CA1135005A - Bone connective prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticity - Google Patents
Bone connective prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticityInfo
- Publication number
- CA1135005A CA1135005A CA000345346A CA345346A CA1135005A CA 1135005 A CA1135005 A CA 1135005A CA 000345346 A CA000345346 A CA 000345346A CA 345346 A CA345346 A CA 345346A CA 1135005 A CA1135005 A CA 1135005A
- Authority
- CA
- Canada
- Prior art keywords
- prosthesis
- elasticity
- layer
- modulus
- polymer layer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 188
- 230000002787 reinforcement Effects 0.000 title claims abstract description 88
- 210000000988 bone and bone Anatomy 0.000 title claims abstract description 46
- 230000007423 decrease Effects 0.000 claims abstract description 7
- 239000002639 bone cement Substances 0.000 claims description 38
- 239000002131 composite material Substances 0.000 claims description 25
- 239000000945 filler Substances 0.000 claims description 18
- 239000004014 plasticizer Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 13
- 238000003780 insertion Methods 0.000 claims description 8
- 230000037431 insertion Effects 0.000 claims description 8
- 239000011800 void material Substances 0.000 claims description 7
- 230000001788 irregular Effects 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000011236 particulate material Substances 0.000 claims 1
- 239000007943 implant Substances 0.000 description 16
- 239000004926 polymethyl methacrylate Substances 0.000 description 13
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 12
- 239000007789 gas Substances 0.000 description 11
- 229910001092 metal group alloy Inorganic materials 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000009826 distribution Methods 0.000 description 8
- 239000002775 capsule Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229920001169 thermoplastic Polymers 0.000 description 7
- 239000004416 thermosoftening plastic Substances 0.000 description 7
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 6
- 210000001624 hip Anatomy 0.000 description 6
- 210000000629 knee joint Anatomy 0.000 description 6
- 239000002861 polymer material Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000004088 foaming agent Substances 0.000 description 5
- 230000003014 reinforcing effect Effects 0.000 description 5
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 210000004394 hip joint Anatomy 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229910001182 Mo alloy Inorganic materials 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229910001069 Ti alloy Inorganic materials 0.000 description 2
- -1 UHMWPE Chemical compound 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000007792 gaseous phase Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 210000001503 joint Anatomy 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000399 orthopedic effect Effects 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 210000002303 tibia Anatomy 0.000 description 2
- 210000000689 upper leg Anatomy 0.000 description 2
- 206010068975 Bone atrophy Diseases 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- FCDDQRGFNZZTMQ-UHFFFAOYSA-N chromium cobalt molybdenum Chemical compound [Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Cr].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Co].[Mo].[Mo].[Mo].[Mo].[Mo].[Mo] FCDDQRGFNZZTMQ-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 229940102838 methylmethacrylate Drugs 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/28—Materials for coating prostheses
- A61L27/34—Macromolecular materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/3094—Designing or manufacturing processes
- A61F2/30965—Reinforcing the prosthesis by embedding particles or fibres during moulding or dipping
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/36—Femoral heads ; Femoral endoprostheses
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- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/36—Femoral heads ; Femoral endoprostheses
- A61F2/3601—Femoral heads ; Femoral endoprostheses for replacing only the epiphyseal or metaphyseal parts of the femur, e.g. endoprosthetic femoral heads or necks directly fixed to the natural femur by internal fixation devices
- A61F2/3603—Femoral heads ; Femoral endoprostheses for replacing only the epiphyseal or metaphyseal parts of the femur, e.g. endoprosthetic femoral heads or necks directly fixed to the natural femur by internal fixation devices implanted without ablation of the whole natural femoral head
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/38—Joints for elbows or knees
- A61F2/389—Tibial components
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- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/28—Materials for coating prostheses
-
- A—HUMAN NECESSITIES
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- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/3094—Designing or manufacturing processes
-
- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/34—Acetabular cups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/36—Femoral heads ; Femoral endoprostheses
- A61F2/3662—Femoral shafts
-
- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/38—Joints for elbows or knees
-
- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30003—Material related properties of the prosthesis or of a coating on the prosthesis
- A61F2002/30004—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis
- A61F2002/30011—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis differing in porosity
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30003—Material related properties of the prosthesis or of a coating on the prosthesis
- A61F2002/30004—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis
- A61F2002/30014—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis differing in elasticity, stiffness or compressibility
-
- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2002/30906—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth shot- sand- or grit-blasted
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- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2002/30925—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth etched
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- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2002/30929—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth having at least two superposed coatings
-
- A—HUMAN NECESSITIES
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/36—Femoral heads ; Femoral endoprostheses
- A61F2/3609—Femoral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic femoral shafts
- A61F2002/3625—Necks
- A61F2002/3631—Necks with an integral complete or partial peripheral collar or bearing shoulder at its base
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/46—Special tools for implanting artificial joints
- A61F2002/4631—Special tools for implanting artificial joints the prosthesis being specially adapted for being cemented
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0014—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
- A61F2250/0018—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in elasticity, stiffness or compressibility
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0014—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
- A61F2250/0023—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in porosity
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00017—Iron- or Fe-based alloys, e.g. stainless steel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00023—Titanium or titanium-based alloys, e.g. Ti-Ni alloys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00029—Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00389—The prosthesis being coated or covered with a particular material
- A61F2310/00952—Coating, pre-coating or prosthesis-covering structure made of bone cement, e.g. pre-applied PMMA cement mantle
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- Health & Medical Sciences (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Manufacturing & Machinery (AREA)
- Physical Education & Sports Medicine (AREA)
- Prostheses (AREA)
Abstract
Abstract of the Disclosure Improved bone connective prostheses are disclosed. The prostheses comprise a reinforcement element carrying a polymer layer having a varying modulus of elasticity. The exterior sur-face of the polymer layer constitutes the bone attachment surface of the prostheses and has the lowest modulus of elasticity. The interior surface of the polymer layer is attached to reinforce-ment element and has the highest modulus of elasticity. Portions of the polymer layer lying between the exterior and the interior surface of the polymer layer have moduli of elasticity which are intermediate with respect to the moduli of elasticity of the ex-terior and interior surface of the layer, The modulus of elas-ticity of the layer decreases in the direction of interior to exterior. The decrease in modulus of elasticity may be either continuous or incremental. The reinforcement element may have either a simple or a complex structure.
Description
~35~ 35 . .
IMPROVED BONE CONNECTIVE PROSTHESIS COMPRISING A
REINFORCEMENT ELEMENT CARRYING A POLYMER LAYER
HAVING A VARYING MODULUS OF ELASTICITY
Background of the Invention Field of the Invention The present invention relates to prostheses adapted to be fixedly attached to bone by means of bone cement. Specifically, the present invention is directed to prostheses adapted to maximize the durability of the prosthesis-bone cement adherence.
Description of the Prior Art In the field of orthopedic surgery, metal alloys such as ZIMALOY, a chromium-cobalt-molybdenum alloy, stainless steel and titanium alloys, and highly rigid plastics such as ultra-high mole-cular weight polyethylene ~hereinafter U~MWPE) have been ~sed suc-cessfully to replace the ends of long bones and joints including the hip joint. However, there exists a severe limitation with respect to this type of orthopedic surgery, namely, coupling of the pros-theses to bone~ Due to such factors as mechanical stress, fatigue, corrosion~ etc., the prostheses-bone cement joints have been prone to failure. As disclosed in applicant's co-pending patent applica-tion, Serial No.~ 6~, filed ~
entitled "Bone Connective Prostheses Adapted to ~laximize Strength 1~ 5~' and Durability of Prosthese-B~ne Cement Interface; and Methods of Forming Same", improved bone-connective prostheses may be prepared by treating a rigid prosthetic element, adapted to be joined to bone by means of bone cement, to provide an adherent polymethyl-methacrylate film on the surface thereof. Prosthetic elements bearing a polymethylmethacrylate film as disclosed in applicant's co-pending application can more readily be joined to bone cement and provide a stronger and more durable joint.
~ owever, an additional problem with respect to bone con-nective prostheses relates to the differences between the rigidity of the prosthetic element and the bone cement. Thus, prosthetic elements designed to be attached to bone, e.g., ~tem insert pros-theses and bone resurfacing prostheses, are generally composed of a very rigid material such as a metal alloy or UHMWPE. On the other hand, bone cement, which normally comprises a mixture of polymethylmethacrylate and methyl methacrylate monomer and which may additionally include a styrene copolymer of methyl meth-acrylate, is typically a less rigid, porous material. Accordingly, when such a rigid prosthetic element is joined to bone by means of bone cement and the resultant composite subjected to force, e.g., walking in the case of a hip ball joint implant, the inter-face between the rigid implant and the less rigid bone cement is subjected to a high degree of mechanical stress. Moreover, ex-treme non-physiological force distribution (in the bone) can occur as well as extreme stress concentration in the prosthesis-cement complex, resulting in bone atrophy, weakening of the bone, loss of interfacial integrity and subsequent fracture of one or more of ~he components. Additionally, these forces can result in a atigue or brittle fracture of the bone cement since the cement typically includes fiaws such as voids, thus leading to failure of the prosthesis.
r .
1~35005 - Summary of the Invention _ It has now been discovered that prostheses fixation ~r~l.lems may be overcome by the utilization of the improved pros-thes~ of the present invention wherein the surface of the pros-thetic element, which is designed to be attached to bone, consists ~f a polymer layer having substantial thickness and being disposed upon a reinforcement element. The polymer layer is designed so as to have a varying modulus of elasticity such that the exterior surface, which is designed to be attached to bone, is less rigid, i.e., has a lower modulus of elasticity, and the interior surface of the polymer layer which is attached to the reinforcement element is more rigid, i.e., has a greater modulus of elasticity. The por-tions of the layer which lie between the exterior and interior sur-face of the polymer layer have moduli of elasticity which are in-termediate with respect to the moduli of elasticity of the exterior and interior surfaces of the polymer layer. Additionally, the modulus of elasticity varies throughout the layer such that the modulus of elasticity decreases in the direction of interior to exterior. Preferably, the modulus of elasticity of the exterior surface of the polymer layer is designed so that it is approximately equal to the modulus of elasticity of bone cement while the modulus of elasticity of the interior surface of the polymer layer is designed so that it is approximately equal to the modulus of elas-ticity of the reinforcement ele~ent. Thus, a more even force dis-tribution can occur as the force is distributed throughout the polymer layer rather than being concentrated at the interface be-tween a rigid prosthesis and a less rigid bone cement.
