JPH08259433A - Cosmetic or preparation for external use containing humectant composition - Google Patents

Cosmetic or preparation for external use containing humectant composition

Info

Publication number
JPH08259433A
JPH08259433A JP7088666A JP8866695A JPH08259433A JP H08259433 A JPH08259433 A JP H08259433A JP 7088666 A JP7088666 A JP 7088666A JP 8866695 A JP8866695 A JP 8866695A JP H08259433 A JPH08259433 A JP H08259433A
Authority
JP
Japan
Prior art keywords
water
composition
lecithin
cosmetic
butylene glycol
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
JP7088666A
Other languages
Japanese (ja)
Other versions
JP3159622B2 (en
Inventor
Keiichi Oyama
慶一 大山
Masaaki Fujisawa
正明 藤澤
Rie Kobayashi
利恵 小林
Naoko Fujimoto
直子 藤本
Misako Tsuji
美佐子 辻
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.)
Nisshin Oil Mills Ltd
Original Assignee
Nisshin Oil Mills 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 Nisshin Oil Mills Ltd filed Critical Nisshin Oil Mills Ltd
Priority to JP08866695A priority Critical patent/JP3159622B2/en
Priority to EP96931290A priority patent/EP0863192B1/en
Priority to US09/068,671 priority patent/US6117434A/en
Priority to PCT/JP1996/002739 priority patent/WO1998013436A1/en
Priority claimed from PCT/JP1996/002739 external-priority patent/WO1998013436A1/en
Publication of JPH08259433A publication Critical patent/JPH08259433A/en
Priority to US09/621,327 priority patent/US6416771B1/en
Application granted granted Critical
Publication of JP3159622B2 publication Critical patent/JP3159622B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • A61K8/553Phospholipids, e.g. lecithin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE: To obtain a cosmetic or skin preparation for external use which comprises a water-soluble polyhydric alcohol, lecithin, butylene glycol and the like and shows excellent moisture retention and high stability. CONSTITUTION: This humectant composition comprises a tri- or more polyhydric alcohol such as glycerol, lecithin and 3-methyl-1,3-butylene glycol and, when needed, further water. Additionally, an oily substance, water, a surfactant, a colorant, a flavor and an antioxidant are properly formulated to prepare the objective cosmetic or dermal preparation for external use of viscous, get- form, oil-in-water type emulsion or solubilized composition. The lecithin is preferably hydrogenated and its concentration is 0.1-50wt.% in the humectant composition and the weight ratio of the alcohol/the butylene glycol is 1/10-20/1 and the amount of the water is some 10wt.%. This cosmetic or skin composition for external use gives good feeling when and after it is applied.

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、特定の成分からなる保
湿剤組成物を含有してなる化粧料または外用剤に係り、
詳しくは、3価以上の水溶性多価アルコール、レシチン
および3−メチル−1,3−ブチレングリコール、所望
により少量の水からなる保湿剤組成物を利用した化粧料
または外用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 cosmetic composition or an external preparation containing a moisturizing agent composition containing specific components,
More specifically, the present invention relates to a cosmetic or an external preparation using a moisturizer composition consisting of a water-soluble polyhydric alcohol having 3 or more valences, lecithin and 3-methyl-1,3-butylene glycol, and optionally a small amount of water.

【0002】[0002]

【従来の技術】若々しい皮膚の保持には水分が深く関係
しており、皮膚の保湿は化粧品の品質にとって重要な機
能の1つであることがよく知られている。化粧料または
外用剤に用いられる公知の保湿剤としては、グリセリ
ン、1,3−ブチレングリコール、ソルビトールなどの
多価アルコールがあり、この他にNMF(天然保湿因
子)の主成分であるピロリドンカルボン酸塩や乳酸塩な
どがある。近年では微生物生産によるヒアルロン酸ナト
リウムも使用されるようになってきた。
BACKGROUND OF THE INVENTION It is well known that moisture is closely related to the retention of youthful skin, and that moisturizing the skin is one of the important functions for the quality of cosmetics. Known moisturizers used in cosmetics or external preparations include polyhydric alcohols such as glycerin, 1,3-butylene glycol and sorbitol, and in addition to them, pyrrolidonecarboxylic acid which is the main component of NMF (natural moisturizing factor). There are salts and lactates. In recent years, sodium hyaluronate produced by microorganisms has also been used.

【0003】また、保湿剤は化粧料や外用剤そのものの
水分保留剤として働いて、系の安定性の保持にも寄与す
る重要な役割も担っている。グリセリンやソルビトール
などの3価以上の多価アルコールは、優れた保湿性、水
分保留性を有し、安全性、安定性、価格などの点からも
っとも汎用性の高い保湿剤として使用されている。
Further, the moisturizer acts as a water retention agent for the cosmetics and the external preparation itself, and also plays an important role of contributing to maintaining the stability of the system. Trihydric or higher polyhydric alcohols such as glycerin and sorbitol have excellent moisturizing properties and water retention properties, and are used as the most versatile moisturizing agents in terms of safety, stability, and price.

【0004】保湿剤として具備すべき必要条件として、
環境条件(温度、湿度、風など)に影響を受けない、特
に周囲の湿度に関わらず、水分を長い間、保持できるこ
とが望ましい。しかしながら、一般に、どのような保湿
剤でも蒸気圧の関係から吸湿量および放出量は周囲の湿
度に影響を受ける。例えば、グリセリンの場合、温度2
5℃での平衡水分量は相対湿度が75%のとき60%、
相対湿度が33%のとき15%、ソルビトールの場合で
は同様に、相対湿度が75%のとき50%、相対湿度が
33%のとき5%となり、周囲の相対湿度の程度によ
り、含水率に差異が生じる。
As a necessary condition to be provided as a moisturizer,
It is desirable to be able to retain moisture for a long time without being affected by environmental conditions (temperature, humidity, wind, etc.), particularly regardless of the ambient humidity. However, generally, the moisture absorption amount and the release amount of any humectant are affected by the ambient humidity because of the vapor pressure. For example, in the case of glycerin, the temperature is 2
The equilibrium water content at 5 ° C is 60% when the relative humidity is 75%,
When the relative humidity is 33%, it is 15%, and in the case of sorbitol, when the relative humidity is 75%, it is 50%, and when the relative humidity is 33%, it is 5%. Occurs.

【0005】このように周囲の湿度が低い場合は、保湿
剤そのものが保留している水分を放出し、保水量が低く
なってしまうという問題点がある。このため、保湿剤を
配合した化粧料や外用剤を使用する際にも、低湿度下で
は経時的に皮膚から水分が失われ、保湿機能の低下を招
くことになる。したがって保湿剤としては、低湿度環境
下における水分の蒸散が緩慢であることが必要である。
本発明者らは、このような状況に鑑み、通常、保湿剤が
配合される化粧料または外用剤の保湿性能を向上せしめ
るべく、鋭意検討を行った。
When the ambient humidity is low as described above, there is a problem in that the moisturizing agent itself releases the retained water and the water retention amount becomes low. Therefore, even when a cosmetic or an external preparation containing a moisturizing agent is used, moisture is lost from the skin over time under low humidity, and the moisturizing function is deteriorated. Therefore, as a moisturizer, it is necessary that the evaporation of water in a low humidity environment is slow.
In view of such a situation, the present inventors have earnestly studied to improve the moisturizing performance of cosmetics or external preparations to which a moisturizing agent is usually added.

【0006】[0006]

【発明が解決しようとする課題】本発明の目的は、上記
の問題を改善し、保湿特性に優れ、かつ、安定性に優れ
た化粧料または外用剤を提供することにある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a cosmetic composition or an external preparation which solves the above problems and has excellent moisturizing properties and stability.

【0007】[0007]

【課題を解決するための手段】本発明の要旨は、3価以
上の水溶性多価アルコール、レシチンおよび3−メチル
−1,3−ブチレングリコール、さらに所望により水か
らなる保湿剤組成物を含有してなる化粧料または外用剤
である。
Means for Solving the Problems The gist of the present invention comprises a moisturizer composition comprising a water-soluble polyhydric alcohol having a valence of 3 or more, lecithin and 3-methyl-1,3-butylene glycol, and optionally water. It is a cosmetic or an external preparation.

