JPH06212186A - Production of eicosapentaenoic acid from red alga fudaraku - Google Patents

Production of eicosapentaenoic acid from red alga fudaraku

Info

Publication number
JPH06212186A
JPH06212186A JP4195829A JP19582992A JPH06212186A JP H06212186 A JPH06212186 A JP H06212186A JP 4195829 A JP4195829 A JP 4195829A JP 19582992 A JP19582992 A JP 19582992A JP H06212186 A JPH06212186 A JP H06212186A
Authority
JP
Japan
Prior art keywords
extraction
eicosapentaenoic acid
fudaraku
red alga
organic solvent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP4195829A
Other languages
Japanese (ja)
Other versions
JPH0765066B2 (en
Inventor
Kiyotaka Hatada
畑田清隆
Shota Ito
伊東祥太
Isao Saito
斎藤功夫
Osamu Sato
佐藤  修
Tomio Goto
後藤富雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP4195829A priority Critical patent/JPH0765066B2/en
Publication of JPH06212186A publication Critical patent/JPH06212186A/en
Publication of JPH0765066B2 publication Critical patent/JPH0765066B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/54Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids

Abstract

PURPOSE:To provide eicosapentaenoic acid, which is known as a substance functioning to prevent thrombosis, cerebral embolism, myocardial infarction, etc., by effectively utilizing fudaraku, a red alga, which has been unutilized. CONSTITUTION:The production method of eicosapentaenonic acid comprises a combination of extraction with an organic solvent as an extraction means and supercritical extraction with carbon dioxide as a means for extraction and extractant removal.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、これまであまり返り見
られなかった未利用海藻である紅藻フダラク中より血清
脂質改善作用や血液凝固抑制作用などを有する高機能油
脂エイコサペンタエン酸(以下EPAと記す)を分離精
製し、健康食品、医療用原料、飼料等の機能性製品分野
に応用展開出来るものである。
BACKGROUND OF THE INVENTION The present invention relates to a highly functional oil, eicosapentaenoic acid (hereinafter referred to as EPA), which has serum lipid-improving action and blood coagulation-inhibiting action from the red seaweed Fudarac which is an unused seaweed which has not been returned so far. Can be applied and developed in the field of functional products such as health foods, medical raw materials, and feeds.

【0002】[0002]

【従来の技術】EPA等の高度不飽和の高機能油脂は体
内で形成されない。このEPAは血栓症、脳梗塞、心筋
梗塞等を防止する作用のあることで知られている。この
様な高級高度不飽和脂肪酸の供給源量として肝油など魚
類等がその主なものである。供給原料の拡大と未利用海
洋バイオマス資源の利用技術が求められている現状に於
て海洋に植生する海藻の脂質部は未だその有効利用法が
無く、有効利用法開発が急務の課題となっている。
2. Description of the Related Art Highly unsaturated and highly functional fats and oils such as EPA are not formed in the body. This EPA is known to have an action of preventing thrombosis, cerebral infarction, myocardial infarction and the like. The main sources of such higher polyunsaturated fatty acids are fish such as liver oil. In the current situation where expansion of supply materials and utilization technology of unused marine biomass resources are required, the lipid part of seaweed vegetation in the ocean does not yet have an effective utilization method, and the development of an effective utilization method is an urgent issue. There is.

【0003】[0003]

【発明が解決しようとする課題】未利用海藻より血栓
症、脳梗塞、心筋梗塞等を防止する作用のあることで知
られるEPAを提供することを目的とする。
An object of the present invention is to provide an EPA known to have an action of preventing thrombosis, cerebral infarction, myocardial infarction and the like from unused seaweed.

【0004】[0004]

【課題を解決するための手段】本発明者らはEPAの供
給原料の拡大と未利用海洋バイオマス資源を利用するた
めに鋭意探索研究を重ねた結果、これまで全くこれらの
高級高度不飽和脂肪酸の含有が知られていなかった紅藻
フダラクに、このEPAが主要な構成成分として存在
し、しかも、SC−CO2抽出を介在した抽出分離の場
合の好適な材料であることを解明するに至った。
[Means for Solving the Problems] As a result of extensive research conducted by the present inventors in order to expand the feedstock of EPA and utilize unused marine biomass resources, as a result, it has hitherto been possible to completely eliminate these higher polyunsaturated fatty acids. It has been clarified that this EPA is present as a main constituent component in the red alga Fudarac, which was not known to be contained, and is a suitable material in the case of extraction and separation mediated by SC-CO 2 extraction. .

