EP0308231B1 - Liquid-collecting device - Google Patents
Liquid-collecting device Download PDFInfo
- Publication number
- EP0308231B1 EP0308231B1 EP88308558A EP88308558A EP0308231B1 EP 0308231 B1 EP0308231 B1 EP 0308231B1 EP 88308558 A EP88308558 A EP 88308558A EP 88308558 A EP88308558 A EP 88308558A EP 0308231 B1 EP0308231 B1 EP 0308231B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aperture
- compartment
- liquid
- slide valve
- compartments
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004793 Polystyrene Substances 0.000 claims abstract description 9
- 229920002223 polystyrene Polymers 0.000 claims abstract description 9
- 230000003068 static effect Effects 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims description 13
- 239000000427 antigen Substances 0.000 claims description 7
- 102000036639 antigens Human genes 0.000 claims description 7
- 108091007433 antigens Proteins 0.000 claims description 7
- 238000011084 recovery Methods 0.000 claims description 7
- 229920001971 elastomer Polymers 0.000 claims description 5
- 239000013642 negative control Substances 0.000 claims description 5
- 239000013641 positive control Substances 0.000 claims description 5
- 239000000806 elastomer Substances 0.000 claims description 4
- 238000003018 immunoassay Methods 0.000 claims description 4
- 239000011358 absorbing material Substances 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims 2
- 238000011144 upstream manufacturing Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 15
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- 239000013610 patient sample Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical class NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
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- 239000005018 casein Substances 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
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- 230000005499 meniscus Effects 0.000 description 1
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- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
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- 239000002964 rayon Substances 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5025—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures for parallel transport of multiple samples
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5025—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures for parallel transport of multiple samples
- B01L3/50255—Multi-well filtration
Definitions
- This invention relates to a construction used to open and close vents in a liquid-collecting compartment, particularly such compartments used in assay devices.
- vent hole is commonly provided in each of the lower compartments, to allow air to escape as liquid is entering.
- an air lock can be created which will allow, or stop, respectively, liquid flow into the lower compartment from above. (Air cannot pass out through the filter either, once it is wetted.)
- the stoppage of flow is appropriate to allow the liquid to incubate first at the filter, before passing down into the lower compartment, as is well-known.
- a liquid-collecting device comprising at least one liquid-collecting compartment, means in that one compartment defining a vent aperture fluidly connecting the compartment to the atmosphere, the aperture-defining means including a portion of a wall in which the aperture is located, and closure means for shutting off the vent aperture, characterized in that a) the closure means comprise a slide valve, b) one of the slide valve and the wall portion comprises an elastomeric member, and c) there is included means for slidably mounting the slide valve and the wall portion relative to each other to move the slide valve between a first position covering the aperture and a second position which uncovers the aperture, the member being formed of an elastomer having the following properties: a durometer valve no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6.
- a liquid-collecting device comprising three separate but adjacent liquid-collecting compartments, means in each of the compartments defining a vent aperture fluidly connecting each compartment to the atmospehre, the aperture-defining means including a portion of a wall in which the aperture is located, and closure means for each of the compartments for shutting off the respective aperture.
- each of the three closure means comprises a slide valve comprising an elastomeric member and means for slidably mounting the member over the aperture to move between a first position covering the aperture and a second position in which the member uncovers the aperture, the member being formed of an elastomer having the following properties: a durometer value no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6.
- a device useful in immunoassays is provided with a valve for closing the necessary vent, that is manually operable with a minimum of effort.
- such a device is provided with a plurality of liquid-collecting compartments, each independently vented, and a slide valve that opens and closes each vent simultaneously, with a minimum of effort.
- the invention is described herein in the context of the preferred embodiments, in which the device has three pairs of upper/lower compartments, to assay a) the patient sample, b) a positive control and c) a negative control, all more or less simultaneously.
- aspects of the invention are useful with only a single pair of compartments, and even without the upper compartment if one simply desires control over the rate of flow into a liquid-receiving compartment.
- the chemistries provide for an immunoassay, in which there is separately received at three filters in three compartments, a patient antigen complexed with an antigen, a positive control for the complex so formed, and a negative control for the complex so formed, respectively.
- a device 10 constructed in accord with at least one aspect of the invention comprises, Figure 1, a frame 12 having a top surface 14, and a front edge 16. Mounted on edge 16 is a slide valve 50 in accord with the invention.