According to one aspect of the present invention, the moduius of elasticity is continuously varied throughout the poly-mer layer. This may be accomplished by the provision of a polymer .
so()s layer containing vo.ds wherein the voids are distributed throughout the layer such that the percentage of volume occupied by voids in portions of the layer adjacent its exterior surface is greater than the percentage of volume occupied by voids in portions of the layer adjacent the interior surface, and wherein the void volume percentage continuously increases from the interior of the layer to the exterior of the layer.
According to another aspect of the present invention, the polymer layer having a varying modulus of elasticity may be pro-vided such that the modulus of elasticity varies incrementally.
This may be accomplished by providing a polymer layer which is composed of several discrete layers, and wherein each layer has a different modulus of elasticity. Thus, each layer may contain varying amounts of plasticizer to provide layers having different moduli of elasticity. Aiternatively, the different layers may contain varying amounts of reinforcement fillers such as fibers (wound or dispersed3, or particulàte fillers such as glass beads, etc. The modulus of elasticity of each layer may also be varied by varying the chemical and physical constituency of the different layers.
According to another aspect of the present invention, ~he reinforcement element carrying the polymer layer may be designed so that it has a more complex shape than the exterior of the polymer layer. Thus, in the case of prior art stem in-sertion prostheses, the stem was required to have a frustoconical shape with a regular surface in order that it could be inserted into the interior of the bone cement. By utiliz~tion of the present invention, a reinforcement element may be designed so that it has a complex shape designed to give even distribution of forces and be covered with a polymer layer such that the composite stem insertion prosthesis comprising the reinforcement element and the polymer layer has a simple frustoconical shape with a smooth surface.
In accordance with another aspect of this invention there is provided a prosthesis adapted to be fixedly attached to bone by means of bone cement, said prosthesis comprising a reinforcement element, at least a portion of the surface of said reinforcement element carrying a polymer layer having substantial thickness, the exterior surface of said polymer layer constituting the bone attachment surface of said prosthesis, the interior surface of said polymer layer being secured - to said reinforcement element, said polymer layer having a varying modulus of elasticity such that the modulus of elasticity of portions of said layer adjacent said interior surface is essentially constant and the modulus of elasticity of portions adjacent said exterior surface is essentially constant, said modulus of elasticity of said portions adjacent said interior surface being greater than said modulus of elasticity of said portions adjacent said exterior surface, portions of said layer which are between said portions adjacent said exterior surface and said portions and adjacent said interior surface having a modulus of elasticity which is in~ermediate with respect to the moduli of said portions adjacent said exterior and interior surfaces and wherein the modulus of elasticity of said layer decreases in the direction of interior to exterior.
Brief Description of the Drawings In the drawings which form a part of the orig-inal disclosure of the present invention:
1135()05 Fi~. 1 is a side elevational view in longitudinal section of a hip prosthesis designed in accordance with the present invelltion wherein a reinforcement element is covered by a polymer layer which is constructed such that the rigidity of the layer is grea~er at the interior than at the exterior.
Fig. 2 is an enlarged top plan view in section taken along lines 2-2 in Fig. 1 and illustrates the varying porosity of the polymer layer shown in Fig. 1.
Fig. 3 diagrammatically illustrates a fragmentary cross-section of an encapsulated implant as in Figs. 1 and 2 which has been fixedly attached to bone by means of bone cement, beneath which there is shown a graph of the elastic moduli of the different components of the reinforcement element/
polymer layer/bone-cement/bone composite.
Fig. 4 is a side elevational view in longitudinal section of a polymer encapsulated hip prosthesis wherein the polymer layer is a composite of several discrete polymer layers and wherein the modulus of elasticity of each of the discrete polymer layers is different.
Fig. 5 is an enlarged top plan view in section taken along lines 5-5 in Fig. 4 illustrating the multi-layered poly-mer layer shown in Fig. 4.
- 5a -50t~5 Fig. 6 diagrammatically illustrates a fragmentary cross-section of an encapsulated implant as in Figs. 5 and 6, which has been fixedly attached to bone by means of bone cement, beneath which there is shown a graph of the elastic moduli of the dif-ferent components of the reinforcement element/discrete polymer layers/bone cement/bone composite.
Fig. 7 is a side elevational view in longitudinal sec-tion of a polymer encapsulat~d hip prosthesis prepared in accord-ance with another aspect of the present invention.
Fig. 8 is an exploded perspective view in vertical sec-tion of a human knee joint wherein the tibial component of the knee joint has been replaced by a prosthesis prepared in accordance with the present invention.
Detailed Description of the Invention . .
A~cording to the present invention, prostheses designed to be fixedly attached to bone by means of bone cement are provided whereby the force distribution between the bone, bone cement and prosthesis may be morle evenly and properly distributed than in prior art prostheses. Such prostheses comprise a reinforcement element, which is composed of a rigid material such as a chromium-O
~obalt-molybdenum alloy, e.g., ZIMALOY~ or a titanium or stainless steel alloy or a polymer such as UHMWPE, with at least a portion of the surface of the reinforcement eiement carrying a polymer layer havinq substantial thickness. The exterior surface of the polymer layer constitutes the bone attachment surface of the pros-thesis. The interior surface of the polymer layer is secured to the reinforcement element. The polymer layer is designed so as to have a varying modulus of elasticity such that the modulus of elasticity in portions of the layer adjacent the interior surface t ~ ~ J /~1 6 1~3SOO~
of the layer is essentially constant and the modulus of elasticity of portions of the layer adjacen~ the exterior surface of the layer i~ likewise essentially constant. The modulus of elasticity of the portions of the layer adjacent the interior surface is greater than the modulus of elasticity of the portions of the layer adiacent the exterior surface while the modulus of elasticity of portions of the layer lying between the exterior and the interior portions decreases in the direction of interior to exterior. Preferably, the modulus of elasticity of the exterior surface of the layer is approximately equal to the modulus of elasticity of hardened bone cement. It is also preferred that the modulus of elasticity of the interior portion of the layer be approximately equal to the modulus-of elasticity of the reinforcement element.
The polymer layer having a varying modulus of elasticity may be a single continuous layer or it may be composed of several discrete polymer layers, each having a different modulus of elas-ticity. A prosthesis having a single, continuous polymer layer disposed upon a reinforcing element is shown in Figs. 1, 2 and 3. Fig. 1 is an elevational side view in longitudinal section of a stem insertion hip prosthesis 10 comprising a reinforcement element 11 carrying a high strength polymer layer 12 which has substantial thickness and which is preferably composed of poly-methylmethacrylate. This layer includes voids 14 within the in-terior thereof.
In Fig. 2 there is illustrated a top plan view of a cross-section of the bone implant prosthesis of Fig 1 taken at line 2-2. The implant reinforcement element 10 is a rigid material such as a metal alloy or UHMWPE. The polymer layer 12 is shown to include voids 14a, 14b and 14c. The voids nearer the interior of the polymer layer represented by 14a are shown to be smaller 1~3SOOS
than the voids located at the exterior of the polymer layer repre-sented by void 14c. Void 14b, which lies linearly between voids 14a and 14c, is shown to be of an intermediate size. Accordingly, it will be seen that the rigidity of the polymer layer is continu-ously varied from a high rigidity at the interior of the polymer capsule where the degree of porosity approaches zero, to a low rigidity at the exterior of the polymer capsule where the degree of porosity is much greater. In fact, rigidity of the polymer capsule is con rolled not only by the size of the individual voids but also by the number of individual voids in a given portion of the capsule. Thus~ whea the percentage of volume occupied by voids in a given portion of the capsule is great, that portion of the layer will be relatively flexible, i.e., will have a low modulus of elasticity. On the other hand, when the void volume percentage is low or near zero in a portion of the layer, such portion of the polymer layer will ~e highly rigid, i.e., have a high modulus of elasticity.
In Fig. 3, there is a shown a diagrammatic fragmen-tary cross-section of an implant as in Figs. 1 and 2 which has been fixedly attached to bone by means of bone cement. Also shown in the lower portion of Fig. 3 is a graph of the elastic moduli of the different components of the reinforcement element/polymer layer/bone cement/bone composite. Thus, reinforcement element 10 is shown to have a relatively high elastic modulus represented by the straight line 20. The polymer layer 12 having a contin-uously varying porosity is shown to have a continuously varying modulus of elasticity represented by line 22 in the graph. At the interior of the polymer layer where the porosity closely approaches zero, it can be seen that the modulus of elasticity of the polymer layer is nearly that of the reinforcement element. At the exterior ~135005 of the polymer layer where the voids volume percentage is muchgreater, it can be seen that the elastic modulus is of a much lower value, preferably closely approximating the modulus of elas-ticity of hardened bone cement. Hardened bone cement 16 is shown lying between the polymer layer 12 and bone 18. The modulus of elasticity of the hardened bone cement is shown to have a con-stant value as indicated by line 24. Thus, ideally, the rigidi~y of the polymer layer 12 is varied so that at the interior of the layer, its modulus of elasticity is approximately equal to the modulus of elasticity of the implant reinforcement element while at the exterior of the layer, which constitutes the bone attachment surface of the prosthesis, its modulus of elasticity is approxi-mately equal to the modulus of elasticity of the bone cement which is low due to the nature of bone cement itself and due to the presence o~ voids and flaws in bone cement.
As indicated previously, the polymer layer has substan-tial thickness. By the term "substantial thickness", it is meant that the polymer layer is sufficiently thick that the modulus of elsticity of the layer may be varied either continuously or incre-mentally as hereinbefore and hereinafter described. Polymer layers which can be utilized in the present invention should have a mini-mum thickness of about 0.1 cm., preferably about 0.5 cm., most preferably about 0.5 - 1.0 cm.
