CN113727693A - Composition for cleaning and/or removing make-up from keratin materials - Google Patents

Composition for cleaning and/or removing make-up from keratin materials Download PDF

Info

Publication number
CN113727693A
CN113727693A CN201980095624.7A CN201980095624A CN113727693A CN 113727693 A CN113727693 A CN 113727693A CN 201980095624 A CN201980095624 A CN 201980095624A CN 113727693 A CN113727693 A CN 113727693A
Authority
CN
China
Prior art keywords
group
composition
alkyl
composition according
glucoside
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201980095624.7A
Other languages
Chinese (zh)
Inventor
沈頔
李琳珊
胡璠
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOreal SA
Original Assignee
LOreal SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LOreal SA filed Critical LOreal SA
Publication of CN113727693A publication Critical patent/CN113727693A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/14Preparations for removing make-up
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)

Abstract

Composition for cleansing and/or removing make-up from keratin materials, comprising a) at least one anionic surfactant chosen from dialkyl sulfosuccinates; and b) at least one nonionic surfactant selected from alkylpolyglycosides of formula (I): R-O-Gx’(I) Wherein R is C6‑C40Alkyl, G is a moiety derived from a reducing sugar containing from 5 to 6 carbon atoms, and X' is the average degree of polymerization of an alkylpolyglycoside of from 1 to 10.

