WO2025105213A1 - Cosmetic containing hydrophobized powder - Google Patents
Cosmetic containing hydrophobized powder Download PDFInfo
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- WO2025105213A1 WO2025105213A1 PCT/JP2024/039040 JP2024039040W WO2025105213A1 WO 2025105213 A1 WO2025105213 A1 WO 2025105213A1 JP 2024039040 W JP2024039040 W JP 2024039040W WO 2025105213 A1 WO2025105213 A1 WO 2025105213A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
Definitions
- the present invention relates to a cosmetic comprising a hydrophobically treated powder. More specifically, the present invention relates to a cosmetic comprising a hydrophobically treated powder in an aqueous phase, the secondary particles of which have an average diameter of 150 nm or less.
- sunscreen cosmetics are to block ultraviolet rays in sunlight and protect the skin from the harmful effects of ultraviolet rays.
- SPF Sun Protection Factor
- Cosmetics have been proposed that have a high SPF value while reducing the feeling of strain on the skin by dispersing powders such as ultraviolet scattering agents in an oil phase by a dispersion method using cavitation (Patent Document 1).
- Powder made of metal oxides or the like with hydrophobic surfaces is known as an ultraviolet scattering agent.
- Such powders are usually present in large amounts in the oil phase, and in order to make them exist in the aqueous phase, it is necessary to improve the dispersion state.
- the inventors' research has surprisingly revealed that by dispersing hydrophobically treated powder with an average secondary particle size of 150 nm or less in the aqueous phase of a cosmetic, it is possible to achieve good stability and a high UV protection effect.
- the present invention is based on these findings.
- a cosmetic comprising (A1) a first hydrophobized powder and (B) water, A cosmetic preparation, comprising: an (A1) component dispersed in an aqueous phase; and an average particle size of secondary particles of the (A1) component in the aqueous phase being 150 nm or less.
- a second hydrophobized powder and (D) an oil component are further included;
- the cosmetic according to [3] or [4], wherein the combined amount of the (A1) component and the (A2) component is 30 mass% or less relative to the total amount of the cosmetic.
- [6] The cosmetic preparation according to any one of [3] to [5], wherein the blending amount of the (A1) component is 10 to 100 mass% relative to the combined blending amount of the (A1) component and the (A2) component.
- An oily mixture preparation step of mixing the (A2) component and an oil to prepare an oily mixture The method according to [9], further comprising an oil phase dispersion step of passing the oil mixture through a throttle passage as a high-pressure fluid of 50 to 200 MPa and dispersing the component (A2) in the oil phase by cavitation generated in the throttle passage.
- the present invention provides a cosmetic preparation that has good stability and can achieve a high UV protection effect. Furthermore, the cosmetic preparation of the present invention can suppress the decrease in transparency of the base, reduce the burden on the skin, and improve the feel when used.
- the present invention relates to a cosmetic preparation comprising (A1) a first hydrophobized powder (hereinafter sometimes referred to as component (A1), the same applies to other components) and (B) water.
- Component (A1) is dispersed in an aqueous phase, and the average particle size of its secondary particles is 150 nm or less, preferably 10 to 130 nm.
- One of the features of the cosmetic preparation according to the present invention is that the aggregation of powder particles is greatly suppressed and the secondary particle size of the powder particles is small.
- the cosmetic preparation according to the present invention includes those in which the powder maintains a dispersed state over a normal storage period, and further includes those in which the powder settles during a normal storage period in the art, but can be redispersed by stirring the cosmetic preparation or shaking the container by a method normal in the art.
- the cosmetic preparation according to the present invention may further comprise an oil phase.
- the cosmetic according to the present invention further comprises (A2) a second hydrophobized powder and (D) an oil component.
- the component (A2) is dispersed in the oil phase, and the average particle size of the secondary particles is 150 nm or less, preferably 10 to 130 nm.
- the components (A1) and (A2) are dispersed in both the aqueous phase and the oil phase, respectively, with average particle sizes of 150 nm or less.
- the average particle size and particle size distribution of the submicron particles dispersed in a liquid can be measured using dynamic light scattering.
- the average particle size of the primary particles can be measured by a nitrogen adsorption method.
- the (A1) component is a hydrophobized powder, dispersed in the aqueous phase of the cosmetic, and has an average particle size of the secondary particles of 150 nm or less.
- the hydrophobized powder is preferably a hydrophobized metal oxide powder.
- the hydrophobized powder is preferably a powder having an ultraviolet scattering function, i.e., an ultraviolet scattering agent.
- the average primary particle size of the hydrophobized powder is generally 10 nm or more and 100 nm or less.
- hydrophobized metal oxides include titanium oxide, zinc oxide, cerium oxide, talc, silica, mica, sericite, kaolin, mica titanium, black iron oxide, yellow iron oxide, red ocher, ultramarine, iron blue, chromium oxide, chromium hydroxide, etc.
- titanium oxide and zinc oxide are preferred because of their high ultraviolet scattering function.
- a composite powder in which particles made of a material other than titanium oxide are coated with titanium oxide can also be used.
- the hydrophobic treatment applied to the powder may be a treatment that introduces hydrophobic groups to the particle surface or forms a coating of a hydrophobic substance.
- the hydrophobic treatment may be a wet method using a solvent, a gas phase method, a mechanochemical method, or the like.
- silicones such as methylhydrogenpolysiloxane, dimethylpolysiloxane, and triethoxycaprylylsilane, dextrin fatty acid esters, higher fatty acids, higher alcohols, fatty acid esters, metal soaps, alkyl phosphate ethers, fluorine compounds, or hydrocarbons such as squalane and paraffin, etc. can be used. Since component (A1) is dispersed in the aqueous phase, silicone treatment is preferred as the hydrophobic treatment.
- the (A1) component may be used alone or in combination with two or more other components.
- the amount of the (A1) component is preferably 0.1 to 30% by mass, more preferably 0.5 to 10% by mass, and even more preferably 1 to 3% by mass, based on the total amount of the cosmetic.
- the cosmetic according to the present invention may further contain (A2) a second hydrophobized powder.
- the (A2) component is a hydrophobized powder that is dispersed in the oil phase in the cosmetic, and the average particle size of the secondary particles is 150 nm or less.
- the (A1) component and the (A2) component may be the same or different.
- the preferred (A2) component is the same as the above-mentioned (A1) component.
- the (A2) component may be used alone or in combination with two or more other components.
- the amount of the (A2) component is preferably 0.5 to 15% by mass, and more preferably 1 to 10% by mass, based on the total amount of the cosmetic.
- the combined amount of the components (A1) and (A2) is preferably 30% by mass or less, more preferably 1 to 20% by mass, and even more preferably 2 to 12% by mass, relative to the total amount of the cosmetic.
- aggregation of the hydrophobized powder is suppressed and the secondary particle size is small, so that a high UV protection effect can be achieved with a smaller amount than the amount of powder normally blended.
- the cosmetic preparation according to the present invention comprises water (B).
- water water used in cosmetics, quasi-drugs, etc., can be used, such as purified water, ion-exchanged water, tap water, etc.
