WO2001028460A1 - Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device - Google Patents

Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device Download PDF

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Publication number
WO2001028460A1
WO2001028460A1 PCT/US2000/027884 US0027884W WO0128460A1 WO 2001028460 A1 WO2001028460 A1 WO 2001028460A1 US 0027884 W US0027884 W US 0027884W WO 0128460 A1 WO0128460 A1 WO 0128460A1
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WO
WIPO (PCT)
Prior art keywords
set forth
self
repeating
orthopaedic implant
dimensional structure
Prior art date
Application number
PCT/US2000/027884
Other languages
French (fr)
Inventor
Jens Peter Timm
Original Assignee
Interpore Cross International
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Interpore Cross International filed Critical Interpore Cross International
Priority to JP2001531057A priority Critical patent/JP2004507274A/en
Priority to EP00972040A priority patent/EP1225847A1/en
Priority to AU10758/01A priority patent/AU777462B2/en
Priority to KR1020027004948A priority patent/KR20020068038A/en
Publication of WO2001028460A1 publication Critical patent/WO2001028460A1/en

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    • AHUMAN NECESSITIES
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/4455Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages
    • A61F2/4465Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages having a circular or kidney shaped cross-section substantially perpendicular to the axis of the spine
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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Definitions

  • the present invention relates generally to a three-dimensional structure for use as a bone mass replacement or fusion augmentation device.
  • this structure is specifically engineered from interconnecting, non-random metallic segments so as to minimize the volume of the metal to void and thereby maximize potential volume for reconstructive bone growth.
  • the metallic segments or filaments are joined to form regular repeating geometric shapes to provide maximum strength and minimize potential shear planes through the structure.
  • a particularly favored geometric shape is a modified dodecahedron based on pentagons.
  • the resulting structure may have a general rectangular block configuration, a cylindrical configuration which can include a larger defined void area in the center.
  • the present invention provides an engineered three-dimensional structure, which has a goal of providing a structure for bone to grow through for fusion or reconstructive surgery.
  • the structure is further intended to be strong enough to provide support to the skeletal and muscular structure during bone rehabilitation, i.e. during the healing process when bone reconstruction occurs.
  • the present invention provides a structure which is self-supporting meaning that no further substrate or support is required to provide the necessary support characteristics during rehabilitation.
  • implants such as acetabular cups having porous coatings.
  • these coatings can also be distinguished since the pores tend to be random and substantially smaller (by at least a magnitude or more of size) than the pores of the present invention.
  • the structure is constructed of discrete subcomponents which are repeating geometric shapes, constructed of filamentary elements so as to provide regular intersticial pores and/or voids of an appropriate shape and size to allow for bone.
  • the filamentary segments are providing structural support, slow in-growth can occur into the void area.
  • the structure has a central void area to accommodate the bone graft or bone substitute.
  • An additional aspect of the invention is the provision of a structure, which is "space-filling" meaning that structure can be expanded to any size and will maintain its shape as a repeating structure.
  • the structure is ordered and not random. It is homogeneous and provides multiple planes of symmetry.
  • the implant is preferably constructed from a bio-compatible cast metal such as titanium or a titanium alloy so as to maximize strength and minimize the metal artifact which would appear on sectional CT scans.
  • the structure can be modified to generate the desired implant stiffness for a variety of applications.
  • the structure can also be modified to increase its strength and resistance to fatigue as is necessary.
  • individual filamentary members may be modified or eliminated to provide for functional structures including for example voids for bone growth voids or means to attach fasteners.
  • spinal fusions such as posterior lumbar inter-body fusion ("PLIF"), anterior lumbar and inter-body fusion (“ALIF”), inter-body fusion ring, long-bone reconstruction such as humoral or femoral reconstruction, tibial-plateau reconstruction, cranial facial applications including mixillo-facial reconstruction, and pelvic- defect reconstruction.
  • PLIF posterior lumbar inter-body fusion
