JPS61227517A - Skin cosmetic - Google Patents

Skin cosmetic

Info

Publication number
JPS61227517A
JPS61227517A JP6957885A JP6957885A JPS61227517A JP S61227517 A JPS61227517 A JP S61227517A JP 6957885 A JP6957885 A JP 6957885A JP 6957885 A JP6957885 A JP 6957885A JP S61227517 A JPS61227517 A JP S61227517A
Authority
JP
Japan
Prior art keywords
water
cyclodextrin polymer
soluble
cosmetic
oil
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP6957885A
Other languages
Japanese (ja)
Inventor
Hiroshi Deura
出浦 浩
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP6957885A priority Critical patent/JPS61227517A/en
Publication of JPS61227517A publication Critical patent/JPS61227517A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • A61K8/738Cyclodextrins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/56Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/74Biological properties of particular ingredients
    • A61K2800/75Anti-irritant

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dermatology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:A skin cosmetic having improved feeling in use free from skin irritation, blending a slightly water-soluble cosmetic component with a cyclodextrin polymer in the form of an inclusion compound of it with the cyclodextrin polymer. CONSTITUTION:A slightly water-soluble cosmetic component (e.g., natural animal or vegetable fats and oils such as olive oil, mink oil, jujube oil, lanolin, hydrocarbon such as liquid paraffin, squalane, etc., wax such as whale wax, bees wax, etc., higher alcohol such as cetanol, etc., higher fatty acid, etc. such as myristic acid, etc., silicone oil, etc.) is blended with a cyclodextrin polymer [having >=20 water-solubility in 100ml water at 25 deg.C; preferably compound shown by the formula (n is 3-4)] in the form of an inclusion compound of it and the cyclodextrin polymer, to give a cosmetic for the skin wherein a large amount of the slightly water-soluble cosmetic component is uniformly blended. The amount of the cosmetic component used is 0.001-0.5pt.wt. based on 1pt.wt. cyclodextrin polymer and the treatment temperature is 10-70 deg.C.

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、水難溶性ないし水不溶性の化粧料成分を水溶
性のシクロデキストリンポリマーとの包接化合物の形態
で配合した皮膚化粧料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to a skin cosmetic composition containing sparingly water-soluble or water-insoluble cosmetic ingredients in the form of an inclusion compound with a water-soluble cyclodextrin polymer.

〔従来技術〕[Prior art]

一般に、皮膚化粧料には、油分補給の目的で。 Generally, it is used in skin cosmetics for the purpose of oil replenishment.

油脂類、炭化水素などの油性物質や、皮膚医学的に優れ
た作用を持つ油溶性の生理活性物質、さらには使用性を
高めるため香料などが使用されている。一方、使用性等
の点から見ると、水を主基剤とした化粧料が多く、この
ようなものとしては、例えば、化粧水、低粘度の乳液、
ボディーローション等がある。近年、このような水性基
剤の製品に、皮膚に対する効果を高めるためにビタミン
A、 E及びD等の脂溶性ビタミン類を配合したり、香
りを楽しむためのボディーローションとするために多量
の香料を配合することが望まれる。しかしながら、この
ような化粧料成分は、油溶性で水難溶性のものであるこ
とから、水性基剤の皮膚化粧料に多量配合することは困
難であった。従って、水性基剤に水難溶性物質を均一に
混合するためには。
Oil-based substances such as fats and oils and hydrocarbons, oil-soluble physiologically active substances with excellent dermatological effects, and fragrances are used to enhance usability. On the other hand, from the viewpoint of usability, there are many cosmetics that are mainly water-based, such as lotions, low-viscosity emulsions,
There are body lotions etc. In recent years, such water-based products have been combined with fat-soluble vitamins such as vitamins A, E, and D to enhance their effects on the skin, and large amounts of fragrances have been added to make body lotions with scents. It is desirable to incorporate However, since such cosmetic ingredients are oil-soluble and poorly water-soluble, it has been difficult to incorporate them in large amounts into aqueous-based skin cosmetics. Therefore, in order to uniformly mix a poorly water-soluble substance into an aqueous base.

