Title of Invention	AN AQUEOUS CONDITIONING SHAMPOO COMPOSITION
Abstract	An aqueous conditioning shampoo composition comprising an anionic cleansing surfactant and a gel network comprising: (i) a fatty material selected from C12-C22 fatty alcohol, C12-C22 fatty acid, C12-C22 fatty amide or mixtures thereof and (ii) particles having platelet morphology and melting point greater than that of the fatty material.

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FORM - 2 THE PATENTS ACT, 1970 (39 of 1970) & The Patents Rules, 2003 COMPLETE SPECIFICATION (See Section 10 and Rule 13) CONDITIONING SHAMPOO COMPOSITIONS HINDUSTAN UNILEVER LIMITED, a company incorporated under the Indian Companies Act, 1913 and having its registered office at 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India The following specification particularly describes the invention and the manner in which it is to be performed WO 2008/055815 PCT/EP2007/061677 CONDITIONING SHAMPOO COMPOSITIONS FIELD OF THE INVENTION 5 This invention relates to aqueous conditioning shampoo compositions comprising a cleansing surfactant and a gel network. BACKGROUND AND PRIOR ART 10 Conditioning shampoo compositions comprising various combinations of cleansing surfactant and conditioning agents are known. These products typically comprise an anionic cleansing surfactant in combination with a conditioning 15 agent. Amongst the most popular conditioning agents used in shampoo compositions are oily materials such as mineral oils, naturally occurring oils such as triglycerides and silicone polymers. These are generally present in the shampoo as dispersed hydrophobic emulsion droplets. 20 Conditioning is achieved by the oily material being deposited onto the hair resulting in the formation of a film. Such compositions often have a relatively low viscosity and may be perceived to be low quality as a result. 25 Other conditioning shampoo compositions use gel networks comprising fatty alcohol to structure or thicken the product and also to deliver a conditioning benefit. US 2003/0223952 (P&G) discloses conditioning shampoos comprising detersive 30 surfactant and a gel network made from fatty alcohol and a cationic surfactant. WO 2008/055815 PCT/EP2007/061677 - 2 - The use of particulate materials in conditioning shampoos is not common. US 6,617,292 B2 (L'Oreal) discloses conditioning shampoos comprising aluminium oxide, an amphoteric or nonionic surfactant, a fatty acid or fatty 5 alcohol, and a cationic surfactant. A problem that arises with many of the conditioners disclosed in the prior art is that they do not give good sensory benefits both when the hair is wet, i.e., during 10 and/or immediately after application and also when the hair is subsequently dried. SUMMARY OF THE INVENTION 15 The present inventors have found that excellent sensory benefits may be given to both wet and subsequently dried hair by use of conditioning shampoos comprising an anionic cleansing surfactants and a particularly structured gel network. These conditioning shampoos also have the benefit 20 of having a rich, creamy appearance, enhancing their perception of being high quality products. Conditioning shampoo compositions of the invention give good wet feel and ease of wet combing. In addition they give 25 good dry feel, ease of dry combing, and manageability. In a first aspect of the invention, there is provided an aqueous conditioning shampoo composition comprising an anionic cleansing surfactant and a gel network comprising: WO 2008/055815 PCT/EP2007/061677 - 3 - (i) a fatty material selected from C12-C22 fatty alcohol, C12-C22 fatty acid, C12-C22 fatty amide or mixtures thereof; and (ii) particles having platelet morphology and melting 5 point greater than that of the fatty material. In a second aspect of the invention, there is provided a method of cleansing and conditioning the hair comprising the application of an aqueous conditioning shampoo composition 0 according to the first aspect of the invention. In a third aspect of the invention, there is provided the use of a gel network comprising a fatty material selected from C12-C22 fatty alcohol, C12-C22 fatty acid, C12-C22 fatty 5 amide or mixtures thereof and particles having platelet morphology and melting point greater than that of the fatty material to give structure and/or conditioning benefits to an aqueous shampoo composition comprising an anionic cleansing surfactant. 