Description

Composition for cleaning and/or removing make-up from keratin materials
Technical Field
The present invention relates to cosmetic compositions. More particularly, the present invention relates to a composition for cleansing and/or removing makeup from keratin materials. The invention also relates to a method for cleaning and/or removing makeup from keratin materials.
Background
Cleansing the skin and removing color cosmetics from the skin are very important for skin care. In particular, it is very important for consumers of cosmetic products to have an effective makeup remover. It must be as effective as possible, since greasy residues (e.g. dirt, excess sebum), residues of cosmetic and make-up products in daily use (especially water-repellent products) accumulate in the skin folds and can block the skin pores, leading to the appearance of spots.
Several types of makeup removal or cleansing products are known, such as flushable cleansing anhydrous oils and gels, solid makeup removers, or dual phase makeup removers and wipe-type makeup removers.
Flushable anhydrous oils and gels have a make-up removal effect by virtue of the oils present in these formulations. These oils make it possible to dissolve the fatty residues and to disperse the cosmetic pigments. These products are effective and well tolerated. However, they exhibit the disadvantages of being massive and not imparting a fresh feel upon application, which is disadvantageous from a cosmetic point of view.
Two-phase makeup removers are effective, but are inconvenient to use because shaking is required before each use, and the two phases are consumed at different rates.
The makeup remover leaves a fresh feeling, but is inefficient. Cleansing milks are also considered inefficient. Balms/creams have a greasy feel, are not suitable for use in the eye region and are not hygienic. The wipe-type makeup remover is convenient but inefficient against water-repellent makeup and is not hygienic.
In the field of make-up removing compositions, "soft solid" compositions constitute a class of products which are appreciated by consumers for their cleansing efficacy, make-up removing ability, rinsing ability, and their cosmetic qualities (softness, dry feel, ease of use, etc.). They are known as solid compositions which soften under stress, such as by spreading on the skin surface or, for example, by extrusion from a device with perforated walls (a grid). Some known soft solid compositions useful for cleansing the skin and/or removing makeup comprise silica aerogel particles, a wax, a hydrocarbon-based oil, and a nonionic surfactant. However, it is difficult to apply the soft solid composition to the skin.
Today, cleansing compositions provide effective cleansing of keratin materials and mildness to the eye and keratin materials, making it increasingly important that the keratin materials be fresh and clean.
There is therefore a need for compositions formulated for cleaning and/or removing make-up from keratin materials, which have a texture that is easy to use, good cleaning performance, no irritation to the eyes and to the keratin materials, and which make the keratin materials fresh and clean.
Summary of The Invention
The aim of the present invention is to provide a composition for cleaning and/or removing makeup from keratin materials, which has a texture that is easy to use, good cleaning properties, is non-irritating to the eyes and to the keratin materials, and leaves the keratin materials fresh and clean.
Thus, according to one aspect, the present invention provides a composition for cleaning and/or removing makeup from keratin materials, comprising:
a) at least one anionic surfactant selected from dialkyl sulfosuccinates; and
b) at least one nonionic surfactant selected from alkylpolyglycosides of formula (I):
R-O-Gx’ (I)
wherein
R is C6-C40An alkyl group, a carboxyl group,
g is a moiety derived from a reducing sugar containing from 5 to 6 carbon atoms,
x' is the average degree of polymerization of the alkylpolyglycoside of 1 to 10.
Such compositions are intended for cleaning and/or removing make-up from keratin materials, in particular the skin.
Thus, according to another aspect, the present invention provides a method for cleansing and/or removing make-up from keratin materials, in particular the skin, comprising applying to the keratin materials, in particular the skin, a composition according to the invention and rinsing off the composition after a random period of time.
The composition according to the invention enables the skin to be refreshed and cleaned without any harsh feeling.
The composition according to the invention also exhibits cream-oil-foam transition and delivers good rinsability during application.
It can be used as daily face cleaning agent. The compositions of the present invention are rinse-off products. Thus, such compositions are applied to the skin (i.e., face and/or body) and then rinsed with rinse water.
Other objects and features, aspects and advantages of the present invention will become even more apparent upon reading the following detailed description and examples.
Detailed Description
Hereinafter and unless otherwise indicated, the upper and lower limits of the range of values are included in the range, especially in the expressions "between … …" and "in the range … … to … …".
Furthermore, the expression "at least one" as used in the present specification is equivalent to the expression "one or more".
Throughout this application, the expression "comprising" should be interpreted as covering all the specifically mentioned features as well as optional, additional, not specifically mentioned features. As used herein, the use of the term "comprising" also discloses embodiments in which no features other than those specifically mentioned are present (i.e., "consisting of … …").
By "keratin materials", we intend to denote human keratin materials, and more particularly the skin and scalp, and more particularly the facial skin.
According to one aspect, the present invention provides a composition for cleansing and/or removing makeup from keratin materials, comprising:
a) at least one anionic surfactant selected from dialkyl sulfosuccinates; and
b) at least one nonionic surfactant selected from alkylpolyglycosides of formula (I):
R-O-Gx’ (I)
wherein
R is C6-C40An alkyl group, a carboxyl group,
g is a moiety derived from a reducing sugar containing from 5 to 6 carbon atoms,
x' is the average degree of polymerization of the alkylpolyglycoside of 1 to 10.
Dialkyl sulfosuccinates
The composition according to the invention comprises at least one anionic surfactant chosen from dialkyl sulfosuccinates.
Preferably, the dialkyl sulfosuccinate salts present in the compositions according to the invention are selected from dialkyl sulfosuccinate salts in which the alkyl group has from 4 to 24 carbon atoms, preferably from 6 to 18 carbon atoms, particularly preferably from 6 to 14 carbon atoms. Different or the same alkyl groups may be present in one molecule of dialkyl sulfosuccinate, wherein the same alkyl groups are preferred.