Formation of the prostheses illustrated in Figs. 1, 2 and 3 wherein a single polymer layer containing voids is disposed upon a reinforcement element, and wherein the modulus of elasticity of the polymer layer is varied from interior to exterior by varia-tion of the percentage of volume occupied by the voids from interior to exterior may be accomplished by any suitable means. One method which may be utilized is to vary the rate of solidification of ~L~3500S
, th~ r layer linearly from the exterior to the interior or frcm .~ interior to the exterior, while at the same time varying ~he degree of porosity within the non-solid polymer.
Thus, the polymer capsule may be formed from a molten PMMA
thermoplastic and the rate of solidification of the thermoplastic may be controlled ~y controlling the temperature of the thermo-plastic. The molten thermoplastic is confined in a closed mold having the desired shape for the bone implan The reinforcement portion or stem of the implant, comprising a metal alloy will also be enclosed in the mold at the center thereof. A portion of the metal alloy comprising a non-reinforcing portion of the implant is not enclosed in the mold. The metal alloy exhibits a high degree of heat conductivity and may be contacted with a cooling means such as a forced supply of cool air, a liquid nitrogen stream, etc.
tilizing this arrangement, the polymer at the interior of the mold, which is in contact with the cool reinforcement stem will harden first while the polymer at the exterior of the mold will be cooled at a later point and thus will solidify at a later point.
The molten polymer within the mold has an inert gas such as, for instance, nitrogen or carbon dioxide dissolved therein.
The amount of gas dissolved in the polymer is controlled such that at high pressures all of the gas is dissolved in the liquid polymer while at lower pressures the gas will exist as discrete bubbles or voids. The mold is designed so that pressure within the mold may be continuously varied. Accordingly, utilizing such an arrange-ment, the pressure within the mold is continuously varied from a higher value wherein all the gas is dissolved in the polymer to a ~ower value wherein only a small percentage of the gas is dissolved in the polymer. At the same time a cooling means is applied to the 'eat conductive reinforcing stem in the center of the mold.
~ 10 --~135005 Therefore, when the polymer in the interior of the mold hardens, it will contain no voids since at that time the pressure in the mold is such that all of the gas is dissolved in the polymer. However, when the polymer at the exterior of the mold hardens it will con-tain voids since the pressure in the mold is, at that time, at a value such that the gas in the polymer exists in the gaseous phase.
Another method of forming the varying porosity polymer layer of the present invention may be utilized when it is desired to form the polymer layer from a polymerizable material such as a crosslinkable PMMA polymer, a monomer, or a polymer-monomer admixture containinq a heat sensitive polymer catalyst or initiator.
In such a case, a gas is again dissolved in the polymerizable material and a closed mold is likewise utilized. However, the implant reinforcement element should be heated and thus the heated material at the interior of the mold will polymerize first. As with the above example, if the pressure at the interior of the mold is continuously decreased as a function of the rate of poly-merization, the material at the interior of the mold will contain no voids while the material at the exterior of the mold will contain a high degree of voids.
In the foregoing discussionsl reference has been made to dissolving gases in polymers and polymerizable liquids in order to promote void formation. However, in the case of some polymeriz-able liquids, such as a mixture of methyl methacrylate monomer and PMMA, porosity is inherently produced when such mixtures are allowed to polymerize in the absence of pressure. When such a polymerizAble mixture is used, no special gas dissolving step will be required.
5till another method which may be utilized to form the polymer layer having a varying porosity involves the use of a temperature sensitive foaming agent. Thus, a non-heat sensitive ~3500~
polymerizable material containing a heat sensitive blowing a~ent m~y be enclosed in the mold under conditions such that polymeriza-tion is initiated by, e.g., inclusion of an ambient temperature polymerization catalyst. Heat is applied to the exterior portion of the mold so that the polymer thereat containing the heat sensi-tive foaming agent will include voids while the relatively cooler material at the interior of the mold will contain no voids. The heat sensitive foaming agent and the gas produced thereby should be non-physiologically active in order that the polymer layer not interact negatively with bone.
Finally, the process of post expansion may be utilized to form the polymer layer having varying porosity. Thus, a layer of thermoplastic material comprising a dissolved foaming agent such as pentane or nitrogen is molded to the exterior of the reinforcing element and allowed to harden. The exterior of the hardened layer is exposed to a heat means such as an infrared radiation source, thus warming and softening the exterior portion of the thermo-plastic layer. At this point, the dlssolved foaming agent reverts to a gaseous phase producing voids in the polymer layer. Upon completion of sufficie~t foaming, the heat source is removed and the layer allowed to harden.
As previously indicated, the polymer layer having a vary-ing modulus of elasticity may comprise several discrete layers rather than a single continuous layer. In such a case, the most exterior discrete layer of the composite polymer layer will have a low modulus of elasticity and thus be relatively flexibleO Prefer-ably, this discrete layer which comprises the bone attachment surface will have a modulus of elasticity which is approximately equal to that of hardened bone cement. The most interior discrete layer of the composite polymer layer which comprises the layer ~ 12 -~35005 directly secured to the reinforcement element, will have a highmodulus of elasticity and thus be relatively rigid. It is pre-ferred that modulus of elasticity of this most interior discrete layer be approximately equal to the modulus of elasticity of the reinforcement element. The intervening polymer layers have moduli of elasticity intermediate of the moduli of the exterior and in-terior layers such that each layer has a smaller modulus than that of the adjacent, more interior layer.
A prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticity wherein the polymer layer is a composite of discrete polymer layers is illustrated in Figs. 4, 5 and 6. Fig. 4 is an elevational side view in longitudinal section of a stem insertion hip joint prosthesis wherein the reinforcement element carries a composite polymer layer comprising four discrete polymer layers. Thus, in Fig. 4 there is shown a stem insertion prosthesis 30 comprising a rigid reinforcement element 31 carrying a multi-layered composite polymer layer 32. The polymer layer is composed of four layers 32a, 32b, 32c and 32d, each of which has a different modulus of elasticity.
~ ig. 5 is an enlarged top plan view in section taken along lines 5-5 in Fig. 4 and illustrates the different layers of the polymer layer 32 shown in Fig. 4. The reinforcement element 31 comprises a metal alloy or UHMWPE which has a high modulus of elasticity. The most interior polymer layer 32a is constructed to have a high modulus of elasticity, preferably closely approxi-mating that of the reinforcement element. The most exterior polymer layer 32d has the lowest modulus of elasticity, preferably approxi-mating that of hardened bone cement. The two polymer layers 32b and 32c are shown lying between the interior and exterior polymer 1135(0~
layers 32a and 32d, respectively. Polymer layer 32c has a modulus of elasticity which is lesser than that of layer 32b while being greater than that of polymer layer 32d. Polymer layer 32b has a modulus of elastic~ty which is lesser than that of polymer layer 32a while being greater than that of polymer layer 32c.
The modulus of elasticity of the different discrete polymer layers can be varied by varying the amount of plasticizer included in each layer. Thus, for example, polymer layer 32a may be composed of p~lymethylmethacrylate with no plasticizer. Polymer layer 32b may be composed of polymethylmethacrylate including a small amount of plasticizer. Polymer layer 32c may be composed of polymethylmethacrylate having a greater amount of plasticizer than that included in layer 32b. Polymer layer 32d may be composed of polymethylmethacrylate having an even greater amount of plasti-cizer than the amount included in layer 32c.
In a like manner, the modulus of elasticity of each layer can be varied by including varying amounts of reinforcement fillers, either fiberous or particulate, in each layer. Generally, the inclusion of reinforcement fillers, either fiberous or particu-late, in polymer compositions will increase the elastic modulus or stiffness of the composition. The degree of increase, however, is dependent on numerous factors including the polymer composi-tion utilized, the chemical make-up of the filler and the physi-cal characteristics of the filler such as size, shape and density in the case of particulate fillers or, in the case of fiberous fillers, the length, diameter and stiffness of the particular fiber. Further information regarding the inclusion of reinforce-ment fillers in polymers and the effect on stiffness or elastic modulus may be found in "Reinforced Thermoplastics" by W.V.
Titow and B.J. Lanham; Halsted Press, a Division of John Wiley &
SC~05 Sons, Inc. (New York, 1975), especially pages 9-16 and 111-116 and references cited therein.
Fiberous reinforcements, either wound or dispersed, which may be utilized include glass fibers, carbon fibers, boron fibers, etc. Particulate reinforcements which may be utilized include glass or metal microspheres and flakes, talc, Wallastonite, chalk, clays, etc.
Since generally the elastic modulus or stiffness of a polymer increases with increasing amounts of reinforce-ment fillers, the elastic modulus of each discrete layerof the composite polymer layer such as is shown in Fig.
5, may be varied by varying the amount of filler, of the same type, in each layer. However, if desired, the type of filler in each layer may be varied. Similarly, amounts and types of filler in each layer may be varied in combination with, if desired, either a constant or varying amount of plasticizer in each layer.
Moreover, the modulus of elasticity of each layer can be varied by varying the chemical constituents of each layer. Thus, the most interior layer, layer 32a, may be composed of a relatively hard polymer such as polymethyl-methacrylate or a melamine-formaldehyde resin. Layer 32b may be composed of a softer polymer or copolymer such as polymethylmethacrylate having been modified by a softer copolymer such as, for example, polybutylacrylate. Layer 32c will be composed of an even more elastic polymer or copolymer, and finally, layer 32d will be composed of the most elastic polymer or copolymer. Similarly, a very effective method of increasing polymer rigidity is by cross-linking. Thus, the innermost layer can be fully cross-linked with intermediate layers having varying amounts ~1350()5 of cross-linking, and the exterior layer having no cross-linking.
Fig. 6 diagrammatically illustrates a fragmentary cross-section of an implant comprising a reinforcement element carrying a multi-layer polymer layer as in Figs.
