System for autonomous monitoring of bioagents
An autonomous monitoring apparatus for monitoring air, water, soil, or other substance for bioagents. A collector gathers a quantity of the air, water, soil, or other substance being monitored. A sample preparation system prepares a sample of the selected potential bioagent particles. The sample is analyzed by a system for detecting said bioagents.
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This application is a Continuation-in-Part of U.S. patent application Ser. No. 10/643797 filed Aug. 19, 2003 and titled, “System for Autonomous Monitoring of Bioagents” which claims the benefit of U.S. Provisional Patent Application No. 60/406159 filed Aug. 26, 2002 titled “System for Autonomous Monitoring of Bioagents.” U.S. patent application Ser. No. 10/643797 filed Aug. 19, 2003 and U.S. Provisional Patent Application No. 60/406159 filed Aug. 26, 2002, both titled, “System for Autonomous Monitoring of Bioagents,” are incorporated herein by this reference.
The United States Government has rights in this invention pursuant to Contract No. W-7405-ENG-48 between the United States Department of Energy and the University of California for the operation of Lawrence Livermore National Laboratory.
BACKGROUND1. Field of Endeavor
The present invention relates to bioagents and more particularly to monitoring bioagents.
2. State of Technology
There exists a critical need to develop distributed biothreat agent sensor networks that can operate in civilian applications. To operate in “Detect to Protect/Warn” type detection architectures, these platforms need to have several key properties. They need to be capable of detecting pathogens within a 1-2 hour time window, allowing for enough time to respond to an event. They need to be extremely low cost to maintain, since continuous monitoring is essential for many applications. These platforms need to have sufficient sensitivity to cover a broad geographical area (limiting the necessary number of sensors) and have sufficient selectivity to virtually eliminate false positives. Currently available bioweapons detection systems are designed primarily for military use on the battlefield. These systems are often expensive to deploy and ultimately unsuited for civilian protection.
In an article titled, “U.S. Is Deploying a Monitor System for Germ Attacks,” by Judith Miller in The New York Times on Jan. 22, 2003, it was reported, “To help protect against the threat of bioterrorism, the Bush administration on Wednesday will start deploying a national system of environmental monitors that is intended to tell within 24 hours whether anthrax, smallpox and other deadly germs have been released into the air, senior administration officials said today. The system uses advanced data analysis that officials said had been quietly adapted since the September 11 attacks and tested over the past nine months. It will adapt many of the Environmental Protection Agency's 3,000 air quality monitoring stations throughout the country to register unusual quantities of a wide range of pathogens that cause diseases that incapacitate and kill . . . . The new environmental surveillance system uses monitoring technology and methods developed in part by the Department of Energy's national laboratories. Samples of DNA are analyzed using polymerase chain reaction techniques, which examine the genetic signatures of the organisms in a sample, and make rapid and accurate evaluations of that organism . . . . Officials who helped develop the system said that tests performed at Dugway Proving Ground in Utah and national laboratories showed that the system would almost certainly detect the deliberate release of several of the most dangerous pathogens. ‘Obviously, the larger the release, the greater the probability that the agent will be detected,’ an official said. ‘But given the coverage provided by the E.P.A. system, even a small release, depending on which way the wind was blowing and other meteorological conditions, is likely to be picked up.’”
In an article titled, “Biodetectors Evolving, Monitoring U.S. Cities,” by Sally Cole in the May 2003 issue of Homeland Security Solutions, it was reported, “The anthrax letter attacks of 2001, and subsequent deaths of five people, brought home the reality of bioterrorism to Americans and provided a wake-up call for the U.S. government about the need for a method to detect and mitigate the impact of any such future attacks. Long before the anthrax letter attacks, scientists at two of the U.S. Department of Energy's national laboratories, Lawrence Livermore National Laboratory (LLNL) and Los Alamos National Laboratory (LANL), were busy pioneering a “biodetector” akin to a smoke detector to rapidly detect the criminal use of biological agents. This technology is now expected to play a large role in the U.S. government's recently unveiled homeland security counter-terrorism initiative, Bio-Watch, which is designed to detect airborne bioterrorist attacks on major U.S. cities within hours. Announced back in January, Bio-Watch is a multi-faceted, multi-agency program that involves the U.S. Department of Energy, the Environmental Protection Agency (EPA), and the U.S. Department of Health and Human Services' Centers for Disease Control and Prevention (CDC). Many of the EPA's 3,000 air-quality monitoring stations throughout the country are being adapted with biodetectors to register unusual quantities of a wide range of pathogens that cause diseases that incapacitate and kill, according to the EPA. The nationwide network of environmental monitors and biodetectors, which reportedly will eventually monitor more than 120 U.S. cities, is expected to detect and report a biological attack within 24 hours. Citing security reasons, the EPA declined to disclose further details about the program at this time . . . . The Autonomous Pathogen Detection System (APDS) is a file-cabinet-sized machine that sucks in air, runs tests, and reports the results itself. APDS integrates a flow cytometer and real-time PCR detector with sample collection, sample preparation, and fluidics to provide a compact, autonomously operating instrument capable of simultaneously detecting multiple pathogens and/or toxins. The system is designed for fixed locations, says Langlois, where it continuously monitors air samples and automatically reports the presence of specific biological agents. APDS is targeted for domestic applications in which the public is at high risk of exposure to covert releases of bioagents—subway systems, transportation terminals, large office complexes, and convention centers . . . . APDS provides the ability to measure up to 100 different agents and controls in a single sample,’ Langlois says. ‘It's being used in public buildings right now.’ The latest evolution of the biodetector, APDS-II, uses bead-capture immunoassays and a compact flow cytometer for the simultaneous identification of multiple biological simulants. Laboratory tests have demonstrated the fully autonomous operation of APDS-II for as long as 24 hours.”
SUMMARYFeatures and advantages of the present invention will become apparent from the following description. Applicants are providing this description, which includes drawings and examples of specific embodiments, to give a broad representation of the invention. Various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this description and by practice of the invention. The scope of the invention is not intended to be limited to the particular forms disclosed and the invention covers all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the claims. (0008) The present invention provides an autonomous monitoring apparatus for monitoring air, water, soil, or other substance for bioagents. A collector gathers a quantity of the air, water, soil, or other substance being monitored. The collector separates selected potential bioagent particles from the air, water, soil, or other substance that is being collected. A sample preparation system prepares a sample of the selected potential bioagent particles. The sample is analyzed by a system for detecting said bioagents.
One embodiment includes a wash assay sample preparation system for preparing a sample of the selected potential bioagent particles. The wash assay sample preparation system is operatively connected to the collector and prepares the sample from the air, water, soil, or other substance gathered by the collector. The wash assay sample preparation system includes optically-encoded beads, a number of reagents, a washing buffer, and a detector for detecting any bioagents in the sample.