0 In a fourth aspect of the invention, there is provided a method of manufacturing an aqueous conditioning shampoo composition comprising the preparation of a gel network comprising a fatty material selected from C12-C22 fatty 5 alcohol, C12-C22 fatty acid, C12-C22 fatty amide or mixtures thereof and particles having platelet morphology and melting point greater than that of the fatty material, the gel network being subsequently added to an aqueous solution of an anionic cleansing surfactant. 8 MAY 2009 WO 2008/055815 PCTVEP2007/061677 - 4 - DETAILED DESCRIPTION OF THE INVENTION The compositions of the invention are suitable for application to the human hair. They are typically used as 5 rinse off products, that is to say their application is usually followed by a rinsing stage with water. The invention uses a gel network as described hereinafter to deliver structure and conditioning benefits to a shampoo 10 composition comprising an anionic cleansing surfactant. The term "structure", when used in this context, should be understood to mean "thicken", i.e. increase the viscosity thereof. 15 The preferred viscosity for products according to the invention is from 3000 to 9000 cP (mPa.s), more preferably from 5000 to 7000 cP (mPa.s), and most preferably from 5500 to 6500 cP (mPa.s) at 30°C, as measured by a Brookfield viscometer equipped with a RVT pin number 5 at a measuring 20 speed of 20 rpm. By "aqueous conditioning shampoo composition" is meant a composition which has water or an aqueous solution or a lyotropic liquid crystalline phase as its major component. 25 Typically, the composition will comprise at least 50%, preferably at least 60%, at most preferably at least 75% by weight of water. 8MAY2009 WO 2008/055815 PCT/EP2007/061677 - 5 - Anionic cleansing surfactant Conditioning shampoo compositions according to the invention comprise one or more anionic cleansing surfactants, which are 5 cosmetically acceptable and suitable for topical application to the hair. Examples of suitable anionic cleansing surfactants are the alkyl sulphates, alkyl ether sulphates, alkaryl sulphonates, 10 alkanoyl isethionates, alkyl succinates, alkyl sulphosuccinates, alkyl ether sulphosuccinates, N-alkyl sarcosinates, alkyl phosphates, alkyl ether phosphates, and alkyl ether carboxylic acids and salts thereof, especially their sodium, magnesium, ammonium and mono-, di- and 15 triethanolamine salts. The alkyl and acyl groups generally contain from 8 to 18, preferably from 10 to 16 carbon atoms and may be unsaturated. The alkyl ether sulphates, alkyl ether sulphosuccinates, alkyl ether phosphates and alkyl ether carboxylic acids and salts thereof may contain from 1 20 to 20 ethylene oxide or propylene oxide units per molecule. Typical anionic cleansing surfactants for use in shampoo compositions of the invention include sodium oleyl succinate, ammonium lauryl sulphosuccinate, sodium lauryl sulphate, 25 sodium lauryl ether sulphate, sodium lauryl ether sulphosuccinate, ammonium lauryl sulphate, ammonium lauryl ether sulphate, sodium dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate, sodium cocoyl isethionate, sodium lauryl isethionate, lauryl ether 30 carboxylic acid and sodium N-lauryl sarcosinate. 8 MAY 2009, WO 2008/055815 PCT/EP2007/06:I677 - 6 - Preferred anionic cleansing surfactants are sodium lauryl sulphate, sodium lauryl ether sulphate(n)EO, (where n is from 1 to 3), sodium lauryl ether sulphosuccinate(n)EO, (where n is from 1 to 3), ammonium lauryl sulphate, ammonium lauryl 5 ether sulphate (n)EO, (where n is from 1 to 3), sodium cocoyl isethionate and lauryl ether carboxylic acid (n) EO (where n is from 10 to 20). Mixtures of any of the foregoing anionic cleansing 10 surfactants may also be suitable. The total amount of anionic cleansing surfactant preferably ranges from 0.5 to 45%, more preferably from 1 to 30%, and most preferably from 5 to 20% by total weight of the 15 composition. Gel Network The gel network is formed by combining the components at a 20 temperature above the melting point of the fatty material in the presence of water. In a preferred method of manufacture in accordance with the fourth aspect of the invention, the fatty material is melted in water and the particulate material is then added. In a more preferred method of 25 manufacture, a quaternary ammonium compound is also added, preferably after the particulate material. A dispersion of liquid crystalline phase droplets is typically produced. It will be realised- that, in effect, the gel network has another component: water. In preferred embodiments, the gel 30 network comprises an LB lamellar phase dispersion at 25°C. 8 MAY 2009 WO 2008/055815 PCT/EP2007/061677 - 7 - The composition according to the invention can only be formed with a separately made gel network. Mixing the components of the gel network together without premixing and heating does not form a gel network. 