FR2777195A1 - Stable water-in-oil cosmetic emulsion with non-greasy feel - Google Patents
Stable water-in-oil cosmetic emulsion with non-greasy feel Download PDFInfo
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- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
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- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
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- A61K8/00—Cosmetics or similar toiletry preparations
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
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- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/553—Phospholipids, e.g. lecithin
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/63—Steroids; Derivatives thereof
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- A61K8/671—Vitamin A; Derivatives thereof, e.g. ester of vitamin A acid, ester of retinol, retinol, retinal
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- A61K8/678—Tocopherol, i.e. vitamin E
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Abstract
Description
La présente invention concerne de nouvelles compositions cosmétiques ouThe present invention relates to new cosmetic compositions or
dermatologiques sous forme d'émulsions de type eau-dans-huile renfermant des hydrocarbures ramifiés liquides et des phospholipides et leur dermatological in the form of water-in-oil emulsions containing liquid branched hydrocarbons and phospholipids and their
procédé de préparation.preparation process.
Les formulations cosmétiques sont, d'une façon générale, destinées à apporter à la peau des substances susceptibles d'améliorer son état ou de la Cosmetic formulations are, in general, intended to provide the skin with substances capable of improving its condition or the
protéger.protect.
Ces substances sont, d'une façon générale, des substances hydratantes, protectrices, régulatrices, nutritives, etc.. Elles sont de nature chimique très variée These substances are, generally, hydrating, protective, regulating, nutritive substances, etc. They are of very varied chemical nature
et peuvent être soit plutôt hydrosolubles, soit plutôt liposolubles. and can be either rather water-soluble or rather liposoluble.
On connaît tout l'intérêt des phospholipides, en particulier des phospholipides naturels tels que ceux que l'on trouve dans les lécithines, pour certains types de formulations cosmétiques telles que les dispersions de liposomes. On connaît, par ailleurs, des émulsions de triglycérides stabilisées par We know all the interest of phospholipids, in particular natural phospholipids such as those found in lecithins, for certain types of cosmetic formulations such as liposome dispersions. Furthermore, triglyceride emulsions stabilized by
de la lécithine.lecithin.
Tous ces produits laissent bien souvent sur la peau un toucher jugé All these products often leave a judged touch on the skin
trop gras lors d'applications dans le domaine de la cosmétique. too greasy during applications in the cosmetic field.
On a maintenant découvert que les phospholipides naturels, en We have now discovered that natural phospholipids, in
particulier les lécithines, permettaient de réaliser des émulsions de type eau-dans- in particular lecithins, made it possible to produce water-in-type emulsions
huile entre l'eau et une phase hydrophobe constituée essentiellement d'hydrocarbures liquides ramifiés en C20 à C40, en particulier, des émulsions de oil between water and a hydrophobic phase consisting essentially of C20 to C40 branched liquid hydrocarbons, in particular, emulsions of
type eau-dans-huile, d'eau dans du perhydrosqualène. water-in-oil type, water in perhydrosqualene.
De telles émulsions de type eau-dans-huile sont remarquablement Such water-in-oil type emulsions are remarkably
stables et présentent d'excellentes qualités cosmétiques. stable and have excellent cosmetic qualities.
Un autre avantage de ces émulsions est qu'elles peuvent être utilisées pour véhiculer dans la peau des actifs cosmétiques ou dermatologiques aussi bien hydrosolubles que liposolubles et présentent, en outre, l'avantage de conduire à des compositions cosmétiques ou dermatologiques particulièrement agréables au toucher. Une des caractéristiques essentielles des compositions décrites dans ce document est qu'elles sont sous forme d'émulsions. C'est pourquoi on les Another advantage of these emulsions is that they can be used to convey cosmetic or dermatological active agents, both water-soluble and liposoluble, into the skin and, moreover, have the advantage of leading to cosmetic or dermatological compositions which are particularly pleasant to the touch. One of the essential characteristics of the compositions described in this document is that they are in the form of emulsions. That's why we
désignera ci-après indifféremment par émulsions ou compositions. will denote below indifferently by emulsions or compositions.
