IP Library Granted Patent US 11,633,443
Granted Patent B2
US 11,633,443 · App. 17/028,768 · Granted Apr 25, 2023

Algal extract comprising sulphated and non-sulphated polyanionic polysaccharides and uses thereof

Inventors: Hervé Demais (Merlevenez, FR); Sebastien Balusson (Saint Etienne du Gue de l'Isle, FR)
Assignee: Amadeite
A61K36/05A61K31/737
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Quick Facts
Patent No.
US 11,633,443
App. No.
17/028,768
Granted
Apr 25, 2023
Kind
B2
Abstract

The present invention relates to an algal extract comprising sulphated and non-sulphated polyanionic polysaccharides, to a method for preparing an algal extract as well as to its therapeutic and prophylactic applications.

Claims (46)

1. A method for treating anxiety, the method comprising the administration of an effective amount of an algal extract from the order of Ulvales comprising sulphated and non-sulphated polyanionic polysaccharides, the size of which is less than or equal to 50 kDa, wherein the algal extract is prepared by a process comprising the following steps:

a) washing the algae and freeing the algae of sand;

b) crushing the washed and freed algae to create a crushed product comprising a solid phase and a liquid phase;

c) separating the solid phase of the crushed product from the liquid phase of the crushed product;

d) clarifying the separated liquid phase to form a juice;

e) filtering the juice with a membrane of less than 50 kDa; and

f) concentrating the filtered juice; and

g) drying the concentrated juice.

2. The method according to claim 1 , wherein the extract is an extract of green algae of the type Ulva.

3. The method according to claim 1 , wherein said polysaccharides comprise mannose and/or arabinose.

4. The method according to claim 3 , wherein said polysaccharides comprise at least 0.005% of mannose and/or at least 0.005% of arabinose, by weight based on the weight of the total dry material of the algal extract.

5. The method according to claim 4 , wherein said polysaccharides comprise mannose at an amount in a range from 0.01 to 0.20% and arabinose at an amount in the range of 0.01 to 0.5%, by weight based on the weight of the total dry material of the algal extract.

6. The method according to claim 1 , wherein said polysaccharides further comprise galactose, glucose, rhamnose, xylose, and glucuronic acid.

7. The method according to claim 6 , wherein:

the galactose is at an amount in the range of 0.05 to 0.5%;

the glucose is at an amount in the range of 0.005 to 0.05%;

the rhamnose is at an amount in the range of 2 to 15%;

the xylose is at an amount in the range of 0.1 to 1%; and

the glucuronic acid is at an amount in the range of 1 to 7%;

by weight based on the weight of the total dry material of the algal extract.

8. The method according to claim 1 , wherein said polysaccharides have a size of less than or equal to 15 kDa.

9. The method according to claim 1 , wherein the algal extract comprises:

carbon at an amount in the range of 10 to 50%;

hydrogen at an amount in the range of 1 to 10%;

nitrogen at an amount in the range of 1 to 5%;

oxygen at an amount in the range of 20 to 50%; and

sulphur at an amount in the range of 1 to 15%;

in weight percentage of the total dry material of the algal extract.

10. The method according to claim 1 , wherein the algal extract comprises:

carbon at an amount in the range of 15 to 30%;

hydrogen at an amount in the range of 3 to 6%;

nitrogen at an amount in the range of 1 to 3%;

oxygen at an amount in the range of 25 to 40%; and

sulphur at an amount in the range of 2.5 to 10%;

in weight percentage of the total dry material of the algal extract.

11. The method according to claim 1 , wherein membrane is a 15 kDa membrane.

12. The method according to claim 1 , wherein solid phase is separate from the liquid phase by pressing the crushed product.

13. The method according to claim 1 , wherein:

the algae is washed in freshwater;

the algae are crushed with a refiner;

the solid phase of the crushed product is separated from the liquid phase of the crushed product by pressing the crushed product with a belt press;

the separated liquid phase is clarified with a clarifier with disc stacks;

the membrane is a 15 kDa ceramic membrane;

the filtered juice is concentrated by evaporation; and/or

the concentrated juice is dried by freeze-drying or atomization.

14. The method according to claim 1 , wherein the composition further comprises for at least one pharmaceutically acceptable excipient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2020
From: DEMAIS, HERVE; BALUSSON, SEBASTIEN
To: AMADEITE
Reel/Frame 054317/0682 →
Priority Claims (1)
FR 1261909 · Dec 11, 2012 · national
Continuity (3)
Continuation 16017862 · Jun 25, 2018
Division 14651345
Related Publication 20210038662A1 · Feb 11, 2021
Cited By (1)
US 12,377,126