JP2010150165A5 - - Google Patents

Description

The present invention relates to emulsifier-shaped skin external preparation, and more particularly, relates to skin external agent having an ultraviolet protective effect, it has a good feeling of use without stickiness relates UV protection effect is high skin external preparation.

Blended with powder-based emulsifier type, powder-containing external preparation for skin by the action of aqueous component and an oily component contained in the emulsifier type, prone dry feeling when powder like is applied to the skin, etc. It can be suppressed and has gained solid support. On the other hand, it is derived from the fact that a powder having a specific gravity of 4 must be stably dispersed for a long period of time in an emulsified structure formed by an oil agent having a specific gravity of 1 and an aqueous phase having a specific gravity of about 1. The problem exists. As a means for solving such a problem, a method using a gel structure formed by a fatty acid soap has been conventionally used. However, according to such a method, a fatty acid soap for forming a structure and an emulsion for emulsification are used. a surfactant, and a surfactant for stable dispersion of the powder is required, reality is the amount of surfactant is well above the 5 wt% required in such systems Met. The reduction in the amount of the surfactant has been desired from the viewpoints of safety and prevention of makeup collapse, but it has not been achieved from the viewpoint of ensuring such stability.

In view of such a situation, the inventors of the present invention have an emulsifier-type skin external preparation containing a metal oxide composite that may be surface-treated, and have a long-lasting use under severe conditions. As a result of repeated earnest research efforts in search of means to improve, by containing an anionic surfactant and a polyglycerin fatty acid ester as a surfactant, the total amount of the surfactant is adjusted to 3% by mass or less, of it found that is significantly improved retention粧, thereby completing the invention. That is, the present invention is as follows.
<1> An emulsifier-type skin external preparation containing a metal oxide composite that may be surface-treated, comprising an anionic surfactant and a polyglycerin fatty acid ester as a surfactant, and the surfactant A skin external preparation in the form of an emulsifier, characterized in that the total amount of is 0.01 to 3% by mass.
<2> The metal oxide composite is one or two selected from the group consisting of a metal oxide and a carboxylic acid represented by the general formula (1), a carboxylic acid derivative, a carboxylic acid polymer, and a carboxylic acid derivative polymer. The emulsifier-type skin external preparation according to <1>, which is a composite of at least a seed.

一般式（１）

尚、一般式（１）の化合物は炭素数１０以下のモノ、ジ又はトリカルボン酸のアルカリ塩及び炭素数１０以下のモノ、ジ又はトリカルボン酸のポリオキシエチレン付加物からなる群から選ばれる一種又は二種以上であり、Ｒは水素原子、又はカルボキシル基及びヒドロキシ基の一方又は両方を有しても良いアルキル基又はアルケニル基を表し、Ｘは水素、アルカリ金属又は炭素数２３以下のポリオキシエチレンを表す。

General formula (1)

Incidentally, one or a compound of the general formula (1) is selected from the group consisting of the number 10 following mono-, di- or alkali salts and having 10 or less of mono-carbon of a tricarboxylic acid, polyoxyethylene adducts of di- or tricarboxylic acids carbon or at two or more, R represents a hydrogen atom, or a carboxyl group and one or may have both alkyl or alkenyl group of hydroxy group, X is hydrogen, an alkali metal or having 23 or less carbon atoms Represents polyoxyethylene.

<3> From the group consisting of the carboxylic acid derivative polymer represented by the general formula (1) consisting of polyacrylic acid or an alkali salt of polymethacrylic acid, and a polyoxyethylene adduct of polyacrylic acid or polymethacrylic acid. characterized in that it chosen one or two or more, <1> or emulsifying dosage form of skin external preparation as described in <2>.
<4> metal constituting the metal oxide composite compound, characterized in that mainly comprising titanium and / or zinc, emulsifiers form according to any one of <1> to <3> Skin Topical agent.
<5> as the anionic surfactant, characterized by containing the acyl lactates and / or fatty acid glyceryl sulfate, <1> to <4> of emulsifying dosage form according to any one of Skin external preparation.
<6> as polyglycerol fatty acid esters of the emulsifier type, degree of polymerization 5 to 15, characterized in that it contains at least two things degree of esterification 1-7 polyglycerol, <1> to the <5> emulsifiers form of skin external preparation according to any one.

