WO1997036166A1 - Apparatus and method for handling fluid samples of body materials - Google Patents
Apparatus and method for handling fluid samples of body materials Download PDFInfo
- Publication number
- WO1997036166A1 WO1997036166A1 PCT/US1997/004354 US9704354W WO9736166A1 WO 1997036166 A1 WO1997036166 A1 WO 1997036166A1 US 9704354 W US9704354 W US 9704354W WO 9736166 A1 WO9736166 A1 WO 9736166A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- viewing
- specimen
- fluid
- liquid
- chambers
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 12
- 239000012530 fluid Substances 0.000 title claims description 35
- 239000000463 material Substances 0.000 title description 7
- 239000007788 liquid Substances 0.000 claims abstract description 36
- 239000012192 staining solution Substances 0.000 claims abstract description 13
- 230000003287 optical effect Effects 0.000 claims abstract description 11
- 238000011010 flushing procedure Methods 0.000 claims description 22
- 238000010926 purge Methods 0.000 claims description 13
- 239000011521 glass Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 3
- 230000000712 assembly Effects 0.000 claims description 2
- 238000000429 assembly Methods 0.000 claims description 2
- 230000000717 retained effect Effects 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims 5
- 238000010168 coupling process Methods 0.000 claims 5
- 238000005859 coupling reaction Methods 0.000 claims 5
- 238000002360 preparation method Methods 0.000 claims 2
- 210000001124 body fluid Anatomy 0.000 claims 1
- 239000010839 body fluid Substances 0.000 claims 1
- 230000009977 dual effect Effects 0.000 abstract description 12
- 230000002550 fecal effect Effects 0.000 abstract description 11
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 15
- 230000002572 peristaltic effect Effects 0.000 description 9
- 230000002441 reversible effect Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 230000003213 activating effect Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 241000224483 Coccidia Species 0.000 description 1
- 108010034145 Helminth Proteins Proteins 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 208000031513 cyst Diseases 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 244000000013 helminth Species 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000003250 oocyst Anatomy 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B21/00—Microscopes
- G02B21/34—Microscope slides, e.g. mounting specimens on microscope slides
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
- G01N1/31—Apparatus therefor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/493—Physical analysis of biological material of liquid biological material urine
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1095—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices for supplying the samples to flow-through analysers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
- G01N1/31—Apparatus therefor
- G01N1/312—Apparatus therefor for samples mounted on planar substrates
-
- 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
- Y10T436/11—Automated chemical analysis
-
- 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
- Y10T436/11—Automated chemical analysis
- Y10T436/112499—Automated chemical analysis with sample on test slide
-
- 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
- Y10T436/11—Automated chemical analysis
- Y10T436/117497—Automated chemical analysis with a continuously flowing sample or carrier stream
Definitions
- This invention generally relates to a method and apparatus for automating the viewing of a sample of body material and more specifically to the transfer of a prepared body material sample to a viewing chamber and subsequently to a disposal.
- U.S. Patents 5,248,480 and 5,393,494 to Greenfield et al. describe an apparatus and method for drawing a fluid sample into a slide assembly for viewing through a microscope.
- the fluid is drawn from a container by way of a reversible pump.
- the fluid such as a urine sample, is drawn in from the container through a glass slide and after viewing purged from the slide by reversing the pump so that it can draw flushing liquid back through the slide into the fluid sample container.
- U.S.Patent 3,352,280 describes an automatic stain apparatus for staining biological specimen.
- a dyeing apparatus is described in U.S. Patent 4,025,393.
- An apparatus wherein a slide is moved to a staining station and then to a buffer station and thence to a rinsing station is described in U.S. Patent 4,034,700.
- an automatic handling and staining or other treatment of a prepared sample is obtained and a transfer into a slide assembly can be made so that the sample can be viewed through a microscope and evaluated without having the operator contact the specimen.
- the sample is automatically treated with an appropriate chemical solution such a staining solution so that an operator can view an untreated sample in one chamber and a treated or stained sample in another adjacent chamber. It is, therefore, an object of the invention to provide an efficient apparatus and method for automatic treatment and handling of a body material in a convenient, economic manner that is safe for the operator.
