JPH0731416A - Food and its preparation - Google Patents

Food and its preparation

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Publication number
JPH0731416A
JPH0731416A JP5195537A JP19553793A JPH0731416A JP H0731416 A JPH0731416 A JP H0731416A JP 5195537 A JP5195537 A JP 5195537A JP 19553793 A JP19553793 A JP 19553793A JP H0731416 A JPH0731416 A JP H0731416A
Authority
JP
Japan
Prior art keywords
food
acid
fatty acid
derivative
saponified
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.)
Pending
Application number
JP5195537A
Other languages
Japanese (ja)
Inventor
Shuichiro Ueda
修一郎 上田
Shinichi Inada
進一 稲田
Yoichi Kobayashi
洋一 小林
Tatsuhiko Suga
辰彦 菅
Kazuyoshi Yazawa
一良 矢澤
Sei Kondo
聖 近藤
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.)
Sagami Chemical Research Institute
Viox Inc
Original Assignee
Sagami Chemical Research Institute
Viox Inc
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 Sagami Chemical Research Institute, Viox Inc filed Critical Sagami Chemical Research Institute
Priority to JP5195537A priority Critical patent/JPH0731416A/en
Publication of JPH0731416A publication Critical patent/JPH0731416A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a food having excellent handleability and storage stability and enabling easy compounding of an omega-3 fatty acid or its derivative and to provide its production process. CONSTITUTION:At least one kind of omega-3 fatty acid such as docosahexaenoic acid, eicosapentaenoic acid and alpha-linolenic acid or their derivative is saponified with an alkaline agent and preferably neutralized with an acid. The treated fatty acid is added to a food such as powdered milk, processed milk and dressing.

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、ω−3系脂肪酸又はそ
の誘導体のケン化物を含有する食品及びその製造方法に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a food containing a saponified omega-3 fatty acid or a derivative thereof and a method for producing the food.

【0002】[0002]

【従来の技術】近年、ドコサヘキサエン酸(以下、DH
Aと略す)、エイコサペンタエン酸(以下、EPAと略
す)、α−リノレン酸等のω−3系脂肪酸が有する、心
血管系疾患の予防効果や、抗腫瘍効果、記憶学習能の低
下予防効果など、各種の生理活性効果が注目されている
(「食品と開発」、VOL.27、NO.8)。このた
め、例えばDHAをカプセル化して健康食品としたり、
あるいはDHAを飼料に添加して鶏等の体内で生体移行
させることにより、DHA強化卵を得ることが行われて
いる。
2. Description of the Related Art Recently, docosahexaenoic acid (hereinafter referred to as DH
A), eicosapentaenoic acid (hereinafter abbreviated as EPA), and ω-3 fatty acids such as α-linolenic acid have a cardiovascular disease preventive effect, an antitumor effect, and a memory learning ability decrease preventive effect. Various bioactive effects such as “Food and Development”, VOL.27, NO.8 have been attracting attention. For this reason, for example, DHA is encapsulated into a health food,
Alternatively, DHA-enriched eggs have been obtained by adding DHA to the feed and allowing it to migrate into the body of chickens and the like.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、ω−3
系脂肪酸は常温で液体であるため、食品への配合や、配
合後の食品の取り扱いが面倒であり、また、水和性が低
いため、液状食品に添加する場合には、乳化剤等を併用
する必要があった。
However, ω-3
Since the fatty acids are liquid at room temperature, it is troublesome to mix them in foods and the foods after mixing are complicated, and since they have low hydration properties, they are used in combination with emulsifiers when added to liquid foods. There was a need.

【0004】また、ω−3系脂肪酸のような高級不飽和
脂肪酸を食品に配合した場合、製造工程中又は保存中に
不飽和脂肪酸が酸化されやすいため、生成された過酸化
物、酸、アルデヒド類が人体に悪影響を及ぼしたり、製
品が酸敗臭を放つなど品質の低下を生じる虞れがあっ
た。
Further, when higher unsaturated fatty acids such as ω-3 fatty acids are mixed in foods, the unsaturated fatty acids are easily oxidized during the production process or during storage, so that the generated peroxide, acid or aldehyde is generated. There is a risk that the kind may adversely affect the human body and that the product may give off a rancid odor, resulting in deterioration in quality.

【0005】したがって、本発明の目的は、ω−3系脂
肪酸又はその誘導体を高濃度で配合でき、取り扱いが容
易で、保存安定性にも優れた食品及びその製造方法を提
供することにある。
Therefore, an object of the present invention is to provide a food product which can contain ω-3 fatty acid or its derivative at a high concentration, is easy to handle, and has excellent storage stability, and a method for producing the food product.

