JPH0753351A - Compound for bathing agent and cosmetic - Google Patents

Compound for bathing agent and cosmetic

Info

Publication number
JPH0753351A
JPH0753351A JP5229418A JP22941893A JPH0753351A JP H0753351 A JPH0753351 A JP H0753351A JP 5229418 A JP5229418 A JP 5229418A JP 22941893 A JP22941893 A JP 22941893A JP H0753351 A JPH0753351 A JP H0753351A
Authority
JP
Japan
Prior art keywords
divalent
iron
rice extract
fermented rice
added
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
JP5229418A
Other languages
Japanese (ja)
Other versions
JP2846799B2 (en
Inventor
Akihiro Saito
明宏 斉藤
Kenji Shirata
健志 白田
Koichiro Muramatsu
浩一郎 村松
Shinji Makino
伸治 牧野
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.)
I B II KK
Aioi Hakko KK
Sekisui Chemical Co Ltd
Original Assignee
I B II KK
Aioi Hakko KK
Sekisui Chemical 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 I B II KK, Aioi Hakko KK, Sekisui Chemical Co Ltd filed Critical I B II KK
Priority to JP5229418A priority Critical patent/JP2846799B2/en
Publication of JPH0753351A publication Critical patent/JPH0753351A/en
Application granted granted Critical
Publication of JP2846799B2 publication Critical patent/JP2846799B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To promote the effect of fermented rice extract to be used as a component of a bathing agent and a cosmetic. CONSTITUTION:A ferro-soferric salt is added to a fermented rice extract to improve the moisture-retaining effect of a bathing agent and cosmetic on the skin and promote the effect of the fermented rice extract.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は入浴剤および化粧品用の
配合物に関するものである。
FIELD OF THE INVENTION The present invention relates to formulations for bath salts and cosmetics.

【0002】[0002]

【従来の技術】従来から米発酵エキスは美容や健康に良
いと云われている。特に最近では米発酵エキスはアトピ
ー性皮膚炎に効果があることが大学病院や国立小児病院
等の研究で明らかになっている。このような米発酵エキ
スの特性を利用して最近入浴剤および化粧品への利用が
検討されている。
Conventionally, fermented rice extract is said to be good for beauty and health. In particular, recently, it has been revealed that studies on rice fermented extract are effective for atopic dermatitis, such as at university hospitals and national children's hospitals. Utilizing such characteristics of the fermented rice extract, it has recently been investigated for use in bath salts and cosmetics.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、米発酵
エキスは入浴剤や化粧品に使用した場合、肌の保温効果
は認められるが、保湿効果の点で十分と言えなかった。
However, when fermented rice extract is used in bath salts and cosmetics, the effect of keeping the skin warm is recognized, but it cannot be said to be sufficient in terms of the moisturizing effect.

【0004】[0004]

【課題を解決するための手段】本発明は上記従来の課題
を解決するための手段として、米発酵エキスと二価三価
鉄塩との混合物を主体とした入浴剤および化粧品用の配
合物を提供するものである。
[Means for Solving the Problems] As a means for solving the above-mentioned conventional problems, the present invention provides a bath agent and a cosmetic composition mainly comprising a mixture of fermented rice extract and divalent and trivalent iron salts. It is provided.

【0005】〔米発酵エキス〕米発酵エキスとは通常米
糠を蒸すか炊くかしてこれに酵素、酵母等を添加し、発
酵して得られた発酵生成物を圧搾濾過し加熱することに
よって得られるものである。上記米発酵エキスにはアル
コール、各種アミノ酸等が含まれる。
[Fermented rice extract] A fermented rice extract is usually obtained by steaming or cooking rice bran, adding enzymes, yeast, etc. to the rice bran, and fermenting the fermented product obtained by fermentation and heating. It is what is done. The above-mentioned fermented rice extract contains alcohol, various amino acids and the like.

