Titanium mesh covered with biocompatible polypropylene film for covering and protecting bone grafts/biomaterials and process for obtaining same
US-2024398571-A1 · Dec 5, 2024 · US
US9775933B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9775933-B2 |
| Application number | US-201313773937-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2013 |
| Priority date | Mar 2, 2012 |
| Publication date | Oct 3, 2017 |
| Grant date | Oct 3, 2017 |
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The invention is an improved biocompatible surface for a variety of medical purposes. The biocompatible surface employs a unique tight microstructure that demonstrates enhanced cellular response in the body, particularly when placed in contact with blood. As a blood contact surface, the present invention can be beneficially employed in a wide variety of implantable devices and in many other devices and equipment that come in contact with blood.
Opening claim text (preview).
What is claimed is: 1. A blood contact surface comprising a polytetrafluoroethylene microstructure of nodes and fibrils in both an x direction and in a substantially perpendicular y direction; wherein the nodes and fibrils have a mean distance between adjacent nodes of 5 micron or less; and wherein the mean width of the 32 largest nodes in a representative 10,000× SEM micrograph is less than about 1.5 micron. 2. The blood contact surface of claim 1 wherein the nodes and fibrils have a ratio of mean distances between adjacent nodes in the x and y directions of about 2:1 to 1.1. 3. The blood contact surface of claim 2 wherein the ratio of mean distances between adjacent nodes in the x and y directions is about 1:1. 4. The blood contact surface of claim 1 wherein the expanded polytetrafluoroethylene comprises a multi-axially expanded polytetrafluoroethylene. 5. The blood contact surface of claim 4 wherein the expanded polytetrafluoroethylene comprises a bi-axially expanded polytetrafluoroethylene. 6. The blood contact surface of claim 1 wherein the expanded polytetrafluoroethylene comprises fibrils extended outwardly from the nodes in substantially perpendicular directions. 7. The blood contact surface of claim 1 wherein the mean width of the nodes comprises less than about 1.25 micron. 8. The blood contact surface of claim 1 wherein the mean width of the nodes is less than about 1 micron. 9. The blood contact surface of claim 1 wherein the ratio of mean distances between adjacent nodes in the x and y directions is less than 1.5 to 1. 10. The blood contact surface of claim 1 wherein the microstructure substantially prevents cellular in-growth. 11. The blood contact surface of claim 1 wherein the blood contact surface is incorporated in an implantable medical device. 12. The blood contact surface of claim 1 wherein the blood contact surface is incorporated in a non-implantable medical device. 13. The blood contact surface of claim 1 wherein the mean distance between adjacent nodes is less than about 4 micron. 14. The blood contact surface of claim 13 wherein the mean distance between adjacent nodes is less than about 3 micron. 15. The blood contact surface of claim 11 wherein the implantable medical device includes a stent. 16. The blood contact surface of claim 1 wherein endothelial cells attach intimately to the node and fibril microstructure.
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