CN116490161A - Cleansing cosmetic composition containing two surfactants, specific diol and levan - Google Patents

Cleansing cosmetic composition containing two surfactants, specific diol and levan Download PDF

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Publication number
CN116490161A
CN116490161A CN202180070521.2A CN202180070521A CN116490161A CN 116490161 A CN116490161 A CN 116490161A CN 202180070521 A CN202180070521 A CN 202180070521A CN 116490161 A CN116490161 A CN 116490161A
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Prior art keywords
weight
composition
composition according
levan
anionic surfactant
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CN202180070521.2A
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Chinese (zh)
Inventor
I·博桑特
玛歌·卡蒂埃-米隆
弗拉维·梅雷·阿米奥特
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LOreal SA
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LOreal SA
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/345—Alcohols containing more than one hydroxy group
    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • 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
    • A61K8/73—Polysaccharides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/10—Washing or bathing preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/02—Preparations for cleaning the hair

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  • 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)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

A cleansing cosmetic composition comprising two surfactants, a specific diol and levan. The present invention relates to a cosmetic composition comprising, in a physiologically acceptable medium: an aqueous phase; at least one amphoteric surfactant selected from betaines; at least one anionic surfactant selected from alkyl sulfates; pentanediol; and at least 0.9% by weight, relative to the total weight of the composition, of at least one active substance of levan.

