WO2009138485A1 - Sunscreens - Google Patents

Sunscreens Download PDF

Info

Publication number
WO2009138485A1
WO2009138485A1 PCT/EP2009/055902 EP2009055902W WO2009138485A1 WO 2009138485 A1 WO2009138485 A1 WO 2009138485A1 EP 2009055902 W EP2009055902 W EP 2009055902W WO 2009138485 A1 WO2009138485 A1 WO 2009138485A1
Authority
WO
WIPO (PCT)
Prior art keywords
topical composition
phosphate
phosphate ester
ester surfactant
filter substance
Prior art date
Application number
PCT/EP2009/055902
Other languages
French (fr)
Inventor
Christine Mendrok-Edinger
Original Assignee
Dsm Ip Assets B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dsm Ip Assets B.V. filed Critical Dsm Ip Assets B.V.
Priority to US12/991,300 priority Critical patent/US20110052516A1/en
Priority to EP09745817A priority patent/EP2274057A1/en
Priority to AU2009248015A priority patent/AU2009248015A1/en
Priority to BRPI0911849A priority patent/BRPI0911849A2/en
Priority to CN2009801177241A priority patent/CN102026683A/en
Priority to JP2011508934A priority patent/JP2011520842A/en
Publication of WO2009138485A1 publication Critical patent/WO2009138485A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds

Definitions

  • the present invention relates to the use of phosphate ester surfactants for increasing the sun protection factors (SPF's) of topical compositions which comprise at least one UV-filter substance. Furthermore, the invention relates to topical compositions comprising a phosphate ester surfactant and at least 4 wt-% of butyl methoxydibenzoylmethane in combination with further UV-filter substances.
  • SPPF's sun protection factors
  • UV-B radiation UV-A radiation
  • UVA UV-A radiation
  • the SPF (Sun Protection Factor) rating system has been developed to provide consumer guidance in selecting sun care products. SPF is measured in the laboratory with a solar simulator that induces UV erythema. However, erythema is primarily caused by UVB, making SPF testing primarily a measurement of UVB - not UVA - protection.
  • UVA protection performance is determined according to the 'Method for the in vitro determination of UVA protection provided by sunscreen products' (COLIPA Guideline 2007) which is labeled as UVAPF (UVA protection factor).
  • UV-filter substances have been developed in the past protecting against the harmful effect of UVA and / or UV-B radiation and even shorter radiation (UVC). These substances are usually incorporated either alone or in combination with each other into cosmetic or pharmaceutical preparations which are widely known and used.
  • UVA-filter substances In order to obtain a UVA protection complying with the above mentioned standards high concentrations of at least one UVA filter substance has to be incorporated into the sun care products.
  • UVA-filter substances are commercially available and all of them exhibit more or less severe downsides e.g. in view of stability, solubility and/ or suitable absorption profile in order to achieve the recommended UVA protection at a reasonable concentration level.
  • the frequently used butyl methoxydibenzoylmethane is difficult to be formulated in high amounts into sun care products as it often renders the formulation instable and as it is incompatible with many other UV-filter substances.
  • ingredients which improve the functionality of UV-filter substances in order to achieve higher
  • phosphate ester surfactants are able to enhance the in vivo SPF at given UV-filter substance concentrations. This surprising effect helps to overcome the problems of the prior art outlined above. Furthermore it has been found that the incorporation of high levels of butyl methoxydibenzoylmethane is facilitated which makes it possible to achieve the recommended UVA protection at high SPF levels.
  • the in vivo SPF according to the invention is tested according to the Colipa, International Test Method for the in vivo determination of the Sun Protection Factor SPF provided by sunscreen products, guideline 2006.
  • the invention relates in one aspect to the use of a phosphate ester surfactant for increasing the SPF of a topical composition comprising at least one UV-filter substance.
  • the at least one UV-filter substance is a UVB and/ or broadband-filter substance.
  • the invention relates to the use of a phosphate ester surfactant for increasing the SPF of a topical composition comprising butyl methoxydibenzoylmethane and at least one UV-filter substance selected from a UVB and/ or broadband-filter substance.
  • Phosphate esters surfactants suitable for incorporation into the compositions of the present invention have the formula
  • the phosphate ester surfactant has the general structure wherein R, R 1 and R 2 may be hydrogen, an alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, or an alkoxylated alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, and having 1 or more, preferably from about 2 to about 25, most preferably 2 to 12, moles ethylene oxide, with the proviso that at least one of R, R 1 and R 2 is an alkyl or alkoxylated alkyl as previously defined but having at least 6 alkyl carbons in said alkyl or alkoxylated alkyl group.
  • Monoesters in which R 1 and R 2 are hydrogen and R is selected from alkyls of 10 to 18 carbons and alkoxylated fatty alcohols of 10 to 18 carbons and 2 to 12 moles ethylene oxide are preferred.
  • phosphate ester surfactants mention may be made of, C8-10 Alkyl Ethyl Phosphate, C9-15 Alkyl Phosphate, Ceteareth-2 Phosphate, Ceteareth-5 Phosphate, Ceteth-8 Phosphate, Ceteth-10 Phosphate, Cetyl Phosphate, C6-10 Pareth-4 Phosphate, C12-15 Pareth-2 Phosphate, C12-15 Pareth-3 Phosphate, DEA-Ceteareth-2 Phosphate, DEA-Cetyl Phosphate, DEA-Oleth-3 Phosphate, Potassium cetyl phosphate, Deceth-4 Phosphate and
  • the phosphate ester surfactant is generally present in the topical compositions according to the invention in proportions ranging from 0.1 to 5 wt.-%, preferably from 0.5 to 5 wt.-%, most preferably from 1 to 3 wt.-%, such as particularly from 2 to 3 wt.-% with respect to the total weight of the topical composition.
  • the at least one UV-filter substance is preferably selected from conventional UVA and/or UVB and/ or broad spectrum UV-filter substances known to be added into topical compositions such as cosmetic or dermatological sun care products.
  • Such UV-filter substances comprise all groups which absorb light in the range of wavelengths 400 nm to 320 nm (UVA) and 320 nm to 280 nm (UVB) or of even shorter wavelengths (UVC) and which are or can be used as cosmetically acceptable UV-filter substances.
  • UV-filter substances are e.g. listed in the CTFA Cosmetic ingredient Handbook or "The Encyclopedia of Ultraviolet Filters" (ISBN: 978-1-932633-25-2) by Nadim A. Shaath.
  • Suitable UV-filter substances may be organic or inorganic compounds.
  • organic UV-filter substances encompass e.g. acrylates such as e.g. 2-ethylhexyl 2-cyano-3,3- diphenylacrylate (octocrylene, PARSOL ® 340), ethyl 2-cyano-3,3-diphenylacrylate; Camphor derivatives such as e.g.
  • ethylhexyl methoxycinnamate PARSOL ® MCX
  • ethoxyethyl methoxycinnamate isoamyl methoxycinnamate as well as cinnamic acid derivatives bond to siloxanes
  • p-Aminobenzoic acid derivatives such as e.g. p-aminobenzoic acid, 2-ethylhexyl p-dimethylaminobenzoate, N-oxypropylenated ethyl p-aminobenzoate, glyceryl p-aminobenzoate
  • Benzophenones such as e.g.