- the blending amount of water is preferably 10 to 35% by mass, more preferably 10 to 25% by mass, based on the total amount of the cosmetic according to the present invention.
- the cosmetic preparation according to the present invention preferably further comprises (C) a polyether-modified silicone or a polyoxyethylene alkyl ether in the aqueous phase.
- Component (C) can improve the dispersion state of component (A1) in the aqueous phase.
- the HLB (hydrophile-lipophile balance) of component (C) is 5 to 18, more preferably 5 to 16, and even more preferably 6 to 10. Within this range, the initial dispersibility and dispersion stability of component (A1) in the aqueous phase can be improved.
- the HLB value is a value calculated by the Griffin method.
- the component (C) is preferably a polyether-modified silicone.
- the polyether-modified silicone is preferably a dimethicone having a PEG chain and/or a PPG chain, more preferably a dimethicone having a PEG chain.
- the average number of moles of alkylene oxide added may be 8 or more and 40 or less. It may also be an alkyl ether of dimethicone having a PEG and/or PPG chain terminal.
- a preferred example of a polyether-modified silicone is PEG-12 dimethicone.
- the silicone chain of the polyether-modified silicone may be either a straight chain or a branched chain, but is preferably a straight chain. It may be a polyether-modified alkyl-modified silicone further having an alkyl side chain, but is preferably unalkyl-modified.
- the (C) component may be blended in one or more types.
- the blended amount of the (C) component is preferably 0.01 to 10 mass % relative to the total amount of the cosmetic, more preferably 0.05 to 5 mass %, and even more preferably 0.05 to 1 mass %.
- the cosmetic composition according to the present invention may further comprise an oil component (D).
- oil component (D) examples include silicone oils, hydrocarbon oils, higher fatty acids, higher alcohols, ester oils, and liquid fats and oils, and preferably silicone oils, hydrocarbon oils, and ester oils.
- silicone oils include dimethicone, methylphenylpolysiloxane, methylhydrogenpolysiloxane, methicone hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexadecamethylheptasiloxane, and caprylyl methicone.
- hydrocarbon oils examples include isododecane, isohexadecane, isoparaffin, liquid paraffin, ozokerite, squalane, pristane, paraffin, ceresin, squalene, petrolatum, and microcrystalline wax.
- ester oil examples include octyl octanoate, nonyl nonanoate, cetyl octanoate, isopropyl myristate, octyldodecyl myristate, isopropyl palmitate, ethylhexyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyldecyl dimethyloctanoate, cetyl lactate, myristyl lactate, lanolin acetate, isocetyl stearate, isocetyl isostearate, cholesteryl 12-hydroxystearate, ethylene glycol di-2-ethylhexanoate, dipentaerythritol fatty acid ester, N-alkyl glycol monoisostearate, neopentyl glycol dicaprate, tripropylene glyco
- the (D) component may be blended in one or more types.
- the blended amount of the (D) component is preferably 10 to 80 mass % relative to the total amount of the cosmetic, and more preferably 20 to 60 mass %.
- the cosmetic preparation according to the present invention may further comprise (E) glycerin modified at both ends with silicone.
- Component (E) can improve the dispersion state of component (A2) in the oil phase.
- the component (E) is preferably represented by formula (1).
- R 1 is a C 1-12 alkyl group or a phenyl group, preferably a methyl group
- R2 is a C2-11 alkylene group, preferably a trimethylene group
- m is 10 to 120
- n is 1 to 11.
- the alkyl and alkylene groups can be straight-chained or branched.
- the weight average molecular weight of the component (E) is preferably 2,000 to 30,000. The weight average molecular weight can be calculated, for example, by gel permeation chromatography using polystyrene standards.
- Examples of component (E) include bisbutyldimethicone polyglyceryl-3.
- the component (E) may be used alone or in combination with two or more other components.
- the amount of component (E) used is preferably 0.1 to 20% by mass, and more preferably 0.5 to 10% by mass, based on the total amount of the cosmetic.
- the cosmetic preparation according to the present invention may contain ingredients other than those mentioned above that are commonly used in cosmetics, provided that the ingredients do not impair the effects of the present invention.
- these ingredients include thickeners, moisturizers, UV absorbers, medicines, stabilizers, pH adjusters, preservatives, pigments, dyes, surfactants, powdered ingredients, fragrances, etc.
- the method for producing a cosmetic according to the present invention is not particularly limited, but in a preferred embodiment, the method comprises the following steps: The method comprises: (I) an aqueous mixture preparation step of mixing component (A1) and water to prepare an aqueous mixture; and (II) an aqueous phase dispersion step of passing the aqueous mixture as a high-pressure fluid of 50 to 200 MPa through a throttle passage and dispersing component (A1) in an aqueous phase by cavitation generated in the throttle passage.
- the method for producing a cosmetic preparation according to the present invention can further include the following steps: (III) an oily mixture preparation step of mixing the (A2) component and an oil to prepare an oily mixture; and (IV) an oil phase dispersion step of passing the oily mixture as a high-pressure fluid of 50 to 200 MPa through a throttle flow path and dispersing the (A2) component in an oil phase by cavitation generated in the throttle flow path.
- component (I) Aqueous mixture preparation step
- water as a dispersion medium, component (A1), and optional components as required are mixed while stirring to prepare an aqueous mixture.
- component (C) as an optional component for improving dispersibility.
- Other optional components include, for example, moisturizers, stabilizers, preservatives, thickeners, etc.
- step (II) Aqueous Phase Dispersion Step
- the aqueous mixture prepared in step (I) is homogenized based on the principle of cavitation to prepare an aqueous phase dispersion.
- Cavitation is a physical phenomenon in which bubbles are generated and disappear in a short time due to pressure differences in a liquid flow.
- the mixture obtained in step (I) is given a flow velocity, and the liquid is passed through a throttle channel to generate fine bubbles due to cavitation, and the aqueous phase dispersion is obtained by the impact force.
- the flow velocity is given by an ultra-high pressure flow of 50 to 200 MPa. If it is less than 50, the dispersion effect may be insufficient, which is not preferable.
- (III) Oily mixture preparation step In this step, the oil as a dispersion medium, the (A2) component, and any other component as necessary are mixed while stirring to prepare an oily mixture.
- the (E) component As the optional component for improving dispersibility.
- Other optional components include, for example, moisturizers, stabilizers, preservatives, thickeners, etc., but it is also a preferred embodiment to not include any other optional components than the (E) component.
- step (IV) Oil phase dispersion step
- the oil mixture prepared in step (III) is homogenized based on the principle of cavitation to prepare an oil phase dispersion.
- the method of homogenization by cavitation is the same as that in step (II).
- the prepared aqueous phase dispersion, and if necessary, the oil phase dispersion, can be used to manufacture cosmetics in accordance with conventional manufacturing methods.
- the cosmetic according to the present invention may be an oil-in-water emulsion cosmetic, a water-in-oil emulsion cosmetic, or an unemulsified aqueous cosmetic, but is preferably an oil-in-water emulsion cosmetic or a water-in-oil emulsion cosmetic, and more preferably a water-in-oil emulsion cosmetic.
