WO2011119557A2

WO2011119557A2 - Kit and method for removing hair

Info

Publication number: WO2011119557A2
Application number: PCT/US2011/029353
Authority: WO
Inventors: Charles Robert Smith; Stuart Andrew Hewlins; Michael John Goffe; Andrew David Watson
Original assignee: The Procter & Gamble Company
Priority date: 2010-03-26
Filing date: 2011-03-22
Publication date: 2011-09-29
Also published as: WO2011119557A3; US20110232006A1

Abstract

A method of removing hair from skin, preferably facial skin, is provided, comprising the steps of: (a) applying a hydrophobic protective composition to an area of skin, preferably facial skin, on which unwanted hair is growing, the hydrophobic protective composition having a thermal transition from solid to liquid within the range from -60°C to 80°C, wherein the enthalpy of thermal transition (ΔH_f(20-50°C)) measured within the range from 20°C to 50°C represents from 10% to 50% of the total enthalpy of thermal transition (ΔH_f) in the range from -60°C to 80°C; (b) applying a depilatory composition to the area of skin to which the hydrophobic protective composition has been applied, the depilatory composition comprising a keratin reducing agent.

Description

KIT AND METHOD FOR REMOVING HAIR

FIELD OF THE INVENTION The present invention relates to a depilatory method and kit.

BACKGROUND OF THE INVENTION

Depilatory compositions are cosmetic hair removal formulations. They comprise keratin reducing agents, which attack the disulphide bonds in hair to weaken it, such that subsequent gentle scraping and/or wiping completes severance of the hair from the skin and effects hair removal. Commercially, the most common keratin reducing agents are thioglycolates, which are typically formulated at high pH. An unwanted side effect of chemical depilation is that the depilatory composition comes into contact with and must have a relatively long residence time on skin to achieve effective hair removal and this long residence time combined with the alkaline conditions needed for effective hair removal may give rise to skin irritation. The above problem has been recognized in the art. Reference is made to US 2004/0219118, which discloses treatment with a "lipophilic" material before application of a thioglycolate -based reactive depilatory compostion. Lipophilic materials exemplified in this patent application are oils, such as mineral oil. As shown hereinbelow, the present applicants have tested a range of lipophilic materials to determine their ability to prevent thioglycolate penetration and, thereby, their ability to reduce or prevent skin irritation Applicants have surprisingly found that oils, such as mineral oil, have no or a low ability to prevent thioglycolate penetration to the skin. There thus exists a need to develop a pre-treatment composition which better reduces skin irritation.

SUMMARY OF THE INVENTION According to a first aspect of the invention, a method of removing hair from skin, preferably facial skin, is provided, comprising the steps of:

(a) applying a hydrophobic protective composition to an area of skin, preferably facial skin, on which unwanted hair is growing, the hydrophobic protective composition having a thermal transition from solid to liquid within the range from -60°C to 80°C, wherein the enthalpy of thermal transition (AH^oso'c ) measured within the range from 20°C to 50°C represents from 10% to 50% of the total enthalpy of thermal transition (Δ¾) in the range from -60°C to 80°C;

(b) applying a depilatory composition to the area of skin to which the hydrophobic protective composition has been applied, the depilatory composition comprising a keratin reducing agent.

According to a second aspect of the invention, depilatory kit is provided comprising:

(a) a hydrophobic protective composition, the hydrophobic protective composition having a thermal transition from solid to liquid within the range from -60°C to 80°C, wherein the enthalpy of thermal transition (AH^oso'c ) measured within the range from 20°C to 50°C represents from 10% to 50% of the total enthalpy of thermal transition (Δ¾) in the range from -60°C to 80 °C;

(b) a depilatory composition comprising an effective amount of a keratin reducing agent. BRIEF DESCRIPTION OF THE DRAWINGS

Fig.1 is a graph teaching how to mix waxes and triglycerides according to the invention

Fig.2 is a schematic view of a Franz Cell apparatus.

DETAILED DESCRIPTION OF THE INVENTION

Applicants have established that it is important for the hydrophobic protective composition to have semi-solid properties in order that it may melt, at least slightly, and spread evenly on skin to form a protective barrier. This explains why the temperature of 20°C has been found to be important, when considering the enthalpy of thermal transition. That said, the product requires a certain amount of solid material to give the barrier the structural properties it requires to enable it to remain intact when the depilatory is applied. This explains why the temperature of 50°C has been found to be important, when considering the enthalpy of thermal transition. Similarly, if the enthalpy of thermal transition in the range from 20°C to 50°C does not represent at least 10% of the total enthalpy of thermal transition, then the product may be too mobile, making it difficult to apply and unlikely that it will maintain a continuous barrier on skin. Furthermore, if the enthalpy of thermal transition in the range from 20°C to 50°C represents more than 50% of the total enthalpy of thermal transition, then the product may be either inhomogenous or too solid to spread evenly on skin and form a protective barrier.

The barrier formed by a hydrophobic protective composition according to the invention has been found to reduce the penetration of thioglycolic acid. In order to establish this, applicants have developed a test method, referred to herein as the "Franz Cell Method" and defined hereinbelow, to establish the penetration of thioglycolate through skin. Applicants have established that hydrophobic protective compositions according to the invention reduce penetration of thioglycolic acid according to the Franz Cell Method by over 45%. A reduction of thioglycolic acid penetration of 45% or more may be shown to correlate to a significant and user- noticeable reduction in irritation. Reference is made to the examples below which demonstrate how compositions according to the invention significantly reduce thioglycolate penetration.

At the same time as reducing contact between the depilatory active ingredient and the skin, the present compositions are observed not noticeably to reduce the ability of the depilatory composition to attack and degrade the unwanted hair growing on that skin. Why this should be is not understood, but it may simply be due to the fact that less of the hydrophobic protective composition adheres to the hairs than to the skin.