  • ALIF anterior lumbar and inter-body fusion
  • inter-body fusion ring long-bone reconstruction such as humoral or femoral reconstruction
  • tibial-plateau reconstruction cranial facial applications including mixillo-facial reconstruction
  • pelvic- defect reconstruction cranial facial applications for mixillo-facial reconstruction.
  • Figure 1 shows a side view of first embodiment of the invention
  • Figure 2 shows an end view of first embodiment shown in Fig. 1
  • Figure 3 shows a top view of the embodiment shown in Fig. 1
  • Figure 4 shows a second embodiment of the invention for use in anterior lumbar inner-body fusion
  • Figure 5 shows a third, annular, embodiment of the invention
  • Figure 6 shows a different view of the third embodiment
  • Figure 7 shows a view of a fourth embodiment
  • Figure 8 shows a different view and scale of the embodiment of
  • Figure 1 illustrates a three-dimensional, geometric-porous engineered structure for use as a bone mass replacement for fusion augmentation device.
  • the structure shown generally at 1 0 is formed from a series of inter-connected filaments 1 2, which form one or more types of repeating geometric shapes.
  • a first shape 1 5 is pentagonal, while a second repeating shape is a modified dodecahedron 1 7.
  • the shapes interconnect so as to define porous areas of intersticial voids 20. These areas provide space for bone to grow into during bone reconstruction or fusion.
  • the structure is intended ultimately to become redundant and/or subplanted by the bone that grows into the area.
  • the structure 1 0 has a generally regular overall shape.
  • the structure has a block configuration with the top 25, bottom 27, side 29 and end 31 geometric structures substantially defining planes.
  • the structure is generally lacking "shear planes", i.e. planes predisposed to shear failure within the structure.
  • This aspect of the invention allows for the maximization of strength in every direction, including characteristics for axial, shear, and torsional stresses 1 0 to which bones are subjected, while minimizing the metallic, scaffolding or substructure.
  • Figure 4 illustrates an embodiment of the invention for use in spinal inter-body fusion.
  • this disc or kidney-shaped device has inner 41 an outer 40 top rings and inner 43 and outer 42 bottom rings inter-connected by filamentary struts 44 to provide the desired strength characteristics. Further, this device has a larger void 46 defined by interior rings to allow bone graft, or bone substitute to be implanted within the structure.
  • FIG. 5 A similar ring implant for reinforcing weak, bony tissue is shown at 50 in Figs. 5 and 6.
  • This structure is illustrated as having filamentary pentagons constructed of individual filaments 52 defining pores 51 and dodecahedron shapes similar to those shown in the first embodiment shown in Figs. 1 -3.
  • the implant in Figs. 5 and 6 is ring shaped and thus includes an interior void 54 intended for the same purpose as in Fig. 4.
  • Figures 7 and 8 illustrate a block-shaped structure 60 again constructed from filaments 62 joined at regular repeating angles 63 to form modified pentagons and highly modified dodecahedrons.
  • modified is meant that one or more angles of the basic shape or one or more filamentary segment length has been modified from the general understanding of this geometric shape to allow the figure to close and to connect the pieces of the three-dimensional space-filling structure.
  • a pentagon is a regular five-sided shape while a dodecahedron is a spherical structure formed by joining ten pentagons. This structure also has a central void 64 defined by closed octagonal inner rings 66.
  • the filaments generally have a thickness of from about 0.25 millimeters to 2 millimeters preferably 0.5 to 1 .5 millimeters and most preferably 0.5 to 1 millimeter.
  • the length of these filaments in a pentagonal shape is generally from about 1 millimeter to about 10 millimeters and, preferably 1 to 6 millimeters and most preferably 1 .5 to 3 millimeters.
  • the dodecahedron shape has a maximum size of 20 millimeters. While cast titanium or titanium alloy are envisioned as a preferable material, the invention could be made of other bio-compatible substances including for example, PEEK, other metals, and ceramic bone substitutes could also be envisioned.
  • the geometry used for the present invention envisions regular repeating convex polyhedra in three-dimensional space including for example the tetrahedron, the cube, the regular octahedron, the pentagonal dodecahedron bounded by 1 2 regular pentagons and the icosahedron, bounded by 20 regular triangles.
  • the filamentary structures are joined together to form geometric shapes, which are the building blocks to form a larger configuration, meaning the general overall profile of the structure.
  • the present invention would envision other configurations or structures based on these kinds of geometric shapes as well.