As the counter ion of the sulfonic acid group, an alkali metal cation, an alkaline earth metal cation, or an ammonium ion, particularly sodium (ion), can be used.
Preferably, the dialkyl sulfosuccinate salt is selected from dialkyl sulfosuccinates wherein the alkyl group has from 6 to 14 carbon atoms and the counterion of the sulfonic acid group is selected from the alkali metal cation and the ammonium ion.
Particularly preferably present dialkyl ester salts of sulfosuccinic acid are selected from the group consisting of sodium diethylhexyl sulfosuccinate, sodium dinonyl sulfosuccinate, sodium diisononyl sulfosuccinate, sodium dioctyl sulfosuccinate, sodium diheptyl sulfosuccinate, sodium dihexyl sulfosuccinate, sodium dipentyl sulfosuccinate, sodium diisopentyl sulfosuccinate, sodium dipentyl sulfosuccinate, sodium dibutyl sulfosuccinate, sodium diisobutyl sulfosuccinate, sodium dioctyl sulfosuccinate, sodium didecyl sulfosuccinate, sodium diundecyl sulfosuccinate, sodium dilauryl sulfosuccinate, sodium coco sulfosuccinate, sodium dicocosyl sulfosuccinate, sodium didecyl sulfosuccinate, sodium tridecyl sulfosuccinate, sodium dihexyl sulfosuccinate, sodium dodecyl sulfosuccinate, sodium coco sulfosuccinate, sodium diisodecyl sulfosuccinate, sodium tridecyl sulfosuccinate, Dicyclohexylammonium sulfosuccinate, diethylhexyl ammonium sulfosuccinate, dinonyl ammonium sulfosuccinate, diisononyl ammonium sulfosuccinate, dioctyl sodium ammonium sulfosuccinate, diheptyl ammonium sulfosuccinate, dihexyl ammonium sulfosuccinate, dineopentyl ammonium sulfosuccinate, diisopentyl ammonium sulfosuccinate, diamyl ammonium sulfosuccinate, dibutyl ammonium sulfosuccinate, diisobutyl ammonium sulfosuccinate, dioctyl ammonium sulfosuccinate, didecyl ammonium sulfosuccinate, diundecyl ammonium sulfosuccinate, dilauryl ammonium sulfosuccinate, dicetyl ammonium sulfosuccinate, ditridecyl ammonium sulfosuccinate, dicyclohexyl ammonium sulfosuccinate, and dicyclohexyl ammonium sulfosuccinate, Potassium diethylhexyl sulfosuccinate, potassium dinonyl sulfosuccinate, potassium diisononyl sulfosuccinate, potassium dioctyl sulfosuccinate, potassium diheptyl sulfosuccinate, potassium dipentyl sulfosuccinate, potassium diisopentyl sulfosuccinate, potassium dipentyl sulfosuccinate, potassium diamyl sulfosuccinate, potassium dibutyl sulfosuccinate, potassium diisobutyl sulfosuccinate, potassium dioctyl sulfosuccinate, potassium didecyl sulfosuccinate, potassium diundecyl sulfosuccinate, potassium dilauryl sulfosuccinate, potassium dicocosulfosuccinate, potassium ditridecyl sulfosuccinate, potassium dipropylheptyl sulfosuccinate, potassium dicyclohexyl sulfosuccinate, with sodium diethylhexyl sulfosuccinate being very particularly preferred.
Preferably, the amount of dialkyl sulfosuccinate salt in the composition ranges from 0.5 to 15 wt. -%, preferably from 1 to 10 wt. -%, and more preferably from 2 to 8 wt. -%, relative to the total weight of the composition according to the present invention.
Alkyl polyglycosides
The composition according to the invention comprises at least one nonionic surfactant chosen from alkylpolyglycosides of formula (I):
R-O-Gx’ (I)
wherein
R is C6-C40An alkyl group, a carboxyl group,
g is a moiety derived from a reducing sugar containing from 5 to 6 carbon atoms, preferably a glucose unit, and
x' represents the average degree of polymerization of the alkylpolyglycoside.
Preferably, R is C8-C34An alkyl group.
For a particular alkylpolysaccharide molecule, x' may only take an integer value. In any physical sample of alkylpolyglycoside, there will generally be molecules with different values of x'. The physical sample may be characterized by an average value of x', which may take on a non-integer value. In the present description, the value of x' is to be understood as an average value.
The polysaccharide hydrophilic portion of the alkylpolyglycoside contains, on average, from about 1 to about 10 saccharide units, preferably from 1.4 to 3 saccharide units. The sugar units may be galactoside, glucoside, lactoside, fructoside, glucosyl, fructosyl, lactosyl and/or galactosyl units, and are preferably glucoside units. Mixtures of these sugar moieties may be used in the alkylpolysaccharide. Glucosides are the preferred sugar moieties and other sugar moieties will function similarly, but because glucosides are the preferred sugar moieties, the remaining disclosure will focus on alkyl polyglucosides.
The hydrophobic groups on the alkylpolyglycoside are hydrocarbyl groups (alkyl groups) which are branched or straight chain, unsaturated or saturated, containing an average of from about 6 to about 40 carbon atoms. Preferably, the hydrocarbyl group is predominantly straight chain saturated C8To C34A hydrocarbyl group.
Useful alkylpolyglycosides of the present invention are also disclosed in U.S. Pat. No. 4,565,647(Llenado), issued on 21/1/1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms, and a polysaccharide (e.g., polyglycoside) hydrophilic group containing from about 1.3 to about 10 (preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7) saccharide units. Any reducing sugar containing 5 or 6 carbon atoms may be used, for example glucose, galactose and galactosyl moieties may be substituted for the glucosyl moieties (optionally the hydrophobic group is attached at the 2-, 3-, 4-, etc. position thus producing glucose or galactose rather than glucoside or galactoside). The intersaccharide linkage may, for example, be between one position of the additional saccharide unit and the 2-, 3-, 4-and/or 6-position on the preceding saccharide unit.
Examples of alkyl polyglycosides include, but are not limited to: octyl/decyl glucoside, lauryl glucoside, octyl glucoside, sodium lauryl glucarate (and) lauryl glucoside, and coco glucoside.
Typically, the nonionic surfactant is selected from octyl/decyl glucoside, coco glucoside, lauryl glucoside, and decyl glucoside, and more typically octyl/decyl glucoside and decyl glucoside.
Preferred alkylpolyglycosides are available, for example, under the following trade names:
for coco glucoside: marketed by Cognis
Figure BDA0003312553490000051
818UP,
For decyl glucoside: marketed by Cognis
Figure BDA0003312553490000052
2000UP,
For octyl/decyl glucoside: oramix sold by SeppicTMCG 110,
For lauryl glucoside: marketed by Cognis
Figure BDA0003312553490000061
1200N UP,
For octyl glucoside: rewosan sold by Rewo,
for sodium lauryl glucarate:
Figure BDA0003312553490000062
LGC SORB。
preferably, the amount of nonionic surfactant in the composition ranges from 0.5% to 15% by weight, preferably from 1% to 10% by weight, and more preferably from 2% to 5% by weight, relative to the total weight of the composition according to the invention.
Amphoteric surface active
The composition according to the invention may comprise at least one amphoteric surfactant chosen from secondary or tertiary, optionally quaternized, aliphatic amine derivatives.
