The present disclosure pertains to medical devices, and methods for manufacturing medical devices. More particularly, the present disclosure pertains to separation devices for biological samples.
A wide variety of medical devices have been developed for medical use, for example for collecting, separating, and/or processing biological samples. Some of these devices include separation devices.
An example medical device includes a device for physically separating a biological sample. The device comprises: a vessel for holding a biological sample, the biological sample includes a plurality of cells and a fluid; a filter membrane disposed within the vessel and positioned adjacent to an end region of the vessel; and an auger member disposed within the vessel, the auger member being designed to drive cells within the biological sample into contact with the filter membrane.
An example medical device includes a device for separating a sample. The device comprises: a vessel for holding a sample, the sample includes a plurality of cells; a filter membrane within the vessel and positioned adjacent to an end region of the vessel; and an auger member within the vessel, the auger member designed to place the plurality of cells into contact with the filter membrane.
Alternatively or additionally to any of the embodiments above, the vessel includes an open first end region and a second end region positioned substantially opposite the open first end region.
Alternatively or additionally to any of the embodiments above, further comprising a fluid passageway formed along the second end region.
Alternatively or additionally to any of the embodiments above, at least a portion of the filter membrane is positioned against a bottom end surface of the vessel.
Alternatively or additionally to any of the embodiments above, the filter membrane is spaced from a bottom end surface of the vessel.
Alternatively or additionally to any of the embodiments above, the auger member includes a central shaft and a helical thread disposed about the central shaft.
Alternatively or additionally to any of the embodiments above, the auger member is designed to rotate within the vessel.
Alternatively or additionally to any of the embodiments above, the auger member includes a central shaft and a compression member disposed at an end region of the central shaft, wherein the filter membrane is coupled to the compression member.
A device for physically separating a biological sample is disclosed. The device comprises: a vessel for holding a biological sample, the biological sample includes a plurality of cells and a fluid; a filter membrane disposed within the vessel, the filter membrane having a first end disposed along a bottom wall surface of the vessel and a second end spaced from the bottom wall surface; and a one-way filter disposed within the vessel and positioned adjacent to the second end of the filter membrane, the one-way filter being designed to allow cells within the biological sample to pass therethrough in a first direction and the one-way filter being designed to substantially prevent cells within the biological sample to pass therethrough in a second direction substantially opposite the first direction.
A device for separating a sample is disclosed. The device comprises: a vessel for holding a biological sample, the biological sample includes a plurality of cells; a filter membrane disposed within the vessel, the filter membrane having a first end along a bottom wall surface of the vessel and a second end spaced from the bottom wall surface; and a one-way filter within the vessel and positioned adjacent to the second end of the filter membrane, the one-way filter designed to allow cells within the biological sample to pass therethrough in a first direction and the one-way filter being designed to prevent cells within the sample to pass therethrough in a second direction opposite the first direction.
Alternatively or additionally to any of the embodiments above, the filter membrane is substantially cylindrical.
Alternatively or additionally to any of the embodiments above, an opening is formed in the vessel along the bottom wall surface.
Alternatively or additionally to any of the embodiments above, at least a portion of the filter membrane extends about the opening.
Alternatively or additionally to any of the embodiments above, the filter membrane extends circumferentially about the opening.
Alternatively or additionally to any of the embodiments above, the one-way filter includes a one-way baffle.
Alternatively or additionally to any of the embodiments above, the one-way filter includes a one-way membrane.
Alternatively or additionally to any of the embodiments above, the vessel includes a removable tray region.
Alternatively or additionally to any of the embodiments above, the bottom wall surface is disposed along the removable tray region.
A method for separating a biological sample is disclosed. The method comprises: disposing a biological sample within a centrifuge tube, the biological sample includes a plurality of cells and a fluid; centrifuging the centrifuge tube so that the cells in the biological sample migrate to a bottom wall surface of the centrifuge tube and the fluid within the biological sample is separated from the cells; disposing a barrier member adjacent to the cells along the bottom wall surface to define a physical barrier between the cells and the fluid; and removing the fluid.
Alternatively or additionally to any of the embodiments above, the barrier member comprises a stopcock and wherein disposing a barrier member adjacent to the cells along the bottom wall surface to define a physical barrier between the cells and the fluid includes shifting the stopcock from an open configuration to a closed configuration.
Alternatively or additionally to any of the embodiments above, the barrier member comprises a ball member and wherein disposing a barrier member adjacent to the cells along the bottom wall surface to define a physical barrier between the cells and the fluid includes placing the ball member within the centrifuge tube.
The above summary of some embodiments is not intended to describe each disclosed embodiment or every implementation of the present disclosure. The Figures, and Detailed Description, which follow, more particularly exemplify these embodiments.
