JPH0210803B2 - - Google Patents

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Publication number
JPH0210803B2
JPH0210803B2 JP56101397A JP10139781A JPH0210803B2 JP H0210803 B2 JPH0210803 B2 JP H0210803B2 JP 56101397 A JP56101397 A JP 56101397A JP 10139781 A JP10139781 A JP 10139781A JP H0210803 B2 JPH0210803 B2 JP H0210803B2
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JP
Japan
Prior art keywords
oil
lipid
composition according
agents
aqueous phase
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
JP56101397A
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Japanese (ja)
Other versions
JPS5777613A (en
Inventor
Zuabotsuto Arufuretsuto
Guria Jakuriinu
Hanjani Roozuumarii
Uanreberugu Gii
Ribie Aren
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LOreal SA
Original Assignee
LOreal SA
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Publication of JPS5777613A publication Critical patent/JPS5777613A/en
Publication of JPH0210803B2 publication Critical patent/JPH0210803B2/ja
Granted legal-status Critical Current

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    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/42Ethers, e.g. polyglycol ethers of alcohols or phenols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/127Liposomes
    • A61K9/1277Processes for preparing; Proliposomes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
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    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
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    • C11D17/0026Structured liquid compositions, e.g. liquid crystalline phases or network containing non-Newtonian phase
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10M2203/022Well-defined aliphatic compounds saturated
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10M2203/024Well-defined aliphatic compounds unsaturated
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

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  • Crystallography & Structural Chemistry (AREA)
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  • Textile Engineering (AREA)
  • Toxicology (AREA)
  • Biophysics (AREA)
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  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
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Description

