KRILL OIL PREPARATIONS WITH OPTIMAL MINERAL AND METAL COMPOSITION, LOW IMPURITIES AND LOW AND STABLE TMA LEVELS
A Krill oil preparation including a reduced amount of trimethylamine of 5 mgN/100 g or less, or more than 700 ppm by weight of endogenous calcium and/or less than 1200 ppm by weight of sodium. A process of making such a Krill oil preparation that includes a step of extracting Krill oil from Krill with a solvent mixture of one or more polar solvents and one or more non-polar solvents. A method of treating a human in need of treatment that includes administering to the human an amount of such a Krill oil preparation.
1 . A Krill oil preparation comprising Krill oil, wherein the Krill oil has a trimethylamine concentration of 5 mg Nitrogen per 100 g (mg N/100 g) or less.
2 . The Krill oil preparation of claim 1 , wherein the Krill oil has a trimethylamine concentration of 5 mg N/100 g or less after three months of storage at 40° C. or less.
3 . The Krill oil preparation of claim 1 , wherein the Krill oil has a concentration of endogenous calcium greater than 700 ppm by weight and/or a concentration of sodium of less than 1200 ppm by weight.
4 . The Krill oil preparation of claim 1 , wherein the Krill oil has a concentration of endogenous magnesium greater than 500 ppm by weight.
5 . The Krill oil preparation of claim 1 , wherein the Krill oil has a concentration of free choline of less than 450 ppm by weight and/or a concentration of betaine of less than 1000 ppm by weight and/or a total amino acid concentration of less than 0.3 g/100 g.
6 . The Krill oil preparation of claim 1 , wherein the Krill oil has a concentration of free choline of less than 450 ppm by weight and/or a concentration of betaine of less than 1000 ppm by weight and/or a concentration of less than 0.15 g per 100 g for each of the following amino acids: Alanine, Arginine, Aspartic acid, Cystine, Glutamic acid, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Ornithine, Phenylalanine, Proline, Serine, Hydroxyproline, Threonine, Tryptophan, Tyrosine, and Valine.
7 . A Krill oil preparation comprising Krill oil, wherein the Krill oil has a concentration of endogenous calcium greater than 700 ppm by weight and/or a concentration of sodium of less than 1200 ppm by weight.
8 . The Krill oil preparation of claim 7 , wherein the Krill oil has a concentration of endogenous magnesium greater than 500 ppm by weight.
9 . The Krill oil preparation of claim 7 , wherein the Krill oil has a concentration of free choline of less than 450 ppm by weight, and/or a concentration of betaine of less than 1000 ppm by weight and/or a total amino acid concentration of less than 0.3 g/100 g.
10 . The Krill oil preparation of claim 7 , wherein the Krill oil has a concentration of free choline less than 450 ppm by weight, and/or a concentration of betaine of less than 1000 ppm by weight and/or a concentration of less than 0.15 g per 100 g for each of the following amino acids: Alanine, Arginine, Aspartic acid, Cystine, Glutamic acid, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Ornithine, Phenylalanine, Proline, Serine, Hydroxyproline, Threonine, Tryptophan, Tyrosine and Valine.
11 . A composition comprising the Krill oil preparation of claim 1 .
12 . The composition of claim 11 , wherein the composition does not contain minerals or metals from non-Krill sources.
13 . The composition of claim 11 , wherein the composition is a capsule.
14 . The composition of claim 11 , wherein the composition is a nutraceutical.
15 . The composition claim 11 , wherein the composition is a dietary supplement.
16 . The composition claim 11 , wherein the composition is a pharmaceutical composition and comprises one or more pharmaceutical excipients.
17 . A process of making a Krill oil preparation, comprising a step of extracting Krill oil from Krill with a solvent mixture comprising one or more polar solvents and one or more non-polar solvents.
18 . The process of claim 17 , wherein the process is effective to reduce endogenous sodium levels in the Krill oil preparation to levels that are below endogenous calcium levels in the Krill oil preparation.
19 . The process of claim 17 , wherein the process is effective to reduce endogenous sodium in the Krill oil preparation to less than 1200 ppm by weight and/or to maintain endogenous calcium in the Krill oil preparation at more than 700 ppm by weight.
20 . The process of claim 17 , wherein the solvent mixture comprises hexane and ethanol.
21 . The process of claim 20 , wherein the volume ratio of hexane to ethanol in the solvent mixture is about 9:1.
22 . The process of claim 17 , further comprising at least one step of washing the extracted Krill oil with water.
23 . The process of claim 22 , wherein the extracted Krill oil is dissolved in an organic solvent mixture when the at least one step of washing the extracted Krill oil with water is conducted.
24 . A method of reducing a CVD risk factor, the method comprising administering to a human in need thereof an amount of the Krill oil preparation according to claim 1 effective to reduce the CVD risk factor.
25 . A method of reducing a CVD risk factor, the method comprising administering to a human in need thereof an amount of the Krill oil preparation according to claim 7 effective to reduce the CVD risk factor.
26 . The method according to claim 24 , wherein reducing the CVD risk factor is selected from reducing an amount of total cholesterol, reducing the amount of triglycerides, and increasing the amount of HDL-cholesterol.
27 . The method according to claim 24 , wherein reducing the CVD risk factor is selected from reducing an amount of total cholesterol, reducing the amount of triglycerides, and increasing the amount of HDL-cholesterol.