- Figure 1 is an overall block diagram of a system in accordance with the invention for use in the analysis of fecal specimen
- Figure 2 is an enlarged view of a fluid flow section of the system shown in Figure 1;
- Figure 3 is an enlarged view of a control segment of the system of Figure 1;
- Figure 4 is a plan view of a slide assembly in accordance with the invention and is an enlargement of a portion of the view in Figure 1.
- FIG. 5 is a flow diagram showing the described operation of the fluid handling system in accordance with the invention.
- an apparatus 10 is shown with which a prepared fecal specimen 20 is drawn from a holding container 22 via a dual aspirator assembly 24 and transferred to a slide assembly 26 having dual optical viewing chambers 30, 32.
- the slide assembly 26 is of a flat configura ⁇ tion having a general shape as more particularly described in the aforemen ⁇ tioned U.S. Patent 5,393,494 to Greenfield et al. This patent is, therefore, incorporated herein by reference thereto subject to such modifications as are described herein.
- decimals serves to denote specific items with the numerals on the right side of the decimal point while reference to the numeral on the left side of the decimal refers to the same item, or items, in a general way.
- the slide assembly 26 can be mounted to the stage of any standard, upright microscope 34 as described in the '494 Greenfield patent.
- the slide assembly's viewing chambers 30, 32 have end located ports 36.1-36.4, see Figure 4.
- Ports 36.1 and 36.2 are coupled by tubings 38.1 and 38.2 to dual aspirator assembly 24 and extend into the specimen solution 20.
- Ports 36.3 and 36.4 are in turn coupled by tubings 40.1 and 40.2, via solenoid controlled pinch valves 42.1 and 42.2.
- Valve 42.1 is normally closed and valve 42.2 is normally open.
- the tubes 40 are joined at a junction 43 to merge into a single tubing 46.
- the tubing 46 in turn is passed through a pressure sensor 48 to a reversible peristaltic pump 50 and thence into a reservoir 52 containing a flushing liquid 54.
- a treating liquid supply tube 60 is connected to junction 62 in tubing 38.2 so as to provide a mixing point, preferably ahead of the viewing chamber 32, for a treating solution into the specimen containing tube 38.2.
- the treating solution is obtained by passing tubing 60 through a normally closed solenoid controlled pinch valve 64 and connecting the tubing 60 to an aspirator assembly 66 attached to container 68 having a treating solution 70.
- the treating solution can be any suitable material useful for the treatment of specimen 20 to enhance its observation by a microscope and in the case of a fecal specimen can be a staining solution.
- Operation of system 10 involves a microcontroller 72, which in turn controls a valve control 74 coupled to operate valves 42, and 64, senses overpressure conditions sensed by pressure sensor 48 and controls a pump control 78 coupled to drive a motor 82 connected to peristaltic pump 50.
- Activation of the system is begun with a sample switch 84 and completion of a visual analysis is followed by activating purge switches 86 and 88 to respectively purge the stain solution from tubing 40.2 and cleanse the junction 60 as described below.
- An input/output control 90 is connected to microcon ⁇ troller 72 and operates suitable system status conditions by illuminating led's 92.1-92.6 for the conditions as noted in Figure 1.
- Operation of system 10 is initiated by actuation of the sample switch 84 by the user.
- the microcontroller 72 commands the valve control circuitry 74 to open both of the internal pinch valves 42.1 and 42.2. This opens both of the normally-closed hydraulic systems represented by tubes 40.1 and 40.2.
- the microcontroller 72 also actuates motor control 78 so as to activate the pump 50 in a sample direction, as indicated by arrow 79.1, as will cause an aspiration of specimen liquid 20 from container 22.
- another pinch valve 64 which is housed in an enclosure 65, external to the apparatus, is activated.
- This activation opens yet another portion of the hydraulic system and allows transfer of a stain solution 70 from its holding container 68, to Y-fitting 62, where the stain naturally mixes with some portion of the fecal specimen 20 and enters the optical viewing chamber 32 of the dual optical viewing chamber assembly 26.
- the dual optical viewing chamber assembly 26 will from here on out be referred to as the slide assembly 26. While a portion of the fecal specimen 20 is being mixed with the stain solution 70 and drawn into chamber 32 of the slide assembly 26, another portion of the specimen is simultaneously drawn unmixed into the other viewing chamber 30 of the slide assembly 26. This procedure is made possible by maintaining two, isolated hydraulic systems within the slide assembly 26.
