Two-component cosmetic
11147750 · 2021-10-19
Assignee
Inventors
Cpc classification
International classification
Abstract
The purpose of the present invention is to provide a two-component cosmetic which, when a first formulation and a second formulation are sequentially applied, forms a uniform gel film on the skin while imparting a feeling of moisture permeating the skin, thereby providing an ideal skin feel. The present invention pertains to a two-component cosmetic containing: (1) a first formulation containing a gel formation-promoting substance; and (2) a second formulation containing a gel-forming substance. The two-component cosmetic is characterized in that the first formulation is applied to the skin, and then the second formulation is applied thereto.
Claims
1. A method for providing human skin with a barrier having an occlusive effect on moisture evaporation, comprising the ordered steps of: (1) applying to the skin a first component, which comprises a first substance consisting of a metal ion selected from the group consisting of Na.sup.+, K.sup.+, Ca.sup.2+, Mg.sup.2+ and Al.sup.3+; and (2) applying to the skin, over the first component, a second component, which comprises a second substance consisting of a water-soluble polymer selected from the group consisting of soluble alginate and gellan gum; whereby a barrier having an occlusive effect on moisture evaporation is formed on the skin.
2. The method of claim 1, wherein: the first substance is Ca.sup.2+ or Mg.sup.2+, and the second substance is a soluble alginate.
3. The method of claim 1, wherein: the first substance is Ca.sup.2+ or Mg.sup.2+, and the second substance is gellan gum.
Description
BRIEF DESCRIPTION OF DRAWINGS
(1)
(2)
(3)
(4)
DESCRIPTION OF EMBODIMENTS
(5) The two-component cosmetic of the present invention includes (1) a first component containing a gel formation promoting substance and (2) a second component containing a gel-forming substance.
(6) The “gel-forming substance” in the present invention means a substance which can be brought into contact with the “gel formation promoting substance” to thereby form gel. For example, “the state where a large amount of a solvent is included in a polymer network” is called “gel” in the cosmetic field (Japanese Patent Office, “Standard Techniques”, “Perfume”, 2007). Such gel can be classified to hydrogel with water as a solvent, oil gel with an organic solvent as a solvent, and xerogel with gas as a solvent. The gel in the present invention is preferably hydrogel (polymer hydrogel).
(7) The “polymer hydrogel” can be defined as gel which has a three-dimensional network structure (polymer network) formed by mutual connection of a plurality of polymers at crosslinking points, and which includes water or an aqueous medium as a solvent.
(8) A mechanism for gel formation by a polymer is considered to involve forming a network structure by mere entanglement of polymer chains or forming a network structure by partial binding (crosslinking) of polymer chains. Examples of factors for crosslinking of polymer chains include a covalent bond, an ionic bond, a coordination bond and a hydrogen bond by a crosslinking agent. Gel is then classified to chemical gel and physical gel depending on the crosslinking system (for example, Fumihiko TANAKA, “Polymer Physics”, pages 91 to 97, issued by Shokabo, 2004,). The chemical gel refers to gel where a crosslinking point is formed by a covalent bond, and the physical gel refers to gel where crosslinking is formed by an ionic bond, a coordination bond, a hydrogen bond, or any intermolecular interaction such as an electrostatic force.
(9) The gel in the present invention is crosslinked gel, preferably physical gel, and is desirably obtained by an ionic bond, a coordination bond, or a hydrogen bond as a crosslinking factor (gelling factor). That is, the gel in the present invention is gel obtained by gelling due to formation of crosslinking by mixing the first component and the second component, thus is in the state of being a gel dispersion where gelling partially progresses in macroscopic observation of a mixture, and is applied to thereby provide a uniform gel film.
(10) The “gel” is herein defined as the above-defined polymer hydrogel (preferably physical gel) in which crosslinking is formed by mixing of the first component and the second component and the viscosity as measured according to the following measurement method is 400 cps or more.