【0006】〔二価三価鉄塩〕本発明の二価三価鉄塩は
二価鉄と三価鉄との中間の性質を示す鉄の塩酸塩、硫酸
塩、燐酸塩、硝酸塩等の無機塩、蟻酸塩、酢酸塩、プロ
ピオン酸塩等の有機塩であり、三価鉄の塩類を多量の水
酸化ナトリウム、水酸化カリウム、水酸化リチウム、水
酸化カルシウム等の強アルカリの水溶液に投入して二価
鉄への原子価変換を起させた場合あるいは二価鉄の塩類
を多量の塩酸、硫酸等の強酸の水溶液に投入して三価鉄
への原子価変換を起こさせた場合の遷移形態として得ら
れるものである。以下に二価三価鉄塩の製造方法の具体
例を示す。
[Divalent and trivalent iron salt] The divalent and trivalent iron salt of the present invention is an inorganic substance such as an iron hydrochloride, a sulfate, a phosphate, a nitrate, etc. showing an intermediate property between divalent iron and trivalent iron. Organic salts such as salts, formates, acetates, propionates, etc., in which a large amount of iron (III) salts are added to an aqueous solution of a strong alkali such as sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide. Transition when valence conversion to ferric iron is caused, or when ferric iron salts are added to a large amount of an aqueous solution of a strong acid such as hydrochloric acid or sulfuric acid to cause valence conversion to ferric iron It is obtained as a form. Specific examples of the method for producing a divalent and trivalent iron salt are shown below.

【0007】1.三価鉄塩より 1.0mgの塩化第二鉄(Fe Cl3・6H2 O)を100
mlの0.5N水酸化ナトリウム水溶液中に投入し攪拌溶
解した後一夜静置する。生じた不溶性物質を濾別し濾液
を塩酸で中和した後減圧濃縮してデシケーター中で乾燥
結晶化する。かくして塩化ナトリウムに担持された二価
三価鉄の塩化物(以下塩化鉄(II,III)と云う)が得
られるが、該担持物から塩化鉄(II,III )を分離する
には更に50mlのイソプロピルアルコール80%の水溶
液を加えて溶出成分を集め、減圧濃縮し溶媒を除去、乾
燥させる。上記抽出−濃縮−乾燥操作を数回繰返すこと
によって0.25mgの塩化鉄(II,III )が得られる。
[0007] 1. Trivalent iron salt than 1.0mg of ferric chloride (Fe Cl 3 · 6H 2 O ) 100
Pour into 0.5 ml of 0.5N aqueous sodium hydroxide solution, stir to dissolve, and leave to stand overnight. The resulting insoluble material is filtered off, the filtrate is neutralized with hydrochloric acid and then concentrated under reduced pressure to dry and crystallize in a desiccator. Thus, a chloride of divalent and trivalent iron supported on sodium chloride (hereinafter referred to as iron chloride (II, III)) is obtained, and 50 ml of iron chloride (II, III) is separated from the supported product. 80% aqueous solution of isopropyl alcohol is added to collect the eluted components, which are concentrated under reduced pressure to remove the solvent and dried. By repeating the above-mentioned extraction-concentration-drying operation several times, 0.25 mg of iron (II, III) chloride is obtained.

【0008】2.二価鉄塩より 1.0mgの硫酸第一鉄(Fe SO4 ・7H2 O)を10
0mlの0.5N塩酸水溶液中に投入し攪拌溶解した後一
夜静置する。生じた不溶性物質を濾別し濾液を減圧濃縮
しデシケーター中で乾燥する。得られた乾燥粉末に10
mlのイソプロピルアルコール80%の水溶液を加えて溶
出成分を集め、減圧濃縮し溶媒を除去、乾燥させる。上
記抽出−濃縮−乾燥操作を数回繰返すことによって0.
6mgの塩化鉄(II,III )が得られる。
[0008] 2. Bivalent iron salt than the 1.0mg ferrous sulfate (Fe SO 4 · 7H 2 O ) 10
It is poured into 0 ml of a 0.5 N hydrochloric acid aqueous solution, dissolved by stirring, and left to stand overnight. The resulting insoluble material is filtered off, the filtrate is concentrated under reduced pressure and dried in a desiccator. 10 to the obtained dry powder
80 ml of 80% isopropyl alcohol aqueous solution is added to collect the eluted components, which are concentrated under reduced pressure to remove the solvent and dried. By repeating the above extraction-concentration-drying operation several times,
6 mg of iron chloride (II, III) are obtained.

