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JPS6231902B2 - - Google Patents
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JPS6231902B2 - - Google Patents

Info

Publication number
JPS6231902B2
JPS6231902B2 JP57154020A JP15402082A JPS6231902B2 JP S6231902 B2 JPS6231902 B2 JP S6231902B2 JP 57154020 A JP57154020 A JP 57154020A JP 15402082 A JP15402082 A JP 15402082A JP S6231902 B2 JPS6231902 B2 JP S6231902B2
Authority
JP
Japan
Prior art keywords
water
tocopherol
antioxidant
acid
monoglyceride
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.)
Expired
Application number
JP57154020A
Other languages
Japanese (ja)
Other versions
JPS5945860A (en
Inventor
Haruo Yoshinaga
Itaru Murase
Masanori Yonetani
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 JP57154020A priority Critical patent/JPS5945860A/en
Publication of JPS5945860A publication Critical patent/JPS5945860A/en
Publication of JPS6231902B2 publication Critical patent/JPS6231902B2/ja
Granted 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)

Description

【発明の詳細な説明】 本発明は水産加工食品等に用いる乳液状酸化防
止製剤に関するものである。従来、水産加工食品
の酸化防止にはBHA(ブチルヒドロキシアニソ
ール)が用いられていたが、安全性が問題視さ
れ、最近、食品への使用を禁止する行政処置がと
られている。このため、BHAに替る安全な酸化
防止剤の開発が強く望まれていた。水産加工食品
に用いる酸化防止剤は魚の浸漬液に溶解させた
り、すり身魚に練り込んだりして使用するのが一
般的用法であり、このため水溶性もしくは水に対
する分散性がかなり良好でなければ充分な酸化防
止能が得られないので、トコフエロールのような
油溶性の酸化防止剤は水と乳化しなければ使用で
きなかつた。しかしながら、トコフエロールのみ
を乳化したものは、十分な酸化防止能が得られ
ず、所定の効果を得るためには、相当量の添加を
必要とし、経済的な面および他の点で不都合があ
つた。 本発明の目的は、前記のようなトコフエロール
の欠点である低酸化防止能を高め、これを乳液状
の製剤とすることにある。 本発明者らは、トコフエロールに没食子酸およ
びL−アスコルビン酸を加えることによつて、ト
コフエロールの酸化防止能が著しく向上すること
に着目し、これらの乳化物について種々の検討を
重ねた結果、本発明を完成した。 没食子酸やL−アスコルビン酸は共に酸性であ
り、トコフエロールの乳化を困難にする物質であ
るが、乳化剤としてモノグリセリドを用いること
により乳化状態が良好な乳液を得られることが判
明し、本発明を現実的に可能にした。 すなわち、本発明はトコフエロール1〜40重量
%(以下%は重量を示す)、没食子酸0.1〜5%、
L−アスコルビン酸0.1〜5%、水20〜95%、モ
ノグリセリド0.2〜5%を主成分とする乳液状酸
化防止製剤を提供するものである。 本発明においては、トコフエロール、没食子
酸、L−アスコルビン酸、水、モノグリセリドの
必須成分を上記割合で混合したものが、水分散性
酸化防止剤としてのトコフエロールの効果が著し
く高く、かつ乳化安定性が良好である。上記配合
範囲外では酸化防止効果が充分でないか、乳化安
定性が不良になるかいずれかの欠を生ずる。 本発明に用いるトコフエロールとは、天然濃縮
トコフエロールおよびこれを油脂で希釈したも
の、天然トコフエロールからδ−トコフエロール
を濃縮したもの、dl−αトコフエロールなど一般
市販のものであつて、これらは単独で、または適
宜組み合せて用いることができる。 また、本発明に用いるモノグリセリドは、ステ
アリン酸モノグリセリドやオレイン酸モノグリセ
リドのようなグリセリン脂肪酸モノエステル、ク
エン酸モノグリセリドやコハク酸モノグリセリド
やジアセチル酒石酸モノグリセリドのような有機
酸モノグリセリドなどであつて、これらは単独
で、または適宜組み合せて用いることができる。 本発明の乳液状酸化防止製剤には、トコフエロ
ール、没食子酸、L−アスコルビン酸、水、モノ
グリセリドの必須成分のほかに、必要に応じて油
脂(トコフエロールの希釈を目的とする)、ガム
質(乳化の安定化を目的とする)、BHT(ジブチ
ルヒドロキシトルエン:酸化防止剤)などを目的
に応じて適宜配合することができる。 本発明の乳液状酸化防止製剤を得るには、これ
ら原料を高速撹拌機やホモジナイザーを用い、公
知の方法で混合、乳化すればよい。 本発明の乳液状酸化防止製剤は、酸化防止効果
が極めて強く、かつ乳液の乳化状態が良好である
ため速やかに分散し、特に煮干等の水産加工品に
用いるとき、製品の褐変を防止する効果が優れて
おり、また一般食品の酸化防止にも有効に用いら
れる。 次に本発明の実施例を示す。 実施例 1 油相部 (重量%) 天然トコフエロール(40%純度品) 40 クエン酸モノグリセリド 2 水相部 L−アスコルビン酸 2 没食子酸 1 キサンタンガム 0.05 水 54.95 キサンタンガムを溶解させた水を65℃に加熱し
てから、没食子酸とL−アスコルビン酸を混合
し、あらかじめ65℃で混合、溶解しておいた油相
部を混合、撹拌後、ホモジナイザー(圧力180
Kg/cm2)を通し、均質化後10℃まで冷やして上記
配合の乳液状酸化防止製剤を得た。このものは5
℃、常温、35℃で1ケ月間静置しても、いずれの
温度でも乳化状態が良好で、水によく分散した。 実施例 2 油相部 (重量%) dl−αトコフエロール(98%純度品) 20 ナタネ油 20 ジアセチル酒石酸モノグリセリド 1.5 水相部 L−アスコルビン酸 3 没食子酸 2 キサンタンガム 0.1 水 53.4 上記配合の乳液状酸化防止製剤を実施例1と同
様にして得た。このものは5℃、常温、35℃で1
ケ月静置しても、いずれの温度でも乳化状態が良
好で水によく分散した。 実施例 3 油相部 (重量%) dl−αトコフエロール(前出) 3 BHT 10 大豆油 20 ジアセチル酒石酸モノグリセリド 1 オレイン酸モノグリセリド 0.5 水相部 L−アスコルビン酸 2 没食子酸 0.5 アラビアガム 5 水 58 上記配合の乳液状酸化防止製剤を実施例1と同
様にして得た。このものは5℃、常温、35℃で1
ケ月間静置しても、いずれの温度でも乳化状態が
良好で水によく分散した。 比較配合例 1 油相部 (重量%) dl−αトコフエロール(前出) 20 ナタネ油 20 クエン酸モノグリセリド 2 水相部 キサンタンガム 0.05 水 57.95 比較配合例 2 油相部 (重量%) dl−αトコフエロール(前出) 20 ナタネ油 20 クエン酸モノグリセリド 2 水相部 L−アスコルビン酸 5 キサンタンガム 0.05 水 52.95 比較配合例 3 油相部 (重量%) dl−α−トコフエロール(前出) 20 ナタネ油 20 クエン酸モノグリセリド 2 水相部 没食子酸 5 キサンタンガム 0.05 水 52.95 この配合では、L−アスコルビン酸がないの
で、没食子酸が鉄イオンと反応して暗紫色に発色
し商品価値が低下する。 比較配合例 4 油相部 (重量%) dl−α−トコフエロール(前出) 20 ナタネ油 20 水相部 L−アスコルビン酸 3 没食子酸 2 キサンタンガム 0.1 水 54.9 この配合例では、乳化剤であるモノグリセリド
が配合してないので、乳化状態が不安定であり、
調製後2日で油相部が分離してきた。 実施例 4 10の水を入れた鍋に、実施例1で得た乳液状
酸化防止製剤を5g入れ、沸騰させた後、水洗い
した真いわし(体長約7cmのもの)を0.5Kg入
れ、5分間煮沸したものを40℃の温風で乾燥し、
煮干を得た。実施例2、実施例3、比較配合例
1、比較配合例2および比較配合例3の乳液状酸
化防止製剤についても同一添加量で別々に煮干を
