JPH02173183A - Antioxidant - Google Patents
AntioxidantInfo
- 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
Links
- 239000003963 antioxidant agent Substances 0.000 title abstract description 32
- 230000003078 antioxidant effect Effects 0.000 title abstract description 26
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims abstract description 16
- 235000017491 Bambusa tulda Nutrition 0.000 claims abstract description 16
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims abstract description 16
- 239000000284 extract Substances 0.000 claims abstract description 11
- 239000011732 tocopherol Substances 0.000 claims abstract description 11
- 229930003799 tocopherol Natural products 0.000 claims abstract description 11
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000787 lecithin Substances 0.000 claims abstract description 10
- 235000010445 lecithin Nutrition 0.000 claims abstract description 10
- 235000010384 tocopherol Nutrition 0.000 claims abstract description 10
- 229960001295 tocopherol Drugs 0.000 claims abstract description 10
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims abstract description 10
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims abstract description 9
- 229940067606 lecithin Drugs 0.000 claims abstract description 9
- 241001330002 Bambuseae Species 0.000 claims description 10
- 239000011425 bamboo Substances 0.000 claims description 10
- 239000003921 oil Substances 0.000 abstract description 7
- 241000209128 Bambusa Species 0.000 abstract description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
- 235000013305 food Nutrition 0.000 abstract description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002904 solvent Substances 0.000 abstract description 5
- 239000003925 fat Substances 0.000 abstract description 4
- 235000003570 Phyllostachys pubescens Nutrition 0.000 abstract description 3
- 239000002994 raw material Substances 0.000 abstract description 3
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 abstract description 2
- 241001520913 Phyllostachys edulis Species 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000010298 pulverizing process Methods 0.000 abstract 1
- 235000006708 antioxidants Nutrition 0.000 description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 2
- 239000002211 L-ascorbic acid Substances 0.000 description 2
- 235000000069 L-ascorbic acid Nutrition 0.000 description 2
- 244000302661 Phyllostachys pubescens Species 0.000 description 2
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- -1 melanoidin Natural products 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000467 phytic acid Substances 0.000 description 2
- 229940068041 phytic acid Drugs 0.000 description 2
- 235000002949 phytic acid Nutrition 0.000 description 2
- PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 description 1
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- SPSPIUSUWPLVKD-UHFFFAOYSA-N 2,3-dibutyl-6-methylphenol Chemical compound CCCCC1=CC=C(C)C(O)=C1CCCC SPSPIUSUWPLVKD-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 235000003840 Amygdalus nana Nutrition 0.000 description 1
- 244000296825 Amygdalus nana Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 235000011432 Prunus Nutrition 0.000 description 1
- 240000001010 Semiarundinaria fastuosa Species 0.000 description 1
- 235000006577 Semiarundinaria fastuosa Nutrition 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930003935 flavonoid Natural products 0.000 description 1
- 150000002215 flavonoids Chemical class 0.000 description 1
- 235000017173 flavonoids Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 235000014774 prunus Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Abstract
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.
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.
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.
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.
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)
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.
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)
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 |
-
1988
- 1988-12-27 JP JP63330258A patent/JPH02173183A/en active Pending
Cited By (4)
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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