AUTOMATED PARTICULATE CONCENTRATION SYSTEM

• US 20110059462A1
• Filed: 11/12/2010
• Published: 03/10/2011
• Est. Priority Date: 02/21/2006
• Status: Abandoned Application

• Current Assignee: University of South Florida (State University System of Florida)
• Original Assignee: University of South Florida (State University System of Florida)
• Inventors: Lim, Daniel V., Magaña, Sonia, Kearns, Elizabeth A., Leskinen, Stephaney D.
• Application Number:
  US12/945,444
• Publication Number:
  US 20110059462A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C02F 1/44 by dialysis, osmosis or reverse osmosis general membrane separation processes B01D61/00, membrane modules B01D63/00, electrodialysis C02F1/4693, combination of membrane modules and bioreactors C02F3/1268
• CPC Class Codes: C02F 2209/001 Upstream control, i.e. monitoring for predictive control
• CPC Class Codes: C02F 2209/003 Downstream control, i.e. outlet monitoring, e.g. to check the treating agents, such as halogens or ozone, leaving the process
• CPC Class Codes: C02F 2303/16 Regeneration of sorbents, filters
• CPC Class Codes: G01N 1/4077 by other techniques involving separation of suspended solids
• CPC Class Codes: G01N 2001/4088 filtration
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]
• CPC Class Codes: Y10T 436/20 Oxygen containing
• CPC Class Codes: Y10T 436/24 Nuclear magnetic resonance, electron spin resonance or other spin effects or mass spectrometry
• CPC Class Codes: Y10T 436/255 including use of a solid sorbent, semipermeable membrane, or liquid extraction

Abstract

An automated system for concentrating potentially harmful substances from various water types or other non-viscous liquids to facilitate detection of those substances is disclosed herein. The automated system comprises a water pressure driven or pump driven concentration unit that filters the test fluid through a hollow-fiber filter. Material collected on the filter is backflushed into a collection vessel by passing a small volume of sterile solution through the filter in the reverse direction. The automated system can be configured to be portable or to be integrated into a continuous liquid stream for online monitoring of test fluids. Optionally, an electronic signal at the end of the backflush sequence triggers a detector, such as an automated array biosensor, to begin processing and analyzing the sample.

Claims

1. An apparatus for extracting an analyte from a test fluid, comprising:

a concentration subsystem further comprising a filter having a first side and a second side, wherein the filter is selected to separate at least one analyte from the test fluid;

a test fluid input port disposed on the first side of the filter and in fluid communication with the test fluid source;

a test fluid output port disposed on the second side of the filter;

a plurality of backflush subsystems in fluid communication with the concentration subsystem, wherein the backflush subsystem further includes

a liquid backflush in fluid communication with the second side of the filter;

an air backflush comprising an air source in fluid communication with the first side of the filter;

said backflush subsystem adapted to remove at least one analyte from the filter thereby providing a sample, and

a sample output disposed on the first side of the filter.

2. The apparatus of claim 1, wherein the test fluid output port is in fluid communication with a filtrate output line.

3. The apparatus of claim 1, further comprising at least one pump disposed in fluid communication with at least the liquid backflush or air backflush, wherein the pumps are selected from the group consisting of a metering pump, a bellow, a double-diaphragm, a flexible impeller, a rotary lobe, a rotary vane, an oscillating, piston, a syringe, a nutating disc, a flexible liner, a progressing cavity, and a peristaltic pump.

4. The apparatus of claim 1, further comprising a plurality of valves disposed along at least one path of the test fluid, wherein the valves are selected from the group consisting of butterfly valves, trunnions, ball valves, plug valves, globe valves, needle valves, check valves, gate valves, angle seat piston valves, angle valves, ceramic disc valves, piston valves, pinch valves, or solenoid valves adapted to control the flow of the test fluid through the apparatus, and mass flow controllers.

5. The apparatus of claim 1, further comprising at least one pressure monitor disposed along at least one path of the test fluid, wherein the pressure monitor is selected from the group consisting of a transducer, piezo-resistive pressure sensor, piezo-resistive pressure transducer, miniature cylindrical pressure transducer, silicon strain gauge pressure transducer, pressure transmitter, digital pressure gauge, and analog pressure gauge.

