
34. A method as claimed in claim 25 wherein the radiation signal has a wavelength greater than a particle size in the sample such that the radiation reflected, from the particles is isotropic.
35. A method as claimed in claim 25 wherein the signal from the sample reflects radiation over a solid angle range selected between about 45° and about 135° relative to the axis of the surface of revolution.
PCT/US1992/008274 1991-10-08 1992-09-29 Detecting a radiation signal WO1993007471A1 (en)

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0582865A1 (en) * 1992-07-24 1994-02-16 Sumitomo Electric Industries, Limited Method of detecting foreign matter in fluid
WO1994029695A1 (en) * 1993-06-08 1994-12-22 Gjelsnes Oddbjoern Liquid flow cytometer
US5495333A (en) * 1992-07-24 1996-02-27 Sumitomo Electric Industries, Ltd. Method and apparatus of detecting impurities in fluid
EP0704699A3 (en) * 1994-09-29 1996-08-21 Hitachi Software Eng Electrophoresis apparatus of capillary type
WO1997030338A1 (en) * 1996-02-16 1997-08-21 Inphocyte, Inc. System and method for rapid analysis of cells using spectral cytometry
WO2001027590A2 (en) * 1999-10-12 2001-04-19 Becton Dickinson And Company Optical element for flow cytometry
WO2004059312A1 (en) * 2002-12-20 2004-07-15 Corning Incorporated Capillary assay device and method
WO2007011726A1 (en) * 2005-07-14 2007-01-25 Battelle Memorial Institute Aerosol trigger device and methods of detecting particulates of interest using and aerosol trigger device
US7518710B2 (en) 2005-07-14 2009-04-14 Battelle Memorial Institute Optical devices for biological and chemical detection
DE102009045075A1 (en) 2009-09-28 2011-04-07 Carl Zeiss Ag Nanostructured filling material dispersion condition e.g. sample agglomeration, measuring device for dispersion production or preparation device, has processing unit detecting measured variable assigned to condition of filling material
US8101426B2 (en) 2007-03-02 2012-01-24 Icyt Mission Technology, Inc. System and method for the measurement of multiple fluorescence emissions in a flow cytometry system
CN106594553A (en) * 2017-01-11 2017-04-26 哈尔滨理工大学 Newborn nostril illumination device
CN106641799A (en) * 2017-01-11 2017-05-10 哈尔滨理工大学 Nostril illumination device for baby
US9746412B2 (en) 2012-05-30 2017-08-29 Iris International, Inc. Flow cytometer
CN110553955A (en) * 2019-08-30 2019-12-10 华中科技大学 Particle size distribution measuring method and system based on light scattering field

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551542A (en) * 1948-11-10 1951-05-01 Charles R Marsh Fluorophotometer
US2852693A (en) * 1953-01-13 1958-09-16 Standard Oil Co Method and apparatus for measuring the optical properties of liquids
US3248551A (en) * 1962-10-22 1966-04-26 Joseph C Frommer Optical arrangement for sensing very small particles
US4088407A (en) * 1974-03-13 1978-05-09 Schoeffel Instrument Corp. High pressure fluorescence flow-through cuvette
US4200802A (en) * 1979-03-28 1980-04-29 The United States Of America As Represented By The United States Department Of Energy Parabolic cell analyzer
US4606636A (en) * 1983-10-25 1986-08-19 Universite De Saint-Etienne Optical apparatus for identifying the individual multiparametric properties of particles or bodies in a continuous flow
EP0421156A2 (en) * 1989-09-12 1991-04-10 Packard Instrument Company, Inc. Method and apparatus for fluorescence measurements