(11) (Measurement Method)
(12) 25 g of the first component and 25 g of the second component are weighed and placed in a 100-mL container, and mixed by use of a handy mixer for 10 seconds and then transferred to a 50-mL container, and the viscosity is measured by use of a B-type viscometer at 30° C.
(13) While “gel”, “jelly”, and the like are used as terms expressing the form of a cosmetic product, one satisfying the above viscosity condition is encompassed in the “gel” in the present invention.
(14) It, however, goes without saying that a system where no crosslinking is formed by mixing of the first component and the second component, for example, a system where the first component is water and the second component is an aqueous water-soluble polymer solution (chemical gel) are not encompassed in the “gel” in the present invention even in the case where a mixture of both the components has a viscosity of 400 cps or more.
(15) The “substance that forms a gel (gel-forming substance)” in the present invention is a substance which is to be brought into contact with the “substance that promotes a gel formation (gel formation promoting substance)” described below and thus gelled. A representative example of a gel-forming substance for formation of a hydrogel is a water-soluble polymer which is a substance serving as a main agent of a network structure for gelling.
(16) The water-soluble polymer preferably used in the present invention is not particularly limited, and is selected from a synthetic or natural water-soluble polymer which can be used for cosmetics and which can interact with a gel formation promoting substance to thereby form a crosslinking point and thus form a three-dimensional network structure.
(17) Specific examples include a carboxy vinyl polymer, a (meth)acrylic acid polymer, gellan gum, alginic acid, carrageenan, pectin, xanthan gum, locust bean gum, and tamarind seed gum.
(18) The “gel formation promoting substance” in the present invention is a substance which generates gelling of the gel-forming substance. That is, in the case where the gel-forming substance is a water-soluble polymer, the substance is a substance which can form a crosslinking point for binding of the polymer chain.
(19) For example, in the case where the water-soluble polymer is a polymer having a carboxyl group, such as a carboxy vinyl polymer or a (meth)acrylic acid polymer, the gel formation promoting substance is a substance which can allow for crosslinking by a hydrogen bond or an ionic bond, for example, polyethylene glycol or a di- or higher valent cation.
(20) In the case where the gel-forming substance (water-soluble polymer) is gellan gum, alginic acid, carrageenan, or LM pectin, the gel formation promoting substance is a cationic substance such as a metal ion. The metal ion is preferably a metal cation selected from the group consisting of Na.sup.+, K.sup.+, Ca.sup.2+, Mg.sup.2+ and Al.sup.3+, and among them, particularly preferably a mono- or divalent metal cation.
(21) Such a metal cation is not particularly limited in terms of the source thereof, and can be contained in the form of halide, nitrate, sulfate, lactate, or the like. Such a metal cation, which is contained in the first component, in the form of a salt type agent such as Na 4-methoxysalicylate, and which is released from the salt type agent, can also be adopted as the gel formation promoting substance. The salt type agent here used is not particularly limited as long as it is a water-soluble agent which can be taken together with the metal cation to form a salt and which can be usually contained in a cosmetic or the like. Examples include salts of L-ascorbic acid and a derivative thereof, salts of tranexamic acid and a derivative thereof, salts of alkoxysalicylic acid and a derivative thereof, and salts of glutathione and a derivative thereof.
(22) Examples of the L-ascorbic acid derivative include L-ascorbic acid monoesters such as L-ascorbic acid monophosphate and L-ascorbic acid-2-sulfate; L-ascorbic acid triesters such as L-ascorbic acid triphosphate; and L-ascorbic acid glucosides such as L-ascorbic acid2-glucoside.
(23) Examples of the tranexamic acid derivative include dimers of tranexamic acid (for example, trans-4-(trans-aminomethylcyclohexanecarbonyl)aminomethylcyclohexanecarboxylic acid hydrochloride), esters of tranexamic acid and hydroquinone (for example, 4-(trans-aminomethylcyclohexanecarboxylic acid 4′-hydroxyphenyl ester), esters of tranexamic acid and gentisic acid (for example, 2-(trans-4-aminomethylcyclohexylcarbonyloxy)-5-hydroxybenzoic acid), and amides of tranexamic acid (for example, trans-4-aminomethylcyclohexanecarboxylic acid methylamide, trans-4-(p-methoxybenzoyl)aminomethylcyclohexanecarboxylic acid, and trans-4-guanidinomethylcyclohexanecarboxylic acid).
