US20050189286A1 - Filter device to capture a desired amount of material and methods of use - Google Patents
Filter device to capture a desired amount of material and methods of use Download PDFInfo
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- US20050189286A1 US20050189286A1 US11/112,186 US11218605A US2005189286A1 US 20050189286 A1 US20050189286 A1 US 20050189286A1 US 11218605 A US11218605 A US 11218605A US 2005189286 A1 US2005189286 A1 US 2005189286A1
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- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
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- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/06—Investigating concentration of particle suspensions
- G01N15/0606—Investigating concentration of particle suspensions by collecting particles on a support
- G01N15/0618—Investigating concentration of particle suspensions by collecting particles on a support of the filter type
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
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- G—PHYSICS
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- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
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- G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
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- G—PHYSICS
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- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/2813—Producing thin layers of samples on a substrate, e.g. smearing, spinning-on
- G01N2001/2826—Collecting by adsorption or absorption
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
- Y10T436/25375—Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
Definitions
- particulate material suspended in a liquid or gas, on a filter for purification, enrichment, observation or subsequent analysis.
- the quantity and characteristics of particulate material is important in manufacturing, for example, processes that utilize powders, pigments, fuels or lubricants. Particle evaluations are also used to assess contaminants in water or air such as pollen, asbestos and soot. Particulate material is sometimes used indirectly to assess proteins or chemicals, for example, beads coated with monoclonal antibody may be interacted with blood. Then these beads may be captured on a filter and assessed for bound protein.
- sample suspension means particulate material suspended in a liquid or gas.
- samplerial as used herein means biological cells, organisms, bacteria, viruses, or components of these, as well as organic and inorganic particulates or any other matter which may be captured or isolated on a filter. This captured material may be subsequently used to provide diagnostic and/or analytical information or be re-suspended or otherwise used. For example, captured material may be analyzed chemically or may be placed on a receiving surface, such as a microscope slide for analysis.
- the present invention is a filter device that provides a means to collect a desired amount of material.
- a pressure sensor is used substantially to monitor the flow rate through the filter.
- the pressure sensor may be combined with a valve that provides control over sample flow, and thus the collection of material.
- a pressure sensor and valve are integrated to form a pressure-sensitive check valve.
- the membrane filter or filter assembly themselves deform, acting as a pressure sensor and flow control mechanism.
- the present invention provides a novel apparatus incorporating a pressure transducer and means to substantially halt or otherwise adjust sample flow, providing a simple, reliable device to capture a desired amount of material without complex electronics.
- the present invention is easily automated to allow material from a plurality of samples to be captured on a membrane filter, simultaneously.
- a variety of pressure sensors are available with appropriate characteristics for exploitation within the present invention.
- material captured on a filter is intended for contract-transfer to a receiving surface, such as a microscope slide. Accordingly, for some applications when a relatively large filter is required, or the suspending fluids are viscous, for example, a filter support structure may be desirable.
- the present invention provides a filter apparatus using means to measure or sense the flow rate of a gas or liquid through a filter.
- pressure is sensed, however, the flow rate of a fluid or gas could also be sensed.
- the present invention terminates or otherwise adjusts sample flow when a predetermined amount of material has been captured on a filter for example by venting the pressure differential responsible for sample flow, or closing the flow pathway, for example with a valve.
- material collection on a filter is substantially reduced by restricting access to the filter, for example, by changing its position or deforming its shape.
- Filter types include fibrous and mesh membranes, porous and capillary porous membranes, and fabric and gel lattices, for example.
- filters are commonly made from paper, nylon, glass fibers, nitrocellulose, polypropylene, chemical gels etc.
- filters are further treated to enhance certain properties such as capture capacity, flexibility, selectivity or adherence by coating them or incorporating other compounds such as PTFE or protein binding compounds.
- filters can be formed in various shapes such as planar, conical, pyramidal, hemispherical, or spherical, or filters may have their shape imposed by a carrier or other support structure.
- FIG. 1 a (Prior art) Method to collect and monitor the concentration of material captured on a membrane filter.
- FIG. 1 b (Prior art) Membrane filter device used in conjunction with FIG. 1 .
- FIG. 2 a shows an embodiment of the present invention capturing a desired amount of material.
- FIG. 2 b shows another embodiment of the present invention capturing a desired amount of particulate material from a fluid suspension.
- FIG. 2 c shows the embodiment of FIG. 2 b used to capture a desired amount of material suspended in a gas.
- FIG. 3 a shows a membrane filter apparatus with pressure-sensitive check valve.
- FIG. 3 b shows another configuration of membrane filter apparatus.
- FIG. 3 c shows an embodiment of the present invention, incorporating a pressure-sensitive check valve in the form of spring tabs arranged around the periphery of a filter apparatus.
- FIG. 4 shows an embodiment of the present invention utilized to process a plurality of samples.
- FIG. 5 a shows a syringe filter assembly of an embodiment of the present invention where a deformable filter provides flow rate monitoring (pressure detection) and flow rate control.
- FIG. 5 b shows a desired amount of material collected on the syringe filter associated with FIG. 5 a.
- FIG. 6 a show yet another embodiment of a filter assembly to monitor and control or otherwise adjust flow rate through a filter.
- FIG. 6 b further describes the filter assembly associated with FIG. 6 a.
- FIG. 6 c shows an embodiment of a filter assembly at rest (under normal operating conditions).
- FIG. 6 d shows the filter assembly embodiment of FIG. 6 c in an activated state having responded to pressure changes indicative of collecting a desired amount of material.
- FIG. 1 a illustrates a system 10 to collect a desired quantity of cells onto the underside of a screen-type filter 12 .
- a pressure sensor 26 is in communication with both sides of a membrane filter 12 . Accordingly, one side of the membrane 12 in the collection vessel 18 is shown at ambient pressure with pressure sensor 26 provided on the opposite side of the membrane.
- Pressure unit 30 typically responds to electrical control signals from a control unit, which can be microprocessor-controlled, to apply selected fluid conditions to the interior of the collection vessel.
- FIG. 1 b (Prior art) further illustrates the collection vessel 18 with screen-type filter 12 as used in this apparatus, and as described in U.S. Pat. No. 6,010,909 and again in U.S. Pat. No. 6,225,125. In this manner, a desired quantity of material may be captured.
- FIG. 2 a shows an embodiment of the present invention with filter apparatus 205 comprised of filter 215 deposed between a top body member 210 and a bottom body member 220 .
- open container 235 contains sample suspension 230 (e.g. particulate material suspended in a liquid), which is introduced via pickup tube 245 .
- sample suspension 230 e.g. particulate material suspended in a liquid
- This pickup tube may comprise part of the bottom body member 220 or pickup tube 245 may be a separate member attached to body member 220 .
- the object of the device is to provide a means to monitor or otherwise sense the flow rate of this sample suspension 230 and to provide a means to alter, adjust, halt or otherwise influence that flow rate when indicated by a sensor 250 , which is in communication (mechanically or electro-mechanically) with the means to control flow.
- Sample suspension 230 is drawn by application of pressure from vacuum source 200 therefore providing a means to cause sample suspension 230 to flow as further indicated by flow directional arrow 240 , which as diagrammed, is in the inlet port 221 of the pickup tube 245 , into the bottom body member 220 , through the filter 215 , which is this instance is a membrane filter, through a flow control element 212 (in this instance a valve) and then out through the outlet port 211 .
- vacuum is used to cause the sample suspension to flow.
- sample suspension 230 flows in this manner, particulate material in the sample suspension 230 begins to be captured by membrane filter 215 .
