WO2005027801A1 - Prosthetic devices employing oxidized zirconium and other abrasion resistant surfaces contacting surfaces of cross-linked polyethylene - Google Patents

Prosthetic devices employing oxidized zirconium and other abrasion resistant surfaces contacting surfaces of cross-linked polyethylene Download PDF

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Publication number
WO2005027801A1
WO2005027801A1 PCT/US2004/030524 US2004030524W WO2005027801A1 WO 2005027801 A1 WO2005027801 A1 WO 2005027801A1 US 2004030524 W US2004030524 W US 2004030524W WO 2005027801 A1 WO2005027801 A1 WO 2005027801A1
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WIPO (PCT)
Prior art keywords
zirconium
black
prosthesis
oxidized
blue
Prior art date
Application number
PCT/US2004/030524
Other languages
French (fr)
Inventor
David L. Evans
Gordon Hunter
Shilesh C. Jani
Robert E. Brosnahan, Iii
Original Assignee
Smith & Nephew Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Smith & Nephew Inc. filed Critical Smith & Nephew Inc.
Priority to EP04784397A priority Critical patent/EP1670397A1/en
Priority to AU2004273968A priority patent/AU2004273968A1/en
Priority to JP2006527062A priority patent/JP2007508855A/en
Priority to CA002535879A priority patent/CA2535879A1/en
Publication of WO2005027801A1 publication Critical patent/WO2005027801A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/28Materials for coating prostheses
    • A61L27/30Inorganic materials
    • A61L27/306Other specific inorganic materials not covered by A61L27/303 - A61L27/32
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/442Intervertebral or spinal discs, e.g. resilient
    • A61F2/4425Intervertebral or spinal discs, e.g. resilient made of articulated components
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14Macromolecular materials
    • A61L27/16Macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L31/00Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
    • A61L31/04Macromolecular materials
    • A61L31/048Macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L31/00Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
    • A61L31/08Materials for coatings
    • A61L31/082Inorganic materials
    • A61L31/088Other specific inorganic materials not covered by A61L31/084 or A61L31/086
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2002/30769Special external or bone-contacting surface, e.g. coating for improving bone ingrowth madreporic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30841Sharp anchoring protrusions for impaction into the bone, e.g. sharp pins, spikes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30907Nets or sleeves applied to surface of prostheses or in cement
    • A61F2002/30909Nets
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/442Intervertebral or spinal discs, e.g. resilient
    • A61F2/4425Intervertebral or spinal discs, e.g. resilient made of articulated components
    • A61F2002/443Intervertebral or spinal discs, e.g. resilient made of articulated components having two transversal endplates and at least one intermediate component
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00029Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00035Other metals or alloys
    • A61F2310/00089Zirconium or Zr-based alloys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00389The prosthesis being coated or covered with a particular material
    • A61F2310/00395Coating or prosthesis-covering structure made of metals or of alloys
    • A61F2310/00419Other metals
    • A61F2310/00485Coating made of zirconium or Zr-based alloys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00389The prosthesis being coated or covered with a particular material
    • A61F2310/00592Coating or prosthesis-covering structure made of ceramics or of ceramic-like compounds
    • A61F2310/00598Coating or prosthesis-covering structure made of compounds based on metal oxides or hydroxides
    • A61F2310/00634Coating made of zirconium oxide or hydroxides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/38Materials or treatment for tissue regeneration for reconstruction of the spine, vertebrae or intervertebral discs
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking
    • C08L2312/06Crosslinking by radiation