Abstract

The invention provides a three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device. The structure is a space-filling, self-supporting structure constructed or rigid filaments (12) joined together to form regular, repeating geometric shapes. The structure supports the skeletal structure as well as the surrounding tissue during rehabilitation and/or bone fusion. Further, the structure provides many open intersticial areas (20), which are appropriately shaped and sized for bone in-growth. One preferred geometric structure is based on repeating modified dodecahedrons which are built from pentagons. The resulting structure has two transverse planes of bilateral symmetry. Other embodiments include disc shaped structures and structures having open internal areas to allow the possibility of auto graft, allograft, or artificial bone substitute.

Description

THREE-DIMENSIONAL GEOMETRIC POROUS ENGINEERED STRUCTURE
FOR USE AS A BONE MASS REPLACEMENT OR FUSION
AUGMENTATION DEVICE
FIELD OF THE INVENTION
The present invention relates generally to a three-dimensional structure for use as a bone mass replacement or fusion augmentation device. In particular, this structure is specifically engineered from interconnecting, non-random metallic segments so as to minimize the volume of the metal to void and thereby maximize potential volume for reconstructive bone growth. The metallic segments or filaments are joined to form regular repeating geometric shapes to provide maximum strength and minimize potential shear planes through the structure. A particularly favored geometric shape is a modified dodecahedron based on pentagons. The resulting structure may have a general rectangular block configuration, a cylindrical configuration which can include a larger defined void area in the center.
SUMMARY OF THE INVENTION
The present invention provides an engineered three-dimensional structure, which has a goal of providing a structure for bone to grow through for fusion or reconstructive surgery. The structure is further intended to be strong enough to provide support to the skeletal and muscular structure during bone rehabilitation, i.e. during the healing process when bone reconstruction occurs.
Thus, it is a goal of the present invention to provide a structure which is self-supporting meaning that no further substrate or support is required to provide the necessary support characteristics during rehabilitation. This contrast with implants such as acetabular cups having porous coatings. Likewise, these coatings can also be distinguished since the pores tend to be random and substantially smaller (by at least a magnitude or more of size) than the pores of the present invention. Further, the structure is constructed of discrete subcomponents which are repeating geometric shapes, constructed of filamentary elements so as to provide regular intersticial pores and/or voids of an appropriate shape and size to allow for bone. Thus, while the filamentary segments are providing structural support, slow in-growth can occur into the void area. This growth, can be encouraged and/or augmented through the use of bone graft or bone substitutes. By "regular" it is meant that the component parts are uniform, or of the same kind or structure or shape or size, or having repeating units of the same size and/or angle. By "geometric" it is meant that at least some of the component parts are formed of straight lines, bars, or crosses. By "ordered" it is meant that the shapes are arranged in a sequence or pattern which is not random but which possesses symmetry and/or repetition. In a further embodiment the structure has a central void area to accommodate the bone graft or bone substitute.
An additional aspect of the invention is the provision of a structure, which is "space-filling" meaning that structure can be expanded to any size and will maintain its shape as a repeating structure. Thus, the structure is ordered and not random. It is homogeneous and provides multiple planes of symmetry.
The implant is preferably constructed from a bio-compatible cast metal such as titanium or a titanium alloy so as to maximize strength and minimize the metal artifact which would appear on sectional CT scans. The structure can be modified to generate the desired implant stiffness for a variety of applications. The structure can also be modified to increase its strength and resistance to fatigue as is necessary. Further, once the fundamental structure has been established by constructing the component repeating shapes, individual filamentary members may be modified or eliminated to provide for functional structures including for example voids for bone growth voids or means to attach fasteners.
Potential applications include spinal fusions such as posterior lumbar inter-body fusion ("PLIF"), anterior lumbar and inter-body fusion ("ALIF"), inter-body fusion ring, long-bone reconstruction such as humoral or femoral reconstruction, tibial-plateau reconstruction, cranial facial applications including mixillo-facial reconstruction, and pelvic- defect reconstruction. Thus, in general, the present structure has many orthopaedic applications for reinforcing weak, bony tissue.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 shows a side view of first embodiment of the invention; Figure 2 shows an end view of first embodiment shown in Fig. 1 ; Figure 3 shows a top view of the embodiment shown in Fig. 1 ; Figure 4 shows a second embodiment of the invention for use in anterior lumbar inner-body fusion;