(1) Metal oxide composite that is an essential component of the skin external preparation of the present invention The skin external preparation of the present invention contains a metal oxide composite that may be surface-treated as an essential component. The content of the metal oxide composite in the external preparation for skin is 0.1% by mass to 30% by mass, more preferably 1% by mass to 20% by mass in terms of metal oxide. In such metal oxide composite compound, the particle size of the metal oxide portion is in a state before conjugation, the grain size measured by a co-chromatography Luther counter is preferably 0.001 [mu] m ~ 0.1 [mu] m. This is because when too small, because enough if complexed stability can not be obtained resides resides may not have sufficient water-dispersible too large. Here, the metal oxide composite is a composite of the fine metal oxide and a water-soluble polymer, and the water-soluble polymer includes a carboxylic acid represented by the following general formula (1). A polymer or a copolymer is preferably exemplified. Whether or not it is complexed is defined by the fact that the stretching peak of the carbonyl derived from the carboxyl group is shifted by the weak bond with the metal oxide by the infrared absorption spectrum. That is, a peak derived from stretching of the carbonyl groups is not shifted is estimated to simple mixture, it does not belong to the composite compound in the present invention. Such a complex is obtained by neutralizing a metal water-soluble salt, for example, a halide such as chloride or nitrate with a water-soluble base in the presence of a water-soluble polymer in an aqueous carrier. It is produced by ion exchange between a residue and a hydroxide ion. The metal of the metal oxide or constituting a hydroxide, e.g., zinc, iron, aluminum, magnesium, titanium, barium, manganese, cerium, cobalt, calcium, cadmium, strontium, copper, Kurominiumu, zirconium, gold, Silver etc. can be illustrated, Among these, what belongs to an amphoteric metal is preferable, and titanium, zinc, and cerium can illustrate suitably. In particular, titanium is preferable because of the hiding effect. It These metals may be used only species, it may be used a material obtained by forming a complex with the water-soluble polymer with two or more. In addition, as the metal oxide in the present invention, a commercially available metal oxide that has been surface-treated with an organic material such as silicone or fatty acid, or an inorganic material such as silica or alumina can also be used. Examples of such commercially available powders include “titanium oxide MT-100TV (average primary particle size : 15 nm, surface treatment: aluminum hydroxide, fatty acid; manufactured by Teika Co., Ltd.)”, “titanium oxide TTO-V-4” (Primary particle diameter : 5 to 15 nm, surface treatment: aluminum hydroxide, stearic acid; manufactured by Ishihara Sangyo Co., Ltd.) "and the like. When such a commercially available metal oxide is used, it is neutralized in the presence of a water-soluble polymer in a solution of a water-soluble salt such as a chloride of the metal, and a complex of the water-soluble polymer and the metal oxide. In this form, it is preferably deposited on a commercially available metal oxide to form a composite. By taking such a deposition step, a composite having a weak bond between the metal oxide and the water-soluble polymer can be obtained. Such complexation can be detected as a shift in the peak of the carbonyl stretch of the carboxyl group in the infrared absorption spectrum.