【0005】本発明は多くの海藻を研究対象にして研究
した結果、当該海藻の有機溶剤抽出物の分析ならびに抽
出物の構造面の研究の結果、当該紅藻フダラクの脂質部
が主要成分として高級高度不飽和脂肪酸をリン脂質の主
要構成脂肪酸とする材料であることを明からかにするこ
とによって本発明をなすに至った。
The present invention has been conducted on many seaweeds, and as a result of the analysis of the organic solvent extract of the seaweed and the structural study of the extract, the lipid portion of the red alga Fudarac is the major component. The present invention has been accomplished by making it clear that polyunsaturated fatty acids are the main constituent fatty acids of phospholipids.

【0006】有機溶媒抽出は、全行程を通じて操作は低
温で行なうのが好ましい。例えば最初にクロロホルム・
メタノール抽出し、それより飽和脂肪酸などをSC−C
2抽出法等で除去した形で当該目的物を分離精製す
る。フダラクを凍結乾して直接SC−CO2 抽出し、飽
和脂肪酸及び炭化水素等の除去行った後、直接有機溶媒
(有機溶剤等)で抽出し蛋白部および糖部を除去した
後、その物自体からSC−CO2抽出で飽和脂肪酸及び
炭化水素等の除去抽出しする行程をも含ませることがで
きる。本発明によって得られるEPAは有機溶媒法その
ものだけに比較してパルミチン酸を10パーセント程度
除去することが出来る。結果としてEPAは約40パー
セント以上の高濃度を含有する。
The organic solvent extraction is preferably carried out at a low temperature throughout the entire process. For example, first chloroform
Extract with methanol and add saturated fatty acid to SC-C
The target product is separated and purified in a form removed by the O 2 extraction method or the like. Fudaraku is freeze-dried and directly subjected to SC-CO 2 extraction to remove saturated fatty acids and hydrocarbons, and then directly extracted with an organic solvent (organic solvent, etc.) to remove protein and sugar moieties, and then the product itself. The process of removing saturated fatty acids and hydrocarbons and extracting by SC-CO 2 extraction can be included. The EPA obtained by the present invention can remove about 10% of palmitic acid as compared with the organic solvent method itself. As a result, EPA contains high concentrations of about 40 percent or more.

【0007】[0007]

【作用】本発明方法によると血栓症、脳梗塞、心筋梗
塞、血清脂質改善作用や、血液凝固抑制作用などを有す
る高機能油脂EPAを、これまで発見されなかった紅藻
フダラクを原料としてよりよく製造することができるの
で、本発明方法はEPAの工業的製法として好適であ
る。
According to the method of the present invention, a highly functional fat EPA having thrombosis, cerebral infarction, myocardial infarction, serum lipid improving action, blood coagulation inhibiting action, etc. Since it can be produced, the method of the present invention is suitable as an industrial production method of EPA.

【実施例】【Example】

【0008】紅藻フダラク200〜500gを十分水洗
し低温に保ってブレンダーにかけ、フダラク部の砕片を
得た。この砕片は低温下に凍結乾燥し有機溶媒抽出(ク
ロロホルム・メタノール等)を行い高濃度高級不飽和脂
肪酸部を得た。得られる抽出物の量は約50mg/g
(フダラク凍結乾燥試料)であり淡い黄色を呈してい
る。その脂肪酸組成の分析は常法に従いメチルエステル
化したサンプルをガスクロマトグラフイ−によって分析
した。当該抽出物の構成脂肪酸の主な構成は次の通りで
ある。14:0(2.3%)、16:0(34.0
%)、16:1(4.1%)、18:1(8.2%)2
0:4(15.9%)、20:5(35.3%)であ
る。
200 to 500 g of the red alga Fudarac was thoroughly washed with water, kept at a low temperature, and then subjected to a blender to obtain fragments of the Fudarac part. This crushed piece was freeze-dried at a low temperature and extracted with an organic solvent (chloroform / methanol, etc.) to obtain a high-concentration higher unsaturated fatty acid moiety. The amount of extract obtained is about 50 mg / g
(Fudarak freeze-dried sample) and has a pale yellow color. The fatty acid composition was analyzed by gas chromatography of a methyl esterified sample according to a conventional method. The main constituents of the constituent fatty acids of the extract are as follows. 14: 0 (2.3%), 16: 0 (34.0)
%), 16: 1 (4.1%), 18: 1 (8.2%) 2
It is 0: 4 (15.9%) and 20: 5 (35.3%).