Figure 5 shows a third, annular, embodiment of the invention; Figure 6 shows a different view of the third embodiment; Figure 7 shows a view of a fourth embodiment; and Figure 8 shows a different view and scale of the embodiment of
Fig. 7.
DESCRIPTION OF THE INVENTION Figure 1 illustrates a three-dimensional, geometric-porous engineered structure for use as a bone mass replacement for fusion augmentation device. The structure, shown generally at 1 0 is formed from a series of inter-connected filaments 1 2, which form one or more types of repeating geometric shapes. In the structure shown in Figs. 1 - 3, a first shape 1 5 is pentagonal, while a second repeating shape is a modified dodecahedron 1 7. The shapes interconnect so as to define porous areas of intersticial voids 20. These areas provide space for bone to grow into during bone reconstruction or fusion. Thus, the structure is intended ultimately to become redundant and/or subplanted by the bone that grows into the area. As can be seen in particular in Figs. 1 -3, the structure 1 0 has a generally regular overall shape. In this instance, the structure has a block configuration with the top 25, bottom 27, side 29 and end 31 geometric structures substantially defining planes. However, as is also evident, the structure is generally lacking "shear planes", i.e. planes predisposed to shear failure within the structure. This aspect of the invention allows for the maximization of strength in every direction, including characteristics for axial, shear, and torsional stresses 1 0 to which bones are subjected, while minimizing the metallic, scaffolding or substructure. Figure 4 illustrates an embodiment of the invention for use in spinal inter-body fusion. In particular, this disc or kidney-shaped device has inner 41 an outer 40 top rings and inner 43 and outer 42 bottom rings inter-connected by filamentary struts 44 to provide the desired strength characteristics. Further, this device has a larger void 46 defined by interior rings to allow bone graft, or bone substitute to be implanted within the structure.
A similar ring implant for reinforcing weak, bony tissue is shown at 50 in Figs. 5 and 6. This structure is illustrated as having filamentary pentagons constructed of individual filaments 52 defining pores 51 and dodecahedron shapes similar to those shown in the first embodiment shown in Figs. 1 -3. However, similar to the embodiment shown in Fig. 4, the implant in Figs. 5 and 6 is ring shaped and thus includes an interior void 54 intended for the same purpose as in Fig. 4. Figures 7 and 8 illustrate a block-shaped structure 60 again constructed from filaments 62 joined at regular repeating angles 63 to form modified pentagons and highly modified dodecahedrons. By "modified" is meant that one or more angles of the basic shape or one or more filamentary segment length has been modified from the general understanding of this geometric shape to allow the figure to close and to connect the pieces of the three-dimensional space-filling structure. A pentagon is a regular five-sided shape while a dodecahedron is a spherical structure formed by joining ten pentagons. This structure also has a central void 64 defined by closed octagonal inner rings 66.
Characteristics which may be considered in the design of specific structures for a particular application include compression, shear rotations and torsion as tested in accordance with ASTM draft of medical testing. The filaments generally have a thickness of from about 0.25 millimeters to 2 millimeters preferably 0.5 to 1 .5 millimeters and most preferably 0.5 to 1 millimeter. The length of these filaments in a pentagonal shape is generally from about 1 millimeter to about 10 millimeters and, preferably 1 to 6 millimeters and most preferably 1 .5 to 3 millimeters. The dodecahedron shape has a maximum size of 20 millimeters. While cast titanium or titanium alloy are envisioned as a preferable material, the invention could be made of other bio-compatible substances including for example, PEEK, other metals, and ceramic bone substitutes could also be envisioned.
In general, the geometry used for the present invention envisions regular repeating convex polyhedra in three-dimensional space including for example the tetrahedron, the cube, the regular octahedron, the pentagonal dodecahedron bounded by 1 2 regular pentagons and the icosahedron, bounded by 20 regular triangles. Thus, the filamentary structures are joined together to form geometric shapes, which are the building blocks to form a larger configuration, meaning the general overall profile of the structure. Thus, the present invention would envision other configurations or structures based on these kinds of geometric shapes as well.
While in accordance with the patent statutes the best mode and preferred embodiment have been set forth, the scope of the invention is not limited thereto, but rather by the scope of the attached claims.

