CN112165928A - Temperature-sensitive cosmetic - Google Patents

Temperature-sensitive cosmetic Download PDF

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Publication number
CN112165928A
CN112165928A CN201980035277.9A CN201980035277A CN112165928A CN 112165928 A CN112165928 A CN 112165928A CN 201980035277 A CN201980035277 A CN 201980035277A CN 112165928 A CN112165928 A CN 112165928A
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cosmetic
oil
temperature
mass
sensitive
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白神裕人
大道口则子
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Shiseido Co Ltd
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Shiseido Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25Silicon; Compounds thereof
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • 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
    • A61K8/89Polysiloxanes
    • 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
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin

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Abstract

The purpose of the present invention is to provide a water-in-oil type temperature-sensitive cosmetic that exhibits an excellent temperature-sensitive imparting effect, has a good feeling of use, and has excellent storage stability. The invention relates to a temperature-sensitive cosmetic which is characterized by containing polyol, an oil phase thickener, an emulsifier and water.

Description

Temperature-sensitive cosmetic
Technical Field
The present invention relates to a temperature-sensitive cosmetic that imparts a temperature-sensitive feel when applied to the skin. More particularly, the present invention relates to a water-in-oil type temperature-sensitive cosmetic which has excellent emulsion stability, exerts a cosmetic effect, and has a good feeling of use.
Background
Generally, it is known that imparting a moderate temperature sensation to the skin promotes blood circulation of the skin, increases metabolism, and provides a blood color improving effect, a relaxing effect, a fatigue recovery effect, and the like. Therefore, these effects are expected to be expected to allow the blending of a heat-generating substance into a cosmetic. As a heat-generating substance to be blended in cosmetics, a moisturizing agent such as a polyhydric alcohol, zeolite, a metal salt, a metal oxide, or the like has been widely used. These are all hygroscopic and generate heat when they come into contact with moisture on the skin, thereby giving a feeling of warmth to the skin.
Patent document 1 proposes a polyol-in-oil type temperature-sensitive cosmetic prepared by emulsifying a polyol with a specific nonionic surfactant, in order to obtain an appropriate viscosity and an excellent temperature-sensitive effect. Further, patent document 2 proposes that zeolite having high heat build-up is dispersed in a polyol solvent to improve the effect of imparting a temperature sensation.
As described above, various bases have been proposed as a temperature-sensitive cosmetic, and the cosmetic of patent document 1 is an oil-in-water type base and has a remarkably high slimy feeling because a polyhydric alcohol is directly in contact with the skin. Therefore, it is a rinse-off type cleanser used by being applied to the skin and rinsed after a certain time has elapsed. The cosmetic of patent document 2 is a Leave-on (Leave-on) type, but is nonaqueous, and therefore it is difficult to stably mix an aqueous solution containing a salt type drug having a cosmetic effect.
Therefore, there is a need for a water-in-oil base which can be blended with a cosmetic agent having a skin-beautifying effect such as a whitening component which exhibits an excellent effect of imparting a warm feeling and is excellent in stability and usability.
Documents of the prior art
Patent document
Patent document 1: japanese patent application laid-open No. 2014-37404
Patent document 2: japanese patent laid-open publication No. 2016 & 193841
Disclosure of Invention
Problems to be solved by the invention
The purpose of the present invention is to provide a water-in-oil type temperature-sensitive cosmetic that exhibits an excellent temperature-sensitive imparting effect, has a good feeling of use, and has excellent storage stability.
Means for solving the problems
The present inventors have made extensive studies and, as a result, have found that the above object can be achieved by blending a polyol, an oil phase thickener, an emulsifier and water, and have completed the present invention.
That is, the present invention is a water-in-oil type temperature-sensitive cosmetic comprising:
a polyhydric alcohol,
An oil phase thickener,
An emulsifier, and
and (3) water.