【0008】本発明の化粧料または外用剤は、前記特定
成分からなる保湿剤組成物を配合してなることを特徴と
する。この保湿剤組成物を得るために用いられるレシチ
ンは、通常の市販品や試薬として入手できる大豆レシチ
ン、卵黄レシチンを始めとして、これらを溶剤分別、抽
出、分画などの処理を施し加工して得られる精製レシチ
ン、水素添加レシチン、分画レシチンなどが使用され
る。レシチンを3価以上の水溶性多価アルコール中に速
やかに溶解させ、共存させるためには、中性油分を除去
した精製レシチン(混合リン脂質)が好ましい。また酸
化安定性の点を考慮すると、水素添加レシチンが好まし
い。リゾレシチンに関しては、リゾ化率すなわち脱アシ
ル化率の低い(例えばリゾ化率が70%以下)ものが好
ましく、リゾ化率の高いものは通常のレシチンと併用し
て用いることができる。なお、高純度の合成ジアシルホ
スファチジルコリンなどのホスファチジルコリンのみの
単一品は本発明に係る保湿剤組成物中で沈澱が析出し、
該組成物の安定性が良くないため適さない。
The cosmetic or external preparation of the present invention is characterized by being blended with a moisturizing agent composition comprising the above specific components. Lecithin used to obtain this moisturizing composition, soybean lecithin that can be obtained as a normal commercial product or reagent, including egg yolk lecithin, these are subjected to processing such as solvent fractionation, extraction, fractionation, etc. Purified lecithin, hydrogenated lecithin, fractionated lecithin and the like are used. In order to quickly dissolve lecithin in a water-soluble polyhydric alcohol having a valence of 3 or more and make it coexist, purified lecithin (mixed phospholipid) from which neutral oil is removed is preferable. Further, hydrogenated lecithin is preferable in consideration of oxidative stability. As for lysolecithin, those having a low lysolysis rate, that is, a deacylation rate (for example, a lysolysis rate of 70% or less) are preferable, and those having a high lysolysis rate can be used in combination with ordinary lecithin. Incidentally, a single product of only phosphatidylcholine such as high-purity synthetic diacylphosphatidylcholine precipitates in the moisturizer composition of the present invention,
It is not suitable because the stability of the composition is not good.

【0009】3価以上の水溶性多価アルコールは特に限
定されず、代表的なものとしてグリセリン、ソルビトー
ル、ジグリセリン、トリグリセリン、ポリグリセリン、
エリトリトール、ペンタエリトリトール、グルコース、
ガラクトース、フルクトース、シュクロース、マルトー
ス、キシロース、キシロビオース、オリゴ糖の還元物な
どがあり、これらは単独であるいは混合して使用でき
る。これらのうちグリセリンおよび/またはソルビトー
ルが好ましい。
The water-soluble polyhydric alcohol having a valence of 3 or more is not particularly limited, and typical ones include glycerin, sorbitol, diglycerin, triglycerin, polyglycerin,
Erythritol, pentaerythritol, glucose,
There are galactose, fructose, sucrose, maltose, xylose, xylobiose, reduced products of oligosaccharides and the like, and these can be used alone or in combination. Of these, glycerin and / or sorbitol are preferred.

【0010】3−メチル−1,3−ブチレングリコール
は市販品(例えば(株)クラレ製)を利用するのが簡便
である。この3−メチル−1,3−ブチレングリコール
を配合することにより、これと3価以上の水溶性多価ア
ルコールとレシチンとの組成物(保湿剤組成物)の保湿
特性が著しく向上する。
It is convenient to use a commercially available 3-methyl-1,3-butylene glycol (for example, manufactured by Kuraray Co., Ltd.). By blending this 3-methyl-1,3-butylene glycol, the moisturizing property of the composition (moisturizer composition) of the water-soluble polyhydric alcohol having 3 or more valences and lecithin is remarkably improved.

【0011】本発明に係る保湿剤組成物において、レシ
チンの濃度は0.1〜50重量%、望ましくは0.5〜
40重量%がよい。レシチンの濃度が0.1重量%未満
の場合、保湿剤組成物の保湿特性が不十分になる傾向に
あり、逆に50重量%超過の場合、該組成物の系中にレ
シチンが均一に溶存せず、不溶分が析出する傾向がみら
れる。
In the humectant composition of the present invention, the concentration of lecithin is 0.1 to 50% by weight, preferably 0.5 to.
40% by weight is preferred. When the concentration of lecithin is less than 0.1% by weight, the moisturizing properties of the moisturizer composition tend to be insufficient, and when it exceeds 50% by weight, lecithin is uniformly dissolved in the system of the composition. However, the insoluble matter tends to precipitate.

【0012】また3価以上の水溶性多価アルコールと3
−メチル−1,3−ブチレングリコールとの重量比は
1:10〜20:1、望ましくは1:4〜10:1がよ
い。この比率が1:10より大きい場合、水溶性多価ア
ルコール中でレシチンが安定的に溶存できなくなり、室
温(例えば20℃)ないしは低温(例えば5℃)で沈澱
を生じる傾向が大きくなる。また、20:1より小さい
場合は、該組成物は高粘性とならず、保湿特性は満足で
きる程度にまで達しない。
Further, a water-soluble polyhydric alcohol having a valence of 3 or more and 3
The weight ratio with -methyl-1,3-butylene glycol is 1:10 to 20: 1, preferably 1: 4 to 10: 1. When this ratio is larger than 1:10, lecithin cannot be stably dissolved in the water-soluble polyhydric alcohol, and the tendency to cause precipitation at room temperature (eg 20 ° C.) or low temperature (eg 5 ° C.) becomes large. On the other hand, when it is less than 20: 1, the composition does not become highly viscous and the moisturizing property does not reach a satisfactory level.

【0013】本発明の化粧料または外用剤に配合する保
湿剤組成物は、前記した3価以上の水溶性多価アルコー
ル、レシチンおよび3−メチル−1,3−ブチレングリ
コールを所望により加熱、攪拌して混合、均一に溶解せ
しめることにより調製できる。かくして得られる組成物
は、そのままを保湿剤組成物として使用できる。あるい
は以下に述べるように、適宜、少量の水(組成物全体の
約10重量%程度)を加えて前記配合成分を均一に溶解
せしめ、これを保湿剤組成物とすることもできる。
The humectant composition to be blended with the cosmetic or external preparation of the present invention contains the above-mentioned trihydric or higher polyhydric alcohol, lecithin and 3-methyl-1,3-butylene glycol, if desired, with stirring. Then, it can be prepared by mixing and dissolving uniformly. The composition thus obtained can be used as it is as a moisturizer composition. Alternatively, as described below, a small amount of water (about 10% by weight of the total composition) may be appropriately added to uniformly dissolve the above-mentioned components, and this may be used as a humectant composition.

【0014】本発明に係る保湿剤組成物における水分量
は、実質的に非水系のままでよく、あるいは適宜に少量
の必要量(下記)を配合せしめればよい。通常、市販の
レシチンでは0.1〜3重量%程度、また、3価以上の
水溶性多価アルコールでは0.1重量%以上(市販品に
は、水分0.1〜20重量%のグリセリン、水分30重
量%のソルビトールなどの含水品もある)、3−メチル
−1,3−ブチレングリコールでは0.1〜2重量%程
度の水が含まれているため、これをそのまま用いて、改
めて新たに水を添加しなくともよい場合がある。また、
3価以上の水溶性多価アルコールが固体状の糖あるいは
糖アルコール(ショ糖、グルコース、フルクトース、ソ
ルビトールなど)の場合、該組成物全体の約10〜約5
0重量%の適量の水を加えて均一に溶解させる必要があ
る。
The amount of water in the humectant composition according to the present invention may remain substantially non-aqueous, or a small amount of the necessary amount (described below) may be appropriately added. Usually, commercially available lecithin is about 0.1 to 3% by weight, and water-soluble polyhydric alcohol having a valence of 3 or more is 0.1% by weight or more (commercially available glycerin having a water content of 0.1 to 20% by weight, Some water-containing products such as sorbitol have a water content of 30% by weight) and 3-methyl-1,3-butylene glycol contains about 0.1 to 2% by weight of water. In some cases it may not be necessary to add water. Also,
When the water-soluble polyhydric alcohol having a valence of 3 or more is a solid sugar or sugar alcohol (sucrose, glucose, fructose, sorbitol, etc.), about 10 to about 5 of the entire composition is used.
It is necessary to add an appropriate amount of water of 0% by weight and dissolve it uniformly.

【0015】なお本発明で用いる保湿剤組成物は、前記
三成分、さらに必要に応じて少量の水を溶解せしめてな
るものであるが、該組成物が偏光性を有するものが望ま
しい。偏光性をもつ組成物とすることにより、この組成
物が顕著な保湿特性を示すようになる。またこの保湿剤
組成物に水を配合せしめていくと、共存する各成分の相
互作用により、レシチンが特異的な会合構造をとり、高
粘性の液晶を形成させるため、該組成物から水分の蒸散
が抑制されると考えられる。
The humectant composition used in the present invention comprises the above-mentioned three components and, if necessary, a small amount of water dissolved therein, and it is desirable that the composition has a polarizing property. The composition having a polarizing property allows the composition to exhibit remarkable moisturizing properties. When water is added to the moisturizer composition, lecithin takes a specific association structure due to the interaction of the coexisting components to form a highly viscous liquid crystal, so that water evaporation from the composition occurs. Is thought to be suppressed.