Definitions

  • This application claims priority to U.S. application Ser. No. 10,666,477, filed September 18, 2003.
  • This invention relates to metallic implants with load bearing surfaces coated with a thin, dense, low friction, highly wear-resistant, uniformly thick coating of oxidized zirconium.
  • This invention also relates generally to metallic implants with load bearing, abrasion resistant surfaces.
  • the load bearing oxidized zirconium surfaces or abrasion resistant surfaces contact counter bearing surfaces of cross- linked polyethylene (XLPE).
  • XLPE has superior wear characteristics compared with other conventional polymer materials used in prostheses.
  • Oxidized zirconium has thermal conductivity characteristics that are particularly advantageous when used in a prosthetic device in which it articulates against XLPE.
  • the invention overcomes the major disadvantage generally inherent in prosthetic devices having hard surfaces articulating against soft surfaces.
  • the basic technology upon which the improvement described herein is based, is described in U.S. Patent 5,037,438 to Davidson and U.S. Patent 6,447,550 to Hunter, et al., both of which are fully incorporated by reference herein.
  • the longevity of medical implant devices is of prime importance as it is desirable that the implant should function for the complete lifetime of a patient. This is particularly true if the patient is young and the number of surgical revisions is to be kept to a minimum and preferably zero.
  • orthopedic implant materials should preferably combine high strength, corrosion resistance and tissue compatibility.
  • One of the variables affecting the longevity of load-bearing implants such as hip-joint implants is the rate of wear of the articulating surfaces and long-term effects of metal ion release.
  • a typical hip-joint prosthesis includes a stem, a femoral head and an acetabular cup against which the femoral head articulates. Wear of either or both of the articulating surfaces results in an increasing level of wear particulates and "play" between the femoral head and the cup against which it articulates. Wear debris can contribute to adverse tissue reaction leading to bone resorption, and ultimately the joint must be replaced.
  • the rate of wear of the acetabular cup and the femoral head surfaces of artificial hips is dependent upon a number of factors which include the relative hardness and surface finish of the materials which constitute the femoral head and the acetabular cup, the factional coefficient between the materials of the cup and head, the load applied and the stresses generated at the articulating surfaces.
  • hip-joint implants include femoral heads of cobalt, titanium, or zirconium alloys articulating against acetabular cups lined with organic polymers or composites of such polymers including, for instance, ultra-high molecular weight polyethylene (UHMWPE) and femoral heads of polished alumina in combination with acetabular cups lined with an organic polymer or composite or made of polished alumina.
  • UHMWPE ultra-high molecular weight polyethylene
  • femoral heads of polished alumina in combination with acetabular cups lined with an organic polymer or composite or made of polished alumina.
  • UHMWPE being a polymeric material
  • UHMWPE is more susceptible to creep at higher temperatures than the commonly used metal alloys or ceramics due to its relatively lower melting point and is consequently more susceptible to wear than the alloys or ceramics.
  • the original impetus for the inclusion of surfaces such as UHMWPE was that they would act sacrificially; they would fail slowly and fail before the harder surface, allowing for an overall extension of the useful life of the device. Additionally, polyethylene was thought to absorb shock much better than harder surfaces, thereby simulating the effect of real cartilage.
  • the instant invention represents another advancement in the art, namely, a further improvement in wear and a simultaneous significant improvement of the creep problem associated with the prior art prostheses comprising polyethylene articulating against harder surfaces.
  • metal prostheses are not completely inert in the body. Body fluids act upon the metals causing them to slowly corrode by an ionization process thereby releasing metal ions into the body.
  • Metal ion release from the prosthesis is also related to the articulation and rate of wear of load bearing surfaces because, as may be expected, when a metallic femoral head, for instance, is articulated against UHMWPE, the passive oxide film which forms on the femoral head is constantly removed. The repassivation process constantly releases metal ions during this process. Furthermore, the presence of third-body wear (cement or bone debris) accelerates this process and micro- fretted metal particles can increase friction. Consequently, the UHMWPE liner inside the acetabular cup, against which the femoral head articulates, is subjected to accelerated levels of creep, wear, and torque. A reduction in these deleterious effects will also improve the problem of metal ion release.
  • the method is said to produce a prosthetic device which has "excellent compatibility with body tissue and is non-thrombogenic".
  • Bokros does not address the issues of friction, heating, creep and wear of orthopedic implant bearing surfaces, or changes induced in the mechanical properties of the underlying metal due to this high- temperature treatment.
  • the aforementioned failings of the prior art were addressed in part by Davidson in U.S. Patent 5,037,438.
  • Davidson teaches a zirconium or zirconium-containing metal alloy prosthesis coated via in-situ oxidation with a surface of blue-black or black oxidized zirconium which articulates against an organic polymer or polymer-based composite.
  • the oxidized zirconium coating provides the prosthesis with a thin, dense, low friction, wear resistant, biocompatible surface ideally suited for use on articulating surfaces of joint prostheses wherein a surface or surfaces of the joint articulates, translates or rotates against mating joint surfaces.
  • the oxidized zirconium coating described the '438 patent may therefore be usefully employed on the femoral heads or inside surfaces of acetabular cups of hip-joint implants or on the articulating surfaces of other types of prostheses, such as knee joints.
  • the oxidized zirconium coating of the '438 patent was a specific type of oxidized zirconium.
  • Oxidized zirconium presents itself in many forms, among them are white, beige, and blue-black.
  • the white variety is particularly disfavored in the present application, as it tends to separate and break off of the substrate.
  • Conventional oxidized zirconium surfaces formed, for example, by simple air oxidation will not be of the blue-black or black variety and will not possess the superior properties of the same which are recited in the '438 patent. The most important of these properties high hardness, low friction that results from the presence of the surface oxide.
  • the specific blue-black or black oxidized zirconium coatings of the '438 patent were known in the art of mechanical bearings, having been described in U.S.
  • Patent 2,987,352 which teaches a 700-1100 °F oxidation method to produce the specific blue-black or blue oxidized zirconium coating.
  • a later issuing patent to Haygarth U.S. Patent 4,671,824 teaches an alternative, salt-bath method to produce the desired coating.
  • the blue- black or black oxidized zirconium of the instant invention possessing the necessary properties is primarily monoclinic crystal structure. This has been characterized by Hunter et al. (Hunter, G, et al., Mat. Res. Symp. Proc, (1999), 550, 337).
  • vertebral disc implants Another prosthetic device which benefits from the novel oxidized zirconium/XLPE couple described herein are vertebral disc implants. These devices are an increasingly popular alternative to the spinal fusion surgical procedure. This alternative typically results in the maintenance of range of motion at the operative level once a damaged disc has been replaced with an implant.
  • One type of vertebral disc implant, described in U.S. Patent No. 5,410,269 is that with two terminal plates which are connected to the endplates of the relevant vertebrae, and with a prosthesis core which cooperates with at least one terminal plate via an articular surface which permits a pivoting movement.
  • the core material of these implants is high density polyethyelene, while the opposing plates are made of materials commonly found in conventional prosthetic devices, such as ceramic or metal.
  • the use of disc implants having XLPE articulating against oxidized zirconium surfaces will not only decrease wear and improve the useful life of the device, but will also better maintain motion at the operative level upon removal of the damaged disc, relative to that of vertebral disc implants fabricated from conventional materials.
  • XLPE devices have exhibited other deficiencies, with which the prior art has largely been concerned about. Free radicals formed during irradiation, however, can exist indefinitely if termination by cross-linking or other forms of recombination do not occur.
  • reacted inte ⁇ nediates are continuously formed and decayed. Exposure of these free radical species at any time (e.g., during irradiation, shelf-aging, or in vivo aging) to molecular oxygen or any other reactive oxidizing agent can result in their oxidation. Extensive oxidation leads to a reduction in molecular weight, and subsequent changes in physical properties, including wear resistance. Many attempts have been made to improve the characteristics of XLPE. These attempts include radiation induced cross linked polyethylene (See U.S. Patents Nos.
  • the advantages of the instant invention will be the preservation of the desirable properties of XLPE with a simultaneous elimination of some of its negative properties.
  • the '438 patent did not contemplate and nowhere does it teach, the use of the oxidized zirconium surfaces directly contacting surfaces of XLPE.
  • the inventors have discovered that the unique properties of oxidized zirconium accentuate the inherent advantages of XLPE as a counter bearing surface.
  • the superior strength and hardness, low friction, wear resistance, thermal conductivity, and biocompatibility characteristics of the blue-black or black oxidized zirconium is sufficient in itself to considerably slow and possibly prevent the degradative wear processes to which the prosthetic devices of the prior art have been subject.
  • the invention is directed to forming prosthetic devices of oxidized zirconium-on-XLPE, which represents a special species of oxidized zirconium-on-polymer devices, exhibiting even longer overall useful service life relative to conventional prostheses materials-on-UHMWPE.
  • the invention is not limited to prostheses formed of zirconium or zirconium alloy.
  • the prostheses substrate may itself be a composite material, only requiring that zirconium or zirconium alloy be present in the substrate layer immediately adjacent to the surface upon which the oxidized zirconium coating is to be formed.
  • a or “an” may mean one or more. As used herein in the claim(s), when used in conjunction with the word “comprising”, the words “a” or “an” may mean one or more than one. As used herein “another” may mean at least a second or more.
  • abrasion resistant surface is defined as a material surface having a greater hardness than the underlying substrate. When used in reference to the underlying substrate material, it is synonymous with “surface hardened”. An oxidized zirconium surface is one example of an abrasion resistant surface. Others include, but are not limited to substrates coated with ceramic materials.
  • base material is defined as the material upon which a layer of oxidized zirconium is to be formed. It may be homogeneous, consisting of a single phase material, or it may be heterogeneous, consisting of a composite material of one or more substrate layers.
  • contacting surface refers to any two surfaces of the prosthetic device or medical implant that contact one another in either a load bearing (articulating) or non-load bearing (non-articulating) manner.
  • substrate layer is defined as a distinct chemical region or domain within the base material. A substrate layer may or may not be comprised of zirconium or zirconium alloy.
  • vertebral disc prosthesis is defined as any prosthetic device for implantation into the vertebra, regardless of configuration or design.
  • zirconium alloy is defined as any metal alloy containing zirconium in any amount greater than zero. Thus, an alloy in which zirconium is a minor constituent is considered a “zirconium alloy” herein.
  • a knee prosthesis for implantation in a patient comprises a prosthesis body formed of zirconium or zirconium alloy.
  • the prosthesis body has an implant portion for inserting into the body tissue of a patient, a bearing surface having at least one condyle on the prosthesis body, a tibial component comprised of cross-linked polyethylene and having a surface adapted to cooperate with the bearing surface, and a thin coating of blue-black or black oxidized zirconium directly on the bearing surface of the condyle portion.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick.
  • the blue- black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the knee prosthesis has an implant portion of the prosthesis body that has, at least in part, an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface st ⁇ icture can have zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue-black or black oxidized zirconium.
  • a hip prosthesis for implantation in a patient includes a hip prosthesis body for implantation into a femur which has a head portion formed at least in part of zirconium or zirconium alloy, a bearing surface on the head portion of the prosthesis body, and an acetabular cup having an inner surface comprising cross-linked polyethylene.
  • a cooperating surface is adapted to engage and articulate with the bearing surface on the head portion.
  • a thin coating of blue-black or black oxidized zirconium is formed directly on the exposed bearing surface of the head portion.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure is formed of zirconium or zirconium alloy beads connected to the outer surface of the prosthesis body.
  • a prosthesis for implantation in a patient includes a prosthesis body formed at least in part of zirconium or zirconium alloy.
  • the prosthesis body includes an implant portion for insertion into the body tissue of the patient, a bearing surface on the prosthesis body, the bearing surface being sized and shaped to engage and articulate with a second bearing surface on another prosthesis portion.
  • the second bearing surface is formed of a cross-linked polyethylene.
  • the prosthesis also includes a coating of blue-black or black oxidized zirconium from about 1 to about 5 microns in thickness on the bearing surface.
  • the prosthesis body is a hip joint having a head portion as a bearing surface and another prosthesis portion is an acetabular cup, the head portion being adapted to cooperate with the inner surface of the acetabular cup, and the inner surface of the acetabular cup is also the second bearing surface.
  • the prosthesis body is a knee joint and the bearing surface of the prosthesis body includes at least one condyle, and another prosthesis portion including a tibial component, with at least one condyle being adapted to cooperate with the tibial component.
  • the prosthesis body has an irregular surface structure adapted to accommodate tissue in-growth on at least a portion of the prosthesis body.
  • the irregular surface structure is formed of zirconium or zirconium alloy beads connected to the outer surface of the prosthesis body, where at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium.
  • the irregular surface structure prosthesis has an irregular surface structure formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium.
  • the invention is directed towards a prosthesis for implantation in a patient which includes a prosthesis body formed at least in part of zirconium or zirconium alloy, the prosthesis body includes an implant portion for inserting into the body tissue of the patient, a bearing surface on the prosthesis body, a counter-bearing surface formed of cross-linked polyethylene and adapted to cooperate with the bearing surface and, a thin coating of blue-black or black oxidized zirconium directly on the bearing surface.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium.
  • a prosthesis for implantation in a patient includes a prosthesis body comprising a substrate material.
  • the prosthesis body includes an implant portion for inserting into the body tissue of the patient, a bearing surface on the prosthesis body formed of any abrasion resistant surface, and a counter-bearing surface formed of cross- linked polyethylene and adapted to cooperate with the bearing surface.
  • the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure has beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium.
  • the irregular surface structure is formed wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium.
  • the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium.
  • a prosthesis for implantation in a patient comprising (a) a prosthesis body comprising a substrate material, said prosthesis body comprising an implant portion for inserting into the body tissue of the patient; (b) a bearing surface on the prosthesis body comprised of an abrasion resistant surface; and, (c) a counter-bearing surface comprising cross-linked polyethylene and adapted to cooperate with the bearing surface.
  • the implant portion of the prosthesis body further comprises an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure comprises beads attached to the outer surface of the prosthesis body, wherein at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium.
  • the irregular surface structure comprises wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium.
  • the prosthesis body further comprises at least one substrate layer.
  • the prosthesis body further comprises at least one substrate layer having a depth-dependent variable concentration of zirconium.
  • a vertebral disc prosthesis for implantation in a patient, the prosthesis comprising at least one surface of cross-linked polyethylene; at least one component formed of zirconium or zirconium alloy, said component having at least one surface of blue-black or black oxidized zirconium; and wherein at least one of the cross- linked polyethylene surfaces cooperates with at least one of the surfaces of blue-black or black oxidized zirconium.
  • the vertebral disc prosthesis further comprises two prosthesis plates; and a prosthesis core; the prosthesis core cooperates with at least one prosthesis plate at surface permitting a rotational movement around a vertical axis.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Most preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the implant portion of the prosthesis body may further include an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium.
  • the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium.
