IP Library Granted Patent US 10,597,608
Granted Patent B2
US 10,597,608 · App. 15/750,485 · Granted Mar 24, 2020

Cetylated fatty acids, system for the preparation thereof and use thereof

Inventors: Andrea Lacorte (Pisa, IT); Germano Tarantino (Pisa, IT); Paolo Bondioli (Milan, IT)
Assignee: PHARMANUTRA S.P.A.
C11C3/003A61K31/23C07C67/08C07C69/24A61P9/00A61P19/02A61P37/02Y02P20/582
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Quick Facts
Patent No.
US 10,597,608
App. No.
15/750,485
Granted
Mar 24, 2020
Kind
B2
Abstract

The present invention relates to a process for preparing a mixture of cetylated fatty acids and a system for carrying out said process. Furthermore, the present invention relates to a composition comprising, or alternatively, consisting of said mixture of cetylated fatty acids. Finally, the present invention relates to said composition for use in the treatment and/or prevention of: (i) rheumatoid arthritis of inflammatory and non-inflammatory origin, in particular osteoarthritis; (ii) other inflammatory joint conditions; (iii) psoriasis, lupus, periodontal diseases or cardiovascular or heart diseases; (iv) all post-traumatic osteoarticular pathologies including sports injuries; (v) all degenerative joint pathologies (arthrosis, gonarthrosis, coxarthrosis, etc.), and (vi) inflammatory-traumatic tendon and muscular conditions. Furthermore, it is envisaged that the composition of the present invention be used in the treatment and/or prevention of the above-mentioned pathologies and disorders (i)-(vi) in association with a rehabilitative therapy. The composition comprising said mixture is formulated in a pharmaceutical form for oral use (novel food, supplement or medical device), i.e. in the form of a pill, pastille, capsule, tablet, granules, dispersible powder, syrup, solution or sprayable solution; for topical use, i.e. in the form of a cream, unguent, ointment, gel or spray to be used as such for application on the skin, or else for trans dermal use in the form of a patch.

Claims (12)

1. A process for preparing a mixture of cetylated fatty acids (MI) comprising the steps of:

placing in contact, in a container ( 3 ) of a reactor ( 2 ), at least one fatty acid selected from the group comprising or, alternatively, consisting of myristic acid, oleic acid or mixtures thereof, with a cetyl alcohol and a metal catalyst, in the absence of a solvent, so as to yield a reaction mixture ( 15 );

heating said reaction mixture ( 15 ) to a reaction temperature comprised from 150° C. to 200° C. and a reaction pressure of about 1 atmosphere, so as to give rise to an esterification reaction with the initial formation of esters of cetylated fatty acids and esterification water;

allowing said reaction mixture ( 15 ) to react for a reaction time comprised from 1 hour to 8 hours until completion of said esterification reaction so as to obtain the complete formation of a mixture of cetylated fatty acids (MI) and the complete removal of said esterification water, the latter being achieved by introducing a flow of inert gas into the container ( 3 ) of said reactor ( 2 ) for the whole reaction time.

2. The process according to claim 1 , wherein said complete removal of esterification water is achieved by maintaining the reaction pressure constant at about 1 atm and introducing said flow of inert gas, via a blowing means ( 7 ), into the portion of volume above the reaction mixture ( 15 ), thus allowing the esterification water to be drawn out of the container ( 3 ).

3. The process according to claim 2 , wherein the esterification water drawn out of the container ( 3 ) during the esterification reaction at a constant reaction pressure is condensed in a horizontal condenser ( 11 ) and collected in a container ( 13 ).

4. The process according to claim 1 , wherein said complete removal of esterification water is achieved by using a vacuum program that applies a reduction in the reaction pressure in a non-linear manner and introducing said flow of inert gas, via the blowing means ( 7 ), into the reaction mixture ( 15 ), thus allowing the esterification water to be drawn out of the container ( 3 ).

5. The process according to claim 4 , wherein the vacuum program applies a reduction in the reaction pressure to 600 mbar after the first hour of reaction in a non-linear manner.

6. The process according to claim 5 , wherein the esterification water, drawn out of the container ( 3 ) during the esterification reaction with the vacuum program, is condensed in a horizontal condenser ( 11 ) and collected in a container ( 13 ) after having passed through a vertical condenser ( 16 ).

7. The process according to claim 6 , wherein said condenser ( 11 ) is maintained at a temperature comprised from 10° C. to 40° C. and is connected to said container ( 3 ) via the vertical condenser ( 16 ).

8. The process according to claim 1 , wherein said mixture of cetylated fatty acids (MI) is subjected to a subsequent refinement treatment, which comprises diatomaceous earth filtration in a filter press ( 23 ), so as to yield a filtered mixture Mf in which the metal catalyst present therein is removed or greatly reduced in amount.

9. The process according to claim 8 , wherein the filtered mixture Mf is treated in a reactor ( 27 ), at a temperature comprised from 150° C. to 200° C. and a pressure comprised from 5 mbar to 15 mbar in the presence of water vapour for a period of time comprised from 1 hour to 5 hours, so as to yield a final refined mixture (MF) based on cetylated fatty acids.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2018
From: LACORTE, ANDREA; TARANTINO, GERMANO; BONDIOLI, PAOLO
To: PHARMANUTRA S.P.A.
Reel/Frame 045673/0427 →
Priority Claims (1)
IT 102015000044822 · Aug 14, 2015 · national
Continuity (1)
Related Publication 20190016991A1 · Jan 17, 2019
Cited By (2)
US 12,383,525 US 12,691,091