  • Esters of benzalmalonic acid such as e.g. di-(2-ethylhexyl) 4-methoxybenzalmalonate
  • Organosiloxane compounds carrying chromophore groups such as e.g. polysilicones-15 (PARSOL ® SLX), drometrizole trisiloxane (Mexoryl ® XL); Imidazole derivatives such as e.g.
  • PARSOL ® HS 2-phenyl benzimidazole sulfonic acid
  • salts thereof such as e.g. sodium- or potassium salts, ammonium salts, morpholine salts, salts of primary, sec. and tert. amines like monoethanolamine salts, diethanolamine salts; Salicylate derivatives such as e.g.
  • ethylhexyl triazone Uvinul ® T-150
  • diethylhexyl butamido triazone Uvasorb ® HEB
  • bis- ethylhexyloxyphenol methoxyphenyl triazine Teinosorb ® S
  • Benzotriazole derivatives such as e.g. 2,2'-methylene-bis-(6-(2H-benzotriazole-2-yl)-4-(1 ,1 ,3,3,-tetramethylbutyl)-phenol
  • Encapsulated UV-filters such as e.g.
  • encapsulated ethylhexyl methoxycinnamate (Eusolex ® UV-pearls) or microcapsules loaded with UV-filters as e.g. dislosed in EP 1471995; Dibenzoylmethane derivatives such as e.g. 4-tert.-butyl-4'- methoxydibenzoyl-methane (PARSOL ® 1789), dimethoxydibenzoylmethane, isopropyldibenzoylmethane; Phenylene-1 ,4-bis-benzimidazolsulfonic acids or salts such as e.g.
  • Inorganic UV-filter substances encompass pigments such as e.g. microparticulated Zink oxide or Titanium dioxide (e.g. commercially available as PARSOL ® TX)
  • microparticulated refers to a particle size from about 5 nm to about 200 nm, particularly from about 15 nm to about 100 nm.
  • the particles may also be coated by other metal oxides such as e.g. aluminum or zirconium oxides or by organic coatings such as e.g. polyols, methicone, aluminum stearate, alkyl silane. Such coatings are well known in the art.
  • photostabilizers known to a skilled person in the art encompass e.g. 3,3-diphenylacrylate derivatives such as e.g. octocrylene (PARSOL ® 340) or
  • Polyester-8 (Polycrylene ® ); Benzylidene camphor derivatives such as e.g. 4-methyl benzylidene camphor (PARSOL ® 5000); Benzalmalonate derivatives such as e.g. polysilicones-15 (PARSOL ® SLX) or diethylhexyl syringylidene malonate (Oxynex ST liquid);
  • Benzylidene camphor derivatives such as e.g. 4-methyl benzylidene camphor (PARSOL ® 5000)
  • Benzalmalonate derivatives such as e.g. polysilicones-15 (PARSOL ® SLX) or diethylhexyl syringylidene malonate (Oxynex ST liquid);
  • Dialkyl naphthalates such as diethylhexyl naphthalate (Corapan TQ) without being limited thereto.
  • An overview on further stabilizers is e.g. given in 'SPF Boosters & Photostability of
  • the photostabilizers are generally used in an amount of 0.05 to 10 wt.-% with respect to the total weigh of the topical composition.
  • the amount of each UV-filter substance in the topical compositions according to the invention is selected in the range of about 0.1 to 10 wt.-%, preferably in the range of about 0.2 to 7 wt.-%, most preferably in the range of about 0.5 to 5 wt.-% with respect to the total weigh of the topical composition.
  • the total amount of UVA-filter substance(s), in particular of butyl methoxydibenzoylmethane, in the topical compositions according to the invention is preferable selected in the range of about 2 to 8 wt.-%, in particular in the range of about 4 to 6 wt.-%, most particular in the range of about 3 to 5 wt.-%, such as 4 to 5 wt.-% with respect to the total weight of the topical composition.
  • the total amount of UV-filter substances in the topical compositions according to the invention is preferably in the range of about 1 to 40 wt.-%, preferably in the range of about 5 to 30 wt.-%, in particular in the range of 10 to 30 wt.-%, such as 20 to 30 wt.-% with respect to the total weight of the topical composition.
  • Preferred UVB-filter substances according to the invention encompass polysilicones-15, phenylbenzimidazol sulfonic acid, octocrylene, ethylhexyl methoxycinnamate, ethyl hexylsalicylate and/ or homosalate.
  • Preferred broadband UV-filter substances according to the invention encompass unsymmetrical s-triazine derivatives such 2,4-Bis- ⁇ [4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl ⁇ - 6-(4-methoxyphenyl)-1 ,3,5-triazin, certain benzophenones such as e.g. 2-Hydroxy-4- methoxy-benzophenon, 2,2'-Methylen-bis-(6-(2H-benzotriazol-2-yl)-4-(1 , 1 ,3,3-tetramethyl- butyl)-phenol), and/ or titanium dioxide.
  • unsymmetrical s-triazine derivatives such 2,4-Bis- ⁇ [4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl ⁇ - 6-(4-methoxyphenyl)-1 ,3,5-triazin
  • certain benzophenones such as e.g. 2-Hy
  • the preferred UVA-filter substance according to the invention is butyl methoxydibenzoylmethane.
  • butyl methoxydibenzoylmethane is the only UVA- filter substance in the topical compositions according to the invention.
  • the invention relates to the use of a phosphate ester surfactant selected from cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate for increasing the SPF of a topical composition comprising butyl methoxydibenzoylmethane and at least one UV-filter substance selected from a UVB and/ or broadband-filter substance.
  • the topical composition comprises butyl methoxydibenzoylmethane, polysilicones-15 and phenylbenzimidazol sulfonic acid and at least one further UV-B and/ or broadband filter substances selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • the topical composition comprises at least 4.5 wt.-% butyl methoxydibenzoylmethane, at least 2 wt.-% of polysilicones-15 and at least 2 wt.-% of phenylbenzimidazol sulfonic acid, at least 3.6 wt- % of octocrylene and at least one further UV-B and/ or broadband filter substances selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • photostable, high SPF compositions which comply with the above mentioned UVA standards can be achieved by combining at least 4.5 wt. -% of butyl methoxydibenzoylmethane with at least 2 wt.-% of polysilicones-15 and at least 2 wt.-% phenylbenzimidazol sulfonic in combination with at least one further UVB or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate in the presence of a phosphate ester surfactant.
  • the invention relates to a topical composition
  • a topical composition comprising a phosphate ester surfactant, at least 4.5 wt.-% of butyl methoxydibenzoylmethane, preferably about 4.5 to 6 wt-
  • the topical composition further comprises at least one further UVB and/ or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • the phosphate ester surfactant is cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate and is used in a concentration of about 1 to 3 wt.-%, such as particularly
  • the topical composition further contains at least 3.6 wt.-% of octocrylene.
  • the total amount of the at least one further UVB and/ or broadband filter substance is at least 8 wt.-%, preferably in the range of about 8 to 20 wt.-% and the total amount of UV-filter substances is in the range of about 20 to 30 wt.-% with respect to the total weight of the topical composition.
