Bone delivery system having a therapeutic agent
US-2015343114-A1 · Dec 3, 2015 · US
US9623044B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9623044-B2 |
| Application number | US-201314414994-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 16, 2013 |
| Priority date | Jul 19, 2012 |
| Publication date | Apr 18, 2017 |
| Grant date | Apr 18, 2017 |
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The present invention relates to chitosan hydrogel microparticles of a median size d50 comprised between 1 and 500 μm (obtained from a number distribution), the chitosan having a degree of acetylation of less than equal to 20% and its concentration in the hydrogel being comprised between 0.25 and 5% by weight based on a total weight of the hydrogel, for use in neuron regeneration and/or in the repair of the nervous system, advantageously of the central nervous system, and/or in the grafting of neurons and/or in the treatment of neurodegenerative diseases and/or in the treatment of paralyses. It also relates to an implant comprising an aqueous suspension of microparticles mixed with Schwann cells and/or stem cells and/or trophic factors.
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The invention claimed is: 1. A method of neuron regenerating and/or repairing of the nervous system, and/or grafting of neurons or precursors of neural cells, and/or treatment of neurodegenerative diseases, and/or treatment of ischemic wounds and/or treatment of paralyses, the method comprising: administering, to a mammal in need thereof, an effective amount of chitosan hydrogel microparticles; wherein said microparticles have a median size d50, obtained from a number distribution, of from 1 to 500 μm; wherein said chitosan has a degree of acetylation of less than or equal to 20%; wherein the concentration of chitosan in the hydrogel is from 0.25 to 5% by weight, based on the total weight of the hydrogel; and wherein the microparticles are administered subsequent to a traumatic lesion of the nervous system of the mammal, which is a traumatic lesion of the spinal cord. 2. The method according to claim 1 , wherein the median size d50 of the microparticles is from 5 to 300 μm. 3. The method according to claim 1 wherein the degree of acetylation of the chitosan is less than 5%. 4. The method according to claim 1 , wherein the concentration of the chitosan in the hydrogel is less than 4% by weight, based on the total weight of the hydrogel. 5. The method according to claim 1 , wherein the hydrogel is a physical chitosan hydrogel, such that interactions responsible for the inter-chain cross-linking in the hydrogel are of a physical type. 6. The method according to claim 1 , comprising administering the microparticles in an aqueous suspension having a viscosity greater than 1000 Pa·s measured in a continuous mode at 22° C. for a shear rate of 0.001 s −1 . 7. The method according to claim 6 , wherein the aqueous suspension is in an injectable form or an implantable form. 8. The method according to claim 6 , comprising mixing the microparticles with a member selected from the group consisting of Schwann cells, stem cells, trophic factors, and a combination thereof. 9. The method according to claim 1 , wherein the mammal is a human being.
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