JPH07188042A - Hot compress - Google Patents

Hot compress

Info

Publication number
JPH07188042A
JPH07188042A JP5347113A JP34711393A JPH07188042A JP H07188042 A JPH07188042 A JP H07188042A JP 5347113 A JP5347113 A JP 5347113A JP 34711393 A JP34711393 A JP 34711393A JP H07188042 A JPH07188042 A JP H07188042A
Authority
JP
Japan
Prior art keywords
rice
product
present
germinated
extraction
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.)
Granted
Application number
JP5347113A
Other languages
Japanese (ja)
Other versions
JP3678435B2 (en
Inventor
Takashi Tokuyama
孝 徳山
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.)
Soken Co Ltd
Original Assignee
Soken 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 Soken Co Ltd filed Critical Soken Co Ltd
Priority to JP34711393A priority Critical patent/JP3678435B2/en
Publication of JPH07188042A publication Critical patent/JPH07188042A/en
Application granted granted Critical
Publication of JP3678435B2 publication Critical patent/JP3678435B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Thermotherapy And Cooling Therapy Devices (AREA)

Abstract

(57)【要約】 【目的】 有効性に優れ、しかも、人体に対して完全に
安全で、簡単に使用できる温湿布剤を提供する。 【構成】 発芽させた米の粉砕物、米または発芽さ
せた米の抽出物、米または発芽させた米の加水物を酵
素分解または麹を作用させたもの、米または発芽させ
た米を抽出するに当たり、その抽出前、抽出と同時また
は抽出後に酵素分解または麹を作用させたもの、米ま
たは発芽させた米の抽出物あるいは酵素分解または麹を
作用させたものに、アルコール発酵あるいは有機酸発酵
を行なったもの、以上それぞれをそのまま、あるいはこ
れを含有してなる温湿布剤。
(57) [Summary] [Purpose] To provide a hot poultice which is highly effective, completely safe for the human body, and easy to use. [Structure] Smashed germinated rice, rice or germinated rice extract, rice or germinated rice hydrolyzed with enzymatic decomposition or koji, rice or germinated rice are extracted Prior to the extraction, at the same time as or after the extraction, those subjected to enzymatic decomposition or koji, the extract of rice or sprouted rice or those subjected to enzymatic decomposition or koji, were subjected to alcohol fermentation or organic acid fermentation. What was done, the above-mentioned each as it is, or a hot compress containing the same.

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、米または発芽させた米
を用いることを特徴とし、温度上昇効果、血管拡張等の
血液循環をよくする効果を有する温湿布剤に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a warm poultice which is characterized by using rice or sprouted rice and has an effect of increasing temperature and improving blood circulation such as vasodilation.

【0002】[0002]

【従来の技術】従来から血行が悪くなることによる手足
の冷え、肩こりなどは重要な問題となっていた。これに
加えて、最近では従来のような体を動かす健康的な生活
から、無理な姿勢、連続した作業、さらには冷房、大気
汚染などのような生活環境の悪化およびストレス等が原
因で血行が悪くなることによる健康上の問題が多くなっ
てきた。これらの問題を解決するために、従来から極所
的なものについては、熱水を利用した温湿布が用いられ
てきた。しかし、これらは手間がかかること、経時的に
効果が落ちること、継続的に使用することにより皮膚が
ただれる等の欠点があることから、あまり用いられてい
ない。
2. Description of the Related Art Conventionally, cold limbs and stiff shoulders due to poor blood circulation have been important problems. In addition to this, recently, from a healthy physical activity as in the past, blood circulation is caused due to stress, etc., such as uncomfortable posture, continuous work, deterioration of living environment such as cooling, air pollution, etc. There are more and more health problems due to worsening. In order to solve these problems, hot compresses that use hot water have been used in the past for extreme ones. However, these are not often used because they are troublesome, their effects are deteriorated over time, and the skin is sore by continuous use.

【0003】そこで、手軽に利用できるカンフル、メン
トールなどを有効成分として含有する温湿布剤、さらに
は、トウガラシチンキなどのような生薬エキスを含有す
る温湿布剤が利用されている。しかし、単離した物質を
混合して効果を求めているものでは、直接的な効果が出
るために、使用中においては効果が認められるものの、
使用中止後においては極端に効果がなくなり、根本的な
改善にはなっていない。さらに、効果はあっても皮膚に
対してかゆみ等の刺激がある場合、あるいは発疹が出た
り、発赤膨張がひどくなったりする場合がある。また、
生薬成分を原料としているものでは、体質を改善してゆ
き、ゆるやかな効果を有するものもあるが、原料が安定
しなかったり、簡単に製造できなかったりするために、
利用は限られた分野でしかなされていないのが現状であ
る。
Therefore, hot compresses containing easily usable camphor, menthol, etc. as active ingredients, as well as warm compresses containing crude drug extracts such as capsicum tincture, have been used. However, in the case of seeking the effect by mixing the isolated substances, the effect is recognized during use because the direct effect is exerted,
After the discontinuation of use, the effect became extremely insignificant and not a fundamental improvement. In addition, although it is effective, it may cause irritation such as itch on the skin, or a rash may appear or redness and swelling may become severe. Also,
Some crude drug ingredients are used as raw materials to improve the constitution and have a gradual effect, but because the raw materials are not stable or cannot be easily manufactured,
At present, it is used only in a limited field.

【0004】[0004]

【発明が解決しようとする課題】前記のように、血管拡
張効果等の血液循環をよくする効果をもつ温湿布剤の利
用機会が急速に増加している。このように利用機会が急
速に増加しているにもかかわらず、安全で有効性に優れ
た温湿布剤は未だ開発されていない。そこで、本発明
は、有効性に優れ、しかも、人体に対して完全に安全
で、簡単に使用できる温湿布剤を提供することを目的と
するものである。
As described above, there are rapidly increasing opportunities to use hot compresses having an effect of improving blood circulation such as a vasodilator effect. In spite of the rapid increase in the use opportunities, safe and effective hot compresses have not been developed yet. Therefore, an object of the present invention is to provide a hot compress which is highly effective, completely safe for the human body, and easy to use.