【0016】本発明は、前述の保湿剤組成物を配合して
なる化粧料または外用剤であることを特徴とする。そし
て本発明の化粧料または外用剤は、前記特定の保湿剤組
成物と少なくとも油性物質および/または水とを必須成
分として含有し、粘稠ないしゲル状、水中油型乳化状ま
たは可溶化状の形態となる。すなわち前記保湿剤組成物
に攪拌下で油性物質、さらに所望により界面活性剤、顔
料、色素、香料、酸化防止剤などを配合せしめることに
より、粘稠状ないしはゲル状の化粧料または外用剤を得
ることができ、例えばアイジェルやクレンジングジェル
などの化粧料またはゲル状外用剤として使用できる。保
湿剤組成物に対する油性物質の配合量は10倍(重量)
以下が望ましく、これを超えると保湿剤組成物の分離を
招く。
The present invention is characterized in that it is a cosmetic or external preparation prepared by blending the aforementioned moisturizer composition. The cosmetic or external preparation of the present invention contains the specific moisturizing agent composition and at least an oily substance and / or water as essential components, and is a viscous or gel-like, oil-in-water emulsified or solubilized form. Form. That is, a viscous or gel-like cosmetic or external preparation is obtained by adding an oily substance to the above moisturizer composition under stirring and, if desired, a surfactant, a pigment, a dye, a fragrance, an antioxidant or the like. For example, it can be used as a cosmetic such as eye gel or cleansing gel or as a gel external preparation. The amount of oily substance mixed with the moisturizer composition is 10 times (weight)
The following is desirable, and when it exceeds this, separation of the moisturizing agent composition is caused.

【0017】ここに油性物質は特に限定されず、炭化水
素類、エステル類、油脂類、ワックス類、高級脂肪酸、
高級アルコール、シリコーン系物質、ステロール類、樹
脂類などがこれに含まれる。これらの例としては、流動
パラフィン、イソパラフィン、ワセリン、スクワラン、
ミリスチン酸イソプロピル、ミリスチン酸オクチルドデ
シル、イソオクチル酸セチル(2−エチルヘキサン酸セ
チル)、トリイソオクチル酸グリセリル(トリ−2−エ
チルヘキサン酸グリセリル)、トリカプリル酸グリセリ
ル、ジイソオクチル酸ネオペンチルグリコールエステル
(ジ−2−エチルヘキサン酸ネオペンチルグリコールエ
ステル)、リンゴ酸ジイソステアリル、イソノナン酸イ
ソノニル(3,5,5−トリメチルヘキサン酸3,5,
5−トリメチルヘキシルアルコールエステル)、12−
ヒドロキシステアリン酸コレステリル、エメリー社製イ
ソステアリン酸を用いるモノないしヘキサイソステアリ
ン酸ジペンタエリスリトールエステル、o,mまたはp
−メトキシケイ皮酸イソオクチル、ユーカリ油、大豆
油、綿実油、ゴマ油、米胚芽油、米ヌカ油、サフラワー
油、ヒマワリ油、パーム油、オリーブ油、ホホバ油、マ
カデミアンナッツ油、アボガド油、ヒマシ油、月見草
油、タートル油、ミンク油、オレンジラフィー油、ラノ
リン、ミリスチン酸、パルミチン酸、ステアリン酸、オ
レイン酸、12−ヒドロキシステアリン酸、ベヘニン
酸、ステアリルアルコール、オレイルアルコール、セタ
ノール、ラノリンアルコール、パラフィンワックス、マ
イクロクリスタリンワックス、セレシンワックス、ミツ
ロウ、カルナウバワックス、キャンデリラワックス、セ
ラックロウ、大豆硬化油、菜種硬化油、トリステアリン
酸グリセリル、ロジン、コレステロール、フィトステロ
ール、ジメチルポリシロキサン、メチルフェニルポリシ
ロキサン、動植物起源の精油成分などがある。これらは
単独であるいは混合して用いることができる。
Here, the oily substance is not particularly limited, and includes hydrocarbons, esters, oils and fats, waxes, higher fatty acids,
These include higher alcohols, silicone materials, sterols, resins and the like. Examples of these are liquid paraffin, isoparaffin, petrolatum, squalane,
Isopropyl myristate, octyldodecyl myristate, cetyl isooctylate (cetyl 2-ethylhexanoate), glyceryl triisooctylate (glyceryl tri-2-ethylhexanoate), glyceryl tricaprylate, neopentyl glycol diisooctylate (di- 2-ethylhexanoic acid neopentyl glycol ester), diisostearyl malate, isononyl isononanoate (3,5,5-trimethylhexanoic acid 3,5,5)
5-trimethylhexyl alcohol ester), 12-
Cholesteryl hydroxystearate, mono- or hexaisostearic acid dipentaerythritol ester using isostearic acid manufactured by Emery Co., o, m or p
-Isooctyl methoxycinnamate, eucalyptus oil, soybean oil, cottonseed oil, sesame oil, rice germ oil, rice bran oil, safflower oil, sunflower oil, palm oil, olive oil, jojoba oil, macadamian nut oil, avocado oil, castor oil , Evening primrose oil, turtle oil, mink oil, orange laffy oil, lanolin, myristic acid, palmitic acid, stearic acid, oleic acid, 12-hydroxystearic acid, behenic acid, stearyl alcohol, oleyl alcohol, cetanol, lanolin alcohol, paraffin wax , Microcrystalline wax, Ceresin wax, Beeswax, Carnauba wax, Candelilla wax, Shellac wax, Hardened soybean oil, Hardened rapeseed oil, Glyceryl tristearate, Rosin, Cholesterol, Phytosterol, Dimethylpolysiro Sun, and the like methylphenyl polysiloxane, essential oil component of the flora and fauna origin. These can be used alone or as a mixture.

【0018】また、前記保湿剤組成物に攪拌下で前記の
油性物質および水、さらに所望により界面活性剤、顔
料、色素、香料、酸化防止剤、防腐剤などを配合せしめ
ることにより、水中油型乳化状の化粧料または外用剤と
なり、例えばクリーム、乳液、乳化化粧水などの化粧料
や軟膏などの外用剤として使用できる。このとき水の配
合量は、保湿剤組成物に対して10重量%〜100倍
(重量)が望ましく、好ましくは10重量%〜20倍
(重量)である。なお、この水には公知の界面活性剤や
保湿剤などの水溶性ないし水分散性成分を配合しておい
てもよい。
The humectant composition may be mixed with the above-mentioned oily substance and water with stirring, and if desired, a surfactant, a pigment, a dye, a fragrance, an antioxidant, an antiseptic agent, etc. It becomes an emulsified cosmetic or external preparation, and can be used as an external preparation such as a cosmetic such as cream, emulsion or emulsion lotion, or an ointment. At this time, the blending amount of water is desirably 10% by weight to 100 times (weight), and preferably 10% by weight to 20 times (weight), with respect to the humectant composition. The water may be mixed with a water-soluble or water-dispersible component such as a known surfactant or moisturizer.

【0019】さらにまた、前記保湿剤組成物に攪拌下で
水、さらに所望により界面活性剤、色素、香料、酸化防
止剤、防腐剤などを添加していくと、しだいに粘度が低
下していき、可溶化状の水性化粧料または外用剤(水分
含量:50重量%以上)を調製することができ、例えば
化粧水、美容液などの化粧料やローション状の外用剤と
して使用できる。なお、この水に公知の界面活性剤や保
湿剤などの水溶性ないし水分散性成分を配合してもよ
い。
Furthermore, when water and, if desired, surfactants, pigments, fragrances, antioxidants, preservatives and the like are added to the above moisturizer composition with stirring, the viscosity gradually decreases. A solubilized aqueous cosmetic or an external preparation (water content: 50% by weight or more) can be prepared, and it can be used as a cosmetic such as lotion or beauty essence or as a lotion-like external preparation. The water may be mixed with a water-soluble or water-dispersible component such as a known surfactant or humectant.

【0020】かくして本発明によれば、前記特定成分か
らなる保湿剤組成物を配合したクリーム、乳液、化粧
水、美容液、クレンジングジェルなどの化粧料や軟膏、
ゲルなどの外用剤が得られるほか、モイスチャージェ
ル、パック剤などのスキンケア化粧料、乳化型ファンデ
ーション、乳化アイシャドー、ネイルトリートメントな
どの保湿効果を期待するメイクアップ化粧料も調製する
ことが可能となる。また、あかぎれ、ひび、かゆみやア
トピーなど皮膚の乾燥を伴う皮膚炎症用の医薬部外品、
医薬品の軟膏、ゲル製剤などの外用剤とすることもでき
る。
Thus, according to the present invention, cosmetics and ointments such as creams, emulsions, lotions, beauty essences, and cleansing gels containing the moisturizer composition comprising the above-mentioned specific components,
In addition to external preparations such as gels, it is also possible to prepare skincare cosmetics such as moisture gels and packs, and make-up cosmetics that are expected to have a moisturizing effect such as emulsified foundations, emulsified eye shadows and nail treatments. . In addition, quasi-drugs for skin irritation with dry skin such as cracks, cracks, itch and atopy,
It can also be used as an external preparation such as a pharmaceutical ointment or gel preparation.

