The present invention is directed to a device for collecting a biological sample, and more specifically, to a device for collecting a biological sample, such as tissue, cells, protein, RNA and/or DNA from an esophagus of a patient.
A known tissue collection device includes an expandable device with longitudinally extending folds. The expandable device expands radially at a collection site within a body lumen, such as an esophagus. After the device is expanded, tissue is collected from the collection site. The expandable device is deflated after tissue is collected. The folds trap collected tissue when the device is deflated after collection of the tissue. The known tissue collection device may be inserted through an endoscope to the collection site or via standard catheter intubation techniques.
The present invention relates to a device for collecting a biological sample in an esophagus of a patient. The device includes a swallowable collection portion for collecting a sample at a collection site in the esophagus. A stylet connected with the collection portion helps place the collection portion into the back of a throat of a patient for swallowing.
In another aspect of the present invention, a device for collecting a biological sample in an esophagus of a patient includes a collection portion having a first axial end portion and a second axial end portion. The second axial end portion has a collapsed position and an expanded position. The second axial end portion moves in an axial direction relative to the first axial end portion when the second axial end portion moves between the collapsed position and the expanded position. The second axial end portion extends axially into the first axial end portion and has a concave shape when the second axial end portion is in the collapsed position. A sleeve is in the first axial end portion.
In another aspect of the present invention, a device for collecting a biological sample in an esophagus of a patient includes a collection portion having a collapsed position and an expanded position. At least one tissue collecting projection extends from an outer surface of the collection portion. A first side wall of the tissue collecting projection extends generally perpendicular to the outer surface of the collection portion when the collection portion is in a non-inflated position between the collapsed and expanded positions. A second wall of the tissue collecting projection tapers toward the first side wall as the side walls extend radially outward from the outer surface when the collection portion is in the non-inflated position between the collapsed and expanded positions.
In another aspect of the present invention, a method for collecting a biological sample includes moving a swallowable collection portion with a stylet into the back of a throat of a patient for swallowing. The collection portion is moved to a collection site in the esophagus with a portion of the collection portion in a collapsed position. The portion of the collection portion is expanded when the collection portion is at the collection site. A biological sample is collected with the portion of the collection portion in the expanded position. The portion of the collection portion is collapsed after collecting the sample. The device is removed from the esophagus of the patient
The foregoing and other features of the present invention will become apparent to those skilled in the art to which the present invention relates upon reading the following description with reference to the accompanying drawings, in which:
A collection device 10 for collecting a biological sample constructed in accordance with the present invention is illustrated in
The collection device 10 includes a generally hollow longitudinally extending collection portion 12. The collection portion 12 has a first or proximal axial end portion 14 connected to a second or distal axial end portion 16. The distal end portion 16 has a first axial end portion 22 connected to the proximal axial end portion 14. The first end portion 22 may be connected to the proximal end portion 14 in any desired manner, such as by using an adhesive or bonding. The first axial end portion 22 engages a shoulder 24 on the proximal axial end portion 14. Therefore, the collection portion 12 has a smooth outer surface. The distal axial end portion 16 may be connected to the proximal end portion 14 in any desired manner. The proximal axial end portion 14 and the distal axial end portion 16 may be made of a flexible polymer, such as silicone or polyurethane. The distal axial end portion 16 has a lower durometer than the proximal axial end portion 14. The distal axial end portion 16 may have a durometer between 5-90 Shore A. The durometer of the distal axial end portion 16 is preferably between 20-70 Shore A, and more specifically, approximately 30 Shore A.
The distal axial end portion 16 may expand and contract. The first or proximal axial end portion 14 is relatively rigid. Therefore, the proximal end portion 14 has a fixed radial extent. The first axial end portion 14 and the second axial end portion 16 may be formed as separate pieces that are connected together in any desire manner or may be integrally formed as one-piece. Although the proximal end portion 14 is illustrated as having a cylindrical shape, the proximal end portion may have any desired shape.
The proximal axial end portion 14 is connected to a support member 20, such as a catheter. The support member 20 may be a tubular member in fluid communication with the interior of the collection portion 12. The proximal axial end portion 14 conducts fluid, such as air, from the support member 20 to the distal axial end portion 16. The support 20 resists collapsing when a vacuum is applied to the support member and resists stretching during withdrawal of the collection device 10 from the collection site.
The second or distal end portion 16 of the collection portion 12 has an expanded or inflated position (
The distal end portion 16 extends into the first or proximal axial end portion 14 and has a concave shape, shown in
The proximal end portion 14 has a relatively high durometer so that the proximal end portion does not collapse when a vacuum is applied to the proximal end portion through the support 20. The shape of the proximal end portion 14 does not change when the distal end portion 16 moves between the deflated and inflated positions. The proximal end portion 14 does not move radially when the distal end portion 16 moves between the deflated and inflated positions.
