IMPLANTABLE SEALABLE MEMBER WITH MESH LAYER

Abstract

The provided technologies provide an implant closure device having a mesh layer formed on a flexible substrate, collectively forming a sealable member, that improves a seal formed over an aperture in a body lumen. The mesh facilitates a faster and more secure adherence of the sealable member to the surrounding edges at the puncture site. Furthermore, the provided technology may promote platelet-capture and encourage localized platelet aggregation at the exposed collagen in the wound edges on the mesh layer. The platelet impregnated mesh layer can facilitate cellular adhesion, enabling the sealable member that is local to the wound opening to act, in essence, as a “biological glue.”

Claims

1. An implantable device for sealing an aperture in a tissue of a body lumen, the implantable device comprising: a sealable member, comprising a flexible substrate; and a mesh layer on the flexible substrate; wherein, when the implantable device is an a sealing position, the sealable member is disposed against an internal surface of the tissue adjacent to the aperture such that the mesh layer is in contact with the internal surface.

2. The implantable device of claim 1, wherein the flexible substrate comprises an extruded layer comprising a thickness in a range from about 5 μm and about 4000 μm.

3. The implantable device of claim 2, wherein the extruded layer comprises a thickness in a range from about 60 μm and about 120 μm.

4. The implantable device of claim 1, wherein the sealable member comprises a bioabsorbable polymer film, wherein the bioabsorbable polymer film, when introduced into cells, is broken down by cellular machinery.

5. The implantable device of claim 4, wherein the bioabsorbable polymer film is broken down via enzymatic degradation.

6. The implantable device of claim 4, wherein bioabsorbable polymer film is broken down via hydrolysis.

7. The implantable device of claim 4, wherein the cells either reuse, reabsorb, or dispose of the bioabsorbable polymer film without significant toxic effects to the cells, and wherein breakdown of the bioabsorbable polymer film does not induce inflammation of the cells.

8. The implantable device of claim 4, wherein breakdown of the bioabsorbable polymer film comprises at least one of: (i) breakdown of the bioabsorbable polymer film into component polymers, monomers, or both polymers and monomers, (ii) hydrolysis of ester bonds, and (iii) cleavage of urethane linkages.

9. The implantable device of claim 1, wherein both the mesh layer and the flexible substrate comprise at least one material selected from the group consisting of Poly-L-lactide, Poly-D-lactide, Poly-DL-lactide, Polyglycolide, ε-Caprolactone, Polyethylene glycol, and a copolymer thereof.

10. The device according to claim 1, wherein at least one of the mesh layer and the flexible substrate is formed at least in part of a material having an inherent viscosity in a range from 0.5 to 7.0 dl/g.

11. The implantable device of claim 1, wherein the sealable member is structured to flexibly roll when in a delivery configuration such that a delivery cross-sectional area of the rolled sealable member has a diameter smaller than that of the aperture.

12. The implantable device of claim 1, wherein a thickness of the mesh layer is equal to a thickness of the flexible substrate.

13. The implantable device of claim 1, wherein thicknesses of each of the mesh layer and the flexible substrate are less than 50% of a diameter of the aperture.

14. The implantable device of claim 1, wherein a thickness of the sealable member is at least one (1) mm smaller than a diameter of the aperture, and wherein a minimum thickness of the mesh layer is smaller than a minimum thickness of the flexible substrate.

15. The implantable device of claim 1, wherein a maximum thickness of the mesh layer is at least 100 times greater than a minimum thickness of the mesh layer, and wherein a maximum thickness of the flexible substrate is at least 10 times greater than a minimum thickness of the flexible substrate.

16. The implantable device of claim 1, wherein the mesh layer comprises a plurality of fibers each having a diameter in a range from 0.3 μm to 8 μm, wherein a first portion of the plurality of fibers comprises a random orientation, wherein a second portion of the plurality of fibers comprises a patterned orientation, and wherein at least one of the flexible substrate and the mesh layer comprises biocompatible material, the biocompatible material, when added to cells in vitro, results in less than or equal to 20% cell death.

17. The implantable device of claim 1, wherein the mesh layer comprises a product of activated platelets.

18. The implantable device of claim 17, wherein the mesh layer comprises a copolymer.

19. The implantable device of claim 1, wherein the mesh layer comprises a plurality of fibers each shaped and sized to promote platelet capture, and wherein, when in contact with collagen from an exposed wound, one or more captured platelets encourages localized platelet activation.

20. The implantable device of claim 19, wherein one or more activated platelets adhere to a surface of the collagen creating fibrins.

21. The implantable device of claim 1, wherein the mesh layer comprises a material with low thrombogenicity, and wherein the mesh layer comprises a non-thrombogenic surface.

Description

BRIEF DESCRIPTION OF THE DRAWING

[0067] The Drawing, which is comprised of at least the following Figures, is for illustration purposes only, not for limitation.