【0006】[0006]

【課題を解決するための手段】上記目的を達成するた
め、本発明の食品は、ω−3系脂肪酸又はその誘導体の
ケン化物を少なくとも1種類含むことを特徴とする。
To achieve the above object, the food of the present invention is characterized by containing at least one saponified omega-3 fatty acid or derivative thereof.

【0007】また、本発明の食品の製造方法は、ω−3
系脂肪酸又はその誘導体を少なくとも1種類含む原料油
脂及び/又は脂肪酸に、不活性ガスの雰囲気下でアルカ
リ剤を添加してケン化させた後、酸を添加して中和させ
て得られたケン化物を、食品原料中に添加することを特
徴とする。
Further, the method for producing food according to the present invention is ω-3.
A saponification product obtained by adding an alkaline agent to a raw material oil and / or fatty acid containing at least one type of fatty acid or its derivative in an inert gas atmosphere for saponification, and then adding an acid for neutralization. The compound is added to the food material.

【0008】以下、本発明について好ましい具体例を挙
げて更に詳細に説明する。
The present invention will be described in more detail below with reference to preferred specific examples.

【0009】本発明の食品は、ω−3系脂肪酸又はその
誘導体のケン化物を少なくとも1種類配合したことを特
徴とするものである。本発明は食品の種類に限定される
ものではないが、特に好ましい食品として、粉ミルク、
加工牛乳、ドレッシング等が挙げられる。ここで、粉ミ
ルクとは、粉乳を主成分とし、必要に応じて糖類、無機
塩、ビタミン等の補助栄養源を加えたもので、水、湯等
を加えてミルクにするものをいい、また、加工牛乳と
は、牛乳を主成分とし、これに糖類、無機塩、ビタミン
等の補助栄養原等を添加したり、あるいは牛乳から脂肪
分など特定の成分を除去したりして、成分を調整したも
のをいう。更に、ドレッシングとは、食酢、食塩、香辛
料等に、油脂を加えたものをいう。
The food of the present invention is characterized by containing at least one saponified ω-3 fatty acid or derivative thereof. The present invention is not limited to the type of food, as a particularly preferred food, milk powder,
Examples include processed milk and dressing. Here, the powdered milk is composed mainly of powdered milk and optionally supplemented with nutritional sources such as sugars, inorganic salts, vitamins, etc., which means that milk is prepared by adding water, hot water, etc. Processed milk is made up of milk as the main ingredient, and sugar, inorganic salts, supplemental nutrients such as vitamins, etc. are added to this, or specific ingredients such as fat are removed from the milk to adjust the ingredients. Say something. Furthermore, dressing means vinegar, salt, spices, etc. to which fats and oils are added.

【0010】食品中への上記ケン化物の添加量は、食品
の種類や、目的に応じて調整することができるが、通常
は上記ケン化物の1日当たりの摂取量が50〜300m
gとなるようにすることが好ましく、強化タイプ食品と
して用いる場合には、1日当たりの摂取量が300〜8
00mgとなるようにすることが好ましい。具体的に
は、例えば粉ミルクの場合には全体に対し0.2〜0.
5重量%、加工牛乳の場合には0.5〜2.0重量%、
ドレッシングの場合には10〜35重量%程度が好まし
い。また、上記ケン化物と併せて、無機塩、ビタミン、
アミノ酸等の補助栄養原や、調味料等を添加することも
できる。
The amount of the saponified product added to the food can be adjusted according to the type of the food and the purpose, but the daily intake of the saponified product is usually 50 to 300 m.
g is preferable, and when used as a fortified food, the daily intake is 300 to 8
It is preferably set to 00 mg. Specifically, for example, in the case of powdered milk, 0.2 to 0.
5% by weight, 0.5-2.0% by weight in the case of processed milk,
In the case of dressing, about 10 to 35% by weight is preferable. In addition to the above saponified products, inorganic salts, vitamins,
Supplementary nutrients such as amino acids and seasonings can also be added.

【0011】本発明の食品に配合されるケン化物の原料
となるω−3系脂肪酸又はその誘導体としては、DH
A、EPA、α−リノレン酸又はこれらの誘導体のう
ち、少なくとも1種類を用いることが好ましい。
As the ω-3 fatty acid or its derivative which is a raw material of the saponified product blended in the food of the present invention, DH
It is preferable to use at least one of A, EPA, α-linolenic acid, or a derivative thereof.