Claims

WHAT IS CLAIMED IS:
1 . A self-supporting bio-compatible porous three dimensional structure for skeletal rehabilitation comprising; inter-connected rigid filaments collectively defining a series of repeating ordered open shapes.
2. A self-supporting porous three-dimensional structure a set forth in claim 1 , wherein said filaments are connected so as to define repeating geometric shapes.
3. A self-supporting porous three-dimensional structure a set forth in claim 2, wherein at least one of said repeating shapes are five-sided.
4. A self-supporting porous three-dimensional structure a set forth in claim 3, wherein at least one of said repeating shapes is a pentagon.
5. A self-supporting porous three-dimensional structure a set forth in claim 2, wherein at least one of said repeating shapes is 1 0 sided.
6. A self-supporting porous three-dimensional structure a set forth in claim 5, wherein said shape is a modified dodecahedron.
7. A self-supporting porous three-dimensional structure a set forth in claim 1 , wherein the filament is metal.
8. A self-supporting porous three-dimensional structure a set forth in claim 7, wherein the filament is titanium.
9. A self-supporting porous three-dimensional structure a set forth in claim 8, wherein said structure is a bone implant.
10. A self-supporting porous three-dimensional structure a set forth in claim 9, wherein said structure is a three-dimensional, self-supporting, space-filling structure having interconnected solid elements together defining repeating open structures and having no shear planes.
1 1 . An orthopaedic implant comprising; a structure formed of non-random inter-connected bio- compatible filaments which define pores, said structure being substantially free from planes predisposed to shear failure.
1 2. An orthopaedic implant as set forth in claim 1 1 further comprising a void internal to said structure for bone graft or bone substitute.
1 3. An orthopaedic implant as set forth in claim 1 1 , wherein said structure has a top which defines a substantially planar first surface and a bottom, which defines a substantially planar surface substantially parallel to said first surface.
1 4. An orthopaedic implant as set forth in claim 1 3, wherein said filaments are connected so as to define repeating geometric shapes.
1 5. An orthopaedic implant as set forth in claim 1 4, wherein at least one of said repeating shapes are five-sided.
1 6. An orthopaedic implant as set forth in claim 1 5, wherein at least one of said repeating shapes is a pentagon.
1 7. An orthopaedic implant as set forth in claim 1 6, wherein at least one of said repeating shape is 10 sided.
18. An orthopaedic implant as set forth in claim 1 7, wherein said shape is a modified dodecahedron.
1 9. An orthopaedic implant as set forth in claim 1 1 , wherein the filament is metal.
20. An orthopaedic implant as set forth in claim 1 9, wherein the filament is titanium.
PCT/US2000/027884 1999-10-20 2000-10-10 Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device WO2001028460A1 (en)

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JP2001531057A JP2004507274A (en) 1999-10-20 2000-10-10 Three-dimensional geometrically porous designed structures for use as bone mass substitutes or joint addition devices
EP00972040A EP1225847A1 (en) 1999-10-20 2000-10-10 Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device
AU10758/01A AU777462B2 (en) 1999-10-20 2000-10-10 Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device
KR1020027004948A KR20020068038A (en) 1999-10-20 2000-10-10 Three-dimensional geometric porous engineered structure for use as a bone mass replacement or fusion augmentation device

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