Biocompatible crosslinked coating and crosslinkable coating polymer composition for forming such a coating

a crosslinkable coating and coating technology, applied in the field of implantable stents, can solve the problems of increasing the complexity of manufacturing and deployment, increasing the difficulty of braided stents, and increasing the complexity of the axial length between radially expanded and radially compressed conditions

Inactive Publication Date: 2009-06-30
BIOCOMPATIBLES UK LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0012]A new radially self-expanding stent according to a first aspect of the invention adapted for implantation in a body passage comprises first and second sets of mutually counter-rotating metallic filaments which are braided together and define a tubular stent body having two ends which is mechanically biased towards a first radially expanded configuration in which it is unconstrained by externally applied forces and can be retained in a second radially compressed configura

Problems solved by technology

There are difficulties with the braided stent of this type.
One difficulty is that with a high angle α the change in axial length between the radially expanded and the radially compressed condition is generally high.
This arrangement, however, adds complexity to the manufacture and deployment and it is difficult to allow for the mutual sliding between stent segments without snagging.
Anothe

Method used

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  • Biocompatible crosslinked coating and crosslinkable coating polymer composition for forming such a coating
  • Biocompatible crosslinked coating and crosslinkable coating polymer composition for forming such a coating
  • Biocompatible crosslinked coating and crosslinkable coating polymer composition for forming such a coating

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Embodiment Construction

[0013]Although the ends of the filaments may be fixed together by other means, for instance by swaging as disclosed in GB-A-1,205,743, mentioned above, it is most convenient for the fixing to be by welding. Although the welding can be by resistance welding and / or by pressure, it is preferred for heat to be used, generally by plasma welding. Preferably the welding softens the metal such that it forms a globule before resolidifying to form a bead.

[0014]For some embodiments and applications it may be adequate to weld some but not all of the filament ends. For instance it may be convenient to weld every third pair of counter-rotating filaments at the end of one or both ends of the stent body. Preferably at least every other pair is welded at both ends, more preferably every pair at one, or preferably, both ends.

[0015]Preferably no filler wire is used in the welding although it may, for some purposes, be useful to include filler wire, for instance where the filler has different, usually ...

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Abstract

A braided stent (1) for transluminal implantation in body lumens is self-expanding and has a radial expanded configuration in which the angle α between filaments is acute. Some or all of filaments (6,7) are welded together in pairs at each end (4,5) of the stent to provide beads (8), thereby strengthening the stent and assisting its deployment from a delivery device. The stent is preferably completely coated using a biocompatible polymeric coating, said polymer preferably having pendant phosphoryl choline groups. A method of making the stent by braiding and welding is described as well as a delivery device for deploying the device.The present invention provides a biocompatible crosslinked coating and a crosslinkable coating polymer composition for forming such a coating. The biocompatible crosslinked coating may be formed by curing a polymer of 23 mole % (methacryloyloxy ethyl)-2-(trimethylammonium ethyl) phosphate inner salt, 47 mole % lauryl methacrylate, 5 mole % γtrimethoxysilyl propyl methacrylate and 25 mole % of hydroxy propyl methacrylate. The crosslinkable coating polymer may include 23 mole % (methacryloyloxy ethyl)-2-(trimethylammonium ethyl) phosphate inner salt, 47 mole % lauryl methacrylate, 5 mole % γtrimethoxysilyl propyl methacrylate and 25 mole % of hydroxy propyl methacrylate.<?insert-end id="INS-S-00001" ?>

Description

[0001]More than one reissue application has been filed. This reissue application is a divisional of reissue application No. 10 / 180,060, filed Jun. 27, 2002, which is a reissue application of U.S. Pat. No. 6,083,257, which issued on Jul. 4, 2000. The entire disclosure of the prior application, application Ser. No. 10 / 180,060, is considered part of the disclosure of the accompanying divisional reissue application and is hereby incorporated by reference.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention relates to an implantable stent for transluminal implantation in body lumen, especially found in peripheral and coronary blood vessels, but also for use in bile ducts, urethras or ileums.[0004]2. Description of the Related Art[0005]There are several designs of stents, permanently implantable devices, for transluminal insertion into blood vessels and other lumen to prevent or reverse occlusion thereof. There are three basic categories of device, namely ...

Claims

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Application Information

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IPC IPC(8): A61F2/06C08F230/02A61F2/00A61F2/90A61F2/95A61F2/966B21F45/00
CPCA61F2/0077A61F2/90A61F2/95A61F2/966A61F2002/9665A61F2210/0019B21F45/00B21F45/008A61F2220/0058A61F2220/0075D04C1/02D10B2401/046D10B2509/06A61L2400/18
Inventor TAYLOR, ALISTAIR STEWARTSTRATFORD, PETER WILLIAMYIANNI, YIANNAKIS PETROUWOODROFFE, MATTHEW JOHNROWAN, LEE
Owner BIOCOMPATIBLES UK LTD
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