【0009】本発明の二価三価鉄塩は塩化ナトリウム、
硫酸ナトリウム、塩化アンモニウム、硫酸アンモニウ
ム、塩化亜鉛、硫酸亜鉛、酸化亜鉛、水酸化亜鉛、酢酸
亜鉛、珪藻土、ベントナイト、シリカ、アルミナ等の無
機化合物、ビタミン、ホルモン、蛋白質、脂質等の有機
化合物に担持されてもよく、その場合においても二価三
価鉄塩の作用は変化することがない。
The divalent and trivalent iron salts of the present invention are sodium chloride,
Supported on inorganic compounds such as sodium sulfate, ammonium chloride, ammonium sulfate, zinc chloride, zinc sulfate, zinc oxide, zinc hydroxide, zinc acetate, diatomaceous earth, bentonite, silica, alumina, and organic compounds such as vitamins, hormones, proteins, and lipids. However, even in that case, the action of the divalent and trivalent iron salt does not change.

【0010】〔配合〕上記米発酵エキス中に二価三価鉄
塩を添加配合するのであるが、上記米発酵エキス中に二
価三価鉄は通常10-2〜10-18g/mlの濃度で添加せら
れる。上記配合物には所望なれば更にビタミン、ミネラ
ル、香料、色素、清涼剤等の第三成分が適宜添加されて
もよい。
[Blending] Divalent and trivalent iron salts are added and blended in the above-mentioned fermented rice extract, and divalent and trivalent iron is usually contained in the above-mentioned fermented rice extract in an amount of 10 -2 to 10 -18 g / ml. It is added at a concentration. If desired, a third component such as vitamins, minerals, fragrances, pigments, and cooling agents may be appropriately added to the above composition.

【0011】[0011]

【作用】二価三価鉄塩は水に溶解させると水分子相互の
水素結合を切断し、クラスターを小さくすることによっ
て水を活性化させる作用がある。このように二価三価鉄
塩によって活性化させた水は本発明の入浴剤や化粧品に
おいて、皮膚に円滑に吸収されて皮膚に適度な湿気を与
え、しかも米発酵エキス中の有効成分の皮膚への吸収を
促進させる。また二価三価鉄自身が生理活性作用を有す
るので皮膚に対してあるいは健康に対して顕著な効果を
有する。
When the divalent and trivalent iron salt is dissolved in water, it has a function of activating water by breaking hydrogen bonds between water molecules and reducing clusters. The water thus activated by the divalent and trivalent iron salt is smoothly absorbed by the skin in the bath preparation and cosmetics of the present invention to give proper moisture to the skin, and the skin of the active ingredient in the fermented rice extract is also skin. Promotes absorption into. Further, since divalent and trivalent iron itself has a physiologically active action, it has a remarkable effect on the skin or health.

【0012】[0012]

【実施例】【Example】

〔米発酵エキスの製造〕100kgの米糠に水160リッ
トルを加え糖化酵素により60℃、12時間の条件で糖
化させた後、酵母を繁殖させ、酵母によるアルコール発
酵を23日間させる。発酵完了後、塩化ナトリウムを加
え圧搾、濾過、加熱殺菌後、200リットルの米発酵エ
キスを得る。
[Production of fermented rice extract] To 100 kg of rice bran, 160 liters of water is added and saccharified with a saccharifying enzyme at 60 ° C for 12 hours, and then yeast is propagated and alcohol fermentation by the yeast is carried out for 23 days. After completion of fermentation, sodium chloride is added, and the mixture is squeezed, filtered, and sterilized by heating to obtain 200 liters of fermented rice extract.