【0012】本発明において、ω−3系脂肪酸又はその
誘導体としては、遊離酸としてのω−3系脂肪酸のほ
か、そのエステル、グリセリド、リン脂質、コリン誘導
体、アミノ酸誘導体、アスコルビン酸誘導体等、各種の
ものを用いることができる。また、ω−3系脂肪酸又は
その誘導体だけを含むように高純度に精製されたものだ
けでなく、例えば魚油のようにDHA、EPA含量の高
い油脂や、シソ油のようにα−リノレン酸含量の高い油
脂を用いることができる。
In the present invention, as the ω-3 fatty acid or its derivative, in addition to the ω-3 fatty acid as a free acid, its ester, glyceride, phospholipid, choline derivative, amino acid derivative, ascorbic acid derivative and the like can be used. Can be used. Further, not only those purified to a high purity so as to contain only ω-3 fatty acids or derivatives thereof, but also fats and oils having a high DHA and EPA content such as fish oil, and α-linolenic acid content such as perilla oil. Higher fats and oils can be used.

【0013】上記ω−3系脂肪酸又はその誘導体をケン
化するために使用されるアルカリ剤としては、例えば水
酸化ナトリウム、水酸化カリウム、水酸化カルシウム、
トリエタノールアミンなど、従来からケン化剤として用
いられているものなどを使用することができる。
Examples of the alkaline agent used for saponifying the ω-3 fatty acid or its derivative include sodium hydroxide, potassium hydroxide, calcium hydroxide,
Those conventionally used as a saponification agent such as triethanolamine can be used.

【0014】本発明においては、ケン化反応を行う前
に、ω−3系脂肪酸又はその誘導体を少なくとも1種類
含む原料油脂及び/又は脂肪酸に、BHT、BHA、ト
コフェロール等の抗酸化剤を添加することが好ましい。
これによって、ケン化反応中のω−3系脂肪酸又はその
誘導体の酸化を防止することができる。
In the present invention, before the saponification reaction, an antioxidant such as BHT, BHA, tocopherol or the like is added to the raw material fat and / or fatty acid containing at least one ω-3 fatty acid or its derivative. It is preferable.
This makes it possible to prevent the ω-3 fatty acid or its derivative from being oxidized during the saponification reaction.

【0015】本発明に用いられるω−3系脂肪酸又はそ
の誘導体のケン化物は、上記ω−3系脂肪酸又はその誘
導体を少なくとも1種類含む原料油脂及び/又は脂肪酸
に、好ましくは窒素等の不活性ガスの雰囲気下でアルカ
リ剤を添加してケン化させることによって製造すること
ができる。ここで、不活性ガスの雰囲気下でケン化を行
う理由は、ω−3系脂肪酸やその誘導体の酸化を防ぐた
めである。不活性ガスの雰囲気下にする方法としては、
例えば反応釜、反応槽を囲む空間に存在する空気を不活
性ガスで置き換える方法などが好ましく採用される。
The saponified ω-3 fatty acid or its derivative used in the present invention is preferably an inert gas such as nitrogen for the raw material oil and / or fatty acid containing at least one ω-3 fatty acid or its derivative. It can be produced by adding an alkali agent in a gas atmosphere and saponifying. Here, the reason why saponification is performed in an atmosphere of an inert gas is to prevent oxidation of the ω-3 fatty acid and its derivative. As a method of setting the atmosphere of an inert gas,
For example, a method of replacing the air existing in the space surrounding the reaction kettle and the reaction tank with an inert gas is preferably adopted.

【0016】この場合、ケン化反応の温度は50〜80
℃が好ましく、50〜65℃がより好ましい。反応温度
が80℃を超えると、ω−3系脂肪酸やその誘導体の酸
化が進行しやすくなり、一方、反応温度が50℃未満で
は、原料に含まれる油脂や脂肪酸の融点等によっても異
なるが、ケン化物の製造が困難となる。
In this case, the temperature of the saponification reaction is 50-80.
C. is preferable, and 50 to 65.degree. C. is more preferable. If the reaction temperature is higher than 80 ° C, the ω-3 fatty acid or its derivative is easily oxidized, while if the reaction temperature is lower than 50 ° C, it depends on the melting point of the fat or oil or the fatty acid contained in the raw material. The production of saponified products becomes difficult.

