Patent Application
20130336908
The present invention relates to an oil-in-water emulsion composition, and more specifically to an oil-in-water emulsion composition that contains an oil-soluble ultraviolet absorbent in the outer phase (water phase) to exhibit stable and good ultraviolet protection ability.
Sunscreen cosmetics are intended to cut off ultraviolet rays in sunlight to protect the skin from adverse influence of ultraviolet rays. Examples of sunscreen cosmetic bases include emulsion type, lotion type, and oil type. Among these, oil-in-water emulsion type is widely used because it has a moist feel on use and can be formulated into a broad range of products including low SPF to high SPF products (Non Patent Document 1).
Meanwhile, the ultraviolet absorbents added to sunscreen cosmetics are classified into oil-soluble ones and water-soluble ones. To achieve high protection ability by absorption of ultraviolet rays in the OVA region (wavelengths from 320 to 400 nm) and the UVB region (wavelengths from 290 to 320 nm), well balanced amounts of a UVB absorbent and a UVA absorbent have to be added.
However, OVA absorbents, which absorb the OVA wavelength longer than the UVB wavelength, tend to have a conjugated bond longer than that of UVB absorbents to temporarily absorb energy. Thus, UVA absorbents generally have larger molecular weight than UVB absorbents, and accordingly, often become poorly soluble in oils. Dissolution of such absorbents requires addition of highly polar oil in a large amount. This has caused loss of a moist feel on use specific to oil-in-water emulsions or has resulted in a stability problem such as precipitation of the ultraviolet absorbent in the oil phase at low temperatures.
Patent Document 1 suggests addition of a specific polyether-modified silicone and hydrophobization of surface of a metal oxide powder to stably add diethylamino hydroxybenzoyl hexyl benzoate, which is an ultraviolet absorbent with poor solubility, and the metal oxide powder, which is an ultraviolet scattering agent. The document states that the resulting cosmetic composition has an excellent feeling on use and water resistance.
Patent Document 2 discloses that adding partially-crosslinked polyether-modified organopolysiloxane, organic titanate-treated zinc oxide or titanium oxide particulates, a silicone oil, a specific oil component, and an inulin fatty acid ester in combination provides a sunscreen cosmetic that exhibits excellent dispersion and emulsion stability as well as has a good feel on use.
The polyether-modified silicones (crosslinked type) used in Patent Documents 1 and 2, which are added also in the sunscreen cosmetics described in Patent Documents 3 and 4, is suggested to contribute to enhancing the dispersion of titanium oxide or the stability of the emulsion.
However, the cosmetics described in Patent Documents 1 to 3 use powders such as titanium oxide as essential components, which are inevitably accompanied by excessive white masking and a reduced feeling on use. Examples of co-addition of crosslinked polyether-modified silicone into a formulation containing a poorly soluble ultraviolet absorbent in the water phase have been neither disclosed nor suggested.
Accordingly, an object of the present invention is to provide a sunscreen cosmetic composition that effectively protects from both UVA and UVB, has moist and cool texture well as excellent stability, and is able to form a film having a good ultraviolet protection effect when applied to skin.
To solve the problems described above, the present invention provides an oil-in-water sunscreen cosmetic composition, comprising:
(a) an aqueous dispersion of an oil-soluble ultraviolet absorbent;
(b) one or two or more selected from crosslinked polyether-modified silicones and crosslinked alkyl-polyether-modified silicones;
(c) a low-viscosity silicone oil; and
(d) water.
In the present invention, the component (a) is preferably an aqueous dispersion of composite particles of an oil-soluble ultraviolet absorber and an organic polymer.
The sunscreen cosmetic composition of the present invention has been able to improve the stability of the system by adding a poorly oil-soluble ultraviolet absorbent in the water phase. Additionally, the cosmetic composition also has a beneficial effect of enhancing ultraviolet protection ability relative to a case in which the ultraviolet absorbent is added in the oil phase. The system of the cosmetic composition has further been stabilized by addition of agar microgel. Therefore, the cosmetic composition of the present invention is particularly suitable to use as a sunscreen cosmetic that has a moist feel on use specific to an oil-in-water emulsion as well as excellent ultraviolet protection ability.
