US2022176021A1PendingUtilityA1
Platelet-derived growth factor compositions and methods of use thereof
Assignee: BIOMIMETIC THERAPEUTICS LLCPriority: Oct 14, 2004Filed: Sep 16, 2021Published: Jun 9, 2022
Est. expiryOct 14, 2024(expired)· nominal 20-yr term from priority
Inventors:Samuel E. Lynch
A61L 2430/06A61L 2400/06A61L 27/12A61L 27/24A61F 2210/0004A61L 2430/02A61L 27/58A61P 19/00A61L 27/54A61K 38/1858A61F 2002/2835A61K 38/17A61K 9/0063A61L 27/425A61L 2300/414A61L 27/56A61P 19/04A61L 2430/12A61F 2/28A61L 27/227A61L 27/40A61K 38/18A61P 1/02A61L 2430/10A61L 27/025A61L 2300/252A61P 19/08A61K 9/14C07K 14/49A61L 2300/412
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Claims
Abstract
A method for promoting growth of bone, periodontium, ligament, or cartilage in a mammal by applying to the bone, periodontium, ligament, or cartilage a composition comprising platelet-derived growth factor at a concentration in the range of about 0.1 mg/mL to about 1.0 mg/mL in a pharmaceutically acceptable liquid carrier and a pharmaceutically-acceptable solid carrier.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 - 78 . (canceled)
79 . An implant material comprising a porous calcium phosphate having incorporated therein a solution comprising platelet derived growth factor (PDGF) having a concentration ranging from about 0.1 mg/mL to about 1.0 mg/mL in a buffer, wherein the calcium phosphate comprises interconnected pores, a porosity greater than 40%, and particles having a size ranging from about 100 microns to about 5000 microns,
wherein the calcium phosphate is chosen from one or more of tricalcium phosphate, hydroxyapatite, amorphous calcium phosphate, calcium metaphosphate, dicalcium phosphate dihydrate, heptacalcium phosphate, calcium pyrophosphate dihydrate, calcium pyrophosphate, and octacalcium phosphate, and wherein the implant material does not comprise demineralized freeze-dried bone allograft.
80 . The implant material of claim 79 , wherein the PDGF comprises recombinant PDGF.
81 . The implant material of claim 79 , wherein the PDGF comprises recombinant human PDGF-BB.
82 . The implant material of claim 79 , wherein the solution comprises PDGF at a concentration of about 0.3 mg/mL.
83 . The implant material of claim 79 , wherein the solution comprises PDGF having a concentration ranging from about 0.25 mg/mL to about 0.5 mg/mL.
84 . The implant material of claim 79 , wherein the solution comprises PDGF having a concentration ranging from about 0.2 mg/mL to about 0.75 mg/mL.
85 . The implant material of claim 79 , wherein the calcium phosphate comprises particles having a size ranging from about 100 microns to about 3000 microns.
86 . The implant material of claim 79 , wherein the calcium phosphate comprises particles having a size ranging from about 250 microns to about 1000 microns.
87 . The implant material of claim 79 , wherein the hydroxyapatite comprises carbonated hydroxyapatite.
88 . The implant material of claim 79 , wherein the calcium phosphate comprises poorly crystalline hydroxyapatite.
89 . The implant material of claim 79 , wherein the calcium phosphate is capable of absorbing an amount of the solution comprising PDGF that is equal to at least about 200% of the calcium phosphate's own weight.
90 . An implant material comprising collagen and a porous calcium phosphate having incorporated therein a solution comprising platelet derived growth factor (PDGF) having a concentration ranging from about 0.1 mg/mL to about 1.0 mg/mL in a buffer, wherein the calcium phosphate comprises interconnected pores, a porosity greater than 40%, and particles having a size ranging from about 100 microns to about 3000 microns,
wherein the calcium phosphate is chosen from one or more of tricalcium phosphate, hydroxyapatite, amorphous calcium phosphate, calcium metaphosphate, dicalcium phosphate dihydrate, heptacalcium phosphate, calcium pyrophosphate dihydrate, calcium pyrophosphate, and octacalcium phosphate, and wherein the implant material does not comprise demineralized freeze-dried bone allograft.
91 . The implant material of claim 90 , wherein the PDGF comprises recombinant PDGF.
92 . The implant material of claim 90 , wherein the PDGF comprises recombinant human PDGF-BB.
93 . The implant material of claim 90 , wherein the calcium phosphate comprises particles having a size ranging from about 250 microns to about 1000 microns.
94 . The implant material of claim 90 , wherein the solution comprises PDGF having a concentration ranging from about 0.25 mg/mL to about 0.5 mg/mL.
95 . The implant material of claim 90 , wherein the solution comprises PDGF having a concentration ranging from about 0.2 mg/mL to about 0.75 mg/mL.
96 . The implant material of claim 90 , wherein the solution comprises PDGF at a concentration of about 0.3 mg/mL.
97 . The implant material of claim 90 , wherein the hydroxyapatite comprises carbonated hydroxyapatite.
98 . The implant material of claim 90 , wherein the calcium phosphate comprises poorly crystalline hydroxyapatite.Join the waitlist — get patent alerts
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