  • cetyl phosphate 2 to 3 wt. -% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate, 4.5 to 5 wt. -% of butyl methoxydibenzoylmethane,
  • topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • compositions as outlined above comprising
  • cetyl phosphate 2 to 3 wt.-% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
  • topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • photostable, high SPF compositions which comply with the above mentioned UVA standards can also be achieved by combining at least 4 wt.-% of butyl methoxydibenzoylmethane with at least 2 wt.-% of bis- ethylhexyloxyphenol methoxyphenol triazine and at least 2 wt.-% phenylbenzimidazol sulfonic in combination with at least one further UVB or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate in the presence of a phosphate ester surfactant.
  • the invention in another embodiment relates to a topical composition
  • a topical composition comprising a phosphate ester surfactant, at least 4 wt.-% of butyl methoxydibenzoylmethane, preferably about 4 to 6 wt.-%, in particular about 4 wt.-%, at least 2 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, preferably about 2 to 5 wt.-%, in particular about 3 wt.-%, at least 2 wt.-% of phenylbenzimidazol sulfonic, preferably about 2 to 8 wt.-%, in particular about 4 wt.-% in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UVB and/ or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate, ethylhexy
  • the phosphate ester surfactant is cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate and is used in a concentration of about 2 to 3 wt.-% with respect to the total weigh of the topical composition.
  • the topical composition further contains at least 3.6 wt.-% of octocrylene.
  • the total amount of the at least one further UVB and/ or broadband filter substance is at least 8 wt.-%, preferably in the range of about 8 to 20 wt.-% and the total amount of UV-filter substances is in the range of about 20 to 30 wt.-% with respect to the total weight of the topical composition.
  • Particular preferred are topical compositions as outlined above comprising
  • cetyl phosphate 2 to 3 wt. -% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
  • topical composition 3.6 to 10 wt.-% of octocrylene in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate .
  • topical compositions as outlined above comprising 2 to 3 wt.-% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
  • topical composition further at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
  • all topical compositions according to the invention further comprise a co-surfactant in an amount of 1 to 4 wt.-%, in particular about 2 wt.-% in order to further improve the stability of the formulation.
  • the co-surfactant is selected from Lanette O (Cetearyl Alcohol (mixture of C16 and C18 alcohol)), Lanette 16 / Lorol C 16 (Cetyl Alcohol) and/ or Estol 3650 (Glyceryl Myristate).
  • topical composition refers in particular to cosmetic compositions that can be topically applied to mammalian keratinous tissue such as e.g. human skin or hair, particularly human skin.
  • cosmetic composition refers to cosmetic compositions as defined under the heading "Kosmetika” in Rompp Lexikon Chemie, 10th edition 1997, Georg Thieme Verlag Stuttgart, New York as well as to cosmetic preparations as disclosed in A. Domsch, "Cosmetic Preparations”, Verlag fur chemische Industrie (ed. H. Ziolkowsky), 4 th edition, 1992.
  • cosmetically acceptable carrier refers to all carriers and/or excipients and/ or diluents conventionally used in topical preparations
  • the topical preparations according to the present invention are in the form of a suspension or dispersion in solvents or fatty substances, or alternatively in the form of an emulsion or micro emulsion (in particular of O/W-type), PIT-emulsion, multiple emulsion (e. g. O/W/0-type and W/O/W), pickering emulsion, one- or multiphase solution or vesicular dispersion or other usual forms, which can also be applied by pens, as masks or as sprays.
  • the topical preparation is or comprises an emulsion it can also contain one or more anionic, nonionic, cationic or amphoteric surfactant(s).
  • the topical compositions according to the invention are 0/W emulsions.
  • the oil phase of the O/W emulsions according to the invention preferably comprises oils selected from butylenglykoldicaprylatV-dicaprat, dicaprylylether, C 12-15 -Alkylbenzoat,
  • Ci ⁇ -38-fatty acid triglyceride dibutyladipate, cyclomethicone, 2-phenylethylbenzoat, isopropyl lauroyl sarkosinate, diisopropyl sebacate as well as mixtures thereof.
  • the amount of the oil isopropyl lauroyl sarkosinate, diisopropyl sebacate as well as mixtures thereof.
  • (one or several) in the O/W emulsion according to the invention is generally selected in the range of about 0,1 bis 40 wt.-%, in particular in the range of about 1 ,0 to 30 wt.-%, most in particular in the range of about 5% to 20 wt.-% with respect to the total weight of the topical composition.
  • Preferred topical compositions according to the invention are sun care preparations.
  • Topical compositions in accordance with the invention can be in the form of a liquid, lotion, a thickened lotion, a gel, a cream, a milk, an ointment, a paste or a make-up, and can be optionally be packaged as an aerosol and can be provided in the form of a mousse such as a aerosol mousse, a foam or a spray foam, a spray, a stick.
  • a mousse such as a aerosol mousse, a foam or a spray foam, a spray, a stick.
  • the topical compositions according to the invention may optionally be combined with further ingredients such as ingredients for skin lightening; tanning prevention; treatment of hyperpigmentation; preventing or reducing acne, wrinkles, lines, atrophy and/or inflammation; chelators and/or sequestrants; anti-cellulites and slimming (e.g. phytanic acid), firming, moisturizing and energizing, self tanning, soothing, as well as agents to improve elasticity and skin barrier and/or further UV-filter substances and carriers and/or excipients or diluents conventionally used in topical compositions. If nothing else is stated, the excipients, additives, diluents, etc.
  • further ingredients such as ingredients for skin lightening; tanning prevention; treatment of hyperpigmentation; preventing or reducing acne, wrinkles, lines, atrophy and/or inflammation; chelators and/or sequestrants; anti-cellulites and slimming (e.g. phytanic acid), firming, mois
  • cosmetic and dermatological adjuvants and additives can, based on the desired product, easily be determined by the skilled person.
  • the cosmetically active ingredients useful herein can in some instances provide more than one benefit or operate via more than one mode of action.
  • vitamin C ascorbic acid
  • vitamin A and/or its derivatives e.g., retinoid derivatives such as retinyl palmitate or retinyl propionate
  • vitamin E and/or its derivatives e.g., tocopherol acetate
  • vitamin B 6 vitamin B 12
  • biotin, co-enzyme Q10 EGCG
  • hydroxytyrosol and/or olive extract shea butter, algae extract, cocoa butter, aloe extract, jojoba oil, echinacea extract, chamomile extract
  • Glycyrrhetinic Acid Glycyryca Glabra extract, in particular vitamin E and/or its derivatives, shea butter, algae extract, cocoa butter, aloe extract and/ or vitamin A and/or its derivatives.
  • the additional cosmetically active ingredient is typically included in an amount of at least 0.001 wt. % based on the total weight of the topical preparation. Generally, an amount of about 0.001 wt. % to about 30 wt. %, preferably from about 0.001 wt. % to about 10 wt. % of an additional cosmetically active agent is used.
  • a vitamin E derivative for use in the present invention is tocopheryl acetate.
  • Tocopheryl acetate may be present in the topical preparations in an amount from about 0.05 wt.-% to about 25 wt.-%, in particular 0.5 wt.-% to 5 wt.-%.
  • Another vitamin E derivative of interest is tocopheryl linoleate.
