US2014199414A1PendingUtilityA1

Krill and/or marine extracts for prevention and/or treatment of cardiovascular diseases, arthritis, skin cancer, diabetes, premenstrual syndrome and transdermal transport

Assignee: NEPTUNE TECHNOLOGIES & BIORESSOURCES INCPriority: Jun 18, 2001Filed: Jan 10, 2014Published: Jul 17, 2014
Est. expiryJun 18, 2021(expired)· nominal 20-yr term from priority
Inventors:Tina Sampalis
A61P 9/12A61P 3/06A61P 9/10A61P 5/24A61P 7/02A61P 9/00A61P 37/06A61P 9/06A61P 3/08A61P 29/00A61P 3/10A61P 35/00A61K 31/685A61K 31/688A61K 31/20A61K 31/015A61K 31/07A61K 33/30A61P 15/08A61K 31/23A61K 31/683A61K 31/122A61K 31/202A61K 33/00A61K 35/612A61K 31/575A61P 19/02A61P 17/00A61P 17/02A61K 31/201A61K 31/355A61K 31/232A61K 9/48A61P 15/00A61K 9/0053
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Claims

Abstract

The present invention relates to a method of treatment and/or prevention of cardiovascular disease, rheumatoid arthritis, skin cancer, premenstrual syndrome, diabetes and transdermal transport enhancement. The method comprises the administration of a therapeutically effective amount of krill and/or marine oil to a patient. The present invention also relates to a composition for the treatment and/or prevention of these diseases.

Claims

exact text as granted — not AI-modified
1 - 57 . (canceled) 
     
     
         58 . A method for reducing cholesterol, comprising administrating a krill oil extract to a human subject, wherein:
 the krill oil is administered to the human subject in a quantity in a range of about 1 to about 4.8 grams per day, and   the krill oil is obtainable by a process comprising the steps of:
 a) placing krill in a ketone solvent to achieve extraction of the soluble lipid fraction from said krill; 
 b) separating the liquid and solid phases; 
 c) recovering a first lipid rich fraction from the liquid phase obtained at step (b) by evaporation of the solvent present in the liquid phase; 
 d) placing the solid phase in an organic solvent selected from the group consisting of alcohol and esters of acetic acid to achieve extraction of the remaining soluble lipid fraction from the solid phase; 
 e) separating the liquid and solid phases; and 
 f) recovering a second lipid rich fraction from the liquid phase obtained at step (e) by evaporation of the solvent present in the liquid phase. 
   
     
     
         59 . The method of  claim 58 , wherein the ketone solvent used in step (a) of the process is acetone. 
     
     
         60 . The method of  claim 58 , wherein the organic solvent used in step (d) of the process is selected from ethanol, isopropanol and t-butanol. 
     
     
         61 . The method of  claim 58 , wherein the organic solvent used in step (d) of the process is ethyl acetate. 
     
     
         62 . The method of  claim 58 , wherein the quantity is about 1 gram per day. 
     
     
         63 . The method of  claim 58 , wherein said krill oil comprises Eicosapentanoic acid, Docosahexanoic acid, Phosphatidylcholine, Phosphatidylinositol, Phosphatidylserine, Phosphatidylethanolamine, Sphingomyelin, α-tocopherol, all-trans retinol, Astaxanthin and flavonoid. 
     
     
         64 . The method of  claim 58 , wherein said krill oil comprises Eicosapentanoic acid, Docosahexanoic acid, Linolenic acid, α-linolenic acid, Arachidonic acid, oleic acid, palmitic acid, palmitoleic acid, stearic acid, nervonic acid, Phosphatidylcholine, Phosphatidylinositol, Phosphatidylserine, Phosphatidylethanolamine, Sphingomyelin, cholesterol, triglycerides, monoglycerides, α-tocopherol, all-trans retinol, Astaxanthin, canthaxanthin, β-carotene, flavonoid, zinc, selenium, sodium, potassium and calcium. 
     
     
         65 . The method of  claim 58 , wherein said patient is a patient suffering from hyperlipidemia. 
     
     
         66 . The method of  claim 58 , wherein said composition is administered orally. 
     
     
         67 . The method of  claim 62 , wherein said composition is administered orally.

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