Composition of and method for treating injury and/or skin conditions
US-2024139138-A1 · May 2, 2024 · US
US9827279B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9827279-B2 |
| Application number | US-200913001814-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 7, 2009 |
| Priority date | Jul 7, 2008 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A xanthine oxidase inhibitor and a uric acid-producing inhibitor, each containing an extract from at least one member selected from the group consisting of Zanthoxylum bungeanum, Sorghum nervosum, Cuminum cyminum, Rosa centifolia, Pimenta officinalis, Origanum majorana, Psidium guajava, Pimpinella anisum, Olea europaea, Illicium verum, Canavalia gladiata, Hyssopus officinalis, Ribes nigrum, Vaccinium myrtillus, Artemisia princeps and Haematoxylon campechianum L.
Opening claim text (preview).
What is claimed is: 1. A method of controlling or reducing a patient's blood uric acid level in a hyperuricemia patient in need of the same which comprises orally administering to the hyperuricemia patient a therapeutically effective amount of a Sorghum nervosum extract, wherein said extract is prepared by a method comprising extracting Sorghum nervosum with an extraction solvent selected from the group consisting of water, ethanol, and a mixture of water and ethanol. 2. The method of claim 1 , wherein the dose of the extract that is administered to the patient is 0.001 to 10 g/kg of body weight per day. 3. The method of claim 1 , wherein the patient's blood uric acid concentration is more than 7 mg/dL. 4. The method of claim 1 , wherein the extraction solvent is water, or a mixture of water and ethanol that contains up to 50% ethanol. 5. The method of claim 1 , wherein the hyperuricemia patient has gout or is in need of reducing the probability of developing gout. 6. The method of claim 5 , wherein the dose of the extract that is administered to the patient is 0.001 to 10 g/kg of body weight per day. 7. The method of claim 5 , wherein the patient's blood uric acid concentration is more than 7 mg/dL. 8. The method of claim 5 , wherein the extraction solvent is water, or a mixture of water and ethanol that contains up to 50% ethanol. 9. The method of claim 5 , wherein the hyperuricemia patient is in need of reducing the probability of developing gout.
Drugs for disorders of the cardiovascular system · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title
Antihypertensives · CPC title
Food compositions, function of food ingredients or processes for food or foodstuffs · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.