Title of Invention

PHOTOSTABLE COSMETIC COMPOSITIONS

Abstract

Photostable cosmetic compositions comprising sunscreens, more particularly to cosmetic compositions comprising dibenzoylmethane sunscreens are provided. It is know that dibenzoylmethane and its derivatives are relatively sensitive to ultraviolet radiation and they decompose rapidly under the effect of sunlight. This decomposition is accelerated in the presence of UV –B sunscreens, especially p-methoxycinnamic acid and its derivatives. The present inventors have surprisingly found that cosmetic compositions comprising dibenzoylmethane ot its derivative and p- methoxycinnamic acid or its derivative, can be stabilized by incorporating a combination of fatty alcohol ethoxylates and polyalkyleneglycol.

Full Text

J2124 FORM -2 THE PATENTS ACT, 1970 (39 of 1970) & The Patent Rules, 2003 PROVISIONAL SPECIFICATION (See Section 10 and Rule 13) PHOTOSTABLE COSMETIC COMPOSITIONS HINDUSTAN LEVER LIMITED, a company incorporated under the Indian Companies Act, 1913 and having its registered office at Hindustan Lever House, 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India The following specification describes the invention Technical field The present invention relates to photostable cosmetic compositions comprising sunscreens, more particularly to cosmetic compositions comprising dibenzoylmethane sunscreens. Background and prior art It is generally known that UV-A rays having wavelengths between 320 and 400 nm cause tanning of the skin, localized irritation, sun-burn and melanoma. It is also known that UV-B radiation, having wavelength between 280 nm and 320 nm also promotes tanning of the human epidermis, in addition to causing various other short and long-term damages, such as photoaging of skin, dryness, deep wrinkle formation, mottled pigmentation and the breakdown of elastic tissues and collagen. Therefore, it is desirable to protect the skin from the harmful effects of ultraviolet radiation. Various cosmetic preparations have been reported for preventing and/or protecting the skin from harmful effects of ultraviolet radiation. Numerous organic sunscreen agents, capable of absorbing harmful UV-A rays are also reported in the field of cosmetics, among which, a particularly advantageous being dibenzoylmethane and its derivatives. This is because they exhibit high intrinsic absorption power. On the other hand p-methoxy cinnamic acid and its derivatives are also used extensively as they are highly effective UV-B sunscreens. It is essential that cosmetic compositions contain both UV-A and UV-B sunscreens so as to provide protection over the entire range of UV radiation. It is known that dibenzoylmethane and its derivatives are relatively sensitive to ultraviolet radiation and they decompose rapidly under the effect of sunlight. This decomposition is accelerated in the presence of UV-B sunscreens, especially p-methoxycinnamic acid and its derivatives. Owing to photochemical instability of dibenzoylmethane and its derivatives in the presence of UV-B sunscreens, especially p-methoxycinnamic acid and its derivatives, one cannot guarantee constant protection during prolonged exposure to the sun. This therefore, warrants repeated applications at regular and frequent intervals by the user in order to maintain effective protection against UV rays. 2 On the other hand, it is also known that the protection afforded by cosmetic sunscreen compositions, reduces over a period of time and typically by the end of 1 hour from application, the protection is almost negligible. Stabilization of dibenzoylmethane and its derivatives therefore becomes important so that the user achieves complete advantage of its' efficacy and he does not have to resort to frequent applications. Various methods have been reported for stabilization of dibenzoylmethane and its derivatives in cosmetic formulations, which include the use of stabilizers such as thickening copolymers, amphiphilic copolymers and micronized insoluble organic UV sunscreen agents. In an alternative approach, US 5985251 (Roche Vitamins, 1999) describes light screening cosmetics wherein compositions comprising dibenzoylmethane derivatives and p-methoxy cinnamic acid derivatives are stabilized by incorporating 0.5 to 12% by weight 3-3-diphenylacrylate derivatives or benzylidene camphor derivatives. It can be readily seen that the formulation must necessarily contain an additional UV-B sunscreen of the diphenylacrylate class to stabilize UV-A sunscreens, a large part of which ends up getting utilized for stabilizing the UV-A sunscreen, without providing protection, which is its' primary role. Incorporation of the additional sunscreen would also add to the cost of the formulation. Therefore, there exists the need for cosmetic compositions comprising dibenzoylmethane or its derivatives, which are stabilized, especially in the presence of p-methoxy cinnamic acid or its derivatives, wherein specialty polymers and/or additional sunscreen stabilizers are not essentially required. It is highly desirable to have cosmetic compositions, which are stabilized with ingredients that are conventionally used in cosmetics, thereby reducing the complexities of formulation and substantially reduce costs. The present inventors have surprisingly found that cosmetic compositions comprising dibenzoylmethane or its derivative and p-methoxycinnamic acid-or its derivative, can be stabilized by incorporating a combination of fatty alcohol ethoxylates and polyalkyleneglycol. 