WO2013190114A1 - Cosmetic composition comprising non-interference scattering particles and aerogel particles, and cosmetic lightening method - Google Patents
Cosmetic composition comprising non-interference scattering particles and aerogel particles, and cosmetic lightening method Download PDFInfo
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- WO2013190114A1 WO2013190114A1 PCT/EP2013/063046 EP2013063046W WO2013190114A1 WO 2013190114 A1 WO2013190114 A1 WO 2013190114A1 EP 2013063046 W EP2013063046 W EP 2013063046W WO 2013190114 A1 WO2013190114 A1 WO 2013190114A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
Definitions
- Cosmetic composition comprising non-interference scattering particles and aerogel particles, and cosmetic lightening method
- the invention relates to a composition for topical application comprising, in a physiologically acceptable medium, at least non-interference scattering particles and at least hydrophobic aerogel particles.
- a subject of the invention is also a cosmetic method for lightening and/or homogenizing the skin and/or the lips, comprising the topical application of this composition to the skin or the lips, in particular facial skin and the shadows around the eyes.
- cosmetic or dermatological compositions which make it possible to lighten and to homogenize the complexion.
- cosmetic compositions containing whitening agents it is known practice to use cosmetic compositions containing whitening agents.
- the substances most commonly used as a whitening agent are hydroquinone and derivatives thereof, kojic acid and derivatives thereof, azelaic acid, arbutin and derivatives thereof, vitamin C and derivatives thereof (for example, magnesium ascorbyl phosphate, or ascorbyl glucoside), alone or in combination with other active agents.
- the powders are generally white or coloured pigments depending on the desired effect and/or fillers of different shapes (lamellar, spherical) depending on the desired effect.
- the complexion is made uniform essentially by virtue of the covering power provided by the pigments and the fillers.
- the drawback of such compositions is that the softening of the skin defects is provided by the covering power of the compositions. The skin thus made up loses its natural appearance due to the lack of transparency of these compositions.
- cosmetic compositions containing fluorescent compounds such as stilbene derivatives, coumarin derivatives, oxazole and benzoxazole derivatives and imidazole derivatives, described in applications EP-A-0 962 224 or WO- 00/71085, in particular come to mind.
- optical brighteners such as stilbene derivatives, coumarin derivatives, oxazole and benzoxazole derivatives and imidazole derivatives, described in applications EP-A-0 962 224 or WO- 00/71085, in particular come to mind.
- cosmetic compositions for topical application which make it possible to obtain an immediate lightening effect, in particular on the complexion, or more generally a correction of dyschromias, in particular a concealer effect, which are not very covering and not very coloured and which do not give the skin a shiny or opaque and artificial appearance.
- they are polyvalent and readily suitable for varied types of skin since it is not necessary for the formula to have the exact same shade as the complexion of the individuals.
- a subject of the present invention is a cosmetic composition which lightens and homogenizes the skin or the lips, in particular the complexion, and which is characterized by great comfort on application.
- These compositions contain, in a physiologically acceptable medium containing oil, an effective amount of an aerogel (preferentially of hydrophobic silica) and of boron nitride particles.
- compositions according to the invention can be in the form of a gel, of a serum, of direct, inverse and multiple emulsions, of hot-cast sticks, or of loose or compacted powders.
- a subject of the invention is therefore a cosmetic composition which is in particular suitable for topical application to the skin and/or the lips, comprising, in a physiologically acceptable medium, at least one oil, at least 0.1 % by weight of particular non-interference scattering particles relative to the total weight of said composition, and at least hydrophobic aerogel particles.
- compositions according to the invention make it possible to immediately confer on the skin to which they are applied, and in particular on the complexion, improved qualities in terms of uniformity, homogeneity, transparency and whiteness. These compositions can also have concealing properties. These compositions can also lighten the lips.
- a subject of the present invention is thus also a cosmetic method intended for immediate lightening and/or homogenizing of the skin and/or of the lips, in particular of the skin.
- a subject of the present invention is thus also a use of the combination of at least hydrophobic silica aerogel particles and of at least 0.1 % by weight of non-interference scattering white particles characterized by 0.3 ⁇ " ⁇ 50 ⁇ 40 ⁇ and 1 .7 ⁇ RI ⁇ 2.2 in a cosmetic composition for softening skin defects.
- compositions according to the invention can also make it possible to reduce the perception of the skin defects at the surface of the skin, and in particular to mask the wrinkles and pores and/or to camouflage the coloured defects of the skin, namely red blotches or blemishes.
