Laser diode-excited biological particle detection system

• US 20030098421A1
• Filed: 11/27/2001
• Published: 05/29/2003
• Est. Priority Date: 11/27/2001
• Status: Active Grant

• 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
• Granted Patent: US 6,831,279 B2
• Time in Patent Office: Days
• US Class Current: 250/458.1
• CPC Class Codes: G01N 21/6486 Measuring fluorescence of biological material, e.g. DNA, RNA, cells G01N21/6428 takes precedence

Abstract

Apparatus is provided for detection of viable and potentially hazardous biological particles in a population which may be dispersed in fluid flow. The particles are characterized as biological and viable by contacting particles with laser light from a laser diode and then looking for the emission of fluorescence which is typically emitted from bacteria or bacterial spore. Biomolecules which are representative of viability are now known to be excited in range of 320 nm and longer. The resulting apparatus is economical, compact and has low-power requirements enabling portable operation. Preferably, the laser diode is combined with an aerodynamic particle sizer to separate particles for sequential contacts, or with additional timing lasers for establishing particle size.

Claims

1. An improved apparatus for identifying the existence of viable biological particles from a particle population containing a mixture of biologically viable and biologically inert particles, the improvement comprising:

a solid state excitation source wherein said source is a laser diode for emitting a light beam being directed to contact particles of the particle population and having a wavelength above about 320 nm which is operative to excite biomolecules contained therein to produce fluorescence;

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

a microprocessor for comparing each contacted particle'"'"'s fluorescent intensity signal against predetermined criteria and establishing whether that particle is a biologically viable particle or an inert particle.

2. The improved apparatus of claim 1 wherein the laser diode has a wavelength operative to excite biomolecules from the group consisting of NADH and flavinoids.

3. The improved apparatus of claim 2 wherein the laser diode has a wavelength in the range of about 320 nm to about 420 nm.

4. The improved apparatus of claim 3 wherein the laser diode has a wavelength operative to excite NADH.

5. The improved apparatus of claim 4 wherein the laser diode has a wavelength in the range of about 320 nm to about 360 nm.

6. The improved apparatus of claim 3 wherein the laser diode has a wavelength operative to excite flavinoids.

7. The improved apparatus of claim 6 wherein the laser diode has a wavelength in the range of about 360 nm to about 420 nm.

8. The improved apparatus of claim 6 further comprising:

means for measuring the size of the contacted particle as indicative of a biological characteristic; and

means for establishing the contacted particle as a candidate particle if its size is within the range of particles which are respirable.

9. The improved apparatus of claim 8 wherein the size measuring means comprises:

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

an instrument for determining the position of each particle in the airstream as a function of time and the particle'"'"'s time of flight between two points along the linear path so as to establish the particle'"'"'s size.

10. The improved apparatus of claim 1 wherein the laser diode light beam is emitted at a power of about 8-15 mW.

11. The improved apparatus of claim 10 wherein the laser diode has a wavelength operative to excite biomolecules from the group consisting of NADH and flavinoids.

12. The improved apparatus of claim 10 wherein the laser diode has a wavelength in the range of about 320 nm to about 420 nm.

13. The improved apparatus of claim 12 wherein the laser diode has a wavelength operative to excite NADH.

14. The improved apparatus of claim 13 wherein the laser diode has a wavelength in the range of about 320 nm to about 360 nm.

15. The improved apparatus of claim 12 wherein the laser diode has a wavelength operative to excite flavinoids.

16. The improved apparatus of claim 15 wherein the laser diode has a wavelength in the range of about 360 nm to about 420 nm.

17. An improved apparatus for identifying the existence of viable biological particles from a particle population containing a mixture of biologically viable and biologically inert particles, the improvement comprising:

a solid state excitation source wherein said source is a laser diode for emitting a light beam being directed to contact particles of the particle population and having a wavelength above about 320 nm which is operative to excite biomolecules contained therein to produce fluorescence;

means for measuring the intensity of 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 biologically viable or an inert particle.

18. The improved apparatus of claim 17 wherein the intensity measuring means comprise a photon counter.

19. The improved apparatus of claim 17 wherein the intensity measuring means comprise a microprocessor.

20. A method for identifying the existence of viable biological particles from a particle population containing a mixture of biologically viable and biologically inert particles, the method comprising:

providing a solid state excitation source wherein said source is a laser diode for emitting a light beam having a wavelength from about 320 nm to 500 nm and a detector for measuring fluorescence emission and producing a signal indicative of the intensity thereof;

contacting the laser beam and particles of the population so as to excite biomolecules contained in a contacted particle to produce fluorescence;

using the detector to measure the intensity of fluorescence from the contacted particle;

comparing each particle'"'"'s fluorescence intensity signal against predetermined criteria and establishing whether that particle is biologically viable or an inert particle.

21. The method of claim 20 further comprising:

measuring the size of the contacted particle as a biological characteristic; and

establishing the contacted particle as a candidate particle if its size is within the range of particles which are respirable.

22. The method of claim 20 wherein the laser diode has a wavelength operative to excite biomolecules from the group consisting of NADH and flavinoids.

23. The method of claim 20 wherein the laser diode has a wavelength operative to excite NADH.

24. The method of claim 20 wherein the laser diode has a wavelength operative to excite riboflavin.