WO2022215492A1 - Produit cosmétique de revêtement des lèvres - Google Patents
Produit cosmétique de revêtement des lèvres Download PDFInfo
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- WO2022215492A1 WO2022215492A1 PCT/JP2022/012550 JP2022012550W WO2022215492A1 WO 2022215492 A1 WO2022215492 A1 WO 2022215492A1 JP 2022012550 W JP2022012550 W JP 2022012550W WO 2022215492 A1 WO2022215492 A1 WO 2022215492A1
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- Prior art keywords
- cosmetic
- mass
- present
- lip
- phenyl
- Prior art date
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- 239000002537 cosmetic Substances 0.000 title claims abstract description 76
- 239000011248 coating agent Substances 0.000 title abstract description 7
- 238000000576 coating method Methods 0.000 title abstract description 7
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 29
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims abstract description 29
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 29
- 229940008099 dimethicone Drugs 0.000 claims abstract description 26
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 18
- 239000000344 soap Substances 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 7
- 239000008346 aqueous phase Substances 0.000 claims description 4
- 239000002562 thickening agent Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 238000012546 transfer Methods 0.000 abstract description 20
- 238000009472 formulation Methods 0.000 abstract description 6
- 239000003921 oil Substances 0.000 description 16
- 239000012071 phase Substances 0.000 description 14
- 238000011156 evaluation Methods 0.000 description 10
- 239000000839 emulsion Substances 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- CIRIDXMVWMITFK-UHFFFAOYSA-N 11-[methyl-bis(trimethylsilyloxy)silyl]undecanoic acid Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)CCCCCCCCCCC(O)=O CIRIDXMVWMITFK-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 208000025721 COVID-19 Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 208000001528 Coronaviridae Infections Diseases 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- BWURADDOONCTEV-UHFFFAOYSA-N [Zn].OC(=O)CCCCCCCCCC[SiH2]O[SiH2]O[SiH3] Chemical compound [Zn].OC(=O)CCCCCCCCCC[SiH2]O[SiH2]O[SiH3] BWURADDOONCTEV-UHFFFAOYSA-N 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229960001631 carbomer Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940090934 diphenylsiloxy phenyl trimethicone Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- -1 fatty acid salts Chemical class 0.000 description 1
- 239000011737 fluorine Chemical group 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000008384 inner phase Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007934 lip balm Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- PHLASVAENYNAOW-UHFFFAOYSA-N methyl-bis[[methyl(diphenyl)silyl]oxy]-phenylsilane Chemical compound C=1C=CC=CC=1[Si](C)(C=1C=CC=CC=1)O[Si](C=1C=CC=CC=1)(C)O[Si](C)(C=1C=CC=CC=1)C1=CC=CC=C1 PHLASVAENYNAOW-UHFFFAOYSA-N 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000008385 outer phase Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229940057874 phenyl trimethicone Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229940117985 trimethyl pentaphenyl trisiloxane Drugs 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
Classifications
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
Definitions
- the present invention relates to a lip coat cosmetic excellent in transfer resistance. More specifically, it relates to a lip coat cosmetic that exhibits excellent transfer resistance, is glossy, and does not give a feeling of film.
- lip coat cosmetics that impart transfer resistance by coating on top of lipstick etc. It is known to use a "overcoat”).
- Conventional lip coat cosmetics prevent secondary adhesion by blending a film agent or powder with a water-repellent or oil-repellent oil component to form a film layer on the lipstick layer (Patent Document 1). ).
- Such a lip coat cosmetic can suppress secondary adhesion, but cannot avoid feeling like a film after application, and sometimes the finish becomes matte and loses "gloss”.
- Patent Document 2 an oil-based lip coat containing predetermined amounts of methylphenylpolysiloxane, silicic anhydride, and polymethylsilsesquioxane particles each having a predetermined viscosity is excellent in transfer resistance, usability, and stability. It is stated that However, in the oil-based lip coat of Patent Document 2, polymethylsilsesquioxane is the only powder that can be stably blended with methylphenylpolysiloxane used to suppress bleeding.
- An object of the present invention is to provide a lip coat cosmetic of a new formulation that can impart excellent transfer resistance by top coating to lipstick, and can impart luster to the lips without giving a filmy feeling after application. do.
- the present invention (a) 30-99% by weight of non-volatile dimethicone, and (b) A lip coat cosmetic containing 5% by mass or less of metallic soap.
- the lip coat cosmetic of the present invention is an emulsified cosmetic containing (c1) phenyl-modified silicone or (c2) water in addition to (a) non-volatile dimethicone and (b) metallic soap. can be done.
- the lip coat cosmetic of the present invention is excellent in transfer resistance (no secondary adhesion) effect, and is easy to use as a tool with an applicator.