Description

Cleansing cosmetic composition containing two surfactants, specific diol and levan
Technical Field
The present invention relates to cosmetic compositions, in particular cleansing cosmetic compositions for skin and skin appendages, preferably body washes or cleansing products for the face, body, hands and/or hair, comprising an aqueous phase, two specific surfactants (one betaine type amphoteric surfactant, the other alkyl sulfate type anionic surfactant), a specific glycol and a levan.
Background
Skin cleansing is very important for skin care. It must be as effective as possible because fat residues, such as excess sebum or residues of cosmetics used daily, accumulate in skin folds and clog skin pores, leading to the appearance of acne. The correct way to clean the skin is to use a foaming cleaning product.
Currently marketed lathering cleansing products have either a bulk form, a gel form or a liquid form of air bubbles. They generally contain soaps which have the advantage of providing creaminess and a large amount of foam, but which can give rise to a tautness due to their excessive detergency, or which contain synthetic detergent-type lathering surfactants and stabilisers which are inter-coupled with each other. Furthermore, the use of currently marketed lathering cleansing products can result in eye stinging and/or eye irritation.
Users are increasingly looking for new cleaning and/or care products for keratin materials, preferably for the skin of the face and/or body and/or hands.
Thus, there is a need for cleansing and/or care compositions for keratin materials, preferably for the skin of the face and/or body and/or hands, which exhibit good ocular tolerance, while foaming, being stable, having a sufficient rinse rate, and giving the skin protection and/or moisturization films. There is also a need for cleansing and/or care compositions for keratin materials, preferably the skin of the face and/or body and/or hands, which exhibit the aforementioned advantages and adequate flowability.
Disclosure of Invention
The object of the present invention is to provide such a composition which does not have the disadvantages of the prior art, has good quality of use (foam quality, consistency, skin moisturization after drying) and good eye resistance.
The inventors have demonstrated that compositions comprising an amphoteric surfactant selected from betaines, an anionic surfactant selected from alkyl sulphates, specific diols and levans enable to obtain cosmetic compositions, in particular body washes, which respond to these needs while remaining stable. The compositions according to the invention have in particular an enhanced ocular tolerance. The composition according to the invention also has an optimal viscosity for its use.
More specifically, the present invention relates to a cosmetic composition comprising, in a physiologically acceptable medium:
the aqueous phase of the water-based polymer,
at least one amphoteric surfactant selected from betaines,
at least one anionic surfactant selected from alkyl sulphates,
pentanediol, and
at least 0.9% by weight, relative to the total weight of the composition, of at least one active substance of levan.
The invention also relates to a method for cleansing keratin materials, in particular the skin of the body or the skin of the face or the hair or the hands, comprising the application to said keratin materials of a cosmetic composition as defined above.
The term "keratin materials" refers to the skin (body, face, eye contours), hair, eyelashes, eyebrows, body hair, nails, lips, and/or mucous membranes.
The term "cosmetically acceptable medium" refers to any medium compatible with the skin and/or its coverings, having a pleasant color, smell and texture, and which does not cause unacceptable discomfort (stinging, tightening, redness) that prevents the consumer from using the composition.
Aqueous phase
The composition according to the invention comprises at least one aqueous phase.
The aqueous phase comprises water.
The water used may be sterile demineralised and/or floral water, such as rose water, cornflower water, chamomile water or basswood water, and/or spring or natural mineral water, such as: vittel water, water from Vichy (Vichy) basin, uria water, la Roche Posay water, la Bourdoule water, enghien-les-Bains water, saint Gervais-les-Bains water, naeris-les-Bains water, allevar-les-Bains water, digne water, maizire water, neyrac-les-Bains water, lons-le-Saunier water, les Eaux Bonnes, rochefort water, saint Christau water, fumades water, and Tercis-les-Bains water, av ene water.
The aqueous phase may comprise at least one organic solvent that is soluble or miscible with water.
Suitable water-soluble or water-miscible solvents for use in the present invention include short chain monohydric alcohols, e.g., C1-C4 alcohols, such as ethanol, isopropanol; diols or polyols, such as ethylene glycol, 1, 2-propanediol, 1, 3-butanediol, hexanediol, diethylene glycol, dipropylene glycol, 2-ethoxyethanol, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, sorbitol; and mixtures thereof.
