Patent Application
20100135947
The present invention relates to hair conditioning compositions which comprise a polygalactomannan having hydrophilic and hydrophobic substituents.
Hair conditioning compositions are typically applied to the hair immediately after shampooing and rinsing the hair. The conditioning composition is worked through the hair, and may then be left to penetrate the hair for a period of time before rinsing it from the hair with water.
Traditionally such conditioning compositions have used a combination of cationic surfactants and fatty materials such as long chain fatty alcohols. This combination forms a lamellar gel phase which imparts a desirable viscosity to the product and deposits on the hair during use of the product to provide a conditioning benefit.
Many consumers desire a “lighter” conditioning product which imparts less of a slippery and coated feel to their hair.
This has led to the development of “low-fat” formulations with a reduced content of fatty material.
However, reducing the content of fatty material can also reduce the viscosity of the product to an unacceptable level. Consequently, it has been found to be necessary to incorporate a thickener.
Examples of thickeners which have been used for this purpose are nonionic cellulose ethers such as hydroxyethylcellulose.
Hydrophobically-modified cellulose ethers such as cetyl hydroxyethylcellulose have also been used. Materials of this type are described in EP 412 705, EP 412 706 and EP 412 710 as providing a rheology very much like the gel-network structure of typical hair conditioners without the slimy feel associated with most polymeric thickeners, and without using a typical quaternary ammonium compound/fatty alcohol gel-network thickening system.
A problem associated with the use of the above-described cellulosic thickeners is that it is difficult to obtain the right viscosity profile under different conditions of product usage. For example, a thick, creamy product viscosity is desirable to enable controlled pouring and product dosage onto the hair. A lower product viscosity is preferred to facilitate spreading of the product through the hair and rinsing, but not to the extent that the product is perceived to “disappear” into the hair.
The inventors have found that this problem can be solved if a polygalactomannan having hydrophilic and hydrophobic substituents is used to thicken the hair conditioning composition.
Substituted polygalactomannans of the above type have been proposed for the stabilisation of lathering compositions such as shower gels and shampoos in WO99/01105. The formulations in that publication are based on insoluble silicones and detergent surfactants.
The invention provides a hair conditioning composition comprising a cationic surfactant, a fatty material, a polygalactomannan having hydrophilic and hydrophobic substituents, and an aqueous carrier.
The invention also provides the use of a polygalactomannan having hydrophilic and hydrophobic substituents as a viscosity modifier in a hair conditioning composition comprising cationic surfactant and fatty material.
Cationic Surfactant
Compositions according to the invention comprise one or more cationic surfactants which are cosmetically acceptable and suitable for topical application to the hair.
Suitable cationic surfactants for use in compositions of the invention contain amino or quaternary ammonium hydrophilic moieties which are positively charged when dissolved in the composition.
Suitable quaternary ammonium cationic surfactants correspond to the following general formula (I):
[N(R1)(R2)(R3)(R4)]+(X)− (I)
in which R1, R2, R3, and R4 are each independently selected from (a) an aliphatic group of from 1 to 22 carbon atoms, or (b) an aromatic, alkoxy, polyoxyalkylene, alkylamido, hydroxyalkyl, aryl or alkylaryl group having up to 22 carbon atoms; and X is a salt-forming anion such as those selected from halogen, (e.g. chloride, bromide), acetate, citrate, lactate, glycolate, phosphate nitrate, sulphate, and alkylsulphate radicals.
The aliphatic groups can contain, in addition to carbon and hydrogen atoms, ether linkages, and other groups such as amino groups. The longer chain aliphatic groups, e.g., those of about 12 carbons, or higher, can be saturated or unsaturated.
In a suitable class of cationic surfactant of general formula (I), R1 and R2 are each independently selected from C16 to C22 hydrocarbyl chains comprising at least one ester linkage in both R1 and R2, and R3 and R4 are each independently selected from CH3 and CH2CH2OH.
In another suitable class of cationic surfactant of general formula (I), R1 and R2 are each independently selected from C16 to C22 saturated or unsaturated, preferably saturated, chains, and R3 and R4 are each independently selected from CH3 and CH2CH2OH, preferably CH3.
In a preferred class of cationic surfactant of general formula (I), R1 is a C16 to C22 alkyl chain and R2, R3 and R4 are each independently selected from CH3 and CH2CH2OH, preferably CH3.
