IE863064L

IE863064L - Refined fish oil concentrate

Info

Publication number: IE863064L
Application number: IE863064A
Authority: IE
Inventors: Harald Breivik; Bernt Borretzen; Erling Tore
Original assignee: Norsk Hydro As
Priority date: 1985-12-19
Filing date: 1986-11-21
Publication date: 1987-06-19
Also published as: NZ218500A; NO855147L; MA20840A1; MX168698B; EP0255824A1; EP0255824B1; NO157302B; IS3159A7; PT83991B; CA1303416C; WO1987003899A1; ZA868927B; IE59171B1; IS1425B6; NO157302C; AU6621186A; DE3668467D1; DD261805A1; AR242111A1; PT83991A

Abstract

Refining of fish waste product so that a concentrate of omega 3-fatty acid alkyl ester is formed with 20-30% eicosapentaenoic acid alkyl ester and 35-50% docosahexaenoic acid alkyl ester (both by weight) free from cholesterol. The omega 3-concentrate is produced through urea precipitation of the non- omega 3-fatty acid esters so that the filtrate from the precipitation may be extracted by means of hexane for the transmission of the omega 3-fatty acid esters and the cholesterol to the hexane extract. Hexane is thereafter removed. The remaining concentrate of the fatty acid esters with the cholesterol is cooled to a temperature of not lower than -50<o>C, whereby the cholesterol is crystallized. The remainder is a omega 3-concentrate with the composition mentioned above. [WO8703899A1]

Description

591 71 - 2 - The present Invention concerns a process for producing refined fish oil concentrate™ In the refining process, cholesterol and useful by products such as urea adducts of fatty acid compounds are produced, in addition to higher 5 unsaturated fatty acids.

It is known that waste products from the fish refining industry contain usable productst among others fatty acidsf cholesterol, proteins and enzymes* These are either fat-soluble or water-soluble„ Such waste products are normally 10 referred to as fish entrails.

Through the processing of fish entrails, the water-soluble portion containing proteins and enzymes may be separated from the fat-soluble portion. The present indention concerns the fat-soluble portion of the waste products but 15 it can also use other refined fish oils such as occur for instance in the fish product industry. In the following these basic raw materials will be called «fish oil product» It is k^oim that certain essential fatty acids in fish oil have a medicinal effect and are useful in the prevention and 20 cure of thrombotic illnesses^ for instance ischemic heart disease- In addition, these compounds lower the cholesterol level in the blood * Among the above-mentioned fatty acids t the following may be I specified as suitable for the medicinal purposes referred 25 tos eicosapsntaenoic acid (EPA) and docosahexaenoic acid - 3 - (DH&). Both fatty acids are u 3-fatty acids of the C-20 and C22 acids. Their nomenclature according to the XUPAC system is s for the eicosapentaenoic acid (EPA)s I 5 cis - 5f lit- 14f 17 - eicosapentaenoic acid? and for the docosaheaeaenoic acid (DHA)s cis - 7 f io, 13, 16 3 where 20 and 22 indicate the number of C-atoms respectively in the molecule of the fatty acid,? 5 and S the nuaaher of unsaturated bondings, and oj 3 that the last unsaturated bonding is positioned at a distance of 3 carbon atoms from 15 the io-position,, In the following we will be using the designations EPA and 20 s 5 u>3 for the eicosapentaenoic acid and DMA and 22 : S bJ3 for the docosaheasaenoic acid.

The fat soluble portion of cod entrails g for instance t, 20 usually contains 10 25% of the fatty acid compounds EPA and DH&i? sometimes referred to herein as the essential fatty acid compounds,, as well as 2-4% cholesterol* The remainder is mainly fatty acid compounds with lower imsaturation, such as pur® fatty acids or their glycerides* 25 The purpose of the indention is to treat fish oil product so as to separate the fatty acid compounds SPA and DBA from cholesterol and other fatty acid compounds and thereby from a concentrate containing high concentrations of EPA and DHA. - 4 - It has long been known that the easiest way to separate fatty acids is by means of extraction or distillation when they appear in the foioxi of esters , for instance as methyl or ethyl esters,. Before treatment, fatty waste products from 5 the fish industry must have been subjected to trans-esterification and asterification, for instance with methanol for production of fatty acid methyl esters.

This basic material is well suited for further separation of EPA and DBA and cholesterol from the remaining less 10 important fatty acid compounds.