界面活性剤や、エタノール、ポリオール等の溶剤を可溶
化剤として用いること等が行われている。
Surfactants and solvents such as ethanol and polyols are used as solubilizers.

しかしながら、このような場合、界面活性剤が皮膚に対
する刺激の原因になったり、また溶剤の使用により皮膚
化粧料本来の使用感が損われる等の問題があった。
However, in such cases, there have been problems such as the surfactant causing irritation to the skin and the use of a solvent impairing the original feel of the skin cosmetic.

一方、環状オリゴ糖であるシクロデキストリンの包接作
用を利用して、水に鑑溶性の物質を水溶性とする方法が
盛んに研究されている。シクロデキストリンは、現在、
3種の同族体(α、β、γ体)が利用されている。その
うち、β−シクロデキストリンは入手が容易で、各種の
物質を包接するため、最も広く利用されている。しかし
、β体は。
On the other hand, a method of making water-soluble substances water-soluble by utilizing the inclusion effect of cyclodextrin, which is a cyclic oligosaccharide, is being actively researched. Cyclodextrins are currently
Three types of homologues (α, β, and γ forms) are used. Among them, β-cyclodextrin is the most widely used because it is easily available and clathrates various substances. However, the β-body.

それ自身の水に対する溶解度が低いため、その可溶化効
果には限界があり、可溶化したい物質を高濃度に可溶化
し、製品に配合することは回道であった。
Due to its low solubility in water, its solubilizing effect is limited, and it has been a roundabout way to solubilize the substance to be solubilized at a high concentration and incorporate it into products.

〔目  的〕〔the purpose〕

本発明者らは、シクロデキストリンを9例えばエピクロ
ルヒドリンにより架橋することにより得られるシクロデ
キストリンポリマーが、シクロデキストリン本来の包接
能を持つと共に、その重合度の低いポリマーは水溶性で
、水と任意の割合で混合することの経験的事実に基づい
て、鋭意検討した結果、このポリマーを水難溶性の化粧
料成分と予め混合し、この化粧料成分を包接化合物とす
ることによって、製品中に多量かつ均一に配合できるこ
とを見い出し、本発明に到ったものである・従って1本
発明の目的は、水難溶性化粧料成分を均一かつ多量に配
合した皮膚化粧料を提供することにある。
The present inventors have discovered that a cyclodextrin polymer obtained by cross-linking cyclodextrin with, for example, epichlorohydrin, has the inherent inclusion ability of cyclodextrin, and that the polymer with a low degree of polymerization is water-soluble and can be used with water and any desired material. As a result of intensive study based on the empirical fact of mixing in proportions, we found that by pre-mixing this polymer with a poorly water-soluble cosmetic ingredient and making this cosmetic ingredient a clathrate compound, a large amount of the polymer can be mixed in the product. The present invention was developed based on the discovery that the cosmetic ingredients can be uniformly blended.Therefore, an object of the present invention is to provide a skin cosmetic containing a large amount of sparingly water-soluble cosmetic ingredients uniformly blended therein.

〔構  成〕〔composition〕

本発明は、水難溶性の化粧料成分をシクロデキストリン
ポリマーとの包接化合物の形態で配合したことを特徴と
する水性基剤皮膚化粧料が提供される。
The present invention provides an aqueous-based skin cosmetic composition containing a poorly water-soluble cosmetic ingredient in the form of an inclusion compound with a cyclodextrin polymer.

本発明で用いるシクロデキストリンポリマーは、シフロ
ブキストンをエピクロルヒドリンにより架橋化すること
によって製造される従来公知の物質であり、次の式で表
わされるものが使用される。
The cyclodextrin polymer used in the present invention is a conventionally known substance produced by crosslinking cyphlobuxtone with epichlorohydrin, and is represented by the following formula.

本発明で用いるシクロデキストリンポリマーとしては、
水に対する溶解性が、25℃の水100mfiに対し2
0g以上であるものが好ましく、そのためには上記化学
式における重合度nが3〜4のものがよ<、nが小さい
程シクロデキストリンポリマー自身の水溶性及び可溶化
効果が高い。
The cyclodextrin polymer used in the present invention includes:
Solubility in water is 2 for 100 mfi of water at 25°C.
It is preferable that the polymerization degree is 0 g or more, and for this purpose, it is preferable that the degree of polymerization n in the above chemical formula is 3 to 4. The smaller n is, the higher the water solubility and solubilization effect of the cyclodextrin polymer itself.