In order make a hydrophobic protective composition having a thermal transition from solid to liquid within the range from -60°C to 80°C, wherein the enthalpy of this thermal transition

(AH_f(2o-5o°c₎) measured within the range from 20°C to 50°C represents from 10% to 50% of the total enthalpy of thermal transition (Δ¾) in the range from -60°C to 80°C, applicants have established that the hydrophobic protective composition may comprise defined amounts of one or more hydrophobic components which are solid at 25 °C. The solid hydrophobic component(s) may comprise, but are not limited to, wax, triglyceride, and mixtures thereof. Without wishing to be bound by theory, applicants believe that the presence of defined amounts of one or more solid hydrophobic components may militate against the tendency otherwise exhibited by oils to ball up and reduce their surface area on skin when in contact with a mainly aqueous depilatory composition and therefore disrupt the barrier. The solid hydrophobic component(s) may also ensure that a thin and continuous barrier of the hydrophobic protective composition can be evenly distributed across the skin, even at a low dosage per unit area. In addition, the solid hydrophobic component(s) may enable the formation of a barrier across the skin that is chemically resistant to ingress from the thioglycolate (or other reducing) actives, therefore physically reducing the ability for the harsh chemistry to come into contact with the skin. This reduction in contact means that the stratum corneum may be maintained in a better state than if no barrier were present with correspondingly reduced signs of irritation, such as erythema, tingling and stinging.

As used herein, the term "wax" includes, but is not limited to, any hydrophobic material that is:

• Solid at 25 °C

• practically insoluble in water according to the United States' Pharmacopeia (USP) definition in 31/NF 26 Vol. 2 General Notices, Page Xvii. (which, according to that definition, means that more than 10,000 parts of water are needed to dissolve 1 part solute);

• has an onset temperature measured according to the DSC Method, defined hereinbelow, which is 10°C or greater; and

• comprises lipids, silicones or mixtures thereof.

As used herein, the term "triglyceride" refers to a material having the following formula:

wherein R, R' and R" may be the same as or different from one or both of the others and wherein each of R, R' and R" is a fatty acid and wherein the or each triglyceride is solid at 25°C.

Suitable waxes may comprise natural wax, synthetic wax, silicone wax, or mixtures thereof. Non-limiting examples of suitable natural waxes include Abies Alba Leaf Wax, Acacia Dealbata Leaf Wax, Acacia Farnesiana Flower Wax, Beeswax, Ceresin, Cetyl Esters, Cistus Labdaniferus Flower Wax, Aurantium Amara (Bitter Orange) Flower Wax, Aurantium Dulcis (Orange) Peel Wax, Copernicia Cerifera (Carnauba) Wax, Eclipta Prostrata Wax, Euphorbia Cerifera (Candelilla) Wax, Helichrysum Angustifolium Wax, Jasminum Officina le (Jasmine) Flower Wax, Jasminum Sambac (Jasmine) Flower Wax, Jojoba Esters, Jojoba Wax, Lanolin Wax, Lavandula Angustifolia (Lavender) Hower Wax, Lawsonia Inermis Wax, Mink Wax, Montan Acid Wax, Montan Wax, Myrica Cerifera (Bayberry) Fruit Wax, Ocimum Tenuiflorum Wax, Olive Wax, Oryza Sativa (Rice) Bran Wax, Ouricury Wax, Palm Kernel Wax, Persea Gratissima (Avocado) Wax, Pistacia Lentiscus Leaf Wax, Polianthes Tuberosa Flower Wax, Pyrus Malus (Apple) Peel Wax, Ribes Nigrum (Black Currant) Wax, Rosa Centifolia Flower Wax, Salvia Sclarea (Clary) Wax, Shellac Wax, Simmondsia Chinensis (Jojoba) Butter, Soft Olive Wax, Spent Grain Wax, Stipa Tenacissima Wax, Sunflower Seed Wax, Vegetable Wax, Vitis Vinifera (Grape) Leaf Wax and mixtures thereof. Non-limiting examples of suitable synthetic waxes include Hydrogenated Japan Wax, Hydrogenated Jojoba Oil, Hydrogenated Jojoba Wax, Hydrogenated Microcrystalline Wax, Hydrogenated Rice Bran Wax, Hydrolyzed Beeswax, Microcrystalline Wax, Oxidized Beeswax, Oxidized Microcrystalline Wax, Ozokerite, Paraffin, PEG-6 Beeswax, PEG-8 Beeswax, PE G-12 Beeswax, PEG-20 Beeswax, PEG- 12 Carnauba, Potassium Oxidized Microcrystalline Wax, Sulfurized Jojoba Oil, Synthetic Beeswax, Synthetic Candelilla Wax, Synthetic Carnauba, Synthetic Japan Wax, Synthetic Jojoba Oil, Synthetic Wax and mixtures thereof.

Non-limiting examples of suitable silicone waxes include DC2503 Cosmetic Wax, DC580 wax, DC AMS-C30 Cosmetic Wax, C30-45 Alkyl Methicone, DC Silkywax 10, Hexamethyldisiloxane, DC ST- Wax 30, C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane, DC SW-8005 resin wax, C26 - 28 Alkyl Dimethicone, C26 - 28 Alkyl Methicone, Polyphenylsilsesquioxane and mixtures thereof.

Advantageously, the wax comprises beeswax, carnauba wax, candelilla wax, jojoba wax, paraffin wax, microcrystalline wax, ozokerite, arachidyl behenate, or mixtures thereof.

