Method and apparatus for treating bone fractures, and/or for fortifying and/or augmenting bone, including the provision and use of composite implants
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61B-017/70
A61B-017/72
A61F-002/28
A61K-047/02
A61K-047/32
A61K-047/34
A61L-027/44
A61L-027/48
A61L-027/50
A61L-027/58
A61B-017/00
출원번호
US-0893441
(2014-05-23)
등록번호
US-10010609
(2018-07-03)
국제출원번호
PCT/US2014/039394
(2014-05-23)
국제공개번호
WO2014/190289
(2014-11-27)
발명자
/ 주소
D'Agostino, Jeffrey A.
Whitehouse, Robert S.
Carter, Andrew J.
Watterson, Arthur
Lane, Joseph P.
McRury, Ian D.
Marchetti, Samantha
Seil, Nikole
출원인 / 주소
206 ORTHO, Inc.
대리인 / 주소
Pandiscio & Pandiscio
인용정보
피인용 횟수 :
0인용 특허 :
76
초록▼
A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the
A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone. A method for treating a bone comprising: selecting at least one reinforcing element to be combined with an injectable matrix material to form a composite implant capable of supporting the bone; positioning the at least one reinforcing element in a cavity in the bone; flowing the injectable matrix material into the cavity wherein the injectable matrix material interfaces with the at least one reinforcing element; and transforming the injectable matrix material from a flowable state to a nonflowable state to establish a static structure that supports the adjacent bone.
대표청구항▼
1. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient stre
1. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin comprises an acrylic resin;wherein the acrylic resin comprises a mixture of prepolymerized acrylic resins or styrene acrylic resins having molecular weights from about 200 to 20,000 daltons, and acrylic monomers selected from the group consisting of methacrylic acid, methyl methacrylate, ethyl methacrylate, butyl methacrylate, acrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate ethylene glycol diacrylate, ethylene glycol dimethacrylate, trimethylol propane triacrylate and trimethylol propane triamethacrylate, and an organic peroxide free radical initiator, with the mixture having an initial viscosity from about 200 cps to about 5000 cps at 20-25 degrees C. 2. A composite implant according to claim 1 wherein the acrylic resin further comprises at least one from the group consisting of inorganic fillers, stabilizers to prevent cure of the acrylic monomers during storage and activators to accelerate the free radical cure of the acrylic resin. 3. A composite implant according to claim 1 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 4. A composite implant according to claim 1 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 5. A composite implant according to claim 1 wherein the acrylic resin comprises a mixture of prepolymerized acrylic resins (or styrene acrylic resins) having molecular weights from about 200 to 20,000 daltons, and acrylic monomers selected from the group consisting of methacrylic acid, methyl methacrylate, ethyl methacrylate, butyl methacrylate, acrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate ethylene glycol diacrylate, ethylene glycol dimethacrylate, trimethylol propane triacrylate and trimethylol propane triamethacrylate, and an organic peroxide free radical initiator, with the mixture having an initial viscosity from about 200 cps to about 5000 cps at 20-25 degrees C. 6. A composite implant according to claim 5 further comprising additional additives selected from the group consisting of inorganic fillers, stabilizers to prevent cure of the acrylic monomers during storage, and/or activators to accelerate the free radical cure of the acrylic resin. 7. A composite implant according to claim 1 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 8. A composite implant according to claim 7 wherein the at least one reinforcing element is surface coated with a sizer or primer. 9. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin comprises a polyurethane having terminal isocyanate functionality and a viscosity from about 800 cps to about 10,000 cps at the temperature when the resin is applied to the at least one reinforcing element and a viscosity of at least 50,000 cps at 20-25 degrees C. 10. A composite implant according to claim 9 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 11. A composite implant according to claim 9 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 12. A composite implant according to claim 9 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 13. A composite implant according to claim 12 wherein the at least one reinforcing element is surface coated with a sizer or primer. 14. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin has a terminal isocyanate functionality and is applied to the at least one reinforcing element at a temperature from about 100 degrees C. to about 200 degrees C., the at least one reinforcing element having been surface coated with a size or prime that provides additional adhesion between the resin and the at least one reinforcing element and can optionally act as a secondary catalyst for further molecular weight increase of the resin and adhesion to the at least one reinforcing element. 15. A composite implant according to claim 14 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 16. A composite implant according to claim 14 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 17. A composite implant according to claim 14 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 18. A composite implant according to claim 17 wherein the at least one reinforcing element is surface coated with a sizer or primer. 19. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the compressive modulus ratio between the cured resin and the at least one reinforcing element is from about 1:3 to about 1:20, and the flexural modulus ratio between the cured resin and the at least one reinforcing element is about 1:3 to about 1:10. 20. A composite implant according to claim 19 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 21. A composite implant according to claim 19 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 22. A composite implant according to claim 19 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 23. A composite implant according to claim 22 wherein the at least one reinforcing element is surface coated with a sizer or primer. 24. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin is applied to the at least one reinforcing element in a continuous process, with the resin having a viscosity (at application temperature) of from about 2 Pas to about 2000 Pas, with fiber content of the at least one reinforcing element being from about 5 volume percent to about 75 volume percent. 