Freeze-dried fibrin matrices and methods for preparation thereof
Methods for treating diseased or injured tissue by implanting into the tissue at a site of the disease or injury a porous freeze-dried fibrin matrix formed from plasma proteins. The proteins include fibrinogen cleaved by the action of thrombin at varying concentrations sufficient to cleave the fibrinogen and Factor XIII. The matrix has less than 10% residual moisture and is devoid of exogenous anti-fibrinolytic agents, plasminogen and of organic chelating agents. Alternatively, the plasma proteins comprise partially purified plasma proteins that are devoid of plasminogen.
1. A method of treating diseased or injured tissue, comprising:
implanting into the tissue at a site of disease or injury a porous freeze-dried fibrin matrix formed from plasma proteins comprising Factor XIII and fibrinogen cleaved by thrombin, wherein the matrix has less than 10% residual moisture and is devoid of exogenous anti-fibrinolytic agents, plasminogen and organic chelating agents, and wherein the diseased or injured tissue is selected from the group consisting of cartilage, bone, liver, pancreas, and cardiac tissue.
2. The method according to claim 1 , wherein said plasma proteins are partially purified.
3. The method according to claim 1 , wherein said plasma proteins comprise less than 20% of plasminogen normally present in plasma.
4. The method according to claim 1 , wherein said porous freeze-dried fibrin matrix further comprises a glycosaminoglycan and a growth factor.
5. The method according to claim 4 , wherein the glycosaminoglycan is crosslinked or non-crosslinked hyaluronic acid.
6. The method according to claim 4 , wherein the growth factor is a fibroblast growth factor.
7. The method according to claim 6 , wherein the fibroblast growth factor is selected from the group consisting of FGF2, FGF4, FGF9, and FGF18.
8. The method according to claim 1 , wherein said porous freeze-dried fibrin matrix further comprises cells.
9. The method according to claim 8 , wherein the cells are selected from the group consisting of: stem cells, progenitor cells, chondrocytes, osteoblasts, hepatocytes, and mesenchymal, endothelial, epithelial, urothelial, endocrine, neuronal, pancreatic, renal and ocular cell types.
10. The method according to claim 1 , wherein at least one of said plasma proteins is autologous or is recombinant.
11. The method according to claim 1 , wherein before implanting, the matrix is prepared by a process comprising the steps of: providing a thrombin solution and a plasma protein solution wherein the plasma protein solution comprises fibrinogen and Factor XIII and is devoid of exogenous anti-fibrinolytic agents and organic chelating agents; introducing the thrombin solution and the plasma protein solution to a solid receptacle or mold in the presence of calcium ions; incubating under conditions appropriate to achieve clotting; freezing the clotted mixture; and lyophilizing the clotted mixture, to obtain the porous freeze-dried fibrin matrix for implanting.
12. A method of treating diseased or injured tissue comprising:
implanting into the tissue at a site of disease or injury a porous freeze-dried fibrin matrix formed from plasma proteins comprising Factor XIII and fibrinogen cleaved by thrombin, wherein the matrix has less than 10% residual moisture and is devoid of exogenous anti-fibrinolytic agents and organic chelating agents, wherein said plasma proteins are partially purified to be devoid of plasminogen and wherein the diseased or injured tissue is selected from the group consisting of cartilage, bone, liver, pancreas, and cardiac tissue.
13. The method according to claim 12 , wherein said plasma proteins comprise less than about 5% of plasminogen normally present in plasma.
14. The method according to claim 12 , wherein said porous freeze-dried fibrin matrix further comprises a glycosaminoglycan and a growth factor.
15. The method according to claim 14 , wherein the glycosaminoglycan is crosslinked or non-crosslinked hyaluronic acid.
16. The method according to claim 14 , wherein the growth factor is a fibroblast growth factor.
17. The method according to claim 16 , wherein the fibroblast growth factor is selected from the group consisting of FGF2, FGF4, FGF9, and FGF18.
18. The method according to claim 12 , wherein said porous freeze-dried fibrin matrix further comprises cells.
19. The method according to claim 18 , wherein the cells are selected from the group consisting of: stem cells, progenitor cells, chondrocytes, osteoblasts, hepatocytes, and mesenchymal, endothelial, epithelial, urothelial, endocrine, neuronal, pancreatic, renal and ocular cell types.
20. The method according to claim 12 , wherein at least one of said plasma proteins is autologous or is recombinant.