【0021】[0021]

【実施例】【Example】

参考例1〜8 グリセリンおよび/またはソルビトール、精製水素添加
大豆レシチン(日清製油(株)製、ベイシスLS−60
H)、および3−メチル−1,3−ブチレングリコール
((株)クラレ製)を用い、該レシチン濃度が5重量
%、かつグリセリンおよび/またはソルビトールと3−
メチル−1,3−ブチレングリコールとが所定の重量比
率となるように、各成分を混合し、80℃に加温して溶
解後、室温に冷却して本発明の保湿剤組成物を調製し
た。次に、該組成物の各20gを80℃に再加温し、同
温度の精製水10gを混合して十分に攪拌し、室温に冷
却後、シャーレに入れ、温度25℃、相対湿度30%の
室内に放置し、その水分の減少量を経時的に測定した。
その結果を表1に示す。本発明に係る組成物はいずれ
も、後述する比較例に対して水分の減少速度がゆるやか
であり、水分の保持性能に優れており、保湿剤組成物と
して有用であることが認められた。
Reference Examples 1 to 8 Glycerin and / or sorbitol, purified hydrogenated soybean lecithin (manufactured by Nisshin Oil Co., Ltd., Basis LS-60)
H) and 3-methyl-1,3-butylene glycol (manufactured by Kuraray Co., Ltd.), the lecithin concentration is 5% by weight, and glycerin and / or sorbitol and 3-
Each component was mixed so that methyl-1,3-butylene glycol had a predetermined weight ratio, heated to 80 ° C. and dissolved, and then cooled to room temperature to prepare a moisturizing composition of the present invention. . Next, each 20 g of the composition is reheated to 80 ° C., 10 g of purified water at the same temperature is mixed and sufficiently stirred, and after cooling to room temperature, put in a petri dish, temperature 25 ° C., relative humidity 30%. The sample was left to stand in the room, and the amount of water loss was measured over time.
Table 1 shows the results. It was confirmed that each of the compositions according to the present invention had a slower rate of water decrease than the Comparative Examples described later and excellent water retention performance, and was useful as a moisturizer composition.

【0022】[0022]

【表1】 注)3−M−1,3−BG:3−メチル−1,3−ブチレングリコールを示す (以下、同じ)。[Table 1] Note) 3-M-1,3-BG: Indicates 3-methyl-1,3-butylene glycol (hereinafter the same).

【0023】参考例9〜14 参考例1と同じ原料を用い、グリセリン:3−メチル−
1,3−ブチレングリコール=1:1(重量比)とし、
かつ所定のレシチン濃度となるように、同例記載の方法
で保湿剤組成物を調製した。その後、参考例1と同様の
方法および条件下で、該組成物20gと精製水10gと
の混合物からの水分の減少量を測定した(表−2参
照)。いずれの組成物も、後述の比較例に比べて水分の
減少速度がゆるやかで、保湿剤組成物として適するもの
であることが認められた。
Reference Examples 9 to 14 Using the same starting materials as in Reference Example 1, glycerin: 3-methyl-
1,3-butylene glycol = 1: 1 (weight ratio),
And the moisturizing agent composition was prepared by the method described in the same example so that the predetermined lecithin concentration was obtained. Then, under the same method and conditions as in Reference Example 1, the amount of water loss from the mixture of 20 g of the composition and 10 g of purified water was measured (see Table-2). It was confirmed that each of the compositions had a slower rate of water loss as compared with Comparative Examples described later and was suitable as a moisturizing composition.

【0024】[0024]

【表2】 [Table 2]

【0025】参考比較例1〜8 レシチン無添加の例で、参考例1と同様の実験を行った
(表−3参照)。いずれの組成物でも水分の減少速度が
大きく、該組成物では周囲の湿度によりその保水量が影
響を受けやすいことが明らかになった。
Reference Comparative Examples 1 to 8 The same experiment as in Reference Example 1 was carried out using lecithin-free examples (see Table 3). It was clarified that the rate of water loss was high in any of the compositions, and that the water retention capacity of the composition was easily affected by the ambient humidity.

【0026】[0026]

【表3】 [Table 3]

【0027】参考比較例9〜11 組成物中のレシチン濃度を5重量%とし、3−メチル−
1,3−ブチレングリコールを用いることなく、あるい
はその代替グリコール類を用いて、参考例1と同様の実
験を行った(表−4参照)。これらの例の組成物でも水
分の減少速度が大きく、該組成物では周囲の湿度により
その保水量が影響を受けやすいことが明らかになった。
Reference Comparative Examples 9 to 11 The lecithin concentration in the composition was 5% by weight, and 3-methyl-
The same experiment as in Reference Example 1 was carried out without using 1,3-butylene glycol or using substitute glycols thereof (see Table 4). It was revealed that the compositions of these examples also had a large rate of water loss, and that the water retention capacity of the compositions was easily affected by the ambient humidity.

【0028】[0028]

【表4】 [Table 4]

【0029】参考例15〜16、参考比較例12〜13 参考例1と同じ原料を用い、グリセリン:3−メチル−
1,3−ブチレングリコール=1:1(重量比)とし、
かつ組成物中のレシチン濃度が5重量%(参考例15,
16)または0(参考比較例12,13)となるよう
に、同例記載の方法で組成物を調製した。該組成物20
gと所定量の精製水(5gまたは20g)とを混合し、
参考例1と同様の方法および条件下で、各混合物からの
水分の減少量を測定した(表−5参照)。レシチンが無
添加の比較例に比べて、本参考例では水分の減少速度が
ゆるやかで、保湿剤組成物として適することが認められ
た。
Reference Examples 15 to 16 and Reference Comparative Examples 12 to 13 Using the same starting materials as in Reference Example 1, glycerin: 3-methyl-
1,3-butylene glycol = 1: 1 (weight ratio),
And the lecithin concentration in the composition is 5% by weight (Reference Example 15,
16) or 0 (Reference Comparative Examples 12 and 13) were prepared by the method described in the same example. The composition 20
g and a predetermined amount of purified water (5 g or 20 g) are mixed,
Under the same method and conditions as in Reference Example 1, the amount of water loss from each mixture was measured (see Table-5). Compared to the comparative example in which lecithin was not added, in this reference example, the rate of water decrease was slow, and it was confirmed that the composition was suitable as a moisturizing composition.

【0030】[0030]

【表5】 [Table 5]

【0031】参考例17〜22、参考比較例14〜18 所定の組成で保湿剤組成物を調製し、これに水を加えた
混合物を作成し、室温(20℃)および低温(5℃)に
おける各混合物の安定性を調べるため、それぞれの24
時間経過後の状態を観察した。また偏光顕微鏡を用い
て、それらの60℃、20℃および5℃における偏光性
の有無を調べた。その結果を表−6に示す。表−6から
本発明に係る組成物は、室温および低温において安定性
に優れることが認められた。また本発明に係る組成物で
はいずれも偏光性を有することが認められた。
Reference Examples 17 to 22 and Reference Comparative Examples 14 to 18 Moisturizer compositions were prepared with predetermined compositions, and water was added to the compositions to prepare a mixture, and the mixture was prepared at room temperature (20 ° C.) and low temperature (5 ° C.). To check the stability of each mixture,
The state after a lapse of time was observed. Moreover, the presence or absence of the polarizability at 60 ° C., 20 ° C. and 5 ° C. was examined using a polarization microscope. The results are shown in Table-6. From Table-6, it was confirmed that the composition according to the present invention had excellent stability at room temperature and low temperature. Further, it was confirmed that each of the compositions according to the present invention has a polarization property.

【0032】[0032]

【表6】 注)1)ソルビトールを70重量%含有する水溶液であ
る。 2)安定性の評価は、析出物なし:○、析出物あり:×
[Table 6] Note) 1) An aqueous solution containing 70% by weight of sorbitol. 2) Stability was evaluated as follows: No precipitate: ○, Precipitate: ×

【0033】なお前記の参考例および参考比較例のう
ち、参考例3および6、参考比較例2、4、7、8、1
0および11の各組成物と精製水との混合物の偏光性の
有無および粘度(BL型粘度計にて測定)は表−7のと
おりであった。このことから明らかなように、本発明に
係る組成物は水を添加することにより著しく高粘度状態
となることが特徴である。
Among the above-mentioned Reference Examples and Reference Comparative Examples, Reference Examples 3 and 6, Reference Comparative Examples 2, 4, 7, 8, 1
The presence or absence of polarizability and the viscosity (measured with a BL type viscometer) of the mixture of each composition of 0 and 11 and purified water are shown in Table 7. As is clear from this, the composition according to the present invention is characterized by having a remarkably high viscosity state by adding water.

【0034】[0034]

【表7】 [Table 7]

【0035】実施例1 以下に示す基本処方(表−8参照)により試料(乳液タ
イプのモデル化粧料)を調製し、これを塗布した皮膚の
表面のコンダクタンスを測定して、各試料の皮膚に対す
る保湿効果を評価した。試料の調製法:温度80℃に
て、攪拌しながらB成分にA成分を混合し、ついでC成
分を徐々に添加し、さらに精製水を加えて乳化させ、2
0℃に冷却した。皮膚表面のコンダクタンスの測定法:
女性健常人の上腕内側部をエタノールで清拭後、試料
0.02gを半径3cmの領域に塗布し、そのまま60分
経過した時点で当該部のコンダクタンスを、高周波伝導
度計(IBS社製、IB−355型)を用い、温度19
〜21℃、相対湿度30〜40%の室内で測定した。測
定値は被験者3名の平均値とした。
Example 1 Samples (milky-type model cosmetics) were prepared according to the following basic formulation (see Table 8), and the conductance of the surface of the skin to which the sample was applied was measured to measure the skin of each sample. The moisturizing effect was evaluated. Sample preparation method: A component is mixed with B component with stirring at a temperature of 80 ° C., then C component is gradually added, and purified water is further added to emulsify the mixture.
Cooled to 0 ° C. How to measure skin surface conductance:
After wiping the inner part of the upper arm of a healthy female with ethanol, 0.02 g of the sample was applied to a region with a radius of 3 cm, and when 60 minutes had elapsed, the conductance of the part was measured by a high frequency conductivity meter (IBS, IB). -355 type) and a temperature of 19
It was measured in a room at -21 ° C and a relative humidity of 30-40%. The measured value was the average value of 3 subjects.

