# US 9,750,866 B2 · Cannula lined with tissue in-growth material > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 9,750,866 B2 - Document ID: US9750866B2 - Status: Granted - Kind: B2 - Application number: 13/204,201 - Filed: 2011-08-05 - Published: 2012-01-05 - Granted: 2017-09-05 - Earliest claimed: 2010-02-11 - Assignees: CircuLite, Inc. - Applicants: Robert C. Farnan; Oliver Marseille - Inventors: Robert C. Farnan; Oliver Marseille - Web page: https://patentgrep.com/patent/US9750866B2 ## CPC - A61M 1/3653: {Interfaces between patient blood circulation and extra-corporal blood circuit} - A61M 1/3659: {Cannulae pertaining to extracorporeal circulation} - A61M 60/178: drawing blood from a ventricle and returning the blood to the arterial system via a cannula external to the ventricle, e.g. left or right ventricular assist devices - A61M 60/857: Implantable blood tubes - A61M 60/861: Connections or anchorings for connecting or anchoring pumps or pumping devices to parts of the patient's body - A61B 2017/00252: {for by-pass connections, i.e. connections from heart chamber to blood vessel or from blood vessel to blood vessel} - A61M 2025/0293: {Catheter, guide wire or the like with means for holding, centering, anchoring or frictionally engaging the device within an artificial lumen, e.g. tube} - A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)} - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) ## Abstract A cannula for moving fluids between a pump and the circulatory system of a patient. The cannula includes a liner having an intermediate portion between a proximal portion and a distal portion, and a lumen extending between the proximal and distal portions. At least the intermediate portion of the liner is constructed from a tissue in-growth material for supporting the growth of endothelial cells. A jacket surrounds at least part of the liner. ## Claims ### Claim 1 A cannula configured to move blood between a pump and a circulatory system of a patient, the cannula comprising: a liner comprising an intermediate portion between a proximal portion and a distal portion and a lumen extending between the proximal and distal portions, wherein at least the intermediate portion is constructed from a tissue in-growth material adapted to contact blood flowing through the lumen configured to support the growth of endothelial cells, the proximal portion is configured for connecting to the pump and the distal portion is configured for connecting to the circulatory system; a jacket fully encapsulating the liner; an outer layer surrounding at least a part of the jacket, wherein the outer layer is constructed from the tissue in-growth material; wherein the outer layer has a proximal and a distal end and an intermediate portion therebetween; and a polymeric layer extending along a partial length of the liner and the outer layer, the polymeric layer having a first portion that extends proximally from the proximal end of the outer layer to a proximal end of the cannula and a second portion that extends distally from the distal end of the outer layer to the distal end of the cannula such that the first and second portions of the polymeric layer encapsulate the proximal and distal ends of the outer layer to prevent delamination of the outer layer from the jacket, the first and second portions of the polymeric layer further encapsulating a proximal and a distal portion of the jacket without encapsulating the intermediate portion of the outer layer. ### Claim 2 (depends on 1) The cannula of claim 1, wherein the tissue in-growth material is an expanded polytetrafluoroethylene, a porous polymeric material, a woven polyester material, or a velour. ### Claim 3 (depends on 1) The cannula of claim 1, wherein the proximal and distal portions of the liner are constructed from an elastomeric material. ### Claim 4 (depends on 1) The cannula of claim 1, wherein the jacket is constructed from a polymeric material and is bonded to the liner. ### Claim 5 (depends on 1) The cannula of claim 1, wherein the distal portion of the liner is constructed from the tissue in-growth material. ### Claim 6 (depends on 1) The cannula of claim 1, wherein the liner is constructed as a unitary structure having the distal, intermediate, and proximal portions constructed from the tissue in-growth material. ### Claim 7 (depends on 1) The cannula of claim 1 further comprising: a reinforcing structure surrounding at least a part of the intermediate portion of the liner and configured to resist kinks along the length of the cannula, wherein the liner and the jacket encapsulate the reinforcing structure. ### Claim 8 (depends on 1) The cannula of claim 1 further comprising: one or more longitudinal strengtheners positioned between the liner and the jacket, and extending at least partially between the proximal and distal portions. ### Claim 9 (depends on 1) The cannula of claim 1, wherein the outer layer is bonded to the jacket. ### Claim 10 A cannula configured to move blood between a pump and the circulatory system of a patient, the cannula comprising: a liner comprising an intermediate portion between a proximal portion and a distal portion and a lumen extending between the proximal and distal portions, wherein at least the intermediate portion is constructed from a tissue in-growth material adapted to contact blood flowing through the lumen configured to support the growth of endothelial cells, the proximal portion is configured for connecting to the pump and the distal portion is configured for connecting to the circulatory system; a reinforcing structure surrounding at least a part of the intermediate portion of the liner and configured to resist kinks along the length of the cannula; and a jacket surrounding the reinforcing structure and fully encapsulating the liner; an outer layer surrounding at least a part of the jacket, wherein the outer layer is constructed from the tissue in-growth material, the outer layer including a proximal and a distal end and an intermediate portion therebetween; and a polymeric layer extending along a partial length of the liner and the outer layer, the polymeric layer having a first portion that extends proximally from the proximal end of the outer layer to a proximal end of the cannula and a second portion that extends distally from the distal end of the outer layer to a distal end of the cannula such that the first and second portions of the polymeric layer encapsulate the proximal and distal