【実施例】【Example】

【0009】有機溶剤抽出物のSC−CO2抽出除去操
作によるEPAの高濃度化は有機溶剤抽出物をクロロホ
ルム、有機溶剤などの有機溶媒に溶解し10〜35メッ
シュの海砂に一様にコーテイングした。抽出除去条件は
液化二酸化炭素を高圧ポンプで流通式の抽出槽(100
ml)に送り超臨界状態とした。抽出槽内は圧力調整器
で一定圧に保ち、大気圧下にフラッシュされたガスを分
離槽に誘導し除去物を捕手した。又使用ガス量は積算流
量計で測定した。圧力:25.0MPa、温度313
K、CO2流量:1.05〜3.00dm3/min抽出
除去時間10〜30時間、抽出試料:10g。抽出除去
される物の量は約0.1g/gであり白色を呈してい
る。除去処理された物質はパルミチン酸の含有量が減少
しEPAの分析値が高くなっている。その結果は14:
0(2.4%)16:0(37.1%)16:1(1.
7%)18:1(8.0%)20:4(7.9%)2
0:5(40.6%)である。
To increase the concentration of EPA by the SC-CO 2 extraction and removal operation of the organic solvent extract, the organic solvent extract is dissolved in an organic solvent such as chloroform or an organic solvent and uniformly coated on 10-35 mesh sea sand. did. Extraction and removal conditions are liquefied carbon dioxide with a high-pressure pump and a flow-type extraction tank (100
ml) and brought to a supercritical state. The inside of the extraction tank was kept at a constant pressure by a pressure regulator, and the gas flushed under atmospheric pressure was guided to the separation tank to catch the removed substance. The amount of gas used was measured with an integrating flow meter. Pressure: 25.0 MPa, temperature 313
K, CO 2 flow rate: 1.05 to 3.00 dm 3 / min extraction removal time 10 to 30 hours, extracted sample: 10 g. The amount of the substance to be extracted and removed is about 0.1 g / g, which is white. The substance subjected to the removal treatment has a reduced content of palmitic acid and an increased EPA analysis value. The result is 14:
0 (2.4%) 16: 0 (37.1%) 16: 1 (1.
7%) 18: 1 (8.0%) 20: 4 (7.9%) 2
It is 0: 5 (40.6%).

【0010】[0010]

【発明の効果】本発明方法によると血栓症、脳梗塞、心
筋梗塞、血清脂質改善作用や、血液凝固抑制作用などを
有する高機能油脂EPAが、これまで発見されなかった
紅藻フダラクを原料としてよりよく製造することができ
ることで、海洋未利用バイオマス資源のさらなる利用研
究に本発明方法は寄与することが出来る。
EFFECTS OF THE INVENTION According to the method of the present invention, a highly functional fat EPA having thrombosis, cerebral infarction, myocardial infarction, serum lipid improving action, blood coagulation inhibiting action and the like is prepared from the red alga Fudarac, which has not been discovered so far. By being able to be manufactured better, the method of the present invention can contribute to further utilization research of unused marine biomass resources.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 31/20 ABS ACB 9283−4C C11B 1/10 2115−4H (72)発明者 後藤富雄 宮城県塩釜市藤倉三丁目17−26─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI Technical display location A61K 31/20 ABS ACB 9283-4C C11B 1/10 2115-4H (72) Inventor Tomio Goto Miyagi Prefecture 3-17-26 Fujikura, Shiogama City