If the hydrophobic protective composition used in the method and comprised within the kit according to the invention comprises wax, then the hydrophobic composition should comprise from 1% to 60%, preferably from 2% to 24% and, more preferably, 3% to 15% wax by weight of the hydrophobic protective composition. At wax levels above 60% by weight, the hydrophobic protective composition may become difficult to handle and apply and may also be brittle, crack and fall off the skin. At wax levels below 1 % the benefits of the invention may not be achieved, unless triglycerides are also present. In such a case, it is possible to operate with as little as 0.5% wax by weight of the hydrophobic protective composition, as discussed below. In relation to the triglycerides, suitable oils from which triglycerides may be formed from include, but are not limited to, the oils listed herein. Suitable fatty acids for formation of the triglycerides include, but are not limited to, Myristoleic acid, Palmitoleic acid, Sapienic acid, Oleic acid, Linoleic acid, a-Linolenic acid ,Arachidonic acid , Eicosapentaenoic acid,

Docosahexaenoic acid, Laurie acid (Ci₂), Myristic acid (Ci₄), Palmitic acid (Ci₆), Stearic acid (Cig), Arachidic acid (C₂o) and mixtures thereof.

Specific sources of triglycerides suitable for inclusion in the protective composition include include Butter, Shea Butter, Butyrospermum Parkii, Theobroma Cacao (Cocoa) Seed Butter, Cocoa Butter, Hydrogenated Shea Butter, Hydrogenated Cocoa Butter, Irvingia Gabonensis Kernel Butter, Tallow, Lard, Mangifera Indica (Mango) Seed Butter, Kokum Butter and mixtures thereof.

If the hydrophobic protective composition used in the method and comprised within the kit according to the invention comprises triglyceride(s), then the hydrophobic composition should comprise 20% or more, preferably 50% or more and more preferably from 75% to 99% of triglyceride(s) by weight of the protective composition. At triglyceride levels below 20%, the benefits of the invention may not be achieved, unless waxes are also present. In the case in which wax is mixed with the triglyceride, then, as discussed below, it is possible to operate with less than 20% triglyceride by weight of the hydrophobic protective composition.

Advantageously, the or each triglyceride has an onset temperature of less than 65 °C as measured by Differential Scanning Calorimetry, using the method defined hereinbelow. If the composition comprises triglycerides having an onset temperature outside this range, then it may become increasingly difficult to apply and may even crack and fall off in use.

Hydrophobic protective compositions according to the invention may comprise a homogenous mixture of wax, in the above-defined amounts, with triglyceride, in the above-defined amounts. More broadly, to make a hydrophobic protective composition comprising a mixture of wax and triglyceride, one may operate in one of the shaded regions shown in Figure 1, in which the order of preference for operation is region A being preferred, region B being less preferred and region C being less preferred still. Very specifically, when operating with a hydrophobic protective composition comprising from 0.5% to 3% wax by weight of the hydrophobic protective composition, combination with triglyceride is desirable, particularly in a weight ratio range of wax to triglyceride of 1:8 to 1:25, preferably 1:10 to 1:20, more preferably 1:15 to 1:20. The combination of the waxes and triglycerides may improve barrier-formation on skin, thereby reducing barrier mobility and therefore the ability for the actives within the depilatory composition to penetrate and cause damage to the skin.

The hydrophobic protective composition used in the method and comprised within the kit according to the invention may comprise oil. The oil may be selected from natural oil, synthetic oil, silicone oil and mixtures thereof.

Non-limiting examples of suitable natural oils include Acetylated Castor Oil, Acetylated Hydrogenated Castor Oil, Actinidia Chinensis (Kiwi), Seed Oil, Adansonia Digitata Oil, Aleurites Moluccana Seed Oil, Anacardium Occidentale (Cashew) Seed Oil, Arachis Hypogaea (Peanut) Oil, Arctium Lappa Seed Oil, Argania Spinosa Kernel Oil, Argemone Mexicana Oil, Avena Sativa (Oat) Kernel Oil, Bertholletia Excelsa Seed Oil, Borago Officinalis Seed Oil, Brassica Campestris (Rapeseed) Seed Oil, Calophyllum Tacamahaca Seed Oil, Camellia Japonica Seed Oil, Camellia Kissi Seed Oil, Camellia Oleifera Seed Oil, Canola Oil,

Caprylic/Capric/Lauric Triglyceride, Caprylic/Capric/Linoleic Triglyceride,

Caprylic/Capric/Myristic/Stearic Triglyceride, Caprylic/Capric/Stearic Triglyceride,

Caprylic/Capric Triglyceride, Carthamus Tinctorius (Hybrid Safflower) Seed Oil, Carthamus Tinctorius (Safflower) Seed Oil, Carum Carvi (Caraway) Seed Oil, Carya Illinoensis (Pecan) Seed Oil, Castor Oil Benzoate, Chenopodium Quinoa Seed Oil, Cibotium Barometz Oil, Citrullus Vulgaris (Watermelon) Seed Oil, Cocos Nucifera (Coconut) Oil, Cod Liver Oil, Coffea Arabica (Coffee) Seed Oil, Coix Lacryma-Jobi (Job's Tears) Seed Oil, Corylus Americana (Hazel) Seed Oil, Corylus Avellana (Hazel) Seed Oil, Cucumis Sativus (Cucumber) Oil, Cucurbita Pepo (Pumpkin) Seed Oil, Daucus Carota Sativa (Carrot) Seed Oil, Elaeis Guineensis (Palm) Kernel Oil, Elaeis Guineensis (Palm) Oil, Gossypium (Cotton) Seed Oil, Helianthus Annuus (Hybrid Sunflower) Oil, Helianthus Annuus (Sunflower) Seed Oil, Hippophae Rhamnoides Oil, Human Placental Lipids, Hydrogenated Canola Oil, Hydrogenated Castor Oil, Hydrogenated Castor Oil Laurate, Hydrogenated Castor Oil Triisostearate, Hydrogenated Coconut Oil, Hydrogenated Cottonseed Oil, Hydrogenated CI 2- 18 Triglycerides, Hydrogenated Fish Oil, Hydrogenated Lard, Hydrogenated Menhaden Oil, Hydrogenated Mink Oil, Hydrogenated Olive Oil,