- both internal pinch valves 42.1 and 42.2 are closed by the valve control 74 and an operator can begin the actual visual analysis of the stained and unstained portions of the specimen.
- the specimen 20 in the other viewing chamber 32 of the slide assembly 26 continues to react with the stain causing clinically significant, but normally transparent matter to take on color thus making it easily visible under microscopic examination.
- the analysis of the unstained portion of the specimen 20 can be flushed out of its chamber, through half of the dual aspirator assembly 24, and either back out into the original holding container 22 or into another waste container followed by a larger volume of flush solution 54.
- This purge operation is initiated by the assertion of the unstained purge switch 88 by the user.
- the purging of the unstained portion of the specimen is performed without disturbing the stained portion of the specimen, by opening the unstained system pinch valve 42.1, and keeping the stained system pinch valve 42.2 closed.
- the purging action is obtained by activating the motor with pump control 78 so that the pump is operated in a reverse flush direction, as indicated by arrow 79.2, causing a flow of flushing liquid 54 to move through the tubing 46 into tubing 40.1 and thence into container 22.
- the stained portion of the specimen can then be analyzed in an identical method as with the unstained specimen.
- the unstained system pinch valve 42.1 remains closed and the stained system pinch valve 42.2 opens after the stained specimen has passed beyond the Y junction 62.
- the normally closed external pinch valve 64 is then opened.
- the peristaltic pump motor 30 is operated to pump in the direction of arrow 79.1 to draw a small volume of stain back into or towards viewing chamber 32 of slide assembly 26. This action cleans out any residual matter that may have gotten trapped in the Y-fitting during the sample cycle.
- the external pinch valve 64 then closes and peristaltic pump 50 resumes purging of the stained hydraulic system by pumping flushing solution from supply 52 through the viewing chamber 32. While the stained specimen is flushed from its hydraulic system, the results of the analysis can be recorded. Upon completion of this flushing operation, the apparatus is ready to draw the next fecal specimen.
- the main electrical portion of system 10 receives electrical power from either a regulated or unregulated AC-DC wallmount adapter 96, or a 12Vdc battery, or any other direct current source capable of providing a minimum of 1.5A of current while maintaining a 12V potential difference.
- the normally- closed pinch valve 64 which is external of the system enclosure 98, is powered from a regulated 12Vdc source within the system workstation's main enclosure.
- valve control 74 The microcontroller 72 requires a clock oscillator signal source 73, see Figure 3, and which serves the function as an incremental time reference for successive operations.
- the internal hydraulic system of system 10 consists of a reversible, peristaltic pump assembly, two 3-way pinch valve assemblies 42.1, 42.2, and a pressure/vacuum sensor 48.
- the peristaltic pump assembly is comprised of a three-rotor impeller 100 mounted directly to the shaft of a reversible, unipolar stepper motor 82, a stainless steel tube mounting bracket 102, and a section of elastomeric tubing 104 in communication with tube 46 and which is stretched a calibrated distance between two, forked ends of the tube mounting bracket 102.
- Total control of the peristaltic pump assembly resides with the pump control circuitry 78.
- This circuitry can alter the angular velocity and direction of the pump impeller 50 to comply with desired flow rate commands sent to it by the workstation's microcontroller 72.
- the control of this hydraulic system is what is commonly referred to as "closed-loop".
- the term "closed-loop" most accurately describes the fact that the microcontroller 72 issues a command to the pump control assembly 78, which responds by energizing the individual coils or phases of the unipolar stepper motor 82 in such a manner to turn the peristaltic pump impeller 50 in a direction and angular velocity to achieve a flow rate which is appropriate for the operation underway.
- Feedback is then obtained by the microcontroller 72, polling the pressure sensor interface circuitry 76, which reads the pressure sensor 48, to determine the sign and magnitude of the actual pressure within the hydraulic system.
- the microcontroller 72 uses this data along with previously collected data to calculate the approximate flow rate of the liquid in the system. If the commanded flow rate varies from the actual flow rate, then an updated command is sent to the pump control circuitry 78, which will work towards eliminating the difference between these two values.
