Method and device for selective addition of a bioactive agent to a multi-phase implant

• US 20070041950A1
• Filed: 02/01/2006
• Published: 02/22/2007
• Est. Priority Date: 02/01/2005
• Status: Abandoned Application

• Current Assignee: OsteoBiologics Inc. (Smith & Nephew PLC)
• Original Assignee: OsteoBiologics Inc. (Smith & Nephew PLC)
• Inventors: Leatherbury, Neil, Blandford, Joseph
• Application Number:
  US11/345,115
• Publication Number:
  US 20070041950A1
• Time in Patent Office: Days
• US Class Current: 424/93.700
• CPC Class Codes: A61F 2/08 Muscles; Tendons; Ligaments sutures A61B17/04
• CPC Class Codes: A61F 2/28 Bones joints A61F2/30
• CPC Class Codes: A61F 2/30744 End caps, e.g. for closing an endoprosthetic cavity
• CPC Class Codes: A61F 2/30756 Cartilage endoprostheses A61F2/3603 takes precedence
• CPC Class Codes: A61F 2/4601 for introducing bone substitute, for implanting bone graft implants or for compacting them in the bone cavity
• CPC Class Codes: A61F 2/4618 of cartilage
• CPC Class Codes: A61F 2002/30004 the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis
• CPC Class Codes: A61F 2002/30011 differing in porosity
• CPC Class Codes: A61F 2002/30014 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2002/30028 differing in tissue ingrowth capacity, e.g. made from both ingrowth-promoting and ingrowth-preventing parts
• CPC Class Codes: A61F 2002/30062 (bio)absorbable, biodegradable, bioerodable, (bio)resorbable, resorptive
• CPC Class Codes: A61F 2002/30065 thermoplastic, i.e. softening or fusing when heated, and hardening and becoming rigid again when cooled
• CPC Class Codes: A61F 2002/30115 circular-O-shaped
• CPC Class Codes: A61F 2002/30235 tubular, e.g. sleeves
• CPC Class Codes: A61F 2002/30354 Cylindrically-shaped protrusion and recess, e.g. cylinder of circular basis
• CPC Class Codes: A61F 2002/30405 made by screwing complementary threads machined on the parts themselves
• CPC Class Codes: A61F 2002/30448 using adhesives
• CPC Class Codes: A61F 2002/30451 soldered or brazed or welded
• CPC Class Codes: A61F 2002/30487 Circumferential cooperating grooves and beads on cooperating lateral surfaces of a mainly longitudinal connection
• CPC Class Codes: A61F 2002/305 Snap connection
• CPC Class Codes: A61F 2002/30589 : Sealing means
• CPC Class Codes: A61F 2002/30594 : slotted, e.g. radial or meridian slot ending in a polar aperture, non-polar slots, horizontal or arcuate slots
• CPC Class Codes: A61F 2002/30604 : modular
• CPC Class Codes: A61F 2002/30677 : Means for introducing or releasing pharmaceutical products, e.g. antibiotics, into the body
• CPC Class Codes: A61F 2002/3068 : the pharmaceutical product being in a reservoir
• CPC Class Codes: A61F 2002/30822 : Circumferential grooves
• CPC Class Codes: A61F 2002/4696 : optical
• CPC Class Codes: A61F 2210/0004 : bioabsorbable
• CPC Class Codes: A61F 2210/0071 : thermoplastic
• CPC Class Codes: A61F 2220/0025 : Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
• CPC Class Codes: A61F 2220/0033 : made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit
• CPC Class Codes: A61F 2220/005 : using adhesives
• CPC Class Codes: A61F 2220/0058 : soldered or brazed or welded
• CPC Class Codes: A61F 2230/0006 : circular
• CPC Class Codes: A61F 2230/0069 : cylindrical
• CPC Class Codes: A61F 2250/0014 : having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
• CPC Class Codes: A61F 2250/0018 : differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0023 : differing in porosity
• 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: A61F 2250/0068 : the pharmaceutical product being in a reservoir
• CPC Class Codes: A61F 2310/00011 : Metals or alloys

Abstract

A method and device for assembling a multi-phase implant for insertion into a patient defect site that spans more than one tissue type. The assembly device comprises a base and cover portion for constructing a two-phase implant separated by a membrane. A repeating intermediate portion that connects the base and cover can be used to construct implants with more than two phases, with each phase separated by a membrane. The invention is also for multi-phase implants, wherein adjacent phases are separated by a membrane. In an embodiment, the implant phases are selectively loaded with a bioactive agent selected to promote tissue repair in the tissue surrounding each phase.