- the lip coat cosmetic of the present invention does not cause the base lipstick to bleed when it is applied over lipstick, and it does not give a filmy feeling after application, does not turn white (does not become white and cloudy), and can give a glossy finish. .
- the lip coat cosmetic of the present invention has an appropriate viscosity, it is easy to remove from the container and does not drip.
- the lip coat cosmetic of the present invention (hereinafter also simply referred to as “cosmetics”) contains (a) non-volatile dimethicone and (b) metallic soap as essential components.
- Non-Volatile Dimethicone used in the cosmetic of the present invention is liquid at room temperature and is a non-volatile linear or branched silicone oil (dimethylpolysiloxane). is.
- Non-volatile as used herein means not exhibiting volatility at normal temperature and normal pressure.
- a non-volatile oil can be defined as an oil having an evaporation rate of less than 0.01 mg/cm 2 /min at normal temperature and pressure, without any particular limitation.
- the (a) non-volatile dimethicone in the present invention is, for example, dimethylpolysiloxane having a degree of polymerization of 6 or more, and optionally part of the trimethylsilyl groups may be substituted with alkyl, alkoxyl, fluorine, or the like.
- phenyl-modified silicones substituted with phenyl groups are not included in (a) non-volatile dimethicone.
- the (a) non-volatile dimethicone used in the cosmetic of the present invention preferably has a viscosity within the range of 100 to 5,000 cs (centistokes) as measured with a Brookfield viscometer at 30°C.
- the amount of (a) nonvolatile dimethicone blended in the cosmetic of the present invention is 30 to 99% by mass, preferably 35 to 90% by mass, based on the total amount of the cosmetic.
- the "metallic soap” blended in the cosmetic of the present invention is generally understood as higher fatty acid salts of non-alkali metals such as calcium, zinc and magnesium.
- carboxysilicone metal salt having a structure represented by the following general formula (1) in the cosmetic of the present invention.
- X is Ra or a group represented by the following formula (2)
- R a and R b are each independently selected from a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a phenyl group, and may be the same or different.
- alkyl groups having 1 to 6 carbon atoms include straight groups such as methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, pentyl, neopentyl, hexyl and cyclopentyl.
- a chain, branched or cyclic alkyl group can be mentioned.
- Each of m and n is an integer of 1 or more and is not particularly limited, but preferably 1, 2 or 3.
- A is a linear or branched alkylene group represented by C q H2 q , where q is an integer of 0-20, preferably 2-10.
- M is a metal atom other than alkali metals, and includes divalent alkaline earth metals and divalent or higher metal atoms. Examples of divalent alkaline earth metals include Mg, Ca, and Ba, and examples of other metal atoms include Mn, Fe, Co, Al, Ni, Cu, V, Mo, Nb, Zn, and Ti. be done.
- the metal atom M in the metal soap (carboxysilicone metal salt) used in the present invention is particularly preferably Ca, Zn, Mg or Al.
- p is an integer of 2 or more corresponding to the valence of the metal atom (M).
- a particularly preferred carboxysilicone in the present invention is 3-(10-carboxydecyl)-1,1,1,3,5,5,5-heptamethyltrisiloxane (hereinafter also referred to as "carboxydecyltrisiloxane”).
- the content of (b) metallic soap in the cosmetic of the present invention is 5% by mass or less, preferably 4% by mass or less, relative to the total amount of the cosmetic. If the amount of the metallic soap exceeds 5% by mass, the viscosity of the cosmetic becomes high and the applicator tends not to stick to it.
- the lower limit of the amount of the metal soap (b) is not particularly limited, but is usually 0.01% by mass or more, preferably 0.05% by mass or more.
- the cosmetic of the present invention preferably has a viscosity of 1 to 14 Pa ⁇ s (Brookfield viscometer) at 30°C of the entire cosmetic. If the viscosity of the cosmetic is less than 1 Pa ⁇ s, it tends to drip from the applicator, and if it exceeds 14 Pa ⁇ s, it tends not to adhere to the applicator.
- the cosmetic of the present invention can contain (c1) phenyl-modified silicone or (c2) water in addition to (a) non-volatile dimethicone and (b) metal soap.
- (c1) phenyl-modified silicone or (c2) water is blended, it can be provided as an oil-in-oil, oil-in-water, or water-in-oil emulsified cosmetic.
- the phenyl-modified silicone in the present invention is a non-volatile silicone oil that is liquid at room temperature and has a structure in which some of the methyl groups of dimethylpolysiloxane (dimethicone) are substituted with phenyl groups.
- phenyl-modified silicone examples include, but are not limited to, phenyltrimethicone, diphenyldimethicone, diphenylsiloxyphenyltrimethicone, and trimethylpentaphenyltrisiloxane.