【0017】また、アルカリ剤の添加に要する時間(ア
ルカリ剤の添加を開始してから終了するまでの時間)
は、1時間以上とすることが好ましく、ケン化時間いっ
ぱいを使って徐々に添加することが最も好ましい。
The time required to add the alkaline agent (time from the start of the addition of the alkaline agent to the end)
Is preferably 1 hour or more, and most preferably gradually added using the entire saponification time.

【0018】なお、本発明においては、上記のようにし
て製造されたω−3系脂肪酸をそのまま食品に配合して
もよいが、クエン酸等の有機酸、塩酸等の鉱酸などの酸
により中和した後、配合するのが好ましい。
In the present invention, the ω-3 fatty acid produced as described above may be blended into food as it is, but it may be mixed with an organic acid such as citric acid or an acid such as mineral acid such as hydrochloric acid. It is preferable to mix after neutralization.

【0019】こうして得られた本発明の食品は、通常の
食品と同様にして保存、調理、飲食することができる。
The thus obtained food of the present invention can be stored, cooked and eaten in the same manner as ordinary foods.

【0020】[0020]

【作用】本発明では、ω−3系脂肪酸又はその誘導体を
ケン化してペースト状又は固形状にすることにより、食
品への配合時における取り扱いが容易となり、得られた
食品も取り扱いやすいものになる。
In the present invention, by saponifying the ω-3 fatty acid or its derivative into a paste or solid form, it becomes easy to handle when blending into food, and the obtained food becomes easy to handle. .

【0021】また、ω−3系脂肪酸又はその誘導体は、
親油性の物質であるが、これをケン化することにより水
和性が向上し、清涼飲料や乳飲料、ドレッシング等の液
状食品にも容易に添加することができる。
The ω-3 fatty acid or its derivative is
Although it is a lipophilic substance, its saponification improves the hydration property and can be easily added to liquid foods such as soft drinks, milk drinks and dressings.

【0022】更に、ケン化によって、空気中の酸素によ
る酸化が抑制され、過酸化物質の生成が抑制されるの
で、人体に悪影響を与える虞れがなく、保存安定性に優
れた食品を得ることができる。
Furthermore, saponification suppresses the oxidation by oxygen in the air and suppresses the production of peroxides, so that there is no possibility of adversely affecting the human body and a food product having excellent storage stability is obtained. You can

【0023】[0023]

【実施例】【Example】

試験例1 DHA混合油(DHA含有量27%)400g中に、エ
タノール180gを加え、窒素ガス雰囲気下の反応釜中
で、80℃で加熱混合した。これに別途水酸化ナトリウ
ム64gを水200gに溶解させた水溶液を、30〜6
0分間かけて少しずつ滴下し、温度を80℃に保ちなが
らケン化反応を終了した。反応終了後、温度を80℃に
保ったままで、クエン酸を添加して中和を行い、ケン化
組成物を製造した。
Test Example 1 180 g of ethanol was added to 400 g of DHA mixed oil (DHA content 27%), and heated and mixed at 80 ° C. in a reaction vessel under a nitrogen gas atmosphere. Separately, an aqueous solution prepared by dissolving 64 g of sodium hydroxide in 200 g of water was added to 30 to 6
The solution was gradually added dropwise over 0 minutes, and the saponification reaction was completed while maintaining the temperature at 80 ° C. After the reaction was completed, while maintaining the temperature at 80 ° C., citric acid was added for neutralization to produce a saponified composition.

【0024】上記試料を小型シャーレに入れ、70℃の
空気が還流する恒温機中に置いて、POV(過酸化物
価)を経時的に測定した。また、比較のために、ケン化
していないDHA混合油(DHA含有量27%)につい
ても、同様にして測定を行った。その結果を表1に示
す。なお、POVは基準油脂分析試験法に準じて測定
し、ケン化組成物については、塩酸を添加した後、エー
テル抽出、脱水して得られた脂肪酸のPOVを測定し
た。
The above sample was placed in a small petri dish, placed in a thermostat at 70 ° C. under which air was refluxed, and POV (peroxide value) was measured with time. Further, for comparison, the same measurement was carried out for an unsaponified DHA mixed oil (DHA content 27%). The results are shown in Table 1. The POV was measured according to the standard oil and fat analysis test method. For the saponified composition, hydrochloric acid was added, followed by extraction with ether and dehydration to obtain the POV of the fatty acid.