The aqueous phase of the composition according to the invention comprises pentanediol.
Preferably, the active substance content of pentanediol is between 0.05% and 10% by weight, preferably between 0.1% and 5% by weight, relative to the total weight of the composition.
Pentanediol is sold, inter alia, by MINASOLVE under the name A-LEEN 5, or by SYMRISE under the name HYDROLITE 5GREEN, by AROMA HOLLY LIMITED under the name PENTYLENE GLYCOL, by MINASOLVE under the name PENTIOL, by LANXESS under the name PUROLAN PD-LO, or by SYMRISE under the name HYDROLITE-5.
The presence of pentanediol in the composition according to the invention helps to reduce the viscosity of the composition. Pentanediol has a higher fluidization efficiency than other known vulcanizing agents. Thus, it helps to reduce the amount of fluidizer contained in the composition while maintaining a comparable or even lower viscosity.
Advantageously, the composition according to the invention has a viscosity of 20s to 100s, preferably 30s to 70s, measured by the following test a:
a consistency cup, such as a Labomat VF2050 consistency cup, is used with a diameter of 6 millimeters ("CF 6"). 150mL of the composition was placed in a cup and the whole was thermostated at 25 ℃ +/-0.5 ℃.
The cup was then placed on a horizontal stand and the beaker was placed under a balance. The flow time was timed such that 90 grams +/-0.5 grams of the composition fell into the beaker at a standard height of 20 cm. The standard height of 20 cm is the distance from the lower end of the consistency cup to the surface of the balance.
This measurement is only significant at these 90 grams of continuous flow.
According to a preferred embodiment, the composition according to the invention is free of glycerol or comprises glycerol, such that the weight ratio of active substances between levan and glycerol is strictly greater than 1.
The term "glycerol-free" means that the composition according to the invention does not comprise glycerol.
According to a particular embodiment of the invention, the aqueous phase represents from 15% to 97% by weight, preferably from 30% to 90% by weight, more preferably from 45% to 90% by weight, relative to the total weight of the composition.
Preferably, the composition according to the invention comprises at least 50% by weight, preferably at least 55% by weight, of water.
Betaine type amphoteric surfactant
The composition according to the invention further comprises at least one amphoteric surfactant selected from betaines.
The amphoteric or zwitterionic surfactant according to the invention is preferably selected from:
alkylbetaines, especially lauryl betaines, e.g. GENAGEN of CLARIANTThe product is either cocobetaine, e.g. Dehyton +.of BASF>30 or Evonik Goldschmidt GmbH TEGO Betaiin AB 1214;
n-alkylamide betaines and derivatives thereof, and in particularIs cocamidopropyl betaine (e.g. LEBON of SANYO)EMPIGEN of HG or ALBRIGHT AND WILSON->) Lauramidopropyl betaine (e.g. REWOTERIC +.>) Or the N-disodium salt of N-carboxyethoxyethyl N-cocoamidoethylamino acetic acid (INCI name: disodium cocoamphodiacetate salts, e.g. MIRANOL C2M CONCENTRE of RHODIA CHIMIE)；
Sulfobetaines, e.g. cocamidopropyl hydroxysulfobetaine (e.g. CRODA CROSULTANE C-)；
And mixtures thereof.
Preferably, the betaine type amphoteric surfactant is selected from the group consisting of alkyl betaines and N-alkyl amidobetaines, preferably from the group consisting of N-alkyl amidobetaines, more preferably coco amidopropyl betaine, coco betaine, and mixtures thereof.
The content of active substance of the amphoteric surfactant selected from alkyl betaines is preferably comprised between 1% and 20% by weight, preferably between 1% and 10% by weight, preferably between 1% and 5% by weight, relative to the total weight of the composition.
Anionic surfactants selected from alkyl sulphates
The composition according to the invention further comprises at least one anionic surfactant selected from alkyl sulphates.
Among the alkyl sulfate anionic surfactants, alkyl sulfates and mixtures thereof are preferably used, especially in the form of alkali metal (Na or K) salts or alkaline earth metal (e.g., mg) salts, or ammonium, amine or amino alkoxides, and mixtures thereof.
Preferably, the anionic surfactant is selected from ammonium salts.
Advantageously, the anionic surfactant is ammonium lauryl sulfate.
Ammonium lauryl sulfate is an ammonium salt of lauryl sulfate, which is generally of the formula CH 3 (CH 2 ) 10 CH 2 OSO 3 NH 4 。
INCI name is ammonium lauryl sulfate.
Preferred ammonium lauryl sulfates according to the present invention are sold by ZSCHIMMER & SCHWARZ under the names SULFETAL LA B-RSPO-MB or SULFETAL LA B, by PCC EXOL under the names ROSLFAN A MB or ROSLFAN A, or by INNOSPEC ACTIVE CHEMICALS under the names EMPICOL AL 30/FL3/MB or EMPICOL AL 30/FL 3.