【0013】〔二価三価鉄塩の製造〕1g の硫酸第一鉄
(Fe SO4 ・6H2 O)を12N塩酸水溶液5ml中に
入れ、攪拌後、不溶性成分を濾紙(No.5C)で濾過
する。該溶液部分の一部をサンプリングして減圧濃縮し
てデシケーター中で乾燥する。得られた乾燥粉末に10
mlのイソプロピルアルコール80%の水溶液を加えて溶
出成分を集め、減圧濃縮し溶媒を除去、乾燥させる。上
記抽出−濃縮−乾燥操作を数回繰返すことによって結晶
が得られる。該結晶の5%水溶液を作成し、その0.0
1mlをペーパークロマトグラフ用濾紙No.51A(2
cm×40cm)下端から3cm内側の個所にスポットし、n
−ブタノール:酢酸:水=5:1:4容量比混合物を展
開溶媒として20℃、15時間の上方展開を行なう。展
開後該濾紙を乾燥させてから1%フエリシアン化カリウ
ム水溶液を発色試薬として濾紙に噴霧発色させると該結
晶の展開位置は1スポットでRf=0.07であること
が確認された。次いで同様のペーパークロマトグラフテ
ストをFe Cl2およびFe Cl3の1:1当量混合物につ
いて行なった折り、展開の結果は2スポットとなりRf
=0.095(Fe Cl2)と、Rf=0.36(Fe C
l3)であることが確認された。上記ペーパークロマトグ
ラフテストにより該結晶は混合物ではなく単一化合物で
あることが確認された。次いで該結晶の0.1g を蒸留
水に溶かして100mlとし可検液を作成する。その2.
5mlを50mlのメスフラスコにとり、0.1%オルソフ
ェナントロリン水溶液2.5ml、および酢酸ナトリウム
−酢酸緩衝液(pH 4.5)2.5mlを加え、蒸留水で
標線まで充たす。30分間室温に静置した後510nmで
吸光度を測定する。Fe Cl2水溶液について同様の方法
で得た標準曲線から可検液の二価鉄を求めると0.01
9g /100mlであった。次いで上記操作においてメス
フラスコに可検液を添加した際、予め10%ヒドロキシ
ルアミン塩酸塩水溶液1.0mlを添加して三価鉄を二価
鉄に還元する。この場合に得られた二価鉄量は0.03
8g /100mlであった。したがって三価鉄量は0.0
38g /100ml−0.019g /100ml=0.01
9g /100mlとなり、該結晶中には二価鉄と三価鉄と
が当量含まれていることが判明した。以上のテストによ
り該結晶はFe2Cl5・x H2 Oであることが推定され
る。
[Production of divalent and trivalent iron salt] 1 g of ferrous sulfate (Fe SO 4 .6H 2 O) was put in 5 ml of 12N hydrochloric acid aqueous solution, and after stirring, insoluble components were filtered off with a filter paper (No. 5C). Filter. A part of the solution portion is sampled, concentrated under reduced pressure, and dried in a desiccator. 10 to the obtained dry powder
80 ml of 80% isopropyl alcohol aqueous solution is added to collect the eluted components, which are concentrated under reduced pressure to remove the solvent and dried. Crystals are obtained by repeating the above-mentioned extraction-concentration-drying operation several times. A 5% aqueous solution of the crystal was prepared, and its 0.0
1 ml of filter paper for paper chromatograph No. 51A (2
cm × 40 cm) Spot 3 cm inside from the bottom edge, n
-Butanol: acetic acid: water = 5: 1: 4 volume ratio The mixture is mixed with a developing solvent at 20 ° C. for 15 hours for upward development. After the development, the filter paper was dried and then spray-developed with a 1% potassium ferricyanide aqueous solution as a coloring reagent on the filter paper, and it was confirmed that the developed position of the crystal was Rf = 0.07 at one spot. Then, a similar paper chromatographic test was performed on a 1: 1 equivalent mixture of Fe Cl 2 and Fe Cl 3 , and the result of folding and development was 2 spots Rf
= 0.095 (Fe Cl 2 ) and Rf = 0.36 (Fe C
l 3 ) was confirmed. The above paper chromatographic test confirmed that the crystal was not a mixture but a single compound. Then, 0.1 g of the crystal is dissolved in distilled water to make 100 ml to prepare a test solution. Part 2.
5 ml is placed in a 50 ml volumetric flask, 2.5 ml of 0.1% orthophenanthroline aqueous solution and 2.5 ml of sodium acetate-acetate buffer (pH 4.5) are added, and the whole is filled with distilled water up to the marked line. After standing at room temperature for 30 minutes, the absorbance is measured at 510 nm. The divalent iron in the test solution was 0.01 from the standard curve obtained by the same method for the FeCl 2 aqueous solution.
It was 9 g / 100 ml. Next, when the test solution was added to the volumetric flask in the above operation, 1.0 ml of 10% hydroxylamine hydrochloride aqueous solution was added in advance to reduce ferric iron to ferrous iron. The amount of divalent iron obtained in this case is 0.03
It was 8 g / 100 ml. Therefore, the amount of trivalent iron is 0.0
38 g / 100 ml-0.019 g / 100 ml = 0.01
It was 9 g / 100 ml, and it was found that the crystals contained equivalent amounts of divalent iron and trivalent iron. From the above test, it is estimated that the crystal is Fe 2 Cl 5 .x H 2 O.

