JPH0477725B2 - - Google Patents

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Publication number
JPH0477725B2
JPH0477725B2 JP60130421A JP13042185A JPH0477725B2 JP H0477725 B2 JPH0477725 B2 JP H0477725B2 JP 60130421 A JP60130421 A JP 60130421A JP 13042185 A JP13042185 A JP 13042185A JP H0477725 B2 JPH0477725 B2 JP H0477725B2
Authority
JP
Japan
Prior art keywords
culture
white fungus
cells
white
cosmetics
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP60130421A
Other languages
Japanese (ja)
Other versions
JPS61289011A (en
Inventor
Hiroaki Konishi
Akira Niwa
Tomonori Katada
Kazutomi Hasegawa
Kazuhisa Oosumi
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.)
Nonogawa Shoji Ltd
Original Assignee
Nonogawa Shoji 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 Nonogawa Shoji Ltd filed Critical Nonogawa Shoji Ltd
Priority to JP60130421A priority Critical patent/JPS61289011A/en
Publication of JPS61289011A publication Critical patent/JPS61289011A/en
Publication of JPH0477725B2 publication Critical patent/JPH0477725B2/ja
Granted legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9728Fungi, e.g. yeasts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9794Liliopsida [monocotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Dermatology (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、液体培養によつて得られるシロキク
ラグの粘性物を配合したことを特徴とする化粧料
に関するものであり、さらに詳しくは、シロキク
ラゲの菌体の液体培養により、菌体外へ排出され
る粘性物を配合した化粧料に関するものである。 従来から化粧料に用いられてきた水溶性の高分
子としては、アラビアゴム、キサンタンガム、ア
ルギン酸ナトリウム、カルボキシビニルポリマー
等が汎用されている。これらが使用される目的と
しては、製品粘度の調整、なめらかな使用感を得
ること、皮膚への好ましい保護膜をつくること等
である。しかし、アラビアゴム、キサンタンガム
等は、使用感として、べたつきがあり、また、ア
ルギン酸ナトリウムの場合、化粧料に配合した
時、経時的な粘度低下を生じ製品の品質を落とす
という欠点があつた。カルボキシビニルポリマー
の場合、PHによつて粘度が変化し、通常、PH5.5
〜8.0の範囲しか使用できないという問題があつ
た。 本発明者らは、こうした事情にかんがみ、上記
の欠点を解決すべく鋭意研究を重ねた結果、キク
ラゲ類の子実体または菌体の抽出成分を配合した
化粧料は、皮膚に対して安全性が高く、経時的に
安定で、PHの依存性もなく、従来の水溶性高分子
には見られない優れた効果、すなわち、なめらか
な使用感、さつぱりしたあと残り感と高い整肌効
果が得られることを先に見出した(弊社昭和60年
5月14日提出の特許願(1))。 化粧料へ配合する場合、シロキクラゲの子実体
または菌体の水抽出成分が、最も適しているが、
子実体の原料価格が高く、また、菌体からの抽出
率が非常に低い(例えば、熱水抽出した場合、子
実体から50〜60%の抽出成分が得られるのに比
べ、菌体からは5〜10%の抽出成分しか得られな
い)等の実用面での問題があつた。 本発明者らは、かかる問題についてさらに鋭意
研究の結果、シロキクラゲの菌体の液体培養によ
り、菌体外へ排出される粘性物が、上記のシロキ
クラゲの子実体または菌体の熱水抽出成分と同様
に、皮膚に塗擦した場合、皮膚を刺激することな
く、大変なめらかに伸び、乾燥後にべたつきもか
さつきもない非常にさつぱりとした被膜が得られ
ることを見出した。さらに、皮膚の水分保留性
や、皮膚の色つやを良くし、小ジワの防止および
改善等の優れた整肌効果が得られることを見出し
た。 すなわち、本発明は、シロキクラゲの菌体の液
体培養により、菌体外へ排出される粘性物を配合
した化粧料に関するものである。 本発明によつて得られる化粧料の特徴は、皮膚
の色つやを良くし、小ジワの防止および改善等の
優れた整肌効果が得られるとともに使用感の非常
にさつぱりした保護膜をのこすことができ、しか
も、水分の保留性が高いことである。また、皮膚
に刺激を与えず、安全性に優れた化粧料である。 本発明で必須成分として配合されるシロキクラ
ゲの粘性物は、シロキクラゲの菌体を液体培養し
たとき、シロキクラゲ菌体外へ排出される粘性物
であり、季節をとわず、比較的容易に、かつ大量
に生産することができる。 本発明のシロキクラゲ菌体の液体培養により、
菌体外へ排出される粘性物の有効成分は、キシロ
ース、マンノース、グルクロン酸、およびこれら
の分子内にアセチル基をもつた構造からなる酸性
多糖類が主である。 本発明のシロキクラゲ菌体の液体培養により、
菌体外へ排出される粘性物は、下記のごとくによ
り製造することができる。液体培養条件は、シロ
キクラゲ菌体が増殖する条件であれば特に限定さ
れない。通常液体培養の培地としては、炭素源、
窒素源、無機塩を含有する培地が利用でき、その
他、天然栄養源、ビタミン、アミノ酸等を加えた
ものも用いることができる。炭素源としては、シ
ヨ糖、ブドウ糖、果糖、麦芽糖などの糖類を挙げ
ることができる。窒素源としては、ペプトン、尿
素、アンモニウム塩などが例示できる。また、無
機塩としては、塩化カリウム、硫酸鉄、硫酸マグ
ネシウム、リン酸塩などが挙げられ、これらは必
要に応じて添加することができる。天然栄養源と
しては、麦芽エキス、酵母エキス、カゼイン加水
分解物、ココナツツミルク、ポテトエキスなどが
例示される。培養条件として、温度20〜32℃、PH
5〜7で、5〜20日間振盪培養、通気撹拌培養な
どの方法により好気的条件下で行なうのが好まし
い。最初から本培養を行なうこともできるが、あ
らかじめ小規模な前培養を行ない、これを本培養
に接種して行なうのが好ましい。 液体培養後の培養液は、通常の方法により、除
菌を行ない、そのまま化粧料原料とすることがで
きる。例えば、液体培養後の培養液を加熱殺菌し
た後、遠心分離またはセライト545やハイフロス
ーパーセル等の剤を用いての過などにより、
シロキクラゲ菌体を除菌し、得られた液、すな
わち、シロキクラゲ菌体が菌体外に排出した粘性
物を含む培養液をそのまま化粧料原料とすること
ができる。また、前記液をさらに、透析、限外
過等による低分子成分の除去、除タンパクの操
