IP Library Granted Patent US 11,020,438
Granted Patent B2
US 11,020,438 · App. 16/582,618 · Granted Jun 1, 2021

Phospholipid compositions and their preparation

Inventors: Finn Myhren (Oslo, NO); Nils Hoem (Oslo, NO); Håvard Thøgersen (Oslo, NO)
Assignee: Aker BioMarine Antarctic AS
A61K35/612A61K31/122A61K31/20A61K31/201A61K31/575A61K31/683A61K31/685
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Quick Facts
Patent No.
US 11,020,438
App. No.
16/582,618
Granted
Jun 1, 2021
Kind
B2
Abstract

The invention provides improved processes for extracting and preparing polar lipids (in particular, desirable phospholipids) from krill and other biological sources. The inventors have discovered processes through which it is possible to extract phospholipids to give high phospholipid content and a reduction of undesired components.

Claims (27)

1. A composition comprising a mixture of phospholipid compounds of formula (I):

wherein:

R 1 and R 2 are each independently selected from a fatty acid moiety of formula —COC n H m , a fatty acid moiety of formula —CH 2 C n H m , and —H, wherein n is from 11 to 22 and for any value of n, m=2n+1;

R 1 and R 2 include omega-3 fatty acid moieties, such that at least 30% by weight of the phospholipid compounds is composed of omega-3 fatty acid moieties;

at least 90% by weight of total omega-3 fatty acid moieties are at position R 2 ;

R 1 and R 2 are not both H in a phospholipid compound, and R 1 or R 2 is H in less than 3% by weight of the compounds of formula (I);

R 3 is selected from —H, a choline moiety, an ethanolamine moiety, a N-acetylethanolamine moiety, an inositol moiety, and a serine moiety; and

R 3 is a choline moiety in at least 85% by number of the compounds of formula (I), and wherein the composition also has one three or more of the following properties:

(a) at least 85% by weight of the composition consists of phospholipid compounds of formula (I);

(b) the weight ratio of C16:0/C14:0 fatty acid moieties in the mixture is between 10:1 and 18:1 and/or the weight ratio of C18:4 n-3/C18:3 n-3 fatty acid moieties is between 1:1 and 3:2;

(c) the composition includes less than 300 μg astaxanthins per gram of phospholipid;

(d) the composition comprises less than 0.01% by weight trimethylamine N-oxide;

(e) the composition comprises less than 0.01% by weight homarine;

(f) the composition includes less than 5% by weight water;

(g) the composition has less than about 0.03% by weight PUFA polymers

(h) the mixture includes both phospholipids where R 1 is a fatty acid moiety of formula —COC n H m and phospholipids where R 1 is a fatty acid moiety of formula —CH 2 C n H m ;

(i) the mixture includes both phospholipids where R 1 is an omega-3 fatty acid moiety and phospholipids where R 2 is an omega-3 fatty acid moiety;

(j) the composition includes less than 5% by weight sphingomyelin;

(k) the composition is free from chloroform and hexane; and/or

(l) less than 0.9% by weight of phospholipids in the composition is formed of compounds where R 1 or R 2 is —H, or more than 1.1% by weight of phospholipids in the composition is formed of compounds where R 1 or R 2 is —H.

2. The composition of claim 1 , wherein less than 0.9% by weight of phospholipids in the composition is formed of compounds where R 1 or R 2 is —H.

3. The composition of claim 1 , having at least properties (h) and (i).

4. The composition of claim 3 , having at least properties (a), (c), (d), (e), (g) and (j).

5. The composition of claim 4 , having at least properties (a), (b), (c), (d), (e), (g) and (j).

6. The composition of claim 3 , having at least properties (a), (c), (d), (e), (f), (h), (j), and (k).

7. The composition of claim 6 , having properties (a), (b) (c), (d), (e), (f), (h), (j), and (k), and wherein: with reference to property (h) fatty acid moieties of formula —CH 2 C n C m are either saturated or mono-unsaturated, and not polyunsaturated; the compounds of formula (I) include C16:0, C14:0, C18:4 n-3 and C18:3 n-3 fatty acid moieties at R 1 and/or R 2 ; the amount of water is less than 2% by weight; the composition has less than 1% by weight free fatty acids; the composition has less than 0.005% by weight trimethylamine; the composition is free from canthaxanthin and flavonoid; and, optionally, wherein the phospholipids of formula (I) include EPA and DHA moieties in a molar ratio (EPA:DHA) from 1.8:1 to 2.2:1.

8. A composition comprising (1) a pharmaceutically-acceptable solvent and (2) a mixture of phospholipid compounds of formula (I), as defined in claim 1 , and further having three or more of properties (b) to (I) as defined in claim 1 , wherein the phospholipid compounds of formula (I) are dissolved, suspended or emulsified in the pharmaceutically-acceptable solvent, and wherein the composition is liquid when at 20° C.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2024
From: AKER BIOMARINE ANTARCTIC AS
To: AKER BIOMARINE HUMAN INGREDIENTS AS
Reel/Frame 066703/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 5, 2021
From: MYHREN, FINN; HOEM, NILS; THOGERSEN, HAVARD
To: AKER BIOMARINE ANTARCTIC AS
Reel/Frame 054809/0331 →
Priority Claims (1)
GB 1400431 · Jan 10, 2014 · national
Continuity (3)
Continuation 15869579 · Jan 12, 2018
Continuation 15110554
Related Publication 20200016214A1 · Jan 16, 2020