Adhesive-Free Bonded Balloon for a Balloon Guide Catheter With Minimal Outer Profile
20220031341 · 2022-02-03
Inventors
Cpc classification
A61M2025/1059
HUMAN NECESSITIES
A61L29/06
HUMAN NECESSITIES
A61B17/22
HUMAN NECESSITIES
B29K2075/00
PERFORMING OPERATIONS; TRANSPORTING
B29C66/71
PERFORMING OPERATIONS; TRANSPORTING
B29C66/71
PERFORMING OPERATIONS; TRANSPORTING
B29C65/02
PERFORMING OPERATIONS; TRANSPORTING
B29K2075/00
PERFORMING OPERATIONS; TRANSPORTING
B29C66/0222
PERFORMING OPERATIONS; TRANSPORTING
A61B2017/22051
HUMAN NECESSITIES
A61L29/06
HUMAN NECESSITIES
A61M2025/109
HUMAN NECESSITIES
B29C66/30325
PERFORMING OPERATIONS; TRANSPORTING
B29C66/7392
PERFORMING OPERATIONS; TRANSPORTING
A61M2025/1068
HUMAN NECESSITIES
International classification
A61B17/22
HUMAN NECESSITIES
Abstract
A balloon guide catheter with a catheter shaft having an outer layer made of a reflowable material and a balloon having a bond interface area with a plurality of punctures defined therein secured about the outer layer of the catheter shaft via seepage of the reflowable material of the outer layer into the plurality of punctures forming a radially outward reflow bond between the catheter shaft and the balloon without the use of an adhesive. One or more reflow jackets made of a reflowable material may also be disposed about the bond interface area of the balloon seeping into the plural punctures forming a radially inward reflow bond.
Claims
1. A balloon guide catheter comprising: a catheter shaft having an outer layer made of a reflowable material; and a balloon having a bond interface area with a plurality of punctures defined therein secured about the outer layer of the catheter shaft via seepage of the reflowable material of the outer layer into the plurality of punctures forming a radially outward reflow bond between the catheter shaft and the balloon; wherein the balloon is secured to the catheter shaft without an adhesive.
2. The balloon guide catheter according to claim 1, wherein the reflowable material of the outer layer comprises a medical grade thermoplastic polyurethane.
3. The balloon guide catheter according to claim 1, wherein the balloon is a sleeve and the bond interface area comprises a proximal bond interface area and an opposite distal bond interface area; wherein the plurality of punctures is arranged 360° radially in the proximal and distal bond interface areas of the balloon sleeve.
4. The balloon guide catheter according to claim 3, each of the proximal and distal bond interface areas of the balloon sleeve having the plurality of punctures defined therein is approximately 2 mm in an axial direction.
5. The balloon guide catheter according to claim 3, further comprising: a proximal reflow jacket disposed about the balloon covering the proximal bond interface area; and a distal reflow jacket disposed about the balloon covering the distal bond interface area; the distal reflow jacket being separated in an axial direction from the proximal reflow jacket forming a 360° radial gap therebetween through which a portion of the balloon is exposed; wherein each of the proximal and distal reflow jackets is made of a reflowable material; the proximal and distal reflow jackets being securable to the balloon via the reflowable material of the proximal and distal outer jackets seepable into the plural punctures forming a radially inward reflow bond; wherein the proximal and distal reflow jackets are secured to the balloon without an adhesive.
6. The balloon guide catheter according to claim 5, wherein the reflowable material of the proximal and distal reflow jackets is the same as the reflowable material of the outer layer of the catheter shaft.
7. The balloon guide catheter according to claim 1, wherein the balloon is a patch or a sleeve.
8. The balloon guide catheter according to claim 7, further comprising: a single reflow jacket made of a reflowable material; the single reflow jacket having an opening defined therein aligned with the balloon; and wherein along the bond interface area about the perimeter of the opening in the balloon, the single reflow jacket is secured to the balloon via seepage of the reflowable material of the single reflow jacket into the plural punctures of the balloon forming a radially inward reflow bond.
9. The balloon guide catheter according to claim 8, wherein the reflowable material of the single reflow jacket is the same as the reflowable material of the outer layer of the catheter shaft.