  • the irregular surface may also comprise a textured surface. Such texturing methods include, but are not limited to, chemical etching, electrochemical etching, photoetching. These procedures may or may not utilize maskant materials.
  • the irregular surface may also comprise a surface having anchoring projections or teeth extending from the outer surface of the top and bottom plate. These anchoring projections or teeth improve fixation when they act against adjacent bone or tissue.
  • FIG. 1 is a schematic diagram depicting a hip joint prosthesis in position.
  • FIG. 2 is a schematic diagram showing a typical hip joint prosthesis.
  • FIG. 3 is a schematic diagram of a knee joint prosthesis in place.
  • FIG. 4 is a schematic diagram of the parts of a typical knee joint.
  • FIG. 5 is a schematic diagram of the vertebral disc prosthesis.
  • the present invention provides low friction, wear and creep resistant, articulating, interfacial bearing surfaces for prosthetic devices.
  • the invention provides for a prosthetic device in which one contacting surface is formed of blue-black or black oxidized zirconium and another contacting surface is formed of XLPE.
  • one contacting surface is formed of an abrasion resistant material and another contacting surface is XLPE.
  • Oxidized zirconium presents itself in many forms, among them are white, beige, and blue-black. The white variety is particularly disfavored in the present application, as it tends to separate and break off of the substrate readily.
  • the blue-black or black oxidized zirconium of the instant invention possessing the necessary properties is primarily monoclinic crystal structure and may include tetragonal zirconia. Its microstructure has been characterized by Hunter et. al.
  • the specific blue-black or black oxidized zirconium coatings used herein were known in the art of mechanical bearings, having been originally taught by Watson in U.S. Patent 2,987,352. Davidson, in U.S. Patent 5,037,428, first taught the application of this form of oxidized zirconium to prosthetic devices.
  • the base materials upon which the oxidized zirconium coating is formed need not be fabricated totally of zirconium or zirconium alloy.
  • the only requirement for the formation of an oxidized zirconium surface is zirconium or zirconium alloy material in the surface before the formation of the oxidized zirconium layer.
  • the former surface becomes the first substrate layer.
  • composite materials are possible embodiments of the present invention. This allows one to realize strength and weight advantages of prostheses having one or more different core materials.
  • a synthetic core material having high strength and being of light weight and having a zirconium or zirconium alloy veneer or outer layer is envisioned by the present invention.
  • the interior of the base material may be of one or more than one material, allowing for varying degrees of heterogeneity in the overall fabrication, depending upon the application. Alternatively, a lesser degree of heterogeneity is possible.
  • a base material being relatively rich in zirconium or zirconium alloy at the surface and exhibiting a continuously decreasing zirconium content as a depth into the substrate increases is another possibility. In this latter example, no abrupt macroscopic phase boundary exists within the base material.
  • the XLPE useful in the present invention is polyethylene cross-linked by any means, irradiative or chemical being illustrative examples which are generally known in the art. Illustrative examples of the prosthetic devices for which the contact interfaces disclosed hererin find use are shown in the schematic diagrams, FIGS. 1-4.
  • a typical hip joint assembly is shown in situ in FIG. 1 and FIG. 2. The hip joint stem 2 fits into the femur while the femoral head 6 of the prosthesis fits into and articulates against the inner lining 8 of an acetabular cup 10 which in turn is affixed to the pelvis as shown in FIG. 1.
  • a porous metal bead or wire mesh coating 12 may be incorporated to allow stabilization of the implant by in-growth of surrounding tissue into the porous coating. Similarly, such a coating can also be applied to the acetabular component.
  • the femoral head 6 may be an integral part of the hip joint stem 2 or may be a separate component mounted upon a conical taper at the end of the neck 4 of the hip joint prosthesis. This allows the fabrication of a prosthesis having a metallic stem and neck but a femoral head of a different material. [0053] This method of construction is often desirable because the use of composite materials allows for the localized optimization of a variety of parameters such as , weight, strength and wear resistance.
  • the femoral head articulates against the inner surface of the acetabular cup thereby causing wear and, in the long term, this may necessitate prosthesis replacement.
  • the inner lining 8 is preferably formed of XLPE and the femoral head 6 is coated with a surface of blue-black or black oxidized zirconium.
  • the oxidized zirconium surface coating is 1-20 ⁇ m thick, but may be outside this range. It may alternatively be from about 1-5 ⁇ m thick.
  • the wire mesh or metal bead surface 12 may be at least partially coated with a surface of blue-black or black oxidized zirconium to promote in-growth of tissue or bone into the device, thereby stabilizing its position.
  • a typical knee joint prosthesis is shown in situ in FIG. 3 and FIG. 4.
  • the knee joint includes a femoral component 20 and a tibial component 30.
  • the femoral component includes condyles 22 which provide the articulating surface of the femoral component and pegs 24 for affixing the femoral component to the femur.
  • the tibial component 30 includes a tibial base 32 with a peg 34 for mounting the tibial base onto the tibia.
  • a tibial platform 36 is mounted atop the tibial base 32 and is supplied with grooves 38 similar to the shape of the condyles 22.
  • the bottom surfaces of the condyles 26 contact the tibial platform's grooves 38 so that the condyles articulate within these grooves against the tibial platform.
  • the condyles 22 are coated with a surface of blue- black or black oxidized zirconium and the grooves 38 on the tibial platform 36 are comprised of XLPE.
  • Part or all of the remainder of the femoral component 20 and a tibial component 30 may have a surface coating of blue-black or black oxidized zirconium.
  • the surface coatings are 1-20 ⁇ m thick, but may be outside this range. They may alternatively be from about 1-5 ⁇ m thick.
  • porous bead or wire mesh coatings can also be applied to either the tibial or femoral components of the knee or both. These porous bead or wire mesh coatings of the knee prosthesis may also be at least partially coated with a surface of blue-black or black oxidized zirconium to promote in-growth of tissue or bone into the device, thereby stabilizing its position.
  • the base (i.e., substrate) zirconium containing metal alloys are cast or machined by conventional methods to the shape and size desired to obtain a prosthesis substrate.
  • the substrate is then subjected to process conditions which cause the natural (in situ) formation of a tightly adhered, diffusion-bonded coating of oxidized zirconium on its surface.
  • the process conditions include, for instance, air, steam, or water oxidation or oxidation in a salt bath.
  • the base materials need not be formed totally of zirconium or zirconium alloy.
  • zirconium or zirconium alloy material comprises the surface layer of the base material before the formation of the oxidized zirconium layer.
  • composite materials are possible embodiments of the present invention. This allows one to realize strength and weight advantages of prostheses having one or more different core materials.
  • a synthetic core material having high strength and being of light weight surrounded by a zirconium or zirconium alloy veneer or outer layer is a possible embodiment of the present invention.
  • One or more substrata may comprise the base material and these substrata may be comprised of any suitable material which may or may not include zirconium or zirconium alloy.
  • the base material may consist of a continuous phase in which the concentration of zirconium or zirconium alloy varies with depth into the base material.
  • the surface at which the coating of oxidized zirconium is formed may be relatively rich in zirconium, with this concentration falling off as the distance into the base material (i.e., away from the surface) increases. Variations on the general embodiment are within the scope of the present invention in light of the disclosure. [0058] Representative methods for the formation of the surface coating of blue- black or black oxidized zirconium have been described previously in U.S.
  • a coating thickness of 1 to 5 ⁇ m is preferred.
  • Conditions useful for the fabrication of surfaces of varying thickness are described in U.S. Patent 5,037,428.
  • Methods for controlling the uniformity of the oxidized zirconium coating are described in U.S. Patent 6,447,550, which is incorporated by reference as though fully set forth herein.
  • Oxygen, niobium, and titanium are common alloying elements in the alloy with oftentimes the presence of hafnium.
  • zirconium containing alloys may be custom formulated by conventional methods known in the art of metallurgy, a number of suitable alloys are commercially available. Illustrative examples of these commercial alloys include among others Zircadyne 705, Zircadyne 702, and Zircalloy.
  • These diffusion-bonded, low friction, highly wear resistant oxidized zirconium coatings are applied to one of the contacting surfaces of orthopedic implants subject to conditions of wear. Such surfaces include the articulating surfaces of knee joints, elbows and hip joints. In the case of hip joints, the femoral head and stem are typically fabricated of metal alloys while the acetabular cup may be fabricated from ceramics.
  • the surface of the base material of the contacting surface of the device must be of zirconium or zirconium alloy such that upon surface oxidation under the appropriate conditions, measurable surface concentrations of oxidized zirconium are formed.
  • Substrate layers extending into the interior of the base material may consist of one or more materials, any, or, or none of which may be of zirconium or zirconium alloy.
  • XLPE For instance as the roughness of the counter bearing surface increases, XLPE approaches conventional polyethylene in its wear resistance (See, e.g., McKellop et al., "Wear of Gamma-Crosslinked Polyethylene Acetabular Cups against Roughened Femoral Balls", Clin. Orthop., (1999) 369, pp. 73-82).
  • the wear advantage of XLPE over conventional polyethylene enhanced by using a low roughness, abrasion resistant articulating surfaces against the XLPE.
  • cross-linked polyethylene is more prone to creep than conventional polyethylene.
  • Creep is a relatively slow plastic deformation process which is more prominent at higher temperatures as a material more closely approaches its melting point.
  • a contacting surface that is a thermal conductor will diminish the creep resistance advantage of conventional polyethylene over XLPE through its ability to pass heat and avoid a localized rise in temperature. As the temperature of either polymer rises, its ability to withstand protracted stress-strain loads decreases, such that prostheses made of either conventional polyethylene or XLPE are subject to failure.
  • Oxidized zirconium is unique with respect to the excellent thermal conductivity it possesses relative to other conventional prosthetic materials. It combines excellent surface roughness characteristics with very high thermal conductivity. In this way, it possesses the relevant beneficial characteristics (in terms of XLPE) of metal and ceramics while avoiding the relevant disadvantages of the former and outperforming the latter.
  • XLPE XLPE
  • oxidized zirconium would enjoy both a significant reduced wear and a significant reduced creep susceptibility. Table 1 below schematically illustrates these characteristics.
  • the prostheses of the instant invention exhibit design advantages in a variety of applications. Importantly, the wear resistance characteristics of XLPE, already superior relative to UHMWPE is fully realized while the creep characteristics are improved when XLPE articulates against abrasion resistant surfaces. These improvements are further enhanced when XLPE articulates against oxidized zirconium, allowing for the polymer lining to be constructed of lower thickness than in conventional prostheses. The superiority of oxidized zirconium counter bearing surfaces in terms of low friction and high thermal conductivity allows for polymer linings that are thinner still.
  • the synergistic result is a potentially smaller prosthesis having weight advantages over conventional prostheses, which requires less bone resection, greater conformity and contact area, and exhibits reductions in contact stress, an increase in range of motion, and a decreased chance of dislocation.
  • a smaller amount of polymer material is expected to result in a lower likelihood of osteolysis (resulting from a lesser likelihood of material migration) while having the same or greater component service life.
  • Decreases in mass of the prosthesis is expected to be of greater significance in hip applications which are typically larger than knee prostheses and have a smaller range of motion.
  • the present invention is also useful in knee prostheses. Knee prostheses typically are of two varieties: mobile bearing knees (MBK) and fixed bearing knees (FBK).
  • the MBK is characterized by having its articulating tibial component 30 movable relative to the tibial platform 36. This results in wear and creep on both the top and bottom of the tibial component 30. In contrast, this interface in the FBK is fixed and the only movement is between the top of the tibial component and the condyles 22. As a result, the MBK has a greater range of motion but suffers from greater wear and creep than an FBK.
  • XLPE generally offers greater wear and comparable creep resistance over UHMWPE when articulating against abrasion resistant surfaces. This characteristic is enhanced where the tibial tray is formed of oxidized zirconium.
  • Zirconium or zirconium alloy can also be used to provide an irregular surface such as, but not limited to, porous bead or wire mesh surface to which surrounding bone or other tissue may integrate to stabilize the oxidized zirconium-on-oxidized zirconium prosthesis.
  • porous coatings can be treated simultaneously by the oxidation treatment in a manner similar to the oxidation of the base prosthesis for the elimination or reduction of metal ion release.
  • zirconium or zirconium alloy can also be used as a surface layer applied over conventional implant materials prior to in situ oxidation and formation of the oxidized zirconium coating.
  • the present invention also finds utility in the area of vertebral disc implants.
  • One common cause of low lumbar back pain is "degenerative disc disease.”
  • the condition may take many different forms (e.g. a herniated disc or a collapsed disc). Any of these conditions can result from a disc that has lost its proper form and therefore does not function properly, causing significant pain when you move or attempt to perform normal daily activities. The purpose, then, of any spinal surgery or disc surgery is to relieve this recurring back pain.
  • spinal fusion surgery For relieving this type of back pain is to stop the movement of the afflicted disc or motion segment by fusing the vertebrae together in that specific area.
  • metal implants e.g. plates, rods and screws
  • This type of procedure may also involve placing bone or fusion cages into the disc space to assist in fusing the spine bones together.
  • disc implantation is intended to maintain motion at the operative level.
  • total disc replacement whereby the damaged disc has been removed and replaced by a disc implant.
  • Total disc replacement theoretically protects the discs at adjacent levels by sharing or distributing the stress through the lower back during normal activities such as lifting and bending.
  • Surgeons have explored the idea of prosthetic replacements for damaged or degenerated intervertebral discs.
  • intervertebral disc and its biomechanical behavior are very complex, the engineering a disc replacement has been challenging.
  • a typical vertebral disc implant is described in U.S. Patent No. 5,401,269 which is incorporated by reference as though fully disclosed herein. [0069]
  • the present invention improves upon the present state of the art by incorporating cooperating surfaces of blue-black or black oxidized zirconium and XLPE.
  • a vertebral disc prosthesis for implantation in a patient, the device comprising at least one surface of cross-linked polyethylene and at least one surface of blue-black or black oxidized zirconium in which at least one of the cross-linked polyethylene surfaces cooperates with at least one of the surfaces of blue-black or black oxidized zirconium.
  • the vertebral disc prosthesis comprises a top plate, a bottom plate, and a core, in which the top and bottom plates are comprised of zirconium alloys and the top and bottom plates further comprise surfaces of blue-black or black oxidized zirconium, and the core comprises cross-linked polyethylene.
  • the core (42) of the implant is typically constructed of a relatively soft material, usually conventional high molecular weight polyethylene.
  • the top (44) and bottom (46) plates are typically constructed of conventional materials such as cobalt-chromium.
  • the top (44) and bottom (46) plates are made from zirconium or a zirconium alloy wherein at least a part its surface which contacts the core (42) is oxidized to blue-black or blue oxidized zirconium.
  • the core (42) is made from XLPE.
  • the oxidized zirconiurn/XLPE couple has all the advantages described above, including improved creep resistance, decreased wear, etc.
  • the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Most preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick.
  • the implant portion of the prosthesis body may further include an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
  • the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue-black or black oxidized zirconium.
  • the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium.
  • the irregular surface when used, is ideally located on the outside surfaces (48) of the top plate (44) and the bottom plate (46). However, the irregular surface may be located in any area where improved adhesion to bone or tissue is desirable.
  • the irregular surface may also comprise a textured surface. The surface is both textured and oxidized. Non-limiting examples of such surfaces are described in copending U.S. Application Serial No. 10,313,205, filed Dec.
  • the resulting surface is a textured, oxidized zirconium surface.
  • texturing methods include, but are not limited to, chemical etching, electrochemical etching, photoetching. These procedures may or may not utilize maskant materials.
  • the irregular surface may also comprise a surface having anchoring projections or teeth extending from the outer surface of the top and bottom plate. These optional components (50) are shown in FIG. 5. These anchoring projections or teeth improve fixation when they act against adjacent bone or tissue.