The sunscreen cosmetic composition of the present invention is characterized in that it comprises an aqueous dispersion of an oil-soluble ultraviolet absorbent (component a) in the water phase.
The oil-soluble ultraviolet absorbent is preferably selected from, but not particularly limited to, ultraviolet absorbents that are insoluble in water and poorly soluble in oil. However, absorbents substantially insoluble in oil, such as methylene bis-benzotriazole tetramethyl butylphenol are not contained. When an oil-in-water emulsion composition, which has been prepared using an aqueous dispersion of an oil-insoluble ultraviolet absorbent, is applied to the skin, the resultant skin may look unnaturally whitish.
Poorly soluble ultraviolet absorbents include those described in Patent Document 1, specifically, such as benzophenone derivatives and triazine derivatives. Especially preferred are triazine derivatives, among which 2,4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]phenyl}-6-(4-methoxyphenyl)-(1,3,5)-triazine (hereinafter, referred to as “bis-ethylhexyloxyphenol methoxyphenyl triazine” in the present specification) is preferred. This bis-ethylhexyloxyphenol methoxyphenyl triazine is commercially available from BASF SE under the trade name Tinosorb S, and the commercially available product can be used.
Furthermore, the aqueous dispersion of the oil-soluble ultraviolet absorbent of the present invention is particularly preferably an aqueous dispersion of composite particles of an oil-soluble ultraviolet absorbent and an organic polymer. When the water phase containing the aqueous dispersion coexists with an oil phase, making of the composite particles suppress dissolution of the oil-soluble ultraviolet absorbent from the water phase into the oil phase.
The aqueous dispersion of composite particles of an oil-soluble ultraviolet absorber and an organic polymer can be prepared, for example, in accordance with the method described in WO2009/007264. In short, a mixture of an ultraviolet absorbent and an organic monomer dispersed in water can be emulsion-polymerized to provide an aqueous dispersion having composite particles of the ultraviolet absorbent and the organic polymer dispersed therein.
Preferable examples of organic monomers include monomers having an ethylenically unsaturated bond, for example, acrylic acid, methacrylic acid, alkyl acrylate, alkyl methacrylate, styrene monomers, and nylon monomers.
As an aqueous dispersion of such composite particles, a commercially available product from BASF SE under the trade name Tinosorb S aqua can be used. Tinosorb S aqua contains composite particles of bis-ethylhexyloxyphenol methoxyphenyl triazine and polymethylmethacrylate (PMMA) dispersed in water. The contents of bis-ethylhexyloxyphenol methoxyphenyl triazine and PMMA are 20% by mass and 19% by mass, respectively.
The amount of the oil-soluble ultraviolet absorbent to be added in the cosmetic of the present invention is 5% by mass or less, preferably 3% by mass or less, and more preferably 0.01 to 3% by mass, on a dry mass basis. If the amount is less than 0.01% by mass, sufficient ultraviolet absorption ability cannot be achieved; whereas, if the amount is more than 5% by mass, a problem in texture such as stickiness tends to arise.
If the amount is converted to an amount of a water dispersion containing 20% by mass of an ultraviolet absorbent (component a) to be added, for example, the aqueous dispersion will be added at 25% by mass or less, preferably at 15% by mass or less, and more preferably at 0.05 to 15% by mass.
The cosmetic composition of the present invention contains one or two or more selected from crosslinked polyether-modified silicones and crosslinked alkyl polyether-modified silicones (component b) as essential components.
Examples of crosslinked polyether silicones (also referred to as polyether-modified crosslinked silicones) are polyether-modified crosslinked silicones such as (dimethicone/(PEG-10/15)) crosspolymer. Crosslinked alkyl-polyether-modified silicones, which are products obtained by further alkyl modification of crosslinked polyether-modified silicones (alkyl co-modification type), include, for example, (PEG-10/lauryl dimethicone) crosspolymer and (PEG-15/lauryl dimethicone) crosspolymer.
As these crosslinked polyether-modified silicones and crosslinked alkyl polyether-modified silicones, commercially available products may be used. Examples of these silicones include gelled dispersions kneaded with various cosmetic oils (for example, dimethicone, mineral oils, trioctanoin, and squalane), which are marketed from Shin-Etsu Silicone under product numbers KSG21, KSG210, KSG240, KSG310, KSG330, and KSG340.