In US-A-4,145,446 a method is described for precipitation of fatty acid compounds in raw material by means of urea» The purpose is to obtain a product containing proteins and fats, suitable for fodder,, The production of the urea adduct is 15 brought about by providing a solution of melted urea at SO 140°C to which is added melted fatty acid or a mixture of fats heated to a temperature of 35-105° so that the ratio fat/fatty acids to urea will be from 40/60 to 60/40 units by weight. 20 Another patent, SU-A-S501393 describes a method for production of cholesterol from, for instance, fish waste products by hydrolysing the fatty acid compounds and converting them to soaps* These are then subjected to an extraction of trichloroethylene at room temperature, whereby 25 the cholesterol is combined with the trichloroethylene and this compound is then subject to further separation.

GB-A-1,240 513 also concerns a separation technique by means of urea where the raw material consists of pure methyl and ethyl esters of the C16-C10 fatty acids. Urea precipitation 30 occurs in a neutral environment with a surplus - 5 - of the relevant alcohol. The purpose is to be able to obtain a stronger concentration of y-linolenic acid„ The above-mentioned fatty acid esters do not contain any higher fatty acids other than C-18 in the form of stearic acid, 5 oleic acid, linoleic acid and linolenic acid, which after the urea precipitation and separation of the urea adduct from the rest of the material has obtained a higher content of acid by means of chromatography.

The higher unsaturated fatty acid compounds 20 : 5 c>3 and 22 10 : 6 fc>3 may be concentrated according to a method described in Japanese Patent Publication Mo» 59-071395 where the fatty acid compounds mentioned are extracted by means of polar solvents, such as acetone, methyl ethyl ketone, methanol, ethanol, and similar solvents, whereby a soluble and an 15 insoluble extract are formed. Thereafter the extract is further processed to obtain essential fatty acid compounds.

According to the present invention it is now possible - in a remarkably simple manner - to optimise the procedure to increase the concentration of «> 3-fatty acid compounds and 20 cholesterol. This is based on. a fractionated precipitation of the less interesting fatty acid compounds with urea, since urea tends to form an adduct with fatty acids which do not belong to the «s3 type, whereas fatty acids of o3 type do not. Mor does cholesterol form an adduct with urea. The 25 procedure used previously was to isolate the fatty acid compounds before these were esterified separately, and then they were subjected to a fractionated precipitation with urea. This procedure is unnecessary with our invention. r Thus, the present invention provides a process for the 30 production of a refined fish oil concentrate containing at least 20% eicosapentaenoic acid (SPA) and at least 35% docosahexaenoic acid (EPA) and at least 35% docosahexaenoic (DHA) by weight, the remainder of the concentrate including other unsaturated fatty acid compounds, and fatty acid compounds of the concentrate being mainly present as alkyl esters of lower alcohols, which comprises the steps ofs (a) esterifying and/or trans-esterifying the fat/fatty acid fraction of fish oil product at room temperature with a lower alcohol in an alkaline environment containing amounts of base sufficient only to catalyze the esterification and/or trans-esterification reaction; (b) heating the resulting alkyl ester product with an excess of urea in an alkanol to from 55-.90°C, (c) cooling the product of step (b) to 0°C to precipitate urea fatty acid alkyl ester adduct, and thereafter separating off said adduct to leave a solution mainly containing 6>3-fatty acid esters and an unsaponifiable portion; (d) separating from the solution remaining from step (c) the &j3-fatty acid alkyl esters and the unsaponifiable portion, preferably by extracting with a solvent; (e) removing any solvent from the mixture obtained in step (d); and (f) cooling the concentrate obtained in step (e) to crystallise out cholesterol and to precipitate out other undefined unsaponifiable compounds, thereby to leave a refined fish oil concentrate. - 7 - A one special feature of this process is that fatty acid compounds are not separated prior to precipitation of the urea adduct/ but instead precipitate from the same nonuniform mixture of components like they are found in the 5 basic raw material- Another special feature is that the precipitation of the urea adduct takes place in an alkaline environment# and in such a way that the alkaline environment is created through applying the base only in catalytic quantities such as a 10 catalytic agent for the trans-esterification of glycerides to methyl esters and not as a means of saponification of the fatty acids.

A third special feature is that the esterification and/or trans-esterification takes place at room temperature. 15 A result of esterification or trans-esterification at low temperature and in an environment with low alkalinity is that isomer!sation of the double bonds is avoided, which results in a more uniform product with no toxic effect At the same time transconfigurations are avoided. The 20 remaining solution is thereafter extracted by means of a non-polar solvent„ for example hexane? whereby the 3-fatty acids as well as cholesterol will be found in the non-polar phase.