- hydrophobic aerogel particles and of non-interference scattering particles makes it possible to obtain compositions which are comfortable and soft on application, and which have matting and soft focus properties.
- scattering particles is intended to mean particles exhibiting light scattering which does not show a favoured direction. Consequently, particles which exhibit an optical interference effect, termed “interference” particles, are most particularly excluded therefrom. Likewise, particles which show a shiny effect, such as metal particles or else particles with a metallic effect, such as bismuth oxychloride, are excluded therefrom.
- white is intended to mean particles having the colour white and its derivatives (off-white, alabaster white, etc.), as opposed to primary colours and derivatives.
- the white particles have a lightness value L * close to 100 in the CIELab76 system.
- the scattering white particles according to the invention have an average refractive index of between 1 .7 and 2.2. This is because, if the particle has a refractive index above 2.2, the opacity of the composition is too high, and if this index is below 1 .7, the lightening effect is not sufficient.
- the white particles according to the invention have a continuous effect, which is controlled by the resolution capacity of the eye. Since said capacity is around 40 ⁇ , particles having a volume average size (D50) of less than 40 ⁇ , preferably less than 25 ⁇ and even better still less than or equal to 6 ⁇ are therefore considered. However, it is ensured that particles of which the D50 is greater than 0.3 ⁇ and preferentially 0.5 ⁇ are taken, so as not to have too great a loss of opacity, which would be extremely detrimental to the desired effect.
- D50 volume average size
- the composition of the invention comprises at least white particles having an average refractive index of between 1.7 and 2.2 and a volume size (D50) of less than 40 ⁇ , preferably between 0.3 and 25 ⁇ and better still between 0.3 and 6 ⁇ , or even between 0.5 and 3 ⁇ .
- D50 volume size
- These particles may be made of one material or else be composites.
- these particles may be of boron nitride with an average refractive index of 1.74.
- They may also be chosen from composite particles comprising titanium dioxide and a substrate chosen from alumina, silica, barium sulfate, glass, mica and synthetic mica, poly(methyl methacrylate) (PMMA) particles, polytetrafluoroethylene (PTFE) particles, or mixtures thereof, the average refractive index of which is between 1.7 and 2.2.
- a substrate chosen from alumina, silica, barium sulfate, glass, mica and synthetic mica, poly(methyl methacrylate) (PMMA) particles, polytetrafluoroethylene (PTFE) particles, or mixtures thereof, the average refractive index of which is between 1.7 and 2.2.
- the particles are boron nitride particles.
- the particles are composite particles comprising titanium dioxide and an alumina substrate.
- the particles are composite particles comprising titanium dioxide and a mica substrate.
- the non-interference scattering white particles are advantageously boron nitride particles, preferentially having a volume average size of from 0.3 to 6 ⁇ .
- the average refractive index is defined as being the sum of the refractive indices weighted by the weight content in the particle.
- composite particles mention may, for example, be made of platelets of mica (60%) covered with Ti0 2 (40%), with an average refractive index of 1.9 (0.6x1 .5+0.4x2.5); inclusions of titanium oxide (40%) in a matrix of alumina (60%), with an average refractive index of 1 .96 (0.6x1 .6+0.4x2.5).
- the refractive index of bismuth oxychloride is here given by way of indication.
- said bismuth oxychloride in its conventional form, does not correspond to a particle for the purposes of the invention, since it is a favoured-reflection particle.
- boron nitride particles such as PUHP1030L from Saint Gobain Ceramics and UHP-1010 from Carborundum.
- boron nitride particles having a volume average size D50 of less than 6 ⁇ such as the boron nitride particles sold under the name PUHP1030L by Saint Gobain Ceramics, having a volume average size of 3 ⁇ .
- Said non-interference white particles according to the invention are present in the composition in an effective amount for lightening and/or homogenizing the skin and/or the lips, in other words in a content of at least 0.1 % by weight of the total composition, in particular at least 0.5% by weight and preferably at least 1 % by weight.
- Said non-interference scattering white particles according to the invention are present in the cosmetic composition in a total amount of active material ranging from 0.1 % to 20% by total weight of the composition and preferably from 0.5% to 10%.
- colour whether it is provided by dyes, or else pigments, lakes, nacres, goniochromatic pigments, etc.
- a cosmetic composition in accordance with the invention advantageously does not contain additional white particle(s) (i.e. particle(s) other than non-interference white particles in accordance with the invention), and in particular does not comprise titanium dioxide.
