JPS62111676A - Antioxidation agent - Google Patents

Antioxidation agent

Info

Publication number
JPS62111676A
JPS62111676A JP60252091A JP25209185A JPS62111676A JP S62111676 A JPS62111676 A JP S62111676A JP 60252091 A JP60252091 A JP 60252091A JP 25209185 A JP25209185 A JP 25209185A JP S62111676 A JPS62111676 A JP S62111676A
Authority
JP
Japan
Prior art keywords
tocopherol
gum
phytic acid
antioxidant
water
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
JP60252091A
Other languages
Japanese (ja)
Inventor
Atsuro Nishina
淳良 仁科
Masakatsu Kakizaki
柿崎 正勝
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.)
NOF Corp
Original Assignee
Nippon Oil and Fats Co Ltd
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 Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP60252091A priority Critical patent/JPS62111676A/en
Publication of JPS62111676A publication Critical patent/JPS62111676A/en
Pending 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
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/90Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation

Landscapes

  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)

Abstract

PURPOSE:To obtain a safe antioxidation agent of an O/W-type emulsion having extremely strong antioxidation effect and storable stably for a long period, by using tocopherol and phytic acid as anti-oxidants and a natural gum as an emulsion stabilizer. CONSTITUTION:The objective agent can be produced by mixing and emulsifying (A) 1-60wt%, preferably 10-40wt% tocopherol, (B) 0.1-40wt%, preferably 1-5wt% phytic acid, (C) 0.01-50wt%, preferably 0.2-10wt% natural gum such as gum arabic, xanthan gum, etc., and (D) 20-95wt% water with a high- speed agitator or a homogenizer.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、食品及び飼料、特に水産物の酸化防止に有効
な乳液状の酸化防止製剤に関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a milky lotion-like antioxidant preparation effective in preventing the oxidation of foods and feeds, particularly marine products.

〈従来の技術〉 食品や飼料を酸素による酸化から保護することは産業上
大変重要な事でおり、現在まで数多くの酸什詫11−橢
四(部器シ剥イ各4 を晶、? Δ→ハ馳化防止剤の中
に毒性を持つものがあり、広く用いきた。そこで、安全
性の高い天然の酸化防止剤0開発が行われ、トコフェロ
ール、フラボン誘導体。
<Prior art> Protecting food and feed from oxidation by oxygen is very important in industry, and to date there have been many methods for protecting food and feed from oxidation by oxygen. →Some antioxidants are toxic and have been widely used.Therefore, highly safe natural antioxidants were developed, including tocopherol and flavone derivatives.

没食子酸誘導体、NDGA (ノルジヒドログアヤレチ
ックアシド)、ボンボール、セサモール、香辛料、アミ
ノ酸々どの天然酸化防止剤の中の1種又は複数と、シネ
ルギストを組合わせた酸化防止製剤が開発されてきた。
Antioxidant formulations have been developed that combine synergists with one or more of the natural antioxidants such as gallic acid derivatives, NDGA (nordihydroguaiaretic acid), bombol, sesamol, spices, amino acids, and the like.

〈発明が解決しようとする問題点〉 上記の天然酸化防止剤は安全■で問題はないが一種類の
みの使用では酸化防止力が十分でなく複数の使用により
酸化防止力を向上させる方法がとられてきた。その中で
トコフェロールにシネルギストとしてフェチン散を組合
わせると強い酸化防止効果が得られるが、油相圧トコフ
ェロール、水相にフィチン酸を含み0/W(水中油)型
とした長期間安定な乳液状酸防止製剤は見当たらない。
<Problems to be solved by the invention> The above-mentioned natural antioxidants are safe and there are no problems, but using only one type of antioxidant does not provide sufficient antioxidant power, and there is a method to improve the antioxidant power by using multiple types. I've been exposed to it. Among them, a strong antioxidant effect can be obtained by combining tocopherol with Fetin Powder as a synergist. No acid inhibitors were found.