【0014】〔実施例1〕 〔入浴剤〕表1に示す処方(単位g)により定法に従っ
て液体入浴剤を製造した。
Example 1 [Bathing Agent] A liquid bathing agent was prepared according to a conventional method according to the formulation (unit: g) shown in Table 1.

【表1】 上記液体入浴剤を家庭に通常の浴槽を持つ健常者50人
に100リットルの温水(さら湯)を充たしかつ各試料
を60gづつ添加した浴槽に、一日一回7日間連続して
入浴してもらい、美肌効果を評価した。その結果表2に
入浴後の肌のすべすべ感を、表3に入浴後の肌のしっと
り感を示した。
[Table 1] Fifty healthy people with a normal bathtub at home were filled with 100 liters of hot water (sarayu) and 60 g of each sample was added to the bath bath once a day for 7 consecutive days. , And evaluated the skin beautifying effect. As a result, Table 2 shows the smoothness of the skin after bathing, and Table 3 shows the moisturization of the skin after bathing.

【表2】 [Table 2]

【表3】 表2および表3の結果から実施例1では美肌効果・保湿
効果ともにかなり改善することが出来る。
[Table 3] From the results shown in Tables 2 and 3, in Example 1, both the skin beautifying effect and the moisturizing effect can be considerably improved.

【0015】実施例1の入浴剤を通常の家庭でアトピー
性皮膚炎の患者10人に連続して一日一回1ヶ月間使用
してもらい、評価した結果を表4に示した。
The bathing agent of Example 1 was used by 10 patients with atopic dermatitis in ordinary households once a day continuously for 1 month, and the evaluation results are shown in Table 4.

【表4】 表4の結果からアトピー性皮膚炎の患者の90%に改善
効果がみられた。
[Table 4] From the results of Table 4, 90% of the patients with atopic dermatitis showed an improving effect.

【0016】〔実施例2〕 〔ボデーシャンプー〕表5の処方(単位g)により、定
法に従ってボデーシャンプーを製造した。
[Example 2] [Body shampoo] A body shampoo was prepared according to a conventional method according to the formulation (unit: g) shown in Table 5.