一般式（１）

但し、一般式（１）の化合物は炭素数１０以下のモノ、ジ又はトリカルボン酸のアルカリ塩及び炭素数１０以下のモノ、ジ又はトリカルボン酸のポリオキシエチレン付加物からなる群から選ばれる一種又は二種以上であり、Ｒは水素原子、又はカルボキシル基及びヒドロキシ基の一方又は両方を有しても良いアルキル基又はアルケニル基を表し、Ｘは水素、アルカリ金属又は炭素数２３以下のポリオキシエチレンを表す。

General formula (1)

However, one or compounds of the general formula (1) is selected from the group consisting of the number 10 following mono-, di- or alkali salts and having 10 or less of mono-carbon of a tricarboxylic acid, polyoxyethylene adducts of di- or tricarboxylic acids carbon or at two or more, R represents a hydrogen atom, or a carboxyl group and one or may have both alkyl or alkenyl group of hydroxy group, X is hydrogen, an alkali metal or having 23 or less carbon atoms Represents polyoxyethylene.

Water-soluble salts of metals, such as halides such as chlorides, and aqueous carriers such as nitrates, neutralize with water-soluble bases in the presence of water-soluble polymers, and anion residues and hydroxides of metal salts Manufactured by ion exchange with ions. The water-soluble salt of the metal is neutralized with a water-soluble base in the presence of a water-soluble monomer in an aqueous carrier to ion-exchange the anion residue of the metal salt with a hydroxide ion, and then the water-soluble monomer is removed. Manufactured by polymerization. The water-soluble polymer, as long as the "soluble" in a transparent property in water but are not otherwise limited, it is preferable that the carboxyl groups or those having a group in the form of their salts, in particular the , also acrylic acid or polymers and monomers constituting the methacrylic acid copolymers and / or their salts can be preferably exemplified. The “melting” means having a uniform distribution. Preferred examples of the polymer salt include alkali metal salts such as sodium salt and potassium salt. As other water-soluble polymers, for example, alginic acid and / or a salt thereof, carboxymethyl cellulose and / or a salt thereof can be preferably exemplified. And the metal salt, by weight of the water-soluble polymer, a metal salt metal oxide or in terms of a hydroxide, such that the metal oxides or hydroxides becomes more than 60 mass%, more Preferably, it is set to 60 mass% to 99 mass% , more preferably 85 mass% to 99 mass% . It is essential that the aqueous carrier contains water, and it is preferable to use a mixture of water and a soluble organic solvent. In general, it is known that when a small amount or a large amount of an organic solvent is mixed in a process of hydrolyzing a metal salt in an aqueous system to produce a hydroxide or oxide, the hydrolyzate of the metal salt becomes an oxide. ing. Furthermore, as a base for the metal oxide or to produce hydroxide, sodium hydroxide, alkali metal hydroxides such as potassium hydroxide, can be preferably exemplified, the amount of such base is the metal salt and the like A slight or excessive amount is preferred. Thus to, in an aqueous carrier, a water-soluble polymer, and water soluble metal salts, metal oxides obtained by reacting the base or hydroxide and a water-soluble polymer complex, centrifugation It precipitates by performing etc. Such precipitation once or several times, by washing with an aqueous carrier containing an organic solvent, it is possible to remove unwanted reaction products. After such a treatment is performed, the precipitate is dried to obtain the fine-particle metal oxide-polymer complex of the present invention. Drying is performed by air drying for about 1 to 24 hours under heating at 30 to 100 ° C. Thus, a complex in which a water-soluble polymer and a metal oxide or hydroxide are intertwined is obtained under observation under an electron microscope. Since such a complex is complexed with a water-soluble polymer, this complex alone is excellent in the effect of being uniformly dispersed in an aqueous carrier. Further, the metal oxide may have a regular shape such as a whisker shape or an indeterminate lump shape, but any shape can be used in use. In addition, as the metal oxide in the present invention, a commercially available metal oxide that has been surface-treated with an organic material such as silicone or fatty acid, or an inorganic material such as silica or alumina can also be used. Alternatively, the surface treatment can be performed after compounding. The metal oxide coating such as silica is preferably not performed prior to complexing with the water-soluble polymer. This is because there are cases where the complexing of the metal oxide and the carboxyl group is inhibited. Examples of such commercially available metal oxides that have been surface-treated in advance include, for example, “titanium oxide MT-100TV (average primary particle size : 15 nm, surface treatment: aluminum hydroxide, fatty acid; manufactured by Teika Co., Ltd.)”, “oxidation” Titanium TTO-V-4 (primary particle diameter : 5 to 15 nm, surface treatment: aluminum hydroxide, stearic acid; manufactured by Ishihara Sangyo Co., Ltd.) "and the like can be exemplified. The water-soluble polymer is preferably 0.1 to 10 times the metal oxide.