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

本発明は脂質小球の分散液から成る化粧用分散
液に関する。この種の水性分散液についてはフラ
ンス特許第2315991号明細書(特開昭52−6375)
に記載されている。 前記分散液中の脂質小球は、水相の層によつて
互いに隔てられている2個またはそれ以上の脂質
層から成る構造に特徴がある。従つて、水溶性活
性物質例えば薬学的または化粧用物質を脂質層の
間の水性部分にとじこめて(封入して)外部の環
境から保護するのに、この脂質小球は役立つ。 前記フランス特許には脂質小球の水性分散液の
新規な製法も記載されている。それによれば、ま
ず小球の同心円状の膜を形成することになる脂質
と小球中にとりこまれるべき水性溶液とを接触さ
せ、その際脂質の親油性/親水性の比はとりこま
れることになる水または水性相中で脂質がふくら
んで薄膜相を形成する程度にし、次に分散液の小
球の外側の連続相となるべき水性溶液を薄膜相に
加え、三番目に全体をはげしくかきまぜて、前記
のとりこまれるべき水性相を同心円状の膜の間に
とじこめている形の小球の分散液を得る。 前記フランス特許によれば小球の同心円状薄膜
を形成するためにはイオン性または非イオン性の
両親媒性(amphiphilic)脂質を使うことができ
る。非イオン性両親媒性脂質の中で好ましいのは
次のものである。 直鎖または分枝鎖のそれぞれ次の式 R―(OCH2―CHOHCH2)―oOH および (この式では1〜6までの整数、Rは炭素原子
12〜30個を含む飽和または不飽和の直鎖または分
枝鎖状の脂肪鎖、ラノリンアルコールの炭化水素
残基または長鎖α―ジオールの2―ヒドロキシア
ルキル残基である) で表わされるポリグリセロールエーテル、ポリオ
キシエチレン化された脂肪アルコール、オキシエ
チレン化されたかまたはされていないポリオール
エステルとりわけポリオキシエチレン化されたソ
ルビツトのエステルおよび天然または合成糖脂質
例えばセレブロシド。 脂質小球にとじこめることのできる化粧用活性
物質の中でフランス特許明細書に挙げられている
のは例えば皮膚の手入れ用品例えば湿潤剤、人工
日焼け剤、皮膚着色剤、水溶性日焼け防止剤、発
汗防止剤、防臭剤、収れん剤、清涼剤、養毛剤、
癒創薬、角質溶解剤、脱毛剤、香水および動物ま
たは植物組織からの抽出物である。 脂質小球の水性分散液の形の前記の化粧用組成
物は、油と水の乳剤の形の従来の組成物に比べ
て、攻撃性が少ないすなわち皮膚に施した時に刺
激が少ないという長所がある。 本発明の目的は、小球の分散液が持つ利点と化
粧用油による利点とを一緒に持つことができる、
脂質小球の水性分散液から成る化粧用組成物を開
示することである。 従つて本発明は少なくとも1種の非イオン性両
親媒性脂質から成る分子層により水性相を内部に
封入した脂質小球をその外側の水性相中に分散さ
せた脂質小球分散液において、液体トリグリセリ
ド、式R―COOR′(式中、Rは炭素原子8〜20個
を含む高級脂肪酸残基であり、R′は炭素原子3
〜20個を含む分枝炭化水素鎖である)で表わされ
る分枝鎖アルコールの脂肪酸エステルおよびジヨ
ジヨバ油から成る群から選んだ少なくとも1種の
油を、前記した脂質小球の外側の水性相中に分散
させたことを特徴とする、化粧用組成物に関す
る。 驚くべきことに、非イオン性両親媒性脂質の小
球を使うと、通常の乳化剤の添加なしに、しかも
小球の破壊を起こすことなく水中油型分散液を安
定化できることがわかつた。しかしよく知られて
いるように乳剤の安定性は主に乳化剤の存在に依
存するものであり、乳化剤の分子は油滴の表面に
吸着して一種の連続した膜を形成し、この膜は例
えばシヨツクを受けた時にとなりあつた2つの小
滴が直接接触するのを防ぐ。従つて当業者は本発
明の場合は小球中の非イオン性両親媒性脂質が乳
化剤と同様の役割をして油滴の表面に吸着すると
考えるであろうがこのような安定化では小球の同
心円状膜が破壊される効果がある。本発明の場合
はそのようなものではなく、驚くべきことに本発
明の非イオン性両親媒性脂質は小球は無傷のまま
油滴のまわりに分散し、外側の水性相中の前記の
植物油少なくとも1種の分散液を安定化すること
ができる。 米国特許第3957971号明細書にはイオン性両親
媒性物質の小球またはリポソームの分散液が記載
されており、これは化粧用クリームまたはローシ
ヨン組成物の一部すなわち油中水型または水中油
乳剤をなすものである。本発明の小球はイオン性
両親媒性物質ではなく非イオン性両親媒性物質か
ら成る。さらに前記の種類の植物油の水中分散液
安定化させることはリポソームにはできないこと
がわかつたのに対して、本発明による非イオン性
両親媒性物質の小球はそのような分散液を安定化
できる。 本発明による化粧用組成物は2段階で製造す
る。第一段階ではフランス特許第2315991号また
は同第2221122号明細書のいずれかに記載の方法
により非イオン性両親媒性脂質から小球の水性分
散液を製造する。第2段階では小球の水性分散液
を製造した後に特に油を加える。振とうしてこの
油を外側の水性相に分散させる。 好ましくは本発明の化粧用組成物は、全組成物
重量に対して、小球の壁を構成する非イオン性両
親媒性脂質2〜10重量%および分散した油2〜40
重量%を含む。非イオン性両親媒性脂質と分散し
た油との比は有利には0.2〜1:1である。 本発明の組成物に含ませることのできる油は、
液体トリグリセリド、式―COO―R′(式中、Rは
炭素原子8〜20個を含む高級脂肪酸の残基、
R′は炭素原子3〜20訣個を含む分枝状炭化水素
鎖を表わす)で表わされる分枝鎖アルコールの脂
肪酸から成る群から選ぶ。液体トリグリセリドの
うち特に挙げられるのはヒマワリ油、トウモロコ
シ油、大豆油、ヒヨウタン油、ブドウ種子油、お
よびグリセリントリカプロカプリレートである。
式R―COO―R′の分枝鎖アルコール脂肪酸エス
テルの中ではとりわけパーセリン油が挙げられ
る。 本発明の組成物の化粧用活性物質は小球の内側
または外側にとじこめることがでる。従つて好ま
しい具体例においては組成物の油性相は1種また
はそれ以上の脂溶性化粧用物質を含む。本発明の
組成物の製造においてはこれらの物質をあらかじ
め油に溶かし、それを脂質小球の分散液に加え
る。これら脂溶性化粧用活性物質の中で特に挙げ
られるのは日焼け防止フイルター例えば2―エチ
ルヘキシル―パラ―ジメチルアミノベンゾエート
または乾燥したり老衰した皮膚の状態を改善する
物質とりわけけん化できない物質例えば大豆およ
びアボガドからの誘導体、トコフエロール、ビタ
ミンEおよびFおよび酸化防止剤である。 小球の分散液の媒質を構成している水中油型分
散液は添加剤少なくとも1種とりわけゲル化剤ま
たは香料を含むことができる。添加剤は油と同時
に分散液に加える。ゲル剤は組成物の全重量に対
して0.1〜2重量%の範囲内の濃度で加えること
ができる。使うことのできるゲル化剤の中で特に
挙げられるのはセルロース誘導体例えばヒドロキ
シエチルセルロース、合成ポリマー、藻類誘導体
例えばサテイアゴム(satiagum)またはさらに
天然ゴム例えばトラガカントである。ヒドロキシ
エチルセルロース、〓CARBOPOL 940〓の名で
市販されているカルボキシビニル酸の混合物、サ
テイアゴムまたはトラガカントをゲル化剤として
使うのが好ましい。 本発明の化粧用組成物の中の小球の同心円状薄
膜を構成する非イオン性両親媒性脂質は、 それぞれ式 R―(OCH2CHOH―CH2o―OH または (式中、nは2〜6の数であり、Rは炭素原子16
〜20個を含む直鎖または分枝鎖状飽和脂肪鎖また
はラノリンアルコールの炭化水素残基である) で表わされる直鎖または分枝鎖ポリグリセリンエ
ーテルまたは(式中のR脂肪鎖右端接続部のメチ
レン基がカルボニル基である)エステル、および ポリオキシエチレン化されたステリン である。 非イオン性両親媒性脂質と、とじこめられる水
性相とを接触させて平らな薄膜相を形成する時、
例えば小球の透過性や表面電荷を変えるために脂
質と一緒に種種の助剤を組み合わせておくことが
できる。このような助剤として所望により加えら
れるのは、長鎖アルコールおよびジオール、ステ
リンとりわけコレステリンおよびβ―シトステリ
ン、長鎖アミンおよびその第四アンモニウム誘導
体とりわけジドデシルジメチルアンモニウムブロ
ミド、ヒドロキシアルキルアミン、ポリオキシエ
チル化脂肪アミン、長鎖アミノアルコールエステ
ルおよびその塩および第四アンモニウム誘導体、
脂肪アルコールのリン酸エステルとりわけジセチ
ルホスフエート、アルキル硫酸塩例えばセチル硫
酸ナトリウム、およびポリマー例えばポリペプチ
ドおよびタンパク質である。 前記の助剤のほか、防腐剤例えばメチル―パラ
―ヒドロキシベンゾエートを加えることができ
る。 小球の内側または外側の水性相は通常、顔、手
または体の手入れに使う水溶性化粧用物質を含む
ことができる。これらの物質の中で特に挙げるこ
とできるのは湿潤剤例えばグリセリン、ソルビツ
ト、ペンタエリトリツト、イノシツトおよびピロ
リドンカルボン酸およびその塩、人工日焼け剤例
えばジヒドロキシアセトン、エリトルロース、グ
リセルアルデヒドおよびγ―ジアルデヒド例えば
酒石酸アルデヒド、皮膚着色剤、日焼け防止剤、
発汗防止剤、防臭剤、収れん剤、清涼剤、養毛
剤、癒創薬、角質溶解剤、脱毛剤、香水、動物ま
たは植物からの抽出物例えばタンパク質、羊水お
よび多糖類さらに抗脂漏剤である。 次にいくつかの具体例を挙げて本発明をさらに
説明するが、これらは決して本発明の範囲を限定
するものではない。 以下の例に記載の化粧用組成物は2段階で製造
する。第1段階ではフランス特許第2315991号に
記載の方法に従つて水性分散液を製造する。 脂質小球の水性分散液は、 非イオン性両親媒性脂質、 ステリン例えばコレステリンまたはβ―シトス
テリン、 所望によりジセチルホスフエート、 所望により水溶性の化粧用活性物質、および防
腐剤を含んでいてもよい、脱イオン水から製造す
る。 第2段階では、油を加え、雰囲気温度好ましく
は約40℃で機械的にはげしくかきまぜ、分散させ
る。この第2段階で脂溶性化粧用物質、香料およ
び(または)ゲル化剤を所望によつて加える。 例 1 本発明による化粧用組成物と公知のタイプの化
粧用組成物との比較実験 2種類の組成物(A)と(B)とを製造する。組成物(B)
の製造においては油を加える第2段階を行なわな
いことのほかは、(A)と(B)とは全く同じである。 組成物(A)は次の成分を含む。 第1段階 式 (式中、Rはヘキサデシル基でありの統計的な
平均値は3である) で表わされる非イオン性両親媒性脂質 3.8g β―シトステリン 3.8g ジセチルホスフエート 0.4g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 66.7g 第2段階 前記分散液にヒマワリ油25gを加え、全体を機
械的に激しくかきまぜて完成した分散液を得る。 化粧用組成物(B)も同じ方法で製造するが第2段
階でヒマワリ油25gを加える代わりに同量の脱イ
オン水を加える。 従つて化粧用組成物(A)はヒマワリ油25%を含む
点で、化粧用組成物(B)と異なる。 (1) 化粧用組成物(A)および(B)を広げる時の皮膚の
摩擦係数の測定 化粧用組成物(A)または(B)を広げる時の皮膚の
摩擦係数は被検者の前腕で回転運動している感
知器により測定する。感知器がそれ自身回転す
る間、感知器の動く範囲内の抵抗力の変化を記
録する。感知器には一定の力(20または50g)
をかける。 次の結果を得る。
The present invention relates to cosmetic dispersions consisting of dispersions of lipid globules. This type of aqueous dispersion is described in French Patent No. 2315991 (Japanese Unexamined Patent Publication No. 52-6375).
