Radiovisible hydrogel intervertebral disc nucleus

a radiovisible hydrogel and disc nucleus technology, applied in the field of prosthetic intervertebral disc nucleus, can solve the problems of degeneration of intervertebral disc, final pathological changes, back pain, etc., and achieve the effect of preventing fluid leakage, restoring the normal function of the nucleus, and preventing fluid leakag

Inactive Publication Date: 2006-11-16
HOWMEDICA OSTEONICS CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0018] The primary disadvantage of the invention of Substad et al., Patil, Kenna and Lee et al., is that use of their prosthesis requires complete replacement of the natural disc which involves numerous surgical difficulties. Secondly, the intervertebral disc is a complex joint, anatomically and functionally, comprising the aforementioned three component structures, each of which has its own unique structural characteristics. Designing and fabricating such a complicated prosthesis from acceptable materials, which will mimic the function of the natural disc, is very difficult. A further problem is the difficulty of preventing the prosthesis from dislodging. Fourthly, even for prostheses which are only intended for replacing the nucleus, a major obstacle has been to find a material which is similar to the natural and is also able to restore the normal function of the nucleus. Hydrophobic elastomers and thermoplastic polymers are not desirable for use in the prosthetic nuclei due to their significant inherent differences from the natural nucleus e.g., lack of hydrophilicty, in the elastomers, and lack of flexibility in their thermoplasts.
[0019] These problems are not solved by Kuntz, who uses elastic rubber plugs, or by Froning and Ray et al., who use bladders, or capsules, respectively, which are filled with a fluid or thixotropic gel. According to the Ray and Froning patents, liquid was used to fill the capsules and bladders, respectively, thereby requiring that their membranes be completely sealed to prevent fluid leakage. As a consequence, those devices cannot completely restore the function of the nucleus which allows body fluid to diffuse in and out during cyclic loading thereby providing the nutrients the disc needs.
[0020] The Bao et al., prosthetic lumbar disc nuclei are made from hydrogels. Hydrogels have been used in biomedical applications, such as contact lenses. Among the advantages of hydrogels is that they are more biocompatible than hydrophobic elastomers and metals. This biocompatibility is largely due to the unique characteristics of hydrogels in that they are soft and contain water like the surround tissues and have relatively low frictional coefficients with respect to the surrounding tissues. The biocompatibility of hydrogels results in prosthetic nuclei which are more easily tolerated in the body. Furthermore, hydrophobic elastomeric and metallic gels will not permit diffusion of aqueous compositions, and their solutes, therethrough.
[0021] An additional advantage of some hydrogels is their good mechanical strength which permits them to withstand the load on the disc and restore the normal space between the vertebral bodies. The aforementioned nuclei of Bao et al. have high mechanical strength and are able to withstand the body loads and assist in the healing of the defective annuli.
[0022] Other advantages of the hydrogels, used in Bao et al. nuclei, are their excellent viscoelastic properties and shape memory. Hydrogels contain a large amount of water which acts as a plasticizer. Part of the water is available as free water which has more freedom to leave the hydrogel when the hydrogel is partially dehydrated under mechanical pressure. This characteristic of the hydrogels enables them to creep, in the same way as the natural nucleus, under compression and to withstand cyclic loading for long periods without any significant degradation or loss of their elasticity. This is because water in the hydrogel behaves like a cushion whereby the polymeric network of a hydrogel with a high equilibrium water content (EWC) is less susceptible to damage under mechanical load.
[0023] Another advantage of hydrogels is their permeability to water and water-soluble substances, such as nutrients, metabolites and the like. It is know that body fluid diffusion, under cycle loading, is the major source of nutrients to the natural disc. If the route of this nutrient diffusion is blocked, e.g., by a water-impermeable nucleus, further deterioration of the disc will ensure.

Problems solved by technology

Although the nucleus plays an important role in the biomechanical function of the disc, the mechanical properties of the disc are not well known, largely because of the loose hydrogel nature of the nucleus.
Degeneration of the intervertebral disc is believed to be a common cause of final pathological changes and back pain.
These changes cause the nucleus to lose part of its water binding capability which decreases the maximum swelling pressure it can exert.
The excess load on the annulus, of the degenerated disc, causes reduction of the disc height and excessive movement of the spinal segments.
The flexibility of the disc produces excessive movement of the collagenous fibers which in turn, injures the fiber attachments and causes delamination of the well organized fibers of the annulus ring.
The delamination annulus can be further weakened by stress on the annulus and in severe cases this stress will cause tearing of the annulus.
The spinal disc may also be displaced or damaged due to trauma or diseases.
This disc may in turn press upon the spinal nerve that exits the vertebral canal through the partially obstructed foramen, causing pain or paralysis in the area of its distribution.
However, it is not necessarily true that conservative care is the most efficient and economical way to solve the low back pain problem.
Clearly, a discectomy is not desirable from a biomechanical point of view.
That is why discectomy yields poor long term benefits and results in a high incidence of reherniation.
The primary disadvantage of the invention of Substad et al., Patil, Kenna and Lee et al., is that use of their prosthesis requires complete replacement of the natural disc which involves numerous surgical difficulties.
Designing and fabricating such a complicated prosthesis from acceptable materials, which will mimic the function of the natural disc, is very difficult.
A further problem is the difficulty of preventing the prosthesis from dislodging.
Fourthly, even for prostheses which are only intended for replacing the nucleus, a major obstacle has been to find a material which is similar to the natural and is also able to restore the normal function of the nucleus.
Hydrophobic elastomers and thermoplastic polymers are not desirable for use in the prosthetic nuclei due to their significant inherent differences from the natural nucleus e.g., lack of hydrophilicty, in the elastomers, and lack of flexibility in their thermoplasts.
As a consequence, those devices cannot completely restore the function of the nucleus which allows body fluid to diffuse in and out during cyclic loading thereby providing the nutrients the disc needs.
Furthermore, hydrophobic elastomeric and metallic gels will not permit diffusion of aqueous compositions, and their solutes, therethrough.
However, it is normally difficult to implant a fully hydrated hydrogel prosthesis in the cavity, of a disc, through the small window provided in the disc, for removing the herniated nucleus, especially in a percutaneous surgery by virtue of their bulkiness in a fully in a fully hydrated state.

