JPH02173183A - Antioxidant - Google Patents

Antioxidant

Info

Publication number
JPH02173183A
JPH02173183A JP63330258A JP33025888A JPH02173183A JP H02173183 A JPH02173183 A JP H02173183A JP 63330258 A JP63330258 A JP 63330258A JP 33025888 A JP33025888 A JP 33025888A JP H02173183 A JPH02173183 A JP H02173183A
Authority
JP
Japan
Prior art keywords
antioxidant
tocopherol
bamboos
stems
lecithin
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
JP63330258A
Other languages
Japanese (ja)
Inventor
Atsuro Nishina
淳良 仁科
Motoharu Arai
基晴 新井
Takeshi Uchibori
内堀 毅
Hajime Kiyono
清野 肇
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 JP63330258A priority Critical patent/JPH02173183A/en
Publication of JPH02173183A publication Critical patent/JPH02173183A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a strong antioxidant, containing an extract of bamboos, tocopherol and lecithin at a specific ratio, excellent in safety for human bodies and used for foods or feeds. CONSTITUTION:The objective antioxidant containing (A) 0.1-50wt.% (preferably 1-10wt.%) extract of bamboos, especially preferably using leaves and stems of Phyllostachys pubescens as a raw material, (B) 1-20wt.% (preferably 5-10wt.%) tocopherol, especially preferably consisting of natural concentrated tocopherol or diluted with fats and oils and (C) 1-50wt.% (preferably 5-20wt.%) lecithin consisting of phosphatidylcholine, N-acylphosphatidylethanolamine, etc. Furthermore, the component (A) is produced by a method for pulverizing leaves or stems of the bamboos which are raw materials using a ball mill, etc., then extracting the pulverized leaves or stems with a solvent, such as ethanol or n-hexane, and subsequently evaporating the solvent.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、食品、又は飼料に用いる、強力で、かつ人体
に対する安全性に優れた酸化防止剤に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a powerful antioxidant that is used in food or feed and has excellent safety for the human body.

〔従来の技術〕[Conventional technology]

従来から、酸化防止剤としては、安価で酸化防止力の優
れたものとして、ブチルヒドロキシアニソール(BHA
)やジブチルヒドロキシトルエン(BHT)などの合成
酸化防止剤が、また、天然酸化防II:、剤として、ト
コフェロール、L−アスコルビン酸、クエン酸、メラノ
イジン、フラボノイド、アミノ酸、フィチン酸などの単
独物またはそれらの混合物が用いられてきた。
Conventionally, butylated hydroxyanisole (BHA) has been used as an antioxidant that is inexpensive and has excellent antioxidant power.
) and dibutylhydroxytoluene (BHT), as well as natural antioxidants such as tocopherol, L-ascorbic acid, citric acid, melanoidin, flavonoids, amino acids, and phytic acid alone or as agents. Mixtures thereof have been used.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら、これらのうち、BHAやB HTなどの
合成酸化防止剤は、近時人体に対する安全性の面から食
品への使用が問題視されるようになってきており、一方
、天然酸化防止剤は、安全性の面では問題は生じないが
、酸化防止効果が十分でないなど、それぞれ一長一短で
あり、さらに優れた酸化防止剤の開発が要望されていた
However, among these, synthetic antioxidants such as BHA and BHT have recently become problematic for use in food products due to their safety to the human body, while natural antioxidants Although they do not pose any safety problems, they each have advantages and disadvantages, such as insufficient antioxidant effects, and there has been a demand for the development of even better antioxidants.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、これら従来の問題点を解決すべく鋭意研
究した結果、酸化防止剤として竹類抽出物とトコフェロ
ール、レシチンを併用することにより、上記の欠点をす
べて解消し、十分に業界の要望にこたえ得る酸化防止剤
が得られることを知り、本発明を完成させるに至った。
As a result of intensive research to solve these conventional problems, the present inventors have found that by using bamboo extract, tocopherol, and lecithin together as antioxidants, all of the above-mentioned drawbacks have been eliminated, and the product has become fully effective in the industry. Having learned that it is possible to obtain an antioxidant that meets these needs, we have completed the present invention.

すなわち、本発明は、竹類抽出物とトコフェロール、レ
シチンを含有してなる酸化防止剤に関する。
That is, the present invention relates to an antioxidant containing a bamboo extract, tocopherol, and lecithin.