Claims

1. An implant assembly for constructing a two-phase implant comprising:

a. a base comprising;

i. a bottom portion;

ii. a top portion;

iii. a lower implant compartment having a cross-sectional shape, said lower implant compartment extending through said top portion and said bottom portion;

b. a cover secured to said base comprising;

i. an upper portion having an upper implant compartment, wherein the upper implant compartment cross-sectional shape is equivalent to the cross-sectional shape of the lower implant compartment; and

ii. a lower portion having a lower receiving compartment sized to receive the top portion of the base.

2. The implant assembly of claim 1 further comprising a well formed at the top of the lower implant compartment for receiving a membrane.

3. The implant assembly of claim 2 further comprising an o-ring on a surface of the top portion of the base for contacting a membrane positioned between the cover and the base.

4. The implant assembly of claim 3 further comprising an o-ring on a surface of the lower portion of the cover for contacting a membrane positioned between the cover and the base.

5. The implant assembly of claim 1, wherein the cover is secured to the base by one or more of welds, adhesives, and fastening means on the base removably engaged with fastening means on the cover.

6. The implant assembly of claim 5 wherein the fastening means comprises a snap bead, wherein said snap bead comprises:

a. a circumferential undercut, wherein said undercut is located between the base bottom portion and base top portion;

b. a compartment overhang, wherein said compartment overhang is located at the bottom of the cover lower portion, for engaging the cover lower portion to the circumferential undercut;

c. a plurality of slots positioned along the cover lower portion to facilitate engaging the cover lower portion to the circumferential undercut.

7. The implant assembly of claim 1 wherein said lower and upper implant compartment cross-sectional shape is circular.

8. The implant assembly of claim 1 further comprising a membrane located between the base and the cover, said membrane having a lower surface and an upper surface.

9. The implant assembly of claim 8 wherein said membrane is impermeable.

10. The implant assembly of claim 8 wherein said membrane is permeable or selectively permeable.

11. The implant assembly of claim 8 further comprising:

a. a first phase of an implant located within the lower compartment and attached to the lower surface of the membrane, and

b. a second phase of an implant located within the upper compartment and attached to the upper surface of the membrane.

12. The implant assembly of claim 11 wherein said first phase and said second phase each comprise different materials.

13. The implant assembly of claim 11 wherein said first phase is adapted for bone implantation and said second phase is adapted for cartilage implantation.

14. The implant assembly of claim 11 wherein the first phase and/or second phase contain one or more bioactive agent.

15. The implant assembly of claim 14 wherein the one or more bioactive agent is selected from the group consisting of growth factors, extracellular matrix, pharmaceutical drugs, and suspension of cells.

16. An implant assembly for constructing a three-or-more-phase implant comprising the device of claim 1, and further comprising one or more intermediate units positioned between the cover and the base, wherein the intermediate unit comprises:

a. an intermediate upper portion secured to the cover, the intermediate upper portion comprising;

i. an intermediate implant compartment having a cross-sectional shape equivalent to the cross-sectional shape of the lower implant compartment;

ii. an upper intermediate portion sized to engage the lower receiving compartment of the cover;

iii. a port for the addition of one or more bioactive agents to the intermediate implant compartment;

b. an intermediate lower portion secured to the base, the intermediate lower portion having an intermediate receiving compartment sized to receive the base top portion.

17. The implant assembly of claim 16 further comprising one or more additional intermediate units identical to said intermediate unit, positioned between said cover and said base.

18. The implant assembly of claim 16 further comprising a membrane between each of the adjacent implant compartments.

19. The implant assembly of claim 18 further comprising a well formed at the top of the upper intermediate compartment for receiving a membrane.