3 Objects of the invention It is therefore, an object of the present invention to obviate atleast some drawbacks of the prior art and provide photostable cosmetic compositions having sunscreens. Another object of the present invention is to provide photostable compositions comprising dibenzoylmethane sunscreens, wherein the stabilization is brought about by using conventionally used ingredients. Summary of the invention According to an aspect, the present invention relates to a photostable cosmetic composition comprising, 0.1 % to 10 % by weight dibenzoylmethane or its derivative; 0.1 % to 10 % by weight p-methoxy cinnamic acid or its derivative, wherein said composition comprises from 0.5 % to 8 % by weight C8-C18 fatty alcohol ethoxylate and 0.5 % to 8 % by weight polyalkyleneglycol. Preferably, dibenzoylmethane or its derivative is present from 0.1 % to 5 % by weight. It is also preferred that p-methoxy cinnamic acid or its derivative is present from 0.1 % to 5 % by weight. According to a most preferred aspect, the dibenzoylmethane derivative is 4-tert.-butyl-4'-methoxydibenzoylmethane and p-methoxy cinnamic acid derivative is 2-ethyl-hexyl-p-methoxy cinnamate. As used herein, the term "cosmetic composition" is intended to describe compositions for topical application to human skin, including leave-on and wash-off products. The term "skin" as used herein includes the skin on the face, neck, chest, back, arms, hands, legs, and scalp. 4 For the avoidance of doubt the word "comprising" is intended to mean including but not necessarily consisting of or composed of. In other words the listed options need not be exhaustive. Other characteristics, aspects and advantages of the invention and the essential, preferred and optional features of the invention will emerge on reading the detailed description that follows. Detailed description The present invention relates to a photostable cosmetic composition comprising, a) 0.1 % to 10 % by weight dibenzoylmethane or its derivative; b) 0.1 % to 10 % by weight p-methoxy cinnamic acid or its derivative, wherein said composition comprises from 0.5 % to 8 % by weight C8-C18 fatty alcohol ethoxylate and 0.5 % to 8 % by weight polyalkyleneglycol. It is preferred that dibenzoylmethane or its derivative is present from 0.1 to 5 % by weight, more preferably from 0.1 % to 2 % by weight. Preferred dibenzoylmethane derivative is selected from 4-tert-butyl-4'-methoxydibenzoylmethane, 2-methyldibenzoylmethane, 4-methyl-dibenzoyl-ethane, 4-isopropyldibenzoyl-methane, 4-tert-butyldibenzoylmethane, 2,4-dimethyldibenzoylmethane, 2,5-dimethyldibenzoylmethane, 4,4-diisopropyl-dibenzoylmethane, 2-methyl-5-isopropyl-4'-methoxydibenzoylmethane, 2-methyl-5-tert-butyl-4'-methoxy-dibenzoylmethane, 2)4-dimethyl-4'-methoxydibenzoylmethane or 2,6-dimethyl-4-tert-butyl-4'-methoxy-dibenzoylmethane. The most preferred dibenzoylmethane derivative is 4-tert.-butyl-4'-methoxydibenzoylmethane. Preferably, the p-methoxy cinnamic acid derivative is present from 0.1 % to 5 % by weight, more preferably from 0.1 % to 2 % by weight of the composition. The preferred p-methoxy cinnamic acid derivative is selected from 2-ethylhexyl-p-methoxy cinnamate, ammonium- p-methoxycinnamate, sodium- p-methoxycinnamate, 5 potassium-p-methoxycinnamate, or salts of primary, secondary or tertiary amines of p-methoxycinnamic acid and more preferably it is 2-ethylhexyl-p-methoxy cinnarriate. Fatty alcohol ethoxylates (also known as ethoxylated fatty alcohols) have the general formula: R~0-(CH2-CH2--0)n H where R is a saturated or unsaturated, linear or branched hydrocarbon-based chain having from 10 to 24 carbon atoms, and n is an integer ranging from 8 to 50. Fatty alcohol ethoxylates are products of the addition of ethylene oxide onto primary alcohols. The ethoxylates are produced by known methods and are basically mixtures. Depending on their production, they may have a conventional broad homolog distribution or a narrow homolog distribution. The degree of ethoxylation (EO: number of ethylene oxide units added on) represents a Gauss distribution, the maximum of the Gauss curve being referred to here as the average degree of ethoxylation "n". Preferred are products of the addition of ethylene oxide onto caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and technical mixtures