Method used

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  • Radiovisible hydrogel intervertebral disc nucleus
  • Radiovisible hydrogel intervertebral disc nucleus
  • Radiovisible hydrogel intervertebral disc nucleus

Examples

Experimental program
Comparison scheme
Effect test

example i

[0077] A PVA solution was formed by mixing 15 g of PVA powder (Kuraray 117 or equivalent), having a molecular weight about 78000 and about 99.7% hydrolysed (Cat. No. 15129, Polysciences Inc., Warrington, Pa.), with 85 ml of a solvent comprising 15% water in DMSO. The mixture was heated at about 110° C. until a homogenous viscous solution formed.

example ii

[0078] 0.1 gram of gold powder (maximum diameter 75 μm) per cc of liquid-phase of PVA solution of Example I were mixed. The two ingredients were combined in the following manner to create a metal-filled polymer solution. A plunger from a 5 cc first syringe was removed and the first syringe was slowly filled half way with PVA solution, 0.5 g of the gold powder was poured into the syringe. The first syringe was then completely filled with PVA solution, and the plunger replaced. A two-way luer connector was screwed onto the tip of the first syringe and the connector was primed with PVA solution from the syringe. The first syringe and a second syringe of equal size were connected using the connector. The gold powder solution from the first syringe was squeezed into the empty syringe. This was repeated until the solution was uniformly mixed. A third syringe was filled with PVA solution without any gold. 5 cc of the PVA solution of the third syringe was injected into a nucleus mold having...

example iii

[0079] About 20 cc of the gold solution was prepared as described in Example II using two 20 cc syringes and 2 grams of gold powder. The metal filled polymer solution was slowly injected into a 20 cc implant mold (for a #5 size implant), filling the mold completely. The mold reservoir was capped so that the metal-filled PVA solution will not leak out of the mold if the mold is inverted. The mold was pressurized and placed in a Turbula Mixer which was placed into a programmable freezer. The mixer used must be able to both rotate and tip the mold during gelation of the metal filled PVA solution to keep the powder in the solution uniformly distributed. The mixer can rotate the mold about a central axis, tilt the mold back and forth through a 90° arc about an axis perpendicular to the central axis. This kept the metal particles uniformly suspended in the solution until it gelled.

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Abstract

A spinal implant for replacing the natural nucleus of the disc made from a polymer such as hydrogel having a radiopaque material located within the polymer. The material may be in the form of a powder dispersed throughout the polymer or may be in he form of a powder dispersed in layers or in other specific locations within the polymer. The radiopaque material is metal such as gold, tungsten, titanium, tantalum or platinum. The metal may also be in the form of a foil or wire located within the hydrogel such as polyurethane, thereby making the implant visible on x-rays. Other polymers besides hydrogel may be used with the radiopaque material being dispersed therein.

Description

[0001] This application is a divisional of U.S. application Ser. No. 10 / 244,306, filed on Sep. 16, 2002, the disclosure of which is incorporated herein by reference.BACKGROUND OF THE INVENTION [0002] This invention relates to a prosthetic intervertebral disc nucleus. More particularly, it relates to an artificial disc nucleus made of a hydrogel material having a radiovisible material therein. [0003] The intervertebral disc is a complex joint anatomically and functionally. It is composed of three component structures; the nucleus pulposus (the nucleus), the annulus fibrosus (the annulus) and the vertebral end-plates. The biochemical composition and anatomical arrangements within these component structures are related to the biomechanical function of the disc. [0004] The nucleus occupies about 25-40% of the total disc cross-sectional area. It is primarily composed of mucoid material containing mainly proteoglycans with a small amount of collagen. The proteoglycans consist of a protein...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): B29C41/22A61L27/00A61F2/00A61F2/30A61F2/44A61L27/50A61L27/52
CPCA61F2/30965A61L2430/38A61F2/442A61F2002/3008A61F2002/30616A61F2002/30971A61F2002/444A61F2250/0064A61F2250/0098A61F2310/00023A61F2310/00131A61F2310/00137A61F2310/00149A61F2310/00155A61L27/50A61L27/52A61F2/441
Inventor HIGHAM, PAULNGO, CHAUDEMARIA, CHRISTOPHERWILLIAMS, PHILIP F. III
Owner HOWMEDICA OSTEONICS CORP
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