本発明において、竹類抽出物を得るための原料となる竹
類としては、ホウオウチク属、シホウチク属、マダケ属
、メダケ属、シュドザサ属、ササモルファ属、ナリヒラ
ダケ属、トウチク属などに属する竹類があり、中でも孟
宗竹の葉および茎が特に好適である。
In the present invention, bamboos that can be used as raw materials for obtaining a bamboo extract include bamboos belonging to the genus Prunus spp., genus P. spp., genus Madake, genus Medake, genus P. genus, genus Sasamorpha, genus Narihiradake, genus P. genus, etc. Among them, leaves and stems of Moso bamboo are particularly suitable.

これらの竹類から竹類抽出物を得るには、まず原料の竹
類の葉または、茎をボールミルなどを用いて粉砕し、つ
いでエタノール、n−ヘキサン。
In order to obtain a bamboo extract from these bamboos, first, the leaves or stems of the raw bamboo are ground using a ball mill or the like, and then ethanol and n-hexane are added.

エーテル、アセトンなどの溶媒で抽出したのち。After extraction with a solvent such as ether or acetone.

溶媒を蒸発せしめればよい。All you have to do is evaporate the solvent.

また、この際必要に応じて、クロマトグラフィーを用い
てさらに精製することもできる。
Further, at this time, if necessary, further purification can be performed using chromatography.

竹類抽出物の配合量は0.1〜50重量%、好ましくは
1〜10重量%とである。
The amount of bamboo extract is 0.1 to 50% by weight, preferably 1 to 10% by weight.

0.1重量%未満では酸化防止力が不十分であり、50
重量%を超える場合はコストの点で高くなるので不利で
ある。
If it is less than 0.1% by weight, the antioxidant power is insufficient;
If it exceeds % by weight, it is disadvantageous because it increases the cost.

本発明で用いられるトコフェールは、α、β。The tocopheres used in the present invention are α and β.

γ、δ、のいずれの型のものでも使用できるが、天然濃
縮トコフェールおよびそれを油脂で希釈したものが特に
好ましい。
Although either γ or δ type tocopheres can be used, naturally concentrated tocopheres and those diluted with fats and oils are particularly preferred.

さらに、これらのトコフェロールは、市販品で十分であ
り、それぞれ単独でも、または適宜組み合わせても用い
ることができる。
Furthermore, commercially available products are sufficient for these tocopherols, and they can be used alone or in appropriate combinations.

トコフェロールの配合量は1〜20重量%、好ましくは
5〜10重量%である。
The amount of tocopherol blended is 1 to 20% by weight, preferably 5 to 10% by weight.

1重量%未満では酸化防止力が不十分であり、20重量
%を超える場合はコスト的に不利である。
If it is less than 1% by weight, the antioxidant power is insufficient, and if it exceeds 20% by weight, it is disadvantageous in terms of cost.

本発明で用いるレシチンとしては、ホスファチジルコリ
ン、ホスファチジルエタノールアミン、ホスファチジル
イノシトール、ホスファチジン酸。
Lecithins used in the present invention include phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, and phosphatidic acid.

N−アシルホスファチジルエタノールアミンなどを単独
で、また適宜組合わせて用いることができる。
N-acylphosphatidylethanolamine and the like can be used alone or in appropriate combinations.

また、上記のレシチンを酸素処理したリゾ型(モノアシ
ルリン脂質)レシチンなども使用可能である。
Furthermore, lyso-type (monoacyl phospholipid) lecithin obtained by treating the above lecithin with oxygen can also be used.

レシチンの配合量は1〜50重量%、好ましくは5〜2
0重量%である。
The amount of lecithin is 1 to 50% by weight, preferably 5 to 2% by weight.
It is 0% by weight.

1重量%未満では酸化防止効果が十分でなく。If it is less than 1% by weight, the antioxidant effect will not be sufficient.

50重量%以上配合しても酸化防止力は向上しなし)a 本発明の酸化防止剤には、さらに他の添加剤として、他
の酸化防止剤や相乗剤、例えばL−アスコルビン酸、没
食子酸、フィチン酸、クエン酸など、また、溶媒として
水、エタノール、アセトン。
Even if 50% by weight or more is added, the antioxidant power is not improved)a) The antioxidant of the present invention may further contain other antioxidants and synergists as other additives, such as L-ascorbic acid and gallic acid. , phytic acid, citric acid, etc., and also water, ethanol, acetone as solvents.

n−ヘキサンなどを単独で又は適宜組合わせて添加する
ことかできる。
N-hexane and the like can be added alone or in appropriate combinations.

