IP Library › Granted Patent US 12,303,581
Granted Patent B2
US 12,303,581 · App. 16/760,191 · Granted May 20, 2025

Cosmetic emulsion containing a gemini surfactant and a lipophilic polymer

Inventors: Raluca Lorant (Chevilly la Rue, FR); Laure Fageon (Chevilly la Rue, FR); Carole Guiramand (Chevilly la Rue, FR); Karl Boutelet (Chevilly la Rue, FR)
Assignee: L'OREAL
A61K8/44A61K8/06A61K8/062A61K8/42A61K8/45A61K8/463A61K8/466A61K8/8152A61K8/86A61Q1/14A61Q17/04A61Q19/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,303,581
App. No.
16/760,191
Granted
May 20, 2025
Kind
B2
Abstract

Cosmetic emulsion containing a gemini surfactant and a lipophilic polymer The invention relates to a composition in the form of an emulsion, in particular in the form of an oil-in-water emulsion, comprising a gemini surfactant having a specific chemical structure with at least two fatty amide groups and at least one lipophilic polymer comprising at least hydroxyethyl acrylate units and acrylate units bearing a lipophilic group, wherein the weight ratio of the sum of all the hydroxyethyl acrylate units to the sum of all the acrylate units bearing a lipophilic group ranges from 1:30 to 1:1 and wherein the lipophilic polymer has a number-average molecular weight Mn ranging from 2000 to 9000 g/mol. The composition in accordance with the invention makes it possible to obtain a cosmetic emulsion having an increased sun protection factor, while at the same time having good cosmetic properties, such as a non-greasy and non-tacky feel, while at the same time being stable, in particular from the physicochemical viewpoint.

Claims (25)

1. A composition in the form of an emulsion comprising 0.1% to 45% by weight based upon the weight of the composition of at least one UV-screening agent, 0.01% to 5% by weight based upon the weight of the composition of at least one gemini surfactant having the Chemical Formula (II) shown below, or stereoisomers thereof:

in which:

R 1 and R 3 denote, independently of each other, an alkyl radical containing from 1 to 25 carbon atoms;

R 2 denotes a spacer constituted of a linear or branched alkylene chain containing from 1 to 12 carbon atoms;

X and Y denote, independently of each other, —(C 2 H 4 O)a —(C 3 H 6 O) b Z, in which

Z denotes a hydrogen atom or a radical —CH 2 —COOM, —SO 3 M, —P(O)(OM) 2 , —C 2 H 4 —SO 3 M, —C 3 H 6 —SO 3 M or —CH 2 (CHOH) 4 CH 2 OH, where M represents H or an alkali metal or alkaline-earth metal or ammonium or alkanolammonium ion,

a ranges from 0 to 15,

b ranges from 0 to 10, and

the sum of a +b ranges from 1 to 25; and

n ranges from 1 to 10;

and

0.1% to 10% by weight based upon the weight of the composition of at least one lipophilic polymer chosen from copolymers of behenyl acrylate and 2-hydroxyethyl acrylate having a number-average molecular weight Mn ranging from 5000 to 9000 g/mol and a weight ratio of the 2-hydroxyethyl acrylate to behenyl acrylate from 1:15 to 1:1; and wherein the sum of the total units of the 2-hydroxyethyl acrylate and behenyl acrylate is 100% by weight of the total weight of the copolymer.

2. The composition according to claim 1 , in which, for the at least one gemini surfactant of formula (II), each of the R 1 —CO— and R 3 —CO— groups is a residue from a fatty acid that comprises from 8 to 20 carbon atoms.

3. The composition according to claim 1 , in which, for the at least one gemini surfactant of formula (II), each of the R 1 —CO— and R 3 —CO— groups denotes a coconut fatty acid residue.

4. The composition according to claim 1 , in which, for the at least one gemini surfactant of formula (II), for each of the X and Y radicals, the sum of a and b has a mean value ranging from 10 to 20.

5. The composition according to claim 1 , in which, for the at least one gemini surfactant of formula (II), Z is the —SO 3 M group, where M is an alkali metal ion.