(24) Alkoxysalicylic acid is obtained by substituting any hydrogen atom of salicylic acid at the 3-, 4-, or 5-position with an alkoxy group, and such an alkoxy group as a substituent is preferably any of a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, and an isobutoxy group, further preferably a methoxy group or an ethoxy group. Specific examples include 3-methoxysalicylic acid, 3-ethoxysalicylic acid, 4-methoxysalicylic acid, 4-ethoxysalicylic acid, 4-propoxysalicylic acid, 4-isopropoxysalicylic acid, 4-butoxysalicylic acid, 5-methoxysalicylic acid, 5-ethoxysalicylic acid, and 5-propoxysalicylic acid.
(25) The salt of the salt type agent described above is not particularly limited, and examples include not only alkali metal salts or alkali earth metal salts such as a sodium salt, a potassium salt, a calcium salt, and a magnesium salt, but also salts such as an ammonium salt and an amino acid salt.
(26) A polysaccharide polymer such as gellan gum or carrageenan is considered to be gelled by forming a spiral structure from each polysaccharide polymer randomly present and then forming steric network structure and binding region.
(27) The content of gellan gum as the gel-forming substance of the second component is preferably 0.1 to 1.0% by mass, more preferably 0.2 to 0.7% by mass, and the content of the cationic substance as the gel formation promoting substance of the first component is preferably 0.01 to 3% by mass, more preferably 0.05 to 1% by mass, from the viewpoint that favorable gel formation and an excellent occlusion effect are achieved.
(28) While alginic acid by itself is insoluble in water, an alkali metal salt such as a sodium salt, an ammonium salt, an organic amine salt, and the like (hereinafter “sodium salt and the like”) are soluble in water. Sodium alginate or the like in an aqueous solution, which is dissociated as an alginic acid ion, generates calcium alginate by addition of any ion of a divalent metal (alkali earth metal) such as calcium or magnesium, thereby allowing for the occurrence of gelling. That is, it is considered that such a divalent metal ion promotes association of alginic acid molecules to form a steric structure, and a structure where such an ion serves as a bridge to bind molecules is called egg-box.
(29) The content of sodium alginate in the second component is preferably 0.1 to 5% by mass, more preferably 0.3 to 2% by mass, and the content of the cationic substance (calcium salt) as the gel formation promoting substance in the first component is preferably 0.1 to 5% by mass, from the viewpoint that favorable gel formation and an excellent occlusion effect are achieved.
(30) In the case where the gel-forming substance (water-soluble polymer) is xanthan gum, the gel formation promoting substance can be locust bean gum, or, on the contrary, a case can also be adopted where the gel-forming substance is locust bean gum and the gel formation promoting substance is xanthan gum. It is considered that such a system allows for gel formation due to intermolecular interaction.
(31) The ratio (weight ratio) of the contents of xanthan gum to locust beam gum is preferably 2:8 to 8:2, more preferably 4:6 to 6:4, from the viewpoint that favorable gel formation and an excellent occlusion effect are achieved.
(32) In the case where the gel-forming substance (water-soluble polymer) is tamarind seed gum, it is considered that a reduction in moisture activity due to the presence of a sugar or an alcohol as the gel formation promoting substance and a reduction in electric repulsion in an acidic condition with an acid allow gelling to occur due to association of molecules by a hydrogen bond. The gel formation promoting substance is suitably ethanol, concentrated glycerin, 1,3-butylene glycol, dipropylene glycol, sorbit, or the like, and the content of such each substance is preferably 5 to 35% by mass, more preferably 10 to 30% by mass.