- Top surface 14 has three wells or upper compartments 17, 18 and 19.
- a filter 24 At the bottom of each of the compartments is a filter 24, Figures 2 and 3, of appropriate pore size and pore volume.
- Filters 24 have an upper surface 25 and an under surface 26, Fig. 3.
- Surface 26 is in liquid-flow contact with an absorbent material 28 that preferably occupies each of three lower compartments 30, 32 and 34, Fig. 2, paired with the upper ones.
- liquid-flow contact means, in sufficient proximity such that a liquid meniscus emanating from surface 26 will also wet material 28 and flow into it, if no air lock exists in the lower compartment.
- Material 28 is any bibulous material, having a sufficient pore volume to soak up about 2 cc of liquid.
- Useful materials include cellulose acetate, cotton, and rayon.
- Useful materials for filters 24 include polyamides, such as nylons, and for example nylon-66 microporous membranes manufactured under the tradenames BIODYNE A or ULTIPOR N-66 by Pall Corporation. Most preferably, the membranes are precoated (prior to use) with one or more water-soluble proteins, such as casein derivatives obtained from acylation, alkylation or sulfonylation of the casein.
- the device can contain (between the filter and the absorbent material) a porous member which restricts flow back up to the filter, but allows flow from the filter to the absorbent material.
- the filter can be treated with a water-soluble polymeric overcoat selected to provide an induction time of from about 30 to about 300 seconds of delay, for a liquid head of pressure of about 6 mm of water.
- This treatment allows aqueous-based reagents to be coated thereafter onto the filter, and dried in less than 30 seconds, without having the reagents pass through the filter.
- Useful examples of such polymers include polyvinyl alcohol, polyvinyl pyrrolidone, carboxymethyl cellulose, and carboxyethyl cellulose.
- a liquid level indicator ridge 38 is provided in the wall 40 of each well, as a circular ring.
- such an indicator can be one or two fragments of a ring vertically spaced on wall 40, or a vertical bar (not shown).
- Vent aperture 44 is provided in each compartment 30, 32 and 34, Figures 2 and 3, to allow air passage out of the compartment as liquid flows in. Without such vents, or when the vent apertures are closed, an air lock precludes liquid from flowing through filter 24 into the lower compartments.
- the vent apertures extend to a wall surface 46, Figure 4, each of which comprises the end face of a stud 47 extending from edge 16. Stud 47 is grooved at 48 and 49, Fig. 4, to slidably accommodate mating lips from valve 50, as will be apparent. There are three studs 47, one for each aperture, Figure 2.
- stops 51 are pendent from frame 12, Figure 3, in a position interposed between material 28 and aperture 44.
- valve 50 is provided to alternately open and close vent apertures 44.
- Valve 50 comprises mounting member 52, and three valve seats 54, 56 and 58 that correspond to each of studs 47.
- Lips 60, 62 are provided at the side edges of member 52, to ride in grooves 48 and 49, respectively, and to force studs 47 against the valve seats.
- valve seats or the contacting wall surface 46 there is an elastomeric material, and in the other contacting member there is a relatively rigid material such as polystyrene.
- the elastomeric member is preferably in the valve seats and is especially selected for durometer hardness, cold flow, and coefficient of friction that will ensure that, when the valve seats are to be slid to the side of studs 47, having been compressed by the studs an amount of about 0.15 mm, they can be slid with a force that is between about 0.15 newtons and 20 newtons. (Anything less than about 0.15 newtons will cause member 52 to slide uncontrollably under its own weight. A force in excess of 10, and certainly in excess of 20, newtons is too high for easy manual manipulation.). The most preferred range is 0.15 to 10 newtons.
- the noted properties for the elastomeric material are preferably within the following ranges: Durometer (a measure of hardness) of no greater than about 70 Shore A, and most preferably from 55 to 65 Shore A.
- Cold flow (a measure of loss of recovery after being deformed, also known as "compression set") of between about 10 and about 40% lost recovery when compressed at 25°C, and most preferably, 23% lost recovery.
- a specific gravity of from 0.95 to 1.0 a tensile strength of from 45 Kg/cm2 to 70 Kg/cm2, ultimate elongation of from 300% to 400%, a 100% modulus value of from 20 to 25 Kg/cm2, a tear strength at 25°C of from 19 to 25 kN/m, a tension set of from 5 to 10%, flex fatigue to failure that is greater than 3.4 million, and a brittle point less than 60°C.
- thermoplastic rubber available under the tradename Santoprene Neutral 201-55 and 201-64, from Monsanto Corp. These two rubbers have the following specific properties: Neutral 201-55 201-64 Hardness 55 Shore A 64 Shore A Spec.
- seats 54, 56 and 58 are each chamfered at 70, Figure 5, to aid in sliding the seats onto studs 47.
- studs 47 are optionally chamfered at 72, Figure 2, to aid in assembling slide valve 50 onto the studs during manufacturing.
- stops 80 and 82 are preferably provided at edge 16. These stops cooperate with surfaces 84 and 86 on mounting member 52, Figure 5.
- slide valve 50 is first kept in place with seats 54, 56 and 58 sealed over apertures 44, the position shown in Figures 1-4. This position prevents liquid from entering compartments 30, 32 and 34 because of the air lock. (Each lower compartment is fluidly isolated from the others.)
- member 52 is slid to the left, Figures 1 and 2, to the position shown on studs 47 in phantom, Figure 5.
- apertures 44 are uncovered simultaneously in this position, so that air can flow out. At the same time, any liquid on filter 24 flows into the lower compartment.
- Filters 24 act as follows, in the preferred embodiment: In compartment 18, the patient sample's antigens, if any, complex with antibodies coated on wall 40 or added by the user, some of which are labeled, so that the complex is unable to pass through the filter. If no antigen is present, all the labeled antibodies pass through and are not available for detection. In compartment 19, antigen is supplied on the filter or on upper chamber wall 40 as manufactured, and when antibody is added by the filter, a complex forms as a positive control, and remains on the filter for detection.
- Device 10 is not a large device, having a length for valve 50, Figure 2, and thus for the entire device, of no more than about 6.5 cm.
- a length for valve 50, Figure 2 and thus for the entire device, of no more than about 6.5 cm.
- the elastomeric member can comprise at least the surface portion 46 of stud 47, Figure 4, with the member 56 being formed of a relatively rigid material, for example, polystyrene. In that case, it is the surface portion 46 that is preferably compressed distance "d" when the slide valve is on the studs.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Sampling And Sample Adjustment (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Measuring And Recording Apparatus For Diagnosis (AREA)
- Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
Abstract
Description
- This invention relates to a construction used to open and close vents in a liquid-collecting compartment, particularly such compartments used in assay devices.
- In the analysis for infectious diseases or pregnancy conditions, it is common to do an immunoassay in a device having an upper compartment, a lower compartment paired with the upper one and containing a liquid-absorbing material, and a filter between them. Examples are shown in US-A-3,888,629. In such devices, a trio of such paired compartments, side-by-side, allows the patient sample to be tested in one, a positive control in another, and a negative control in a third.
- In such devices, a vent hole is commonly provided in each of the lower compartments, to allow air to escape as liquid is entering. By appropriately opening and closing such vent holes, an air lock can be created which will allow, or stop, respectively, liquid flow into the lower compartment from above. (Air cannot pass out through the filter either, once it is wetted.) The stoppage of flow is appropriate to allow the liquid to incubate first at the filter, before passing down into the lower compartment, as is well-known.
- Thus, prior to this invention, there has been an unsolved problem of convenient, manual operation of the opening and closing of each of the vents in a liquid-collecting and -assaying device. The opening and closing of each vent heretofore has not been conducive to easy use of such devices. Particularly this has been troublesome where the devices are sold for home use, such as in home pregnancy kits. Additionally, it is necessary, particularly in the home kits, that the vent closure be operable manually. Materials that give negligible resistance to hand movement also tend to not reliably seal off the vent. Conversely, those that provide a secure seal tend to give high resistance to a manual opening of the vent. Such problems are magnified if all three compartments are vented at once.
- In accord with one aspect of the invention, the above problem is addressed by a liquid-collecting device comprising at least one liquid-collecting compartment, means in that one compartment defining a vent aperture fluidly connecting the compartment to the atmosphere, the aperture-defining means including a portion of a wall in which the aperture is located, and closure means for shutting off the vent aperture, characterized in that a) the closure means comprise a slide valve, b) one of the slide valve and the wall portion comprises an elastomeric member, and c) there is included means for slidably mounting the slide valve and the wall portion relative to each other to move the slide valve between a first position covering the aperture and a second position which uncovers the aperture, the member being formed of an elastomer having the following properties: a durometer valve no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6.
- In accord with another aspect of the invention, the above problem is addressed by a liquid-collecting device comprising three separate but adjacent liquid-collecting compartments, means in each of the compartments defining a vent aperture fluidly connecting each compartment to the atmospehre, the aperture-defining means including a portion of a wall in which the aperture is located, and closure means for each of the compartments for shutting off the respective aperture. The device is improved in that each of the three closure means comprises a slide valve comprising an elastomeric member and means for slidably mounting the member over the aperture to move between a first position covering the aperture and a second position in which the member uncovers the aperture, the member being formed of an elastomer having the following properties: a durometer value no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6.
- Thus, it is an advantageous feature of the invention that a device useful in immunoassays is provided with a valve for closing the necessary vent, that is manually operable with a minimum of effort.
- It is a further advantageous feature of the invention that such a device is provided with a plurality of liquid-collecting compartments, each independently vented, and a slide valve that opens and closes each vent simultaneously, with a minimum of effort.
- The present invention will now be described by way of example with reference to the accompanying drawings in which:
- Figure 1 is a perspective view of a device constructed in accord with the invention;
- Figure 2 is a plan view, partially broken away, and with the slide valve exploded away, of the device;
- Figure 3 is a section view taken along line III-III of Figure 2;
- Figure 4 is an enlarged section view of the portion of Figure 3 encircled as "Fig. 4"; and
- Figure 5 is a section view taken generally along line V-V of Figure 4, of only the
slide valve 50. - The invention is described herein in the context of the preferred embodiments, in which the device has three pairs of upper/lower compartments, to assay a) the patient sample, b) a positive control and c) a negative control, all more or less simultaneously. In addition, aspects of the invention are useful with only a single pair of compartments, and even without the upper compartment if one simply desires control over the rate of flow into a liquid-receiving compartment.
- The actual chemistries of the assay are not described in detail, primarily because the mechanics of the device are applicable to any, or even no, chemistry provided it is appropriate that flow not take place instantaneously into the liquid-receiving compartment. If the flow should proceed instantaneously, there is no need to have a valve to close the vents, as provided for by this invention.
- In the most preferred embodiment, the chemistries provide for an immunoassay, in which there is separately received at three filters in three compartments, a patient antigen complexed with an antigen, a positive control for the complex so formed, and a negative control for the complex so formed, respectively.
- A
device 10 constructed in accord with at least one aspect of the invention comprises, Figure 1, a frame 12 having atop surface 14, and afront edge 16. Mounted onedge 16 is aslide valve 50 in accord with the invention.Top surface 14 has three wells orupper compartments filter 24, Figures 2 and 3, of appropriate pore size and pore volume.Filters 24 have an upper surface 25 and an undersurface 26, Fig. 3.Surface 26 is in liquid-flow contact with anabsorbent material 28 that preferably occupies each of threelower compartments surface 26 will alsowet material 28 and flow into it, if no air lock exists in the lower compartment.Material 28 is any bibulous material, having a sufficient pore volume to soak up about 2 cc of liquid. Useful materials include cellulose acetate, cotton, and rayon. Useful materials forfilters 24 include polyamides, such as nylons, and for example nylon-66 microporous membranes manufactured under the tradenames BIODYNE A or ULTIPOR N-66 by Pall Corporation. Most preferably, the membranes are precoated (prior to use) with one or more water-soluble proteins, such as casein derivatives obtained from acylation, alkylation or sulfonylation of the casein. - Optionally the device can contain (between the filter and the absorbent material) a porous member which restricts flow back up to the filter, but allows flow from the filter to the absorbent material.
- Various optional treatments can be given the filter's upper surface 25, depending on the assays to be used. For example, the filter can be treated with a water-soluble polymeric overcoat selected to provide an induction time of from about 30 to about 300 seconds of delay, for a liquid head of pressure of about 6 mm of water. This treatment allows aqueous-based reagents to be coated thereafter onto the filter, and dried in less than 30 seconds, without having the reagents pass through the filter. Useful examples of such polymers include polyvinyl alcohol, polyvinyl pyrrolidone, carboxymethyl cellulose, and carboxyethyl cellulose.
- Optionally, a liquid
level indicator ridge 38, Figure 3, is provided in thewall 40 of each well, as a circular ring. Alternatively, such an indicator can be one or two fragments of a ring vertically spaced onwall 40, or a vertical bar (not shown). -
Vent aperture 44 is provided in eachcompartment filter 24 into the lower compartments. The vent apertures extend to awall surface 46, Figure 4, each of which comprises the end face of astud 47 extending fromedge 16.Stud 47 is grooved at 48 and 49, Fig. 4, to slidably accommodate mating lips fromvalve 50, as will be apparent. There are threestuds 47, one for each aperture, Figure 2. - To insure that
absorbent material 28 does not come in contact withaperture 44, and thus leak liquid,stops 51 are pendent from frame 12, Figure 3, in a position interposed betweenmaterial 28 andaperture 44. - In accord with the invention,
slide valve 50 is provided to alternately open andclose vent apertures 44. Valve 50 comprisesmounting member 52, and threevalve seats studs 47.Lips member 52, to ride ingrooves studs 47 against the valve seats. - In either the valve seats or the contacting
wall surface 46, there is an elastomeric material, and in the other contacting member there is a relatively rigid material such as polystyrene. The elastomeric member is preferably in the valve seats and is especially selected for durometer hardness, cold flow, and coefficient of friction that will ensure that, when the valve seats are to be slid to the side ofstuds 47, having been compressed by the studs an amount of about 0.15 mm, they can be slid with a force that is between about 0.15 newtons and 20 newtons. (Anything less than about 0.15 newtons will causemember 52 to slide uncontrollably under its own weight. A force in excess of 10, and certainly in excess of 20, newtons is too high for easy manual manipulation.). The most preferred range is 0.15 to 10 newtons. - The above test is not intended to imply that seats 54-58 are only to be compressed 0.15 mm when
member 52 is mounted onstuds 47. Instead, the compression can be distance "d", Figure 4, which can be from about 0 to as much as 0.3 mm, measured atsurface 64 of the seat shown in phantom for its uncompressed position. Practically speaking, however, some compression is preferred to ensure thatsurface 64 of seats 54-58 is in fact sealed overaperture 44. For the measurement of the force required to slide the valve, 0.15 mm compression is preferred. - To achieve the desired sliding force, the noted properties for the elastomeric material are preferably within the following ranges: Durometer (a measure of hardness) of no greater than about 70 Shore A, and most preferably from 55 to 65 Shore A. Cold flow (a measure of loss of recovery after being deformed, also known as "compression set") of between about 10 and about 40% lost recovery when compressed at 25°C, and most preferably, 23% lost recovery. Coefficient of friction (static) against polystyrene (the preferred material for stud 47) of between about 0.3 and about 0.6, and most preferably about 0.35. Other useful properties are: a specific gravity of from 0.95 to 1.0, a tensile strength of from 45 Kg/cm² to 70 Kg/cm², ultimate elongation of from 300% to 400%, a 100% modulus value of from 20 to 25 Kg/cm², a tear strength at 25°C of from 19 to 25 kN/m, a tension set of from 5 to 10%, flex fatigue to failure that is greater than 3.4 million, and a brittle point less than 60°C.
- Useful materials falling within these ranges include thermoplastic rubber available under the tradename Santoprene Neutral 201-55 and 201-64, from Monsanto Corp. These two rubbers have the following specific properties:
Neutral 201-55 201-64 Hardness 55 Shore A 64 Shore A Spec. Gravity 0.97 0.97 Tensile Strength 47 Kg/ cm² 70 Kg/cm² Ultimate Elongation 330% 400% 100% Modulus 21 Kg/cm² 25 Kg/cm² Tear Strength (25°C) 19 kN/m 24.5 kN/m Tension Set 6% 10% Cold Flow at 25°C 23% 23% Flex Fatigue (cycles to fail) >3.4 million >3.4 million Brittle Point Not Available <60°C Static Coefficient of Friction (against polystyrene) 0.59 0.35 - Optionally, seats 54, 56 and 58 are each chamfered at 70, Figure 5, to aid in sliding the seats onto
studs 47. Additionally,studs 47 are optionally chamfered at 72, Figure 2, to aid in assemblingslide valve 50 onto the studs during manufacturing. - To assist in keeping
slide valve 50 from being slid too far in either direction, stops 80 and 82 are preferably provided atedge 16. These stops cooperate withsurfaces member 52, Figure 5. - In use,
slide valve 50 is first kept in place withseats apertures 44, the position shown in Figures 1-4. This position prevents liquid from enteringcompartments apertures 44,member 52 is slid to the left, Figures 1 and 2, to the position shown onstuds 47 in phantom, Figure 5. As is readily apparent,apertures 44 are uncovered simultaneously in this position, so that air can flow out. At the same time, any liquid onfilter 24 flows into the lower compartment. -
Filters 24 act as follows, in the preferred embodiment: Incompartment 18, the patient sample's antigens, if any, complex with antibodies coated onwall 40 or added by the user, some of which are labeled, so that the complex is unable to pass through the filter. If no antigen is present, all the labeled antibodies pass through and are not available for detection. Incompartment 19, antigen is supplied on the filter or onupper chamber wall 40 as manufactured, and when antibody is added by the filter, a complex forms as a positive control, and remains on the filter for detection. Incompartment 17, no complexing will occur unless the test conditions are improper, such as due to the presence of high amounts of salt, in which case a special anti-complexing agent such as N-acetylglucosamine is overcome and complexing forms for detection as a negative control. -
Device 10 is not a large device, having a length forvalve 50, Figure 2, and thus for the entire device, of no more than about 6.5 cm. Thus, with the properties of the valve seats 54, 56 and 58 described above, it is readily feasible to slideslide valve 50 back and forth manually, by using finger pressure. - Alternatively (not shown), the elastomeric member can comprise at least the
surface portion 46 ofstud 47, Figure 4, with themember 56 being formed of a relatively rigid material, for example, polystyrene. In that case, it is thesurface portion 46 that is preferably compressed distance "d" when the slide valve is on the studs.
Claims (8)
- A liquid-collecting device (10) comprising at least one liquid-collecting compartment (17, 30; 18, 32; 19, 34), means (44) in said at least one compartment defining a vent aperture fluidly connecting said compartment (17, 30; 18, 32; 19, 34) to the atmosphere, said aperture-defining means (44) including a portion of a wall (46, 47) in which said aperture (44) is located, and closure means (50, 52) for shutting off said vent aperture (44);
characterized in that a) said closure means (50, 52) comprise a slide valve (54; 56; 58), b) one of said slide valve (54; 56; 58) and said wall portion (46, 47) comprises an elastomeric member, and c) further including means (48, 49, 60, 62) for slidably mounting said slide valve (54; 56; 58) and said wall portion (46, 47) relative to each other to move said slide valve (52) between a first position covering said aperture (44) and a second position which uncovers said aperture (44);
said member being formed of an elastomer having the following properties: a durometer value no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6. - A device as defined in Claim 1, wherein said elastomeric member is in said slide valve (54; 56; 58).
- A device as defined in Claim 1 or 2, and further including at least one additional liquid collecting compartment (17, 28; 18, 30; 19, 32), means (44) in said at least one additional compartment (17, 28; 18, 30; 19, 32) defining a vent aperture fluidly connecting said compartment (17, 28; 18, 30; 19, 32) to the atmosphere, said aperture-defining means (44) including a portion (47) of a wall (46) in which said aperture (44) is located, and closure means (50, 52) for shutting off said vent aperture (44); said closure means (50, 52) of said additional compartment (17, 28; 18, 30; 19, 32) comprising a slide valve (54; 56; 58) substantially identical to said slide valve of said at least one compartment.
- A liquid-collecting device (10) comprising three separate but adjacent liquid-collecting compartments (17, 28; 18, 30; 19, 32), means (44) in each of said compartments defining a vent aperture fluidly connecting said each compartment (17, 28; 18, 30; 19, 32) to the atmosphere, said aperture-defining means (44) including a portion (47) of a wall (46) in which said aperture (44) is located, and closure means (50, 52) for each of said compartments (17, 28; 18, 30; 19, 32) for shutting off said respective aperture (44);
characterized in that each of said three closure means (50, 52) comprise a slide valve (54; 56; 58) comprising an elastomeric member and means (48, 49, 60, 62) for slidably mounting said member over said aperture (44) to move between a first position covering said aperture (44) and a second position in which said member uncovers said aperture (44),
said member being formed of an elastomer having the following properties: a durometer value no greater than 70 Shore A, cold flow at 25°C that is between 10% and 40% lost recovery and a static coefficient of friction against polystyrene that is between 0.3 and 0.6. - A device as defined in Claim 4, and further including filtering means (24, 25, 26) for each of said compartments (17, 30; 18, 32; 19, 34), constructed to receive on said filtering means (24, 25, 26), each at one of the respective compartments (17, 30; 18, 32; 19, 34), a patient antigen complexed with an antibody, and positive and negative controls for the complex formed by the patient antigen;
whereby said device is useful in an immunoassay. - A device as defined in Claim 3, 4 or 5, wherein said slide valves (54, 56, 58) comprise an integral member (52), said valves (54, 56, 58) being disposed on said member (52) to simultaneously cover and simultaneously uncover said apertures (44) as said integral member (52) is moved between said first and second positions.
- A device as defined in any one of the preceding claims, and further including a water-absorbing material (28) in the or each compartment (30; 32; 34).
- A device as defined in Claim 7, and further including a filter (24, 25, 26) disposed upstream of, and in liquid-flow contact with, said water-absorbing material (28).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT88308558T ATE78194T1 (en) | 1987-09-18 | 1988-09-16 | DEVICE FOR COLLECTING LIQUIDS. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9824887A | 1987-09-18 | 1987-09-18 | |
US98248 | 1987-09-18 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0308231A2 EP0308231A2 (en) | 1989-03-22 |
EP0308231A3 EP0308231A3 (en) | 1989-07-19 |
EP0308231B1 true EP0308231B1 (en) | 1992-07-15 |
Family
ID=22268350
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88308558A Expired - Lifetime EP0308231B1 (en) | 1987-09-18 | 1988-09-16 | Liquid-collecting device |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0308231B1 (en) |
JP (1) | JPH021551A (en) |
AT (1) | ATE78194T1 (en) |
CA (1) | CA1302247C (en) |
DE (1) | DE3872811T2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6439303U (en) * | 1987-08-31 | 1989-03-09 | ||
US5147609A (en) * | 1989-05-19 | 1992-09-15 | Pb Diagnostic Systems, Inc. | Assay element |
CA2041050A1 (en) * | 1990-10-29 | 1992-04-30 | Kerinchan Babaoglu | Batch test apparatus with adjacent negative control and patient sample rows |
DE19725894A1 (en) * | 1997-06-19 | 1998-12-24 | Biotechnolog Forschung Gmbh | Differential vacuum chamber |
JP6247391B2 (en) * | 2013-07-15 | 2017-12-13 | サイトゲン カンパニー リミテッド | Slide assembly |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4246339A (en) * | 1978-11-01 | 1981-01-20 | Millipore Corporation | Test device |
AU2991384A (en) * | 1983-06-29 | 1985-01-03 | Precision Valve Australia Pty Limited | Self sealing caps |
US4632901A (en) * | 1984-05-11 | 1986-12-30 | Hybritech Incorporated | Method and apparatus for immunoassays |
DE3535292A1 (en) * | 1985-10-03 | 1987-04-09 | Bramlage Gmbh | DEVICE FOR PORTIONED ISSUE OF GRINED MEDIA, TABLETS OR THE LIKE |
US4719085A (en) * | 1985-12-24 | 1988-01-12 | Eastman Kodak Company | Mount for ammonia-sensitive test elements |
-
1988
- 1988-04-07 CA CA000563473A patent/CA1302247C/en not_active Expired - Fee Related
- 1988-09-16 AT AT88308558T patent/ATE78194T1/en active
- 1988-09-16 DE DE8888308558T patent/DE3872811T2/en not_active Expired - Lifetime
- 1988-09-16 EP EP88308558A patent/EP0308231B1/en not_active Expired - Lifetime
- 1988-09-18 JP JP63234692A patent/JPH021551A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE3872811T2 (en) | 1992-12-17 |
CA1302247C (en) | 1992-06-02 |
JPH021551A (en) | 1990-01-05 |
EP0308231A2 (en) | 1989-03-22 |
EP0308231A3 (en) | 1989-07-19 |
ATE78194T1 (en) | 1992-08-15 |
DE3872811D1 (en) | 1992-08-20 |
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