PATHOGEN DETECTION BY SIMULTANEOUS SIZE/FLUORESCENCE MEASUREMENT
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.
This application claims priority from U.S. Provisional Application Ser. No. 60/805,962 filed Jun. 27, 2006.
FIELD OF THE INVENTIONThe present invention relates generally to a system and method for detecting airborne or waterborne particles, and more particularly to a system and method for detecting airborne or waterborne particles and classifying the detected particles. The invention has particular utility in detecting and classifying allergens and biological warfare agents and will be described in connection with such utility, although other utilities are contemplated.
BACKGROUND OF THE INVENTIONAn urban terrorist attack involving release of biological warfare agents such as bacillus anthracis (anthrax) is presently a realistic concern. Weaponized anthrax spores are extremely dangerous because they can gain passage into the human lungs. A lethal inhalation dose of anthrax spores for humans, LD50 (lethal dose sufficient to kill 50% of the persons exposed) is estimated to be 2,500 to 50,000 spores (see T. V. Inglesby, et al., “Anthrax as a Biological Weapon”, JAMA, vol. 281, page 1735, 1999). Some other potential weaponized bio-agents are yersinia pestis (plague), clostridium botulinum (botulism), and francisella tularensis. In view of this potential threat, there is currently a need for an early warning system to detect such an attack. In the pharmaceutical, healthcare and food industries, a real time detector of environmental microbial level is useful for public health, quality control and regulatory purposes. For example, parenteral drug manufacturers are required to monitor the microbial levels in their aseptic clean rooms. In these applications, an instrument which can detect microbes in the environment instantaneously will be a useful tool and have advantages over conventional nutrient plate culture methods which requires days for microbes to grow and to be detected.
Particle size measurement and ultraviolet (UV) induced fluorescence detection have been used to detect the presence of biological substances in the air. There exist various patents describing using these techniques as early warning sensors for bio-terrorist attack release of weaponized bio-agents. Among these devices are Biological Agent Warning Sensor (BAWS) developed by MIT Lincoln Laboratory, fluorescence biological particle detection system of Ho (Jim yew-Wah Ho, U.S. Pat. Nos. 5,701,012; 5,895,922; 6,831,279); FLAPS and UV-APS by TSI of Minnesota (Peter P. Hairston; and Frederick R. Quant; U.S. Pat. No. 5,999,250), and a fluorescence sensor by Silcott (U.S. Pat. No. 6,885,440).
A proposed bio-sensor based on laser-induced fluorescence using a pulsed UV laser is described by T. H. Jeys, et al., Proc. IRIS Active Systems, vol. 1, p. 235, 1998. This is capable of detecting an aerosol concentration of five particles per liter of air, but involves expensive and delicate instruments. Other particle counters are manufactured by Met One Instrument, Inc, of Grants Pass, Oreg., Particle Measurement Systems, Inc., of Boulder, Colo., and Terra Universal Corp., of Anaheim, Calif.
Various detectors have been designed to detect airborne allergen particles and provide warning to sensitive individuals when the number of particles within an air sample exceeds a predetermined minimum value. These are described in U.S. Pat. Nos. 5,646,597, 5,969,622, 5,986,555, 6,008,729, 6,087,947, and 7,053,783, all to Hamburger et al. These detectors all involve direction of a light beam through a sample of environmental air such that part of the beam will be scattered by any particles in the air, a beam blocking device for transmitting only light scattered in a predetermined angular range corresponding to the predetermined allergen size range, and a detector for detecting the transmitted light.
SUMMARY OF THE INVENTIONFor the purpose of detection of microbes in air or water, it is of importance to devise an effective system to measure both particle size and fluorescence generated intrinsically by the microbes. The present invention provides a sensor system which is capable of simultaneously measuring particle size and detecting the presence of intrinsic fluorescence from metabolites and other bio-molecules, on a particle-by-particle basis. The advantages of this detection scheme over the prior art are several. For one it provides a deterministic particle measurement methodology for characterizing particles rather than relying on statistical models employed in prior art for particle characterization. The deterministic measurement methodology enables more definitive assignment of particle characters than the prior art and less reliance on statistical models. It also reduces the possibility of false positives in microbial detection, for example, pollen (larger sizes than microbes) and smoke particles (smaller sizes than microbes) can be excluded from detection. And, it allows detailed analyses of data collected on each individual particle for characterizing the particle, such as intensity of fluorescence signal from a particle as a function of its cross-sectional area or volume, for the purpose of determining the biological status of the particles.
The current invention comprises three main components: (1) a first optical system for measuring an individual particle size; (2) a second optical system to detect a UV laser-induced intrinsic fluorescence signal from an individual particle; and (3) a data recording format for assigning both particle size and fluorescence intensity to an individual particle, and computer readable program code for differentiating microbes from non-microbes (e.g. inert dust particles).
