In situ bioprosthetic filler and methods, particularly for in situ formation of vertebral disc bioprosthetics
View Patent ↗Bioprosthetic devices include an exterior biological tissue member which at least partly defines a cavity, and a proteinaceous biopolymer which fills the cavity, and intercalates and is chemically bound (fixed) to the tissue of the surrounding biological tissue member. In preferred forms, the bioprosthetic device is a bioprosthetic vertebral disc having a fibrillar outer annulus which surrounds and defines an interior cavity and is formed by removal of at least a substantial portion of the natural gelatinous core therefrom. The cavity defined by the fibrillar outer annulus may then be filled with a flowable proteinaceous biopolymer. Preferably, the proteinaceous biopolymer is a liquid mixture comprised of human or animal-derived protein material and a di- or polyaldehyde, which are allowed to react in situ to form a cross-linked biopolymer within the cavity. The liquid mixture may be formed in advance of being introduced into the cavity, or may be formed simultaneously during introduction into the cavity.
1. A compressible prosthetic core for a vertebral disc having a cavity bound by a fibrillar outer annulus, the cavity being formed by the removal of the vertebral disc's natural gelatinous core comprising:
a proteinaceous biopolymeric material comprising a cross-linked reaction product of human or animal-derived protein material and a di- or polyaldehyde the proteinaceous biopolymeric material being load distributing and compressible without exhibiting substantial deformation and being dimensioned to fill the cavity of the vertebral disc.
2. The compressible prosthetic core of claim 1 , wherein the proteinaceous biopolymeric material further comprises a fibrous or particulate filler material.
3. The compressible prosthetic core of claim 1 , wherein the protein comprises bovine or human serum albumin or hemoglobin.
4. The compressible prosthetic core of claim 1 , wherein the aldehyde comprises glutaraldehyde.
5. The compressible prosthetic core of claim 1 , wherein when the biopolymeric material is provided within the cavity of the vertebral disc, the vertebral disc remains intact and flexible after being subjected to 5 million cycles of a cyclic load of 0.85 MPa.
6. The compressible prosthetic core of claim 1 , wherein the proteinaceous biopolymeric material is configured to chemically bind to the tissue of the vertebral disc.
7. A compressible prosthetic core for a vertebral disc having an exterior biological tissue member which at least partly defines a cavity comprising:
a proteinaceous biopolymeric material which is dimensioned to fill the cavity of the vertebral disc;
wherein the proteinaceous biopolymeric material is the reaction product of at least two reactable components and is load distributing and compressible without exhibiting substantial permanent deformation, and one of the components comprises human or animal-derived serum albumin or hemoglobin.
8. The compressible prosthetic core of claim 7 , wherein the proteinaceous biopolymeric material further comprises a fibrous or particulate filler material.
9. The compressible prosthetic core of claim 7 , wherein the vertebral disc exhibits flexibility comparable to the biologically natural vertebral disc after being subjected to 5 million cycles of cyclic load of 0.85 MPa when the compressible prosthetic core is provided in the cavity of vertebral disc.
10. The compressible prosthetic core of claim 7 , wherein the proteinaceous biopolymeric material is configured to chemically bind to the tissue of the vertebral disc.
11. The compressible prosthetic core of claim 8 , wherein the proteinaceous biopolymeric material is configured to chemically bind to the tissue of the vertebral disc.
12. A compressible prosthetic core for a vertebral disc having a fibrillar outer annulus which remains following removal of a gelatinous core from a biologically natural vertebral disc to thereby define an interior cavity comprising:
a proteinaceous biopolymeric material which is dimensioned to fill the interior cavity of the vertebral disc,
the proteinaceous biopolymeric material being the reaction product of at least two reactable components, one of which comprises human or animal-derived serum albumin or hemoglobin,
wherein the proteinaceous biopolymeric material is capable of withstanding compression for 100 and 1000 cycles at a compression rate of 100 mm/min between a minimum stress of 200 kPa and a maximum stress of 800 kPa without exhibiting fracture, permanent deformation, and loss of hydration, and
wherein the vertebral disc is capable of withstanding a constant load of 700 N for 10 minutes when the proteinaceous biopolymeric material is provided in the interior cavity of the vertebral disc.