(2) Surfactant which is an essential component of the external preparation for skin of the present invention The external preparation for skin of the present invention contains an anionic surfactant and a polyglycerin fatty acid ester as surfactants as essential components, and is surface active. The total amount of the agent is 0.01 to 3% by mass. The polyglycerol-based surfactant as the acyl group, straight chain having 8 to 30 carbon atoms, branched or has alkyloyl group or Arukeroiru group that have a cyclic structure can be preferably exemplified. Specific examples of such acyl group include, for example, 2-ethylhexanoyl group, lauroyl group, myristoyl group, palmitoyl group, stearoyl group, isostearoyl group, behenoyl group, oleoyl group, linoloyl group, linolenoyl group. Etc. can be suitably exemplified. Of these, stearoyl groups are particularly preferred. Moreover, as polyglycerol, the polyglycerol of 5-15 of a polymerization degree is preferable, and 7-12 are especially preferable. Such among free hydroxyl groups of the polyglycerol, preferably those modified with the acyl group is less than half, preferably has at least a plurality of the acyl group in the same molecule. Specifically, in the skin external preparation of the present invention, monoacylated decaglycerin, triacylated decaglycerin, pentaacylated decaglycerin and the like can be suitably exemplified. Such polyglycerin type surfactants can contain only one species, or two or more species can be contained in combination. A combination of two or more types is preferable because it improves emulsification stability, powder dispersibility, and powder dispersion stability. In order to exert such effects, the polyglycerin surfactant is contained in a total amount of 0.1 to 2% by mass, more preferably 0.2 to 1.8% by mass, based on the total amount of the external preparation for skin. It is preferable. In addition, as a combination of polyglycerin fatty acid esters, it is preferable to combine those having an average difference in the number of acyl groups of 2 or more and 4 or less. That is, a combination of monoacyl polyglycerol and triacyl glycerol, a combination of monoacyl polyglycerol and tetraacyl glycerol, a combination of diacyl polyglycerol and tetraacyl glycerol, a combination of diacyl polyglycerol and pentaacyl polyglycerol, and a triacyl polyglycerol Preferred examples include a combination of pentaacyl polyglycerol and a combination of triacyl polyglycerol and hexaacyl polyglycerol.

Further, in addition to the fatty acid esters of polyglycerol, the skin external preparation of the present invention, containing an anionic surfactant as an essential component. Examples of the anionic surfactant include fatty acid soaps, carboxylic acid salt type anionic surfactants such as acyl oxycarboxylic acid salts, alkyl sulfates, POE alkyl sulfates, fatty acid glyceryl sulfate, sulfuric acid, such as sulfosuccinic acid ester salt Anionic surfactants such as phosphoric acid anionic surfactants such as alkyl phosphates, alkyl phosphates, POE alkyl phosphates, and the like. Among these, carboxylic acid anionic surfactants and sulfate anions It is particularly preferable to combine them. In addition, in the carboxylic acid anionic surfactant, it is not preferable to select a fatty acid soap as such a surfactant because it leads to a decrease in usability due to formation of a gel structure as described in the background art. It is preferable to exclude from the choice of the anionic surfactant.