−+−AJ−,也漕エヒi)−ル客11噂トナ −フ 
、 4− ソにロ ズー今す、−一十日の王が低いため
に乳化が破壊されて、どうして本保存中に離れ、オイル
オフを起こして安定な乳液が得られなかった。
-+-AJ-, Yakoehi i) -ru customer 11 rumored tona -f
, 4- The emulsion is destroyed due to the low value of the 10th day, so why did it separate during storage and cause oil-off, making it impossible to obtain a stable emulsion?

史企垂立圭相) 本発明は以上の実情に鑑み完成されたもので、従来品よ
υもさらに強い酸化防止力を有し、安全で、かつ長期間
安定なO/W聾乳液状の酸化防止製剤を提供する事を目
的とする。
The present invention was completed in view of the above-mentioned circumstances, and is a safe and long-term stable O/W emulsion that has even stronger antioxidant power than conventional products. The purpose is to provide antioxidant preparations.

く問題点を解決するための手段〉 して含有することを特徴とする乳液状の酸化防止製剤に
関するものである。
The present invention relates to an emulsion-like antioxidant preparation characterized by containing:

本発明においてフィチン酸としては、ミオイノシトール
のへキサリン酸エステルを用いる。またトコフェロール
としては、天然濃縮トコフェロールおよび、これらを油
脂で希釈したものなどであυ、必要に応じてa−αトコ
フェロールを用いることも可能でおる。
In the present invention, myo-inositol hexaphosphate is used as phytic acid. In addition, tocopherols include naturally concentrated tocopherols and those diluted with fats and oils, and it is also possible to use a-α tocopherol if necessary.

本発明ではトコフェロールを1〜60重量係、量俤未満
では酸化防止力が不足し、60重−ii俤を越えると乳
化が困1になる。また、フィチン酸は0.1〜40i1
Lit9!+、好ましくは1〜511係を含有する。こ
の量が06lli’1未満では酸化防止力が不足し、4
0i[4を越えると油相を乳化する事が困難となる。
In the present invention, if the amount of tocopherol is less than 1 to 60 weight, the antioxidant power will be insufficient, and if it exceeds 60 weight, emulsification will be difficult. In addition, phytic acid is 0.1 to 40i1
Lit9! +, preferably 1 to 511. If this amount is less than 06lli'1, the antioxidant power will be insufficient, and 4
If it exceeds 0i[4, it becomes difficult to emulsify the oil phase.

天然ガム質としては一般市販のS藻抽出物、種子粘質物
、植物分泌粘質物、果実粘質物、微生物粘質物、澱粉と
その加工品、繊維素系粘質物などを単独で又は適宜組合
わせて用いることができるが、特に乳化力を有するアラ
ビアガム、キサンタンガム、トラガントガムが望ましく
、他にタマリンドガム、ローカストビーンガム、カラギ
ーナン等が使用できる。天然ガム質の含有量は0.01
〜50重量%、好ましくは0.2〜10iJlチである
As natural gums, commercially available S-algae extracts, seed mucilages, plant secreted mucilages, fruit mucilages, microbial mucilages, starch and its processed products, cellulose mucilages, etc. may be used singly or in appropriate combinations. Although gum arabic, xanthan gum, and gum tragacanth having emulsifying power are particularly preferred, tamarind gum, locust bean gum, and carrageenan can also be used. Natural gum content is 0.01
-50% by weight, preferably 0.2-10 iJl.

この量が0、O1重量係未満では安定な乳液が得られず
、50TIL量チを越えるとゲル化して好ましくない。
If this amount is less than 0.01 by weight, a stable emulsion cannot be obtained, and if it exceeds 50 TIL, it will undesirably turn into a gel.

本発明の乳液状の酸化防止製剤には上記必須成分の他K
L−アスコルビン酸、クエン駿、没食子酸などを酸化防
止力向上の目的で適宜配合できる。
In addition to the above-mentioned essential ingredients, the emulsion-like antioxidant preparation of the present invention contains K.
L-ascorbic acid, citric acid, gallic acid, etc. can be appropriately blended for the purpose of improving antioxidant power.

本発明の乳液状の酸化防止製剤を得るには、上記の原料
を高速攪拌機やホモジナイザーを用い、公知の方法で混
合乳化す九ばよい。
In order to obtain the emulsion-like antioxidant preparation of the present invention, the above-mentioned raw materials may be mixed and emulsified using a high-speed stirrer or homogenizer by a known method.