It is described in. The lipid globules in the dispersion are characterized by a structure consisting of two or more lipid layers separated from each other by a layer of aqueous phase. The lipid globules thus serve to protect water-soluble active substances, such as pharmaceutical or cosmetic substances, from the external environment by entrapping them in the aqueous part between the lipid layers. The French patent also describes a new method for preparing aqueous dispersions of lipid globules. According to this, the lipids that will form the concentric membranes of the globules are brought into contact with the aqueous solution to be incorporated into the globules, and the lipophilic/hydrophilic ratio of the lipids is maintained. The lipids swell in the water or aqueous phase to such an extent that they form a thin film phase, then the aqueous solution that is to become the continuous phase outside the globules of the dispersion is added to the thin film phase, and third the whole is stirred vigorously. A dispersion of globules is thus obtained in which the aqueous phase to be incorporated is confined between concentric membranes. According to the French patent, ionic or nonionic amphiphilic lipids can be used to form concentric thin films of globules. Among the nonionic amphiphilic lipids, the following are preferred. Straight-chain or branched, respectively, with the following formulas R—(OCH 2 —CHOHCH 2 )— o OH and (In this formula, an integer from 1 to 6, R is a carbon atom
12 to 30 saturated or unsaturated linear or branched aliphatic chains, hydrocarbon residues of lanolin alcohols or 2-hydroxyalkyl residues of long-chain α-diols) Ethers, polyoxyethylated fatty alcohols, oxyethylated or non-oxyethylated polyol esters, especially polyoxyethylated esters of sorbitol, and natural or synthetic glycolipids such as cerebrosides. Among the cosmetic active substances that can be entrapped in lipid globules, the French patent specification mentions, for example, skin care products such as humectants, artificial tanning agents, skin colorants, water-soluble sunscreens, perspiration. Preventive agents, deodorants, astringents, refreshing agents, hair tonics,
Healing medicines, keratolytic agents, depilatory agents, perfumes and extracts from animal or plant tissues. Said cosmetic composition in the form of an aqueous dispersion of lipid globules has the advantage, compared to conventional compositions in the form of an oil and water emulsion, of being less aggressive, i.e. less irritating when applied to the skin. be. The object of the present invention is to combine the advantages of a dispersion of globules with those of a cosmetic oil.
A cosmetic composition comprising an aqueous dispersion of lipid globules is disclosed. Accordingly, the present invention provides a lipid globule dispersion in which lipid globules having an aqueous phase encapsulated inside by a molecular layer composed of at least one nonionic amphipathic lipid are dispersed in an aqueous phase outside the lipid globule dispersion. Triglyceride, formula R-COOR', where R is a higher fatty acid residue containing 8 to 20 carbon atoms, and R' is a
At least one oil selected from the group consisting of fatty acid esters of branched chain alcohols (which are branched hydrocarbon chains containing up to 20 branched hydrocarbon chains) and bittersweet oil is added to the aqueous phase outside the lipid globules as described above. It relates to a cosmetic composition, characterized in that it is dispersed in. Surprisingly, it has been found that oil-in-water dispersions can be stabilized using nonionic amphiphilic lipid globules without the addition of conventional emulsifiers and without globule destruction. However, as is well known, the stability of emulsions mainly depends on the presence of emulsifiers, whose molecules adsorb to the surface of oil droplets and form a kind of continuous film, which can be e.g. Prevents direct contact between two droplets that form when being shot. Therefore, those skilled in the art would think that in the case of the present invention, the nonionic amphipathic lipids in the globules play a role similar to that of an emulsifier and are adsorbed onto the surface of the oil droplets; The effect is that the concentric membranes of the membrane are destroyed. This is not the case with the present invention, and surprisingly, the nonionic amphiphilic lipids of the present invention disperse around the oil droplets with the globules intact, leaving the aforementioned vegetable oil in the outer aqueous phase. At least one dispersion can be stabilized. U.S. Pat. No. 3,957,971 describes globular or liposomal dispersions of ionic amphiphiles, which may be part of cosmetic cream or lotion compositions, i.e. water-in-oil or oil-in-water emulsions. It is something that does. The globules of the present invention consist of non-ionic rather than ionic amphiphiles. Furthermore, it has been found that liposomes are not able to stabilize dispersions of vegetable oils in water of the type mentioned above, whereas spherules of nonionic amphiphiles according to the invention can stabilize such dispersions. can. The cosmetic composition according to the invention is produced in two stages. In the first step, an aqueous dispersion of globules is prepared from nonionic amphiphilic lipids by the method described in either FR 2 315 991 or FR 2 221 122. In the second stage, especially after the preparation of the aqueous dispersion of the globules, oil is added. Shake to disperse this oil into the outer aqueous phase. Preferably, the cosmetic composition of the invention contains 2 to 10% by weight of nonionic amphipathic lipids constituting the walls of the globules and 2 to 40% of dispersed oil, based on the total composition weight.
Including weight %. The ratio of nonionic amphiphilic lipid to dispersed oil is advantageously from 0.2 to 1:1. Oils that can be included in the compositions of the invention include:
Liquid triglyceride, formula -COO-R', where R is a residue of a higher fatty acid containing 8 to 20 carbon atoms;
R' represents a branched hydrocarbon chain containing from 3 to 20 carbon atoms. Among liquid triglycerides, particular mention may be made of sunflower oil, corn oil, soybean oil, calabash oil, grapeseed oil, and glycerin tricaprocaprylate.