ADVANTAGEOUS EFFECTS OF INVENTION
The temperature-sensitive cosmetic of the present invention exhibits an excellent temperature-sensitive imparting effect and also has excellent emulsion stability. Further, the temperature-sensitive cosmetic of the present invention is a water-in-oil type temperature-sensitive cosmetic, and can prevent the polyol from directly contacting the skin, so that the viscosity can be suppressed as compared with conventional oil-in-water or oil-in-polyol type temperature-sensitive cosmetics, although the humectant (polyol) is highly blended. Therefore, the temperature-sensitive cosmetic of the present invention can also be used as a leave-on type temperature-sensitive cosmetic base. In addition, a salt-type drug having a skin-beautifying effect such as a whitening component can be added because water can be added.
Detailed Description
The temperature-sensitive cosmetic of the present invention is characterized by containing a polyol, an oil phase thickener, an emulsifier and water as essential components. The present invention will be described in detail below.
< polyol >
The polyhydric alcohol used in the warm cosmetic of the present invention is one which imparts a warm feeling when applied to the skin. Specific examples, without limitation, include: glycerin, diglycerin, polyglycerol, 1, 3-butanediol, ethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol (PEG-8 and the like), polypropylene glycol, polyethylene glycol-polypropylene glycol, methyl glucitol polyether-10, trimethylolethane, trimethylolpropane, erythritol, pentaerythritol, sorbitan, glucose, sorbitol, maltitol, sucrose, raffinose, hexanediol, 1, 2-pentanediol, trehalose and the like.
Among these, glycerin, dipropylene glycol, polyethylene glycol, 1, 3-butanediol, methyl gluceth-10, and the like are preferably used in an appropriate amount.
In addition, the compounding of the polyhydric alcohol can also produce a warming effect to introduce the skin with a bright and good bloody color, and prevent removal of makeup due to dryness by utilizing a high moisturizing effect.
The amount of the polyol to be blended in the cosmetic of the present invention is 20% by mass or more, preferably 20 to 80% by mass, and more preferably 30 to 70% by mass, based on the total amount of the cosmetic. If the amount of the polyol to be blended is less than 20% by mass, the feeling of warmth at the time of use cannot be sufficiently obtained.
< oil phase thickener >
The oil phase thickener used in the temperature-sensitive cosmetic of the present invention is one that can impart viscosity to an oil phase. By way of example, mention may be made of: emulsifying or non-emulsifying crosslinked silicone elastomer, dextrin fatty acid ester, hydrophobic modified polysaccharide, fatty acid, wax, etc. Among these, in the present invention, a non-emulsifying crosslinked siloxane elastomer is preferably used from the viewpoint of suppressing a sticky feeling.
The non-emulsifying crosslinked silicone elastomer is not particularly limited, and examples thereof include: methyl polysiloxane crosspolymer, methyl phenyl polysiloxane crosspolymer, vinyl dimethicone/lauryl dimethicone crosspolymer, lauryl dimethicone alkoxyethyl dimethicone/divinyl dimethicone crosspolymer, alkyl (C30-45) cetearyl dimethicone crosspolymer, and the like. These non-emulsifying crosslinked silicone elastomers are commercially available in the form of a swollen product that swells in various oil components such as silicone oil, mineral oil, glyceryl triisooctanoate, and squalane. Specific examples thereof include the following.
As the methylpolysiloxane crosslinked polymer, there can be mentioned: polydimethylsiloxane cross-linked polymers such as 9040 silicone elastomer blend, 9041 silicone elastomer blend, 9045 silicone elastomer blend and EL-8040ID silicone organic blend (manufactured by Dow Corning Toray Co., Ltd.), polydimethylsiloxane/vinyl polydimethylsiloxane cross-linked polymers such as KSG-15, KSG-16 and KSG-1610 (manufactured by shin-Etsu chemical Co., Ltd.), vinyl polydimethylsiloxane/polymethylsiloxane silsesquioxane cross-linked polymers such as KSP-100 (manufactured by shin-Etsu chemical Co., Ltd.), polymethylsilsesquioxane such as PEARL 150KA (manufactured by MoTOSE Performance Materials Co., Ltd.), and the like.