  • Tocopheryl linoleate may be present in the skin care composition in an amount from about 0.05 wt.-% to about 25 wt.-% in particular .05 wt.-% to 5 wt.-%.
  • Vitamin A and/or its derivatives in particular retinoid derivatives such as retinyl palmitate or retinyl propionate is preferably used in the topical preparations according to the invention in an amount of 0.01 - 5 wt.-%, in particular 0.01 - 0.3 wt.-%
  • the topical cosmetic compositions of the invention can also contain usual cosmetic adjuvants and additives, such as preservatives/ antioxidants, fatty substances/ oils, water, organic solvents, silicones, thickeners, softeners, emulsifiers, sunscreens, antifoaming agents, moisturizers, aesthetic components such as fragrances, surfactants, fillers, sequestering agents, anionic, cationic, nonionic or amphoteric polymers or mixtures thereof, propellants, acidifying or basifying agents, dyes, colorings/colorants, abrasives, absorbents, essential oils, skin sensates, astringents, antifoaming agents, pigments or nanopigments, e.g.
  • cosmetic adjuvants and additives such as preservatives/ antioxidants, fatty substances/ oils, water, organic solvents, silicones, thickeners, softeners, emulsifiers, sunscreens, antifoaming agents, moisturizers, aesthetic components such as fragrances, surfactants
  • cosmetic ingredients those suited for providing a photoprotective effect by physically blocking out ultraviolet radiation, or any other ingredients usually formulated into cosmetic compositions.
  • Such cosmetic ingredients commonly used in the skin care industry, which are suitable for use in the compositions of the present invention are e.g. described in the CTFA Cosmetic Ingredient Handbook, Second Edition (1992) without being limited thereto.
  • the cosmetic and/ or dermatological compositions according to the invention have a pH in the range of 3-10, preferably in the range of pH of 4-8, most preferred in the range of pH 6- 8.
  • UV-filter substances were incorporated in two different standard cosmetic bases using Potassium Cetyl Phosphate, respectively Polyester-5 & Water & Butylene Glycol & Glycerin as emulsifier.
  • the in vivo SPF was tested according to the Colipa, International Test Method for the in vivo determination of the Sun Protection Factor SPF provided by sunscreen products, guideline 2006. Table 1
  • Procedure for preparation of the formulations Heat part A to 85°C and stir until homogeneous then heat part B to 75°C and add to part A under agitation, then cool down to 55 0 C and add TEA. When everything is homogenous add part C pre-heated to 50 0 C. Be sure that the pH of Phenylbenzimidazole Sulfonic Acid solution is 7.0 (adjusted with TEA). If traces remain, add small quantities of the used neutralizing base until the particles are dissolved. Homogenize thoroughly and then with continued mixing cool down to ambient temperature. It is generally recommended to use vacuum while producing the emulsion.
  • a composition according to the invention with a total amount of UV-filter substances in the range of 20 to 30 wt.-% comprising a phosphate ester surfactant, 4 wt.-% of butyl methoxydibenzoylmethane, 3 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, and 4 wt.-% of phenylbenzimidazol sulfonic acid in combination with further UVB and/ or broadband filter substances realize the criteria of an SPF> 50 while achieving the UVA standards, i.e. EU recommendation and critical wavelength whereas the compositions comprising a non phosphate ester surfactant, i.e. Arlacel 165 (A) with the same UV-filter substance concentrations does not achieve the required in vivo SPF (see formulation 7 & 8).

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

The present invention relates to the use of phosphate ester surfactants for increasing the sun protection factors (SPF's) of topical compositions which comprise at least on UV-filter substance. Furthermore, the invention relates to topical compositions comprising a phosphate ester surfactant and at least 4 wt-% of butyl methoxydibenzoylmethane in combination with further UV-filter substances.

Description

Sunscreens
The present invention relates to the use of phosphate ester surfactants for increasing the sun protection factors (SPF's) of topical compositions which comprise at least one UV-filter substance. Furthermore, the invention relates to topical compositions comprising a phosphate ester surfactant and at least 4 wt-% of butyl methoxydibenzoylmethane in combination with further UV-filter substances.
Sun care products have evolved considerably over the years. Earlier formulations were intended to protect the user from UV-B radiation (UVB) as was once thought that UV-B rays were the most important contributors to wrinkling, skin disease, and skin cancer. However, more recent studies have shown that UV-A radiation (UVA) is equally or even more important in the development of solar damage and skin diseases, such as lupus erythematosus and melanoma and non-melanoma skin cancers. Thus, today's focus is toward eliminating as much of UVA (320-400 nm) and / or UVB (280-320 nm) light as possible. Consequently, there's a constantly increasing need for sun care products exhibiting high SPF's up to 50+ and high UVA protection.
The SPF (Sun Protection Factor) rating system has been developed to provide consumer guidance in selecting sun care products. SPF is measured in the laboratory with a solar simulator that induces UV erythema. However, erythema is primarily caused by UVB, making SPF testing primarily a measurement of UVB - not UVA - protection.
Colipa has developed a method for testing the UVA performance of sun care products that meet the European Commission's Recommendation of 22 September 2006 on the efficacy of sunscreen products. The UVA protection performance according to the invention is determined according to the 'Method for the in vitro determination of UVA protection provided by sunscreen products' (COLIPA Guideline 2007) which is labeled as UVAPF (UVA protection factor).
Many UV-filter substances have been developed in the past protecting against the harmful effect of UVA and / or UV-B radiation and even shorter radiation (UVC). These substances are usually incorporated either alone or in combination with each other into cosmetic or pharmaceutical preparations which are widely known and used.
Due to the increasing demand for high SPF sun care products with a UVA protection complying with the above mentioned standards, more UV-filter substances at elevated levels have to be incorporated into the sun care products; this, however, is not always feasible, as high UV-filter substance concentrations add considerable cost to the formulation and often lead to an unpleasant skin feel and/ or aesthetic appearance.
Furthermore, high sunscreen levels can promote increased irritancy. In order to obtain a UVA protection complying with the above mentioned standards high concentrations of at least one UVA filter substance has to be incorporated into the sun care products. However, not many UVA-filter substances are commercially available and all of them exhibit more or less severe downsides e.g. in view of stability, solubility and/ or suitable absorption profile in order to achieve the recommended UVA protection at a reasonable concentration level. For example, the frequently used butyl methoxydibenzoylmethane is difficult to be formulated in high amounts into sun care products as it often renders the formulation instable and as it is incompatible with many other UV-filter substances. Thus, there is an ongoing need for ingredients which improve the functionality of UV-filter substances in order to achieve higher
SPF at a given concentration of UV-filter substances and furthermore allow the incorporation of high amounts of butyl methoxydibenzoylmethane in order to achieve the recommended UVA protection.
Surprisingly, it has been found that phosphate ester surfactants are able to enhance the in vivo SPF at given UV-filter substance concentrations. This surprising effect helps to overcome the problems of the prior art outlined above. Furthermore it has been found that the incorporation of high levels of butyl methoxydibenzoylmethane is facilitated which makes it possible to achieve the recommended UVA protection at high SPF levels.