【0036】各試料の処方および各試料を適用した皮膚
表面のコンダクタンス測定値を表−8に示す。この結
果、本発明のモデル化粧料(試料No.1〜3および8〜
11)では、皮膚表面のンダクタンスが大きい値とな
り、皮膚に対する優れた保湿効果が認められた。これに
対して3−メチル−1,3−ブチレングリコールを併用
しないもの(試料No.4〜7)やレシチンを併用しない
もの(試料No. 12〜16)では、同コンダクタンスが
小さく、保湿効果は弱い。
The formulation of each sample and the measured conductance value of the skin surface to which each sample is applied are shown in Table-8. As a result, the model cosmetics of the present invention (Sample Nos. 1 to 3 and 8 to
In 11), the conductance of the skin surface was large, and an excellent moisturizing effect on the skin was recognized. On the other hand, in the case of not using 3-methyl-1,3-butylene glycol (Sample No. 4 to 7) and the case of not using lecithin (Sample No. 12 to 16), the conductance is small and the moisturizing effect is weak.

【0037】[0037]

【表8】 [Table 8]

【0038】実施例2 以下に示す基本処方(表−9参照)により試料(化粧水
タイプのモデル化粧料)を調製し、これを塗布した皮膚
の表面のコンダクタンスを測定して、各試料の皮膚に対
する保湿効果を評価した。試料の調製法:温度80℃に
て、攪拌しながらB成分にA成分を混合し、ついでpH
調整剤を加えた精製水を徐々に添加した後、20℃に冷
却した。皮膚表面のコンダクタンスの測定法:実施例1
と同じ。各試料の処方および各試料を適用した皮膚表面
のコンダクタンス測定値を表−9に示す。この結果、本
発明のモデル化粧料(試料No.1〜3および8〜11)
では、皮膚表面のコンダクタンスが大きく、皮膚に対す
る優れた保湿効果が認められた。これに対して3−メチ
ル−1,3−ブチレングリコールを併用しないもの(試
料No.4〜7)やレシチンを併用しないもの(試料12
〜18)では、同コンダクタンスが小さく、保湿効果は
弱い。
Example 2 A sample (lotion-type model cosmetic) was prepared by the following basic formulation (see Table 9), and the conductance of the surface of the skin to which the sample was applied was measured to measure the skin of each sample. The moisturizing effect was evaluated. Sample preparation method: A component is mixed with B component while stirring at a temperature of 80 ° C., and then pH
Purified water containing a regulator was gradually added, and then cooled to 20 ° C. Skin Conductance Measurement Method: Example 1
Same as. The formulation of each sample and the measured conductance value of the skin surface to which each sample is applied are shown in Table-9. As a result, the model cosmetics of the present invention (Sample Nos. 1 to 3 and 8 to 11)
, The conductance of the skin surface was large, and an excellent moisturizing effect on the skin was observed. On the other hand, those not using 3-methyl-1,3-butylene glycol (Sample Nos. 4 to 7) and those not using lecithin (Sample 12)
In 18 to 18), the conductance is small and the moisturizing effect is weak.

【0039】[0039]

【表9】 [Table 9]

【0040】実施例3 以下に示す基本処方(表−10参照)により試料(クレ
ンジング料タイプのモデル化粧料)を調製し、これを塗
布後、水で洗い流した後の皮膚の表面のコンダクタンス
を測定して、各試料の皮膚に対する保湿効果を評価し
た。試料の調製法:温度80℃にて、攪拌しながらB成
分にA成分を混合し、さらにC成分を徐々に加えた後、
20℃に冷却した。皮膚表面のコンダクタンスの測定
法:実施例1記載の方法に準じ、試料を塗付、マッサー
ジした後、水洗し、水分を拭きとり60分経過した時点
で測定した。各試料の処方および各試料を適用した皮膚
表面のコンダクタンス測定値を表−10に示す。この結
果、本発明のモデル化粧料(試料No.1〜3)では、ク
レンジング処理後の皮膚表面のコンダクタンスが大き
く、保湿効果が低下しなかった。これに対して水のみ、
ラウリン酸カリウム水溶液、および通常のクレンジング
オイル(試料No.4〜6)では、クレンジング処理後の
皮膚表面のコンダクタンスは小さかった。
Example 3 A sample (cleansing-type model cosmetic) was prepared by the following basic formulation (see Table 10), and after applying this, the conductance of the surface of the skin was measured after rinsing with water. Then, the moisturizing effect on the skin of each sample was evaluated. Sample preparation method: A component was mixed with B component while stirring at a temperature of 80 ° C., and then C component was gradually added,
Cooled to 20 ° C. Method of measuring conductance of skin surface: According to the method described in Example 1, the sample was applied, massaged, washed with water, and water was wiped off. After 60 minutes, the measurement was performed. The formulation of each sample and the conductance measurement value of the skin surface to which each sample is applied are shown in Table-10. As a result, in the model cosmetics of the present invention (Sample Nos. 1 to 3), the conductance of the skin surface after cleansing treatment was large, and the moisturizing effect was not lowered. On the other hand, only water,
In the potassium laurate aqueous solution and the usual cleansing oil (Sample Nos. 4 to 6), the conductance on the skin surface after the cleansing treatment was small.

【0041】[0041]

【表10】 1)表−8の1)と同じ。 2)ソルビトールの70重量%水溶液。 3)表−8の4)と同じ。 4)組成は、ツイーン80:5重量%、スパン80:5
重量%、流動パラフィン:40重量%およびミリスチン
酸イソプロピル:50重量%。
[Table 10] 1) Same as 1) in Table-8. 2) 70% by weight aqueous solution of sorbitol. 3) Same as 4) in Table-8. 4) The composition is 80: 5% by weight of tween, 80: 5 span.
% By weight, liquid paraffin: 40% by weight and isopropyl myristate: 50% by weight.

【0042】実施例4 〔クリーム〕下記(1)〜(10)の原料成分を用い、
保湿クリームを試作した。(1)〜(3)を80℃に加
温、混合し、均一に溶解した保湿剤組成物を作成した。
一方、(4)〜(9)を85℃に加温、混合して、油相
とした。温度80℃で攪拌しながら、保湿剤組成物に油
相を徐々に添加し、粘稠な組成物を得た。この粘稠組成
物に80℃に加温した(10)を注ぎ、攪拌して乳化液
とした後、室温まで冷却し、水中油型クリームを得た。
本クリームは、乾性肌の女性に対してしっとり感の優れ
たものであった。また1年間、室内(20〜25℃、湿
度40〜60%、以下同じ。)で成分の分離や析出物を
生じることなく安定性は良好であった。
Example 4 [Cream] Using the following raw material components (1) to (10),
A moisturizing cream was prototyped. (1) to (3) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved.
On the other hand, (4) to (9) were heated to 85 ° C. and mixed to obtain an oil phase. The oil phase was gradually added to the humectant composition while stirring at a temperature of 80 ° C. to obtain a viscous composition. (10) heated to 80 ° C. was poured into this viscous composition, and the mixture was stirred to form an emulsion, and then cooled to room temperature to obtain an oil-in-water cream.
The cream had an excellent moisturizing effect on women with dry skin. In addition, for one year, the stability was good in the room (20 to 25 ° C., humidity 40 to 60%, the same applies hereinafter) without separation of components or formation of precipitates.

【0043】 (1)ソルビトール液(70%) 10 (重量%) (2)精製水素添加大豆レシチン 2 (3)3−メチル−1,3−ブチレングリコール 5 (4)ステアリルアルコール 2 (5)マイクロクリスタリンワックス 2 (6)スクワラン 5 (7)トリオクタン酸グリセリル 10 (8)ミリスチン酸オクチルドデシル 5 (9)パラオキシ安息香酸メチル 0.3 (10)精製水 残量 ───────────── 100.0(1) Sorbitol liquid (70%) 10 (% by weight) (2) Purified hydrogenated soybean lecithin 2 (3) 3-Methyl-1,3-butylene glycol 5 (4) Stearyl alcohol 2 (5) Micro Crystalline wax 2 (6) Squalane 5 (7) Glyceryl trioctanoate 10 (8) Octyldodecyl myristate 5 (9) Methyl paraoxybenzoate 0.3 (10) Purified water Residual amount ─────────── ─── 100.0

【0044】実施例5 〔乳液〕下記(1)〜(11)の原料成分を用い、乳液
を試作した。(1)〜(3)を80℃に加温、混合し、
均一に溶解した保湿剤組成物を作成した。一方、(4)
〜(10)を85℃に加温、混合して、油相とした。温
度80℃で、攪拌しながら、保湿剤組成物に油相を徐々
に添加し、粘稠な組成物を得た。この粘稠組成物に80
℃に加温した(11)を注ぎ、攪拌して乳化液とした
後、室温まで冷却し、水中油型乳液を得た。本乳液は、
使用時に違和感なく、使用後1日経過してもしっとり感
が十分に残っており、また1年間、室内で安定であっ
た。
Example 5 [Emulsion] An emulsion was prepared by using the following raw material components (1) to (11). (1) to (3) are heated to 80 ° C. and mixed,
A humectant composition that was uniformly dissolved was prepared. On the other hand, (4)
(10) was heated to 85 ° C. and mixed to obtain an oil phase. The oil phase was gradually added to the humectant composition at a temperature of 80 ° C. with stirring to obtain a viscous composition. 80 to this viscous composition
(11) heated to 0 ° C. was poured, the mixture was stirred to form an emulsion, and then cooled to room temperature to obtain an oil-in-water emulsion. This emulsion is
There was no discomfort at the time of use, a sufficient moist feeling remained even after 1 day of use, and it was stable in the room for one year.