The amount of one or two or more selected from crosslinked polyether-modified silicones and crosslinked alkyl polyether-modified silicones (component b) to be added in the cosmetic of the present invention is 5% by mass or less, preferably 3% by mass or less, and more preferably 0.01 to 3% by mass. If the amount to be added is less than 0.01% by mass, a stable emulsion is difficult to obtain; whereas, if the amount is more than 5% by mass, a problem in texture such as stickiness may arise.
The cosmetic composition of the present invention also contains a low-viscosity silicone oil (component c). Preferable low-viscosity silicone oils include low-viscosity dimethicones with a viscosity of 10 mPa·s or less, preferably 5 mPa·s or less, such as decamethylcyclopentasiloxane. Addition of the low-viscosity silicone oil can reduce stickiness and squeakiness on application.
The amount of the low-viscosity silicone oil in the cosmetic composition of the present invention is 30% by mass or less, preferably 15% by mass or less, and more preferably 0.01 to 10% by mass. If the amount is more than 30% by mass, a stability problem such as separation or a problem in texture such as loss of a moist feeling on use may arise.
The cosmetic of the present invention further contains water (component d) as an essential component.
The amount of water to be added in the cosmetic composition of the present invention is 80% by mass or less, preferably 50% by mass or less, and more preferably 0.01 to 30% by mass. If the amount is more than 80% by mass, a stability problem such as separation or a problem in texture such as loss of a moist feeling on use may arise.
Furthermore, the cosmetic composition of the present invention preferably has methylene bisbenzotriazolyl tetramethylbutylphenol (component e) added in the water phase. Addition of methylene bisbenzotriazolyl tetramethylbutylphenol further enhances the ultraviolet protection effect.
Methylene bisbenzotriazolyl tetramethylbutylphenol, which is insoluble in water, is preferably dispersed in the water phase before admixture. For example, an aqueous dispersion of methylene bisbenzotriazolyl tetramethylbutylphenol, commercially available from BASF SE under the trade name Tinosorb M, can be used.
The amount of methylene bisbenzotriazolyl tetramethylbutylphenol to be added in the cosmetic of the present invention is 20% by mass or less, preferably 10% by mass or less, and more preferably 1 to 9% by mass. If the amount is more than 20% by mass, a problem such as squeakiness on application may arise.
Other ultraviolet absorbents may be further added to the compositions of the present invention, in addition to the aqueous dispersion of the oil-soluble ultraviolet absorbent (component a) and methylene bisbenzotriazolyl tetramethylbutylphenol (component e) added in the water phase.
Other ultraviolet absorbents, which are oil soluble, preferably dissolve into the oil phase and absorb ultraviolet radiation synergistically with the ultraviolet absorbent in the water phase.
Such ultraviolet absorbents include, but not particularly limited to, methoxy cinnamic acid derivatives, diphenyl acrylic acid derivatives, salicylic acid derivatives, para-aminobenzoic acid derivatives, triazine derivatives, benzophenone derivatives, benzal malonate derivatives, anthranilic derivatives, imidazoline derivatives, 4,4-diaryl butadiene derivatives, and phenylbenzimidazole derivatives. Specific examples include 2-ethylhexyl p-methoxycinnamate, homosalate, octyl salicylate, oxybenzone, 4-t-butyl-4′-methoxydibenzoylmethane, octyltriazone, bis-ethylhexylphenol methoxyphenyl triazine, 2-hydroxy-4-methoxybenzophenone, dihydroxy dimethoxybenzophenone, dihydroxybenzophenone, tetrahydroxybenzophenone, diethylamino hydroxybenzoyl hexyl benzoate, 2-cyano-3,3-diphenylacrylic acid-2′-ethylhexyl ester, polysilicone-15, and drometrizole polysiloxane.
The cosmetic composition of the present invention may also contain powders of metal oxides that serve as ultraviolet scattering agents, including titanium oxide and zinc oxide.