Thereafter the non-polar phase is treated to remove the 25 solvent, as by being subjected to evaporation of the solvent under moderate conditions, for instance by means of vacuum distillation. The remaining ^3-concentrate now contains all the cholesterol, and it becomes apparent that the cholesterol does not dissolve easily in this concentrate and - 8 - will crystallize on cooling- The 0^3-concentrate which is left will contain 20-30 per cent EPA by weight and 35-50% DHA by weight. The remainder of the concentrate consists mainly of non-essential fatty acid compounds which are not 5 important for our purpose.

For a better understanding of the invention, we refer to the block diagram in Fig. 1 which shows diagrammatically one way of carrying out the invention and where each block represents a step in the process and is marked with a 10 reference number. The flow of the material to and from each block and between the blocks is marked by solid and dotted lines. In addition, each material is characterized by a letter.

The basic material is fat and/or fatty acids from fish and 15 especially fat and/or fatty acids obtained from the fish processing industry in connection with ensilage and or auto-catalysis processes, but the process may also be used with other forms of marine fat. This fatty raw material is called fish oil product in the claims. 20 Such fat/fatty acids have a high content of saturated, unsaturated and polyunsaturated fatty acids with a chain length C 18, C 20 and C 22 as well as a certain amount of cholesterol, vitamins and other fat soluble products which are indefinable, usually characterised as unsaponifiable, as 25 well as fatty acid compounds with shorter chain lengths* Boss 1.

I Fat/fatty acids (A) from fish with a content of i.a. cholesterol, also called the fish oil product,, is placed in a container for trans-esterification with an alcohol with a - 9 - low boiling point (B), for instance methanol or ethanol, preferably methanol, and a catalytic agent as well as auxiliary compounds (C) to obtain a faster esterification and trans-esterification in order to prevent oxidization and 5 dis-coloration. Potassium hydroxide may be used as a catalytic agents and in order to prevent oxidization, especially when heavy metals such as chromium, iron, cobalt, nickel and copper are present, small amounts of the sodium salt of ethylenediaminetetra-acetic acid (EDTA-Ma3) may be 10 added. The esterification and trans-esterification take place under moderate conditions and stirring at about 20°C for some hours. The formation of alkyl esters is nearly complete when the ester product has changed its appearance from opalescent to clear. The clear solution (Dl) therefore 15 contains alkyl esters of the fatty acids, glycerol, alkanol, as well as some water from the esterification of the free fatty acids.

Box 2 .

The clear solution is then heated to a temperature of 55-20 90*% preferably 30-80°, most preferably 55-68°C£. whereafter a fisted amount of urea (E) and alkanol (B) is added and stirred in until everything is completely dissolved. The amount of urea depends on the composition of the fatty acids go that if the raw material (A) contains 6-8% EPA by weight, 25 urea is added in the ratio 3 parts urea by weight to 1 part alkyl ester. In order to ensure that the components are completely soluble, 9 parts alkanol by weight is added. r When everything is dissolved;, the solution is slowly cooled to approx. 20°C An adduct of urea fatty ester (F) is ( 30 crystallized and then removed by means of for instance decanting and filtration„ whereafter the filter mass is - 10 - cooled to 0°C in order to crystallize a larger portion of the adduct (F). The adduct is then separated by a known method so that the remaining filter mass (G) contains the essential fatty acid fractions and the unsaponifiable 5 fractions.

Box 3.

The slightly alkaline filter mass (G) is saturated with hexane or other non-polar solvent, preferably hexane, and is extracted by means of this solvent through a known 10 technique* as, for instance, by a continuing fluid-to-fluid counter current process t, whereafter a further quantity of adduct of urea fatty ester may be crystallized. By means of this extraction two fluids are formed, consisting of hexane (1) and a residue (K) 15 Box 4.

The hexane extract (I), which contains the alkyl-fatty esters of the polyunsaturated fatty acids 18 : 4 6)3,20 : 5 &>3- and 22 : 6 6)3 as well as cholesterol as the most important components, is washed in dilute hydrochloric acid 20 (L) in order to neutralise possible potassium soaps of the essential polyunsaturated fatty acids in the hexane extract. The washing water is decanted.

Hexane (H) is thereafter removed by evaporation of the extract (1) so that a concentrate is produced which is free A 25 from solvents (M) and which contains the compounds that are I essential for the invention, the fatty acid compounds EPA, i and DH& as well as cholesterol. - 11 - The dehydrated extract normally contains 20-30% EPA, 35-45% DHA, 10-20% other polyunsaturated fatty acids, as well as 5-15% cholesterol and undefined compounds, all by weighty but the e^act composition referred to will depend on the type of 5 fish used, the time of year the fish is caught, and the type and condition of the raw material.