10. A method for assembling a balloon guide catheter, the method comprising the steps of: piercing a plurality of punctures in a bond interface area of a balloon where securable to an outer layer made of a reflowable material of a catheter shaft; arranging the balloon with the plurality of punctures pierced therein about the outer layer of the catheter shaft; and subjecting to heat along the bond interface area causing the reflowable material of the outer layer of the catheter shaft to seep into the plurality of punctures creating a radially outward reflow bond between the outer layer of the catheter shaft and the balloon; wherein the balloon is secured to the catheter shaft without an adhesive.
11. The method according to claim 10, wherein the reflowable material of the outer layer comprises a medical grade thermoplastic polyurethane.
12. The method according to claim 10, wherein the balloon is a sleeve and the bond interface area comprises a proximal bond interface area and an opposite distal bond interface area; wherein the plurality of punctures is arranged 360° radially in the proximal and distal bond interface areas of the balloon sleeve.
13. The method according to claim 12, wherein each of the proximal and distal bond interface areas of the balloon sleeve having the plurality of punctures defined therein is approximately 2 mm in an axial direction.
14. The method according to claim 13, further comprising the step of: positioning a proximal reflow jacket disposed about the balloon covering the proximal bond interface area and a distal reflow jacket disposed about the balloon covering the distal bond interface area; wherein the distal reflow jacket is separated in an axial direction from the proximal reflow jacket forming a 360° radial gap therebetween through which a portion of the balloon is exposed; wherein each of the proximal and distal reflow jackets is made of a reflowable material; further securing the balloon to the outer layer of the catheter shaft by heating of the reflow material of the proximal and distal reflow jackets causing seepage into the plurality of punctures forming a radially inward reflow bond.
15. The method according to claim 14, wherein the reflowable material of the proximal and distal reflow jackets is the same as the reflowable material of the outer layer of the catheter shaft.
16. The method according to claim 15, further comprising the step of: positioning a single reflow jacket made of a reflowable material disposed about the balloon covering the bond interface area; the single reflow jacket having an opening defined therein aligned with the balloon; and wherein along the bond interface area about a perimeter of the opening in the balloon, securing the single reflow jacket to the balloon by heating of the reflowable material of the single reflow jacket causing seepage into the plural punctures of the balloon forming a radially inward reflow bond.
17. The method according to claim 16, wherein the reflowable material of the single reflow jacket is the same as the reflowable material of the outer layer of the catheter shaft.
Description
BRIEF DESCRIPTION OF THE DRAWING
[0009] The foregoing and other features of the present invention will be more readily apparent from the following detailed description and drawings illustrative of the invention wherein like reference numbers refer to similar elements throughout the several views and in which:
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DETAILED DESCRIPTION OF THE INVENTION
[0018] The terms “distal” or “proximal” are used in the following description with respect to a position or direction relative to the treating physician or medical interventionalist. “Distal” or “distally” are a position distant from or in a direction away from the physician or interventionalist. “Proximal” or “proximally” or “proximate” are a position near or in a direction toward the physician or medical interventionalist. The terms “occlusion”, “clot” or “blockage” are used interchangeably.
[0019] Balloons are typically adhered via adhesive to the exterior surface of the catheter shaft of an assembled balloon guide catheter. The use of an adhesive for securing the balloon poses several disadvantages: increased bond profile and difficulty controlling/constraining the boundaries in which the adhesive remains. It is therefore an aspect of the present invention to eliminate the use of the adhesive (adhesive free bond or non-adhesive bond) where the compliant inflatable balloon is secured to the outer layer of the catheter shaft without sacrificing bond integrity or strength.