〈発明の効果〉 本発明の乳液状の酸化防止製剤は、酸化防止効果が極め
て強く、−iた、乳化状態および安定性が良好なため、
水分散性に優れ、高温で長期間放置しても油相と水相が
分離する事がない。
<Effects of the Invention> The emulsion-like antioxidant preparation of the present invention has an extremely strong antioxidant effect, -i, and good emulsification state and stability;
It has excellent water dispersibility, and the oil phase and water phase will not separate even if left at high temperatures for a long period of time.

〈実施例〉 つぎに実施例、比較例および試敗例によシ、本発明を説
明する。以下係はX量係を示す。
<Examples> Next, the present invention will be explained with reference to Examples, Comparative Examples, and Trial/Failure Examples. The following coefficients indicate the X quantity coefficient.

実施例1 油相部 天然トコフェロール(40%純度品)4o%(トコフェ
ロールとして16チ) 水相部 フィチン酸            10チキサンクン
ガム          0.5チ水        
              49.5優上記の成分を
混合して65“Cに加熱した水相部に、あらかじめ65
°Cに加熱し九油相部を添加して攪拌後、ホモジナイザ
ーを通して均質化した。
Example 1 Oil phase: Natural tocopherol (40% purity product) 4o% (16 t as tocopherol) Aqueous phase: Phytic acid 10 thixan gum 0.5 t water
49.5% The above ingredients were mixed and heated to 65"C.
After heating to °C and adding the 9 oil phase and stirring, the mixture was homogenized using a homogenizer.

実施例2 油相部 天然トコフェロール(80係純度品)40彊(トコフェ
ロールとして32チ) 水相部 フィチン酸            0.5係トラガン
トガム          109II水      
                34,5%上記の成
分について、実施例1と同様にして酸化防止製剤を得た
Example 2 Oil phase natural tocopherol (80 purity product) 40 degrees (32 degrees as tocopherol) Aqueous phase phytic acid 0.5 degree gum tragacanth 109II water
34.5% An antioxidant preparation was obtained in the same manner as in Example 1 using the above ingredients.

実施例3 油相部 a−αトコフェロール       10チ水相部 フィチン酸             2慢アラビアガ
ム            1チクエン酸      
        1チ水              
         86張上記の成分について、実施例
1と同様にして酸化防止製剤を得た。
Example 3 Oil phase: a-α tocopherol 10: Water phase: phytic acid 2: Gum arabic 1: citric acid
1 inch water
An antioxidant preparation was obtained in the same manner as in Example 1 using the above ingredients.

なお、以下にテす比較例1〜5尤ついても実施例1と同
様にして製剤を得た。
In Comparative Examples 1 to 5 below, preparations were obtained in the same manner as in Example 1.

比較例1 油相部 天然トコフェロール(40チ純度品)40チ水相部 フィチン酸            10係デカグリセ
リンモノラクレート    3チ水         
              47チ比較例2 油相部 天然トコフェロール(SO*純度品)40慢水相部 フィチン酸             0.5チ没食子
1!2             10チ比較例3 油相部 a−αトコフェロール       10チクエン酸モ
ノステアレート       5チ水相部 フィチン酸              2%デカグリ
セリンモノラウレート     3係クエン酸    
          1憾水            
          79僑比較例4 油相部 脱臭ナタネ油           40チ水相部 フィチン酸            10優キサンタス
ガム          0.51水        
               49.5饅比較例5 油相部 天然トコフェロール(404純度品)40憾水相部 キサンタンガム          0.5俤水   
                   59.5畳試
験例1 実施例1〜3、比較例1〜5で得た乳液t−100dの
メスシリンダーに入n、30°Cと60゛Cの恒温槽に
1ケ月静置し、乳化状態を観察した。結果は表1に示し
たが、天然ガム質を用いたものは、乳化安定性が良好で
あることがわかる。
Comparative Example 1 Oil phase: natural tocopherol (40% pure product): 40% water phase: phytic acid: 10% decaglycerin monolacrate: 3% water
47-chi Comparative Example 2 Oil phase natural tocopherol (SO*purity product) 40-hydrohydric phase phytic acid 0.5-chi gallic acid 1!2 10-chi Comparative Example 3 Oil phase a-α tocopherol 10-thicitric acid monostearate 5 Aqueous phase: phytic acid, 2% decaglycerin monolaurate, 3: citric acid
1 bitter water
79 Comparative Example 4 Oil phase deodorized rapeseed oil 40% Water phase phytic acid 10xanthus gum 0.51 water
49.5 Comparative Example 5 Oil phase natural tocopherol (404 purity product) 40 Water phase xanthan gum 0.5 water
59.5 tatami Test Example 1 The emulsions obtained in Examples 1 to 3 and Comparative Examples 1 to 5 were placed in a t-100d measuring cylinder and left standing in a constant temperature bath at 30°C and 60°C for one month to emulsify. I observed the condition. The results are shown in Table 1, and it can be seen that the emulsion stability using natural gum is good.