4 and 5 which has been fixedly attached to bone by means of bone cement, beneath which there is illustrated a graph of the elastic modulus of the different components of the reinforcement element/multi-layer polymer layer/bone cement/
bone composite. Thus, reinforcement element 31 is shown to have a constant, high modulus of elasticity represented by line 34. The polymer layer is shown to be composed of four layers 32a, 32b, 32c and 32d, each having an incre-mentally lower but substantially constant modulus of elast-icity as shown by lines 36a, 36b, 36c and 36d. Hardened bone cement 16 is shown to have a constant but lower modulus of elasticity represented by line 24. It can be seen that the outermost layer of the polymer layer, layer 32d, has a modulus of elasticity approximately equal to the modulus of elasticity of the bone cement while the innermost layerof the polymer layer 32a, has the highest modulus of elas-ticity which is approximately equal to the modulus of elasticity of the reinforcement element.
Formation of the multi-layered polymer layer on the reinforcement element may be accomplished by any suitable means, such as by dipping or the utilization of by a series of molds after treatment of the reinforcement element to insure proper adhesion of the polymer layer.
Such treatment of the reinforcement element may comprise removal of weak boundary layers as described in applicant's previously referred-to copending application, Serial No.
345,630.
1135~05 Where the reinforcement element has a relatively simple shape, such as the reinforcement element shown in Fig. 4, formation ~ 16a ~3500~
of the multi-layered polymer layer may be accomplished by dipping.
Thus, there may be provided, for example, four containers contain ing a molten polymer, such as polymethylmethacrylate. The molten polymer in the first container has no plasticizer. The molten polymer in the second container includes a small amount of plasti-cizer. The molten polymer in the third container includes a greater amount of plasticizer, while the molten polymer in the fourth and final container contains the greatest amount of plasti-cizer. A reinforcement element is dipped into the molten polymer in the first container and removed. After the polymer has hardened on the reinforcement element, it is again dipped into the first ~ontainer. The is continued until there is a layer having a thick-ness of approximately 0.125 cm. Thereafter, th~ reinforcement element which now has the ~irst discrete polymer layer thereon . . _ .
is dipped into the second container. This is continued as with dipping in the first container until the second layer has a thick-ness of about 0.125 cm.; thus, the composite polymer layer now has a thickness of 0.250 cm. In a like manner, the reinforcement element having the two-layer polymer layer is dipped in the third container until a layer-of approximately 0.125 cm. is formed.
Thus, the polymer composite layer now has a thickness of about 0.375 cm. Finally, the reinforcement element having the polymer layer thereon is dipped in the fourth container until the com-posite polymer layer has a total thickness of 0.50 cm~
The composite polymer layer may be composed of more or less than four discrete polymer layers, and, as shown in Fig. 5, it is not necessary that each discrete polymer layer have the same thickness. In fact, it may be desired in some instances that no layer have the same thickness.
1~3S005 Another method of forming the multi-layered polymer layer disposed upon the reinforcement element comprises the utilization of a series of molds. Thus, there can be provided a series of progressively larger molds. The reinforcement ele-ment is placed in the first mold and a polymer is likewise placed into the first mold to provide a first layer of polymer material having a relatively high modulus of elasticity, preferably closely approximating that of the reinforcement element. The reinforcement element having one polymer layer thereon is thereafter placed into the second mold, which is larger than the first mold and a polymer material having a lower modulus of elasticity when hardened due to, e.g., the inclusion of a greater amount of plasticizer or a smaller amount of filler, is provided in the second mold. The polymer material which may be either a thermoplastic or thermosetting resin is allowed to harden, thus providing a second layer of polymer material. Thereafter, the reinforcing element having two layers of polymer material thereon is treated in a third, larger mold, and the process may be continued using progressively larger molds containing progressively less rigid polymer material, until the desired degree of thickness and flexibility is obtained.
According to another aspect of the present invention, the use of a polymer layer or capsule allows for a complex reinforce-ment element shape in the provision of e.g., a bone insert pros-thesis, while the external surface of the insert, i.e., the bone attachment surface, can have a simple shape. Fig. 7 illustrates such a prosthesis wherein the reinforcement element has a complex, physiologically designed reinforcement structure whereby the force distribution throughout the prosthesis may be more properly con-trolled, while the external polymer layer covering the complexly shaped surface provides a simple, nearly frustoconical external i~3SV05 surface, suitable for insertion into a bone cavity. Thus, Fig.
7 is a side elevational view in longitudinal section of a polymer encapsulated hip prosthesis 40. Reinforcement element 41, which is composed of a highly rigid material such as a metal alloy or UHMWPE, is shown to have a main finger-like portion 41a and a smaller finger-like appendage 41b. The provision of the multiple appendages 41a and 41b can accomplish a more even force distribution. However, due to the irregular shape of the reinforcement element, it cannot be suitably inserted into a bone cavity containins bone cement.
By encapsulating the irregular reinforcement element 41 with polymer layer 42, the insert may be provided with a regular shape as shown in Fig. 7. Thus, irregularly shaped reinforcement elements, i.e~, having multiple concave and convex portions, may be designed and may thereafter be encapsulated or covered by a polymer layer so that the entire composite has a simple, regular shape. By the term "re~ular", it is meant a generally smooth, three-dimen-sional surface havi~g no significant concave or convex portions other than the overall, e.g., frustoconical, shape.
It will be noted that the polymer layer 42 shown in Fig.
7 is composed of four layers 42a, 42b, 42c and 42d. Thus, the poly-mer layer is designed so as to have a varying modulus of elasticity as hereinbefore described. If desired, the polymer layer may be a single, continuous layer wherein the modulus of elasticity is varied by means of, e.g., a varying void volume as hereinbefore discussed.
Formation of prosthetic elements wherein the reinforcement element has an irregular, complex shape which complex shape is covered by a polymer layer, the external surface of which has a regular, simple shape, may be accomplished by any suitable meansr particularly the means hereinbefore described. It should be noted 1135~05 that where a multi~layered, composite polymer layer is desir~d, the use of the dipping technique herein described will normally not be suitable.
Fig. 8 is an exploded perspective view in vertical sec-tion of a human knee joint wherein the tibial component of the knee joint has been replaced by a prosthesis prepared in accordance with the present invention. Thus, a vertical section of the femur component of the knee joint is shown at 51. Tibia 52 has been treated so as to remove the damaged knee joint component. The prosthetic element 50 which is to be joined to the damaged tibia, is composed of rigid reinforcement element 53 and a composite polymer layer composed of four discrete layers 54, 55, 56 and 57.
Reinforcement el~ment 53 is composed of a rigid material such as a metal alloy or U~MWPE. The reinforcement element is shown as having a complex shape including two depressions for receiving the condyles of the femur and two corresponding convex protrusions or bulges on the opposite side of the reinforcement element. While such a complex shape provides for an even force distribution across the prosthesis, great difficulties would be encountered in joining such a complex shape to bone. Thus~ a composite polymer layer com-prising discrete polymer layers 54, 55, 56 and 57, and together which form a regular convex surface, are provided as the bone attachment surface. As previously described, the polymer layers are designed ~o that the composite polymer layer has a varying modulus of elasticity. Thus, polymer layer 54 has the greatest modulus of elasticity while polymer layer 57 has the least modulus of elasticity. Polymer layer 55 has a modulus of elasticity greater than that of polymer layer 56 but less than that of polymer layer 54. Pclymer layer 56 has a modulus of elasticity greater than that of polymer layer 57 but less than that o~ polymer layer 54.
.. ~
s~s If desired, a continuous polymer layer having a varying modulus of elasticity may be substituted for the composite polymer layer shown in Fig. 8.
Other resurfacing implants may be designed in accordance with the present invention. Thus, for instance, an acetabalum or hip joint socket implant may be designed in accordance with the teachings hereinbefore set forth. A hemispherical or cup-shaped prosthetic element having a concave surface designed to receive a f~mur head is provided. The element îs composed of a rigid alloy such as ZIMALOY or plastic such as U~MWPE. The convex surface of the implant, designed to be attached to bone, includes a polymer layer having a varying modulus of elasticity as previously des cribed. The convex surface of the rigid reinforcement element may be a simple, regular hemisphere or it may have a complex shape, including protrusions and concave surfaces designed in accordance with engineering principles so as to provide an even force distri-bution throughout the implant~ Such convex surface, either regular or complex, of the reinforcement element will be covered with a polymer layer having a varying modulus of elasticity, which layer constitutes the bone attachment surface. The polymer layer may be a continuous layer or a composite layer as hereinbefore shown.
IMPROVED BONE CONNECTIVE PROSTHESIS COMPRISING A
REINFORCEMENT ELEMENT CARRYING A POLYMER LAYER
HAVING A VARYING MODULUS OF ELASTICITY
Background of the Invention Field of the Invention The present invention relates to prostheses adapted to be fixedly attached to bone by means of bone cement. Specifically, the present invention is directed to prostheses adapted to maximize the durability of the prosthesis-bone cement adherence.
Description of the Prior Art In the field of orthopedic surgery, metal alloys such as ZIMALOY, a chromium-cobalt-molybdenum alloy, stainless steel and titanium alloys, and highly rigid plastics such as ultra-high mole-cular weight polyethylene ~hereinafter U~MWPE) have been ~sed suc-cessfully to replace the ends of long bones and joints including the hip joint. However, there exists a severe limitation with respect to this type of orthopedic surgery, namely, coupling of the pros-theses to bone~ Due to such factors as mechanical stress, fatigue, corrosion~ etc., the prostheses-bone cement joints have been prone to failure. As disclosed in applicant's co-pending patent applica-tion, Serial No.~ 6~, filed ~
entitled "Bone Connective Prostheses Adapted to ~laximize Strength 1~ 5~' and Durability of Prosthese-B~ne Cement Interface; and Methods of Forming Same", improved bone-connective prostheses may be prepared by treating a rigid prosthetic element, adapted to be joined to bone by means of bone cement, to provide an adherent polymethyl-methacrylate film on the surface thereof. Prosthetic elements bearing a polymethylmethacrylate film as disclosed in applicant's co-pending application can more readily be joined to bone cement and provide a stronger and more durable joint.