Another embodiment includes a no-wash assay sample preparation system for preparing a sample of the selected potential bioagent particles. The no-wash assay sample preparation system is operatively connected to the collector for preparing the sample from the air, water, soil, or other substance gathered by the collector. The no-wash assay sample preparation system includes optically-encoded beads, a number of reagents, and a detector for detecting any bioagents in the sample.
Another embodiment of the present invention provides an apparatus for sampling air and collecting sample particles of a predetermined particle size range from the air for autonomous monitoring air, water, soil, or other substance for bioagents. A low pass section has an opening for gathering said air. A prescreen unit is positioned in the opening that prevents large particles from blocking the opening.
The invention is susceptible to modifications and alternative forms. Specific embodiments are shown by way of example. It is to be understood that the invention is not limited to the particular forms disclosed. The invention covers all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the claims.
BRIEF DESCRIPTION OF THE DRAWINGSThe accompanying drawings, which are incorporated into and constitute a part of the specification, illustrate specific embodiments of the invention and, together with the general description of the invention given above, and the detailed description of the specific embodiments, serve to explain the principles of the invention.
Referring now to the drawings, to the following detailed description, and to incorporated materials, detailed information about the present invention is provided including the description of specific embodiments. The detailed description and the specific embodiments serve to explain the principles of the invention. The invention is susceptible to modifications and alternative forms. The invention is not limited to the particular forms disclosed. The invention covers all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the claims.
Terrorists sending anthrax-contaminated packages. Militant organizations obtaining potassium cyanide. Religious cult members poisoning local residents to fix an election. Sadly, these scenarios are not the plots of the three latest bestsellers, but rather, very real incidents with a very real danger. By the mid-1990s, the U.S. Congress began to assess the vulnerability of the U.S. civilian population to biological terrorism and found us considerably lacking in our ability to cope with even a small-scale biological event. Initial thinking was that Department of Defense technology could be readily transferred to the civilian arena. However, upon further reflection, it was concluded that although there was overlap between military and civilian defense needs, in the case of a biological threat, there are marked differences: (1) the soldier is trained and equipped with protective gear so he may respond to a threat quickly enough to prevent a lethal dose; (2) military intelligence usually reduces the potential threat to a relatively small number of biological agents; and, (3) military battlefield tactics are designed to minimize the density of soldiers. The civilian population, however, is neither trained nor equipped, is vulnerable to any conceivable pathogen and often gathers in large crowds (special events, sporting venues, etc.) where a small release could potentially infect thousands. In response to these differences, federal agencies, including Department of Energy, have recently begun funding directed research efforts to reduce civilian biological terrorist vulnerabilities.
At present there are more than 30 pathogens and toxins on various agency threat lists. Public health personnel rarely see most, of the pathogens so they have difficulty identifying them quickly. In addition, many pathogenic infections aren't immediately symptomatic, with delays as long as several days, limiting options to control the disease and treat the patients. The lack of a practical monitoring network capable of rapidly detecting and identifying multiple pathogens or toxins on current threat lists translates into a major deficiency in the United States ability to counter biological terrorism.
Referring now to
After the collection 101, the sample is transferred as shown by arrow 102 for sample preparation 103. The sample preparation 103 provides an automated sample, an immunoassay sample, and/or a nucleic acid assay sample. In sample preparation 103 the sample may be concentrated, purified, lysed, pulverized or otherwise made to have smaller particulates, mixed, and/or amplified.
After sample preparation 103, the sample is transferred as shown by arrow 104 for detection. In one embodiment of the autonomous pathogen detection system 100, the detection is by a multiplex immunoassay detector. In another embodiment of the autonomous pathogen detection system 100, the detection is by a multiplex PCR detector. The detection may also be performed in the same location as the sample preparation, in which case the transfer arrow 104 is not required.
The autonomous pathogen detection system 100 provides an apparatus and method for monitoring air, water, soil, or other substance for particles containing bioagents. The autonomous pathogen detection system 100 comprises a collector for gathering the air, water, soil, or other substance being monitored; sample preparation system for preparing a sample from the air, water, soil, or other substance gathered by the collector; and a detector for detecting any bioagents in the sample. In one embodiment the collector is an aerosol collector. In other embodiments the collector gathers water, soil, or other substances. The collector in one embodiment includes separator system for separating the particles of interest from other particles. The particles of interest are of a predetermined size range.
In one embodiment the collector is an aerosol collector that collects air and includes a system for separating the air into a bypass air flow that does not contain the particles of a predetermined particle size range and a product air flow that does contain the sample particles of a predetermined particle size range. A wetted-wall cyclone collector receives the product air flow and traps and concentrates the particles of a predetermined particle size range in a liquid.
In one embodiment the sample preparation system is automated. In one embodiment the sample preparation system provides an immunoassay sample. In another embodiment the sample preparation system provides a nucleic acid assay sample. In another embodiment the sample preparation system includes concentration of the air, water, soil, or other substance. In another embodiment the sample preparation system includes purification of the air, water, soil, or other substance. In another embodiment the sample preparation system includes lysis of the air, water, soil, or other substance. In another embodiment the sample preparation system includes mixing of the air, water, soil, or other substance. In another embodiment the sample preparation system includes amplification.
In one embodiment of the autonomous pathogen detection system 100, the detector is a multiplex immunoassay detector. In one embodiment of the autonomous pathogen detection system 100, the detector is a multiplex PCR detector.
The primary focus of the autonomous pathogen detection system 100 is the protection of civilians from terrorist attacks; however, the system also has a role in protecting military personnel from biological warfare attacks. The autonomous pathogen detection system 100 also has uses in medical facilities and research and development facilities. The autonomous pathogen detection system 100 has uses in medical monitoring. There are a variety of medical applications where monitoring for biological pathogens would be useful. A good example of this is monitoring in hospitals and clinics for highly infectious agents such as tuberculosis or nosocomial diseases that can threaten the well being of patients and health care professionals. The autonomous pathogen detection system 100 also has uses in environmental monitoring, that is, any application that would benefit from environmental monitoring of biological species. One example is continuous aerosol monitoring of bacterial and other pathogens that could affect the health of livestock (such as the recent hoof and mouth disease outbreak). Another example is continuous aerosol monitoring of viruses that could affect the health of large portions of the population (such as the recent SARS outbreak).
Referring now to
After the collection 201, the sample is transferred as illustrated by arrow 202 for sample preparation 203. The sample preparation 203 provides an automated sample, an immunoassay sample, and/or a nucleic acid assay sample. In the sample preparation 203 the sample may be concentrated, purified, lysed, pulverized or otherwise made to have smaller particulates, mixed, and/or amplified.
After sample preparation 203, the sample is transferred as illustrated by arrow 204 for detection. In one embodiment of the autonomous pathogen detection system 200, the detection is by a multiplex immunoassay detector. In another embodiment of the autonomous pathogen detection system 200, the detection is by a multiplex PCR detector.
