Classifications

• • 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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/0216—Solid or semisolid forms
  • A61K8/022—Powders; Compacted Powders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/0216—Solid or semisolid forms
  • A61K8/0233—Distinct layers, e.g. core/shell sticks
  • A61K8/0237—Striped compositions
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/04—Dispersions; Emulsions
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/11—Encapsulated compositions
• • 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
• • 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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin

Definitions

• the invention relates to a water containing powder composition and a process to produce a creamy composition from this powdery composition.
• Solid cosmetic preparations such as powders, having a high water content are known in the prior art.
• the basis of some patent applications is the long-known fact that in the presence of a hydrophobic powder, such as a hydrophobic silicon dioxide powder, water can be dispersed into fine droplets and enveloped by the hydrophobic material, thus preventing the droplets from rejoining.
• a powdery substance having a high water content known as "dry water” is formed in this way (Fine Particles series no. 1 1 , Evonik Degussa).
• Cosmetic formulations based on "dry water” are described in Seifen, Fette, Ole, Wachse (SOFW), 8 (2003), pages 1 -8.
• US 4274883 discloses an aqueous dispersion of a hydrophobic silica consisting of 0.1 to 50 parts of hydrophobic silica, in a given case up to 3 parts of wetting agent and 99.9 to 50 parts of water. It is produced by intensive mixing of hydrophobic silica with water with the known "dry-water-phase" as an intermediate step. In a given case there can additionally be used a wetting agent in which case the "dry-water-phase" does not occur.
• the dispersion of hydrophobic silicas can be mixed without additional steps or materials with rubber latex.
• DE-A-1467023 discloses the use of aqueous solutions comprising cosmetic ingredients instead of pure water for the preparation of dry water.
• EP-A-1206928 discloses a water-containing powder composition comprising aqueous gel cores coated with hydrophobic particles.
• JP 2000-309505 discloses a cosmetic powder being liquefied by embrocation including 2-20 wt.% of a hydrophobic silica having a specific surface area of at least 60 m2/g and an oil-in-water type emulsion composition.
• EP-A-1235554 discloses a cosmetic or pharmaceutical powder-to-liquid composition
• a cosmetic or pharmaceutical powder-to-liquid composition comprising hydrophobically coated silica particles into which are incorporated water and a water soluble polymer, the composition containing less than 1 % oil.
• EP-A-1386599 discloses a method for producing dry water composed of an aqueous ingredient coated with a hydrophobic powder to form a powder state capable of liquefying upon embrocation at the time of use, comprising charging a hydrophobic powder and an aqueous ingredient into a hollow container forming a hydrophobic enclosed space in the inside thereof, followed by agitating at a high speed in the hydrophobic hollow container to form fine aqueous droplets, and then allowing the surface of the fine aqueous droplets to be uniformly adsorbed with the hydrophobic powder.
• WO 01/85138 A2 discloses an encapsulation system comprising a core of aqueous liquid having at least 5% by weight water therein, and an encapsulant surrounding the core to form stable encapsulated particles, the encapsulant comprising at least one layer of hydrophobic particles in contact with and surround ing the core, the core and hydrophobic particles provid ing an encapsulated system that has a volume weighted mean particle diameter of from 0.05 to 25 micrometers, at least 25% of the encapsulated particles are spherical and can support its own weight.
• EP-A-855177 discloses a whitening powder comprising 0.1 to 7 wt.% trimethylsiloxylated silica having a specific surface area of at least 80 m 2 /g and a hydrophobicization degree of at least 50%, 5 to 40 wt.% of a polyhydric alcohol, 50 to 94 wt.% water and 0.01 to 5 wt.% of a whitening ingredient.
• WO 2005/058256 discloses cosmetic preparations of creme- or paste-like consistency, comprising 50 - 95 wt. % water, hydrophobized silicon dioxide powder, at least one cosmetically-relevant active ingredient, or adjunct which is water soluble or which may be dispersed or emulsified in an aqueous medium and a viscosity regulator.