~ owever, an additional problem with respect to bone con-nective prostheses relates to the differences between the rigidity of the prosthetic element and the bone cement. Thus, prosthetic elements designed to be attached to bone, e.g., ~tem insert pros-theses and bone resurfacing prostheses, are generally composed of a very rigid material such as a metal alloy or UHMWPE. On the other hand, bone cement, which normally comprises a mixture of polymethylmethacrylate and methyl methacrylate monomer and which may additionally include a styrene copolymer of methyl meth-acrylate, is typically a less rigid, porous material. Accordingly, when such a rigid prosthetic element is joined to bone by means of bone cement and the resultant composite subjected to force, e.g., walking in the case of a hip ball joint implant, the inter-face between the rigid implant and the less rigid bone cement is subjected to a high degree of mechanical stress. Moreover, ex-treme non-physiological force distribution (in the bone) can occur as well as extreme stress concentration in the prosthesis-cement complex, resulting in bone atrophy, weakening of the bone, loss of interfacial integrity and subsequent fracture of one or more of ~he components. Additionally, these forces can result in a atigue or brittle fracture of the bone cement since the cement typically includes fiaws such as voids, thus leading to failure of the prosthesis.
r .
1~35005 - Summary of the Invention _ It has now been discovered that prostheses fixation ~r~l.lems may be overcome by the utilization of the improved pros-thes~ of the present invention wherein the surface of the pros-thetic element, which is designed to be attached to bone, consists ~f a polymer layer having substantial thickness and being disposed upon a reinforcement element. The polymer layer is designed so as to have a varying modulus of elasticity such that the exterior surface, which is designed to be attached to bone, is less rigid, i.e., has a lower modulus of elasticity, and the interior surface of the polymer layer which is attached to the reinforcement element is more rigid, i.e., has a greater modulus of elasticity. The por-tions of the layer which lie between the exterior and interior sur-face of the polymer layer have moduli of elasticity which are in-termediate with respect to the moduli of elasticity of the exterior and interior surfaces of the polymer layer. Additionally, the modulus of elasticity varies throughout the layer such that the modulus of elasticity decreases in the direction of interior to exterior. Preferably, the modulus of elasticity of the exterior surface of the polymer layer is designed so that it is approximately equal to the modulus of elasticity of bone cement while the modulus of elasticity of the interior surface of the polymer layer is designed so that it is approximately equal to the modulus of elas-ticity of the reinforcement ele~ent. Thus, a more even force dis-tribution can occur as the force is distributed throughout the polymer layer rather than being concentrated at the interface be-tween a rigid prosthesis and a less rigid bone cement.
According to one aspect of the present invention, the moduius of elasticity is continuously varied throughout the poly-mer layer. This may be accomplished by the provision of a polymer .
so()s layer containing vo.ds wherein the voids are distributed throughout the layer such that the percentage of volume occupied by voids in portions of the layer adjacent its exterior surface is greater than the percentage of volume occupied by voids in portions of the layer adjacent the interior surface, and wherein the void volume percentage continuously increases from the interior of the layer to the exterior of the layer.
According to another aspect of the present invention, the polymer layer having a varying modulus of elasticity may be pro-vided such that the modulus of elasticity varies incrementally.
This may be accomplished by providing a polymer layer which is composed of several discrete layers, and wherein each layer has a different modulus of elasticity. Thus, each layer may contain varying amounts of plasticizer to provide layers having different moduli of elasticity. Aiternatively, the different layers may contain varying amounts of reinforcement fillers such as fibers (wound or dispersed3, or particulàte fillers such as glass beads, etc. The modulus of elasticity of each layer may also be varied by varying the chemical and physical constituency of the different layers.
According to another aspect of the present invention, ~he reinforcement element carrying the polymer layer may be designed so that it has a more complex shape than the exterior of the polymer layer. Thus, in the case of prior art stem in-sertion prostheses, the stem was required to have a frustoconical shape with a regular surface in order that it could be inserted into the interior of the bone cement. By utiliz~tion of the present invention, a reinforcement element may be designed so that it has a complex shape designed to give even distribution of forces and be covered with a polymer layer such that the composite stem insertion prosthesis comprising the reinforcement element and the polymer layer has a simple frustoconical shape with a smooth surface.
In accordance with another aspect of this invention there is provided a prosthesis adapted to be fixedly attached to bone by means of bone cement, said prosthesis comprising a reinforcement element, at least a portion of the surface of said reinforcement element carrying a polymer layer having substantial thickness, the exterior surface of said polymer layer constituting the bone attachment surface of said prosthesis, the interior surface of said polymer layer being secured - to said reinforcement element, said polymer layer having a varying modulus of elasticity such that the modulus of elasticity of portions of said layer adjacent said interior surface is essentially constant and the modulus of elasticity of portions adjacent said exterior surface is essentially constant, said modulus of elasticity of said portions adjacent said interior surface being greater than said modulus of elasticity of said portions adjacent said exterior surface, portions of said layer which are between said portions adjacent said exterior surface and said portions and adjacent said interior surface having a modulus of elasticity which is in~ermediate with respect to the moduli of said portions adjacent said exterior and interior surfaces and wherein the modulus of elasticity of said layer decreases in the direction of interior to exterior.
Brief Description of the Drawings In the drawings which form a part of the orig-inal disclosure of the present invention:
1135()05 Fi~. 1 is a side elevational view in longitudinal section of a hip prosthesis designed in accordance with the present invelltion wherein a reinforcement element is covered by a polymer layer which is constructed such that the rigidity of the layer is grea~er at the interior than at the exterior.
Fig. 2 is an enlarged top plan view in section taken along lines 2-2 in Fig. 1 and illustrates the varying porosity of the polymer layer shown in Fig. 1.
Fig. 3 diagrammatically illustrates a fragmentary cross-section of an encapsulated implant as in Figs. 1 and 2 which has been fixedly attached to bone by means of bone cement, beneath which there is shown a graph of the elastic moduli of the different components of the reinforcement element/
polymer layer/bone-cement/bone composite.
Fig. 4 is a side elevational view in longitudinal section of a polymer encapsulated hip prosthesis wherein the polymer layer is a composite of several discrete polymer layers and wherein the modulus of elasticity of each of the discrete polymer layers is different.
Fig. 5 is an enlarged top plan view in section taken along lines 5-5 in Fig. 4 illustrating the multi-layered poly-mer layer shown in Fig. 4.
- 5a -50t~5 Fig. 6 diagrammatically illustrates a fragmentary cross-section of an encapsulated implant as in Figs. 5 and 6, which has been fixedly attached to bone by means of bone cement, beneath which there is shown a graph of the elastic moduli of the dif-ferent components of the reinforcement element/discrete polymer layers/bone cement/bone composite.
Fig. 7 is a side elevational view in longitudinal sec-tion of a polymer encapsulat~d hip prosthesis prepared in accord-ance with another aspect of the present invention.
Fig. 8 is an exploded perspective view in vertical sec-tion of a human knee joint wherein the tibial component of the knee joint has been replaced by a prosthesis prepared in accordance with the present invention.
Detailed Description of the Invention . .
A~cording to the present invention, prostheses designed to be fixedly attached to bone by means of bone cement are provided whereby the force distribution between the bone, bone cement and prosthesis may be morle evenly and properly distributed than in prior art prostheses. Such prostheses comprise a reinforcement element, which is composed of a rigid material such as a chromium-O
~obalt-molybdenum alloy, e.g., ZIMALOY~ or a titanium or stainless steel alloy or a polymer such as UHMWPE, with at least a portion of the surface of the reinforcement eiement carrying a polymer layer havinq substantial thickness. The exterior surface of the polymer layer constitutes the bone attachment surface of the pros-thesis. The interior surface of the polymer layer is secured to the reinforcement element. The polymer layer is designed so as to have a varying modulus of elasticity such that the modulus of elasticity in portions of the layer adjacent the interior surface t ~ ~ J /~1 6 1~3SOO~
of the layer is essentially constant and the modulus of elasticity of portions of the layer adjacen~ the exterior surface of the layer i~ likewise essentially constant. The modulus of elasticity of the portions of the layer adjacent the interior surface is greater than the modulus of elasticity of the portions of the layer adiacent the exterior surface while the modulus of elasticity of portions of the layer lying between the exterior and the interior portions decreases in the direction of interior to exterior. Preferably, the modulus of elasticity of the exterior surface of the layer is approximately equal to the modulus of elasticity of hardened bone cement. It is also preferred that the modulus of elasticity of the interior portion of the layer be approximately equal to the modulus-of elasticity of the reinforcement element.
The polymer layer having a varying modulus of elasticity may be a single continuous layer or it may be composed of several discrete polymer layers, each having a different modulus of elas-ticity. A prosthesis having a single, continuous polymer layer disposed upon a reinforcing element is shown in Figs. 1, 2 and 3. Fig. 1 is an elevational side view in longitudinal section of a stem insertion hip prosthesis 10 comprising a reinforcement element 11 carrying a high strength polymer layer 12 which has substantial thickness and which is preferably composed of poly-methylmethacrylate. This layer includes voids 14 within the in-terior thereof.
In Fig. 2 there is illustrated a top plan view of a cross-section of the bone implant prosthesis of Fig 1 taken at line 2-2. The implant reinforcement element 10 is a rigid material such as a metal alloy or UHMWPE. The polymer layer 12 is shown to include voids 14a, 14b and 14c. The voids nearer the interior of the polymer layer represented by 14a are shown to be smaller 1~3SOOS
than the voids located at the exterior of the polymer layer repre-sented by void 14c. Void 14b, which lies linearly between voids 14a and 14c, is shown to be of an intermediate size. Accordingly, it will be seen that the rigidity of the polymer layer is continu-ously varied from a high rigidity at the interior of the polymer capsule where the degree of porosity approaches zero, to a low rigidity at the exterior of the polymer capsule where the degree of porosity is much greater. In fact, rigidity of the polymer capsule is con rolled not only by the size of the individual voids but also by the number of individual voids in a given portion of the capsule. Thus~ whea the percentage of volume occupied by voids in a given portion of the capsule is great, that portion of the layer will be relatively flexible, i.e., will have a low modulus of elasticity. On the other hand, when the void volume percentage is low or near zero in a portion of the layer, such portion of the polymer layer will ~e highly rigid, i.e., have a high modulus of elasticity.