作、アルコール等の溶媒を用いた分画などの方法
により、分画、精製して使用することもできる。
また、菌体除去後の培養液または培養をさらに分
画、精製した培養成分は必要に応じて濃縮あるい
は希釈することもできる。さらに、凍結乾燥ある
いはスプレードライ等の方法により、乾燥粉末の
状態で化粧料原料として使用することも可能であ
る。 本発明によれば、シロキクラゲの菌体の液体培
養により、菌体外へ排出される粘性物(除菌後の
培養液または培養成分)は、種々の化粧料基材と
ともに、化粧水、乳液、クリームなどの基礎化粧
料、フアンデーシヨンなどのメイクアツプ化粧
料、ヘアーリキツド、ヘアークリームなどの頭髪
化粧料等の形で用いることができる。また、これ
らの化粧料は常法により製造できる。 本発明で用いるシロキクラゲの菌体の液体培養
によつて、菌体外に排出される粘性物の配合量
は、化粧料基材に対して0.001〜20.0重量%使用
するのが適当である。また、シロキクラゲの菌体
を除いた培養液を直接使用する場合、ほぼ100%
の配合も可能である。配合量が、0.001重量%よ
り少ない量では充分な効果が得らられず、また、
20.0重量%を超える量では効果の増強がないので
不経済である。 次に、実施例を示しながら本発明の化粧料の有
効性について説明する。なお、本発明の内容は、
これらに限定されるものではない。実施例および
比較例に示す配合量の部とは重量部を示す。実施
例中のシロキクラゲ培養液とシロキクラゲ培養成
分は、次の方法で製造したものを使用しており、
いずれも、シロキクラゲ菌体の液体培養により、
菌体外へ排出される粘性物を含むものである。 シロキクラゲの液体培養実施例 麦芽エキス2部、シヨ糖2部に精製水を加えて
100部とした培地(PH5.5)を殺菌後、シロキクラ
ゲ Tremella fuciformis IFONo.8890を接種し、
30℃で6日間振盪培養(110回/分)した。培養
終了後、遠心分離機(12000rpm/min)により
菌体を除去し、得られた上澄液をさらに、セライ
ト545を用いて過して、液すなわちシロキク
ラゲ培養液80部を得た。上記シロキクラゲ培養液
の限外過を行ない、分子量8000以下の低分子の
ものを取り除いた後、凍結乾燥し、シロキクラゲ
培養成分(培地100部に対して、収量0.1〜1.0部)
を得た。 実施例1 化粧水 処方 配合量 A シロキクラゲ培養成分 0.6部 1,3−ブチレングリコール 5.0 グリセリン 2.0 キサンタンガム 0.2 精製水 46.9 B エタノール 5.0 p−ヒドロキシ安息香酸メチル 0.1 ポリオキシエチレン(40)硬化ヒマシ油 0.2 香料 適量 精製水 10.0 製造方法:成分Aおよび成分Bをそれぞれ均一
に溶解後、混合し製品とする。 比較例1 化粧水 実施例1からシロキクラゲ培養成分を除いた処
方で、化粧水を調製した。 実施例2 スキンクリーム A ステアリン酸 4.0部 セチルアルコール 3.0 ステアリルアルコール 1.0 流動パラフイン 6.5 ワセリン 10.0 ソルビタンモノステアレート 1.5 ポリオキシエチレン(25)モノステアレート
3.0 B 1,3−ブチレングリコール 5.0 水酸化カリウム 0.1 シロキクラゲ培養成分 1.0 p−ヒドロキシ安息香酸メチル 0.2 精製水 64.7 C 香料 適量 製造方法:油相成分Aおよび水相成分Bをそれ
ぞれ70〜75℃に加熱溶解した後、成分Aに成分B
を加えて乳化し、冷却途上で成分cを加えて混合
し、30℃まで冷却し製品とする。 実施例3 乳液 A ステアリン酸 5.0部 セチルアルコール 5.0 流動パラフイン 2.0 グリセリンモノステアレート 1,3 ソルビタンモノオレート 1.5 ポリオキシエチレン(10)ソルビタンモノオレ
ート 0.8 B グリセリン 6.0 シロキクラゲ培養液 6.0 p−ヒドロキシ安息香酸メチル 0.2 精製水 72.2 C 香料 適量 製造方法:実施例2と同様にして、製品とす
る。 実施例4 パツク A グリセリン 15.0 1,3−ブチレングリコール 10.0 p−ヒドロキシ安息香酸メチル 0.2 ポリオキシエチレン(40)硬化ヒマシ油 0.5 シロキクラゲ培養液 10.0 クエン酸 0.1 クエン酸ナトリウム 0.3 香料 適量 精製水 63.9 製造方法:各成分を均一に溶解し製品とする。 本発明のシロキクラゲ菌体の液体培養により、
菌体外へ排出される粘性物の安全性を明らかにす
るため、人体に対する一次刺激性試験を閉塞パツ
チテストにより行なつた。すなわち、フインチヤ
ンバー(大正製薬)を用い、健康人30名に対し、
前腕屈側部に48時間閉塞貼布を行ない、パツチテ
スト用絆創膏除去後、1時間後、24時間後、およ
び48時間後の判定の平均値を用いて判定した。シ
ロキクラゲ培養液およびシロキクラゲ培養成分の
いずれの場合も、紅斑等は、認められず一次刺激
性がないことが確認された。
The present invention relates to a cosmetic product characterized by containing a viscous material of white fungus obtained by liquid culture, and more specifically, the present invention relates to a cosmetic product containing a viscous substance of white fungus that is obtained by liquid culture, and more specifically, a viscous substance of white fungus that is excreted from the fungal body by liquid culture of white fungus. The present invention relates to cosmetics containing viscous substances. As water-soluble polymers that have been conventionally used in cosmetics, gum arabic, xanthan gum, sodium alginate, carboxyvinyl polymer, and the like are commonly used. The purposes for which they are used include adjusting the viscosity of the product, providing a smooth feeling of use, and creating a favorable protective film for the skin. However, gum arabic, xanthan gum, etc. have a sticky feel when used, and sodium alginate has the disadvantage that when incorporated into cosmetics, the viscosity decreases over time, degrading the quality of the product. For carboxyvinyl polymers, the viscosity changes depending on the pH, typically PH5.5.
