SOFT FILLED PROSTHESIS SHELL WITH DISCRETE FIXATION SURFACES

• US 20100042211A1
• Filed: 05/01/2009
• Published: 02/18/2010
• Est. Priority Date: 08/13/2008
• Status: Abandoned Application

• Current Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Original Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Inventors: Powell, Thomas E., Van Epps, Dennis
• Application Number:
  US12/434,445
• Publication Number:
  US 20100042211A1
• Time in Patent Office: Days
• US Class Current: 623/8
• CPC Class Codes: A61F 2/12 Mammary prostheses and implants
• CPC Class Codes: A61F 2210/0057 stretchable
• CPC Class Codes: A61F 2210/0061 swellable
• CPC Class Codes: A61F 2250/0003 having an inflatable pocket filled with fluid, e.g. liquid or gas
• CPC Class Codes: A61F 2250/0051 differing in tissue ingrowth capacity, e.g. made from both ingrowth-promoting and ingrowth-preventing parts
• CPC Class Codes: B29C 2791/001 Shaping in several steps
• CPC Class Codes: B29C 41/14 Dipping a core B29C41/10 takes precedence
• CPC Class Codes: B29L 2031/7532 Artificial members, protheses

Abstract

A soft prosthetic implant shell, such as a silicone breast implant shell, that has discrete fixation surfaces thereon for tissue adhesion. The fixation surfaces may be provided on the posterior face of the shell, as well as either on the periphery or at discrete areas on the anterior face. Band-shaped fixation surfaces may be provided on the anterior face of the shell to generally match the angle of pectoralis major or pectoralis minor muscle groups. The fixation surfaces may be roughened areas of the shell, or may be separate elements adhered to the shell.

Claims

1. A breast prosthesis for implantation in a human being, the device comprising

a shell having an exterior structured to contact tissue, the shell including a first fixation surface having a first open cell structure, and a second fixation surface having a second open cell structure different than said first open cell structure;

the first fixation surface and the second fixation surface being positioned to encourage respectively different degrees of tissue ingrowth or tissue adhesion by the body at a body-shell interface.

2. The prosthesis of claim 1 wherein the first and second fixation surfaces are positioned to be effective to disrupt or disorient capsular tissue formation about the prosthesis after the prosthesis has been implanted in the body.

3. The prosthesis of claim 1 wherein the first open cell structure comprises relatively large open cells and the second open cell structure comprises relatively smaller open cells.

4. The prosthesis of claim 1 wherein the first open cell structure comprises a first distribution of cells and the second open cell structure comprises a second distribution of cells wherein the first distribution of cells is relatively more dense than the second distribution of cells.

5. The prosthesis of claim 1 wherein the first open cell structure comprises relatively large rounded open cells and the second open cell structure comprises relatively small rounded open cells.

6. The prosthesis of claim 1 wherein the first open cell structure comprises relatively rounded open cells and the second open cell structure comprises relatively angular open cells.

7. The prosthesis of claim 1 further comprising a gel core enveloped by the shell.

8. The prosthesis of claim 1 wherein the shell is fillable with saline after implantation in the body.

9. A breast prosthesis shell for implantation in a human being, the shell manufactured by the steps of:

(a) providing a shell precursor;

(b) applying a layer of silicone elastomer to the shell precursor;

(c) applying solid particles of a first configuration to a portion of the layer of silicone elastomer before the layer is fully cured;

(d) applying solid particles of a second configuration to another portion of the layer of silicone elastomer before the layer is fully cured, the second configuration being different from the first configuration; and

(e) fully curing the layer; and

(f) dissolving the solid particles with a solvent that does not dissolve the silicone elastomer to any appreciable extent to thereby form an elastomer shell having a first open cell texture region formed by said application of the solid particles of the first configuration, and a second open cell texture region formed by said application of the solid particles of the second configuration.

10. The prosthesis of claim 9 structured such that tissue adhesion or ingrowth by the body engages the first open cell texture region differently than the second open cell texture region.