(33) The pectin for use as the gel-forming substance (water-soluble polymer) is classified to HM (high methoxylated) pectin having a degree of esterification of 50% or more and LM (low methoxylated) pectin having a degree of esterification of less than 50%, and the gel formation promoting substance corresponding to HM pectin is an acid and the gel formation promoting substance corresponding to LM pectin is a divalent metal ion such as a calcium ion.
(34) The first component in the two-component cosmetic of the present invention contains the gel formation promoting substance and is preferably formulated to include no gel-forming substance so that no gelling occurs before application to the skin. On the contrary, the second component is preferably formulated not to contain any substance for promotion of gelling of the gel-forming substance contained, for example, a metal ion.
(35) The two-component cosmetic of the present invention is preferably in the form of an aqueous composition including the first component and the second component. An aqueous composition means a composition which includes 50% by mass or more of an aqueous cosmetic ingredient based on the total weight of the composition and which is in the form of an aqueous solution, an oil-in-water emulsion, or the like.
(36) The two-component cosmetic of the present invention allows an ideal skin feeling to be realized by applying (1) a first component containing a gel formation promoting substance, to the skin, and then applying (2) a second component containing a gel-forming substance, onto the first component, thereby imparting moist feeling and elasticity to the skin.
(37) The first component is usually applied to the skin immediately after washing, to impart a fresh moist feeling, and thus is preferably in the form of a composition having a low viscosity (for example, 100 mPa.Math.s or less), for example, a lotion or an emulsion. A cosmetic ingredient which increases a penetration feeling to the skin and improves comfortability to the skin is also preferably contained therein. Accordingly, the first component preferably contains a moisturizing agent, a lower alcohol, an oil content, a surfactant, and the like. On the other hand, it is preferable that a film forming agent such as polyvinyl alcohol is not contained or the content thereof is minimized (for example, about 1% by mass or less).
(38) The moisturizing agent may be any ingredient applicable for skincare cosmetics and the like, and examples include polyhydric alcohols such as glycerin, dipropylene glycol, 1,3-butylene glycol and polyethylene glycol, sugars such as erythritol, trehalose and sorbitol, and polysaccharides such as hyaluronic acid.
(39) The oil content is polar oil, non-polar oil, silicone oil, or the like, and examples include polar oil such as glyceryl tri-2-ethylhexanoate, non-polar oil such as an α-olefin oligomer, and silicone oil such as methylpolysiloxane.
(40) The surfactant which can be contained is a nonionic surfactant, an ionic surfactant, an amphoteric surfactant, or the like, and examples include nonionic surfactants such as polyoxyethylene hydrogenated castor oil, ionic surfactants such as N-stearoyl-N-methyl taurine sodium, and amphoteric surfactants such as N-lauryldimethylaminoacetic acid betaine.
(41) The second component that is applied onto the skin to which the first component is applied, forms a gel film on the skin to impart tension, elasticity, plump feeling, and the like. The form of the second component is not particularly limited, and the second component can be in the form of a composition having viscous properties depending on the application form (for example, a viscosity of about 1 to 100,000 mPa.Math.s, preferably 1 to 10,000 mPa.Math.s), for example, a mist lotion, an emulsion or a cream. The second component may contain a film forming agent, such as polyvinyl alcohol, which can impart tension feeling. Furthermore, the second component may contain a moisturizing agent for enhancing moisturization effect, an oily ingredient for supplying the skin with an oil content, and also the surfactant together. A thickener for adjusting the viscosity of the second component may also be additionally contained.
(42) The moisturizing agent may be any applicable agent for skincare cosmetics and the like, and examples include polyhydric alcohols such as glycerin, dipropylene glycol (DPG), 1,3-butylene glycol (BG) and polyethylene glycol, sugars such as erythritol, trehalose and sorbitol, and polysaccharides such as hyaluronic acid.
(43) The oily ingredient (oil content) is polar oil, non-polar oil, silicone oil, or the like, and examples include polar oil such as glyceryl tri-2-ethylhexanoate, non-polar oil such as an α-olefin oligomer, and silicone oil such as methylpolysiloxane.