【0025】[0025]

【表1】 [Table 1]

【0026】表1の結果より、DHAをケン化すること
により、空気中の酸素によるDHAの酸化を抑制できる
ことが確認された。
From the results shown in Table 1, it was confirmed that saponification of DHA can suppress the oxidation of DHA by oxygen in the air.

【0027】試験例2 α−リノレン酸混合油(α−リノレン酸含有量55%)
250g中に、エタノール112gを加え、窒素ガス雰
囲気下の反応釜中で、80℃で加熱混合した。これに別
途水酸化ナトリウム40gを水125gに溶解させた水
溶液を、30〜60分間かけて少しずつ滴下し、温度を
80℃に保ちながらケン化反応を終了した。反応終了
後、温度を80℃に保ったままで、クエン酸を添加して
中和を行い、ケン化組成物を製造した。
Test Example 2 α-linolenic acid mixed oil (α-linolenic acid content 55%)
112 g of ethanol was added to 250 g, and heated and mixed at 80 ° C. in a reaction kettle under a nitrogen gas atmosphere. Separately, an aqueous solution prepared by dissolving 40 g of sodium hydroxide in 125 g of water was added dropwise little by little over 30 to 60 minutes to complete the saponification reaction while maintaining the temperature at 80 ° C. After the reaction was completed, while maintaining the temperature at 80 ° C., citric acid was added for neutralization to produce a saponified composition.

【0028】上記試料を小型シャーレに入れ、70℃の
空気が還流する恒温機中に置いて、試験例1と同じ方法
でPOV(過酸化物価)を経時的に測定した。また、比
較のために、ケン化していないα−リノレン酸混合油
(α−リノレン酸含有量55%)についても、同様にし
て測定を行った。その結果を表2に示す。
The above sample was placed in a small petri dish, placed in a thermostat at 70 ° C. under which air was refluxed, and the POV (peroxide value) was measured over time by the same method as in Test Example 1. Further, for comparison, the same measurement was carried out for an unsaponified α-linolenic acid mixed oil (α-linolenic acid content 55%). The results are shown in Table 2.

【0029】[0029]

【表2】 [Table 2]

【0030】表2の結果より、α−リノレン酸について
も、ケン化することによって、空気中の酸素による酸化
を抑制できることが確認された。
From the results shown in Table 2, it was confirmed that the saponification of α-linolenic acid can also suppress the oxidation by oxygen in the air.

【0031】実施例1(粉ミルク) 全脂粉乳70g、ショ糖20g、デンプン分解物8g
に、上記試験例1の製造方法で得られたDHAケン化物
を300mg添加して、粉ミルクを製造した。
Example 1 (Powdered milk) 70 g of whole milk powder, 20 g of sucrose, 8 g of decomposed starch
To the above, 300 mg of the DHA saponification product obtained by the production method of Test Example 1 was added to produce a milk powder.

【0032】実施例2(加工牛乳) 生乳198.9g、ミルクフレーバー0.1gに、上記
試験例1の製造方法で得られたDHAケン化物を1.0
g添加して、加工牛乳を製造した。
Example 2 (Processed milk) To 198.9 g of raw milk and 0.1 g of milk flavor, 1.0 part of the DHA saponification product obtained by the production method of Test Example 1 was added.
g was added to produce processed milk.

【0033】実施例3(ドレッシング) 砂糖4.5g、食塩2.0g、原酢5.3g、卵黄4.
5g、サラダオイル10.0g、香辛料2.0g、水5
3.5gに、上記試験例2の製造方法で得られたα−リ
ノレン酸ケン化物を20.0g添加して、ドレッシング
を製造した。
Example 3 (dressing) Sugar 4.5 g, salt 2.0 g, raw vinegar 5.3 g, egg yolk 4.
5g, salad oil 10.0g, spice 2.0g, water 5
20.0 g of the saponified α-linolenic acid obtained by the production method of Test Example 2 was added to 3.5 g to produce a dressing.

【0034】[0034]