[0068] FIG. 1A is a diagram of an exemplary closure device with a material system comprising a mesh layer and a substrate that, collectively, form a sealable member for closing an aperture in a body lumen, according to an illustrative embodiment.

[0069] FIG. 1B is a diagram of an exemplary closure device of FIG. 1A during deployment into a body lumen.

[0070] FIG. 2 is a diagram of an exemplary closure device with a material system comprising a mesh layer and a substrate that, collectively, form a sealable member for closing an aperture in a body lumen, according to another illustrative embodiment.

[0071] FIGS. 3A, 3B, 3C, 3D, and 3E are diagrams of a material system comprising a mesh layer and a substrate that, collectively, form a sealable member, according to various embodiments.

[0072] FIG. 4A is an image of the extruded side of the sealable member.

[0073] FIG. 4B is an image of the electrospun side of the sealable member.

[0074] FIG. 5 is a SEM image of the electrospun side of the sealable member under magnification.

[0075] FIGS. 6, 7A and 7B are diagrams of an exemplary closure device deployed at an arteriotomy.

[0076] FIG. 8 is a diagram of the sealable member comprising the mesh layer and substrate folded in a delivery cannula of a closure device delivery system.

[0077] FIG. 9A is a diagram of the sealable member, in the delivery state, being introduced into a vessel.

[0078] FIG. 9B is a diagram of the sealable member, in the deployed state, being deployed in the vessel.

[0079] FIG. 9C is a diagram of the sealable member being positioned, at the sealing position.

[0080] FIGS. 10A and 10B illustrate direct comparison of histograms of data used to generate Table 4. The data are of an in vitro leakage test on bovine artery, comparing (i) a baseline closure device having a rigid base core and a non-mesh sealable member and (ii) a closure device configured with a flexible support member and a sealable member comprising the mesh layer and substrate.

[0081] FIGS. 11A and 11B illustrate direct comparison of histograms of data used to generate Table 5. The data are of an in vitro leakage test on a flexible tube, comparing (i) a baseline closure device having a rigid base core and a non-mesh sealable member and (ii) a closure device configured with a flexible support member and a sealable member comprising the mesh layer and substrate.

[0082] FIG. 12 is a diagram of a process for fabricating the material system comprising a mesh layer and a substrate, forming a sealable member, according to illustrative embodiments.

[0083] FIG. 13 shows an image of a flexible wing with the mesh layer having been deployed at the site of a 24 (F) French arteriotomy in a pig aorta. The image was captured, after the aorta was explanted, approximately 24 hours after the flexible wing has been deployed at the arteriotomy. The image shows the wing being pulled back at the arteriotomy site. Remarkably, as shown, activated platelets have adhered to the collagen surface of the arteriotomy, creating fibrins at the site. The flexible wing with the mesh layer thus, has facilitated formation of a biological glue which adheres the flexible wing to the arteriotomy site.

DETAILED DESCRIPTION

[0084] As described herein, illustrative embodiments provide a vascular closure implantable device for sealing an aperture in a tissue of a body lumen. Examples of the blood vessel includes, but not limited to, the femoral artery, subclavian artery, ascending and descending aorta, auxiliary and brachial arteries, femoral vein, iliac vein, subclavian vein, and vena cava. In some embodiments, the systems, devices, and methods are used to close a surgical perforation in a body cavity, such as the gastrointestinal tract, heart, peritoneal cavity, esophagus, vagina, rectum, trachea, bronchi, and blood vessel.

[0085] FIG. 1A is a diagram of an exemplary closure device 100 with a material system comprising a mesh layer 102 and a substrate 104 that, collectively, form a sealable member 106 for closing an aperture 108 in a tissue 110 of a body lumen 112.

[0086] Examples of the flexible sealable member (also referred to as a “flexible wing”) are described in U.S. Patent Application Publication No. 2014/0018847, titled “Percutaneous Perforation Closure Systems, Devices, and Methods,” the content of which is incorporated by reference herein in its entirety. Among other things, this disclosure provides details of a variant of the flexible wing design.

[0087] The sealable member 106 with the mesh layer 102 and substrate 104 forms, in some embodiments, a flexible bilayer bioabsorbable polymer film. The sealable member 106 is deployable at a sealing position in the body lumen 112. In some embodiments, the mesh layer 102 is formed of a bioabsorbable or biodegradable polymer that is electrospun onto a substrate material 104. The electrospinning process creates and/or forms a textured surface 114, by the mesh layer 102, for contacting the interior surface 116 of the 110 tissue.