- a composition according to the invention can comprise from 0 to 3% by weight, relative to the total weight of the composition, of particles of Rl > 2.3, in particular of iron oxides.
- Silica aerogels are porous materials obtained by replacing (by drying) the liquid component of a silica gel with air.
- sol-gel processes are generally synthesized via a sol-gel process in liquid medium and then dried, usually by extraction with a supercritical fluid, the one most commonly used being supercritical C0 2 . This type of drying makes it possible to avoid shrinkage of the pores and of the material.
- the sol-gel process and the various drying operations are described in detail in Brinker C.J. and Scherer G.W., Sol-Gel Science, New York, Academic Press, 1990.
- the hydrophobic silica aerogel particles used in the present invention exhibit a specific surface area per unit of mass (S M ) ranging from 500 to 1500 m 2 /g, preferably from 600 to 1200 m 2 /g and better still from 600 to 800 m 2 /g, and a size, expressed as the volume average diameter (D[0.5]), ranging from 1 to 1500 ⁇ , better still from 1 to 1000 ⁇ , preferably from 1 to 100 ⁇ , in particular from 1 to 30 ⁇ , more preferably from 5 to 25 ⁇ , better still from 5 to 20 ⁇ and even better still from 5 to 15 ⁇ .
- S M specific surface area per unit of mass
- D[0.5] volume average diameter
- the hydrophobic silica aerogel particles used in the present invention have a size, expressed as volume average diameter (D[0.5]), ranging from 1 to 30 ⁇ , preferably from 5 to 25 ⁇ , better still from 5 to 20 ⁇ and even better still from 5 to 15 ⁇ .
- D[0.5] volume average diameter
- the specific surface area per unit of mass can be determined by the nitrogen absorption method, known as the BET (Brunauer-Emmett-Teller) method, described in The Journal of the American Chemical Society, Vol. 60, page 309, February 1938 and corresponding to the international standard ISO 5794/1 (appendix D).
- BET Brunauer-Emmett-Teller
- the BET specific surface area corresponds to the total specific surface area of the particles under consideration.
- the sizes of the silica aerogel particles can be measured by static light scattering using a commercial particle size analyser of MasterSizer 2000 type from Malvern.
- the data are processed on the basis of the Mie scattering theory.
- This theory which is exact for isotropic particles, makes it possible to determine, in the case of non-spherical particles, an "effective" particle diameter.
- This theory is in particular described in the publication by Van de Hulst, H.C., "Light Scattering by Small Particles", Chapters 9 and 10, Wiley, New York, 1957.
- the hydrophobic silica aerogel particles used in the present invention have a specific surface area per unit of mass (S M ) ranging from 600 to 800 m 2 /g and a size, expressed as the volume average diameter (D[0.5]), ranging from 5 to 20 ⁇ and even better still from 5 to 15 ⁇ .
- the silica aerogel particles used in the present invention may advantageously have a tapped density p ranging from 0.02 g/cm 3 to 0.10 g/cm 3 , preferably from 0.03 g/cm 3 to 0.08 g/cm 3 and in particular from 0.05 g/cm 3 to 0.08 g/cm 3 .
- this density may be assessed according to the following protocol, known as the tapped density protocol:
- the hydrophobic silica aerogel particles used in the present invention have a specific surface area per unit of volume S v ranging from 5 to 60 m 2 /cm 3 , preferably from 10 to 50 m 2 /cm 3 and better still from 15 to 40 m 2 /cm 3 .
- the hydrophobic silica aerogel particles according to the invention have an oil-absorbing capacity, measured at the wet point, ranging from 5 to 18 ml/g, preferably from 6 to 15 ml/g and better still from 8 to 12 ml/g.
- the absorption capacity measured at the wet point corresponds to the amount of oil which it is necessary to add to 100 g of particles in order to obtain a homogeneous paste.
- the oil uptake corresponds to the ratio Vs/m.
- the aerogels used according to the present invention are aerogels of hydrophobic silica, preferably of silylated silica (INCI name: silica silylate).
- hydrophobic silica is intended to mean any silica whose surface is treated with silylating agents, for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with silyl groups Si-Rn, for example trimethylsilyl groups.
- silylating agents for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes
- Use will preferably be made of hydrophobic silica aerogel particles that are surface- modified with trimethylsilyl groups.