Specific examples of suitable quaternary ammonium cationic surfactants of general formula (I) are cetyltrimethylammonium chloride, behenyltrimethylammonium chloride (BTAC), cetylpyridinium chloride, tetramethylammonium chloride, tetraethylammonium chloride, octyltrimethylammonium chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octyldimethylbenzylammonium chloride, decyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride, didodecyldimethylammonium chloride, dioctadecyldimethylammonium chloride, tallowtrimethylammonium chloride, cocotrimethylammonium chloride, dipalmitoylethyldimethylammonium chloride, PEG-2 oleylammonium chloride and salts of these, where the chloride is replaced by halogen, (e.g., bromide), acetate, citrate, lactate, glycolate, phosphate nitrate, sulphate, or alkylsulphate.
Particularly preferred quaternary ammonium cationic surfactants for use in the invention are cetyltrimethylammonium chloride, available commercially, for example as GENAMIN CTAC, ex Hoechst Celanese and Arquad 16/29 supplied by Akzo Nobel, and behenyltrimethylammonium chloride (BTAC) such as Genamin KDM-P supplied by Clariant.
Mixtures of any of the foregoing materials may also be suitable.
Salts of primary, secondary, and tertiary fatty amines are also suitable cationic surfactants for use in the invention. The alkyl groups of such amines preferably have from about 12 to about 22 carbon atoms, and can be substituted or unsubstituted. These amines are typically used in combination with an acid to provide the cationic species.
A preferred class of amine corresponds to the following general formula (II):
R1—C(O)—N(H)—R2—N(R3)(R4) (II)
in which R1 is a fatty acid chain containing from 12 to 22 carbon atoms, R2 is an alkylene group containing from one to four carbon atoms, and R3 and R4 are, independently, an alkyl group having from one to four carbon atoms.
Specific examples of suitable materials of general formula (II) are stearamidopropyldimethylamine, stearamidopropyldiethylamine, stearamidoethyldiethylamine, stearamidoethyldimethylamine, palmitamidopropyldimethylamine, palmitamidopropyldiethylamine, palmitamidoethyldiethylamine, palmitamidoethyldimethylamine, behenamidopropyldimethylamine, behenamidopropyldiethylamine, behenamidoethyldiethylamine, behenamidoethyldimethylamine, arachidamidopropyldimethylamine, arachidamidopropyldiethylamine, arachidamidoethyldiethylamine, arachidamidoethyldimethylamine, and diethylaminoethylstearamide.
Also useful are dimethylstearamine, dimethylsoyamine, soyamine, myristylamine, tridecylamine, ethylstearylamine, N-tallowpropane diamine, ethoxylated (with 5 moles of ethylene oxide) stearylamine, dihydroxyethylstearylamine, and arachidyl behenylamine.
Particularly preferred is stearamidopropyldimethylamine.
Mixtures of any of the foregoing materials may also be suitable.
The acid used to provide the cationic species can be any organic acid or mineral acid of sufficient acid strength to neutralise a free amine nitrogen. Such acids include hydrochloric acid, sulphuric acid, nitric acid, phosphoric acid, lactic acid, citric acid, tartaric acid, acetic acid, gluconic acid, glycolic acid and propionic acid, or combinations thereof. In general, a sufficient amount of acid is added to neutralise the amidoamine compound and to adjust the final pH of the composition to within a range of from about 2.5 to about 6, preferably in a pH range of from about 3 to about 5. The molar ratio of protonatable amine groups to H+ from the acid is preferably from about 1:0.3 to 1:1.2, and more preferably from about 1:0.5 to about 1:1.1.
Mixtures of any of the above-described cationic surfactants may also be suitable.
In the composition of the invention, the level of cationic surfactant preferably ranges from 0.1 to 10%, more preferably 0.2 to 5%, most preferably 0.25 to 4% by total weight of cationic surfactant based on the total weight of the composition.
Fatty Material
Compositions of the invention comprise a fatty material. The fatty material, together with the cationic surfactant and an aqueous carrier, forms a lamellar gel phase which is suitable for providing various hair conditioning attributes.
By “fatty material” is meant a compound having the general formula R—X, wherein R is an aliphatic carbon chain and X is a functional group (e.g. alcohol, acid, or derivative).
R is preferably a fully saturated aliphatic carbon chain comprising from 8 to 30 carbon atoms, more preferably from 16 to 22 carbon atoms.
X is preferably an alcohol group.
Most preferably, the fatty material is selected from cetyl alcohol, stearyl alcohol, behenyl alcohol, and mixtures thereof.
The level of fatty material in conditioners of the invention suitably ranges from 0.01 to 15%, preferably from 0.1 to 10%, and more preferably from 0.1 to 5% by total weight fatty material based on the total weight of the composition.
The weight ratio of cationic surfactant to fatty material is suitably from 10:1 to 1:10, preferably from 4:1 to 1:8, more preferably from 1:1 to 1:7.