Abstract

Orthopedic implants which include the components of zirconium or zirconium-based alloys having surfaces coated with oxidized zirconium or alternatively, other orthopedic implants comprising abrasion resistant surfaces contacting surfaces of cross­linked polyethylene are disclosed. Such implants provide low friction, highly wear resistant coatings especially useful in artificial joints, such as hip joints, knee joints, elbows, etc., but also useful in other implant devices as well. The implants also find use as vertebral disc prostheses.

Description

PROSTHETIC DEVICES EMPLOYING OXIDIZED ZIRCONIUM AND OTHER ABRASION RESISTANT SURFACES CONTACTING SURFACES OF CROSS-LINKED POLYETHYLENE
BACKGROUND OF THE INVENTION
[0001] This application claims priority to U.S. application Ser. No. 10,666,477, filed September 18, 2003. [0002] This invention relates to metallic implants with load bearing surfaces coated with a thin, dense, low friction, highly wear-resistant, uniformly thick coating of oxidized zirconium. This invention also relates generally to metallic implants with load bearing, abrasion resistant surfaces. In the present invention, the load bearing oxidized zirconium surfaces or abrasion resistant surfaces contact counter bearing surfaces of cross- linked polyethylene (XLPE). XLPE has superior wear characteristics compared with other conventional polymer materials used in prostheses. Oxidized zirconium has thermal conductivity characteristics that are particularly advantageous when used in a prosthetic device in which it articulates against XLPE. The unique advantages of oxidized zirconium and abrasion resistant surfaces in combination with those of XLPE result in a synergy which allows one to accentuate the superior properties of XLPE as a counter bearing surface, resulting in a superior prosthetic device. [0003] Historically prostheses of articulating surfaces were constructed of materials of differing hardness for the contacting surfaces. By having one "yielding" surface, such prior art devices eventually form an optimal fit, i.e., a tight tolerance, whereby galling, fretting, and other erosive phenomena are minimized, resulting in longer-lasting prosthetic devices. An example of these early-generation devices is the femoral head of a hip-stem prosthesis which engages a counter-bearing surface in an acetabular cup which is often made of a softer material such as ultra-high molecular weight polyethylene. However, use of contacting surfaces of different hardness is not a perfect solution. The softer surface is, by nature sacrificial; it will eventually fail, its main virtue is the realization of an overall increase in the useful life of the prostheses. Additionally, fretting of the softer surface results in debris that may have deleterious effects on the health on the patient. [0004] The invention described herein is a particular type of ceramic-on-polymer prosthesis. Its unique compositional properties affords the traditional advantages of ceramic- on-polymer systems while avoiding their major disadvantage. [0005] The invention overcomes the major disadvantage generally inherent in prosthetic devices having hard surfaces articulating against soft surfaces. The basic technology upon which the improvement described herein is based, is described in U.S. Patent 5,037,438 to Davidson and U.S. Patent 6,447,550 to Hunter, et al., both of which are fully incorporated by reference herein. [0006] The longevity of medical implant devices is of prime importance as it is desirable that the implant should function for the complete lifetime of a patient. This is particularly true if the patient is young and the number of surgical revisions is to be kept to a minimum and preferably zero. To this end, orthopedic implant materials should preferably combine high strength, corrosion resistance and tissue compatibility. One of the variables affecting the longevity of load-bearing implants such as hip-joint implants is the rate of wear of the articulating surfaces and long-term effects of metal ion release. A typical hip-joint prosthesis includes a stem, a femoral head and an acetabular cup against which the femoral head articulates. Wear of either or both of the articulating surfaces results in an increasing level of wear particulates and "play" between the femoral head and the cup against which it articulates. Wear debris can contribute to adverse tissue reaction leading to bone resorption, and ultimately the joint must be replaced. [0007] The rate of wear of the acetabular cup and the femoral head surfaces of artificial hips is dependent upon a number of factors which include the relative hardness and surface finish of the materials which constitute the femoral head and the acetabular cup, the factional coefficient between the materials of the cup and head, the load applied and the stresses generated at the articulating surfaces. The most common material combinations currently used in the fabrication of hip-joint implants include femoral heads of cobalt, titanium, or zirconium alloys articulating against acetabular cups lined with organic polymers or composites of such polymers including, for instance, ultra-high molecular weight polyethylene (UHMWPE) and femoral heads of polished alumina in combination with acetabular cups lined with an organic polymer or composite or made of polished alumina. [0008] Of the factors which influence the rate of wear of conventional hip-joint implants, the most significant are patient weight and activity level. Additionally, heat generated by friction in the normal use of the implant has been shown to cause accelerated creep and wear of the polyethylene cup. Furthermore, there is a correlation between the factional moment which transfers torque loading to the cup and the frictional coefficient between the femoral head and the surface of the acetabular cup against which the head articulates. Cup torque has been associated with cup loosening. Thus, in general, the higher the coefficient of friction for a given load, the higher the level of torque generated. Ceramic bearing surfaces have been shown to produce significantly lower levels of frictional torque. It is also noteworthy that two of the three commonly used hip-joint systems as indicated above include a metallic femoral head articulating against an ultra high molecular weight polyethylene (UHMWPE) liner inside the acetabular cup. UHMWPE, being a polymeric material, is more susceptible to creep at higher temperatures than the commonly used metal alloys or ceramics due to its relatively lower melting point and is consequently more susceptible to wear than the alloys or ceramics. [0009] The original impetus for the inclusion of surfaces such as UHMWPE was that they would act sacrificially; they would fail slowly and fail before the harder surface, allowing for an overall extension of the useful life of the device. Additionally, polyethylene was thought to absorb shock much better than harder surfaces, thereby simulating the effect of real cartilage. While the advance in the art which was realized by the use of oxidized zirconium surfaces articulating against UHMWPE surfaces was a lessening of wear and cup loosening between the surface of the metallic component and the UHMWPE, the problem was not completely eliminated. Thus, the instant invention represents another advancement in the art, namely, a further improvement in wear and a simultaneous significant improvement of the creep problem associated with the prior art prostheses comprising polyethylene articulating against harder surfaces. [0010] It has also been found that metal prostheses are not completely inert in the body. Body fluids act upon the metals causing them to slowly corrode by an ionization process thereby releasing metal ions into the body. Metal ion release from the prosthesis is also related to the articulation and rate of wear of load bearing surfaces because, as may be expected, when a metallic femoral head, for instance, is articulated against UHMWPE, the passive oxide film which forms on the femoral head is constantly removed. The repassivation process constantly releases metal ions during this process. Furthermore, the presence of third-body wear (cement or bone debris) accelerates this process and micro- fretted metal particles can increase friction. Consequently, the UHMWPE liner inside the acetabular cup, against which the femoral head articulates, is subjected to accelerated levels of creep, wear, and torque. A reduction in these deleterious effects will also improve the problem of metal ion release. [0011] A number of attempts to correct these problems were the subject of much of the early work in this area. U.S. Pat. No. 4,145,764 to Suzuki taught a metal prosthesis plasma sprayed with a bonding agent which is in turn covered with a porous ceramic coating which would allow the in-growth of bone spicules into the pores. However, the Suzuki patent did not address the issue of friction or wear of orthopedic implant bearing surfaces but confined itself to the single issue of the biocompatibility of metal prostheses and did not address the issue of dimensional changes that occur when applying such a coating. U.S. Pat. No. 3,677,795 to Bokros is directed to the application of a carbide coating over a metallic prosthetic device. The method is said to produce a prosthetic device which has "excellent compatibility with body tissue and is non-thrombogenic". However, Bokros does not address the issues of friction, heating, creep and wear of orthopedic implant bearing surfaces, or changes induced in the mechanical properties of the underlying metal due to this high- temperature treatment. [0012] The aforementioned failings of the prior art were addressed in part by Davidson in U.S. Patent 5,037,438. In the '438 patent, Davidson teaches a zirconium or zirconium-containing metal alloy prosthesis coated via in-situ oxidation with a surface of blue-black or black oxidized zirconium which articulates against an organic polymer or polymer-based composite. The oxidized zirconium coating provides the prosthesis with a thin, dense, low friction, wear resistant, biocompatible surface ideally suited for use on articulating surfaces of joint prostheses wherein a surface or surfaces of the joint articulates, translates or rotates against mating joint surfaces. The oxidized zirconium coating described the '438 patent may therefore be usefully employed on the femoral heads or inside surfaces of acetabular cups of hip-joint implants or on the articulating surfaces of other types of prostheses, such as knee joints. Notably, the oxidized zirconium coating of the '438 patent was a specific type of oxidized zirconium. Oxidized zirconium presents itself in many forms, among them are white, beige, and blue-black. The white variety is particularly disfavored in the present application, as it tends to separate and break off of the substrate. Conventional oxidized zirconium surfaces formed, for example, by simple air oxidation will not be of the blue-black or black variety and will not possess the superior properties of the same which are recited in the '438 patent. The most important of these properties high hardness, low friction that results from the presence of the surface oxide. [0013] The specific blue-black or black oxidized zirconium coatings of the '438 patent were known in the art of mechanical bearings, having been described in U.S. Patent 2,987,352, which teaches a 700-1100 °F oxidation method to produce the specific blue-black or blue oxidized zirconium coating. A later issuing patent to Haygarth (U.S. Patent 4,671,824) teaches an alternative, salt-bath method to produce the desired coating. The blue- black or black oxidized zirconium of the instant invention possessing the necessary properties is primarily monoclinic crystal structure. This has been characterized by Hunter et al. (Hunter, G, et al., Mat. Res. Symp. Proc, (1999), 550, 337). [0014] The introduction of XLPE as a counter bearing surface in articulating prostheses was another unrelated attempt to address the problem of the relatively short service life of the UHMWPE component. Cross- linking of UHMWPE forms covalent bonds between polymer chains which retard the process of wear through the internal reinforcement of the individual polymer chains. However, XLPE is not without problems. The advantages of XLPE over other forms of polyethylene diminish as the roughness of the counter bearing surface increases and the operating temperature of device increases. Thus, a counter bearing surface, which possesses properties that prevent or improve the aforementioned conditions, would accentuate the advantages of XLPE over conventional forms of polyethylene. Additionally, there is anecdotal evidence that the improvement of wear characteristics comes at a cost of greater susceptibility to creep, particularly at elevated temperatures. [0015] Another prosthetic device which benefits from the novel oxidized zirconium/XLPE couple described herein are vertebral disc implants. These devices are an increasingly popular alternative to the spinal fusion surgical procedure. This alternative typically results in the maintenance of range of motion at the operative level once a damaged disc has been replaced with an implant. One type of vertebral disc implant, described in U.S. Patent No. 5,410,269 is that with two terminal plates which are connected to the endplates of the relevant vertebrae, and with a prosthesis core which cooperates with at least one terminal plate via an articular surface which permits a pivoting movement. Typically, the core