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 紅藻フダラクを原料としてエイコサペン
タエン酸を分離製造する方法。
1. A method for separating and producing eicosapentaenoic acid from the red alga Fudarac.
【請求項2】 前記フダラクの溶媒抽出物に超臨界二酸
化炭素抽出処理を行い、得られるリン脂質部の処理行程
に超臨界二酸化炭素抽出分離行程を入れエイコサペンタ
エン酸を製造する方法。
2. A method for producing eicosapentaenoic acid, wherein the solvent extract of Fudarak is subjected to a supercritical carbon dioxide extraction treatment, and a supercritical carbon dioxide extraction separation step is added to the treatment step of the resulting phospholipid part.
JP4195829A 1992-05-28 1992-05-28 Method for producing eicosapentaenoic acid-containing substance using red alga Fudarac Expired - Lifetime JPH0765066B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4195829A JPH0765066B2 (en) 1992-05-28 1992-05-28 Method for producing eicosapentaenoic acid-containing substance using red alga Fudarac

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4195829A JPH0765066B2 (en) 1992-05-28 1992-05-28 Method for producing eicosapentaenoic acid-containing substance using red alga Fudarac

Publications (2)

Publication Number Publication Date
JPH06212186A true JPH06212186A (en) 1994-08-02
JPH0765066B2 JPH0765066B2 (en) 1995-07-12

Family

ID=16347707

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4195829A Expired - Lifetime JPH0765066B2 (en) 1992-05-28 1992-05-28 Method for producing eicosapentaenoic acid-containing substance using red alga Fudarac

Country Status (1)

Country Link
JP (1) JPH0765066B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004047554A1 (en) * 2002-11-26 2004-06-10 Phares Pharmaceutical Research N.V. Marine lipid compositions
KR20040057909A (en) * 2002-12-25 2004-07-02 시라코 가부시키가이샤 Health foods having a blood liquidity-improving action
JP2004536059A (en) * 2001-05-14 2004-12-02 マーテック バイオサイエンシズ ボールダー コーポレーション Generation and use of polar lipid-rich fractions containing ω-3 and / or ω-6 polyunsaturated fatty acids from microorganisms, genetically modified plant seeds and marine organisms
KR20150020513A (en) * 2013-08-13 2015-02-26 (주)다인내추럴 Method for Microencapsulation of Fat-Soluble Materials and Method for Functional Beverage by Using Microencapsulated Fat-Soluble Materials
CN107904016A (en) * 2017-11-10 2018-04-13 海南三元星生物科技股份有限公司 A kind of red algae essential oil and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6055096A (en) * 1983-09-06 1985-03-29 岩谷産業株式会社 Manufacture of neutral lipid from fishes and shells
JPS6272793A (en) * 1985-09-26 1987-04-03 バブコツク日立株式会社 Method for concentrating and separating eicosapentaenic acidfrom fish oil
JPS6479191A (en) * 1987-09-22 1989-03-24 Ishikawajima Harima Heavy Ind Production of fat-soluble component by mass cultivation of order laminariales
JPH01294649A (en) * 1988-05-21 1989-11-28 Agency Of Ind Science & Technol Method for extracting docosahexaenoic acid and eicosapentaenoic acid in high concentration from spermary of walleye pollack

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6055096A (en) * 1983-09-06 1985-03-29 岩谷産業株式会社 Manufacture of neutral lipid from fishes and shells
JPS6272793A (en) * 1985-09-26 1987-04-03 バブコツク日立株式会社 Method for concentrating and separating eicosapentaenic acidfrom fish oil
JPS6479191A (en) * 1987-09-22 1989-03-24 Ishikawajima Harima Heavy Ind Production of fat-soluble component by mass cultivation of order laminariales
JPH01294649A (en) * 1988-05-21 1989-11-28 Agency Of Ind Science & Technol Method for extracting docosahexaenoic acid and eicosapentaenoic acid in high concentration from spermary of walleye pollack