The active substance content of the alkyl sulphate type anionic surfactant is preferably at least equal to 5% by weight, preferably between 5% and 20% by weight, preferably between 5% and 15% by weight, relative to the total weight of the composition.
Furthermore, it is preferred that in the composition according to the invention the weight ratio of active substance between anionic surfactant and amphoteric surfactant is less than or equal to 4.5, preferably between 2.5 and 4.5, preferably between 3 and 4, preferably between 3.1 and 3.9.
Preferably, in the composition according to the invention, the total active mass of the surfactant is between 6% and 30% by weight, preferably between 6% and 20% by weight.
Levan (Fructan)
The composition of the present invention further comprises: at least 0.9% by weight, relative to the total weight of the composition, of at least one active substance of levan.
Fructans (fructosan or fructicans) are oligosaccharides or polysaccharides comprising a chain of anhydrofructose units optionally linked to one or more different sugar residues of fructose. Levan may be linear or branched. Levan may be a product obtained directly from a plant or microbial source, or a product in which the chain length has been modified (increased or decreased) by fractionation, synthesis or hydrolysis, in particular enzymatic hydrolysis. The degree of polymerization of the levan is generally from 2 to about 1000, preferably from 3 to about 60.
Among levan, there is a unique group which includes products in which fructose units are bound mainly by beta bonds (2→1). These are essentially linear fructans such as inulin.
Preferably, the levan comprised in the composition of the invention is inulin. Inulin may be obtained from, for example, chicory (chicory), dahlia or Jerusalem artichoke (Jerusalem artichoke). Preferably, the inulin used in the composition according to the invention is obtained from chicory, for example.
Inulin is particularly abundant in plant rhizomes, in particular jerusalem artichoke and chicory, from which inulin is industrially extracted. Inulin is also found in other plants belonging to the family of the chrysanthemum (Asteraceae), such as artichoke (Jerusalem artichokes), dahlia corm and burdock.
Inulin is a polydisperse linear polymer of the general formula GFn (g=glucose, f=fructose, n ranging from 2 to 60 or more), the fructose units being bound together by β -linkages (2→1). Inulin thus corresponds to a chain of fructose units terminated by glucose units.
Inulin may be represented by the following formula (I):
[ chemical formula 1]
Where n varies between 2 and 60.
Among the inulin materials suitable and commercially available, mention may be made of Inutec H25P (between 2 and 7) and Inutec N25 (average n=25) produced by Orafti.
According to one embodiment, the cosmetic composition according to the invention may comprise salts, in particular electrolytes.
The electrolyte may be selected from sodium chloride or sodium sulfate. The electrolyte is preferably sodium chloride.
Preferably, the active substance content of the electrolyte is between 0.2% and 5% by weight, preferably between 0.5% and 3% by weight, preferably between 1% and 2% by weight, relative to the total weight of the composition.
The electrolyte is used in particular to correct the final viscosity of the composition according to the invention.
The composition according to the invention may further comprise conventional cosmetic additives, in particular selected from preservatives, pH regulators, oils, ionic or nonionic thickeners, wetting agents, defoamers, fragrances, active ingredients, fillers, propellants or any other ingredients commonly used in the cosmetic and/or dermatological field.
Among the pH adjusters, mention may be made of inorganic or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids (such as acetic acid, tartaric acid, citric acid, lactic acid, sulfonic acid). Among the alkalizing agents, mention may be made, for example, of ammonia, alkaline carbonates, alkanolamines (such as monoethanolamine, diethanolamine and triethanolamine and derivatives thereof), sodium hydroxide and potassium hydroxide.
To obtain an acceptable pH, these pH adjusters may be present in an amount of between 0.01% and 1% of active substance. Typically, the pH of the composition according to the invention is between 4 and 7, preferably between 4 and 6.
Among these oils, mention may be made of vegetable oils such as olive oil, safflower oil, cumin oil, in particular black seed (nigellan) oil, sweet almond oil, or essential oils such as peppermint essential oil or peppermint essential oil. These oils may be present in an amount of between 0.0001% and 1% by weight, preferably between 0.001% and 0.5% by weight of active substance.
