US2022105245A1PendingUtilityA1
Bone-like prosthetic implants
Est. expiryApr 10, 2028(~1.7 yrs left)· nominal 20-yr term from priority
Inventors:Shai Meretzki
A61L 27/3886A61L 2430/02A61L 27/3843A61L 27/3804A61P 43/00
63
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Claims
Abstract
A prosthetic implant comprising a biocompatible three-dimensional scaffold and at least two cell types selected from the group consisting of osteoblasts, osteoclasts, and endothelial cells or progenitors thereof.
Claims
exact text as granted — not AI-modified1 . A composition comprising an injectable medium and a mineral implant having a biocompatible, three-dimensional mineral scaffold comprising ex vivo expanded mesenchymal cells and at least one cell type selected from the group consisting of: osteoblasts, osteoclasts, chondrocytes, endothelial cells and progenitors thereof, wherein said mesenchymal cells and said at least one cell type are organized in more than one layer in a 3-D interaction, wherein said mesenchymal cells comprise a combination of osteoprogenitor cells and mesenchymal stem cells.
2 . The composition of claim 1 , further comprising osteoblasts, osteoclasts, chondrocytes, endothelial cells, or any combination thereof.
3 . The composition of claim 1 , wherein said mineral implant comprises an extracellular matrix.
4 . The composition of claim 1 , wherein said mesenchymal cells and at least one cell type are at a density of at least 10 6 cells/ml in said implant.
5 . The composition of claim 1 , wherein said scaffold comprises a bone particle selected from the group consisting of: a dry bone particle, a frozen bone particle and a dematerialized bone particle.
6 . The composition of claim 1 , wherein said scaffold comprises a material selected from the group consisting of: calcium phosphate derivatives, calcium sulfate derivatives, calcium hydroxyapatite, silicate matrices, hydroxyapatite, and beta-3 calcium phosphate.
7 . The composition of claim 1 , wherein said scaffold comprises a coating layer.
8 . The composition of claim 1 , comprising a material selected from the group consisting of: poly-D-lysine, collagen, fibronectin, hydrogel, or a combination thereof.
9 . The composition of claim 1 , wherein said scaffold has a pore size in the range of from about 50 microns to about 2000 microns.
10 . A method for repairing a bone lesion in a subject in need thereof, comprising inserting the composition of claim 1 into said bone lesion, thereby repairing a bone lesion in a subject in need thereof.
11 . The method of claim 10 , wherein said cells further comprise osteoblasts, osteoclasts, chondrocytes, endothelial cells, or any combination thereof.
12 . The method of claim 10 , wherein said cells are at a density of at least 10 6 cells/ml of said implant.
13 . The method of claim 10 , wherein said cells are arranged within more than one layer.
14 . The method of claim 10 , wherein said cells are derived from bone marrow, placenta, adipose tissue, cord blood, cord vein, peripheral blood, mobilized peripheral blood, embryonic stem cells, or any combination thereof.
15 . The method of claim 10 , wherein said scaffold has a pore size in the range of from about 50 microns to about 2000 microns.
16 . The method of claim 10 , wherein said scaffold comprises a bone particle selected from the group consisting of: a dry bone particle, a frozen bone particle a dematerialized bone particle, or any combination thereof.
17 . The method of claim 10 , wherein said scaffold comprises: a calcium phosphate derivative, a calcium sulfate derivative, calcium hydroxyapatite, a silicate matrice, hydroxyapatite, beta-3 calcium phosphate, or any combination thereof.
18 . The method of claim 10 , wherein said composition further comprises poly-D-lysine, collagen, fibronectin, extra-cellular-matrix, hydrogel, or any combination thereof.Join the waitlist — get patent alerts
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