material of these implants is high density polyethyelene, while the opposing plates are made of materials commonly found in conventional prosthetic devices, such as ceramic or metal. The use of disc implants having XLPE articulating against oxidized zirconium surfaces will not only decrease wear and improve the useful life of the device, but will also better maintain motion at the operative level upon removal of the damaged disc, relative to that of vertebral disc implants fabricated from conventional materials. [0016] XLPE devices have exhibited other deficiencies, with which the prior art has largely been concerned about. Free radicals formed during irradiation, however, can exist indefinitely if termination by cross-linking or other forms of recombination do not occur. Furthermore, reacted inteαnediates are continuously formed and decayed. Exposure of these free radical species at any time (e.g., during irradiation, shelf-aging, or in vivo aging) to molecular oxygen or any other reactive oxidizing agent can result in their oxidation. Extensive oxidation leads to a reduction in molecular weight, and subsequent changes in physical properties, including wear resistance. Many attempts have been made to improve the characteristics of XLPE. These attempts include radiation induced cross linked polyethylene (See U.S. Patents Nos. 5,728,748; 5,650,485; 5,543,471; 5,414,049; and 5,449,745 to Howmedica; Johnson & Johnson's EP 0737481 Al, see also Hamilton, J.V. et al, Scientific Exhibit, 64th AAOS Meeting, February 1997; Hamilton, J. V. et al, Trans 43rd ORS, 782, 1997; Biomet's World Patent Application No. 97/29787; see also Oonishi, H. et al, Radiat. Phys. Chem., 39(6), 495, 1992; Oonishi, H. et al, Mat. Sci: Materials in Medicine, 7, 753-63, 1966, Oonishi, H. et al, J. Mat. Sci: Materials in Medicine, 8, 11-18, 1997; U.S. Patent No. 5,879,400; World Patent Application WO 98/01085; U.S. Patent No. 6,165,220; EP 0729981 Al; U.S. Patent No. 6,017,975; and U.S. Patent 6,228,900, for chemical cross-linking of polyethylene (See EP 0722973 Al)). [0017] In the present invention, the improvement in the performance of XLPE is realized not through improvements in the XLPE composition itself, but rather through the use of oxidized zirconium or other abrasion resistant surface as a counter bearing surface against which the XLPE component articulates. The advantages of the instant invention will be the preservation of the desirable properties of XLPE with a simultaneous elimination of some of its negative properties. The '438 patent did not contemplate and nowhere does it teach, the use of the oxidized zirconium surfaces directly contacting surfaces of XLPE. The inventors have discovered that the unique properties of oxidized zirconium accentuate the inherent advantages of XLPE as a counter bearing surface. The superior strength and hardness, low friction, wear resistance, thermal conductivity, and biocompatibility characteristics of the blue-black or black oxidized zirconium is sufficient in itself to considerably slow and possibly prevent the degradative wear processes to which the prosthetic devices of the prior art have been subject. An unapparent synergy is realized because the unique properties of oxidized zirconium serve to improve the performance of XLPE as a counter bearing surface. These unexpected advantages are also present, to a lesser degree, when other abrasion resistant surfaces are used. [0018] The invention is directed to forming prosthetic devices of oxidized zirconium-on-XLPE, which represents a special species of oxidized zirconium-on-polymer devices, exhibiting even longer overall useful service life relative to conventional prostheses materials-on-UHMWPE. This is due not only to the advantages which inure upon the substitution of oxidized zirconium for conventional prosthesis materials, but also from the synergistic improvement in XLPE performance that is seen when XLPE articulates against oxidized zirconium. The invention is not limited to prostheses formed of zirconium or zirconium alloy. The prostheses substrate may itself be a composite material, only requiring that zirconium or zirconium alloy be present in the substrate layer immediately adjacent to the surface upon which the oxidized zirconium coating is to be formed.
SUMMARY OF THE INVENTION
[0019] As used herein, "a" or "an" may mean one or more. As used herein in the claim(s), when used in conjunction with the word "comprising", the words "a" or "an" may mean one or more than one. As used herein "another" may mean at least a second or more. [0020] As used herein, "abrasion resistant surface" is defined as a material surface having a greater hardness than the underlying substrate. When used in reference to the underlying substrate material, it is synonymous with "surface hardened". An oxidized zirconium surface is one example of an abrasion resistant surface. Others include, but are not limited to substrates coated with ceramic materials. [0021] As used herein, "base material" is defined as the material upon which a layer of oxidized zirconium is to be formed. It may be homogeneous, consisting of a single phase material, or it may be heterogeneous, consisting of a composite material of one or more substrate layers. [0022] As used herein, the term "contacting surface" refers to any two surfaces of the prosthetic device or medical implant that contact one another in either a load bearing (articulating) or non-load bearing (non-articulating) manner. [0023] As used herein, "substrate layer" is defined as a distinct chemical region or domain within the base material. A substrate layer may or may not be comprised of zirconium or zirconium alloy. [0024] As used herein, "vertebral disc prosthesis" is defined as any prosthetic device for implantation into the vertebra, regardless of configuration or design. [0025] As used herein, "zirconium alloy" is defined as any metal alloy containing zirconium in any amount greater than zero. Thus, an alloy in which zirconium is a minor constituent is considered a "zirconium alloy" herein. [0026] The following discussion contains illustration and examples of preferred embodiments for practicing the present invention. However, they are not limiting examples. Other examples and methods are possible in practicing the present invention and would be apparent to one of skill in the art upon reading the present disclosure. [0027] In another embodiment of the present invention, there is a knee prosthesis for implantation in a patient comprises a prosthesis body formed of zirconium or zirconium alloy. The prosthesis body has an implant portion for inserting into the body tissue of a patient, a bearing surface having at least one condyle on the prosthesis body, a tibial component comprised of cross-linked polyethylene and having a surface adapted to cooperate with the bearing surface, and a thin coating of blue-black or black oxidized zirconium directly on the bearing surface of the condyle portion. [0028] In specific embodiments of a knee prosthesis, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Preferably, the blue- black or black oxidized zirconium coating is from about 1 to about 5 microns thick. In a further embodiment, the knee prosthesis has an implant portion of the prosthesis body that has, at least in part, an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface stracture prosthesis, the irregular surface stαicture can have zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue-black or black oxidized zirconium. In another embodiment of the irregular surface structure prosthesis, the irregular surface structure can have zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium. [0029] In another embodiment of the invention, a hip prosthesis for implantation in a patient includes a hip prosthesis body for implantation into a femur which has a head portion formed at least in part of zirconium or zirconium alloy, a bearing surface on the head portion of the prosthesis body, and an acetabular cup having an inner surface comprising cross-linked polyethylene. A cooperating surface is adapted to engage and articulate with the bearing surface on the head portion. A thin coating of blue-black or black oxidized zirconium is formed directly on the exposed bearing surface of the head portion. [0030] In a specific embodiment of the hip prosthesis, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick. In another embodiment, the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed of zirconium or zirconium alloy beads connected to the outer surface of the prosthesis body. At least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium. In yet another embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body. At least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium. [0031] In another embodiment of the invention, a prosthesis for implantation in a patient includes a prosthesis body formed at least in part of zirconium or zirconium alloy. The prosthesis body includes an implant portion for insertion into the body tissue of the patient, a bearing surface on the prosthesis body, the bearing surface being sized and shaped to engage and articulate with a second bearing surface on another prosthesis portion. The second bearing surface is formed of a cross-linked polyethylene. The prosthesis also includes a coating of blue-black or black oxidized zirconium from about 1 to about 5 microns in thickness on the bearing surface. [0032] In a specific embodiment, the prosthesis body is a hip joint having a head portion as a bearing surface and another prosthesis portion is an acetabular cup, the head portion being adapted to cooperate with the inner surface of the acetabular cup, and the inner surface of the acetabular cup is also the second bearing surface. In another embodiment the prosthesis body is a knee joint and the bearing surface of the prosthesis body includes at least one condyle, and another prosthesis portion including a tibial component, with at least one condyle being adapted to cooperate with the tibial component. In a specific embodiment, the prosthesis body has an irregular surface structure adapted to accommodate tissue in-growth on at least a portion of the prosthesis body. In another embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed of zirconium or zirconium alloy beads connected to the outer surface of the prosthesis body, where at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium. In a specific embodiment, the irregular surface structure prosthesis has an irregular surface structure formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium. [0033] In another embodiment, the invention is directed towards a prosthesis for implantation in a patient which includes a prosthesis body formed at least in part of zirconium or zirconium alloy, the prosthesis body includes an implant portion for inserting into the body tissue of the patient, a bearing surface on the prosthesis body, a counter-bearing surface formed of cross-linked polyethylene and adapted to cooperate with the bearing surface and, a thin coating of blue-black or black oxidized zirconium directly on the bearing surface. [0034] In a specific embodiment, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick. In another embodiment, the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium. In yet another specific embodiment of the irregular surface structure, the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium. [0035] In another embodiment, a prosthesis for implantation in a patient, includes a prosthesis body comprising a substrate material. The prosthesis body includes an implant portion for inserting into the body tissue of the patient, a bearing surface on the prosthesis body formed of any abrasion resistant surface, and a counter-bearing surface formed of cross- linked polyethylene and adapted to cooperate with the bearing surface. In a specific embodiment, the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure prosthesis, the irregular surface structure has beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium. In another specific embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium. [0036] In a specific embodiment, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick. In another embodiment, the implant portion of the prosthesis body further includes an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure prosthesis, the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium. In yet another specific embodiment of the irregular surface structure, the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium. [0037] In another embodiment of the present invention, there is a prosthesis for implantation in a patient, comprising (a) a prosthesis body comprising a substrate material, said prosthesis body comprising an implant portion for inserting into the body tissue of the patient; (b) a bearing surface on the prosthesis body comprised of an abrasion resistant surface; and, (c) a counter-bearing surface comprising cross-linked polyethylene and adapted to cooperate with the bearing surface. In a specific embodiment, the implant portion of the prosthesis body further comprises an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In another embodiment, the irregular surface structure comprises beads attached to the outer surface of the prosthesis body, wherein at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium. In yet another embodiment, the irregular surface structure comprises wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium. In another embodiment, the prosthesis body further comprises at least one substrate layer. In another embodiment, the prosthesis body further comprises at least one substrate layer having a depth-dependent variable concentration of zirconium. [0038] In another embodiment, there is a vertebral disc prosthesis for implantation in a patient, the prosthesis comprising at least one surface of cross-linked polyethylene; at least one component formed of zirconium or zirconium alloy, said component having at least one surface of blue-black or black oxidized zirconium; and wherein at least one of the cross- linked polyethylene surfaces cooperates with at least one of the surfaces of blue-black or black oxidized zirconium. [0039] In a preferred embodiment, the vertebral disc prosthesis further comprises two prosthesis plates; and a prosthesis core; the prosthesis core cooperates with at least one prosthesis plate at surface permitting a rotational movement around a vertical axis. [0040] Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Most preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick. In another embodiment, the implant portion of the prosthesis body may further include an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure disc prosthesis, the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue- black or black oxidized zirconium. In yet another specific embodiment of the irregular surface structure, the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium. In another embodiment, the irregular surface may also comprise a textured surface. Such texturing methods include, but are not limited to, chemical etching, electrochemical etching, photoetching. These procedures may or may not utilize maskant materials. [0041] In another embodiment, the irregular surface may also comprise a surface having anchoring projections or teeth extending from the outer surface of the top and bottom plate. These anchoring projections or teeth improve fixation when they act against adjacent bone or tissue.