(44) It is noted that, even if the content of the gel-forming substance in the entire preparation is constant, an increase in the content of the oil content in the preparation may naturally decrease the amount of moisture, resulting in an increase in the concentration of the gel-forming substance in an aqueous phase and progression of gelling to thereby cause a hard film to be formed. Thus, the amount of the oil content contained, such as non-volatile hydrocarbon oil (for example, liquid paraffin), is preferably less than 15% by mass, more preferably less than 10% by mass, further preferably less than 5% by mass.
(45) The surfactant which can be contained is a nonionic surfactant, an ionic surfactant, an amphoteric surfactant, or the like, and examples include nonionic surfactants such as polyoxyethylene hydrogenated castor oil, ionic surfactants such as N-stearoyl-N-methyl taurine sodium, and amphoteric surfactants such as N-lauryldimethylaminoacetic acid betaine.
(46) The two-component cosmetic of the present invention is particularly suitable as a skin-care cosmetic which enables an ideal skin feel to be actually felt by spreading the first component and then spreading the second component, but is not limited thereto and can also be provided as a sun-care cosmetic, a haircare cosmetic, a makeup cosmetic, or the like which is excellent in moisture retention (occlusion effect).
(47) Any other ingredient which a cosmetic, in particular, a skincare cosmetic or the like can contain may be arbitrarily contained in the two-component cosmetic of the present invention as long as the effect of the present invention is not impaired. Examples of such any other ingredient include an antioxidant, a preservative agent, an ultraviolet absorber, a powdery ingredient, and various agents (skin-whitening agent, skin quality improver, and the like), but are not limited thereto.
(48) The forms of the containers and the application forms of the first component and the second component are not particularly limited. For example, a common form of a cosmetic container, such as a dispenser container, an aerosol container, or a jar container can be arbitrarily adopted. Any application form (application method) can also be adopted, for example, common application by hand (application by fingers), application by cotton, or spraying by mist or the like.
EXAMPLES
(49) Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not intended to be limited to such Examples at all. The content of any ingredient is expressed by “% by mass” based on the total amount of any composition in which such an ingredient is contained, unless specifically noted.
(50) (Example 1)
(51) A first component (lotion) was prepared in a formulation presented in Table 1 below, and a second component (emulsion) was prepared in a formulation presented in Table 2 below.
(52) TABLE-US-00001 TABLE 1 Ingredient Content (%) Ion exchanged water Balance Ethanol 7 Concentrated glycerin 8 Dipropylene glycol 7 1,3-Butylene glycol 4 Polyoxyethylene methyl glucoside 0.5 Polyethylene glycol 1000 1 Erythritol 0.1 Trehalose 1 Magnesium chloride 0.03 Sodium chloride 1 Polyoxyethylene (14) polyoxypropylene (7) dimethyl ether 3 Polyoxyethylene polyoxypropylene 2-diethyl tetradecyl 0.2 ether Sodium lactate 0.4 Trisodium ethylenediaminetetraacetate 0.03 Phenoxyethanol 0.5 Perfume q.s. Total 100
(53) TABLE-US-00002 TABLE 2 Ingredient Content (%) Ion exchanged water Balance Ethanol 2 Concentrated glycerin 4 Dipropylene glycol 5 Polyvinyl alcohol 0.1 Polyoxyethylene hydrogenated castor oil (60E.O.) 0.1 Acrylic acid/alkyl methacrylate copolymer 0.05 Carboxy vinyl polymer 0.1 Xanthan gum 0.05 Gellan gum 0.4 Potassium hydroxide 0.05 α-Olefin oligomer 3 Pentaerythrityl tetra2-ethylhexanoate 1 Macadamia nut oil fatty acid phytosteryl 0.3 Di(phytosteryl/2-octyldodecyl) N-lauroyl-L-glutamate 1 Polybutene 1 Phenoxyethanol 0.5 Sodium metaphosphate 0.03 Perfume q.s. Total 100
(54) The first component and the second component were applied to evaluate the ability of retention of moisture on the skin surface (occlusion ability) and the surface roughness of a formed gel film, with respect to the respective applications when (1) the first component was first applied and next, the second component, (2) the second component was first applied and next, the first component, and case (3) the first component and the second component were pre-mixed in advance and the resulting mixture was applied.