【0005】[0005]

【課題を解決するための手段】本発明者らは、動植物合
和すの観点から、主食である米を中心に種々の植物成分
の研究を進めてきた。その過程で、米には今まで予測で
きなかった数多くの可能性、効果があることが判明して
きた。そこで、主食として用いられ安全性が最も高いこ
とが実証されている米をテーマとしてとりあげ、米の総
合利用研究を行ってきた。そのうちの一つのテーマとし
て、米からの温湿布剤について鋭意研究を重ねてきた。
その過程で、本発明者らは、米の水抽出または有機溶媒
抽出により得られる米からの温湿布剤を発明した(特願
平4−145034)。しかし、米から、より安価に、
より効果の高い温湿布剤を見出し、本発明を完成するに
至った。すなわち、本発明は、米あるいは米の発芽物を
用いることにより、簡単に安価に、しかも、安全な血液
循環をよくする効果を有する温湿布剤に関するものであ
る。
[Means for Solving the Problems] From the viewpoint of animal and plant harmony, the present inventors have conducted research on various plant components centering on rice, which is a staple food. In the process, it has become clear that rice has many unpredictable possibilities and effects. Therefore, we have conducted comprehensive research on the utilization of rice with the theme of rice, which is used as a staple food and proved to have the highest safety. As one of the themes, we have earnestly studied hot compresses from rice.
In the process, the present inventors invented a hot compress for rice obtained by extracting rice with water or organic solvent (Japanese Patent Application No. 4-145034). But cheaper from rice,
The present invention has been completed by finding a more effective warm poultice. That is, the present invention relates to a hot poultice which has an effect of improving safe blood circulation easily and inexpensively by using rice or a germinated product of rice.

【0006】本発明において、米および発芽させた米に
含有されている温湿布効果を有する成分は未だ解明する
に至っていないが、米および発芽させた米を下記のよう
に処理したものは温湿布効果を示すことが判明した。 発芽させた米の粉砕物をそのまま、あるいはこれを
含有してなるもの。 米または発芽させた米の抽出物をそのまま、あるい
はこれを含有してなるもの。 米または発芽させた米の加水物を酵素分解または麹
を作用させたものをそのまま、あるいはこれを含有して
なるもの。 米または発芽させた米を抽出するに当たり、その抽
出前、抽出と同時または抽出後に酵素分解または麹を作
用させたものをそのまま、あるいはこれを含有してなる
もの。 米または発芽させた米の抽出物あるいは酵素分解ま
たは麹を作用させたものに、アルコール発酵あるいは有
機酸発酵を行なったものをそのまま、あるいはこれを含
有してなるもの。
[0006] In the present invention, the components having a hot compress effect contained in rice and germinated rice have not yet been clarified, but rice and germinated rice treated as described below are warm compresses. It turned out to be effective. Sprouted crushed rice as it is or containing it. Rice or germinated rice extract as it is or containing it. Enzyme-decomposed or hydrolyzed rice hydrolyzed as it is, or containing it. When extracting rice or sprouted rice, the one that has been subjected to enzymatic decomposition or koji before or at the same time as or after the extraction is used as it is or containing it. An extract of rice or germinated rice or a product of enzymatic decomposition or koji which has been subjected to alcohol fermentation or organic acid fermentation as it is or containing it.

【0007】本発明で使用される米とは、ジャポニカ、
インディカ米を問わず、うるち米、および餅米等の玄米
および白米を指し、品種、種類は問わない。さらに、精
白時に出てくる92%以上の赤糠、あるいは92%以下
の白糠を使用してもよく、安価で経済的である。また、
発芽させた米が使用される。なお、有効成分は、熱およ
び光に対して安定であるため、上記の原料は、浸漬、蒸
煮、焙煎(砂焙り、網焙り、熱風焙煎等全てを指す)、
蒸煮焙煎、凍結乾燥等の表面変性、UV照射等の光変
性、パットライス等の加圧焙煎、揚げる等の原料処理を
してもよく、また、効果も変わらなかった。米および発
芽させた米は、そのまま用いても有効であるが、実用上
の面から粉砕して用いるのが好ましい。米および発芽さ
せた米を粉砕して粉体化するには、粉砕機または精米機
を用い、一般的な方法で行えばよい。
The rice used in the present invention is Japonica,
Regardless of indica rice, it refers to non-glutinous rice, brown rice such as sticky rice, and white rice, regardless of variety and type. Further, 92% or more of red rice bran or 92% or less of white rice bran, which appears during whitening, may be used, which is inexpensive and economical. Also,
Germinated rice is used. In addition, since the active ingredient is stable to heat and light, the above raw materials are dipping, steaming, roasting (all sand roasting, net roasting, hot air roasting, etc.),
The raw material treatment such as steam roasting, surface modification such as freeze-drying, photo-modification such as UV irradiation, pressure roasting such as Patrice, and frying may be performed, and the effect was not changed. Although rice and germinated rice are effective as they are, they are preferably crushed and used from the viewpoint of practical use. In order to pulverize the rice and the sprouted rice into powder, a pulverizer or a rice mill may be used and a general method may be used.

【0008】米を発芽させる場合、胚芽のついた米を水
に浸漬あるいは水を噴霧して発芽させる。発芽させる時
の温度は5〜70℃である。ただし、発芽さえすれば、
温度および時間は問わない。また、発芽中に水が腐敗す
る危険性がある場合は、腐敗しないように水を取り替え
るか、何らかの防腐を行うのが好ましい。ここで、発芽
とは、発芽する直前から発芽したものまで全てを指す。
この発芽させた米をよく洗浄して用いる。この時、乾燥
して用いてもよい。米または発芽させた米を抽出、ある
いは酵素分解または麹を作用させる場合、原料の米を粉
砕して顆粒あるいは粉体化すると、表面積が大きくなる
ため効率がよくなる。粉砕しなくてもよいが、この場合
には、米組織の分解および抽出に長時間を要する。
In the case of germinating rice, germinated rice is soaked in water or sprayed with water to germinate. The temperature for germination is 5 to 70 ° C. However, as long as it germinates,
Temperature and time do not matter. Further, when there is a risk of water spoiling during germination, it is preferable to replace the water so that it does not spoil, or to perform some kind of preservative. Here, germination refers to everything from just before germination to germinated ones.
The germinated rice is washed well before use. At this time, it may be dried before use. When extracting rice or sprouted rice, or subjecting it to enzymatic decomposition or koji, the raw material rice is pulverized into granules or powder to increase the surface area, resulting in higher efficiency. Although it is not necessary to grind, in this case, it takes a long time to decompose and extract the rice tissue.