- Pressure sensor or pressure transducer 250 in this instance contained substantially within the top body member 210 , communicates with the upper surface of membrane filter 215 . This communication is further indicated by communication arrow 270 .
- Pressure sensor 250 is also in communication with flow control element 212 so as to provide a means to adjust or otherwise control flow when certain pressures are sensed. This communication between pressure sensor 250 and flow control element 212 is further indicated by communication arrow 260 .
- a pressure differential is established across the membrane filter 215 , thereby providing a means for the pressure sensor 250 to monitor the flow rate of the sample suspension.
- particulate material that is smaller than the pore size of the membrane filter 215 passes through the membrane (to waste or to another vessel—not shown) while material larger than the pore size of the membrane filter 215 is captured. Since filter pores provide the actual pathway through a filter, material captured by the membrane filter 215 typically blocks pores, which in turn restricts flow.
- pressure sensor 250 responds (at a predetermined pressure based on the application, filter characteristic, amount of desired material etc.
- pressure sensor 250 activates and in turn activates flow control element 212 .
- the flow control element 212 may halt the flow of sample suspension 230 and hence stop further capture of material on the membrane filter 215 , which has now captured the desired amount of material. While such a valve (flow control element 212 ) could be implemented in various positions of within the filter assembly 205 , generally communication with pressure sensor 250 is simpler and provides more options when these two functions are relatively closely related. Further examples of this will be provided in the descriptions accompanying FIGS. 2 b and 2 c .
- Activation of the flow control element 212 may be mechanical, electromechanical or may be accomplished via further integration of the pressure sensor and valve (as will be further discussed).
- top body member 210 and bottom body member of filter apparatus 205 are preferably made separable, by employing threads or a press-fit assembly, for example.
- FIG. 2 b shows another embodiment of the present invention with sample suspension 230 being drawn through filter 215 by application of vacuum 200 .
- filter 215 is sealed to the bottom of upper body member 210 , thereby providing access to material captured by membrane filter 215 .
- the sensor 250 is integrated with flow control element 213 , which in this instance provides flow control using a valve to vent the pressure source 200 through vent port 214 or flow control valve 213 , rather than adjusting the sample flow pathway, as described in association with FIG. 2 a .
- the vent may substantially release the vacuum supplied by source 200 to halt flow, or the drop in vacuum provided by this venting may be sensed and the vacuum source, shut off.
- FIG. 2 c shows application of the device and configuration of the present invention described in association with FIG. 2 b where sample suspension 221 consists of particulate matter, for example, soot, suspended in a gas, for example air.
- sample suspension 221 consists of particulate matter, for example, soot, suspended in a gas, for example air.
- FIG. 3 a shows an embodiment of the present invention 300 comprised of a hollow main body 310 and a pressure-sensitive check valve 320 extending into the main body 310 so as to communicate with one side of a membrane filter 330 , which is attached to the underside of the main body 310 .
- a protrusion 335 may be provided on the bottom of the main body 310 or may be fashioned appropriately to stop the membrane filter 330 from contacting the bottom of a sample vessel (not shown) and disrupting flow during use.
- a vacuum source 360 is provided for sample aspiration. Initially, the vent portion 340 of the pressure-sensitive check valve 320 is closed and typically, the membrane filter 330 is fresh (free of sample material).
- sample suspension (not shown) through the membrane filter 330 causing material to collect on the underside of the membrane filter 330 . Accordingly, as material collects, the pores become occluded and the rate of flow of sample suspension decreases.
- the pressure-sensitive check value 320 monitors flow rate through the membrane filter 320 and when the flow rate falls to a desired level, thus indicating that a desired amount of material has been collected, the pressure-sensitive check valve 320 triggers (at a predetermined pressure) and sample flow (and material collection) is halted.
- the membrane filter 330 typically has relatively uniformly-distributed pores of a uniform size, intended to capture material larger than the pore size, while passing particulate material that is small.
- syringe filters a filter apparatus that is adapted to a syringe
- the sensor portion of the pressure-sensitive check valve 320 has been adjusted to trigger at a desired, predetermined pressure which is established to indicate capture of a desired quantity of material on the bottom surface of the membrane filter 330 .
- a desired, predetermined pressure which is established to indicate capture of a desired quantity of material on the bottom surface of the membrane filter 330 .
- a pathway is opened which vents off the vacuum, thereby stopping the aspiration of sample. While it is one object of the present invention to minimize or eliminate electronics that communicate with the pressure transducer or control systems, a battery-powered pressure transducer and/or valve assembly is consistent with this objective.
- the pressure-sensitive check valve 320 could be implemented in a variety of other ways so as to monitor and control sample flow, for example upon triggering it could close a fluid pathway.
- vacuum could be provided by a stepper-driven syringe, with one syringe for each sample.
- a vacuum pump and vacuum isolators may be preferred.
- material capture by the present invention may be transferred by contacting an appropriate receiving surface.
- monolayer deposition may be made to the underside of a cover-glass or other relatively thin, uniform material, such as transparent tape, thereby providing material at approximately the same distance from the top surface to facilitate focus.
- the thin receiving surface may be placed or affixed to a second surface as desired, or required.
- FIG. 3 b shows an alternative configuration of present filter device 300 , this time having upper body portion 315 and lower body portion 316 .
- a membrane filter 330 is shown to be sealed with the formed body by o-rings 325 .
- the upper and lower body portions 315 and 316 are designed so as to join and seal with the o-rings 325 , establishing conditions for sample flow to be substantially through the membrane filter 330 .
- it may be useful to re-suspend this material by back-flushing the filter.
- another filter device may be used to isolate a sub-component of the material collected.
- the upper body 315 and the lower body 316 should be made separable using a press-fit, threads or other convenient form of assembly.
- a pressure-sensitive check valve 320 is shown in communication with the upper body portion 315 of the filter 335 . Again, flow through the membrane filter 330 decreases with time due to progressive obstruction of the pores by material as it collects. The pressure-sensitive check valve 320 senses flow rate therefore, providing a measure of the amount of material captured by the membrane filter 330 .
- FIG. 3 c shows an embodiment of the present invention having a membrane filter 330 (not shown) attached on the lower surface of the device body 310 .
- a standoff 335 may be provided.
- the pressure-sensitive check valve 370 is integrated and implemented around the periphery of the apparatus with plastic spring tabs that operate as poppet valves. These are further diagrammed in expanded view.
- Plastic spring tab 376 has contact area 374 , tension sealed into vent hole 372 in the wall of the device body 310 .
- a single poppet valve of this type could function as a pressure-sensitive check valve for the intended use, such functionality has been implemented using a plurality of plastic poppet valves 370 distributed around the periphery of filter device 300 .
- applied vacuum 360 initiates the flow of sample suspension (not shown) through the membrane filter 330 .
- the pressure-sensitive poppet valves 370 are in communication with the upper side of the membrane filter 330 , so positioned so as to monitor the flow rate of material through the membrane filter 330 .
- the poppet valve(s) are set to trigger at a predetermined pressure to indicate when a desired quantity of material has been collected on the membrane filter 330 .
- the pressure-sensitive check valve 370 may be implemented with one or more contact tabs. Compound valves of this type may be adjusted to trigger or otherwise activate at a predetermined pressure. Similarly, the characteristics of the valve portion may also be made adjustable, for example, when used as a vent or fluid pathway the diameter of the valve could be adjusted. For some applications or reasons of manufacture, size, operating range, reliability, sensitivity, trigger rate, etc. it may be desirable to distribute a plurality of these plastic spring tabs around the periphery of the device, as shown. Such tab(s) may be affixed as separate units, be fabricated as a ring of units designed for insertion into the device body or it may be preferable to establish these pressure-sensitive check valve components as part of a molding process. Again, the application, costs and other factors may influence implementation.