前記方法にて試作した。また、酸化防止剤無添加
の煮干も同時に試作し、それぞれを常温に保管
し、油焼けによる褐変の度合を経日的に観察し
た。結果は表−1の通りであつた。 なお、比較配合例3では鍋の中の水が暗紫色に
淡く着色した。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an emulsion-like antioxidant preparation for use in processed marine foods and the like. BHA (butylated hydroxyanisole) has traditionally been used to prevent oxidation in processed seafood foods, but safety has been raised as a problem, and administrative measures have recently been taken to ban its use in foods. For this reason, there has been a strong desire to develop a safe antioxidant to replace BHA. Antioxidants used in processed seafood foods are generally used by dissolving them in the fish soaking liquid or kneading them into minced fish, so they must have very good water solubility or dispersibility in water. Since sufficient antioxidant ability cannot be obtained, oil-soluble antioxidants such as tocopherols cannot be used unless they are emulsified with water. However, emulsifying only tocopherols does not have sufficient antioxidant ability and requires the addition of a considerable amount to achieve the desired effect, which is disadvantageous from an economical and other point of view. . The purpose of the present invention is to improve the low antioxidant ability of tocopherols as described above, and to formulate them into a milky lotion preparation. The present inventors noticed that the antioxidant ability of tocopherols was significantly improved by adding gallic acid and L-ascorbic acid to tocopherols, and as a result of various studies on these emulsions, the present invention was developed. Completed the invention. Both gallic acid and L-ascorbic acid are acidic substances that make it difficult to emulsify tocopherols, but it was found that a milky lotion with good emulsification can be obtained by using monoglyceride as an emulsifier, which led to the realization of the present invention. made it possible. That is, the present invention contains tocopherol 1 to 40% by weight (hereinafter % indicates weight), gallic acid 0.1 to 5%,
The present invention provides an emulsion-like antioxidant preparation whose main components are 0.1-5% L-ascorbic acid, 20-95% water, and 0.2-5% monoglyceride. In the present invention, a mixture of the essential components of tocopherol, gallic acid, L-ascorbic acid, water, and monoglyceride in the above proportions has a significantly high effect of tocopherol as a water-dispersible antioxidant and has high emulsion stability. In good condition. Outside the above blending range, either the antioxidant effect is insufficient or the emulsion stability becomes poor. The tocopherols used in the present invention are commonly commercially available products such as naturally concentrated tocopherol, diluted with oil and fat, δ-tocopherol concentrated from natural tocopherol, and dl-α tocopherol, which may be used alone or They can be used in appropriate combinations. Furthermore, the monoglycerides used in the present invention include glycerin fatty acid monoesters such as stearic acid monoglyceride and oleic acid monoglyceride, organic acid monoglycerides such as citric acid monoglyceride, succinic acid monoglyceride, and diacetyl tartaric acid monoglyceride, and the like. , or can be used in appropriate combination. In addition to the essential components of tocopherol, gallic acid, L-ascorbic acid, water, and monoglyceride, the emulsion antioxidant preparation of the present invention also contains oil (for the purpose of diluting tocopherol), gum (emulsifying ), BHT (dibutylhydroxytoluene: antioxidant), etc. can be blended as appropriate depending on the purpose. In order to obtain the milky antioxidant formulation of the present invention, these raw materials may be mixed and emulsified using a high-speed stirrer or homogenizer by a known method. The emulsion-like antioxidant preparation of the present invention has an extremely strong antioxidant effect, and