Hydrogenated Orange Roughy Oil, Hydrogenated Palm Kernel Oil, Hydrogenated Palm Oil, Hydrogenated Peanut Oil, Hydrogenated Rapeseed Oil, Hydrogenated Shark Liver Oil,

Hydrogenated Soybean Oil, Hydrogenated Sunflower Seed Oil, Hydrogenated Tallow,

Hydrogenated Vegetable Oil, lsatis Tinctoria Seed Oil, Juglans Regia (Walnut) Seed Oil, Lauric/Palmitic/Oleic Triglyceride, Umnanthes Alba (Meadowfoam) Seed Oil, Unum

Usitatissimum (Linseed) Seed Oil, Lupinus Albus Seed Oil, Macadamia Integrifolia Seed Oil, Macadamia Ternifolia Seed Oil, Maleated Soybean Oil, Mangifera Indica (Mango) Seed Oil, Marmot Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Melia Azadirachta Seed Oil, Melissa Officina lis (Balm Mint) Seed Oil, Menhaden Oil, Mink Oil, Moringa pterygosperma Seed Oil, Mortierella Oil, Neatsfoot Oil, Nelumbium Speciosum Flower Oil, Nigella Sativa Seed Oil, Oenothera Biennis (Evening Primrose) Oil, Olea Europaea (Olive) Fruit Oil, Olea Europaea (Olive) Husk Oil, Orange Roughy Oil, Orbignya Cohune Seed Oil, Orbignya Oleifera Seed Oil, Oryza Sativa (Rice) Bran Oil, Oryza Sativa (Rice) Germ Oil, Ostrich Oil, Oxidized Corn Oil, Oxidized Hazel Seed Oil, Papaver Orientale (Poppy) Seed Oil, Passiflora Edulis Seed Oil, Persea Gratissima (Avocado) Oil, Pistacia Vera Seed Oil, Placental Lipids, Prunus Amygdalus Amara (Bitter Almond) Kernel Oil, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Prunus Armeniaca (Apricot) Kernel Oil, Prunus Avium (Sweet Cherry) Seed Oil, Prunus Cerasus (Bitter Cherry) Seed Oil, Prunus Persica (Peach) Kernel Oil, Pyrus Malus (Apple) Oil, Ribes Nigrum (Black Currant) Seed Oil, Ricinus Communis (Castor) Seed Oil, Rosa Canina Fruit Oil, Rosa Moschata Seed Oil, Salmon Oil, Salvia Hispanica Seed Oil, Santalum Album (Sandalwood) Seed Oil, Sesamum Indicum (Sesame) Seed Oil, Shark Liver Oil, Solanum Lycopersicum (Tomato) Seed Oil, Soybean Lipid, Sphingolipids, Taraktogenos Kurzii Seed Oil, Telphairia Pedata Oil, Vegetable Oil, Vitis Vinifera (Grape) Seed Oil, Zea Mays (Corn) Germ Oil, Zea Mays (Corn) Oil and mixtures thereof.

Non-limiting examples of suitable synthetic oils include mineral oil, isopropyl pamitate, isopropyl stearate, isohexadecane, isododecane, polyglyceryl triisostearate and mixtures thereof. Non-limiting examples of suitable silicone oils include dimethicones (including partial esters of dimethicones and fatty acids derived from natural/synthetic oils), cyclomethicones, polydimethlysiloxanes (e.g. DC200 from Dow Corning), phenyl trimethicones, trimethyl pentaphenyl trisiloxane, dimethicone copolyols and mixtures thereof.

The hydrophobic protective c omposition used in the method and comprised within the kit according to the invention may comprise skin active agents such as, but not limited to oil soluble vitamins, such as vitamin E derivatives, including vitamin E acetate and tocopherol nicotinate; oil-soluble vitamin A derivatives, such as retinyl palmitate; lanolin; ceramides; sterols and sterol esters; salicylic acid; camphor; eucalyptol; essential oils and mixtures thereof. These materials may also fall under the definition of "wax" or "triglyceride" as used herein and, in such a case, should be included as a wax or triglyceride for the purposes of determining the proportions of these materials.

The hydrophobic protective composition used in the method and comprised within the kit according to the invention may include further ingredients such as, but not limited to metal oxides, organic and inorganic dyes, lakes, micas, flavourings, perfumes and mixtures thereof.

Any depilatory composition comprising a suitable keratin reducing agent may be used in the present method and included in the present kit. Non-limiting examples of suitable keratin reducing agents include: sulphide salts such as L1₂S, Na₂S, K₂S, MgS, CaS, SrS or BaS, hydrogen sulphide salts such as NaSH or KSH; thioglycol; thioglycerol; thioglycolamide;

thioglycolhydrazide; thioglycolic acid; thioglycolate salts (such as potassium thioglycolate, calcium thioglycolate, ammonium thioglycolate, diammonium dithioglycolate, glyceryl monothioglycolate, or monoethanolamine thioglycolate); thiosalicylic acid; thiomalic acid;

ammonium thiolactate; monoethanolamine thiolactate; dithioerythritol; 2-mercaptopropionic acid; 1,3-dithiopropanol; glutathione; dithiothreitol; cysteine; homocysteine; N-acetyl-L-cysteine and cysteamine. Advantageously, the keratin reducing agent is comprised within the depilatory composition in an amount from 0.3% to 20%, preferably from 0.8% to 15%, more preferably from 1% to 10% by weight of the depilatory composition.