DESCRIPTION OF THE DRAWINGS
[0042] FIG. 1 is a schematic diagram depicting a hip joint prosthesis in position. [0043] FIG. 2 is a schematic diagram showing a typical hip joint prosthesis. [0044] FIG. 3 is a schematic diagram of a knee joint prosthesis in place. [0045] FIG. 4 is a schematic diagram of the parts of a typical knee joint. [0046] FIG. 5 is a schematic diagram of the vertebral disc prosthesis.
DETAILED DESCRIPTION OF THE INVENTION
[0047] The present invention provides low friction, wear and creep resistant, articulating, interfacial bearing surfaces for prosthetic devices. Preferably, the invention provides for a prosthetic device in which one contacting surface is formed of blue-black or black oxidized zirconium and another contacting surface is formed of XLPE. Alternatively, one contacting surface is formed of an abrasion resistant material and another contacting surface is XLPE. [0048] Oxidized zirconium presents itself in many forms, among them are white, beige, and blue-black. The white variety is particularly disfavored in the present application, as it tends to separate and break off of the substrate readily. Conventional oxidized zirconium surfaces formed, for example, by simple air oxidation will not be of the blue-black or black variety. [0049] The blue-black or black oxidized zirconium of the instant invention possessing the necessary properties is primarily monoclinic crystal structure and may include tetragonal zirconia. Its microstructure has been characterized by Hunter et. al. The specific blue-black or black oxidized zirconium coatings used herein were known in the art of mechanical bearings, having been originally taught by Watson in U.S. Patent 2,987,352. Davidson, in U.S. Patent 5,037,428, first taught the application of this form of oxidized zirconium to prosthetic devices. [0050] Importantly, the base materials upon which the oxidized zirconium coating is formed need not be fabricated totally of zirconium or zirconium alloy. The only requirement for the formation of an oxidized zirconium surface is zirconium or zirconium alloy material in the surface before the formation of the oxidized zirconium layer. Upon formation of the oxidized zirconium surface the former surface becomes the first substrate layer. For example, composite materials are possible embodiments of the present invention. This allows one to realize strength and weight advantages of prostheses having one or more different core materials. For example, a synthetic core material having high strength and being of light weight and having a zirconium or zirconium alloy veneer or outer layer is envisioned by the present invention. The interior of the base material may be of one or more than one material, allowing for varying degrees of heterogeneity in the overall fabrication, depending upon the application. Alternatively, a lesser degree of heterogeneity is possible. For example, a base material being relatively rich in zirconium or zirconium alloy at the surface and exhibiting a continuously decreasing zirconium content as a depth into the substrate increases is another possibility. In this latter example, no abrupt macroscopic phase boundary exists within the base material. These examples are meant to be merely illustrative and not exhaustive; variations in the possible embodiments which would be apparent to one of ordinary skill in the art upon a reading of this disclosure are part of the present invention. [0051] The XLPE useful in the present invention is polyethylene cross-linked by any means, irradiative or chemical being illustrative examples which are generally known in the art. Illustrative examples of the prosthetic devices for which the contact interfaces disclosed hererin find use are shown in the schematic diagrams, FIGS. 1-4. [0052] A typical hip joint assembly is shown in situ in FIG. 1 and FIG. 2. The hip joint stem 2 fits into the femur while the femoral head 6 of the prosthesis fits into and articulates against the inner lining 8 of an acetabular cup 10 which in turn is affixed to the pelvis as shown in FIG. 1. A porous metal bead or wire mesh coating 12 may be incorporated to allow stabilization of the implant by in-growth of surrounding tissue into the porous coating. Similarly, such a coating can also be applied to the acetabular component. The femoral head 6 may be an integral part of the hip joint stem 2 or may be a separate component mounted upon a conical taper at the end of the neck 4 of the hip joint prosthesis. This allows the fabrication of a prosthesis having a metallic stem and neck but a femoral head of a different material. [0053] This method of construction is often desirable because the use of composite materials allows for the localized optimization of a variety of parameters such as , weight, strength and wear resistance. Regardless of the materials, however, the femoral head articulates against the inner surface of the acetabular cup thereby causing wear and, in the long term, this may necessitate prosthesis replacement. This is especially the case where the femoral head is of metal and the acetabular cup is lined with an organic polymer or composite thereof. While these polymeric surfaces provide good, relatively low friction surfaces and are biocompatible, they are, as explained above, subject to wear and accelerated creep due to the frictional heat and torque to which they are subjected during ordinary use. [0054] In the present invention, the inner lining 8 is preferably formed of XLPE and the femoral head 6 is coated with a surface of blue-black or black oxidized zirconium. Preferably, the oxidized zirconium surface coating is 1-20 μm thick, but may be outside this range. It may alternatively be from about 1-5 μm thick. The wire mesh or metal bead surface 12 may be at least partially coated with a surface of blue-black or black oxidized zirconium to promote in-growth of tissue or bone into the device, thereby stabilizing its position. [0055] A typical knee joint prosthesis is shown in situ in FIG. 3 and FIG. 4. The knee joint includes a femoral component 20 and a tibial component 30. The femoral component includes condyles 22 which provide the articulating surface of the femoral component and pegs 24 for affixing the femoral component to the femur. The tibial component 30 includes a tibial base 32 with a peg 34 for mounting the tibial base onto the tibia. A tibial platform 36 is mounted atop the tibial base 32 and is supplied with grooves 38 similar to the shape of the condyles 22. The bottom surfaces of the condyles 26 contact the tibial platform's grooves 38 so that the condyles articulate within these grooves against the tibial platform. In the present invention, the condyles 22 are coated with a surface of blue- black or black oxidized zirconium and the grooves 38 on the tibial platform 36 are comprised of XLPE. Part or all of the remainder of the femoral component 20 and a tibial component 30 may have a surface coating of blue-black or black oxidized zirconium. Preferably, the surface coatings are 1-20 μm thick, but may be outside this range. They may alternatively be from about 1-5 μm thick. As in the case of the hip joint, porous bead or wire mesh coatings can also be applied to either the tibial or femoral components of the knee or both. These porous bead or wire mesh coatings of the knee prosthesis may also be at least partially coated with a surface of blue-black or black oxidized zirconium to promote in-growth of tissue or bone into the device, thereby stabilizing its position. [0056] The base (i.e., substrate) zirconium containing metal alloys are cast or machined by conventional methods to the shape and size desired to obtain a prosthesis substrate. The substrate is then subjected to process conditions which cause the natural (in situ) formation of a tightly adhered, diffusion-bonded coating of oxidized zirconium on its surface. The process conditions include, for instance, air, steam, or water oxidation or oxidation in a salt bath. These processes ideally provide a thin, hard, dense, blue-black or black, low- friction wear-resistant oxidized zirconium film or coating of thickness typically on the order of several microns (10~6 meters) on the surface of the prosthesis substrate. Below this coating, diffused oxygen from the oxidation process increases the hardness and strength of the underlying substrate metal. [0057] Importantly, the base materials need not be formed totally of zirconium or zirconium alloy. The only requirement for the formation of an oxidized zirconium surface is that zirconium or zirconium alloy material comprises the surface layer of the base material before the formation of the oxidized zirconium layer. For example, composite materials are possible embodiments of the present invention. This allows one to realize strength and weight advantages of prostheses having one or more different core materials. For example, a synthetic core material having high strength and being of light weight surrounded by a zirconium or zirconium alloy veneer or outer layer is a possible embodiment of the present invention. One or more substrata may comprise the base material and these substrata may be comprised of any suitable material which may or may not include zirconium or zirconium alloy. Alternatively, the base material may consist of a continuous phase in which the concentration of zirconium or zirconium alloy varies with depth into the base material. For example, the surface at which the coating of oxidized zirconium is formed may be relatively rich in zirconium, with this concentration falling off as the distance into the base material (i.e., away from the surface) increases. Variations on the general embodiment are within the scope of the present invention in light of the disclosure. [0058] Representative methods for the formation of the surface coating of blue- black or black oxidized zirconium have been described previously in U.S. Patents, 2,987,352 to Watson and 5,037,428 to Davidson, which are incorporated by reference as though fully set forth herein. A coating thickness of 1 to 5 μm is preferred. Conditions useful for the fabrication of surfaces of varying thickness are described in U.S. Patent 5,037,428. Methods for controlling the uniformity of the oxidized zirconium coating are described in U.S. Patent 6,447,550, which is incorporated by reference as though fully set forth herein. [0059] Oxygen, niobium, and titanium are common alloying elements in the alloy with oftentimes the presence of hafnium. While such zirconium containing alloys may be custom formulated by conventional methods known in the art of metallurgy, a number of suitable alloys are commercially available. Illustrative examples of these commercial alloys include among others Zircadyne 705, Zircadyne 702, and Zircalloy. [0060] These diffusion-bonded, low friction, highly wear resistant oxidized zirconium coatings are applied to one of the contacting surfaces of orthopedic implants subject to conditions of wear. Such surfaces include the articulating surfaces of knee joints, elbows and hip joints. In the case of hip joints, the femoral head and stem are typically fabricated of metal alloys while the acetabular cup may be fabricated from ceramics. The only requirement is that the surface of the base material of the contacting surface of the device must be of zirconium or zirconium alloy such that upon surface oxidation under the appropriate conditions, measurable surface concentrations of oxidized zirconium are formed. Substrate layers extending into the interior of the base material may consist of one or more materials, any, or, or none of which