Examples of the methylphenylpolysiloxane crosslinked polymer include a polydimethylsiloxane/phenylpolydimethylsiloxane crosslinked polymer such as KSG-18A (polydimethylsiloxane/phenylvinyl polydimethylsiloxane crosslinked polymer, manufactured by shin-Etsu chemical Co., Ltd.).
Examples of vinyl dimethicone/lauryl dimethicone crosspolymer include: KSG-41A, KSG-42A, KSG-43, KSG-44 (manufactured by shin-Etsu chemical Co., Ltd.).
Examples of the swollen product of the lauryl polydimethylsiloxyethyl dimethicone/bisvinyl dimethicone crosspolymer include KSG-042Z, KSG-045Z (manufactured by shin-Etsu chemical Co., Ltd.).
Examples of the alkyl (C30-45) cetearyl dimethicone crosspolymer include VELVESIL 125 and VELVESIL 034 (manufactured by Momentive Performance Materials Co., Ltd.).
The cross-linked polymer of cetearyl dimethicone may be, for example, VELVESIL DM (manufactured by Momentive Performance Materials).
The amount of the oil phase thickener to be blended in the cosmetic of the present invention is more than 1.25 mass% and 15 mass% or less, preferably 1.26 to 12 mass%, more preferably 1.27 to 10 mass%, and still more preferably 1.28 to 10 mass% with respect to the total amount of the cosmetic. When the amount of the oil phase thickener added is 1.25% by mass or less, emulsion stability tends to be poor or usability tends to be poor, while when it is added in an amount exceeding 15% by mass, it may be difficult to produce a stable cosmetic.
The oil phase thickener of the present invention may be used in combination with one or more than 2 kinds selected from the aforementioned non-emulsifying crosslinked siloxane elastomers.
< emulsifier >
The emulsifier used in the temperature-sensitive cosmetic of the present invention is a relatively high lipophilicity and can exert an emulsion stabilizing effect of an aqueous component and an oily component highly blended with a polyhydric alcohol. In the present invention, polyether-modified silicone or organically modified clay mineral having specific properties can be preferably used.
The so-called polyether-modified silicone having the above-mentioned specific properties, which is used as the emulsifier of the present invention, is one having an HLB of 8.0 or less and a viscosity of 10000mm at 25 ℃2More than s, preferably 15000mm2A thickness of 20000mm or more2More than s. If the viscosity is less than 10000mm2And/s, good emulsion stability cannot be obtained.
Specific examples of the polyether-modified silicone include PEG/PPG (Poly Propylene Glycol) -19/19 polydimethylsiloxane (trade name "BY 11-030", HLB: 3, and viscosity of 30000mm2S; manufactured by Dow Corning Toray corporation), and the like.
The organically modified clay mineral used in the present invention is one of colloidal hydrous aluminum silicates having a three-layer structure, and a clay mineral represented by the following general formula (1) can be modified with a quaternary ammonium salt cationic surfactant.
(x,Y)2-3(Si,Al)4O10(OH)2Z1/3·nH2O (1)
In the formula, X is Al, Fe (III), Mn (III) or Cr (III), Y is Mg, Fe (II), Ni, Zn or Li, and Z is K, Na or Ca.
Specifically, the cationic surfactant can be obtained by treating clay minerals such as natural or synthetic smectites (in this case, those in which the (OH) group in the formula is substituted with fluorine) such as montmorillonite, saponite and hectorite (commercially available products such as magnesium aluminum silicate, Kunipia and synthetic hectorite), and synthetic micas (commercially available products such as Dimonite and manufactured by TOPY INDUSTRIES) known under the name of sodium silicate mica, sodium mica or laponite.
The quaternary ammonium salt cationic surfactant used here is represented by the following general formula (2).
Figure BDA0002797758290000051
In the formula, R1Represents C10-22 alkyl or benzyl, R2Represents a methyl group or an alkyl group having 10 to 22 carbon atoms, R3And R4Represents an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms, and X represents a halogen atom or a methyl sulfate residue.