Advantageously, the depilatory composition may comprise at least one thioglycolate salt or thioglycollic acid acting as a hair removal agent when the depilatory composition is applied to unwanted hair. Preferably, the depilatory composition comprises sodium, potassium, magnesium, calcium, beryllium, strontium, zinc, monoethanolamine, ammonium,

tetralkylammonium, imidazolium, pyridinium, phosphonium or glyceryl thioglycolate salts, or mixtures thereof, which may include dianion forms of thioglycolate. More preferably, the depilatory composition comprises at least one of sodium, potassium, magnesium or calcium thioglycolate, or mixtures thereof. Even more preferably the depilatory composition comprises potassium or calcium thioglycolate, or mixtures thereof.

The pH of the depilatory composition may advantageously be in the range of from 6 to 13.8, preferably from greater than 7 to 13, more preferably from 9 to 12.9, even more preferably from 10 to 12.8, even more preferably still from 12 to 12.75 and yet more preferably from 12.3 to 12.6 to improve the efficacy of the active ingredient. The depilatory composition may, in a preferred embodiment, comprise at least one base to control the pH. Preferably, the depilatory composition comprises potassium hydroxide; sodium hydroxide; lithium hydroxide; calcium hydroxide; barium hydroxide; caesium hydroxide; sodium hydroxide; ammonium hydroxide; strontium hydroxide; rubidium hydroxide; magnesium hydroxide; zinc hydroxide; sodium carbonate; pyridine; ammonia; alkanolamides (including monoethanolamine, diethanolamine, triethanolamine), phosphates (including tetrasodium phosphate), arginine or mixtures thereof. More preferably, the depilatory composition comprises at least one buffering base, even more preferably the depilatory composition comprises calcium hydroxide, magnesium hydroxide; barium hydroxide; strontium hydroxide; zinc hydroxide; arginine or mixtures thereof. Still more preferably the depilatory composition comprises calcium hydroxide; magnesium hydroxide, zinc hydroxide, sodium hydroxide, potassium hydroxide or mixtures thereof. Even more preferably still, the depilatory composition comprises calcium hydroxide, sodium hydroxide or mixtures thereof.

In an advantageous embodiment, the base is present at a concentration of from 0.1% to 10.0%, more preferably from 0.5% to 8.0% and even more preferably from 1.0% to 5.0%, by weight of the depilatory composition.

The concentration of water in the depilatory composition is preferably at least 40%, more preferably from 50% to 98%, even more preferably from 60% to 95% and even more preferably still from 70% to 90%, by weight of the depilatory composition.

The depilatory composition may optionally comprise a thickening agent. A representative but not exhaustive list can be found in "The Encyclopaedia of Polymers and Thickeners for Cosmetics" compiled and edited by Robert Y. Lochhead, PhD and William R. Fron, Department of Polymer Science, University of Southern Mississippi. Exemplary classes of thickening agents include gums, carbomers, polymers and copolymers of acrylic acid, associated thickeners, layered silicates/clays and natural polymers (including polysaccharides). One or more thickening agents may be included in the aqueous depilatory composition. The thickening agent may be present at a level of from about 0.01% to about 20%, preferably from about 0.1% to about 10% by weight of the depilatory composition.

The depilatory composition may also include other skin care ingredients such as conditioning agents selected from the group consisting of humectants, moisturizers, or skin conditioners (including mineral oil; almond oil; chamomile oil; jojoba oil; avocado oil; shea butter, niacinamide and glycerine); skin rejuvenation compositions (for example targeted for fine lines, wrinkles and uneven skin tone, including retinoids), cosmetic compositions; anti-inflammatory agents (including corticosteroids); anti-oxidants (including flavonoids) radical scavengers; sunscreen agents; skin cooling or warming agents and the like. The depilatory composition may comprise one or more skin care ingredients present in an amount of from about 0.001% to about 10%, more preferably from about 0.01% to about 7%, and even more preferably from about 0.025% to about 5%, by weight of the depilatory composition.

An accelerant may be employed in the depilatory composition. This optional component accelerates the rate of depilatory action of the depilatory agent. Suitable accelerants include, but are not limited to, urea; thiourea; dimethyl isosorbide; arginine salts; ethoxydiglycol; propylene glycol and methylpropyldiol. The accelerant may be present in a concentration range of from 0.5% to 10%, more preferably from 2% to 8% and even more preferably from 2% to 5% by weight of the depilatory composition.

The depilatory composition may further comprise components known, conventionally used, or otherwise effective for use in cosmetic compositions, such as dyes; pigments (including ultra marines and talc); anionic, cationic, non-ionic and/or amphoteric or zwitterionic surfactants, polymers (including hydrophobically modified polymers); dispersing agents; solvents; lubricants; fragrances; preservatives; chelants, proteins and derivatives thereof, plant materials (e.g. aloe, chamomile and henna extracts); silicones (volatile or non- volatile, modified or non-modified); film-forming agents; film forming promoters and mixtures thereof. The depilatory composition may be formulated in any common delivery form, such as a cream or lotion. Alternatively, it may be delivered on a substrate, such as a thin layer of depilatory composition coated onto the substrate. The substrate may be configured in any suitable form, such as a strip, mask or patch.

In addition to the hydrophobic protective composition and the depilatory composition, the kit according to the second aspect of the invention may comprise one or more of:

(a) A make-up removal composition and/or a make-up removal wipe;

(b) Means for removal of the hydrophobic protective composition and the depilatory

composition following use, which means may comprise one or more of a tool, such as a scraper or a spatula; or a wipe; (c) A post-treatment composition skin care composition to be applied to the area of skin from which hair has been removed. Such a post-treatment skin care composition may comprise ingredients to promote skin conditioning; moisturizers, skin rejuvenation compositions (targeted for fine lines, wrinkles and uneven skin tone, for example), cosmetic compositions (e.g., foundation, rouge), sunscreens and the like. The post- treatment skin care composition may be leave-on or a rinse-off composition.