[0088] Electrospinning employs, in some embodiments, electrical force to draw very fine fibers (e.g., micro or nano-scale) of polymers, ceramics, metals, carbon and/or composite materials from a liquid and/or a solution/melt. Electrospinning typically generates a jet in a high-voltage field to produce elongated fibers. A high-voltage electrical field is applied between a capillary where a suitable solution or melt is stored and a collection screen on which an electrically charged jet solidifies. For example, one electrode from a high-voltage source may be contacted with the solution/melt (e.g., needle, capillary) and the other attached to the collection screen. When a voltage is applied to a droplet of the solution/melt, the droplet is stretched into a jet due to electrostatic repulsion and surface tension. The jet is whipped by electrostatic repulsion until it is deposited on the collection screen. Electrospinning can be adjusted to produce continuous liquid jets by controlling parameters (e.g., molecular weight, viscosity, conductivity, surface tension, and electric potential, flow rate, concentration, distance between capillary and collection screen, temperature, needle gauge, etc.). The method beneficially ensures, among other benefits as described herein (e.g., combined with secondary processing (e.g., reduced pressure processing), that no solvent made from the manufacturing process is carried over into the final product. Of course, other methods of generating very fine fibers may be employed. The mesh layer 102 and/or the substrate 104 comprise, in some embodiments, at least one material selected from the group consisting of Polydioxanone, Poly-L-lactide, Poly-D-lactide, Poly-DL-lactide, Polyglycolide, ε-Caprolactone, Polyethylene glycol, and a copolymer thereof. In some embodiments, the material of the mesh layer 102 and/or substrate layer 104 is a copolymer of, for example, but not limited to, Polydioxanone, Poly-L-lactide, Poly-D-lactide, Poly-DL-lactide, Polyglycolide, ε-Caprolactone, and Polyethylene glycol. In some embodiments, the copolymer includes (a) monomers of Polydioxanone, Poly-L-lactide, Poly-D-lactide, Poly-DL-lactide, Polyglycolide, ε-Caprolactone, or Polyethylene glycol, and (b) one or more additional monomers. In some embodiments, the (a) and (b) monomers form a polymer that is bioabsorbable. One of ordinary skill in the art will appreciate that other bioabsorbable and/or biodegradable material may be employed.

[0089] A bioabsorbable polymer can have crystalline and amorphous regions and are therefore, in general, semi-crystalline in nature. Degradation of a bioabsorbable polymer, in certain embodiments, initiates in the amorphous regions, with the crystalline regions degrading at a slower rate relative to the amorphous regions. Without wishing to be tied to a particular theory, and for illustrative purposes only, degradation of a polymer such as Polydioxanone (PDO) occurs along the polymer back bone by hydrolysis of the ester bonds. This non-specific ester bond scission may occur randomly along the polymer chain with water penetration initially breaking the chemical bonds and converting the long polymer chains into natural monomeric acids found in the body, such as lactic acid. Such monomeric acids are then phagocytized by the enzymatic action of special types of mononuclear and multinuclear white blood cells. The polymer is, thus, degraded into non-toxic, low molecular weight residues that are capable of being eliminated from the body by normal metabolic pathways, e.g., via exhalation and/or excretion. Such a pathway thereby enables reference to the breakdown of such polymers in-vivo through terminology such as absorbable, bioabsorbable, degradation, biodegradation, resorbtion, bioresorbtion, among others.

[0090] In certain embodiments, the extruded layer 104 preferably has a range between about 60 μm and about 120 μm in thickness. The range of thicknesses may be between 5 μm and 4000 μm. In certain embodiments, the electrospun layer 102 substantially consists of fibers in the range from 0.3 μm to 8 μm diameter, with a layer thickness preferably in the range from 10 μm to 60 μm. The fibers may be arranged in a random or patterned orientation. The range of thicknesses of the mesh layer 102 may be between 5 μm and 4000 μm, e.g., depending on the size of aperture being sealed and/or the size of blood vessel/hollow vessel.

[0091] The thickness of the mesh layer 102 and the substrate 104 is such that the sealable member 106 can bend, in some embodiments, to conform to the interior surface of the blood vessel while sufficiently rigid to maintain the tamponade at the aperture 108 when the device 100 is in the sealing position. In some embodiments, the mesh layer 102 and substrate 104 can roll, e.g., such that the tips of the sealable member touch each other, or bend beyond the curvature required to conform to the interior surface of the blood vessel, allowing the sealable member to fit within a delivery cannula to be deployed into the body lumen.

[0092] FIG. 1B is a diagram of the closure device 100 with a material system comprising the mesh layer 102 and the substrate 104, when introduced into a vessel 112. Without wishing to be bounded to a particular theory, from the mesh structure, the electrospun side 114 of the flexible wing 106 has a larger (textured) surface area compared to an untreated smooth surface of the substrate 104, on the other side of the wing 106. This large surface area promotes platelet capture due to the pore size in the textured surface (e.g., whereby the captured platelet encourages localized platelet activation, e.g., due to contact with the collagen from the exposed wound, at the wound surface). During closing of the hole in the blood vessel 110, the wing 106 is appositioned against the tissue 110 at the hole 108 such that the textured flexible wing surface 114 is positioned against the inner lumen 116 of the vessel tissue 110. The textured surface 114 facilitates a faster and more secure adherence of the flexible wing 106 to the surrounding edges at the puncture site. The electrospun surface 114 of the wing 106 promotes a faster hemostatic seal between the wing 106 and the vessel inner luminal surface 116. The nature of the flexible wing 106 means it has a significant capability, beyond the state of the art, to provide sealing across a wide variety of blood vessel inner lumen surface topography. This topography can be in various states of disrepair due to disease and systemic diseases (e.g., diabetes). The electrospun surface 114 facilitates cellular adhesion, thereby acting as a “biological glue” and would aid encapsulation of the implant 100 in the vessel 110.