thereof. Representative examples of ethoxylated fatty alcohols are the addition products of ethylene oxide with lauryl alcohol, in particular those containing from 9 to 50 oxyethylenated groups (having CTFA names Laureth-9 to Laureth-50); the addition products of ethylene oxide with behenyl alcohol, in particular those containing from 9 to 50 oxyethylenated groups (having CTFA names Beheneth-9 to Beheneth-50); the addition products of ethylene oxide with cetearyl alcohol (mixture of cetyl alcohol and of stearyl alcohol) in particular those containing from 9 to 30 oxyethylenated groups (having CTFA names Ceteareth-9 to Ceteareth-30); the addition products of ethylene oxide with cetyl alcohol, in particular those containing from 9 to 30 oxyethylenated groups (having CTFA names Ceteth-9 to Ceteth-30); the addition products of ethylene oxide with stearyl alcohol, in particular those containing from 9 to 30 oxyethylenated groups (having CTFA names Steareth-9 to Steareth-30; the addition 6 products of ethylene oxide with isostearyl alcohol, in particular those containing from 9 to 50 oxyethylenated groups (having CTFA names lsosteareth-9 to lsosteareth-50); and mixtures thereof. The more preferred alcohol ethoxylates are addition products of ethylene oxide onto fatty alcohol having 8 to 12 carbon atoms, i.e. C8-C18 fatty alcohol ethoxylates, and in a highly preferred aspect; it is lauryl alcohol, which has 12 Carbon atoms. It is marketed under the name Brij® 35 (laureth-35, lauryl alcohol with 35 EO units). Several grades of Brij are available, depending upon the degree of ethoxylation. It is preferred that the fatty alcohol ethoxylate is present from 0.5 % to 4 % by weight of the composition. According to a preferred aspect, the polyalkyleneglycol is present from 0.5 to 4 % by weight. Suitable polyalkyleneglycol is selected from polyethyleneglycol, polypropyleneglycol or polybutyleneglycol and preferably it is polyethyleneglycol. According to a preferred aspect, the molecular weight of polyethyleneglycol is between 200 to 100000 Daltons, more preferably between 200 to 10000 Daltons. The present composition can include any cosmetic vehicle/carrier known in the art. Suitable vehicles include, but are not limited to, one or more of the following: vegetable oils; esters such as octyl palmitate, isopropyl myristate and isopropyl palmitate; ethers such as dicapryl ether and dimethyl isosorbide; alcohols such as ethanol and isopropanol; fatty alcohols such as cetyl alcohol, stearyl alcohol and behenyl alcohol; isoparaffins such as isooctane, isododecane and isohexadecane; silicone oils such as dimethicones, cyclic silicones, and polysiloxanes; hydrocarbon oils such as mineral oil, petrolatum, isoeicosane and polyisobutene; polyols such as propylene glycol, ethoxydiglycol, glycerin, butylene glycol, pentylene glycol and hexylene glycol; as well as water, or any combinations of the above. Fatty acids having from 10 to 30 carbon atoms may also be included as cosmetically acceptable carriers for compositions of this invention. Illustrative of this category are pelargonic, lauric, myristic, palmitic, stearic, isostearic, hydroxystearic, oleic, linoleic, ricinoleic, arachidic, behenic and erucic acids. 7 Humectants of the polyhydric alcohol-type may also be employed as cosmetically acceptable carriers in compositions of this invention. The humectant aids in increasing the effectiveness of the emollient, reduces skin dryness and improves skin feel. Typical polyhydric alcohols include glycerol, polyalkylene glycols and more preferably alkylene polyols and their derivatives, including propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol and derivatives thereof, sorbitol, hydroxypropyl sorbitol, hexylene glycol, 1,3-butylene glycol, 1,2, 6-hexanetriol, ethoxylated glycerol, propoxylated glycerol and mixtures thereof. The amount of humectant may range anywhere from 0.5% to 30%, preferably between 1% and 15% by weight of the composition. The amount of cosmetically acceptable vehicle in the present composition will vary considerably based upon product form, but typically will range from about 20 wt % to about 70 wt % and preferably from about 20 wt % to about 40 wt %, based upon the total weight of the composition. The cosmetically acceptable vehicle acts as a dilutant, dispersant or carrier for the in the composition, so as to facilitate the distribution of the sunscreens when the composition is applied to the skin. The present composition, when in emulsion form, could optionally have one or more additional emulsifiers, without deviating from the scope of the invention, which are preferably selected from sorbitan esters dimethicone copolyols; polyglyceryl-3-diisostearate; such as sorbitan monooleate and sorbitan monostearate; glycerol esters such as glycerol monostearate and glycerol monooleate; polyoxyethylene phenols such as polyoxyethylene octyl phenol and