In Fig. 3, there is a shown a diagrammatic fragmen-tary cross-section of an implant as in Figs. 1 and 2 which has been fixedly attached to bone by means of bone cement. Also shown in the lower portion of Fig. 3 is a graph of the elastic moduli of the different components of the reinforcement element/polymer layer/bone cement/bone composite. Thus, reinforcement element 10 is shown to have a relatively high elastic modulus represented by the straight line 20. The polymer layer 12 having a contin-uously varying porosity is shown to have a continuously varying modulus of elasticity represented by line 22 in the graph. At the interior of the polymer layer where the porosity closely approaches zero, it can be seen that the modulus of elasticity of the polymer layer is nearly that of the reinforcement element. At the exterior ~135005 of the polymer layer where the voids volume percentage is muchgreater, it can be seen that the elastic modulus is of a much lower value, preferably closely approximating the modulus of elas-ticity of hardened bone cement. Hardened bone cement 16 is shown lying between the polymer layer 12 and bone 18. The modulus of elasticity of the hardened bone cement is shown to have a con-stant value as indicated by line 24. Thus, ideally, the rigidi~y of the polymer layer 12 is varied so that at the interior of the layer, its modulus of elasticity is approximately equal to the modulus of elasticity of the implant reinforcement element while at the exterior of the layer, which constitutes the bone attachment surface of the prosthesis, its modulus of elasticity is approxi-mately equal to the modulus of elasticity of the bone cement which is low due to the nature of bone cement itself and due to the presence o~ voids and flaws in bone cement.
As indicated previously, the polymer layer has substan-tial thickness. By the term "substantial thickness", it is meant that the polymer layer is sufficiently thick that the modulus of elsticity of the layer may be varied either continuously or incre-mentally as hereinbefore and hereinafter described. Polymer layers which can be utilized in the present invention should have a mini-mum thickness of about 0.1 cm., preferably about 0.5 cm., most preferably about 0.5 - 1.0 cm.
Formation of the prostheses illustrated in Figs. 1, 2 and 3 wherein a single polymer layer containing voids is disposed upon a reinforcement element, and wherein the modulus of elasticity of the polymer layer is varied from interior to exterior by varia-tion of the percentage of volume occupied by the voids from interior to exterior may be accomplished by any suitable means. One method which may be utilized is to vary the rate of solidification of ~L~3500S
, th~ r layer linearly from the exterior to the interior or frcm .~ interior to the exterior, while at the same time varying ~he degree of porosity within the non-solid polymer.
Thus, the polymer capsule may be formed from a molten PMMA
thermoplastic and the rate of solidification of the thermoplastic may be controlled ~y controlling the temperature of the thermo-plastic. The molten thermoplastic is confined in a closed mold having the desired shape for the bone implan The reinforcement portion or stem of the implant, comprising a metal alloy will also be enclosed in the mold at the center thereof. A portion of the metal alloy comprising a non-reinforcing portion of the implant is not enclosed in the mold. The metal alloy exhibits a high degree of heat conductivity and may be contacted with a cooling means such as a forced supply of cool air, a liquid nitrogen stream, etc.
tilizing this arrangement, the polymer at the interior of the mold, which is in contact with the cool reinforcement stem will harden first while the polymer at the exterior of the mold will be cooled at a later point and thus will solidify at a later point.
The molten polymer within the mold has an inert gas such as, for instance, nitrogen or carbon dioxide dissolved therein.
The amount of gas dissolved in the polymer is controlled such that at high pressures all of the gas is dissolved in the liquid polymer while at lower pressures the gas will exist as discrete bubbles or voids. The mold is designed so that pressure within the mold may be continuously varied. Accordingly, utilizing such an arrange-ment, the pressure within the mold is continuously varied from a higher value wherein all the gas is dissolved in the polymer to a ~ower value wherein only a small percentage of the gas is dissolved in the polymer. At the same time a cooling means is applied to the 'eat conductive reinforcing stem in the center of the mold.
~ 10 --~135005 Therefore, when the polymer in the interior of the mold hardens, it will contain no voids since at that time the pressure in the mold is such that all of the gas is dissolved in the polymer. However, when the polymer at the exterior of the mold hardens it will con-tain voids since the pressure in the mold is, at that time, at a value such that the gas in the polymer exists in the gaseous phase.
Another method of forming the varying porosity polymer layer of the present invention may be utilized when it is desired to form the polymer layer from a polymerizable material such as a crosslinkable PMMA polymer, a monomer, or a polymer-monomer admixture containinq a heat sensitive polymer catalyst or initiator.
In such a case, a gas is again dissolved in the polymerizable material and a closed mold is likewise utilized. However, the implant reinforcement element should be heated and thus the heated material at the interior of the mold will polymerize first. As with the above example, if the pressure at the interior of the mold is continuously decreased as a function of the rate of poly-merization, the material at the interior of the mold will contain no voids while the material at the exterior of the mold will contain a high degree of voids.
In the foregoing discussionsl reference has been made to dissolving gases in polymers and polymerizable liquids in order to promote void formation. However, in the case of some polymeriz-able liquids, such as a mixture of methyl methacrylate monomer and PMMA, porosity is inherently produced when such mixtures are allowed to polymerize in the absence of pressure. When such a polymerizAble mixture is used, no special gas dissolving step will be required.
5till another method which may be utilized to form the polymer layer having a varying porosity involves the use of a temperature sensitive foaming agent. Thus, a non-heat sensitive ~3500~
polymerizable material containing a heat sensitive blowing a~ent m~y be enclosed in the mold under conditions such that polymeriza-tion is initiated by, e.g., inclusion of an ambient temperature polymerization catalyst. Heat is applied to the exterior portion of the mold so that the polymer thereat containing the heat sensi-tive foaming agent will include voids while the relatively cooler material at the interior of the mold will contain no voids. The heat sensitive foaming agent and the gas produced thereby should be non-physiologically active in order that the polymer layer not interact negatively with bone.
Finally, the process of post expansion may be utilized to form the polymer layer having varying porosity. Thus, a layer of thermoplastic material comprising a dissolved foaming agent such as pentane or nitrogen is molded to the exterior of the reinforcing element and allowed to harden. The exterior of the hardened layer is exposed to a heat means such as an infrared radiation source, thus warming and softening the exterior portion of the thermo-plastic layer. At this point, the dlssolved foaming agent reverts to a gaseous phase producing voids in the polymer layer. Upon completion of sufficie~t foaming, the heat source is removed and the layer allowed to harden.
As previously indicated, the polymer layer having a vary-ing modulus of elasticity may comprise several discrete layers rather than a single continuous layer. In such a case, the most exterior discrete layer of the composite polymer layer will have a low modulus of elasticity and thus be relatively flexibleO Prefer-ably, this discrete layer which comprises the bone attachment surface will have a modulus of elasticity which is approximately equal to that of hardened bone cement. The most interior discrete layer of the composite polymer layer which comprises the layer ~ 12 -~35005 directly secured to the reinforcement element, will have a highmodulus of elasticity and thus be relatively rigid. It is pre-ferred that modulus of elasticity of this most interior discrete layer be approximately equal to the modulus of elasticity of the reinforcement element. The intervening polymer layers have moduli of elasticity intermediate of the moduli of the exterior and in-terior layers such that each layer has a smaller modulus than that of the adjacent, more interior layer.
A prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticity wherein the polymer layer is a composite of discrete polymer layers is illustrated in Figs. 4, 5 and 6. Fig. 4 is an elevational side view in longitudinal section of a stem insertion hip joint prosthesis wherein the reinforcement element carries a composite polymer layer comprising four discrete polymer layers. Thus, in Fig. 4 there is shown a stem insertion prosthesis 30 comprising a rigid reinforcement element 31 carrying a multi-layered composite polymer layer 32. The polymer layer is composed of four layers 32a, 32b, 32c and 32d, each of which has a different modulus of elasticity.
~ ig. 5 is an enlarged top plan view in section taken along lines 5-5 in Fig. 4 and illustrates the different layers of the polymer layer 32 shown in Fig. 4. The reinforcement element 31 comprises a metal alloy or UHMWPE which has a high modulus of elasticity. The most interior polymer layer 32a is constructed to have a high modulus of elasticity, preferably closely approxi-mating that of the reinforcement element. The most exterior polymer layer 32d has the lowest modulus of elasticity, preferably approxi-mating that of hardened bone cement. The two polymer layers 32b and 32c are shown lying between the interior and exterior polymer 1135(0~
layers 32a and 32d, respectively. Polymer layer 32c has a modulus of elasticity which is lesser than that of layer 32b while being greater than that of polymer layer 32d. Polymer layer 32b has a modulus of elastic~ty which is lesser than that of polymer layer 32a while being greater than that of polymer layer 32c.
The modulus of elasticity of the different discrete polymer layers can be varied by varying the amount of plasticizer included in each layer. Thus, for example, polymer layer 32a may be composed of p~lymethylmethacrylate with no plasticizer. Polymer layer 32b may be composed of polymethylmethacrylate including a small amount of plasticizer. Polymer layer 32c may be composed of polymethylmethacrylate having a greater amount of plasticizer than that included in layer 32b. Polymer layer 32d may be composed of polymethylmethacrylate having an even greater amount of plasti-cizer than the amount included in layer 32c.