The distal end portion 16 has an outer surface 32 for collecting tissue when the distal portion is in the expanded position. The outer surface 32 faces radially outwardly when the distal end portion 16 is in the expanded position and may face radially inwardly when the distal end portion is in the collapsed or inverted position. It is contemplated that the outer surface 32 of the distal end portion 16 may have any desired construction for collecting tissue. The outer surface 32 of the distal end portion 16 may have a plurality of projections or bristles 40 for collecting tissue. The distal end portion 16 may have any desired number of projections or bristles 40.
The projections or bristles 40 may have a V-shape (
The first and second sides 42, 44 may extend at an angle of approximately 90° relative to each other. It is contemplated that the first and second sides 42 and 44 may extend at any desired angle relative to each other. The desired angle may be determined based on the type of biological sample to be collected. Alternatively, the projections 40 may be cup shaped or have a semi-circular shape.
Each of the projections or bristles 40 has side walls 54 and 56 (
The side wall 56 may form a flap, hood or lip 59 (
The distal end portion 16 may include a plurality of projections or bristles 60 (
The projections or bristles 40, 60 are arranged in circumferentially extending rows (
The catheter 20 may have a stylet 100 (
A proximal end 106 (
The Y-fitting 102 has a second branch 120 extending at an angle to the first branch 110. The second branch 120 may have a stopcock 122 for opening and closing the second branch. A syringe may be connected to the second branch 120 for introducing a fluid, such as air, into the Y-fitting 102 and catheter 20 to expand the distal end portion 16 of the collection portion 12 and apply a vacuum to remove the fluid to collapse the distal end portion 16 after collecting a sample. The stopcock 122 may be used to retain the fluid in the catheter 20 and collection portion 12 when obtaining a sample. The stopcock 122 and syringe help to control the injection of fluid to move the distal end portion 16 between the collapsed and expanded positions.
A disk 126 may be connected to a proximal end of the catheter 20 or the distal end of the connector 102. The disk 126 extends radially away from the catheter 20 to prevent the connector 102 from being inserted into a patient's mouth and/or throat.
The collection portion 12 is moved to a collection site within a body lumen, such as an esophagus, with the distal end portion 16 in the collapsed or deflated position. The collection portion 12 may be swallowed by a patient. The stylet 100 may be manipulated to place the collection portion 12 into the back of the throat of the patient to help with the swallowing of the collection portion. It is also contemplated that the patient may be intubated with the collection portion 12 attached to the catheter. The distal end portion 16 may be held in the collapsed or deflated position by applying a vacuum to the collection portion 12 through the support 20. The support member 20 or catheter may have depth markings to determine the collection site within the patient's anatomy. The collection portion 12 may be moved past a lower esophageal sphincter (LES) and pulled in a proximal direction toward the LES. The operator or physician may sense the increased tension in the catheter 20 when the collection portion 12 engages the LES. The distal end portion 16 of the collection portion 12 may be expanded when the LES is sensed. The distal end portion 16 is moved from the collapsed position to the expanded position when the collection portion 12 is at or near the collection site. The syringe connected to the Y-fitting 102 may be activated to apply pressurized fluid, such as air, to the distal end portion 16 to cause the distal end portion to move axially from the collapsed position to the expanded position.
The collection portion 12 is moved in the esophagus or body lumen to collect a biological sample, such as, tissue, cells, protein, RNA and/or DNA from the collection site when the distal end portion 16 is in the expanded position. It is contemplated that the collection portion 12 is only moved in a proximal direction so that the expanded distal end portion 16 engages the collection site to collect biological samples. The depth markings on the support member 20 or catheter may be used as a guide. After the biological sample is collected, the distal end portion 16 is moved from the expanded position to the collapsed or inverted position. The distal end portion 16 may be moved from the expanded position to the collapsed position by applying a vacuum to the collection portion 12 with the syringe connected to the Y-fitting 102. As the collection portion 12 moves out of the body lumen, the distal end portion 16 does not engage the body lumen and prevents the collected biological samples from being contaminated by tissue from areas along the body lumen different from the collection site. Once the collection device 10 is removed from the patient, the biological samples are collected via a wash and/or the collection portion 12 or the distal end portion 16 may be cut from the support member 20 and deposited in a biological sample vial.