- hydrophobic silica aerogels that may be used in the invention
- an example that may be mentioned is the aerogel sold under the name VM-2260 or VM-2270 (INCI name: Silica silylate) by the company Dow Corning, the particles of which have a mean size of about 1000 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g.
- Aerogel TLD 201 Mention may also be made of the aerogels sold by the company Cabot under the references Aerogel TLD 201 , Aerogel OGD 201 and Aerogel TLD 203, Enova® Aerogel MT 1 100 and Enova Aerogel MT 1200.
- Use will preferably be made of the aerogel sold under the name VM-2270 (I NCI name: Silica silylate), by the company Dow Corning, the particles of which have an average size ranging from 5-15 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g.
- VM-2270 I NCI name: Silica silylate
- the hydrophobic silica aerogel particles represent from 0.1 % to 20% by weight, preferably from 0.5% to 10% by weight, better still from 1 % to 10% by weight and more preferably from 1 .5% to 5% by weight relative to the total weight of the composition.
- compositions used according to the invention may in particular constitute cosmetic compositions. They contain, for such an application, a physiologically acceptable medium.
- physiologically acceptable medium is intended to mean here a medium which is compatible with the skin, and optionally the lips, the scalp, the eyelashes, the eyes and/or the hair.
- This physiologically acceptable medium may be more particularly constituted of a physiologically acceptable organic solvent and optionally water.
- the organic solvent may be chosen, for example, from lower alcohols containing from 1 to 4 carbon atoms, for instance ethanol, isopropanol, propanol or butanol; polyethylene glycols containing from 6 to 80 ethylene oxide units; and polyols, for instance propylene glycol, isoprene glycol, butylene glycol, glycerol and sorbitol.
- the physiologically acceptable medium of the composition according to the invention has a pH which is compatible with the skin, and preferably ranging from 3 to 8 and better still from 5 to 7.
- compositions are in the form of an oil-in- water or water-in-oil emulsion, of a triple emulsion, or else of a gel.
- Makeup galenical forms loose powders, compacted powders, sticks, etc. are also envisaged.
- the emulsion is an oil-in-water emulsion.
- compositions according to the present invention comprise at least one oily phase comprising at least one oil.
- This oily phase may be present in an amount ranging, for example, from 10% to 95% by weight, preferably from 10% to 80% by weight, better still from 15% to 70% by weight and even better still from 20% to 60% by weight relative to the total weight of the composition.
- This oily phase contains at least one oil, in particular one cosmetic oil, and it may contain several oils and optionally one or more other fatty substances.
- mineral oils liquid petroleum jelly
- vegetable oils animal oils
- synthetic oils non-volatile or volatile silicone oils (cyclomethicones such as cyclopentasiloxane and cyclohexasiloxane) and fluoro oils (perfluoropolyethers).
- cyclomethicones such as cyclopentasiloxane and cyclohexasiloxane
- fluoro oils perfluoropolyethers
- fatty substances use may also be made of fatty alcohols, fatty acids and waxes.
- the oily phase of the emulsion may also contain gums, such
- compositions of the invention may also contain adjuvants that are common in the cosmetics or dermatological fields, such as hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic active agents, preservatives, antioxidants, solvents, fragrances, fillers, screening agents, bactericides, odour absorbers, colorants and salts.
- the composition according to the invention may comprise, as cosmetic adjuvants, nacres, pigments, dyes, biological active agents (anti- ageing, oily skin, whitening, antiperspirant, antioxidant, etc.), sunscreens, film-forming polymers, scattering and/or lightening fillers, oils and fatty substances, moisturizers and emollients.
- these various adjuvants are those conventionally used in the field under consideration, for example from 0.01 % to 20% of the total weight of the composition and preferably from 0.01 % to 10% of the total weight of the composition. Depending on their nature, these adjuvants may be introduced into the fatty phase, into the aqueous phase and/or into lipid spherules.