After sample preparation 203 and detection 205 when a pathogen has been detected, a sample is transferred from sample preparation 203 to the confirmation module 207. This is illustrated by arrow 206 in
The autonomous pathogen detection system 200 provides an apparatus and method for monitoring air, water, soil, or other substance for particles containing bioagents. The autonomous pathogen detection system 200 comprises a collector for gathering the air, water, soil, or other substance being monitored; sample preparation system for preparing a sample from the air, water, soil, or other substance gathered by the collector; a detector for detecting a bioagents in the sample; and a system for confirmation of a bioagent in the sample. In one embodiment the collector is an aerosol collector. In other embodiments the collector gathers water, soil, or other substances. The collector in one embodiment includes separator system for separating the particles of interest from other particles. The particles of interest are of a predetermined size range.
In one embodiment the collector is an aerosol collector that collects air and includes system for separating the air into a bypass air flow that does not contain the particles of a predetermined particle size range and a product air flow that does contain the sample particles of a predetermined particle size range. A wetted-wall cyclone collector receives the product air flow and traps and concentrates the particles of a predetermined particle size range in a liquid.
In one embodiment the sample preparation system is automated. In one embodiment the sample preparation system provides an immunoassay sample. In another embodiment the sample preparation system provides a nucleic acid assay sample. In another embodiment the sample preparation system includes concentration of the air, water, soil, or other substance. In another embodiment the sample preparation system includes purification of the air, water, soil, or other substance. In another embodiment the sample preparation system includes lysis of the air, water, soil, or other substance. In another embodiment the sample preparation system includes mixing of the air, water, soil, or other substance. In another embodiment the sample preparation system includes amplification of the sample.
In one embodiment of the autonomous pathogen detection system 200, the detector 205 is a multiplex immunoassay detector. In one embodiment of the autonomous pathogen detection system 200, the detector 205 is a multiplex PCR detector.
In one embodiment of the autonomous pathogen detection system 200, the system 207 for confirmation of a bioagent in the sample is a multiplex immunoassay detector. In one embodiment of the autonomous pathogen detection system 200, the system 207 for confirmation of a bioagent in the sample is a multiplex PCR detector. In one embodiment of the autonomous pathogen detection system 200, the system 207 for confirmation of a bioagent in the sample is a real-time PCR detector.
Referring now to
The APDS 300 provides a stand-alone pathogen detection system capable of rapid, continuous, low cost environmental monitoring of multiple airborne biological threat agents. The system 300 provides a “Detect to Protect/Warn” system with a number of key properties. The system 300 is capable of detecting pathogens within a 1-2 hour time window, allowing for enough time to respond to an event. The system 300 is extremely low cost to maintain, since continuous monitoring is essential for many applications. The system 300 has sufficient sensitivity to cover a broad geographical area (limiting the necessary number of sensors) and has sufficient selectivity to virtually eliminate false positives.
Multiplexed assays are used to reduce reagent costs, making long term monitoring operations possible. An orthogonal detection section combines antibody-based and nucleic acid-based assays and reduces false positives to a very low level. Antibody assays allow the detector to respond to all types of bioagents, including those without nucleic acids such as protein toxins. Nucleic acid assays allow much more sensitive detection, reducing the number of sensors needed to protect a given area. The fully autonomous aerosol collection and sample preparation capabilities limit maintenance requirements and makes integration into a central security or monitoring network possible.
Referring again to
In the “detection” sub-system, a collected sample is mixed with optically encoded microbeads. Each color of microbead contains a capture assay that is specific for a given bioagent. Fluorescent labels are added to identify the presence of each agent on the bound bead. Each optically encoded and fluorescently labeled microbead is individually read in a flow cytometer, and fluorescent intensities are then correlated with bioagent concentrations.
In the “confirmation” sub-system, PCR amplification and detection of nucleic acids confirms the presence of the bioagent. An archived sample is mixed with the TaqMan real-time PCR reagent, and then introduced by a SIA system into a flow-through polymerase chain reaction (PCR) system. Specific nucleic acid signatures associated with the targeted bioagent are amplified and detected using fluorescence generated from nucleic acid replication from the TaqMan probes.
In the “Integrated Remote Control and Feedback” sub-system, a central computer uses a simple serial based LabVIEW control system to control all instrument functions. A software system provides data acquisition, real-time data analysis, and result reporting via a graphical user interface.
The APDS 300 is integrated into a self-contained “ATM” style chassis. All fluids and reagents are contained in the instrument. The ADPS 300 includes the following subsystems: Aerosol Collection 301, In-Line Sample Preparation 302, Detection—Liquid-Array Based Multiplex Immunoassay Detection and/or Nucleic Assays Detection 303, Confirmation—In-Line Nucleic Acid Amplification and Detection 304, and Integrated Remote Control and Feedback 305. The subsystem will be described in greater detail.
APDS Aerosol Collection—301
The first stage of the APADS 300 is “aerosol collection” that provides collection of airborne particles that could contain targeted bioagents. Aerosol release of bioagents is considered one of the possible scenarios of a terrorist organization. One of the methods of rapidly exposing a large population to a biowarfare agent is through use of an aerosol (witness the effect of the recent, relatively small-scale anthrax mailroom releases). The aerosol collection system 301 continuously samples the air and traps particles in a swirling liquid solution. Particles of a given size distribution are selected by varying the flow rate across a virtual impactor unit.
The aerosol collection system 301 is a multi-stage aerosol collector that utilizes a low pass aerosol section and a virtual impactor preconcentration that delivers the particles of interest to a wetted wall cyclone collector. The virtual impactor preferentially captures particles 1-10 micrometer (micron) which is the size of particles most likely to be captured in the human lung. In the wetted wall cyclone collector, the particles are collected in a fluid, making downstream processing much easier. The fans and inputs to the obtain high collection rates, up to 3000 liters of air per minute flow through the detection system, allowing many particles to be collected over a short period. The aerosol collection system provides improved sensitivity and reduced collection times. An on-board computer controls air flow rates and the size range of particles collected.
As shown by
As best illustrated by
Referring now to
As best illustrated by
To efficiently pass the smaller particulate, the cap 402B is a “passive” device in that is has no moving parts and uses the fact that particulate with a finite mass and moving in a flow stream (in this case air) will not follow the streamlines exactly due to their inertia. If the curvature of a streamline is sufficiently large and the mass of the particulate is correspondingly high, the particle deviates far enough from the streamline to impact with a surface. The particles are drawn through the pre-screen 404B into the annular slot 401B and directed into the transition section 409B. In operation of the embodiment 300B, nightly clean-in-place protocols are implemented to keep the walls of the wetted-wall-cyclone clean using reagents such as dilute bleach and surfactant solutions. Also, the optical bubble counter is cleaned periodically with a pipe-cleaner, catheter, or other such tool.
The APDS 300A has the capability to measure particle sizes in the sampling environment via a built in particle counter with four size ranges, and can store and display the results in real-time. The system is entirely self-contained requiring only a 110 V ac power connection. The on-board computer has high-speed communications capability allowing networks of these sampling systems to be remotely operated.