Examples of the quaternary ammonium salt cationic surfactant include: dodecyl trimethyl ammonium chloride, myristyl trimethyl ammonium chloride, cetyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride, arachidyl trimethyl ammonium chloride, behenyl trimethyl ammonium chloride, myristyl dimethyl ethyl ammonium chloride, cetyl dimethyl ethyl ammonium chloride, stearyl dimethyl ethyl ammonium chloride, arachidyl dimethyl ethyl ammonium chloride, behenyl dimethyl ethyl ammonium chloride, myristyl diethyl methyl ammonium chloride, cetyl diethyl methyl ammonium chloride, stearyl diethyl methyl ammonium chloride, arachidyl diethyl methyl ammonium chloride, behenyl diethyl methyl ammonium chloride, benzyl dimethyl myristyl ammonium chloride, benzyl dimethyl cetyl ammonium chloride, benzyl dimethyl stearyl ammonium chloride, benzyl dimethyl behenyl ammonium chloride, benzyl methyl ethyl cetyl ammonium chloride, benzyl methyl ethyl stearyl ammonium chloride, benzyl dimethyl behenyl ammonium chloride, benzyl dimethyl lauryl ammonium chloride, benzyl methyl ethyl stearyl ammonium chloride, Dibehenyl dihydroxyethyl ammonium chloride, a bromide equivalent thereto, dipalmitoylpropylethylammonium methylsulfate, and the like. In the practice of the present invention, one or more than 2 of these are arbitrarily selected.
Representative examples of the organically modified clay mineral include: dimethyl distearyl ammonium hectorite (distearyl dimethyl ammonium hectorite), dimethyl alkyl ammonium hectorite, benzyl dimethyl stearyl ammonium hectorite, distearyl dimethyl ammonium chloride-treated aluminum magnesium silicate, and the like. Among them, dimethyl distearyl ammonium hectorite is particularly preferable. Commercially available products include Bentonine 27 (benzyldimethylstearylammonium chloride-treated hectorite, manufactured by Elementis Japan) and Bentonine 38VCG (distearyldimethylammonium chloride-treated hectorite, manufactured by Elementis Japan).
The amount of the emulsifier blended in the cosmetic of the present invention is 0.1 to 5% by mass, preferably 0.2 to 4% by mass, and more preferably 0.4 to 3% by mass based on the total amount of the cosmetic. When the amount is less than 0.1% by mass, the viscosity is not easily developed and the stability is poor, and when it exceeds 5% by mass, a sticky feeling or powdery feeling is generated from the emulsifier, which is not preferable in terms of usability.
< water >)
In the temperature-sensitive cosmetic composition of the present invention, water (ion-exchanged water, purified water, natural water, or the like) may be used as the aqueous solvent. Among these, since the effect of temperature sensitivity is reduced when the aqueous solvent is present, when the aqueous solvent is blended, the content should be suppressed to 10% by mass or less, preferably 8% by mass or less, and more preferably 5% by mass or less, relative to the total amount of the temperature sensitive cosmetic. Therefore, in the temperature-sensitive cosmetic of the present invention, the amount of water to be added is preferably 0.1 to 10% by mass, or 1 to 10% by mass, more preferably 0.1 to 8% by mass, or 1 to 8% by mass, and still more preferably 1 to 5% by mass, from the viewpoint of sufficiently dissolving the drug such as the whitening agent and obtaining a temperature-sensitive feeling.
< whitening agent >
In contrast to conventional leave-on type temperature sensitive cosmetics which are nonaqueous and difficult to incorporate water-soluble drugs, the temperature sensitive cosmetics of the present invention are characterized in that they can incorporate water-soluble drugs because they contain water.