In a like manner, the modulus of elasticity of each layer can be varied by including varying amounts of reinforcement fillers, either fiberous or particulate, in each layer. Generally, the inclusion of reinforcement fillers, either fiberous or particu-late, in polymer compositions will increase the elastic modulus or stiffness of the composition. The degree of increase, however, is dependent on numerous factors including the polymer composi-tion utilized, the chemical make-up of the filler and the physi-cal characteristics of the filler such as size, shape and density in the case of particulate fillers or, in the case of fiberous fillers, the length, diameter and stiffness of the particular fiber. Further information regarding the inclusion of reinforce-ment fillers in polymers and the effect on stiffness or elastic modulus may be found in "Reinforced Thermoplastics" by W.V.
Titow and B.J. Lanham; Halsted Press, a Division of John Wiley &
SC~05 Sons, Inc. (New York, 1975), especially pages 9-16 and 111-116 and references cited therein.
Fiberous reinforcements, either wound or dispersed, which may be utilized include glass fibers, carbon fibers, boron fibers, etc. Particulate reinforcements which may be utilized include glass or metal microspheres and flakes, talc, Wallastonite, chalk, clays, etc.
Since generally the elastic modulus or stiffness of a polymer increases with increasing amounts of reinforce-ment fillers, the elastic modulus of each discrete layerof the composite polymer layer such as is shown in Fig.
5, may be varied by varying the amount of filler, of the same type, in each layer. However, if desired, the type of filler in each layer may be varied. Similarly, amounts and types of filler in each layer may be varied in combination with, if desired, either a constant or varying amount of plasticizer in each layer.
Moreover, the modulus of elasticity of each layer can be varied by varying the chemical constituents of each layer. Thus, the most interior layer, layer 32a, may be composed of a relatively hard polymer such as polymethyl-methacrylate or a melamine-formaldehyde resin. Layer 32b may be composed of a softer polymer or copolymer such as polymethylmethacrylate having been modified by a softer copolymer such as, for example, polybutylacrylate. Layer 32c will be composed of an even more elastic polymer or copolymer, and finally, layer 32d will be composed of the most elastic polymer or copolymer. Similarly, a very effective method of increasing polymer rigidity is by cross-linking. Thus, the innermost layer can be fully cross-linked with intermediate layers having varying amounts ~1350()5 of cross-linking, and the exterior layer having no cross-linking.
Fig. 6 diagrammatically illustrates a fragmentary cross-section of an implant comprising a reinforcement element carrying a multi-layer polymer layer as in Figs.
4 and 5 which has been fixedly attached to bone by means of bone cement, beneath which there is illustrated a graph of the elastic modulus of the different components of the reinforcement element/multi-layer polymer layer/bone cement/
bone composite. Thus, reinforcement element 31 is shown to have a constant, high modulus of elasticity represented by line 34. The polymer layer is shown to be composed of four layers 32a, 32b, 32c and 32d, each having an incre-mentally lower but substantially constant modulus of elast-icity as shown by lines 36a, 36b, 36c and 36d. Hardened bone cement 16 is shown to have a constant but lower modulus of elasticity represented by line 24. It can be seen that the outermost layer of the polymer layer, layer 32d, has a modulus of elasticity approximately equal to the modulus of elasticity of the bone cement while the innermost layerof the polymer layer 32a, has the highest modulus of elas-ticity which is approximately equal to the modulus of elasticity of the reinforcement element.
Formation of the multi-layered polymer layer on the reinforcement element may be accomplished by any suitable means, such as by dipping or the utilization of by a series of molds after treatment of the reinforcement element to insure proper adhesion of the polymer layer.
Such treatment of the reinforcement element may comprise removal of weak boundary layers as described in applicant's previously referred-to copending application, Serial No.
345,630.
1135~05 Where the reinforcement element has a relatively simple shape, such as the reinforcement element shown in Fig. 4, formation ~ 16a ~3500~
of the multi-layered polymer layer may be accomplished by dipping.
Thus, there may be provided, for example, four containers contain ing a molten polymer, such as polymethylmethacrylate. The molten polymer in the first container has no plasticizer. The molten polymer in the second container includes a small amount of plasti-cizer. The molten polymer in the third container includes a greater amount of plasticizer, while the molten polymer in the fourth and final container contains the greatest amount of plasti-cizer. A reinforcement element is dipped into the molten polymer in the first container and removed. After the polymer has hardened on the reinforcement element, it is again dipped into the first ~ontainer. The is continued until there is a layer having a thick-ness of approximately 0.125 cm. Thereafter, th~ reinforcement element which now has the ~irst discrete polymer layer thereon . . _ .
is dipped into the second container. This is continued as with dipping in the first container until the second layer has a thick-ness of about 0.125 cm.; thus, the composite polymer layer now has a thickness of 0.250 cm. In a like manner, the reinforcement element having the two-layer polymer layer is dipped in the third container until a layer-of approximately 0.125 cm. is formed.
Thus, the polymer composite layer now has a thickness of about 0.375 cm. Finally, the reinforcement element having the polymer layer thereon is dipped in the fourth container until the com-posite polymer layer has a total thickness of 0.50 cm~
The composite polymer layer may be composed of more or less than four discrete polymer layers, and, as shown in Fig. 5, it is not necessary that each discrete polymer layer have the same thickness. In fact, it may be desired in some instances that no layer have the same thickness.
1~3S005 Another method of forming the multi-layered polymer layer disposed upon the reinforcement element comprises the utilization of a series of molds. Thus, there can be provided a series of progressively larger molds. The reinforcement ele-ment is placed in the first mold and a polymer is likewise placed into the first mold to provide a first layer of polymer material having a relatively high modulus of elasticity, preferably closely approximating that of the reinforcement element. The reinforcement element having one polymer layer thereon is thereafter placed into the second mold, which is larger than the first mold and a polymer material having a lower modulus of elasticity when hardened due to, e.g., the inclusion of a greater amount of plasticizer or a smaller amount of filler, is provided in the second mold. The polymer material which may be either a thermoplastic or thermosetting resin is allowed to harden, thus providing a second layer of polymer material. Thereafter, the reinforcing element having two layers of polymer material thereon is treated in a third, larger mold, and the process may be continued using progressively larger molds containing progressively less rigid polymer material, until the desired degree of thickness and flexibility is obtained.
According to another aspect of the present invention, the use of a polymer layer or capsule allows for a complex reinforce-ment element shape in the provision of e.g., a bone insert pros-thesis, while the external surface of the insert, i.e., the bone attachment surface, can have a simple shape. Fig. 7 illustrates such a prosthesis wherein the reinforcement element has a complex, physiologically designed reinforcement structure whereby the force distribution throughout the prosthesis may be more properly con-trolled, while the external polymer layer covering the complexly shaped surface provides a simple, nearly frustoconical external i~3SV05 surface, suitable for insertion into a bone cavity. Thus, Fig.
7 is a side elevational view in longitudinal section of a polymer encapsulated hip prosthesis 40. Reinforcement element 41, which is composed of a highly rigid material such as a metal alloy or UHMWPE, is shown to have a main finger-like portion 41a and a smaller finger-like appendage 41b. The provision of the multiple appendages 41a and 41b can accomplish a more even force distribution. However, due to the irregular shape of the reinforcement element, it cannot be suitably inserted into a bone cavity containins bone cement.
By encapsulating the irregular reinforcement element 41 with polymer layer 42, the insert may be provided with a regular shape as shown in Fig. 7. Thus, irregularly shaped reinforcement elements, i.e~, having multiple concave and convex portions, may be designed and may thereafter be encapsulated or covered by a polymer layer so that the entire composite has a simple, regular shape. By the term "re~ular", it is meant a generally smooth, three-dimen-sional surface havi~g no significant concave or convex portions other than the overall, e.g., frustoconical, shape.
It will be noted that the polymer layer 42 shown in Fig.
7 is composed of four layers 42a, 42b, 42c and 42d. Thus, the poly-mer layer is designed so as to have a varying modulus of elasticity as hereinbefore described. If desired, the polymer layer may be a single, continuous layer wherein the modulus of elasticity is varied by means of, e.g., a varying void volume as hereinbefore discussed.
Formation of prosthetic elements wherein the reinforcement element has an irregular, complex shape which complex shape is covered by a polymer layer, the external surface of which has a regular, simple shape, may be accomplished by any suitable meansr particularly the means hereinbefore described. It should be noted 1135~05 that where a multi~layered, composite polymer layer is desir~d, the use of the dipping technique herein described will normally not be suitable.
Fig. 8 is an exploded perspective view in vertical sec-tion of a human knee joint wherein the tibial component of the knee joint has been replaced by a prosthesis prepared in accordance with the present invention. Thus, a vertical section of the femur component of the knee joint is shown at 51. Tibia 52 has been treated so as to remove the damaged knee joint component. The prosthetic element 50 which is to be joined to the damaged tibia, is composed of rigid reinforcement element 53 and a composite polymer layer composed of four discrete layers 54, 55, 56 and 57.
Reinforcement el~ment 53 is composed of a rigid material such as a metal alloy or U~MWPE. The reinforcement element is shown as having a complex shape including two depressions for receiving the condyles of the femur and two corresponding convex protrusions or bulges on the opposite side of the reinforcement element. While such a complex shape provides for an even force distribution across the prosthesis, great difficulties would be encountered in joining such a complex shape to bone. Thus~ a composite polymer layer com-prising discrete polymer layers 54, 55, 56 and 57, and together which form a regular convex surface, are provided as the bone attachment surface. As previously described, the polymer layers are designed ~o that the composite polymer layer has a varying modulus of elasticity. Thus, polymer layer 54 has the greatest modulus of elasticity while polymer layer 57 has the least modulus of elasticity. Polymer layer 55 has a modulus of elasticity greater than that of polymer layer 56 but less than that of polymer layer 54. Pclymer layer 56 has a modulus of elasticity greater than that of polymer layer 57 but less than that o~ polymer layer 54.
.. ~
s~s If desired, a continuous polymer layer having a varying modulus of elasticity may be substituted for the composite polymer layer shown in Fig. 8.
