Amphiphilic peptides and hydrogel matrices thereof for bone repair
View Patent ↗The present invention relates to the field of tissue engineering and more specifically to amphiphilic peptides and peptide matrices thereof useful in vitro and in situ biomineralization and inducing bone repair. The present invention provides peptides, which are useful in hydrogels and other pharmaceutical compositions, and methods and kits of use for bone repair and promotion of biomineralization. Certain hydrogels according to the invention comprise cells within or adhered to the peptide matrix.
1. A hydrogel composition comprising an amphiphilic peptide having the amino acid sequence selected from the group consisting of:
Pro-Glu-(Leu-Glu)5-Pro;
(SEQ ID NO: 6)
Pro-Asp-(Leu-Asp)5-Pro;
(SEQ ID NO: 7) and
Pro-Asp-(Phe-Asp)5-Pro.
(SEQ ID NO: 22)
2. The hydrogel composition of claim 1 wherein the peptide has the amino acid sequence Pro-Glu-(Leu-Glu)5-Pro (SEQ ID NO:6).
3. The hydrogel composition of claim 1 wherein the peptide has the amino acid sequence Pro-Asp-(Leu-Asp)5-Pro (SEQ ID NO:7).
4. The hydrogel composition of claim 1 wherein the peptide has the amino acid sequence Pro-Asp-(Phe-Asp)5-Pro (SEQ ID NO:22).
5. The hydrogel composition of claim 1 comprising one or more of a pre-loaded mineral-salt solution or aggregate or a pre-loaded polysaccharide.
6. The hydrogel composition of claim 5 wherein the pre-loaded mineral salt is a calcium phosphate mineral selected from the group consisting of amorphous calcium phosphate, tricalcium phosphate and hydroxyapatite or the pre-loaded polysaccharide is selected from the group consisting of hyaluronic acid, alginate and sulfated polysaccharide.
7. A pharmaceutical composition comprising at least one amphiphilic peptide according to claim 1 and a pharmaceutically acceptable carrier or excipient.
8. An implant comprising a hydrogel composition according to claim 7 and optionally further comprising a metal structure.
9. The implant of claim 8 wherein the hydrogel further comprises at least one mineral or at least one polysaccharide.
10. The implant of claim 9 wherein the mineral is a calcium phosphate mineral selected from the group consisting of amorphous calcium phosphate, tricalcium phosphate and hydroxyapatite or the polysaccharide is selected from the group consisting of hyaluronic acid, alginate and sulfated polysaccharide.
11. A method for preparing a hydrogel composition according to claim 1 which comprises:
providing a liquid solution comprising at least one amphiphilic peptide according to claim 1 in a vessel;
providing a solution comprising ionic calcium, optionally further comprising a therapeutic agent;
mixing together the peptide composition and the solution;
allowing the mixture to form a hydrogel; and
separating a peptide/precipitate solid composition from the solution.
12. The method of claim 11 wherein the ionic calcium is selected from the group consisting of calcium chloride salt, phosphate salt, particles or particulates of calcium phosphate mineral, tricalcium phosphate and hydroxyapatite.
13. The method of claim 11 wherein the peptide is provided in powder form and the solution is an alkaline solution.
14. A kit comprising at least one amphiphilic peptide according to claim 1 and optionally further comprising a pharmaceutically acceptable carrier or excipient and an optional means for delivery of the peptide or peptide and carrier or excipient.