Ainsi, selon un premier aspect, l'invention concerne une composition cosmétique ou dermatologique pour application topique, sous forme d'émulsion de type eau-dans-huile, caractérisée en ce qu'elle contient, exprimé en pourcentage en poids: - 8 à 50 %, de préférence 15 à 35 %, d'un hydrocarbure ramifié saturé en C20 à C40 ou d'un mélange de tels hydrocarbures, - 1 à 43 %, de préférence 5 à 30 %, d'un phospholipide naturel ou d'un mélange de phospholipides naturels, Thus, according to a first aspect, the invention relates to a cosmetic or dermatological composition for topical application, in the form of an emulsion of the water-in-oil type, characterized in that it contains, expressed as a percentage by weight: - 8 to 50%, preferably 15 to 35%, of a branched hydrocarbon saturated with C20 to C40 or a mixture of such hydrocarbons, - 1 to 43%, preferably 5 to 30%, of a natural phospholipid or a mixture of natural phospholipids,
-46 à 85 %, de préférence 65 à 75 %, d'eau. -46 to 85%, preferably 65 to 75%, of water.
L'hydrocarbure ou les hydrocarbures liquides ramifiés saturés utilisés pour la préparation des émulsions de l'invention peuvent être tout hydrocarbure ou mélange d'hydrocarbures liquides ramifiés en C20 à C4o, toutefois on utilisera The saturated branched liquid hydrocarbon or hydrocarbons used for the preparation of the emulsions of the invention can be any hydrocarbon or mixture of branched liquid hydrocarbons at C20 to C40, however use will be made
avantageusement l'hexaméthyltétracosane (ou perhydrosqualène). advantageously hexamethyltetracosane (or perhydrosqualene).
Comme phospholipide ou mélange de phospholipides, on pourra utiliser tout phospholipide naturel. On utilisera toutefois de préférence la lécithine de soja ou la lécithine d'oeuf La phase aqueuse de l'émulsion de l'invention contient avantageusement au moins un alcool en C2 à C6 ou un polyol en C2 à C6 ou encore un mélange de tels alcools et polyols. A titre d'alcools ou polyols préférés en C2 à C6, on citera l'éthanol, le propanol, le propylèneglycol, le butylèneglycol, le glycérol et le sorbitol. Ces alcools et/ou polyols et/ou mélanges d'alcools et de polyols, lorsqu'ils sont introduits dans les émulsions de l'invention représentent de préférence de 0,1 à 15 %, de préférence de 1 à 5 % en poids par rapport au poids As phospholipid or mixture of phospholipids, any natural phospholipid may be used. However, soy lecithin or egg lecithin will preferably be used. The aqueous phase of the emulsion of the invention advantageously contains at least one C2 to C6 alcohol or a C2 to C6 polyol or a mixture of such alcohols. and polyols. As preferred alcohols or polyols in C2 to C6, mention will be made of ethanol, propanol, propylene glycol, butylene glycol, glycerol and sorbitol. These alcohols and / or polyols and / or mixtures of alcohols and polyols, when introduced into the emulsions of the invention preferably represent from 0.1 to 15%, preferably from 1 to 5% by weight per relative to weight
total de ladite composition.total of said composition.
L'émulsion de l'invention peut contenir, en outre, 0,5 à 30 % en poids, de préférence 1 à 10 % en poids d'un autre composé liquide hydrophobe ou d'un mélange d'autres composés liquides hydrophobes, lesdits liquides hydrophobes étant de préférence choisis dans le groupe constitué des hydrocarbures en C6 à C16, par exemple l'isododécane, des esters liquides d'acides et d'alcools gras, par The emulsion of the invention may also contain 0.5 to 30% by weight, preferably 1 to 10% by weight of another hydrophobic liquid compound or of a mixture of other hydrophobic liquid compounds, said hydrophobic liquids preferably being chosen from the group consisting of C6 to C16 hydrocarbons, for example isododecane, liquid esters of fatty acids and alcohols, for example
exemple l'huile de jojoba et des triglycérides d'acides gras. example jojoba oil and triglycerides of fatty acids.
Les esters liquides d'acide gras et d'alcool gras entrant éventuellement dans la composition des émulsions de l'invention sont avantageusement choisis parmi les esters liquides naturels. A ce titre, on utilisera avantageusement l'huile The liquid esters of fatty acid and of fatty alcohol optionally entering into the composition of the emulsions of the invention are advantageously chosen from natural liquid esters. As such, the oil will advantageously be used
de jojoba. Mais, on peut également recourir à l'huile de jojoba synthétique. of jojoba. But, one can also resort to synthetic jojoba oil.
Par acide gras au sens de l'invention, on entend des acides contenant By fatty acid within the meaning of the invention is meant acids containing
de 8 à 30 atomes de carbone.from 8 to 30 carbon atoms.
Par alcool gras au sens de l'invention, on entend des alcools contenant By fatty alcohol within the meaning of the invention means alcohols containing
de 8 à 30 atomes de carbone.from 8 to 30 carbon atoms.