Of the carboxylic acid anionic surfactants, citric acid, lactic acid, glycolic acid and the like can be preferably exemplified as the oxycarboxylic acid serving as the basic skeleton of the acyloxycarboxylate, and among these, lactic acid is particularly preferred. As the acyl group to modify the hydroxyl group of lactic acid, those having 10 to 24 carbon atoms are preferable, for example, lauroyl group, myristoyl group, palmitoyl group, stearoyl group, isostearoyl group, oleoyl group and the like can be suitably exemplified. A stearoyl group is particularly preferred. These salts can be used without any particular limitation as long as they are used in skin external preparations, for example, alkali metal salts such as sodium salts and potassium salts, alkaline earth metal salts such as calcium salts and magnesium salts. Preferred examples include organic amine salts such as ammonium salt, triethylamine salt, triethanolamine salt, and monoethanolamine salt, and basic amino acid salts such as lysine salt and alginate. Particularly preferred salts are alkali metal salts, especially sodium salts. The preferable content of such components with respect to the total amount of the external preparation for skin is 0.1 to 0.6% by mass, and more preferably 0.2 to 0.5% by mass.

Examples of the sulfate anionic surfactant, preferably contains a fatty acid glyceryl sulfate and / or a salt thereof. The fatty acid residue (acyl group) constituting the fatty acid glyceryl sulfate is preferably one having 10 to 30 carbon atoms, such as lauroyl group, myristoyl group, palmitoyl group, stearoyl group, isostearoyl group, behenoyl group, oleoyl. Preferred examples include groups such as coconut oil fatty acid residues, beef tallow fatty acid residues, and palm oil fatty acid residues, which are natural mixtures thereof. Of these, coconut oil fatty acid glyceryl sulfate is most preferable. These salts can be used without any particular limitation as long as they are used in skin external preparations, for example, alkali metal salts such as sodium salts and potassium salts, alkaline earth metal salts such as calcium salts and magnesium salts. Preferred examples include organic amine salts such as ammonium salt, triethylamine salt, triethanolamine salt, and monoethanolamine salt, and basic amino acid salts such as lysine salt and alginate. Particularly preferred salts are alkali metal salts, especially sodium salts. The preferred content of one kind or two or more kinds of the total amount of the skin treatment composition selected from the fatty acid glyceryl sulfate and / or its salt is 0.01 to 0.3 wt%, more preferably, 0.05 It is 0.25% by mass. This is the emulsion stability and too small, the powder dispersibility and do not bring out the effects of improving the powder dispersion stability resides, because resides may be impaired too large the stability of the system. As such sulfate anionic surfactant, it can be used commercially available ones can be used Nikkol SGC-80 N that are released, for example, from Nikko Chemicals Company.