表  −1 0は離水力し、Xは水相と油相が完全に分離試験例2 試験例1において乳化安定性が良好でおった実施例1〜
3および比較例4.5についで下記の試験を行なった。
Table-1 0 indicates water separation force, X indicates complete separation of aqueous phase and oil phase Test Example 2 Examples 1 to 2 where emulsion stability was good in Test Example 1
3 and Comparative Example 4.5, the following tests were conducted.

それぞれの酸化防止製剤を0.1%溶解した海水を用意
し、その中に即殺した天然調を浸漬し退色(表皮の赤色
)の経日変化を観察した。また、比較のために製剤無添
加の海水についても同様の試験を行った。なお、海水の
温度は約3 ”C前後に保った。この結果は表2【示し
た。表2の結果から、トコフェロールとフィチン酸とを
含む実施例のものは比較例の本のより酸化防止効果が優
れているので、州の表皮の退色が遅くなり新鮮さを保持
していることがわかる。
Seawater in which 0.1% of each antioxidant preparation was dissolved was prepared, and immediately-killed natural seawater was immersed in the seawater to observe changes in color fading (red skin) over time. For comparison, a similar test was also conducted using seawater without any additives. The temperature of the seawater was maintained at around 3"C. The results are shown in Table 2. From the results in Table 2, it can be seen that the example containing tocopherol and phytic acid has a higher antioxidant content than the comparative example book. It can be seen that the effect is excellent, which slows down the fading of the epidermis of the state and preserves its freshness.

◎は鮮赤色、O赤色、Δわずかに退色、X退色試験例3 水洗した真イワシ(体長9clL程度)を約20尾入れ
、6分間煮沸したものを冷風乾燥し煮干しを作比較例4
1.5を用いて上述の方法により煮干しを作製した。
◎ is bright red, O is red, Δ is slightly faded,
1.5 was used to prepare dried sardines by the method described above.

乾燥終了後、そnぞれの煮干しを37°Cの恒温槽に入
九、油焼けによる褐変の度合いを経時的に観察した。結
果は表3に示した。
After drying, each dried sardine was placed in a constant temperature bath at 37°C, and the degree of browning due to oil burn was observed over time. The results are shown in Table 3.

m:褐変せず、±:微かに褐変、十:褐変、+:明らか
に褐変、++ひど〈褐変 表3より実施例のものは比較例のものより優れた油焼は
防止力を有することがわかる。
m: No browning, ±: Slight browning, 10: Browning, +: Obvious browning, ++ Severe (browning Table 3 shows that the examples have better anti-burning ability than the comparative examples. Recognize.

