SOFT PROSTHESIS SHELL TEXTURING METHOD

• US 20130053956A1
• Filed: 10/24/2012
• Published: 02/28/2013
• Est. Priority Date: 11/05/2007
• Status: Active Grant

• Current Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Original Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Inventors: Powell, Thomas, Dang, Loantrang
• Granted Patent: US 9,138,310 B2
• Time in Patent Office: Days
• US Class Current: 623/8
• CPC Class Codes: A61F 2/0077 Special surfaces of prostheses, e.g. for improving ingrowth A61F2/30767 takes precedence
• CPC Class Codes: A61F 2/12 Mammary prostheses and implants
• CPC Class Codes: A61F 2002/0086 for preferentially controlling or promoting the growth of specific types of cells or tissues of bone tissue onto implantable joints A61F2002/3093

Abstract

A method of texturing a soft prosthetic implant shell, such as a silicone breast implant shell. A soft prosthetic implant with a textured external surface layer of silicone elastomer and having an open-cell structure is made by adhering and then dissolving round salt crystals. The resulting roughened surface has enhanced physical properties relative to surfaces formed with angular salt crystals. An implant having such a textured external surface layer is expected to help prevent capsular contraction, to help prevent scar formation, and to help in anchoring the implant within the body.

Claims

1. A breast implant comprising:

a closed envelope of silicone elastomer having an exterior surface and a thickness, wherein the exterior surface has an undulating topography and an open-pored structure comprising round open cavities defined by impressions of round particles, wherein the open-pored structure does not extend through the entire thickness of the silicone elastomer.

2. The implant of claim 1 wherein said round open cavities are defined by impressions of round particles having a substantially uniform particle size within a particle size range selected from a group of ranges consisting of (1) a range between 180 microns and 425 microns, (2) a range between 425 microns and 850 microns, and (3) a range between 850 microns and 1450 microns.

3. The implant of claim 2 wherein the selected particle size range is the range between 850 microns and 1450 microns.

4. The implant of claim 2 wherein the selected particle size range is the range between 180 microns and 425 microns.

5. The implant of claim 2 wherein the selected particle size range is the range between 425 microns and 850 microns.