초록 ▼

A method for selectively bonding layers of polymeric material, especially expanded polytetrafluoroethylene (ePTFE), to create endoluminal vascular devices. In a preferred method the selective bonding is achieved by applying pressure to selected areas using a textured mandrel. This permits a stent de

A method for selectively bonding layers of polymeric material, especially expanded polytetrafluoroethylene (ePTFE), to create endoluminal vascular devices. In a preferred method the selective bonding is achieved by applying pressure to selected areas using a textured mandrel. This permits a stent device to be encapsulated between two layers of ePTFE with unbonded slip pockets to accommodate movement of the structural members of the stent. This allows stent compression with minimal force and promotes a low profile of the compressed device. Unbonded regions of ePTFE allow enhanced cellular penetration for rapid healing and can also contain bioactive substance that will diffuse through the ePTFE to treat the vessel wall.

대표청구항 ▼

1. A method for making an endoluminal prosthesis, comprising the steps of: positioning a first covering member composing a biocompatible polymer material over a mandrel; positioning at least one radially expandable support member, having a plurality of openings passing through a wall thereof, ov

1. A method for making an endoluminal prosthesis, comprising the steps of: positioning a first covering member composing a biocompatible polymer material over a mandrel; positioning at least one radially expandable support member, having a plurality of openings passing through a wall thereof, over said first covering member; positioning a second covering member comprising a biocompatible polymer material over said support member and said first covering member; and attaching said first covering member to said second covering member at a plurality of predetermined bonding locations, wherein said bonding locations are positioned in said openings in said support member, and wherein a plurality of unbonded regions are formed between said first and second covering members. 2. The method according to claim 1, wherein said attaching step further comprises applying an adhesive to a surface of at least one of said first and second covering members facing said support member at said bonding locations. 3. The method according to claim 2, wherein said adhesive is an ultraviolet curable adhesive, further comprising the step of utilizing an ultraviolet laser or a photolithography system to attach said first covering member to said second covering member at said bonding locations by curing said ultraviolet adhesive. 4. The method according to claim 2, wherein said adhesive is activatable, further comprising the steps of utilizing electromagnetic energy to activate the adhesive and applying pressure to the endoluminal prosthesis to bring the first covering member in contact with the second covering member at said bonding locations. 5. The method according to claim 1, wherein said attaching step further comprises applying a thermoplastic polymer to a surface of at least one of said first and second covering members facing said support member at said bonding locations. 6. The method according to claim 1, wherein said attaching step further comprises applying heat to said bonding locations by using a heating tool having a tip that is attached to a numerically controlled machine, wherein said machine is programmed to move said heating tool to said bonding locations. 7. The method according to claim 1, wherein said radially expandable support member comprises a first diameter and a second diameter, said first diameter being greater than said second diameter, wherein said support member is positioned over said first covering member at said first diameter.