(d) Instructions regarding how to use the various elements of the kit, which instructions may comprise one or more elements of the method as defined herein.

Prior to applying the method or using the kit according to the present invention, a user should advantageously remove all make-up from the skin, to ensure good adherence and effective application of both the hydrophobic protective composition and the depilatory composition.

The method according to the first aspect of the invention comprises the step of applying the above-defined hydrophobic protective composition to an area of skin on which unwanted hair is growing. The area of skin may be located on any part of the human body, but is preferably on the face, more preferably on an area of skin adjacent to the vermillion lip and more preferably still on an area above the upper vermillion lip.

Advantageously, the hydrophobic protective composition is not just applied to the area to be depilated, but also to an immediately juxtaposing area thereabout (that is, the hydrophobic protective composition is applied to an area of skin which is greater than just the area which is to be depilated).

Advantageously, the user will apply from 0.3 - 2mg of hydrophobic protective composition per square centimetre of skin, preferably from 0.4 - lmg/cm², more preferably from 0.4 to

0.7mg/cm².

Following application, the hydrophobic protective composition is advantageously massaged into the skin. Preferably, massaging is effected for at least 10 seconds, and, more preferably, massaging is effected as a circular motion. Without wishing to be bound by theory, it is believed that the hydrophobic protective composition may trap hair within it thereby shielding it from the to-be-applied depilatory composition; massaging may help to release the hairs from the skin and ensure improved access thereto by the depilatory composition. The method according to the first aspect of the invention comprises the subsequent step of applying the above-defined depilatory composition to an area of skin on which unwanted hair is growing and to which hydrophobic protective composition has already been applied.

Advantageously, the user will apply a layer of depilatory composition which is from 0.1mm to 5mm, preferably from 0.3 to 3mm, more preferably from 0.5 to 2mm in thickness.

Subsequently, according to the method of the first aspect of the invention, the depilatory composition is advantageously left in place for at least 1 minute, preferably from 1 to 10 minutes, more preferably from 3 to 10 minutes, depending on the thickness of the hair and the hair removal efficacy of the depilatory composition (which, in turn, is dependent upon the

concentration of keratin reducing agent in the depilatory composition).

Subsequently, according to the method of the first aspect of the invention, the hydrophobic protective composition and the depilatory composition are advantageously removed. This may be achieved using one or more of a cotton wool ball, pad or wand, a tissue, a cloth, or a tool, such as a spatula or a scraper. Advantageously, the skin from which hair has been removed is then rinsed with water.

In an advantageous subsequent step, a post-treatment skin care composition may be applied to the area of skin from which hair has been removed. Such a post-treatment skin care composition may comprise ingredients to promote skin conditioning; moisturizers, skin rejuvenation compositions (targeted for fine lines, wrinkles and uneven skin tone, for example), cosmetic compositions (e.g., foundation, rouge), sunscreens and the like. The post-treatment skin care composition may be leave-on or a rinse-off composition.

Differential Scanning Calorimetry (DSC) Melting Method

This method is the American Oil Chemists' Society Method Cj 1-94, as reapproved in 2009 and it determines the "onset temperature" (that is the temperature of onset of melting) and thermal properties of oils and fats by differential scanning calorimetry (DSC").

Apparatus

1. Aluminum capsules.

2. DSC instrument, capable of holding temperature at -60°C and achieving a temperature of 80 r. Reagents

1. Indium, powder 60 mesh, 99.999%, such as Aldrieh Chemical Co., Milwaukee, Wi

53233, or equivalent.

2. n-Decane, 99+%, such as Aldrieh Chemical Co., Milwaukee, WI 53233, or equivalent. 3. Methyl stearate, 99%, such as Aldrieh Chemical Co., Milwaukee, WI 53233, or equivalent.

Procedure

1. Standardization of equipment Proceed with the normal standardization using both indium and n-decane as reference standards. Follow instrument manual for adjustment to lock onto these two reference points and flatten the baseline slope as much as possible when empty pans are analyzed. Analyze the secondary standard (methyl stearate). Weigh 5 mg of the standard into the same kind of pan which will be used for the test portion (if hermetically sealed, it may be reused at a later date). Use the method sequence in Procedure, 2-7 to obtain the melting point onset (because of the high purity, only a 2 niin hold is necessary for the standard after crystallization). Be certain that the heating rate during the definitive heating pattern is at 5°C/min. The melting point onset should be within ±2.00°C of 36.5°C. If not, recheck calibration.

Note -be certain to use identical capsules for the test portion as those used for reference standards and the instrument blank reference, 2. Melt each test portion completely and weigh 7 ± 0.200 mg of each test portion into the same kind of capsule used for the blank and reference samples (aluminum) and seal to minimize oxidation and other changes.

3. Place capsules in DSC at room temperature,

4. Heat rapidly to 80°C and hold for 10 min. 5. Cool to -60°C at 10°C/min and hold for 30 min.

6. Heat to 80°C at 5°C/min.

7. Use the baseline obtained for an empty capsule analysis from the final melt segment of the program to define the position of the baseline under the sample peaks. Overlay the final melting curve of the test portion over the curve for the empty capsule with a flexible ruler or other curve guide to define the baseline of the test portion back to where it intersects the initial deviation of the melting curve from its baseline. The baseline beneath the test portion should be a continuation of the baseline where there are no sample components present, if a shift has occurred in the heat capacity of the test portion after the melt, it will be evident relative to the baseline of the empty capsule. Have the instrument calculate the sigmoid baseline if it can, or connect the end of the peak point with the last point in which the test portion was in conjunction with the baseline of the empty capsule. Results

Determine the onset temperature in °C, which, if not computer generated, is an extrapolation to baseline of the steepest slope of the principal peak.