Amphoteric surfactants selected from optionally quaternized secondary or tertiary aliphatic amine derivatives contain at least one anionic group, such as carboxylate, sulfonate, sulfate, phosphate or phosphonate, wherein at least one of the aliphatic group or aliphatic groups is a linear or branched chain comprising from 8 to 22 carbon atoms.
Mention may in particular be made of (C)8-C20) Alkyl betaines, sulfobetaines, (C)8-C20Alkyl) amide (C)2-C8Alkyl) betaines and (C)8-C20Alkyl) amide (C)2-C8Alkyl) sulfobetaine.
In (C)8-C20) Among the alkyl betaines, behenyl betaine, cetyl betaine, cocoyl betaine, decyl betaine may be mentioned. Among the alkyl betaines, coco betaines are preferred, for example under the trade name Rhodia
Figure BDA0003312553490000063
Products sold by BB/FLA.
Among the optionally quaternized secondary or tertiary aliphatic amine derivatives which may be used, mention may also be made of the compounds of formula (II) below and of the compounds of formula (III) below:
Ra-CON(Z)CH2-(CH2)m-N+(Rb)(Rc)(CH2COO-) (II)
wherein:
Rarepresents a derivative derived from the acid R preferably present in hydrolysed coconut oilaC of-COOH10-C30Alkyl or C10-C30Alkenyl, heptyl, nonyl or undecyl,
Rbrepresents a beta-hydroxyethyl group, and the beta-hydroxyethyl group,
Rcrepresents a carboxymethyl group;
m is equal to 0, 1 or 2,
z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group;
Ra’-CON(Z)CH2-(CH2)m’-N(B)(B’) (III)
wherein:
b represents-CH2CH2OX ', wherein X' represents-CH2-COOH、CH2-COOZ’、-CH2CH2-COOH、-CH2CH2-COOZ' or a hydrogen atom,
b' represents- (CH)2)z-Y ', wherein z ═ 1 or 2, and Y ' represents-COOH, -COOZ ', -CH2-CHOH-SO3H or-CH2-CHOH-SO3Z’,
m' is equal to 0, 1 or 2,
z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group,
z' represents an ion derived from an alkali metal or alkaline earth metal (e.g., sodium, potassium or magnesium); an ammonium ion; or ions derived from organic amines, and in particular from amino alcohols such as monoethanolamine, diethanolamine and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1, 3-propanediol and tris (hydroxymethyl) aminomethane.
Ra’Typical excellenceAcid R selected from hydrolyzed linseed oil or hydrolyzed coconut oila’C of COOH10-C30Alkyl or C10-C30An alkenyl group; alkyl, especially C17Alkyl and isomeric forms thereof; or unsaturated C17A group.
Preference is given to compounds corresponding to formula (II).
Among the compounds corresponding to formula (II) mention may be made of cocamidopropyl betaine, for example the product sold under the trade name Dehyton PK 45 by cognis (basf).
Compounds of formula (IV) may also be used:
Ra”-NH-CH(Y”)-(CH2)n-C(O)-NH-(CH2)n’-N(Rd)(Re) (IV)
wherein:
-Ra”represents the acid R preferably present in hydrolysed linseed oil or hydrolysed coconut oila”C of-C (O) OH10-C30Alkyl or C10-C30An alkenyl group;
y represents a group-C (O) OH, -C (O) OZ ", -CH2-CH(OH)-SO3H or a group CH2-CH(OH)-SO3-Z ", wherein Z" represents a cationic counterion derived from an alkali or alkaline earth metal (e.g. sodium), an ammonium ion, or an ion derived from an organic amine;
-Rdand ReIndependently of one another represent C1-C4An alkyl or hydroxyalkyl group; and is
-n and n' independently of each other represent an integer ranging from 1 to 3.
Among the compounds corresponding to formula (IV), mention may be made in particular of the compounds classified under the name diethylaminopropyl coco-asparagine sodium in the CTFA dictionary, such as the product sold under the name Chimexane HB by the Chimex company.
Preferably, the amphoteric surfactant is selected from (C)8-C20) Alkyl betaines, (C)8-C20) Alkylamide group (C)1-C6) Alkyl betaines, and mixtures thereof.
More preferably, the amphoteric surfactant is selected from cocamidopropyl betaine, cocobetaine, or mixtures thereof.
Preferably, the amount of amphoteric surfactant in the composition ranges from 0.5% to 20% by weight, preferably from 1% to 10% by weight, more preferably from 2% to 5% by weight, relative to the total weight of the composition according to the invention.
Oil
The composition according to the invention may comprise at least one non-volatile polar oil.
Here, "oil" means a fatty compound or substance in the form of a liquid or paste (non-solid) at room temperature (25 ℃) under atmospheric pressure (760 mmHg). As the oil, those generally used in cosmetics may be used alone or in combination thereof.
Preferably, the oil used is a non-silicone oil, i.e. the composition according to the invention does not comprise a silicone oil.
The oil may be selected from oils of vegetable origin and synthetic oils.
As examples of vegetable oils, mention may be made of, for example, linseed oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, avocado oil, camellia oil, castor oil, safflower oil, jojoba oil, sunflower oil, almond oil, rapeseed oil, sesame oil, soybean oil, peanut oil, and mixtures thereof.
As examples of synthetic oils, mention may be made of alkane oils, such as ester oils, ether oils and artificial triglycerides.
The ester oil is preferably saturated or unsaturated, linear or branched C1-C26Aliphatic mono-or poly-acids with saturated or unsaturated, straight-chain or branched C1-C26Liquid esters of aliphatic monohydric or polyhydric alcohols, the total number of carbon atoms of the esters being greater than or equal to 10.
Preferably, for esters of monohydric alcohols, at least one of the alcohol and the acid from which the ester of the invention is derived is branched.
Among the monoesters of monobasic acids with monobasic alcohols, mention may be made of ethyl palmitate, ethylhexyl palmitate, isopropyl palmitate, dioctyl carbonate, alkyl myristate (for example isopropyl myristate or ethyl myristate), isocetyl stearate, 2-ethylhexyl isononanoate, isononyl isononanoate, isodecyl neopentanoate and isostearyl neopentanoate.
Also can use C4-C22Di-or tricarboxylic acids with C1-C22Esters of alcohols, and monocarboxylic, dicarboxylic or tricarboxylic acids with non-sugar C4-C26Esters of dihydric, trihydric, tetrahydric or pentahydric alcohols.
Mention may be made in particular of: diethyl sebacate, isopropyl lauroyl sarcosinate, diisopropyl sebacate, bis (2-ethylhexyl) sebacate, diisopropyl adipate, di-n-propyl adipate, dioctyl adipate, bis (2-ethylhexyl) adipate, diisostearyl adipate, bis (2-ethylhexyl) maleate, triisopropyl citrate, triisocetyl citrate, triisostearyl citrate, glycerol trilactate, glycerol trioctanoate, trioctyl dodecyl citrate, trioleate citrate, neopentyl glycol diheptanoate, diethylene glycol diisononanoate.
As ester oil, C can be used6-C30Fatty acids and preferably C12-C22Sugar esters and diesters of fatty acids. The term "saccharide" herein denotes an oxygen-bearing hydrocarbon-based compound containing several alcohol functional groups, with or without aldehyde or ketone functional groups, and which comprises at least 4 carbon atoms. These sugars may be monosaccharides, oligosaccharides or polysaccharides.
Examples of suitable sugars which may be mentioned include sucrose (or saccharose), glucose, galactose, ribose, fucose, maltose, fructose, mannose, arabinose, xylose and lactose, and derivatives thereof, in particular alkyl derivatives, such as methyl derivatives, for example methyl glucose.