The optical assembly of the present invention has two optical sub-assemblies: (a) an optical setup to measure the particle size. As an example, the preferred embodiment of the current invention uses the well-known and often used Mie scattering detection scheme, but applies it in a novel way, enabling the system to make highly accurate measurements of airborne particles with size ranges from 0.5 microns to 20 microns. This capability to make fine distinctions in size is important in order to determine the class of microbe, because different classes of microbes have different size ranges; (b) simultaneous to the particle size measurement, an optical apparatus is used to measure the fluorescence level from the particle being interrogated. As an example, the preferred embodiment of the current invention uses an elliptical mirror which is positioned to collected fluorescence emission from the same particle as it is being measured for size.
Further features and advantages of the present invention will be seen from the following detailed description, taken in conjunction with the accompanying drawings, wherein:
The term “fluid borne particles” as used herein means both airborne particles and waterborne particles.
The term “pathogen” as used herein refers to any airborne or waterborne particles, biological agent, or toxin, which could potentially harm or even kill humans exposed to such particles if present in the air or water in sufficient quantities.
The term “biological agent” is defined as any microorganism, pathogen, or infectious substance, toxin, biological toxin, or any naturally occurring, bioengineered or synthesized component of any such micro-organism, pathogen, or infectious substance, whatever its origin or method of production. Such biological agents include, for example, biological toxins, bacteria, viruses, rickettsiae, spores, fungi, and protozoa, as well as others known in the art.
“Biological toxins” are poisonous substances produced or derived from living plants, animals or microorganisms, but also can be produced or altered by chemical means. A toxin, however, generally develops naturally in a host organism (i.e., saxitoxin is produced by marine algae), but genetically altered and/or synthetically manufactured toxins have been produced in a laboratory environment. Compared with microorganisms, toxins have a relatively simple biochemical composition and are not able to reproduce themselves. In many aspects, they are comparable to chemical agents. Such biological toxins are, for example, botulinum and tetanus toxins, staphylococcal enterotoxin B, tricothocene mycotoxins, ricin, saxitoxin, Shiga and Shiga-like toxins, dendrotoxins, erabutoxin b, as well as other known toxins.
The detector system of the present invention is designed to detect airborne or waterborne particles and produce outputs indicating, for instance, the number of particles of each size within the range, which is detected in a sample, and indicate whether the particles are biologic or non-biologic. The system also may produce an alarm signal or other response if the number of particles exceeds a predetermined value above a normal background level, and/or biological organisms or biological agents and potentially dangerous.
In the system 10 illustrated in
Off axis from the laser beam 14, an elliptical mirror 30 is placed at the particle-sampling region in such a way that the intersection of the incoming particle stream and the laser beam is at one of the two foci of the ellipsoid, while a fluorescence detector 32 (in this case a photo-multiplier tube) occupies the other focus. This design utilizes the fact that a point source of light emanating from one of the two foci of an ellipsoid will be focused onto the other. In this optical design, the elliptical mirror 30 concentrates the fluorescence signal from microbe and focus it onto the fluorescence detector 32. An optical filter 34 is placed in front of the fluorescence detector to block the scattered UV light and pass the induced fluorescence.
The beam blocker lens 22 is designed to reflect non-scattered elements of the laser beam 14, and may have a material, such as vinyl, attached a front surface to reflect the non-scattered elements of the beam of electromagnetic radiation. Other features and considerations for the beam blocker lens 22 are disclosed in some of the earlier U.S. patents to Hamburger et al. listed above, and in PCT Application Serial No. PCT/US2006027638, incorporated herein by reference.
The particle detector 20 may comprise, for example, a photodiode for sizing the particles, e.g. as described in the earlier U.S. patent to Hamburger et al., listed above, and incorporated herein by reference.
The present invention's use of Mie scattering also facilitates the placement of optical components for the detection of UV light illumination to concurrently examine individual particles for the presence of the metabolites NADH, riboflavin and other bio-molecules, which are necessary intermediates for metabolism of living organisms, and therefore exist in microbes such as bacteria and fungi. If these chemical compounds exist in a bio-aerosol, they are excited by the UV photon energy and subsequently emit auto-fluorescence light which may be detected by an instrument based on the detection scheme outlined above. While this detection scheme is not capable of identifying the genus or species of microbes, and viruses may be too small and lack the metabolism for detection, this detection scheme's ability to simultaneously and for each particle determine the size of the particle and if it is biologic or inert indicates to the user the presence or absence of microbial contamination.