since the emulsification state of the emulsion is good, it is quickly dispersed, and is particularly effective in preventing browning of the product when used in processed marine products such as dried sardines. It is also effective in preventing the oxidation of general foods. Next, examples of the present invention will be shown. Example 1 Oil phase (% by weight) Natural tocopherol (40% purity) 40 Citric acid monoglyceride 2 Aqueous phase L-ascorbic acid 2 Gallic acid 1 Xanthan gum 0.05 Water 54.95 Water in which xanthan gum was dissolved was heated to 65°C. Then, gallic acid and L-ascorbic acid were mixed, and the oil phase, which had been mixed and dissolved at 65℃ in advance, was mixed and stirred, and then heated using a homogenizer (pressure 180℃).
Kg/cm 2 ), homogenized, and then cooled to 10° C. to obtain an emulsion-like antioxidant preparation with the above formulation. This one is 5
℃, room temperature, and 35℃ for one month, the emulsification state was good at all temperatures, and it was well dispersed in water. Example 2 Oil phase (% by weight) dl-α tocopherol (98% purity product) 20 Rapeseed oil 20 Diacetyl tartrate monoglyceride 1.5 Aqueous phase L-ascorbic acid 3 Gallic acid 2 Xanthan gum 0.1 Water 53.4 Antioxidant emulsion with the above formulation A formulation was obtained in the same manner as in Example 1. This product is 1 at 5℃, room temperature, and 35℃.
Even after standing for several months, the emulsification state was good at all temperatures and it was well dispersed in water. Example 3 Oil phase (weight %) dl-α tocopherol (as above) 3 BHT 10 Soybean oil 20 Diacetyl tartaric acid monoglyceride 1 Oleic acid monoglyceride 0.5 Water phase L-ascorbic acid 2 Gallic acid 0.5 Gum arabic 5 Water 58 Above formulation An emulsion-like antioxidant preparation was obtained in the same manner as in Example 1. This product is 1 at 5℃, room temperature, and 35℃.
Even after being left standing for several months, the emulsification state was good at all temperatures and it was well dispersed in water. Comparative formulation example 1 Oil phase (wt%) dl-α tocopherol (as above) 20 Rapeseed oil 20 citric acid monoglyceride 2 Aqueous phase xanthan gum 0.05 Water 57.95 Comparative formulation example 2 Oil phase (wt%) dl-α tocopherol ( 20 Rapeseed oil 20 Citric acid monoglyceride 2 Water phase L-Ascorbic acid 5 Xanthan gum 0.05 Water 52.95 Comparative formulation example 3 Oil phase (wt%) dl-α-tocopherol (Previous) 20 Rapeseed oil 20 Citric acid monoglyceride 2 Aqueous phase gallic acid 5 Xanthan gum 0.05 Water 52.95 In this formulation, since there is no L-ascorbic acid, gallic acid reacts with iron ions to develop a dark purple color, reducing the commercial value. Comparative formulation example 4 Oil phase (wt%) dl-α-tocopherol (mentioned above) 20 Rapeseed oil 20 Aqueous phase L-ascorbic acid 3 Gallic acid 2 Xanthan gum 0.1 Water 54.9 In this formulation example, monoglyceride as an emulsifier is blended. Since the emulsification state is unstable,
Two days after preparation, the oil phase separated. Example 4 Put 5g of the emulsion-like antioxidant preparation obtained in Example 1 into a pot filled with water, bring to a boil, then add 0.5kg of washed Japanese sardines (about 7cm long) and boil for 5 minutes. Dry the boiled material with warm air at 40℃,
I got dried sardines. The emulsion-like antioxidant preparations of Example 2, Example 3, Comparative Formulation Example 1, Comparative Formulation Example 2, and Comparative Formulation Example 3 were also trial-produced using the same method in the same manner. At the same time, we also produced a trial version of dried sardines without the addition of antioxidants, stored them at room temperature, and observed the degree of browning due to oil burn over time. The results were as shown in Table-1. In addition, in Comparative Formulation Example 3, the water in the pot was slightly colored dark purple. 【table】