- the microcontroller 72 detects one of the preprogrammed error conditions such as overpressure or underpressure in either the stained or unstained portions of the hydraulic system, the operation is ceased, the system error light-emitting diode 92.2 is illuminated along with another appropriate error-indicating LED 92, and an audible warning indicator is pulsed.
- the system error LED 92.2 four other light indicating errors are provided such as are labelled in Figures 1 and 3 with a stained overpressure 92.3, a stained underpressure 92.4, an unstained overpressure 92.5, and unstained underpressure 92.6, to inform the operator of such a fault condition.
- the pinch valves 42 are dual acting in that they each act on a tubing 40 with a normally closed pinch section and when this section is opened another tube 106 is pinched closed.
- Tube 106 provides a parallel connection from a junction 108 to flushing solution container 52 so as to enable the flushing fluid to be pumped back into the container 52 in case one of the pinch valves 42 malfunctions.
- the slide assembly 26 includes viewing chambers 30, 32 which are each similar to the transparent glass enclosures as shown and described in the aforementioned and incorporated by reference US Patent 5,393,494 in its Figures 17-22.
- the slide assembly 26 of the instant invention has a frame 110, see Figure 4 herein, with a pair of elongate side by side parallel recesses 111.1 and 111.2 in which the glass enclosures 30, 32 are placed and retained. Each glass enclosure 30, 32 overlies an opening 112 in the frame 110 to enable a back lighting for enhanced viewing.
- the frame 110 has a groove 114 to receive the tube 60, though this could be passed around the frame.
- the junction 62 is formed of suitable plastic or glass material.
- Figure 5 illustrates a simplified flow chart 120 for the operation of the microcontroller 72.
- the controller is initialized with the appropriate signals such as the durations for the respective pump cycles, x seconds to draw a sample, y seconds for flushing the samples from the slide assembly 26 and z seconds to draw a cleansing sample of the staining solution.
- Other initial values are stored as well and the various controls are place in their respective reset conditions.
- the treated line valve 42.2 is opened at 142 and the pump activated in the flushing direction at 144 for y seconds, enough to assure that the sample is flushed from the slide assembly and into the container 22.
- the pump is then, at 146 operated a short time to draw a staining solution into tubing 40.2 sufficient to use it for flushing of the junction 62.
- the pump is then reactivated at 148 in the flushing direction to purge the treating solution back into container 22.
- a return is made at 152 to step 124 to enable another fecal specimen sample to be taken and reviewed as described.
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97916825A EP0890106A4 (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling fluid samples of body materials |
JP53447997A JP3316574B2 (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling fluid sample of human body material |
AU25340/97A AU719091B2 (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling fluid samples of body materials |
BR9708250-3A BR9708250A (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling body material fluid samples |
CA002249235A CA2249235C (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling fluid samples of body materials |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1409696P | 1996-03-25 | 1996-03-25 | |
US60/014,096 | 1996-03-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1997036166A1 true WO1997036166A1 (en) | 1997-10-02 |
WO1997036166A9 WO1997036166A9 (en) | 1997-12-04 |
Family
ID=21763507
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1997/004354 WO1997036166A1 (en) | 1996-03-25 | 1997-03-06 | Apparatus and method for handling fluid samples of body materials |
Country Status (7)
Country | Link |
---|---|
US (1) | US5895762A (en) |
EP (1) | EP0890106A4 (en) |
JP (1) | JP3316574B2 (en) |
AU (1) | AU719091B2 (en) |
BR (1) | BR9708250A (en) |
CA (1) | CA2249235C (en) |
WO (1) | WO1997036166A1 (en) |
Cited By (2)
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JP2003525454A (en) * | 2000-02-29 | 2003-08-26 | デイアシス コーポレーシヨン | Method and apparatus for handling various body fluids |
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Also Published As
Publication number | Publication date |
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CA2249235C (en) | 2002-05-07 |
US5895762A (en) | 1999-04-20 |
BR9708250A (en) | 2000-01-04 |
AU2534097A (en) | 1997-10-17 |
CA2249235A1 (en) | 1997-10-02 |
EP0890106A4 (en) | 2002-08-28 |
JP2002504986A (en) | 2002-02-12 |
JP3316574B2 (en) | 2002-08-19 |
EP0890106A1 (en) | 1999-01-13 |
AU719091B2 (en) | 2000-05-04 |
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