Among the branched alcohol fatty acid esters of the formula R--COO--R', mention may be made, inter alia, of parcellin oil. The cosmetically active substance of the composition according to the invention can be confined inside or outside the globule. Accordingly, in preferred embodiments, the oily phase of the composition comprises one or more lipophilic cosmetic substances. In preparing the compositions of the invention, these substances are dissolved in oil beforehand and added to the dispersion of lipid globules. Among these fat-soluble cosmetic active substances, mention may be made in particular of sunscreen filters, such as 2-ethylhexyl-para-dimethylaminobenzoate, or of substances that improve the condition of dry and aged skin, especially from non-saponifiable substances such as soybean and avocado. derivatives, tocopherols, vitamins E and F and antioxidants. The oil-in-water dispersion constituting the medium for the dispersion of globules can contain at least one additive, especially a gelling agent or a perfume. Additives are added to the dispersion at the same time as the oil. Gel agents can be added in concentrations ranging from 0.1 to 2% by weight relative to the total weight of the composition. Among the gelling agents that can be used, particular mention may be made of cellulose derivatives such as hydroxyethylcellulose, synthetic polymers, algal derivatives such as satiagum or even natural gums such as tragacanth. Hydroxyethylcellulose, a mixture of carboxyvinylic acids sold under the name CARBOPOL 940, gum satya or tragacanth are preferably used as gelling agents. The nonionic amphiphilic lipids constituting the concentric thin films of globules in the cosmetic composition of the present invention have the formula R-( OCH2CHOH - CH2 ) o -OH or respectively (In the formula, n is a number from 2 to 6, R is a carbon atom 16
A straight or branched polyglycerin ether represented by (which is a straight or branched saturated fatty chain containing ~20 hydrocarbon residues of lanolin alcohol) or (where the methylene group is a carbonyl group), and polyoxyethylenated sterine. When a nonionic amphiphilic lipid is brought into contact with an entrapped aqueous phase to form a flat thin film phase,
For example, various auxiliaries can be combined with the lipids to alter the permeability or surface charge of the globules. Optionally added as such auxiliaries are long-chain alcohols and diols, sterine, especially cholesterin and β-sitosterine, long-chain amines and their quaternary ammonium derivatives, especially didodecyldimethylammonium bromide, hydroxyalkylamines, polyoxy Ethylated fatty amines, long chain amino alcohol esters and their salts and quaternary ammonium derivatives,
Phosphate esters of fatty alcohols are especially dicetyl phosphate, alkyl sulfates such as sodium cetyl sulfate, and polymers such as polypeptides and proteins. In addition to the auxiliaries mentioned above, preservatives such as methyl-para-hydroxybenzoate can be added. The aqueous phase inside or outside the globule can typically contain water-soluble cosmetic substances for use in caring for the face, hands or body. Among these substances, mention may be made in particular of humectants such as glycerin, sorbitol, pentaerythritol, inosytate and pyrrolidone carboxylic acids and their salts, artificial tanning agents such as dihydroxyacetone, erythrulose, glyceraldehyde and gamma-dialdehydes such as tartaric aldehyde, skin colorants, sunscreens,
Antiperspirants, deodorants, astringents, cooling agents, hair nourishing agents, healing agents, keratolytic agents, depilatory agents, perfumes, extracts from animals or plants such as proteins, amniotic fluid and polysaccharides, and also antiseborrheic agents. Next, the present invention will be further explained by giving some specific examples, but these are not intended to limit the scope of the present invention. The cosmetic compositions described in the examples below are manufactured in two stages. In the first step, an aqueous dispersion is prepared according to the method described in French Patent No. 2,315,991. The aqueous dispersion of lipid globules comprises a nonionic amphipathic lipid, a sterin such as cholesterin or β-sitosterin, optionally dicetyl phosphate, optionally a water-soluble cosmetic active substance, and a preservative. It is also made from deionized water. In the second stage, the oil is added and dispersed by vigorous mechanical stirring at an ambient temperature, preferably about 40°C. In this second step, fat-soluble cosmetic substances, fragrances and/or gelling agents are optionally added. Example 1 Comparative experiments between the cosmetic composition according to the invention and cosmetic compositions of the known type Two compositions (A) and (B) are prepared. Composition (B)
(A) and (B) are exactly the same except that the second step of adding oil is not performed in the production of. Composition (A) contains the following ingredients. 1st stage formula (In the formula, R is a hexadecyl group and the statistical average value is 3) Nonionic amphipathic lipid represented by 3.8g β-sitosterin 3.8g dicetyl phosphate 0.4g Methyl-para-hydroxybenzoate 0.3 g Deionized water 66.7 g 2nd step Add 25 g of sunflower oil to the above dispersion and stir the whole vigorously mechanically to obtain the finished dispersion. Cosmetic composition (B) is prepared in the same way, but instead of adding 25 g of sunflower oil in the second stage, the same amount of deionized water is added. Cosmetic composition (A) thus differs from cosmetic composition (B) in that it contains 25% sunflower oil. (1) Measurement of the skin friction coefficient when spreading cosmetic compositions (A) and (B) The skin friction coefficient when spreading cosmetic compositions (A) or (B) was measured on the forearm of the subject. Measured by a rotating sensor. While the sensor rotates itself, it records the change in resistance force within the range of movement of the sensor. Constant force on the sensor (20 or 50g)
multiply. I get the following result:

【表】 脂質小球の油を含有しない水性分散液である
組成物(B)は皮膚の摩擦係数が実質的に増すのに
対して、本発明による、脂質小球の油を含有す
る水性分散液である組成物(A)では(B)とは反対の
効果を得る。皮膚の摩擦係数がこのように実質
的に減少するということは、化粧品としては本
発明の組成物(A)でやわらかさが得られることに
なる。 (2) 前記化粧用組成物(A)および(B)の適用前または
適用後における、ヒト角質層の弾性係数の生体
外での測定 皮膚の弾性係数を測定するための実験装置を
使つて測定を行なつた。この種の実験装置はフ
ランス特許出願第78/25149号明細書に開示さ
れている。 実験条件は次のようである。 相対湿度:72±2% 温 度:30±0.2℃ 適用した組成物の量:5mg/cm2 次の結果を得る。
Table: Composition (B), which is an oil-free aqueous dispersion of lipid globules, substantially increases the skin friction coefficient, whereas composition (B), which is an oil-free aqueous dispersion of lipid globules, substantially increases the coefficient of friction of the skin. Composition (A), which is a liquid, has the opposite effect to (B). This substantial reduction in the coefficient of friction of the skin means that the composition (A) of the present invention provides softness as a cosmetic product. (2) In vitro measurement of the elastic modulus of the human stratum corneum before or after application of the cosmetic compositions (A) and (B) Measured using an experimental device for measuring the elastic modulus of the skin I did this. An experimental device of this type is disclosed in French patent application no. 78/25149. The experimental conditions were as follows. Relative humidity: 72±2% Temperature: 30±0.2°C Amount of composition applied: 5 mg/cm 2 The following results are obtained.