The sugar esters of fatty acids may be chosen in particular from the sugars described above and linear or branched, saturated or unsaturated C6-C30(and preferably C)12-C22) Esters or mixtures of esters of fatty acids. If these compounds are unsaturated, thenThey may have from one to three conjugated or nonconjugated carbon-carbon double bonds.
The esters according to this variant may also be selected from monoesters, diesters, triesters, tetraesters and polyesters, and mixtures thereof.
These esters may be, for example, C1-C26Alkyl (preferably C)1-C10Alkyl) oleate, laurate, palmitate, myristate, behenate, cocoate, stearate, linoleate, linolenate, caprate and arachidonate, or mixtures thereof, such as, in particular, the mixed esters of oleyl palmitate (oleopalate), oleostearate and palmitostearate (palmitanate), and pentaerythritol tetra (ethylhexanoate).
More particularly, mono-and diesters are used, and in particular sucrose, glucose or methylglucose mono-or dioleate, stearate, behenate, oleyl palmitate, linoleate, linolenate and oleyl stearate.
Examples which may be mentioned are the names given by the company Amerchol
Figure BDA0003312553490000091
DO, which is methyl glucose dioleate.
As examples of preferred ester oils, mention may be made, for example, of diisopropyl adipate, dioctyl adipate, 2-ethylhexyl caproate, ethyl laurate, cetyl octanoate, octyl dodecyl octanoate, isodecyl pivalate, myristyl propionate, 2-ethylhexyl 2-ethylhexanoate, 2-ethylhexyl octanoate/decanoate, methyl palmitate, ethyl palmitate, isopropyl palmitate, dioctyl carbonate, isopropyl lauroyl sarcosinate, isononyl isononanoate, ethylhexyl palmitate, isohexyl laurate, hexyl laurate, isocetyl stearate, isopropyl isostearate, isopropyl myristate, isodecyl oleate, glyceryl tri (2-ethylhexanoate), pentaerythritol tetra (2-ethylhexanoate), 2-ethylhexyl succinate, ethyl hexanoate, isopropyl myristate, isopropyl palmitate, isopropyl laurate, isopropyl palmitate, glyceryl tri (2-ethylhexanoate), glyceryl tetra (2-ethylhexanoate), pentaerythritol tetra (2-ethylhexyl ethylhexanoate), ethyl succinate, ethyl hexanoate, octyl octanoate, ethyl hexanoate, isopropyl palmitate, isopropyl, Diethyl sebacate, and mixtures thereof.
As examples of artificial triglycerides, mention may be made, for example, of caprylocaproyl glyceride (capryl glycerol), trimyristin, tripalmitin, trilinolein, trilaurin, tricaprin, tricaprylin, tri (capric/caprylic) glyceride and tri (capric/caprylic/linolenic) glyceride.
Preferably, the oil is selected from oils of vegetable origin, such as linseed oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, avocado oil, camellia oil, castor oil, safflower oil, jojoba oil, sunflower oil, almond oil, rapeseed oil, sesame oil, soybean oil, peanut oil; and ester oils, such as oleate, laurate, palmitate, myristate, behenate, cocoate, stearate, linoleate, linolenate, decanoate and arachidonate, or mixtures thereof, such as in particular oil palmitate, mixed oil stearate and palmitostearate, and pentaerythritol tetra (ethylhexanoate).
In a preferred embodiment, the composition according to the invention comprises an oil of vegetable origin, palmitic acid C1-C10Alkyl esters and myristic acid C1-C10A combination of alkyl esters.
In a preferred embodiment, the composition according to the invention comprises a combination of sunflower oil, ethylhexyl palmitate and isopropyl myristate.
Preferably, the amount of oil in the composition according to the invention is not limited and may range from 10 to 60 wt. -%, preferably from 20 to 60 wt. -%, and more preferably from 40 to 60 wt. -%, relative to the total weight of the composition.
Hydrophilic gelling agent
The composition according to the invention may comprise at least one hydrophilic gelling agent.
Gelling agents useful in the compositions according to the invention may include water-soluble polymers, such as high molecular weight crosslinked acrylic acid homopolymers and acrylates/C10-30Alkyl acrylate cross-linked copolymers, e.g.
Figure BDA0003312553490000101
And
Figure BDA0003312553490000102
anionic acrylate polymers, e.g.
Figure BDA0003312553490000103
AST, and cationic acrylate polymers, e.g.
Figure BDA0003312553490000104
SC 96; acrylamidopropyltrimethylammonium chloride/acrylamide; hydroxyethyl methacrylate polymers, steareth-10 allyl ether/acrylate copolymers; acrylate/beheneth-25 methacrylate copolymers, known as
Figure BDA0003312553490000105
28; poly (glycerol methacrylate), acrylate/steareth-25 methacrylate copolymers; bentonite; gums, such as alginate, carageenan, acacia, gum arabic, ghatti, karaya, tragacanth, guar gum; guar hydroxypropyltrimonium chloride, xanthan gum or gellan gum; cellulose derivatives, such as sodium carboxymethylcellulose, hydroxyethylcellulose, hydroxymethylcarboxyethylcellulose, hydroxymethylcarboxypropylcellulose, ethylcellulose, cellulose sulfate, hydroxypropylcellulose, methylcellulose, hydroxypropylmethylcellulose, microcrystalline cellulose; agar; pectin; gelatin; starch and its derivatives; chitin and its derivatives, such as hydroxyethyl chitin; polyvinyl alcohol, PVM/MA copolymers, PVM/MA decadiene crosspolymers, polyethylene oxide-based gelling agents, sodium carbomer, and mixtures thereof.
Preferably, the amount of hydrophilic gelling agent in the composition ranges from 0.1 to 5 wt. -%, preferably from 0.15 to 3 wt. -%, and more preferably from 0.2 to 1 wt. -%, relative to the total weight of the composition according to the present invention.
Aqueous phase
Generally, the compositions of the present invention comprise at least one aqueous phase.
The aqueous phase of the composition according to the invention comprises water and optionally one or more water-miscible or at least partially water-miscible compounds, for example C2To C8Lower polyols or monohydric alcohols, such as ethanol and isopropanol.
The term "polyol" is understood to mean any organic molecule comprising at least two free hydroxyl groups. Examples of polyols that may be mentioned include diols such as butanediol, propylene glycol and isoprene glycol, octaethylene glycol, glycerol (i.e. glycerol) and polyethylene glycol.
The aqueous phase may also contain any of the common water-soluble or water-dispersible additives mentioned below.
The aqueous phase may represent from 20% to 80% by weight, preferably from 20% to 60% by weight and better still from 30% to 60% by weight, relative to the total weight of the composition.
Other ingredients
The composition according to the invention may also comprise other ingredients previously known elsewhere in cosmetic compositions, such as cosmetic active ingredients, for example hydroxyacetophenone; and various common adjuvants such as chelating agents (e.g., EDTA and etidronic acid), preservatives (e.g., phenoxyethanol and salicylic acid), opacifiers, fragrances, and the like.
According to a preferred embodiment, the present invention relates to a composition for cleansing and/or removing makeup from keratin materials, comprising, in an aqueous phase, with respect to the total weight of the composition:
a) from 2 to 8% by weight of at least one anionic surfactant selected from dialkyl sulfosuccinates, wherein the alkyl group has from 6 to 14 carbon atoms and the counterion of the sulfonic acid group is selected from alkali metal cations and ammonium ions;
b)2 to 5% by weight of at least one nonionic surfactant selected from octyl/decyl glucoside, lauryl glucoside, octyl glucoside, sodium lauryl glucarate (and) lauryl glucoside, and coco glucoside.
According to a preferred embodiment, the present invention relates to a composition for cleansing and/or removing makeup from keratin materials, comprising, in an aqueous phase, with respect to the total weight of the composition:
a) from 2 to 8% by weight of at least one anionic surfactant selected from dialkyl sulfosuccinates wherein the alkyl group has from 6 to 14 carbon atoms and the counterion of the sulfonic acid group is selected from alkali metal cations and ammonium ions;
b) 2% to 5% by weight of at least one nonionic surfactant selected from octyl/decyl glucoside, lauryl glucoside, octyl glucoside, sodium lauryl glucarate (and) lauryl glucoside, and coco glucoside; and
c)2 to 5% by weight of at least one member selected from the group consisting of (C)8-C20) Alkyl betaines, (C)8-C20) Alkylamide group (C)1-C6) Alkyl betaines, and mixtures thereof.
Method and use
The compositions according to the invention can be used in a method for cleansing and/or removing makeup from keratin materials, by application to the keratin materials (for example the skin, in particular the face).
The composition according to the invention can be applied by any means that enables uniform distribution, in particular using a finger, or a cotton ball, a stick, a brush, a gauze or a spatula, and can be removed by rinsing with water.
Thus, according to another aspect, the present invention relates to a method for cleansing and/or removing makeup from keratin materials, in particular the skin, comprising applying to the keratin materials, in particular the skin, a composition according to the invention and rinsing off said composition after a random period of time.
The invention is illustrated in more detail by the examples described below, which are given as non-limiting illustrations.
Examples
Example 1: preparation of compositions according to inventive and comparative formulations
Compositions according to the inventive formulation (inv.) and compositions according to the comparative formulation (comp.) listed in table 1 were prepared. The numerical values of the amounts of the ingredients shown in table 1 are all based on "wt%" of the active ingredient relative to the total weight of the composition.
TABLE 1
Figure BDA0003312553490000131
The preparation procedure is as follows:
the composition was prepared as follows:
the ingredients for phase A were mixed with a dispenser at a stirring speed of 200rpm and heated to 65 ℃. The heating was stopped and the ingredients for phase B were added to phase A and emulsified for 10 minutes. Once the mixture was cooled to 50 ℃, the stirring speed was increased to 500rpm, the ingredients for phase C were added and mixed for 10 minutes. The mixture was cooled to room temperature under a stirring speed of 200 rpm.
Example 2: evaluation examples
The compositions prepared in example 1 were evaluated for texture, makeup removal ability, foaming properties and skin/eye irritation.
The makeup removal ability was evaluated based on the following protocol.
(i) Pretreatment of biological skin:
biological skin was washed with Shu Uemura Ultima 8 cleansing oil (Shu Uemura Ultima 8 cleansing oil) and then with Lifuquan super Anjie cleansing foam cream (LRP toleriane cleansing foaming cream).
(ii) Application of waterproof mascara:
megbaolian (Maybelline) (Hyper Curl volume Express waterproof mascara) was applied to biological skin at 0.05g per 5cmx5cm biological skin.
(iii) Drying was carried out at 32 ℃ for 10 minutes.
1g of the composition to be tested is applied with a gentle massage of 100 cycles, rinsed off with running water and dried with a paper towel by patting.
Photographs were taken with dermoscore + and the images were analyzed to detect the percentage of dark pixels in the photographs. A lower score indicates less makeup residue left on the biological skin and therefore better makeup removal.
The score of makeup removal ability was given based on the following criteria.
Dark pixel% 0-0.5% 0.5-1% >1%
Makeup removing ability Good taste In Difference (D)
Skin/eye irritation was evaluated based on the following protocol.
The compositions were tested by 10 consumers as follows:
(i) applying the composition to be tested on dry face with dry hands;
(ii) massaging in a looping way to dissolve color cosmetics on the face;
(iii) adding water to foam and completely washing;
(iv) the consumer is asked whether the composition has skin/eye irritation during each step.
The score for skin stimulation is given based on the following criteria.
Number of consumers claiming irritation 0 1-3 >3
Level of stimulation Is low in In Height of
The presence or absence of cream-to-oil transition was observed by sensory perception during application.
Foaming performance was evaluated by 10 consumers aged 20 to 40 years using the following procedure:
(i) applying the composition to be tested on dry face and massaging in a loop;
(ii) wetting the face with water creates lather for better cleansing;
(iii) washed off with water.
The score for foaming performance is given based on the following criteria:
and 5, dividing: at least 80% of consumers believe the effect is good and expected;
and 4, dividing: 60% to 80% (excluding 80%) of the consumers considered to be good and expected;
and 3, dividing: at least 50% of consumers believe the effect is good and expected;
and 2, dividing: over 60% of consumers consider the effect poor and unacceptable;
1 minute: results that are considered poor and unacceptable by more than 80% of consumers are as follows:
item Inv.1 Inv.2 Comp.1 Comp.2
Texture of Elastic cream Elastic cream Fluid emulsions N/A, cannot be prepared
Removal capability Good taste Good taste In N/A
Skin/eye irritation Is low in Is low in N/A N/A
Cream-to-oil conversion Is that Is that Whether or not N/A
Volume of foam 5 4 4 N/A
N/A: not tested.
From the results listed above it is clear that the composition according to the invention shows a much better rinse stability compared to the comparative composition. At the same time, the compositions according to the invention do not cause irritation to the skin and the eyes.
It has also been found that the composition according to the invention shows a cream-to-oil transition during application and is capable of refreshing and cleansing the skin.
While illustrative embodiments of the invention have been described above, it will be understood, of course, from the foregoing description that various modifications will be apparent to those of ordinary skill in the relevant art or may become apparent as the technology advances. Such modifications are to be considered within the spirit and scope of one or more of the inventions disclosed in this specification.