may be of zirconium or zirconium alloy. [0061] The wear advantages of XLPE over conventional polyethylene are diminished under certain conditions. For instance as the roughness of the counter bearing surface increases, XLPE approaches conventional polyethylene in its wear resistance (See, e.g., McKellop et al., "Wear of Gamma-Crosslinked Polyethylene Acetabular Cups Against Roughened Femoral Balls", Clin. Orthop., (1999) 369, pp. 73-82). The wear advantage of XLPE over conventional polyethylene enhanced by using a low roughness, abrasion resistant articulating surfaces against the XLPE. [0062] There is anecdotal evidence that cross-linked polyethylene is more prone to creep than conventional polyethylene. Thus, there is a potential trade-off to be made in gaining the superior wear characteristics of XLPE over conventional PE in medical implants. However, the articulating bearing surfaces unexpectedly diminished this disadvantage. Creep is a relatively slow plastic deformation process which is more prominent at higher temperatures as a material more closely approaches its melting point. (See "Metallurgy Fundamentals", D.A. Brandt and J.C. Warner, Goodheart-Wilcox Pub. Co., Inc., p. 57, 1999). A contacting surface that is a thermal conductor will diminish the creep resistance advantage of conventional polyethylene over XLPE through its ability to pass heat and avoid a localized rise in temperature. As the temperature of either polymer rises, its ability to withstand protracted stress-strain loads decreases, such that prostheses made of either conventional polyethylene or XLPE are subject to failure. At temperatures significantly lower than the melting point, the two polymers more closely approach one another in their creep resistance. [0063] Oxidized zirconium, is unique with respect to the excellent thermal conductivity it possesses relative to other conventional prosthetic materials. It combines excellent surface roughness characteristics with very high thermal conductivity. In this way, it possesses the relevant beneficial characteristics (in terms of XLPE) of metal and ceramics while avoiding the relevant disadvantages of the former and outperforming the latter. Thus, while all abrasion resistant surfaces such as zirconia and alumina would enjoy the benefit of reduced wear of XLPE and at least some improvement in creep resistance, oxidized zirconium would enjoy both a significant reduced wear and a significant reduced creep susceptibility. Table 1 below schematically illustrates these characteristics.
Table 1 : Relative Performance of Various Prostheses Surfaces with Respect to Various Characteristics and Overall Degradative Effects on Counter Bearing Surfaces
Figure imgf000019_0001
Figure imgf000020_0001
3 = Excellent 2 = Good 1 = Fair 0 = Poor [0064] The prostheses of the instant invention exhibit design advantages in a variety of applications. Importantly, the wear resistance characteristics of XLPE, already superior relative to UHMWPE is fully realized while the creep characteristics are improved when XLPE articulates against abrasion resistant surfaces. These improvements are further enhanced when XLPE articulates against oxidized zirconium, allowing for the polymer lining to be constructed of lower thickness than in conventional prostheses. The superiority of oxidized zirconium counter bearing surfaces in terms of low friction and high thermal conductivity allows for polymer linings that are thinner still. The synergistic result is a potentially smaller prosthesis having weight advantages over conventional prostheses, which requires less bone resection, greater conformity and contact area, and exhibits reductions in contact stress, an increase in range of motion, and a decreased chance of dislocation. A smaller amount of polymer material is expected to result in a lower likelihood of osteolysis (resulting from a lesser likelihood of material migration) while having the same or greater component service life. Decreases in mass of the prosthesis is expected to be of greater significance in hip applications which are typically larger than knee prostheses and have a smaller range of motion. [0065] The present invention is also useful in knee prostheses. Knee prostheses typically are of two varieties: mobile bearing knees (MBK) and fixed bearing knees (FBK). Referring to FIGs 3 and 4, the MBK is characterized by having its articulating tibial component 30 movable relative to the tibial platform 36. This results in wear and creep on both the top and bottom of the tibial component 30. In contrast, this interface in the FBK is fixed and the only movement is between the top of the tibial component and the condyles 22. As a result, the MBK has a greater range of motion but suffers from greater wear and creep than an FBK. XLPE generally offers greater wear and comparable creep resistance over UHMWPE when articulating against abrasion resistant surfaces. This characteristic is enhanced where the tibial tray is formed of oxidized zirconium. This same advantage is also seen in FBK prostheses, but is limited to the articulating interface between the tibial component 30 and the condyles 22. [0066] Zirconium or zirconium alloy can also be used to provide an irregular surface such as, but not limited to, porous bead or wire mesh surface to which surrounding bone or other tissue may integrate to stabilize the oxidized zirconium-on-oxidized zirconium prosthesis. These porous coatings can be treated simultaneously by the oxidation treatment in a manner similar to the oxidation of the base prosthesis for the elimination or reduction of metal ion release. Furthermore, zirconium or zirconium alloy can also be used as a surface layer applied over conventional implant materials prior to in situ oxidation and formation of the oxidized zirconium coating. [0067] The present invention also finds utility in the area of vertebral disc implants. One common cause of low lumbar back pain is "degenerative disc disease." The condition may take many different forms (e.g. a herniated disc or a collapsed disc). Any of these conditions can result from a disc that has lost its proper form and therefore does not function properly, causing significant pain when you move or attempt to perform normal daily activities. The purpose, then, of any spinal surgery or disc surgery is to relieve this recurring back pain. One common surgical method, referred to as "spinal fusion surgery", for relieving this type of back pain is to stop the movement of the afflicted disc or motion segment by fusing the vertebrae together in that specific area. There are different methods of spinal fusion surgery, but most involve placing metal implants (e.g. plates, rods and screws) into the vertebrae or bones of the spine to hold them still and achieve what is referred to as a "fusion". This type of procedure may also involve placing bone or fusion cages into the disc space to assist in fusing the spine bones together. [0068] As an alternative to current spine fusion techniques, disc implantation is intended to maintain motion at the operative level. The most common for of this is total disc replacement, whereby the damaged disc has been removed and replaced by a disc implant. Total disc replacement theoretically protects the discs at adjacent levels by sharing or distributing the stress through the lower back during normal activities such as lifting and bending. Surgeons have explored the idea of prosthetic replacements for damaged or degenerated intervertebral discs. As the intervertebral disc and its biomechanical behavior are very complex, the engineering a disc replacement has been challenging. A typical vertebral disc implant is described in U.S. Patent No. 5,401,269 which is incorporated by reference as though fully disclosed herein. [0069] The present invention improves upon the present state of the art by incorporating cooperating surfaces of blue-black or black oxidized zirconium and XLPE. In another embodiment, there is a vertebral disc prosthesis for implantation in a patient, the device comprising at least one surface of cross-linked polyethylene and at least one surface of blue-black or black oxidized zirconium in which at least one of the cross-linked polyethylene surfaces cooperates with at least one of the surfaces of blue-black or black oxidized zirconium. [0070] Preferably, the vertebral disc prosthesis comprises a top plate, a bottom plate, and a core, in which the top and bottom plates are comprised of zirconium alloys and the top and bottom plates further comprise surfaces of blue-black or black oxidized zirconium, and the core comprises cross-linked polyethylene. FIG. 5 shows a schematic of a vertebral disc implant (40) to which the present invention may be applied. The core (42) of the implant is typically constructed of a relatively soft material, usually conventional high molecular weight polyethylene. The top (44) and bottom (46) plates are typically constructed of conventional materials such as cobalt-chromium. In the present invention the top (44) and bottom (46) plates are made from zirconium or a zirconium alloy wherein at least a part its surface which contacts the core (42) is oxidized to blue-black or blue oxidized zirconium. The core (42) is made from XLPE. The oxidized zirconiurn/XLPE couple has all the advantages described above, including improved creep resistance, decreased wear, etc. [0071] Preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 20 microns thick. Most preferably, the thin blue-black or black oxidized zirconium coating is from about 1 to about 5 microns thick. Like the oxidized zirconium implants discussed above, the implant portion of the prosthesis body may further include an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body. In a specific embodiment of the irregular surface structure disc prosthesis, the irregular surface structure is formed at least in part of zirconium or zirconium alloy beads attached to the outer surface of the prosthesis body, with at least a portion of the surface of the beads being oxidized to blue-black or black oxidized zirconium. In yet another specific embodiment of the irregular surface structure, the irregular surface structure is formed of zirconium or zirconium alloy wire mesh connected to the outer surface of the prosthesis body, with at least a portion of the surface of the mesh being oxidized to blue-black or black oxidized zirconium. The irregular surface, when used, is ideally located on the outside surfaces (48) of the top plate (44) and the bottom plate (46). However, the irregular surface may be located in any area where improved adhesion to bone or tissue is desirable. [0072] The irregular surface may also comprise a textured surface. The surface is both textured and oxidized. Non-limiting examples of such surfaces are described in copending U.S. Application Serial No. 10,313,205, filed Dec. 6, 2002, and incorporated by reference as though fully described herein. The resulting surface is a textured, oxidized zirconium surface. Such texturing methods include, but are not limited to, chemical etching, electrochemical etching, photoetching. These procedures may or may not utilize maskant materials. [0073] The irregular surface may also comprise a surface having anchoring projections or teeth extending from the outer surface of the top and bottom plate. These optional components (50) are shown in FIG. 5. These anchoring projections or teeth improve fixation when they act against adjacent bone or tissue. [0074] While only a specific configuration and design of a vertebral disc implant was discussed in detail, it is understood by one of ordinary skill in the art that any configuration that is amenable to one or more cooperating surfaces of blue-black or black oxidized zirconium and cross-linked polyethylene is encompassed by the present invention. [0075] Although the invention has been described with reference to its preferred embodiments, those of ordinary skill in the art may, upon reading this disclosure, appreciate changes and modifications which may be made and which do not depart from the scope and spirit of the invention as described above or claimed hereafter. Moreover, the scope of the present application is not intended to be limited to the particular embodiments described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure of the present invention, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present invention. Accordingly, the appended claims are intended to include within their scope such processes, machines, manufacture, compositions of matter, means, methods, or steps.
REFERENCES
[0076] All patents and publications mentioned in the specification are indicative of the level of those skilled in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference. U.S. Patent 5,037,438 8/1991 Davidson
U.S. Patent 4,145,746 3/1979 Suzuki et al.
U.S. Patent 3,677,795 7/1972 Bokros et al.
U.S. Patent 2,987,352 2/1958 Watson
U.S. Patent 4,671,824 6/1987 Haygarth
U.S. Patent 6,447,550 9/2002 Hunter et al.
U.S. Patent 5,401,269 3/1995 Buttner-Janz et al
U.S. Patent 4,932,969 6/1990 Frey et al.
U.S. Patent 6,562,072 5/2003 Fuss et al.
U.S. Patent 5,514,180 5/1996 Heggeness et al.
Hunter, G. et al., Mat. Res. Soc. Symp. Proc, 1999, 550, 337.
McKellop et al., "Wear of Garnma-Crosslinked Polyethylene Acetabular Cups Against Roughened Femoral Balls", Clin. Orthop., (1999) 369, pp. 73-82.
Hunter et al., "Abrasive Wear of Oxidized Zr-2.5Nb, CoCrMo, and Ti-6A1-4V Against Bone Cement", 6th World Biomaterials Cong. Trans., Society for Biomaterials, Minneapolis, MN, (2000), p. 835