【0009】米または発芽させた米を水抽出する場合、
抽出温度は、高温が効率的であるが、低温でも十分に抽
出を行うことができる。ただし、40℃以下の低温の場
合は、PHを酸性あるいはアルカリ性にするか、防腐剤
あるいはアルコールを加えて、米が腐敗しないように処
理することが望ましい。抽出時間は、有効成分さえ抽出
できれば、長くても短くてもよく、抽出温度により定め
ればよい。また、抽出は、加圧下または常圧下で行って
も、減圧下で行ってもよい。水抽出の場合、最も問題に
なるのは糊化現象である。糊状になれば、抽出効率が悪
くなるばかりでなく、実作業においては困難を極める。
これを防ぐためには、アミラーゼを加えて反応させる
か、塩酸などで酸性にして澱粉を切ってやればよく、こ
の方法を用いることにより、十分に解決でき、実用上も
全く問題はない。
When water or sprouted rice is extracted with water,
High extraction temperature is efficient, but extraction can be sufficiently performed even at low temperature. However, in the case of a low temperature of 40 ° C. or lower, it is desirable to make PH acidic or alkaline, or add a preservative or alcohol to treat the rice so that it does not spoil. The extraction time may be long or short as long as the active ingredient can be extracted, and may be determined depending on the extraction temperature. The extraction may be carried out under pressure, at normal pressure, or under reduced pressure. In the case of water extraction, the most problematic is the gelatinization phenomenon. If it becomes pasty, not only the extraction efficiency will deteriorate, but it will be extremely difficult in actual work.
In order to prevent this, the reaction may be carried out by adding amylase or acidification may be carried out with hydrochloric acid or the like to cut the starch. By using this method, it can be sufficiently solved and there is no problem in practice.

【0010】抽出物中の有効成分は、酸、アルカリに安
定であるためか、酸分解抽出あるいはアルカリ分解抽出
を行うのも有効である。この場合、必要により中和、脱
塩を行う。有機溶媒で抽出する場合も、米はなるべく微
粉砕または粉体化して抽出することが望ましい。有機溶
媒はアルコール、アセトン、n−ヘキサン、メタノール
等の一般的な有機溶媒でよいが、人体に対して有害なも
のは抽出後、溶媒を完全に除去する必要があるので安全
なものがよい。また、米あるいは発芽させた米を酵素分
解、または麹を作用させてもよい。ここで言う酵素分解
とは、澱粉分解酵素、蛋白分解酵素、脂肪分解酵素、繊
維分解酵素、リグニン分解酵素、ペクチン分解酵素等米
に働く酵素を1種または2種以上作用させることをい
う。また、麹として麹菌の種類および米の品種、種類は
問わない。
Since the active ingredient in the extract is stable to acid and alkali, it is also effective to carry out acid decomposition extraction or alkali decomposition extraction. In this case, neutralization and desalting are performed if necessary. Also when extracting with an organic solvent, it is desirable to pulverize or pulverize rice as much as possible before extracting. The organic solvent may be a general organic solvent such as alcohol, acetone, n-hexane and methanol, but those harmful to the human body are preferably safe because it is necessary to completely remove the solvent after extraction. In addition, rice or germinated rice may be enzymatically decomposed or koji may be allowed to act. The term "enzymatic degradation" as used herein refers to the action of one or more enzymes that act on rice, such as starch degrading enzymes, proteolytic enzymes, lipolytic enzymes, fiber degrading enzymes, lignin degrading enzymes, and pectin degrading enzymes. The type of koji mold and the variety and type of rice as koji do not matter.

【0011】さらに、前記の抽出を行うに当り、抽出の
前、抽出と同時、または抽出の後に、上記の酵素分解お
よび麹を作用させてもよい。本発明においては、さらに
上記の処理を行なうと同時または処理後、アルコール発
酵あるいは乳酸発酵、酢酸発酵等の有機酸発酵を行う
と、さらに有効である。アルコール発酵を行なえば、塗
布時にベタツキがないばかりか、濃縮がしやすく、有効
成分の濃縮が容易になる。なお、必要により酵母による
通気発酵、アルコール沈澱、合成吸着剤等で除糖を行な
ってもよい。また、92%以上の赤糠部分を調べてみた
ところ、効果はあるが、弱いことが判明した。
Further, in carrying out the above-mentioned extraction, the above-mentioned enzymatic decomposition and koji may be applied before the extraction, at the same time as the extraction, or after the extraction. In the present invention, it is more effective to carry out the organic acid fermentation such as alcohol fermentation, lactic acid fermentation, or acetic acid fermentation at the same time as or after the above treatment. If alcohol fermentation is carried out, not only there is no stickiness at the time of application, but also the concentration is easy and the active ingredient can be easily concentrated. If necessary, aeration fermentation with yeast, alcohol precipitation, sugar removal with a synthetic adsorbent and the like may be performed. Further, when the red bran portion of 92% or more was examined, it was found that it was effective but weak.

【0012】以上のようにして得られた本発明品は、残
渣を分離することなく、そのまま、あるいは圧搾、濾過
して用いる。そのまま用いるときは、殺菌あるいは除菌
して製品にする。なお、本発明品を配合する場合、実際
の用途に応じ、常法にしたがってクリーム、洗顔料、乳
液、化粧水、クレンジング、パック、石鹸などの化粧
料、軟膏剤、貼布剤、パスタ剤、ローション剤、チキン
剤、リエメント剤、ゼリー剤、エアゾール剤などの外用
医薬品のような剤型にする。他の配合成分は、通常用い
られるものいずれでもよく、さらに、他の薬効剤を併用
してもよい。
The product of the present invention obtained as described above is used as it is, or after being squeezed and filtered without separating the residue. When used as is, sterilize or sterilize the product. In addition, when blending the product of the present invention, depending on the actual application, creams, facial cleansers, emulsions, lotions, cleansing, packs, cosmetics such as soaps, ointments, patches, pasta agents, etc. Formulations such as lotions, chicken agents, liment agents, jellies, aerosols and other external medicines. The other compounding ingredients may be any of those usually used, and further, other medicinal agents may be used in combination.