- the cosmetics in this specification include cosmetics with enhanced ultraviolet absorbing function, basic cosmetics (foundation, base makeup, etc.), makeup cosmetics (eye shadow, blush, etc.), and of course sunscreen cosmetics (sunscreen compositions).
- the cosmetics according to the present invention can achieve a high ultraviolet ray protection effect and have an excellent feeling when used, so they are preferably sunscreen cosmetics.
- aqueous phase dispersion W1 to W6 Using the compositions shown in Table 1, aqueous phase dispersions W1 to W5 were prepared by a dispersion method using cavitation, and aqueous phase dispersion W6 was prepared by a dispersion method using a homomixer.
- Table 1 (*1): "STR 100C-LP", manufactured by Sakai Chemical Industry Co., Ltd., average primary particle size 15 nm.
- Average secondary particle size The average secondary particle size of the dispersion prepared above was measured by dynamic scattering method, and the results are shown in Tables 1 and 2.
- Example 1 to 6 and Comparative Examples 1 and 2 Using the dispersions prepared above, water-in-oil emulsion cosmetics of Examples 1 to 6 and Comparative Examples 1 and 2 were prepared according to the formulations shown in Table 3.
- UV protection effect and stability were performed using the same method as the measurement method for the dispersion described above, using the cosmetics prepared in Table 3.
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Abstract
Description
本発明は、疎水化処理粉末を含んでなる化粧料に関する。より詳細には、水相に二次粒径の平均粒径が150nm以下である疎水化処理粉末を含んでなる化粧料に関する。 The present invention relates to a cosmetic comprising a hydrophobically treated powder. More specifically, the present invention relates to a cosmetic comprising a hydrophobically treated powder in an aqueous phase, the secondary particles of which have an average diameter of 150 nm or less.
日焼け止め化粧料は、太陽光線中の紫外線をカットし、紫外線による悪影響から肌を守ることを目的としている。皮膚への紫外線照射を遮断して高いSPF(Sun Protection Factor)値を得るために、紫外線散乱剤を高配合することが考えられるが、その場合に、基剤の透明性が低下したり、肌への塗布の際に肌に負担感を与えたり、塗布後の肌が白くなったりすることがある。
紫外線散乱剤等の粉体を、キャビテーションを用いた分散方法により油相中に分散させて、肌への負担感を軽減しつつ、高いSPF値を有する化粧料が提案されている(特許文献1)。
The purpose of sunscreen cosmetics is to block ultraviolet rays in sunlight and protect the skin from the harmful effects of ultraviolet rays. In order to block ultraviolet rays from reaching the skin and obtain a high SPF (Sun Protection Factor) value, it is conceivable to incorporate a high amount of ultraviolet scattering agents, but in that case, the transparency of the base may decrease, the skin may feel burdensome when applied to the skin, or the skin may become white after application.
Cosmetics have been proposed that have a high SPF value while reducing the feeling of strain on the skin by dispersing powders such as ultraviolet scattering agents in an oil phase by a dispersion method using cavitation (Patent Document 1).
紫外線散乱剤等として、金属酸化物等の表面が疎水化処理された粉末が知られている。このような粉末は、通常、油相中に多く存在し、水相中で存在させるには、分散状態の改善が必要とされている。 Powder made of metal oxides or the like with hydrophobic surfaces is known as an ultraviolet scattering agent. Such powders are usually present in large amounts in the oil phase, and in order to make them exist in the aqueous phase, it is necessary to improve the dispersion state.
本発明者らの検討によると、驚くべきことに、化粧料の水相に二次粒子の平均粒径が150nm以下である疎水化処理粉末を分散させることで、安定性が良好であり、かつ高い紫外線防御効果を達成できることを発見した。本発明はこれらの知見に基づくものである。 The inventors' research has surprisingly revealed that by dispersing hydrophobically treated powder with an average secondary particle size of 150 nm or less in the aqueous phase of a cosmetic, it is possible to achieve good stability and a high UV protection effect. The present invention is based on these findings.
本発明によれば、以下の発明が提供される。
[1](A1)第1の疎水化処理粉末および(B)水を含んでなる化粧料であって、
(A1)成分が水相に分散されており、前記水相における(A1)成分の二次粒子の平均粒径が150nm以下である、化粧料。
[2]前記水相が、(C)HLBが5~18の、ポリエーテル変性シリコーンまたはポリオキシエチレンアルキルエーテルをさらに含んでなる、[1]に記載の化粧料。
[3](A2)第2の疎水化処理粉末および(D)油分をさらに含んでなり、
(A2)成分が油相に分散されており、前記油相における(A2)成分の二次粒子の平均粒径が150nm以下である、[1]または[2]に記載の化粧料。
[4]前記油相に、(E)両末端シリコーン変性グリセリンをさらに含んでなる、[3]に記載の化粧料。
[5](A1)成分および(A2)成分の合計配合量が、前記化粧料の総量に対して、30質量%以下である、[3]または[4]に記載の化粧料。
[6](A1)成分の配合量が、(A1)成分と(A2)成分との合計の配合量に対して、10~100質量%である、[3]~[5]のいずれかに記載の化粧料。
[7]水中油型乳化化粧料または油中水型乳化化粧料である、[1]~[6]のいずれかに記載の化粧料。
[8]日焼け止め化粧料である、[1]~[7]のいずれかに記載の化粧料。
[9][1]に記載の化粧料の製造方法であって、
(A1)成分および水を混合し、水性混合物を調製する水性混合物調製工程と、
前記水性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A1)成分を水相に分散させる水相分散工程と
を含んでなる、製造方法。
[10](A2)成分および油分を混合し、油性混合物を調製する油性混合物調製工程と、
前記油性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A2)成分を油相に分散させる油相分散工程と
をさらに含んでなる、[9]に記載の製造方法。
According to the present invention, the following inventions are provided.
[1] A cosmetic comprising (A1) a first hydrophobized powder and (B) water,
A cosmetic preparation, comprising: an (A1) component dispersed in an aqueous phase; and an average particle size of secondary particles of the (A1) component in the aqueous phase being 150 nm or less.
[2] The cosmetic preparation according to [1], wherein the aqueous phase further comprises (C) a polyether-modified silicone or polyoxyethylene alkyl ether having an HLB of 5 to 18.
[3] (A2) A second hydrophobized powder and (D) an oil component are further included;
The cosmetic preparation according to [1] or [2], wherein the component (A2) is dispersed in an oil phase, and the average particle size of secondary particles of the component (A2) in the oil phase is 150 nm or less.
[4] The cosmetic preparation according to [3], further comprising (E) glycerin modified at both ends with silicone in the oil phase.
[5] The cosmetic according to [3] or [4], wherein the combined amount of the (A1) component and the (A2) component is 30 mass% or less relative to the total amount of the cosmetic.
[6] The cosmetic preparation according to any one of [3] to [5], wherein the blending amount of the (A1) component is 10 to 100 mass% relative to the combined blending amount of the (A1) component and the (A2) component.
[7] The cosmetic preparation according to any one of [1] to [6], which is an oil-in-water emulsion cosmetic preparation or a water-in-oil emulsion cosmetic preparation.
