Composition and method for the treatment of neurological diseases and cerebral injury
US-2015359762-A1 · Dec 17, 2015 · US
US11065272B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11065272-B2 |
| Application number | US-201615766314-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 6, 2016 |
| Priority date | Oct 6, 2015 |
| Publication date | Jul 20, 2021 |
| Grant date | Jul 20, 2021 |
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Methods and compositions for treating traumatic brain injury. The methods and compositions utilize a multi-functional oxygen reactive polymer (ORP) that includes repeating units that include a reactive oxygen species (ROS) scavenging group and a polyalkylene oxide group. For theranostic applications, the oxygen reactive polymer further includes a diagnostic group.
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The invention claimed is: 1. A method for treating traumatic brain injury, comprising administering a therapeutically effective amount of an oxygen reactive copolymer to a subject in need thereof, wherein the oxygen reactive copolymer has the formula wherein n is an integer from 1 to 12, m is an integer from 0 to 12, and p is an integer from 6 to 40; and *represents the remainder of the copolymer. 2. The method of claim 1 , wherein treating traumatic brain injury comprises reducing neurodegeneration. 3. The method of claim 1 , wherein treating traumatic brain injury comprises altering gliosis. 4. The method of claim 1 , wherein treating traumatic brain injury comprises treating the secondary effects of traumatic brain injury. 5. The method of claim 1 , wherein treating traumatic brain injury comprises treating one or more of reperfusion injury, delayed cortical edema, blood-brain barrier breakdown, local electrolyte imbalance, neurovascular unit dysfunction, and intracranial pressure. 6. The method of claim 1 , wherein administering the oxygen reactive polymer comprises intravenous, intranasal, intrathecal/intraventrical, or intracranial administration. 7. The method of claim 1 , wherein the oxygen reactive polymer is in the form of a nanoparticle. 8. The method of claim 7 , wherein the nanoparticle comprises a single oxygen reactive polymer. 9. The method of claim 1 , wherein the diagnostic group is a magnetic resonance imaging group, a radiolabel group, a fluorescent group, a luminescent group, an X-ray/CT group, or an ultrasound group. 10. The method of claim 1 , wherein the copolymer is a random copolymer. 11. The method of claim 1 , wherein the copolymer has a hydrodynamic diameter from about 4 to about 100 nm. 12. The method of claim 1 , wherein the copolymer has a molar mass dispersity from about 1.05 to about 1.30. 13. The method of claim 1 , wherein the copolymer has a number average molecular weight (M n ) from about 5,000 to about 100,000.
Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates · CPC title
Particulate form, e.g. powders, {Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles (microspheres A61K9/16; microcapsules A61K9/50; nanocapsules, nanoparticles of the matrix type A61K9/51)} · CPC title
for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia · CPC title
Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title
Polymers containing oxygen · CPC title
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