The APDS 300A is useful for most environmental sampling. It is particularly useful with biological material collection, but can be used for collecting any airborne matter. The APDS 300A can be used to sample air quality in public buildings such as convention centers and sports arenas, for sampling in food processing facilities, sampling animal pens (such as poultry houses), or for use in monitoring orchards or agricultural areas for the presence of pollens or pesticides. Because of its relatively compact size and weight it can be used to sample in confined spaces such as found in aircraft or subway systems.
Referring now to
The flow forms streamlines 605. Small particles with low inertia 606 follow the flow streamlines and are carried away radially with the major flow 603. Large particles with greater inertia 607 deviate from the flowlines but they continue moving axially in their forward path down the collection probe 602 with the minor or “product” flow 604. The separation efficiency is determined by the ratio of the major and minor flows (or Bypass to Product) and the physical dimensions of the nozzle D0 and collection probe D1. The key is particulate larger than the cut size become concentrated in the minor flow. The concentration factor is the ratio of the total flow to the minor flow.
Referring now to
The product flow particles enter a stainless steel funnel section into the input of a multistage, wetted-wall cyclone collector section 700. The system includes a cyclone collector 701, peristaltic pump 707, an air pump 704, a vent 706, wash 705, 8 liter DD-H2O (double deionized water) reservoir 702, and 1 liter bleach reservoir 703. The reservoirs 702 and 703 are provided as external tanks outside of the front panel interface 708. The multistage, wetted-wall cyclone collector section 700 directs the particles of interest to the sample preparation system 302.
The on-board computer monitors and controls the flow of air through the system using built in hot wire anemometers that have been mounted in the two exhaust ports of the sampler. The computer and control software also act to control the liquid level in the cyclone, and monitor all status indicators of the sampling system. At a selected time the computer will stop the flow of air and turn on a built-in peristaltic pump to deliver the collected liquid sample via an external sample port. The system also has the capability to measure particle sizes in the background environment via a built in particle counter such as particle counter Biotest APC-1000, with four size ranges, and can store and display the results in real-time.
The system 300 is entirely self-contained requiring only a 110 vac power connection. The on-board computer has high-speed communications capability allowing networking of multiple sampling systems to be remotely operated. The computer has extra RS-232 or RS-485 serial ports that can be used to control other instrumentation. A keyboard, mouse, printer, displays, and other peripherals can be “plugged” in at the rear of the system, or it can be started “headless” (headless=Without a display, mouse, etc.)
Referring now to
The HiCRASS system provides a very high volume flow of aerosol particles (e.g., up to 3313 Lpm) that are drawn into the annular slot 401 formed in the cap 402 that is designed to limit the upper or larger particulate size range as they enter the collector. The annular slot 401 allows the passage of particles smaller than 10 microns. To efficiently pass the smaller particulate, the cap 402 is a “passive” device in that is has no moving parts and uses the fact that particulate with a finite mass and moving in a flowstream (in this case air) will not follow the streamlines exactly due to their inertia. The curvature of the streamline is sufficiently large and the mass of the particulate is correspondingly high that the particle deviates far enough from the streamline to impact with a surface. The accepted particles continue around the corner and onto the dichotomous virtual impaction section 403 that returns substantially all the aerosol particles smaller than 1-micron back into the environment.
The virtual impactor 403 works as the aerosol passes through an accelerating nozzle 601 and is directed toward a collection probe 602 where a major portion of the flow 603 is diverted 90° away from it. The flow forms streamlines 605. Small particles with low inertia 606 follow the flow streamlines and are carried away radially with the major flow 603. Large particles with greater inertia 607 deviate from the flowlines but they continue moving axially in their forward path down the collection probe 602 with the minor or “product” flow 604. The separation efficiency is determined by the ratio of the major and minor flows (or Bypass to Product) and the physical dimensions of the nozzle D0 and collection probe D1. Particulate larger than the cut size become concentrated in the minor flow. The concentration factor is the ratio of the total flow to the minor flow. (If the minor flow is 25% of the total flow, then the concentration factor is 4).
The remaining particles (1-10 microns) now known as the product 604, flow down a stainless steel funnel section into the input of the multistage, wetted-wall cyclone collector section 700. In this stage of the system 301 the product particles are trapped and concentrated into a liquid, typically water, in a volume between 2 and 7 cc. The wetted-wall cyclone collector section 700 is a system that causes the product flow particles 604 to be collected by a liquid. The wetted-wall cyclone collector section 700 operates by forcing the air stream tangentially into a cylinder causing the air stream to circulate around the inside of the cylinder. Particles in the air stream having sufficient inertia will collide with the interior wall where they are collected by the liquid that circulates along the interior wall.
The on-board computer 714 monitors and controls the flow of air through the system using built-in hot wire anemometers, as well as controlling the liquid level in the cyclone 700. At a selected time the computer 714 will stop the flow of air and turn on a built-in peristaltic pump to deliver the sample via an external sample port. The on-board computer 714 monitors and controls the flow of air through the system using built in hot wire anemometers that have been mounted in the two exhaust ports of the sampler. The computer and control software also act to control the liquid level in the cyclone, and monitor all status indicators of the sampling system. At a selected time the computer will stop the flow of air and turn on a built-in peristaltic pump to deliver the collected liquid sample via an external sample port.
The system also has the capability to measure particle sizes in the sampling environment via a built in particle counter such as particle counter Biotest APC-1000, with four size ranges, and can store and display the results in real-time. The system is entirely self-contained requiring only a 110 vac power connection. The on-board computer has high-speed communications capability allowing networks of these sampling systems to be remotely operated.
Referring now to
A low pass section 902 has an opening of a preselected size for gathering the air 901 but excluding particles larger than the sample particles. In one embodiment, the opening of a preselected size is an annular slot that only allows the passage of particles smaller than 10 microns. The low pass section 902 produces a total air flow 903 that contains the sample particles of a predetermined particle size range. The low pass section 902 allows a very high volume flow of air to be drawn through the preselected size opening. In one embodiment, the very high volume flow of air is 3313 Lpm or less.
An impactor section 904 is connected to the low pass section 902 and receives the total air flow 903. The impactor section 904 separating the total air flow 903 into a bypass air flow 905 that does not contain the sample particles and a product air flow 906 that does contain the sample particles. An accelerating nozzle and a collection probe in the impactor section 904 diverts the bypass air flow 90° from the product air flow thereby separating the bypass air flow and the product air flow. In one embodiment, the bypass air flow and the product air flow separation is determined by the ratio of the bypass air flow and the product air flow. In one embodiment, the bypass air flow and the product air flow separation is determined by the physical dimensions of the accelerating nozzle and the collection probe. In one embodiment, the bypass air flow and the product air flow separation is determined by the ratio of the bypass air flow and the product air flow and the physical dimensions of the accelerating nozzle and the collection probe.