The in vivo SPF according to the invention is tested according to the Colipa, International Test Method for the in vivo determination of the Sun Protection Factor SPF provided by sunscreen products, guideline 2006. Thus, the invention relates in one aspect to the use of a phosphate ester surfactant for increasing the SPF of a topical composition comprising at least one UV-filter substance. Preferably, the at least one UV-filter substance is a UVB and/ or broadband-filter substance.
In another aspect the invention relates to the use of a phosphate ester surfactant for increasing the SPF of a topical composition comprising butyl methoxydibenzoylmethane and at least one UV-filter substance selected from a UVB and/ or broadband-filter substance.
Phosphate esters surfactants suitable for incorporation into the compositions of the present invention have the formula
O
Il 2
RO-P-OR
I 1
OR
The phosphate ester surfactant has the general structure wherein R, R1 and R2 may be hydrogen, an alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, or an alkoxylated alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, and having 1 or more, preferably from about 2 to about 25, most preferably 2 to 12, moles ethylene oxide, with the proviso that at least one of R, R1 and R2 is an alkyl or alkoxylated alkyl as previously defined but having at least 6 alkyl carbons in said alkyl or alkoxylated alkyl group. Monoesters in which R1 and R2 are hydrogen and R is selected from alkyls of 10 to 18 carbons and alkoxylated fatty alcohols of 10 to 18 carbons and 2 to 12 moles ethylene oxide are preferred. Among the preferred phosphate ester surfactants, mention may be made of, C8-10 Alkyl Ethyl Phosphate, C9-15 Alkyl Phosphate, Ceteareth-2 Phosphate, Ceteareth-5 Phosphate, Ceteth-8 Phosphate, Ceteth-10 Phosphate, Cetyl Phosphate, C6-10 Pareth-4 Phosphate, C12-15 Pareth-2 Phosphate, C12-15 Pareth-3 Phosphate, DEA-Ceteareth-2 Phosphate, DEA-Cetyl Phosphate, DEA-Oleth-3 Phosphate, Potassium cetyl phosphate, Deceth-4 Phosphate and Deceth-6 Phosphate. Particular preferred phosphate ester surfactants according to the invention are cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate. - A -
The phosphate ester surfactant is generally present in the topical compositions according to the invention in proportions ranging from 0.1 to 5 wt.-%, preferably from 0.5 to 5 wt.-%, most preferably from 1 to 3 wt.-%, such as particularly from 2 to 3 wt.-% with respect to the total weight of the topical composition.
The at least one UV-filter substance is preferably selected from conventional UVA and/or UVB and/ or broad spectrum UV-filter substances known to be added into topical compositions such as cosmetic or dermatological sun care products. Such UV-filter substances comprise all groups which absorb light in the range of wavelengths 400 nm to 320 nm (UVA) and 320 nm to 280 nm (UVB) or of even shorter wavelengths (UVC) and which are or can be used as cosmetically acceptable UV-filter substances. Such UV-filter substances are e.g. listed in the CTFA Cosmetic ingredient Handbook or "The Encyclopedia of Ultraviolet Filters" (ISBN: 978-1-932633-25-2) by Nadim A. Shaath. Suitable UV-filter substances may be organic or inorganic compounds. Exemplary organic UV-filter substances encompass e.g. acrylates such as e.g. 2-ethylhexyl 2-cyano-3,3- diphenylacrylate (octocrylene, PARSOL® 340), ethyl 2-cyano-3,3-diphenylacrylate; Camphor derivatives such as e.g. 4-methyl benzylidene camphor (PARSOL® 5000), 3-benzylidene camphor, camphor benzalkonium methosulfate, polyacrylamidomethyl benzylidene camphor, sulfo benzylidene camphor, sulphomethyl benzylidene camphor, terephthalylidene dicamphor sulfonic acid (Mexoryl® SX); Cinnamate derivatives such as e.g. ethylhexyl methoxycinnamate (PARSOL® MCX), ethoxyethyl methoxycinnamate, isoamyl methoxycinnamate as well as cinnamic acid derivatives bond to siloxanes; p-Aminobenzoic acid derivatives such as e.g. p-aminobenzoic acid, 2-ethylhexyl p-dimethylaminobenzoate, N-oxypropylenated ethyl p-aminobenzoate, glyceryl p-aminobenzoate; Benzophenones such as e.g. benzophenone-3, benzophenone-4, 2,2',4,4'-tetrahydroxy-benzophenone, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone; Esters of benzalmalonic acid such as e.g. di-(2-ethylhexyl) 4-methoxybenzalmalonate; Organosiloxane compounds carrying chromophore groups such as e.g. polysilicones-15 (PARSOL® SLX), drometrizole trisiloxane (Mexoryl® XL); Imidazole derivatives such as e.g. 2-phenyl benzimidazole sulfonic acid (PARSOL®HS) and salts thereof such as e.g. sodium- or potassium salts, ammonium salts, morpholine salts, salts of primary, sec. and tert. amines like monoethanolamine salts, diethanolamine salts; Salicylate derivatives such as e.g. isopropylbenzyl salicylate, benzyl salicylate, butyl salicylate, ethylhexyl salicylate (PARSOL® EHS, Neo Heliopan® OS), isooctyl salicylate or homomenthyl salicylate (homosalate, PARSOL® HMS, Neo Heliopan® HMS); Triazine derivatives such as e.g. ethylhexyl triazone (Uvinul® T-150), diethylhexyl butamido triazone (Uvasorb® HEB), bis- ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb® S); Benzotriazole derivatives such as e.g. 2,2'-methylene-bis-(6-(2H-benzotriazole-2-yl)-4-(1 ,1 ,3,3,-tetramethylbutyl)-phenol (Tinosorb® M); Encapsulated UV-filters such as e.g. encapsulated ethylhexyl methoxycinnamate (Eusolex® UV-pearls) or microcapsules loaded with UV-filters as e.g. dislosed in EP 1471995; Dibenzoylmethane derivatives such as e.g. 4-tert.-butyl-4'- methoxydibenzoyl-methane (PARSOL® 1789), dimethoxydibenzoylmethane, isopropyldibenzoylmethane; Phenylene-1 ,4-bis-benzimidazolsulfonic acids or salts such as e.g. 2,2-(1 ,4-phenylene)bis-(1 H-benzimidazol-4,6-disulfonic acid) (Neoheliopan AP); Amino substituted hydroxybenzophenones such as e.g. 2-(4-diethylamino-2-hydroxy-benzoyl)- benzoic acid hexylester (Aminobenzophenon, Uvinul® A Plus); Benzoxazol-derivatives such as e.g. 2,4-bis-[5-1 (dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino- 1 ,3,5-triazin [Uvasorb® K2A);
Inorganic UV-filter substances encompass pigments such as e.g. microparticulated Zink oxide or Titanium dioxide (e.g. commercially available as PARSOL® TX) The term "microparticulated" refers to a particle size from about 5 nm to about 200 nm, particularly from about 15 nm to about 100 nm. The particles may also be coated by other metal oxides such as e.g. aluminum or zirconium oxides or by organic coatings such as e.g. polyols, methicone, aluminum stearate, alkyl silane. Such coatings are well known in the art.