Box 5 The concentrate of alkyl fatty acid ester (N) is thereafter cooled to approac. minus 25°C, whereafter cholesterol (O) is 10 crystallized. This is centrifuged and/or filtered.

Further impurities which are present in the concentrate (M) may be removed by cooling the mixture to a temperature of lower than minus 25°C, whereafter certain undefined compounds are precipitated and filtered by means of a known 15 method. The remaining w3-concentrate (P) thus contains 20-35% EPA, 35-50% DHA and 15-25% of other polyunsaturated a 3-fatty acid compounds (all by weight) as well as unsaturated fatty acid compounds which are not essential for the invention. 20 Product (p) which contains the alkyl esters of the corresponding3-fatty acids may be utilised as it is or if desired the concentration of EPA and DHA may be increased.

Since the product contains only small amounts of other fatty acids with the same chain length as EPA and DHA, it is well 25 suited for separation of the essential fatty acids, EPA and DHA, by means of supercritical fluid extraction. - 12 - Another method for increasing the concentration is by means of preparative liquid chromatography by which method a more than 90% purity of the essential fatty acids is obtained.

Box 5. 5 The alkaline residue (K) is acidified by means of concentrated hydrochloric acid (L) to a pH = 2, whereafter a hexane fraction (R) is precipitated in an upper layer which is separated. One may also subject the acid solution (S) to further extraction by means of hexane if this should 10 be necessarye whereafter the hexane extracts are gathered. The hexane fractions (R) contain free fatty acids as well as some of their alkyl esters and fairly high percentages of EPA and but also a fairly substantial portion of C 18-, C 20- and C 22-fatty acids with lower unsaturation-15 This acid solution contains water, alcohol,, alkanol, glycerol* urea and other products which may be retrieved by a separate process which is not described here.

Box 7.

The fatty acid components of the hexane fraction are 20 increased by evaporating hexane (H) in a separate piece of equipment.

Box 8.

The remaining solution is esterified using lower alkemols ^ for instance methanol or ethanol by means of an appropriate 25 catalytic agent (V) which for instance may be dehydrated I hydrochloric acidt, acetic acid chloride or boron- trichloride. - 13 - The resultant alkyl ester (D2) from the fatty acid components (T) from boa: 7 may be processed in various ways, for instance returned to box 2 for urea precipitation of the less unsaturated fatty acids. ji 5 Example To 50 kg fish oil product (.a) from cod entrails (containing 8% EPikff 11% DHA? and 2 33 cholesterol all by weight) 400 1 methanol (B) and 10 g EDTA Ma3 (C) were added in a reactor,, Potassium hydroxide (C) dissolved in methanol i?j&s added for 10 neutralisation of free fatty acids in a quantity corresponding to a colour reaction of pH 12 on a moist pH-paper. Thereafter 50 1 methanol (B) %?ere added.

The whole mixture was subjected to stirring for 15 hours at 20°C in order to bring about a trans-esterification of the 15 glycerides to methyl esters and esterification of the free fatty acids to methyl esters™ When the trans-esterification was complete, the temperature was increased to 65-S8°C and XiO kg urea (E) e as well as a fixed amount of methanol (B) were stirred in while being 20 heated until everything seemed to be dissolved,, Then the solution was slowly cooled to room temperature (appros„ 20°C)f whereafter a urea addiaet. of fatty acid was precipitated (F) It contained the major portion of the saturated and lo%rer unsaturated fatty acid methyl esters. 25 The urea adduct was separated from the solution by decanting and filtering according to an ordinary, known technicrue. (i* Result s 100«1 kg urea adduct (F) - 14 1 Thereafter the solution was cooled to 0-4°C, whereby an additional 5.1 kg urea adduct (F) could be filtrated from the solution.

This filtrate (G) contained gj 3-polyunsaturated fatty acid 5 methyl esters* cholesterol and a residue of unwanted fatty acid fractions with lower unsaturated C 18, C 20 and C 22 fatty acid methyl esters. To this filtrate we added hexane for saturation, whereby a further amount of urea adduct (22 kg) could be separated. This hexana - saturated solution was 10 extracted in a counter-current with hexane so that the hexane extract (1) finally made up approx. 300 1. The remaining unextracted solution is called (K). The hexane extract was thereafter evaporated. The yield of t,>3-fatty acid methyl ester concentrate : 10.2 kilos. 15 The concentrate (N) which contained 23% EPA, 41% DHA and 8% cholesterol* all by weight, was thereafter cooled to minus 25°C, whereby pure cholesterol (O) crystallized and was removed by means of centrifuging during which time the residue in the centrifuge was washed with hexane with a 20 lower temperature in order to remove the fatty acid methyl esters from the cholesterol crystals. Yield : 750 g pure cholesterol. The concentrated filtrate (P) contained 25% EPA-methylester* 43% DHA-methylester by weight based on the fatty acid portion, and traces of cholesterol. 25 The above-mentioned extracted residue (K) was cleansed with a solution of concentrated hydrochloric acid,, whereby one hexane phase could be filtered of f. Additional hexane was added to the batch, stirred and then precipitated. The I hexane fractions were put together and the hexane 30 evaporated. To 7.7 kilos of the remaining fatty acid and - 15 - the methyl fatty acid fraction, 15 liter 2% methanolic solution of boron trichloride were added.