A wetted-wall cyclone collector section 907 is connected to the impactor section 904. The wetted-wall cyclone collector section 907 receives the product air flow 906 and traps the sample particles in a liquid. The sample particles of a predetermined particle size range are concentrated in the liquid. In one embodiment, the wetted-wall cyclone collector section 907 traps and concentrates the sample particles into a liquid in a volume between 2 and 7 cc. In one embodiment, the liquid is water.
The system 900 is useful for most environmental sampling. It is particularly useful with biological material collection, but can be used for collecting any airborne matter. The system 900 can be used to sample air quality in public buildings such as convention centers and sports arenas, for sampling in food processing facilities, sampling animal pens (such as poultry houses), or for use in monitoring orchards or agricultural areas for the presence of pollens or pesticides. Because of its relatively compact size and weight it can be used to sample in confined spaces such as found in aircraft or subway systems.
APDS In-Line Sample Preparation—302
As best illustrated in
The prior art sample preparation instrumentation uses robotic manipulation of micropipettes coupled to disposable filter wells. Robotics are inherently complex and difficult to scale. The sample preparation module 302 uses Zone fluidics. Zone fluidics is the precisely controlled physical, chemical, and fluid-dynamic manipulation of zones of miscible and immiscible fluids in narrow bore conduits to accomplish sample conditioning and chemical analysis. A zone is a volume region within a flow conduit containing at least one unique characteristic. A unit operation in zone fluidics comprises of a set of fluid handling steps intended to contribute to the transformation of the sample into a detectable species or prepare it for manipulation in subsequent unit operations. Examples of unit operations include sample filtering, dilution, enrichment, medium exchange, headspace sampling, solvent extraction, matrix elimination, de-bubbling, amplifying, hybridizing, and reacting. In current analytical practice many of these steps are handled manually or in isolated pieces of equipment. Integration is scant at best, and there is a high degree of analyst involvement. In zone fluidics, sample and reagent zones are subjected to these unit operations in a sequential manner being transported from one unit operation to the next under fluidic control.
Samples in zone fluidics are not limited to liquids. Rather, gases, and suspensions containing solids or cells are also included. Where solid samples are used, particles are limited to a size that ensures no blockages. In most cases, reagents are prepared and then coupled to the zone fluidics manifold. The metering capability of the pump and mixing unit operations allow for reagents and standards to be prepared in situ. Reagents can therefore be presented to the zone fluidics manifold in an appropriately designed cartridge as ready-made, reagent concentrates, lyophilized, or crystalline form. Standards can be plumbed to the multi-position valve as discrete reservoirs providing the required range of concentrations. As for reagents though, standards can also be prepared in situ or diluted to cover a larger dynamic range.
The sample preparation module 302 uses a powerful, highly flexible technique called sequential injection analysis (SIA). Automation is achieved through the manipulation of small solution zones under conditions of controlled dispersion in narrow bore tubing. Zone fluidics makes use of a multi-position selection valve and a high precision, bi-directional pump to construct a stack of well-defined sample and reagent zones in a holding coil of narrow bore tubing. By appropriate manipulation of this zone stack, a wide range of sample handling unit operations can be accommodated. The pump is used to move the sample from one device to the next achieving the required sample manipulation in the process. Once a detectable species has been formed, the zone stack is transported to the immunoassay detector 303 and to the nucleic acid detector 304.
Various embodiments of system for sample preparation and detection have been described in connection with
The wash assay system embodiment uses a number of reagents in addition to the liquid sample. The reagents include detector antibody, and fluorescent reporter (streptavidin-phycoerythrin). In the wash assay system, a bed of beads is deposited on a filter then exposed to the sample, washing buffer, detector antibody, washing buffer, fluorescent reporter, washing buffer, and then the beads are released to the detector. For the wash assay system, the bead filter performance in releasing beads is improved by implementing frequent clean-in-place protocols using reagents such as bleach for cleaning and morpholine propane sulfonic acid (MOPS) citrate buffer for reconditioning the filter. This extends the time between servicing the instrument and thus reduces operating cost.
In the no-wash assay embodiment, the reagents are sequentially mixed but the embodiment does not include the filter or the wash steps. It has been shown that the wash assays are more sensitive and selective, providing better signal-to-noise ratios in response to bioagents.
Referring now to
The first stage of the system 1400 is “sample collection 1401” that provides collection of particles that could contain targeted bioagents. The sample collection 1401 gathers air, water, soil, or other substance being monitored. The sample collection 1401 separates selected potential bioagent particles from the air, water, soil, or other substance.
The “sample preparation 1402” moves the sample from the sample collection to appropriate modules within the system 1400 and provides sample preparation. In one mode, the sample preparation 1402 prepares the sample (Lysis, Concentration, Purification, Mixing, etc.) and delivers the sample to “Multiplex Amplification PCR 1403.” One mode provides “Multiplex, Liquid Array Based Detection of PCR Amplicons 1404.” An example of a flow cytometric detection method for DNA samples is shown in U.S. patent application 2002/0155482 by Shanavaz Nasarabadi, Richard G. Langlois, and Kodumudi Venkateswaran published Oct. 24, 2002. The disclosure of U.S. patent application 2002/0155482 is incorporated herein by reference.
Referring now to
The system 1501 for injecting and or aspirating a sample provides injection and/or aspiration of the sample. In one embodiment the injecting/aspirating system 1501 consists of a zone fluidics system. In another embodiment the injecting/aspirating system 1501 consists of an FIA system. The system 1501 for injecting and or aspirating a sample can be, for example, a injecting/aspirating device available under the trademark milliGAT™ pump, Global FIA, Inc., Fox Island, Wash.
The system 1502 for adding PCR reagent to the sample is operatively connected to the system 1501 for injecting and or aspirating a sample. The system 1502 for adding PCR reagent to the sample can be, for example, a unit for adding PCR reagent to the sample such as an injection or multi position selection valve, available from VICI, Houston, Tex.
The system 1503 for mixing the sample and the reagent is operatively connected to the system 1502 for adding PCR reagent to the sample. The mixing system 1503 mixes the sample with a PCR reagent. In one embodiment the PCR reagent includes primers. In another embodiment the PCR reagent includes oligos. The system 1503 for mixing the sample and the reagent can be, for example, a super serpentine reactor, available from Global FIA, Inc., Fox Island, Wash.
The system 1504 for transporting the sample and the reagent to a PCR reactor is operatively connected to the system 1503 for mixing the sample and the reagent. The system 1504 for transporting the sample and the reagent to a PCR reactor consists of a fluidics system. The system 1504 for transporting the sample and the reagent to a PCR reactor can be, for example, FEP tubing available from Cole-Parmer, Vernon Hills, Ill.