[0093] FIG. 13 shows an image of a flexible wing 106 with the mesh layer 102 having been deployed at the site of a 24 (F) French arteriotomy in a pig aorta. The image was captured, after the aorta was explanted, approximately 24 hours after the flexible wing 106 has been deployed at the arteriotomy. The image shows the wing being pulled back at the arteriotomy site. Remarkably, as shown, activated platelets have adhered to the collagen surface of the arteriotomy, creating fibrins at the site. The flexible wing 106 with the mesh layer 102 has, thus, biologically glued the tissue together within a short period of time following the closure procedure.

[0094] As further shown in FIG. 13, little or no adhesion of the sealable member 106 is observed, in this image, at the unbroken surfaces surrounding the arteriotomy. The activated platelets aggregated on the mesh layer 102 are observed to adhere to the collagen surface of the arteriotomy only.

[0095] It is further observed, in this image, within this post-procedure time period, that little or no platelet aggregates on the non-mesh surface of the substrate of the sealable member.

[0096] In certain embodiments, the mesh layer 102 preferably has a thickness in the range of about 10 μm (microns) to about 60 μm, including 10, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 um. The mesh layer 102, in some embodiments, comprises electrospun fibers that are substantially (e.g., greater than 50% of the fibers) in the range of about 0.3 μm to about 8 μm in diameter. In some embodiments, the spacing between the fibers may be about or greater than 2-3 um. It should be appreciated that other thicknesses and spacing among the fibers may be employed so as to promote platelet capture and/or aggregation (e.g., thereby encouraging localized platelet activation, e.g., due to the contact with the collagen from the exposed wound, at the wound surface).

[0097] In certain embodiments, the thickness of the mesh and substrate layers, as deployed in the lumen/vessel, is selected based on the size of the aperture to be sealed and/or the size of the blood vessel/hollow vessel. Table 1 lists exemplary ranges of thicknesses of the mesh and substrate layer that may be selected for a sealable member to close an aperture based on the aperture/incision size that is formed. Table 2 lists exemplary ranges of thicknesses of the mesh and substrate layer that may be selected for a sealable member to close an aperture based on the vessel diameter size. Table 3 lists exemplary ranges of thicknesses of the mesh and substrate layer that may be selected for a sealable member to close an aperture base on the size of the hollow vessel.

TABLE-US-00001 TABLE 1 Example thicknesses of the mesh and substrate layers of a sealable member for closure of a blood vessel (e.g., having an internal diameter between about 6 and 12 mm), selected based on the incision/puncture size at the blood vessel. Hole Mesh Layer Substrate Layer French Size Thickness (mm) Thickness (mm) size (mm) Min Max Min Max 6 2 0.005 0.5 0.04 0.5 9 3 0.005 0.75 0.04 0.75 12 4 0.005 1 0.04 1 15 5 0.005 1.5 0.04 1.5 18 6 0.005 2 0.04 2 21 7 0.005 2.5 0.04 2.5 24 8 0.005 3 0.04 3 27 9 0.005 4 0.04 4

TABLE-US-00002 TABLE 2 Example thicknesses of the mesh and substrate layers of a sealable member for closure of a blood vessel, selected based on the size of the blood vessel. Vessel Size Mesh Layer Substrate Layer (Internal Thickness (mm) Thickness (mm) Diameter, mm) Min Max Min Max 5 0.005 0.5 0.04 0.5 6 0.005 0.75 0.04 0.75 7 0.005 1 0.04 1 9 0.005 1.5 0.04 1.5 11 0.005 2 0.04 2 15 0.005 3 0.04 3 20 0.005 3.5 0.04 3.5 30 0.005 4 0.04 4

TABLE-US-00003 TABLE 3 Example thicknesses of the mesh and substrate layers of a sealable member for closure of a non-blood carrying hollow vessel (e.g., having an internal diameter between 15 and 100+ mm), selected based on the size of the hollow vessel. Vessel Size Mesh Layer Substrate Layer (Internal Thickness (mm) Thickness (mm) Diameter, mm) Min Max Min Max 15 0.005 3  0.04 3  40 0.005 8  0.04 8  >100 0.005 20+ 0.04 20+

[0098] Referring still to FIG. 1B, in certain embodiments, the sealable member 106 is maintained in the sealing position at the aperture 108 by the hemostatic pressure of the blood of the vessel 112 (or hydraulic pressure of the fluid of the vessel/lumen). The sealable member 106 may operate, in some embodiments, in conjunction with an anchorable member 120 (as part of the closure device 100), which maintains the sealable member 106 at the sealing position and prevents the inadvertent dislodgment and/or movement of the sealable member 106 from such position, e.g., due to a physical impact near the aperture 108 and/or movements of the patient. Put another way, the anchorable member 120 acts, in some embodiments, as a safety device to prevent the closure device 100 from forming an embolism in the vessel/lumen if the closure device (or portion thereof) is inadvertently dislodged from its deployed position.