【0045】 (1)グリセリン 8 (重量%) (2)精製レシチン 1 (3)3−メチル−1,3−ブチレングリコール 10 (4)セタノール 1 (5)キャンデリラワックス 1 (6)流動パラフィン 5 (7)パルミチン酸イソプロピル 5 (8)ノナン酸イソノニル 5 (9)メチルフェニルポリシロキサン 1 (10)パラオキシ安息香酸エチル 0.1 (11)精製水 残量 ───────────── 100.0(1) Glycerin 8 (% by weight) (2) Purified lecithin 1 (3) 3-Methyl-1,3-butylene glycol 10 (4) Cetanol 1 (5) Candelilla wax 1 (6) Liquid paraffin 5 (7) Isopropyl palmitate 5 (8) Isononyl nonanoate 5 (9) Methylphenylpolysiloxane 1 (10) Ethyl paraoxybenzoate 0.1 (11) Purified water Remaining amount ──────────── ── 100.0

【0046】実施例6 〔化粧水1〕下記の(1)〜(8)の原料成分を用い、
化粧水を試作した。(1)〜(6)を80℃に加温、混
合し、均一に溶解した保湿剤組成物を作成した。一方、
(7)、(8)を80℃に加温、混合して水溶液を得
た。温度80℃で攪拌しながら、保湿剤組成物に水溶液
を徐々に添加し、等方性の可溶化液とした後、室温まで
冷却し、化粧水を得た。本化粧水は、使用時の感触が良
く、使用後1日経過してもしっとり感があり、また1年
間、室内で安定であった。
Example 6 [Lotion 1] Using the following raw material components (1) to (8),
A lotion was made as a trial. (1) to (6) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. on the other hand,
(7) and (8) were heated to 80 ° C. and mixed to obtain an aqueous solution. The aqueous solution was gradually added to the humectant composition while stirring at a temperature of 80 ° C. to prepare an isotropic solubilizing solution, which was then cooled to room temperature to obtain a lotion. This lotion had a good feel during use, had a moist feeling even after 1 day of use, and was stable in the room for one year.

【0047】 (1)グリセリン 10 (重量%) (2)精製水素添加大豆レシチン 5 (3)3−メチル−1,3−ブチレングリコール 10 (4)精製水 1 (5)スクワラン 0.1 (6)パラオキシ安息香酸エチル 0.1 (7)クインスシード 0.1 (8)精製水 残量 ───────────── 100.0(1) Glycerin 10 (wt%) (2) Purified Hydrogenated Soybean Lecithin 5 (3) 3-Methyl-1,3-butylene glycol 10 (4) Purified Water 1 (5) Squalane 0.1 (6 ) Ethyl paraoxybenzoate 0.1 (7) Quinceseed 0.1 (8) Purified water Residual amount ────────────── 100.0

【0048】実施例7 〔化粧水2〕下記(1)〜(8)の原料成分を用い、化
粧水を試作した。(1)〜(6)を80℃に加温、混合
し、均一に溶解した保湿剤組成物を作成した。一方、
(7)(8)を80℃に加温、混合して水溶液を得た。
温度80℃で攪拌しながら、保湿剤組成物に水溶液を徐
々に添加し、白濁状の乳化液とした後、室温まで冷却
し、化粧水を得た。本化粧水は、使用時の感触が良く、
使用後1日経過してもしっとり感が十分に残っており、
また室内で1年間、安定であった。
Example 7 [Lotion 2] A lotion was prepared by using the following raw material components (1) to (8). (1) to (6) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. on the other hand,
(7) and (8) were heated to 80 ° C. and mixed to obtain an aqueous solution.
While stirring at a temperature of 80 ° C., the aqueous solution was gradually added to the humectant composition to form a cloudy emulsion, which was then cooled to room temperature to obtain a lotion. This lotion has a good feel when used,
Even after 1 day has passed, a sufficient moist feeling remains.
It was stable indoors for one year.

【0049】 (1)濃グリセリン 5 (重量%) (2)ジグリセリン 5 (3)精製水素添加卵黄レシチン 2 (4)3−メチル−1,3−ブチレングリコール 10 (5)ジカプリル酸ネオペンチルグリコールエステル 1 (6)パラオキシ安息香酸エチル 0.1 (7)ヒアルロン酸ナトリウム 0.1 (8)水 残量 ──────────── 100.0(1) Concentrated glycerin 5 (% by weight) (2) Diglycerin 5 (3) Purified hydrogenated egg yolk lecithin 2 (4) 3-Methyl-1,3-butylene glycol 10 (5) Neopentyl glycol dicaprylate Ester 1 (6) Ethyl paraoxybenzoate 0.1 (7) Sodium hyaluronate 0.1 (8) Water Remaining amount ───────────── 100.0

【0050】実施例8 〔クレンジングジェル〕下記(1)〜(11)の原料成
分を用い、クレンジングジェルを試作した。(1)〜
(5)を80℃に加温、混合し、均一に溶解した保湿剤
組成物を作成した。一方、(6)〜(11)を80℃に
加温、混合して油相とした。温度80℃で攪拌しなが
ら、保湿剤組成物に油相を徐々に添加し、ゲル状の組成
物とした後、室温まで冷却し、クレンジングジェルを得
た。本クレンジングジェルは、クレンジング性に優れ、
水による洗い流し性も良好であり、洗い流しの肌のしっ
とり感が十分にあり、つっぱり感の少ないものであっ
た。
Example 8 [Cleansing Gel] A cleansing gel was produced by using the following raw material components (1) to (11). (1) ~
(5) was heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. On the other hand, (6) to (11) were heated to 80 ° C. and mixed to form an oil phase. While stirring at a temperature of 80 ° C., the oil phase was gradually added to the humectant composition to give a gel composition, which was then cooled to room temperature to obtain a cleansing gel. This cleansing gel has excellent cleansing properties,
The washability with water was also good, the skin after washing had a sufficient moist feeling, and the feeling of tightness was small.

【0051】 (1)濃グリセリン 25 (重量%) (2)精製水素添加大豆レシチン 2 (3)3−メチル−1,3−ブチレングリコール 10 (4)水 2 (5)カミツレエキス 1 (6)スクワラン 10 (7)流動パラフィン 10 (8)トリオクタン酸グリセリル 20 (9)ミリスチン酸オクチルドデシル 5 (10)パルミチン酸イソオクチル 10 (11)ホホバ油 5 ──────────── 100(1) Concentrated glycerin 25 (% by weight) (2) Purified hydrogenated soybean lecithin 2 (3) 3-Methyl-1,3-butylene glycol 10 (4) Water 2 (5) Chamomile extract 1 (6) Squalane 10 (7) Liquid paraffin 10 (8) Glyceryl trioctanoate 20 (9) Octyldodecyl myristate 5 (10) Isooctyl palmitate 10 (11) Jojoba oil 5 ───────────── 100

【0052】実施例9 〔モイスチャージェル〕下記(1)〜(7)の原料成分
を用い、モイスチャージェルを試作した。(1)〜
(3)を80℃に加温、混合し、均一に溶解した保湿剤
組成物を作成した。これに80℃に加温した(4)を混
合した後、さらに(5)〜(7)の混合溶液を加えて混
合し、透明状のモイスチャージェルを得た。本モイスチ
ャージェルは、安定性が良好で、使用後1日目のしっと
り感は極めて優れたものであった。
Example 9 [Moisture gel] Using the following raw material components (1) to (7), a moisture gel was experimentally produced. (1) ~
(3) was heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. This was mixed with (4) heated to 80 ° C., and then the mixed solutions of (5) to (7) were added and mixed to obtain a transparent moisture gel. The present moisture gel had good stability and had a very moist feeling on the first day after use.