5 Fatty material A fatty material selected.from fatty alcohol, fatty acid, fatty amide, or mixtures thereof is an essential component 0 of the gel network. Preferably, the fatty material comprises a C12-C22 fatty alcohol. The fatty alcohol is preferably a primary alcohol. The fatty alcohol and/or fatty acid and/or fatty amide preferably has a linear (i.e. non-branched) C12-C22 hydrocarbon chain. Preferably, said 5 chain is saturated. Preferably, the fatty alcohol and/or fatty acid is C16-C22 and more preferably it is C16-C18-Most preferably the fatty material is cetyl alcohol and/or stearyl alcohol. 0 The total amount of fatty material selected from C3.2-C22 fatty alcohol, C12-C22 fatty acid, or mixtures thereof, is preferably from 0.01 to 20%, more preferably from 0.1 to 10%, and most preferably from 0.5 to 5% by weight of the total composition. In preferred embodiments, these 5 preferred amounts apply to the level of C12-C22 fatty alcohol in the total composition. 8MAY2009 WO 2008/055815 PCT/EP2007/061677 - 8 - Particles having platelet morphology Particles having platelet morphology are a second essential component of the gel network. Without wishing to be bound 5 by theory, it is believed that such particles act as templates that help sustain the ordered structure of the gel network within the shampoo composition, despite the presence of anionic surfactant therein. The particles are believed to enhance the stability and performance of the gel network 10 as a result. The particles should be understood to be solid and to have a melting point greater than that of the fatty material. When the gel network also comprises a quaternary ammonium 15 compound (vide infra), the particles also have a melting point higher than this component. Typically, the solid particles have an inorganic core, although they may be surface-modified with organic groups (vide infra). Preferably, the particles have a melting point of greater 20 than 150°C. ^Platelet morphology" should be understood to mean that the particles have a plate-like" shape, i.e. their lengths in two orthogonal directions are considerably greater than 25 their length in the third orthogonal direction. Typically, the particles have length and breadth that are each independently at least 10 times greater their depth; where "length", "breadth", and "depth" are expressions for the three orthogonal directions. 30 ' 8MAY2009 WO 2008/055815 PCT/EP2007/061677 - 10 - having the general formula Mg3 (Si20s)2(OH)2-nH20, and derivatives thereof, for example in which a proportion of the aluminium ions are replaced with magnesium ions or a proportion of the magnesium ions are replaced with lithium 5 ions and/or some of the hydroxyl ions are replaced by fluoride ions; the derivatives may comprise a further metal ion to balance the overall charge. Specific examples of suitable smectite clays are 10 montmorillonites, volchonskoites, nontronites, saponites, beidelites and sauconites, particularly those having an alkali or alkaline earth metal ion within the crystal lattice structure. Preferred smectite clays are montmorillonites, nontronites, saponites, beidelites, 15 sauconites and mixtures thereof. Particularly preferred are montmorillonites, e.g. bentonites and hectorites, with bentonites being especially preferred. Particularly preferred particles having platelet morphology 20 are hydrophobically-modified anionic clays; especially, hydrophobically-modified bentonite clay. When used, hydrophobically-modified clays typically have organic cations replacing at least a proportion of the 25 inorganic metal ions of the unmodified clay. Preferred organic cations for this purpose comprising one or more Cg- C30 alkyl groups. The cationic group is preferably a quaternary ammonium group. Particularly preferred organic cations have two C6_C3o alkyl groups, for example: 30 distearyldimethylammonium; 8 MAY 2009, WO 2008/055815 PCT7EP2007/061677 - 11 - dicetyldimethylammonium; dimethyldi(hydrogenated tallow)ammonium; dicetylmethylbenzylammonium; dicocodimethylammonium; 5 dibehenyl/diarachidyldimethylammonium; hydroxypropyl bis-stearylammonium; dibehenyldimethy1ammonium; dibehenylmethylbenzylammonium; and dimyristyldimethylammonium. 