There was a problem that only the range ~8.0 could be used. In view of these circumstances, the present inventors have conducted extensive research to resolve the above-mentioned drawbacks, and have found that cosmetics containing extracts of the fruiting bodies or fungal bodies of wood ear fungi are safe for the skin. It is stable over time, has no PH dependence, and has excellent effects not found in conventional water-soluble polymers, such as a smooth feeling of use, a refreshing aftertaste, and a high skin conditioning effect. We first discovered what could be obtained (patent application (1) filed by our company on May 14, 1985). When blended into cosmetics, the water-extracted components of the fruiting bodies or fungal cells of the white fungus are most suitable;
The cost of raw material for fruiting bodies is high, and the extraction rate from bacterial cells is very low (for example, when hot water is extracted, 50-60% of the extracted components can be obtained from fruiting bodies, but There were practical problems such as only 5 to 10% of extracted components could be obtained. As a result of further intensive research into this problem, the present inventors discovered that the viscous substance discharged outside the bacterial cells by liquid culture of the bacterial cells of the white wood fungus is the above-mentioned fruiting body or hot water extracted component of the bacterial cells of the white wood jellyfish. Similarly, it has been found that when rubbed on the skin, it spreads very smoothly without irritating the skin, and after drying, a very crisp film is obtained that is neither sticky nor bulky. Furthermore, it has been found that excellent skin conditioning effects such as improved skin moisture retention, improved skin color and luster, and prevention and improvement of fine wrinkles can be obtained. That is, the present invention relates to a cosmetic containing a viscous substance that is excreted from the cells of the white fungus through liquid culture of the cells. The cosmetics obtained by the present invention are characterized by improving skin color and luster, providing excellent skin conditioning effects such as preventing and improving fine wrinkles, and leaving behind a protective film with a very refreshing feel. Moreover, it has a high water retention property. In addition, it is a cosmetic that does not irritate the skin and has excellent safety. The viscous substance of white fungus that is blended as an essential ingredient in the present invention is a viscous substance that is excreted outside the white fungus body when the white fungus body is cultured in liquid, and can be easily and easily produced regardless of the season. Can be produced in large quantities. By liquid culturing the white fungus cells of the present invention,
The active ingredients of the viscous substance excreted from the bacterial body are mainly xylose, mannose, glucuronic acid, and acidic polysaccharides having a structure with an acetyl group in these molecules. By liquid culturing the white fungus cells of the present invention,
The viscous substance excreted outside the bacterial cells can be produced as follows. The liquid culture conditions are not particularly limited as long as they allow the white fungus cells to proliferate. Usually, the liquid culture medium includes a carbon source,