本発明において用いられる水難溶性化粧料成分とは、実
質的に水に全く溶解しないか、あるいは僅かに溶解する
化粧料成分を意味し、このようなものには、従来化粧料
に一般的に使用されている油溶性物質が用いられ、その
具体例としては、例えば、オリーブ油、ミンク油、ホホ
バ油、ラノリン、スクワレン等の天然動植物油脂類;流
動パラフィン、パラフィンワックス、スクワラン等の炭
化水素類;鯨ロウ、蜜ロウ等のワックス類;セタノール
、インセタノール、スアタリルアルコール、インステア
リルアルコール等の高級アルコール類;ミリスチン酸、
パルミチン酸、ステアリン酸、ベヘニン酸、イソステア
リン酸等の高級脂肪酸類;イソプロピルミリスチン酸、
イソプロピルパルミチン酸、イソプロピルイソステアリ
ン酸等のエステル類の他、シリコーン油等を挙げること
ができる。さらに、ビタミンA、ビタミンD、ビタミン
E、酢酸1−コフェロール、アスコルビン酸、パルミチ
ン酸エステル等のビタミン類及びγ−オリザノール、葉
酸などのビタミン様作用物質類;安息香酸エストラジオ
ール、吉草酸エストラジオール、エチニルエストラジオ
ール、プロスタグランジン。
The poorly water-soluble cosmetic ingredient used in the present invention means a cosmetic ingredient that is substantially completely insoluble in water or only slightly soluble in water. Specific examples include natural animal and vegetable oils such as olive oil, mink oil, jojoba oil, lanolin, and squalene; hydrocarbons such as liquid paraffin, paraffin wax, and squalane; and whale oil. Waxes such as wax and beeswax; Higher alcohols such as cetanol, incetanol, suataryl alcohol, and instearyl alcohol; myristic acid,
Higher fatty acids such as palmitic acid, stearic acid, behenic acid, isostearic acid; isopropyl myristic acid,
Examples include esters such as isopropyl palmitic acid and isopropyl isostearic acid, as well as silicone oil and the like. Furthermore, vitamins such as vitamin A, vitamin D, vitamin E, 1-copherol acetate, ascorbic acid, and palmitic acid ester; and vitamin-like active substances such as γ-oryzanol and folic acid; estradiol benzoate, estradiol valerate, and ethinyl estradiol. , prostaglandin.

プロピオン酸テストステロンのホルモン類;ρ−アミノ
安息香酸エステル、サリチル酸フェニル等の紫外線吸収
剤類、その他グアイスアズレン、グリチルレチン酸など
の生理活性物質;オイルレッドxO(赤色5号)、ナフ
トールイエローS(黄色1号)、タートラジン(黄色4
号)等の油溶性色素類、さらに香料類を挙げることがで
きる。これらの成分は単独又は2種以上の混合物の形で
用いられる。
Hormones such as testosterone propionate; UV absorbers such as ρ-aminobenzoic acid ester and phenyl salicylate; other physiologically active substances such as guaice azulene and glycyrrhetinic acid; Oil Red xO (red No. 5), naphthol yellow S (yellow No. 1), tartrazine (yellow No. 4)
Examples include oil-soluble pigments such as No.), and fragrances. These components may be used alone or in the form of a mixture of two or more.

前記のような水難溶性化粧料成分の包接化合物を製造す
るには、シクロデキストリンポリマーの水溶液に所要の
化粧料成分を添加混合すればよい。
In order to produce the above-mentioned clathrate compound of poorly water-soluble cosmetic ingredients, necessary cosmetic ingredients may be added to and mixed with an aqueous solution of a cyclodextrin polymer.