10 Especially preferred particulate materials having platelet morphology are Quaternium-18 Bentonite, i.e. bentonite hydrophobically-modified by dimethyldi(hydrogenated tallow)ammonium cations) and Quaternium-90 Bentonite, an 15 analogous material with two vegetable-derived fatty chains. TM Examples of such clays are Tixogel MP 100 and Tixogel MP TM 100V from Sud Chemie. Other similar materials include Quaternium benzalkonium bentonite, Quaternium-18 hectorite, stearalkonium bentonite, stearalkonium hectorite and 20 dihydrogenated tallow benzylmonium hectorite. The particles having platelet morphology have a particle size such that preferably at least 50% and more preferably at least 80% of them are able to pass through a 90 micron 25 screen, such as an air sieve as commonly used in the art. The total amount of particles having platelet morphology is preferably from 0.005 to 10%, more preferably from 0.01 to 5%, and most preferably from 0.01 to 1% by weight of the 30 total composition. 8 MAY 2009, WO 2008/055815 PCT/EP2007/061677 - 12 - The weight ratio of particles having platelet morphology to the fatty material is preferably from 1:100 to 1:2, more preferably from 1:50 to 1:5, and most preferably from 1:30 to 1:10. 5 Quaternary ammonium compound A quaternary ammonium compound having at least one carbon chain of length C12-C30 is a highly preferred component of 10 the gel network. In preferred embodiments, the quaternary ammonium compound has only one carbon chain of length C12 C30 Typically, the one carbon chain of length C12-C30 is a linear {i.e. non-branched) hydrocarbon chain. Preferably, the one carbon chain of length C12-C30 is saturated. 15 Preferably, the one carbon chain of length C12-C30 is of chain length C12-C22 and more preferably it is of chain length C16-C22 The quaternary ammonium compound having at least one carbon 20 chain of length C12-C30 has three other carbon-containing substituents attached to the quaternary nitrogen atom. These are typically C1-C4 alkyl groups and are preferably methyl and/or ethyl groups; most preferably they are methyl groups. 25 Most preferably, the quaternary ammonium compound having at least one carbon chain of length C12-C30 is '8 MAY 2OO9 WO 2008/055815 PCT/EP2007/061677 - 13 - cetyltrimethylammonium chloride or benhenyltrimethylammonium chloride. When present, the total amount of quaternary ammonium 5 compound having at least one carbon chain of length C12-C30 is preferably from 0.005 to 10%, more preferably from 0.01 to 5%, and most preferably from 0.01 to 1% by weight of the total composition. 0 The weight ratio of quaternary ammonium compound having at least one carbon chain of length C12-C30 to particles having platelet morphology is preferably from 30:1 to 5:1. The molar ratio of quaternary ammonium compound having at 5 least one carbon chain of length C12-C30 to fatty material selected from C12-C22 fatty alcohol, C12-C22 fatty acid, or mixtures thereof is preferably from 1:100 to 5:1, more preferably from 1:50 to 1:2, and most preferably from 1:30 to 1:10. These molar ratios apply particularly when the 0 quaternary ammonium compound has only one carbon chain of length C12-C30 and the fatty material is a C12-C22 fatty alcohol. Silicone oils 5 A preferred additional component in conditioning shampoo compositions according to the invention is silicone oil. Silicone oil can enhance the conditioning benefit found with compositions of the invention. 