Thixotropic oxidized cellulose solutions and medical applications thereof
US-2016346316-A1 · Dec 1, 2016 · US
US9579346B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9579346-B2 |
| Application number | US-201414271054-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 6, 2014 |
| Priority date | Aug 6, 2009 |
| Publication date | Feb 28, 2017 |
| Grant date | Feb 28, 2017 |
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The present invention provides a method of treating a macrophage related disease comprising administering to a subject in need thereof an effective amount of an oxidative agent or an immunosuppressive agent. The present invention also provides a method of modulating macrophage accumulation or activation comprising administering to a subject in need thereof an effective amount of an oxidative agent or an immunosuppressive agent. The oxidative agent can be chlorite or a chlorite containing compound.
Opening claim text (preview).
What is claimed is: 1. A sodium chlorite compound, wherein said compound is a crystalline solid of greater than 95% purity; wherein said compound has an x-ray powder diffraction pattern with peaks expressed in degrees 2θ at about 21, 30, 32, 34, and 39; and wherein said compound has an x-ray powder diffraction (XRPD) pattern as shown in FIG. 6 . 2. A compound of claim 1 , wherein said compound is a crystalline solid of greater than 99% purity. 3. A compound of claim 1 , wherein said compound is a crystalline solid of greater than 99.9% purity. 4. The compound of claim 1 , wherein said compound is substantially free of chlorate. 5. The compound of claim 1 , wherein said compound is substantially free of sulfate. 6. A pharmaceutical composition comprising: a) the compound of claim 1 ; b) a pH adjusting agent; and c) a pharmaceutically acceptable excipient or carrier; wherein said composition is a liquid that exhibits 25% less pH drift compared to an identical composition without said pH adjusting agent. 7. The composition of claim 6 , wherein said pH adjusting agent is sodium phosphate dibasic. 8. The composition of claim 6 , wherein said compound is substantially free of chlorate. 9. The composition of claim 6 , wherein said compound is substantially free of sulfate. 10. A solid pharmaceutical composition comprising: a) the compound of claim 1 ; and b) a pharmaceutically acceptable excipient or carrier. 11. The composition of claim 10 , wherein said compound is substantially free of chlorate. 12. The composition of claim 10 , wherein said compound is substantially free of sulfate. 13. A method of treating a disease associated with migration of monocytes or activated macrophages, said method comprising administering a therapeutically-effective amount of the compound of claim 1 . 14. The method of claim 13 , wherein said disease is characterized by elevated CD16 expression levels in CD14+cells. 15. The method of claim 13 , wherein said disease is characterized by migration of PBMCs in response to a chemoattractant. 16. A method of treating a disease associated with excess activation of monocytes to activated macrophages, said method comprising administering a therapeutically-effective amount of the compound of claim 1 . 17. The method of claim 16 , wherein said disease is associated with excess CD14CD16 expression. 18. The method of claim 16 , wherein said disease is a neurodegenerative disease selected from the group consisting of amyotrophic lateral sclerosis (ALS), Parkinson's Disease (PD), Alzheimer's Disease (AD), and complications thereof. 19. A method of treating Type II diabetes or related complications comprising administering to a subject in need thereof an effective amount of the compound of claim 1 .
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