polyoxyethylene nonyl phenol; polyoxyethylene ethers such as polyoxyethylene cetyl ether and polyoxyethylene stearyl ether; polyoxyethylene glycol esters; polyoxyethylene sorbitan esters; dimethicone copolyols; polyglyceryl-3-diisostearate; or any combinations thereof. An oil or oily material may be present, together with an emulsifier to provide either a water-in-oil emulsion or an oil-in-water emulsion, depending largely on the average hydrophilic-lipophilic balance (HLB) of the emulsifier employed. Preferred anionic surfactants include soap, alkyl ether sulfate and sulfonates, alkyl sulfates and sulfonates, alkylbenzene sulfonates, alkyl and dialkyl sulfosuccinates, C9-C20 acyl isethionates, acyl glutamates,C8-C20 alkyl ether phosphates and combinations thereof. Typically, the additional emulsifier could be present from 1 wt % to about 12 wt %, based upon the total weight of the composition. 8 Water when present will be in amounts which could range from 5% to 75%, preferably from 20% to 70%, optimally between 40% and 70% by weight of said composition. Besides water, relatively volatile solvents may also serve as carriers within compositions of the present invention. Most preferred are monohydric C1-C3 alkanols. These include ethyl alcohol and isopropyl alcohol. Preferred cream bases are, for example, beeswax, cetyl alcohol, stearic acid, glycerine, propylene glycol, propylene glycol monostearate, polyoxyethylene cetyl ether and the like. Preferred lotion bases include, for example, oleyl alcohol, ethanol, propylene glycol, glycerine, lauryl ether, sorbitan monolaurate and the like. When the composition of the present invention is in the form of film-forming skin packs or masks it could comprise film formers known in the art. These include acrylate copolymers, acrylates C12-22 alkyl methacrylate copolymer, acrylate/octylacrylamide copolymers, acrylate/VA copolymer, amodimethicone, AMP/acrylate copolymers, behenyl beeswax, behenyl/isostearyl, beeswax, butylated PVP, butyl ester of PVM/MA copolymers, calcium/sodium PVM/MA copolymers, dimethicone, dimethicone copolyol, dimethicone/mercaptopropyl methicone copolymer, dimethicone propylethylenediamine behenate, dimethicolnol ethylcellulose, ethylene/acrylic acid copolymer, ethylene/MA copolymer, ethyleneA/A copolymer, fluoro C2-8 alkyldimethicone, hexanediol beeswax, C30-38 olefin/isopropyl maleate/MA copolymer, hydrogenated styrene/butadiene copolymer, hydroxyethyl ethylcellulose, isobutylene/MA copolymer, laurylmethicone copolyol, methyl methacrylate crosspolymer, methylacryloyl ethyl betaine/acrylates copolymer, microcrystalline wax, nitrocellulose, octadecene/MA copolymer, octadecene/maleic anhydride copolymer, octylacrylamide/acrylate/butylaminoethyl methacrylate copolymer, oxidized polyethylene, perfluoropolymethylisopropyl ether, polyacrylic acid, polyethylene, polymethyl methacrylate, polypropylene, polyquaternium-10, polyquaternium-11, polyquaternium-28, polyquaternium-4, PVM/MA decadiene crosspolymer, PVM/MA copolymer, PVP, PVP/decene copolymer, PVP/eicosene copolymer, PVP/hexadecene copolymer, PVP/MA copolymer, PVPA/A copolymer, silica, silica dimethyl silylate, sodium acrylate/vinyl alcohol copolymer, stearoxy dimethicone, stearoxytrimethylsilane, stearyl alcohol, stearylvinyl ether/MA copolymer, styrene/DVB copolymer, styrene/MA copolymer, tetramethyl tetraphenyl trisiloxane, tricontanyl 9 trimethyl pentaphenyl trisiloxane, trimethylsiloxysilicate, VA/crotonates copolymer, VA/crotonates/vinyl proprionate copolymer, VA/butyl maleate/isobornyl acrylate copolymer, vinyl caprolactam/PVP/dimethylaminoethyl methacrylate copolymer, and vinyldimethicone. The film former is preferably present in an amount from about 0.5 wt % to about 5 wt %, and more preferably from about 1 wt % to about 5 wt %, based upon the total weight of the composition. More preferably, the film former is present in an amount about 3 wt % of the total weight of the composition. Optionally, the present composition may include one or more ingredients selected from chelating agents, botanical extracts, colorants, depigmenting agents, emollients, exfollients, fragrances, humectants, moisturizers, preservatives, skin protectants, skin penetration enhancers, stabilizers, thickeners, viscosity modifiers, vitamins, anti-aging, wrinkle- reducing, skin whitening, anti-acne, and sebum reduction agents or any combinations thereof. Examples of these include alpha-hydroxy acids and esters, beta-hydroxy acids and ester, polyhydroxy acids and esters, kojic acid and esters, ferulic acid and ferulate derivatives, vanillic acid and esters, dioic acids (such as sebacid and azoleic acids) and esters, retinol, retinal, retinyl esters, hydroquinone, t-butyl hydroquinone, mulberry extract, licorice extract, and resorcinol derivatives such as 4-substituted resorcinol derivatives, as well as additional sunscreens such UV diffusing agents, typical of which