US2016143886A1PendingUtilityA1
Compositions And Method For Treatment Of Ischemic Neuronal Reperfusion Injury
Individually held — no corporate assignee on recordPriority: May 8, 2013Filed: Jan 28, 2016Published: May 26, 2016
Est. expiryMay 8, 2033(~6.8 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 9/10A61K 31/59A61K 45/06A61K 31/765A61K 38/05A61K 31/4178A61K 31/5513A61K 31/355A61P 25/00A61K 31/40A62B 17/00A61K 31/5517C07D 405/12A61K 31/13Y10T428/2982
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Claims
Abstract
A method and composition for the treatment of ischemic neuronal reperfusion injury are provided. The composition can include a compound which is a combination of dantrolene and a residue of FMOC-valine. This composition can be used to provide a faster and higher CNS penetration than heretofore experienced with dantrolene. In another form, dantrolene may be formulated as a pro-drug, a pro-pro-drug and the like.
Claims
exact text as granted — not AI-modified1 .- 18 . (canceled)
19 . A method of treatment of neuronal reperfusion injury with ischemic neuropathy, the method comprising:
administering an effective amount of at least one compound selected from the group consisting of a pro-drug form of dantrolene, a pro-pro-drug form of dantrolene, and mixtures thereof.
20 . The method of claim 19 wherein the step of administering is performed intranasally using a positive pulsating pressure with pulses occurring about every 5 seconds to 3 minutes.
21 . The method of claim 19 wherein the at least one compound is in the form of nanoparticles.
23 . The method of claim 19 wherein the at least one compound is administered via a nebulizer.
24 . The method of claim 19 wherein the at least one compound is administered in combination with at least one of Vitamin D, Vitamin E, and pluronic acid.
25 . The method of claim 19 wherein the at least one compound is in the form of a suspension or emulsion.
26 . The method of claim 19 wherein the at least one compound is delivered to a patient via an administration selected from the group consisting of orally, subcutaneously, parenterally, intravenously, intranasally, intrathecally, sublingually, rectally, and topically.
27 . The method of claim 19 wherein the at least one compound is administered in a dosage of about 100 ng/kg per day to about 100 mg/kg per day.
28 . A gas mask which includes at least one of a compound being deliverable to a wearer, the compound selected from the group consisting of a pro-drug form of dantrolene, a pro-pro-drug form of dantrolene, and mixtures thereof.
29 . The gas mask of claim 28 further comprising at least one of Vitamin D, Vitamin E, and pluronic acid in combination with the compound.
30 . The gas mask of claim 28 wherein the compound is in the form of a suspension or emulsion.
31 . The gas mask of claim 28 wherein the at least one compound is in the form of nanoparticles.
32 . A method of protecting a human from a nerve gas, the method comprising administering at least one of a compound through the lungs or intranasally, the compound selected from the group consisting of a pro-drug form of dantrolene, a pro-pro-drug form of dantrolene, and mixtures thereof.
33 . The method of claim 32 wherein the step of administering is performed intranasally using a positive pulsating pressure with pulses occurring about every 5 seconds to 3 minutes.
34 . The method of claim 32 wherein the at least one compound is in the form of nanoparticles.
35 . The method of claim 32 wherein the at least one compound is administered via a nebulizer.
36 . The method of claim 32 wherein the at least one compound is administered in combination with at least one of Vitamin D, Vitamin E, and pluronic acid.
37 . The method of claim 32 wherein the at least one compound is in the form of a suspension or emulsion.Join the waitlist — get patent alerts
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