In order to enhance the photostability of sun care products it may be desirable to add a photostabilizer. Exemplary photostabilizers known to a skilled person in the art encompass e.g. 3,3-diphenylacrylate derivatives such as e.g. octocrylene (PARSOL® 340) or
Polyester-8 (Polycrylene®); Benzylidene camphor derivatives such as e.g. 4-methyl benzylidene camphor (PARSOL® 5000); Benzalmalonate derivatives such as e.g. polysilicones-15 (PARSOL® SLX) or diethylhexyl syringylidene malonate (Oxynex ST liquid);
Dialkyl naphthalates such as diethylhexyl naphthalate (Corapan TQ) without being limited thereto. An overview on further stabilizers is e.g. given in 'SPF Boosters & Photostability of
Ultraviolet Filters', HAPPI, October 2007, p. 77-83 which is included herein by reference. The photostabilizers are generally used in an amount of 0.05 to 10 wt.-% with respect to the total weigh of the topical composition.
Generally, the amount of each UV-filter substance in the topical compositions according to the invention is selected in the range of about 0.1 to 10 wt.-%, preferably in the range of about 0.2 to 7 wt.-%, most preferably in the range of about 0.5 to 5 wt.-% with respect to the total weigh of the topical composition.
The total amount of UVA-filter substance(s), in particular of butyl methoxydibenzoylmethane, in the topical compositions according to the invention is preferable selected in the range of about 2 to 8 wt.-%, in particular in the range of about 4 to 6 wt.-%, most particular in the range of about 3 to 5 wt.-%, such as 4 to 5 wt.-% with respect to the total weight of the topical composition.
The total amount of UV-filter substances in the topical compositions according to the invention is preferably in the range of about 1 to 40 wt.-%, preferably in the range of about 5 to 30 wt.-%, in particular in the range of 10 to 30 wt.-%, such as 20 to 30 wt.-% with respect to the total weight of the topical composition.
Preferred UVB-filter substances according to the invention encompass polysilicones-15, phenylbenzimidazol sulfonic acid, octocrylene, ethylhexyl methoxycinnamate, ethyl hexylsalicylate and/ or homosalate.
Preferred broadband UV-filter substances according to the invention encompass unsymmetrical s-triazine derivatives such 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}- 6-(4-methoxyphenyl)-1 ,3,5-triazin, certain benzophenones such as e.g. 2-Hydroxy-4- methoxy-benzophenon, 2,2'-Methylen-bis-(6-(2H-benzotriazol-2-yl)-4-(1 , 1 ,3,3-tetramethyl- butyl)-phenol), and/ or titanium dioxide.
The preferred UVA-filter substance according to the invention is butyl methoxydibenzoylmethane. Preferably, butyl methoxydibenzoylmethane is the only UVA- filter substance in the topical compositions according to the invention. In a particular embodiment the invention relates to the use of a phosphate ester surfactant selected from cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate for increasing the SPF of a topical composition comprising butyl methoxydibenzoylmethane and at least one UV-filter substance selected from a UVB and/ or broadband-filter substance. Preferably, the topical composition comprises butyl methoxydibenzoylmethane, polysilicones-15 and phenylbenzimidazol sulfonic acid and at least one further UV-B and/ or broadband filter substances selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate. In a most preferred embodiment, the topical composition comprises at least 4.5 wt.-% butyl methoxydibenzoylmethane, at least 2 wt.-% of polysilicones-15 and at least 2 wt.-% of phenylbenzimidazol sulfonic acid, at least 3.6 wt- % of octocrylene and at least one further UV-B and/ or broadband filter substances selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
Surprisingly, it has furthermore been found that photostable, high SPF compositions which comply with the above mentioned UVA standards can be achieved by combining at least 4.5 wt. -% of butyl methoxydibenzoylmethane with at least 2 wt.-% of polysilicones-15 and at least 2 wt.-% phenylbenzimidazol sulfonic in combination with at least one further UVB or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate in the presence of a phosphate ester surfactant.
Thus, in another aspect the invention relates to a topical composition comprising a phosphate ester surfactant, at least 4.5 wt.-% of butyl methoxydibenzoylmethane, preferably about 4.5 to 6 wt-
%, in particular about 5 wt.-%, at least 2 wt.-% of polysilicone-15, preferably about 2 to 10 wt.-%, in particular about 3 wt.-%, at least 2 wt.-% of phenylbenzimidazol sulfonic, preferably about 2 to 8 wt.-%, preferably about 3 to 4 wt.-%, in particular about 4 wt.-% in a cosmetically acceptable carrier. and wherein the topical composition further comprises at least one further UVB and/ or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate. Preferably, the phosphate ester surfactant is cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate and is used in a concentration of about 1 to 3 wt.-%, such as particularly
2 to 3 wt.-% with respect to the total weigh of the topical composition. Preferably, the topical composition further contains at least 3.6 wt.-% of octocrylene. Preferably, the total amount of the at least one further UVB and/ or broadband filter substance is at least 8 wt.-%, preferably in the range of about 8 to 20 wt.-% and the total amount of UV-filter substances is in the range of about 20 to 30 wt.-% with respect to the total weight of the topical composition. Particular preferred are topical compositions as outlined above comprising
2 to 3 wt. -% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate, 4.5 to 5 wt. -% of butyl methoxydibenzoylmethane,
2 to 3 wt.-% of polysilicone-15,
3 to 4 wt.-% of phenylbenzimidazol sulfonic and
3.6 to 10 wt.-% of octocrylene in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
Further preferred are topical compositions as outlined above comprising
2 to 3 wt.-% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
5 wt.-% of butyl methoxydibenzoylmethane, 3 wt.-% of polysilicone-15,
4 wt.-% of phenylbenzimidazol sulfonic and
3.6 to 10 wt.-% of octocrylene in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
Unexpectedly, it has furthermore been found that photostable, high SPF compositions which comply with the above mentioned UVA standards can also be achieved by combining at least 4 wt.-% of butyl methoxydibenzoylmethane with at least 2 wt.-% of bis- ethylhexyloxyphenol methoxyphenol triazine and at least 2 wt.-% phenylbenzimidazol sulfonic in combination with at least one further UVB or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate in the presence of a phosphate ester surfactant. In another embodiment the invention relates to a topical composition comprising a phosphate ester surfactant, at least 4 wt.-% of butyl methoxydibenzoylmethane, preferably about 4 to 6 wt.-%, in particular about 4 wt.-%, at least 2 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, preferably about 2 to 5 wt.-%, in particular about 3 wt.-%, at least 2 wt.-% of phenylbenzimidazol sulfonic, preferably about 2 to 8 wt.-%, in particular about 4 wt.-% in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UVB and/ or broadband filter substance which preferably is selected from octocrylene, titanium dioxide, ethyl hexylsalicylate, ethylhexylmethoxycinnamate and/ or homosalate a cosmetically acceptable carrier. Preferably, the phosphate ester surfactant is cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate and is used in a concentration of about 2 to 3 wt.-% with respect to the total weigh of the topical composition. Preferably, the topical composition further contains at least 3.6 wt.-% of octocrylene.