The system 1505 for performing PCR amplification is operatively connected to the system 1504 for transporting the sample and the reagent to a PCR reactor. This results in an amplified sample. In one embodiment the PCR amplification system 1505 includes an embedded thermocouple calibration conduit. PCR amplification devices are described in publications such as U.S. Pat. No. 5,589,136 for silicon-based sleeve devices for chemical reactions, assigned to the Regents of the University of California, inventors: M. Allen Northrup, Raymond P. Mariella, Jr., Anthony V. Carrano, and Joseph W. Balch, patented Dec. 31, 1996 and many are commercially available such as ABI PRISM® 7700 Sequence Detection System by Applied Biosystems; iCycler iQ Real-Time PCR Detection System by Bio-Rad; and Smart Cycler® System by Cepheid.
The system 1506 for transporting the amplified sample from the PCR reactor is operatively connected to the system 1205 for performing PCR amplification. The system 1506 for transporting the amplified sample from the PCR reactor can be, for example, FEP tubing available from Cole-Parmer, Vernon Hills, Ill.
The system 1507 for detection of PCR amplicons is operatively connected to the system 1506 for transporting the amplified sample from the PCR reactor. The system 1507 for detection of PCR amplicons can be, for example, a detection system described in publications and products produced by Cepheid and Baltimore-based Environmental Technologies Group, Inc. (ETG), a part of London-based Smiths Aerospace.
Conduits are included within the system 1501 for injecting and or aspirating a sample, system 1502 for adding PCR reagent to the sample, system 1503 for mixing the sample and the reagent, system 1504 for transporting the sample and the reagent to a PCR reactor, system 1505 for performing PCR amplification, system 1506 for transporting the amplified sample from the PCR reactor, and system 1507 for detection of PCR amplicons. A system 1508 for decontamination and conditioning the conduits is directly connected to the system 1507 for detection of PCR amplicons. The system 1508 for decontamination and conditioning the conduits is operatively connected to the system 1501 for injecting and or aspirating a sample, system 1502 for adding PCR reagent to the sample, system 1503 for mixing the sample and the reagent, system 1504 for transporting the sample and the reagent to a PCR reactor, system 1505 for performing PCR amplification, system 1506 for transporting the amplified sample from the PCR reactor, and system 1507 for detection of PCR amplicons. The decontamination and conditioning of all exposed conduits can be, for example, be performed by using a decontaminant, such as bleach, which is pumped through the exposed conduits and then washed from the system with a suitable wash solution.
Referring now to
In operation, a water sample collection unit 1601 continuously samples a water source. Water sampling systems are known in the art. For example, a water sampling system is shown in U.S. Pat. No. 6,306,350 issued Oct. 23, 2001 titled “Water Sampling Method and Apparatus With Analyte Integration.” The disclosure of U.S. Pat. No. 6,306,350 is incorporated herein by reference.
The in-line sample preparation unit 1602 concentrates the sample in a swirling buffer solution. Particles of a given size distribution are selected by varying the flow rate across a separator unit. The in-line sample preparation system 1602 provides all sample preparation steps (i.e., mix, wash, incubation, etc.), and performing multiplex detection using a Luminex flow cytometer.
In the “detection” sub-system 1603, a collected sample is mixed with optically encoded microbeads. Each color of microbead contains a capture assay that is specific for a given bioagent. Fluorescent labels are added to identify the presence of each agent on the bound bead. Each optically encoded and fluorescently labeled microbead is individually read in a flow cytometer, and fluorescent intensities are then correlated with bioagent concentrations.
In the “confirmation” sub-system 1604, PCR (nucleic acid) amplification and detection confirms the presence of the bioagent. An archived sample is mixed with the Taqman reagent, and then introduced by a SIA system into a flow through polymerase chain reaction (PCR) system. Specific nucleic acid signatures associated with the targeted bioagent are amplified and detected using fluorescence generated from nucleic acid replication from the Taqman probes. In the “Integrated Remote Control and Feedback” sub-system 1605, a central computer uses a simple serial based LabVIEW control system to control all instrument functions. A software system provides data acquisition, real-time data analysis, and result reporting via a graphical user interface.
The first stage of the system 1600 is “water sample collection 1601” that provides collection of particles from a source of water that could contain bioagents. The water sample collection system 1601 and in-line sample preparation 1602 provide preconcentration and delivery of the particles of interest to a wetted wall cyclone collector. The separator system captures particles of interest.
In the wetted wall cyclone collector, the particles are collected in a fluid, making downstream processing much easier. An on board computer controls water flow rates and the size range of particles collected. A particle counter provides real-time feedback on the size and quantity of particles collected.
Particles are drawn into the system that is designed to only allow the collection of particles of a pre-set size. The pre-set size can be selected as desired. The system is designed to only collect particles that are desired. The accepted particles continue on into a separator section that returns all the particles that are not of the desired size back into the environment. The remaining particles are known as the product flow. The product flow continues into the detection sections.
The system 1600 has the capability to measure particle sizes in the sampling environment via a built in particle counter with four size ranges, and can store and display the results in real-time. The system is entirely self-contained requiring only a power connection. The on-board computer has high-speed communications capability allowing networks of these sampling systems to be remotely operated.
The 1600 is useful for many application of water sampling. The system 1600 can be used to sample water quality in public buildings, for sampling in food processing facilities, for use in monitoring agricultural areas for the presence of pollens or pesticides and other water sampling uses.
Referring now to
In operation, a soil sample collection unit 1701 continuously samples a soil source. Soil sampling systems are known in the art. For example, a soil sampling system is shown in U.S. Pat. No. 6,363,803 titled “Vehicle Mounted Soil Sampler,” invented by Elmer Hubers, patented Apr. 2, 2002. The disclosure of U.S. Pat. No. 6,363,803 is incorporated herein by reference.
The in-line sample preparation unit 1702 concentrates the sample in a swirling buffer solution. Particles of a given size distribution are selected by varying the flow rate across a separator unit. The in-line sample preparation system 1702 provides all sample preparation steps (i.e., mix, wash, incubation, etc.), and performing multiplex detection using a Luminex flow cytometer.
In the “detection” sub-system 1703, a collected sample is mixed with optically encoded microbeads. Each color of microbead contains a capture assay that is specific for a given bioagent. Fluorescent labels are added to identify the presence of each agent on the bound bead. Each optically encoded and fluorescently labeled microbead is individually read in a flow cytometer, and fluorescent intensities are then correlated with bioagent concentrations.
In the “confirmation” sub-system 1704, PCR (nucleic acid) amplification and detection confirms the presence of the bioagent. An archived sample is mixed with the TaqMan reagent, and then introduced by a SIA system into a flow through polymerase chain reaction (PCR) system. Specific nucleic acid signatures associated with the targeted bioagent are amplified and detected using fluorescence generated from nucleic acid replication from the TaqMan probes. In the “Integrated Remote Control and Feedback” sub-system 1705, a central computer uses a simple serial based LabVIEW control system to control all instrument functions. A software system provides data acquisition, real-time data analysis, and result reporting via a graphical user interface.
The first stage of the system 1700 is “soil sample collection 1701” that provides collection of particles from a source of soil that could contain bioagents. The soil sample collection system 1701 and in-line sample preparation 1702 provide preconcentration and delivery of the particles of interest to a wetted wall cyclone collector. The separator system captures particles of interest.