In the external preparation for skin of the present invention, in addition to the complex of the present invention, an optional component usually used in external preparations for skin can be contained. Examples of such optional ingredients include macadamia nut oil, avocado oil, corn oil, olive oil, rapeseed oil, sesame oil, castor oil, safflower oil, cottonseed oil, jojoba oil, coconut oil, palm oil, liquid lanolin, and hardened coconut oil. Oil, wax, oils such as beeswax, molasses, hydrogenated castor oil, beeswax, candelilla wax, carnauba wax, ibotarou, lanolin, reduced lanolin, hard lanolin, jojoba wax; , Hydrocarbons such as microcrystalline wax; higher fatty acids such as oleic acid, isostearic acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, undecylenic acid; cetyl alcohol, stearyl alcohol, isostearyl Higher alcohols such as alcohol, behenyl alcohol, octyldodecanol, myristyl alcohol, cetostearyl alcohol; cetyl isooctanoate, isopropyl myristate, hexyldecyl isostearate, diisopropyl adipate, di-2-ethylhexyl sebacate, cetyl lactate, malic acid Diisostearyl, di-2-ethylhexanoic acid ethylene glycol, dicaprate neopentyl glycol, di-2-heptylundecanoic acid glycerin, tri-2-ethylhexanoic acid glycerin, tri-2-ethylhexanoic acid trimethylolpropane, tri Synthetic ester oils such as trimethylolpropane isostearate and pentane erythritol tetra-2-ethylhexanoate; dimethylpolysiloxane, methylphenylpoly Linear polysiloxanes such as oxane and diphenylpolysiloxane; cyclic polysiloxanes such as octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexanesiloxane; amino-modified polysiloxane, polyether-modified polysiloxane, alkyl-modified polysiloxane, oil such silicone oils of modified polysiloxanes and fluorine-modified polysiloxane; fatty acid soap (sodium laurate, sodium palmitate), potassium lauryl sulfate, an anionic surfactant such as alkyl sulfate, triethanolamine ether; stearyl trimethyl ammonium chloride, benzalkonium chloride, cationic surfactants such as lauryl amine oxide; imidazoline amphoteric surface active agent (2-cocoyl-2-y Amphoteric surfactants such as midazolinium hydroxide-1-carboxyethyloxy disodium salt), betaine surfactants (alkyl betaine, amide betaine, sulfobetaine, etc.), acylmethyl taurine; sorbitan fatty acid esters ( Sorbitan monostearate, sorbitan sesquioleate, etc.), glycerin fatty acids (such as glyceryl monostearate), propylene glycol fatty acid esters (such as propylene glycol monostearate), hardened castor oil derivatives, glycerin alkyl ether, POE sorbitan fatty acid ester (POE sorbitan monooleate, polyoxyethylene sorbitan monostearate, etc.), POE sorbite fatty acid esters (POE-sorbitol monolaurate, etc.), POE glycerin fat Esters (POE-glycerol monoisostearate, etc.), POE fatty acid esters (polyethylene glycol monooleate, POE distearate, etc.), POE alkyl ethers (POE2-octyldodecyl ether, etc.), POE alkylphenyl ethers (POE nonylphenyl) Ethers, etc.), Pluronic types, POE / POP alkyl ethers (POE / POP2-decyltetradecyl ether, etc.), Tetronics, POE castor oil / hardened castor oil derivatives (POE castor oil, POE hardened castor oil, etc.), Nonionic surfactants such as sucrose fatty acid esters and alkyl glucosides; polyethylene glycol, glycerin, 1,3-butylene glycol, erythritol, sorbitol, xylitol, maltitol, propylene Polyhydric alcohols such as polyglycol, dipropylene glycol, diglycerin, isoprene glycol, 1,2-pentanediol, 2,4-hexanediol, 1,2-hexanediol, 1,2-octanediol; pyrrolidonecarboxylic acid Moisturizing ingredients such as sodium, lactic acid, sodium lactate; surface may be treated, such as mica, talc, kaolin, synthetic mica, calcium carbonate, magnesium carbonate, anhydrous silicic acid (silica), aluminum oxide, barium sulfate, etc. Powders ; surface may be treated, bengara, yellow iron oxide, black iron oxide, cobalt oxide, ultramarine, bitumen, titanium oxide, zinc oxide inorganic pigments; surface may be treated, mica Pearl agents such as titanium, fish phosphorus foil, bismuth oxychloride; red 202 which may be raked, Red 228, Red 226, Yellow 4, Blue 404, Yellow 5, Red 505, Red 230, Red 223, Orange 201, Red 213, Yellow 204, Yellow 203, Blue 1 No., green 201, purple 201, red 204, etc .; organic powders such as polyethylene powder, polymethyl methacrylate, nylon powder, organopolysiloxane elastomer; para-aminobenzoic acid UV absorbers; anthranils Acid UV absorbers; salicylic acid UV absorbers ; cinnamic acid UV absorbers ; benzophenone UV absorbers; sugar UV absorbers; 2- (2′-hydroxy-5′-t-octylphenyl) benzotriazole; UV absorbers such as 4-methoxy-4'-t-butyldibenzoylmethane; lower alcohols such as ethanol and isopropanol Vitamin B such as vitamin A or derivatives thereof, vitamin B ₆ hydrochloride, vitamin B ₆ tripalmitate, vitamin B ₆ dioctanoate, vitamin B ₂ or derivatives thereof, vitamin B ₁₂ , vitamin B ₁₅ or derivatives thereof Α-tocopherol, β-tocopherol, γ-tocopherol, vitamin E such as vitamin E acetate, vitamin D, vitamin H, vitamins such as pantothenic acid, panthetin, pyrroloquinoline quinone, etc .; antibacterial agents such as phenoxyethanol Preferred examples can be given. The skin external preparation of this invention can be manufactured by processing these components according to a conventional method.