【0013】次に、本発明品の温湿布剤としての効果を
調べた試験結果について以下に示す。まず、本発明品
0.5mlを各パネラー6人の手の甲に直接塗布したと
ころ、本発明品全てに、6人中4人以上の者がポカポカ
と温湿布効果があるとした。また、パネラー6人中2人
以上の者は、わずかに血管が拡張したようだとした。そ
こで、本発明品の温湿布効果を実験的に例証するため
に、本発明品塗布後の皮膚表面温度をサーモグラフィー
装置を用いて検討した。パネラーは各15名を用い、サ
ーモグラフィーから読み取った本試験と対照試験(水塗
布)との皮膚表面温度の経過の平均値を表1に記載し
た。
Next, the test results for examining the effect of the product of the present invention as a hot compress are shown below. First, when 0.5 ml of the product of the present invention was directly applied to the backs of the hands of 6 panelists, all of the products of the present invention showed that 4 or more people out of 6 had a warm and compress effect. Also, 2 or more of the 6 panelists said that the blood vessels seemed to have expanded slightly. Therefore, in order to experimentally demonstrate the hot compress effect of the product of the present invention, the skin surface temperature after application of the product of the present invention was examined using a thermography device. 15 panelists were used, and Table 1 shows the average values of the progress of the skin surface temperature of the main test and the control test (water application) read from the thermography.

【0014】サーモグラフィーの測定方法を以下に記載
する。室温20℃±1℃程度で空気の流れのない検査室
において、被験者の前腕部を30分程度露出した状態で
室温に順応させ、その後、人体表面から放射される赤外
線を検知し、その強度から温度情報を検出するサーモグ
ラフィー装置を用いて、被験者の右前腕上背部のサーモ
グラフを撮影した。次に、被験者の右前腕肘部までに本
発明品5mlを均一に塗布した。撮影の間隔は、本発明
品塗布後2分、5分、10分、15分、20分、25
分、30分、40分とし、皮膚表面温度の経時変化を観
察した。対照試験としては、本発明品の代わりに水を塗
布した後、同様にサーモグラフを撮影した。対照試験と
本試験の同時間の温度を表1に記載した。
The method of measuring thermography will be described below. In an examination room at room temperature of 20 ° C ± 1 ° C with no air flow, the subject's forearm is exposed to room temperature for about 30 minutes and then acclimated to room temperature, and then infrared rays radiated from the human body surface are detected. A thermograph of the subject's right forearm and upper back was photographed using a thermographic device that detects temperature information. Next, 5 ml of the product of the present invention was evenly applied to the right forearm elbow of the subject. The shooting interval is 2 minutes, 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes after application of the product of the present invention.
Minutes, 30 minutes, 40 minutes, and changes in skin surface temperature with time were observed. As a control test, water was applied instead of the product of the present invention, and then a thermograph was similarly taken. The temperatures during the control test and the main test are shown in Table 1.

【0015】[0015]

【表1】 [Table 1]

【0016】表1から明らかなように、前腕部を測定部
位として測定した結果で、全ての実施例で得られた本発
明品において、10分後からは水を塗布した場合との差
が出てきはじめ、20分後には明らかな差が認められ
た。また、パネラーの個別な経時データーにおいては、
2分後から即座に効果が出た人もおり、10分後に差が
出た人もいたが、40分後には、水塗布の場合に処理前
の表面温度と同じなのに対して、本発明品塗布の場合に
は、処理前より0.5〜2.2℃も高い表面温度を示し
た。この結果、本発明品は、表皮の温度を上昇させる優
れた温湿布効果を持っていることが判明した。
As is clear from Table 1, the results obtained by measuring the forearm as the measurement site showed that the products of the present invention obtained in all the examples showed a difference from the case where water was applied after 10 minutes. A clear difference was observed after 20 minutes from the beginning. Also, in the individual time series data of the panelists,
Some people showed the effect immediately after 2 minutes, and some people showed the difference after 10 minutes, but after 40 minutes, the surface temperature before treatment was the same as in the case of water application, while the product of the present invention was used. In the case of coating, the surface temperature was 0.5 to 2.2 ° C. higher than that before the treatment. As a result, it was found that the product of the present invention has an excellent warm compress effect of raising the temperature of the epidermis.

【0017】さらに、ネズミの耳に実施例30で得られ
た本発明品を塗布し、本発明品添加による血管拡張作用
を客観的に観察した。試験方法は、DDY系マウス10
匹の耳に、本発明品を1日3回2週間塗布した。1回の
塗布量は、片方の耳に綿棒に2回分の本発明品を塗布し
た。また、対照実験としては、本発明品の代わりに生理
食塩水を用いた。なお、判定は専門の医師により行っ
た。その結果、コントロールとして生理食塩水を用いた
ものでは、塗布前後において目視ではまったく差が認め
られなかったのに対して、本発明品を塗布したもので
は、早いものでは塗布5分後くらいから効果が認めら
れ、塗布60分後まで明らかにはっきりした効果がみら
れた。また、本発明品を2週間続けて塗布したもので
は、本発明品塗布による血管拡張作用が長く続いている
ことが判明した。他の実施例において得られた本発明品
においても同様の効果が認められた。これらの結果よ
り、本発明品は、きわめて優れた血管拡張作用等の血液
循環をよくする効果、さらには、血液循環をよくするこ
とによる温湿布作用を有することが判明した。
Further, the product of the present invention obtained in Example 30 was applied to the ear of a mouse, and the vasodilatory action by the addition of the product of the present invention was objectively observed. The test method is DDY mouse 10
The product of the present invention was applied to the ears of the animal three times a day for two weeks. The application amount of one time was such that the product of the present invention was applied twice to a swab on one ear. Further, as a control experiment, physiological saline was used instead of the product of the present invention. The judgment was made by a specialist doctor. As a result, in the case where physiological saline was used as a control, no difference was visually observed before and after application, whereas in the case where the product of the present invention was applied, the effect was obtained about 5 minutes after application in the case of early application. Was observed, and a clear effect was observed until 60 minutes after application. Further, it was found that when the product of the present invention was applied for 2 weeks continuously, the vasodilatory action by the application of the product of the present invention continued for a long time. Similar effects were observed in the products of the present invention obtained in other examples. From these results, it was revealed that the product of the present invention has an extremely excellent effect of improving blood circulation such as a vasodilatory effect, and further has a hot compress effect by improving blood circulation.