In the wetted wall cyclone collector, the particles are collected in a fluid, making downstream processing much easier. An on board computer controls soil flow rates and the size range of particles collected. A particle counter provides real-time feedback on the size and quantity of particles collected.
Particles are drawn into the system that is designed to only allow the collection of particles of a pre-set size. The pre-set size can be selected as desired. The system is designed to only collect particles that are desired. The accepted particles continue on into a separator section that returns all the particles that are not of the desired size back into the environment. The remaining particles are known as the product flow. The product flow continues into the detection sections.
The system 1700 has the capability to measure particle sizes in the sampling environment via a built in particle counter with four size ranges, and can store and display the results in real-time. The system is entirely self-contained requiring only a power connection. The on-board computer has high-speed communications capability allowing networks of these sampling systems to be remotely operated. The 1700 is useful for many application of soil sampling. The system 1700 can be used to sample soil quality in monitoring agricultural areas for the presence of pollens or pesticides and other soil sampling uses.
Referring now to
The liquid-array based immunoassay detection system 1802 measures multiple pathogen targets in the sample. The immunoassay system 1802 can use either “wash assay” system or “no-wash assay” system. The “wash assay” system and the “no-wash assay” system use optically-encoded beads. The beads are kept in a small (˜15 mL) stirred tank. Bead loss from agglomeration is reduced by using dispersing agents such as ethanol in the bead slurry. This reduces reagent cost.
The wash assay system embodiment uses a number of reagents in addition to the liquid sample. The reagents include detector antibody, and fluorescent reporter (streptavidin-phycoerythrin). In the wash assay system, a bed of beads is deposited on a filter then exposed to the sample, washing buffer, detector antibody, washing buffer, fluorescent reporter, washing buffer, and then the beads are released to the detector. For the wash assay system, the bead filter performance in releasing beads is improved by implementing frequent clean-in-place protocols using reagents such as bleach for cleaning and morpholine propane sulfonic acid (MOPS) citrate buffer for reconditioning the filter. This extends the time between servicing the instrument and thus reduces operating cost.
In the no-wash assay embodiment, the reagents are sequentially mixed but the embodiment does not include the filter or the wash steps. It has been shown that the wash assays are more sensitive and selective, providing better signal-to-noise ratios in response to bioagents.
The PCR (nucleic acid) amplification and detection system 1803 confirms the presence of any bioagent. An archived sample is mixed with the TaqMan reagent, and then introduced by a system into a flow through polymerase chain reaction (PCR) system. Specific nucleic acid signatures associated with the targeted bioagent are amplified and detected using fluorescence generated from nucleic acid replication from the TaqMan probes.
The PCR assays for confirming immunoassay positives are implemented using real-time PCR and the TaqMan process. Both FAM and TAMRA dyes are used as TaqMan reporters and TAMRA and BHQ (Black Hole Quencher) dyes are used as TaqMan quenchers. In one embodiment the FAM-BHQ is used for the bioagent probe and TAMRA-BHQ for an internal control probe. This allows an internal control to be used on a two-color detector. Internal controls are critical in PCR due to the delicacy of the reaction; otherwise, negative results are not definitive. In one embodiment, two color excitation is used to give strong signals for duplexed TaqMan PCR (agent plus internal control).
In some embodiments, the PCR reagents for TaqMan PCR are stored on the system together as MasterMix (enzyme, buffer, dNTPs) mixed with primers and probes. In another embodiment it was found that storing the MasterMix in one reservoir and primers plus probes in another reservoir made the reagents more stable, potentially eliminating the need for cooling in the instrument. In one embodiment, extraction of DNA onto microfabricated silica pillars is used as a means of purifying DNA from PCR inhibitors.
Sample preparation moves the sample from the sample collection 1801 to appropriate modules within the system. The nucleic acid assay system 1803 includes a number of components including system for injecting/aspirating a sample, system for adding PCR reagent, system for mixing sample and reagent, system for transport to PCR reactor, system for performing PCR amplification, system for transport of amplified sample from PCR reactor for detection of PCR amplicons. A central computer 1805 uses a simple serial based LabVIEW control system to control all instrument functions. A software system provides data acquisition, real-time data analysis, and result reporting via a graphical user interface.
In operation of the pathogen detection system, the in-line nucleic acid amplification and detection system provides nucleic acid assay methods. The methods include a number of steps. One step consists of automatically injecting and or aspirating a sample. Another step consists of automatically adding PCR reagent to the sample. Another step consists of automatically mixing the sample and the reagent. Another step consists of automatically transporting the sample and the reagent to a PCR reactor. The PCR reactor consists of a fluidics system. Another step consists of automatically performing PCR amplification resulting in an amplified sample. Another step consists of automatically transporting the amplified sample from the PCR reactor. Another step consists of automatically detecting PCR amplicons. The method is performed in a nucleic acid assay system and the nucleic acid assay system is decontaminated and conditioned before a new sample is analyzed.
The system includes both real-time and post-PCR detection. The system is ideal for monitoring type systems, such as those currently being developed to detect terrorist releases of aerosolized bioagents. On-site detection systems for infectious diseases under development will need to incorporate sample preparation and analysis functions. The system allows relatively unskilled personnel, such as early responders, to perform real-time field or point-of-care nucleic acid assays. In various other embodiments of the autonomous pathogen detection system, the confirmation of bioagent(s) in the sample is provided by a multiplex immunoassay detector, a multiplex PCR detector, and a real-time PCR detector.
The present invention provides an Autonomous Pathogen Detection System (APDS) for monitoring the environment to protect the public from the release of hazardous biological agents. The Autonomous Pathogen Detection System is a countermeasure to bioterrorism, one of the most serious threats to the safety of United States citizens, citizens of other countries, and the military.
The APDS program was initiated to fill the requirement of a distributed environmental monitoring system for civilian applications. Multiplexed assays are used to reduce reagent costs, making long term monitoring operations possible (e.g., U.S. Postal Service mail screening). A unique, orthogonal detection approach that combines antibody-based and nucleic acid-based assays reduces false positives to a very low level. Antibody assays allow the detector to respond to all types of bioagents, including those without nucleic acids such as protein toxins. Nucleic acid assays allow much more sensitive detection, reducing the number of sensors needed to protect a given area. The fully autonomous aerosol collection and sample preparation capabilities limit maintenance requirements and makes integration into a central security or monitoring network possible.
There are other environmental or clinical pathogen detection system needs. Mobile units could be transported to suspected “sick buildings” to test for mold or fungal spores that might be causing tenant illnesses. Units with reagents for animal diseases could be placed in livestock transport centers or feedlots to rapidly detect airborne pathogens and protect against disease outbreaks. Monitors in hospitals could be used to test for airborne spread of contagious materials among patients. The system could be used at high profile events such as the Olympics for short-term, intensive monitoring or more permanent installation in major public buildings or transportation nodes. All of the individual units can be networked to a single command center so that a small group of technical experts can maintain and respond to alarms at any of the units. The system is capable of meeting all of these needs.