6. The composition according to claim 1 , in which, for the at least one gemini surfactant of formula (II), n is equal to 1.

7. The composition according to claim 1 , in which the at least one gemini surfactant of formula (II) has the following structure:

8. The composition according to claim 1 , in which the at least one gemini surfactant of formula (II) is mixed with (a) a glyceryl ester of a C 6 -C 22 fatty acid, (b) a diester of a C 6 -C 22 fatty acid and of citric acid and of glycerol, and (c) a C 10 -C 30 fatty alcohol.

9. The composition according to claim 1 , in which the at least one lipophilic polymer has a melting point ranging from 60° C. to 69° C.

10. The composition according to claim 9 in which the at least one gemini surfactant of formula (II) has the following structure:

11. The composition according to claim 1 , in which the at least one lipophilic polymer is present in an amount ranging from 0.1% to 3% by weight relative to the total weight of the composition.

12. A process for caring for and/or removing makeup from and/or cleansing keratin materials which comprises applying to the keratin materials the composition according to claim 1 .

13. A cosmetic process for treating a keratin material, in which the composition as defined in claim 1 is applied to the keratin material.

14. The composition according to claim 1 , which is an oil-in-water emulsion.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2021
From: LORANT, RALUCA; FAGEON, LAURE; GUIRAMAND, CAROLE; BOUTELET, KARL
To: L'OREAL
Reel/Frame 055639/0830 →
Priority Claims (1)
FR 1760735 · Nov 15, 2017 · national
Continuity (1)
Related Publication 20210177719A1 · Jun 17, 2021
References Cited (39)
US 4128634A · Hase et al. · 1978 [cited by applicant]
US 4128635A · Hase et al. · 1978 [cited by applicant]
US 20040005279A1 · Lorant et al. · 2004 [cited by applicant]
US 20070264204A1 · Noor et al. · 2007 [cited by applicant]
US 20090105353A1 · Lorant · 2009 [cited by examiner]
US 20100202985A1 · Sengupta · 2010 [cited by applicant]
US 20110097288A1 · Janssen · 2011 [cited by applicant]
US 20120244202A1 · Simonnet · 2012 [cited by applicant]
US 20130052148A1 · Chavan · 2013 [cited by applicant]
US 20160250137A1 · Noor · 2016 [cited by examiner]
US 20170348219A1 · Uyama · 2017 [cited by applicant]
CN 101442979A · 2009 [cited by applicant]
CN 102762186A · 2012 [cited by applicant]
CN 104936575A · 2015 [cited by applicant]
CN 107250181A · 2017 [cited by applicant]
DE 2608875A1 · 1977 [cited by applicant]
DE 2608834A1 · 1977 [cited by applicant]
EP 1386600A1 · 2004 [cited by applicant]
EP 2039339A2 · 2009 [cited by applicant]
EP 3235839A1 · 2017 [cited by applicant]
FR 2843020A1 · 2004 [cited by applicant]
FR 2921262A1 · 2009 [cited by applicant]
FR 3046076A1 · 2017 [cited by applicant]
GB 1560428A · 1980 [cited by applicant]
JP 52108030A · 1977 [cited by applicant]
JP 2009120493A · 2009 [cited by applicant]
JP 2009536949A · 2009 [cited by applicant]
JP 2012144580A · 2012 [cited by applicant]
JP A2012144580A · 2012 [cited by applicant]
JP 2013520464A · 2013 [cited by applicant]
JP 2015131767A · 2015 [cited by applicant]
JP 2015164970A · 2015 [cited by applicant]
WO WO2007133720A2 · 2007 [cited by applicant]
WO WO2011104228A1 · 2011 [cited by applicant]
WO WO2016098456A1 · 2016 [cited by applicant]
JPO English abstract for JP 2015-131767 (Sase et al) (Year: 2015). [cited by examiner]
Derwent English abstract for JP 2012-144580 (Sekiguchi et al) (Year: 2012). [cited by examiner]
Machine-assisted English translation for JP 2015-131767 (Sase et al) (Year: 2015). [cited by examiner]
Machine-assisted English translation for JP 2012-144580 (Sekiguchi et al) (Year: 2012). [cited by examiner]