8MAY2009 WO 2008/055815 PCT/EP2007/061677 - 14 - When used, silicone oil is typically present as emulsified droplets having a mean droplet diameter {D3,2) of 4 micrometres or less. Preferably the mean droplet diameter (D3,2) is 1 micrometre or less, more preferably 0.5 5 micrometre or less, and most preferably 0.25 micrometre or less. A suitable method for measuring the mean droplet diameter (D3,2) is by laser light scattering using an instrument such 10 as a Malvern Mastersizer. Preferably the silicone oil is non-volatile, meaning that it has a vapour pressure of less than 1000 Pa at 25°C. 15 Suitable silicone oils are polydiorganosiloxanes, in particular polydimethylsiloxanes (dimethicones), polydimethyl siloxanes having hydroxyl end groups (dimethiconols), and amino-functional polydimethylsiloxanes (amodimethicones). 20 Suitable silicones preferably have a molecular weight of greater than 100,000 and more preferably a molecular weight of greater than 250,000. 25 Suitable silicones preferably have a kinematic viscosity of 2 -1 greater than 50,000 cS (mm ,s ) and more preferably a 2 -1 kinematic viscosity of greater than 500,000 cS {mm .s ). Silicone oil kinematic viscosities as referred to in this specification are measured at 25°C and can be measured by 8 MAY 2009,' WO 2008/0558 J 5 PCT/EP2O07/O61677 - 15 - means of a glass capillary viscometer as set out further in Dow Corning Corporate Test Method CTM004 July 20, 1970. Suitable silicones for use in compositions of the invention 5 are available as pre-formed silicone emulsions from suppliers 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 10 comprise a suitable emulsifier, 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 15 are generally termed microemulsions. Examples of suitable pre-formed silicone emulsions include emulsions DC2-1766, DC2-1784, DC-1785, DC-1786, DC-1788, DC-1310, DC-7123 and microemulsions DC2-1865 and DC2-1870, all 20 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). 25 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. 30 Mixtures of any of the above described silicone emulsions may also be used. 8 MAY 2009 WO 2008/055815 PCT7EP2007/061677 - 16 - The total amount of silicone oil in compositions of the invention may suitably range from 0.05 to 10%, particularly from 0.2 to 8%, and especially from 0.5 to 5% by weight of the composition. 5 Hydrocarbon oils and ester oils A further component that may be used in compositions of the invention is a hydrocarbon oil or ester oil. Like silicone 10 oils, these materials may enhance the conditioning benefits found with compositions of the invention. Suitable hydrocarbon oils have at least 12 carbon atoms, and include paraffin oil, mineral oil, saturated and unsaturated 15 dodecane, saturated and unsaturated tridecane, saturated and unsaturated tetradecane, saturated and unsaturated pentadecane, saturated and unsaturated hexadecane, and mixtures thereof. Branched-chain isomers of these compounds, as well as of higher chain length hydrocarbons, 20 can also be used. Also suitable are polymeric hydrocarbons of C2-6 alkenyl monomers, such as polyisobutylene. Suitable ester oils have at least 10 carbon atoms, and include esters with hydrocarbyl chains derived from fatty 25 acids or alcohols. Typical ester oils are formula R'COOR in which R' and R independently denote alkyl or alkenyl radicals and the sum of carbon atoms in R' and R is at least 10, preferably at least 20. Di- and trialkyl and alkenyl esters of carboxylic acids can also be used. 30 Preferred fatty esters are mono-, di- and triglycerides, more specifically the mono-, di-, and tri-esters of glycerol 8 MAY 2009 WO 2008/055815 PCT/EP2007/061677 - 17 - with long chain carboxylic acids such as C1-22 carboxylic acids. Examples of such materials include cocoa butter, palm stearin, sunflower oil, soyabean oil and coconut oil. 5 Mixtures of any of the above described hydrocarbon/ester oils also be used. The total combined amount of hydrocarbon oil and ester oil in compositions of the invention may suitably range from 10 0.05 to 10%, particularly from 0.2 to 5%, and especially from 0.5 to 3% by weight of the composition. Cationic polymer A preferred additional component in conditioning shampoo compositions according to the invention is a cationic polymer. Such components may enhance the deliver of conditioning agents and thereby improve the conditioning benefits obtained. Cationic polymers typically contain cationic nitrogen-containing groups such as quaternary ammonium or protonated amino groups. The cationic protonated amines can be primary, secondary, or tertiary amines (preferably secondary or tertiary). The average molecular weight of the cationic polymer is preferably from 5,000 