TISSUE-TREATING IMPLANTABLE COMPOSITIONS

• US 20100266663A1
• Filed: 04/26/2010
• Published: 10/21/2010
• Est. Priority Date: 09/10/2003
• Status: Abandoned Application

• Current Assignee: MAST Biosurgery AG
• Original Assignee: MAST Biosurgery AG
• Inventors: Calhoun, Christopher J., Bluecher, Lukas
• Application Number:
  US12/767,716
• Publication Number:
  US 20100266663A1
• Time in Patent Office: Days
• US Class Current: 424/426
• CPC Class Codes: A61F 2/0063 Implantable repair or support meshes, e.g. hernia meshes
• CPC Class Codes: A61L 27/18 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• CPC Class Codes: A61L 31/06 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds A61L31/041 takes precedence
• CPC Class Codes: C08L 67/04 Polyesters derived from hydroxycarboxylic acids, e.g. lactones C08L67/06 takes precedence

Abstract

A prosthesis for repairing a hernia includes an adhesion-resistant biodegradable region and an opposing tissue-ingrowth biodegradable region. When the prosthesis is implanted into the patient, the adhesion-resistant biodegradable region covers a fascial defect of the hernia, and the tissue-ingrowth biodegradable region is located above the adhesion-resistant biodegradable region while being exposed substantially only to the host'"'"'s subcutaneous tissue layer. This orientation allows the tissue-ingrowth biodegradable region to become firmly incorporated with the host'"'"'s body tissue. The adhesion-resistant biodegradable region faces the internal organs and decreases the incidence of adhesions and/or bowel obstruction.

Claims

1. A method for governing tissue growth, the method comprising providing a substantially planar barrier membrane of resorbable polymer base material having a tissue-growing substantially-smooth side that comprises a tissue-inductive factor and a non-tissue growing substantially-smooth side, the substantially planar barrier membrane of resorbable polymer base material comprising a single layer of resorbable polymer base material between the tissue-growing side and the non-tissue growing side, the single layer of resorbable polymer base material having a substantially uniform composition, wherein a thickness of the single layer of resorbable polymer base material, measured between the tissue-growing side and the non-tissue growing side, is between about 10 microns and about 300 microns, wherein the single layer of resorbable polymer base material is non-porous, wherein the single layer of resorbable polymer base material consists essentially of a material selected from the group consisting of a poly-lactide polymer and a copolymer of two or more cyclic esters, and wherein the single layer of resorbable polymer base material is adapted to maintain a smooth-surfaced barrier between the tissue growing side and the non-tissue growing side, and is adapted to be resorbed into a mammalian body within a period of approximately 18 to 24 months from an initial implantation of the substantially planar barrier membrane of resorbable polymer base material into the mammalian body;

and forming a spatial barrier with the substantially planar barrier membrane of resorbable polymer base material, the substantially planar barrier membrane of resorbable polymer base material separating a tissue-growth area, which faces the tissue-growing side having the tissue-inductive factor, from a non-tissue-growth area, which faces the non-tissue growing side having a pre-implantation compositional characteristic different from a pre-implantation compositional characteristic of the tissue growing side, wherein the compositional characteristic is defined by an amount or concentration of one or more of a tissue growth inhibitor or anti-tissue agent, an anti-tissue agent or factor, an anti-angiogenic factor, a monoclonal or polyclonal antibody, an antibody fragment, a substance for cellular control, a chemotactic substance for influencing cell-migration, an inhibitory substance for influencing cell-migration, a mitogenic growth factor for influencing cell proliferation, a tissue-inductive factor, a growth factor for influencing cell differentiation, and a factor which promotes angiogenesis.

2. The method of claim 1, wherein the resorbable polymer base material is about 70:

30 poly (L-lactide-co-D,L-lactide).

3. The method of claim 1, wherein the spatial barrier is formed in a cavity of a tissue of a patient.

4. The method of claim 1, wherein a thickness of the single layer of resorbable polymer base material, measured between the tissue-growing side and the non-tissue growing side, is about 100 microns.

5. The method of claim 1, wherein a thickness of the single layer of resorbable polymer base material, measured between the tissue-growing side and the non-tissue growing side, is about 200 microns.

6. The method of claim 1, wherein the single layer of resorbable polymer base material is not fluid permeable.

11. The method of claim 1, wherein the governing of tissue growth is in a spinal canal and wherein the forming of a spatial barrier comprises positioning the substantially planar barrier membrane of resorbable polymer base material to form a spatial barrier between a tissue-growth area, which faces the tissue-growing side, and the spinal canal, which faces the non-tissue growing side having a characteristic different from a characteristic of the tissue-growing side.

12. The method of claim 1, wherein:

the governing of tissue growth comprises governing tissue growth in a cavity in a tissue;

the forming of a spatial barrier comprises inserting the substantially planar barrier membrane of resorbable polymer base material into the cavity so that the at least one resorbable barrier membrane defines the tissue-growth area and the non-tissue-growth area, each of the tissue-growth area and the non-tissue-growth area being disposed on opposite sides of the substantially planar barrier membrane of resorbable polymer base material before the substantially planar barrier membrane of resorbable polymer base material is resorbed; and

the method further comprises administering at least one tissue growth inhibitor to inhibit tissue growth in a vicinity only of the non-tissue-growth area, wherein the substantially planar barrier membrane of resorbable polymer base material governs tissue growth by reducing tissue-growth in the non-tissue-growth area.