L'émulsion de l'invention peut contenir en outre au moins un composé liquide hydrophobe et/ou au moins un composé hydrophobe cireux. Plus précisément, l'émulsion contiendra avantageusement 0,1 à 10 % en poids, de préférence 0,5 à 5 % en poids d'un composé hydrophobe cireux ou d'un mélange de composés hydrophobes cireux, lesdits composés hydrophobes cireux étant de préférence choisis dans le groupe constitué des cires microcristallines The emulsion of the invention may also contain at least one hydrophobic liquid compound and / or at least one waxy hydrophobic compound. More specifically, the emulsion will advantageously contain 0.1 to 10% by weight, preferably 0.5 to 5% by weight of a waxy hydrophobic compound or of a mixture of waxy hydrophobic compounds, said waxy hydrophobic compounds being preferably chosen from the group consisting of microcrystalline waxes
d'hydrocarbures, de la cire d'abeille et des stérols. hydrocarbons, beeswax and sterols.
Enfin, les émulsions de l'invention pourront contenir différents adjuvants tant hydrophiles que lipophiles classiquement utilisés dans les Finally, the emulsions of the invention may contain various adjuvants, both hydrophilic and lipophilic, conventionally used in
compositions cosmétiques ou dermatologiques. cosmetic or dermatological compositions.
Ainsi, les émulsions de l'invention pourront contenir avantageusement: de 0,1 à 1 % en poids d'additifs choisis parmi les conservateurs, les bactéricides et les fongicides, - de 1 à 5 % en poids d'un filtre UV ou d'un mélange de filtres UV, - de 0, 1 à 5 % en poids de parfums, -de 1 à 10 % en poids de particules solides choisies parmi les Thus, the emulsions of the invention may advantageously contain: from 0.1 to 1% by weight of additives chosen from preservatives, bactericides and fungicides, - from 1 to 5% by weight of a UV or d filter '' a mixture of UV filters, - from 0.1 to 5% by weight of perfumes, - from 1 to 10% by weight of solid particles chosen from
pigments, les micropigments et les charges minérales. pigments, micropigments and mineral fillers.
L'intérêt des émulsions décrites précédemment est essentiellement de pouvoir véhiculer dans la peau des substances aussi bien hydrophobes qu'hydrophiles. Les substances hydrophiles ou hydrophobes visées peuvent être tout agent cosmétique ou dermatologique soluble dans l'eau, dans les hydrocarbures ou The advantage of the emulsions described above is essentially that of being able to carry substances both hydrophobic and hydrophilic in the skin. The hydrophilic or hydrophobic substances targeted can be any cosmetic or dermatological agent soluble in water, in hydrocarbons or
dans des huiles.in oils.
Par conséquent, l'invention concerne des compositions sous forme d'émulsions telles que définies précédemment contenant 0,001 à 5 % en poids d'agents actifs cosmétiques ou dermatologiques choisis parmi les agents cosmétiques ou dermatologiques solubles dans l'eau, ou dans les hydrocarbures ou Consequently, the invention relates to compositions in the form of emulsions as defined above containing 0.001 to 5% by weight of cosmetic or dermatological active agents chosen from cosmetic or dermatological agents soluble in water, or in hydrocarbons or
dans les huiles.in oils.
A titre d'exemples non limitatifs de ces substances actives cosmétiques ou dermatologiques, on citera tout particulièrement celles choisies dans le groupe constitué des vitamines et dérivés de vitamines, des oligoéléments, des acides aminés, des céramides, des stérols, de l'acide rétinoique, des ecdystéroides tels que la 20-hydroxyecdysone, de l'acide 13-glycyrrhétinique, du glycyrrhizinate d'ammonium, de l'hydroquinone et de ses dérivés, de l'acide kojique, de l'urée, du pyroglutamate de sodium, des triterpènes, des ginsenosides, des dérivés des acides By way of nonlimiting examples of these cosmetic or dermatological active substances, particular mention will be made of those chosen from the group consisting of vitamins and vitamin derivatives, trace elements, amino acids, ceramides, sterols, retinoic acid , ecdysteroids such as 20-hydroxyecdysone, 13-glycyrrhetinic acid, ammonium glycyrrhizinate, hydroquinone and its derivatives, kojic acid, urea, sodium pyroglutamate, triterpenes, ginsenosides, acid derivatives
asiatique et madécassique, du séricoside, de la visnadine, de la caféine, des mono- asian and madecassic, sericoside, visnadine, caffeine, mono-
et diméthylxanthines, des extraits végétaux, des extraits d'algues, des extraits de levures, des extraits de bactéries, des extraits de champignons, de la mélatonine, de la DHEA, des protéines, des alcools gras, des sucres, des a-hydroxyacides, des and dimethylxanthines, plant extracts, algae extracts, yeast extracts, bacteria extracts, mushroom extracts, melatonin, DHEA, proteins, fatty alcohols, sugars, α-hydroxy acids ,
huiles essentielles, du panthénol, de l'acide salicylique. essential oils, panthenol, salicylic acid.