この場合、シクロデキストリンポリマー水溶液の濃度は
5〜80重量%、好ましくは20〜40重量%程度であ
り、化粧料成分の使用割合は、シクロデキストリンポリ
マー1重量部に対し、0.001〜0.5重量部、好ま
しくは0.01〜0.15重量部である。処理温度は1
0〜70℃、好ましくは30〜50℃である。この処理
により、水難溶性化粧料成分とシクロデキストリンポリ
マーの包接化合物の水溶液が得られ、これを水性基剤添
加成分として用いる。
In this case, the concentration of the cyclodextrin polymer aqueous solution is about 5 to 80% by weight, preferably about 20 to 40% by weight, and the proportion of the cosmetic ingredients used is 0.001 to 0.00% to 1 part by weight of the cyclodextrin polymer. 5 parts by weight, preferably 0.01 to 0.15 parts by weight. The processing temperature is 1
The temperature is 0 to 70°C, preferably 30 to 50°C. Through this treatment, an aqueous solution of a poorly water-soluble cosmetic component and a cyclodextrin polymer clathrate compound is obtained, and this is used as an additive component to the aqueous base.

本発明の皮膚化粧料は、前記の成分の他、その製品の目
的に応じて、他の化粧料成分1例えば、粘度調節剤、保
湿剤、薬効剤、防腐剤、香料、色素等を配合することが
できる。この場合、粘度調節剤としては、例えば、ヒド
ロキシエチルセルロース、カチオン化セルロース、メチ
ルセルロース、カルボキシメチルセルロース リマー ム、ゼラチン等の高分子物質が用いられ、保湿剤として
は,例えば、グリセリン、プロピレングリコール、ジプ
ロピレングリコール、1.3−ブチレンゲリコール、ソ
ルビトール、ピロリドンカルボン酸ナトリウム等が用い
られ,薬効剤としては、例えば、ビタミンB群等の水溶
性ビタミン類,アラントイン等が用いられ、防腐剤とし
ては,例えば、パラオキシ安息香酸のメチル、エチル、
プロピル又はブチルエステル、安息香酸又はその塩、ソ
ルビン酸又はそのナトリウム塩等が用いられる。
In addition to the above-mentioned ingredients, the skin cosmetic of the present invention may contain other cosmetic ingredients such as viscosity modifiers, humectants, medicinal agents, preservatives, fragrances, pigments, etc., depending on the purpose of the product. be able to. In this case, the viscosity modifier used is, for example, a polymeric substance such as hydroxyethyl cellulose, cationized cellulose, methyl cellulose, carboxymethyl cellulose rimam, gelatin, etc., and the humectant used is, for example, glycerin, propylene glycol, dipropylene glycol. , 1.3-butylene gellicol, sorbitol, sodium pyrrolidonecarboxylate, etc. are used, and as medicinal agents, for example, water-soluble vitamins such as vitamin B group, allantoin, etc. are used, and as preservatives, for example, Methyl, ethyl paraoxybenzoic acid,
Propyl or butyl ester, benzoic acid or its salt, sorbic acid or its sodium salt, etc. are used.

本発明の皮膚化粧料において5前記水難溶性化粧料酸分
とシクロデキストリンポリマーとの包接化合物は、少な
くとも0.1重量%であり,水難溶性化粧料成分の含量
がo.oot重量%以上になるように添加するのがよい
In the skin cosmetic of the present invention, the inclusion compound of the poorly water-soluble cosmetic acid and the cyclodextrin polymer is at least 0.1% by weight, and the content of the poorly water-soluble cosmetic component is o. It is preferable to add it in an amount of oot weight % or more.

(効  果〕 本発明の皮膚化粧料は,水性基剤とするにもかかわらず
,従来配合が困難とされていた水難溶性化粧料成分又は
油溶性物質を多量かつ均一に含有するものであり,その
油溶性物質の添加効果を十分に発揮し得るものである。
(Effects) Although the skin cosmetics of the present invention are aqueous-based, they uniformly contain a large amount of poorly water-soluble cosmetic ingredients or oil-soluble substances, which were conventionally difficult to incorporate. The effect of adding the oil-soluble substance can be fully exhibited.

本発明の皮膚化粧料は、皮膚刺激性もなく、水性基剤皮
膚化粧料本来のすぐれた使用感を有するものであり,化
粧水、低粘度の乳液,ボディーローション等として利用
される。
The skin cosmetics of the present invention have no skin irritation and have the excellent feeling of use inherent to water-based skin cosmetics, and can be used as lotions, low-viscosity milky lotions, body lotions, and the like.