- FIG. 4 shows a configuration of filter devices of the present invention for processing a plurality of samples.
- a vacuum manifold 400 distributes vacuum which is further isolated via vacuum chambers 410 .
- Material in suspension 430 begins to be aspirated into filter device(s) 420 . Accordingly, by selecting appropriate components, a plurality of similar or different samples may be processed simultaneously. Alternatively, each station may be established to capture the same amount of material, or different amounts of material as desired, or required.
- FIG. 5 a shows a filter device 500 of the present invention with a membrane filter 530 interposed between upper body 510 and lower body 520 .
- Sample suspension (not shown) enters through inlet port 525 , passes through the membrane filter 530 and exits via outlet port 515 .
- the membrane filter 530 is selected with sufficient deformability so as to generally conform to the interior surface 535 of the upper device body 510 when a desired amount of material (indicated by the reduced flow rate through the membrane filter 530 ) has been captured. Accordingly, flow is subsequently restricted to a smaller area of the membrane filter 530 , for example a single central fluid pathway, as diagrammed.
- FIG. 5 b shows such a filter 530 , as described in association with FIG. 5 a , having captured a desired amount of material in region 540 and providing reduced flow through a more restricted area of the filter 545 .
- sample flow may continue or be allowed to continue, for example, until area 545 occludes so as to slow or substantially reduce or stop sample flow, as such continuation has no subsequent effect as the desired amount of material has been captured in area 540 of the filter.
- the device may continue to draw sample as desired without substantially affecting the desired amount of material collected in region 540 .
- the upper body 315 and lower body 316 may be made separable to provide filter access.
- FIG. 6 a shows a filter device 600 of the present invention with a membrane filter assembly 650 interposed between upper body 610 and lower body 620 .
- Sample suspension (not shown) enters through inlet port 625 , passes through the membrane filter assembly 650 and exits via outlet port 615 .
- the membrane filter assembly 650 is comprised of a filter 660 and surrounding non-porous support structure 655 .
- the membrane filter assembly 650 acts as a pressure transducer, responding to a reduction in flow rate through the filter 660 as particulate material collects on the underside of the filter 660 .
- deformation of the filter, or in this instance the membrane filter assembly 650 provides the means to alter flow in response to the pressure differential across the membrane filter assembly 650 .
- FIG. 6 b shows the membrane filter assembly 650 having a filter area 660 supported by a surrounding non-porous support structure 655 .
- the support structure 655 has striations 665 allowing it to deform in a triggered motion when a predetermined pressure is sensed.
- material collecting on the underside of the filter 660 begins to occlude the filter 660 , contributing to a reduction in flow rate through the filter 660 and a pressure change across the membrane filter assembly 650 .
- the support structure triggers so as to conform to the inner surface as described in association with FIG. 5 a or the support structure may contact a valve as described in association with FIGS. 3 a, b and c so as to substantially stop sample flow and therefore halt material collection.
- FIG. 6 c shows a membrane filter assembly 670 having a filter area 680 in surrounding non-porous support structure 675 .
- the support structure 675 has striations 685 .
- the membrane assembly is diagrammed in a first state which is substantially maintained until the pressure differential across the membrane filter assembly 670 reaches a predetermined trigger point at which time the structure toggles or deforms to a second state.
- FIG. 6 d shows the membrane filter assembly 670 as discussed in association with FIG. 6 c in a triggered or deformed state.
- the membrane filter assembly 670 may itself provide a means to alter flow when the state toggles, indicating collection of a desired amount of material on the filter 680 .
- the state change may contact a valve, a switch or value interfaced to a switch so that flow through the membrane may be adjusted, or halted.
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Abstract
The present invention is a filter device with methods to capture a desired amount of material suspended in a liquid or gas. These filter capture methods may be used for the purification or enrichment of various sample constituents or captured material may be observed or analyzed. The filter device employs a deformable filter to provide a simple reliable device to capture a desired amount of material, with minimal electronic intervention.
Description
- This application is a divisional of U.S. patent application Ser. No. 10/263,129, filed on Oct. 2, 2002, and published as United States Published Patent Application No. 2004/0065622 A1, and claims priority from that application.
- In industry and biology it is often advantageous to capture particulate material suspended in a liquid or gas, on a filter for purification, enrichment, observation or subsequent analysis. The quantity and characteristics of particulate material is important in manufacturing, for example, processes that utilize powders, pigments, fuels or lubricants. Particle evaluations are also used to assess contaminants in water or air such as pollen, asbestos and soot. Particulate material is sometimes used indirectly to assess proteins or chemicals, for example, beads coated with monoclonal antibody may be interacted with blood. Then these beads may be captured on a filter and assessed for bound protein.
- As used herein, “sample suspension” means particulate material suspended in a liquid or gas. “Material” as used herein means biological cells, organisms, bacteria, viruses, or components of these, as well as organic and inorganic particulates or any other matter which may be captured or isolated on a filter. This captured material may be subsequently used to provide diagnostic and/or analytical information or be re-suspended or otherwise used. For example, captured material may be analyzed chemically or may be placed on a receiving surface, such as a microscope slide for analysis.
- Although there are a number of established methods to deposit mono-layers of material on a receiving surface for observation or analysis, controlling the amount of material collected on a filter is more difficult to achieve. Typically, electronic control and intervention is required to monitor and control the collection of material on a filter apparatus and/or other laboratory methods (employing particle counters and dilution techniques) are used to adjust the concentration of the material in suspension. Unfortunately, these methods require additional apparatus and electronics, and are relatively complex or expensive in terms of supplies, and time. Therefore, a simple, reliable method of capturing a desired amount of material on a filter would be advantageous.
- The present invention is a filter device that provides a means to collect a desired amount of material. To accomplish this, a pressure sensor is used substantially to monitor the flow rate through the filter. In addition, the pressure sensor may be combined with a valve that provides control over sample flow, and thus the collection of material. In one embodiment of the present invention, a pressure sensor and valve are integrated to form a pressure-sensitive check valve. In other embodiments the membrane filter or filter assembly themselves deform, acting as a pressure sensor and flow control mechanism.
- It would be beneficial to provide a simple filter apparatus to capture a desired amount of material on a filter that does not rely on relatively complex electronics and sensors. In addition, it would be advantageous to provide a filter capture method that can be automated to prepare a plurality of samples, simultaneously. Accordingly, as will be further described, the present invention provides a novel apparatus incorporating a pressure transducer and means to substantially halt or otherwise adjust sample flow, providing a simple, reliable device to capture a desired amount of material without complex electronics. In addition, the present invention is easily automated to allow material from a plurality of samples to be captured on a membrane filter, simultaneously.
- As previously discussed herein, a variety of pressure sensors are available with appropriate characteristics for exploitation within the present invention. For some applications material captured on a filter is intended for contract-transfer to a receiving surface, such as a microscope slide. Accordingly, for some applications when a relatively large filter is required, or the suspending fluids are viscous, for example, a filter support structure may be desirable.
- The present invention provides a filter apparatus using means to measure or sense the flow rate of a gas or liquid through a filter. In some embodiments pressure is sensed, however, the flow rate of a fluid or gas could also be sensed. In some embodiments, the present invention terminates or otherwise adjusts sample flow when a predetermined amount of material has been captured on a filter for example by venting the pressure differential responsible for sample flow, or closing the flow pathway, for example with a valve. In other embodiments of the present invention material collection on a filter is substantially reduced by restricting access to the filter, for example, by changing its position or deforming its shape.