The disclosure may be more completely understood in consideration of the following detailed description in connection with the accompanying drawings, in which:
While the disclosure is amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit the disclosure to the particular embodiments described. On the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the disclosure.
For the following defined terms, these definitions shall be applied, unless a different definition is given in the claims or elsewhere in this specification.
All numeric values are herein assumed to be modified by the term “about”, whether or not explicitly indicated. The term “about” generally refers to a range of numbers that one of skill in the art would consider equivalent to the recited value (e.g., having the same function or result). In many instances, the terms “about” may include numbers that are rounded to the nearest significant figure.
The recitation of numerical ranges by endpoints includes all numbers within that range (e.g. 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5).
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
It is noted that references in the specification to “an embodiment”, “some embodiments”, “other embodiments”, etc., indicate that the embodiment described may include one or more particular features, structures, and/or characteristics. However, such recitations do not necessarily mean that all embodiments include the particular features, structures, and/or characteristics. Additionally, when particular features, structures, and/or characteristics are described in connection with one embodiment, it should be understood that such features, structures, and/or characteristics may also be used connection with other embodiments whether or not explicitly described unless clearly stated to the contrary.
The following detailed description should be read with reference to the drawings in which similar elements in different drawings are numbered the same. The drawings, which are not necessarily to scale, depict illustrative embodiments and are not intended to limit the scope of the disclosure.
There are a number of methods for the collection of biological samples by a biopsy and/or other surgical processes. Such processes typically result in a tissue sample that can be routinely processed for pathological analysis. In some endoscopic procedures such as those where a fine needle aspiration device is utilized, the sample that is collected includes loose cells and fluids. Prior to tissue processing and/or analysis, additional steps may be necessary to gather the desired cells/tissue and allow the cells/tissue to be further processed. Disclosed herein are devices and methods that allow cells/tissue to be efficiently processed and/or analyzed including cells/tissue gathered by fine needle aspiration devices and/or other devices that collect cells/tissue along with fluids.
The vessel 14 may vary in form. In some instances, the vessel 14 may take the form of a beaker, flask, tube (e.g., test tube, conical tube, centrifuge tube, or the like), or any other suitable container. A first end region or “top” 21 of the vessel 14 may be open or otherwise include an opening that allows the sample 12 to be transferred into the vessel 14. A second end region or “bottom” 23 of the vessel 14 may be closed, meaning that the bottom 23 of the vessel 14 has a solid wall that can contain the sample 12. In some instances, the vessel 14 may include one or more openings (not shown in
In at least some instances, the filter membrane 16 may be positioned adjacent to the bottom 23 of the vessel 14. For example, at least a portion of the filter membrane 16 may be disposed along or otherwise in contact with the bottom 23 of the vessel 14. In some instances, the entire filter membrane 16 is disposed along and lines the bottom 23 of the vessel 14. Alternatively, a portion or all of the filter membrane 16 may be spaced from the bottom 23 of the vessel 14. The filter membrane 16 may include a porous material with openings sized to allow the desired cells/tissue 12a to be collected thereon while allowing fluid 12b to pass therethrough. For example, the filter membrane 16 have pores that are about 1-50 microns, or about 1-20 microns, or about 2-10 microns, or about 5 microns, or smaller than about 10 microns, or smaller than about 5 microns, or the like. Alternatively, the filter membrane 16 may be impervious to both the cells/tissue 12a and the fluid 12b.
The auger member 18 may include central shaft 32 and one or more helical threads 34 disposed thereon. The word “auger” in the auger member 18 is not intended to be limiting as other structures are contemplated that may be used in a manner similar to the auger member 18 in order to drive the cells/tissue 12a into contact with the filter membrane 16. For example, the “auger member” 18 may take the form of a plunger or syringe mechanism for driving the cells/tissue 12a into contact with the filter membrane 16.
In order to separate the biological sample 12, the biological sample 12 may be transferred from the fine needle aspiration device 20 into the vessel 14. The auger member 18 may be rotated in order to generate a force that drives the cells/tissue 12a into contact with the filter membrane 16 as shown in
In at least some instances, the vessel 114 may include a tray region 124 that is removable from the vessel 114 as shown in
It should be understood that this disclosure is, in many respects, only illustrative. Changes may be made in details, particularly in matters of shape, size, and arrangement of steps without exceeding the scope of the disclosure. This may include, to the extent that it is appropriate, the use of any of the features of one example embodiment being used in other embodiments. The invention's scope is, of course, defined in the language in which the appended claims are expressed.
This application claims priority under 35 U.S.C. § 119 to U.S. Provisional Application Ser. No. 62/527,610, filed Jun. 30, 2017, the entirety of which is incorporated herein by reference.
Number | Date | Country | |
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62527610 | Jun 2017 | US |