- the composition may contain active agents conventionally used in the cosmetics industry, and for example chosen from desquamating agents, moisturizing agents, depigmenting agents, pro-pigmenting agents, anti-glycation agents, NO-synthase inhibitors, 5oc-reductase inhibitors, lysyl and/or prolyl hydroxylase inhibitors, agents for stimulating the synthesis of dermal or epidermal macromolecules and/or preventing their degradation, agents for stimulating fibroblast or keratinocyte proliferation and/or keratinocyte
- the whitening agents capable of being incorporated into the composition according to the present invention comprise, for example, the following compounds: kojic acid; ellagic acid; arbutin and derivatives thereof, such as those described in applications EP-895 779 and EP- 524 109; hydroquinone; aminophenol derivatives, such as those described in applications WO 99/10318 and WO 99/32077, and in particular N-cholesteryloxycarbonyl-para- aminophenol and N-ethyloxycarbonyl-para-aminophenol; iminophenol derivatives, in particular those described in application WO 99/22707; L-2-oxothiazolidine-4-carboxylic acid or procysteine, and also salts and esters thereof; calcium D-pantetheine sulfonate, ascorbic acid and derivatives thereof, in particular ascorbyl glucoside, and extracts of plants, in particular of liquorice, of blackberry, of skullcap and of Bacopa monnieri, without this list being limiting.
- compositions used may also comprise at least one organic photoprotective agent and/or at least one inorganic photoprotective agent that is active in the UVA and/or UVB range (absorbers), which may be water-soluble or liposoluble, or else insoluble in the commonly used cosmetic solvents.
- organic photoprotective agent and/or at least one inorganic photoprotective agent that is active in the UVA and/or UVB range (absorbers), which may be water-soluble or liposoluble, or else insoluble in the commonly used cosmetic solvents.
- photoprotective agents are different from optical brighteners.
- the photoprotective agents are generally present in the compositions according to the invention in proportions ranging from 0.1 % to 20% by weight, relative to the total weight of the composition, and preferably ranging from 0.2% to 15% by weight relative to the total weight of the composition.
- compositions used according to the invention may be more or less fluid and may have the appearance of a white or coloured cream, an ointment, a balm, a milk, a serum, a paste or a foam. They can optionally be applied to the skin in the form of an aerosol. They can also be in solid form, for example in the form of a stick, suitable in particular for application to the lips.
- the present invention also relates to a cosmetic method for lightening and/or homogenizing the skin and/or the lips, in particular facial skin and/or the shadows around the eyes, comprising the topical application to the skin of a composition according to the invention as defined previously.
- This cosmetic method will be more particularly intended for immediate lightening and/or homogenizing of the skin and/or of the lips, in particular of the skin.
- composition of the invention may be used as it is or as a care and/or makeup base, applied to the skin before a care product or a makeup product.
- the invention also relates to a method for making up and/or for non-therapeutic care of the skin and/or the lips, comprising at least one step of applying to the skin a cosmetic composition according to the invention as defined previously.
- Another aspect of the invention relates to the combined use of hydrophobic silica aerogel particles as defined previously and of non-interference scattering white particles as defined previously, as an agent for lightening and/or homogenizing the skin and/or the lips, in particular the complexion, and/or for softening skin defects.
- the amounts are expressed as percentage by weight, relative to the total weight of the composition. Unless otherwise mentioned, the amounts are not indicated as amount of active material, but as crude amount introduced into the composition.
- Example 1 Demonstration of the lightening, homogenizing and dvschromia-correcting effects of formulae containing the combination of hydrophobic silica aerogel particles and boron nitride particles
- the formula-spreading protocol consists in producing 50 ⁇ spreads on a standard contrast chart. The measurements are carried out on white background. Colour measurements are carried out using a colorimeter. This is a Konica Minolta CR-400 chroma meter. The colorimeter provides numerical data representing the absolute value and the difference in colour between a reference sample and a sample to be controlled. The values obtained on the bare chart without film are used as reference.
- the operating conditions are as follows:
- the instrument has an optical device which produces a diffuse light, placed in a spherical cavity coated with a white layer which generates multiple light reflection.
- An anti-glare trap eliminates the effects of glare of the surface of the sample. Initially, a "white plate" calibration of the instrument is carried out.
- an average ⁇ 0 is calculated from the measurements L * , a * b * of the bare ethnic chart. This is the difference in colour between a zone of small surface area and the corresponding large zone. For example, on the African-American chart (contrast chart 32 described below), the average of the colour differences between B1 1 and B1 1 +, B12 and B1 1 +, and so on, is calculated:
- n 1 , 2, ... , n
- a transparency bearing a spread (referred to as a film) is then placed over the ethnic chart. The same measurements are carried out and the average ⁇ is obtained. Finally, H, which corresponds to the homogenizing power of the formula spread on the transparency, is determined according to the equation:
- the contrast chart 32 comprises a square coloured zone B1 1 + and four rectangular coloured zones B1 1 , B12, B12+ and XXX.