- the cosmetic containing (c1) phenyl-modified silicone is an oil-in-oil type in which one of (a) non-volatile dimethicone and (c1) phenyl-modified silicone is an external phase (continuous phase) and the other is an internal phase (dispersed phase). It becomes an oily cosmetic.
- the content of (c1) phenyl-modified silicone in the cosmetic of the present invention is 60% by mass or less, preferably 58% by mass or less, relative to the total amount of the cosmetic. If the amount of the phenyl-modified silicone (c1) exceeds 60% by mass, the stability of the emulsion tends to decrease.
- the content of (c2) water in the cosmetic of the present invention is 60% by mass or less, preferably 58% by mass or less, relative to the total amount of the cosmetic.
- (a) non-volatile dimethicone and (c2) water mixing ratio (mass ratio), [(a) / (c2)] 0.5 ⁇ 5.0 in the range of emulsification It is preferable from the viewpoint of stability.
- Aqueous phase thickeners include natural or synthetic organic modified clay minerals such as bentonite, agar, xanthan gum, succinoglycan, carboxyvinyl polymer (carbomer), (dimethylacrylamide/acryloyldimethyltaurate Na) crosspolymer, and the like. can be exemplified.
- the amount of the aqueous phase thickener is not particularly limited as long as the viscosity of the cosmetic is within the above range (1 to 14 Pa ⁇ s at 30°C). Usually, it is 0.05 to 6% by mass, preferably 0.1 to 5% by mass, more preferably 0.5 to 3% by mass, based on the total amount of the cosmetic.
- Silicic anhydride The cosmetic of the present invention preferably further contains (e) silicic anhydride. (e) Addition of silicic anhydride further improves stability. (e) Silicic anhydride is preferably ultrafine silicic anhydride having an average primary particle size of 1 to 50 nm, such as Aerosil 200, 300, R972, R974, RY200 (manufactured by Nippon Aerosil Co., Ltd.). The silicic anhydride used in the present invention may be hydrophilic or hydrophobized by silylation or the like.
- the content of (e) silicic anhydride in the cosmetic of the present invention is 0.5 to 5% by mass, preferably 1 to 4% by mass, based on the total amount of the cosmetic.
- the cosmetic of the present invention may contain other ingredients that are commonly used in lip coat cosmetics as long as they do not impair the effects of the present invention.
- other ingredients include coloring materials, oils (other than silicone oils), powders, dyes, moisturizers, perfumes, surfactants, antioxidants, preservatives, cosmetic ingredients, and the like.
- oils other than silicone oils
- the cosmetics of the present invention also include embodiments in which no hydrocarbon oil is blended.
- the cosmetic of the present invention can be provided as a liquid lip coat (lipstick overcoat), lip balm, or the like.
- a lip coat cosmetic having good usability and excellent transfer resistance and gloss.
- the present invention will be described in more detail below with reference to examples, but the present invention is not limited by these. Unless otherwise specified, the blending amount is shown in % by mass.
- Lip coat cosmetics were prepared according to the usual method with the formulations shown in Tables 2 to 5 below.
- the cosmetics of each example were evaluated for "transfer resistance (secondary adhesion resistance effect)", "ease of use” and “finishing” based on the following methods and criteria.
- "Ease of use” means ease of taking the cosmetic from the container using the applicator (no defects such as dripping due to too low viscosity or sticking to the applicator due to too high viscosity)
- finish means that the lip coat cosmetic does not turn white but is glossy after being applied.
- the viscosity at 30° C. of some cosmetics was measured using a Brookfield viscometer (rotor M4, number of revolutions 12 rpm).
- "-" in the table means unmeasured.
- lip coat cosmetics having formulations shown in Tables 2 to 5 below were applied over the lipstick.
- the application method was a method in which, after applying the cosmetics of each example and each comparative example to the lips, the upper and lower lips were rubbed together and pressure was applied for about 5 seconds. Transfer resistance was evaluated based on the absence of color transfer to the cup. Ease of use was evaluated based on ease of application with the applicator and ease of application with the applicator. The finish was evaluated by a sensory test and visual observation by each specialized panel.
- Evaluation criteria A: Evaluation value (average value) 4.0 or more B: Evaluation value (average value) 3.0 or more and less than 4.0 points C: Evaluation value (average value) less than 3.0 points
- Non-volatile dimethicone is not compatible with the oil commonly used in lipstick, so it can be applied over the lipstick without bleeding the base lipstick, giving it excellent transfer resistance.
- Comparative Example 1-1 containing no metal soap had too low a viscosity and dripped from the applicator and could not be applied. was too high to stick to the applicator and could not be removed from the container with the applicator.