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551542A (en) * 1948-11-10 1951-05-01 Charles R Marsh Fluorophotometer
US2852693A (en) * 1953-01-13 1958-09-16 Standard Oil Co Method and apparatus for measuring the optical properties of liquids
US3248551A (en) * 1962-10-22 1966-04-26 Joseph C Frommer Optical arrangement for sensing very small particles
US4088407A (en) * 1974-03-13 1978-05-09 Schoeffel Instrument Corp. High pressure fluorescence flow-through cuvette
US4200802A (en) * 1979-03-28 1980-04-29 The United States Of America As Represented By The United States Department Of Energy Parabolic cell analyzer
US4606636A (en) * 1983-10-25 1986-08-19 Universite De Saint-Etienne Optical apparatus for identifying the individual multiparametric properties of particles or bodies in a continuous flow
EP0421156A2 (en) * 1989-09-12 1991-04-10 Packard Instrument Company, Inc. Method and apparatus for fluorescence measurements

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 14, no. 534 (P-1135)26 November 1990 & JP,A,22 27 637 ( SHIMADZU ) 10 September 1990 *

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0582865A1 (en) * 1992-07-24 1994-02-16 Sumitomo Electric Industries, Limited Method of detecting foreign matter in fluid
US5495333A (en) * 1992-07-24 1996-02-27 Sumitomo Electric Industries, Ltd. Method and apparatus of detecting impurities in fluid
WO1994029695A1 (en) * 1993-06-08 1994-12-22 Gjelsnes Oddbjoern Liquid flow cytometer
EP0704699A3 (en) * 1994-09-29 1996-08-21 Hitachi Software Eng Electrophoresis apparatus of capillary type
WO1997030338A1 (en) * 1996-02-16 1997-08-21 Inphocyte, Inc. System and method for rapid analysis of cells using spectral cytometry
WO2001027590A2 (en) * 1999-10-12 2001-04-19 Becton Dickinson And Company Optical element for flow cytometry
WO2001027590A3 (en) * 1999-10-12 2001-12-13 Becton Dickinson Co Optical element for flow cytometry
WO2004059312A1 (en) * 2002-12-20 2004-07-15 Corning Incorporated Capillary assay device and method
US7110107B2 (en) 2002-12-20 2006-09-19 Corning Incorporated Capillary assay device and method
US7532314B1 (en) 2005-07-14 2009-05-12 Battelle Memorial Institute Systems and methods for biological and chemical detection
US7499167B2 (en) 2005-07-14 2009-03-03 Battelle Memorial Institute Aerosol trigger device and methods of detecting particulates of interest using an aerosol trigger device
US7518710B2 (en) 2005-07-14 2009-04-14 Battelle Memorial Institute Optical devices for biological and chemical detection
WO2007011726A1 (en) * 2005-07-14 2007-01-25 Battelle Memorial Institute Aerosol trigger device and methods of detecting particulates of interest using and aerosol trigger device
US7993585B2 (en) 2005-07-14 2011-08-09 Battelle Memorial Institute Biological and chemical monitoring
US8101426B2 (en) 2007-03-02 2012-01-24 Icyt Mission Technology, Inc. System and method for the measurement of multiple fluorescence emissions in a flow cytometry system
DE102009045075A1 (en) 2009-09-28 2011-04-07 Carl Zeiss Ag Nanostructured filling material dispersion condition e.g. sample agglomeration, measuring device for dispersion production or preparation device, has processing unit detecting measured variable assigned to condition of filling material
US9746412B2 (en) 2012-05-30 2017-08-29 Iris International, Inc. Flow cytometer
US10126227B2 (en) 2012-05-30 2018-11-13 Iris International, Inc. Flow cytometer
US10209174B2 (en) 2012-05-30 2019-02-19 Iris International, Inc. Flow cytometer
US10330582B2 (en) 2012-05-30 2019-06-25 Iris International, Inc. Flow cytometer
US11255772B2 (en) 2012-05-30 2022-02-22 Iris International, Inc. Flow cytometer
US11703443B2 (en) 2012-05-30 2023-07-18 Iris International, Inc. Flow cytometer
CN106641799A (en) * 2017-01-11 2017-05-10 哈尔滨理工大学 Nostril illumination device for baby
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CN106594553B (en) * 2017-01-11 2019-03-29 哈尔滨理工大学 A kind of newborn nostril lighting device
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