[0020] During a thrombectomy procedure balloon guide catheters are often employed to arrest blood flow by introducing an inflation fluid into a compliant inflatable balloon (rather than inflating via pressure) made of an elastomeric material, for example, polyurethane, polyblend, or latex. Its ability to conform to the shape of the vasculature makes the compliant inflatable balloon particularly suited for use in arresting of blood flow. In other applications such as dilating of a vessel or opening an occlusion, balloon guide catheters may employ a non-compliant or semi-compliant balloon that is inflated by pressure, rather than using an inflation fluid. Specifically, non-compliant balloons typically made of polyester or nylon when inflated at a high pressure dilate a vessel or open an occlusion; whereas semi-compliant balloons made of material such as Pebax or higher durometer polyurethanes when inflated in pressure are more compliant than that of non-compliant balloons providing greater flexibility during delivery. Regardless of the type of balloon (compliant, semi-compliant, or non-compliant), bonding of the balloon to the exterior surface of the catheter shaft during manufacture has two competing criteria, i.e., minimization of the outer profile/diameter at the bonding interface area(s) in which the balloon is mounted to the catheter shaft while maximizing bond strength and integrity. By way of example, the present inventive balloon guide catheter is illustrated and described using a compliant inflatable balloon for arresting blood flow through the vessel. It is understood that the present invention is applicable for use with any type of balloon (e.g., compliant, semi-compliant, or non-compliant).
[0021] The compliant inflatable balloon 105 with the plural punctures 120 made in each of the proximal and distal bond interface areas 110, 115, respectively, is positioned exteriorly about a catheter shaft 125 as shown in
[0022] Specific regions of the compliant inflatable balloon 105, preferably restricted only to those areas to be bonded to the catheter shaft (e.g., proximal and distal bond interface areas 110, 115 of the balloon sleeve; or a perimeter of a balloon patch), are subject to heat (e.g., thermal and/or laser generated) causing reflow/melting of the outer layer 130 of the catheter shaft 125 which seeps/oozes upwards through the punctures 120 (piercings, holes, openings) forming a radially outward reflow bond therebetween. By way of illustrative example, heated jaws may be applied only about those areas of the compliant inflatable balloon to be bonded thereby restricting the heat to a certain area or distance.
[0023] To further strengthen the bond of the balloon to the catheter shaft, an additional step may be performed in sequence or simultaneously with the forming of the radially outward reflow bond to create a supplemental radially inward reflow bond using one or more reflow jacket(s)/sleeve(s) made of a reflow material (a material that preferably includes medical grade thermoplastic polyurethane (TPU)). Preferably, the reflow material of the one or more reflow jacket(s)/sleeve(s) and that of the outer layer of the catheter shaft is the same to ensure the reflow of both materials when subject to heat at a predetermined temperature. Thus, the reflow bond is created both radially inward and radially outward of the proximal and distal interface bond areas of the compliant inflatable balloon. That is, when heated the reflow/melted outer layer 130 of the catheter shaft 125 seeps radially outwards through the punctures 120 creating a radially outward reflow bond, while the reflow/melted reflow jackets/sleeves 135, 140 ooze radially inwards through the punctures 120 creating a radially inward reflow bond. The enhanced reflow bonds (radially inward and radially outward) created between the reflowing/melting of the material for the reflow jackets/sleeves 135, 140 and outer layer 130 of the catheter shaft 125 into the punctures 120 on either side of the compliant inflatable balloon 105 optimizes bond integrity and strength while minimizing the potential for leakage without increasing the outer diameter/profile.
[0024] In one configuration shown in
[0025] An alternative design employing a single reflow jacket/sleeve 137 with a cut-out or opening 138 defined therein is set forth in the longitudinal cross-sectional and top views of
[0026] The different aspects, features, designs and configurations of the invention may be combined, as desired, for a given intravascular catheter with the intended goals of enhancing the integrity and strength of the bond between the balloon and the catheter shaft, while simultaneously minimizing the outer profile or outer diameter of the assembled catheter.
[0027] Thus, while there have been shown, described, and pointed out fundamental novel features of the invention as applied to a preferred embodiment thereof, it will be understood that various omissions, substitutions, and changes in the form and details of the systems/devices illustrated, and in their operation, may be made by those skilled in the art without departing from the spirit and scope of the invention. For example, it is expressly intended that all combinations of those elements and/or steps that perform substantially the same function, in substantially the same way, to achieve the same results be within the scope of the invention. Substitutions of elements from one described embodiment to another are also fully intended and contemplated. It is also to be understood that the drawings are not necessarily drawn to scale, but that they are merely conceptual in nature. It is the intention, therefore, to be limited only as indicated by the scope of the claims appended hereto.
[0028] Every issued patent, pending patent application, publication, journal article, book or any other reference cited herein is each incorporated by reference in their entirety.