Claims (13)

1. Composition for cleansing and/or removing makeup from keratin materials, comprising:
a) at least one anionic surfactant selected from dialkyl sulfosuccinates; and
b) at least one nonionic surfactant selected from alkylpolyglycosides of formula (I):
R-O-Gx’ (I)
wherein
R is C6-C40An alkyl group, a carboxyl group,
g is a moiety derived from a reducing sugar containing from 5 to 6 carbon atoms,
x' is the average degree of polymerization of the alkylpolyglycoside of 1 to 10.
2. The composition according to claim 1, wherein the dialkyl sulfosuccinate salt is selected from dialkyl sulfosuccinates wherein the alkyl group has from 6 to 14 carbon atoms and the counterion to the sulfonic acid group is selected from the group consisting of an alkali metal cation and an ammonium ion.
3. The composition according to claim 1 or 2, wherein the amount of dialkyl sulfosuccinate salt in the composition ranges from 0.5 to 15 wt. -%, preferably from 1 to 10 wt. -%, and more preferably from 2 to 8 wt. -%, relative to the total weight of the composition according to the invention.
4. The composition according to any one of claims 1 to 3, wherein the non-ionic surfactant is selected from octyl/decyl glucoside, coco glucoside, lauryl glucoside, and decyl glucoside.
5. The composition according to any one of claims 1 to 4, wherein the amount of nonionic surfactant in the composition ranges from 0.5% to 15% by weight, preferably from 1% to 10% by weight, and more preferably from 2% to 5% by weight, relative to the total weight of the composition according to the invention.
6. The composition according to any one of claims 1 to 5, further comprising at least one amphoteric surfactant selected from optionally quaternized secondary or tertiary aliphatic amine derivatives.
7. The composition of claim 6, wherein the amphoteric surfactant is selected from the group consisting of a compound of formula (II) below and a compound of formula (III) below:
Ra-CON(Z)CH2-(CH2)m-N+(Rb)(Rc)(CH2COO-) (II)
wherein:
Rarepresentative derived from hydrolyzed coconut oilAcid RaC of-COOH10-C30Alkyl or C10-C30Alkenyl, heptyl, nonyl or undecyl,
Rbrepresents a beta-hydroxyethyl group, and the beta-hydroxyethyl group,
Rcrepresents a carboxymethyl group;
m is equal to 0, 1 or 2,
z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group;
Ra’-CON(Z)CH2-(CH2)m’-N(B)(B’) (III)
wherein:
b represents-CH2CH2OX ', wherein X' represents-CH2-COOH、CH2-COOZ’、-CH2CH2-COOH、-CH2CH2-COOZ' or a hydrogen atom,
b' represents- (CH)2)z-Y ', wherein z ═ 1 or 2, and Y ' represents-COOH, -COOZ ', -CH2-CHOH-SO3H or-CH2-CHOH-SO3Z’,
m' is equal to 0, 1 or 2,
z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group,
z' represents an ion derived from an alkali metal or alkaline earth metal such as sodium, potassium or magnesium; an ammonium ion; or ions derived from organic amines, and in particular from amino alcohols such as monoethanolamine, diethanolamine and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1, 3-propanediol and tris (hydroxymethyl) aminomethane,
Ra’represents the acid R preferably present in hydrolysed linseed oil or hydrolysed coconut oila’C of COOH10-C30Alkyl or C10-C30An alkenyl group; alkyl, especially C17Alkyl, and isomeric forms thereof; or unsaturated C17A group.
8. The composition of claim 6 wherein the amphoteric surfactant is selected from (C)8-C20) Alkyl betaines, (C)8-C20) Alkylamide group (C)1-C6) Alkyl betaines, and mixtures thereof, preferably selected from cocamidopropyl betaine, cocoyl betaine, or mixtures thereof.
9. The composition according to any one of claims 1 to 8, further comprising at least one non-volatile polar oil.
10. The composition of any one of claims 1 to 9, further comprising at least one hydrophilic gelling agent.
11. The composition of any one of claims 1 to 10, further comprising at least one aqueous phase.
12. Composition for cleansing and/or removing makeup from keratin materials, comprising, in an aqueous phase, with respect to the total weight of the composition:
a) from 2 to 8% by weight of at least one anionic surfactant selected from dialkyl sulfosuccinates wherein the alkyl group has from 6 to 14 carbon atoms and the counterion of the sulfonic acid group is selected from alkali metal cations and ammonium ions;
b) 2% to 5% by weight of at least one nonionic surfactant selected from octyl/decyl glucoside, lauryl glucoside, octyl glucoside, sodium lauryl glucarate (and) lauryl glucoside, and coco glucoside; and
c)2 to 5% by weight of at least one member selected from the group consisting of (C)8-C20) Alkyl betaines, (C)8-C20) Alkylamide group (C)1-C6) Alkyl betaines, and mixtures thereof.
13. Method for cleansing and/or removing make-up from keratin materials, in particular the skin, comprising the application to the keratin materials, in particular the skin, of a composition according to any one of claims 1 to 12 and the rinsing off of the composition after a random period of time.
CN201980095624.7A 2019-04-22 2019-04-22 Composition for cleaning and/or removing make-up from keratin materials Pending CN113727693A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2019/083678 WO2020215178A1 (en) 2019-04-22 2019-04-22 A composition for cleansing and/or removing makeup from keratin materials