〔実施例〕〔Example〕

次に本発明を実施例によりさらに詳細に説明する。 Next, the present invention will be explained in more detail with reference to Examples.

実施例1 〔油溶性エモリエント剤、香料を安定配合した化粧水〕
A液 フローラル系香料           0.2部β−
シクロデキストリンポリマー    2.0II水  
                        8
,QnB液 パルミチン酸イソプロピル       1.0部β−
シクロデキストリンポリマー    9.0〃水   
                     20.0
#C液 グリセリン              7.0部エタ
ノール              10.0#安息香
酸メチル           0.1//クエン酸 
              o.llIクエン酸ナト
リウム          o.1〃水       
                  42.5//β
−シクロデキストリンポリマー(3部4量体)2.0部
を水8.0部に溶かし、フローラル系香料0.2部を加
えて攪拌し、香料・シクロデキストリンポリマー複合体
(包接化合物)溶液Aを調した。
Example 1 [Lotion with stable combination of oil-soluble emollient and fragrance]
A liquid floral fragrance 0.2 part β-
Cyclodextrin polymer 2.0II water
8
, QnB liquid isopropyl palmitate 1.0 part β-
Cyclodextrin polymer 9.0 water
20.0
#C liquid glycerin 7.0 parts Ethanol 10.0 #Methyl benzoate 0.1//Citric acid
o. llI Sodium Citrate o. 1. Water
42.5//β
-Dissolve 2.0 parts of cyclodextrin polymer (3 parts tetramer) in 8.0 parts of water, add 0.2 parts of floral fragrance, stir, and solution of fragrance/cyclodextrin polymer complex (clathrate compound). I played A.

また、A液と同様に、香料をパルミチン酸イソプロピル
におきかえた他は同様にしてパルミチン酸イソプロピル
・シクロデキストリンポリマー結合体溶液Bを調製した
In addition, an isopropyl palmitate/cyclodextrin polymer conjugate solution B was prepared in the same manner as in Solution A except that the fragrance was replaced with isopropyl palmitate.

次に,前記溶液Cに、A液及びB液を加えて、エモリエ
ント剤,香料を安定に配合した化粧水を得た。なお、上
記組成物からシクロデキストリンポリマーを除いたもの
は、香料とパルミチン酸イソプロピルが分離して、均一
で使用性の良い化粧水とはならない。
Next, liquid A and liquid B were added to the solution C to obtain a lotion stably containing an emollient and a fragrance. It should be noted that when the cyclodextrin polymer is removed from the above composition, the fragrance and isopropyl palmitate separate, resulting in a lotion that is not uniform and easy to use.

実施例2 〔消炎剤を安定配合したボディローション〕A液 グリチルレチン酸・シクロデキストリンポリマー複合体
(グリチルレチン酸2%v/w含有)1.0部水   
                      3.0
〃B液 ウツディ用香料・シクロデキストリンポリマー複合体(
香料5%w/v含有)2.0部水          
               5.0nC液 エタノール              20.0部1
.3−ブチレングリコール       8.OII水
                         
61.OII色素                微
量〃β−シクロデキストリンポリマー(3部4量体)0
.98重量部を水3.0部に溶かし、グリチルレチン酸
0.02部を加えて攪拌し、グリチルレチン酸・シクロ
デキストリンポリマー複合体溶液^を得た。
Example 2 [Body lotion with stable blend of anti-inflammatory agent] Liquid A glycyrrhetinic acid/cyclodextrin polymer complex (contains 2% v/w glycyrrhetinic acid) 1.0 part water
3.0
〃B liquid fragrance/cyclodextrin polymer complex (
Contains 5% w/v fragrance) 2.0 parts water
5.0nC liquid ethanol 20.0 parts 1
.. 3-Butylene glycol 8. OII water
61. OII dye trace amount β-cyclodextrin polymer (tripartite tetramer) 0
.. 98 parts by weight were dissolved in 3.0 parts of water, and 0.02 parts of glycyrrhetinic acid was added and stirred to obtain a glycyrrhetinic acid/cyclodextrin polymer composite solution^.