• the above is produced by continuously adding hydrophobized silicon dioxide powder with mixing, to a solution or a dispersion of at least one cosmetical ly-relevant active ingredient and the mixing is continued until a paste-like consistency is achieved.
• the present invention provides a powdery composition comprising
• the water soluble liquid and the water reactive substrate are reversibly bound to the carrier by capillary action/absorption/adsorption and can be flushed or dissolved from the carrier, in part or completely, by the liquid water or the liquid aqueous phase of the core-shell particles.
• the carrier itself can be water soluble or not.
• the core shell particles as part of the composition according to the invention refer to a powdered material, that contains liquid water or a liquid aqueous phase, but where the coalescence of the individual water droplets is prevented by a shell of hydrophobic or hydrophobized particles.
• the shell is able to release the liquid aqueous phase or liquid water from the core when activated by pressure, shear, temperature, vibration and/or addition of one or more solvents or one or more surfactants.
• core shell particles are known as "dry water".
• the aqueous phase may be an aqueous solution, an aqueous dispersion or an aqueous emulsion.
• Hydrophobic particles are understood to be hydrophobic particles per se, whereas hydrophobized particles are those obtained by reacting the surface of a hydrophilic particle with a hydrophobic surface modifying agent. Usually a covalent bond is formed between reactive groups at the surface of the particles, e.g. hydroxyl groups, and reactive groups of the surface modifying agent.
• hydrophobic means that there is only a small or no interaction with water and the affinity with water is small or zero.
• a methanol wettability may be used as a quantitative measure of the hydrophobicity.
• the shell particles of the present invention should have a methanol wettability of at least 40, preferably 50 to 80, more preferably 60 to 70.
• 0.2 g ( ⁇ 0.005 g) of hydrophobic or hydrophobized particles are weighed into transparent centrifuge tubes. 8.0 ml portions of a methanol/water mixture with 10, 20, 30, 40, 50, 60, 70 or 80 vol.% methanol are added to each sample. The tubes are shaken for 30 seconds and then centrifuged at 2500 min "1 for 5 minutes.
• the methanol wettability is the defined as the volume per cent of methanol for which the sediment volume is 100%. The higher the number the higher the hydrophobicity.
• the hydrophobic or hydrophobized shell of the core shell particles usable in the present invention comprise for example inorganic powders such as talc, kaolin, mica, sericite, dolomite, phlogopite, synthetic mica, lepidolite, biotite, lithia mica, vermiculite, magnesium carbonate, calcium carbonate, aluminum silicate, barium sil icate, calcium sil icate, magnesium sil icate, strontium sil icate, tungstenic acid metal salts, magnesium, silica, zeolite, barium sulfate, calcined calcium sulfate, calcium phosphate, fluorapatite, hydroxyapatite, titania, fumed titania, alumina and fumed alumina.
• inorganic powders such as talc, kaolin, mica, sericite, dolomite, phlogopite, synthetic mica, lepidolite, biotite, lith
• hydrophobized silica particles which form a three dimensional network, an aggregated structure are a preferred shell material.
• the silica may be a precipitated silica or a fumed silica, the latter being preferred.
• Fumed silica is obtained in a flame hydrolysis or flame oxidation process. Its purity is higher than 99 wt.-%, usually higher than 99.8 wt.-%. Fumed silica usually forms a three-dimensional network of aggregated primary particles.
• the fumed silica primary particles bear hydroxyl groups at their surface and are nonporous.
• Precipitated and fumed silica particles, as well as other particles suitable as shell particles are hydrophilic particles which need to be hydrophobized in a subsequent step. Procedures for this step are known for the person skilled in the art.
• Suitable surface modifying agents can be the following silanes, which may be used individually or as a mixture.
• X CI, Br
• R' alkyl, such as methyl-, ethyl-, n-propyl-, isopropyl-, butyl-
• R' cycloalkyl
• n 1 - 20.