to 10 million. The cationic polymer preferably has a cationic charge density of from 0.2 meq/gm to 7 meq/gm. 30 The cationic nitrogen-containing moiety of the cationic polymer is generally present as a substituent on all, or 8MAY2009 WO 2008/055815 PCT/EP2007/06T677 - 18 - more typically on some, of the repeat units thereof. The cationic polymer may be a homo-polymer or co-polymer of quaternary ammonium or cationic amine-substituted repeat units, optionally in combination with non-cationic repeat 5 units. Non-limiting examples of such polymers are described in the CTFA Cosmetic Ingredient Dictionary, 6th edition, edited by Wenninger, JA and McEwen Jr, GN, (The Cosmetic, Toiletry, and Fragrance Association, 1995). Particularly suitable cationic polymers for use in the composition 10 include polysaccharide polymers, such as cationic cellulose derivatives, cationic starch derivatives, and cationic guars. Examples of cationic cellulose derivatives are salts of 15 hydroxyethyl cellulose reacted with trimethylammonium substituted epoxide, referred to in the industry (CTFA) as Polyquaternium 10. Further examples of cationic cellulose derivatives are prepared from hydroxyethyl cellulose and lauryldimethylammonium-substituted epoxide and are referred 20 to in the industry (CTFA) as Polyquaternium 24. Especially preferred cationic polymers are cationic guar gum derivatives, such as guar hydroxypropyltrimonium chloride, specific examples of which include the JAGUAR series 25 commercially available from Rhodia Corp. (e.g., JAGUAR C17 or JAGUAR C13S). Other suitable cationic polymers include quaternary nitrogen-containing cellulose ethers, examples of which are 30 described in US 3,962,418. Other suitable cationic polymers include derivatives of etherified cellulose, guar and 8 MAY 2009 WO 2008/055815 PCT7EP2007/061677 - 19 - starch, some examples of which are described in US 3,958,581. Synthetic cationic polymers may also be employed. Examples 5 include co-polymers of vinyl monomers having cationic protonated amine or quaternary ammonium functionality with water soluble spacer repeat units, typically derived from monomers such as acrylamide, methacrylamide, N-alkyl and N,N-dialkyl acrylamides and methacrylamides, alkyl acrylate, 0 allyl methacrylate, vinyl caprolactone, vinyl acetate,/alcohol. Other spacer repeat units may be derived from maleic anhydride, propylene glycol, or ethylene glycol. Other suitable synthetic cationic polymers include co-5 polymers of l-vinyl-2-pyrrolidone and l-vinyl-3- methylimidazolium salt (e.g., chloride salt), referred to in the industry (CTFA) as Polyquaternium-16; co-polymers of 1-vinyl-2-pyrrolidone and dimethylaminoethyl methacrylate, refereed to in the industry (CTFA) as Polyquaternium-11; 0 cationic diallyl quaternary ammonium-containing polymers, including, for example, dimethyldiallylammonium chloride homo-polymer and co-polymers of acrylamide and dimethyldiallylammonium chloride, referred to in the industry (CTFA) as Polyquaternium 6 and Polyquaternium 7, 5 respectively; and mineral acid salts of amino-alkyl esters of homo-polymers and co-polymers of unsaturated carboxylic acids having from 3 to 5 carbon atoms. The total amount of cationic polymer in the composition is 0 preferably from 0.05% to 2% and more preferably from 0.1 to 0.5% by weight of the composition. 8 MAY 2009 WO 2008/055815 PCT/EP2007/061677 - 20 - Amphoteric surfactant An amphoteric surfactant is a preferred additional ingredient in compositions of the invention. Suitable 5 amphoteric surfactants are betaines, such as those having the general formula R(CH3)2N CH2CO2 , where R is an alkyl or alkylamidoalkyl group, the alkyl group preferably having 10-16 carbon atoms. Particularly suitable betaines are oleyl betaine, caprylamidopropyl betaine, lauramidopropyl betaine, 10 isostearylamidopropyl betaine, and cocoamidopropyl betaine. Other suitable betaine amphoteric surfactants are sulfobetaines, such as those having the general formula R' (CH3)2N+CH2CH(OH)CH2S03-, where R' is an alkyl or 15 alkylamidoalkyl group, the alkyl group preferably having 10-16 carbon atoms. Particularly suitable sulfobetaines are laurylainidopropyl hydroxysultaine and cocoamidopropyl hydroxysultaine. 