Claims

What is claimed is:
1. A vertebral disc prosthesis for implantation in a patient, said prosthesis comprising: at least one surface of cross-linked polyethylene; and, at least one component formed of zirconium or zirconium alloy and having at least one surface of blue-black or black oxidized zirconium, said vertebral disc implant further characterized by at least one surface of cross-linked polyethylene cooperating with at least one surface of blue-black or black oxidized zirconium.
2. The vertebral disc prosthesis of claim 1, further characterized by: two prosthesis plates; and, a prosthesis core, wherein said prosthesis core cooperates with at least one prosthesis plate permitting a rotational movement around a vertical axis.
3. The vertebral disc prosthesis of claim 1 or 2, characterized by a surface of blue-black or black oxidized zirconium having a thickness from about 1 to 20 microns thick.
4. The vertebral disc prosthesis of claim 1 or 2, characterized by a surface of blue-black or black oxidized zirconium having a thickness from 1 to 5 microns thick.
5. The vertebral disc prosthesis of claim 1 or 2, characterized by an irregular surface structure adapted to accommodate tissue in-growth on a portion of the prosthesis body.
6. The vertebral disc prosthesis of claim 5, characterized by an irregular surface structure having beads attached to the outer surface of the prosthesis body, wherein at least a portion of the surface of the beads is oxidized to blue-black or black oxidized zirconium.
7. The vertebral disc prosthesis of claim 5 characterized by an irregular surface structure having wire mesh connected to the outer surface of the prosthesis body, wherein at least a portion of the surface of the mesh is oxidized to blue-black or black oxidized zirconium.
8. The vertebral disc prosthesis of claim 5 characterized by an irregular surface structure having a textured surface.
9. The vertebral disc prosthesis of claim 5 characterized by an irregular surface structure having anchoring projections or teeth.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007103519A3 (en) * 2006-03-08 2007-11-15 Reell Prec Mfg Corp Shearing-force mechanism with cross-linked thermoplastic
JP2008061897A (en) * 2006-09-08 2008-03-21 Saga Univ Living body implant
US8257438B2 (en) 2005-04-12 2012-09-04 Warsaw Orthopedic, Inc. Methods and devices for preserving motion in an articulating prosthetic disc
US8523476B2 (en) 2010-06-01 2013-09-03 Reell Precision Manufacturing Corporation Positioning and damper device using shear force from cyclic differential compressive strain of a cross-linked thermoplastic
US8959717B2 (en) 2012-03-12 2015-02-24 Reell Precision Manufacturing Corporation Circumferential strain rotary detent
US10004604B2 (en) 2006-09-08 2018-06-26 Kyocera Corporation Bioimplant for artifical joint with evanescent coating film
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Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2824261B1 (en) 2001-05-04 2004-05-28 Ldr Medical INTERVERTEBRAL DISC PROSTHESIS AND IMPLEMENTATION METHOD AND TOOLS
US20030153979A1 (en) * 2002-02-11 2003-08-14 Dean Hughes Posterior stabilized knee system prosthetic devices employing diffusion-hardened surfaces
US6824278B2 (en) * 2002-03-15 2004-11-30 Memx, Inc. Self-shadowing MEM structures
EP2002805A3 (en) * 2002-09-19 2009-01-07 Malan De Villiers Intervertebral prosthesis
FR2846550B1 (en) 2002-11-05 2006-01-13 Ldr Medical INTERVERTEBRAL DISC PROSTHESIS
EP2329778A3 (en) * 2003-01-31 2012-06-20 Spinalmotion, Inc. Spinal midline indicator
WO2004066884A1 (en) 2003-01-31 2004-08-12 Spinalmotion, Inc. Intervertebral prosthesis placement instrument
WO2004084742A1 (en) * 2003-03-24 2004-10-07 Theken Surgical Llc Spinal implant adjustment device
WO2004089240A2 (en) * 2003-04-04 2004-10-21 Theken Disc, Llc Artificial disc prosthesis
US20090076614A1 (en) * 2007-09-17 2009-03-19 Spinalmotion, Inc. Intervertebral Prosthetic Disc with Shock Absorption Core
US10052211B2 (en) 2003-05-27 2018-08-21 Simplify Medical Pty Ltd. Prosthetic disc for intervertebral insertion
WO2004105638A2 (en) 2003-05-27 2004-12-09 Spinalmotion, Inc. Prosthetic disc for intervertebral insertion
US7575599B2 (en) * 2004-07-30 2009-08-18 Spinalmotion, Inc. Intervertebral prosthetic disc with metallic core
US7621956B2 (en) * 2003-07-31 2009-11-24 Globus Medical, Inc. Prosthetic spinal disc replacement
US7288115B2 (en) * 2004-01-02 2007-10-30 Zimmer Technology, Inc. Multipart component for an orthopaedic implant
PT2113227E (en) 2004-02-04 2015-10-16 Ldr Medical Intervertebral disc prosthesis
FR2865629B1 (en) 2004-02-04 2007-01-26 Ldr Medical INTERVERTEBRAL DISC PROSTHESIS
US7585326B2 (en) 2004-08-06 2009-09-08 Spinalmotion, Inc. Methods and apparatus for intervertebral disc prosthesis insertion
WO2006042486A1 (en) * 2004-10-18 2006-04-27 Buettner-Janz Karin Intervertebral disk endoprosthesis having a motion-adapted edge for the lumbar and cervical spine
FR2879436B1 (en) 2004-12-22 2007-03-09 Ldr Medical INTERVERTEBRAL DISC PROSTHESIS
US8083797B2 (en) * 2005-02-04 2011-12-27 Spinalmotion, Inc. Intervertebral prosthetic disc with shock absorption
FR2887762B1 (en) 2005-06-29 2007-10-12 Ldr Medical Soc Par Actions Si INTERVERTEBRAL DISC PROSTHESIS INSERTION INSTRUMENTATION BETWEEN VERTEBRATES
FR2891135B1 (en) 2005-09-23 2008-09-12 Ldr Medical Sarl INTERVERTEBRAL DISC PROSTHESIS
FR2893838B1 (en) 2005-11-30 2008-08-08 Ldr Medical Soc Par Actions Si PROSTHESIS OF INTERVERTEBRAL DISC AND INSTRUMENTATION OF INSERTION OF THE PROSTHESIS BETWEEN VERTEBRATES
US20070135923A1 (en) * 2005-12-14 2007-06-14 Sdgi Holdings, Inc. Ceramic and polymer prosthetic device
US7867279B2 (en) * 2006-01-23 2011-01-11 Depuy Spine, Inc. Intervertebral disc prosthesis
US8734519B2 (en) * 2006-04-12 2014-05-27 Spinalmotion, Inc. Posterior spinal device and method
US20080027431A1 (en) * 2006-07-29 2008-01-31 Williams James M Coated medical device and method of making
US20080195221A1 (en) * 2007-01-22 2008-08-14 Zimmer Gmbh Implant and a method for partial replacement of joint surfaces
US8465546B2 (en) 2007-02-16 2013-06-18 Ldr Medical Intervertebral disc prosthesis insertion assemblies
US9370427B2 (en) * 2007-04-13 2016-06-21 Christopher G. Sidebotham Bone-compliant femoral stem
FR2916956B1 (en) 2007-06-08 2012-12-14 Ldr Medical INTERSOMATIC CAGE, INTERVERTEBRAL PROSTHESIS, ANCHORING DEVICE AND IMPLANTATION INSTRUMENTATION
US20090043391A1 (en) 2007-08-09 2009-02-12 Spinalmotion, Inc. Customized Intervertebral Prosthetic Disc with Shock Absorption
WO2009029207A1 (en) * 2007-08-27 2009-03-05 Vladimir Shur Knee prosthesis
US8758441B2 (en) * 2007-10-22 2014-06-24 Spinalmotion, Inc. Vertebral body replacement and method for spanning a space formed upon removal of a vertebral body
WO2009094477A1 (en) * 2008-01-25 2009-07-30 Spinalmotion, Inc. Compliant implantable prosthetic joint with preloaded spring
US8764833B2 (en) * 2008-03-11 2014-07-01 Spinalmotion, Inc. Artificial intervertebral disc with lower height
US9034038B2 (en) * 2008-04-11 2015-05-19 Spinalmotion, Inc. Motion limiting insert for an artificial intervertebral disc
KR20110009216A (en) * 2008-05-05 2011-01-27 스피날모우션, 인코포레이티드 Polyaryletherketone artificial intervertebral disc
US9220603B2 (en) * 2008-07-02 2015-12-29 Simplify Medical, Inc. Limited motion prosthetic intervertebral disc
WO2010000766A2 (en) * 2008-07-03 2010-01-07 Ceramtec Ag Intervertebral disc endoprosthesis
US8642112B2 (en) * 2008-07-16 2014-02-04 Zimmer, Inc. Thermally treated ceramic coating for implants
EP2299944A4 (en) 2008-07-17 2013-07-31 Spinalmotion Inc Artificial intervertebral disc placement system
EP2299941A1 (en) * 2008-07-18 2011-03-30 Spinalmotion Inc. Posterior prosthetic intervertebral disc
US9408718B2 (en) * 2009-12-31 2016-08-09 Rhausler, Inc. Inter-vertebral implant with angled plate
US8945226B2 (en) * 2009-12-31 2015-02-03 Rhausler Vertebral spacer
US20120116457A1 (en) * 2010-11-06 2012-05-10 Limited Liability Company; Stabilizer for assisting stabilization of a spinal implant and method of using the stabilizer
US8496713B2 (en) * 2010-12-10 2013-07-30 Globus Medical, Inc. Spine stabilization device and methods
US8998991B2 (en) * 2011-02-23 2015-04-07 Globus Medical, Inc. Six degree spine stabilization devices and methods
RU2550973C2 (en) 2011-03-11 2015-05-20 Фбс Девайс Апс Vertebral implant, instrument for manufacturing and application method
CN107361885A (en) * 2017-07-31 2017-11-21 北京爱康宜诚医疗器材有限公司 Intervertebral disk prosthesis

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401269A (en) * 1992-03-13 1995-03-28 Waldemar Link Gmbh & Co. Intervertebral disc endoprosthesis
WO2003008008A1 (en) * 2001-07-18 2003-01-30 Smith & Nephew, Inc. Prosthetic devices employing oxidized zirconium surfaces contacting surfaces of cross-linked polyethylene
US20030078667A1 (en) * 1999-06-04 2003-04-24 Depuy Acromed, Incorporated Orthopedic implant

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4281420A (en) * 1979-02-15 1981-08-04 Raab S Bone connective prostheses adapted to maximize strength and durability of prostheses-bone cement interface; and methods of forming same
US4944974A (en) * 1984-10-24 1990-07-31 Zachariades Anagnostis E Composite structures of ultra-high-molecular-weight polymers, such as ultra-high-molecular-weight polyethylene products, and method of producing such structures
CH671691A5 (en) * 1987-01-08 1989-09-29 Sulzer Ag
US5152794A (en) * 1989-07-25 1992-10-06 Smith & Nephew Richards Inc. Zirconium oxide and nitride coated prothesis for reduced microfretting
CA2021814C (en) * 1989-07-25 2002-04-02 James A. Davidson Zirconium alloy-based prosthesis with zirconium oxide or zirconium nitride coating
US5370694A (en) * 1989-07-25 1994-12-06 Smith & Nephew Richards, Inc. Zirconium oxide and nitride coated endoprostheses for tissue protection
US5037438A (en) * 1989-07-25 1991-08-06 Richards Medical Company Zirconium oxide coated prosthesis for wear and corrosion resistance
EP0562782A3 (en) * 1992-03-24 1994-05-25 Smith & Nephew Richards Inc Dual composition coupler for modular medical implants
JPH06327705A (en) * 1993-05-26 1994-11-29 Kobe Steel Ltd Artificial joint
US5414049A (en) * 1993-06-01 1995-05-09 Howmedica Inc. Non-oxidizing polymeric medical implant
GB9322962D0 (en) 1993-11-08 1994-01-05 Gillette Co Antiperspirants
US5514180A (en) * 1994-01-14 1996-05-07 Heggeness; Michael H. Prosthetic intervertebral devices
US6290726B1 (en) * 2000-01-30 2001-09-18 Diamicron, Inc. Prosthetic hip joint having sintered polycrystalline diamond compact articulation surfaces
WO1996009330A1 (en) * 1994-09-21 1996-03-28 Bmg Incorporated Ultrahigh-molecular-weight polyethylene molding for artificial joint and process for producing the molding
US6051751A (en) * 1995-01-20 2000-04-18 Spire Corporation Arthroplasty process for securely anchoring prostheses to bone, and arthroplasty products therefor
CA2166450C (en) * 1995-01-20 2008-03-25 Ronald Salovey Chemically crosslinked ultrahigh molecular weight polyethylene for artificial human joints
US5577368A (en) 1995-04-03 1996-11-26 Johnson & Johnson Professional, Inc. Method for improving wear resistance of polymeric bioimplantable components
US5674293A (en) * 1996-01-19 1997-10-07 Implant Sciences Corp. Coated orthopaedic implant components
US5879400A (en) * 1996-02-13 1999-03-09 Massachusetts Institute Of Technology Melt-irradiated ultra high molecular weight polyethylene prosthetic devices
US6228900B1 (en) * 1996-07-09 2001-05-08 The Orthopaedic Hospital And University Of Southern California Crosslinking of polyethylene for low wear using radiation and thermal treatments
EP1795212A3 (en) 1996-07-09 2007-09-05 Orthopaedic Hospital Crosslinking of polyethylene for low wear using radiation and thermal treatments
US6017975A (en) * 1996-10-02 2000-01-25 Saum; Kenneth Ashley Process for medical implant of cross-linked ultrahigh molecular weight polyethylene having improved balance of wear properties and oxidation resistance
EP1028760B1 (en) 1996-10-15 2004-04-14 Orthopaedic Hospital Wear resistant surface-gradient cross-linked polyethylene
JP4491076B2 (en) * 1997-03-27 2010-06-30 スミス アンド ネフュー インコーポレーテッド Zirconium alloy surface oxidation method and product by this method
AT405367B (en) * 1998-01-23 1999-07-26 Fuss Franz K Dipl Biomech Dr Implant
CA2256963A1 (en) * 1998-12-23 2000-06-23 Nigel Copner Three port resonant optical cavity
US6113638A (en) * 1999-02-26 2000-09-05 Williams; Lytton A. Method and apparatus for intervertebral implant anchorage
US6818172B2 (en) * 2000-09-29 2004-11-16 Depuy Products, Inc. Oriented, cross-linked UHMWPE molding for orthopaedic applications
US6726725B2 (en) * 2001-06-01 2004-04-27 Smith & Nephew, Inc. Prosthetic devices employing contacting oxidized zirconium surfaces

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401269A (en) * 1992-03-13 1995-03-28 Waldemar Link Gmbh & Co. Intervertebral disc endoprosthesis
US20030078667A1 (en) * 1999-06-04 2003-04-24 Depuy Acromed, Incorporated Orthopedic implant
WO2003008008A1 (en) * 2001-07-18 2003-01-30 Smith & Nephew, Inc. Prosthetic devices employing oxidized zirconium surfaces contacting surfaces of cross-linked polyethylene

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8257438B2 (en) 2005-04-12 2012-09-04 Warsaw Orthopedic, Inc. Methods and devices for preserving motion in an articulating prosthetic disc
WO2007103519A3 (en) * 2006-03-08 2007-11-15 Reell Prec Mfg Corp Shearing-force mechanism with cross-linked thermoplastic
JP2008061897A (en) * 2006-09-08 2008-03-21 Saga Univ Living body implant
US10004604B2 (en) 2006-09-08 2018-06-26 Kyocera Corporation Bioimplant for artifical joint with evanescent coating film
US10610614B2 (en) 2006-09-08 2020-04-07 Kyocera Corporation Bioimplant with evanescent coating film
US11278642B2 (en) 2006-09-08 2022-03-22 Takao Hotokebuchi Bioimplant with evanescent coating film
US8523476B2 (en) 2010-06-01 2013-09-03 Reell Precision Manufacturing Corporation Positioning and damper device using shear force from cyclic differential compressive strain of a cross-linked thermoplastic
US8959717B2 (en) 2012-03-12 2015-02-24 Reell Precision Manufacturing Corporation Circumferential strain rotary detent

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