[0099] In certain embodiments, the anchorable member 120 has a column portion 118 that is disposed in the aperture 108 when the device 100 is in the sealing position. The anchorable member 120 includes, in some embodiments, a rigid or flexible portion 132 to retain the sealable member 106 at the position. In some embodiments, the portion 132 does not exert a force on the sealable member 106 when the device is deployed at the sealing position. In other embodiments, the core portion 132 provides a force to push the sealable member 106 against the tissue 110. In certain embodiments, the force is compressive.

[0100] In certain embodiments, the column portion 118 (or portions thereof) and/or core portion 132 (or portions thereof) of the anchorable member 120 comprise a mesh layer, as described herein. In other embodiments, the column portion 118 and/or core portion 132 comprises a body having mesh properties of the mesh layer 102, as described herein.

[0101] In certain embodiments, the sealable member 106 forms a solid flexible structure. It does not include a hole. FIG. 2 is a diagram of an exemplary closure device 100 with a material system comprising the mesh layer 102 and the substrate 104 that, collectively, form the sealable member 106 for closing an aperture in a body lumen, according to another illustrative embodiment.

[0102] In certain embodiments, the closure device 100 is employed for endoscopic procedures.

[0103] FIGS. 3A, 3B, 3C, 3D, and 3E are diagrams of material systems comprising a mesh layer 102 and a substrate 104 that, collectively, form a sealable member 106, according to various embodiments. As shown, in FIG. 3A, the mesh layer 102 is formed over a surface 302 of the substrate 104. The sealable member 106 may include a center through-hole 130 for assembly onto the closure device 100. In some embodiments, the material of the mesh layer 102 and the substrate 104 are the same.

[0104] As shown in FIG. 3B, the mesh layer 102 is formed over the surface 302 of the substrate 104. In addition, a second mesh layer 304 is formed over a second surface 306 on the underside of the substrate 104.

[0105] As shown in FIG. 3C, the mesh layer 102 is formed over the substrate 104 so as to encapsulate the substrate 104.

[0106] As shown in FIG. 3D, the mesh layer 102 is formed over the substrate 104 so as to encapsulate one side of the substrate 104, including the surface 302 and the side surface 308.

[0107] In some embodiments, the sealable members 106 shown in FIGS. 3C and 3D are cut to form the respective sealable members 106 shown in FIGS. 3A and 3B.

[0108] As shown, in FIG. 3E, the mesh layer 102 is formed over a surface 302 of a solid substrate 310 so as to form a single solid structure. In certain embodiments, the single solid structure is employed as the sealable member 106. In some embodiments, the hole 130, e.g., as shown in FIG. 3A, is formed, e.g., by removing and/or cutting the material from the structure, to form the sealable member.

[0109] It should be appreciated that in some embodiments, the material of the mesh layer 102 and the substrate 104 are different. In such embodiments, the mesh layer 102, when formed over the substrate 104, has sufficient bond strength to not delaminate when bent during the delivery of the sealable member 106 into the lumen 112 or during the deployment of the sealable member 106 over the aperture of the tissue 110 when the device is in the seal position. In some embodiments, a bioabsorbable and/or biodegradable intermediary material is used between the mesh layer 102 and the substrate 104.

[0110] In addition, it should be appreciated that, in certain embodiments, the mesh layer 102 may form within the hole 130 of the sealable member 106.

[0111] FIG. 4A is an image of the extruded side 104 of an exemplary sealable member. This sealable member has a diameter of 16 mm. The extruded side of the substrate 104 is about 0.1 mm thick.

[0112] FIG. 4B is an image of the electrospun side 102 of the sealable member 106. The electrospun side of the mesh layer 102 is about 0.02 mm thick.

[0113] FIG. 5 is a SEM image of the electrospun side 102 under magnification. The fibers of the mesh layer have diameters in the range between about 0.1 μm and 8 μm.

[0114] In some embodiments, the systems, devices, and methods may be used for closing a surgical perforation in, and/or repairing, smaller blood vessels (e.g., small arteries and small veins). The dimensions of devices may be adjusted to be delivered in the smaller blood vessels.

Example 1: Closure of Holes in Blood-Carrying Vessels

[0115] In certain embodiments, the flexible wing 106 is designed to seal the arteriotomy when positioned juxtaposed to the artery lumen 110. The flexible bilayer wing 106 is delivered into the vessel 100 in a folded or constricted state. Once in the vessel 110, the flexible wing 106 is positioned at the arteriotomy with the electrospun surface 102 next to the vessel lumen 110, where it regains its original structure forming a seal.