【0053】 (1)濃グリセリン 10 (重量%) (2)精製水素添加大豆リゾレシチン(リゾ化率50%) 5 (3)3−メチル−1,3−ブチレングリコール 10 (4)カルボキシビニルポリマー1%水溶液 40 (5)水酸化カリウム1%水溶液 10 (6)ヒアルロン酸ナトリウム10%水溶液 1 (7)水 残量 ──────────── 100(1) Concentrated glycerin 10 (% by weight) (2) Purified hydrogenated soybean lysolecithin (lysation rate 50%) 5 (3) 3-Methyl-1,3-butylene glycol 10 (4) Carboxyvinyl polymer 1 % Aqueous solution 40 (5) potassium hydroxide 1% aqueous solution 10 (6) sodium hyaluronate 10% aqueous solution 1 (7) water remaining amount ───────────── 100

【0054】実施例10 〔パック剤〕下記(1)〜(10)の原料成分を用い、
パック剤を試作した。(1)〜(4)を80℃に加温、
混合し、均一に溶解した保湿剤組成物を作成した。一
方、(10)に(5)、(6)を加え、分散させた後、
次に保湿剤組成物を分散させ、最後に(7)〜(9)を
分散させ、泥状のパック剤を得た。本パック剤は、使用
後の肌の柔軟感、うるおい感に優れるものであった。
Example 10 [Packing agent] Using the following raw material components (1) to (10),
A pack agent was made as a prototype. (1) to (4) are heated to 80 ° C,
A humectant composition that was mixed and uniformly dissolved was prepared. On the other hand, after adding (5) and (6) to (10) and dispersing,
Next, the moisturizing agent composition was dispersed, and finally (7) to (9) were dispersed to obtain a mud-like pack agent. This pack was excellent in the softness and moisture of the skin after use.

【0055】 (1)ソルビトール(70%) 10 (重量%) (2)トリグリセリン 10 (3)精製水素添加卵黄レシチン 5 (4)3−メチル−1,3−ブチレングリコール 10 (5)モンモリロナイト 1 (6)エタノール 5 (7)酸化チタン 5 (8)カオリン 10 (9)タルク 5 (10)精製水 残量 ──────────── 100(1) Sorbitol (70%) 10 (wt%) (2) Triglycerin 10 (3) Purified Hydrogenated Egg Yolk Lecithin 5 (4) 3-Methyl-1,3-butylene glycol 10 (5) Montmorillonite 1 (6) Ethanol 5 (7) Titanium oxide 5 (8) Kaolin 10 (9) Talc 5 (10) Purified water Remaining amount ───────────── 100

【0056】実施例11 〔乳化ファンデーション〕下記(1)〜(14)の原料
成分を用い、乳化ファンデーションを試作した。(1)
〜(4)を80℃に加温、混合し、均一に溶解した保湿
剤組成物を作成した。一方、(9)〜(13)を85℃
に加温、混合して、油相とした。温度80℃で攪拌しな
がら、保湿剤組成物に油相を徐々に添加し、粘稠な組成
物を得た。この粘稠組成物に80℃に加温した(14)
を注ぎ、攪拌して乳化液とした後、(5)〜(8)を分
散させ、室温まで冷却し、乳化ファンデーションを得
た。本乳化ファンデーションは、使用して拭きとった後
の肌のかさつき感が極めて少ないものであった。
Example 11 [Emulsified foundation] An emulsified foundation was prepared by using the following raw material components (1) to (14). (1)
(4) was heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. On the other hand, (9) to (13) are 85 ° C.
The mixture was heated and mixed to obtain an oil phase. The oil phase was gradually added to the humectant composition while stirring at a temperature of 80 ° C. to obtain a viscous composition. The viscous composition was heated to 80 ° C. (14)
After pouring and stirring to make an emulsion, (5) to (8) were dispersed and cooled to room temperature to obtain an emulsion foundation. The emulsified foundation had very little feeling of bulkiness on the skin after being wiped off by using.

【0057】 (1)濃グリセリン 10 (重量%) (2)精製水素添加大豆レシチン 1 (3)3−メチル−1,3−ブチレングリコール 10 (4)精製水 5 (5)タルク 3 (6)酸化チタン 5 (7)ベンガラ 0.5 (8)黄酸化鉄 1 (9)流動パラフィン 5 (10)オクタン酸セチル 10 (11)乳酸オクチルドデシル 3 (12)ラノリン 2 (13)セタノール 2 (14)精製水 残量 ────────────── 100.0(1) Concentrated glycerin 10 (% by weight) (2) Purified hydrogenated soybean lecithin 1 (3) 3-Methyl-1,3-butylene glycol 10 (4) Purified water 5 (5) Talc 3 (6) Titanium oxide 5 (7) Red iron oxide 0.5 (8) Yellow iron oxide 1 (9) Liquid paraffin 5 (10) Cetyl octanoate 10 (11) Octyldodecyl lactate 3 (12) Lanolin 2 (13) Cetanol 2 (14) Purified water Remaining amount ────────────── 100.0

【0058】実施例12 〔浴用剤〕下記(1)〜(9)の原料成分を用い、浴用
剤を試作した。(1)〜(6)を80℃に加温、混合
し、均一に溶解した保湿剤組成物を作成した。一方、
(7)〜(9)を80℃に加温、混合して油相とした。
温度80℃で攪拌しながら、保湿剤組成物に油相を徐々
に添加し、ゲル状の組成物とした後、室温まで冷却し、
白濁浴用剤を得た。本浴用剤は、これを用いた入浴の後
の肌のしっとり感が十分に残っておりべたつき感のない
ものであった。
Example 12 [Bath agent] A bath agent was prepared by using the following raw material components (1) to (9). (1) to (6) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. on the other hand,
(7) to (9) were heated to 80 ° C. and mixed to form an oil phase.
While stirring at a temperature of 80 ° C., the oil phase was gradually added to the humectant composition to give a gel composition, which was then cooled to room temperature,
A cloudy bath preparation was obtained. The bath preparation had a sufficient moisturizing feel of the skin after bathing using it and was not sticky.

【0059】 (1)濃グリセリン 30 (重量%) (2)精製大豆レシチン 2 (3)3−メチル−1,3−ブチレングリコール 10 (4)カミツレエキス 2 (5)トウキエキス 2 (6)ショウブエキス 1 (7)流動パラフィン 10 (8)トリオクタン酸グリセリル 38 (9)メチルフェニルポリシロキサン 5 ───────────── 100(1) Concentrated glycerin 30 (% by weight) (2) Purified soybean lecithin 2 (3) 3-methyl-1,3-butylene glycol 10 (4) Chamomile extract 2 (5) Touki extract 2 (6) Shobu Extract 1 (7) Liquid paraffin 10 (8) Glyceryl trioctanoate 38 (9) Methylphenylpolysiloxane 5 ────────────── 100

【0060】実施例13 〔軟膏剤〕下記(1)〜(12)の原料成分を用い、軟
膏剤を試作した。(1)〜(4)を80℃に加温、混合
し、均一に溶解した保湿剤組成物を作成した。一方、
(5)〜(11)を85℃に加温、混合して油相とし
た。温度80℃で攪拌しながら、保湿剤組成物に油相を
徐々に添加し、粘稠な組成物を得た。この粘稠組成物に
80℃に加温した(12)を注ぎ、攪拌して乳化液とし
た後、室温まで冷却し、親水軟膏剤を得た。本軟膏剤
は、肌になじみやすく、しっとり感を与えるものであ
り、また1年間、室内で成分が分離することなく安定性
に優れていた。
Example 13 [Ointment] An ointment was trial-produced using the following raw material components (1) to (12). (1) to (4) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. on the other hand,
(5) to (11) were heated to 85 ° C. and mixed to form an oil phase. The oil phase was gradually added to the humectant composition while stirring at a temperature of 80 ° C. to obtain a viscous composition. (12) heated to 80 ° C. was poured into this viscous composition, and the mixture was stirred to form an emulsion, and then cooled to room temperature to obtain a hydrophilic ointment. The ointment was easily adapted to the skin and gave a moist feeling, and the stability was excellent for one year without separation of the components indoors.

【0061】 (1)グリセリン 10 (重量%) (2)精製水素添加大豆レシチン 1 (3)3−メチル−1,3−ブチレングリコール 15 (4)精製水 5 (5)モノステアリン酸グリセリド 1 (6)ステアリルアルコール 5 (7)ワセリン 10 (8)ミリスチン酸イソプロピル 10 (9)パラオキシ安息香酸プロピル 0.1 (10)パラオキシ安息香酸メチル 0.1 (11)グリチルレチン酸 0.3 (12)精製水 残量 ───────────── 100.0(1) Glycerin 10 (% by weight) (2) Purified hydrogenated soybean lecithin 1 (3) 3-Methyl-1,3-butylene glycol 15 (4) Purified water 5 (5) Monostearic acid glyceride 1 ( 6) Stearyl alcohol 5 (7) Vaseline 10 (8) Isopropyl myristate 10 (9) Propyl paraoxybenzoate 0.1 (10) Methyl paraoxybenzoate 0.1 (11) Glycyrrhetinic acid 0.3 (12) Purified water Remaining amount ───────────── 100.0

【0062】実施例14 〔ゲル剤〕下記の(1)〜(9)の原料成分を用い、ゲ
ル剤を試作した。(1)〜(3)を80℃に加温、混合
し、均一に溶解した保湿剤組成物を作成した。一方、8
0℃に加温した(4)〜(6)の混合溶液を保湿剤組成
物と混合した後、冷却し、(7)〜(9)をそれぞれ加
えてゲル剤を得た。本ゲル剤は、使用時の感触が良く、
肌にしっとりした感じ、湿潤感を与え、また1年間、室
内で成分分離、析出物や異臭の発生のない安定性に優れ
たものであった。
Example 14 [Gel agent] A gel agent was experimentally produced using the following raw material components (1) to (9). (1) to (3) were heated to 80 ° C. and mixed to prepare a humectant composition that was uniformly dissolved. On the other hand, 8
The mixed solution of (4) to (6) heated to 0 ° C. was mixed with the humectant composition and then cooled, and (7) to (9) were added to obtain a gel agent. This gel has a good feel when used,
The skin had a moist feeling and a moist feel, and was excellent in stability for one year without separation of components, generation of precipitates and offensive odors.