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004536059A (en) * 2001-05-14 2004-12-02 マーテック バイオサイエンシズ ボールダー コーポレーション Generation and use of polar lipid-rich fractions containing ω-3 and / or ω-6 polyunsaturated fatty acids from microorganisms, genetically modified plant seeds and marine organisms
EP1392623A4 (en) * 2001-05-14 2005-05-04 Martek Biosciences Corp Production and use of a polar lipid-rich fraction containing omega-3 and/or omega-6 highly unsatruated fatty acids from microbes, genetically modified plant seeds and marine organisms
JP2008088181A (en) * 2001-05-14 2008-04-17 Martek Biosciences Corp PRODUCTION AND USE OF POLAR LIPID-RICH FRACTION CONTAINING omega-3 AND/OR omega-6 HIGHLY UNSATURATED FATTY ACID(S) DERIVED FROM MICROORGANISM, GENETICALLY-MODIFIED PLANT SEED AND MARINE ORGANISM
JP2010065048A (en) * 2001-05-14 2010-03-25 Martek Biosciences Corp PRODUCTION AND USE OF POLAR LIPID-RICH FRACTION CONTAINING omega-3 AND/OR omega-6 HIGHLY UNSATURATED FATTY ACID FROM MICROBE, GENETICALLY MODIFIED PLANT SEED AND MARINE ORGANISM
EP2255668A3 (en) * 2001-05-14 2012-04-04 Martek Biosciences Corporation Production and Use of a Polar Lipid-Rich Fraction Containing Omega-3 and/or Omega-6 Highly Unsaturated Fatty Acids from Microbes, Genetically Modified Plant Seeds and Marine Organisms
WO2004047554A1 (en) * 2002-11-26 2004-06-10 Phares Pharmaceutical Research N.V. Marine lipid compositions
KR20040057909A (en) * 2002-12-25 2004-07-02 시라코 가부시키가이샤 Health foods having a blood liquidity-improving action
KR20150020513A (en) * 2013-08-13 2015-02-26 (주)다인내추럴 Method for Microencapsulation of Fat-Soluble Materials and Method for Functional Beverage by Using Microencapsulated Fat-Soluble Materials
CN107904016A (en) * 2017-11-10 2018-04-13 海南三元星生物科技股份有限公司 A kind of red algae essential oil and preparation method thereof

Also Published As

Publication number Publication date
JPH0765066B2 (en) 1995-07-12

Similar Documents

Publication Publication Date Title
CA1303416C (en) Refined fish oil concentrate and the production process for same
Gbogouri et al. Analysis of lipids extracted from salmon (Salmo salar) heads by commercial proteolytic enzymes
JP4181305B2 (en) Methods for extracting lipids from marine and freshwater animal tissues
EP2024473B1 (en) Extraction of highly unsaturated lipids with liquid dimethyl ether
JP2021121676A (en) Very long chain polyunsaturated fatty acids from natural oils
RU2242505C2 (en) Method for removing free fatty acids from fat and oil of biological origin or their vapor distillate (variants)
KR100972703B1 (en) Improvements in or relating to separation technology
US9409851B2 (en) Long chain monounsaturated fatty acid composition and method for the production thereof
FR2702773A1 (en) Process for the preparation of vegetable fat fractions enriched with unsaponifiable matter
JP6573241B2 (en) Lipid composition and method for producing the same
JPH08511547A (en) Method for obtaining highly purified phosphatidylcholine
CN114058438A (en) Krill oil preparation method and krill oil composition
JPH06212186A (en) Production of eicosapentaenoic acid from red alga fudaraku
JPS6333387A (en) Production of phospholipid containing lysophospholipid having reduced neutral lipid content
CA2628304C (en) Method of refining episesamin
US3869482A (en) Method of producing highly purified phosphatides
JPH05230494A (en) Method for removing sterol from vegetable and animal fat
JP2009227765A (en) Manufacturing method of plasmalogen containing lipid
Hessel Marine biotoxins: II. The extraction and partial purification of ciguatera toxin from Lutjanus bohar (Forskål)
CA2288469A1 (en) Production process, used in particular for obtaining lecithin from dehydrated egg
JP3531876B2 (en) Method for obtaining phospholipid composition containing docosahexaenoic acid
JPH01294649A (en) Method for extracting docosahexaenoic acid and eicosapentaenoic acid in high concentration from spermary of walleye pollack
JP2005112819A (en) Method for production of phospholipid derived from fish and shellfish
FR2633936A1 (en) PROCESS FOR THE EXTRACTION OF CHOLESTEROL CONTAINED IN FATTY MATTER OF ANIMAL ORIGIN
JPH0649480A (en) Separation of unsaturated compound

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term