- Filter types include fibrous and mesh membranes, porous and capillary porous membranes, and fabric and gel lattices, for example. Such filters are commonly made from paper, nylon, glass fibers, nitrocellulose, polypropylene, chemical gels etc. In some cases filters are further treated to enhance certain properties such as capture capacity, flexibility, selectivity or adherence by coating them or incorporating other compounds such as PTFE or protein binding compounds. Accordingly, filters can be formed in various shapes such as planar, conical, pyramidal, hemispherical, or spherical, or filters may have their shape imposed by a carrier or other support structure.
- The organization and manner of the structure and operation of the preferred embodiments of the invention, together with further objects and advantages thereof, may best be understood by reference to the following description, taken in connection with the accompanying drawings, wherein like reference numerals identify like elements in which:
-
FIG. 1 a (Prior art) Method to collect and monitor the concentration of material captured on a membrane filter. -
FIG. 1 b (Prior art) Membrane filter device used in conjunction withFIG. 1 . -
FIG. 2 a shows an embodiment of the present invention capturing a desired amount of material. -
FIG. 2 b shows another embodiment of the present invention capturing a desired amount of particulate material from a fluid suspension. -
FIG. 2 c shows the embodiment ofFIG. 2 b used to capture a desired amount of material suspended in a gas. -
FIG. 3 a shows a membrane filter apparatus with pressure-sensitive check valve. -
FIG. 3 b shows another configuration of membrane filter apparatus. -
FIG. 3 c shows an embodiment of the present invention, incorporating a pressure-sensitive check valve in the form of spring tabs arranged around the periphery of a filter apparatus. -
FIG. 4 shows an embodiment of the present invention utilized to process a plurality of samples. -
FIG. 5 a shows a syringe filter assembly of an embodiment of the present invention where a deformable filter provides flow rate monitoring (pressure detection) and flow rate control. -
FIG. 5 b shows a desired amount of material collected on the syringe filter associated withFIG. 5 a. -
FIG. 6 a show yet another embodiment of a filter assembly to monitor and control or otherwise adjust flow rate through a filter. -
FIG. 6 b further describes the filter assembly associated withFIG. 6 a. -
FIG. 6 c shows an embodiment of a filter assembly at rest (under normal operating conditions). -
FIG. 6 d shows the filter assembly embodiment ofFIG. 6 c in an activated state having responded to pressure changes indicative of collecting a desired amount of material. - While the invention may be susceptible to embodiment in different forms, there is shown in the drawings, and herein will be described in detail, specific embodiments with the understanding that the present disclosure is to be considered an exemplification of the principles of the invention, and is not intended to limit the invention to that as illustrated and described herein.
-
FIG. 1 a (prior art) illustrates asystem 10 to collect a desired quantity of cells onto the underside of a screen-type filter 12. As diagrammed, a pressure sensor 26 is in communication with both sides of amembrane filter 12. Accordingly, one side of themembrane 12 in thecollection vessel 18 is shown at ambient pressure with pressure sensor 26 provided on the opposite side of the membrane.Pressure unit 30 typically responds to electrical control signals from a control unit, which can be microprocessor-controlled, to apply selected fluid conditions to the interior of the collection vessel. -
FIG. 1 b (Prior art) further illustrates thecollection vessel 18 with screen-type filter 12 as used in this apparatus, and as described in U.S. Pat. No. 6,010,909 and again in U.S. Pat. No. 6,225,125. In this manner, a desired quantity of material may be captured. -
FIG. 2 a shows an embodiment of the present invention withfilter apparatus 205 comprised offilter 215 deposed between atop body member 210 and abottom body member 220. In this instance,open container 235 contains sample suspension 230 (e.g. particulate material suspended in a liquid), which is introduced viapickup tube 245. This pickup tube, as required or desired, may comprise part of thebottom body member 220 orpickup tube 245 may be a separate member attached tobody member 220. The object of the device, which will now be further described, is to provide a means to monitor or otherwise sense the flow rate of thissample suspension 230 and to provide a means to alter, adjust, halt or otherwise influence that flow rate when indicated by asensor 250, which is in communication (mechanically or electro-mechanically) with the means to control flow.Sample suspension 230 is drawn by application of pressure fromvacuum source 200 therefore providing a means to causesample suspension 230 to flow as further indicated by flowdirectional arrow 240, which as diagrammed, is in theinlet port 221 of thepickup tube 245, into thebottom body member 220, through thefilter 215, which is this instance is a membrane filter, through a flow control element 212 (in this instance a valve) and then out through theoutlet port 211. (In this embodiment, as well as in subsequently-described and illustrated embodiments, vacuum is used to cause the sample suspension to flow. Other means can be used for this purpose in this and subsequent embodiments, such as gravity or mechanical means such as a pump.) Accordingly, assample suspension 230 flows in this manner, particulate material in thesample suspension 230 begins to be captured bymembrane filter 215. Pressure sensor orpressure transducer 250, in this instance contained substantially within thetop body member 210, communicates with the upper surface ofmembrane filter 215. This communication is further indicated bycommunication arrow 270.Pressure sensor 250 is also in communication withflow control element 212 so as to provide a means to adjust or otherwise control flow when certain pressures are sensed. This communication betweenpressure sensor 250 andflow control element 212 is further indicated bycommunication arrow 260. Accordingly, a pressure differential is established across themembrane filter 215, thereby providing a means for thepressure sensor 250 to monitor the flow rate of the sample suspension. As sample continues to flow, and as described in association with the description of prior art inFIGS. 1 and 2 , particulate material that is smaller than the pore size of themembrane filter 215 passes through the membrane (to waste or to another vessel—not shown) while material larger than the pore size of themembrane filter 215 is captured. Since filter pores provide the actual pathway through a filter, material captured by themembrane filter 215 typically blocks pores, which in turn restricts flow. When the flow rate drops to a certain level,pressure sensor 250 responds (at a predetermined pressure based on the application, filter characteristic, amount of desired material etc. as previously described herein and in the prior art cited),pressure sensor 250 activates and in turn activatesflow control element 212. Theflow control element 212 may halt the flow ofsample suspension 230 and hence stop further capture of material on themembrane filter 215, which has now captured the desired amount of material. While such a valve (flow control element 212) could be implemented in various positions of within thefilter assembly 205, generally communication withpressure sensor 250 is simpler and provides more options when these two functions are relatively closely related. Further examples of this will be provided in the descriptions accompanyingFIGS. 2 b and 2 c. Activation of theflow control element 212 may be mechanical, electromechanical or may be accomplished via further integration of the pressure sensor and valve (as will be further discussed). Similarly, these elements may be physically separate or may be functionally integrated. For applications, such as monolayer deposition, that may require access to the filter for touch or other material transfer method, thetop body member 210 and bottom body member offilter apparatus 205 are preferably made separable, by employing threads or a press-fit assembly, for example. -