【0063】 (1)グリセリン 20 (重量%) (2)水素添加卵黄レシチン 10 (3)3−メチル−1,3−ブチレングリコール 20 (4)ポリエチレングリコール400 20 (5)カルボキシビニルポリマー10%水溶液 4 (6)水酸化ナトリウム10%水溶液 1 (7)エタノール 2 (8)グリチルリチン酸ジカリウム 0.3 (9)水 残量 ───────────── 100.0(1) Glycerin 20 (wt%) (2) Hydrogenated egg yolk lecithin 10 (3) 3-Methyl-1,3-butylene glycol 20 (4) Polyethylene glycol 400 20 (5) Carboxyvinyl polymer 10% aqueous solution 4 (6) Sodium hydroxide 10% aqueous solution 1 (7) Ethanol 2 (8) Dipotassium glycyrrhizinate 0.3 (9) Water remaining amount ────────────── 100.0

【0064】[0064]

【発明の効果】本発明の化粧料または外用剤は、前記特
定成分からなる保湿剤組成物を含有し、保湿性に優れ
る。使用時および使用後の感触も良好である。また粘稠
ないしゲル状、水中油型乳化状または可溶化状などの種
々の形態に調製することが可能であり、しかも安定性に
富む。
The cosmetic or external preparation of the present invention contains a moisturizing agent composition containing the above-mentioned specific components and has excellent moisturizing properties. Feels good during and after use. Further, it can be prepared in various forms such as viscous or gel form, oil-in-water emulsion form or solubilization form, and is highly stable.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 7/00 A61K 7/00 K ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display area A61K 7/00 A61K 7/00 K

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 3価以上の水溶性多価アルコール、レシ
チンおよび3−メチル−1,3−ブチレングリコールか
らなる保湿剤組成物を含有してなる化粧料または外用
剤。
1. A cosmetic or external preparation containing a humectant composition comprising a water-soluble polyhydric alcohol having a valence of 3 or more, lecithin and 3-methyl-1,3-butylene glycol.
【請求項2】 保湿剤組成物が少量の水を含むものであ
る請求項1に記載の化粧料または外用剤。
2. The cosmetic or external preparation according to claim 1, wherein the humectant composition contains a small amount of water.
【請求項3】 保湿剤組成物が偏光性を有するものであ
る請求項1または2に記載の化粧料または外用剤。
3. The cosmetic or external preparation according to claim 1, wherein the humectant composition has a polarizing property.
【請求項4】 保湿剤組成物中の3価以上の水溶性多価
アルコールがグリセリンおよび/またはソルビトールで
ある請求項1〜3のいずれか1項に記載の化粧料または
外用剤。
4. The cosmetic or external preparation according to any one of claims 1 to 3, wherein the water-soluble polyhydric alcohol having 3 or more valences in the humectant composition is glycerin and / or sorbitol.
【請求項5】 保湿剤組成物中のレシチンが水素添加レ
シチンである請求項1〜3のいずれか1項に記載の化粧
料または外用剤。
5. The cosmetic or external preparation according to claim 1, wherein the lecithin in the moisturizing composition is hydrogenated lecithin.
【請求項6】 保湿剤組成物中のレシチンの濃度が0.
1〜50重量%であり、かつ3価以上の水溶性多価アル
コール:3−メチル−1,3−ブチレングリコール=
1:10〜20:1(重量比)である請求項1〜5のい
ずれか1項に記載の化粧料または外用剤。
6. The concentration of lecithin in the moisturizing composition is 0.
Water-soluble polyhydric alcohol of 1 to 50% by weight and having a valence of 3 or more: 3-methyl-1,3-butylene glycol =
It is 1: 10-20: 1 (weight ratio), The cosmetics or external preparation of any one of Claims 1-5.
JP08866695A 1995-03-23 1995-03-23 Cosmetic or external preparation containing humectant composition Expired - Fee Related JP3159622B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP08866695A JP3159622B2 (en) 1995-03-23 1995-03-23 Cosmetic or external preparation containing humectant composition
EP96931290A EP0863192B1 (en) 1995-03-23 1996-09-24 Humectant composition, base containing the same, and cosmetic material or external preparation containing said humectant composition
US09/068,671 US6117434A (en) 1995-03-23 1996-09-24 Humectant composition, base containing the same, and cosmetic material or external preparation containing said humectant composition
PCT/JP1996/002739 WO1998013436A1 (en) 1995-03-23 1996-09-24 Humectant composition, base containing the same, and cosmetic material or external preparation containing said humectant composition
US09/621,327 US6416771B1 (en) 1995-03-23 2000-07-21 Moisturizing composition, base containing the same, and cosmetic or external preparation containing the moisturizing composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP08866695A JP3159622B2 (en) 1995-03-23 1995-03-23 Cosmetic or external preparation containing humectant composition
PCT/JP1996/002739 WO1998013436A1 (en) 1995-03-23 1996-09-24 Humectant composition, base containing the same, and cosmetic material or external preparation containing said humectant composition

Publications (2)

Publication Number Publication Date
JPH08259433A true JPH08259433A (en) 1996-10-08
JP3159622B2 JP3159622B2 (en) 2001-04-23

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ID=29666430

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3159622B2 (en)

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JP2002179565A (en) * 2000-12-15 2002-06-26 Asahi Denka Kogyo Kk Histamine release inhibitor
JP2003095870A (en) * 2001-09-27 2003-04-03 Kose Corp Oil-in-water type unevenness-correcting cosmetic
JP2004269502A (en) * 2003-02-19 2004-09-30 Kose Corp Oil in water type emulsion cosmetic
JP2007314442A (en) * 2006-05-24 2007-12-06 Shiseido Co Ltd Oil-in-water type emulsified cosmetic
KR100787797B1 (en) * 2002-02-08 2007-12-21 주식회사 코리아나화장품 Make-up Cosmetic Composition Containing Lecithin
JP2008007430A (en) * 2006-06-27 2008-01-17 Kracie Home Products Kk Gel-formed cosmetic and method for producing the same
EP1931106A2 (en) 1997-05-01 2008-06-11 Matsushita Electric Industrial Co., Ltd. Information providing system
JP2008530009A (en) * 2005-02-04 2008-08-07 ザ ジレット コンパニー Skin moisturizing composition
JP2009046472A (en) * 2007-07-20 2009-03-05 Rohto Pharmaceut Co Ltd Emulsified composition
JP2011213601A (en) * 2010-03-31 2011-10-27 Kose Corp Oil-in-water type emulsion cosmetic
JP2012082177A (en) * 2010-10-14 2012-04-26 Kao Corp Aqueous cosmetic
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JP2016094363A (en) * 2014-11-13 2016-05-26 ポーラ化成工業株式会社 Liquid crystal emulsion composition
JPWO2018020903A1 (en) * 2016-07-29 2019-05-09 セーレン株式会社 Skin external preparation

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1931106A2 (en) 1997-05-01 2008-06-11 Matsushita Electric Industrial Co., Ltd. Information providing system
JP2002179565A (en) * 2000-12-15 2002-06-26 Asahi Denka Kogyo Kk Histamine release inhibitor
JP2003095870A (en) * 2001-09-27 2003-04-03 Kose Corp Oil-in-water type unevenness-correcting cosmetic
KR100787797B1 (en) * 2002-02-08 2007-12-21 주식회사 코리아나화장품 Make-up Cosmetic Composition Containing Lecithin
JP2004269502A (en) * 2003-02-19 2004-09-30 Kose Corp Oil in water type emulsion cosmetic
JP2008530009A (en) * 2005-02-04 2008-08-07 ザ ジレット コンパニー Skin moisturizing composition
JP2007314442A (en) * 2006-05-24 2007-12-06 Shiseido Co Ltd Oil-in-water type emulsified cosmetic
JP2008007430A (en) * 2006-06-27 2008-01-17 Kracie Home Products Kk Gel-formed cosmetic and method for producing the same
JP2009046472A (en) * 2007-07-20 2009-03-05 Rohto Pharmaceut Co Ltd Emulsified composition
JP2011213601A (en) * 2010-03-31 2011-10-27 Kose Corp Oil-in-water type emulsion cosmetic
JP2012082177A (en) * 2010-10-14 2012-04-26 Kao Corp Aqueous cosmetic
JP2016094363A (en) * 2014-11-13 2016-05-26 ポーラ化成工業株式会社 Liquid crystal emulsion composition
KR101518343B1 (en) * 2014-11-21 2015-05-11 주식회사 나우코스 Gel-type cosmetic composition for moisturizing the skin
JPWO2018020903A1 (en) * 2016-07-29 2019-05-09 セーレン株式会社 Skin external preparation

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