[8] The cosmetic preparation according to any one of [1] to [7], which is a sunscreen cosmetic preparation.
[9] A method for producing the cosmetic composition according to [1],
an aqueous mixture preparation step of mixing the component (A1) with water to prepare an aqueous mixture;
and an aqueous phase dispersion step of passing the aqueous mixture through a throttle passage as a high-pressure fluid of 50 to 200 MPa and dispersing component (A1) in an aqueous phase by cavitation generated in the throttle passage.
[10] An oily mixture preparation step of mixing the (A2) component and an oil to prepare an oily mixture;
The method according to [9], further comprising an oil phase dispersion step of passing the oil mixture through a throttle passage as a high-pressure fluid of 50 to 200 MPa and dispersing the component (A2) in the oil phase by cavitation generated in the throttle passage.
本発明によれば、安定性が良好であり、高い紫外線防御効果を達成できる化粧料を提供することができる。さらに、本発明による化粧料は、基剤の透明性の低下を抑制し、かつ、肌への負担感を軽減し、使用感を向上させることができる。 The present invention provides a cosmetic preparation that has good stability and can achieve a high UV protection effect. Furthermore, the cosmetic preparation of the present invention can suppress the decrease in transparency of the base, reduce the burden on the skin, and improve the feel when used.
[化粧料]
本発明は、(A1)第1の疎水化処理粉末(以下、(A1)成分と称することがある。他の成分についても同様である。)および(B)水を含んでなる化粧料である。(A1)成分は水相中に分散され、その二次粒子の平均粒径が150nm以下、好ましくは10~130nmである。
本発明による化粧料では、粉末粒子の凝集が大きく抑制され、粉末粒子の二次粒子径が小さいことが特徴の一つである。本発明による化粧料は、通常の保管期間にわたって粉末が分散した状態を維持しているものが含まれ、さらに、当分野で通常の保管期間中に粉末が沈積するが、当分野で通常の方法によって化粧料を撹拌したり容器を揺動させたりすることによって再分散が可能であるものも含まれる。
[Cosmetics]
The present invention relates to a cosmetic preparation comprising (A1) a first hydrophobized powder (hereinafter sometimes referred to as component (A1), the same applies to other components) and (B) water. Component (A1) is dispersed in an aqueous phase, and the average particle size of its secondary particles is 150 nm or less, preferably 10 to 130 nm.
One of the features of the cosmetic preparation according to the present invention is that the aggregation of powder particles is greatly suppressed and the secondary particle size of the powder particles is small. The cosmetic preparation according to the present invention includes those in which the powder maintains a dispersed state over a normal storage period, and further includes those in which the powder settles during a normal storage period in the art, but can be redispersed by stirring the cosmetic preparation or shaking the container by a method normal in the art.
本発明による化粧料は、さらに、油相を含むことができる。
好ましくは、本発明による化粧料は、(A2)第2の疎水化処理粉末および(D)油分をさらに含んでなる。この場合、(A2)成分は油相中に分散され、その二次粒子の平均粒径が150nm以下、好ましくは10~130nmである。
本発明の好ましい一形態において、水相および油相ともに、それぞれ(A1)成分および(A2)成分が平均粒径150nm以下で、分散されている。
The cosmetic preparation according to the present invention may further comprise an oil phase.
Preferably, the cosmetic according to the present invention further comprises (A2) a second hydrophobized powder and (D) an oil component. In this case, the component (A2) is dispersed in the oil phase, and the average particle size of the secondary particles is 150 nm or less, preferably 10 to 130 nm.
In a preferred embodiment of the present invention, the components (A1) and (A2) are dispersed in both the aqueous phase and the oil phase, respectively, with average particle sizes of 150 nm or less.
疎水化処理粉末の二次粒子の平均粒径については、動的光散乱法(Dynamic light scattering)を用いて、液体中に分散したサブミクロン粒子の平均粒径及び粒径分布を測定することができる。
一次粒子の平均粒径については、窒素吸着法を用いて測定することができる。
Regarding the average particle size of the secondary particles of the hydrophobized powder, the average particle size and particle size distribution of the submicron particles dispersed in a liquid can be measured using dynamic light scattering.
The average particle size of the primary particles can be measured by a nitrogen adsorption method.
(A1)第一の疎水化処理粉末
(A1)成分は疎水化処理された粉末であり、化粧料中で水相中に分散され、その二次粒子の平均粒径が150nm以下ある。疎水化処理粉末は、好ましくは疎水化処理された金属酸化物粉末である。疎水化処理された粉末は、紫外線散乱機能を有する粉末、すなわち紫外線散乱剤であることが好ましい。疎水化処理粉末の平均一次粒径は、一般に、10nm以上100nm以下である。疎水化処理された金属酸化物の具体例としては、酸化チタン、酸化亜鉛、酸化セリウム、タルク、シリカ、マイカ、セリサイト、カオリン、雲母チタン、黒酸化鉄、黄酸化鉄、ベンガラ、群青、紺青、酸化クロム、水酸化クロム等が挙げられる。このうち、紫外線散乱機能が高いことから、酸化チタン、酸化亜鉛であること好ましい。また、酸化チタン以外の材料からなる粒子を酸化チタンで被覆した複合粉体を用いることもできる。
(A1) First Hydrophobized Powder The (A1) component is a hydrophobized powder, dispersed in the aqueous phase of the cosmetic, and has an average particle size of the secondary particles of 150 nm or less. The hydrophobized powder is preferably a hydrophobized metal oxide powder. The hydrophobized powder is preferably a powder having an ultraviolet scattering function, i.e., an ultraviolet scattering agent. The average primary particle size of the hydrophobized powder is generally 10 nm or more and 100 nm or less. Specific examples of hydrophobized metal oxides include titanium oxide, zinc oxide, cerium oxide, talc, silica, mica, sericite, kaolin, mica titanium, black iron oxide, yellow iron oxide, red ocher, ultramarine, iron blue, chromium oxide, chromium hydroxide, etc. Among these, titanium oxide and zinc oxide are preferred because of their high ultraviolet scattering function. In addition, a composite powder in which particles made of a material other than titanium oxide are coated with titanium oxide can also be used.
粉末に施されている疎水化処理は、粒子表面に、疎水基を導入するか、または疎水性物質の被覆を形成する処理であってよい。疎水処理は、具体的には、溶媒を使用する湿式法、気相法、メカノケミカル法等であってよい。また、疎水化処理における処理剤として、メチルハイドロジェンポリシロキサン、ジメチルポリシロキサン、トリエトキシカプリリルシラン等のシリコーン、デキストリン脂肪酸エステル、高級脂肪酸、高級アルコール、脂肪酸エステル、金属石鹸、アルキルリン酸エーテル、フッ素化合物、またはスクワラン、パラフィン等の炭化水素等を使用することができる。(A1)成分は水相中で分散されるため、疎水化処理としては、シリコーン処理が好ましい。 The hydrophobic treatment applied to the powder may be a treatment that introduces hydrophobic groups to the particle surface or forms a coating of a hydrophobic substance. Specifically, the hydrophobic treatment may be a wet method using a solvent, a gas phase method, a mechanochemical method, or the like. In addition, as a treatment agent for the hydrophobic treatment, silicones such as methylhydrogenpolysiloxane, dimethylpolysiloxane, and triethoxycaprylylsilane, dextrin fatty acid esters, higher fatty acids, higher alcohols, fatty acid esters, metal soaps, alkyl phosphate ethers, fluorine compounds, or hydrocarbons such as squalane and paraffin, etc. can be used. Since component (A1) is dispersed in the aqueous phase, silicone treatment is preferred as the hydrophobic treatment.