FIG. 2 b shows another embodiment of the present invention withsample suspension 230 being drawn throughfilter 215 by application ofvacuum 200. In thisinstance filter 215 is sealed to the bottom ofupper body member 210, thereby providing access to material captured bymembrane filter 215. As diagrammed thesensor 250 is integrated withflow control element 213, which in this instance provides flow control using a valve to vent thepressure source 200 throughvent port 214 or flowcontrol valve 213, rather than adjusting the sample flow pathway, as described in association withFIG. 2 a. As required, or desired, the vent may substantially release the vacuum supplied bysource 200 to halt flow, or the drop in vacuum provided by this venting may be sensed and the vacuum source, shut off. -
FIG. 2 c shows application of the device and configuration of the present invention described in association withFIG. 2 b wheresample suspension 221 consists of particulate matter, for example, soot, suspended in a gas, for example air. -
FIG. 3 a shows an embodiment of thepresent invention 300 comprised of a hollowmain body 310 and a pressure-sensitive check valve 320 extending into themain body 310 so as to communicate with one side of amembrane filter 330, which is attached to the underside of themain body 310. As desired, for use in fluids, aprotrusion 335 may be provided on the bottom of themain body 310 or may be fashioned appropriately to stop themembrane filter 330 from contacting the bottom of a sample vessel (not shown) and disrupting flow during use. Avacuum source 360 is provided for sample aspiration. Initially, thevent portion 340 of the pressure-sensitive check valve 320 is closed and typically, themembrane filter 330 is fresh (free of sample material). To begin collection, vacuum is used to draw sample suspension (not shown) through themembrane filter 330 causing material to collect on the underside of themembrane filter 330. Accordingly, as material collects, the pores become occluded and the rate of flow of sample suspension decreases. The pressure-sensitive check value 320 monitors flow rate through themembrane filter 320 and when the flow rate falls to a desired level, thus indicating that a desired amount of material has been collected, the pressure-sensitive check valve 320 triggers (at a predetermined pressure) and sample flow (and material collection) is halted. Descriptions of filter collection systems that utilize electronics to accomplish a comparable task may be found in U.S. Pat. No. 6,010,909 and U.S. Pat. No. 6,225,125. A portion of this prior art is presented inFIGS. 1 and 2 herein. Although various filters may be employed in such a configuration, for preparing cytological samples, themembrane filter 330 typically has relatively uniformly-distributed pores of a uniform size, intended to capture material larger than the pore size, while passing particulate material that is small. Approximately half a dozen companies provide a filter apparatus that is adapted to a syringe (syringe filters). - For one embodiment of the present invention, the sensor portion of the pressure-
sensitive check valve 320 has been adjusted to trigger at a desired, predetermined pressure which is established to indicate capture of a desired quantity of material on the bottom surface of themembrane filter 330. As diagrammed, when the pressure-sensitive check valve 320 triggers (indicating that a desired amount of material has been captured), a pathway is opened which vents off the vacuum, thereby stopping the aspiration of sample. While it is one object of the present invention to minimize or eliminate electronics that communicate with the pressure transducer or control systems, a battery-powered pressure transducer and/or valve assembly is consistent with this objective. As desired, the pressure-sensitive check valve 320 could be implemented in a variety of other ways so as to monitor and control sample flow, for example upon triggering it could close a fluid pathway. For biological applications, or when other dangers are present, it may be preferable to vent the vacuum as described, which serves to limit the potential for aerosols. - To simultaneously prepare several samples, vacuum could be provided by a stepper-driven syringe, with one syringe for each sample. For higher levels of automation a vacuum pump and vacuum isolators may be preferred. Accordingly, material capture by the present invention may be transferred by contacting an appropriate receiving surface. For some applications, such as machine vision examination of cytological samples, monolayer deposition may be made to the underside of a cover-glass or other relatively thin, uniform material, such as transparent tape, thereby providing material at approximately the same distance from the top surface to facilitate focus. To provide additional rigidity, the thin receiving surface may be placed or affixed to a second surface as desired, or required.
-
FIG. 3 b shows an alternative configuration ofpresent filter device 300, this time havingupper body portion 315 andlower body portion 316. Amembrane filter 330 is shown to be sealed with the formed body by o-rings 325. The upper andlower body portions rings 325, establishing conditions for sample flow to be substantially through themembrane filter 330. For some applications, once a desired quantity of material is captured on the filter, it may be useful to re-suspend this material by back-flushing the filter. Once material is re-suspended, for example, another filter device may be used to isolate a sub-component of the material collected. Alternatively, if access to the filter surface is desired, theupper body 315 and thelower body 316 should be made separable using a press-fit, threads or other convenient form of assembly. - A pressure-
sensitive check valve 320 is shown in communication with theupper body portion 315 of thefilter 335. Again, flow through themembrane filter 330 decreases with time due to progressive obstruction of the pores by material as it collects. The pressure-sensitive check valve 320 senses flow rate therefore, providing a measure of the amount of material captured by themembrane filter 330. -
FIG. 3 c shows an embodiment of the present invention having a membrane filter 330 (not shown) attached on the lower surface of thedevice body 310. As described in association withFIG. 3 a, astandoff 335 may be provided. In this embodiment the pressure-sensitive check valve 370 is integrated and implemented around the periphery of the apparatus with plastic spring tabs that operate as poppet valves. These are further diagrammed in expanded view.Plastic spring tab 376 hascontact area 374, tension sealed intovent hole 372 in the wall of thedevice body 310. Although a single poppet valve of this type could function as a pressure-sensitive check valve for the intended use, such functionality has been implemented using a plurality ofplastic poppet valves 370 distributed around the periphery offilter device 300. As described in association withFIGS. 3 a and 3 b, appliedvacuum 360 initiates the flow of sample suspension (not shown) through themembrane filter 330. And as material is captured on the underside ofmembrane filter 330, the pressure-sensitive poppet valves 370 are in communication with the upper side of themembrane filter 330, so positioned so as to monitor the flow rate of material through themembrane filter 330. The poppet valve(s) are set to trigger at a predetermined pressure to indicate when a desired quantity of material has been collected on themembrane filter 330. - As discussed, the pressure-