また、A液と同様に、グリチルレチン酸を香料におきか
えた他は同様にして、香料・シクロデキストリンポリマ
ー複合体溶液Bを調製した。
In addition, a perfume/cyclodextrin polymer complex solution B was prepared in the same manner as in Solution A except that glycyrrhetinic acid was replaced with a perfume.

次に、前記C液に、A液及びB液を加えて、消炎剤、香
料を安定配合したボディーローションを製造した。なお
、上記組成物からシクロデキストリンポリマーを除いた
ものは、グリチルレチン酸及び香料が分離して均一性が
なくなり、このために使用時常に同一の有効性を発揮し
ない。
Next, liquids A and B were added to liquid C to produce a body lotion stably containing an anti-inflammatory agent and fragrance. In addition, when the above-mentioned composition is removed from the cyclodextrin polymer, the glycyrrhetinic acid and fragrance are separated and the composition is not uniform, so that it does not always exhibit the same effectiveness when used.

実施例3 〔殺菌剤を安定配合したアフターシェーブローション〕
A液 トリクロサン・シクロデキストリンポリマー複合体(ト
リクロサンlO%讐/%1含有)     2.o部水
                         
5.QtyB液 柑橘系香料・シクロデキストリンポリマー複合体(香料
5%%+/w含有)2.0部 水                        
 5.07/C液 エタノール              35.0部ポ
リエチレングリコール       5.OII水  
                      46.
0部色素                微量〃β−
シクロデキストリンポリマー(3部4量体)1.8部を
水5.θ部に溶かし、トリクロサン0.2部を加えて攪
拌し、ドルクロサン・シクロデキストリンポリマー複合
体溶液Aを得た。
Example 3 [Aftershave lotion with a stable blend of fungicides]
Part A triclosan/cyclodextrin polymer complex (contains triclosan 10%/%1) 2. o part water
5. QtyB liquid citrus fragrance/cyclodextrin polymer complex (contains 5% fragrance +/w) 2.0 parts water
5.07/C liquid ethanol 35.0 parts polyethylene glycol 5. OII water
46.
0 part dye Trace amount〃β-
1.8 parts of cyclodextrin polymer (3 parts tetramer) and 5 parts of water. The solution was dissolved in θ part, 0.2 part of triclosan was added and stirred to obtain Dorclosan/Cyclodextrin Polymer Complex Solution A.

また、A液と同様に、トリクロサンを香料におきかえた
他は同様にして香料・シクロデキストリンポリマー複合
体溶液Bを得た。
In addition, a perfume/cyclodextrin polymer composite solution B was obtained in the same manner as in Solution A except that triclosan was replaced with a perfume.

次に、前記C液にA液及びB液を加えて、殺菌剤・香料
を安定配合したアフターシェーブローションを得た。な
お、上記組成物から、シフロブキス1へリンポリマーを
除いたものは、トリクロサン及び香料が分離し、均一性
がなくなっているため、使用時常に同一の有効性を発揮
せず、また、長期保存(6力月)においてトリクロサン
由来の変色が生じ、安定性も劣化した。
Next, liquids A and B were added to the liquid C to obtain an aftershave lotion in which a disinfectant and fragrance were stably blended. In addition, in the above-mentioned composition from which Schiflobukis 1 Herrin Polymer is removed, the triclosan and fragrance are separated and the uniformity is lost, so the same effectiveness is not always exhibited during use, and long-term storage ( (6), discoloration due to triclosan occurred and stability also deteriorated.

Claims (3)