[0116] FIGS. 6, 7A and 7B are diagrams of an exemplary closure device 100 deployed at an arteriotomy. As shown in FIG. 6, the closure device 100 includes the sealable member 106 (e.g., a flexible wing) positionable against an interior surface 116 of the tissue 110 adjacent the aperture 108 in the tissue (e.g., so as to form a tamponade at the aperture 108). FIG. 7A is a diagram of an exemplary anchorable member 120. The anchorable member 120 includes a flexible base 132 having a central portion 128 and lateral portions 130 extending outwardly.

[0117] Although flat or slightly curved when in a relaxed state, the sealable member 106 flexibly curves to conform to the interior surface 108 of the lumen 112 to which it engages, in the deployed state (see FIG. 6). In such state, the flexible base 132 holds, in some embodiments, the sealable member 106 against the tissue 110. Examples of the anchorable members with a flexible base are described in U.S. Provisional Application Nos. 62/092,235 and 62/092,240, titled “Closure Apparatus with Flexible Sealable Member and Flexible Support Member”, the contents of which are incorporated by reference herein in their entirety.

[0118] In some embodiments, the column 118 of the anchorable member 120 has an engagement portion 122 (see FIG. 7B) to secure a guard member 124 (e.g., an insertable or engagable pin or cage) to the support member 120, thereby engaging the guard member 124 against the exterior surface 126 of the tissue 110 when the closure device 100 is in the sealing position. The guard member 124 is moveable, from a stowed state to a deployed state, to engage the exterior surface 126 of the tissue adjacent the aperture 108 such that a portion of the tissue is disposed between the guard member 124 and the sealable member 106 when the closure device 100 is in the sealing position. In certain embodiments, the engagement does not exert a force on the tissue, but merely provides a structure to keep the closure device 100 at its deployed location, e.g., whereby the device 100 is prevented from dislodgement from its deployed location. In certain embodiments, the guard member 124 is an extra-luminal pin. Examples of the extra-luminal pin are described in U.S. Patent Application Publication No. US 2014/0018847, titled “Percutaneous Perforation Closure Systems, Devices, and Methods.”

[0119] In other embodiments, the engagement results in a force being applied on the tissue by the anchorable member 120 and the guard member 124.

[0120] The sealable member 106, in some embodiment, is sized to be larger than the diameter of the aperture, e.g., between 12 French (F) and 30 French (F). In some embodiments, the sealable member 106 is sized to be larger than the diameter of the aperture, e.g., between 6 French (F) and 18 French (F). The sealable member 106 is preferably circular in shape. It should be understood, however, that other geometries may be employed for the sealable member, including, but not limited to, ovals, and other elongate shapes.

[0121] The sealable member 106, in some embodiments, has a hole (e.g., located in the center of the sealable member 106) sized to accept the column 118. In some embodiments, the sealable member 106 is free to rotate relative to the base of the support member 120 about an axis concentric to the column 118. Other examples of the sealable member is described in U.S. Patent Application Publication No. US 2014/0018847, titled “Percutaneous Perforation Closure Systems, Devices, and Methods.”

[0122] In some embodiments, during deployment to close a hole, e.g., in a hollow vessel, the implant 100 is loaded into a delivery cannula through a loading funnel which reduces the cross-sectional area of the implant 100 (e.g., support member 118 and sealable member 106) to make it possible to deliver the implant through the delivery cannula into the hollow vessel (such as an artery or a vein).

[0123] FIG. 8 is a diagram of the sealable member 106 comprising the mesh layer 102 and substrate 104 folded in a delivery cannula 802 of a closure-device delivery system. As shown, the sealable member is folded and assembled onto the closure device, which is connected to a shaft of the delivery system. Both the sealable member 106 and the support member 120 are folded into their delivery state. The support member 120 is positioned, in some embodiments, within the delivery cannula 802 such that it is surrounded by the sealable member 106. In some embodiments, the electrospun layer 102 is oriented to be facing the wall of the delivery cannula 802 such that the substrate layer 104 faces the center of the delivery cannula 802.

[0124] FIG. 9A is a diagram of the sealable member, in the delivery state, being introduced into a vessel 110. A guide wire 901 may be employed to guide the delivery cannula 802 through the tissue 110 and into the lumen 112. To deploy the sealable member 106 in the lumen 112, the cannula 802 is translated back (see arrow 904), in some embodiments, by a mechanical actuation of the delivery system, while the sealable member 106 remains generally stationary with respect to the lumen 112. Consequently, the delivery cannula 802 passes the sealable member 106, whereby the sealable member 106 then unfolds.

[0125] FIG. 9B is a diagram of the sealable member, in the deployed state, being deployed in the vessel 112. As shown, the sealable member 106 has unfolded to a deployed state in the lumen 112. In some embodiments, the support member 120 also unfolds with the sealable member 106 (not shown). The sealable member 106 is now ready to be positioned against the aperture (e.g., the puncture site) in the body lumen.