【発明の効果】以上説明したように、本発明によれば、
ω−3系脂肪酸又はその誘導体をケン化してペースト状
又は固形状にしたものを食品に配合するので、食品の製
造時及び調理時における取り扱い性が良好となる。ま
た、ω−3系脂肪酸又はその誘導体をケン化させたこと
により、水和性が向上して食品への添加が容易になり、
更に、空気中の酸素による酸化が抑制されるので、ω−
3系脂肪酸又はその誘導体を高濃度で含有し、保存安定
性に優れた食品を提供することができる。
As described above, according to the present invention,
The ω-3 fatty acid or its derivative is saponified to form a paste or solid, which is added to the food, so that the handleability during food production and cooking is improved. Further, by saponifying the ω-3 fatty acid or its derivative, the hydration is improved and the addition to foods is facilitated,
Furthermore, since oxidation by oxygen in the air is suppressed, ω−
It is possible to provide a food product containing a high concentration of a 3-fatty acid or its derivative and having excellent storage stability.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小林 洋一 東京都小平市上水本町6−18−18 (72)発明者 菅 辰彦 埼玉県狭山市根岸239−41 (72)発明者 矢澤 一良 神奈川県相模原市鵜野森571 (72)発明者 近藤 聖 神奈川県大和市中央林間5−16−4 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoichi Kobayashi 6-18-18, Kamimizumoto-cho, Kodaira-shi, Tokyo (72) Inventor Tatsuhiko Suga 239-41, Negishi, Sayama-shi, Saitama (72) Inventor Kazuyoshi Yazawa Kanagawa 571 Unomori, Sagamihara-shi, Japan (72) Inventor St. Kondo 5-16-4 Chuorinkan, Yamato-shi, Kanagawa

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 ω−3系脂肪酸又はその誘導体のケン化
物を少なくとも1種類含むことを特徴とする食品。
1. A food comprising at least one saponified omega-3 fatty acid or derivative thereof.
【請求項2】 前記ω−3系脂肪酸が、ドコサヘキサエ
ン酸、エイコサペンタエン酸、α−リノレン酸から選ば
れた少なくとも1種である請求項1記載の食品。
2. The food according to claim 1, wherein the ω-3 fatty acid is at least one selected from docosahexaenoic acid, eicosapentaenoic acid and α-linolenic acid.
【請求項3】 前記食品が、粉ミルク、加工牛乳、ドレ
ッシングから選ばれた1つである請求項1又は2記載の
食品。
3. The food according to claim 1, wherein the food is one selected from powdered milk, processed milk and dressing.
【請求項4】 ω−3系脂肪酸又はその誘導体を少なく
とも1種類含む原料油脂及び/又は脂肪酸に、不活性ガ
スの雰囲気下でアルカリ剤を添加してケン化させた後、
酸を添加して中和させて得られたケン化物を、食品原料
中に添加することを特徴とする食品の製造方法。
4. A raw material oil and / or fatty acid containing at least one ω-3 fatty acid or derivative thereof is saponified by adding an alkali agent in an inert gas atmosphere,
A method for producing a food, characterized in that a saponified product obtained by adding an acid to neutralize is added to a food material.
【請求項5】 前記ω−3系脂肪酸が、ドコサヘキサエ
ン酸、エイコサペンタエン酸、α−リノレン酸から選ば
れた少なくとも1種である請求項3記載の食品の製造方
法。
5. The method for producing a food according to claim 3, wherein the ω-3 fatty acid is at least one selected from docosahexaenoic acid, eicosapentaenoic acid and α-linolenic acid.
【請求項6】 前記食品が、粉ミルク、加工牛乳、ドレ
ッシングから選ばれた1つである請求項4又は5記載の
食品の製造方法。
6. The method for producing a food product according to claim 4, wherein the food product is one selected from powdered milk, processed milk and dressing.
JP5195537A 1993-07-13 1993-07-13 Food and its preparation Pending JPH0731416A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5195537A JPH0731416A (en) 1993-07-13 1993-07-13 Food and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5195537A JPH0731416A (en) 1993-07-13 1993-07-13 Food and its preparation

Publications (1)

Publication Number Publication Date
JPH0731416A true JPH0731416A (en) 1995-02-03

Family

ID=16342744

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5195537A Pending JPH0731416A (en) 1993-07-13 1993-07-13 Food and its preparation

Country Status (1)

Country Link
JP (1) JPH0731416A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6146189A (en) * 1996-06-26 2000-11-14 Alps Electric Co., Ltd. Flexible printed circuit board mounting structure and recording/reproducing apparatus using the same
JP2006514541A (en) * 2002-08-29 2006-05-11 ユニバーシティー オブ マサチューセッツ Using emulsion interface engineering to form an oxidatively stable lipid delivery system

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6146189A (en) * 1996-06-26 2000-11-14 Alps Electric Co., Ltd. Flexible printed circuit board mounting structure and recording/reproducing apparatus using the same
JP2006514541A (en) * 2002-08-29 2006-05-11 ユニバーシティー オブ マサチューセッツ Using emulsion interface engineering to form an oxidatively stable lipid delivery system

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