US2013018014A1PendingUtilityA1
New class of therapeutics that enhance small molecule diffusion
Assignee: DIFFUSION PHARMACEUTICALS LLCPriority: Oct 31, 2007Filed: Jun 22, 2012Published: Jan 17, 2013
Est. expiryOct 31, 2027(~1.3 yrs left)· nominal 20-yr term from priority
Inventors:John L. Gainer
A61P 35/00A61P 3/10A61P 9/00A61P 7/04A61P 7/06A61P 9/10A61P 9/12A61P 25/00A61P 27/02A61P 25/28A61K 47/50A61K 31/7016A61K 31/401A61K 31/14A61P 1/00A61K 31/232A61P 19/02A61P 11/06A61K 47/40A61K 33/42A61P 11/00A61P 13/12A61K 31/70A61K 31/17
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Claims
Abstract
The subject application relates to novel compositions containing a diffusion enhancing compound and their use in treating a variety of disorders.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical composition comprising a diffusion enhancing compound and a pharmaceutically acceptable carrier.
2 . A pharmaceutical composition comprising a unit dose of a diffusion enhancing compound and a pharmaceutically acceptable carrier.
3 . A pharmaceutical composition as in claim 1 wherein the diffusion enhancing compound is selected from the group consisting of trimethylamine N-oxide, proline, ectoine, trehalose and other disaccharides which increase hydrogen bonding, glycine betaine, 3-dimethylsulfoniopropionate, urea, maltose, glycerol, a small or multiply-charged ion with high charge density, t-butanol, and DMSO (dimethylsulfoxide).
4 . A pharmaceutical composition as in claim 1 wherein the diffusion enhancing compound is selected from the group consisting of trehalose, glycine betaine, and proline.
5 . A pharmaceutical composition as in claim 3 wherein the small or multiply-charged ion with high charge density is selected from the group consisting of SO 4 2− , HPO 4 2− , Mg 2+ , Ca 2+ , Li + , Na + , OH − , F − , and Cl − .
6 . A pharmaceutical composition as claim 1 wherein the composition is an aqueous based solution.
7 . A pharmaceutical composition as in claim 1 wherein the pharmaceutically acceptable carrier is selected from the group consisting of cyclodextrins, PEG and glycols.
8 . (canceled)
9 . A method of treating hemorrhagic shock in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
10 . A method of treating a hypoxic condition in a mammal comprising administering to said mammal a diffusion enhancing compound other than a bipolar trans carotenoid in an amount sufficient to increase tissue oxygenation.
11 . A method of treating respiratory disease, asthma, emphysema, ALI, ARDS, COPD in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
12 . A method of treating cardiovascular disease, myocardial infarction, hypertension, ischemia or stroke, in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
13 . A method of treating traumatic brain injury or Alzheimer's disease in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
14 . A method of treating anemia in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
15 . A method of treating chronic renal failure in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
16 . A method of treating cancer in a mammal comprising administering before during or after radiation therapy or chemotherapy to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
17 . A method of treating hypertension or myocardial infarction in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
18 . A method of treating diabetes, diabetic retinopathy, peripheral vascular disease/claudication, or spinal stenosis/neurogenic claudication in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than a bipolar trans carotenoid.
19 . A method as in claim 9 , wherein the diffusion enhancing compound is selected from the group consisting of trimethylamine N-oxide, proline, ectoine, maltose, trehalose and other disaccharides which cause increased hydrogen bonding, glycine betaine, 3-dimethylsulfoniopropionate, urea, glycerol, a small or multiply-charged ion with high charge density, t-butanol, and DMSO (dimethylsulfoxide).
20 . A method as in claim 9 , wherein the diffusion enhancing compound is selected from the group consisting of trehalose, glycine betaine, and proline.
21 . A method as in claim 9 , wherein said administration is selected from the group consisting of nasal, parenteral, transdermal, intramuscular injection and oral delivery.
22 . A method of treating Wegener's granulomatosis in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound.
23 . A method of treating cancer in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound as an adjunct to radiation therapy and/or chemotherapy.
24 . A method of treating arthritis in a mammal comprising administering to said mammal a therapeutically effective amount of a diffusion enhancing compound other than crocetin.
25 . A method as in claim 22 , 23 or 24 , wherein the diffusion enhancing compound is a bipolar trans carotenoid.
26 . A method as in claim 22 , 23 or 24 , wherein the diffusion enhancing compound is TSC.Cited by (0)
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