(A1)成分は、1種または2種以上を配合することができる。(A1)成分の配合量は、化粧料の総量に対して、好ましくは0.1~30質量%であり、より好ましくは0.5~10質量%であり、さらに好ましくは1~3質量%である。 The (A1) component may be used alone or in combination with two or more other components. The amount of the (A1) component is preferably 0.1 to 30% by mass, more preferably 0.5 to 10% by mass, and even more preferably 1 to 3% by mass, based on the total amount of the cosmetic.
(A2)第2の疎水化処理粉末
本発明による化粧料は、(A2)第2の疎水化処理粉末をさらに含むことができる。(A2)成分は疎水化処理粉末であり、化粧料中で油相中に分散され、その二次粒子の平均粒径が150nm以下である。(A1)成分と(A2)成分は、同一であってもよいし、異なっていてもよい。好ましい(A2)成分は、上記の(A1)成分と同様である。
(A2) Second hydrophobized powder The cosmetic according to the present invention may further contain (A2) a second hydrophobized powder. The (A2) component is a hydrophobized powder that is dispersed in the oil phase in the cosmetic, and the average particle size of the secondary particles is 150 nm or less. The (A1) component and the (A2) component may be the same or different. The preferred (A2) component is the same as the above-mentioned (A1) component.
(A2)成分は、1種または2種以上を配合することができる。(A2)成分の配合量は、化粧料の総量に対して、好ましくは0.5~15質量%であり、より好ましくは1~10質量%である。 The (A2) component may be used alone or in combination with two or more other components. The amount of the (A2) component is preferably 0.5 to 15% by mass, and more preferably 1 to 10% by mass, based on the total amount of the cosmetic.
(A1)成分および(A2)成分の合計配合量は、化粧料の総量に対して、好ましくは30質量%以下であり、より好ましくは1~20質量%であり、さらに好ましくは2~12質量%である。
本発明による化粧料では、疎水化処理粉末の凝集が抑制され、二次粒径が小さい状態で分散されており、これにより、通常配合される粉末の配合量よりも少ない量で、高い紫外線防御効果を達成できる。化粧料に配合される疎水化処理粉末を抑制できることで、基剤の透明性の低下を抑制でき、また使用感も向上させることができる。
The combined amount of the components (A1) and (A2) is preferably 30% by mass or less, more preferably 1 to 20% by mass, and even more preferably 2 to 12% by mass, relative to the total amount of the cosmetic.
In the cosmetic preparation according to the present invention, aggregation of the hydrophobized powder is suppressed and the secondary particle size is small, so that a high UV protection effect can be achieved with a smaller amount than the amount of powder normally blended. By suppressing the amount of hydrophobized powder blended in the cosmetic preparation, the decrease in the transparency of the base can be suppressed and the feeling of use can be improved.
(B)水
本発明による化粧料は、(B)水を含んでなる。水としては、化粧品、医薬部外品等に使用される水を使用することができ、例えば、精製水、イオン交換水、水道水等を使用することができる。
水の配合量は、本発明による化粧料の総量に対して、好ましくは10~35質量%であり、より好ましくは10~25質量%である。
The cosmetic preparation according to the present invention comprises water (B). As the water, water used in cosmetics, quasi-drugs, etc., can be used, such as purified water, ion-exchanged water, tap water, etc.
The blending amount of water is preferably 10 to 35% by mass, more preferably 10 to 25% by mass, based on the total amount of the cosmetic according to the present invention.
(C)ポリエーテル変性シリコーンまたはポリオキシエチレンアルキルエーテル
本発明による化粧料は、水相に、(C)ポリエーテル変性シリコーンまたはポリオキシエチレンアルキルエーテルをさらに含むことが好ましい。(C)成分は、水相中で、(A1)成分の分散状態を改善することができる。
(C)成分のHLB(hydrophile-lipophile balance)は、5~18であり、より好ましくは5~16であり、さらに好ましくは6~10である。この範囲にあることで、(A1)成分の水相中での初期分散性および分散安定性を向上することができる。本発明において、HLB値は、グリフィン法によって算出した値である。
(C) Polyether-modified silicone or polyoxyethylene alkyl ether The cosmetic preparation according to the present invention preferably further comprises (C) a polyether-modified silicone or a polyoxyethylene alkyl ether in the aqueous phase. Component (C) can improve the dispersion state of component (A1) in the aqueous phase.
The HLB (hydrophile-lipophile balance) of component (C) is 5 to 18, more preferably 5 to 16, and even more preferably 6 to 10. Within this range, the initial dispersibility and dispersion stability of component (A1) in the aqueous phase can be improved. In the present invention, the HLB value is a value calculated by the Griffin method.
(C)成分は、好ましくはポリエーテル変性シリコーンである。ポリエーテル変性シリコーンは、好ましくはPEG鎖および/またはPPG鎖を有するジメチコンであり、より好ましくはPEG鎖を有するジメチコンである。アルキレンオキサイドの平均付加モル数は8以上40以下であってよい。また、PEGおよび/またはPPG鎖の末端を有するジメチコンのアルキルエーテルであってもよい。好ましいポリエーテル変性シリコーンとしては、例えば、PEG-12ジメチコンが挙げられる。なお、ポリエーテル変性シリコーンのシリコーン鎖は直鎖であってもよいし、分枝していてもよいが、直鎖であることが好ましい。アルキル側鎖をさらに有するポリエーテル変性アルキル変性シリコーンであってもよいが、アルキル未変性であることが好ましい。 The component (C) is preferably a polyether-modified silicone. The polyether-modified silicone is preferably a dimethicone having a PEG chain and/or a PPG chain, more preferably a dimethicone having a PEG chain. The average number of moles of alkylene oxide added may be 8 or more and 40 or less. It may also be an alkyl ether of dimethicone having a PEG and/or PPG chain terminal. A preferred example of a polyether-modified silicone is PEG-12 dimethicone. The silicone chain of the polyether-modified silicone may be either a straight chain or a branched chain, but is preferably a straight chain. It may be a polyether-modified alkyl-modified silicone further having an alkyl side chain, but is preferably unalkyl-modified.
(C)成分は、1種または2種以上を配合することができる。(C)成分の配合量は、化粧料の総量に対して、好ましくは0.01~10質量%であり、より好ましくは0.05~5質量%であり、さらに好ましくは0.05~1質量%である。 The (C) component may be blended in one or more types. The blended amount of the (C) component is preferably 0.01 to 10 mass % relative to the total amount of the cosmetic, more preferably 0.05 to 5 mass %, and even more preferably 0.05 to 1 mass %.