A medium containing a nitrogen source and an inorganic salt can be used, and a medium containing natural nutritional sources, vitamins, amino acids, etc. can also be used. Examples of carbon sources include sugars such as sucrose, glucose, fructose, and maltose. Examples of nitrogen sources include peptone, urea, and ammonium salts. Further, examples of inorganic salts include potassium chloride, iron sulfate, magnesium sulfate, phosphates, and the like, and these can be added as necessary. Examples of natural nutritional sources include malt extract, yeast extract, casein hydrolyzate, coconut milk, and potato extract. Culture conditions: temperature 20-32℃, pH
5 to 7, preferably carried out under aerobic conditions by a method such as shaking culture or aerated agitation culture for 5 to 20 days. Although main culture can be performed from the beginning, it is preferable to perform a small-scale preculture in advance and inoculate the main culture with this preculture. The culture solution after liquid culture can be sterilized by a conventional method and used as a raw material for cosmetics. For example, after heating and sterilizing the culture solution after liquid culture, centrifugation or filtration using an agent such as Celite 545 or Hyflo Super Cell, etc.
The liquid obtained by sterilizing the white jellyfish cells, that is, the culture solution containing the viscous substances excreted outside the white jellyfish cells, can be used as a raw material for cosmetics as it is. In addition, the above-mentioned liquid can be further fractionated and purified by methods such as removal of low-molecular components by dialysis, ultrafiltration, etc., protein removal operation, and fractionation using a solvent such as alcohol. .
Further, the culture solution after bacterial cell removal or culture components obtained by further fractionating and purifying the culture can be concentrated or diluted as necessary. Furthermore, it can also be used as a raw material for cosmetics in the form of a dry powder by freeze-drying, spray-drying, or other methods. According to the present invention, the viscous substances (culture solution or culture components after sterilization) discharged from the cells by liquid culture of the cells of White-eared Fungus can be used as lotions, emulsions, lotions, etc., along with various cosmetic base materials. It can be used in the form of basic cosmetics such as creams, makeup cosmetics such as foundations, hair cosmetics such as hair liquids and hair creams, and the like. Moreover, these cosmetics can be manufactured by conventional methods. The appropriate amount of the viscous substance excreted outside the cells by the liquid culture of the cells of the white fungus used in the present invention is 0.001 to 20.0% by weight based on the cosmetic base material. In addition, when using the culture solution without the fungal cells of the white fungus directly, almost 100%
It is also possible to mix. If the blending amount is less than 0.001% by weight, sufficient effects cannot be obtained, and
If the amount exceeds 20.0% by weight, the effect will not be enhanced and it will be uneconomical. Next, the effectiveness of the cosmetics of the present invention will be explained while showing examples. The content of the present invention is as follows:
It is not limited to these. The amounts shown in Examples and Comparative Examples refer to parts by weight. The white jellyfish culture solution and white jellyfish culture components used in the examples were manufactured by the following method.
In both cases, by liquid culture of white fungus cells,