• Cyclic polysiloxanes D3, D4, D5 and their homologs, with D3, D4 and D5 meaning cyclic polysiloxanes having 3, 4 or 5 units of the type -O-Si(CH 3 ) 2 , e.g. octamethylcyclotetrasiloxane D4.
• octyltrimethoxysilane octyltriethoxysilane, hexamethyldisilazane, hexadecyltrimethoxysilane, hexadecyltriethoxysilane, dimethylpolysiloxane, nonafluorohexyltrimethoxysilane, tridecafluorooctyltrimethoxysilane,
• the shell particles of the powdery composition according to the invention can be hydrophobized silica particles having a BET surface area preferably from 30 m 2 /g to 500 m 2 /g, more preferably of 100 m 2 /g to 350 m 2 /g. Due to the reaction with the surface modifying agent these particles may contain 0.1 to 15 wt.-%, usually 0.5. to 5 wt.-%, of carbon. Typical examples that may be used as shell material are
• AEROSIL ® R104 octamethylcyclotetrasiloxane; 150 m 2 /g; 55;
• AEROSIL ® R106 octamethylcyclotetrasiloxane; 250 m 2 /g; 50
• AEROSIL ® R202 polydimethylsiloxane; 100 m 2 /g; 75
• AEROSIL ® R805 (octylsilane; 150 m 2 /g; 60),
• AEROSIL ® R812 hexamethyldisilazane; 260 m 2 /g; 60
• AEROSIL ® R812S hexamethyldisilazane; 220 m 2 /g; 65
• AEROSIL ® R8200 hexamethyldisilazane; 150 m 2 /g; 65).
• the ind ication in parenthesis refer to the surface mod ifying agent, the approximate BET surface area and the approximate methanol wettability, determined by the procedure given in this specification.
• Particularly useful shell particles material are hydrophobized silica particles which are obtained by reacting a hydrophilic fumed silica particles having a BET surface area of from 270 to 330 m 2 /g with hexamethyldisilazane.
• the obtained hydrophobized silica particles have a BET surface area of from 200 to 290 m 2 /g, a carbon content of 2 to 4 wt.-% and a methanol wettability of at least 50, more preferred 50 to 70.
• hydrophobized fumed silica particles in compacted form or as granules.
• the core contains liquid water, either in form of liquid water itself, or as a liquid aqueous solution, an emulsion containing liquid water or as an aqueous dispersion.
• the dissolved or emulsified material in case of a liquid aqueous solution or emulsion or the solid material in case of an aqueous dispersion should be selected from those materials that neither significantly reduce the surface tension of the core nor cause wetting of the hydrophobic or hydrophobized particles of the shell.
• the liquid aqueous solution this means that the solution should not contain more than 10 wt.-%, preferable not more than 3 wt.-%, of dissolved material.
• Liquid water itself is the most preferred core material.
• the core can consist of a liquid aqueous phase containing up to 10 wt.-% of compounds typically be used in the fields of cosmetic, personal care or household care may be used, as long as they do not reduce the surface tension of the core nor cause wetting of the hydrophobic or hydrophobized particles of the shell. Typical example will be discussed together with the carrier containing a at least partially water soluble liquid and/or a water reactive substrate.
• the water content of the core-shell particles usually is in a range from 75 to 95 wt.-%, based on the core shell particle.
• the powdery composition according to the invention consists of a powder next to the core shell particles that consists of at least one other powder, defined as a carrier containing a at least partially water soluble liquid or a water reactive substrate, each located in and/or on a carrier.
• the water soluble liquid is capable of being flushed or dissolved from the carrier, in part or completely, by the core material of the core-shell particles in case the core shell particles are activated by pressure, shear, temperature, vibration and/or addition of one or more solvents or one or more surfactants. This means that the water soluble liquid is either partially or completely dissolved from carrier by the water or the aqueous phase of the core. Or the water soluble liquid can be flushed, partially or completely, form carrier by the water or the aqueous phase of the core.
• a water reactive substrate is a material which is not water soluble or soluble only to a small amount. When being activated by water or an aqueous phase it is transformed to a reaction product or products that are essentially or completely water soluble.
