Fluorescent biological particle detection system

• US 5,701,012 A
• Filed: 03/19/1996
• Issued: 12/23/1997
• Est. Priority Date: 03/19/1996
• Status: Expired due to Term

• Current Assignee: TSI Incorporated
• Original Assignee: Her Majesty The Queen In Right of Canada As Represented By The Minister of National Defence
• Inventors: Ho, Jim Yew-Wah
• Primary Examiner(s): Hannaher, Constantine
• Application Number:
  US08/616,475
• Time in Patent Office: 644 Days
• Field of Search: 250/461.2
• US Class Current: 250/461.2
• 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 21/64 Fluorescence; Phosphorescence

Abstract

A process and apparatus are provided for detection of viable and potentially hazardous biological particles which may be dispersed in a particulate-containing airstream. The process comprises directing each of the contained particles along a linear path through air, in a sequential manner, and sampling them for determination of their size, whether they are biological and viable, and whether they are present in concentrations greater than background levels. The particle size identifies the particles as respirable or not and the particles are characterized as biological and viable by subjecting each particle in turn, to 340 nm, ultraviolet laser light and looking for the emission of fluorescence which is typically emitted from bacteria or bacterial spore. Fluorescence detected in the 400-540 nm range signals the presence of nicotinamide adenine dinucleotide hydrogen, which is indicative of biological activity or viability.

Claims

1. Apparatus for identifying the existence of viable biological particles within an airstream containing a mixture of biologically viable end biologically inert particles, comprising:

means for directing the particles individually and sequentially along a substantially linear path through air;

a source emitting an ultraviolet laser beam directed to contact each particle moving along its linear path in the air, said beam having a wavelength operative to excite biomolecules contained therein to produce fluorescence;

means for measuring the intensity of the fluorescence emitted from each particle and producing a signal indicative thereof; and

means for comparing each particle'"'"'s fluorescence intensity signal against pre-determined criteria and establishing whether that particle is a biologically viable particle or an inert particle.

2. Apparatus as recited in claim 1 wherein the ultraviolet laser beam has a wavelength between 320 and 360 nm and the means for measuring the intensity of the fluorescence emitted is operative to measure it in the wavelength range of 400-540 nm.

3. Apparatus as recited in claim 1 wherein the ultraviolet laser beam has a wavelength operative to excite nicotinamide adenine dinucleotide hydrogen to produce fluorescence therefrom.

4. Apparatus as recited in claim 3 further comprising:

means for measuring the size of each particle and producing a signal indicative thereof;

means for storing the fluorescence intensity signal and the corresponding particle size signal for each particle;

means for counting the number of particles and producing and storing signals indicative thereof; and

means for processing the stored fluorescence intensity, particle size and particle count signals and establishing the concentration of biologically viable particles as a function of particle size.

5. Apparatus as recited in claim 4 wherein the means for measuring the size of each particle comprises:

an air discharge nozzle capable of accelerating the flow of the particle-containing airstream through the nozzle so that the particles exit the nozzle individually and sequentially along a substantially linear path, the air flow acting to accelerate a particle passing through the nozzle due to the aerodynamic drag acting thereon, said particle resisting the acceleration by its inertia, whereby the velocity of the particle exiting the nozzle is less than that of the airstream;

means for measuring the velocity of the airstream and producing a signal indicative thereof;

means for emitting two spaced apart laser beams, both of which intersect the particle'"'"'s linear path, the first beam intersecting the path adjacent the nozzle, the second beam being spaced a known distance downstream;

means for measuring the time taken for the particle to move between the first and second laser beams and producing a signal indicative thereof; and

means for processing the known distance between the first and second laser beams and the time signal so as to establish the velocity of the particle and producing a signal indicative thereof; and

means for processing the difference between the particle velocity signal and the airstream velocity signal so as to establish the size of the particle.

6. Apparatus as recited in claim 5 wherein the means for emitting two spaced apart laser beams comprises:

the source emitting the ultraviolet laser beam;

end

means for splitting the ultraviolet laser beam into two beams.

7. A process for detecting the existence of viable biological particles within a stream of air containing a mixture of biologically viable and biologically inert particles, comprising the steps of:

(a) continuously processing the stream of air so as to direct the particles along a substantially linear path through air in a sequential manner;

(b) contacting each particle with an ultraviolet laser beam having a wavelength suitable to excite biomolecules contained therein and produce fluorescence;

(c) detecting fluorescence from the particle and establishing its intensity;

(d) comparing the intensity of each particle'"'"'s fluorescence against pre-determined criteria so as to establishing whether that particle is biologically viable or is inert; and

(e) repeating steps (b)-(d) for sequentially following particles.