(D)油分
本発明による化粧料は、(D)油分をさらに含むことができる。(D)成分としては、例えば、シリコーン油、炭化水素油、高級脂肪酸、高級アルコール、エステル油、液体油脂等が挙げられ、好ましくはシリコーン油、炭化水素油、エステル油である。
シリコーン油としては、例えば、ジメチコン、メチルフェニルポリシロキサン、メチルハイドロジェンポリシロキサン、メチコンヘキサメチルジシロキサン、オクタメチルトリシロキサン、デカメチルテトラシロキサン、ヘキサデカメチルヘプタシロキサン、カプリリルメチコン等が挙げられる。
炭化水素油としては、例えば、イソドデカン、イソヘキサデカン、イソパラフィン、流動パラフィン、オゾケライト、スクワラン、プリスタン、パラフィン、セレシン、スクワレン、ワセリン、マイクロクリスタリンワックス等が挙げられる。
エステル油としては、例えば、エステル油としては、例えば、オクタン酸オクチル、ノナン酸ノニル、オクタン酸セチル、ミリスチン酸イソプロピル、ミリスチン酸オクチルドデシル、パルミチン酸イソプロピル、パルミチン酸エチルヘキシル、ステアリン酸ブチル、ラウリン酸ヘキシル、ミリスチン酸ミリスチル、オレイン酸デシル、ジメチルオクタン酸ヘキシルデシル、乳酸セチル、乳酸ミリスチル、酢酸ラノリン、ステアリン酸イソセチル、イソステアリン酸イソセチル、12-ヒドロキシステアリン酸コレステリル、ジ-2-エチルヘキサン酸エチレングリコール、ジペンタエリスリトール脂肪酸エステル、モノイソステアリン酸N-アルキルグリコール、ジカプリン酸ネオペンチルグリコール、ピバリン酸トリプロピレングリコール、リンゴ酸ジイソステアリル、ジ-2-ヘプチルウンデカン酸グリセリン、ジイソステアリン酸グリセリン、トリ-2-エチルヘキサン酸トリメチロールプロパン、トリイソステアリン酸トリメチロールプロパン、テトラ-2-エチルヘキサン酸ペンタエリスリトール、トリ-2-エチルヘキサン酸グリセリン、トリオクタン酸グリセリン、トリイソパルミチン酸グリセリン、トリイソステアリン酸トリメチロールプロパン、セチル2-エチルヘキサノエート-2-エチルヘキシルパルミテート、トリミリスチン酸グリセリン、トリ-2-ヘプチルウンデカン酸グリセライド、ヒマシ油脂肪酸メチルエステル、オレイン酸オレイル、アセトグリセライド、パルミチン酸2-ヘプチルウンデシル、アジピン酸ジイソブチル、N-ラウロイル-L-グルタミン酸-2-オクチルドデシルエステル、アジピン酸ジ-2-ヘプチルウンデシル、エチルラウレート、セバシン酸ジ-2-エチルヘキシル、ミリスチン酸2-ヘキシルデシル、パルミチン酸2-ヘキシルデシル、アジピン酸2-ヘキシルデシル、セバシン酸ジイソプロピル、コハク酸2-エチルヘキシル、クエン酸トリエチル、エチルヘキサン酸セチル等が挙げられる。
The cosmetic composition according to the present invention may further comprise an oil component (D). Examples of the oil component (D) include silicone oils, hydrocarbon oils, higher fatty acids, higher alcohols, ester oils, and liquid fats and oils, and preferably silicone oils, hydrocarbon oils, and ester oils.
Examples of silicone oils include dimethicone, methylphenylpolysiloxane, methylhydrogenpolysiloxane, methicone hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexadecamethylheptasiloxane, and caprylyl methicone.
Examples of hydrocarbon oils include isododecane, isohexadecane, isoparaffin, liquid paraffin, ozokerite, squalane, pristane, paraffin, ceresin, squalene, petrolatum, and microcrystalline wax.
Examples of the ester oil include octyl octanoate, nonyl nonanoate, cetyl octanoate, isopropyl myristate, octyldodecyl myristate, isopropyl palmitate, ethylhexyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyldecyl dimethyloctanoate, cetyl lactate, myristyl lactate, lanolin acetate, isocetyl stearate, isocetyl isostearate, cholesteryl 12-hydroxystearate, ethylene glycol di-2-ethylhexanoate, dipentaerythritol fatty acid ester, N-alkyl glycol monoisostearate, neopentyl glycol dicaprate, tripropylene glycol pivalate, diisostearyl malate, glycerin di-2-heptylundecanoate, glycerin diisostearate, trimethylolpropane tri-2-ethylhexanoate, triisostearate trimethylolpropane, pentaerythritol tetra-2-ethylhexanoate, glycerin tri-2-ethylhexanoate, glycerin trioctanoate, glycerin triisopalmitate, trimethylolpropane triisostearate, cetyl 2-ethylhexanoate-2-ethylhexyl palmitate, glycerin trimyristate, tri-2-heptylundecanoate glyceride, castor oil fatty acid methyl ester, oleyl oleate, acetoglyceride, Examples of the glyceryl ester include 2-heptylundecyl palmitate, diisobutyl adipate, N-lauroyl-L-glutamic acid-2-octyldodecyl ester, di-2-heptylundecyl adipate, ethyl laurate, di-2-ethylhexyl sebacate, 2-hexyldecyl myristate, 2-hexyldecyl palmitate, 2-hexyldecyl adipate, diisopropyl sebacate, 2-ethylhexyl succinate, triethyl citrate, and cetyl ethylhexanoate.
(D)成分は、1種または2種以上を配合することができる。(D)成分の配合量は、化粧料の総量に対して、好ましくは10~80質量%であり、より好ましくは20~60質量%である。 The (D) component may be blended in one or more types. The blended amount of the (D) component is preferably 10 to 80 mass % relative to the total amount of the cosmetic, and more preferably 20 to 60 mass %.
(E)両末端シリコーン変性グリセリン
本発明による化粧料は、(E)両末端シリコーン変性グリセリンをさらに含むことができる。(E)成分は、油相中で、(A2)成分の分散状態を改善することができる。
(E)成分は、好ましくは式(1)で表されるものである。
R1は、C1-12アルキル基またはフェニル基であり、好ましくはメチル基であり、
R2は、C2-11アルキレン基であり、好ましくはトリメチレン基であり、
mは、10~120であり、
nは、1~11である。
アルキル基およびアルキレン基は、直鎖または分岐であってよい。
(E)成分の重量平均分子量は、好ましくは2,000~30,000である。重量平均分子量は、例えば、ゲル浸透クロマトグラフィーにおける、ポリスチレン換算によって算出できる。
(E)成分としては、例えば、ビスブチルジメチコンポリグリセリル-3が挙げられる。
(E) Glycerin modified at both ends with silicone The cosmetic preparation according to the present invention may further comprise (E) glycerin modified at both ends with silicone. Component (E) can improve the dispersion state of component (A2) in the oil phase.
The component (E) is preferably represented by formula (1).