• the carrier is preferably selected from the group consisting of silica, silica-metal mixed oxides, like silica-alumina mixed oxides, silica-titania mixed oxides, phyllosilicate, starch, hollow glass spheres, nylon, sugar, cyclodextrines and polysaccharides.
• the carrier is selected from fumed silica or precipitated silica, good results being obtained with hydrophilic as well as hydrophobized forms.
• the carrier is a precipitated silica having
• a BET surface area from 50 to 1000 m 2 /g, preferably from 100 to 700 m 2 /g, more preferably 150 to 500 m 2 /g,
• a DBP (dibutyl phthalate) absorption in g DBP/100 g silica, of from 200 to 400, preferably 250 to 350.
• the BET surface area is determined according to ISO 5794-1 , annex D, the particle size d 5 o is determined according to ASTM 690-1 992, and the DBP absorption is determined according to ASTM D 2414, based on the substance after drying.
• Special grades of precipitated silica comprise a material having a BET surface area of from 400 to 500 m 2 /g, a particle size d 5 o of 4 to 6 ⁇ and a DBP absorption of 300 to 350 g DBP/100 g silica. Also another material having a BET surface area of from 150 to 250 m 2 /g, a particle size d 5 o of 4 to 7 ⁇ and a DBP absorption of 250 to 300 g DBP/100 g silica. Typical examples are SIPERNAT ® 500 LS and SIPERNAT ® 22 LS, both from Evonik Degussa.
• the weight ratio of the at least partially water soluble liquid and/or water reactive substrate to carrier is determined by multiple factors such as the viscosity of the water soluble liquid, the structure of carrier comprising the pore size, the pore volume and the BET surface area. Usually is in the range of 10 to 90, a range from 60 to 75 being preferred.
• the weight ratio of the carrier including the at least partially water soluble liquid and/or water reactive substrate to the core-shell particles usually is from 1 :1 to 1 :9.
• the average particle size of the carrier and of the core-shell particles usually can vary, independently from each other, from 2 to 20 ⁇ .
• An average particle size of the core shell particles of 50 to 150% of the average particles size of the carrier may be preferred.
• the aqueous phase of the core of the core-shell particles and/or the at least partially water soluble liquid and/or water reactive substrate, each in and/or on the carrier comprises at least one of the materials of the group consisting of comprises at least one of the materials of the group consisting of UV light protection filters, antioxidants, moisturizing substances, deodorant,
• UV light protection filters are organic substances which are liquid or crystalline at room temperature and are capable of absorbing ultraviolet rays and of releasing the absorbed energy again in the form of radiation of longer wavelength, for example heat. UV filters can be oil-soluble or water-soluble. Oil-soluble substances are for example:
• 4-aminobenzoic acid derivatives preferably 4-(dimethylamino)benzoic acid 2-ethylhexyl ester, 4-(dimethylamino)benzoic acid 2-octyl ester and
• 4-(dimethylamino)benzoic acid amyl ester- esters of cinnamic acid preferably 4-methoxycinnamic acid 2-ethylhexyl ester, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid isoamyl ester,
• esters of salicylic acid preferably salicylic acid 2-ethylhexyl ester, salicylic acid 4-isopropyl benzyl ester, salicylic acid homomenthyl ester
• 3-benzylidenecamphor such as, for example, 4-(2-oxo-3-bornylidenemethyl)benzenesulfonic acid and
• UV-A filters are derivatives of benzoylmethane, such as
• UV-A and UV-B filters can of course also be employed in mixtures.
• benzoylmethane for example 4-tert-butyl-4'-methoxydibenzoylmethane and
• 2-phenylbenzimidazole-5-sulfonic acid and alkali metal, alkaline earth metal, ammonium, alkylammonium, alkanolammonium and glucammonium salts thereof.
