US2012136053A1PendingUtilityA1
Copepod oil composition, formulations comprising the oil composition, and the use thereof to reduce accumulation of visceral fat, improve glucose tolerance, and prevent or treat obesity related diseases and disorders
Est. expiryJun 12, 2029(~2.9 yrs left)· nominal 20-yr term from priority
A61P 3/10A61P 43/00A23L 33/30A23L 33/12A23D 9/013A61P 3/00A23L 33/115A61K 31/232A23V 2002/00A23K 20/158A61K 35/612A61K 31/122A61P 3/04A61K 35/63A61K 31/231A61K 31/202A61K 31/201A61K 35/64
33
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Claims
Abstract
This invention relates to an oil composition, preferably obtained from a copepod, and the use thereof to reduce accumulation of visceral fat and counteract impairment of heart function caused by obesity inducing Western diets. The oil composition of the present invention can thus be used to reduce abdominal obesity and improve glucose tolerance and thus to reduce the risk of obesity related diseases such as but not limited to type 2 diabetes or cardiovascular disease, or to prevent or treat such diseases.
Claims
exact text as granted — not AI-modified1 .- 17 . (canceled)
18 . Oil composition comprising 20-100% by weight of wax esters, wherein said wax esters consist of monoesters of mono- or polyunsaturated C16 to C22 fatty acids and monounsaturated C16 to C22 fatty alcohols.
19 . Composition according to claim 18 comprising 40-85% by weight of wax esters.
20 . Composition according to claim 18 wherein 70% or more of the monounsaturated fatty alcohols of the wax esters are C16:1, C20:1 and C22:1.
21 . Composition according to claim 18 wherein 70% or more of the fatty alcohols of the wax esters are monounsaturated, and wherein 50% or more of the fatty acids of the wax ester are either mono- or polyunsaturated n-3 fatty acids.
22 . Composition according to any one of claims 18 to 21 wherein the composition comprises 5-20% by weight of stearidonic acid (SDA).
23 . Composition according to claim 22 wherein the composition comprises 3-20% by weight of eicosapentaenoic acid (EPA) and 2-15% by weight of docosahexaenoic acid (DHA).
24 . Composition according to claim 23 wherein the composition comprises fatty alcohols and SDA, DHA and EPA as monoesters.
25 . Composition according to claim 18 wherein the composition contains 500-4000 ppm of astaxanthin.
26 . Composition according to any one of claim 18 to 21 or 25 wherein said composition is isolated from a copepod of the genus Calanus.
27 . Composition according to claim 26 wherein said copepod is of the species Calanus finmarchicus.
28 . A composition according to any one of claim 18 to 21 or 25 , wherein the composition is provided as a pharmaceutical composition in capsules, tablets, emulsions or tonics.
29 . A composition according to claim 28 , further comprising one or more pharmaceutically acceptable additives selected from the group consisting of adjuvants, stabilizers, antioxidants, emulsifiers, surfactants and carriers.
30 . A method for the prevention or treatment of abdominal obesity and type 2 diabetes comprising administering to a patient in need thereof a clinically effective dosage of composition comprising 20-100% by weight of wax esters, wherein said wax esters consist of monoesters of mono- or polyunsaturated C16 to C22 fatty acids and monounsaturated C16 to C22 fatty alcohols.
31 . A method according to claim 30 , comprising administering to a patient in need thereof a clinically effective dosage of composition comprising 40-85% by weight of wax esters.
32 . A method according to claim 30 , comprising administering to a patient in need thereof a clinically effective dosage of composition wherein 70% or more of the monounsaturated fatty alcohols of the wax esters are C16:1, C20:1 and C22:1.
33 . A method according to claim 30 , comprising administering to a patient in need thereof a clinically effective dosage of composition wherein 70% or more of the fatty alcohols of the wax esters are monounsaturated, and wherein 50% or more of the fatty acids of the wax ester are either mono- or polyunsaturated n-3 fatty acids.
34 . A method according to claim 30 , comprising administering to a patient in need thereof a clinically effective dosage of composition comprising 5-20% by weight of stearidonic acid (SDA
35 . A method according to claim 30 , comprising administering to a patient in need thereof a clinically effective dosage of composition containing 500-4000 ppm of astaxanthin
36 . A method according to any one of claims 30 to 35 , wherein the clinically effective dosage is a daily amount of 0.5 to 5 g of the oil composition.Join the waitlist — get patent alerts
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