R 1 is a C 1-12 alkyl group or a phenyl group, preferably a methyl group;
R2 is a C2-11 alkylene group, preferably a trimethylene group;
m is 10 to 120;
n is 1 to 11.
The alkyl and alkylene groups can be straight-chained or branched.
The weight average molecular weight of the component (E) is preferably 2,000 to 30,000. The weight average molecular weight can be calculated, for example, by gel permeation chromatography using polystyrene standards.
Examples of component (E) include bisbutyldimethicone polyglyceryl-3.
(E)成分は、1種または2種以上を配合することができる。(E)成分の配合量は、化粧料の総量に対して、好ましくは0.1~20質量%であり、より好ましくは0.5~10質量%である。 The component (E) may be used alone or in combination with two or more other components. The amount of component (E) used is preferably 0.1 to 20% by mass, and more preferably 0.5 to 10% by mass, based on the total amount of the cosmetic.
本発明による化粧料は、上記以外の他の成分を本発明の効果を阻害しない範囲で、化粧料に通常用いられる成分を配合することができる。これらの成分としては、例えば、増粘剤、保湿剤、紫外線吸収剤、薬剤、安定化剤、pH調製剤、防腐剤、色素、染料、界面活性剤、粉末成分、香料等が挙げられる。 The cosmetic preparation according to the present invention may contain ingredients other than those mentioned above that are commonly used in cosmetics, provided that the ingredients do not impair the effects of the present invention. Examples of these ingredients include thickeners, moisturizers, UV absorbers, medicines, stabilizers, pH adjusters, preservatives, pigments, dyes, surfactants, powdered ingredients, fragrances, etc.
[化粧料の製造方法]
本発明による化粧料の製造方法は、特に限定されないが、好ましい一形態において、以下の工程:
(I)(A1)成分および水を混合し、水性混合物を調製する水性混合物調製工程;および
(II)前記水性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A1)成分を水相に分散させる水相分散工程
を含んでなる。
本発明による化粧料の製造方法は、さらに、以下の工程
(III)(A2)成分および油分を混合し、油性混合物を調製する油性混合物調製工程;および
(IV)前記油性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A2)成分を油相に分散させる油相分散工程
を含むことができる。
[Production method of cosmetics]
The method for producing a cosmetic according to the present invention is not particularly limited, but in a preferred embodiment, the method comprises the following steps:
The method comprises: (I) an aqueous mixture preparation step of mixing component (A1) and water to prepare an aqueous mixture; and (II) an aqueous phase dispersion step of passing the aqueous mixture as a high-pressure fluid of 50 to 200 MPa through a throttle passage and dispersing component (A1) in an aqueous phase by cavitation generated in the throttle passage.
The method for producing a cosmetic preparation according to the present invention can further include the following steps: (III) an oily mixture preparation step of mixing the (A2) component and an oil to prepare an oily mixture; and (IV) an oil phase dispersion step of passing the oily mixture as a high-pressure fluid of 50 to 200 MPa through a throttle flow path and dispersing the (A2) component in an oil phase by cavitation generated in the throttle flow path.
(I)水性混合物調製工程
この工程では、分散媒である水と、(A1)成分と、必要に応じて任意の成分とを撹拌しながら混合し、水性混合物を調製する。この工程において、分散性向上のために任意の成分としては、(C)成分を含むことが好ましい。その他の任意成分としては、例えば、保湿剤、安定化剤、防腐剤、増粘剤等が挙げられる。
(I) Aqueous mixture preparation step In this step, water as a dispersion medium, component (A1), and optional components as required are mixed while stirring to prepare an aqueous mixture. In this step, it is preferable to include component (C) as an optional component for improving dispersibility. Other optional components include, for example, moisturizers, stabilizers, preservatives, thickeners, etc.
(II)水相分散工程
この工程では、(I)工程で調製された水性混合物をキャビテーションの原理に基づいて均質化させ、水相分散体を調製する。キャビテーションとは、液体の流れの中で圧力差により短時間に泡の発生と消滅が起きる物理現象である。具体的には、(I)工程で得られた混合物に流速を付与した液体を、絞り流路を通過させることによって、液体にキャビテーションによる微細気泡を発生させて、その衝撃力で、水相分散体を得る。付与する流速は、50~200MPaの超高圧流で与える。50未満であると、分散効果が不十分となる場合があるため好ましくない。
(II) Aqueous Phase Dispersion Step In this step, the aqueous mixture prepared in step (I) is homogenized based on the principle of cavitation to prepare an aqueous phase dispersion. Cavitation is a physical phenomenon in which bubbles are generated and disappear in a short time due to pressure differences in a liquid flow. Specifically, the mixture obtained in step (I) is given a flow velocity, and the liquid is passed through a throttle channel to generate fine bubbles due to cavitation, and the aqueous phase dispersion is obtained by the impact force. The flow velocity is given by an ultra-high pressure flow of 50 to 200 MPa. If it is less than 50, the dispersion effect may be insufficient, which is not preferable.
(III)油性混合物調製工程
この工程では、分散媒である油分と、(A2)成分と、必要に応じて任意の成分とを撹拌しながら混合し、油性混合物を調製する。この工程において、分散性向上のために任意の成分としては、(E)成分を含むことが好ましい。その他の任意成分としては、例えば、保湿剤、安定化剤、防腐剤、増粘剤等が挙げられるが、(E)成分以外の任意成分を含まないことも好ましい形態の一つである。
(III) Oily mixture preparation step In this step, the oil as a dispersion medium, the (A2) component, and any other component as necessary are mixed while stirring to prepare an oily mixture. In this step, it is preferable to include the (E) component as the optional component for improving dispersibility. Other optional components include, for example, moisturizers, stabilizers, preservatives, thickeners, etc., but it is also a preferred embodiment to not include any other optional components than the (E) component.
(IV)油相分散工程
この工程では、(III)工程で調製された油性混合物をキャビテーションの原理に基づいて均質化させ、油相分散体を調製する。キャビテーションによる均質化の方法については、(II)工程と同じである。
(IV) Oil phase dispersion step In this step, the oil mixture prepared in step (III) is homogenized based on the principle of cavitation to prepare an oil phase dispersion. The method of homogenization by cavitation is the same as that in step (II).
調製した水相分散体、必要に応じて油相分散体を用いて、従来から使用されている製造方法に準じて、化粧料を製造することができる。 The prepared aqueous phase dispersion, and if necessary, the oil phase dispersion, can be used to manufacture cosmetics in accordance with conventional manufacturing methods.
本発明による化粧料は、水中油型乳化化粧料、油中水型乳化化粧料の他に、乳化をしていない水性化粧料等であってよいが、好ましくは水中油型乳化化粧料または油中水型乳化化粧料であり、より好ましくは油中水型乳化化粧料である。 The cosmetic according to the present invention may be an oil-in-water emulsion cosmetic, a water-in-oil emulsion cosmetic, or an unemulsified aqueous cosmetic, but is preferably an oil-in-water emulsion cosmetic or a water-in-oil emulsion cosmetic, and more preferably a water-in-oil emulsion cosmetic.