20 Other suitable amphoteric surfactants are fatty amine oxides, such as lauryldimethylamine oxide. When included, the total level of amphoteric surfactant is preferably from 0.1% to 20%, more preferably from 1% to 10%, 25 and most preferably from 1% to 5% by weight of the composition. Carbomer 30 A Carbomer may be advantageously employed in particular embodiments of the invention. A Carbomer is a homopolymer 8MAY2009 WO 2008/055815 PCT/EP2007/061677 - 21 - of acrylic acid crosslinked with an allyl ether of pentaerythritol or an allyl ether of sucrose. Such materials may serve as suspending agnets. 5 When included, the total level of Carbomer is preferably from 0.01% to 10%, more preferably from 0.1% to 5%, and most preferably from 0.25% to 1% by weight of the composition. Other Optional Components 10 Compositions according to the invention may contain other ingredients suitable for use in hair cleansing and conditioning compositions. Such ingredients include but are not limited to: fragrance, suspending agents, amino acids 15 and protein derivatives, viscosity modifiers, preservatives, colourants and pearlisers. EXAMPLES 20 Example 1 as indicated in Table 1 was prepared in the following manner. At least 10% of the water was heated to 65°C in a side pot. To this, was added the cetyl alcohol, with high speed 25 stirring. When all of the cetyl alcohol had melted, the Quaternium-18 Bentonite was added, also with high speed stirring, followed by the cetyltrimethylammonium chloride. The uniform dispersion obtained, whilst still at 65°C, was added to an aqueous solution of the sodium laureth sulphate 30 at ambient temperature. Moderate speed stirring was 8 MAY 2009 WO 2008/055815 PCT/EP2007/061677 - 22 - employed to achieve a uniform dispersion without causing aeration of the product. The remaining components were then added with continued moderate speed stirring. 5 Comparative Example A was prepared by methods known in the art. Table 1 10 All ingredients are expressed by weight percent of the total composition, and as level of active ingredient. 1. Sodium lauryl ether sulphate (1EO). 8 MAY 2009/ WO 2008/055815 PCT/EP2007/06J677 - 23 - TM 2. Tixogel MP10 0V1 , ex Sud Chemie. Comparative Example A and Example 1 were compared in a salon halfhead test assessed by hairdressers (n = 36). Example 1 was found to be significantly superior on a wide range of conditioning benefits, including ease of fingering through (wet); slippery feel (wet); soft feel (wet); ease of wet combing; slippery feel (dry); soft feel (dry); more elastic compressed; weighty hair; and retain style. 10 In a subsequent test, Example 1 was compared with an analogous composition in which the Quaternium-18 bentonite was not included. In this test, Example 1 was again found to be significantly superior on a wide range of conditioning 15 benefits, including soft feel (wet); slippery feel (dry); straight weighty (dry); bouncy (dry); retain manageability (next day). 8 MAY 2009, WO 2008/055815 PCT/EP2007/061677 - 24 - CLAIMS 1. An aqueous conditioning shampoo composition comprising an anionic cleansing surfactant and a gel network 5 comprising: (i) a fatty material selected from C12-C22 fatty alcohol, C12-C22 fatty acid, C12-C22 fatty amide or mixtures thereof and (ii) particles having platelet morphology and melting 10 point greater than that of the fatty material. 2. An aqueous conditioning shampoo composition according to claim 1, wherein the gel network comprises a quaternary ammonium compound having at least one carbon 15 chain of length C12-C30 and wherein the particles having platelet morphology have a melting point higher than said quaternary ammonium compound. 3. An aqueous conditioning shampoo composition according 20 to claim 1 or claim 2, wherein the gel network comprises a C12-C22 fatty alcohol. 4. An aqueous conditioning shampoo composition according to any of preceding claims, wherein the gel network 25 comprises a quaternary ammonium compound having only one carbon chain of length C12-C30 and wherein the particles having platelet morphology have a melting point higher than said quaternary ammonium compound. Dated this 8th day of May 2009 HINDUSTAN UNILEVER LIMITED (S. Venkatramanj) Head of Patent Group, India

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906-MUMNP-2009-REPLY TO HEARING(5-11-2014).pdf

906-MUMNP-2009-US DOCUMENT(10-12-2012).pdf

906MUMNP2009-CORRESPONDENCE(13-8-2010).pdf

906MUMNP2009-FORM 18(13-8-2010).pdf