The whitening agent to be blended is not particularly limited as long as it is a whitening agent blended in a usual cosmetic, and examples thereof include: ascorbic acid (vitamin C), tranexamic acid, kojic acid, ellagic acid, arbutin, alkoxysalicylic acid, and salts or derivatives thereof. More specific examples include: sodium L-ascorbate, magnesium L-ascorbate ester, L-ascorbic acid glucoside, 2-O-ethyl-L-ascorbic acid, 3-O-ethyl-L-ascorbic acid, sodium 4-methoxysalicylate, and potassium 4-methoxysalicylate.
In the present invention, 4-methoxysalicylic acid potassium salt can be preferably used.
In addition, agents other than whitening agents may be added. Examples of the drug include: vitamin B compounds such as vitamin A, vitamin A palmitate, vitamin A acetate and the like, vitamin B6 hydrochloride, vitamin B6 tripalmitate, vitamin B6 dicaprylate, vitamin B2 and derivatives thereof, vitamin B12, vitamin B15 and derivatives thereof, vitamin E compounds such as alpha-vitamin E, beta-vitamin E, vitamin E acetate and the like, vitamin D compounds, vitamins such as vitamin H, pantothenic acid, pantethine and the like; gamma-oryzanol, allantoin, glycyrrhizic acid (salt), glycyrrhetinic acid stearyl ester, juniperitol, bisabolol, eucalyptone, thymol, inositol, saikoside, ginsenoside, luffa saponin, soapberry saponin and other saponins, panthenol ethyl ether, arbutin, cepharanthine and other various medicaments, rumex japonicus, sophora flavescens, japanese lotus root, orange, common sage herb, saw-leaved mallow, swertia herb, thyme, angelica, bitter orange, birch, horsetail, luffa, horse chestnut, saxifrage, scutellaria baicalensis, arnica, lily, wormwood, peony, aloe, gardenia, cherry leaf and other plant extracts, and beta-carotene and other pigments.
The amount of the drug of the present invention to be blended is arbitrarily determined within the range of the amount of the drug to be dissolved in the temperature-sensitive cosmetic. In the cosmetic, from the viewpoint of obtaining a sufficient drug effect, the content is preferably 0.5 to 4% by mass, and more preferably 1 to 3% by mass.
< polyether modified Silicone >)
In the present invention, HLB is 8.0 or less and viscosity at 25 ℃ is less than 10000mm2The polyether modified organosilicon of/s can further improve the emulsion stability. Among them, those having no alkyl chain in the side chain and having a polyoxyalkylene group in the side chain of a linear or branched silicone skeleton are preferable.
Specific examples of the polyether-modified silicone having a linear silicone skeleton include: PEG-3 Dimethicone (trade name "KF-6015", HLB 4.5, viscosity 150 mm)2S; manufactured by shin-Etsu chemical Co., Ltd.), PEG-9 methyl ether polydimethylsiloxane (trade name "KF-6016", HLB 4.5, viscosity 150mm2S; manufactured by shin-Etsu chemical Co., Ltd.), PEG-10 polydimethylsiloxane (trade name "KF-6017P", HLB 4.5, viscosity 850mm2S; manufactured by shin-Etsu chemical Co., Ltd.), PEG-12 polydimethylsiloxane (trade name "SH 3772M", HLB 6, viscosity 1050mm2(ii)/s, trade name "SH 3773M", HLB (8), viscosity 650mm2(ii)/s, trade name "SH 3775M", HLB 5, viscosity 1600mm2S; these are all manufactured by Dow Corning Toray Co., Ltd.), PEG/PPG-20/22 butyl ether polydimethylsiloxane (trade name "KF-6012", HLB 7.0, viscosity 1600mm2S; shin-Etsu chemical Co., Ltd.) and the like.
Specific examples of the polyether-modified silicone having a branched silicone skeleton include: PEG-9 Dimethylsilalkoxyethyl polydimethylsiloxane (trade name: KF-6028, HLB: 4, viscosity 900 mm)2S; manufactured by shin-Etsu chemical Co., Ltd.), lauryl PEG-9 Dimethylsilyloxyalkylethyl polydimethylsiloxane (trade name "KF-6038", HLB 3, viscosity 700mm2S; manufactured by shin-Etsu chemical Co., Ltd.), cetyl PEG/PPG-10/1 Dimethicone (trade name "KF-6048", HLB 3.5, viscosity 2700 mm)2S; shin-Etsu chemical Co., Ltd.) and the like.