• insoluble light protection pigments namely finely disperse metal oxide powders, as such or in
• suitable metal oxide powders or hydrophobized metal oxide powders can be titanium dioxide powder, zinc oxide powder and/or a mixed oxide powder of these with the elements Si, Ti, Al, Zn, Fe, B, Zr and/or Ce.
• Typical examples are coated titanium dioxides, such as UV-Titan M212, M 262 and X 1 1 1 (Kemira), AEROXIDE ® TiO2 P25, PF2, T 805 and T 817 (Evonik
• Degussa Micro Titanium Dioxide MT-150 W, MT-100 AQ, MT-100 SA, MT-100 HD, MT-100 TV (Tayca), Eusolex TM T2000 (Merck), Zinc Oxide neutral H&R and Zinc Oxide NDM (Haarmann & Reimer) as well as Z-Cote and Z-Cote HP1 (BASF).
• Dispersions such as, for example, TEGO Sun TAQ 40, a 40 wt.% strength aqueous dispersion of a hydrophobized titanium dioxide (Evonik Goldschmidt) can also be used.
• Typical antioxidants as part of the powdery composition according to the invention can be
• - chelators like alpha-hydroxy-fatty acids, palmitic acid, phytic acid,
• Moisturising substance may be selected from the group consisting of ethylene glycol, butylene glycol, 2,3-butandiol, propylene glycol, dipropylene glycol, tripropylene glycol, hexylene glycol, glycerine, diglycerine, glucose, fructose, lactose, saccharose, maltose, mannitol, mannose, PEG-4 to PEG-800, like PEG-4, PEG-6, PEG-7, PEG-8, PEG-9, PEG-10, PEG-12, PEG-14, PEG-16, PEG-18, PEG-20, sorbitol, polyglyceryl sorbitol, urea, xylitol and mixtures thereof.
• the deodorant and antiperspirant active compounds can be at least one selected from the group consisting of
• germ-inhibiting agents such as chitosan, phenoxyethanol, chlorhexidine gluconate or 5-chloro-2-(2,4-dichlorophenoxy)-phenol
• trial kyl citrates such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, tributyl citrate and triethyl citrate;
• sterol sulfates or phosphates such as lanosterol, cholesterol
• campesterol, stigmasterol and sitosterol sulfate and phosphate iii) dicarboxylic acids and esters thereof, such as, for example, glutaric acid, glutaric acid monoethyl ester, glutaric acid diethyl ester, adipic acid, adipic acid monoethyl ester, adipic acid diethyl ester, malonic acid and malonic acid diethyl ester,
• hydroxycarboxylic acids and esters thereof such as, for example, citric acid, malic acid, tartaric acid or tartaric acid diethyl ester; or
• salicylic acid N-alkylamides such as salicylic acid n-octylamide or salicylic acid n-decylamide.
• absorbers or odour maskers like benzyl acetate, p-tert-butylcyclohexyl acetate, linalyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, allylcyclohexyl propionate, styrallyl propionate and benzyl salicylate, benzyl ethyl ether, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, jonones, methyl cedryl ketone, anethole, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol, terpineol or terpenes.
• the biogenic substances may be selected from at least one of the group consisting of tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, (deoxy)ribonucleic acid and fragmentation products thereof, beta-glucans, retinol, bisabolol, allantoin, phytantriol, panthenol, pantothenic acid, fruit acids, alpha-hydroxy acids, amino acids, ceramides, pseudoceramides, essential oils, plant extracts, such as, for example, prunus extract, bambara nut extract and vitamin complexes.
• the insect repellent active compounds may be selected from the group consisting of N,N-diethyl-m-toluamide, 1 ,2-pentanediol,
• bleaching agents suitable for the present invention are
• hydroquinone zinc peroxide, urea peroxide, hydrogen peroxide and/or organic peroxides.
• the core of the core-shell particles is water, and the shell consists of hydrophobized fumed silica particles that are obtained by reacting a hydrophilic fumed silica having a BET surface area of from 30 to 500 m 2 /g.