[0126] FIG. 9C is a diagram of the sealable member being positioned, at the sealing position. As shown, the sealable member 106 has been withdrawn from the point of insertion such that the sealable member 106 now contacts the tissue 110 of the lumen 112. The sealable member 106 is positioned over the aperture 108 and is then released from the delivery shaft 906. In some embodiments, a guard member (e.g., an extra-luminal pin or slotted cage) is deployed from the delivery system to engage the closure device 100 (see, for example, FIG. 6) so as to secure and/or hold the closure device 100 in the sealing position and, e.g., prevent the inadvertent dislodgement of the device 100 from its sealing position, e.g., due to application of external forces.

Example 2: Fabrication of the Material System Comprising a Mesh Layer and Substrate

[0127] FIG. 12 is a diagram of a process for fabricating a material system comprising a mesh layer and a substrate, forming a sealable member, according to illustrative embodiments.

[0128] The method includes forming (e.g., by an extrusion process, a molding process (e.g., compression molding, injection molding, etc.), or a casting process) a flexible substrate 104 (1202). In some embodiments, the substrate-forming process produces a flexible substrate layer 104 having a thickness in a range from about 60 μm to about 120 The substrate 104 can flexibly bend, in some embodiments, such that opposing ends of the substrate can overlap when under load and to return to an original shape of the substrate when the load is removed. In some embodiments, the forming process produces a thickness (of the substrate) between about 40 μm and about 500 or between about 40 μm and about 750 or between about 40 μm and about 1000 or between about 40 μm and about 1500 or between about 40 μm and about 2,000 or between about 40 μm and about 2500 or between about 40 μm and about 3000 or between about 40 μm and about 4000 μm.

[0129] The method then includes forming (e.g., by an electrospun process) a mesh layer 102 on the substrate 104 (1204) In certain embodiments, the electrospinning produces a mesh layer 102 having a thickness in a range from about 10 μm to about 50 μm. A majority of the fibers of the mesh layer (e.g., greater than 50%, greater than 80%, or greater than 90%) has diameter in a range from about 0.3 μm to about 8 μm.

[0130] In some embodiments, the electrospun process produces a mesh layer having a thickness between about 5 μm and about 500 or between about 5 μm and about 750 or between about 5 μm and about 1000 or between about 5 μm and about 1500 or between about 5 μm and about 2000 or between about 5 μm and about 2500 or between about 5 μm and about 3000 or between about 5 μm and about 4000 μm.

[0131] In some embodiments, the mesh layer is substantially formed (e.g., greater than 50%) with fibers structured (e.g., sized and shaped) to promote platelet capture (e.g., whereby the captured platelets encourages localized platelet activation, e.g., when in contact with collagen from the exposed wound, at the wound surfaces) when the device is in the sealing position.

[0132] Some embodiments of the present invention are directed to a closure system, device, and method of percutaneous closure of an arteriotomy following endovascular/intra S arterial procedures.

[0133] Some embodiments of the present invention are directed to a closure system, device, and method of percutaneous closure of an arteriotomy following endovascular/intra S arterial procedures.

[0134] With regards to the arterial wall morphology, in the context of example embodiments directed to closing arterial perforations, the fibrous adventitial layer of an artery (i.e., the outer layer) is relatively tough, whilst the intimal and medial/endothelial layers are friable. Because of the morphology of the arterial wall, an arteriotomy may be circumferential in nature and perpendicular to the longitudinal axis of the artery.

[0135] One of ordinary skill in the art will recognize that many mammalian lumina are comprised of one or more friable tissues. Thus, a common difficulty associated with surgical closure of a perforation in such lumina is that suture material, used in typical closure systems, tends to cause tears in the friable tissue. Such tearing of the luminal tissue impedes healing and causes scarring. Indeed, such tearing of the friable tissues of the interior lumina of blood vessels can lead to scarring, dislodgment of tissue particles, blockage, or even eventual death of the patient. In view of the fragile nature of luminal tissues, an aspect of example embodiments of the present invention is to provide systems, devices, and methods that allow a seal to be formed over a closure of a tissue perforation in a reliable manner with minimal trauma to the luminal tissue, for example, by providing a sutureless seal.

[0136] In certain embodiments, the invention is used for closing access site holes from abdominal post endoscopic procedures.

[0137] In certain embodiments, the fibers of the mesh layer are impregnated and/or coated with one or more therapeutic agents. Such therapeutic agents may include drugs, e.g., antibiotics (e.g., to control infection), anti-proliferative(s) (e.g., for hyperplasia), among others. In other embodiments, the one or more therapeutic agents may be impregnated within the structure of the mesh layer. Alternatively, or in conjunction with the mesh layer, the substrate layer may be impregnated and/or coated with the one or more therapeutic agents.