6. The apparatus of claim 5, wherein the at least one transducer is disposed before the filter and after the filter.

7. The apparatus of claim 1, further comprising a sample detection system in fluid communication with the sample output port;

wherein the sample detection system is selected from the group consisting of culture-dependent identification, biochemical identification, selective staining, immunoassay, shape-based identification, nucleic acid-based identification, sequence-based identification, carbohydrate-based identification, fatty acid-based identification, size-based identification, mass-selective identification, charge-selective identification, ion-selective identification, optical identification, spectral identification, ELISA, bioluminescence, electrochemiluminescence, growth selective media, growth differential media, fatty acid analysis, carbohydrate analysis, detection of toxin production, electrophoresis, fluorescent labeling with flow cytometry, optical differential staining, antibody capture with fluorescent antibody tagging;

microarrays, nanoarrays, quartz crystal microbalance, nucleic acid sequence-based amplification, polymerase chain reaction, pyrosequencing, ion mobility spectroscopy, Raman spectroscopy, liquid chromatography-mass spectrometry, and combinations thereof.

8. The apparatus of claim 1, further comprising a large-particulate filter disposed along the path of the test fluid and before the test fluid reaches the filter.

9. The apparatus of claim 1, wherein the air source is selected from the group consisting of a pump in fluid communication with an air-intake valve, and a pressurized gas container.

10. The apparatus of claim 9, further comprising an air filter disposed on the air-intake valve.

11. The apparatus of claim 1, wherein the liquid backflush further comprises a pump in fluid communication with a liquid solution reservoir.

12. The apparatus of claim 1, further comprising a spiking port disposed along the path of the test fluid and before the test fluid reaches the filter.

13. The apparatus of claim 12, further comprising a mixing chamber disposed on the test fluid input line after the spiking port, wherein the mixing chamber is adapted to generate mild turbulence and approximate the natural dilution of water contamination.

14. The apparatus of claim 1, further comprising a cleaning subsystem, wherein the cleaning subsystem further comprises a pump and cleaning solution reservoir in fluid communication with the filter.

15. The apparatus of claim 13, further comprising a heating element adapted to heat a cleaning solution before the cleaning solution is introduced to the filter.

16. The apparatus of claim 1, further comprising a purge subsystem in fluid communication with the concentration subsystem, said purge subsystem adapted to release any gas in the filter.

17. The apparatus of claim 1, further comprising a forward flow buffer subsystem;

wherein the forward flow buffer subsystem comprises a solution reservoir in fluid communication with a pump, and wherein the pump is in fluid communication with a test fluid input line and before the test fluid input port.

18. The apparatus of claim 1, further comprising a forward flow air subsystem;

wherein the forward flow air subsystem comprises an air source in fluid communication with a test fluid input line and before the test fluid input port.

19. The apparatus of claim 17, wherein the air source is selected from the group consisting of a pump in fluid communication with an air-intake valve, and a pressurized gas container.

20. A method of extracting an analyte from a test fluid, comprising the steps of:

providing a test fluid source;

providing a filter with a first side and a second side;

collecting an analyte in the filter by passing the test fluid along a first path of travel through a filter whereby the analyte is captured in the first side of the filter;

equilibrating the filter with a recovery fluid by flowing the recovery fluid in the same direction as the test fluid;

removing the equilibrating recovery fluid from the filter by flowing air in the same direction as the test fluid;

forming a retentate by initiating at least one backflush sequence to remove the analyte from the filter, wherein the at least one backflush sequence comprises at least one air backflush followed by a plurality of liquid backflushes; and

collecting the backflush liquid as a sample.

21. The method of claim 20, wherein the gas is ambient air.

22. The method of claim 20, wherein the liquid is selected from the group consisting of water, a buffer and a solution.

23. The method of claim 20, further comprising the step of pumping a cleaning solution through the filter.

24. The method of claim 23, wherein the cleaning solution passes through the filter in the same path of travel as the fluid.

25. The method of claim 20, further comprising the step of purging any gas accumulated in the filter.

26. The method of claim 20, further comprising the step of delivering the sample to a sample detection system adapted to identify the analyte in the retentate;

wherein the sample detection system is selected from the group consisting of culture-dependent identification, biochemical identification, selective staining, immunoassay, shape-based identification, nucleic acid-based identification sequence-based identification, carbohydrate-based identification, fatty acid-based identification, size-based identification, mass-selective identification, charge-selective identification, ion-selective identification, optical identification, spectral identification, ELISA, bioluminescence, electrochemiluminescence, growth selective media, growth differential media, fatty acid analysis, carbohydrate analysis, detection of toxin production, electrophoresis, fluorescent labeling with flow cytometry, optical differential staining, antibody capture with fluorescent antibody tagging;

microarrays, nanoarrays, quartz crystal microbalance, nucleic acid sequence-based amplification, polymerase chain reaction, pyrosequencing, ion mobility spectroscopy, Raman spectroscopy, liquid chromatography-mass spectrometry, and combinations thereof.