Yield : 6 kilos methyl fatty acid esters, containing 13% EPA-methylester, 17% DHA-methylester and approximately 2% 5 cholesterol, all by weight„ The methyl fatty acid concentrate, containing methanol, was returned to the process for treatment with urea.

With the invention it has been possible to produce a very pure 3-concentrats of fatty acid alkyl esters, where the 10 essential anti-thrombotic fatty acid components eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) are present in a high concentration.

Further, by means of the procedure invented, it has been possible in a simple manner to separate very pure and 15 crystalline cholesterol- An additional product is a urea adduct of fatty acid components, but this is not of current interest.

Another advantage with the invention is that it is possible to produce a urea adduct without following the cumbersome 20 procedure of first producing the fatty acids, esterify these with alkanol and then separating them by means of the fractionated urea precipitation.

By following the procedure invented, it is also possible to avoid the formation of emulsions in the phases, and the 25 phase separation is thereby facilitated during later extraction stages. - 16 -

Claims

1. Process for the production of a refined fish oil concentrate containing at least 20% eicosapentaenoic acid (EPA) and at least 35% docosahexaenoic acid (DHA) by weight, the remainder of the concentrate including other unsaturated fatty acid compounds, and the fatty acid compounds of the concentrate being mainly present as alkyl esters of lower alcohols, which process comprises the steps of: (a) esterifying and/or trans-esterifying the fat/fatty acid fraction of fish oil product at room temperature with a lower alcohol in an alkaline environment containing amounts of a base sufficient only to catalyze the esterification and/or trans-esterification reaction; (b) heating the resulting alkyl ester product with an excess of urea in an alkanol to from 55-90°C; (c) cooling the product of step (b) to 0°C to precipitate urea fatty acid alkyl ester adduct and thereafter separating off said adduct to leave a solution mainly containing 3-fatty acid esters and an unsaponifiable portion; (d) separating from the solution remaining from step (c) the 3-fatty acid alkyl esters and the unsaponifiable portion, preferably by extracting with a solvent; (e) removing any solvent from the mixture obtained in step (d); and - 17 - (f) cooling the concentrate obtained in step (e) to crystallize out cholesterol and to precipitate out other undefined unsaponifiable compounds, thereby to leave a refined fish oil concentrate. 5

2. Process according to Claim 1, wherein the concentrate obtained in step (f) is further treated in order to increase the concentration of EPA and DHA therein.

3. Process according to either one of Claims 1 and 2, wherein, in step (b), the fatty acid alkyl esters are 10 treated with urea at a temperature of from 60-80°C, whereby the urea fatty acid alkyl ester adduct in the main does not contain 3-fatty acid compounds and unsaponifiable compounds.

4. Process according to any preceding claim wherein, in 15 step (d), the separation is effected by extraction with hexan®-

5. Process according to Claim 4, wherein, prior to step (e) the hexane extract is cleansed with a dilute acid, preferably hydrochloric acid. 20 S. Process according to any preceding claim, wherein step (f) is carried out by first cooling the 3-fatty acid alkyl ester concentrate to a temperature not lower than -25°C, whereby cholesterol is crystallized out, and thereafter to -50°C whereby the remaining portion of 25 the unsaponifiable compounds precipitates.

6. V

7. Process according to any preceding claim, wherein methanol is used in step (a), whereby the fatty acid - 18 - compounds of the concentrate obtained are mainly present as methyl esters.

8. Process according to any preceding claim, wherein the refined fish oil concentrate obtained in step (f) 5 contains 20-30% by weight of EPA and 35-50% by weight DHA„

9. A process substantially as hereinbefore described with reference to the example and drawing.

10. Refined fish oil concentrate wherever prepared by a 10 process as claimed in any of claims 1 to 9. Dated this 20th day of November, 1986. CRUICKSHAMK & CO., Agents for the Applicants 1 Holies Street, 15 Dublin 2. 1 I \9435 . SPE