Appeal 2007-0532 Application 10/828,316 and cellular material taken from a group consisting of living cells, cell elements such as red blood cells, white blood cells, platelets, blood plasma, pluripotential cells, osteoblasts, osteoclasts, and fibroblasts, epithelial cells, and endothelial cells present at a concentration of 105 to 108 per cc of the carrier, said hydrogel component having a molecular weight ranging from ten thousand to three hundred thousand Daltons with a stable viscosity and said composition having a pH ranging from about 6.8 to about 7.4[.] 26. A sterile formable bone composition as claimed in claim 23 wherein said bone particles are allograft cortical bone ranging from 100 microns to 850 microns in size at a concentration ranging from 20% to 35% by weight of the composition. Claim 21 is directed to a formable composition comprising demineralized bone particles (5-50% w/w) in a viscous, phosphate buffered aqueous carrier. The carrier contains either chitosan or sodium alginate (5- 20% by weight of the carrier) with a molecular weight of 10,000 to 300,000 Daltons and provides a stable viscosity at 22° C to 37° C. The composition also has a pH in the range of 6.8 to 7.4 and comprises at least one of “transforming growth factor (TGF-beta), insulin growth factor (IGF-1), plat[e]let derived growth factor (PDGF), vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF) (numbers 1-23), osteopontin, growth hormones such as somatotropin cellular attractants and attachment agents.” Claim 23 is directed to a similar composition but requires chitosan as the hydrogel, does not require a growth factor, and requires a “cellular material taken from a group consisting of living cells, cell elements such as red blood cells, white blood cells, platelets, blood plasma, pluripotential cells, osteoblasts, osteoclasts, and fibroblasts, epithelial cells, and 3Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 Next
Last modified: September 9, 2013