[go: up one dir, main page]

LU100194B1 - Anhydrous cosmetic composition applicable to the nails - Google Patents

Anhydrous cosmetic composition applicable to the nails Download PDF

Info

Publication number
LU100194B1
LU100194B1 LU100194A LU100194A LU100194B1 LU 100194 B1 LU100194 B1 LU 100194B1 LU 100194 A LU100194 A LU 100194A LU 100194 A LU100194 A LU 100194A LU 100194 B1 LU100194 B1 LU 100194B1
Authority
LU
Luxembourg
Prior art keywords
parts
acid
composition
film
anhydrous
Prior art date
Application number
LU100194A
Other languages
French (fr)
Inventor
Robin Cisneros
Fatima Eddoumy
Frédéric Derosier
Original Assignee
Int Lacquers S A
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 Int Lacquers S A filed Critical Int Lacquers S A
Priority to LU100194A priority Critical patent/LU100194B1/en
Priority to PCT/EP2018/060999 priority patent/WO2018206333A1/en
Priority to EP18721370.7A priority patent/EP3621695A1/en
Application granted granted Critical
Publication of LU100194B1 publication Critical patent/LU100194B1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • A61Q3/02Nail coatings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/85Polyesters
    • 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
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • A61K2800/31Anhydrous

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)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

Composition cosmétique anhydre pour vernis à ongles comprenant au moins un solvant organique cosmétiquement acceptable et au moins un agent filmogène de type biopolyester, le biopolyester étant l'acide polylactique. Utilisation d'acide polylactique, comme agent filmogène dans une composition anhydre pour vernis à onglesAnhydrous cosmetic composition for nail polish comprising at least one cosmetically acceptable organic solvent and at least one film-forming agent of the biopolyester type, the biopolyester being polylactic acid. Use of polylactic acid as a film-forming agent in an anhydrous nail polish composition

Description

Luiuui:Luiuui:

COMPOSITION COSMETIQUE ANHYDRE APPLICABLE SUR LES ONGLESANHYDROUS COSMETIC COMPOSITION APPLICABLE ON NAILS

Domaine technique [0001] La présente invention concerne les vernis à ongles comprenant un nouvel agent filmogène et qui sont au moins partiellement biosourcées.TECHNICAL FIELD [0001] The present invention relates to nail polishes comprising a novel film-forming agent and which are at least partially biosourced.

Etat de la technique [0002] Les filmogènes actuels nitrocellulosiques présentent deux défauts majeurs en formulation, à savoir leur opacité et leur propension à jaunir plus ou moins rapidement dans le temps. Il est important de noter également qu'ils présentent une certaine instabilité qui peut les rendre inflammables voire explosifs, ce qui complique les conditions de stockage et de manipulation.STATE OF THE ART [0002] The current nitrocellulose film-forming agents have two major defects in formulation, namely their opacity and their tendency to yellow more or less rapidly over time. It is important to note also that they have a certain instability that can make them flammable or explosive, which complicates the conditions of storage and handling.

[0003] Malgré que des tentatives aient déjà été faites pour substituer ce produit, il continue d'être la résine de base très largement utilisée dans l'ensemble des formulations de vernis à ongles.Despite attempts have already been made to substitute this product, it continues to be the base resin widely used in all nail polish formulations.

[0004] Il existe donc un besoin de substituer la nitrocellulose par d'autres matériaux plus stables et compatibles dans les formulations de vernis à ongles. Par contre, ce matériau doit toujours permettre d'obtenir les différentes propriétés que l'on demande, aujourd'hui, à un vernis à ongles, à savoir: - une bonne application, lorsque le vernis à ongles est appliqué sur l'ongle, il doit former une surface lisse, sans stries avec une épaisseur constante afin d'obtenir un film et une coloration homogènes, - un étalement facilité sur toute la surface de l'ongle pour rendre son utilisation pratique, - une brillance accrue et qui persiste dans le temps, - un temps de séchage et de durcissement sur l'ongle très courts, et - une bonne tenue du vernis à ongles sur l'ongle, il est en effet souhaité que le vernis s'écaille le moins possible afin de conserver un aspect esthétique.[0004] There is therefore a need to substitute nitrocellulose with other more stable and compatible materials in nail polish formulations. On the other hand, this material must always make it possible to obtain the different properties that are required, today, to a nail polish, namely: - a good application, when the nail polish is applied to the nail, it must form a smooth, streak-free surface with a constant thickness in order to obtain a homogeneous film and coloring, - easy spreading over the entire surface of the nail to make its practical use, - increased gloss and which persists in the time, - a drying time and hardening on the nail very short, and - a good performance of the nail polish on the nail, it is indeed desired that the varnish flakes as little as possible to maintain a aesthetic appearance.

[0005] D'une manière générale dans le domaine des vernis à ongles, il existe une demande constante de nouveaux produits ayant des propriétés améliorées, notamment au niveau de la facilité d'application, de la rapidité de séchage, de la durabilité, de l'esthétique, etc. De plus en plus, on observe aussi une sensibilité croissante des utilisateurs et utilisatrices pour des produits plus respectueux de l’environnement.In general, in the field of nail polish, there is a constant demand for new products with improved properties, especially in terms of ease of application, speed of drying, durability, aesthetics, etc. Increasingly, there is also a growing awareness of users for more environmentally friendly products.

Objet de l'invention [0006] Un objet de la présente invention est donc de proposer des nouvelles compositions de vernis à ongles qui comprennent un nouvel agent filmogène pouvant remédier aux inconvénients mentionnés ci-dessus, de préférence sans devoir utiliser la nitrocellulose, mais de préférence sans altérer (significativement) les autres propriétés importantes du vernis à ongles, notamment la tenue, la brillance, la couvrance, le temps de séchage ou le durcissement.OBJECT OF THE INVENTION [0006] An object of the present invention is therefore to propose novel nail polish compositions which comprise a new film-forming agent which can overcome the drawbacks mentioned above, preferably without having to use nitrocellulose, but preferably without altering (significantly) the other important properties of the nail polish, including strength, gloss, coverage, drying time or hardening.

Description générale de l'invention [0007] Afin de résoudre le problème mentionné ci-dessus, la présente invention propose une composition anhydre pour vernis à ongles comprenant au moins un solvant organique cosmétiquement acceptable et au moins un agent filmogène de type biopolyester, le biopolyester étant l'acide polylactique et la composition cosmétique ne contenant pas de nitrocellulose. Dans une variante préférée, la quantité d'acide polylactique est comprise entre 0,1 % et 45 % en poids sec par rapport au poids total de la composition et de façon encore plus préférée entre 1 % et 25 % en poids, de manière particulièrement préférée entre 5 % et 12 % en poids sec par rapport au poids total de la composition anhydre.General description of the invention [0007] In order to solve the problem mentioned above, the present invention provides an anhydrous composition for nail polish comprising at least one cosmetically acceptable organic solvent and at least one biopolyester-type film-forming agent, the biopolyester. being polylactic acid and the cosmetic composition not containing nitrocellulose. In a preferred variant, the amount of polylactic acid is between 0.1% and 45% by dry weight relative to the total weight of the composition and even more preferably between 1% and 25% by weight, particularly preferably preferred between 5% and 12% by dry weight relative to the total weight of the anhydrous composition.

[0008] De façon surprenante, il a été mis en évidence que l'acide polylactique, qui est un polymère biosourcé totalement biocompatible, offre une alternative très intéressante et tout à fait novatrice à la nitrocellulose.[0008] Surprisingly, it has been demonstrated that polylactic acid, which is a biocompatible biosourced polymer, offers a very interesting and quite innovative alternative to nitrocellulose.

[0009] L'acide polylactique peut être obtenu notamment à partir de l’amidon de maïs. En effet, l’acide polylactique est un produit résultant de la fermentation des sucres ou de l’amidon sous l’effet de bactéries synthétisant l’acide lactique. Dans un second temps, l’acide lactique est polymérisé soit par un nouveau procédé de fermentation, soit chimiquement pour en devenir de l’acide polylactique. Il fait partie de la famille des biopolyesters. Ainsi, l’utilisation de l'acide polylactique conduit à l’obtention d’une composition anhydre pour vernis à ongle qui offre une bonne application, présente une tenue, une brillance, une couvrance ainsi qu’un temps de séchage et de durcissement avantageux. L'acide polylactique utilisé est de préférence celui commercialisé sous les dénominations suivantes: Ingeo Biopolymer 10361 D (faible poids moléculaire) et Ingeo Biopolymer 4060 D (poids moléculaire plus élevé).The polylactic acid can be obtained in particular from corn starch. Indeed, polylactic acid is a product resulting from the fermentation of sugars or starch under the effect of bacteria synthesizing lactic acid. In a second step, the lactic acid is polymerized either by a new fermentation process, or chemically to become polylactic acid. He belongs to the family of biopolyesters. Thus, the use of polylactic acid leads to the production of an anhydrous nail varnish composition which offers good application, has a good hold, gloss, coverage and drying and curing time. . The polylactic acid used is preferably that marketed under the following names: Ingeo Biopolymer 10361 D (low molecular weight) and Ingeo Biopolymer 4060 D (higher molecular weight).

[0010] L'acide polylactique peut être utilisé dans tous les types de compositions anhydres pour vernis à ongles classiques colorés et comme par exemple les vernis à ongles à effet (miroir, craquelé, irisé, martelé, magnétique, mat, métallisé etc.), les vernis à ongles longue tenue (« gel like »), mais également les vernis à ongles dits « top coat » ou « base coat » (destinés à être appliqués sur ou en dessous d’un vernis à ongles).Polylactic acid can be used in all types of anhydrous compositions for conventional nail polish and as for example effect nail polish (mirror, cracked, iridescent, hammered, magnetic, matte, metallized etc.) , long-lasting nail polish ("gel like"), but also nail polish called "top coat" or "base coat" (intended to be applied on or below a nail polish).

[0011] La composition anhydre pour vernis à ongles comprend un solvant organique. Le solvant organique pourra être choisi en fonction de ses propriétés physico-chimiques et en considérations des autres composants présents dans la composition anhydre pour vernis à ongles.The anhydrous composition for nail polish comprises an organic solvent. The organic solvent may be selected according to its physico-chemical properties and in consideration of the other components present in the anhydrous composition for nail polish.

[0012] Ce solvant organique peut être choisi parmi le groupe constitué par le toluène, le xylène, l’acétate de méthyle, l’acétate d’éthyle, l’acétate de butyle, l’acétate d’isobutyle, l’acétate de propyle, une cétone, un ester, un alcool, comme l’éthanol dénaturé (avec la méthyléthylcétone ou le diethyléther), l’isopropanol, le butanol, le diacétone alcool, les hydrocarbures linéaires ou cycliques, comme par exemple l’hexane, le cyclohexane, l’heptane et n’importe quelle combinaison de ceux-ci.This organic solvent may be chosen from the group consisting of toluene, xylene, methyl acetate, ethyl acetate, butyl acetate, isobutyl acetate, ethyl acetate and the like. propyl, a ketone, an ester, an alcohol, such as denatured ethanol (with methyl ethyl ketone or diethyl ether), isopropanol, butanol, diacetone alcohol, linear or cyclic hydrocarbons, such as, for example, hexane, cyclohexane, heptane and any combination thereof.

[0013] De façon préférée, la quantité de solvant organique présente dans la composition anhydre pour vernis à ongles est généralement comprise entre 60% et 80% en poids par rapport au poids total de la composition.Preferably, the amount of organic solvent present in the anhydrous composition for nail polish is generally between 60% and 80% by weight relative to the total weight of the composition.

[0014] Avantageusement, le solvant organique est l’acétate d’éthyle et/ou l’acétate de butyle et/ou un alcool ; ou un de leur mélanges.[0014] Advantageously, the organic solvent is ethyl acetate and / or butyl acetate and / or an alcohol; or one of their mixtures.

[0015] Si nécessaire ou souhaité, la composition peut également comprendre un ou plusieurs autre(s) agent(s) filmogène(s) seul ou une combinaison, de préférence en quantité nettement plus réduite qu'en absence d'acide polylactique. Le pourcentage du/des autre(s) agent(s) filmogène(s) dans la formule peu(ven)t aller de 0,5 % à 15 % en poids sec et de façon préférée de 2 % à 5 % en poids sec par rapport au poids total de la composition.If necessary or desired, the composition may also comprise one or more other film-forming agent (s) alone or a combination, preferably in a much smaller quantity than in the absence of polylactic acid. The percentage of the other film-forming agent (s) in the formula may range from 0.5% to 15% by dry weight and preferably from 2% to 5% by dry weight. relative to the total weight of the composition.

[0016] Le ou les autre(s) agent(s) filmogène(s) éventuellement compris dans la composition de vernis à ongles peu(ven)t être choisi(s) parmi le groupe constitué par la cellulose, un dérivé de cellulose, une résine vinylique, une résine acrylique et n'importe quelle combinaison de ceux-ci. Les dérivés de cellulose sont par exemple l'acétate butyrate cellulose, l'éthylcellulose et l'hydroxypropyl-'cellulose. Préférentiellement, on choisira l'acétate butyrate cellulose comme agent filmogène. D'une manière générale les compositions anhydres pour vernis à ongles de l'invention ne contiennent pas du tout de nitrocellulose.The other film-forming agent (s) optionally included in the nail polish composition may be selected from the group consisting of cellulose, a cellulose derivative, a vinyl resin, an acrylic resin and any combination thereof. The cellulose derivatives are, for example, butyrate acetate cellulose, ethylcellulose and hydroxypropylcellulose. Preferentially, acetate butyrate cellulose will be chosen as film-forming agent. In general, the anhydrous nail polish compositions of the invention do not contain nitrocellulose at all.

[0017] La composition selon l'invention peut également contenir des résines conventionnelles. Les résines conventionnelles utilisables sont les suivantes : • Résines polyester • Résines époxytosylamide • Résine acrylate et styrène-acrylate • Sucrose perbenzoate [0018] Des résines supplémentaires peuvent également être ajoutées dans la composition. En particulier, ces résines supplémentaires permettent d'augmenter le collant et l'adhérence du film sur l'ongle.The composition according to the invention may also contain conventional resins. Conventional resins that can be used are as follows: • Polyester resins • Epoxytosylamide resins • Acrylate and styrene-acrylate resin • Sucrose perbenzoate [0018] Additional resins can also be added to the composition. In particular, these additional resins make it possible to increase the tackiness and the adhesion of the film to the nail.

[0019] Les résines supplémentaires pouvant être utilisées sont les suivantes : • Les résines tosylamide/formaldéhyde ou résines toluènesulfonamide/ formal-dle-hyde, • Les résines tosylamide/époxy ou résines toluènesulfonamide/époxy, • La résine de copolymères d'acide adipique, d'acide fumarique, de néopentylglycol et de cyclohexanediméthanol • Copolymères acide adipique/néopentyl glycol/anhydride triméllitique, • Copolymères d'anhydride phtalique/glycérine/glycidyl décanoate, • Copolymères d'anhydride phtalique/anhydride trimellitique/glycols, • Copolymères de glycérine/acide phtalique, • Copolymères styrène/acrylate/acrylonitrile, • Polymères et copolymères d'acrylates, • Copolymères d'acrylates et de styrène, • Sucrose acétate isobutyrate, • Résine polyvinylbutyral.The additional resins that can be used are as follows: • tosylamide / formaldehyde resins or toluenesulfonamide / formal-d-hyde resins, • tosylamide / epoxy resins or toluenesulfonamide / epoxy resins, • adipic acid copolymer resin , fumaric acid, neopentyl glycol and cyclohexanedimethanol • Copolymers adipic acid / neopentyl glycol / trimellitic anhydride • Copolymers of phthalic anhydride / glycerin / glycidyl decanoate • Copolymers of phthalic anhydride / trimellitic anhydride / glycols • Copolymers of glycerine / phthalic acid, • Styrene / acrylate / acrylonitrile copolymers, • Polymers and copolymers of acrylates, • Copolymers of acrylates and styrene, • Sucrose acetate isobutyrate, • Polyvinylbutyral resin.

[0020] En plus de leur action collante, la plupart de ces résines ont également une action plastifiante. Les résines peuvent être utilisées dans la formule, seules ou sous la forme de mélanges, dans des quantités allant de 1 % à 25 % en poids sec, de préférence 5 % à 15 % en poids sec, en particulier de 7 % à 12 % en poids sec par rapport au poids total de la composition.In addition to their sticky action, most of these resins also have a plasticizing action. The resins can be used in the formula, alone or in the form of mixtures, in amounts ranging from 1% to 25% by dry weight, preferably 5% to 15% by dry weight, in particular from 7% to 12% by weight. in dry weight relative to the total weight of the composition.

[0021] La composition selon l’invention pourra également contenir des plastifiants. Les plastifiants sont des composés ayant une température d'ébullition élevée qui ne s’évaporent pas lors du séchage du vernis à ongles. Ces ingrédients servent de préférence à moduler la dureté de la formule. Ces plastifiants sont généralement des composés non volatiles et compatibles avec les milieux dans lesquels ils sont ajoutés. Ils représentent en général de 1 % à 12 % en poids sec, de préférence de 5 % à 10 % en poids sec, en particulier de 6 % à 8 % en poids sec par rapport au poids total de la composition.The composition according to the invention may also contain plasticizers. Plasticizers are compounds with a high boiling point that do not evaporate when the nail polish dries. These ingredients are preferably used to modulate the hardness of the formula. These plasticizers are generally non-volatile compounds and compatible with the media in which they are added. They generally represent from 1% to 12% by dry weight, preferably from 5% to 10% by dry weight, in particular from 6% to 8% by dry weight relative to the total weight of the composition.

[0022] Des exemples de plastifiants utilisables dans l'invention sont l'acétyl tributyl citrate, l'acétyl triéthyl citrate, le tributyl citrate, le triéthylcitrate, le dibutyl phtalate, le triphénylphosphate, la triacétine, le triméthyl pentanyl diisobutyrate, la triéthyl hexanoïne, le sucrose benzoate, le dibutyl adipate, le diéthyl phthalate, le diisobutyl adipate, le diisopropyl adipate, le dipropylène glycol dibenzoate, N-éthyl toluène sulfonamide, ses isomères ortho et para, le N-(2-hydroxypropyl) benzène sulfonamide et le N-(n-butyl) benzène sulfonamide, etc.Examples of plasticisers used in the invention are acetyl tributyl citrate, acetyl triethyl citrate, tributyl citrate, triethyl citrate, dibutyl phthalate, triphenyl phosphate, triacetin, trimethyl pentanyl diisobutyrate, triethyl hexanoïne , sucrose benzoate, dibutyl adipate, diethyl phthalate, diisobutyl adipate, diisopropyl adipate, dipropylene glycol dibenzoate, N-ethyl toluene sulfonamide, its ortho and para isomers, N- (2-hydroxypropyl) benzene sulfonamide and N- (n-butyl) benzene sulfonamide, etc.

[0023] La composition anhydre pour vernis à ongles peut en outre comprendre divers additifs choisis parmi les agents rhéologiques, les absorbeurs UV, les modificateurs de surface et les agents dits « traitants ».The anhydrous composition for nail polish may further comprise various additives selected from the rheological agents, UV absorbers, surface modifiers and so-called "treating agents".

[0024] Les différents additifs utilisables dans l'invention sont : [0025] Parmi les additifs de rhéologie, on citera notamment les dérivés d'argile modifiés comme le stéaralkonium hectorite ou le stéaralkonium bentonite ou de type silice pyrogénée. Ces additifs de rhéologie seront de préférence utilisés de 0,1 à 4 % en poids sec par rapport au poids total de la composition. Ces additifs permettent notamment la suspension des particules insolubles dans le vernis tels que les pigments ou encore les nacres.The various additives that can be used in the invention are: [0025] Among the rheology additives, mention may be made in particular of modified clay derivatives such as stearalkonium hectorite or stearalkonium bentonite or fumed silica type. These rheology additives will preferably be used from 0.1 to 4% by dry weight relative to the total weight of the composition. These additives allow in particular the suspension of insoluble particles in the varnish such as pigments or nacres.

[0026] La composition anhydre peut également comporter des absorbeurs UV. Parmi ces autres absorbants UV, on citera : la benzophénone-1 (CAS 131-56-6), la benzophénone-3 (CAS 131-57-7), le benzyl salicylate (CAS 118-58-1), l'étocrylène (CAS 5232-99-5), le drométrizole (CAS 2440-22-4), le butyl méthoxydibenzoylméthane (CAS 70356-09-1), etc.The anhydrous composition may also comprise UV absorbers. Other UV absorbers include: benzophenone-1 (CAS 131-56-6), benzophenone-3 (CAS 131-57-7), benzyl salicylate (CAS 118-58-1), etocrylene (CAS 5232-99-5), drometzole (CAS 2440-22-4), butyl methoxydibenzoylmethane (CAS 70356-09-1), etc.

[0027] Les autres absorbants UV seront utilisés seuls ou sous la forme de combinaison dont le pourcentage total dans la formule peut aller de 0 % à 1,5% en poids sec par rapport au poids total de la composition.The other UV absorbers will be used alone or in the form of combination whose total percentage in the formula can range from 0% to 1.5% by dry weight relative to the total weight of the composition.

[0028] Parmi les additifs utilisables selon l'invention, on citera également les modificateurs de surface comme les cyclométhicônes ou cyclopentasiloxane, les diméthicones et le triméthylsiloxysilicate, Butyl Acrylate/hydroxypropyldimethicone Acrylate Copolymer, Amodimethicone, acrylates/dimethicone copolymer...Among the additives that can be used according to the invention, mention may also be made of surface modifiers such as cyclomethicones or cyclopentasiloxane, dimethicones and trimethylsiloxysilicate, butyl acrylate / hydroxypropyldimethicone acrylate copolymer, amodimethicone, acrylates / dimethicone copolymer, etc.

[0029] Ces additifs de surface sont généralement utilisés dans des faibles quantités dans la formulation allant de 0,05 à 10 % en poids sec par rapport au poids total de la composition.These surface additives are generally used in small amounts in the formulation ranging from 0.05 to 10% by dry weight relative to the total weight of the composition.

[0030] On citera également les additifs dits « traitants » de l'ongle utilisables dans la composition selon l'invention. Les additifs traitants peuvent représenter de 0,01 % à 5 % en poids sec, de préférence de 0,05 % à 2 % en poids sec par rapport au poids total de la composition. Parmi ces additifs « traitants », on citera : • le formaldéhyde utilisé comme durcisseur de l'ongle, • la vitamine E acétate (tocophéryl acétate), • la vitamine A palmitate (rétinyl palmitate), • les dérivés organiques ou inorganiques de calcium tels que le chlorure de calcium, le pantothénate de calcium, • le diméthyloxobenzodioxasilane, • la myrrhe, • les acides aminés soufrés comme la cystéine, ses sels et leurs dérivés, la cystine, le glutathion. Les acides aminés soufrés sont en effet capables de créer des ponts de réticulation entre la kératine et les groupes SH libres de ces dérivés soufrés, • la kératine hydrolysée d'origine végétale, • les alpha-hydroxyacides comme l'acide citrique, l'acide ascorbique, • la biotine, et • l'urée et la diméthylurée.Also include the so-called "treating" additives of the nail used in the composition according to the invention. The treating additives may represent from 0.01% to 5% by dry weight, preferably from 0.05% to 2% by dry weight relative to the total weight of the composition. These "treating" additives include: • formaldehyde used as a hardener for the nail, • vitamin E acetate (tocopheryl acetate), • vitamin A palmitate (retinyl palmitate), • organic or inorganic calcium derivatives such as calcium chloride, calcium pantothenate, • dimethyloxobenzodioxasilane, • myrrh, • sulfur-containing amino acids such as cysteine, its salts and derivatives, cystine, glutathione. The sulfur-containing amino acids are indeed capable of creating crosslinking bridges between keratin and the free SH groups of these sulfur-containing derivatives, • hydrolysed keratin of plant origin, • alpha-hydroxy acids such as citric acid, and acid. ascorbic acid, • biotin, and • urea and dimethylurea.

[0031] Pour colorer ou fournir des effets particuliers à la composition anhydre pour vernis à ongles, celle-ci peut comprendre un ou plusieurs agents de coloration choisis parmi les pigments, les nacres, les glitters (paillettes) et/ou les particules métalliques. Ces agents de coloration fournissent l'aspect esthétique recherché par les utilisateurs de vernis à ongles. Ces agents de coloration peuvent produire des effets très différents tels que « irisé », « métallisé », « nacré », « miroir », « crème », « pailleté », craquelé », « mat », « néon », « fluorescent », « holographique », etc.To color or provide particular effects to the anhydrous composition for nail polish, it may comprise one or more coloring agents chosen from pigments, pearlescent agents, glitters (flakes) and / or metal particles. These coloring agents provide the aesthetic appearance sought by nail polish users. These coloring agents can produce very different effects such as "iridescent", "metallic", "pearlescent", "mirror", "cream", "glittery", crackle "," matte "," neon "," fluorescent " , "Holographic", etc.

[0032] En particulier, les pigments utilisés peuvent être sélectionnés parmi le groupe comprenant le dioxyde de titane (Cl 77891), l'oxyde de fer noir (Cl 77499), l'oxyde de fer rouge (Cl 77491 ), le DC Red 6 Ba Lake (Cl 15850), le DC Red 7 Ca Lake (Cl 15850:1), le DC Red 34 Ca Lake (Cl 15880), le FDC Yellow 5 Al Lake (Cl 19140), le FDC Blue 1 Al Lake (Cl 42090), le bleu ultramarine (Cl 77007), le DC Violet 2 (Cl 60725), le DC Black 2 (Cl 77266), etc.In particular, the pigments used may be selected from the group comprising titanium dioxide (Cl 77891), black iron oxide (Cl 77499), red iron oxide (Cl 77491), DC Red. 6 Ba Lake (C 15850), DC Red 7 Ca Lake (C 15850: 1), DC Red 34 Ca Lake (C 15880), FDC Yellow 5 Al Lake (Cl 19140), FDC Blue 1 Al Lake ( Cl 42090), ultramarine blue (Cl 77007), DC Violet 2 (Cl 60725), DC Black 2 (Cl 77266), etc.

[0033] Les nacres sont également utilisables dans l'invention, les nacres sont des particules minérales de différentes natures recouvertes d'une ou plusieurs couches d'oxydes (oxydes de titane ou oxydes de fer) ou encore de pigments. Les nacres peuvent se présenter sous la forme d'une poudre ou de plaque de tailles variées. Parmi les nacres utilisables dans l'invention, on peut citer : • les nacres préparées à partir de mica naturel et ayant subi des opérations de revêtement (coating) successives, • les nacres préparées à partir de mica synthétique appelé également « synthetic fluorphlogopite », • les nacres préparées à partir de calcium sodium borosilicate, • les nacres préparées à partir d'oxyde de silice.The nacres are also used in the invention, the nacres are mineral particles of different kinds covered with one or more layers of oxides (titanium oxides or iron oxides) or pigments. The nacres can be in the form of a powder or plate of various sizes. Among the nacres that can be used in the invention, mention may be made of: • nacres prepared from natural mica and having undergone successive coating operations, • nacres prepared from synthetic mica also called "synthetic fluorphlogopite", • nacres prepared from sodium borosilicate calcium, • nacres prepared from silica oxide.

[0034] Les glitters (paillettes) utilisables dans l'invention peuvent être préparés à partir de plusieurs types de matériaux comme les films polyesters comportant en surface une couche métallique, le polyéthylène téréphtalate, le polybutylène téréphtalate, les copolymères d'acrylates, les copolymères d'acrylates ou encore l'aluminium.The glitters (flakes) used in the invention can be prepared from several types of materials such as polyester films having a metal layer on the surface, polyethylene terephthalate, polybutylene terephthalate, copolymers of acrylates, copolymers acrylates or aluminum.

[0035] Selon un mode de réalisation de l’invention, la composition anhydre pour vernis à ongles comprend une quantité d’agent de coloration comprise de 0,1 % à 20 % en poids sec et de préférence de 0,5 % à 12 % en poids sec par rapport au poids total de la composition.According to one embodiment of the invention, the anhydrous composition for nail polish comprises an amount of coloring agent of from 0.1% to 20% by dry weight and preferably from 0.5% to 12% by weight. % by dry weight relative to the total weight of the composition.

[0036] Tous les modes de réalisation cités précédemment peuvent être combinés sous réserve de leur faisabilité technique.All the embodiments mentioned above can be combined subject to their technical feasibility.

Exemple [0037] Ci-dessous dans le Tableau 1, un exemple de formulation selon l'invention. L'effet de l'acide polylactique sur la brillance, la dureté, l'adhérence, la viscosité, la thixotropie et le hardening du vernis à ongles est illustré dans le Tableau 2 en comparaison à un vernis à ongles classique à base nitrocellulosique.Example [0037] Below in Table 1, an example of a formulation according to the invention. The effect of polylactic acid on the gloss, hardness, adhesion, viscosity, thixotropy and hardening of nail polish is shown in Table 2 in comparison to a conventional nitrocellulose nail polish.

[0038] Tableau 1Table 1

[0039] Pour déterminer la brillance du film formé, l'analyse par brillancemètre est réalisée sur des films secs appliqués sur des cartes de contraste normalisées à l'aide d'un applicateur permettant la formation d'un film humide d'une épaisseur de 100 pm. Le film déposé est séché à 30°C pendant 12 h. La brillance est mesurée sous un angle de 60 par rapport à la normale du film et est réalisée trois fois. La valeur finale obtenue est la moyenne de ces trois mesures.In order to determine the gloss of the film formed, the glossmeter analysis is carried out on dry films applied to standardized contrast cards using an applicator allowing the formation of a wet film with a thickness of 100 pm. The deposited film is dried at 30 ° C. for 12 hours. The gloss is measured at an angle of 60 relative to the normal of the film and is carried out three times. The final value obtained is the average of these three measurements.

[0040] Concernant la mesure de thixotropie, trois mesures différentes sont effectuées correspondant aux différentes contraintes subies par le vernis lors de l'application. Une première mesure est effectuée pour le vernis au repos, le spindle du viscomètre tourne à une vitesse de 6 tr/min pendant une minute. Il passe ensuite à 60 tr/min pour modéliser le mélange dans le flacon puis l'application sur ongle. Enfin, la vitesse de rotation revient à 6 tr/min pour modéliser le comportement du vernis une fois étalé sur ongle et donc au repos. Le rapport entre la troisième viscosité et la seconde donne l'indice thixotropique.Regarding the measurement of thixotropy, three different measurements are made corresponding to the different stresses experienced by the varnish during the application. A first measurement is made for the varnish at rest, the spindle of the viscometer rotates at a speed of 6 rpm for one minute. It then goes to 60 rpm to model the mixture in the bottle and then the nail application. Finally, the speed of rotation returns to 6 rpm to model the behavior of the varnish once spread on nail and therefore at rest. The ratio between the third viscosity and the second gives the thixotropic index.

[0041] La dureté de la base est contrôlée en étalant un film fin de 100 pm sur une plaque en verre à l'aide d'un barcoater. La plaque est mise à l'étuve pendant 12h. La dureté est mesurée grâce à un pendule de Persoz. L'essai de dureté au pendule s'appuie sur le principe selon lequel l'amplitude de l'oscillation d'un pendule qui touche une surface diminue plus rapidement si cette surface est tendre. La plaque de verre est bloquée entre le support du pendule et une plaque de métal. La dureté est donc notée en nombre d'oscillations du pendule avant d'atteindre un angle de 4°.The hardness of the base is controlled by spreading a thin film of 100 .mu.m on a glass plate using a barcoater. The plate is put in the oven for 12 hours. Hardness is measured with a Persoz pendulum. The pendulum hardness test is based on the principle that the amplitude of oscillation of a pendulum which touches a surface decreases more rapidly if this surface is soft. The glass plate is locked between the pendulum support and a metal plate. The hardness is noted in number of oscillations of the pendulum before reaching an angle of 4 °.

[0042] L'adhérence est testée grâce à un couteau avec quatre lames parallèles. La plaque où a été déposée la base est griffée de manière verticale et horizontale de manière à dessiner de petits carrés. C'est en observant le détachement des parties de la base que l'on qualifie l'adhérence de celle-ci.The adhesion is tested with a knife with four parallel blades. The plate where the base was laid is scratched vertically and horizontally so as to draw small squares. It is by observing the detachment of the parts of the base that one qualifies the adhesion of this one.

[0043] Tableau 2[0043] Table 2

[0044] On constate que les propriétés de la composition pour vernis à ongles comprenant l'acide polylactique sont identiques voir très similaires aux propriétés d'une composition pour vernis à ongles classique comprenant de la nitrocellulose.It is found that the properties of the nail polish composition comprising polylactic acid are identical or very similar to the properties of a composition for conventional nail polish comprising nitrocellulose.

[0045] Cela confirme bien que l'acide polylactique représente donc une alternative tout à fait novatrice à la nitrocellulose.This confirms that polylactic acid represents a completely innovative alternative to nitrocellulose.

Claims (6)

1. Composition cosmétique anhydre pour vernis à ongles comprenant au moins un solvant organique cosmétiquement acceptable et au moins un agent filmogène de type biopolyester, le biopolyester étant l'acide polylactique et la composition cosmétique ne contenant pas de nitrocellulose.1. An anhydrous cosmetic composition for nail polish comprising at least one cosmetically acceptable organic solvent and at least one film-forming agent of the biopolyester type, the biopolyester being polylactic acid and the cosmetic composition not containing nitrocellulose. 2. Composition selon la revendication 1, dans laquelle la quantité d'acide polylactique est comprise entre 0,1 % et 45 % en poids sec, de préférence entre 1 % et 25 % en poids, de manière particulièrement préférée entre 5 % et 12 % en poids sec par rapport au poids total de la composition anhydre.2. Composition according to claim 1, wherein the amount of polylactic acid is between 0.1% and 45% by dry weight, preferably between 1% and 25% by weight, particularly preferably between 5% and 12% by weight. % by dry weight relative to the total weight of the anhydrous composition. 3. Composition selon l'une quelconque des revendications 1 ou 2, dans laquelle le solvant organique est choisi parmi le toluène, le xylène, l'acétate d'éthyle, l'acétate de butyle, l'acétate d'isobutyle, l'acétate de propyle, l'acétate de méthyle, une cétone, un ester, l'isopropanol, le butanol, le diacétone alcool, l'éthanol dénaturé avec la méthyléthylcétone ou le diéthyléther, les hydrocarbures linéaires ou cycliques, de préférence l'hexane, le cyclohexane, l'heptane ou n'importe quelle combinaison de ceux-ci.3. Composition according to any one of claims 1 or 2, wherein the organic solvent is selected from toluene, xylene, ethyl acetate, butyl acetate, isobutyl acetate, propyl acetate, methyl acetate, a ketone, an ester, isopropanol, butanol, diacetone alcohol, ethanol denatured with methyl ethyl ketone or diethyl ether, linear or cyclic hydrocarbons, preferably hexane, cyclohexane, heptane or any combination thereof. 4. Composition selon l'une quelconque des revendications 1 à 3, dans laquelle le solvant organique est l'acétate d'éthyle, l'acétate de butyle, de l'alcool ou une combinaison de ceux-ci.The composition of any one of claims 1 to 3, wherein the organic solvent is ethyl acetate, butyl acetate, alcohol or a combination thereof. 5. Composition selon l'une quelconque des revendications 1 à 4, dans laquelle la quantité de solvant organique de la composition est comprise entre 60 % et 80 % en poids par rapport au poids total de la composition anhydre. 6. Composition selon l'une quelconque des revendications 1 à 6 qui comprend un ou plusieurs autres agents filmogènes. 7. Composition selon la revendication 6, dans laquelle le ou les autres agents filmogènes est/sont choisi(s) parmi la cellulose, un dérivé de cellulose, une résine vinylique, une résine acrylique ou n'importe quelle combinaison de ceux-ci, de préférence l'agent filmogène est un dérivé de cellulose choisi parmi l'acétate butyrate cellulose, l'éthylcellulose et l’hydroxypropylcellulose, de manière davantage préférée l'agent filmogène est l'acétate butyrate cellulose.5. Composition according to any one of claims 1 to 4, wherein the amount of organic solvent of the composition is between 60% and 80% by weight relative to the total weight of the anhydrous composition. The composition of any one of claims 1 to 6 which comprises one or more other film-forming agents. The composition of claim 6, wherein the one or more other film-forming agents is / are selected from cellulose, a cellulose derivative, a vinyl resin, an acrylic resin or any combination thereof, preferably the film-forming agent is a cellulose derivative selected from acetate butyrate cellulose, ethylcellulose and hydroxypropylcellulose, more preferably the film-forming agent is acetate butyrate cellulose. 8. Composition selon la revendication 6 ou 7, dans laquelle la quantité du ou des autres agents filmogènes est comprise entre 0,5 % et 15 % en poids sec, de préférence entre 2 % et 5 % en poids sec par rapport au poids total de la composition anhydre. 9. Composition selon l’une quelconque des revendications 1 à 8 comprenant en outre un ou plusieurs additifs choisis parmi les résines, les plastifiants, les agents rhéologiques, les absorbeurs UV, les modificateurs de surface et les agents dits « traitants ». 10. Composition selon l’une quelconque des revendications 1 à 9 comprenant en outre un ou plusieurs agents de coloration choisis parmi les pigments, les nacres, les glitters et/ou les particules métalliques. 11. Vernis à ongles comprenant une composition anhydre selon l'une quelconque des revendications précédentes. 12. Utilisation d'acide polylactique, comme agent filmogène dans une composition anhydre pour vernis à ongles. Abrégé Composition cosmétique anhydre pour vernis à ongles comprenant au moins un solvant organique cosmétiquement acceptable et au moins un agent filmogène de type biopolyester, le biopolyester étant l'acide polylactique et la composition cosmétique ne contenant pas de nitrocellulose. Utilisation d'acide polylactique, comme agent filmogène dans une composition anhydre pour vernis à ongles. Ad point V Déclaration motivée quant à la nouveauté, l’activité inventive et la possibilité . d'application industrielle; citations et explications à l'appui de cette declaration Ί La présente opinion écrite fait mention des documents D1 à D6 suivants cites danste rapport .de . recherche .préliminaire. DI DATABASE WPI Week 201408 Thomson Scientific. London, GB; AN 2012Ό18228 XP002772374, &amp; KR 2012 0123853 A (KUMOH NAT INST TECHNOLOGY IND ACAD COOP) 12 novembre 2012 (2012-11-12) D2. DATABASE WR Week 201653 Thomson Scientific, London, GB; AN 2016-47738Q XP002772375, &amp; WO 2016/121696 Al (DAITO KASEl KOGYO CO LTD) 4 août 2016 (2016-08-04) D3. US A1 .(VALIA: DAVïD'TUS]: -ET AL).2 -mars:2017 (2017-03-02) D4: WO 2014/176275 Al (CREATIVE NAIL DESIGN INC [US]) 30 octobre 2014 (2014-10-30) D5: US 2014/199256' A :(SASIK ÇAMILLE T'IUSÏ:· ET AL) 17: juillet 2014 (2014-07-17) D6 - - DATABASE WPI Week 201159 Thomson Scientific, London, GB; AN 2011-L09203 XP002772376, &amp; JP 2011 168552 A (DAITO KASEl KOGYO KK) 1 septembre 2011 (2011-09-01) 2 La présente revendication indépendante 1 concerne une composition cosmétique anhydre pour vernis à ongles comprenant au moins un solvant organique cosmétlquement acceptable --et--au moins un', agent, filmogène-, 'de type biopolyester, le biopolyester étant î ‘ acide polylactique. L'attention de la Demanderesse est attirée sur le fait, que l'utilisation du libellé "pour vernis à ongles" dans cette revendication 1 n'a pas d'effet limitatif sur la composition cosmétique anhydre, dans la mesure où elle ne modifie pas les caractéristiques physiques de la composition telle quelle. Ainsi, le fait qu'une composition ou qu'un produit d'un document de l'art antérieur est destiné à une utilisation différente ne modifie pas les caractéristiques distinctives qui correspondent ' - : à- : - celles ' de : : la : - présente · revendication ' 1.. - Par conséquent, 'toute - : composition .- -anhydre -.--comprenant --- -un. -: -solvant- --organique .- : -cosmétlqueiment -· acceptable et .de l'acide polylactique, et pouvant 'être: utilisée- dans .-ce- but, pnve l'objet de la revendication 1 de sa nouveauté. 3' La -revendication 'indépendante' "1-1- divulgue.: un -vernfs-à-: ongles-: comprenant : une composition anhydre selon l'une quelconque des revendications précédentes. L'attention de la Demanderesse est attirée sur le fait que, du fait du terme "comprenant” utilisé, le vernis à. ongles peut contenir en plus des composés présents- :dans-:la- composition anhydre, tout-autres ingrédients utilisés-dans le -domaine des vernis à ongles, et en particulier--: de-l'eau.. Par- conséquent,.: ce-vernis-à'ongles-ne présente-pas-forcément -un-caractère' anhydre. 4' Nouveauté 4 1 La présente demande ne remplit pas les conditions de brevetabilité, l'objet des revendications indépendantes 1, 11 et 12 n'étant pas conforme au cntère de nouveauté pour les raisons suivantes: Le document 'D1 décrit une composition de manucure anhydre sous forme -d'un vernis à ongles comprenant un solvant organique cosmétlquement acceptable (cf. alcool isopropylique) et de l'acide polylactique (voir le résumé). Les exemples 1-3 de la traduction anglaise (voir document DI a annexé, paragraphes [0026H0031]) décrivent de tels vernis à ongles anhydres comprenant de l'acétate d'éthyle, de l'acétate de butyle, du toluène et de l'alcool isopropylique comme solvants organiques et de l'acide polyiactique comme agent filmogène. La composition contient de surcroît un agent filmogène supplémentaire. en l'occurrence la nitrocellulose, des plastifiants, : . . des : . agents rhéologiques: et des : agents de . coloration. : .Par· -conséquent, l'objet des revendications indépendantes 1, 11 et 12 n'est pas considéré comme nouveau. Le document D2 divulgue des compositions anhydres pouvant être utilisées comme vernis à ongles comprenant un solvant organique cosmétiquement acceptable (cf. l'acétate d'éthyle) et de l'acide polyiactique (voir le paragraphe [0077] de la traduction anglaise, document D2a annexé). De surcroît, ce document D2a exemplifie un vernis à ongles (voir le paragraphe [0090] de la traduction anglaise) comprenant du 1,3-butylène glycol comme solvant organique, de l'acide polyiactique et d'autres ingrédients tels que desplastifiants, .. : des · · •pigments: :et des · agents. : - · rhéologiques. Par · conséquent, l'objet : : des revendications: indépendantes . : : 1 ' : et ' 11 : : n'est : : pas : : : considéré : comme : nouveau. Les documents D3 et D4 (voir les citations des parties pertinentes dans le rapport de recherche préliminaire) enseignent l'utilisation de l'acide polyiactique comme agent filmogène (polymere filmogène) dans des vernis à ongles anhydres : (une seule sélection dans une liste d'agents filmogènes). Par : .conséquent, l'objet la revendication:, indépendante 12 . n'est pas : considéré-comme nouveau. Le: : : document D5 (voir les citations des parties pertinentes dans : : : te rapport de : recherche préliminaire) décrit une composition anhydre susceptible d'être utilisée comme vernis à ongles et comprenant de l'acide polyiactique comme agent filmogène et un solvant organique cosmétiquement acceptable tel que les alcools en C1-C6, le carbitoi ou l'acétone. Par conséquent, l'objet de la revendication indépendante 1 n'est pas considéré comme nouveau. Le document D6 divulgue : des compositions anhydrescomprenant unmolvant:. organique cosmétiquement acceptable et de l'acide polyiactique comme agent filmogène (voir les paragraphes [0006], [0022] et [0024] de la traduction: anglaise, document D6a annexé). L'acide polyiactique est présent en une concentration de 40% dans de l'acétate d'éthyle. Le document D6a décrit également des compositions de vernis à ongles comprenant de l'acide polyiactique, des solvants organiques (cf. acétate de butyle, toluène, acétate d'éthyle, alcool isopropyiique) ainsi que d'autres ingrédients tels que des plastifiants, des agents rhéologiques et des pigments. Par conséquent, l'objet des revendications indépendantes 1, 11 et 12 n'est pas considéré comme nouveau.8. Composition according to claim 6 or 7, wherein the amount of the other film-forming agent (s) is between 0.5% and 15% by dry weight, preferably between 2% and 5% by dry weight relative to the total weight. of the anhydrous composition. 9. Composition according to any one of claims 1 to 8 further comprising one or more additives selected from resins, plasticizers, rheological agents, UV absorbers, surface modifiers and so-called "treating agents". 10. Composition according to any one of claims 1 to 9 further comprising one or more coloring agents chosen from pigments, nacres, glitters and / or metal particles. 11. Nail polish comprising an anhydrous composition according to any one of the preceding claims. 12. Use of polylactic acid as a film-forming agent in an anhydrous nail polish composition. Anhydrous cosmetic composition for nail polish comprising at least one cosmetically acceptable organic solvent and at least one film-forming agent of biopolyester type, the biopolyester being polylactic acid and the cosmetic composition not containing nitrocellulose. Use of polylactic acid as a film-forming agent in an anhydrous nail polish composition. Ad point V Motivated statement as to novelty, inventive step and possibility. industrial application; citations and explanations in support of this statement Ί This written opinion refers to the following documents D1 to D6 cited in this report. preliminary research. DI DATABASE WPI Week 201408 Thomson Scientific. London, GB; AN 2012Ό18228 XP002772374, &amp; KR 2012 0123853 A (KUMOH NAT INST TECHNOLOGY IND ACAD COOP) November 12, 2012 (2012-11-12) D2. DATABASE WR Week 201653 Thomson Scientific, London, GB; AN 2016-47738Q XP002772375, &amp; WO 2016/121696 A1 (DAITO KASEI KOGYO CO LTD) August 4, 2016 (2016-08-04) D3. US A1 (VALIA: DAVID'TUS): -ET AL) .2 -March: 2017 (2017-03-02) D4: WO 2014/176275 A1 (CREATIVE NAIL DESIGN INC [US]) October 30, 2014 (2014- 10-30) D5: US 2014/199256 A: (SASIK ÇAMILLE T'IUSI: · AND AL) 17: July 2014 (2014-07-17) D6 - - WPI Week DATABASE 201159 Thomson Scientific, London, UK; AN 2011-L09203 XP002772376, &amp; The present independent claim 1 relates to an anhydrous cosmetic composition for nail polish comprising at least one cosmetically acceptable organic solvent - and - at least one a biopolyester-type film-forming agent, the biopolyester being polylactic acid. The attention of the Applicant is drawn to the fact that the use of the wording "for nail polish" in this claim 1 has no limiting effect on the anhydrous cosmetic composition, insofar as it does not modify the physical characteristics of the composition as it is. Thus, the fact that a composition or a product of a prior art document is intended for a different use does not alter the distinguishing characteristics which correspond to those of: Therefore, any composition comprising: an anhydrous composition comprising: The invention relates to a method of the present invention and to the use of the polylactic acid and may be used for the purpose of claim 1 of its novelty. The "independent" claim "1-1- discloses a -vernfs-to-nails comprising: an anhydrous composition according to any one of the preceding claims. fact that, because of the term "comprising" used, the varnish. Nails may contain in addition to the compounds present in the anhydrous composition, any other ingredients used in the field of nail polish, and in particular: water. This nail varnish does not necessarily have an anhydrous character. 4 'Novelty 4 1 This application does not meet the conditions for patentability, the subject matter of independent claims 1, 11 and 12 not being in accordance with the novelty guideline for the following reasons: Document' D1 discloses a manicure composition anhydrous form of a nail polish comprising a cosmetically acceptable organic solvent (see isopropyl alcohol) and polylactic acid (see summary). Examples 1-3 of the English translation (see document DI annexed, paragraphs [0026H0031]) describe such anhydrous nail varnishes comprising ethyl acetate, butyl acetate, toluene, and the like. isopropyl alcohol as organic solvents and polyacetic acid as film-forming agent. The composition additionally contains an additional film-forming agent. in this case nitrocellulose, plasticizers,: . of:. rheological agents and agents. coloring. Therefore, the subject-matter of the independent claims 1, 11 and 12 is not considered new. Document D2 discloses anhydrous compositions that can be used as nail polish comprising a cosmetically acceptable organic solvent (see ethyl acetate) and polyacetic acid (see paragraph [0077] of the English translation, document D2a Annex). In addition, this document D2a exemplifies a nail polish (see paragraph [0090] of the English translation) comprising 1,3-butylene glycol as organic solvent, polyacetic acid and other ingredients such as plasticizers,. : · · • pigments :: and agents. : - · rheological. Therefore, the object:: claims: independent. :: 1 ': and' 11:: is:: not::: considered: as: new. Documents D3 and D4 (see citations of the relevant parts in the preliminary research report) teach the use of polyacetic acid as a film-forming agent (film-forming polymer) in anhydrous nail polish: (only one selection from a list of film-forming agents). By: accordingly, the object the claim :, independent 12. is not: considered-as new. Document D5 (see citations of relevant parts in: the report of: preliminary research) describes an anhydrous composition suitable for use as a nail polish and comprising polyacetic acid as a film-forming agent and a solvent. cosmetically acceptable organic such as C1-C6 alcohols, carbitol or acetone. Therefore, the subject of independent claim 1 is not considered new. D6 discloses: anhydrous compositions comprising a solvent. organic cosmetically acceptable and polyacetic acid as film-forming agent (see paragraphs [0006], [0022] and [0024] of the translation: English, attached document D6a). The polyacetic acid is present in a concentration of 40% in ethyl acetate. D6a also discloses nail polish compositions comprising polyacetic acid, organic solvents (ie, butyl acetate, toluene, ethyl acetate, isopropyl alcohol) as well as other ingredients such as plasticizers, rheological agents and pigments. Therefore, the subject matter of the independent claims 1, 11 and 12 is not considered new. 42. Les caractéristiques supplémentaires des revendications dépendantes 2 à 10 sont également citées dans au meins l'un des documents Di, D2, D5 et D6. Pour - cette .raison,; l'objet· de: ces . .revendications: '2-1'0·· .n'est. pas. considéré· : comme-nouveau.. 5· Àctivité.inenntive 5.1 L'obietessprésnntesreeendication s1-1 2n'étan tpasnuweau . !adiscussic n sur l'activité inventive est repoussée à l'établissement de la nouveauté. les remarques ·suivcetss. .peuvent-être·priésé:sh:compté. 5 2 La présente demande adresse le problème technique· ·de .substituer la niirosslluloés par d'autres agents filmogènes dans les formulations de vernis à ongles sans altérer les autres propriétés du vernis à ongles, notamment la tenue,.ia·bri:liensei la ·. co·u:vranse> ·ls'·tempé·de ééchegs-'na·is du:rsi:sss:meet. 5.3·: · Ce problème···tsshniqus···a···été ····: dené ··: : la · ρrόéenis: ·demcede ·' en' utilisant· ·: de. 1^^ ·pnl.ylestiqae· comme· : 'agent · film'ngèes:· en .·cnmbinai.énn. "avec :un snlvant·nfgeniqas. 5.4·.. Comme indiqué ci-dessus, les documents 03 et D4 enseignent déjà |'utîl·iéetioe· de: '.l'cside·:ρol·ylesΐiqae:·so:mms agent 'dans des vernis· à· ongles anhydres. Par conséquent, shecan:·de··sss documents· D3 .eu 04 peut· être · · considere · comme · · représentant · l'état · : de · la · · : · tssheiqas : : · le · plus proche · · · : de· · · l'objet revendiqué. 5.5· Les documents"03· et "04··exemplifient" des ·sompoéitines de "vernis 'à Ongles · comprenant des solvants organiques, des pigments, des agents plastifiants, des agents rhéologiques et des agents filmogènes. Ces vernis à ongles diffèrent de ceux présentement revendiqués de par la nature de l'agent fImogens, par exemple l'utiliéatine de nitrocellulose ou d'acétate butyrate cellulose à :|c ;pIccs d'un : acide: polylestiqas·. 5.6· O:epé.Ces.·:deaχ:"d:nöumeets, l'acide pnlylaStique est placé au même niveau· que d'autres agents filmogenes couramment utilisés dans des vernis à ongles (comme la nitrossllulnés ou I acétate butyrate cellulose), et par conséquent,· l’homme-du: •métier "serait·, fnrtemsnt·:.:incité à •utiliser -un asids··pnlylactiqas· dans· les vernis à ongles des documents D3 ou D4 en plus ou au lieu de l'agert fllmogène présent dans ladite composition. En tout état de cause, l'acide polylactique a déjà été employé ou proposé dans· le-même.-, but -dans -des -compositions -de vernis- -à-ongles· analogues. Il serait évident pour l'homme du métier désireux de parvenir au même résultat d'utiliser un - adde . polylactique, avec-un-effet-correspondant, dans les vernis à -ongles selon les documents D3 ou 04 afin d'obtenir une composition cosmétique anhydre ou un vernis à ongles conformément aux revendications indépendantes 1 et 11. 5.7 Les présentes revendications dépendantes 2 à 10 ne semblent pas contenir de caractéristiques supplémentaires qui satisfassent aux exigences d'activité inventive en étant combinées aux caractéristiques de la revendication 1 à laquelle lesdites revendications dépendantes sont liées. En effet, les caractéristiques de ces revendications sont soit divulguées dans les documents ' D3 et - 04, . peuvent - - en être - - - : dérivées - - - . ou bien- sont connus dans- - le - -domaine-technique en-question... En-l'absence-d'un -effet.-technique-surprenant-lié à-ces-caractéristiques, la-combinaison de-ces-caractér^^stiques-est donc- le. fruit d'un choix arbitraire parmi l'ensemble de ceux que l'homme du métier avait à sa disposition. 5.8- Par conséquent, la présente demande ne remplit pas les conditions de brevetabilité, l'objet des présentes revendications 1 à 12 n'impliquant pas une-activité inventive.42. The additional features of the dependent claims 2 to 10 are also cited in at least one of the documents D 1, D 2, D 5 and D 6. For this reason,; the object of these. .requests: '2-1'0 ··. not. considered ·: as-new. 5 · Active.activity 5.1. The subject of prescribing s1-1 2 is not relevant. ! adiscussic n on the inventive step is pushed back to the establishment of the novelty. remarks · follow-up. .peuvent be Priese ·: sh: counted. The present application addresses the technical problem of substituting other film-forming agents for nail varnish formulations without altering the other properties of the nail polish, particularly the holding of the nail varnish. ·. co · u: vranse> · rsi: sss: meet. 5.3 ·: · This problem ··· has been ··· ·································································· 1 ~^ · pnl.ylestiqae · as ·: · agent · film'ngèes: · en. · Cnmbinai.énn. 5.4. .. As mentioned above, the documents 03 and D4 already teach the use of: · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · in anhydrous nail polishes, therefore, the following may be considered as representing the condition of: · tseheiqas · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · : · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · · These nail polishes differ from those currently claimed by the nature of the imogenent agent, for example nitrocellulose or acetate butyrate cellulose utilic acid at: ## EQU1 ## the pH of an acid: polylestiqas 5.6 · O: this is the same level as other agents. s filmogens commonly used in nail polish (such as nitrossllulins or acetate butyrate cellulose), and as a result, the "man-of-the-job" would, in particular, be encouraged to use-a-asids. In the nail varnishes of the D3 or D4 documents in addition to or instead of the agglomerative agent present in said composition. In any case, polylactic acid has already been used or proposed in the same way, but in the compositions of similar nail varnish. It would be obvious to a person skilled in the art desiring to achieve the same result of using a - adde. polylactically, with-a-corresponding-effect, in the nail varnishes according to D3 or 04 to obtain an anhydrous cosmetic composition or a nail polish according to independent claims 1 and 11. 5.7 The present dependent claims 2 to 10 do not appear to contain additional features that satisfy the requirements of inventive step by being combined with the features of claim 1 to which said dependent claims are related. Indeed, the features of these claims are either disclosed in documents D3 and -04. can - - in - - - -: derivatives - - -. or else are known in the technical field in question in the absence of a surprisingly technical effect related to these characteristics, the combination of these -characteristic is therefore. the result of an arbitrary choice among all those whom the person skilled in the art had at his disposal. 5.8- Therefore, the present application does not fulfill the conditions of patentability, the subject matter of the present claims 1 to 12 not involving an inventive step. 6- Lobje tee - revendictioios - - à 2 -es - sscepptiei - a’appiicatio - indusi^rit^l- e dans le domaine des compositions cosmétiques. Ad point : : VII j Certaines observations relatives-à-la-demande 1 - - - a - reuendicatie -éPeenaenj e Secure rtl aprevenv-td'n nade eofylai^c^ticiu e en une quantité comprise entre 0,1% et 45% en poids sec par rapport au poids total de la composition anhydre. De -son - -côté, -la- - revendication - - - dépendante - 5, - lié --à . - - '-la reeUedicatiO.e - - : - - 2,.. récite - -que - - la - - quantité - - de-- - solvant - ' - organiq.uu - - est - - comprise· - - entre - 60%. - et : - - 80% : : -en - poids - -par rapport au poids total de la composition anhydre. Ainsi, dans le cas où par exemple la composition anhydre contient 45% en poids sec d'acide polyiactique (ce qui peut être ie cas selon la revendication 2), la quantité maximale de tous les ingrédients supplémentaires est de 55% en poids. Par conséquent, la quantité minimale en solvant organique de 60% en poids selon la revendication 5 ne peut pas être atteinte. Il s'en suit donc qu'une concentration de 45% en poids sec d'acide poiylactique n'est pas possible : en: : : tenant compte de l'objet de: . l a. : revendication. . 5. Ainsi, ::eettè::discprdance entre les revendications dépendantes 2 et Sucrée-un doute quant à l'objet de la protection demandée, au point que les revendications manquent de clarté. 2: La<: présente- revendication 6 est dépendante des-revendïcaions·· 1 Cette dépendance devrait cependant être limitée aux revendications 1 à 5. Machine Translated by ThomsonReuters SUBJECT : OF : THE . INVENTION ..... ...... The .naili cosmetics which are eco-friendly, and were excellent in applicability [paintability using biodegradable film formation resin, excellent in glossiness, and . excellent. . in film strength are provided, PROBLEM to be SOLVED Polylactiq acid which is a natural plant-derived non~crystaliine biodegradable high molecular compound shown by foilowing Chemical formula (1) is mix j blended as a resir component. •EMT : : <ÉMW79817p0éW. : . is loading,, (In formula, R1fR2,R3 is a Cl or more saturated hydrocarbon group, and is same or different. n : : : is an integer greater than or equal to 1.) TECHNICAL FIELD [0001] This invention relates to eco-friendly riaF cosmetics excellent in appllcabiiity | paintability. DESCRIPTION OF .RELATED ART > [0002] Generally, .nail' cosmetics contain organic solvents, such as ethyl acetate, lactic acid ester, and a hydrogen oxide, cellulose nitrate, film formation resin, the plasticizer, the coloring agent, etc. ; The components which actually form a membrane [filmjcoat as nail cosmetics are cellulose nitrate and him formation resin. Cellulose nitrate is a natural origin component which uses a cellulose as a raw material, However, Him formation resin generally used is synthetic macromolecules, such as acrylic resin, an alkyd-type resin, a toluene sulfone type-resin, and a sucrose type-resin derived from a ..half-natural product. Specifically as this film formation resin, co acrylic ester / methacrylic acid ester copoiymur, a phthalate system alkyd resin, an isophthclic-acid typujsystum|group alkyd resin, a succinic acid series alkyd resin, a toldueusulfoecmidu/formclduhydu resins, toluene / sulfonamide / epoxy resin, ....... Sucrose benzo ade, sucrose Acera fgfCf \ butylate[butyrate etc, can be mentioned. Since these resin is synthe^c-macromolecule typu|systum|grodps, it does not have biodegradability. [ÖÖ03]" Each recent-years and industrial field | area WHEREIN: ...... .............. It - has become important to use a biodegradable material and it is just going to desire also in haili cosmetics to use a biodegradable material. However, _________ In the conventional hal'j cosmetics, cellulose nitrate is a component of natural plant- • derived, However, Since film formation resin mix [blended simultaneously with this cellulose nitrate was -a" synt.hutic-macromGlecdlu type] system [group, there existed a trouble that it was not uco-·friuedly. PROBLEM - " " TO ' ' ' - - BE' - , . . SOLVED ' - - BY- " THE INVENTION [0004]" This invention was made [formed in view of the above troubles, and is ecofriendly using biodegradable film formation resin, And it aims at providing the paii cosmetics which were excellent in cppl^cabiîltyJpcintcbility, excellent in glossiness, and excellent in film strength. MEANS TO- SOLVEfTHE- PROBLEM [0005] [Nail cosmetics by this invention in order to achieve the said subject, J, V.-.-.-.-n-.-.-.-.Λ...... ............ Poly lactic acid which is a non-crystalline biodegradable high molecular compound of natural plant-derived shown by following Chemical formula (!) is mix | blended as a resin component, It is characterized by the cbovu-muetioeud. w- «EMôwà’ÂTDi» -is- locdeg... (In formula, &amp;1,Ρ2,Ρ3 is a Cl or more saturated hydrocarbon group, and is same or different. n- ie-ce- integer- gructtuΓ-th:ae-:or equal -to-1.:) INVENTION [0006] According to this invention, biodegradable poîyiactic acid which is a natural plant-derived high molecular compound is used as film formation resin, Therefore It is eco-friendly, And the nail cosmetics which were excellent in applîcabiilty|paintability, excellent in glossiness, and excellent in film strength can be obtained. EMBODIMENT : OF : THE INVENTION [0007] Next, concrete embodiment of theinaU cosmetics by this invention is described. [0008] Biodegradable polylactid acid of natural plant-derived used for this invention is a thing obtained by superposing [polymerizing the lactide mainly refine [purified considering maize as a raw material, By combining the optical isomers of this lactide, a high molecular compound non-crystailine and soluble to the organic solvent used for nail: cosmetics can be superposed[polymerized. .................... Although the glass transition point of this non-crystalline poiyiacttcacid is based also . on the combination ratio of optical isomers, it is preferable that it is the range of 50 degreeC from -10 degreeC. [0009] Moreover, especially the polymerization degree of polylactic acid used for this invention is although it does not restrict [limit, It is... preferable to set it as the polymerization degree which gives a viscosity moderate as nail . cosmetics. Furthermore, pojyiactic. acid used for this invention has the biodee}rackalbilty in which the process by aerobic decomposition and an anaerobic resolution . is possible. Moreover, when mix[blending with naif cosmetics non-crystalline polylactic acid used for this invention, it is good to make it melt [dissolve in a suitable organic solvent, for example, ethyl acetate, butyl acetate, methyl ethyl ketone, acetone etc., beforehand. [0010] That is, this invention is the following component.............. (a) Natural plant-derived, biodegradable non-crystalline poiy'iactic acid (said Chemical formula (1)) (b) Cellulose nitrate (c) Organic pigment (d) Gelatinize (e) Non -aromatic organic solvent These . . are contained, The nai.; cosmetics characterized by the above-mentioned are provided. [0<Ol] Cellulose .nitrats of (b) shown here wili not be specifically limited if used for the cnevsntineal nail; cosmetics,· N!trnssllulnés H 1/2, Hi/4, Hl/8, etc. are used. [0012] Moreover, the organic pigment of (c) is good to kneadlmi* and construct in chip forms beforehand with the said nltrncsllulnés (= ssiiulnés nitrate) and plasticizer, for example, a citrate etc., 3 rolls, etc. About the colored pigment mix [blended, if normally used for cosmetics, it will not specifically limit, A titanium oxide, carbon black, chromium oxide, chromium hydroxide, "a navy] Prussian blue, Lake pigments, such as organic colored pigments, such as inorganic colored pigments, such as pearl pigments, such as ultramarine· blue, · red iron 'oxide, yellow iron oxide or a black iron oxide, and mica titanium, Red No. 226 and Yeilow No. 205, and Blue No. 404, and also red No. 201, Yellow No. 202, Blue No. 1, Yellow No. 4, are msetinesd. Mofsnvsr, . various éurfass treatment, such "as· a· verious·éilίcoeizatine· and· "·αlkyl.éîlaee· process, an alkyl titeeets process, a lauroyl Iysîcs process, the phosphate process, a perfluoro alkyl silane process, and a silica process, may be given to · these : ·colored .pigmsnté [0013] · The gslatinizsrs of (d) ars very littls addition and ths viscosity of KaiL cosmetics is mads to increase. For example, Montmnrillneits groups, such as a mnntmnrillneits, smsctits, or hectorite, Synthetic micas, such as sodium silicic mica, sodium /f/j/I light| write|right, or a lithium taeniolite stc., Or hectorite, a clay mineral like a bentonite, or a silicic acid anhydride is msntinesd. [0014] Oxidation butyl, an oxidation sthyl, msthyl sthyl ketone, acetone, e-baieenl,. isopropyl alcohol, ethyl alcohol etc'. are mentioned as a non-ernmetis organic én!veet oi (s). ........................................................................................... In addition, an oil-based component ·.is m-ix|tip^r^d^€d for ths objective of improving improvement of ths removability of a msmbrene|film|soet, reétnretine [repair property, etc., and ths compatibility of a mixiegjblsedieg raw material, Fdil'hermore, you may add a plasticizer, a cosolvent, a diluent, a sizing [paste agent, · a stabilizer, surfactant, dye, a fregreese|flevnr, water, etc It is [ said ] under mixing[bleedieg arid 0-15 mass % of the compounding quantity of cellulose nitrate is a suitable quantity, When ths compounding quantity of cellulose nitrate is 0 mass %, it is good to knead[mix a colored pigment and a plasticizer to biodegradable eoe-sryétellins Spojyiactic acid of natural plant-derived beforehand. On the other hand, 1-40 mass„%...ie_.sultablu for the compounding quantity of biodegradable eoe-crystcilieu polyiactic" acid of natural plant-derived as film formation -resin. Dye, a fragrancujflavor, etc. can generally mixj^end with the nail] cosmetics of this invention the component other than these which can be mixlblended with nai(-cosmetics. [0015] The foliowing method is mentioned as a manufacturing method of the naij-cosmetics of this invention. (1) 1st method : color pigment and a plasticizer like citrate are knead jmixed by 3 hot calender rolls to commercially available cellulose nitrate including ieopropcnol, Evaporative removal of the isopropanol is carried out and the colorjcollar cellulose nitrate chlp|tip of each coior is prepared. Organic solvents, such as an acetate ester and -a -hydrocarboet -are made-to.mix; dissolve by using natural ρiαet-durieud eon-crystailieu biodegradation polylactic acid of such colorjcoliar cellulose nitrate chip|tips and this invention as film formation resin, and it is made uniform. Moreover, you may mix existing bright big pigment pcrticlu|grcίes and dye, aed-fragraecejflaeor like a pearl pigment simultaneously then. (2) A 2nd method : a color pigment, a plasticizer, etc. are beforehand l<euad|mixud with a biaxial extruder, a heat-type kneader, etc, -to natural plant-derived noncrystalline biodegradation polyiactic acid of this invention, and the color {collar polylactic acid chïpjtip is prepared. Meitjdissolution mixing of this and the ceilulose nitrate swollen by ethanol etc. is carried out with organic solvents, such as an acetate ester. You may mix existing bright big pigment pai'ticlu|graiee and dye, and fragrancelflavor simdltαnuodely- like -a -pearl- pigment - at-this time. EXAMPLES [0016] Hereafter, this invention is not limited by these Examples although an Example demonstrates the --nail cosmetics by this ineuetίoe further in detail. [0017] (Manufacture Examples 1-4) Various coior pigments were knead (mixed by the mixing (blending (a unit is a mass part) shown by Table 1 with nitrocellulose Hi/4 (isopropyl alcohol moisture) using 3 hot-calender-roil machines, and the eitrΌcelldlosu color chipjtip was prepared. In the prepared nitrocellulose color chipjtip, isopropyl alcohol of a several percent remains normally. ....... [0018] EMI <EMI079817007.1> is loading... [0019] (Manufacture Examples . 5-8) It knead I mixes by the mixing [blending (a unit is a mass part) shown by Table 2 using a biaxial extruder by using Toyobo Co., Ltd. polylactic acid "bio-equol BE-400" as base resin. The polylactic acid color chip J tip was prepared. The working temperature at this time was 150-200 degreeC. :[0020] EMI <EMI079817007,1> is loading... [0021] (Example . 1,. 2) As a ilacquer thinner base solvent, what was mixed in 33 mass % of n-butyl acetate, 3 mass % of ethyl acetates, and the ratio of 34 mass % of toluene is prepared beforehand. Meltjdissolution dlspersi-oiijdistributrlon of 70 mass % of this [lacquer thinner base and 30 mass % of the nitrocellulose color chip [tips prepared in manufacture Examples 1-4 was carried out using the disper, and the color| collar blend paste of each color was prepared. On the other hand, the Bentone Gel paste was also beforehand prepared by the following mixing [blending. , Toluene 35 parts n-butyl acetate 26 parts Ethyl acetate 6.75 parts Isopropyl alcohol 8.5 parts Nitrocellulose H 1/4 15 parts Benton 27 8 parts Camphor 0.75 part 100 parts [0022] Moreover, the following paste was prepared as a dispersion [distribution base, n-butyl acetate 23 parts Toluene 17.7 parts Nitrocellulose H 1/4 14.4 parts Acetyl triethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0.8 part Isopropyl alcohol 0.2 part Ethyl alcohol 1.7 parts Bentone Gel (above) . 20 parts ......... 17 parts of 40% of ipoixlactiç acid (BE-400) ethyl-acetate solutions 100· · : · parts · [0023] Colorlcollar Paj.. polish was prepared! by the following mixingl blending using ths said dispersion Idistribution base. (Example 1: Brown n^lj polish) 0.5 part of nitrosellaloss color chipltip prepared in manufacture Example 2 with respect to 100 parts of dispersiιnrr|diétrlhatίnn bases, The solor|snller blend paste which rnixlblendsd 0.61 part of nitrocellulose color chlpltip prepared in manufacture Example 3 and 0.5 part of nitrnsellulnée color stip|tip prepared in manufacture Example 4, respectively was mιxed1end1dlsperéed uniformly at a. disper. (Example 2: Pink nalj polish) The snloΓjsnller bleed paste which mix(bleeded 0.2 pert of nltrnseliulnée color chiplt'lp prepared ie manufacture Example 1 aed 0.4 part of nitrnsellulnée color stip)tip prepared ie manufacture Example 4 with respect to 100 parts of diépersioπ|diétrihutinr bases, respectively was mlxed-and-dispsi'sed uniformly at a disper. [0024] (Example 3, 4) ..... The dispersion I distribution base was prepared by ths following mixleg (bleeding using Bsetoee Gel .similar to the time of ths said Example 1, 2. n-butyl acetate 23 parts Toluene 17.7 parts Nίtrnsellalnss H 1/4 18.4 parts Acetyl trlethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0 8 part Isopropyl ·elsnhnl ·0.2 part:: Ethyl alcohol 1.7 parts Bsetoee Gel .(above) 20 parts The 40% of po'ly'lactic acid (BE-400) ethyl-acetate solution 13 parts 100 parts [0025] Co-iorl collar pai| polish was prepared by the following mixing (bleeding using · ths said dispersion |dίstrihatinn base. (Example 3: Brown hajj polish) 0.5 part of nitrocellulose color stip|tip prepared ie manufacture Example 8 with respect to 100 parts of diépβrs^itπ|dlétrihutinn bases, Ths ssίιnr|snller bleed paste which mlxlWended 0.61 part of eltrncellalose color stίpjtip prepared le manufacture Example 6 and 0.5 part of nitrocellulose color stίp|tlp prepared le manufacture Example 7, respectively was mixsd1end-diépsrésd uniformly · at a disper. ....... (Example 4: Pink nail polish) The color j collar blend paste which mix {blended 0,4 parit for 0,2 part of nitrocellulose color chip{tip prepared in manufacture Example 5 and the nitrocellulose color chipjtip prepared in manufacture Example 7 with respect to 100 parts of dispersion [distribution bases, respectively was mixed-and-dispersed uniformly at a disper. [0026] (Comparative examples 1 and 2) The dispersion [distribution base was prepared by the following mixing {blending. In addition, Bentone Gel used the thing similar to the thing of the said Example, n-butyl acetate 23.09.parts· Toluene 22.18 parts Ethyl acetate 7.23 parts Nitrocellulose H 1/4 14.39 parts Acetyl triethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0.8 part Isopropyl alcohol 0.225 part Ethyl alcohol 0.06 part Benzophenone- 2 0.025 part Bentone Gel (above) 20 parts Alkydoresin .6.8. part's .100:^0 [0027] Colorlcollar Rail polish was prepared by the following mixingjblending using the said dispersion!distribution base. (Comparative example 1: Brown Rail polish) 0.5 part of nitrocellulose color chip {tip prepared in manufacture Example 2 with respect to 100 parts of dispersion|distribution bases, ........ The colorjcoHar blend paste which mix{blended 0.61 part of nitrocellulose color chlpftip prepared in manufacture Example 3 and 0.5 part of nitrocellulose color chip {tip prepared in manufacture Example 4, respectively was mixed-and-dispersed uniformly at a disper. ___ (Comparative example 2: Pink RglT polish) The tolor|tollar blend paste which mix|blended 0.2 part of nitrocellulose color chipltip prepared in manufacture Example 1 and 0.4 part of nitrocellulose color chip {tip prepared in manufacture Example 4 with respect to 100 parts of dispersion [distribution bases, respectively was mixed-and-dispersed uniformly at a disper, ........ . . . ..... [0028] The color I collar Rail polish prepared in Examples 1-4 showed gioss and a glossiness equivalent to what was prepared by the comparative examples 1 and 2, film strength, and coloring property. Moreover, poiyiaCtiÇ acid which the thing of Examples 1-4 can biodegrade by the: method of both aerobic decomposition and an anaerobic resolution is contained to the thing of the comparative examples 1 and 2 not being eco-friendly, , Therefore It is thenaii polish which does not require ioad for an environment. INDUSTRIAL- APPLICATION _ [0029] According to this invention, since the .naij cosmetics which were 1x0111101 in cppllcabiilty|pcietability and glossiness and it is not only eco-friendly, but 1x0111101' in film strength are obtained, the utilization as cosmetics is possible. ['Claims] 1. jPoyjactiÇ acid which -s a -natural pίaπt-durivud nan-crystalline biodegradable high molecular compound shown by following Chemical formula (1) is mix|blundud as a resir component, Nail· cosmetics characterized by the above-mentioned. EMI <EMI079817C08.1> is loading.:.. (In formula, R1,R2,R3 is a Ci or more saturated hydrocarbon group, and is same or different. ..... ...... n is an integer greater than or equal to 1.)6 - Lobje tee - revendictioios - - to 2 -es - sscepppicei - apiicatio - industriality in the field of cosmetic compositions. Ad point:: VII Some demand-side observations 1 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - % by dry weight relative to the total weight of the anhydrous composition. From -its-side, -la- - claim - - - dependent - 5, - bound - to. - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 60%. and: 80% by weight relative to the total weight of the anhydrous composition. Thus, in the case where for example the anhydrous composition contains 45% by dry weight of polyacetic acid (which may be the case according to claim 2), the maximum amount of all the additional ingredients is 55% by weight. Therefore, the minimum amount of organic solvent of 60% by weight according to claim 5 can not be reached. It follows therefore that a concentration of 45% by dry weight of polyolactic acid is not possible: in::: taking into account the object of :. the. : claim. . 5. Thus, there is disagreement between the dependent claims 2 and Sugar-a doubt as to the object of the protection sought, to the extent that the claims are unclear. However, this dependency should be limited to claims 1 to 5. However, this dependency should be limited to claims 1 to 5. INVENTION ..... ...... The cosmetics which are eco-friendly, and were excellent in applicability [paintability using biodegradable film formation resin, excellent in glossiness, and. excellent. . SOLID POLYCLICITY, which is a natural plant-derived non-crystal biodegradable high molecular compound shown by foilowing chemical formula (1). • EMT:: <EMW79817p0éW. :. Injection, R1fR2, R3 is a more saturated hydrocarbon group, and is more or less equal to 1. TECHNICAL FIELD [0001] This invention relates to eco-friendly riaF cosmetics excellent in appllcabiiity | paintability. DESCRIPTION OF THE PREFERRED EMBODIMENTS [0002] Generally, the organic solvent, the acid ester, and a hydrogen oxide, cellulose nitrate, film formation resin, the plasticizer, the coloring agent, and the like. ; The components which actually form a membrane [film] as nitrate and resin formation. Nitrate cellulose is a synthetic material used as a raw material, but it is a synthetic resin, a resin-type resin, a toluene-type resin, and a sucrose-type resin. resin derived from a ..half-natural product. Specifically as this film formation resin, acrylic ester / methacrylic acid ester copolymer, a phthalate system alkyd resin, an isophthylic-acid typujsystum | alkyd resin group, a succinic acid series alkyd resin, a toldueusulfoecmidu / formclduhydu resins, toluene / sulfonamide / epoxy resin, ....... Sucrose benzo ade, sucrose Acera fgfCf / butylate [butyrate etc, can be mentioned. Since these resins are synthesized, they do not have biodegradability. [ÖÖ03] "Each recent-years and industrial field WHEREIN: ...... .............. It is important to use biodegradable material and it is just going However, in the past, cellulose nitrate is a component of natural plant-derived, however, since film formation resin blends with this cellulose nitrate was -a "synt.hutic-macromGlecdlu type] system [group, there existed a disorder that it was not uco- · friuedly. PROBLEM - "" TO '' '- - BE' -,. . SOLVED '- - BY- "THE INVENTION [0004]" This invention has been made using biodegradable film formation resin, and it has been found to provide excellent compatibility in the production of plastics. , excellent in glossiness, excellent in film strength. The present invention relates to the subject matter of the present invention, wherein the present invention provides a method for achieving said subject matter. ............ Poly lactic acid which is a non-crystalline biodegradable high molecular compound of natural plant-derived shown by following chemical formula (!) Is mix | blended as a resin component, It is characterized by the cbovu-muteioeud. w- "EMôwà'DTDi" -is- locdeg ... (In formula, &amp; 1, Ρ2, Ρ3 is a Cl or more saturated hydrocarbon group, and is same or different. n- ie-ce-integer-gructtuΓ- [0006] According to this invention, biodegradable polyacetic acid which is a natural plant-derived high molecular compound is used as film formation resin, Therefore it is eco-friendly, And the nail cosmetics were excellent in excellent performance, excellent in glossiness, and excellent in film strength can be obtained. EMBODIMENT OF THE INVENTION [0007] This invention is described below. [0008] Biodegradable polylactid acid of natural plant-derived used for this invention is obtained by superimposing [polymerizing the lactide mainly by a combination of high molecular compound -crystalline and soluble to the organic solvent used for cosmetics can be superimposed [polymerized. .................... Although the transition transition of this non-crystalline poiyiacttcacid is based also. on the combination ratio of optical isomers, it is preferable that it is the range of 50 degreeC from -10 degreeC. [0009] Moreover, especially the polymerization degree of polylactic acid is used for this invention, it is not preferable to limit the viscosity of the polymer. cosmetics. Furthermore, pojyiactic. The use of biodegradable acid in a biodegradable process in an aerobic decomposition and anaerobic resolution. is possible. Moreover, when mix is used for this invention, it is good to make it melt (dissolving in a suitable organic solvent, for example, ethyl acetate, butyl acetate, methyl ethyl ketone, acetone, etc.). , beforehand. [0010] That is, this invention is the following component .............. (a) Natural plant-derived, biodegradable non-crystalline poiy'iactic acid (said Chemical formula (1)) (b) Cellulose nitrate (c) Organic pigment (d) Gelatinize (e) Non-aromatic organic solvent These. . are contained, The nai .; cosmetics characterized by the above-mentioned are provided. [0 <Ol] Cellulose .nitrats of (b) shown here wili not be specifically limited if used for cnevsntineal nail; cosmetics, · N · trnssllulnes H 1/2, Hi / 4, Hl / 8, etc. are used. [0012] Moreover, the organic pigment of (c) is good to kneadlmi * and construct in chips forms beforehand with the said nltrncsllulnés (= ssiiulnés nitrate) and plasticizer, for example, citrate etc., 3 rolls, etc. The color pigment, a chromium oxide, chromium oxide, chromium oxide, chromium hydroxide, "a navy", Prussian blue, Lake pigments, such as organic colored pigments, as inorganic pigment pigments, such as pearl pigments, such as ultramarine · blue, · red iron 'oxide, yellow iron oxide or a black iron oxide, and mica titanium, Red No. 226 and Yeilow No. 205, and Blue No. 404 Also, No. 201, Yellow No. 202, Blue No. 1, Yellow No. 4, are various agents, and various types of treatment, such as, but are not limited to, · Process, an alkyl process, process, process, process, perfluoroalkyl silane, process, and silica process, may be given to these: · colored .pigmsnty [0013] · The gslatinizsrs of (d) ars for example, Montmnrillneits groups, such as a mnntmnrillneits, smsctits, or hectorite, Synthetic micas, such as sodium silicic acid, sodium / f / j / I light | write | right, or a lithium taeniolite stc., gold hectorite, clay mineral like a bentonite, or a silicic acid anhydride is msntinesd. Butyl oxidation, oxidation sthyl, msthyl sthyl ketone, acetone, e-bayenl. isopropyl alcohol, ethyl alcohol etc. are mentioned as non-ernmetis organic en! veet oi (s). .................................................. ......................................... In addition, an oil-based component · .is m-ix | tip ^ r ^ d ^ d for ths objective of improving improvement of the removability of a film, preservation, etc. You can add a plasticizer, a cosolvent, to dilute, a sizing [paste agent, stabilizer, surfactant, dye, fregreese, water, etc. It is [said] under mixing [arid bleedieg 0-15 mass % of the compounding quantity of cellulose nitrate is a suitable quantity, When is the compounding of cellulose nitrate is 0 mass%, it is good to knead [mix a colored pigment and a plasticizer to biodegradable eoe-sryetellins Spojyiactic acid of natural plant-derived beforehand. On the other hand, 1-40 mass "% ... ie_sultablu for the compounding of biodegradable eoe -crystallieu polyiactic" acid of natural plant-derived as film formation -resin Dye, a fragrancujflavor, etc. can generally mixj The present invention relates to the subject of the present invention, which can be used in combination with other methods of the invention (-cosmetics. [1] The foliowing method is a method for the manufacture of this invention. CIPO - Patent - 2524616 Canadian Intellectual Property Office Symbol of the Government of Canada CA 2313539 such as an acetate ester and -a -hydrocarboet -are made-to.mix; dissolve by using natural ρiαet-durieud eon-crystailieu biodegradation polylactic acid of such colorjcoliar cellulose nitrate chip | tips and this invention as film formation resin, and it is made uniform. Moreover, you may mix existing bright pigment, and a dye, aed-fragraecejflaeor like a pearl pigment simultaneously then. (2) A 2nd method: a color pigment, a plasticizer, etc. are beforehand mixed with a biaxial extruder, a heat-type kneader, etc., and a natural plant-derived noncrystalline biodegradation polyacetic acid of this invention, and the color colloidal polylactic acid is prepared. Meitjdissolution mixing of this and the ceilulose nitrate swollen by ethanol etc. is carried out with organic solvents, such as an acetate ester. You may mix existing bright pigment with great pigment and dye, and fragrance-free simdltαnuodely-like-a-pearl-pigment - at-this time. EXAMPLES [0016] Hereafter, this invention is not limited by these examples of an example. [0017] (Manufacture Examples 1-4) Various pigments were knead (mixed by the mixing) shown by Table 1 with nitrocellulose Hi / 4 (isopropyl alcohol moisture) using 3 hot-calender- In the prepared nitrocellulose color chipjtip, the isopropyl alcohol of a multi-purpose powder is normally used in the preparation of ... [0018] EMI <EMI079817007.1> is loading ... [0019] ] (Manufacture Examples 5-8) It is mixed by the mixing shown by Table 2 using a biaxial extruder by using Toyobo Co., Ltd. polylactic acid "bio-equol BE- The term temperature is 150-200 degree C .: [0020] EMI <EMI079817007.1> is loading ... [0021] (Example 1 2) As a result, it was mixed with solvent, which was mixed in 33% of n-butyl acetate, 3% of ethyl acetates, and the ratio of 34% by weight was prepared. ehand. Meltjdissolution dlspersi-oiijdistributrlon of 70 mass% of this [lacquer thinner base and 30 mass% of the nitrocellulose color chip [tips prepared in manufacture Examples 1-4 was carried out using the disper, and the color | collar paste paste of each color was prepared. On the other hand, the Bentone Gel paste has been prepared by blending. , Toluene 35 parts n-butyl acetate 26 parts Ethyl acetate 6.75 parts Isopropyl alcohol 8.5 parts Nitrocellulose H 1/4 15 parts Benton 27 8 parts Camphor 0.75 part 100 parts [0022] Moreover, the following is prepared for dispersion [distribution base , n-butyl acetate 23 parts Toluene 17.7 parts Nitrocellulose H 1/4 14.4 parts Acetyl triethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0.8 part Isopropyl alcohol 0.2 part Ethyl alcohol 1.7 parts Bentone Gel (above). 20 parts ......... 17 parts of 40% of ipoixlacti acid (BE-400) ethyl acetate solutions 100 · ·: · parts · [0023] Colorlcollar Paj .. polish was prepared! by the following mixingl blending using ths said dispersion Idistribution base. (Example 1: Brown n ^ lj polish) 0.5 part of nitrosellaloss color chipltip prepared in manufacture Example 2 with respect to 100 parts of dispersiιrr | diétrlhatίnn bases, The solor | snller blend paste which rnixlblendsd 0.61 part of nitrocellulose color chlpltip prepared in manufacture Example 3 and 0.5 part of nitritesellulnée color Example 4, respectively was mιxed1end1dlsperéed uniformly at a. disper. (Example 2: Pink nalj polish) The snloΓjsnller bleed paste which mix (bleeded 0.2 pert of nltrnseliule color chiplt'lp prepared ie manufacture Example 1 aed 0.4 part of nitrnsellulnée color stip) tip prepared ie manufacture Example 4 with respect to 100 parts of dieperior base dyes were respectively uniformly dispersed and uniformly dispersed. [0024] (Example 3, 4) ..... The dispersion I distribution base was prepared by ths following mixleg (bleeding using Bsetoee Gel .similar to the time of ths said Example 1, 2. n-butyl acetate 23 parts Toluene 17.7 parts Nίtrnsellalnss H 1/4 18.4 parts Acetyl trlethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0 8 parts Isopropyl · elsnhnl · 0.2 part :: Ethyl alcohol 1.7 parts Bsetoee Gel. (Above) 20 parts The 40% of po ' ly'lactic acid (BE-400) ethyl-acetate solution 13 parts 100 parts [0025] Co-iorl collar is prepared by the following mixing (Example 3: Brown hajj polish) 0.5 part of nitrocellulose color stip | tip prepared ie manufactory Example 8 with respect to 100 parts of dibetry | dlétrihutinn bases, Ths ssίιnr | snller bleed paste which mlxlWended 0.61 part of eltrncellalose color stίpjtip prepared the manufacture Example 6 and 0.5 part of nitrocellulose color stίp | tlp prepared Examp manufacture the 7, respectively was mixsd1end-diépsrésd uniformly · to be disper. ....... (Example 4: Pink nail polish) The color of the collar blend paste which mix (blended 0.4 parit for 0.2 part of nitrocellulose color chip (tip prepared in manufacture Example 5 and nitrocellulose color chipjtip Example 7 with respect to 100 parts of dispersion [distribution bases, respectively was mixed-and-dispersed uniformly at a disper. [Comparative examples 1 and 2] The dispersion [distribution base was prepared by the following mixing {blending. In addition, Bentone Gel used the same Example: n-butyl acetate 23.09.parts · Toluene 22.18 parts Ethyl acetate 7.23 parts Nitrocellulose H 1/4 14.39 parts Acetyl triethyl citrate 4 parts Camphor 1.2 parts n-butyl acetate 0.8 part Isopropyl alcohol 0.225 part Ethyl alcohol 0.06 part Benzophenone- 2 0.025 part Bentone Gel (above) 20 parts Alkydoresin .6.8. part: .100: ^ 0 [0027] Colorlcollar Rail polish was prepared by the following mixingjblending using the said dispersion! distribution base. (Comparative example 1: Brown Rail polish) 0.5 part of nitrocellulose color chip (tip prepared in manufacture Example 2 with respect to 100 parts of dispersion | distribution bases, ........ The colorjcoHar blend paste which mix {blended 0.61 Example 3 and 0.5 part of nitrocellulose color chip Example 4, which is mixed-and-dispersed uniformly at a disper. ___ (Comparative example 2: Pink RglT polish) The tolor | tollar blend paste which mix | blended 0.2 part of nitrocellulose color chipltip prepared in manufacture Example 1 and 0.4 part of nitrocellulose color chip of dispersion [distribution bases, respectively was mixed-and-dispersed uniformly at a disper, ......... . . ..... [0028] The color I collar Rail polish prepared in Examples 1-4 shown in the text and in the glossiness of the text. Moreover, poiyiaCtiÇ acid which the thing of Examples 1-4 can biodegrade by the: method of both aerobic decomposition and anaerobic resolution is contained in the comparison of the comparative examples 1 and 2 not being eco-friendly,, Therefore It is thenaii polish which does not require ioad for an environment. INDUSTRIAL APPLICATION According to this invention, since the invention has not been exclusively eco-friendly, but has not been found to be effective. . ['Claims] 1.JPoyjactiÇ acid which -s a -natural pίaπt-durivud nan-crystalline biodegradable high molecular compound shown by following Chemical formula (1) is a mixture of a component, Nail-cosmetics characterized by the above-mentioned. EMI <EMI079817C08.1> is loading.: .. (In formula, R1, R2, R3 is a Ci or more saturated hydrocarbon group, and is same or different. ..... ...... n is an integer greater than or equal to 1.)
LU100194A 2017-05-08 2017-05-08 Anhydrous cosmetic composition applicable to the nails LU100194B1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
LU100194A LU100194B1 (en) 2017-05-08 2017-05-08 Anhydrous cosmetic composition applicable to the nails
PCT/EP2018/060999 WO2018206333A1 (en) 2017-05-08 2018-04-30 Anhydrous cosmetic composition which can be applied to nails
EP18721370.7A EP3621695A1 (en) 2017-05-08 2018-04-30 Anhydrous cosmetic composition which can be applied to nails

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
LU100194A LU100194B1 (en) 2017-05-08 2017-05-08 Anhydrous cosmetic composition applicable to the nails

Publications (1)

Publication Number Publication Date
LU100194B1 true LU100194B1 (en) 2018-11-26

Family

ID=59034824

Family Applications (1)

Application Number Title Priority Date Filing Date
LU100194A LU100194B1 (en) 2017-05-08 2017-05-08 Anhydrous cosmetic composition applicable to the nails

Country Status (3)

Country Link
EP (1) EP3621695A1 (en)
LU (1) LU100194B1 (en)
WO (1) WO2018206333A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011168552A (en) * 2010-02-19 2011-09-01 Daito Kasei Kogyo Kk Manicure preparation
KR20120123853A (en) * 2011-05-02 2012-11-12 금오공과대학교 산학협력단 Temperature Susceptible Manicure Composition and Method for Preparing the Same
US20140199256A1 (en) * 2012-06-22 2014-07-17 Camille T. Sasik Cosmetic Compositions Including Natural Or Naturally Derived Polyesters
WO2014176275A1 (en) * 2013-04-22 2014-10-30 Creative Nail Design, Inc. Nail coatings having enhanced adhesion
WO2016121696A1 (en) * 2015-01-30 2016-08-04 東洋紡株式会社 Polylactic acid-containing aqueous dispersion
US20170056313A1 (en) * 2012-08-22 2017-03-02 Creative Nail Design, Inc. Nail coatings having enhanced adhesion

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011168552A (en) * 2010-02-19 2011-09-01 Daito Kasei Kogyo Kk Manicure preparation
KR20120123853A (en) * 2011-05-02 2012-11-12 금오공과대학교 산학협력단 Temperature Susceptible Manicure Composition and Method for Preparing the Same
US20140199256A1 (en) * 2012-06-22 2014-07-17 Camille T. Sasik Cosmetic Compositions Including Natural Or Naturally Derived Polyesters
US20170056313A1 (en) * 2012-08-22 2017-03-02 Creative Nail Design, Inc. Nail coatings having enhanced adhesion
WO2014176275A1 (en) * 2013-04-22 2014-10-30 Creative Nail Design, Inc. Nail coatings having enhanced adhesion
WO2016121696A1 (en) * 2015-01-30 2016-08-04 東洋紡株式会社 Polylactic acid-containing aqueous dispersion

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 201159, Derwent World Patents Index; AN 2011-L09203, XP002772376 *
DATABASE WPI Week 201408, Derwent World Patents Index; AN 2012-Q18228, XP002772374 *
DATABASE WPI Week 201653, Derwent World Patents Index; AN 2016-47738Q, XP002772375 *

Also Published As

Publication number Publication date
EP3621695A1 (en) 2020-03-18
WO2018206333A1 (en) 2018-11-15

Similar Documents

Publication Publication Date Title
FR2982155A1 (en) COSMETIC COMPOSITION COMPRISING AT LEAST ONE ALCOXYSILANE
EP2923735A1 (en) Anhydrous cosmetic composition applicable to the nails
WO2021234270A1 (en) Cosmetic nail care composition in the form of a varnish
LU100194B1 (en) Anhydrous cosmetic composition applicable to the nails
EP3426354B1 (en) Compositions for nail varnish
EP3595617B1 (en) Nail enamel composition
EP2234670B1 (en) Anhydrous cosmetic composition
EP2790664B1 (en) Anhydrous cosmetic composition applicable to the nails
FR3134315A1 (en) Inverse emulsion comprising a dedextrin ester, a volatile linear alkane, a natural wax, a natural hydrophilic polymer gelling agent, a non-ionic emulsifier
FR3004932A1 (en) COSMETIC COMPOSITION OF NAILS COATING
LU100108B1 (en) Stabilizing method of nail polish coloring
FR2939659A1 (en) Nail polish, useful for non therapeutic makeup or care of nail, comprises alkylether or an ester of polysaccharide (cellulose acetobutyrate) and plant resin (rosin), in solvent medium containing plant solvent (e.g. ethyl lactate)
EP2926866A1 (en) Use of dipropylene glycol dibenzoate in anhydrous cosmetic compositions applicable to the nails
LU100592B1 (en) Improved compositions applicable to nails
US20260000599A1 (en) Peel-off lip liner stain
FR2964568A1 (en) Nail polish, useful as varnish base, a makeup product for the nails, finishing product to be applied to the makeup product or cosmetic nail care product, comprises shellac, and a solvent system having an alcohol and an acetate
LU100356B1 (en) Improved compositions applicable to nails
LU100889B1 (en) Improved compositions as a makeup product applicable to the nails
LU100275B1 (en) Improved compositions for thick nail polish called &#34;gel-like&#34;
EP3344224A1 (en) Anhydrous cosmetic composition
LU100176B1 (en) Reduce the turbidity of nail polish
LU100323B1 (en) ALCOHOL-LIKE PELLET NAIL VARNISH
EP4450050A1 (en) Composition based on chitosan and a phospholipid
EP4450053A1 (en) Composition based on chitosan and spiculisporic acid or its salts
EP0944380A1 (en) Cosmetic composition in the form of an organic solution or dispersion containing at least a polymeric colouring agent

Legal Events

Date Code Title Description
FG Patent granted

Effective date: 20181126