Experimental Data

[0138] The provided technologies were tested in vitro and in vivo. For the in vitro test, the sealable member was tested on a test bench using either a flexible tube or a bovine artery to simulate the body lumen. The bovine artery has an inner diameter between 7.8 mm and 9 mm and a wall thickness between 1.4 and 1.9 mm. The flexible tube has an inner diameter of 7.1 mm and a wall thickness of 0.55 mm. In each of the flexible tube and the bovine artery, an aperture was created with a diameter of 6-8 mm. A deployment sheath (e.g., the delivery cannula), used in the procedure, has an inner/outer diameter of 20 F/24 F.

[0139] The test was performed with water flowing through each of the respective bovine artery and flexible tube, under physiological conditions with a pulse of approximately 60 hertz, a systolic pressure of about 120 mm-Hg, and a diastolic pressure of about 80 mm-Hg. Ten data samples were collected for each test. The amount of water leaked within 5 minutes from the time of deployment is measured and provided in Table 4 and Table 5 below.

TABLE-US-00004 TABLE 4 Bovine artery: in vitro test comparison of devices, including (i) a baseline closure device having a rigid base core and a non-mesh sealable member (see “Current Device R#1”) and (ii) a closure device configured with an anchorable member comprising a flexible support base and a sealable member (comprising the mesh layer and substrate) (see “New Device R#2”). FIGS. 10A and 10B illustrate a direct comparison of histograms of data used to generate Table 4. Total leak in Current Device New Device 5 ml (ml) R#1 R#2 Mean 5.2 0.9 SD 4.2 0.7 Min 0.8 0.0 Max 12 2.0

TABLE-US-00005 TABLE 5 Flexible tube: in vitro test comparison of devices, including (i) the same baseline closure device having a rigid base core and a non-mesh sealable member (see “Current Device R#1”) and (ii) the same closure device configured with an anchorable member comprising a flexible support base and a sealable member (comprising the mesh layer and substrate) (see “New Device R#2”). FIGS. 11A and 11B illustrate a direct comparison of histograms of data used to generate Table 5. Total leak in Current Device New Device 5 ml (ml) R#1 R#2 Mean 13.6 1.8 SD 12.0 1.2 Min 0 0.6 Max 16 4.1

[0140] The test illustrates a 5x improvement of the closure device, configured with a flexible support member and a sealable member comprising the mesh layer and substrate, in reducing the amount of fluid leakage over a current design employing a sealable with no mesh layer (and having a rigid core). In addition to the seal formed from the R #2 closure device having improved leakage performance, as shown in the plots of the histograms and the standard deviation values of the tables, a more consistent closure is also provided.

[0141] For the in vivo test, the sealable member was tested in animal subjects. A similar 6 mm puncture was made in a pig aorta. The deployment sheath, used in the procedure, also has an inner/outer diameter of 20 F/24 F. Six data samples were collected for each test using the R #1 design and the R #2 design. The total deployment time, tamponade time, time to hemostasis, and total procedure time are provided in Table 6 below.

TABLE-US-00006 TABLE 6 Pig Aorta: in vivo study comparison of devices, including (i) the same baseline closure device having a rigid base core and a non-mesh sealable member (see “R#1”) and (ii) the same closure device configured with an anchorable member with flexible support base and a sealable member (comprising the mesh layer and substrate) (see “R#2”). Deployment Tamponade Time to Total Time Time Hemostasis Procedure (mm:ss) (TT) (TTH) Time ACT n = 6 (IncTT) (mm:ss) (mm:ss) (mm:ss) (sec) R#1 in vivo study Average 07:01 04:08 05:49 12:50 190 Max 07:45 04:30 30:15 37:38 217 Min 06:24 04:00 00:00 07:00 165 R#2 in vivo study Average 02:50 00:57 00:38 03:29 294 Max 03:07 01:37 01:30 04:30 404 Min 02:15 00:20 00:00 02:15 194

[0142] As shown in Table 6, the R #2 design improves the total deployment time by 2.5× over the R #1 design. The total deployment time, used in the observations, includes the time for the device to be positioned and deployed in the pig aorta and for the leakage to stop.

[0143] In addition, the R #2 design improves the time to hemostasis by 9× over the R #1 design. The time to hemostasis (TTH), used in the observations, refers to the time from which a seal is created and the time for leakage to stop. Less variability in the time to hemostasis is also observed.

[0144] In addition, the R #2 design reduces the overall closure procedure time by 3.7× over the R #1 design. The activated clotting time (ACT time) was longer by over 100 seconds. The activated clotting time refers to the time for whole blood to clot upon exposure to an activator.

[0145] Although certain figures and embodiments relate to use of systems and devices for closure of a perforation associated with vascular surgery, one of ordinary skill in the art will appreciate that components of a provided device are not size dependent (i.e., are scalable) and are therefore useful for closure of any perforation in a lumen of a mammal.

[0146] Although the present invention has been described with reference to particular examples and exemplary embodiments, it should be understood that the foregoing description is in no manner limiting. Moreover, the features described herein may be used in any combination.