is finely divided titanium oxide and zinc oxide which generally arebetween 5 nm and 100 nm and preferably between 10 and 50 nm) of coated or uncoated metal oxides, for instance nanopigments of titanium oxide (amorphous or crystallized in rutile and/or anatase form), of iron oxide, of zinc oxide, of zirconium oxide or of cerium oxide, which are all photoprotective agents that are well-known per se, acting by physically blocking out (reflection and/or scattering) UV radiation. Standard coating agents are, moreover, alumina and/or aluminum stearate.. The compositions according to the invention may also contain agents for artificially tanning and/or browning the skin (self-tanning agents), for instance dihydroxy-acetone (DHA). Thickeners may also be utilized as part of the cosmetically acceptable carrier of compositions according to the present invention, without deviating from the scope of the present invention. Typical thickeners include crosslinked acrylates (e. g. Carbopol 982), hydrophobically-modified acrylates (e. g. Carbopol 1382), cellulosic derivatives and 10 natural gums. Among useful cellulosic derivatives are sodium carboxymethylcellulose, hydroxypropyl methylcellulose, hydroxypropyl cellulose, hydroxyethyl cellulose, ethyl cellulose and hydroxymethyl cellulose. Natural gums suitable for the present invention include guar, xanthan, sclerotium, carrageenan, pectin and combinations of these gums. Amounts of the thickener may range from 0. 0001% to.5%, usually from 0. 001% to 1%, optimally from 0.01 % to 0.5% by weight. The inventive cosmetic composition could also optionally contain lathering surfactant. By "lathering surfactant" is meant a surfactant which, when combined with water and mechanically agitated, generates a foam or lather. Preferably, the lathering surfactant should be mild, meaning that it must provide sufficient cleansing or detergent benefits but not overly dry the skin, and yet meet the lathering criteria described above. The cosmetic compositions of the present invention may contain a lathering surfactant in a concentration of about 0.01% to about 50%. This is typically needed, in wash-off products, such as face-washes. The cosmetic compositions according to the invention may also contain, besides the essential elements, one or more additional sunscreens that are different from the preceding sunscreens, which are water-soluble, liposoluble or insoluble in the cosmetic solvents commonly used. These screening agents may be suitably chosen from salicylic derivatives, benzylidenecamphor derivatives, triazine derivatives, benzophenone derivatives, [J3 ], fJ3]'-diphenylacrylate derivatives, phenyl-benzimidazole derivatives, anthranilic derivatives, imidazoline derivatives, methylenebis(hydroxyphenyl-benzotriazole) derivatives, p-aminobenzoic acid derivatives, and screening hydrocarbon-based polymers and screening silicones derivatives. The preferred organic UV-screening agents are chosen from the following compounds: Ethylhexyl salicylate, Octocrylene, Phenylbenzimidazolesulphonic acid, Terephthalylidenedicamphorsulphonic acid, Benzophenone-3, Benzophenone-4, Benzophenone-5, 4-Methylbenzylidene, Benzimidazilate, Anisotriazine, 2,4,6-Tris(diisobutyl4'-aminobenzalmalonate)-s-triazine, Ethylhexyltriazone, Diethylhexylbutamidotriazone, Methylenebis(benzotriazolyl)tetramethylbutyl-phenol, Drometrizole trisiloxane, and mixtures thereof. 11 Specific preparations of the cosmetics to which the present invention is applicable include creams, ointments, emulsions, lotions, oils and face-packs, balm, gel, mousse, stick or hair-gels, hair-creams and the like. The emulsion could be, for example, anhydrous, water-in-oil, oil-in-water, water-in-silicone, or multiple emulsions. In case of protection of the hairs, the suitable formulations are shampoos, conditioners, lotions, gels, emulsions, dispersions, lacquers, and the like. The cosmetic composition of the invention can be formulated as a lotion having a viscosity of from 4,000 to 10,000mPas, a fluid cream having a viscosity of from 10,000 to 20,000 mPas or a cream having a viscosity of from 20,000 to 100,000 mPas or above, all measured at 25 °C. The composition according to the invention is intended primarily as a personal care product for topical application to human skin, as well as to protect exposed skin from the harmful effects of excessive exposure to sunlight. In use, a small quantity of the composition, for example about 0.1 ml to about 5 ml, is applied to exposed areas of the skin, from a suitable container or applicator and, if necessary, it is then spread over and/or rubbed into the skin using the hand or fingers or a suitable device. In order to further illustrate the present invention and the advantages thereof, the following specific examples are given, it being understood that same are intended only as illustrative and in no way limitative. In said examples to follow, all parts and percentages are given by weight, unless otherwise indicated. Examples Example-1: Demonstration of stabilization of dibenzoylmethane derivative using combination of fatty alcohol ethoxylate and polyethyleneglycol, according to the invention. Various cosmetic cream compositions were prepared as per formulation details given in table-1 below. 