<Production Example 1>
An acidic aqueous dispersion of titania fine particles having a rutile crystal structure with an average particle diameter of 10 nm, obtained by treating hydrous titanium oxide obtained by hydrolysis of titania sulfate with alkali and aging in hydrochloric acid. Created. The concentration of this was adjusted to 100 g / L with water, and 1 L of an acidic aqueous dispersion of titania fine particles was measured. The obtained acidic dispersion liquid of titania fine particles was diluted with pure water to obtain 5 L of titania fine particle aqueous dispersion 5 g of 20 g / L in terms of titanium dioxide . 20 g of polyacrylic acid (polymerization degree 5000) (manufactured by Wako Pure Chemical Industries, Ltd.) was dissolved in 8 L of pure water to obtain a B solution. The solution A was gradually added to the solution B at room temperature with stirring, and then aged for 1 hour. Further, the pH was adjusted to 5 with a 2N aqueous sodium hydroxide solution, aged for 1 hour, filtered and washed to obtain a wet cake. The wet cake was repulped into pure water, and then ultrasonically dispersed to obtain a titania fine particle composite (solid content concentration 25%, pH 7.5) (sample A) of the present invention that was stable in a neutral range. .

<Formulation example 1>
With specimen A, according to Table 1 to prepare cosmetic 1,2,3,4,5,6. Ingredient (a) is heated and dissolved to uniformly disperse the powder, then the temperature is adjusted to 70 ° C., and the ingredient (b) that has been heated and dissolved in advance to uniformly disperse the powder is gradually added, and a homogenizer is used. And emulsified. Thereafter, the mixture was cooled to room temperature with stirring to obtain the intended emulsifier-type skin external preparation. Further, according to Table 1, Comparative Examples 1, 2, and 3 were obtained in the same manner.

<Test Example 1> (Viscosity value)
For cosmetic 1 , cosmetic 2, cosmetic 3, cosmetic 4, cosmetic 5, cosmetic 6, Comparative Example 1, Comparative Example 2 and Comparative Example 3, using a B-type viscometer, No. 3 rotor, Viscosity was measured under the measurement conditions of 6 minutes per minute. As a result, as shown in Table 2, it was revealed that the cosmetic of the present invention had a viscosity value of 2000 to 9000 mPa · s and was suitable for an emulsion type. This result means that, when the compound represented by the general formula (1) is used as a monomer, it is combined with a water-soluble polymer, so that even if this is dispersed, the increase in the viscosity of the system is suppressed and the usability is increased. is doing.

< Test Example 2> (UV protective effect)
Cosmetic 1 , Cosmetic 2, Cosmetic 3, Cosmetic 4, Cosmetic 5, Cosmetic 6, Comparative Example 1, Comparative Example 2 and Comparative Example 3 are provided on the inner side of the forearm of 5 female subjects 1 cm × 2 cm 10 mg of the sample was applied to the sample, and the sample was allowed to stay in a constant temperature room at 40 ° C. for 4 hours. Thereafter, the sample was irradiated with ultraviolet rays 15 times the minimum amount of erythema, and the skin reaction at 24 hours after irradiation was determined. Skin reaction was determined according to the Japanese patch test criteria (-: no reaction, ±: reaction with weak erythema, +: reaction with obvious erythema, ++: reaction with edema or papule). The results are shown in Table 3. This shows that the cosmetic of the present invention has an excellent ultraviolet protective effect. This is presumably because the decorative film is not destroyed by sweating under severe conditions.