The amount of polyether-modified silicone blended in the cosmetic of the present invention is 0.1 to 10% by mass or less, preferably 0.3 to 6% by mass, and more preferably 1 to 5% by mass based on the total weight of the cosmetic.
< oil content >
In the cosmetic preparation for warmth of the present invention, it is preferable to blend an oil component in order to improve the feeling of use when it is applied to the skin. The oil component is not particularly limited as long as it can be used in a usual cosmetic.
Examples thereof include: linseed oil, camellia oil, macadamia nut oil, corn oil, olive oil, avocado oil, camellia oil, castor oil, safflower oil, almond oil, cinnamon oil, jojoba oil, grape oil, sunflower oil, almond oil, rapeseed oil, sesame oil, wheat germ oil, rice bran oil, cottonseed oil, soybean oil, peanut oil, tea seed oil, evening primrose oil and other oils; fatty acids such as heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, pentadecanoic acid, heptadecanoic acid, nonadecanoic acid, isostearic acid, oleic acid, linoleic acid, and arachidonic acid; esters such as pentaerythritol tetraoctanoate, cetyl octanoate, hexyl laurate, isopropyl myristate, octyl myristate, dodecyl palmitate, octyl palmitate, isopropyl isostearate, octyl isopalmitate, isodecyl oleate, cetyl ethylhexanoate, and the like; hydrocarbons such as liquid paraffin, squalane, squalene, olefin oligomers, hydrogenated polydecene, paraffin, isoparaffin, octane, decane, dodecane, isododecane, hexadecane, and isohexadecane; higher alcohols such as octanol, isostearyl alcohol, oleyl alcohol and the like; chain silicones such as dimethylpolysiloxane, methylphenylpolysiloxane and methylhydrogenpolysiloxane, cyclic silicones such as octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane, and silicone oils such as octylmethicone.
In the cosmetic of the present invention, a plurality of the above-mentioned oil components may be combined and blended. The amount of the oil component is 10 to 50% by mass, preferably 15 to 40% by mass, and more preferably 15 to 35% by mass, based on the total amount of the cosmetic. If the amount of the oil component is less than 10% by mass, the external oil phase is small, and emulsification is difficult, and lightness and spreadability when the composition is applied to the skin cannot be sufficiently obtained, and if it exceeds 50% by mass, the internal water phase is small, and viscosity is not easily developed, and stability may be impaired.
< other ingredients >
In the temperature-sensitive cosmetic composition of the present invention, other components used in usual cosmetic compositions, for example, a powder component, an ultraviolet ray protective agent, various aqueous solvents, a thickener, a masking agent, a sugar, an amino acid, an organic amine, a pH adjuster, a stabilizer, a skin nutrient, an antioxidant aid, a perfume, and the like may be appropriately blended as necessary within a range not impairing the effects of the present invention.
The average emulsified particle size of the water droplets constituting the temperature sensitive cosmetic of the present invention is 10 μm or less, and more preferably 5 μm or less. By reducing the average emulsified particle size of the water droplets, the emulsion stability is excellent.
The thermal cosmetic of the present invention has a hardness of 6 or more, preferably 8 or more, and more preferably 10 or more as measured at 25 ℃ by a rheometer (11.3 mm. phi., 10mm needle penetration). Can be made into ointment by combining with wax. The emulsion cosmetic of the present invention having such hardness is excellent in stability, and when filled into a bottle container, for example, does not flow and retains an appropriate hardness.
The temperature-sensitive cosmetic of the present invention is characterized by being a one-layer type. The temperature-sensitive cosmetic of the present invention has good emulsion stability even when a water-soluble drug is blended, has no sticky feeling even when a humectant is highly blended, and has excellent use feeling. Therefore, the temperature-sensitive cosmetic of the present invention can be widely applied to cosmetics, and can be provided in any form such as emulsion, lotion, cream, massage cosmetic, sunscreen cosmetic, foundation, pack, lipstick, blusher, eye shadow, and the like.