It will be apparent to those skilled in the art that the optional supplemental compounds and/or amounts thereof described above may be carefully selected so that the beneficial properties inherently associated with the compositions of the present invention are not or substantially not impaired by the envisaged addition.
Unless otherwise indicated, the expressions "between … … and … …" and "range from … … to … …" are to be understood as including the limit values.
Detailed Description
The following examples illustrate the invention but do not limit it in any way. In these examples, the amounts of the ingredients are given in weight% of the active substance relative to the total weight of the composition.
Examples
Example 1: preparation and evaluation of the compositions according to the invention and of the comparative compositions
1.Preparation of the composition:
the composition C1 according to the invention and the comparative compositions C2 to C6 were prepared by mixing the ingredients in the table below in water.
TABLE 1
2. Ocular tolerance measurement protocol and results for compositions
In this example, the ocular tolerance of the composition was evaluated.
For this purpose, an in vitro test for determining the integrity of the cornea and an in vitro test for determining the integrity of the conjunctiva are carried out according to an appropriate protocol based on the following official standards, respectively:
OECD BCOP (bovine corneal opacity and permeability test method, "Bovine Corneal Opacity and Permeability test method") protocol 437 ("OECD test guideline 437, https:// read-ilibrary. Org/environmental/test-no-437-bone-corn-accuracy-and-permeneability-test-method-for-identification-i-chemicals-reduction-service-date-and-ii-chemicals-non-resolution-analysis-for-eye-ir-quality-date-9789264203846-en#patch 7") and
HETCAM (egg test-chorioallantoic membrane) protocol https:// www.legifrance.gouv.fr/jorf/id/JORFTEXT000000369360/, 29:.
In this study, the evaluation of ocular tolerance of the different compositions was based on cornea integrity evaluation and conjunctival integrity evaluation methods. These results are shown in table 2, with the number of "+" appended to indicate the extent of preservation of corneal or conjunctival integrity.
TABLE 2
Composition C1 according to the invention gives the cornea integrity and conjunctival integrity sex is the result of++; thus, in the model used to observe comparative test compositions C2 to C6, they exhibited significantly better ocular tolerability results.
These results obtained in vitro indicate an increase in clinical ocular tolerance in the case of the composition according to the invention.
Example 2: preparation and evaluation of the compositions according to the invention
Composition C7 according to the invention was prepared by mixing the ingredients in the table below in water.
TABLE 3
The moisturizing effect of composition C7 according to the present invention was tested by a moisturizing ability tester (coremeter).
The test panel was as follows:
24 women, aged from 21 to 65 years (average age: 52 years)
Inclusion values on legs: 20 to 40a.u. (after 20 minutes conditioning period), and
is not easy to hot flush.
The test conditions were as follows:
study area: the inner surfaces of the legs. Demarcating 24 x 4cm 2 1 area on each leg, one treated area versus one untreated area.
Number of applications：1
Application amount：2mg/cm 2 Or 32mg
Washing process
1) The area was wetted with 3 pieces of cotton immersed in warm water (38+/-2 ℃), the body wash applied with the fingerstall and gently massaged for 15 seconds. The product was allowed to stand for 30 seconds to function, rinsed with 20 ml of 38 ℃ water, and dried by gentle wiping with a paper towel.
Wetting and rinsing the untreated areas. It was dried by gentle wiping with a paper towel.
2) Rest for 30 minutes in an air conditioned room at 21+ -1 deg.c-45 +/-5% RH.
3) Skin wettability was measured with a CM825 skin moisture tester (corneometer) (high pressure) before washing, then 30 minutes after standardized washing.
The results obtained are given in the table below, representing the average moisturizing ability measurement +/-sd, unit A.U.
TABLE 4
Control area Composition C7 Student inspection
t0 31.1 4.9 30.5 5.2
t＝30min 30.4 6.1 32.5 7.0
T＝4H 31.6 6.3 32.7 5.8
δt 30min-t0 -0.7±2.8 2.0 4.9 S(p<0.05)
δt 4H-T0 -0.5±3.5 2.2 4.6 Ls(p＝0.06)
Composition C7 significantly increased skin wettability (8%) after 30 minutes of application compared to the control area washed with water.
Thus, composition C7 had a significant effect after 30 minutes of application to the skin.
In addition, the viscosity of composition C7 was evaluated; the presence of pentanediol in composition C7 enables a lower viscosity composition to be obtained than when pentanediol is not present.
The viscosity was measured according to the protocol of test a above.
The viscosity of composition C7 was 40s, corresponding to composition C7Does not containViscosity of pentanediol compositionThe degree is 108s.