【0018】[0018]

【実施例】【Example】

(実施例1)胚芽のついたままの米1kgを25℃の水
につけ、3日間浸漬させ、米を発芽させた。この発芽米
をよく洗浄した後、50℃で24時間乾燥し、その後、
細かく微粉砕し、本発明品990gを得た。 (実施例2)玄米を粉砕機にかけ、玄米の粉砕物500
gを得た。この粉砕物に水1500mlを添加、塩酸で
PHを落とし10日間放置した。その後、絞り機で絞
り、得た清澄液を中和して、本発明品1200mlと残
渣760gを得た。 (実施例3)実施例1で得られた本発明品500gを用
いて、実施例3と同様の操作を行い、別の本発明品11
90mlを得た。
(Example 1) 1 kg of rice without germ was soaked in water at 25 ° C for 3 days to germinate rice. After thoroughly washing the germinated rice, it is dried at 50 ° C. for 24 hours, and then,
The product was finely pulverized to obtain 990 g of the product of the present invention. (Example 2) Brown rice was crushed to obtain a crushed brown rice product 500
g was obtained. 1500 ml of water was added to this pulverized product, PH was dropped with hydrochloric acid, and the mixture was left for 10 days. Then, it was squeezed with a squeezing machine to neutralize the resulting clear liquid to obtain 1200 ml of the product of the present invention and 760 g of a residue. (Example 3) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 3 was carried out to obtain another product of the present invention 11
90 ml was obtained.

【0019】(実施例4)玄米を粉砕機にかけ、玄米の
粉砕物500gを得た。この粉砕物に液化酵素10gと
水1500mlを添加した。その後、徐々に温度を上げ
ていき、5分間煮沸抽出した後、冷却した。その後、絞
り機で絞り、本発明品1420mlと残渣560gを得
た。 (実施例5)実施例1で得られた本発明品500gを用
いて、実施例4と同様の操作を行い、別の本発明品14
00mlを得た。 (実施例6)玄米を粉砕機にかけ、玄米の粉砕物500
gを得た。この粉砕物に2N−NaOH1500mlを
添加して5日間放置した。その後、絞り機で絞り、清澄
液1350mlと残渣650gを得た。この清澄液を1
0N−HClで中和して、本発明品1480mlを得
た。
Example 4 Brown rice was crushed to obtain 500 g of crushed brown rice. Liquefaction enzyme 10g and water 1500ml were added to this ground product. Then, the temperature was gradually raised, and the mixture was boiled and extracted for 5 minutes and then cooled. Then, it was squeezed with a squeezing machine to obtain 1420 ml of the product of the present invention and 560 g of a residue. (Example 5) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 4 was carried out to obtain another product of the present invention 14
00 ml was obtained. (Example 6) Brown rice is crushed by a crusher to obtain crushed brown rice 500
g was obtained. 1500 ml of 2N-NaOH was added to this pulverized product and the mixture was left for 5 days. Then, it was squeezed with a squeezing machine to obtain 1350 ml of the clear liquid and 650 g of the residue. 1 of this clarified liquid
Neutralization with 0N-HCl gave 1480 ml of the product of the present invention.

【0020】(実施例7)実施例1で得られた本発明品
500gを用いて、実施例6と同様の操作を行い、別の
本発明品1490mlを得た。 (実施例8)玄米を粉砕機にかけ、玄米の粉砕物500
gを得た。この粉砕物に95%エタノール1500ml
を添加して、5日間放置した。その後、絞り機で絞り、
清澄液1300mlと残渣650gを得た。この清澄液
に水2000mlを添加し、ロータリーエバポレーター
で濃縮し、本発明品1500mlを得た。 (実施例9)実施例1で得られた本発明品500gを用
いて、実施例8と同様の操作を行い、別の本発明品15
00mlを得た。
(Example 7) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 6 was carried out to obtain another 1490 ml of the product of the present invention. (Embodiment 8) Brown rice is crushed to obtain a crushed brown rice product 500
g was obtained. 1500 ml of 95% ethanol is added to this pulverized product.
Was added and left for 5 days. After that, squeeze with a wringer,
1300 ml of clear liquid and 650 g of residue were obtained. 2000 ml of water was added to this clarified solution, and the mixture was concentrated by a rotary evaporator to obtain 1500 ml of the product of the present invention. (Example 9) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 8 was carried out to obtain another invention product 15
00 ml was obtained.

【0021】(実施例10)玄米を粉砕機にかけ、玄米
の粉砕物500gを得た。この粉砕物に麹300g、水
1500mlを加え、55℃で20時間放置した。その
後、絞り機で絞り、本発明品1230mlと残渣100
0gを得た。 (実施例11)実施例1で得られた本発明品500gを
用いて、実施例10と同様の操作を行い、別の本発明品
1210mlを得た。 (実施例12)玄米を粉砕機にかけ、玄米の粉砕物50
0gを得た。この粉砕物に蛋白分解酵素2gと水150
0mlを加え、50℃で20時間放置した。その後、絞
り機で絞り、本発明品1310mlと残渣670gを得
た。
Example 10 Brown rice was crushed to obtain 500 g of crushed brown rice. 300 g of koji and 1500 ml of water were added to this pulverized product, and the mixture was left at 55 ° C. for 20 hours. Then, squeezing with a squeezing machine, 1230 ml of the present invention product and 100 residues
0 g was obtained. (Example 11) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 10 was carried out to obtain another 1210 ml of the present invention product. (Example 12) Brown rice is crushed to obtain a crushed brown rice product 50
0 g was obtained. 2 g of protease and 150 water
0 ml was added and the mixture was left at 50 ° C. for 20 hours. Then, the product was squeezed with a squeezing machine to obtain 1310 ml of the product of the present invention and 670 g of a residue.

【0022】(実施例13)実施例1で得られた本発明
品500gを用いて、実施例12と同様の操作を行い、
別の本発明品1380mlを得た。 (実施例14)玄米を粉砕機にかけ、玄米の粉砕物50
0gを得た。この粉砕物に脂肪分解酵素2gと水150
0mlを加え、50℃で20時間放置した。その後、絞
り機で絞り、本発明品1290mlと残渣680gを得
た。 (実施例15)実施例1で得られた本発明品500gを
用いて、実施例14と同様の操作を行い、別の本発明品
1360mlを得た。
(Example 13) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 12 was carried out,
Another 1380 ml of the product of the present invention was obtained. (Example 14) Brown rice is crushed to obtain 50 crushed brown rice.
0 g was obtained. 2 g of lipolytic enzyme and 150 water
0 ml was added and the mixture was left at 50 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1290 ml of the product of the present invention and 680 g of a residue. (Example 15) The same operation as in Example 14 was carried out using 500 g of the product of the present invention obtained in Example 1 to obtain 1360 ml of another product of the present invention.

【0023】(実施例16)玄米を粉砕機にかけ、玄米
の粉砕物500gを得た。この粉砕物に繊維分解酵素2
gと水1500mlを加え、50℃で20時間放置し
た。その後、絞り機で絞り、本発明品1330mlと残
渣650gを得た。 (実施例17)実施例1で得られた本発明品500gを
用いて、実施例16と同様の操作を行い、別の本発明品
1370mlを得た。 (実施例18)玄米を粉砕機にかけ、玄米の粉砕物50
0gを得た。この粉砕物に澱粉分解酵素2gと水150
0mlを加え、55℃で20時間放置した。その後、絞
り機で絞り、本発明品1380mlと残渣600gを得
た。
(Example 16) Brown rice was crushed by a crusher to obtain 500 g of crushed brown rice. Fiber-degrading enzyme 2 in this crushed product
g and 1500 ml of water were added, and the mixture was left at 50 ° C. for 20 hours. Then, the product was squeezed with a squeezing machine to obtain 1330 ml of the product of the present invention and 650 g of a residue. (Example 17) The same operation as in Example 16 was carried out using 500 g of the product of the present invention obtained in Example 1 to obtain 1370 ml of another product of the present invention. (Example 18) Brown rice was crushed to obtain a crushed brown rice product 50
0 g was obtained. 2g starch degrading enzyme and 150g water
0 ml was added and the mixture was left at 55 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1380 ml of the product of the present invention and 600 g of a residue.

【0024】(実施例19)実施例1で得られた本発明
品500gを用いて、実施例18と同様の操作を行い、
別の本発明品1400mlを得た。 (実施例20)玄米を粉砕機にかけ、玄米の粉砕物50
0gを得た。この粉砕物にペクチン分解酵素2gと水1
500mlを加え、50℃で20時間放置した。その
後、絞り機で絞り、本発明品1320mlと残渣660
gを得た。 (実施例21)実施例1で得られた本発明品500gを
用いて、実施例20と同様の操作を行い、別の本発明品
1300mlを得た。
(Example 19) The same operation as in Example 18 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1400 ml of the product of the present invention was obtained. (Example 20) Brown rice is crushed to obtain a crushed brown rice product 50
0 g was obtained. Add 2 g of pectin-degrading enzyme and 1 part of water to this ground product.
500 ml was added and left at 50 ° C. for 20 hours. After that, squeezing with a squeezing machine, 1320 ml of the present invention product and residue 660
g was obtained. (Example 21) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 20 was carried out to obtain another 1300 ml of the present invention product.

【0025】(実施例22)玄米を粉砕機にかけ、玄米
の粉砕物500gを得た。この粉砕物に蛋白分解酵素2
g、脂肪分解酵素2g、繊維分解酵素2g、澱粉分解酵
素2g、ペクチン分解酵素2gと水1500mlを加
え、50℃で20時間放置した。その後、絞り機で絞
り、本発明品1420mlと残渣560gを得た。 (実施例23)実施例1で得られた本発明品500gを
用いて、実施例22と同様の操作を行い、別の本発明品
1440mlを得た。 (実施例24)実施例22と同様の操作をして、米の酵
素分解物2000gを得た。その後、徐々に温度を上げ
ていき、5分間煮沸抽出した後、冷却した。その後、絞
り機で絞り、本発明品1400mlと残渣550gを得
た。
(Example 22) Brown rice was crushed to obtain 500 g of crushed brown rice. Proteolytic enzyme 2 in this crushed product
g, lipolytic enzyme 2 g, fiber degrading enzyme 2 g, starch degrading enzyme 2 g, pectin degrading enzyme 2 g and 1500 ml of water were added, and the mixture was allowed to stand at 50 ° C. for 20 hours. Then, it was squeezed with a squeezing machine to obtain 1420 ml of the product of the present invention and 560 g of a residue. (Example 23) Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 22 was carried out to obtain another 1440 ml of the product of the present invention. (Example 24) The same operation as in Example 22 was carried out to obtain 2000 g of an enzymatic decomposition product of rice. Then, the temperature was gradually raised, and the mixture was boiled and extracted for 5 minutes and then cooled. Then, it was squeezed with a squeezing machine to obtain 1400 ml of the product of the present invention and 550 g of a residue.

【0026】(実施例25)実施例1で得られた本発明
品500gを用いて、実施例24と同様の操作を行い、
別の本発明品1420mlを得た。 (実施例26)玄米を粉砕機にかけ、玄米の粉砕物50
0gを得た。この粉砕物に麹300gと40%エタノー
ル1500mlを加え、55℃で48時間放置した。そ
の後、絞り機で絞り、清澄液1300mlと残渣850
gを得た。その後、清澄液に1000mlの水を加水
し、ロータリーエバポレーターで濃縮し、本発明品13
00mlを得た。 (実施例27)実施例1で得られた本発明品500gを
用いて、実施例26と同様の操作を行い、別の本発明品
1300mlを得た。
Example 25 Using 500 g of the product of the present invention obtained in Example 1, the same operation as in Example 24 was carried out,
1420 ml of another product of the present invention was obtained. (Example 26) Brown rice was crushed to obtain a crushed brown rice product 50
0 g was obtained. To this crushed product, 300 g of koji and 1500 ml of 40% ethanol were added, and the mixture was left at 55 ° C. for 48 hours. After that, squeeze with a squeezing machine and clarified liquid 1300 ml and residue 850
g was obtained. Then, 1000 ml of water was added to the clarified liquid, and the mixture was concentrated by a rotary evaporator to obtain the product 13 of the present invention.
00 ml was obtained. (Example 27) The same operation as in Example 26 was carried out using 500 g of the present invention product obtained in Example 1 to obtain another 1300 ml of the present invention product.

【0027】(実施例28)実施例4と同様にして、米
の抽出物2000gを得た。この抽出物に蛋白分解酵素
2g、脂肪分解酵素2g、繊維分解酵素2g、澱粉分解
酵素2g、ペクチン分解酵素2gを添加し、50℃で2
4時間放置した。その後、絞り機で絞り、本発明品14
00mlと残渣580gを得た。 (実施例29)実施例1で得られた本発明品500gを
用いて、実施例28と同様の操作を行い、別の本発明品
1390mlを得た。 (実施例30)実施例24と同様にして、米の酵素分解
抽出物2000gを得た。この酵素分解抽出物に酵母を
添加し、16日間アルコール発酵した。その後、絞り機
で絞り、本発明品1880mlと残渣80gを得た。
(Example 28) In the same manner as in Example 4, 2000 g of a rice extract was obtained. To this extract, 2 g of proteolytic enzyme, 2 g of lipolytic enzyme, 2 g of fiber degrading enzyme, 2 g of starch degrading enzyme, 2 g of pectin degrading enzyme were added, and the mixture was heated at 50 ° C for 2
It was left for 4 hours. After that, the product of the present invention 14
00 ml and 580 g of residue were obtained. (Example 29) The same operation as in Example 28 was carried out using 500 g of the present invention product obtained in Example 1 to obtain another 1390 ml of the present invention product. (Example 30) In the same manner as in Example 24, 2000 g of an enzyme-decomposed extract of rice was obtained. Yeast was added to this enzyme-decomposed extract, and alcoholic fermentation was carried out for 16 days. Then, it was squeezed with a squeezing machine to obtain 1880 ml of the product of the present invention and 80 g of a residue.

【0028】(実施例31)実施例1で得られた本発明
品500gを用いて、実施例30と同様の操作を行い、
別の本発明品1800mlを得た。 (実施例32)実施例24と同様にして、米の酵素分解
抽出物2000gを得た。この酵素分解抽出物を煮沸殺
菌した後、37℃まで冷却し、前もって乳酸菌を培養し
たスターター200mlを添加後、よく攪拌密封し、3
7℃で2日間乳酸発酵を行った。その後、絞り機で絞
り、本発明品1380mlと残渣500gを得た。 (実施例33)実施例1で得られた本発明品500gを
用いて、実施例32と同様の操作を行い、別の本発明品
1400mlを得た。
(Example 31) The same operation as in Example 30 was carried out using 500 g of the product of the present invention obtained in Example 1,
Another 1800 ml of the product of the present invention was obtained. (Example 32) In the same manner as in Example 24, 2000 g of an enzyme-decomposed extract of rice was obtained. The enzyme-decomposed extract was sterilized by boiling, cooled to 37 ° C., 200 ml of a starter in which lactic acid bacteria had been cultured in advance was added, and the mixture was well stirred and sealed, and
Lactic acid fermentation was performed at 7 ° C for 2 days. Then, it was squeezed with a squeezing machine to obtain 1380 ml of the product of the present invention and 500 g of a residue. (Example 33) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 32 was carried out to obtain another 1400 ml of the present invention product.

【0029】(実施例34)実施例24で得られた本発
明品1000mlに95%エタノール80mlを添加
し、20日間酢酸発酵を行った。その後、濾過をし、本
発明品990mlを得た。 (実施例35)実施例1で得られた本発明品500gを
用いて、実施例34と同様の操作を行い、別の本発明品
1000mlを得た。以上の実施例で得た本発明品は、
用途に応じて適宜に使用されるが、本発明品を配合して
化粧水および乳液とする場合の実施例について、次に記
載する。なお、配合例は以下の実施例に限定されるもの
ではない。
(Example 34) To 1000 ml of the product of the present invention obtained in Example 24, 80 ml of 95% ethanol was added, and acetic acid fermentation was carried out for 20 days. Then, filtration was performed to obtain 990 ml of the product of the present invention. (Example 35) Using 500 g of the present invention product obtained in Example 1, the same operation as in Example 34 was carried out to obtain another 1000 ml of the present invention product. The products of the present invention obtained in the above examples,
Examples of the case where the product of the present invention is blended into a lotion and a milky lotion, which may be appropriately used depending on the application, will be described below. The formulation examples are not limited to the examples below.

【0030】(実施例36)化粧水 実施例22で得られた本発明品 10.0重量% ソルビトール 3.0重量% グリセリン 5.0重量% 精製水 76.4重量% アラントイン 0.1重量% ポリオキシエチレンヒマシ油誘導体 0.5重量% エタノール 5 重量% 以上の配合材料を常法により混合溶解し、化粧水を得
た。
(Example 36) Toner lotion Product of the present invention obtained in Example 22 10.0% by weight Sorbitol 3.0% by weight Glycerin 5.0% by weight Purified water 76.4% by weight Allantoin 0.1% by weight Polyoxyethylene castor oil derivative 0.5% by weight Ethanol 5% by weight The above ingredients were mixed and dissolved by a conventional method to obtain a lotion.

【0031】(実施例37)乳液 実施例30で得られた本発明品 20.0重量% ステアリン酸 1.3重量% セタノール 0.7重量% ミツロウ 2.0重量% ポリオキシエチレン(11) モノオレイン酸エステル 1.2重量% グリセリンモノステアリン酸エステル 0.8重量% クインスシード抽出液(5%水溶液) 15.0重量% ジプロピレングリコール 5.0重量% エタノール 3.0重量% メチルパラベン 0.3重量% 香料 0.3重量% 精製水 50.4重量% 精製水にジプロピレングリコールを加え、加熱攪拌し、
温度を70℃に保持し、これに本発明品、クインスシー
ド抽出液、香料、エタノール以外の原料を加えて攪拌
し、次に、ホモジナイザーで均一に乳化させる。得られ
た乳化液を冷却しながら攪拌下に、残りのものを徐々に
加え、室温に冷却して乳液を得た。
(Example 37) Emulsion The product of the present invention obtained in Example 2 20.0% by weight Stearic acid 1.3% by weight Cetanol 0.7% by weight Beeswax 2.0% by weight Polyoxyethylene (11) Mono Oleic acid ester 1.2% by weight Glycerin monostearate ester 0.8% by weight Quinceseed extract (5% aqueous solution) 15.0% by weight dipropylene glycol 5.0% by weight Ethanol 3.0% by weight Methylparaben 0.3 % By weight Perfume 0.3% by weight Purified water 50.4% by weight Dipropylene glycol is added to the purified water and heated and stirred,
The temperature is kept at 70 ° C., the product of the present invention, quince seed extract, fragrance and raw materials other than ethanol are added and stirred, and then uniformly emulsified by a homogenizer. While cooling the obtained emulsion, the rest of the emulsion was gradually added to the emulsion and cooled to room temperature to obtain an emulsion.