Publications (1)

Publication Number Publication Date
CN113727693A true CN113727693A (en) 2021-11-30

Family

ID=72940846

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201980095624.7A Pending CN113727693A (en) 2019-04-22 2019-04-22 Composition for cleaning and/or removing make-up from keratin materials

Country Status (3)

Country Link
EP (1) EP3958832A4 (en)
CN (1) CN113727693A (en)
WO (1) WO2020215178A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023044899A1 (en) * 2021-09-27 2023-03-30 L'oreal Foaming composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101095653A (en) * 2006-06-28 2008-01-02 拜尔斯道夫股份有限公司 Hair care cleansing formulations with especially dry hair feel
WO2015163337A1 (en) * 2014-04-24 2015-10-29 L'oreal Cosmetic composition
CN105030556A (en) * 2014-04-17 2015-11-11 赢创工业集团股份有限公司 Surfactant compositions and highly oleaginous formulations containing these

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9018150B1 (en) * 2013-12-09 2015-04-28 L'oreal Cleansing composition with cationic surfactants
DE102014207421A1 (en) * 2014-04-17 2015-10-22 Evonik Degussa Gmbh Surfactant compositions and high oily formulations containing these
WO2017037188A1 (en) * 2015-09-01 2017-03-09 L'oreal Composition comprising at least one anionic surfactant, at least one nonionic surfactant, at least one amphoteric surfactant, at least one cationic polymer and at least one amphoteric polymer

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101095653A (en) * 2006-06-28 2008-01-02 拜尔斯道夫股份有限公司 Hair care cleansing formulations with especially dry hair feel
CN105030556A (en) * 2014-04-17 2015-11-11 赢创工业集团股份有限公司 Surfactant compositions and highly oleaginous formulations containing these
WO2015163337A1 (en) * 2014-04-24 2015-10-29 L'oreal Cosmetic composition

Also Published As

Publication number Publication date
WO2020215178A1 (en) 2020-10-29
EP3958832A1 (en) 2022-03-02
EP3958832A4 (en) 2023-04-12

Similar Documents

Publication Publication Date Title
CN106535869B (en) Foaming cleanser
US6821942B2 (en) Cosmetic cleansing composition
CN105722497B (en) Foaming composition comprising at least one glycinate surfactant
US7749523B2 (en) Emollient skin conditioning cream and method
JP4142272B2 (en) Cleansing cosmetic composition
US5179128A (en) Cosmetic composition for removing make-up
JPH08301725A (en) Cleansing composition having low irritation
WO2010140319A1 (en) Cleansing method
JP2012167035A (en) Creamy skin-cleansing agent
CN1326511C (en) Foam cosmetic composition for cleaning or dress taking off
CN113727693A (en) Composition for cleaning and/or removing make-up from keratin materials
DE60310856T2 (en) Liquid cleaners based on soaps and synthetic surfactants; Their use for cleaning human keratin materials
JP4181153B2 (en) Effervescent cleansing composition
JPH01168612A (en) Liquid detergent composition
JP2019214564A (en) Solubilized skin detergent composition
JP4085667B2 (en) Transparent gel detergent composition
JPH11193213A (en) Composition for cleansing
JP2007246510A (en) Foamable cosmetic composition
JP7156083B2 (en) Cleansing composition for skin
JP2001213740A (en) Detergent composition
JP3446172B2 (en) Cleansing cosmetics
JP7312529B2 (en) Oil-in-water emulsified cosmetic
JP4101827B2 (en) Foaming cleansing composition
CN117545455A (en) Composition for cleaning and/or removing makeup from keratin materials
JPH07179322A (en) Skin detergent

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination