Compound for androgen receptor degradation, and pharmaceutical use thereof
US-2024383877-A1 · Nov 21, 2024 · US
US9713550B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9713550-B2 |
| Application number | US-201414320234-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 30, 2014 |
| Priority date | Nov 18, 2008 |
| Publication date | Jul 25, 2017 |
| Grant date | Jul 25, 2017 |
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A reduced-pressure treatment system for treating a wound on a patient includes a composite manifold that may help prevent or minimize injury to a wound edge of the wound being treated with reduced pressure. The composite manifold includes a perimeter manifold member and an inboard manifold member. The perimeter manifold member is designed to not collapse substantially under reduced pressure in a therapy range. The perimeter manifold member may be more rigid with respect to compressibility than the inboard manifold member. A sealing member is used to form a fluid seal over the wound, and a reduced-pressure subsystem provides reduced pressure to the composite manifold. Other systems, methods, and dressings are presented.
Opening claim text (preview).
What is claimed is: 1. A system for providing reduced-pressure treatment to a wound, the system comprising: an inboard manifold having a first rigidity; a perimeter manifold circumscribing the inboard manifold, the perimeter manifold having a second rigidity that is greater than the first rigidity of the inboard manifold; a sealing member configured to be placed over the inboard manifold and the perimeter manifold to form a sealed space; and a reduced-pressure source configured to be fluidly coupled to the sealed space to provide a therapeutic reduced pressure; wherein the perimeter manifold has adequate strength to resist collapse under compressive force transmitted by the sealing member when under therapeutic reduced pressure. 2. The system of claim 1 , wherein a bulk modulus of the perimeter manifold is greater than a bulk modulus of the inboard manifold. 3. The system of claim 1 , wherein a density of the perimeter manifold is greater than a density of the inboard manifold. 4. The system of claim 1 , further comprising support elements disposed in the perimeter manifold. 5. The system of claim 4 , wherein the support elements comprise filaments. 6. The system of claim 4 , wherein the support elements comprise vertical posts. 7. The system of claim 4 , wherein the support elements comprise struts. 8. The system of claim 1 , further comprising a bio-friendly stiffening substance coating the perimeter manifold. 9. The system of claim 8 , wherein the bio-friendly stiffening substance comprises a gel configured to be applied to an edge of a wound, and the perimeter manifold is configured to be coated by the bio-friendly stiffening substance in situ. 10. The system of claim 1 , wherein the perimeter manifold comprises a tape applied to the periphery of the inboard manifold. 11. The system of claim 1 , wherein the perimeter manifold is configured to support a wound edge. 12. The system of claim 11 , wherein the perimeter manifold is configured to carry a load asserted by the sealing member. 13. The system of claim 1 , wherein the perimeter manifold is configured to carry a load asserted by the sealing member. 14. A manifold for use with a reduced-pressure treatment system, the manifold comprising: an inboard manifold having a first rigidity; and a perimeter manifold circumscribing the inboard manifold, the perimeter manifold having a second rigidity that is greater than the first rigidity of the inboard manifold; wherein the perimeter manifold has adequate strength to resist collapse under compressive force transmitted by a sealing member when under therapeutic reduced pressure. 15. The manifold of claim 14 , wherein a bulk modulus of the perimeter manifold is greater than a bulk modulus of the inboard manifold. 16. The manifold of claim 14 , wherein a density of the perimeter manifold is greater than a density of the inboard manifold. 17. The manifold of claim 14 , further comprising support elements disposed in the perimeter manifold. 18. The manifold of claim 17 , wherein the support elements comprise filaments. 19. The manifold of claim 17 , wherein the support elements comprise vertical posts. 20. The manifold of claim 17 , wherein the support elements comprise struts. 21. The manifold of claim 14 , further comprising a bio-friendly stiffening substance coating the perimeter manifold. 22. The manifold of claim 21 , wherein the bio-friendly stiffening substance comprises a gel configured to be applied to an edge of a wound, and the perimeter manifold is configured to be coated by the bio-friendly stiffening substance in situ. 23. The manifold of claim 14 , wherein the perimeter manifold comprises a tape applied to the periphery of the inboard manifold. 24. The manifold of claim 14 , wherein the perimeter manifold is configured to support a wound edge. 25. The manifold of claim 24 , wherein the perimeter manifold is configured to carry a load asserted by the sealing member. 26. The manifold of claim 14 , wherein the perimeter manifold is configured to carry a load asserted by the sealing member. 27. A method of manufacturing a composite manifold for use in a reduced-pressure treatment system, the method comprising the steps of: forming a perimeter manifold member adapted to support an edge of a wound and carry a load asserted by a sealing member when under therapeutic reduced pressure, the perimeter manifold member having an interior portion and a first bulk modulus K 1 ; forming an inboard manifold member having a second bulk modulus K 2 , wherein K 1 is greater than K 2 ; and disposing the inboard manifold member adjacent the interior portion of the perimeter manifold member. 28. The method of claim 27 , further comprising the step of coupling the perimeter manifold member to the inboard manifold member. 29. The method of claim 27 , wherein the steps of forming a perimeter manifold member and forming an inboard manifold member comprise the steps of: forming the perimeter manifold member from a first manifold material having a first density, ρ 1 ; forming the inboard manifold member from a second manifold material having a second density, ρ 2 ; and wherein the first density is greater than the second density, ρ 1 >ρ 2 . 30. The method of claim 27 , wherein the step of forming a perimeter manifold member comprises the steps of forming the perimeter manifold member from a first manifold material and applying a bioactive material to at least a portion of the first manifold material. 31. The method of claim 27 , wherein the step of forming a perimeter manifold member comprises the steps of forming the perimeter manifold member from a first manifold material and applying a bioactive material to at least a portion of the first manifold material and wherein the bioactive material comprises epinephrine.
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