13. The method of claim 12, further comprising administering a tissue morphogenic protein to the tissue-growth area to enhance tissue growth in the tissue-growth area.

14. The method of claim 13, wherein the tissue morphogenic protein is provided on the surface of the substantially planar barrier membrane of resorbable polymer base material facing the tissue-growth area.

15. The method of claim 12, further comprising administering at least one anti-tissue factor to inhibit tissue growth in the non-tissue-growth area.

16. The method of claim 15, wherein the at least one anti-tissue factor is provided only on a surface of the substantially planar barrier membrane of resorbable polymer base material facing the non-tissue-growth area.

17. The method of claim 12, wherein the substantially planar barrier membrane of resorbable polymer base material is inserted adjacent to the spinal meninges to reduce tissue growth into the spinal canal of the patient.

18. The method of claim 12, wherein the substantially planar barrier membrane of resorbable polymer base material comprises a poly-lactide polymer and a copolymer of at least two lactides.

19. The method of claim 12, wherein the substantially planar barrier membrane of resorbable polymer base material is impermeable to fluid.

20. The method of claim 12, further comprising attaching the substantially planar barrier membrane of resorbable polymer base material to an anatomical structure to provide a fixed border between the tissue-growth area and the non-tissue-growth area.

7. A method for governing tissue growth, the method comprising providing a substantially planar barrier membrane of resorbable polymer base material having a tissue-growing substantially-smooth side and a non-tissue growing substantially-smooth side, the substantially planar barrier membrane of resorbable polymer base material comprising a single layer of resorbable polymer base material between the tissue-growing side and the non-tissue growing side, the single layer of resorbable polymer base material having a substantially uniform composition, wherein a thickness of the single layer of resorbable polymer base material, measured between the tissue-growing side and the non-tissue growing side, is between about 10 microns and about 300 microns, wherein the single layer of resorbable polymer base material is non-porous, wherein the single layer of resorbable polymer base material consists essentially of a material selected from the group consisting of a poly-lactide polymer and a copolymer of two or more cyclic esters, and wherein the single layer of resorbable polymer base material is adapted to maintain a smooth-surfaced barrier between the tissue growing side and the non-tissue growing side, and is adapted to be resorbed into a mammalian body within a period of approximately 18 to 24 months from an initial implantation of the substantially planar barrier membrane of resorbable polymer base material into the mammalian body;

and forming a spatial barrier with the substantially planar barrier membrane of resorbable polymer base material, the substantially planar barrier membrane of resorbable polymer base material separating a tissue-growth area, which faces the tissue-growing side having a tissue inductive factor, from a non-tissue-growth area, which faces the non-tissue growing side having a pre-implantation compositional characteristic, which is defined by an amount or concentration of one or more of a tissue growth inhibitor or anti-tissue agent, an anti-tissue agent or factor, an anti-angiogenic factor, a monoclonal or polyclonal antibody, an antibody fragment, a substance for cellular control, a chemotactic substance for influencing cell-migration, an inhibitory substance for influencing cell-migration, a mitogenic growth factor for influencing cell proliferation, a tissue-inductive factor, a growth factor for influencing cell differentiation, and a factor which promotes angiogenesis, and which is different from a pre-implantation compositional characteristic of the tissue growing side, wherein the substantially planar barrier membrane or resorbable polymer base material is impregnated with at least one of an anti-tissue agent, a chemotactic substance for influencing cell-migration, an inhibitory substance for influencing cell-migration, a mitogenic growth factor for influencing cell proliferation, a growth factor for influencing cell differentiation, and factors which promote angiogenesis.

8. A method for governing tissue growth in a tissue cavity, comprising:

providing a smooth-surfaced resorbable polymer barrier membrane—

which is about 10 to 300 microns thick and adapted to be resorbed in about 18 to 24 months and which has a tissue-growing side with a tissue inductive factor and a non-tissue-growing side substantially free of the tissue inductive factor; and

inserting the resorbable barrier membrane into a tissue cavity of a patient so that the resorbable barrier membrane defines a tissue-growth area and a non-tissue-growth area, each of the tissue-growth area and the non-tissue-growth area being disposed on opposite sides of the resorbable barrier membrane before the resorbable barrier membrane is resorbed, wherein the resorbable barrier membrane comprises an agent that governs tissue growth by limiting tissue-growth in the non-tissue-growth area relative to a growth of tissue in the tissue-growth area.

9. The method of claim 8, wherein the resorbable barrier membrane is impermeable to fluid.

10. The method of claim 9, wherein the implant comprises:

a promoter of cell growth disposed substantially only on the tissue-growing side of the implant; and

an inhibitor of cell growth disposed substantially only on the non-tissue growing side of the implant.