【特許請求の範囲】[Claims] (1)水難溶性の化粧料成分をシクロデキストリンポリ
マーとの包接化合物の形態で配合したことを特徴とする
皮膚化粧料。
(1) A skin cosmetic comprising a poorly water-soluble cosmetic ingredient in the form of an inclusion compound with a cyclodextrin polymer.
(2)該シクロデキストリンポリマーとして、25℃の
水に対する溶解度が5g/100ml以上のものを用い
ると共に、該シクロデキストリンポリマー含量が0.1
重量%以上である特許請求の範囲第1項の皮膚化粧料。
(2) The cyclodextrin polymer used has a solubility in water at 25°C of 5 g/100 ml or more, and the cyclodextrin polymer content is 0.1
% or more by weight of the skin cosmetic according to claim 1.
(3)該化粧料成分が油溶性物質である特許請求の範囲
第1項又は第2項の皮膚化粧料。
(3) The skin cosmetic according to claim 1 or 2, wherein the cosmetic component is an oil-soluble substance.
JP6957885A 1985-04-01 1985-04-01 Skin cosmetic Pending JPS61227517A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6957885A JPS61227517A (en) 1985-04-01 1985-04-01 Skin cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6957885A JPS61227517A (en) 1985-04-01 1985-04-01 Skin cosmetic

Publications (1)

Publication Number Publication Date
JPS61227517A true JPS61227517A (en) 1986-10-09

Family

ID=13406821

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6957885A Pending JPS61227517A (en) 1985-04-01 1985-04-01 Skin cosmetic

Country Status (1)

Country Link
JP (1) JPS61227517A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02196709A (en) * 1988-10-28 1990-08-03 Shiseido Co Ltd Cosmetic and powdery cosmetic
WO1999058104A1 (en) * 1998-05-12 1999-11-18 Interhealth Ab Therapeutic compositions
AU727291B2 (en) * 1996-11-15 2000-12-07 Interhealth Ab Therapeutic and cosmetic compositions, their use and method for the preparation thereof
WO2003026603A1 (en) * 2001-09-21 2003-04-03 Beiersdorf Ag Cosmetic and/or dermatological active ingredient combination of triterpenes and cyclodextrins
KR100832796B1 (en) 2006-08-23 2008-05-27 주식회사 마크로케어 Method for extraction of squalene or squalane using cyclodextrin and cosmetic composition containing squalene or squalane-cyclodextrin inclusion complex prepared thereby
FR2944700A1 (en) * 2009-04-23 2010-10-29 Centre Nat Rech Scient METHOD OF FORMING EMULSIONS BASED ON CYCLODEXTRIN POLYMERS AND LIPOPHILIC COMPOUNDS, EMULSIONS THUS OBTAINED, AND COMPOSITIONS COMPRISING SAID EMULSIONS
EP4070781A4 (en) * 2019-12-06 2024-01-31 H&A Pharmachem Co., Ltd Transdermal delivery composite using covalent organic framework and polymer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02196709A (en) * 1988-10-28 1990-08-03 Shiseido Co Ltd Cosmetic and powdery cosmetic
AU727291B2 (en) * 1996-11-15 2000-12-07 Interhealth Ab Therapeutic and cosmetic compositions, their use and method for the preparation thereof
WO1999058104A1 (en) * 1998-05-12 1999-11-18 Interhealth Ab Therapeutic compositions
WO2003026603A1 (en) * 2001-09-21 2003-04-03 Beiersdorf Ag Cosmetic and/or dermatological active ingredient combination of triterpenes and cyclodextrins
KR100832796B1 (en) 2006-08-23 2008-05-27 주식회사 마크로케어 Method for extraction of squalene or squalane using cyclodextrin and cosmetic composition containing squalene or squalane-cyclodextrin inclusion complex prepared thereby
FR2944700A1 (en) * 2009-04-23 2010-10-29 Centre Nat Rech Scient METHOD OF FORMING EMULSIONS BASED ON CYCLODEXTRIN POLYMERS AND LIPOPHILIC COMPOUNDS, EMULSIONS THUS OBTAINED, AND COMPOSITIONS COMPRISING SAID EMULSIONS
WO2010122246A3 (en) * 2009-04-23 2011-04-07 Centre National De La Recherche Scientifique -Cnrs - Method for forming cyclodextrin polymer and lipophilic compound emulsions, resulting emulsions, and compositions including said emulsions
US8741347B2 (en) 2009-04-23 2014-06-03 Centre National de la Recherche Scientifique—CNRS Method for forming cyclodextrin polymer and lipophilic compound emulsions, resulting emulsions, and compositions including said emulsions
EP4070781A4 (en) * 2019-12-06 2024-01-31 H&A Pharmachem Co., Ltd Transdermal delivery composite using covalent organic framework and polymer

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