sensitive check valve 370 may be implemented with one or more contact tabs. Compound valves of this type may be adjusted to trigger or otherwise activate at a predetermined pressure. Similarly, the characteristics of the valve portion may also be made adjustable, for example, when used as a vent or fluid pathway the diameter of the valve could be adjusted. For some applications or reasons of manufacture, size, operating range, reliability, sensitivity, trigger rate, etc. it may be desirable to distribute a plurality of these plastic spring tabs around the periphery of the device, as shown. Such tab(s) may be affixed as separate units, be fabricated as a ring of units designed for insertion into the device body or it may be preferable to establish these pressure-sensitive check valve components as part of a molding process. Again, the application, costs and other factors may influence implementation. -
FIG. 4 shows a configuration of filter devices of the present invention for processing a plurality of samples. Avacuum manifold 400 distributes vacuum which is further isolated viavacuum chambers 410. Material insuspension 430 begins to be aspirated into filter device(s) 420. Accordingly, by selecting appropriate components, a plurality of similar or different samples may be processed simultaneously. Alternatively, each station may be established to capture the same amount of material, or different amounts of material as desired, or required. -
FIG. 5 a shows afilter device 500 of the present invention with amembrane filter 530 interposed betweenupper body 510 andlower body 520. Sample suspension (not shown) enters throughinlet port 525, passes through themembrane filter 530 and exits viaoutlet port 515. In this instance, themembrane filter 530 is selected with sufficient deformability so as to generally conform to theinterior surface 535 of theupper device body 510 when a desired amount of material (indicated by the reduced flow rate through the membrane filter 530) has been captured. Accordingly, flow is subsequently restricted to a smaller area of themembrane filter 530, for example a single central fluid pathway, as diagrammed. -
FIG. 5 b shows such afilter 530, as described in association withFIG. 5 a, having captured a desired amount of material inregion 540 and providing reduced flow through a more restricted area of thefilter 545. As desired, sample flow may continue or be allowed to continue, for example, untilarea 545 occludes so as to slow or substantially reduce or stop sample flow, as such continuation has no subsequent effect as the desired amount of material has been captured inarea 540 of the filter. The device may continue to draw sample as desired without substantially affecting the desired amount of material collected inregion 540. As desired theupper body 315 andlower body 316 may be made separable to provide filter access. -
FIG. 6 a shows afilter device 600 of the present invention with amembrane filter assembly 650 interposed betweenupper body 610 andlower body 620. Sample suspension (not shown) enters throughinlet port 625, passes through themembrane filter assembly 650 and exits viaoutlet port 615. Themembrane filter assembly 650 is comprised of afilter 660 and surroundingnon-porous support structure 655. In this instance, themembrane filter assembly 650 acts as a pressure transducer, responding to a reduction in flow rate through thefilter 660 as particulate material collects on the underside of thefilter 660. As described in association withFIGS. 5 a and 5 b, deformation of the filter, or in this instance themembrane filter assembly 650, provides the means to alter flow in response to the pressure differential across themembrane filter assembly 650. -
FIG. 6 b shows themembrane filter assembly 650 having afilter area 660 supported by a surroundingnon-porous support structure 655. Thesupport structure 655 has striations 665 allowing it to deform in a triggered motion when a predetermined pressure is sensed. As described, material collecting on the underside of thefilter 660 begins to occlude thefilter 660, contributing to a reduction in flow rate through thefilter 660 and a pressure change across themembrane filter assembly 650. When a desired amount of material has been collected the support structure triggers so as to conform to the inner surface as described in association withFIG. 5 a or the support structure may contact a valve as described in association withFIGS. 3 a, b and c so as to substantially stop sample flow and therefore halt material collection. -
FIG. 6 c shows amembrane filter assembly 670 having afilter area 680 in surroundingnon-porous support structure 675. Thesupport structure 675 has striations 685. The membrane assembly is diagrammed in a first state which is substantially maintained until the pressure differential across themembrane filter assembly 670 reaches a predetermined trigger point at which time the structure toggles or deforms to a second state. -
FIG. 6 d shows themembrane filter assembly 670 as discussed in association withFIG. 6 c in a triggered or deformed state. As desired or required, themembrane filter assembly 670 may itself provide a means to alter flow when the state toggles, indicating collection of a desired amount of material on thefilter 680. Alternatively, the state change may contact a valve, a switch or value interfaced to a switch so that flow through the membrane may be adjusted, or halted. - While preferred embodiments of the present invention are shown and described, it is envisioned that those skilled in the art may devise various modifications of the present invention without departing from the spirit and scope of the appended claims.
Claims (1)
1. An apparatus for capturing a desired quantity of material from a sample suspension on a filter, comprising:
a body member defining a chamber and having opposed ends, an outlet port in one of said ends, and an inlet port;
said inlet port and said outlet port defining a single pathway for sample suspension to flow though said apparatus;
a substantially planar filter mounted within said chamber between said inlet port and said outlet port and completely across said single pathway, so that sample suspension flowing through said apparatus must flow from said inlet port through said filter and to said outlet port;
said filter being deformable toward said outlet end at a predetermined pressure change across said filter and having a first porous portion and a second porous portion concentrically arranged centrally of said first portion, said predetermined pressure change selected so that when a desired quantity of material has been captured by said first portion, said substantially planar filter deforms against said outlet end such that all flow of sample suspension through said apparatus must flow through said more restrictive second portion; and
means for providing a pressure to cause said sample suspension to flow through said apparatus.
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US11/112,186 US20050189286A1 (en) | 2002-10-02 | 2005-04-22 | Filter device to capture a desired amount of material and methods of use |
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US11/112,186 US20050189286A1 (en) | 2002-10-02 | 2005-04-22 | Filter device to capture a desired amount of material and methods of use |
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Citations (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2151538A (en) * | 1937-09-22 | 1939-03-21 | Eric H Swanson | Filter |
US3388800A (en) * | 1965-12-02 | 1968-06-18 | Champion Lab Inc | Axial flow, compressible element, filter unit with bypass means |
US3591003A (en) * | 1970-02-11 | 1971-07-06 | Pall Corp | Differential pressure-responsive signalling device and a filter assembly having same |