- the various zones B1 1 , B1 1 +, B12, B12+ and XXX are preferably made by printing of inks chosen such that these zones appear to an observer to be of the same colour under at least two different illuminants, as described in European patent application EP 1 212 961.
- the contrast chart 32 may be representative of skin of which the lightness is between 30 and 40.
- the various zones B1 1 +, B1 1 , B12, B12+ and XXX may correspond to the average colours observed on a panel of individuals who have dark skin with a dark complexion, for various regions of the face.
- the region B1 1 + may correspond to the average of the colour measured on the forehead in the zones V1 , averaged with that measured on the cheekbones in the zones V2.
- the zone B1 1 may correspond to the colour measured on the cheekbones, in the zone V2, the zone B12 to that measured on the forehead, in the zones V1 , the zone B12+ to the average colour between that measured on the outer shadows in the zones V3, that measured in the middle shadows of the zones V4 and that measured around the lips in the zones V5.
- the zone XXX may correspond to the colour of the inner shadows, measured in the zones V6.
- the contrast chart 32 is characterized, for each zone, by the following values:
- the contrast ratio is calculated by producing the mathematical average of the three values of the Ys on black background, divided by the average of the three Ys on white background, multiplied by 100.
- compositions films of 25 ⁇ are applied on polyethylene (PE) films of 50 ⁇ .
- the film is then measured after one hour of drying at ambient temperature.
- the film is then placed in the instrument and transparency and haze measurements are carried out.
- Control comparative comparative invention invention invention base (ex. 2) (ex. 3) (ex. 4) (ex. 5) (ex. 6) (ex. 1 )
- Myristyl alcohol 0.05 0.05 0.05 0.05 0.05 0.05 0.05 0.05 0.05 0.05 0.05 0.05
- Glyceryl stearate 1.05 1 .05 1 .05 1 .05 1.05 1 .05
- Carbomer (Carbopol 0.2 0.2 0.2 0.2 0.2 0.2 0.2 981 Polymer from Lubrizol)
- PEG-100 Stearate 1.05 1 .05 1 .05 1 .05 1.05 1 .05
- silica aerogel with boron nitride particles makes it possible to obtain high transparency (TH), haze, lightening (E) and homogenizing power (H) levels while at the same time maintaining the coverage (CR) at values below 50.
- this composition When applied to facial skin, this composition gives a lightening effect with transparency.
- weight percentages given for a compound or a family of compounds are always expressed as weight of solids of the compound in question.
Abstract
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CN201380031917.1A CN104379114B (en) | 2012-06-21 | 2013-06-21 | Method is highlighted comprising non-interfering type scattering particles and the cosmetic composition of aerogel particles and cosmetic |
BR112014027027A BR112014027027B8 (en) | 2012-06-21 | 2013-06-21 | cosmetic composition, cosmetic method for lightening and use of a combination |
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US10709647B2 (en) | 2015-10-27 | 2020-07-14 | Conopco, Inc. | Skin care composition comprising turbostratic boron nitride |
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FR3035587B1 (en) * | 2015-04-28 | 2017-05-26 | Oreal | COSMETIC COPOSITION BASED ON CUCURBIC ACID OR DERIVATIVE |
FR3067931B1 (en) * | 2017-06-26 | 2020-08-28 | Oreal | COSMETIC COMPOSITION IN POWDER BASED ON OIL-IN-WATER DISPERSION COATED WITH HYDROPHOBIC SILICA AIROGEL PARTICLES |
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2013
- 2013-06-21 CN CN201380031917.1A patent/CN104379114B/en active Active
- 2013-06-21 BR BR112014027027A patent/BR112014027027B8/en active IP Right Grant
- 2013-06-21 WO PCT/EP2013/063046 patent/WO2013190114A1/en active Application Filing
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CN105451815A (en) * | 2013-08-22 | 2016-03-30 | 默克专利有限公司 | Diffusion pigments in phototherapy |
US10709647B2 (en) | 2015-10-27 | 2020-07-14 | Conopco, Inc. | Skin care composition comprising turbostratic boron nitride |
Also Published As
Publication number | Publication date |
---|---|
CN104379114B (en) | 2018-01-02 |
CN104379114A (en) | 2015-02-25 |
BR112014027027A2 (en) | 2017-06-27 |
BR112014027027B8 (en) | 2019-09-17 |
BR112014027027B1 (en) | 2019-09-03 |
FR2992197A1 (en) | 2013-12-27 |
FR2992197B1 (en) | 2014-06-27 |
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