- Examples 2-1 to 2-4 which were oil-in-oil emulsions of (a) nonvolatile dimethicone and (c1) phenyl-modified silicone, were excellent in transfer resistance, ease of use, and finish. .
- Comparative Example 2-1 in which the amount of phenyl-modified silicone was more than 60% by mass, a stable emulsion could not be prepared.
- Examples 3-1 to 3-7 which were water-in-oil emulsions in which (a) non-volatile dimethicone was the outer phase (continuous phase) and (c2) water was the inner phase (dispersed phase), had excellent transfer resistance. demonstrated its versatility and ease of use. However, when the viscosity of the cosmetic exceeds 14 Pa ⁇ s, although the transfer resistance and ease of use are excellent, the cosmetic may become white after application and the finish may deteriorate (data not shown).
- Example 3-8 as an oil-in-water emulsion with water as an external phase (continuous phase) is easier to use than the water-in-oil type Although the hardness and finish were slightly inferior, the properties were sufficiently satisfactory. On the other hand, in Comparative Examples 3-1 and 3-2 containing no metal soap, stable emulsions could not be prepared in either the water-in-oil type or the oil-in-water type.
- Lip coat cosmetics of the present invention were prepared according to the formulations shown in Tables 6 and 7 below.
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- Cosmetics (AREA)
Abstract
La présente invention a pour objet de réaliser un produit cosmétique de revêtement des lèvres qui est une nouvelle formulation capable de fournir une résistance de transfert supérieure supplémentaire lorsqu'il est utilisé en tant que couche de finition pour un rouge à lèvres, et capable de conférer un brillant aux lèvres sans laisser une sensation de revêtement sur les lèvres après application. La présente invention concerne un produit cosmétique de revêtement des lèvres caractérisé en ce qu'il contient (a) de 30 à 99 % en masse de diméthicone non volatile, et (b) au plus 5 % en masse d'un savon métallique. Le produit cosmétique de revêtement des lèvres selon la présente invention peut être transformé en un produit cosmétique de type émulsion qui contient (c1) une silicone modifiée par un phényle ou (c2) de l'eau, ainsi que (a) la diméthicone non volatile et (b) le savon métallique.
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JP2023512903A JPWO2022215492A1 (fr) | 2021-04-06 | 2022-03-18 |
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JP2021-064827 | 2021-04-06 | ||
JP2021064827 | 2021-04-06 |
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WO2022215492A1 true WO2022215492A1 (fr) | 2022-10-13 |
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PCT/JP2022/012550 WO2022215492A1 (fr) | 2021-04-06 | 2022-03-18 | Produit cosmétique de revêtement des lèvres |
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JP (1) | JPWO2022215492A1 (fr) |
WO (1) | WO2022215492A1 (fr) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5470437A (en) * | 1977-11-16 | 1979-06-06 | Kobayashi Kose Co | Lip overcoat |
JPH07316016A (ja) * | 1994-05-25 | 1995-12-05 | Shiseido Co Ltd | 口紅オーバーコート |
JPH0881335A (ja) * | 1994-09-13 | 1996-03-26 | Kanebo Ltd | 油性リップコート |
JPH08183715A (ja) * | 1994-12-28 | 1996-07-16 | Shiseido Co Ltd | 水中油乳化型リップオーバーコート |
JP2002138017A (ja) * | 2000-10-30 | 2002-05-14 | Kose Corp | 油性化粧料 |
JP2016132650A (ja) * | 2015-01-21 | 2016-07-25 | 株式会社 資生堂 | メーキャップ化粧料 |
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2022
- 2022-03-18 WO PCT/JP2022/012550 patent/WO2022215492A1/fr active Application Filing
- 2022-03-18 JP JP2023512903A patent/JPWO2022215492A1/ja active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5470437A (en) * | 1977-11-16 | 1979-06-06 | Kobayashi Kose Co | Lip overcoat |
JPH07316016A (ja) * | 1994-05-25 | 1995-12-05 | Shiseido Co Ltd | 口紅オーバーコート |
JPH0881335A (ja) * | 1994-09-13 | 1996-03-26 | Kanebo Ltd | 油性リップコート |
JPH08183715A (ja) * | 1994-12-28 | 1996-07-16 | Shiseido Co Ltd | 水中油乳化型リップオーバーコート |
JP2002138017A (ja) * | 2000-10-30 | 2002-05-14 | Kose Corp | 油性化粧料 |
JP2016132650A (ja) * | 2015-01-21 | 2016-07-25 | 株式会社 資生堂 | メーキャップ化粧料 |
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JPWO2022215492A1 (fr) | 2022-10-13 |
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