本明細書における化粧料には、紫外線吸収機能を高めた化粧料、基礎化粧料(ファンデーション、ベースメイク等)、メークアップ化粧料(アイシャドウ、チーク等)はもちろん、日焼け止め化粧料(サンスクリーン組成物)が含まれる。本発明による化粧料は、高い紫外線防御効果を達成でき、使用感にも優れるので、好ましくは、日焼け止め化粧料である。 The cosmetics in this specification include cosmetics with enhanced ultraviolet absorbing function, basic cosmetics (foundation, base makeup, etc.), makeup cosmetics (eye shadow, blush, etc.), and of course sunscreen cosmetics (sunscreen compositions). The cosmetics according to the present invention can achieve a high ultraviolet ray protection effect and have an excellent feeling when used, so they are preferably sunscreen cosmetics.
以下の例に基づいて本発明を具体的に説明するが、本発明はこれらの例に限定されるものではない。配合量は特記しない限り、総量に対する質量%で示す。 The present invention will be specifically explained based on the following examples, but the present invention is not limited to these examples. The blend amounts are shown as mass % of the total amount unless otherwise specified.
[水相分散体W1~W6]
表1に記載の組成で、キャビテーションを用いた分散方法によりW1~W5の水相分散体を、ホモミキサーを用いた分散方法によりW6の水相分散体を調製した。
(*1):「STR 100C-LP」、堺化学工業株式会社製、平均一次粒径15nm。
[Aqueous phase dispersion W1 to W6]
Using the compositions shown in Table 1, aqueous phase dispersions W1 to W5 were prepared by a dispersion method using cavitation, and aqueous phase dispersion W6 was prepared by a dispersion method using a homomixer.
(*1): "STR 100C-LP", manufactured by Sakai Chemical Industry Co., Ltd., average primary particle size 15 nm.
[油相分散体О1およびO2]
表2に記載の組成で、キャビテーションを用いた分散方法によりО1の水相分散体を、ホモミキサーを用いた分散方法によりО2の水相分散体を調製した。
(*2):「ST-485SA」、チタン工業株式会社製、平均一次粒径8nm、
(*3):「MSY-MZ500」、テイカ株式会社製、平均一次粒径25nm。
[Oil phase dispersions O1 and O2]
Using the compositions shown in Table 2, an aqueous phase dispersion of O1 was prepared by a dispersion method using cavitation, and an aqueous phase dispersion of O2 was prepared by a dispersion method using a homomixer.
(*2): "ST-485SA", manufactured by Titan Kogyo Co., Ltd., average primary particle size 8 nm,
(*3): “MSY-MZ500”, manufactured by Teika Corporation, average primary particle size 25 nm.
[平均二次粒径]
上記で調製した分散体の平均二次粒径を動的散乱法により測定した。得られた結果を表1および2に記載する。
[Average secondary particle size]
The average secondary particle size of the dispersion prepared above was measured by dynamic scattering method, and the results are shown in Tables 1 and 2.
[紫外線防御効果の評価]
上記で調製した分散体のSPF値をSPF測定装置「SPF MASTER」(資生堂)を用いて測定し、以下の基準により紫外線防御効果を評価した。得られた結果を表1および2に記載する。
A:SPFが50以上
B:SPFが30以上~50未満
C:SPFが30未満
[Evaluation of UV protection effect]
The SPF value of the dispersion prepared above was measured using an SPF measuring device "SPF MASTER" (Shiseido), and the UV protection effect was evaluated according to the following criteria. The results are shown in Tables 1 and 2.
A: SPF 50 or more B: SPF 30 or more to less than 50 C: SPF less than 30
[安定性評価]
上記で調製した分散体について、調製直後と、10日間室温で保管した後との外観を目視により観察し、以下の基準により、評価した。得られた結果を表1および2に記載する。
A:析出や凝集がみられず、極めて安定であった。
B:大きな析出や凝集がみられず、安定であった。
C:経時的に析出や凝集がみられた。
[Stability evaluation]
The appearance of the dispersion prepared above was visually observed immediately after preparation and after storage at room temperature for 10 days, and was evaluated according to the following criteria. The results are shown in Tables 1 and 2.
A: No precipitation or aggregation was observed, and the composition was extremely stable.
B: No significant precipitation or aggregation was observed and the mixture was stable.
C: Precipitation or aggregation was observed over time.
[実施例1~6および比較例1、2]
上記で調製された分散体を用いて、表3に示される配合で、実施例1~6および比較例1、2の油中水型乳化化粧料を調製した。
(*4):「SA-SB-300」、三好化成株式会社製、平均一次粒径5μm。
[Examples 1 to 6 and Comparative Examples 1 and 2]
Using the dispersions prepared above, water-in-oil emulsion cosmetics of Examples 1 to 6 and Comparative Examples 1 and 2 were prepared according to the formulations shown in Table 3.
(*4): “SA-SB-300”, manufactured by Miyoshi Chemicals Co., Ltd., average primary particle size 5 μm.
紫外線防御効果の評価と安定性評価は、上記の分散体の測定方法と同じ方法で、表3では調製された化粧料を用いて行った。 The evaluation of UV protection effect and stability were performed using the same method as the measurement method for the dispersion described above, using the cosmetics prepared in Table 3.
Claims (10)
(B)水
を含んでなる化粧料であって、
(A1)成分が水相に分散されており、前記水相における(A1)成分の二次粒子の平均粒径が150nm以下である、化粧料。 A cosmetic comprising: (A1) a first hydrophobized powder; and (B) water,
A cosmetic preparation, comprising: an (A1) component dispersed in an aqueous phase; and an average particle size of secondary particles of the (A1) component in the aqueous phase being 150 nm or less.
(D)油分
をさらに含んでなり、
(A2)成分が油相に分散されており、前記油相における(A2)成分の二次粒子の平均粒径が150nm以下である、請求項1に記載の化粧料。 (A2) a second hydrophobized powder; and (D) an oil component,
2. The cosmetic preparation according to claim 1, wherein the component (A2) is dispersed in an oil phase, and the average particle size of secondary particles of the component (A2) in the oil phase is 150 nm or less.
(A1)成分および水を混合し、水性混合物を調製する水性混合物調製工程と、
前記水性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A1)成分を水相に分散させる水相分散工程と
を含んでなる、製造方法。 A method for producing the cosmetic preparation according to claim 1, comprising the steps of:
an aqueous mixture preparation step of mixing the component (A1) with water to prepare an aqueous mixture;
and an aqueous phase dispersion step of passing the aqueous mixture through a throttle passage as a high-pressure fluid of 50 to 200 MPa and dispersing component (A1) in an aqueous phase by cavitation generated in the throttle passage.
前記油性混合物を50~200MPaの高圧流体として絞り流路を通過させ、前記絞り流路内に発生させたキャビテーションにより、(A2)成分を油相に分散させる油相分散工程と
をさらに含んでなる、請求項9に記載の製造方法。 (A2) An oily mixture preparation step of mixing the component and an oil to prepare an oily mixture;
The method according to claim 9, further comprising an oil phase dispersion step of passing the oily mixture through a throttle passage as a high-pressure fluid of 50 to 200 MPa and dispersing the component (A2) in the oil phase by cavitation generated in the throttle passage.
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