It contains viscous substances that are excreted outside the bacterial body. Example of liquid culture of white fungus by adding purified water to 2 parts of malt extract and 2 parts of sucrose.
After sterilizing 100 parts of the medium (PH5.5), inoculate the white fungus Tremella fuciformis IFO No. 8890.
Shaking culture was carried out at 30°C for 6 days (110 times/min). After the cultivation was completed, the bacterial cells were removed using a centrifuge (12,000 rpm/min), and the resulting supernatant was further filtered through Celite 545 to obtain 80 parts of a liquid, that is, a white fungus culture solution. The above-mentioned white fungus culture solution is subjected to ultrafiltration to remove low-molecular substances with a molecular weight of 8000 or less, and then lyophilized to produce white fungus culture components (yield: 0.1 to 1.0 parts per 100 parts of medium).
I got it. Example 1 Lotion formulation Amount A White fungus culture ingredient 0.6 parts 1,3-butylene glycol 5.0 Glycerin 2.0 Xanthan gum 0.2 Purified water 46.9 B Ethanol 5.0 Methyl p-hydroxybenzoate 0.1 Polyoxyethylene (40) hydrogenated castor oil 0.2 Fragrance Appropriate amount Purified water 10.0 Manufacturing method: Uniformly dissolve component A and component B, then mix to form a product. Comparative Example 1 Lotion A lotion was prepared using the formulation of Example 1 except that the white fungus culture component was removed. Example 2 Skin Cream A Stearic acid 4.0 parts Cetyl alcohol 3.0 Stearyl alcohol 1.0 Liquid paraffin 6.5 Vaseline 10.0 Sorbitan monostearate 1.5 Polyoxyethylene (25) monostearate
3.0 B 1,3-butylene glycol 5.0 Potassium hydroxide 0.1 White fungus culture component 1.0 Methyl p-hydroxybenzoate 0.2 Purified water 64.7 C Fragrance Appropriate amount Production method: Heat oil phase component A and water phase component B to 70-75°C, respectively. After dissolving, component A and component B
Add and emulsify, add component c during cooling, mix, and cool to 30°C to form a product. Example 3 Emulsion A Stearic acid 5.0 parts Cetyl alcohol 5.0 Liquid paraffin 2.0 Glycerin monostearate 1,3 Sorbitan monooleate 1.5 Polyoxyethylene (10) Sorbitan monooleate 0.8 B Glycerin 6.0 White fungus culture solution 6.0 Methyl p-hydroxybenzoate 0.2 Purified water 72.2C Perfume Appropriate amount Manufacturing method: Produce a product in the same manner as in Example 2. Example 4 Pack A Glycerin 15.0 1,3-butylene glycol 10.0 Methyl p-hydroxybenzoate 0.2 Polyoxyethylene (40) Hydrogenated castor oil 0.5 White fungus culture solution 10.0 Citric acid 0.1 Sodium citrate 0.3 Fragrance Appropriate amount of purified water 63.9 Production method: Dissolve each component uniformly to form a product. By liquid culturing the white fungus cells of the present invention,
In order to clarify the safety of the viscous substance discharged outside the bacterial cells, a primary irritation test on the human body was conducted using an occlusion patch test. In other words, using Finch Yanvar (Taisho Pharmaceutical), 30 healthy people were given
An occlusive patch was applied to the flexor side of the forearm for 48 hours, and the average value of the results 1 hour, 24 hours, and 48 hours after removal of the patch test adhesive was used for determination. No erythema or the like was observed in either the white fungus culture solution or the white fungus culture component, and it was confirmed that there was no primary irritation.