The temperature-sensitive cosmetic of the present invention can be produced by a conventional method. For example, the aqueous phase component and the oil phase component are stirred and mixed to prepare a uniform aqueous phase portion and an oil phase portion, and the aqueous phase portion is added to the oil phase portion while stirring and mixing.
Examples
The present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. The amount to be blended represents mass% unless otherwise specified. Before the examples, the evaluation method used in the present invention will be described.
(1) Effect of temperature sensing
The prepared test specimens were subjected to actual use tests by 10 professional functional inspectors. Specifically, the prepared samples were applied to the face of each functional examiner, and the temperature sensation was evaluated according to the following criteria.
< evaluation Standard >
A: more than 8 professional functional examiners consider the effect of temperature.
B: the professional sensory examiner was recognized as having a warming effect by 5 or more and less than 8.
C: the professional sensory examiner was considered to have a warming effect by 3 or more and less than 5.
D: less than 3 professional functional examiners consider a warming effect.
(2) Stability of
Each sample was allowed to stand at 0 ℃, 25 ℃ and 50 ℃ for 1 month after preparation, and then returned to room temperature, followed by visual observation and evaluation of the presence or absence of separation. The emulsified particle size of the water droplets after sample preparation was measured by a microscope. The smaller the average emulsified particle is, the better the emulsion stability is, and when it exceeds 10 μm, the tendency of separation is high due to long-term storage.
(3) Hardness of
Here, the "hardness" in the above description is measured by using a rheometer (manufactured by non-industrial corporation) in a needle diameter: 11.3mm φ, penetration distance: 10mm, measurement temperature: measured at 25 ℃.
(4) Usability
The prepared test specimens were subjected to actual use tests by 10 professional functional inspectors. Specifically, the prepared samples were applied to the faces of the functional examiners, and the lightness of the sample, i.e., no stickiness, smoothness, and extension, was evaluated comprehensively in accordance with the following criteria.
< evaluation Standard >
A: more than 8 professional functional inspectors were considered to be excellent in usability.
B: the professional functional examiner 5 or more and less than 8 were considered to be excellent in usability.
C: the professional functional examiner has 3 or more but less than 5 persons who are considered to be excellent in usability.
D: less than 3 professional functional inspectors consider the usability to be excellent.
Examples 1 to 8 and comparative examples 1 to 7
Cosmetics were prepared using the formulations shown in the following tables 1 and 2, and each characteristic was evaluated according to the above evaluation method. The results are shown in tables 1 and 2.
[ Table 1]
Figure BDA0002797758290000121
[ Table 2]
Figure BDA0002797758290000131
1KSG-16 (manufactured by shin-Etsu chemical Co., Ltd.)
2DC9041 (manufactured by Dow Corning Toray Co., Ltd.)
3TOSPEARL 150KA (manufactured by Momentive Performance Materials Co., Ltd.)
4KSG-18A (manufactured by shin-Yue chemical industries Co., Ltd.)
5KSP-100 (manufactured by shin-Yue chemical industries Co., Ltd.)
6BY11-030 (manufactured BY Dow Corning Toray Co.)
7BENTONE 38VCG (manufactured by Elementis Japan)
8KF-6017P (manufactured by shin-Yue chemical Co., Ltd.)
9KF-6048 (manufactured by shin-Etsu chemical Co., Ltd.)
10KF-6028 (manufactured by shin & shin chemical Co., Ltd.)
As shown in the results in the table, the composition containing the moisturizing agent, the oil phase thickener and the emulsifier of the present invention (example 1) can obtain a sufficient temperature-sensitive effect, and also has excellent emulsion stability, no sticky feeling and good feeling in use. Further, the compositions of examples 2 to 8 can be stably mixed with a whitening agent.