12 Table-1 Ingredients % wt Control Form-1 Form-2 Form-3 Form-4 Form-5 Stearic acid 18 18 18 18 18 18 Potassium hydroxide 0.67 0.67 0.67 0.67 0.67 0.67 Cetyl alcohol 0.53 0.53 0.53 0.53 0.53 0.53 Isopropyl myristate 0.75 0.75 0.75 0.75 0.75 0.75 Dimethicone 200 0.5 0.5 0.5 0.5 0.5 0.5 Niacinamide 1 1 1 1 1 1 Parsol 1789 0.8 0.8 0.8 0.8 0.8 0.8 Parsol MCX 0.75 0.75 0.75 0.75 0.75 0.75 Brij-35 - - 4 4 - - Tween-80 - - - - 4 - Span-80 - - - - 4 Polyethylene glycol 200 - 4 - 4 4 4 Water and other minors upto 100 100 100 100 100 100 Tween 80 Polyoxythylene sorbitan monooleate ex Uniquema Span 80 Sorbitan monooleate ex- Uniquema Brij-35 Polyoxyethylene lauryl ether ex Uniquema PARSOL 1789 4-tert.-butyl-4'-methoxydibenzoylmethane ex Merck Parsol MCX 2-ethylhexyl methoxycinnamate ex-Merck Processing 1. Weighed quantities of Water, Potassium hydroxide, EDTA, p-casitose, and glycerin were taken in a 100ml beaker (Vessel A). 2. Weighed quantities of Isopropyl myristate, Parsol-1789, Parsol-MCX, Propyl- paraben, Methyl-paraben, cetyl alcohol, and phenoxyethanol were taken in another beaker. (Vessel B) 3. Stearic acid was melted by heating to 70 °C in a separate vessel. 4. Contents of Vessel-B were melted at 70 °C. 5. Vessel B was heated to 75 degree under continuous homogenization at low shear (500-700 rpm). 6. After attaining 70 °C, molten Stearic acid was added to vessel A, slowly and under continuous stirring. 7. After 1-2 min of stirring Brij was added, followed by the addition of PEG-200 in above rotating mixture, followed by the addition of Ti02. 8. Molten mass of Vessel- B was added to it. 9. Shear rate of homogenization was increased to 1000-1200 rpm and was continued for 5 min. 10. The hot mixture was thereafter allowed to cool at room temperature with continuous stirring at low speed (500-700rpm). 11. At 60 °C, Niacinamide was added. 12. Mixture was allowed to cool to room temperature. Test Method The following test method was used for determining the stability of dibenzoylmethane sunscreens in the compositions of the present invention as well as for all the comparative examples described below. 1. A clean glass slide was taken and its weight was recorded (A). 2. About 10mg of cream was applied and spread on about 2 cm2. 3. The weight of slide with cream was recorded as (B). 4. Subtraction of B from A gave the weight of cream applied (C). 5. Above process was repeated six times for each test formulation. 6. These glass slides were exposed to sun simultaneously for various time intervals: 0 min, 15 min, 30 min and 60 min respectively. 7. After exposure to sunlight the creams were extracted in methanol and the volume was made up to 25ml. 8. The UV-absorbance of each of the samples was recorded on a UV spectrophotometer. 9. Absorbance per unit weight of the sample was calculated by dividing the absorbance at a max (i.e. 357nm, which is A max of dibenzoylmethanes) by weight of the cream (C). 10. The percentage absorbance remaining which is an indicator of the stability of the sample was calculated as follows: Percentage absorbance remaining = [An/ Ao X 100] where Ao is "absorbance per unit weight" of 0 min sample, and Anis "absorbance per unit weight" of nth min sample. Results of the experiment conducted in example-1 are summarized in Table-2 below. 14 It is to be noted that the intensity of sunlight was found to vary from 20-40 mW/Cm2 at the time of exposure of the slides to sun and the experiments were conducted on different days. Therefore, the absolute values of % absorbance for the same/similar experiments conducted over the entire period, e.g. experiments using control samples are different across the tables. Table-2 Sunlight Exposure time/min % Absorbance of Parsol 1789 remaining after exposure, when measured by the procedure given above. Control Form-1 Form-2 Form-3 0 (To) 100 100 100 100 15(T15) 79 91 78. 97 30(T30) 68 91 69 93 45 (T45) 60 80 60 91 60 (T60) 42 69 57 88 The above table indicates that in the formulation containing both PEG 200 and Brij-35, a significantly higher activity of dibenzoylmethane sunscreen is available after 1 hour of application, as evident from the absorbance value. Example 2: To study the effect of combination of polyethyleneglycol with other surfactants on the stability of dibenzolmethane sunscreen and its comparison with the combination of polyethyleneglycol with Brij-35 according to the invention. The results are summarized in table-3 below. 