ends of the outer layer to prevent delamination of the outer layer from the jacket, the first and second portions of the polymeric layer further encapsulating the proximal and distal portions of the jacket without encapsulating the intermediate portion of the outer layer. ### Claim 11 (depends on 10) The cannula of claim 10, wherein the tissue in-growth material is a porous polymeric material, a woven polyester material, expanded polytetrafluoroethylene, or a velour. ### Claim 12 (depends on 10) The cannula of claim 10, wherein the liner is constructed as a unitary structure having the distal, intermediate, and proximal portions constructed from the tissue in-growth material. ### Claim 13 (depends on 10) The cannula of claim 10, wherein the jacket is constructed from a polymeric material and is bonded to the liner. ### Claim 14 (depends on 10) The cannula of claim 10, wherein the jacket fully encapsulates the proximal and distal portions of the liner. ### Claim 15 (depends on 10) The cannula of claim 10, wherein the outer layer is bonded to the jacket. ### Claim 16 An inflow cannula configured to move blood from the heart of a patient to a pump, the inflow cannula comprising: a liner comprising an intermediate portion between a proximal portion and a distal portion and a lumen extending between the proximal and distal portions, wherein at least the intermediate portion is constructed from a tissue in-growth material adapted to contact blood flowing through the lumen configured to support the growth of endothelial cells; wherein the distal and proximal portions are constructed from the tissue in-growth material, and the distal and proximal portions of the liner have an outer diameter that is greater than an outer diameter of the intermediate portion of the liner so as to define a channel at the intermediate portion, the channel having an outer diameter that is smaller than the outer diameter of the distal and proximal portions; an intermediate polymeric layer disposed in the channel; a jacket fully encapsulating the intermediate polymeric layer; a tip coupled to the distal portion and configured to be inserted through a wall of the heart; and a hub coupled to the proximal portion and configured to secure the inflow cannula to the pump. ### Claim 17 (depends on 16) The cannula of claim 16, further comprising: a reinforcement structure positioned in the channel between the liner and the intermediate polymeric layer so as to form a layering of the liner, the reinforcement structure, the intermediate polymeric layer, and the jacket. ### Claim 18 An outflow cannula configured to move blood from a pump to an arterial structure within the vascular network of a patient, the outflow cannula comprising: a liner comprising an intermediate portion between a proximal portion and a distal portion and a lumen extending between the proximal and distal portions, wherein at least the intermediate portion is constructed from a tissue in-growth material adapted to contact blood flowing through the lumen configured to support the growth of endothelial cells; wherein the distal and proximal portions are constructed from the tissue in-growth material, and the distal and proximal portions of the liner have an outer diameter that is greater than an outer diameter of the intermediate portion of the liner so as to define a channel at the intermediate portion, the channel having an outer diameter that is smaller than the outer diameter of the distal and proximal portions; an intermediate polymeric layer disposed in the channel; a jacket fully encapsulating the intermediate polymeric layer; a hub coupled to the proximal portion and configured to secure the outflow cannula to the pump; and a distal end that is configured to be coupled to the arterial structure. ### Claim 19 (depends on 18) The cannula of claim 18, further comprising: a reinforcement structure positioned in the channel between the liner and the intermediate polymeric layer so as to form a layering of the liner, the reinforcement structure, the intermediate polymeric layer, and the jacket. ### Claim 20 A cannula for moving blood between a pump and a circulatory system of a patient, the cannula comprising: a liner constructed from a polymer material and including an inner blood contacting surface; a jacket fully encapsulating the liner and constructed from a polymer material; and an intermediate layer between the liner and the jacket, the intermediate layer being constructed from a porous material; wherein neither the inner blood contacting surface of the liner nor the jacket supports tissue in-growth thereon. ### Claim 21 (depends on 20) The cannula of claim 20, wherein the porous material is an expanded polytetrafluoroethylene, a porous polymeric material, a woven polyester material, or a velour. ### Claim 22 (depends on 20) The cannula of claim 20 further comprising: a reinforcing structure surrounding at least a part of an intermediate portion of the liner configured to resist kinks along a length of the cannula. ### Claim 23 A cannula configured to move blood between a pump and a circulatory system of a patient, the cannula comprising: a liner comprising a proximal portion, a distal portion, an intermediate portion located between the proximal and distal portions, and a lumen extending between the proximal and distal portions, wherein at least the intermediate portion is constructed from a tissue in-growth material adapted to contact blood flowing through the lumen configured to support the growth of endothelial cells, the proximal portion is configured for connecting to the pump and the distal portion is configured for connecting to the circulatory system; a jacket fully encapsulating the liner; wherein the distal and proximal portions are constructed from the tissue in-growth material and each have an outer diameter that is greater than an outer diameter of the intermediate portion of the liner so as to define a channel at the intermediate portion, the channel having an outer diameter that is smaller than the outer diameter of the distal and proximal portions; and an intermediate polymeric layer disposed in the channel and fully encapsulated by the jacket. ### Claim 24 (depends on 23) The cannula of claim 23, further comprising: a reinforcement structure positioned in the channel between the liner and the intermediate polymeric layer so as to form a layering of the liner, the reinforcement structure, the intermediate polymeric layer, and the jacket.