Other resurfacing implants may be designed in accordance with the present invention. Thus, for instance, an acetabalum or hip joint socket implant may be designed in accordance with the teachings hereinbefore set forth. A hemispherical or cup-shaped prosthetic element having a concave surface designed to receive a f~mur head is provided. The element îs composed of a rigid alloy such as ZIMALOY or plastic such as U~MWPE. The convex surface of the implant, designed to be attached to bone, includes a polymer layer having a varying modulus of elasticity as previously des cribed. The convex surface of the rigid reinforcement element may be a simple, regular hemisphere or it may have a complex shape, including protrusions and concave surfaces designed in accordance with engineering principles so as to provide an even force distri-bution throughout the implant~ Such convex surface, either regular or complex, of the reinforcement element will be covered with a polymer layer having a varying modulus of elasticity, which layer constitutes the bone attachment surface. The polymer layer may be a continuous layer or a composite layer as hereinbefore shown.
Claims (21)
1. A prosthesis adapted to be fixedly attached to bone by means of bone cement, said prosthesis comprising a reinforcement element, at least a portion of the surface of said reinforcement element carrying a polymer layer having substantial thickness, the exterior surface of said polymer layer constituting the bone attachment surface of said prosthesis, the interior surface of said polymer layer being secured to said reinforcement element, said polymer layer having a varying modulus of elasticity such that the modulus of elasticity of portions of said layer adjacent said interior surface is essentially constant and the modulus of elasticity of portions adjacent said exterior surface is essentially constant, said modulus of elasticity of said portions adjacent said interior surface being greater than said modulus of elasticity of said portions adjacent said exterior surface, portions of said layer which are between said portions adjacent said exterior surface and said portions and adjacent said interior surface having a modulus of elasticity which is intermediate with respect to the moduli of said portions adjacent said exterior and interior surfaces and wherein the modulus of elasticity of said layer de-creases in the direction of interior to exterior.
2. A prosthesis in accordance with claim 1 wherein the modulus of elasticity of said portions of said layer adjacent said exterior surface is approximately equal to the modulus of elasticity of hardened bone cement.
3. A prosthesis in accordance with claim 2 wherein the modulus of elasticity of said portions of said layer adjacent said interior surface is approximately equal to the modulus of elasticity of said reinforcement element.
4. A prosthesis in accordance with claim 1 wherein said modulus of elasticity of said layer decreases contin-uously in the direction of interior to exterior.
- 22a -
- 22a -
5. A prosthesis in accordance with claim 4 wherein said polymer layer comprises voids, said voids being distributed through-out said polymer layer such that the percentage of volume occupied by voids in portions of said layer adjacent said exterior surface is greater than the percentage of volume occupied by voids in portions of said layer adjacent said interior surface, said void volume percentage continuously increasing in the direction of interior to exterior of said layer.
6. A prosthesis in accordance with claim 5 wherein the percentage of volume occupied by voids in said portions of said layer adjacent said interior surface is about zero.
7. A prosthesis in accordance with claim 5 wherein said reinforcement element consists essentially of metal.
8. A prosthesis in accordance with claim 7 wherein said polymer layer has a thickness of greater tha 0.10 cm.
9. A prosthesis in accordance with claim 8 wherein said prosthesis is a stem insertion prosthesis.
10. A prosthesis in accordance with claim 1 wherein said modulus of elasticity of said polymer layer decreases incrementally in the direction of interior to exterior.
11. A prosthesis in accordance with claim 10 wherein said polymer layer is a composite of discrete polymer layers each having a different modulus of elasticity.
12. A prosthesis in accordance with claim 11 wherein each of said discrete polymer layers comprises a different amount of a plasticizer.
13. A prosthesis in accordance with claim 12 wherein each of said layers has a greater amount of plasticizer than the adjacent, more interior layer.
14. A prosthesis in accordance with claim 11 wherein each of said discrete layers comprises a different amount of a reinforcement filler.
15. A prosthesis in accordance with claim 14 wherein said reinforcement filler is a particulate material.
16. A prosthesis in accordance with claim 14 wherein said reinforcement filler is a fiberous material.
17. A prosthesis in accordance with claim 14 wherein each of said layers has a lesser amount of reinforcement filler than the adjacent, more interior layer.
18. A prosthesis in accordance with claim 1 wherein said reinforcement element has an irregular shape and wherein the external surface of said polymer layer has a simple, regular shape.
19. A prosthesis in accordance with claim 18 wherein said reinforcement element is composed of a metal.
20. A prosthesis in accordance with claim 18 wherein said prosthesis is a stem insertion prosthesis.
21. A prosthesis in accordance with claim 19 wherein said prosthesis is a stem insertion prosthesis.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7905445 | 1979-02-15 | ||
GB79/05445 | 1979-02-15 | ||
US63,434 | 1979-08-03 | ||
US06/063,434 US4280233A (en) | 1979-02-15 | 1979-08-03 | Bone connective prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticity |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1135005A true CA1135005A (en) | 1982-11-09 |
Family
ID=26270589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000345346A Expired CA1135005A (en) | 1979-02-15 | 1980-02-07 | Bone connective prosthesis comprising a reinforcement element carrying a polymer layer having a varying modulus of elasticity |
Country Status (5)
Country | Link |
---|---|
AU (1) | AU527332B2 (en) |
CA (1) | CA1135005A (en) |
DE (1) | DE3005265A1 (en) |
FR (1) | FR2448891B1 (en) |
GB (1) | GB2045082B (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2116848B (en) * | 1982-03-19 | 1984-11-28 | James Michael Sheehan | Element for prosthetic joint |
IE54180B1 (en) * | 1982-04-19 | 1989-07-05 | Vitek Inc | Articulating joint prostheses |
GB8419559D0 (en) * | 1984-08-01 | 1984-09-05 | Field R E | Endoprosthetic bone joint components |
DE3501723A1 (en) * | 1985-01-19 | 1986-07-24 | Bayer Ag, 5090 Leverkusen | SUBSTITUTED FURAZANE |
NL8702626A (en) * | 1987-11-03 | 1989-06-01 | Orthopaedic Tech Bv | METHOD FOR FORMING A GEOMETRY OF AN ENDOPROTHESIS, A FEMUR HEAD PROSTHESIS, AN ACETABULUM PROSTHESIS, A METHOD FOR BOTTING A FEMUR HEAD PROSTHESIS AND AN INSTRUMENT FOR PLACING ACROTHESES |
CH676196A5 (en) * | 1988-08-30 | 1990-12-28 | Sulzer Ag | |
CA2132423A1 (en) * | 1993-01-19 | 1994-07-20 | Robert Mathys Sr. | Shaft for an articulation endoprosthesis |
ES2138699T3 (en) * | 1994-04-11 | 2000-01-16 | Bristol Myers Squibb Co | IMPLANT OF POLYMERIC COMPOSITE MATERIAL AND MANUFACTURING PROCEDURE. |
WO1997032540A1 (en) * | 1996-03-08 | 1997-09-12 | Ao-Forschungsinstitut Davos | Implant for cementing into bone, method for cementing an implant into bone and package for implant |
WO1997041809A1 (en) * | 1996-05-03 | 1997-11-13 | Bmp S.A. | Intra-bone implant |
DE19619166C2 (en) * | 1996-05-11 | 1999-06-02 | Heraeus Kulzer Gmbh | Semi-finished product for the precise manufacture of an implantable prosthesis |
NL1016040C2 (en) * | 2000-08-29 | 2002-03-01 | Giles William Melsom | Porous cell attachment material, method for its manufacture, and applications. |
FR2840039B1 (en) * | 2002-05-22 | 2004-11-12 | Bioprofile | CONICAL COUPLING AND PROSTHESIS COMPRISING SUCH A COUPLING |
WO2008095327A1 (en) * | 2007-02-08 | 2008-08-14 | Woodwelding Ag | Implant, method of preparing an implant, implantation method, and kit of parts |
EP2637609B1 (en) | 2010-11-11 | 2016-02-24 | Zimmer, Inc. | Orthopedic implant with porous polymer bone contacting surface |
DE102013211175A1 (en) * | 2013-06-14 | 2014-12-18 | R + K CAD/CAM Technologie GmbH & Co. KG | Production of semi-finished products for implants based on plastic |
DE102015105100A1 (en) * | 2015-04-01 | 2016-10-06 | Aesculap Ag | Joint implant part, joint endoprosthesis and method for producing a joint implant part and a joint endoprosthesis |
GB201614171D0 (en) * | 2016-08-18 | 2016-10-05 | Fitzbionics Ltd | An implant for repair of bone defects |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3605123A (en) * | 1969-04-29 | 1971-09-20 | Melpar Inc | Bone implant |
US3623164A (en) * | 1969-10-06 | 1971-11-30 | Gulf Oil Corp | Prosthetic device |
US3789029A (en) * | 1970-07-06 | 1974-01-29 | Research Corp | Plastic bone composition and method of making same |
US3986212A (en) * | 1975-04-11 | 1976-10-19 | Glasrock Products, Inc. | Composite prosthetic device with porous polymeric coating |
DE2603456C2 (en) * | 1976-01-30 | 1984-04-05 | Robert Bosch Gmbh, 7000 Stuttgart | Process for the production of a bone implant |
US4164794A (en) * | 1977-04-14 | 1979-08-21 | Union Carbide Corporation | Prosthetic devices having coatings of selected porous bioengineering thermoplastics |
-
1980
- 1980-02-06 GB GB8004015A patent/GB2045082B/en not_active Expired
- 1980-02-07 CA CA000345346A patent/CA1135005A/en not_active Expired
- 1980-02-13 DE DE19803005265 patent/DE3005265A1/en not_active Withdrawn
- 1980-02-14 AU AU55543/80A patent/AU527332B2/en not_active Expired
- 1980-02-14 FR FR8003305A patent/FR2448891B1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2448891A1 (en) | 1980-09-12 |
DE3005265A1 (en) | 1980-08-28 |
AU527332B2 (en) | 1983-02-24 |
FR2448891B1 (en) | 1985-09-20 |
AU5554380A (en) | 1980-08-21 |
GB2045082B (en) | 1983-03-23 |
GB2045082A (en) | 1980-10-29 |
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