25. A composite implant according to claim 24 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 26. A composite implant according to claim 24 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 27. A composite implant according to claim 24 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 28. A composite implant according to claim 27 wherein the at least one reinforcing element is surface coated with a sizer or primer. 29. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the at least one reinforcing element comprises a very high modulus fiber (e.g., a fiber having a modulus greater than about 80 GPa compressive strength) and a low modulus thermoplastic fiber (e.g., a fiber having a modulus less than 8 GPa), wherein the thermoplastic fiber is pre-melted so as to provide a retaining structure for the very high modulus fiber. 30. A composite implant according to claim 29 wherein the very high modulus fiber has a modulus greater than about 80 GPa compressive strength. 31. A composite implant according to claim 29 wherein the low modulus thermoplastic fiber has a modulus less than 8 GPa. 32. A composite implant according to claim 29 wherein the very high modulus fiber has a surface which is coated with a sizing agent, or a primer, which provides additional adhesion between the resin and the at least one reinforcing element. 33. A composite implant according to claim 32 wherein the sizing agent, or primer, acts as a secondary catalyst for the polymerization of the resin. 34. A composite implant according to claim 32 wherein the very high modulus fiber is surface coated with an amino functional material selected from the group consisting of amino silanes, lysine, polyamines, amino acids and polyamino acids. 35. A composite implant according to claim 29 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 36. A composite implant according to claim 29 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 37. A composite implant according to claim 29 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 38. A composite implant according to claim 37 wherein the at least one reinforcing element is surface coated with a sizer or primer. 39. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin comprises a polyurethane having terminal isocyanate functionality and a viscosity from about 800 cps to about 10,000 cps at the temperature when the urethane resin is applied to the at least one reinforcing element and a viscosity of at least 50,000 cps at 20-25 degrees C. 40. A composite implant according to claim 39 wherein the resin comprises a polyurethane having terminal isocyanate functionality, which is applied to the at least one reinforcing element at a temperature of about 100 degrees C. to about 200 degrees C. 41. A composite implant according to claim 39 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 42. A composite implant according to claim 39 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 43. A composite implant according to claim 39 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 44. A composite implant according to claim 43 wherein the at least one reinforcing element is surface coated with a sizer or primer. 45. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element;wherein the surface coating acts as a secondary catalyst for further molecular weight increase of the resin and can facilitate adhesion to the at least one reinforcing element. 46. A composite implant according to claim 45 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 47. A composite implant according to claim 45 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 48. A composite implant according to claim 45 wherein the at least one reinforcing element is surface coated with a sizer or primer. 49. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element;wherein the at least one reinforcing element is surface coated with an amino functional material selected from the group consisting of amino silanes, lysine, polyamines, amino acids, and polyamino acids. 50. A composite implant according to claim 49 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 51. A composite implant according to claim 49 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 52. A composite implant according to claim 49 wherein the at least one reinforcing element is surface coated with a sizer or primer. 53. A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the injectable matrix material comprising a resin, and the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone; wherein the resin is a polyurethane, and the composite implant also contains residual isocyanate groups in the composite implant such that they can be stored in a dry inert atmosphere without further crosslinking reactions, and then, when applied in the body where moisture is present, will further cure until no residual isocyanate groups are present. 54. A composite implant according to claim 53 wherein the composite implant comprises up to about 4% by weight of polymer-bound isocyanate groups. 55. A composite implant according to claim 53 wherein the composite implant provides a foamed surface structure in the body during final cure so as to accommodate the special difference between the polymer implant and the cavity constructed to accommodate the polymer implant, thus providing improved strength and stiffness to the repaired bone area. 56. A composite implant according to claim 53 wherein the at least one reinforcing element comprises at least one from the group consisting of E-glass, bio glass, soluble glass, resorbable glass, carbon fiber, polyaramid fiber, PET fiber, ceramic fiber, PEEK fiber, fibers formed from homopolymers or copolymers of one or more monomers selected from D lactic acid, L lactic acid dilactides of D and L isomers, glycolic acid, and/or combinations thereof. 57. A composite implant according to claim 53 wherein the at least one reinforcing element comprises at least one from the group consisting of a series of single filaments, woven filaments or a composite mesh containing one or more different compositional fibers. 58. A composite implant according to claim 53 wherein the at least one reinforcing element is surface coated so as to provide additional adhesion between the resin and the at least one reinforcing element. 59. A composite implant according to claim 58 wherein the at least one reinforcing element is surface coated with a sizer or primer.
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