Preferably, the total amount of the at least one further UVB and/ or broadband filter substance is at least 8 wt.-%, preferably in the range of about 8 to 20 wt.-% and the total amount of UV-filter substances is in the range of about 20 to 30 wt.-% with respect to the total weight of the topical composition. Particular preferred are topical compositions as outlined above comprising
2 to 3 wt. -% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
3 to 5 wt.-% of butyl methoxydibenzoylmethane
2 to 3 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, 3 to 4 wt. -% of phenylbenzimidazol sulfonic and
3.6 to 10 wt.-% of octocrylene in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate . Further preferred are topical compositions as outlined above comprising 2 to 3 wt.-% of cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate,
4 wt.-% of butyl methoxydibenzoylmethane 3 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine,
4 wt.-% of phenylbenzimidazol sulfonic and 3.6 to 10 wt.-% of octocrylene in a cosmetically acceptable carrier and wherein the topical composition further at least one further UV-filter substance selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
In a particular embodiment all topical compositions according to the invention further comprise a co-surfactant in an amount of 1 to 4 wt.-%, in particular about 2 wt.-% in order to further improve the stability of the formulation. Preferably, the co-surfactant is selected from Lanette O (Cetearyl Alcohol (mixture of C16 and C18 alcohol)), Lanette 16 / Lorol C 16 (Cetyl Alcohol) and/ or Estol 3650 (Glyceryl Myristate).
The term "topical composition" as used herein refers in particular to cosmetic compositions that can be topically applied to mammalian keratinous tissue such as e.g. human skin or hair, particularly human skin.
The term "cosmetic composition" as used in the present application refers to cosmetic compositions as defined under the heading "Kosmetika" in Rompp Lexikon Chemie, 10th edition 1997, Georg Thieme Verlag Stuttgart, New York as well as to cosmetic preparations as disclosed in A. Domsch, "Cosmetic Preparations", Verlag fur chemische Industrie (ed. H. Ziolkowsky), 4th edition, 1992.
The term cosmetically acceptable carrier refers to all carriers and/or excipients and/ or diluents conventionally used in topical preparations
Preferably, the topical preparations according to the present invention are in the form of a suspension or dispersion in solvents or fatty substances, or alternatively in the form of an emulsion or micro emulsion (in particular of O/W-type), PIT-emulsion, multiple emulsion (e. g. O/W/0-type and W/O/W), pickering emulsion, one- or multiphase solution or vesicular dispersion or other usual forms, which can also be applied by pens, as masks or as sprays. If the topical preparation is or comprises an emulsion it can also contain one or more anionic, nonionic, cationic or amphoteric surfactant(s). In a particular preferred embodiment, the topical compositions according to the invention are 0/W emulsions.
The oil phase of the O/W emulsions according to the invention preferably comprises oils selected from butylenglykoldicaprylatV-dicaprat, dicaprylylether, C12-15-Alkylbenzoat,
Ciβ-38-fatty acid triglyceride, dibutyladipate, cyclomethicone, 2-phenylethylbenzoat, isopropyl lauroyl sarkosinate, diisopropyl sebacate as well as mixtures thereof. The amount of the oil
(one or several) in the O/W emulsion according to the invention is generally selected in the range of about 0,1 bis 40 wt.-%, in particular in the range of about 1 ,0 to 30 wt.-%, most in particular in the range of about 5% to 20 wt.-% with respect to the total weight of the topical composition.
Preferred topical compositions according to the invention are sun care preparations.
Topical compositions in accordance with the invention can be in the form of a liquid, lotion, a thickened lotion, a gel, a cream, a milk, an ointment, a paste or a make-up, and can be optionally be packaged as an aerosol and can be provided in the form of a mousse such as a aerosol mousse, a foam or a spray foam, a spray, a stick.
In accordance with the present invention, the topical compositions according to the invention may optionally be combined with further ingredients such as ingredients for skin lightening; tanning prevention; treatment of hyperpigmentation; preventing or reducing acne, wrinkles, lines, atrophy and/or inflammation; chelators and/or sequestrants; anti-cellulites and slimming (e.g. phytanic acid), firming, moisturizing and energizing, self tanning, soothing, as well as agents to improve elasticity and skin barrier and/or further UV-filter substances and carriers and/or excipients or diluents conventionally used in topical compositions. If nothing else is stated, the excipients, additives, diluents, etc. mentioned in the following are suitable for topical preparations according to the present invention. The necessary amounts of the cosmetic and dermatological adjuvants and additives can, based on the desired product, easily be determined by the skilled person. The cosmetically active ingredients useful herein can in some instances provide more than one benefit or operate via more than one mode of action.
Preferred examples of further ingredients are vitamin C (ascorbic acid) and/or its derivatives (e.g. ascorbyl phosphate such as Stay C (sodium ascorbyl monophosphate) from DSM Nutritional Products Ltd.), vitamin A and/or its derivatives (e.g., retinoid derivatives such as retinyl palmitate or retinyl propionate), vitamin E and/or its derivatives (e.g., tocopherol acetate), vitamin B6, vitamin B12, biotin, co-enzyme Q10, EGCG, hydroxytyrosol and/or olive extract, shea butter, algae extract, cocoa butter, aloe extract, jojoba oil, echinacea extract, chamomile extract, Glycyrrhetinic Acid, Glycyryca Glabra extract, in particular vitamin E and/or its derivatives, shea butter, algae extract, cocoa butter, aloe extract and/ or vitamin A and/or its derivatives. The additional cosmetically active ingredient is typically included in an amount of at least 0.001 wt. % based on the total weight of the topical preparation. Generally, an amount of about 0.001 wt. % to about 30 wt. %, preferably from about 0.001 wt. % to about 10 wt. % of an additional cosmetically active agent is used.
A vitamin E derivative for use in the present invention is tocopheryl acetate. Tocopheryl acetate may be present in the topical preparations in an amount from about 0.05 wt.-% to about 25 wt.-%, in particular 0.5 wt.-% to 5 wt.-%. Another vitamin E derivative of interest is tocopheryl linoleate. Tocopheryl linoleate may be present in the skin care composition in an amount from about 0.05 wt.-% to about 25 wt.-% in particular .05 wt.-% to 5 wt.-%.
Vitamin A and/or its derivatives in particular retinoid derivatives such as retinyl palmitate or retinyl propionate is preferably used in the topical preparations according to the invention in an amount of 0.01 - 5 wt.-%, in particular 0.01 - 0.3 wt.-%
The topical cosmetic compositions of the invention can also contain usual cosmetic adjuvants and additives, such as preservatives/ antioxidants, fatty substances/ oils, water, organic solvents, silicones, thickeners, softeners, emulsifiers, sunscreens, antifoaming agents, moisturizers, aesthetic components such as fragrances, surfactants, fillers, sequestering agents, anionic, cationic, nonionic or amphoteric polymers or mixtures thereof, propellants, acidifying or basifying agents, dyes, colorings/colorants, abrasives, absorbents, essential oils, skin sensates, astringents, antifoaming agents, pigments or nanopigments, e.g. those suited for providing a photoprotective effect by physically blocking out ultraviolet radiation, or any other ingredients usually formulated into cosmetic compositions. Such cosmetic ingredients commonly used in the skin care industry, which are suitable for use in the compositions of the present invention are e.g. described in the CTFA Cosmetic Ingredient Handbook, Second Edition (1992) without being limited thereto.