US3662887A (en) * | 1970-01-21 | 1972-05-16 | Ripley Screen And Strainer Co | Oil pump inlet strainer |
US3886968A (en) * | 1974-04-22 | 1975-06-03 | Robertshaw Controls Co | Flow control device |
US3963048A (en) * | 1975-02-27 | 1976-06-15 | General Gas Light Company | Poppet valve assembly |
US4246788A (en) * | 1978-11-30 | 1981-01-27 | Sierra Instruments, Inc. | Method and apparatus for sampling of a particle-bearing gas |
US4250830A (en) * | 1979-10-03 | 1981-02-17 | Leif Robert C | Swinging buckets |
US4284505A (en) * | 1979-10-29 | 1981-08-18 | Baxter Travenol Laboratories, Inc. | Flexible membrane filter assembly |
US4319996A (en) * | 1980-11-10 | 1982-03-16 | Gelman Sciences, Inc. | Filter with initially flat membrane and curved membrane support |
US4395493A (en) * | 1981-05-14 | 1983-07-26 | Coulter Electronics, Inc. | Monolayer device using filter techniques |
US4435507A (en) * | 1980-07-08 | 1984-03-06 | Stenkvist Bjoern G | Process and device for preparation of cell samples for cytological tests |
US4614109A (en) * | 1982-12-27 | 1986-09-30 | Brunswick Corporation | Method and device for testing the permeability of membrane filters |
US4765963A (en) * | 1985-09-24 | 1988-08-23 | Mitsubishi Denki Kabushiki Kaisha | Apparatus for measuring impurities in water |
US4792398A (en) * | 1987-08-10 | 1988-12-20 | Marion Laboratories, Inc. | Manual vacuum filtration device |
US4832840A (en) * | 1982-06-04 | 1989-05-23 | Klinkau Besitzges. Mbh | Membrane filter plate having improved bending characteristics of the membrane |
US4961432A (en) * | 1989-01-10 | 1990-10-09 | Cancer Diagnostics, Inc. | Modular fluid sample preparation assembly |
US4967791A (en) * | 1989-04-26 | 1990-11-06 | The Boeing Company | Pressure activated check valve |
US4969997A (en) * | 1988-02-04 | 1990-11-13 | Sartorius Gmbh | Fluid-impermeable areas on porous membrane filters and their application |
US4996627A (en) * | 1989-01-30 | 1991-02-26 | Dresser Industries, Inc. | High sensitivity miniature pressure transducer |
US5141639A (en) * | 1990-08-14 | 1992-08-25 | Gelman Sciences, Inc. | Vacuum filter assembly |
US5168965A (en) * | 1989-12-22 | 1992-12-08 | August Bilstein Gmbh & Co. Kg | Bypass valve with selective characteristics for controlled and adjustable dashpots |
USD343682S (en) * | 1991-12-02 | 1994-01-25 | Corning Incorporated | Vacuum filter flask |
US5312380A (en) * | 1985-06-06 | 1994-05-17 | Thomas Jefferson University | Endothelial cell procurement and deposition kit |
US5341838A (en) * | 1993-08-23 | 1994-08-30 | Powell Walter W | Direct spring pressure operated valve |
US5358690A (en) * | 1989-01-10 | 1994-10-25 | Lamina, Ltd. | Environmental sample collection and membrane testing device |
US5422273A (en) * | 1993-03-23 | 1995-06-06 | Baal Medical Products, Inc. | Cell collection apparatus |
US5429803A (en) * | 1991-04-18 | 1995-07-04 | Lamina, Inc. | Liquid specimen container and attachable testing modules |
US5469883A (en) * | 1993-11-22 | 1995-11-28 | Daewoo Heavy Industries Ltd. | Flow modulation device having an elastically deformable disk-like flap |
US5471994A (en) * | 1989-01-10 | 1995-12-05 | Guirguis; Raouf A. | Method and apparatus for obtaining a cytology monolayer |
US5480484A (en) * | 1994-03-01 | 1996-01-02 | Statspin Technologies | Cytology centrifuge apparatus |
US5500167A (en) * | 1993-07-12 | 1996-03-19 | Pall Corporation | Method of preparing a supported microporous filtration membrane |
US5561556A (en) * | 1994-04-21 | 1996-10-01 | Compucyte Corporation | Slide analysis system with slide having self contained microscope analysis information |
US5593529A (en) * | 1990-01-18 | 1997-01-14 | Pall Corporation | Cylindrical filters and their manufacture |
US5603827A (en) * | 1994-04-30 | 1997-02-18 | Jv Kunststoffwerk Gmbh | Membrane filter plate |
US5679154A (en) * | 1994-03-01 | 1997-10-21 | Norfolk Scientific, Inc. | Cytology centrifuge apparatus |
US5744034A (en) * | 1995-06-09 | 1998-04-28 | Hydra Tools International Plc | Hydraulic circuit |
US5784193A (en) * | 1996-06-28 | 1998-07-21 | Ferguson; Gary W. | Microscope slide with removable layer and method |
US5792425A (en) * | 1995-05-19 | 1998-08-11 | Millipore Coporation | Vacuum filter device |
US5976824A (en) * | 1993-11-24 | 1999-11-02 | Abbott Laboratories | Method and apparatus for collecting a cell sample from a liquid specimen |
US6010909A (en) * | 1990-03-02 | 2000-01-04 | Cytyc Corporation | Method and apparatus for controlled instrumentation of particles with a filter device |
US6091483A (en) * | 1995-11-03 | 2000-07-18 | Lamina, Inc. | Method and apparatus for preparing substances for optical analysis |
US6106483A (en) * | 1989-01-10 | 2000-08-22 | Lamina, Inc. | Apparatus for obtaining a cytology monolayer |
US6149871A (en) * | 1997-08-25 | 2000-11-21 | Lamina, Inc. | System for processing multiple specimens of biological fluid |
US6162401A (en) * | 1997-05-23 | 2000-12-19 | Shandon Scientific Limited | Cytofunnel arrangement |
US6215892B1 (en) * | 1995-11-30 | 2001-04-10 | Chromavision Medical Systems, Inc. | Method and apparatus for automated image analysis of biological specimens |
US6286372B1 (en) * | 1997-02-28 | 2001-09-11 | Siemens Aktiengesellschaft | Pressure differential measuring transducer |
US6295877B1 (en) * | 1999-03-30 | 2001-10-02 | A-Med Systems, Inc. | Pressure sensing cannula |
US6296764B1 (en) * | 1997-11-04 | 2001-10-02 | Lamina, Inc. | Apparatus for mixing and separating particulate matter from a fluid |
US6309362B1 (en) * | 1992-07-28 | 2001-10-30 | Lamina, Inc. | Method and apparatus for automatically separating particulate matter from a fluid |
US6318190B1 (en) * | 1996-11-01 | 2001-11-20 | Cytyc Corporation | Systems for collecting fluid samples having select concentrations of particles |
US6404906B2 (en) * | 1997-03-03 | 2002-06-11 | Bacus Research Laboratories,Inc. | Method and apparatus for acquiring and reconstructing magnified specimen images from a computer-controlled microscope |
US6425883B1 (en) * | 1998-05-08 | 2002-07-30 | Circuit Tree Medical, Inc. | Method and apparatus for controlling vacuum as a function of ultrasonic power in an ophthalmic phaco aspirator |
US6579447B2 (en) * | 2001-07-25 | 2003-06-17 | Lancer Partnership, Ltd. | Self-cleaning pre-filter system |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH615029A5 (en) * | 1976-05-25 | 1979-12-28 | Inventa Ag | Member for regulating the flowthrough quantity of a pressure medium |
WO2001083089A1 (en) | 2000-05-04 | 2001-11-08 | Bisconte De Saint Julien Jean | Cell control in milk or blood |
-
2002
- 2002-10-02 US US10/263,129 patent/US6884341B2/en not_active Expired - Fee Related
-
2003
- 2003-09-17 JP JP2004540399A patent/JP2006501450A/en active Pending
- 2003-09-17 CN CNA038252228A patent/CN1701225A/en active Pending
- 2003-09-17 CA CA 2501042 patent/CA2501042A1/en not_active Abandoned
- 2003-09-17 WO PCT/CA2003/001417 patent/WO2004031735A1/en not_active Application Discontinuation
- 2003-09-17 AU AU2003266889A patent/AU2003266889A1/en not_active Abandoned
- 2003-09-17 EP EP20030747770 patent/EP1546677A1/en not_active Withdrawn
-
2005
- 2005-04-22 US US11/112,186 patent/US20050189286A1/en not_active Abandoned
Patent Citations (57)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2151538A (en) * | 1937-09-22 | 1939-03-21 | Eric H Swanson | Filter |
US3388800A (en) * | 1965-12-02 | 1968-06-18 | Champion Lab Inc | Axial flow, compressible element, filter unit with bypass means |
US3662887A (en) * | 1970-01-21 | 1972-05-16 | Ripley Screen And Strainer Co | Oil pump inlet strainer |
US3591003A (en) * | 1970-02-11 | 1971-07-06 | Pall Corp | Differential pressure-responsive signalling device and a filter assembly having same |
US3886968A (en) * | 1974-04-22 | 1975-06-03 | Robertshaw Controls Co | Flow control device |
US3963048A (en) * | 1975-02-27 | 1976-06-15 | General Gas Light Company | Poppet valve assembly |
