Graft trussing and suspension construct
US-2024358496-A1 · Oct 31, 2024 · US
US9561304B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9561304-B2 |
| Application number | US-200913001055-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 22, 2009 |
| Priority date | Jun 23, 2008 |
| Publication date | Feb 7, 2017 |
| Grant date | Feb 7, 2017 |
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The invention relates to a biomaterial containing coagulated blood or coagulated bone marrow aspirate and biphasic calcium phosphate ceramic particles, to a production method thereof and to the use of same for the production of an implant that enables bone tissue regeneration.
Opening claim text (preview).
The invention claimed is: 1. A method for manufacturing a biomaterial, the method comprising: (i) mixing a biphasic calcium phosphate (BCP) comprising hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) in an HA/β-TCP weight/weight ratio of between 5/95 and 95/5, in the form of granules whose size is between 40 and 500 μm, with blood or with a bone marrow aspirate, in a proportion ranging from 10 to 90 g by weight of BCP per 100 mL of blood or bone marrow aspirate to give a mixture; (ii) adding to the mixture of (i) at least one coagulating agent in a sufficient quantity to cause coagulation of blood or of the bone marrow aspirate, wherein the concentration of the coagulating agent is from 1 mM to 50 mM; and (iii) mixing under conditions promoting homogenization of the BCP while the coagulation occurs, and wherein the biomaterial is in the form of a malleable homogeneous paste. 2. The method of claim 1 , wherein the at least one coagulating agent comprises calcium and is a biocompatible calcium salt. 3. The method of claim 1 , wherein the blood is employed and is collected beforehand from a donor compatible with a recipient for whom the biomaterial is intended. 4. The method of claim 1 , wherein the blood is employed and is collected beforehand from a recipient for whom the biomaterial is intended. 5. The method of claim 1 , wherein the mixture comprises the BCP, the blood, and the coagulating agent, is allowed to stand during the coagulation so as to allow the BCP to sediment and to form an implant saturated with BCP. 6. The method of claim 1 , wherein (i) to (iii) are carried out in an inner cavity of a syringe or in a tube closed at its ends. 7. The method of claim 1 , which comprises mixing from 50 to 90 g by weight of BCP, per 100 mL of blood or bone marrow aspirate. 8. A biomaterial comprising a BCP in the form of granules having a size of between 40 and 500 μm dispersed substantially homogeneously in a three-dimensional network of blood proteins or in a network of bone marrow proteins obtained by a method consisting essentially of: mixing a biphasic calcium phosphate (BCP) comprising hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) in an HA/β-TCP weight/weight ratio of between 5/95 and 95/5, in the form of granules whose size is between 40 and 500 μm, with blood or with a bone marrow aspirate, and with at least one coagulating agent, in a sufficient quantity to cause coagulation of the blood or of the marrow aspirate, and allowing the mixture comprising the BCP, the blood or bone marrow aspirate and the coagulating agent to coagulate, wherein, in the mixture: BCP is present in a proportion ranging from 10 to 90 g by weight of BCP, per 100 mL of blood or bone marrow aspirate, and the concentration of the coagulating agent is from 1 mM to 50 mM, and wherein the biomaterial is in the form of a malleable homogeneous paste. 9. The biomaterial of claim 8 , wherein the BCP granules have a size ranging from 80 to 200 μm. 10. The biomaterial of claim 8 further comprising at least one additive selected from the group consisting of: a polymer, a ceramic particle, a pharmaceutical molecule, a growth factor, a natural biomarker or a synthetic biomarker, a contrast agent, a tissue preparation and a cell preparation. 11. A method for filling in a bone defect, the method comprising implanting the biomaterial of claim 8 into a bone. 12. A method of producing bone tissue, the method comprising growing the bone tissue upon a support comprising the biomaterial of claim 8 in vitro or ex vivo. 13. A method of producing a bone implant, the method comprising combining the biomaterial of claim 8 in vitro or ex vivo with a bone tissue or prosthesis. 14. The biomaterial of claim 8 , wherein the BCP comprises hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) in an HA/β-TCP weight/weight ratio of between 30/70 and 80/20. 15. The biomaterial of claim 14 , wherein the BCP comprises hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) in an HA/β-TCP weight/weight ratio of between 40/60 and 60/40. 16. The biomaterial of claim 8 , wherein the BCP is porous and the pores have sizes from 50 nm to 150 μm. 17. The biomaterial of claim 8 , wherein the BCP is porous and the pores have sizes from 1 μm to 50 μm. 18. The biomaterial of claim 8 , wherein the at least one coagulating agent comprises calcium and is a biocompatible calcium salt. 19. The biomaterial of claim 8 , wherein blood is employed and is collected beforehand from a donor compatible with a recipient for whom the biomaterial is intended. 20. The biomaterial of claim 8 , wherein blood is employed and is collected beforehand from a recipient for whom the biomaterial is intended. 21. The biomaterial of claim 8 , wherein the mixture comprising the BCP, the blood and the coagulating agent, is allowed to stand during the coagulation so as to allow the BCP to sediment. 22. The biomaterial of claim 8 , wherein BCP is in a proportion ranging from 30 to 90 g by weight of BCP per 100 mL of blood or bone marrow aspirate. 23. The biomaterial of claim 8 , further comprising the step of mixing under conditions promoting homogenization of the BCP while the coagulation occurs. 24. The biomaterial of claim 22 , BCP is in a proportion ranging from 50 to 70 g by weight of BCP, per 100 mL of blood or bone marrow aspirate. 25. The biomaterial of claim 8 , wherein the concentration of the coagulating agent in the mixture is from 3 to 35 mM.
Blood, e.g. platelet-rich plasma · CPC title
Phosphorus-containing materials, e.g. apatite · CPC title
Drugs for skeletal disorders · CPC title
Bones · CPC title
Materials or treatment for tissue regeneration · CPC title
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