Myostatin inhibitor enhancement of musculoskeletal repair
Abstract
The methods and compositions of this invention provide a means of regenerating injured musculoskeletal tissue by inhibition of myostatin function. The invention provides methods of treating a nonunion fracture in an individual comprising delivering to the fracture via a delivery system comprising biodegradable hydrogel, a pharmacological amount of myostatin propeptide effective to inhibit myostatin function. The invention also teaches compositions useful for the treatment of non-union fracture in an individual, said compositions comprising a pharmacological amount of myostatin propeptide effective to inhibit myostatin function; and a delivery system for delivering said myostatin propeptide to said fracture, wherein the delivery system comprises a biodegradable hydrogel or biodegradable nanobeads.
Claims
exact text as granted — not AI-modified1 . A method of regenerating injured musculoskeletal tissue, comprising:
contacting the injured tissue with a myostatin inhibitor, wherein said contact results in musculoskeletal tissue regeneration by inhibition of myostatin function.
2 . The method of claim 1 , wherein the myostatin inhibitor is myostatin propeptide.
3 . The method of claim 1 , wherein the myostatin inhibitor is a soluble myostatin receptor.
4 . The method of claim 1 , wherein said myostatin inhibitor is delivered to said injured musculoskeletal tissue via a biodegradable delivery system.
5 . The method of claim 4 , wherein said delivery system is a biodegradable hydrogel.
6 . The method of claim 5 , wherein said biodegradable hydrogel comprises hyaluronan-gelatin and heparin.
7 . The method of claim 4 , wherein said delivery system is biodegradable nanobeads.
8 . The method of claim 1 , wherein said injured musculoskeletal tissue is a fractured bone.
9 . A method of treating a fracture in an individual comprising:
administering a pharmacological amount of a myostatin inhibitor effective to inhibit myostatin function, thereby treating the fracture.
10 . The method of claim 9 , wherein the myostatin inhibitor is myostatin propeptide.
11 . The method of claim 9 , wherein the myostatin inhibitor is myostatin receptor.
12 . The method of claim 9 , wherein said myostatin inhibitor is delivered to the fractured bone via a biodegradable delivery system.
13 . The method of claim 12 , wherein said delivery system is a biodegradable hydrogel comprising hyaluronan-gelatin and heparin.
14 . The method of claim 12 , wherein said delivery system is biodegradable nanobeads.
15 . The method of claim 9 , wherein said fracture is a nonunion fracture.
16 . A method of treating a fracture in an individual comprising:
contacting said fracture with a biodegradable delivery vehicle containing a pharmacological amount of a myostatin inhibitor effective to inhibit myostatin function, thereby treating the fracture.
17 . The method of claim 16 , wherein the myostatin inhibitor is myostatin propeptide.
18 . The method of claim 16 , wherein said delivery system is a biodegradable hydrogel comprising hyaluronan-gelatin and heparin.
19 . The method of claim 16 , wherein said delivery system is a biodegradable nanobead.
20 . The method of claim 16 , wherein said fracture is a nonunion fracture.
21 . A method of treating a nonunion fracture in an individual comprising:
contacting said fracture with a biodegradable delivery vehicle containing a pharmacological amount of a myostatin propeptide effective to inhibit myostatin function, thereby treating the fracture.
22 . The method of claim 21 , wherein the biodegradable delivery vehicle comprises biodegradable nanobeads.
23 . A biodegradable composition containing a pharmacological amount of myostatin propeptide.
24 . The composition of claim 23 , wherein said composition is a hydrogel.
25 . The composition of claim 24 , wherein said hydrogel comprises hyaluronan-gelatin and heparin.
26 . The composition of claim 23 , wherein said composition is a nanobead.Join the waitlist — get patent alerts
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