On the other hand, when the compositions containing no oil phase thickener (comparative examples 1 to 3) and the oil phase thickener were used in small amounts (comparative examples 4 and 5), the stability was remarkably lowered and separation occurred. In addition, the composition containing neither the polyether-modified silicone having a high viscosity nor the organic-modified clay mineral (comparative example 6) was remarkably low in stability. In addition, when the amount of water added is large (comparative example 7), a sufficient temperature effect cannot be obtained.

Claims (8)

1. A water-in-oil type temperature-sensitive cosmetic comprising:
a polyhydric alcohol,
An oil phase thickener,
An emulsifier, and
and (3) water.
2. The cosmetic according to claim 1, wherein the water content is 0.1 to 10% by mass.
3. The cosmetic according to claim 1, wherein the emulsifier has a viscosity of 10000mm at 25 ℃2Polyether modified organosilicon with a concentration of more than s.
4. The cosmetic of claim 1, wherein the emulsifier is disteardimonium hectorite.
5. The cosmetic according to claim 1, wherein the oil phase thickener is a silicone elastomer.
6. The cosmetic according to claim 1, wherein the amount of the oil phase thickener blended is more than 1.25% by mass and 15% by mass or less.
7. The cosmetic according to claim 1, further comprising a viscosity at 25 ℃ of less than 10000mm2Polyether modified silicone/s.
8. The cosmetic according to claim 1, further comprising a whitening agent.
CN201980035277.9A 2018-05-29 2019-05-24 Temperature-sensitive cosmetic Pending CN112165928A (en)

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Publication number Priority date Publication date Assignee Title
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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001187711A (en) * 1999-12-28 2001-07-10 Nonogawa Shoji Kk Cosmetic
JP2008115358A (en) * 2007-06-18 2008-05-22 Shin Etsu Chem Co Ltd Organopolysiloxane, method for producing the same and cosmetic composition including the same
CN103191027A (en) * 2013-04-27 2013-07-10 珀莱雅化妆品股份有限公司 Solid makeup removing cream having warm sense in using process
CN103608384A (en) * 2011-05-30 2014-02-26 道康宁东丽株式会社 Novel liquid organo polysiloxane and use therefor
CN103619914A (en) * 2011-05-30 2014-03-05 道康宁东丽株式会社 Novel organopolysiloxane elastomer and use therefor
CN108024930A (en) * 2016-03-15 2018-05-11 株式会社漫丹 Warm heat sense makeup removing cosmetic preparation

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001206817A (en) 1999-11-15 2001-07-31 Shiseido Co Ltd Oil-in-polyhydric alcohol type thermal substrate
JP2013129625A (en) 2011-12-21 2013-07-04 Pola Chemical Industries Inc Skin care preparation of water-in-oil type emulsion dosage form
KR102610931B1 (en) * 2016-09-07 2023-12-08 (주)아모레퍼시픽 Cosmetic composition having thermal effects
JP6765951B2 (en) * 2016-12-16 2020-10-07 株式会社 資生堂 Aqueous solvent type thermal skin external preparation in oil
JP6809255B2 (en) * 2017-01-30 2021-01-06 信越化学工業株式会社 Water-in-oil cosmetics

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001187711A (en) * 1999-12-28 2001-07-10 Nonogawa Shoji Kk Cosmetic
JP2008115358A (en) * 2007-06-18 2008-05-22 Shin Etsu Chem Co Ltd Organopolysiloxane, method for producing the same and cosmetic composition including the same
CN103608384A (en) * 2011-05-30 2014-02-26 道康宁东丽株式会社 Novel liquid organo polysiloxane and use therefor
CN103619914A (en) * 2011-05-30 2014-03-05 道康宁东丽株式会社 Novel organopolysiloxane elastomer and use therefor
CN103191027A (en) * 2013-04-27 2013-07-10 珀莱雅化妆品股份有限公司 Solid makeup removing cream having warm sense in using process
CN108024930A (en) * 2016-03-15 2018-05-11 株式会社漫丹 Warm heat sense makeup removing cosmetic preparation

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