Patent Application
20240344945
Blood sampling is a common health care procedure typically used in hospital and laboratory settings to determine the physiological and biochemical condition of a patient. Blood sampling is essential to the diagnosis and treatment of patients suspected of a wide variety of disorders. Blood samples are analyzed by fluid testing devices, such as blood analyzers, to detect clinically significant variations in blood components, e.g., plasma, red blood cells, white blood cells, and platelets, or other characteristics, such as blood gas conditions. Analysis of a blood sample for blood gas conditions provides information, such as the amount of oxygen and carbon dioxide in the blood, and may also determine the pH of a blood sample. Imbalances in the oxygen, carbon dioxide, or pH levels of a blood sample may indicate particular pathological conditions or stage of disease progression.
Blood samples are typically collected from a central or arterial line using blood collection syringes having hypodermic needles or vacuum tubes coupled to a needle assembly. However, blood collection syringes are prone to have bubbles of air within the syringe. The bubbles in the barrel and tip of the syringe may alter the blood sample and interfere with the analysis of blood samples. Regarding blood gas analysis, bubbles trapped in a syringe may cause a blood analyzer to produce erroneous results. To obtain accurate results, blood samples need to be mixed thoroughly and all air must be expelled before mixing. Bubbles are typically expelled by tapping the sides of the syringe to force the air or gas to the top of the syringe. Once the bubbles have reached the top of the syringe, a piece of gauze or tissue is put over the top to force the gas (and some blood) out of the syringe. This method poses not only a biohazard risk because the blood sample is freely flowing out of the top of the syringe, but also an exposure risk, as the tip of the syringe is still open to ambient air. When a sample is in contact with ambient air, the sample begins to equilibrate the surrounding gases. Thus, when an improperly de-bubbled sample is tested on a blood gas analyzer, the results may not reflect the actual patient condition.
Further, blood analyzers often may not permit direct sample input via a syringe or vacuum tube. There, the syringe and/or vacuum tube is merely an intermediate container for the blood sample, and at least a portion of the blood sample must be removed and transferred to a secondary sample container (e.g., an adapter) capable of being accommodated by the blood analyzer. Transferring the blood sample to a secondary sample container presents its own exposure risks and may increase the likelihood of obtaining erroneous results.
A need exists for an apparatus and method for removing bubbles from a fluid sample. It is to such an apparatus and method that the inventive concepts disclosed and claim herein are directed.
The inventive concepts disclosed and claimed herein generally relate to an apparatus for removing bubbles from a fluid sample having a liquid portion and a gas portion. The apparatus includes a barrel and a filter member. The barrel has a first end, a second end, a sidewall, and an inner surface. The sidewall extends between the first end and the second end of the barrel, and the inner surface of the barrel defines an internal chamber. The first end of the barrel has an inlet opening and the second end has an outlet opening. The filter member is disposed within the internal chamber so the filter member defines an inlet side and an outlet side of the internal chamber. The filter member is positioned between the first end and the second end of the filter member. The filter member has at least one gas-permeable, liquid-impermeable membrane to permit at least a portion of the gas portion of the fluid sample to pass across the filter member from the inlet side to the outlet side of the internal chamber. The filter member is slidably disposed in the internal chamber of the barrel so as to be movable from a first position to a second position. In the first position, the filter member cooperates with the barrel to provide a fluid-tight seal across the filter member preventing the liquid portion of the fluid sample from passing from the inlet side to the outlet side as the fluid sample is passed into the internal chamber via the inlet opening to separate at least a portion of the gas portion from the liquid portion of the fluid sample. In the second position, the filter member cooperates with the barrel to provide at least one liquid passage between the filter member and the barrel to allow the liquid portion of the fluid sample to pass from the inlet side to the outlet side. The barrel further includes a second gas-permeable, liquid-impermeable membrane that is secured to the barrel adjacent the second end of the barrel. The second gas-permeable, liquid-impermeable membrane provides a fluid-tight seal across the outlet opening to prevent the liquid portion of the fluid sample from passing into the outlet opening from the internal chamber as the liquid portion of the fluid sample is passed from the inlet side to the outlet side via the liquid passage. The second gas-permeable, liquid-impermeable membrane is pierceable so a probe may be passed through the gas-permeable, liquid-impermeable membrane to the outlet side to withdraw the liquid portion of the fluid sample from the outlet side of the internal chamber.