The primary needs describe above are directed to protection of civilians from terrorist attacks. The system also has uses in protecting military personnel from biological warfare attacks. The military continues to evaluate options to their current biowarfare detection systems and the system meets many of the needs of the military.
While the invention may be susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and have been described in detail herein. However, it should be understood that the invention is not intended to be limited to the particular forms disclosed. Rather, the invention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the following appended claims.
Claims
1. An autonomous monitoring apparatus for monitoring air, water, soil, or other substance for bioagents that could be in potential bioagent particles, comprising:
- collector means for gathering said air, water, soil, or other substance being monitored, said collector separating the potential bioagent particles from said air, water, soil, or other substance;
- sample preparation means for preparing a sample of the potential bioagent particles, said sample preparation means operatively connected to said collector means for preparing said sample from said air, water, soil, or other substance gathered by said collector;
- detector means for detecting said bioagents in said sample, said detector means comprising a liquid-array based multiplex immunoassay detector and a multiplex PCR detector.
2. The apparatus of claim 1 wherein said sample preparation means is a means for providing an immunoassay sample.
3. The apparatus of claim 2 wherein said means for providing an immunoassay sample is a multiplex immunoassay detector that utilizes optically encoded microbeads.
4. The apparatus of claim 1 wherein said sample preparation means is a means for providing a nucleic acid assay sample.
5. The apparatus of claim 1 wherein said multiplex PCR detector is a real time PCR detector.
6. The apparatus of claim 1 wherein said multiplex PCR detector includes means for performing PCR amplification.
7. An autonomous monitoring apparatus for monitoring air, water, soil, or other substance for bioagents, the bioagents potentially being in potential bioagent particles within the air, water, soil, or other substance, comprising:
- a collector for gathering said air, water, soil, or other substance being monitored, said collector separating selected potential bioagent particles from said air, water, soil, or other substance;
- a wash assay sample preparation system for preparing a sample of said selected potential bioagent particles, said wash assay sample preparation system operatively connected to said collector for preparing said sample from said air, water, soil, or other substance gathered by said collector; said wash assay sample preparation system including optically-encoded beads, a number of reagents, and a washing buffer; and
- a detector for detecting the bioagents in said sample, said detector operatively connected to said sample preparation system.
8. The apparatus of claim 7 wherein said reagents include detector antibodies.
9. The apparatus of claim 7 wherein said reagents include fluorescent reporters.
10. The apparatus of claim 7 wherein said wash assay sample preparation system includes a filter.
11. The apparatus of claim 7 wherein said wash assay sample preparation system includes a filter and optically-encoded beads.
12. An autonomous monitoring apparatus for monitoring air, water, soil, or other substance for bioagents, the bioagents potentially being in potential bioagent particles within the air, water, soil, or other substance, comprising:
- a collector for gathering said air, water, soil, or other substance being monitored, said collector separating selected potential bioagent particles from said air, water, soil, or other substance;
- a no-wash assay sample preparation system for preparing a sample of said selected potential bioagent particles, said no-wash assay sample preparation system operatively connected to said collector for preparing said sample from said air, water, soil, or other substance gathered by said collector; said no-wash assay sample preparation system including optically-encoded beads and a number of reagents; and
- a detector for detecting the bioagents in said sample, said detector operatively connected to said sample preparation system.
13. An apparatus for sampling air and collecting sample particles of a predetermined particle size range from said air for monitoring air, water, soil, or other substance for bioagents, the bioagents potentially being in potential bioagent particles within the air, water, soil, or other substance, comprising:
- a low pass section having an opening for gathering said air,
- a pre-screen unit positioned in said opening that prevents large particles from blocking said opening,
- an impactor section operatively connected to said low pass section, said impactor section receiving said air and separating said air into a bypass air flow that does not contain said sample particles and a product air flow that contains said sample particles, and
- a sample preparation system for preparing a sample of the potential bioagent particles, said sample preparation system operatively connected to said impactor section for preparing said sample; and
- a detector for detecting the bioagents in said sample, said detector operatively connected to said sample preparation system.
14. The apparatus of claim 13 wherein said opening in said low pass section size is a slot and said pre-screen unit is a grill positioned in said opening.
15. The apparatus of claim 1 wherein said opening in said low pass section size is a slot and said pre-screen unit is a screen positioned in said opening.
16. The apparatus of claim 13 wherein said opening in said low pass section size is an annular slot and said pre-screen unit is an annular screen positioned in said opening.
17. A method of monitoring air, water, soil, or other substance for bioagents, said air, water, soil, or other substance containing potential bioagent particles of various sizes, comprising the steps of:
- gathering said air, water, soil, or other substance containing potential bioagent particles of various sizes;
- separating said potential bioagent particles by size and collecting said potential bioagent particles of a size range that are likely to contain said bioagents; and
- detecting said bioagents in said potential bioagent particles of a size range that are likely to contain said bioagents, said step of detecting said bioagents comprising mixing optically encoded microbeads with said potential bioagent particles and detecting said bioagents with said optically encoded microbeads.
18. The method of monitoring air, water, soil, or other substance for bioagents of claim 17 wherein said step of detecting said bioagents comprises exposing said microbeads to said air, water, soil, or other substance; depositing said microbeads on a filter; exposing said microbeads to a washing buffer, and releasing said microbeads to a detector.
19. The method of monitoring air, water, soil, or other substance for bioagents of claim 17 wherein said washing buffer comprises buffer solutions.
20. The method of monitoring air, water, soil, or other substance for bioagents of claim 18 wherein steps following releasing said microbeads to a detector includes using cleaning reagents for reconditioning said filter.
21. The method of monitoring air, water, soil, or other substance for bioagents of claim 20 wherein said cleaning reagents include bleach.
22. The method of monitoring air, water, soil, or other substance for bioagents of claim 20 wherein said cleaning reagents include morpholine propane sulfonic acid (MOPS) citrate buffer.
Type: Application
Filed: Nov 29, 2004
Publication Date: Mar 16, 2006
Applicant:
Inventors: John Dzenitis (Danville, CA), Steve Brown (Livermore, CA), Billy Colston (San Ramon, CA), Dora Gutierrez (Livermore, CA), Bruce Henderer (Livermore, CA), Benjamin Hindson (Belmont), Ramakrishna Madabhushi (Fremont, CA), Anthony Makarewicz (Livermore, CA), Don Masquelier (Tracy, CA), Mary McBride (Brentwood, CA), Thomas Metz (Tracy, CA), Shanavaz Nasarabadi (Livermore, CA), Ujwal Setlur (Livermore, CA), Sally Smith (Salida, CA), Kodumudi Venkateswaran (Livermore, CA)
Application Number: 11/000,491
International Classification: C12Q 1/68 (20060101); C12M 1/34 (20060101);