8. The process as set forth in claim 7 further comprising:

measuring the size of each particle;

associating the fluorescence intensity of the particle with the size for that particle;

storing the size and fluorescence intensity for the particle and repeating the process for the next particle in sequence;

identifying the size range of particles which are respirable; and

establishing the concentration of biologically viable particles which are found to be within the respirable range using the stored particles'"'"' sizes and fluorescence intensities.

9. The process as recited in claim 8 comprising:

initially performing the entire process on an ambient stream of air for establishing a background concentration of viable biological particles which appear in the respirable size range;

performing the process for a sample stream of air for establishing the sample'"'"'s concentration of viable biological particles which appear in the respirable size range; and

comparing the background and sample concentrations of biologically viable particles for identifying sample concentrations higher than the background concentrations.

10. The process as set forth in claim 9 wherein the process steps are all conducted sufficiently quickly so as to maintain continuous processing of the sample stream of particle-containing air.

11. The process as recited in claim 10, wherein size and fluorescence intensity signals produced for particles having a size smaller than a threshold size and particles emitting fluorescence at an intensity lower than a threshold fluorescence intensity are suppressed from the background and sample concentrations so as to better distinguish the viable biological particles from the inert particles.

12. The process as recited in claim 9, wherein size and fluorescence intensity signals produced for particles having a size smaller than a threshold size and particles emitting fluorescence at an intensity lower than a threshold fluorescence intensity are suppressed from the background and sample concentrations so as to better distinguish the viable biological particles from the inert particles.

13. The process as recited in claim 8 wherein the stream of air is continuously processed by:

rapidly accelerating the stream of air containing particles to a known velocity wherein each particle accelerates to reach a characteristic velocity, slower than the velocity of the stream of air itself, so that, as a function of the particle'"'"'s inertia and aerodynamic properties, each particle becomes separated from the others and becomes distributed substantially sequentially along a linear path through the air;

directing each particle to intersect two laser beams of known spacing;

measuring the particle'"'"'s transit time between the two laser beams;

establishing measures of the particle'"'"'s velocity from the particle'"'"'s transit time and the laser beam spacing; and

comparing the relative velocities of the particle and stream of air so as to establish the size of the particle.

14. The process as recited in claim 13 wherein the ultraviolet laser beam has a wavelength operative to excite nicotinamide adenine dinucleotide hydrogen to produce fluorescence therefrom.

15. The process as recited in claim 13 wherein the ultraviolet laser beam has a wavelength between 320 and 360 nm and the means for measuring the intensity of the fluorescence emitted is operative to measure in the wavelength range of 400-540 nm.

16. The process as set forth in claim 8 wherein the ultraviolet laser beam has a wavelength operative to excite nicotinamide adenine dinucleotide hydrogen to produce fluorescence therefrom.

17. The process as set forth in claim 8 wherein the ultraviolet laser beam has a wavelength between 320 and 360 nm and the means for measuring the intensity of the fluorescence emitted is operative to measure it in the wavelength range of 400-540 nm.

18. The process as recited in claim 7 wherein the stream of air is continuously processed by:

rapidly accelerating the stream of air containing particles to a known velocity wherein each particle accelerates to reach a characteristic velocity, slower than the velocity of the stream of air itself, so that, as a function of the particle'"'"'s inertia and aerodynamic properties, each particle becomes separated from the others and becomes distributed substantially sequentially along a linear path through the air.

19. The process as set forth in claim 18 wherein the ultraviolet laser beam has a wavelength operative to excite nicotinamide dinucleotide hydrogen to produce fluorescence therefrom.

20. The process as recited in claim 18 wherein the ultraviolet laser beam has a wavelength between 320 and 360 nm and the means for measuring the intensity of the fluorescence emitted is operative to measure it in the wavelength range of 400-540 nm.

21. The process as recited in claim 7 wherein the ultraviolet laser beam has a wavelength operative to excite nicotinamide adenine dinucleotide hydrogen to produce fluorescence therefrom.

22. The process as recited in claim 7 wherein the ultraviolet laser beam has a wavelength between 320 and 360 nm and the means for measuring the intensity of the fluorescence emitted is operative to measure it in the wavelength range of 400-540 nm.