Enfin, selon un deuxième aspect, l'invention concerne un procédé de préparation des compositions sous forme d'émulsions telles qu'elles ont été Finally, according to a second aspect, the invention relates to a process for preparing the compositions in the form of emulsions as they have been
défminies précédemment.previously defined.
Ce procédé comprend les étapes de: - préparation d'une phase dite phase hydrophobe par dissolution de la lécithine dans un mélange comprenant les hydrocarbures ramifiés en C20 à C40 et les éventuels autres adjuvants hydrophobes constituant ladite émulsion, - préparation d'une phase aqueuse comprenant l'eau et les éventuels autres adjuvants hydrophiles constituant ladite émulsion, This process comprises the steps of: - preparation of a phase called hydrophobic phase by dissolving lecithin in a mixture comprising the branched hydrocarbons C20 to C40 and any other hydrophobic adjuvants constituting said emulsion, - preparation of an aqueous phase comprising water and any other hydrophilic adjuvants constituting said emulsion,
- l'addition de ladite phase aqueuse dans ladite phase hydrophobe. - Adding said aqueous phase to said hydrophobic phase.
EXEMPLESEXAMPLES
Les compositions cosmétiques données dans les exemples ci-après avec les proportions de leurs différents constituants exprimées en pourcentages en poids sont préparées de la façon suivante: 1. Les adjuvants hydrophobes sont dissous ou dispersés sous agitation The cosmetic compositions given in the examples below with the proportions of their various constituents expressed in percentages by weight are prepared as follows: 1. The hydrophobic adjuvants are dissolved or dispersed with stirring
dans l'hydrocarbure ou le mélange d'hydrocarbures. in the hydrocarbon or mixture of hydrocarbons.
2. La lécithine est dissoute sous agitation dans le liquide obtenu ci- 2. Lecithin is dissolved with stirring in the liquid obtained above
dessus, en chauffant au besoin à une température de l'ordre de 80 C. On obtient une phase désignée ci-après par phase huileuse A. 3. Les adjuvants hydrophiles sont dissous dans l'eau sous agitation. On obtient une phase aqueuse ci-après désignée par phase B. 4 . La phase aqueuse B est ajoutée lentement sous agitation à la phase A. Exemple 1, Produit de traitement des peaux sèches Phase A: Perhydrosqualène 25 Céramides 0,5 Vitamine F 0,5 Lécithine de soja 5 Parfum 0,5 Phase B: Glycérol 3 Pyroglutamate de sodium 1 Sérine 1 Bêta- ecdysone 0,2 Parahydroxybenzoates 0,5 Eau qsp 100 Exemple 2: Produit de dermatologie anti-acné Phase A: Perhydrosqualène 20 Acide transrétinoïque 0,02 Lécithine de soja 5 Phase B: Glycyrrhizinate d'ammonium 0,1 Butylèneglycol 2 Conservateurs p-hydroxybenzoates 0,5 Eau qsp 100 Exemple 3: Crème anti-âge Phase A: Perhydrosqualène 16 Acide salicylique 1 Filtre UV 3 Lécithine d'oeuf 5 Phase B: Phosphate de vitamine E 0,1 Extrait sec de ginseng 0,3 Propylèneglycol 2 Glycérol 2 Conservateurs p-hydroxybenzoates 0,5 Eau qsp 100 above, heating if necessary to a temperature of the order of 80 C. This gives a phase designated below by oily phase A. 3. The hydrophilic adjuvants are dissolved in water with stirring. An aqueous phase is obtained below, designated by phase B. 4. The aqueous phase B is added slowly with stirring to phase A. Example 1, Dry skin treatment product Phase A: Perhydrosqualene 25 Ceramides 0.5 Vitamin F 0.5 Soy lecithin 5 Fragrance 0.5 Phase B: Glycerol 3 Sodium pyroglutamate 1 Serine 1 Beta-ecdysone 0.2 Parahydroxybenzoates 0.5 Water qs 100 Example 2: Anti-acne dermatology product Phase A: Perhydrosqualene 20 Transretinoic acid 0.02 Soy lecithin 5 Phase B: Ammonium glycyrrhizinate 0 , 1 Butylene glycol 2 Preservatives p-hydroxybenzoates 0.5 Water qs 100 Example 3: Anti-aging cream Phase A: Perhydrosqualene 16 Salicylic acid 1 UV filter 3 Egg lecithin 5 Phase B: Vitamin E phosphate 0.1 Dry extract of ginseng 0.3 Propylene glycol 2 Glycerol 2 Preservatives p-hydroxybenzoates 0.5 Water qs 100
Claims (13)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9904276A FR2777195A1 (en) | 1998-04-10 | 1999-04-06 | Stable water-in-oil cosmetic emulsion with non-greasy feel |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9804542A FR2777194A1 (en) | 1998-04-10 | 1998-04-10 | Stable water-in-oil cosmetic emulsion without greasy feel |
FR9904276A FR2777195A1 (en) | 1998-04-10 | 1999-04-06 | Stable water-in-oil cosmetic emulsion with non-greasy feel |
Publications (1)
Publication Number | Publication Date |
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FR2777195A1 true FR2777195A1 (en) | 1999-10-15 |
Family
ID=26234259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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FR9904276A Pending FR2777195A1 (en) | 1998-04-10 | 1999-04-06 | Stable water-in-oil cosmetic emulsion with non-greasy feel |
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FR (1) | FR2777195A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004000242A1 (en) * | 2002-06-25 | 2003-12-31 | Cosmeceutic Solutions Pty Ltd | Topical cosmetic compositions |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2072016A (en) * | 1980-03-24 | 1981-09-30 | Oreal | Cosmetic and pharmaceutical compositions in the form of stable oil-in-water emulsions |
JPS59122412A (en) * | 1982-12-28 | 1984-07-14 | Kanebo Ltd | Creamy or milky skin cosmetic |
EP0419148A2 (en) * | 1989-09-20 | 1991-03-27 | Shiseido Company Limited | Cosmetic composition |
EP0479121A1 (en) * | 1990-10-01 | 1992-04-08 | FIDIA S.p.A. | Skin treatment compositions containing beta-phosphatidyl choline derivatives |
JPH06179613A (en) * | 1992-12-12 | 1994-06-28 | Taiyo Kagaku Co Ltd | Cosmetic |
FR2706301A1 (en) * | 1993-06-09 | 1994-12-23 | Clarins | Cosmetic night preparation intended for combating skin aging |
JPH07132222A (en) * | 1993-11-10 | 1995-05-23 | Lion Corp | Emulsion type composition |
EP0739623A1 (en) * | 1994-01-19 | 1996-10-30 | Taisho Pharmaceutical Co. Ltd | Dermatologic composition |
-
1999
- 1999-04-06 FR FR9904276A patent/FR2777195A1/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2072016A (en) * | 1980-03-24 | 1981-09-30 | Oreal | Cosmetic and pharmaceutical compositions in the form of stable oil-in-water emulsions |
JPS59122412A (en) * | 1982-12-28 | 1984-07-14 | Kanebo Ltd | Creamy or milky skin cosmetic |
EP0419148A2 (en) * | 1989-09-20 | 1991-03-27 | Shiseido Company Limited | Cosmetic composition |
EP0479121A1 (en) * | 1990-10-01 | 1992-04-08 | FIDIA S.p.A. | Skin treatment compositions containing beta-phosphatidyl choline derivatives |
JPH06179613A (en) * | 1992-12-12 | 1994-06-28 | Taiyo Kagaku Co Ltd | Cosmetic |
FR2706301A1 (en) * | 1993-06-09 | 1994-12-23 | Clarins | Cosmetic night preparation intended for combating skin aging |
JPH07132222A (en) * | 1993-11-10 | 1995-05-23 | Lion Corp | Emulsion type composition |
EP0739623A1 (en) * | 1994-01-19 | 1996-10-30 | Taisho Pharmaceutical Co. Ltd | Dermatologic composition |
Non-Patent Citations (3)
Title |
---|
CHEMICAL ABSTRACTS, vol. 101, no. 16, 1984, Columbus, Ohio, US; abstract no. 136815f, page 376; XP002085664 * |
DATABASE WPI Week 9529, Derwent World Patents Index; AN 95-220155, XP002085665 * |
STN, Serveur de Bases de Données, * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004000242A1 (en) * | 2002-06-25 | 2003-12-31 | Cosmeceutic Solutions Pty Ltd | Topical cosmetic compositions |
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