これらの配合量は1〜97.9重量%が好ましい。The blending amount of these is preferably 1 to 97.9% by weight.

本発明の酸化防止剤の使用に当たっては、食品や飼料な
どの対象物にそのまま添加すればよく、その添加割合は
1食品や飼料などに含まれる油脂の量に対して10〜1
10000pp好ましくは200〜1000 p p 
mである。この量がLoppm未満では酸化防止効果が
なく、110000ppを超えても酸化防止力はそれ程
向上せず不経済である。
When using the antioxidant of the present invention, it is sufficient to add it directly to the object such as food or feed, and the addition ratio is 10 to 1% of the amount of oil and fat contained in the food or feed.
10000 pp preferably 200-1000 pp
It is m. If this amount is less than Loppm, there will be no antioxidant effect, and if it exceeds 110,000 ppm, the antioxidant power will not improve much and it will be uneconomical.

さらに、この場合、酸化防止剤が食品や飼料などの対象
物に不溶なときは、酸化防止剤と水を混合乳化し、O/
W型エマルションとして添加すればよく、その際、グリ
セリン脂肪酸エステルなど適当な乳化剤を使用しても差
し支えない。
Furthermore, in this case, when the antioxidant is insoluble in the target material such as food or feed, the antioxidant and water are mixed and emulsified, and O/
It may be added as a W-type emulsion, and in this case, a suitable emulsifier such as glycerin fatty acid ester may be used.

〔発明の効果〕〔Effect of the invention〕

本発明の酸化防止剤は、従来の天然酸化防止剤に比較し
てはるかに強力な酸化防止力を有し、かつ人体に対する
安全性が高く、有用な酸化防止剤である。
The antioxidant of the present invention has much stronger antioxidant power than conventional natural antioxidants, is highly safe for the human body, and is a useful antioxidant.

〔実施例〕〔Example〕

以下、実施例、比較例および試験例について説明する。 Examples, comparative examples, and test examples will be described below.

例中、%は重量%を示す。In the examples, % indicates weight %.

実施例1 孟宗竹の茎の表皮Logをボールミルで粉砕し、エーテ
ル100ccを添加したのち室温で一昼夜放置した。つ
いで、この混合物をろ過してろ液を得、エーテルを蒸発
せしめて竹抽出物0.3gを製造した。
Example 1 The epidermis Log of the stem of Moso bamboo was ground with a ball mill, 100 cc of ether was added thereto, and then left overnight at room temperature. Then, the mixture was filtered to obtain a filtrate, and the ether was evaporated to produce 0.3 g of bamboo extract.

次いで、得られた竹抽出物を下記に示す構成物と配合割
合で混合溶解させて、酸化防止剤を!8J製した。
Next, the obtained bamboo extract is mixed and dissolved with the constituents shown below in the mixing ratio to create an antioxidant! Made by 8J.

竹抽出物               □%天然トコ
フェロール(40%品)     20%(商品名:ト
コフェロール40、日清製油株式会社)大豆レシチン 
           10%(商品名二日清レシチン
DX、日清製油株式会社)脱臭ナタネ油       
     69%比較例1〜8 実施例1で用いた各構成物を表1に示す配合割合で酸化
防止剤を調整した。
Bamboo extract □% Natural tocopherol (40% product) 20% (Product name: Tocopherol 40, Nisshin Oil Co., Ltd.) Soybean lecithin
10% (Product name Nisshin Lecithin DX, Nisshin Oil Co., Ltd.) Deodorized rapeseed oil
69% Comparative Examples 1 to 8 Antioxidants were prepared using the respective components used in Example 1 in the proportions shown in Table 1.

試験例1 精製ラードに実施例1.及び比較例1〜8の酸化防止剤
をloooppm添加した後、AOM試験を行った。
Test Example 1 Example 1 on purified lard. After adding loooppm of the antioxidants of Comparative Examples 1 to 8, an AOM test was conducted.

POvが100に上昇するまでの時間を表2に示す。Table 2 shows the time required for POv to rise to 100.

表2 表2の結果から、無添加のものは言うにおよばず、また
1本発明の配合割合を逸脱したもの等と比しても本発明
の酸化防IE剤は、これら比較例のものより強力な抗醸
化作用を有していることが明らかである。
Table 2 From the results in Table 2, it can be seen that the antioxidant IE agent of the present invention is superior to those of these comparative examples, not to mention those without additives, and even when compared with those that deviate from the blending ratio of the present invention. It is clear that it has a strong anti-inflammatory effect.