(55) <Evaluation of Occlusion Ability>
(56) (1) A paper filter to which the first component is first applied and then the second component is applied (Paper Sample (1)), (2) a paper filter to which the second component is first applied and then the first component is applied (Paper Sample (2)), and (3) a paper filter to which a mixture, prepared in advance, of the first component and the second component is applied (Paper Sample (3)), were prepared (each component amount: 5 μL/cm.sup.2). Each of the paper filters was sandwiched between a vial bottle charged with a constant amount of water and a punctured lid, and the evaporation amount of moisture was measured over time to evaluate the occlusion ability based on the amount of moisture decreased. The results are illustrated in
(57) It was revealed from the results represented in
(58) <Evaluation of Smoothness of Applied Film>
(59) Each of applied films, (1) an applied film obtained by application of the first component and then application of the second component (Film Sample (1)), (2) an applied film obtained by application of the second component and then application of the first component (Film Sample (2)), and (3) an applied film obtained by application of a sample obtained by pre-mixture of the first component and the second component in advance (Film Sample (1)), was produced on a glass plate by use of a doctor blade (75 μm), and dried at room temperature overnight, and the surface roughness Ra was measured using a laser microscope. The results are illustrated in
(60) As illustrated in
(61) <Usability Test>
(62) The skin texture after first application of the first component and subsequent application of the second component was evaluated according to sensory evaluation by twelve healthy female panelists and was rated according to the following criteria.
(63) 5: very excellent skin texture
(64) 4: excellent skin texture
(65) 3: moderate
(66) 2: no excellent skin texture
(67) 1: no excellent skin texture at all
(68) The rating results obtained (average value at N=12) are illustrated in
(69) (Example 2)
(70) A first component (lotion) was prepared in a formulation presented in Table 3 below, and a second component (emulsion) was prepared in a formulation presented in Table 4 below.
(71) TABLE-US-00003 TABLE 3 Ingredient Content (%) Ion exchanged water Balance Concentrated glycerin 4 1,3-Butylene glycol 7 Dipropylene glycol 4 Polyoxyethylene (14) polyoxypropylene (7) dimethyl ether 1 Carboxymethylcellulose sodium 0.1 Polyoxyethylene hydrogenated castor oil 0.15 Polyglyceryl diisostearate 0.1 Poly(oxyethylene/oxypropylene) methylpolysiloxane 0.5 copolymer Isostearyl alcohol 0.2 Methylphenylpolysiloxane 0.15 Magnesium chloride 0.1 Calcium chloride 0.2 Lactic acid 0.04 Sodium lactate 0.35 Sodium metaphosphate 0.01 Phenoxyethanol 0.5 Perfume q.s. Total 100
(72) TABLE-US-00004 TABLE 4 Ingredient Content (%) Ion exchanged water Balance Ethanol 1.5 Concentrated glycerin 5 Dipropylene glycol 3 Diglycerin 0.3 Xylitol 0.2 Polyoxyethylene (17) polyoxypropylene (4) dimethyl ether 0.2 Gellan gum 0.5 Potassium hydroxide 0.02 Polyoxyethylene glyceryl isostearate 0.3 Polyoxyethylene/methylpolysiloxane copolymer 0.3 Behenyl alcohol 2 Batyl alcohol 0.6 Behenic acid 0.2 Glyceryl tri-2-ethylhexanoate 1 Di(phytosteryl/2-octyldodecyl) N-lauroyl-L-glutamate 0.1 Myristyl myristate 0.2 Methylphenylpolysiloxane 1 Methylpolysiloxane 3 Citric acid 0.01 Sodium citrate 0.04 Disodium edetate 0.01 Phenoxyethanol 0.4 Methylparaben 0.1 Perfume q.s. Total 100
(73) The first component described in Table 3 and the second component described in Table 4 were used to evaluate the ability of retention of moisture on the skin surface (occlusion ability) by the same method as in Example 1, with respect to a filter paper (1) to which only the first component was applied, a filter paper (2) to which a pre-mixture of the first component and the second component in advance was applied, and a filter paper (3) to which the first component was first applied and the second component was then applied. The results are illustrated in
(74) It was confirmed from the results illustrated in
(75) (Example 3)
(76) A first component (lotion) was prepared in a formulation presented in Table 5 below, and a second component (emulsion) was prepared in a formulation presented in Table 6 below.