US4246788A (en) * | 1978-11-30 | 1981-01-27 | Sierra Instruments, Inc. | Method and apparatus for sampling of a particle-bearing gas |
US4250830A (en) * | 1979-10-03 | 1981-02-17 | Leif Robert C | Swinging buckets |
US4284505A (en) * | 1979-10-29 | 1981-08-18 | Baxter Travenol Laboratories, Inc. | Flexible membrane filter assembly |
US4435507A (en) * | 1980-07-08 | 1984-03-06 | Stenkvist Bjoern G | Process and device for preparation of cell samples for cytological tests |
US4319996A (en) * | 1980-11-10 | 1982-03-16 | Gelman Sciences, Inc. | Filter with initially flat membrane and curved membrane support |
US4395493A (en) * | 1981-05-14 | 1983-07-26 | Coulter Electronics, Inc. | Monolayer device using filter techniques |
US4832840A (en) * | 1982-06-04 | 1989-05-23 | Klinkau Besitzges. Mbh | Membrane filter plate having improved bending characteristics of the membrane |
US4614109A (en) * | 1982-12-27 | 1986-09-30 | Brunswick Corporation | Method and device for testing the permeability of membrane filters |
US5312380A (en) * | 1985-06-06 | 1994-05-17 | Thomas Jefferson University | Endothelial cell procurement and deposition kit |
US4765963A (en) * | 1985-09-24 | 1988-08-23 | Mitsubishi Denki Kabushiki Kaisha | Apparatus for measuring impurities in water |
US4792398A (en) * | 1987-08-10 | 1988-12-20 | Marion Laboratories, Inc. | Manual vacuum filtration device |
US4969997A (en) * | 1988-02-04 | 1990-11-13 | Sartorius Gmbh | Fluid-impermeable areas on porous membrane filters and their application |
US4961432A (en) * | 1989-01-10 | 1990-10-09 | Cancer Diagnostics, Inc. | Modular fluid sample preparation assembly |
US6106483A (en) * | 1989-01-10 | 2000-08-22 | Lamina, Inc. | Apparatus for obtaining a cytology monolayer |
US5471994A (en) * | 1989-01-10 | 1995-12-05 | Guirguis; Raouf A. | Method and apparatus for obtaining a cytology monolayer |
US5358690A (en) * | 1989-01-10 | 1994-10-25 | Lamina, Ltd. | Environmental sample collection and membrane testing device |
US4996627A (en) * | 1989-01-30 | 1991-02-26 | Dresser Industries, Inc. | High sensitivity miniature pressure transducer |
US4967791A (en) * | 1989-04-26 | 1990-11-06 | The Boeing Company | Pressure activated check valve |
US5168965A (en) * | 1989-12-22 | 1992-12-08 | August Bilstein Gmbh & Co. Kg | Bypass valve with selective characteristics for controlled and adjustable dashpots |
US5593529A (en) * | 1990-01-18 | 1997-01-14 | Pall Corporation | Cylindrical filters and their manufacture |
US6010909A (en) * | 1990-03-02 | 2000-01-04 | Cytyc Corporation | Method and apparatus for controlled instrumentation of particles with a filter device |
US6225125B1 (en) * | 1990-03-02 | 2001-05-01 | Cytyc Corporation | Method and apparatus for controlled instrumentation of particles with a filter device |
US5141639A (en) * | 1990-08-14 | 1992-08-25 | Gelman Sciences, Inc. | Vacuum filter assembly |
US5849505A (en) * | 1991-04-18 | 1998-12-15 | Lamina, Inc. | Liquid specimen container and attachable testing modules |
US6210909B1 (en) * | 1991-04-18 | 2001-04-03 | Lamina, Inc. | Liquid specimen container and attachable testing modules |
US5429803A (en) * | 1991-04-18 | 1995-07-04 | Lamina, Inc. | Liquid specimen container and attachable testing modules |
USD343682S (en) * | 1991-12-02 | 1994-01-25 | Corning Incorporated | Vacuum filter flask |
US6309362B1 (en) * | 1992-07-28 | 2001-10-30 | Lamina, Inc. | Method and apparatus for automatically separating particulate matter from a fluid |
US5422273A (en) * | 1993-03-23 | 1995-06-06 | Baal Medical Products, Inc. | Cell collection apparatus |
US5500167A (en) * | 1993-07-12 | 1996-03-19 | Pall Corporation | Method of preparing a supported microporous filtration membrane |
US5341838A (en) * | 1993-08-23 | 1994-08-30 | Powell Walter W | Direct spring pressure operated valve |
US5469883A (en) * | 1993-11-22 | 1995-11-28 | Daewoo Heavy Industries Ltd. | Flow modulation device having an elastically deformable disk-like flap |
US5976824A (en) * | 1993-11-24 | 1999-11-02 | Abbott Laboratories | Method and apparatus for collecting a cell sample from a liquid specimen |
US5480484A (en) * | 1994-03-01 | 1996-01-02 | Statspin Technologies | Cytology centrifuge apparatus |
US5679154A (en) * | 1994-03-01 | 1997-10-21 | Norfolk Scientific, Inc. | Cytology centrifuge apparatus |
US5561556A (en) * | 1994-04-21 | 1996-10-01 | Compucyte Corporation | Slide analysis system with slide having self contained microscope analysis information |
US5603827A (en) * | 1994-04-30 | 1997-02-18 | Jv Kunststoffwerk Gmbh | Membrane filter plate |
US5792425A (en) * | 1995-05-19 | 1998-08-11 | Millipore Coporation | Vacuum filter device |
US5744034A (en) * | 1995-06-09 | 1998-04-28 | Hydra Tools International Plc | Hydraulic circuit |
US6091483A (en) * | 1995-11-03 | 2000-07-18 | Lamina, Inc. | Method and apparatus for preparing substances for optical analysis |
US6215892B1 (en) * | 1995-11-30 | 2001-04-10 | Chromavision Medical Systems, Inc. | Method and apparatus for automated image analysis of biological specimens |
US5784193A (en) * | 1996-06-28 | 1998-07-21 | Ferguson; Gary W. | Microscope slide with removable layer and method |
US6318190B1 (en) * | 1996-11-01 | 2001-11-20 | Cytyc Corporation | Systems for collecting fluid samples having select concentrations of particles |
US6286372B1 (en) * | 1997-02-28 | 2001-09-11 | Siemens Aktiengesellschaft | Pressure differential measuring transducer |
US6404906B2 (en) * | 1997-03-03 | 2002-06-11 | Bacus Research Laboratories,Inc. | Method and apparatus for acquiring and reconstructing magnified specimen images from a computer-controlled microscope |
US6162401A (en) * | 1997-05-23 | 2000-12-19 | Shandon Scientific Limited | Cytofunnel arrangement |
US6149871A (en) * | 1997-08-25 | 2000-11-21 | Lamina, Inc. | System for processing multiple specimens of biological fluid |
US6296764B1 (en) * | 1997-11-04 | 2001-10-02 | Lamina, Inc. | Apparatus for mixing and separating particulate matter from a fluid |
US6425883B1 (en) * | 1998-05-08 | 2002-07-30 | Circuit Tree Medical, Inc. | Method and apparatus for controlling vacuum as a function of ultrasonic power in an ophthalmic phaco aspirator |
US6295877B1 (en) * | 1999-03-30 | 2001-10-02 | A-Med Systems, Inc. | Pressure sensing cannula |
US6579447B2 (en) * | 2001-07-25 | 2003-06-17 | Lancer Partnership, Ltd. | Self-cleaning pre-filter system |
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WO2010047726A1 (en) * | 2008-10-22 | 2010-04-29 | David Chanley | Apparatus and method for decomposing bacteria into a waste stream |
US20110233148A1 (en) * | 2008-12-19 | 2011-09-29 | Stemcell Technologies Inc. | Filter apparatus and filter plate system |
US9290731B2 (en) * | 2008-12-19 | 2016-03-22 | Stemcell Technologies Inc. | Filter apparatus and filter plate system |
US20120229287A1 (en) * | 2009-08-31 | 2012-09-13 | Lorne Schuetzle | Gas monitoring system |
US20110290116A1 (en) * | 2010-05-27 | 2011-12-01 | General Electric Company | Long life pyramidal filter for gas turbine inlet system |
US8440002B2 (en) * | 2010-05-27 | 2013-05-14 | General Electric Company | Long life pyramidal filter for gas turbine inlet system |
US8790596B2 (en) | 2011-06-01 | 2014-07-29 | Ventana Medical Systems, Inc. | Dispenser with filter device |
US20150238888A1 (en) * | 2014-02-25 | 2015-08-27 | Thomas A. COMEAU | Apparatus for removing particulate from a filter |
US10632427B2 (en) | 2015-12-14 | 2020-04-28 | Murata Manufacturing Co., Ltd. | Filtration filter |
US10926229B2 (en) | 2015-12-14 | 2021-02-23 | Murata Manufacturing Co., Ltd. | Filtration filter |
Also Published As
Publication number | Publication date |
---|---|
EP1546677A1 (en) | 2005-06-29 |
JP2006501450A (en) | 2006-01-12 |
US20040065622A1 (en) | 2004-04-08 |
US6884341B2 (en) | 2005-04-26 |
CN1701225A (en) | 2005-11-23 |
AU2003266889A1 (en) | 2004-04-23 |
CA2501042A1 (en) | 2004-04-15 |
WO2004031735A1 (en) | 2004-04-15 |
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