PATHOGEN DETECTION BY SIMULTANEOUS SIZE/FLUORESCENCE MEASUREMENT

• US 20110036995A1
• Filed: 12/15/2008
• Published: 02/17/2011
• Est. Priority Date: 12/13/2007
• Status: Abandoned Application

• Current Assignee: Azbil Corporation (Azbil BioVigilant Incorporated)
• Original Assignee: BioVigilant Systems Incorporated (Azbil BioVigilant Incorporated)
• Inventors: Morris, GRegory Scott, Binnie, Erik H.
• Application Number:
  US12/808,170
• Publication Number:
  US 20110036995A1
• Time in Patent Office: Days
• US Class Current: 250/459.1
• CPC Class Codes: G01N 1/2247 Sampling from a flowing stream of gas
• CPC Class Codes: G01N 1/2273 Atmospheric sampling
• CPC Class Codes: G01N 15/1404 Handling flow, e.g. hydrodynamic focusing
• CPC Class Codes: G01N 15/1434 Optical arrangements
• CPC Class Codes: G01N 15/1459 the analysis being performed on a sample stream
• CPC Class Codes: G01N 2015/019 Biological contaminants; Fouling
• CPC Class Codes: G01N 2015/025 Methods for single or grouped particles
• CPC Class Codes: G01N 2015/1486 Counting the particles
• CPC Class Codes: G01N 2015/1493 Particle size
• CPC Class Codes: G01N 21/53 within a flowing fluid, e.g. smoke
• CPC Class Codes: G01N 21/6486 Measuring fluorescence of biological material, e.g. DNA, RNA, cells G01N21/6428 takes precedence
• CPC Class Codes: G01N 2201/06113 Coherent sources; lasers
• CPC Class Codes: G01N 2201/06193 Secundary in-situ sources, e.g. fluorescent particles

Abstract

A method and apparatus for detecting pathogens and particles in a fluid in which particle size and intrinsic fluorescence of a simple particle is determined, comprising a sample cell; a light source on one side of the sample cell for sending a focused beam of light through the sample, whereby portions of the beam of light are scattered at various angles by particles of various sizes present in the sample area; a particle size detector positioned in the light path for detecting a portion of forward scattered light; a pair of fluorescence detectors positioned off axis from the beam of light; and a pair of elliptical mirrors positioned such that an intersection of the incoming particle stream and the light beam are at one foci of each ellipsoid, and one of said pair of fluorescence detectors lies at the other foci.

Claims

1. A method of differentiating biological particles from inert particles in a fluid which comprises simultaneously measuring particle size and detecting intrinsic fluorescence from a particle, wherein fluorescence intensity is measured and assigned a value, and including the step of classifying the particle as either inert or biological based on particle size and fluorescence intensity, and wherein fluorescence is measured using two fluorescence detectors, and further wherein each of said two fluorescence detectors produce a signal, said signals being compared to determine relevant data for classifying particles.

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7. A particle detector system, comprising:

sampling area including particles of various size to be measured;

a light source on one side of the sampling area for sending a beam of light through the sampling area;

a particle size detector positioned in the light path after the sampling area positioned to receive and detect a portion of forward scattered light scattered at various angles by the particles of various sizes, and producing an output including information on the size of particles in the light path;

a pair of opposite facing elliptical mirrors located in particle sampling region, wherein each elliptical mirror has one foci at a point where said light beam and said particles intersect and one foci on one of a pair of fluorescence detectors, and further wherein the elliptical mirrors are out of plane of the particle size detector.

8. The system of claim 7, further comprising a beam blocking device on an opposite side of the sampling area from said light source for blocking at least a portion of unscattered light emerging from the sampling area.

9. The system of claim 7, further comprising a collimating lens on an opposite side of the sampling area from said light source, an optical element positioned after the collimating lens for reflecting a portion of forward scattered light into a condensing lens which focuses said portion of forward scattered light into said particle size detector, wherein said unscattered light is stopped by a beam blocker in front of the condensing lens or passes through said optical element into a light dump.

11. The system of claim 7, wherein the light source emits light with a wavelength in the range of about 270 to about 410 nm.

12. The system of claim 7, further comprising a processing unit for processing particle size distribution and particle fluorescence at a given time, and displaying a signal on an output device.

14. The system of claim 7, further comprising computer readable program code for integrating detected particle size and detected intrinsic fluorescence.

18. The system of claim 7, wherein the fluorescence detectors are positioned orthogonal to the beam of light for detecting intrinsic fluorescence, and wherein said fluorescence detectors are positioned to opposite sides of said light beam.

19. The system of claim 11, wherein the light source is a UV laser, a visible light laser or a LED.

20. The system of claim 9, wherein the collimating lens and condensing lens are orientated 90 degrees from one another, and wherein the optical element is a mirror.

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15. A particle detector system, comprising:

sampling area including particles of various size to be measured;

a light source on one side of a sampling area for sending a beam of light through the sampling area;

a first detector positioned in the light path after the sampling area positioned to receive and detect a portion of forward scattered light scattered at various angles by said particles of various sizes, and producing an output including information on the size of particles in the light path within a predetermined size range;

a second detector positioned orthogonal to the beam of light for detecting intrinsic fluorescence from particles in the light path;

an elliptical mirror located in a particle sampling region such that an intersection of the sampling area and the light beam are at one foci of the ellipsoid, and the second detector is at the other foci; and

a spherical mirror positioned facing said elliptical mirror such that the intersection of the sampling area and the light beam are at the focus of the sphere.

16. The system of claim 15, further comprising a beam blocking device on an opposite side of the sampling area from said light source for blocking at least a portion of unscattered light emerging from the sampling area.

17. The system of claim 15, further comprising a collimating lens on an opposite side of the sampling area from said light source, a mirror for reflecting a portion of forward scattered light into a condensing lens which focuses said portion of forward scattered light into said particle size detector, wherein said unscattered light is not reflected into said condensing lens, wherein said unscattered light is stopped by a beam blocker in front of the condensing lens or passes through said optical element into a light dump.

21. The system of claim 15, further comprising an alarm unit for providing a warning signal when a particle within a predetermined size range is detected which also fluoresces.

22. The system of claim 15, wherein the light source emits light with a wavelength in the range of about 270 to about 410 nm.

24. The system of claim 15, further comprising a processing unit for processing particle size distribution and particle fluorescence at a given time, and displaying a signal on an output device.

25. The system of claim 15, further comprising computer readable program code for integrating detected particle size and detected intrinsic fluorescence.

26. The system of claim 17, wherein the collimating lens and condensing lens are orientated 90 degrees from one another.

27. The system of claim 15, wherein the elliptical and spherical mirrors are position around the particle sampling region such that the surface of the elliptical mirror and special mirror intersect.

23. The system of claim 23, wherein the light source is a UV laser, a visible light laser or a LED.