(77) TABLE-US-00005 TABLE 5 Ingredient Content (%) Ion exchanged water Balance Ethanol 7 Concentrated glycerin 8 1,3-Butylene glycol 4 Polyoxyethylene methyl glucoside 0.2 Polyethylene glycol 1500 1 Erythritol 0.05 Trehalose 0.5 Magnesium chloride 0.02 Calcium chloride 0.02 Sodium chloride 0.5 Polyoxyethylene (14) polyoxypropylene (7) dimethyl ether 3 Polyoxyethylene polyoxypropylene decyl tetradecyl ether 0.2 Sodium lactate 0.1 Trisodium edetate 0.02 Phenoxyethanol 0.5 Perfume q.s. Total 100
(78) TABLE-US-00006 TABLE 6 Ingredient Content (%) Ion exchanged water Balance Ethanol 5 Concentrated glycerin 6 1,3-Butylene glycol 6 Xanthan gum 0.2 Hydrophobically modified alkyl cellulose 0.1 Gellan gum 0.4 Polyoxyethylene behenyl ether 1 PEG/PPG-14/7-dimethyl ether 2 Behenyl alcohol 1 Stearyl alcohol 0.2 Caprylyl methicone 5 Methylpolysiloxane 2 Decamethyltetrasiloxane 10 Isostearic acid 0.1 Octyl methoxycinnamate 3 Octocrylene 5 Oxybenzone 2 Citric acid 0.05 Sodium citrate 0.15 Disodium edetate 0.1 Hydrophobized zinc oxide 10 Total 100
(79) The first component and the second component described in Tables 5 and 6 were used to evaluate the ability of retention of moisture on the skin surface (occlusion ability) by the same method as in Example 2.
(80) As a result, it could be confirmed, as in Example 2, that the filter paper (3) of application of the first component and the application of the second component provided a significantly low moisture evaporation rate constant and an extremely high occlusion ability as compared with other two filter papers (1) and (2).
(81) (Example 4)
(82) A second component (lotion) having a low viscosity was prepared in a formulation presented in Table 7 below. When the second component is paired with the first component (lotion) described in Table 1, 3 or 5, both of the first component and the second component of the resultant two-component cosmetic become applicable by spraying as a mist.
(83) TABLE-US-00007 TABLE 7 Ingredient Content (%) Ion exchanged water Balance Concentrated glycerin 4 Diglycerin 1 Dipropylene glycol 6 Trehalose 3 Gellan gum 0.5 Disodium edetate 0.01 Phenoxyethanol 0.4 Citric acid 0.01 Sodium citrate 0.04 Total 100
(84) (Example 5)
(85) A first component (lotion) was prepared in a formulation presented in Table 8 below, and a second component (lotion) was prepared in a formulation presented in Table 9 below.