特許出願人  日本油脂株式会社 手続補正書(自発) 昭和60年12月11日 特許庁長官 宇 買 道 部 殿 (W許庁審査官        殿) 1 事件の表示 昭和60年特許願1g  25zo 9 z  号2 
発明の名称 酸化防止製剤 3 補正をする者 事件との関係  特許出願人 東京都千代田区有楽町1丁目10番1号4、補正の対象 明細δの発明の詳細な説明の欄 5 補正の内容 (1)明細書2頁7行「ボンポール」を「ボンポール」
と改める。
Patent Applicant Nippon Oil & Fats Co., Ltd. Procedural Amendment (Voluntary) December 11, 1985 Director General of the Japan Patent Office Mr. Ubuya Michibe (Mr. W Patent Office Examiner) 1 Indication of the Case 1985 Patent Application 1g 25zo 9 z No. 2
Name of the invention Antioxidant preparation 3 Relationship with the case of the person making the amendment Patent applicant 1-10-1-4 Yurakucho, Chiyoda-ku, Tokyo Column 5 Detailed explanation of the invention of the specification subject to amendment δ Contents of the amendment (1 ) "Bonpol" on page 2, line 7 of the specification as "Bonpol"
I'll change it to.

(2)明細書3頁2行「離れ」−を「分離し」と改める
(2) Change "separate" to "separate" in line 2 on page 3 of the specification.

Claims (1)

【特許請求の範囲】 1、酸化防止剤としてトコフェロールとフィチン酸とを
含有し、天然ガム質を乳化安定剤として含有することを
特徴とする乳液状の酸化防止製剤。 2、トコフェロール1〜60重量%、フィチン酸0.1
〜40重量%、天然ガム質0.01〜50重量%、水2
0〜95重量%である特許請求の範囲第1項記載の酸化
防止製剤。
[Scope of Claims] 1. An emulsion-like antioxidant preparation containing tocopherol and phytic acid as antioxidants and natural gum as an emulsion stabilizer. 2. Tocopherol 1-60% by weight, phytic acid 0.1
~40% by weight, natural gum 0.01-50% by weight, water 2
The antioxidant preparation according to claim 1, which contains 0 to 95% by weight.
JP60252091A 1985-11-12 1985-11-12 Antioxidation agent Pending JPS62111676A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60252091A JPS62111676A (en) 1985-11-12 1985-11-12 Antioxidation agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60252091A JPS62111676A (en) 1985-11-12 1985-11-12 Antioxidation agent

Publications (1)

Publication Number Publication Date
JPS62111676A true JPS62111676A (en) 1987-05-22

Family

ID=17232414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60252091A Pending JPS62111676A (en) 1985-11-12 1985-11-12 Antioxidation agent

Country Status (1)

Country Link
JP (1) JPS62111676A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326026A2 (en) * 1988-01-29 1989-08-02 BASF Aktiengesellschaft Stable mixture containing oxidation-sensitive compounds, process to obtain it and use of a combination of products to stabilize oxidation-sensitive compounds
JPH02124894A (en) * 1988-11-01 1990-05-14 Sanwa Kagaku Kenkyusho Co Ltd Stabilized phytic acid composition
FR2736803A1 (en) * 1995-07-19 1997-01-24 Franvet Stable compsn. contg. vitamin and inert food gel as carrier - esp. for feeding animals
EP0779915A4 (en) * 1994-09-08 1997-08-13 Multisorb Tech Inc An oxygen absorbing composition
US6156231A (en) * 1994-09-08 2000-12-05 Multisorb Technologies, Inc. Oxygen absorbing composition with cover layer

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326026A2 (en) * 1988-01-29 1989-08-02 BASF Aktiengesellschaft Stable mixture containing oxidation-sensitive compounds, process to obtain it and use of a combination of products to stabilize oxidation-sensitive compounds
JPH02124894A (en) * 1988-11-01 1990-05-14 Sanwa Kagaku Kenkyusho Co Ltd Stabilized phytic acid composition
EP0779915A4 (en) * 1994-09-08 1997-08-13 Multisorb Tech Inc An oxygen absorbing composition
US5746937A (en) * 1994-09-08 1998-05-05 Multiform Desiccants, Inc. Oxygen absorbing composition
US6156231A (en) * 1994-09-08 2000-12-05 Multisorb Technologies, Inc. Oxygen absorbing composition with cover layer
FR2736803A1 (en) * 1995-07-19 1997-01-24 Franvet Stable compsn. contg. vitamin and inert food gel as carrier - esp. for feeding animals

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