試験例2 脱臭ナタネ油に実施例1、及び比較例1〜8で得た酸化
防止剤を11000pp添加した。
Test Example 2 11,000 pp of the antioxidants obtained in Example 1 and Comparative Examples 1 to 8 were added to deodorized rapeseed oil.

次に、これらの油脂それぞれ790gに乳化剤としてモ
ノグリセリンステアレートを溶解させた油相を、水1k
gにアラビアゴム200gを溶解させた水相に混合し、
70℃で予備乳化後、ホモゲナイザーを用いて均質化し
た。
Next, an oil phase obtained by dissolving monoglycerol stearate as an emulsifier in 790 g of each of these oils and fats was added to 1 k of water.
g and 200 g of gum arabic dissolved in the aqueous phase,
After preliminary emulsification at 70°C, homogenization was performed using a homogenizer.

この乳化液をスプレードライすることにより、ナタネ粉
末油脂を得た。
By spray drying this emulsion, powdered rapeseed fat and oil was obtained.

そして、得られた粉末を60℃の恒温槽に保存し、10
日後に粉末から油分を抽出し、その過階化物価を測定し
た。油分の抽出方法は、粉末10gにクロロホルム40
m1を加え、超音波処理を5分間行った後に残っている
粉末をろ別し、ろ液を濃縮して測定サンプルとした。P
Ovの測定の結果を表3に示す。
Then, the obtained powder was stored in a constant temperature bath at 60°C, and
After a day, the oil content was extracted from the powder and its peroxidation value was measured. To extract the oil, add 40 g of chloroform to 10 g of powder.
After adding m1 and performing ultrasonic treatment for 5 minutes, the remaining powder was filtered off, and the filtrate was concentrated to obtain a measurement sample. P
Table 3 shows the results of Ov measurement.

表3 表3の結果から、 本発明の酸化防止剤は比較例 のものより強力な抗酸化作用を有していることが明らか
である。
Table 3 From the results in Table 3, it is clear that the antioxidant of the present invention has a stronger antioxidant effect than that of the comparative example.

Claims (1)

【特許請求の範囲】[Claims] 竹類抽出物0.1〜50重量%、トコフェロール1〜2
0重量%、レシチン1〜50重量%を含有してなる酸化
防止剤。
Bamboo extract 0.1-50% by weight, tocopherol 1-2
0% by weight, and 1 to 50% by weight of lecithin.
JP63330258A 1988-12-27 1988-12-27 Antioxidant Pending JPH02173183A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63330258A JPH02173183A (en) 1988-12-27 1988-12-27 Antioxidant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63330258A JPH02173183A (en) 1988-12-27 1988-12-27 Antioxidant

Publications (1)

Publication Number Publication Date
JPH02173183A true JPH02173183A (en) 1990-07-04

Family

ID=18230629

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63330258A Pending JPH02173183A (en) 1988-12-27 1988-12-27 Antioxidant

Country Status (1)

Country Link
JP (1) JPH02173183A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5523429A (en) * 1991-12-18 1996-06-04 Rhone-Poulenc Rorer-Gmbh N-acylphosphatidylethanolamines as anti-oxidants
KR100454115B1 (en) * 2001-02-28 2004-10-26 애경산업(주) Method for Separating 1,2-di-o-feruloylglycerol and Cosmetic Composition Containing the Same and its Use
KR100486763B1 (en) * 2001-09-07 2005-05-03 학교법인고려중앙학원 Extracts of Phyllostachys edulis leaf having antioxidant activity and the process for preparation thereof
JP2007507437A (en) * 2003-10-08 2007-03-29 杭州浙大力夫生物科技有限公司 Bamboo leaf antioxidant and its uses

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5523429A (en) * 1991-12-18 1996-06-04 Rhone-Poulenc Rorer-Gmbh N-acylphosphatidylethanolamines as anti-oxidants
KR100454115B1 (en) * 2001-02-28 2004-10-26 애경산업(주) Method for Separating 1,2-di-o-feruloylglycerol and Cosmetic Composition Containing the Same and its Use
KR100486763B1 (en) * 2001-09-07 2005-05-03 학교법인고려중앙학원 Extracts of Phyllostachys edulis leaf having antioxidant activity and the process for preparation thereof
JP2007507437A (en) * 2003-10-08 2007-03-29 杭州浙大力夫生物科技有限公司 Bamboo leaf antioxidant and its uses

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