Substituted Polygalactomannan
Polygalactomannans are polysaccharides composed principally of galactose and mannose units and are usually found in the endosperm of certain leguminous seeds such as guar, locust bean, honey locust, flame tree and the like. Guar gum, for example, is composed mostly of a galactomannan with essentially is a straight chain mannan with single membered galactose branches. The ratio of galactose to mannose in the guar polymer is 1:2. Locust bean gum is a polygalactomannan gum of similar molecular structure in which the ratio of galactose to mannose is 1:4.
Guar and locust bean gums are preferred sources of the polygalactomannans, principally because of their commercial availability. Guar gum is a most preferred source.
Polygalactomannans for use in compositions of the invention (hereinafter referred to as “substituted polygalactomannans”) contain hydrophilic substituents and hydrophobic substituents.
Suitably the substituted polygalactomannan is derived from a polygalactomannan having a molecular weight of from 50,000 to 1,600,000, depending on the origin of the polygalactomannan.
Suitable substituted polygalactomannans have a total molar substitution of greater than 0.7. Preferably the total molar substitution ranges from 0.9 to 2.01. By “molar substitution” is meant the average number of moles of substituents on each anhydroglycosidic unit of the polygalactomannan.
Suitable substituted polygalactomannans contain an average of from 0.7 to 4 hydrophilic substituents per anhydroglycosidic unit. Preferred substituted polygalactomannans contain an average of from 0.9 to 2 hydrophilic substituents per anhydroglycosidic unit.
Suitable substituted polygalactomannans contain an average of from 0.0001 to 0.02 hydrophobic substituents per anhydroglycosidic unit. Preferred substituted polygalactomannans contain an average of from 0.0005 to 0.01 hydrophobic substituents per anhydroglycosidic unit.
Suitably the molar ratio of hydrophilic substituents to hydrophobic substituents ranges from 35:1 to 40,000:1. Preferably the molar ratio ranges from 90:1 to 4000:1.
The hydrophilic substituents may suitably be selected from C2-C4 alkyl groups, C2-C4 hydroxyalkyl groups, carboxymethyl, amino and carboxylic groups. Preferably the hydrophilic substituents are C2-C4 hydroxyalkyl groups, most preferably hydroxypropyl groups. Mixtures of any of the above hydrophilic substituents may also be suitable.
The hydrophobic substituents may suitably be chosen from linear or branched alkyl and alkenyl groups containing from 10 to 32 carbon atoms, more preferably from 14 to 28 carbon atoms. The alkyl or alkenyl groups can be substituted with one or more hydroxyl groups. Mixtures of any of the above hydrophobic substituents may also be suitable.
The hydrophilic and hydrophobic substituents can either be linked directly via a carbon-carbon bond to the anhydroglycoside unit, or can be linked via an ether, urethane, ester, amide or acyl bond and preferably via an ether bond.
Preferred substituted polygalactomannans for use in the invention are poly (alkyl ethers) of polygalactomannans having hydrophilic and hydrophobic alkyl ether substituents respectively.
Examples of such materials are poly (alkyl ethers) of polygalactomannans in which the hydrophilic substituent is HOR1—, in which R1 is an alkylene group having two to four carbon atoms and in which the OH group is on the carbon atom beta to the ether group, and the hydrophobic substituent is chosen from R2, HOR3, and R4O—CH2CH(OH)—CH2—, in which R2 is an alkyl group which contains 10 to 32 carbon atoms, R3 is an alkylene group which contains 10 to 32 carbon atoms having the OH group on the carbon atom beta to the ether group and R4 is an alkyl group having from 7 to 29 carbon atoms.
Preferred examples of such materials are poly (alkyl ethers) of polygalactomannans in which the hydrophilic substituent is the hydroxypropyl group and the hydrophobic substituent is a linear alkyl group containing from 14 to 28 carbon atoms or a mixture of such alkyls.
U.S. Pat. No. 4,960,876 and U.S. Pat. No. 4,870,167 describe methods of preparation of substituted polygalactomannans suitable for use in compositions of the invention.
Commercially available examples of substituted polygalactomannans suitable for use in compositions of the invention are guar gums sold under the name Esaflor HM 22 by the company Lamberti or under the name Jaguar XC 95-3 by the company Rhone-Poulenc.
The level of substituted polygalactomannan in conditioners of the invention suitably ranges from 0.001 to 10%, preferably from 0.005 to 5%, and more preferably from 0.01 to 2% by total weight substituted polygalactomannan based on the total weight of the composition.
Aqueous Carrier
The conditioning composition of the present invention comprises an aqueous carrier.
Suitable aqueous carriers are water and water solutions of lower alkyl alcohols and polyhydric alcohols.
Examples of suitable lower alkyl alcohols are monohydric alcohols having 1 to 6 carbons, preferably ethanol and isopropanol.
Examples of suitable polyhydric alcohols are propylene glycol, hexylene glycol, glycerin, and propanediol.