【表】 さらに本発明化粧料の効果を明らかにするため
25〜50才の一般女性30名を対象に使用試験を行な
い、ダブルブラインド法により、整肌効果を中心
にアンケート調査を行なつた。シロキクラゲ培養
成分使用の化粧水(実施例1の化粧水)とシロキ
クラゲ培養成分を含まない従来の化粧水(比較例
1の化粧水)を1カ月間使用した結果を表2にま
とめて示す。なお、使用期間中の皮膚トラブルは
1件も発生しなかつた。
[Table] To further clarify the effects of the cosmetics of the present invention
We conducted a usage test on 30 general women between the ages of 25 and 50, and conducted a double-blind questionnaire survey focusing on the skin conditioning effect. Table 2 summarizes the results of using a lotion containing white jellyfish cultured ingredients (the lotion of Example 1) and a conventional lotion that does not contain white jellyfish cultured ingredients (the lotion of Comparative Example 1) for one month. Furthermore, no skin problems occurred during the period of use.

【表】 表2でも明らかなように、シロキクラゲ培養成
分を添加することにより、優れた整肌効果が得ら
れた。シロキクラゲ培養液についても、同様な試
験を行なつたが、優れた整肌効果が得られた。
[Table] As is clear from Table 2, excellent skin conditioning effects were obtained by adding the white fungus cultured ingredients. A similar test was conducted using a white fungus culture solution, and an excellent skin conditioning effect was obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 シロキクラゲの液体培養により得られる粘性
物を配合したことを特徴とする化粧料。
1. A cosmetic containing a viscous substance obtained by liquid culture of white fungus.
JP60130421A 1985-06-15 1985-06-15 Cosmetic Granted JPS61289011A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60130421A JPS61289011A (en) 1985-06-15 1985-06-15 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60130421A JPS61289011A (en) 1985-06-15 1985-06-15 Cosmetic

Publications (2)

Publication Number Publication Date
JPS61289011A JPS61289011A (en) 1986-12-19
JPH0477725B2 true JPH0477725B2 (en) 1992-12-09

Family

ID=15033846

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60130421A Granted JPS61289011A (en) 1985-06-15 1985-06-15 Cosmetic

Country Status (1)

Country Link
JP (1) JPS61289011A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2578341B2 (en) * 1987-10-29 1997-02-05 ポーラ化成工業株式会社 External preparation for skin
US6383799B1 (en) * 1999-10-15 2002-05-07 Medmyco Ltd. Process for producing, methods and compositions of glucuronoxylomannan as nutriceutical agent from higher basidiomycetes mushroom
JP2006111545A (en) * 2004-10-13 2006-04-27 Nippon Menaade Keshohin Kk Glutathione reductase activity-enhancing agent
CN104366640B (en) * 2014-11-25 2016-11-02 呼伦贝尔蒙天源生物科技有限公司 A kind of preparation method of Auricularia polycose beverage
WO2018095532A1 (en) * 2016-11-25 2018-05-31 Lvmh Recherche Aqueous cosmetic

Also Published As

Publication number Publication date
JPS61289011A (en) 1986-12-19

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