15 Table-3 Sunlight Exposure time/min % Absorbance of Parsol 1789 remaining after exposure, when measured by the procedure given above. Control Form-4 Form-5 Form-3 0(T0) 100 100 100 100 15(T15) 66 73 96 97 30(T30) 66 71 78 94 45(T45) 47 63 78 85 60 (T60) 40 64 75 83 Thus it can be readily seen that a combination of polyethylene glycol and fatty alcohol ethoxylate gives better stability as compared to combination of polyethylene glycol other surfactants/emulsifiers. Example-3 The present inventors have also determined the effect of varying molecular weight of Polyethyleneglycol on stability of dibenzoylmethane. Results of this experiment are summarized in table-4 below. 16 Table-4 SunlightExposuretime/min % Absorbance of Parsol 1789 remaining after exposure, when measured by the procedure given above. Form-3 with Form-3 with Form-3 with 4% PEG 4% PEG 4% PEG Control Form-3 6000 instead of 20000 instead of 100000 instead of 4% PEG 4% PEG 4% PEG 200 200 200 0(T0) 100 100 100 100 100 15(T15) 74 86 91 86 96 30(T30) 57 81 87 80 81 45 (T45) 50 78 78 68 76 60 (T60) 47 72 71 70 72 The above table indicates that with various molecular weights of polyethylene glycol, greater than 70% of the dibenzoylmethane derivative remains available, even after 1 hour from application. This demonstrates that any molecular weight of PEG from 200 to 100000 can be used, without departing from the scope of the invention. Example -4 In yet another set of experiments, the effect of 2 grades of fatty alcohol ethoxylates (Brij) on stability of dibenzoylmethane sunscreen was studied in cosmetic creams, results of which are summarized in table -5 below. 17 Table -5 SunlightExposuretime/min % Absorbance of Parsol 1789 remaining after exposure by the procedure given below. when measured Control Form-1 Form-3 Form-3 with 4% Brij-56 instead of 4% Brij 35. 0(To) 100 100 100 98 15 (T15) 81i 81 99 84 30(T30) 70 69 95 78 45 (T45) 45 68 84 74 60 (T60) 43 59 83 74 Note: Brij56 is Polyethylene glycol hexadecvl ether or (Polyoxvethylene 10 cetyl ether). CAS number 9004-95-9, commercially available from Uniquema, Sigma-Aldrich. Thus, it can be readily seen that different grades of fatty alcohol ethoxylates provide high degree of stability to the dibenzoylmethane sunscreen in the composition. Example -5 The stability of dibenzoylmethane derivative was also studied in the case of cosmetic lotions, to test the invention in a different carrier/vehicle. Details of the formulation are present in table-6 below. Processing details are also given below. Results are summarized in the table-7 below. 18 Table-5 Ingredient Percentage Control lotion Lotion -A Lotion-B Lotion-C Part a Water 84 84 84 84 Part b Brij 35 - 4.00 - 4.00 Peg-200 - - 4.00 4.00 Part c Titanium Dioxide 1.00 1.00 1.00 1.00 Part d Isopropyl Myristate 0.75 0.75 0.75 0.75 Dimethicone DC 200 0.50 0.50 0.50 0.50 Stearic acid 2.00 2.00 2.00 2.00 Cetyl alcohol 0.53 0.53 0.53 0.53 Parsol 1789 0.80 0.80 0.80 0.80 Parsol MCX 0.75 0.75 0.75 0.75 Part e Triethanolamine (99%) 0.50 0.50 0.50 0.50 Total with other minors 100 100 100 100 Processing 1. Disodium EDTA was added to the water and was mixed until dissolution. 2. Carbopol Ultrez was dispersed in the water and was mixed at low speed. 3. Ingredients of PART B were added to the water. 4. Ingredients of PART C were added to the water and was mixed after moderate heating The Titanium dioxide was mixed until it dispersed. 5. The combined PARTS A, B and C were heated to 65 degC. 6. Ingredients of PART D were heated to 65 degC and mixed until all the solids dissolved. 7. This part D was then added to combined PARTS A, B and C. While the temperature was at 65 degC, PART E ingredients were added. 8. The emulsion was missed under moderate agitation until the temperature reached 40 degC. It was later cooled to room temperature and was used as such for analysis. Table -7 Sunlight Exposure time/min % Absorbance of Parsol 1789 remaining after exposure, when measured by the procedure given above. Control (Lotion) Lotion-A Lotion-B Lotion-C 0(T0) 100 100 100 100 15(T15) 81 96 81 86 30(T30) 70 91 69 78 45 (T45) 46 70 68 75 60 (T60) 43 68 59 76 Thus it can be readily seen that the inventive combination of polyethylene glycol and fatty alcohol ethoxylate stabilizes the dibenzoylmethane derivative, even in a lotion based cosmetic composition. 20 Thus it can be seen from the foregoing description and examples that the invention provides for a composition comprising stable sunscreens. The invention also provides for compositions comprising stabilized dibenzoylmethane sunscreens, wherein the stabilization is brought about by using ingredients, which are conventionally used in cosmetic compositions. While the invention has been described in terms of various specific and preferred embodiments, the skilled artisan will appreciate that various modifications, substitutions, omissions, and changes may be made without departing from the spirit thereof. Dated this 23rd day of August 2006 Hindustan Lever Limited S. Venkatramani (Senior Patents Manager) 21

