Corrugated microporous tissue interface for improved performance and infection resistance of vascular grafts and other implantable devices
Provided herein are implantable devices, such as vascular grafts and access port for hemodialysis, that include a microporous sheath layer having a corrugated outer surface, and use therefore for reducing the risk of infection or stenosis.
1. A tubular implantable device comprising a multi-layer composite wall defining a longitudinal passageway, wherein the multi-layer composite wall includes an inner layer and a microporous sheath layer having a corrugated outer surface, and wherein the microporous sheath layer is formed of a biocompatible elastomeric biomaterial having an open-pore network of interconnected pores extending from the corrugated outer surface to an interface between the inner layer and the microporous sheath layer,
wherein the microporous sheath layer includes a base portion and a plurality of ridges extending from the base portion, each two adjacent ridges defining a groove, and wherein the ridges and grooves alternate to provide the corrugated outer surface, and wherein the grooves and ridges are oriented circumferentially or spirally around the tubular implantable device; and
wherein the base portion has a thickness that is 0.8-3 times of a mean height of the ridges.
2. The tubular implantable device of claim 1 , wherein the biocompatible elastomeric biomaterial comprises a plurality of interconnecting pores, and wherein substantially all the interconnected pores are each connected to at least two other pores, the pores having a mean diameter between about 5 and about 90 micrometers, and any two adjacent pores being connected by a throat having a mean throat diameter of at least 5 micrometers.
3. The tubular implantable device of claim 1 wherein the base portion has a thickness between 0.1-2 millimeters, and the ridges have a mean height of between 0.1 and 2 millimeters.
4. The tubular implantable device of claim 1 , wherein the inner layer is made of polyester or expanded polytetrafluoroethylene (ePTFE), and the tubular implantable device is a vascular graft.
5. The tubular implantable device of claim 1 , wherein the inner layer forms a dialysis access port adapted to house one or more cannulas, and wherein the dialysis access port is configured to interface with skin.
6. The tubular implantable device of claim 5 wherein the dialysis access port is further connected to a vascular graft, the vascular graft comprising a microporous sheath layer.
7. A vascular graft comprising a single microporous layer defining an inner luminal surface and having a corrugated outer surface, wherein the single microporous layer is formed of a biocompatible elastomeric biomaterial having an open-pore network of a plurality of interconnected pores extending from the inner luminal surface to the corrugated outer surface; wherein substantially all the plurality of the interconnected pores are each connected to at least two other pores, the pores having a mean diameter between about 5 and about 90 micrometers, and wherein any two adjacent pores are connected by a throat, the throat having a mean diameter of at least 5 micrometers, wherein the single microporous layer includes a base portion defining the inner luminal surface and a plurality of ridges extending from the base portion, each two adjacent ridges defining a groove, and wherein the ridges and grooves alternate to provide the corrugated outer surface, and wherein the grooves and ridges are oriented circumferentially or spirally around the vascular graft, and wherein the ridges have a mean height of between 0.1 and 2 millimeters and wherein the base portion has a thickness of between 0.1 and 2 millimeters.