【表】 この結果から、油相を持たない小球の分散液を
使う場合と、油相を持つ小球の分散液を使う場合
の角質のやわらかさの違いが明らかにわかる。 例 2 体の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 4.5g β―シトステリン 4.5g ジセチルホスフエート 1.0g メチル―パラ―ヒドロキシベンゾエート 0.3g ピロリドンカルボン酸のナトリウム塩 2.0g 脱イオン水 56.5g 第2段階 第1段階で得た脂質小球の分散液に次の物質を
加える。 香 料 0.4g ヒマワリ油 10.0g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.4g トリエタノールアミン 0.4g 脱イオン水 20.0g 例 3 顔の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、nは2であ
る) で表わされる非イオン性両親媒性脂質 6.0g コレステリン 1.6g ジセチルホスフエート 0.4g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 61.1g 第2段階 第1段階で得た脂質小球の分散液に次の物質を
加える。 香 料 0.2g ブドウ種子油 20.0g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.2g トリエタノールアミン 0.2g 脱イオン水 10.0g 例 4 手の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 ポリオキシエチレン化されたフイトステリン
(平均値は5で統計的に分布している) 6.0g コレステリン 2.0g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 45.7g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 香 料 0.2g ジヨジヨバ油 25.0g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.4g トリエタノールアミン 0.4g 脱イオン水 20.0g 例 5 体の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 4.0g コレステリン 4.0g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 45.5g 第2段階 第1段階で得た脂質小球の分散液に次の物質を
加える。 香 料 0.4g トウモロコシ油 25.0g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.4g トリエタノールアミン 0.4g 脱イオン水 20.0g 例 6 顔の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 0.95g β―シトステリン 0.95g ジセチルホスフエート 0.10g メチル―パラ―ヒドロキシベンゾエート 0.30g 脱イオン水 64.80g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 香 料 0.4g 大豆油 10.0g 大豆から誘導されたケン化されない物質 2.0g 〓Natroso 250 HHR〓の名で市販されている
ヒドロキシエチルセルロース 0.5g 脱イオン水 20.0g 例 7 日焼け防止液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 3.6g β―シトステリン 3.6g ジドデシルジメチルアンモニウムブロミド 0.8g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 45.9g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 香 料 0.4g ヒヨウタン油 22.0g 2―エチルヘキシル―パラ―ジメチルアミノベ
ンゾエート 3.0g トラガカントゴム 0.4g 脱イオン水 20.0g 例 8 手の手入れ用液 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 3.8g β―シトステリン 3.8g ジセチルホスフエート 0.4g メチル―パラ―ヒドロキシベンゾエート 0.3g グリセリン 3.0g 脱イオン水 42.5g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 香 料 0.2g パーセリン油 25.0g サテイアゴム 1.0g 脱イオン水 20.0g 例 9 体の手入れ用液 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 3.8g β―シトステリン 3.8g ジセチルホスフエート 0.4g メチル―パラ―ヒドロキシベンゾエート 0.3g 脱イオン水 60.5g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 香 料 0.4g グリセリン―トリカプロカプリレート 10.0g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.4g トリエタノールアミン 0.4g 脱イオン水 20.0g 例 10 顔の手入れ用クリーム 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 (式中、Rはヘキサデシル基であり、の統計的
な平均値は3である) で表わされる非イオン性両親媒性脂質 3.8g β―シトステリン 3.8g ジセチルホスフエート 0.4g 防腐剤 0.3g 脱イオン水 47.6g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 ヒマワリ油 35.0g 香 料 0.6g 〓CARBOPOL 940〓の名で市販されているカ
ルボキシビニル酸混合物 0.2g トリエタノールアミン 0.2g 脱イオン水 8.1g 例 11 顔の手入れ用クリーム 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 C16H33O(CH2CHOHCH2O)―2H で表わされる非イオン性両親媒性脂質 3.80g コレステリン 3.80g ジセチルホスフエート 0.40g 防腐剤 0.30g グリセリン 3.00g 脱イオン水 56.68g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 ゴマ油 16.00g 香 料 0.20g 〓Goodrich社から〓CARBOPOL 940〓の名
で市販されているカルボキシビニル酸混合物
0.42g トリエタノールアミン 0.40g 脱イオン水 15.00g 例 12 顔の手入れ用クリーム 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 式 C15H31COO(CH2CHOHCH2O)―2H で表わされる非イオン性両親媒性脂質 3.80g コレステリン 3.80g ジセチルホスフエート 0.40g 防腐剤 0.30g グリセリン 3.00g 脱イオン水 56.68g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 ゴマ油 16.00g 香 料 0.20g Goodrich社から〓CARBOPOL 940〓の名で
市販されているカルボキシビニル酸混合物
0.42g トリエタノールアミン 0.40g 脱イオン水 15.00g 例 13 顔の手入れ用クリーム 第1段階 前記の方法に従い、次の物質から脂質小球の水
性分散液を製造する。 CapitalCity社から〓CAPROL 6G2S〓の名で
市販されているグリセリン約6モルを含むポリ
グリセリンのジステアリン酸エステル 3.80g コレステリン 3.80g ジセチルホスフエート 0.40g 防腐剤 0.30g グリセリン 3.00g 脱イオン水 47.68g 第2段階 第1段階で得た小球の分散液に次の物質を加え
る。 マカダミア油 25.00g 香 料 0.20g Goodrich社から〓CARBOPOL 940〓の名で
市販されているカルボキシビニル酸混合物
0.42g トリエタノールアミン 0.40g 脱イオン水 15.00g 当然のことながら以上の具体例は本発明を限定
するものではなく、本発明の範囲を逸脱しない限
り、種種の望ましい変化変形が可能である。
[Table] This result clearly shows the difference in the softness of the stratum corneum when using a dispersion of globules without an oil phase and when using a dispersion of globules with an oil phase. Example 2 Body Care Liquid Stage 1 According to the method described above, an aqueous dispersion of lipid globules is prepared from the following materials: formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3) Nonionic amphiphilic lipid represented by 4.5g β-sitosterin 4.5g Dicetyl phosphate 1.0g Methyl-para-hydroxy Benzoate 0.3g Sodium salt of pyrrolidone carboxylic acid 2.0g Deionized water 56.5g Second stage Add the following substances to the dispersion of lipid globules obtained in the first stage. Fragrance 0.4 g Sunflower oil 10.0 g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.4 g Triethanolamine 0.4 g Deionized water 20.0 g Example 3 Facial care liquid 1st stage According to the above method, An aqueous dispersion of lipid globules is prepared from the following materials: formula (In the formula, R is a hexadecyl group and n is 2) Nonionic amphiphilic lipid represented by 6.0g Cholesterin 1.6g Dicetyl phosphate 0.4g Methyl-para-hydroxybenzoate 0.3g Deionized water 61.1g Second stage Add the following substances to the lipid globule dispersion obtained in the first stage. Flavoring 0.2 g Grape seed oil 20.0 g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.2 g Triethanolamine 0.2 g Deionized water 10.0 g Example 4 Hand care liquid Step 1 Follow the above method , prepare an aqueous dispersion of lipid globules from the following materials: Polyoxyethylated phytosterin (average value 5, statistically distributed) 6.0 g Cholesterin 2.0 g Methyl-para-hydroxybenzoate 0.3 g Deionized water 45.7 g Second stage Small particles obtained in the first stage Add the following substances to the sphere dispersion. Fragrance 0.2g Perfume oil 25.0g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.4g Triethanolamine 0.4g Deionized water 20.0g Example 5 Body care liquid 1st stage According to the above method, An aqueous dispersion of lipid globules is prepared from the following materials: formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3) Nonionic amphipathic lipid represented by 4.0 g Cholesterin 4.0 g Methyl-para-hydroxybenzoate 0.3 g Deionized water 45.5 g Second stage Add the following substances to the dispersion of lipid globules obtained in the first stage. Fragrance 0.4 g Corn oil 25.0 g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.4 g Triethanolamine 0.4 g Deionized water 20.0 g Example 6 Facial Care Liquid Stage 1 According to the above method, An aqueous dispersion of lipid globules is prepared from the following materials: formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3.) Benzoate 0.30g Deionized water 64.80g Second stage Add the following substances to the dispersion of globules obtained in the first stage. Fragrance 0.4 g Soybean oil 10.0 g Non-saponifiable substances derived from soybeans 2.0 g Hydroxyethylcellulose, commercially available under the name Natroso 250 HHR 0.5 g Deionized water 20.0 g Example 7 Sunscreen liquid first stage As described above According to the method, an aqueous dispersion of lipid globules is prepared from the following materials: formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3) Nonionic amphiphilic lipid represented by 3.6g β-sitosterin 3.6g Didodecyldimethylammonium bromide 0.8g Methyl-para- Hydroxybenzoate 0.3g Deionized water 45.9g Second stage Add the following substances to the dispersion of globules obtained in the first stage. Fragrance 0.4g Calabash oil 22.0g 2-Ethylhexyl-para-dimethylaminobenzoate 3.0g Gum tragacanth 0.4g Deionized water 20.0g Example 8 Hand care liquid Step 1 According to the method described above, lipid globules were prepared from the following substances: Produce an aqueous dispersion. formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3) Nonionic amphipathic lipid represented by Benzoate 0.3g Glycerin 3.0g Deionized water 42.5g Second stage Add the following substances to the dispersion of globules obtained in the first stage. Perfume 0.2 g Parcellin oil 25.0 g Satya gum 1.0 g Deionized water 20.0 g Example 9 Body care liquid An aqueous dispersion of lipid globules is prepared from the following materials according to the method described above. formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3) Nonionic amphipathic lipid represented by Benzoate 0.3g Deionized water 60.5g Second stage Add the following substances to the dispersion of globules obtained in the first stage. Fragrance 0.4g Glycerin-tricaprocaprylate 10.0g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.4g Triethanolamine 0.4g Deionized water 20.0g Example 10 Facial Care Cream Stage 1 Said An aqueous dispersion of lipid globules is prepared from the following materials according to the method of: formula (In the formula, R is a hexadecyl group, and the statistical average value of is 3.) Ionized water 47.6g Second stage Add the following substances to the dispersion of small spheres obtained in the first stage. Sunflower oil 35.0 g Fragrance 0.6 g Carboxyvinylic acid mixture commercially available under the name CARBOPOL 940 0.2 g Triethanolamine 0.2 g Deionized water 8.1 g Example 11 Facial care cream Stage 1 According to the above method, An aqueous dispersion of lipid globules is prepared from the following materials: Nonionic amphipathic lipids with the formula C 16 H 33 O (CH 2 CHOHCH 2 O) - 2 H 3.80 g Cholesterin 3.80 g Dicetyl phosphate 0.40 g Preservative 0.30 g Glycerin 3.00 g Deionized water 56.68 g Step 2 Add the following substances to the dispersion of globules obtained in step 1. Sesame oil 16.00g Flavoring 0.20g Carboxyvinylic acid mixture commercially available from Goodrich under the name CARBOPOL 940
0.42 g Triethanolamine 0.40 g Deionized water 15.00 g Example 12 Facial Care Cream Stage 1 An aqueous dispersion of lipid globules is prepared from the following materials according to the method described above. Nonionic amphipathic lipids represented by the formula C 15 H 31 COO (CH 2 CHOHCH 2 O) - 2 H 3.80 g Cholesterin 3.80 g Dicetyl phosphate 0.40 g Preservative 0.30 g Glycerin 3.00 g Deionized water 56.68 g Step 2 Add the following substances to the dispersion of globules obtained in step 1. Sesame oil 16.00g Flavoring 0.20g Carboxyvinylic acid mixture commercially available from Goodrich under the name CARBOPOL 940
0.42 g Triethanolamine 0.40 g Deionized water 15.00 g Example 13 Facial Care Cream Stage 1 An aqueous dispersion of lipid globules is prepared from the following materials according to the method described above. Polyglycerin distearate containing approximately 6 moles of glycerin, commercially available from Capital City under the name CAPROL 6G2S 3.80 g Cholesterin 3.80 g Dicetyl phosphate 0.40 g Preservative 0.30 g Glycerin 3.00 g Deionized water 47.68 g Step 2 Add the following substances to the dispersion of globules obtained in step 1. Macadamia oil 25.00g Flavoring 0.20g Carboxyvinylic acid mixture commercially available from Goodrich under the name CARBOPOL 940
0.42 g Triethanolamine 0.40 g Deionized water 15.00 g It will be understood that the above specific examples are not intended to limit the invention, and that various desirable changes and modifications are possible without departing from the scope of the invention.