Referring to
It should be emphasized that the above-described embodiments of the present invention, particularly, any “preferred” embodiments, are merely possible examples of implementations, merely set forth for a clear understanding of the principles of the invention. Many variations and modifications may be made to the above-described embodiments of the invention without departing substantially from the spirit and principles of the invention. All such modifications and variations are intended to be included herein within the scope of this disclosure and the present invention and protected by the following claims.
Claims
1. A method of differentiating biological particles from inert particles in a fluid which comprises simultaneously measuring a particle size and detecting intrinsic fluorescence from that particle.
2. The method of claim 1, 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.
3. The method of claim 2, wherein size information of the particle is used to classify whether that particle is a microorganism.
4. The method of claim 3, wherein size information of the particle is derived from determining cross-section area of the particle, or volume of the particle.
5. The method of claim 4, wherein volume of the particle is derived by first determining the diameter of the particle, and calculating its volume based on said diameter.
6. The method of claim 2, wherein particle size and fluorescence intensity data from an individual particle is used to differentiate between pollen and allergens from microbes.
7. The method of claim 2, wherein particle size and fluorescence signal data from an individual particle is used to estimate relative abundance of biochemical compounds inside the biological particles.
8. The method of claim 2, wherein particle size and fluorescence intensity value from an individual particle is normalized by its size or volume and used to differentiate between inert particles from microbes.
9. The method of claim 2, wherein particle size and fluorescence intensity value from an individual particle is normalized by its size or volume and used to differentiate between pollen and allergens from microbes.
10. The method of claim 1, wherein the fluid comprises air.
11. The method of claim 1, wherein the fluid comprises water.
12. A method for detecting and classifying a particle in a liquid or gas comprising illuminating the particle with a UV light source, and simultaneously measuring a size of the particle and any intrinsic fluorescence from the particle.
13. The method of claim 12, wherein the particle comprises a bioparticle.
14. The method of claim 13, wherein the bioparticle comprises a microbe.
15. The method of claim 12, wherein the bioparticle is selected from the group consisting of a bacterium, a mold, a fungi, and a spore.
16. The method of claim 12, including the step of measuring fluorescence intensity.
17. The method of claim 12, including the step of comparing particle size information and fluorescence intensity to classify the particle as inert or microbial in origin.
18. The method of claim 12, including the step of differentiating the particle as a bacterium, a mold, a fungi or a spore.
19. The method of claim 12, including the step of differentiating the particle as a pollen or an allergen.
20. The method of claim 18, including the step of classifying the particle based on its fluorescence response.
21. The method of claim 19, including the steps of classifying the particle based on its fluorescence response.
22. The method of claim 18, including the steps of classifying the particle based on its diameter or volume.
23. The method of claim 18, including the steps of classifying the particle based on its fluorescence intensity normalized by its diameter or volume.
24. The method of claim 19, including the steps of classifying the particle based on its diameter or volume.
25. The method of claim 19, including the steps of classifying the particle based on its fluorescence intensity normalized by its diameter or volume.
26. A particle detector system, comprising:
- a sample cell;
- a light source on one side of a 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, and an unscattered portion of the beam of light remains unscattered;
- a beam blocking device on an opposite side of the sample cell for blocking at least the portion of the unscattered portion of the beam of light and for limiting a range of particles measured;
- a first detector positioned in the light path after the beam blocking device for detecting a portion of forward scattered light, and producing an output including information on the size of a single particle in the light path within a predetermined size range;
- a second detector positioned off axis from the beam of light for detecting intrinsic fluorescence from said same single particle.
27. The system of claim 26, wherein an elliptical mirror is located in a particle sampling region such that an intersection of the incoming particle stream and the light beam are at one foci of the ellipsoid, and the second detector is at the other foci.
28. The system of claim 26, further comprising an alarm unit for providing a warning signal when a particle within a predetermined size range is detected which also fluoresces.
29. The system of claim 26, wherein the light source emits ultraviolet radiation.
30. The system of claim 26, wherein the light source comprises a LED.
31. The system of claim 30, further comprising a collimator lens optically positioned between the light source and the first detector.
32. The system of claim 26, further comprising a processing unit for processing particle size distribution and particle fluorescence at a give time, and displaying a histogram of the particle on an output device.
33. The system of claim 26, wherein the first detector comprise a photodiode.
34. The system of claim 26, wherein the sample cell comprises an air sample cell.
35. The system of claim 26, wherein the sample cell comprises a water sample cell.
36. The system of claim 26, further comprising computer readable program code for integrating detected particle size and detected intrinsic fluorescence.
Type: Application
Filed: Jun 25, 2007
Publication Date: May 17, 2012
Inventor: Jian-Ping Jiang (Tucson, AZ)
Application Number: 11/768,103
International Classification: G01N 21/00 (20060101);