(86) TABLE-US-00008 TABLE 8 Ingredient Content (%) Water Balance Ethanol 3 Glycerin 4 DPG 9 BG 1 PEG-6, PEG-32 3 PEG/PPG-14/7dimethyl ether 3 PEG/polybutylene glycol-44/15 methyl ether hydrogenated 0.4 dimer dilinoleyl Ca chloride 0.2 Mg chloride 0.1 Na lactate 0.4 EDTA-2Na 0.01 Phenoxyethanol 0.5 Perfume 0.01 Total 100
(87) TABLE-US-00009 TABLE 9 Ingredient Content (%) Water Balance Ethanol 4 Glycerin 3 DPG 4 Trehalose 3 PEG-8 1 PEG/polybutylene glycol-44/15 methyl ether hydrogenated 0.025 dimer dilinoleyl Gellan gum 0.2 Xanthan gum 0.04 Citric acid 0.01 Na citrate 0.09 Phenoxyethanol 0.3 Methylparaben 0.15 Na metaphosphate 0.01 Perfume 0.01 Total 100
(88) When the first component (lotion) described in Table 8 and the second component (lotion) having a formula presented in Table 9 were paired, and respective mists of the first component and the second component were sprayed (in order), gelation took place on the skin, while providing excellent use feeling and moisturizing effect.
(89) (Example 6)
(90) A two-component cosmetic was prepared where Na alginate was used as a gel-forming substance to be contained in a second component and a divalent metal ion was used as a gel formation promoting substance to be contained in a first component.
(91) Sample 1-1 (including calcium chloride and magnesium chloride) and Sample 1-2 (including no divalent metal) were prepared in each formulation presented in Table 10 below, and Sample 1-1 and Sample 1-2 were mixed in proper amounts to produce a variety of the first components having a different concentration of divalent metal ion.
(92) Sample 2-1 (including Na alginate) and Sample 2-2 (including no Na alginate) were prepared in the same manner in each formulation presented in Table 11 below, and Sample 2-1 and Sample 2-2 were mixed in proper amounts to produce a variety of the second components having a different concentration of Na alginate.
(93) TABLE-US-00010 TABLE 10 Ingredient Sample 1-1 Sample 1-2 Ion exchanged water 72.587 75.587 Common alcohol 95% 3 3 Dynamite glycerin 4 4 Dipropylene glycol 9 9 1,3-Butylene glycol 1 1 Polyethylene glycol 1500 3 3 Polyoxyethylene (14) polyoxypropylene (7) 3 3 dimethyl ether Polyoxybutylene (15) polyoxyethylene (44) 0.4 0.4 dimethyl dimer diol ether Calcium chloride 2 — Magnesium chloride 1 — Sakihira mineral water 0.1 0.1 Lactic acid 0.003 0.003 Sodium lactate liquid (50%) 0.4 0.4 EDTA-2Na—2H2O 0.01 0.01 Phenoxyethanol 0.3 0.3 Methylparaben 0.15 0.15 Perfume 0.05 0.05
(94) TABLE-US-00011 TABLE 11 Sample 2-1 Sample 2-2 Ion exchanged water 81.7575 83.7575 Common alcohol 4 4 Dynamite glycerin 3 3 Diglycerin 0.5 0.5 Dipropylene glycol 4 4 Trehalose 3 3 PEG-400 1 1 Polyoxybutylene (15) polyoxyethylene (44) 0.025 0.025 dimethyl dimer diol ether Na alginate 2 — Carboxymethylcellulose sodium 0.05 0.05 Sakihira mineral water 0.1 0.1 Citric acid (food) 0.01 0.01 Sodium citrate 0.09 0.09 Phenoxyethanol 0.3 0.3 Methylparaben 0.15 0.15 Sodium hexametaphosphate (first grade 0.01 0.01 reagent) Perfume 0.0075 0.0075
(95) When the concentration of each divalent metal cation included in the first component and the concentration of Na alginate included in the second component were changed, the occurrence of gelling and the appearance upon mixing of the first component and the second component were evaluated.
(96) It was confirmed in the present Example that, when the concentration of each divalent metal cation in the first component was 0.1 to 5% by mass and the concentration of Na alginate in the second component was 0.1 to 5% by mass, gel formation was favorably made, and in particular, when the concentration of Na alginate was 0.3 to 2% by mass, gel further enhanced in uniformity was formed. On the other hand, when the concentration(s) of Na alginate and/or each divalent metal cation was/were more than 5% by mass, the problems of high stickiness and deterioration in use feeling were caused in some cases.