Claims (1)

【特許請求の範囲】 1 少なくとも1種の非イオン性両親媒性脂質か
ら成る分子層により水性相を内部に封入した脂質
小球をその外側の水性相中に分散させた脂質小球
分散液において、液体トリグリセリド、式R―
COOR′(式中、Rは炭素原子8〜20個を含む高級
脂肪酸残基であり、R′は炭素原子3〜20個を含
む分枝状炭化水素鎖である)で表わされる分枝鎖
アルコールの脂肪酸エステルおよびジヨジヨバ油
から成る群から選んだ少なくとも1種の油を、前
記した脂質小球の外側の水性相中に分散させたこ
とを特徴とする、化粧用組成物。 2 液体トリグリセリドとして、ヒマワリ油、ト
ウモロコシ油、大豆油、ヒヨウタン油、ブドウ種
子油およびグリセリン・トリカプロカプリレート
から成る群から選んだものを使つた、前項1に記
載の組成物。 3 式R―COOR′の分枝鎖アルコール脂肪酸エ
ステルとして、パーセリン(Purcellin)油を使
つた前項1に記載の組成物。 4 組成物の全重量に対して、脂質小球の壁を構
成する非イオン性両親媒性脂質を2〜10重量%使
い脂質小球の外側の水性相中に分散する油を2〜
40重量%使い、そして非イオン性両親媒性脂質と
油との比を0.2:1〜1:1とした、前項1〜3
のいずれかに記載の組成物。 5 脂質小球の外側の水性相中にゲル化剤を組成
物の全重量に対して0.1〜2重量%含ませた、前
項1〜4のいずれかに記載の組成物。 6 ゲル化剤として、セルロース誘導体、合成ポ
リマー、藻類誘導体または天然ゴムから成る群か
ら選んだものを使つた、前項5に記載の組成物。 7 脂質小球の外側の水性相中に少なくとも1種
の香料および(または)1種またはそれ以上の脂
溶性化粧用物質を含ませた、前項1〜6のいずれ
かに記載の組成物。 8 脂溶性化粧用物質として、日焼け防止フイル
ター、乾燥または老衰した皮膚の状態を改良する
物質または酸化防止剤から選んだものを使つた、
前項7に記載の組成物。 9 脂質小球の壁を構成する非イオン性両親媒性
脂質として、 式 R―(OCH2CHOHCH2)―oOH または (式中、nは2〜6の数であり、Rは炭素原子16
〜20個を含む直鎖またはまたは分枝鎖状飽和脂肪
鎖またはラノリンアルコールの炭化水素残基であ
る)で表わされる直鎖または分枝鎖ポリグリセリ
ンエーテルまたは(式中のR脂肪鎖右端接続部の
メチレン基がカルボニル基である)エステル、ま
たはポリオキシエチレン化されたステリンを使つ
た、前項1〜8のいずれかに記載の組成物。 10 長鎖アルコールおよびジオール、ステリ
ン、長鎖アミンおよびその第四アンモニウム誘導
体、ヒドロキシアルキルアミン、ポリオキシエチ
レン化された脂肪アミン、長鎖アミノアルコール
エステルおよびその塩およびその第四アンモニウ
ム誘導体、ポリマーおよび脂肪アルコールのリン
酸エステルから成る群から選んだ助剤と非イオン
性両親媒性脂質とを組み合わせた、前項9に記載
の組成物。 11 内部の水性相または外側の水性相に少なく
とも1種の水溶性化粧用物質を含ませた、前項1
〜10のいずれかに記載の組成物。 12 水溶性化粧用物質として、湿潤剤、人工日
焼け剤、皮膚着色剤、日焼け防止剤、発汗防止
剤、防臭剤、収れん剤、清涼剤、養毛剤、癒創
薬、角質溶解剤、脱毛剤、香水、動物または植物
組織からの抽出物および抗脂漏剤から成る群から
選んだものを使つた、前項11に記載の組成物。
[Scope of Claims] 1. In a lipid globule dispersion in which lipid globules having an aqueous phase encapsulated therein by a molecular layer composed of at least one nonionic amphipathic lipid are dispersed in an aqueous phase outside the lipid globule. , liquid triglyceride, formula R-
A branched chain alcohol represented by COOR' (wherein R is a higher fatty acid residue containing 8 to 20 carbon atoms and R' is a branched hydrocarbon chain containing 3 to 20 carbon atoms) A cosmetic composition, characterized in that at least one oil selected from the group consisting of fatty acid esters of 1 and 100% oil is dispersed in an aqueous phase outside the aforementioned lipid globules. 2. The composition according to item 1 above, wherein the liquid triglyceride is selected from the group consisting of sunflower oil, corn oil, soybean oil, calabash oil, grape seed oil, and glycerin tricaprocaprylate. 3. The composition according to item 1 above, wherein Purcellin oil is used as the branched chain alcohol fatty acid ester of formula R-COOR'. 4 Based on the total weight of the composition, 2 to 10% by weight of nonionic amphipathic lipids constituting the walls of the lipid globules and 2 to 10% of the oil dispersed in the aqueous phase outside the lipid globules.
40% by weight, and the ratio of nonionic amphipathic lipid to oil was 0.2:1 to 1:1, items 1 to 3 above.
The composition according to any one of. 5. The composition according to any one of items 1 to 4 above, wherein the aqueous phase outside the lipid globules contains a gelling agent in an amount of 0.1 to 2% by weight based on the total weight of the composition. 6. The composition according to item 5 above, wherein the gelling agent is selected from the group consisting of cellulose derivatives, synthetic polymers, algae derivatives, or natural rubber. 7. The composition according to any one of items 1 to 6 above, wherein the aqueous phase outside the lipid globules contains at least one fragrance and/or one or more fat-soluble cosmetic substances. 8. As a fat-soluble cosmetic substance, one selected from sunscreen filters, substances that improve the condition of dry or aged skin, or antioxidants is used;
The composition according to item 7 above. 9 As a nonionic amphipathic lipid that constitutes the wall of a lipid globule, the formula R-(OCH 2 CHOHCH 2 )- o OH or (In the formula, n is a number from 2 to 6, R is a carbon atom 16
A straight-chain or branched polyglycerol ether represented by a straight-chain or branched saturated aliphatic chain containing ~20 or a hydrocarbon residue of lanolin alcohol; 9. The composition according to any one of the preceding items 1 to 8, which uses an ester (wherein the methylene group is a carbonyl group) or a polyoxyethylenated sterine. 10 Long-chain alcohols and diols, sterine, long-chain amines and their quaternary ammonium derivatives, hydroxyalkylamines, polyoxyethylated fatty amines, long-chain amino alcohol esters and their salts and their quaternary ammonium derivatives, polymers and fats 10. The composition according to item 9 above, which comprises a combination of an auxiliary agent selected from the group consisting of alcohol phosphate esters and a nonionic amphipathic lipid. 11. Item 1 above, in which the inner aqueous phase or the outer aqueous phase contains at least one water-soluble cosmetic substance.
The composition according to any one of items 1 to 10. 12 Water-soluble cosmetic substances include humectants, artificial tanning agents, skin coloring agents, sunscreen agents, antiperspirants, deodorants, astringents, refreshing agents, hair tonics, healing agents, keratolytic agents, depilatory agents, and perfumes. 12. The composition according to the preceding item 11, wherein the composition is selected from the group consisting of , extracts from animal or plant tissues, and antiseborrheic agents.
JP56101397A 1980-07-01 1981-07-01 Cosmetic composition consisting of aqueous dispersion of lipid vesicles Granted JPS5777613A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8014657A FR2485921A1 (en) 1980-07-01 1980-07-01 COSMETIC COMPOSITION BASED ON AN AQUEOUS DISPERSION OF LIPID SPHERULES