Claims (13)

1. A cosmetic composition comprising, in a physiologically acceptable medium:
the aqueous phase of the water-based polymer,
at least one amphoteric surfactant selected from betaines,
at least one anionic surfactant selected from alkyl sulphates,
pentanediol, and
at least 0.9% by weight, relative to the total weight of the composition, of at least one active substance of levan.
2. The composition according to claim 1, characterized in that the cosmetic composition is free of glycerol or in that the cosmetic composition comprises glycerol such that the active substance weight ratio between levan and glycerol is strictly greater than 1.
3. Composition according to claim 1 or 2, characterized in that the levan is inulin.
4. A composition according to any one of claims 1 to 3, characterized in that pentanediol is present in an active matter content of between 0.05 and 10 wt%, preferably between 0.1 and 5 wt%, relative to the total weight of the composition.
5. The composition according to any one of claims 1 to 4, wherein the active mass ratio between the anionic surfactant and the amphoteric surfactant is less than or equal to 4.5.
6. Composition according to any one of claims 1 to 5, characterized in that the amphoteric surfactant is selected from alkyl betaines and N-alkyl amidobetaines, preferably from N-alkyl amidobetaines, more preferably from cocamidopropyl betaine, coco betaine and mixtures thereof.
7. Composition according to any one of claims 1 to 6, characterized in that the amphoteric surfactant is present in an active substance content of between 1 and 20% by weight, preferably between 1 and 10% by weight, preferably between 1 and 5% by weight, relative to the total weight of the composition.
8. Composition according to any one of claims 1 to 7, characterized in that the anionic surfactant is selected from alkyl sulphates and mixtures thereof, in particular alkali metal or alkaline earth metal salts or ammonium salts, amine salts or amino alkoxides, and mixtures thereof.
9. The composition according to any one of claims 1 to 8, wherein the anionic surfactant is selected from ammonium salts.
10. The composition according to any one of claims 1 to 9, wherein the anionic surfactant is ammonium lauryl sulfate.
11. Composition according to any one of claims 1 to 10, characterized in that the anionic surfactant is present in a content of active substance at least equal to 5% by weight, preferably between 5% and 20% by weight, preferably between 5% and 15% by weight, relative to the total weight of the composition.
12. Composition according to any one of claims 1 to 11, characterized in that the content of pentanediol is between 0.05 and 10% by weight, preferably between 0.1 and 5% by weight, relative to the total weight of the composition.
13. A method for cleaning keratin materials, comprising applying to the keratin materials the cosmetic composition according to any one of claims 1 to 12.
CN202180070521.2A 2020-10-16 2021-10-15 Cleansing cosmetic composition containing two surfactants, specific diol and levan Pending CN116490161A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FRFR2010648 2020-10-16
FR2010648A FR3115198B1 (en) 2020-10-16 2020-10-16 Cosmetic cleansing composition comprising two surfactants, a specific diol and a fructan
PCT/EP2021/078665 WO2022079271A1 (en) 2020-10-16 2021-10-15 Cleansing cosmetic composition comprising two surfactants, a specific diol and a fructan

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US8993792B2 (en) * 2012-02-03 2015-03-31 Evonik Industries Ag Polyglycol ether-free sulphosuccinates based on polyglycerol partial esters and use thereof
FR3063637B1 (en) * 2017-03-07 2021-07-16 Laboratoires De Biologie Vegetale Yves Rocher USE OF AGAVE EXTRACTS FOR A HAIR APPLICATION
FR3086542B1 (en) * 2018-09-28 2021-01-08 Laboratoires De Biologie Vegetale Yves Rocher USE OF AN AGAVE EXTRACT TO STRENGTHEN THE BARRIER FUNCTION OF THE SKIN, SCALP AND / OR MUCOSAUSES AND MODULATE THE SKIN MICROBIOTE

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EP4228591A1 (en) 2023-08-23
WO2022079271A1 (en) 2022-04-21
FR3115198A1 (en) 2022-04-22

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