To assist those of ordinary skill in the relevant art in making and using the inventive concepts disclosed herein, reference is made to the appended drawings and schematics, which are not intended to be drawn to scale, and in which like reference numerals are intended to refer to the same or similar elements for consistency. For purposes of clarity, not every component may be labeled in every drawing. Certain features and certain views of the figures may be shown exaggerated and not to scale or in schematic in the interest of clarity and conciseness. In the drawings:
Before explaining at least one embodiment of the inventive concept(s) in detail by way of exemplary drawings, experimentation, results, and laboratory procedures, it is to be understood that the inventive concept(s) is not limited in its application to the details of construction and the arrangement of the components set forth in the following description or illustrated in the drawings, experimentation and/or results. The inventive concept(s) is capable of other embodiments or of being practiced or carried out in various ways. The language used herein is intended to be given the broadest possible scope and meaning, and the embodiments are meant to be exemplary-not exhaustive. Also, it is to be understood that the phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting.
Unless otherwise defined, scientific and technical terms used in connection with the presently disclosed and claimed inventive concept(s) shall have the meanings commonly understood by those of ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. The foregoing techniques and procedures are generally performed according to conventional methods well known in the art and as described in various general and more specific references cited and discussed throughout the present specification. The nomenclatures utilized in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art. Standard techniques are used for chemical syntheses and chemical analyses.
All the articles, compositions and/or methods disclosed and claimed herein can be made and executed without undue experimentation, given the present disclosure. While the articles, compositions and methods of the inventive concept(s) have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the articles, compositions and/or methods and in the steps or in the sequence of steps of the methods described herein without departing from the concept, spirit and scope of the inventive concept(s). All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the inventive concept(s) as defined by the appended claims.
As utilized under the present disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:
The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.”
The use of the term “or” in the claims is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.”
Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among the study subjects.
The use of the term “at least one” will be understood to include one as well as any quantity more than one, including but not limited to, 2, 3, 4, 5, 10, 15, 20, 30, 40, 50, 100, etc. The term “at least one” may extend up to 100 or 1000 or more, depending on the term to which it is attached, in addition, the quantities of 100/1000 are not to be considered limiting, as higher limits may also produce satisfactory results. In addition, the use of the term “at least one of X, Y, and Z” will be understood to include X alone, Y alone, and Z alone, as well as any combination of X, Y, and Z.
As used in this specification and claim(s), the words “comprising” (and any form of comprising, such as “comprise” and “comprises”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “includes” and “include”) or “containing” (and any form of containing, such as “contains” and “contain”) are inclusive or open-ended and do not exclude additional, unrecited elements or method steps.
The term “or combinations thereof” as used herein refers to all permutations and combinations of the listed items preceding the term. For example, “A, B, C, or combinations thereof” is intended to include at least one of: A, B, C, AB, AC, BC, or ABC, and if order is important in a particular context, also BA, CA, CB, CBA, BCA, ACB, BAC, or CAB. Continuing with this example, expressly included are combinations that contain repeats of one or more item or term, such as BB, AAA, MB, BBC, AAABCCCC, CBBAAA, CABABB, and so forth. The skilled artisan will understand that typically there is no limit on the number of items or terms in any combination, unless otherwise apparent from the context.
As used herein, the term “sample” and variations thereof is intended to include biological tissues, biological fluids, chemical fluids, chemical substances, suspensions, solutions, slurries, mixtures, agglomerations, tinctures, slides, powders, or other preparations of biological tissues or fluids, synthetic analogs to biological tissues or fluids, bacterial cells (prokaryotic or eukaryotic), viruses, single-celled organisms, lysed biological cells, fixed biological cells, fixed biological tissues, cell cultures, tissue cultures, genetically engineered cells and tissues, genetically engineered organisms, and combinations thereof, for example.
In the following detailed description of embodiments of the inventive concept, numerous specific details are set forth in order to provide a more thorough understanding of the inventive concept. However, it will be apparent to one of ordinary skill in the art that the inventive concept within the disclosure may be practiced without these specific details. In other instances, well-known features have not been described in detail to avoid unnecessarily complicating the instant disclosure.
Finally, as used herein any reference to “one embodiment” or “an embodiment” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. The appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
Described herein, and shown in the accompanying figures, are several non-limiting embodiments of the apparatus of the presently claimed and disclosed inventive concepts which may be used in association with collection syringes and fluid sample analyzers for removing bubbles of air or other gases from a fluid sample for analysis by a fluid sample analyzer. The fluid sample is generally from a biological source. A “fluid” refers to any substance that has no fixed shape and yields easily to external pressure.
Referring now to the drawings, and more particularly to
The barrel 12 includes a first end 18, a second end 20, a sidewall 22, and an inner surface 24. The barrel 12 may be of any suitable size and shape, and formed of any suitable material, such as, without limitation, plastics such as polycarbonate, polystyrene, polyacrylates, and polyurethane, or medical-grade polymers. The sidewall 22 of the barrel 12 extends between the first end 18 and the second end 20 of the barrel 12. The inner surface 24 of the barrel 12 defines an internal chamber 26. The first end 18 has an inlet opening 28 and the second end 20 has an outlet opening 30. The internal chamber 26 may be of any suitable size and shape to contain a fluid sample 32. The fluid sample 32 may be, for example, blood, serum, plasma, or other bodily fluids. The fluid sample 32 may contain a gas portion and a liquid portion. The gas portion of the fluid sample 32 may be, for example, air or other gases. A portion of the gas portion may form bubbles in the fluid sample
The inlet opening 28 and the outlet opening 30 may have a cross-section of any suitable geometry, including, but not limited to, circular, oval, square, or rectangular. The inlet opening 28 and the outlet opening 30 may be molded or cut into the barrel 12, or otherwise pre-fabricated. The inlet opening 28 may be formed to prevent coagulation as the fluid sample 32 is passed into the internal chamber 26 via the inlet opening 28.
The outlet opening 30 may be provided with a nozzle cap 14. The nozzle cap 14 includes an annular wall 36 and a tubular portion 38 having a bore 40 extending therethrough. The bore 40 may have a cross-section of any suitable geometry, including, but not limited to, circular, oval, square, or rectangular. The bore 40 may be sized to have a diameter adapted to slidably axially receive a sample probe. The base of the tubular portion 38 flares outwardly and merges with the annular wall 36 at a rim 42, the annular wall 36 tapers downwardly to form an inverted frusto-conical section. The nozzle cap 14 may be releasably coupled to the outlet opening 30 such that the bore 40 is aligned with the outlet opening 30 to permit fluid communication with the internal chamber 26.
Referring now to
As will be discussed below, the groves 27 cooperate with the filter member 16 to define at least one liquid passage between the filter member 16 and the barrel 12 to allow the liquid portion of the fluid sample to pass from the inlet side 44 of the internal chamber 26 to the outlet side 46 thereof. It will be appreciated that the number and size of the grooves 27 may be varied. The grooves 27 may be molded or machined into the inner surface 24, or otherwise pre-fabricated. The grooves 27 terminates at or near the stop member 29. The stop member 29 is positioned intermediate the first end 18 and the second end 20 of the barrel 12. The stop member 29 extends radially from the inner surface 24 into the internal chamber 26. The stop member 29 includes a surface to engage at least one surface of the filter member 16 and prevents the movement of the filter member 16 beyond the stop member 29 and prior to contact of the filter member 16 with the second end 20 of the barrel 12.
The filter member 16 is disposed within the internal chamber 26 so the filter member 16 defines an inlet side 44 and an outlet side 46 of the internal chamber 26. The filter member 16 is positionable between the first end 18 and the second end 20 of the barrel 12. The filter member 16 includes at least one gas-permeable, liquid-impermeable membrane 48.
The filter member 16 is slidable from a first position (
Referring now to
The body 50 of the filter member 16 may be formed of any suitable material, such as, without limitation, a rubber, an elastomer, a polyolefin-based resin, a fluorine-based resin, or a polyester-based resin. The elastomer may include, for example, a polyvinyl chloride-based elastomer, a polyolefin-based elastomer, a styrene-based elastomer, a polyester-based elastomer, a polyamide-based elastomer, a polyurethane-based elastomer, or a mixture thereof.
The filter member 16 further includes a gas-permeable, liquid-impermeable membrane 48 which extends across the entirety of the passageway 58. In one embodiment, the gas-permeable, liquid-impermeable membrane 48 is secured to the body 50 adjacent the second end 54 of the body 50, as shown in
Referring now to
Referring now to
A gas-permeable, liquid impermeable membrane 49 is secured to the barrel 12 adjacent the second end 20 of the barrel 12 to provide a fluid-tight seal across the outlet opening 30 to prevent the liquid portion of the fluid sample 32 from passing into the outlet opening 30 from the internal chamber 26 as the liquid portion of the fluid sample 32 is passed from the inlet side 44 to the outlet side 46 via the liquid passage 47. The gas-permeable, liquid impermeable membrane 49 is pierceable so a sample probe 72 may be passed through the gas-permeable, liquid impermeable membrane 49 from the outlet side 46 of the internal chamber 26 to withdraw the liquid portion of the fluid sample 32 from the outlet side 46 of the internal chamber 26.
The gas-permeable, liquid-impermeable membranes 48 and 49 may be formed of any suitable material, such as, without limitation, polytetrafluoroethylene, polyvinylidene fluoride, polyvinylchloride, polyolefins like polypropylene, polyethylene, polymethylpentene, polyamides, polysulfones, polyetheretherketones, polycarbonates, and combinations including any of these. In one embodiment, the gas-permeable, liquid-impermeable membranes 48 and 49 are formed from a material comprising at least one of polytetrafluorethylene, polypropylene, and polyethylene. The gas-permeable, liquid-impermeable membrane 49 may have a thickness suitable for allowing puncture upon application of a mechanical force. The gas-permeable, liquid-impermeable membrane 48 may permit at least a portion of the gas portion of the fluid sample 32, which forms bubbles, to pass across the filter member 16 from the inlet side 44 to the outlet side 46 of the internal chamber 26. The gas-permeable, liquid-impermeable membrane 48 also provides a fluid-tight seal across the filter member 16 to prevent the liquid portion of the fluid sample 32 from passing from inlet side 44 to the outlet side 46 as the fluid sample 32 is passed into the internal chamber 26 via the inlet opening 28 to separate at least a portion of the gas portion from the liquid portion of the fluid sample 32
As shown in
The fluid sample analyzer 68 includes a sample input port 70 and a sample probe 72. The sample probe 72 may be axially slidable relative to the sample input port 70. The sample input port 70 may be sized to receive and detachably secure at least a portion of the nozzle cap 14, as shown in
The collection syringe 66 includes a syringe body 74 having a front end 76, a rear end 78, and a plunger 80. The syringe body 74 defines a reservoir 82 within which the fluid sample 32 may be contained and later expelled via a dispensing opening 84 positioned at the front end 76 of the syringe body 74. The rear end 78 of the syringe body 74 may be open and provided with a body flange 85 to facilitate the collection and expulsion of the fluid sample 32. The syringe body 74 may be any suitable size or shape for collection of fluid samples, such as, for example, a cylindrical shape. The syringe body 74 may also include a collar 77 formed concentrically with the dispensing opening 84 into a cylindrical shape to surround the dispending opening 84. The collar 77 may include an inner peripheral surface in which a threaded engagement portion 79 is formed for engaging the apparatus 10. The syringe body 74 may be constructed of any suitable material, such as glass or plastic. The syringe body 74 may have an outer diameter adapted to coaxially slide within inlet opening 28 of the apparatus 10.
The plunger 80 may include a shaft 86 that terminates at one end in a plunger flange 88 to facilitate the collection and expulsion of the fluid sample 32. The shaft 86 may, for example, have a cylindrical shape or a columnar shape, and may have a cross-section of a polygonal shape, such as a square, pentagonal, hexagonal, or cruciform shape. The plunger 80 may further include a plunger seal 90 secured to the shaft 86 opposite the plunger flange 88. The plunger 80 may be removably disposed within the syringe body 74 and may be selectively movable within the reservoir 82. The plunger seal 90 has a diameter that permits the plunger seal 90 to create a fluid-tight seal when positioned within the reservoir 82 such that the liquid sample 32 may not move past the plunger seal 90. Further, the plunger seal 90 prevents ambient air from moving from the rear end 78 of the syringe body 74 in a direction past the plunger seal 90. The plunger 80 may be axially displaced relative to the syringe body 74. Movement of the plunger 80 from the rear end 78 to the front end 76 of the syringe body 74 may cause at least a portion of the fluid sample 32 to be expelled from the reservoir 82 and introduced into the inlet opening 28 of the apparatus 10 via the dispensing opening 84. The plunger 80 may be constructed of any suitable polymeric material known in the art.