【0032】[0032]

【発明の効果】前記の結果からも明らかなように、米を
水抽出あるいは有機溶媒抽出することにより、簡単に、
しかも、全く安全に温度上昇効果、血管拡張効果等の血
液循環をよくする効果を併せ持つ非常に優れた温湿布剤
が得られたのである。米は今まで主食であったため、新
規な製法、利用用途はほとんど開発されていなかった。
さらに、米は今まで主食とされてきたものであり、安全
性も実証されているものである。すなわち、本発明は、
温湿布剤として非常に優れた効果を持っているばかりで
なく、安全性も十分に実証されているものを見出したも
のである。また、米の過剰生産といわれている現在、新
たな米の利用用途を見出したこと、および米のイメージ
アップによる消費拡大を図り得ることは、極めて有意義
なことである。
As is apparent from the above results, it is easy to extract rice by water extraction or organic solvent extraction,
Moreover, a very excellent warm poultice having a totally safe effect of improving blood circulation such as a temperature increasing effect and a vasodilatory effect was obtained. Since rice has been the staple food until now, new production methods and uses have hardly been developed.
Furthermore, rice has been the staple food until now, and its safety has been proven. That is, the present invention is
The present inventors have found that not only it has a very excellent effect as a warm poultice, but also its safety is sufficiently demonstrated. In addition, it is extremely significant that the current use of rice is said to be over-produced and that new uses of rice are found and that consumption of rice can be increased by improving the image of rice.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 発芽させた米の粉砕物をそのまま、ある
いはこれを含有してなる温湿布剤。
1. A hot poultice which is a crushed product of germinated rice as it is or contains it.
【請求項2】 米または発芽させた米の抽出物をそのま
ま、あるいはこれを含有してなる温湿布剤。
2. A hot poultice containing the extract of rice or germinated rice as it is or containing it.
【請求項3】 米または発芽させた米の加水物を酵素分
解または麹を作用させたものをそのまま、あるいはこれ
を含有してなる温湿布剤。
3. A hot poultice, which is obtained by enzymatically decomposing or hydrolyzing rice or a hydrolyzed product of germinated rice, or containing the same.
【請求項4】 米または発芽させた米を抽出するに当
り、その抽出前、抽出と同時または抽出後に酵素分解ま
たは麹を作用させたものをそのまま、あるいはこれを含
有してなる温湿布剤。
4. A hot poultice, which is obtained by extracting rice or sprouted rice with enzymatic decomposition or koji before or after the extraction, simultaneously with or after the extraction, or containing the same.
【請求項5】 米または発芽させた米の抽出物あるいは
酵素分解または麹を作用させたものに、アルコール発酵
あるいは有機酸発酵を行なったものをそのまま、あるい
はこれを含有してなる温湿布剤。
5. A hot poultice which comprises the extract of rice or germinated rice or the product of enzymatic decomposition or koji which has been subjected to alcohol fermentation or organic acid fermentation as it is or containing the product.
JP34711393A 1993-12-27 1993-12-27 Hot compress Expired - Lifetime JP3678435B2 (en)

Priority Applications (1)

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JP34711393A JP3678435B2 (en) 1993-12-27 1993-12-27 Hot compress

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2005036240A Division JP2005162765A (en) 2005-02-14 2005-02-14 Hot compress

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JPH07188042A true JPH07188042A (en) 1995-07-25
JP3678435B2 JP3678435B2 (en) 2005-08-03

Family

ID=18388002

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014196280A (en) * 2013-03-29 2014-10-16 三笠製薬株式会社 Percutaneous absorption type tape for reducing uraroma

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60188305A (en) * 1984-03-07 1985-09-25 Nisshin Oil Mills Ltd:The Cosmetic
JPS617208A (en) * 1984-06-22 1986-01-13 Indoneshia Bunka Shinkoukai:Kk Pack and peel preparation containing plant powder
JPS6168404A (en) * 1984-09-13 1986-04-08 Tokuyama Toshie Production of cosmetic from rice
JPH04139132A (en) * 1990-09-28 1992-05-13 Asahi Breweries Ltd Anti-active oxygen action composition, anti-active oxygen agent, food, cosmetic and medicine containing the same as active ingredient
JPH04352716A (en) * 1991-05-30 1992-12-07 Soken:Kk Bath additive
JPH05139983A (en) * 1991-11-25 1993-06-08 Soken:Kk Skin treatment
JPH05221844A (en) * 1992-02-17 1993-08-31 Kyoei Kagaku Kogyo Kk Aging-preventive cosmetic
JPH05310584A (en) * 1992-05-12 1993-11-22 Soken Kk Hot compress

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60188305A (en) * 1984-03-07 1985-09-25 Nisshin Oil Mills Ltd:The Cosmetic
JPS617208A (en) * 1984-06-22 1986-01-13 Indoneshia Bunka Shinkoukai:Kk Pack and peel preparation containing plant powder
JPS6168404A (en) * 1984-09-13 1986-04-08 Tokuyama Toshie Production of cosmetic from rice
JPH04139132A (en) * 1990-09-28 1992-05-13 Asahi Breweries Ltd Anti-active oxygen action composition, anti-active oxygen agent, food, cosmetic and medicine containing the same as active ingredient
JPH04352716A (en) * 1991-05-30 1992-12-07 Soken:Kk Bath additive
JPH05139983A (en) * 1991-11-25 1993-06-08 Soken:Kk Skin treatment
JPH05221844A (en) * 1992-02-17 1993-08-31 Kyoei Kagaku Kogyo Kk Aging-preventive cosmetic
JPH05310584A (en) * 1992-05-12 1993-11-22 Soken Kk Hot compress

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014196280A (en) * 2013-03-29 2014-10-16 三笠製薬株式会社 Percutaneous absorption type tape for reducing uraroma

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