Preferably, the aqueous carrier is substantially water.
Generally, compositions according to the invention comprise at least 60%, preferably at least 65%, more preferably at least 70% water by weight based on the total weight of the composition.
Further Conditioning Agents
Compositions of the invention may comprise further conditioning agents to optimise wet and dry conditioning benefits.
Particularly preferred further conditioning agents are silicone emulsions.
Suitable silicone emulsions include those formed from silicones such as polydiorganosiloxanes, in particular polydimethylsiloxanes which have the CTFA designation dimethicone, polydimethyl siloxanes having hydroxyl end groups which have the CTFA designation dimethiconol, and amino-functional polydimethyl siloxanes which have the CTFA designation amodimethicone.
The emulsion droplets may typically have a Sauter mean droplet diameter (D3,2) in the composition of the invention ranging from 0.01 to 20 micrometer, more preferably from 0.2 to 10 micrometer.
A suitable method for measuring the Sauter mean droplet diameter (D3,2) is by laser light scattering using an instrument such as a Malvern Mastersizer.
Suitable silicone emulsions for use in compositions of the invention are available from suppliers of silicones such as Dow Corning and GE Silicones. The use of such pre-formed silicone emulsions is preferred for ease of processing and control of silicone particle size. Such pre-formed silicone emulsions will typically additionally comprise a suitable emulsifier such as an anionic or nonionic emulsifier, or mixture thereof, and may be prepared by a chemical emulsification process such as emulsion polymerisation, or by mechanical emulsification using a high shear mixer. Pre-formed silicone emulsions having a Sauter mean droplet diameter (D3,2) of less than 0.15 micrometers are generally termed microemulsions.
Examples of suitable pre-formed silicone emulsions include emulsions DC2-1766, DC2-1784, DC-1785, DC-1786, DC-1788 and microemulsions DC2-1865 and DC2-1870, all available from Dow Corning. These are all emulsions/microemulsions of dimethiconol. Also suitable are amodimethicone emulsions such as DC939 (from Dow Corning) and SME253 (from GE Silicones).
Also suitable are silicone emulsions in which certain types of surface active block copolymers of a high molecular weight have been blended with the silicone emulsion droplets, as described for example in WO03/094874. In such materials, the silicone emulsion droplets are preferably formed from polydiorganosiloxanes such as those described above. One preferred form of the surface active block copolymer is according to the following formula:
wherein the mean value of x is 4 or more and the mean value of y is 25 or more.
Another preferred form of the surface active block copolymer is according to the following formula:
wherein the mean value of a is 2 or more and the mean value of b is 6 or more.
Mixtures of any of the above described silicone emulsions may also be used.
Silicone will generally be present in a composition of the invention at levels of from 0.05 to 10%, preferably 0.05 to 5%, more preferably from 0.5 to 2% by total weight of silicone based on the total weight of the composition.
Other Optional Ingredients
Compositions according to the invention may also incorporate other cosmetically suitable ingredients, preferably at a level of 2% by weight or less. Suitable ingredients include: preservatives, colouring agents, chelating agents, antioxidants, fragrances, antimicrobials, antidandruff agents, cationic conditioning polymers, styling ingredients, sunscreens, proteins and hydrolysed proteins.
Use
The compositions of the invention may be used by applying them to wet hair, typically hair which has been shampooed and then rinsed with water.
Generally, the composition is applied to the hair and then worked through the hair. Preferably the composition is then left to penetrate the hair for a period of about one to three minutes before rinsing it from the hair with water.
The invention will now be further described by reference to the following Examples. In the Examples, all percentages are by weight based on total weight, unless otherwise specified. Examples according to the invention are denoted by a number, whereas comparative examples are denoted by a letter.
A series of hair conditioning compositions were prepared having ingredients as shown in the following Table 1:
(1)Hydroxyethylcellulose, ex Aqualon
(2)Cetyl hydroxyethylcellulose, ex Aqualon
(3)Hydrophobically modified hydroxypropyl guar, ex Lamberti
The compositions were evaluated for their viscosity behaviour under varying conditions of shear stress.
The results of the evaluation are shown below in Table 2:
The results show that the Examples according to the invention (1, 2 and 3) have a superior viscosity profile under conditions of low and high shear, when compared to Comparative Examples (A, B, C, D) with the same surfactant base.
Compositions according to the invention have a desirable thick viscosity at low shear, which does not break down too rapidly at high shear. If viscosity breakdown is too rapid at high shear (for example as shown in Comparative Example B), the conditioner will be perceived to “disappear” into the hair when it is spread through the hair by the consumer.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0624132.7 | Dec 2006 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP07/61971 | 11/7/2007 | WO | 00 | 1/15/2010 |