• hydrophobized fumed silica particles are obtained by reacting a hydrophilic fumed silica having a BET surface area from 270 to 330 m 2 /g with
• hydrophobized fumed silica particles having a BET surface area of from 200 to 290 m 2 /g and a carbon content of 2 to 4 wt.-% and methanol wettability of at least 50.
• the special embodiment may further comprise as carrier a precipitated silica having a BET surface area from 400 to 500 m 2 /g, a particle size d 5 o, determined by laser diffraction, from 4 to 6 ⁇ and a DBP (dibutyl phthalate) absorption, in g DBP/ 100 g silica, from 300 to 350.
• the special embodiment may also further comprise as carrier a precipitated silica having a BET surface area from 150 to 250 m 2 /g, a particle size d 5 o, determined by laser diffraction, from 4 to 7 ⁇ and a DBP (dibutyl phthalate) absorption, in g DBP/ 100 g silica, from 250 to 300.
• the special embodiments may further comprise as at least partially water soluble liquid and/or water reactive substrate, each located in and/or on the carrier, and UV light protection filters, antioxidants, moisturizing substances, deodorant, antiperspirant active compounds, biogenic substances, insect repellent active compounds, bleaching agents antioxidant, bleach, antibacterial substances, antifungal substances, flavors, fragrances, acids, alkalis, enzymes or mixtures thereof.
• UV light protection filters antioxidants, moisturizing substances, deodorant, antiperspirant active compounds, biogenic substances, insect repellent active compounds, bleaching agents antioxidant, bleach, antibacterial substances, antifungal substances, flavors, fragrances, acids, alkalis, enzymes or mixtures thereof.
• Another object of the invention is a process for the manufacture of a creamy composition, starting form the powdery composition according to the invention.
• This powdery composition is activated by an energy input in form of pressure, shear, temperature, vibration and/or solvent addition, the energy input being sufficient to release the liquid water or the liquid aqueous phase from the core- shell material, the liquid water or the liquid aqueous phase subsequently is a) dissolving or flushing the at least partially water soluble liquid from the
• Creamy is understood to mean a range from more liquid compositions to more gel like compositions to creamy compositions.
• Example 1 Powder-to-Cream-to-Powder Foundation according to the state-of the-art way
• AEROSIL ® R812S was added at 5.0 wt.-% on top of the water/PEG/Dimethicone/Pigments mixture.
• the lid was placed tightly on the blender and the mixture was blended at the highest setting (Liquefy) at 9,700 RPM for one minute.
• the entire blender was tilted at a 50-60 degree angle from left to right with 10 second hold times.
• the product is a cream/mousse texture that has a clear separation on the bottom after about 30 minutes.
• Example 2 Powder-to-Cream-to-Powder Foundation according to the invention
• the dry water was produced by adding 5 wt.- % of AEROSIL ® R812S, 20 wt.-% iron oxide AC-5 pigments and 75 wt.-% Dl water. The lid was placed tightly on the blender and the mixture was blended at the highest setting (Liquefy) at
• the end product was a cream/ mousse texture that has a clear separation on the bottom after about half an hour.
• a liquid mix of 71 .4 wt.-% of polyethylene glycol (PEG Sentry ® Polyethylene Glycol 400 NF from The Dow Chemical Company), 14.3 wt.-% Vitamin E (from JEEN International Corp.) and 14.3 wt-% Dl water was made.
• the liquid mix was then used to make a 64.0 wt.-% liquid mix, to 36.0 wt.-% SIPERNAT ® 22LS as carrier.
• the liquid mix was slowly added to SIPERNAT ® 22 LS in 3-4 addition steps, using low shear mixing (in this case, by hand) until the mix was uniform.
• the powder obtained (30 wt.-%) was then gently mixed (tumbled, tossed folded in) to 70 wt.-% dry water.
• the powder was then stored in a plastic container.
• Tab. 1 Ingredients of the formulations of Examples 1 to 4 [wt.-%l

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• 2010
  • 2010-11-26 KR KR1020127016449A patent/KR101431932B1/ko active Active
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