Documents:

1322-mum-2006-abstract(14-8-2007).pdf

1322-MUM-2006-CLAIMS(AMENDED)-(13-10-2011).pdf

1322-MUM-2006-CLAIMS(AMENDED)-(23-6-2011).pdf

1322-mum-2006-claims(complete)-(14-8-2007).pdf

1322-mum-2006-correspondence 1(28-5-2008).pdf

1322-mum-2006-correspondence 2(24-9-2007).pdf

1322-mum-2006-correspondence received.pdf

1322-MUM-2006-CORRESPONDENCE(04-05-2009).pdf

1322-MUM-2006-CORRESPONDENCE(13-10-2011).pdf

1322-MUM-2006-CORRESPONDENCE(21-3-2012).pdf

1322-MUM-2006-CORRESPONDENCE(22-08-2008).pdf

1322-MUM-2006-CORRESPONDENCE(23-6-2011).pdf

1322-MUM-2006-CORRESPONDENCE(28-10-2009).pdf

1322-MUM-2006-CORRESPONDENCE(29-3-2010).pdf

1322-MUM-2006-CORRESPONDENCE(30-7-2010).pdf

1322-mum-2006-correspondence(ipo)-(3-11-2008).pdf

1322-mum-2006-description (provisional).pdf

1322-mum-2006-description(complete)-(14-8-2007).pdf

1322-mum-2006-form 13(3-10-2007).pdf

1322-MUM-2006-FORM 13(8-2-2012).pdf

1322-MUM-2006-FORM 18(22-08-2008).pdf

1322-mum-2006-form 2(complete)-(14-8-2007).pdf

1322-mum-2006-form 2(title page)-(complete)-(14-8-2007).pdf

1322-mum-2006-form 2(title page)-(provisional)-(24-8-2006).pdf

1322-MUM-2006-FORM 3(12-8-2011).pdf

1322-mum-2006-form 3(14-8-2007).pdf

1322-MUM-2006-FORM 3(15-2-2011).pdf

1322-MUM-2006-FORM 3(15-2-2012).pdf

1322-MUM-2006-FORM 3(24-2-2010).pdf

1322-MUM-2006-FORM 3(4-8-2010).pdf

1322-mum-2006-form 5(14-8-2007).pdf

1322-mum-2006-form-1.pdf

1322-mum-2006-form-2.doc

1322-mum-2006-form-2.pdf

1322-mum-2006-form-3.pdf

1322-MUM-2006-PETITION UNDER RULE-137(21-3-2012).pdf