Another embodiment of a collection device 140 is shown in
A stiffening sleeve 148 is connected to the proximal end portion 144. The sleeve 148 may be axially inserted into the proximal end portion 144 of the collection portion 142 so that the distal end portion 146 extends into the sleeve when the distal end portion is in the collapsed position. The sleeve 148 is retained in the proximal end portion 144 by a distal undercut rim 150 on the proximal end portion. The sleeve 148 may be inserted axially into the proximal end portion 144 until the undercut rim 150 snaps over the sleeve to retain the sleeve in the proximal end portion. The undercut rim prevents the sleeve 148 form being able to slide out into the distal end portion 146. The sleeve 148 may be a polypropylene molded cylinder that provides additional column strength to the proximal end portion 144 to help prevent column and side wall collapse during vacuum inversion of the distal end portion 146. The sleeve 148 allows for a thinner wall of the proximal end portion 144. The thinner wall of the proximal end portion 144 provides more space on the inside of the proximal end portion for the distal end portion 146 to invert easier. The ease at which the distal end portion 146 inverts may enhance the ability to collect as much of the biological sample as possible. If there is too much friction between the surfaces of the distal end portion 146 as the distal end portion inverts into the proximal end portion 144 it could squeegee off the sample. The sleeve 148 enhances inversion reliability and reduces the surfaces of the distal end portion 146 from rubbing against each other during the inversion. The sleeve 148 may be a polymer and/or metallic thin wall sleeve inserted or insert molded into the proximal end portion 144. The sleeve 148 provides hoop strength and helps prevent the proximal end portion 144 from collapsing under vacuum.
The distal end portion 146 has an outer surface for collecting tissue when the distal portion is in the expanded position. The outer surface faces radially outwardly when the distal end portion 146 is in the expanded position and may face radially inwardly when the distal end portion is in the collapsed or inverted position. The outer surface of the distal end portion 146 may have a plurality of projections or bristles 152 for collecting tissue. The projections 152 may have a V-shape similar to the V-shaped projections 40 illustrated in
Another embodiment of a collection device 160 is illustrated in
The distal end portion 166 has an outer surface for collecting tissue when the distal portion is in the expanded position. The outer surface faces radially outwardly when the distal end portion 166 is in the expanded position and may face radially inwardly when the distal end portion is in the collapsed or inverted position. The outer surface of the distal end portion 166 may have a plurality of projections or bristles 172 for collecting tissue. The projections 172 may form a double V-shape. Each of the projections 172 is similar to the V-shaped projections 40 illustrated in
Another embodiment of a collection device 180 is illustrated in
The distal end portion 186 has an outer surface for collecting tissue when the distal portion is in the expanded position. The outer surface faces radially outwardly when the distal end portion 186 is in the expanded position and may face radially inwardly when the distal end portion is in the collapsed or inverted position. The outer surface of the distal end portion 186 may have a plurality of projections or bristles 192 for collecting tissue. The projections 192 may have a V-shape similar to the V-shaped projections 40 illustrated in
The collection device 180 includes a gelcap or gelatin cover or cap 194 that may be loaded over an end of the collection portion 182. The cap 194 holds the distal end portion 186 in the collapsed position during insertion and movement of the collection portion 182 to the collection site. The cap 194 falls off, pops off and/or dissolves when the collection portion 182 reaches the body lumen. The cap 194 may fall off in response to the movement of the distal end portion 186 from the collapsed position to the expanded position.
Another embodiment of a collection device 200 is illustrated in
The distal end portion 206 has an outer surface for collecting tissue when the distal portion is in the expanded position. The outer surface faces radially outwardly when the distal end portion 206 is in the expanded position and may face radially inwardly when the distal end portion is in the collapsed or inverted position. The outer surface of the distal end portion 206 may have a plurality of projections or bristles 212 for collecting tissue. The projections 212 may have a V-shape similar to the V-shaped projections 40 illustrated in
The collection device 200 includes a weight 214 connected to the proximal end portion 204. The weight 214 may aid in swallowing the collection portion 202. The weight 214 may be made of tungsten and inserted into the proximal end portion 204. It is contemplated that the weight 214 may be insert molded to the proximal end portion 204.
The collection devices 140, 160, 180 and 200 may be used with the catheter 20, stylet 100, and/or connector 102 of
From the above description of the invention, those skilled in the art will perceive improvements, changes and modifications. Such improvements, changes and modifications are intended to be covered by the appended claims.
This application claims priority from U.S. Provisional Patent Application Ser. No. 62/500,933 filed May 3, 2017, the subject matter of which is incorporated herein by reference in its entirety.
This invention was made with government support under Grant Nos. P50CA150964, U01CA152756, U54CA163060 awarded by The National Institutes of Health. The United States government has certain rights to the invention.
Filing Document | Filing Date | Country | Kind |
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PCT/US2018/030907 | 5/3/2018 | WO | 00 |
Number | Date | Country | |
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62500933 | May 2017 | US |