Claims (1)

【特許請求の範囲】 1 トコフエロール1〜40重量%、没食子酸0.1
〜5重量%、L−アスコルビン酸0.1〜5重量
%、水20〜95重量%、モノグリセリド0.2〜5重
量%を主成分とする乳液状酸化防止製剤。 2 油脂、ガム質およびジブチルヒドロキシトル
エンから選ばれる1種以上をさらに加えてなる特
許請求の範囲第1項記載の乳液状酸化防止製剤。
[Claims] 1. Tocopherol 1-40% by weight, gallic acid 0.1
-5% by weight, L-ascorbic acid 0.1-5% by weight, water 20-95% by weight, and monoglyceride 0.2-5% by weight. 2. The emulsion antioxidant preparation according to claim 1, further comprising one or more selected from oils and fats, gums, and dibutylhydroxytoluene.
JP57154020A 1982-09-06 1982-09-06 Milky lotionlike antioxidizing pharmaceutical Granted JPS5945860A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57154020A JPS5945860A (en) 1982-09-06 1982-09-06 Milky lotionlike antioxidizing pharmaceutical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57154020A JPS5945860A (en) 1982-09-06 1982-09-06 Milky lotionlike antioxidizing pharmaceutical

Publications (2)

Publication Number Publication Date
JPS5945860A JPS5945860A (en) 1984-03-14
JPS6231902B2 true JPS6231902B2 (en) 1987-07-10

Family

ID=15575148

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57154020A Granted JPS5945860A (en) 1982-09-06 1982-09-06 Milky lotionlike antioxidizing pharmaceutical

Country Status (1)

Country Link
JP (1) JPS5945860A (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60221032A (en) * 1984-04-16 1985-11-05 Nippon Oil & Fats Co Ltd Freshness preserving agent for fish and shellfish
JPS63137639A (en) * 1986-11-28 1988-06-09 Riken Vitamin Co Ltd Method for improving the quality of joints
JPH01137934A (en) * 1987-11-19 1989-05-30 Nippon Oil & Fats Co Ltd Preparation for preventing oxidation for dried small sardine
JPH01171465A (en) * 1987-12-28 1989-07-06 Takara Shuzo Co Ltd Freshness preservative for food
CH676470A5 (en) * 1988-02-03 1991-01-31 Nestle Sa
JPH01265870A (en) * 1988-04-16 1989-10-23 Nisshin Oil Mills Ltd:The Fats and oils composition
JP2701897B2 (en) * 1988-12-16 1998-01-21 宇野醤油株式会社 Method for producing O / W emulsion containing natural tocopherol
JPH03259034A (en) * 1990-03-09 1991-11-19 Nippon Light Metal Co Ltd Freshness retention liquid for foods and its use
US20040195549A1 (en) * 2003-04-04 2004-10-07 Clifford Adams Lipid-soluble formulations containing mixtures of antioxidants
JP2005298816A (en) * 2004-03-19 2005-10-27 Mitsubishi Chemicals Corp Deterioration preventive
JP5623959B2 (en) * 2011-03-30 2014-11-12 森永乳業株式会社 Formula milk powder, production method thereof, and oxidation inhibitor

Also Published As

Publication number Publication date
JPS5945860A (en) 1984-03-14

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