<Test Example 3> (SPF value)
Cosmetic 1 , Cosmetic 2, Cosmetic 3, Cosmetic 4, Cosmetic 5, Cosmetic 6, Comparative Example 1, Comparative Example 2 and Comparative Example 3 were applied to vitro skin at 2 mg / cm ² , 20 After drying at room temperature for minutes, the SPF value was measured using SPF Analyzer System UV-1000S (manufactured by labsphere). Further, the prepared sample was allowed to stand at 40 ° C. for 1 month, and the SPF value was measured in the same manner, and then the SPF value retention rate after being left was calculated. As a result, as shown in Table 4, it was revealed that the cosmetic of the present invention exhibits a high SPF value. This is considered to be because dispersibility was improved by the compounding and the filling degree of the metal oxide in the decorative film was improved. Further, from the SPF value maintenance rate after standing at 40 ° C. for 1 month in Table 4, when comparing cosmetics 1 to 4 and cosmetic 5, among the anionic surfactants of the present invention, acyl lactate and / or fatty acid glyceryl. It was clarified that those containing sulfate showed a high SPF value retention rate. This is considered to be because the aggregation of metal oxides over time was suppressed by the incorporation of acyl lactate and / or fatty acid glyceryl sulfate.

For 5 panelists, cosmetic 1 , cosmetic 2, cosmetic 3, cosmetic 4, cosmetic 5, cosmetic 6, comparative example 1, comparative example 2, and comparative example 3 were applied to the face three times a day. And, regarding the feeling of use of each sample, the following evaluation criteria were investigated. The results are shown in Table 5. From the results shown in Table 5, it is clear that the present invention is excellent in use feeling and less sticky.
(Evaluation criteria for feeling of use)
1: A feeling of stickiness is not felt 2: A feeling of stickiness is felt a little 3: A feeling of stickiness is felt 4: A feeling of stickiness is felt considerably

Claims (6)

An emulsifier-type skin external preparation containing a metal oxide composite that may be surface-treated, comprising an anionic surfactant and a polyglycerin fatty acid ester as a surfactant, and the total amount of the surfactant is An external preparation for skin in the form of an emulsifier, characterized by being 0.01 to 3% by mass. The metal oxide composite is one or more selected from the group consisting of a metal oxide and a carboxylic acid represented by the general formula (1), a carboxylic acid derivative, a carboxylic acid polymer, and a carboxylic acid derivative polymer. The skin external preparation in the form of an emulsifier according to claim 1, wherein

General formula (1)

Incidentally, one or a compound of the general formula (1) is selected from the group consisting of the number 10 following mono-, di- or alkali salts and having 10 or less of mono-carbon of a tricarboxylic acid, polyoxyethylene adducts of di- or tricarboxylic acids carbon or at two or more, R represents a hydrogen atom, or a carboxyl group and one or may have both alkyl or alkenyl group of hydroxy group, X is hydrogen, an alkali metal or having 23 or less carbon atoms Represents polyoxyethylene. The carboxylic acid derivative polymer represented by the general formula (1) is a kind selected from the group consisting of an alkali salt of polyacrylic acid or polymethacrylic acid, and a polyoxyethylene adduct of polyacrylic acid or polymethacrylic acid or wherein the at two or more, according to claim 1 or 2 emulsifying dosage form of skin external preparation as described in. The emulsifier-type skin external preparation according to any one of claims 1 to 3 , wherein a metal constituting the metal oxide composite is mainly composed of titanium and / or zinc. Examples anionic surfactants, characterized in that it contains an acyl lactate and / or fatty acid glyceryl sulfate, emulsifying dosage form of skin external preparation according to any one of claims 1 to 4. As polyglycerol fatty acid esters of the emulsifier type, those of degree of esterification of the polyglycerol 1-7 polymerization degree 5 to 15, characterized in that it contains at least two, in any one of claims 1 to 5 The emulsifier type skin external preparation as described.