Publications (2)

Publication Number Publication Date
JPS5777613A JPS5777613A (en) 1982-05-15
JPH0210803B2 true JPH0210803B2 (en) 1990-03-09

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ID=9243726

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JP56101398A Granted JPS5794326A (en) 1980-07-01 1981-07-01 Manufacture of stable dispersed liquid in at least one kind of aqueous phase of nonmiscible liquid phase to water and dispersed liquid obtained
JP56101397A Granted JPS5777613A (en) 1980-07-01 1981-07-01 Cosmetic composition consisting of aqueous dispersion of lipid vesicles

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JP (2) JPS5794326A (en)
BE (2) BE889451A (en)
CA (1) CA1168158A (en)
CH (1) CH649915A5 (en)
DE (1) DE3125710A1 (en)
FR (1) FR2485921A1 (en)
GB (1) GB2079179B (en)
IT (1) IT1144739B (en)

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GB2079179A (en) 1982-01-20
CA1168158A (en) 1984-05-29
FR2485921B1 (en) 1983-07-22
CH649915A5 (en) 1985-06-28
JPS6333414B2 (en) 1988-07-05
IT1144739B (en) 1986-10-29
JPS5794326A (en) 1982-06-11
BE889451A (en) 1981-12-30
DE3125710A1 (en) 1982-03-25
DE3125710C2 (en) 1988-09-22
IT8167906A0 (en) 1981-06-30
FR2485921A1 (en) 1982-01-08
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GB2079179B (en) 1984-03-07

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