To remove the gas portion (i.e., bubbles) of the fluid sample 32 from the liquid portion, the collection syringe 66, containing a volume of the fluid sample 32 within the reservoir 82, is releasably attached to the inlet opening 28 of the barrel 12, as shown in
The collection syringe 66 and the apparatus 10 are positioned in an upright orientation with the apparatus 10 above the collection syringe 66 and the bubbles in the fluid sample rise to the top of the fluid sample 32. The plunger 80 of the collection syringe 66 is displaced axially along the reservoir 82 a distance from the rear end 78 towards the front end 76 of the syringe body 74, as shown in
Upon application of sufficient force to overcome the initial resistive force, the plunger 80 is advanced further into the reservoir 82 towards the front end 76 of the syringe body 74, as shown in
The filter member 16 continues to migrate along the length of the internal chamber 26 before contacting the stop member 29 of the barrel 12 and coming to rest in the second position, as shown in
In this position, as the fluid sample 32 enters the inlet side 44 of the internal chamber, the liquid portion of the fluid sample 32 infiltrates into the fluid passage 47 and passes between the filter member 16 and the barrel 12 from the inlet side 44 of the internal chamber 26 to the outlet side 46 of the internal chamber 26. The gas-permeable, liquid-impermeable membrane 49, secured to the barrel 12 adjacent the second end 20, prevents the liquid portion of the fluid sample 32 from being discharged from the internal chamber 26.
This arrangement prevents ambient air from entering the internal chamber 26 and prevents the fluid sample 32 from exiting the internal chamber 26 via the outlet opening 30. In some embodiments, the plunger 80 may be partially extended into the reservoir 82 so less than all of the fluid sample 32 is transferred from the reservoir 82 into the internal chamber 26.
Once the liquid portion of the fluid sample 32 has been expelled from the reservoir 82 and is contained within the internal chamber 26 of the apparatus 10, the sample probe 72 of the fluid sample analyzer 68 may be extended from the sample input port 70 and passed through the gas-permeable, liquid impermeable membrane 49 secured adjacent the second end 20 of the barrel 12 to withdraw the liquid portion of the fluid sample 32 from the outlet side 46 of the internal chamber 26, as shown in
In some embodiments, the barrel 12 may further include a lateral flow strip 96, as shown in
From the above description, it is clear that the inventive concept(s) disclosed herein is well adapted to carry out the objects and to attain the advantages mentioned herein as well as those inherent in the inventive concept disclosed herein. While exemplary embodiments of the inventive concept disclosed herein have been described for purposes of this disclosure, it will be understood that numerous changes may be made which will readily suggest themselves to those skilled in the art and which are accomplished without departing from the scope of the inventive concept disclosed herein and defined by the appended claims.
The following is a list of non-limiting illustrative embodiments of the inventive concepts disclosed herein:
An illustrative apparatus for removing bubbles from a fluid sample having a liquid portion and a gas portion, comprising:
The illustrative apparatus wherein the filter member further comprises a body having a first end, a second end, and a sidewall extending from the first end to the second end, the sidewall of the body defining a passageway extending through the body from the first end to the second end, and wherein the gas-permeable, liquid-impermeable membrane extends across an entirety of the passageway.
The illustrative apparatus wherein the sidewall of the body has at least two annular projections extending radially outwardly in slidable contact with the inner surface of the barrel, and wherein at least one of the projections is in sealing contact with the inner surface of the barrel when the filter member is in the first position.
The illustrative apparatus wherein the filter member cooperates with the barrel to provide at least one liquid passage between the filter member and the barrel.
The illustrative apparatus wherein the liquid passage is defined by the body and a plurality of grooves extending along at least a portion of the inner surface of the barrel.
The illustrative apparatus wherein the grooves extend circumferentially about the inner surface of the barrel.
The illustrative apparatus wherein the grooves are parallel to one another The illustrative apparatus wherein the barrel has a stop member to engage the filter member in the second position. The illustrative apparatus wherein the gas-permeable, liquid-impermeable membrane is secured to the body adjacent the second end of the body.
The illustrative apparatus wherein the gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene.
The illustrative apparatus wherein the body has a plurality of passageways extending through the body from the first end to the second end, and wherein the filter member further has a plurality of gas-permeable, liquid impermeable membranes with at least one of the gas-permeable, liquid impermeable membranes extending across each of the passageways of the body.