Determine the enthalpy of fusion (A¾) in Joules, which, if not computer generated, is a linear integration of the total thermal transition curve area between -60°C and 80°C. Determination of the enthalpy of fusion between 20°C and 50°C (AH_f(2o-so_°c)) in Joules, if not computer generated, is an integration of the total thermal transition curve area between 20°C and 50°C. Determination of the percentage of enthalpy of fusion for the product that is between 20°C and 50°C is made as follows:

AH (20-50°C)

%(AH /(20-50°C) ) =^■ xlOO

AH

Franz cell method Principle and Scope:

This method is applicable for using Franz cell apparatus for the in-vitro assessment of penetration of thioglycolic acid (TGA) and its salts through a skin mimic after the application of a depilatory composition following pre-treatment with a hydrophobic protective composition.

Penetrated TGA is quantified using Reverse Phase High Performance (or Pressure) Liquid Chromatography (RP-HPLC) with external standard quantitation at 240nm. Method

Reference is made to Figure 2 and to the reference numerals therein:

1. Prepare the Vitro-Skin (IMS Vitro-Skin®, Catalogue number: P&G1013, made by IMS Inc., Portland, Maine, USA) samples by cutting 8x6.2cm segments and placing them textured side up on the racks into a hydration chamber (manufactured & sold by IMS) containing a 14.7% glycerol solution. The hydration chamber should be sealed and the vitro-skin left to hydrate at room temperature and a humidity of 80.4% ±3.5% for 24 hours.

2. Prepare the receptor solution for the Franz-cell by mixing 1.90ml formic acid (98%wt+ Fluka, by Sigma Aldrich, or equivalent), 30ml acetonitrile (RP-HPLC grade) and 968.1ml water (RP- HPLC grade). Set up the static Franz cell (Permegear or equivalent, 15mm diameter unjacketed cell with a 12ml receptor volume) by clamping it in place over suitable stirrer plates (not shown) and add a small stirrer bar (6) to each cell, fill the receptor cell (2) to the brim with the required amount of receptor solution.

3. Once hydrated, remove a sheet of vitro-skin from the hydration chamber and lay textured side up on a clean flat surface then dose ΙΟΟμΙ (~2mg/cm²) of hydrophobic protective composition

(not shown) onto the vitro-skin and spread evenly over the surface by rubbing for 30 seconds with a gloved finger.

4. Using a scalpel blade cut the vitro-skin segment (3) into two equal sections, each large enough to completely cover the top of the cell. Place the relevant size o-ring (5) (22mm, for the specified Franz-cell) onto each section of the vitro skin and dose to 150mg/cm² of depilatory composition (4) ("Veet Normal Skin Hair Removal Cream" or an equivalent (an equivalent being a composition comprising 3.7%wt thioglycolic acid)) into the centre then, using a glass rod, evenly spread the cream around the inside of the o-ring (5). Using tweezers pick up the vitro-skin segment and place the vitro-skin segment, depilatory and o-ring centrally over the receptor cell (2), place donor cell (1) over the top and clamp in place. Turn on stirrer plate and start 10 minute countdown timer. After 10 minutes; turn off stirrer and remove the clamp, donor cell (1) and vitro-skin segment and place the receptor solution in a suitable container for analysis.

5. A reference sample should also be run without hydrophobic protective composition treatment on the vitro-skin. Remove a sheet of vitro-skin from the hydration chamber and lay textured side up on a clean flat surface. Repeat step 4 of the protocol to produce the reference sample. Sample Analysis

For RP-HPLC analysis, prepare a 50mM Formic acid (98%+ Fluka) solution and mix 970ml of this solution with 30ml acetonitrile (HPLC grade) to act as a mobile phase during the analysis.

A reference standard solution should be made with a concentration of Calcium Thioglycolate Trihydrate of 0.94 mg/ml.

Install a Waters Atlantis T3 3μηι 4.6 x 50mm column into the HPLC (although any silica- based Ci₈ reversed phase RP-HPLC column may be used), and ensure all solvent lines for the RP- HPLC are primed and free of leaks. Allow the mobile phase to circulate through the system for 25 minutes at 0.7mL/Min in order to equilibrate the column. Detection of the thioglycolic acid is via UV spectroscopy.

The RP-HPLC conditions are as follows:

Injection volume: 20 μL

Mobile phase flow rate: 0.70 ml/min

Run time: 10 minutes

UV Detection wavelength: 240 nm

Column temperature: 35°C

UV sampling rate: > 5 per second

Retention time: Thioglycolic Acid ~ 2.5 min

Calculations:

Calculate the concentration of Thioglycolic Acid in the sample

concentration (mg/ml) = weight of std (mg) x purity x _3

25 25 Calculate the concentration of thioglycolic acid in the sample using the following formula: concentration (mg/ml) = A/B x C x E/F

Where, A = Peak Area of Thioglycolic Acid Sample

B = Average Peak Area of Thioglycolic Acid Standard

C = Thioglycolic Acid final STD concentration in mg/ml (0.94 mg/ml)

E = Molecular weight of Thioglycolic acid (92.12g/mol)

F = Molecular weight of Calcium thioglycolate (184.23g/mol)

The efficacy of the barrier (resistance to TGA penetration) can be calculated as a percentage decrease in TGA in the receptor solution:

%reduction = concentration without barrier - concentration with barrier x 100

concentration without barrier

For example, if TGA in solution without hydrophobic protective composition = 75μg/ml and TGA in solution with barrier = 15 μg/ml

%reduction = 75 - 60 x 100 = 85%

75

A reduction of TGA penetration of 45% or more is believed to correlate to a significant and user- noticeable reduction in irritation. Examples

The following compositions were made by heating all elements of the composition to the melting temperature of the highest melting point material and then mixing until a homogenous mixture was obtained. The compositions were then tested using the Franz Cell method defined above.

