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US 9,445,619 B2Granted
Compositions and methods for utilization of algal compounds
AssigneeAurora Algae, Inc.
InventorsJames Astwood, Michelle L. Collins, Brian Connolly
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AssigneeAurora Algae, Inc.
InventorsJames Astwood, Michelle L. Collins, Brian Connolly
Estimating the term…
Provided herein are exemplary compositions, products, and capsules utilizing POA, EPA, blends of POA and EPA, total algal oil compositions, and/or whole biomass compositions in methods of inhibiting inflammation including in cardiovascular disease, diabetes, obesity, stroke, metabolic syndromes, dementia, Alzheimer's disease, and/or cancer. The exemplary compositions, products, and capsules may be orally, topically, intravenously, and/or subcutaneously administered. The exemplary compositions herein may be used as feed, food, food supplements, beverages, beverage supplements, nutritional products, products for athletic performance, pharmaceutical products, and/or medical products for mammalian use, including humans.
A method for reducing inflammation due to cardiovascular disease in a human subject having a cardiovascular disease, the method comprising administering a pharmaceutically effective dose to the human subject a composition of:
A method for reducing in an obese human subject chronic inflammation due to obesity, the method comprising orally administering to the obese human subject on a daily basis for a treatment period of at least 30 days at least one capsule having at least approximately 25 percent of capsule volume comprising a pharmaceutically effective composition further comprising by dry weight approximately 90% palmitoleic acid, less than approximately 0.5% saturated fatty acids, less than approximately 2% arachidonic acid, substantially no docosahexaenoic acid, and less than approximately 10% eicosapentaenoic acid, wherein each ingredient of the composition is in a form of an ethyl ester (EE).
A method for reducing in a human subject having coronary artery disease inflammation due to coronary artery disease, the method comprising orally administering to the human subject on a daily basis for a treatment period of at least 30 days at least one capsule having at least approximately 25 percent of capsule volume comprising a pharmaceutically effective composition further comprising by dry weight approximately 90% palmitoleic acid, less than approximately 0.5% saturated fatty acids, less than approximately 2% arachidonic acid, substantially no docosahexaenoic acid, and less than approximately 10% eicosapentaenoic acid, wherein each ingredient of the composition is in a form of an ethyl ester (EE).
Dependencies are inferred from the claim text.