However, the sunscreen cosmetic composition of the present invention, which contains essential components such as bis-ethylhexyloxyphenol methoxyphenyl triazine in the water phase and optionally contains methylene bisbenzotriazolyl tetramethylbutylphenol or other ultraviolet absorbents, has good ultraviolet protection ability throughout the UVA to UVB regions. Thus, the cosmetic composition of the present invention may not contain ultraviolet scattering agents, which may be responsible for excessive white masking on application.
In addition to the components described above, the cosmetic composition of the present invention can contain other components usually used in compositions for external use such as cosmetics to the extent where the intended effect of the present invention is not substantially prevented.
The compositions of the present invention can be prepared by separately mixing components constituting the oil phase and components constituting the water phase followed by adding the oil phase into the water phase for emulsification.
The composition of the present invention has a moist feel on use intrinsic to an oil-in-water emulsion, provides excellent stability at low and high temperatures, and exhibits excellent ultraviolet protection ability. As such, the composition is particularly suitable to use as a sunscreen cosmetic composition of oil-in-water emulsion type.
Hereinbelow, the present invention is described in greater detail in view of the specific examples, but the present invention is not limited to the Examples given below. Further, the amounts mentioned in the following Examples indicate % by mass, unless specifically described otherwise.
Oil-in-water emulsion compositions with the composition shown in the following Table 1 were prepared. Specifically, water phase components and oil phase components were separately heated to 70° C. to be completely dissolved, and then, the oil phase was added to the water phase for emulsification by an emulsifier to obtain compositions of Examples.
To a surface of a PMMA film (5 cm×5 cm), 18.87 μL of a sample of each of the compositions of Examples 1, 2, and Comparative Example 1 was uniformly applied at a ratio of 0.75 mg/cm2. After left for 15 minutes, each sample was measured for absorbance by using a spectrophotometer (U-4100: manufactured by Hitachi, Ltd.). The results are shown in
As shown in
Oil-in-water emulsion compositions with the composition shown in the following Tables 2 and 3 were prepared. Specifically, water phase components and oil phase components were separately heated to 70° C. to be completely dissolved, and then, the oil phase was added to the water phase for emulsification by an emulsifier to obtain compositions of Examples.
As described above, each composition was evaluated for absorbance at the wavelength of 310 nm, stability at room temperature, and usability such as excessive whiteness and stickiness. Method and criteria of evaluation are as follows. The results are shown in both Tables 2 and 3.
1. Room Temperature Stability After left at room temperature, the compositions were evaluated by visual observation.
◯: No precipitation of ultraviolet absorbent was observed.
X: Precipitation of ultraviolet absorbent was observed.
Female panelists (N=20) were asked to apply each composition on their skin and to evaluate the presence or absence of excessive white masking based on the following criteria.
◯: Sixteen or more panelists found no excessive white masking.
Δ: Six to fifteen panelists found no excessive white masking.
X: Five or fewer panelists found no excessive white masking.
Female panelists (N=20) were asked to apply each composition on their skin and to evaluate stickiness when the composition blended into their skin based on the following criteria.
◯: Sixteen or more panelists found no stickiness.
Δ: Six to fifteen panelists found no stickiness.
X: Five or fewer panelists found no stickiness.
*1)KF6038 (manufactured by Shin-Etsu Chemical Co., Ltd.)
*2)KSG-210 (manufactured by Shin-Etsu Chemical Co., Ltd.)
*3)Parsol MCX
*4)Uvinul A plus
*5)Tinosorb S (manufactured by BASF SE)
*6)Tinosorb S aqua (20% aqueous dispersion: manufactured by BASF SE)
*7)Tinosorb M (manufactured by BASF SE)
The results in Table 2 and 3 show that Examples 3 to 5, in which bis-ethylhexyloxyphenol methoxyphenyl triazine was added to the water phase, had enhanced ultraviolet protection effect relative to Comparative Example 5, in which bis-ethylhexyloxyphenol methoxyphenyl triazine was added to the oil phase and to Comparative Examples 2 to 4, in which other ultraviolet absorbent was used instead. Additionally, the results reveal that these compositions are superior in formulation stability and feeling on use as well.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-023537 | Feb 2011 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2012/052080 | 1/31/2012 | WO | 00 | 9/5/2013 |