【表5】 上記ボデーシャンプーを健常者50人に各試料を一日一
回7日間連続して使用してもらい、美肌効果を評価し
た。その結果表6に使用後の肌のすべすべ感を、表7に
使用後の肌のしっとり感を示した。
[Table 5] Fifty healthy people were allowed to use the above-mentioned body shampoo once a day for 7 consecutive days to evaluate the skin beautifying effect. As a result, Table 6 shows the smooth feeling of the skin after use, and Table 7 shows the moist feeling of the skin after use.

【表6】 [Table 6]

【表7】 表6および表7の結果から実施例2では美肌効果・保湿
効果ともにかなり改善することが出来る。
[Table 7] From the results shown in Tables 6 and 7, in Example 2, both the skin beautifying effect and the moisturizing effect can be considerably improved.

【0017】実施例2のボデーシャンプーをアトピー性
皮膚炎患者10人に使用してもらい洗い上がり後の影響
について調査した。その結果を表8に示した。
The body shampoo of Example 2 was used by 10 patients with atopic dermatitis and the effect after washing was investigated. The results are shown in Table 8.

【表8】 表8の結果からアトピー性皮膚炎患者への影響は少な
い。
[Table 8] From the results in Table 8, the effect on atopic dermatitis patients is small.

【0018】[0018]

【発明の効果】したがって本発明の配合物を使用すれば
美容や健康に優れた効果を有する入浴剤、化粧品が得ら
れる。
Therefore, the use of the composition of the present invention makes it possible to obtain bath salts and cosmetics having excellent effects on beauty and health.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 白田 健志 大阪府高槻市天神町2丁目5番31号 (72)発明者 村松 浩一郎 愛知県名古屋市中区富士見町15−33 (72)発明者 牧野 伸治 愛知県幡豆郡幡豆町大字西幡豆字郷中18番 地 有限会社 アイ・ビー・イー内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Kenji Shirata 2-53-1, Tenjin-cho, Takatsuki-shi, Osaka (72) Inventor Koichiro Muramatsu 15-33 Fujimi-cho, Naka-ku, Aichi Prefecture (72) Inventor Makino Shinji Aichi Prefecture, Hazu-gun, Hazu-machi, Oaza, Nishi-Hazame, No.18, Gochu, I / E Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】米発酵エキスと二価三価鉄塩との混合物を
主体とした入浴剤および化粧品用の配合物
1. A bathing agent and a cosmetic composition mainly comprising a mixture of fermented rice extract and divalent and trivalent iron salts.
JP5229418A 1993-08-20 1993-08-20 Formulations for bath salts and cosmetics Expired - Fee Related JP2846799B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5229418A JP2846799B2 (en) 1993-08-20 1993-08-20 Formulations for bath salts and cosmetics

Applications Claiming Priority (1)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07187992A (en) * 1993-12-27 1995-07-25 Soken Kk Bathing agent
JPH07242531A (en) * 1994-03-08 1995-09-19 Soken Kk Cosmetic prepared from rice bran
JPH07242533A (en) * 1994-03-08 1995-09-19 Soken Kk Bathing agent prepared from rice bran
KR100479665B1 (en) * 2002-04-03 2005-03-30 주식회사 나우코스 Cosmetic compositions containing fermented extracts of green tea, dehulled rice and taraxacum herb
US7887851B2 (en) * 2004-06-07 2011-02-15 Kao Corporation Aromatase activator

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07187992A (en) * 1993-12-27 1995-07-25 Soken Kk Bathing agent
JPH07242531A (en) * 1994-03-08 1995-09-19 Soken Kk Cosmetic prepared from rice bran
JPH07242533A (en) * 1994-03-08 1995-09-19 Soken Kk Bathing agent prepared from rice bran
KR100479665B1 (en) * 2002-04-03 2005-03-30 주식회사 나우코스 Cosmetic compositions containing fermented extracts of green tea, dehulled rice and taraxacum herb
US7887851B2 (en) * 2004-06-07 2011-02-15 Kao Corporation Aromatase activator
US9222079B2 (en) 2004-06-07 2015-12-29 Kao Corporation Aromatase activator

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