The illustrative apparatus wherein the filter member further comprises a plurality of porous filter material positioned between the first end of the body and each of the gas-permeable, liquid impermeable membranes to prevent solid particulate from contacting the gas-permeable, liquid impermeable membranes.
The illustrative apparatus wherein the plurality of gas-permeable, liquid-impermeable membranes are secured to the body adjacent the second end of the body.
The illustrative apparatus wherein the passageways are in a parallel relationship to one another.
The illustrative apparatus wherein the gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene.
The illustrative apparatus wherein the second gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene.
An illustrative apparatus for removing bubbles from a fluid sample having a liquid portion and a gas portion in combination with a liquid sample analyzer having a sample probe, comprising:
The illustrative combination wherein the filter member further comprises a body having a first end, a second end, and a sidewall extending from the first end to the second end, the sidewall of the body defining a passageway extending through the body from the first end to the second end, and wherein the gas-permeable, liquid-impermeable membrane extends across an entirety of the passageway.
The illustrative combination wherein the sidewall of the body has at least two annular projections extending radially outwardly in slidable contact with the inner surface of the barrel, and wherein at least one of the projections is in sealing contact with the inner surface of the barrel when the filter member is in the first position.
The illustrative combination wherein the filter member cooperates with the barrel to provide at least one liquid passage between the filter member and the barrel.
The illustrative combination wherein the liquid passage is defined by the body and a plurality of grooves extending along at least a portion of the inner surface of the barrel.
The illustrative combination wherein the grooves extend circumferentially about the inner surface of the barrel.
The illustrative combination wherein the grooves are parallel to one another. The illustrative combination wherein the barrel has a stop member to engage the filter member in the second position.
The illustrative combination wherein the gas-permeable, liquid-impermeable membrane is secured to the body adjacent the second end of the body.
The illustrative combination wherein the gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene. The illustrative combination wherein the body has a plurality of passageways extending through the body from the first end to the second end, and wherein the filter member further has a plurality of gas-permeable, liquid impermeable membranes with at least one of the gas-permeable, liquid impermeable membranes extending across each of the passageways of the body.
The illustrative combination wherein the filter member further comprises a plurality of porous filter material positioned between the first end of the body and each of the gas-permeable, liquid impermeable membranes to prevent solid particulate from contacting the gas-permeable, liquid impermeable membranes.
The illustrative combination wherein the plurality of gas-permeable, liquid-impermeable membranes are secured to the body adjacent the second end of the body.
The illustrative combination wherein the passageways are in a parallel relationship to each other.
The illustrative combination wherein the gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene.
The illustrative combination wherein the second gas-permeable, liquid-impermeable membrane is formed from a material comprising at least one of polytetraflyorethylene, polypropylene, and polyethylene
An illustrative method for removing bubbles from a fluid sample having a liquid portion and a gas portion, comprising:
The illustrative method wherein at least a portion of the liquid portion of the fluid sample is collected from the outlet side of the internal chamber by piercing a second gas-permeable, liquid-impermeable membrane secured to the barrel adjacent the second end of the barrel so a sample probe may be passed through the second gas-permeable, liquid-impermeable membrane to the outlet side to withdraw the liquid portion of the fluid sample from the outlet side of the internal chamber.
The illustrative method the filter member further comprises a filter element interposed between the gas-permeable, liquid-impermeable membrane and the inlet side of the internal chamber, the at least one filter element having an inlet port and an outlet port, the inlet port in fluid communication with the inlet side of the internal chamber, the outlet port in fluid communication with the gas-permeable, liquid-impermeable membrane to permit at least a portion of the fluid sample to pass across the at least one filter element and to the gas-permeable, liquid-impermeable membrane.
The illustrative method wherein the gas-permeable, liquid-impermeable membrane is a plurality of gas-permeable, liquid-impermeable membranes.
This application claims benefit under 35 USC § 119(e) of U.S. Provisional Application No. 63/244,987, filed Sep. 16, 2021 and U.S. Provisional Application No. 63/232,365, filed Aug. 12, 2021. The entire contents of the above-referenced patent application(s) are hereby expressly incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2022/074578 | 8/5/2022 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63232365 | Aug 2021 | US | |
| 63244987 | Sep 2021 | US |