20. The implant assembly of claim 19 further comprising an o-ring on a top surface of the intermediate upper portion for contacting a membrane positioned between the intermediate portion and the cover and an o-ring on the bottom surface of the intermediate lower portion for contacting a membrane positioned between the intermediate portion and the base.

21. The implant assembly of claim 11, wherein said implant assembly is disposed within a loading device.

24. A multi-phase implant made using the implant assembly of claim 1, wherein adjacent phases are separated by a membrane.

25. The implant of claim 24 wherein the adjacent phases are separated by a membrane having a thickness between 125 μ

m and 250 μ

m.

22. An implant assembly for constructing a multi-phase implant comprising:

a. a base comprising

i. a bottom portion;

ii. a top portion;

iii. a lower implant compartment having a cross-sectional shape, said lower implant compartment extending through said top portion and said bottom portion;

b. a cover comprising;

i. an upper portion having an upper implant compartment, wherein the upper implant compartment cross-sectional shape is equivalent to the cross-sectional shape of the lower implant compartment; and

ii. a lower portion having a lower receiving compartment sized to receive the top portion of the base;

c. means for positioning a membrane between the base and cover portions; and

d. means for sealingly engaging the base with the cover.

23. The implant assembly of claim 22 further comprising one or more intermediate units placed between the base and cover, wherein the intermediate unit comprises:

a. an intermediate upper portion comprising;

i. an intermediate implant compartment having a cross-sectional shape equivalent to the cross-sectional shape of the lower implant compartment;

ii. an upper intermediate portion sized to engage the lower receiving compartment of the cover;

iii. means for positioning a membrane between said intermediate implant compartment and an adjacent compartment;

iv. means for the intermediate upper portion to sealingly engage the cover lower portion;

b. an intermediate lower portion comprising;

i. an intermediate receiving compartment sized to engage the base top portion;

ii. means for the intermediate lower portion to sealingly engage the base.

26. An implant for insertion into a tissue defect, said implant comprising:

a. a membrane having a top surface and a bottom surface;

b. a first implant phase attached to said membrane top surface; and

c. a second implant phase attached to said membrane bottom surface.

27. The implant of claim 26 wherein the first implant phase has a composition that is different than the second implant phase composition.

28. The implant of claim 26 wherein the first implant phase and/or second implant phase contain one or more bioactive agent.

29. The implant of claim 28 wherein the first implant phase is adapted for bone implantation and the second implant phase is adapted for cartilage implantation.

30. A method of constructing a two-phase implant with the two phases separated by a membrane, said method comprising:

a. providing a first holder for a first implant phase, also comprising a holder for a membrane at a first end of the first holder;

b. providing a second holder for a second implant phase;

c. inserting a first implant phase into said first holder;

d. inserting a membrane into said first end of the first holder and attaching the membrane to said first phase; and

e. inserting a second implant phase into said second holder and attaching it to said membrane

to construct a two-phase implant with the two phases separated by a membrane.

31. The method of claim 30 further comprising sealingly engaging said first and second holders.

32. The method of claim 31 wherein the membrane is impermeable or selectively permeable.

33. The method of claim 32 further comprising inserting one or more bioactive agents into the first implant phase and inserting one or more bioactive agents into the second implant phase.

34. The method of claim 33 wherein the one or more bioactive agents in the first phase promote a first tissue repair by selectively delivering the bioactive agent in the first implant phase to the first tissue and the one or more bioactive agents in the second implant phase promote a second tissue repair by selectively delivering the bioactive agent in the second implant phase to the second tissue.

35. The method of claim 34 wherein the first tissue is cartilage and the second tissue is bone.

36. The method of claim 35 wherein the one or more bioactive agents in the phase to promote cartilage repair comprises a suspension of chondrocytes.

37. The method of claim 30 further comprising inserting the two-phase implant into a delivery device.

38. The method of claim 37 further comprising inserting the implant into a defect in a patient.

39. The method of claim 38 wherein the defect in a patient spans bone tissue and cartilage tissue.