AHf(2o°c - AHf/mJ % AHf(2o°c -

Example Composition % Reduction in 5o°c/mJ 5o°c)/mJ

Thioglycolic

Acid

Penetration

According to

the Franz Cell

Method

Inventive 6% beeswax 99.0 87 191 46

Example 1

6% ozokerite 88% mineral oil

Inventive 12% beeswax 95.0 36 103 35

Example 2

88% DC245 (Dow

Corning)

Inventive 6% beeswax 95.3 55 186 30

Example 3

94% mineral oil

Inventive 6% beeswax 85.9 133 925 14

Example 4

94% coconut oil

Inventive 12% beeswax 94.1 25 87 29

Example 5

88% DC200 Inventive 2% mineral oil 86.3 181 567 32 Example 6

98% shea butter

Inventive 25% olive oil 95.1 46 188 24 Example 7

75% cocoa butter

Comparative 25.0 0 179 0

100% mineral oil

Example 1

Comparative 100% sunflower 10.8 0 852 0 Example 2 seed oil

Comparative 0.0 0 421 0

100% olive oil

Example 3

Comparative 12% shea butter 20.1 11 165 7 Example 4

88% mineral oil

Comparative 12% cocoa butter 21.1 13 611 2 Example 5

88% mineral oil

Comparative 12% DC580 42.0 200 275 73 Example 6

88% mineral oil

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm".

Claims

CLAIMS What is claimed is:

1. A method of removing hair from skin, preferably facial skin, comprising the steps of:

2. The method of claim 1 , wherein the amount of hydrophobic protective composition applied to the skin is from 0.3 - 2mg/cm², preferably from 0.4 - lmg/cm², more preferably from 0.4 to 0.7mg/cm².

3. The method of claim 1 or 2, wherein the depilatory composition is applied as a layer to the skin which has been pre-treated with hydrophobic protective composition, wherein the layer has a thickness from 0.1mm to 5mm, preferably from 0.3 to 3mm, more preferably from 0.5 to 2mm.

4. The method of any of claims 1 to 3, comprising the following additional step between step (a) and step (b):

(al) massaging the hydrophobic protective composition into the skin for at least 10 seconds.

5. The method of any preceding claim, comprising the following additional step immediately following step (b):

(c) leaving the depilatory composition in place on the hydrophobic protective

composition for a period of at least 1 minute, preferably from 1 to 10 minutes, more preferably from 3 to 10 minutes.

6. The method of any preceding claim, comprising the following additional step

immediately following step (c):

(d) removing both the hydrophobic protective composition and the depilatory

composition from the skin, optionally scraping, wiping or rubbing it off.

7. The method of any preceding claim, wherein the hydrophobic protective composition comprises from 1 % to 60%, preferably from 2% to 24%, more preferably from 3% to 15% of wax by weight of the hydrophobic protective composition.

8. The method of any preceding claim, wherein the hydrophobic protective composition comprises from 20% to 99%, preferably from 50% to 99% and more preferably from 75% to 99% of triglyceride by weight of the hydrophobic protective composition.

9. The method of any of claims 1 to 6, wherein the hydrophobic protective composition comprises a homogenous mixture of triglyceride and from 0.5% to 3% wax by weight of the hydrophobic protective composition, wherein the weight ratio of wax : triglyceride is 1 :8 to 1 :25, preferably 1 : 10 to 1 :20, more preferably 1 : 15 to 1 :20.

10. A depilatory kit comprising:

(a) a hydrophobic protective composition, the hydrophobic protective composition having a thermal transition from solid to liquid within the range from -60°C to 80°C, wherein the enthalpy of thermal transition (AH^oso'c ) measured within the range from 20°C to 50°C represents from 10% to 50% of the total enthalpy of thermal transition (AH_f) in the range from -60°C to 80 °C;

(b) a depilatory composition comprising an effective amount of a keratin reducing agent.

11. The depilatory kit of claim 10, wherein the hydrophobic protective composition comprises from 1 % to 60%, preferably from 2% to 24%, more preferably from 3% to 15% of wax by weight of the hydrophobic protective composition.

12. The depilatory kit of claim 10 or 11, wherein the hydrophobic protective composition comprises from 20% to 99%, preferably from 50% to 99% and more preferably from 75% to 99% of triglyceride by weight of the hydrophobic protective composition.

13. The depilatory kit of any of claims 10 to 12, wherein the depilatory composition is in the form of a cream or lotion, or is disposed on a substrate.

14. The depilatory kit of any of claims 10 to 13, additionally comprising a tool, such as a scraper or a spatula, or a wipe.

15. The depilatory kit of any of any of claims 10 to 14, additionally comprising the following instructions:

(a) An instruction to apply the hydrophobic protective composition over an area of skin, preferably facial skin, to be depilated, preferably an instruction to apply the hydrophobic protective composition over an area which is greater than the area of skin to be depilated;

(b) Optionally an instruction to massage the hydrophobic protective composition into the area of skin to be depilated, preferably for at least 10 seconds, more preferably to massage in a circular motion;

(c) An instruction to apply the depilatory composition to the pre-treated area of skin to be depilated;

(d) Optionally, an instruction to leave the depilatory composition in place on top of the hydrophobic protective composition for a period of at least 1 minute, preferably from 1 to 10 minutes, more preferably from 3 to 10 minutes;

(e) Optionally an instruction to remove both the hydrophobic protective composition and the depilatory composition from the skin, by scraping, wiping or rubbing it off.