The necessary amounts of the cosmetic and dermatological adjuvants and additives can - based on the desired product - easily be chosen by a skilled person in this field and will be illustrated in the examples, without being limited hereto.
Of course, one skilled in this art will take care to select the above mentioned optional additional compound or compounds and/or their amounts such that the advantageous properties intrinsically associated with the combination in accordance with the invention are not, or not substantially, detrimentally affected by the envisaged addition or additions.
The cosmetic and/ or dermatological compositions according to the invention have a pH in the range of 3-10, preferably in the range of pH of 4-8, most preferred in the range of pH 6- 8.
The following examples are provided to further illustrate the compositions and effects of the present invention. These examples are illustrative only and are not intended to limit the scope of the invention in any way.
Example 1
The same UV-filter substances were incorporated in two different standard cosmetic bases using Potassium Cetyl Phosphate, respectively Polyester-5 & Water & Butylene Glycol & Glycerin as emulsifier. The in vivo SPF was tested according to the Colipa, International Test Method for the in vivo determination of the Sun Protection Factor SPF provided by sunscreen products, guideline 2006. Table 1
Figure imgf000015_0001
As can bee seen from table 1 the incorporation of a defined amount of UV-filter substances in a standard potassium cetyl phosphate formulation resulted in a significantly higher in vivo SPF compared to the same UV-filter combination in a standard Polyester-5 & Water & Butylene Glycol & Glycerin formulation.
Example 2
Various UV-filter combinations have been incorporated into a cosmetic base as outlined in table 2 using Potassium Cetyl Phosphate (Amphisol K) or Glyceryl Stearate & PEG-100 Stearate (Arlacel 165) as emulsifier. The use of Potassium Cetyl Phosphate significantly increased the in vivo SPF of the formulations.
Table 2:
Figure imgf000015_0002
Figure imgf000016_0001
Figure imgf000017_0001
selected from Behenyl Alcohol, Cetyl Alcohol or Cetearyl Alcohol
2) Phenoxyethanol & Methylparaben & Ethylparaben & Butylparaben & Propylparaben & lsobutylparaben
3) selected from Disodium EDTA or Pentasodium Ethylenediamine Tetramethylene Phosphonate
EU recommendation fulfilled
Procedure for preparation of the formulations: Heat part A to 85°C and stir until homogeneous then heat part B to 75°C and add to part A under agitation, then cool down to 55 0C and add TEA. When everything is homogenous add part C pre-heated to 500C. Be sure that the pH of Phenylbenzimidazole Sulfonic Acid solution is 7.0 (adjusted with TEA). If traces remain, add small quantities of the used neutralizing base until the particles are dissolved. Homogenize thoroughly and then with continued mixing cool down to ambient temperature. It is generally recommended to use vacuum while producing the emulsion.
As can bee seen from table 2, a composition according to the invention with a total amount of UV-filter substances in the range of 20 to 30 wt.-% comprising a phosphate ester surfactant, 5 wt.-% of butyl methoxydibenzoylmethane, 3 wt.-% of polysilicone-15, and 4 wt. -% of phenylbenzimidazol sulfonic acid in combination with further UVB and/ or broadband filter substances and realize the criteria of an SPF> 50 while achieving the UVA standards, i.e. EU recommendation and critical wavelength whereas the compositions comprising a non phosphate ester surfactant, i.e. Arlacel 165 (A) with the same UV-filter substance concentrations does not achieve the required in vivo SPF (see Formulations 1-4)
As can bee seen from table 2, a composition according to the invention with a total amount of UV-filter substances in the range of 20 to 30 wt.-% comprising a phosphate ester surfactant, 4 wt.-% of butyl methoxydibenzoylmethane, 3 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, and 4 wt.-% of phenylbenzimidazol sulfonic acid in combination with further UVB and/ or broadband filter substances realize the criteria of an SPF> 50 while achieving the UVA standards, i.e. EU recommendation and critical wavelength whereas the compositions comprising a non phosphate ester surfactant, i.e. Arlacel 165 (A) with the same UV-filter substance concentrations does not achieve the required in vivo SPF (see formulation 7 & 8).

Claims

Claims
1. Use of a phosphate ester surfactant for increasing the SPF of a topical composition comprising at least one UV-filter substance.
2. Use according to claim 1, characterized in that the topical composition comprises from 0.1 to 5 wt.-% of a phosphate ester surfactant.
3. Use according to claim 1 or 2, characterized in that the topical composition comprises from 1 to 3 wt.-% of a phosphate ester surfactant.
4. Use according to any one of claims 1 to 3, characterized in that the phosphate ester surfactant is selected from cetyl phosphate, potassium cetyl phosphate and/ or DEA cetyl phosphate.
5. Use according to any one of claims 1 to 4, characterized in that the topical composition comprises butyl methoxydibenzoylmethane, polysilicone-15 and phenylbenzimidazol sulfonic acid and at least one further UV-B and/ or broadband filter substances selected from octocrylene, titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
6. Use according to any one of claims 1 to 5, characterized in that the topical composition comprises at least one co -surfactant selected from cetearyl alcohol (mixture of C16 and C18 alcohol), Cetyl Alcohol and/ or Glyceryl Myristate.
7. Topical composition comprising a phosphate ester surfactant, at least 4.5 wt.-% of butyl methoxydibenzoylmethane at least 2 wt.-% of polysilicone-15, at least 2 wt.-% of phenylbenzimidazol sulfonic in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UVB and/ or broadband filter substance.
8. Topical composition comprising a phosphate ester surfactant, at least 4 wt.-% of butyl methoxydibenzoylmethane, at least 2 wt.-% of bis-ethylhexyloxyphenol methoxyphenol triazine, at least 2 wt.-% of phenylbenzimidazol sulfonic in a cosmetically acceptable carrier and wherein the topical composition further comprises at least one further UVB and/ or broadband filter substance.
9. Topical composition according to claim 7 or 8, characterized in that the topical composition further contains at least 3.6 wt.-% of octocrylene.
10. Topical composition according to any one of claims 7 to 9, characterized in that the further UVB and/ or broadband filter substance is selected from titanium dioxide, ethyl hexylsalicylate and/ or homosalate.
11. Topical composition according to any one of claims 7 to 10, characterized in that the total amount of the further UVB and/ or broadband filter substance is in the range of
8 to 20 wt. -% with respect to the total weight of the topical composition.
12. Topical composition according to any one of claims 7 to 11 , further comprising at least 1 wt. -% of cetearyl alcohol (mixture of C16 and C18 alcohol), Cetyl Alcohol and/ or Glyceryl Myristate.
PCT/EP2009/055902 2008-05-16 2009-05-15 Sunscreens WO2009138485A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US12/991,300 US20110052516A1 (en) 2008-05-16 2009-05-15 Sunscreens
EP09745817A EP2274057A1 (en) 2008-05-16 2009-05-15 Sunscreens
AU2009248015A AU2009248015A1 (en) 2008-05-16 2009-05-15 Sunscreens
BRPI0911849A BRPI0911849A2 (en) 2008-05-16 2009-05-15 sunscreens
CN2009801177241A CN102026683A (en) 2008-05-16 2009-05-15 Sunscreens
JP2011508934A JP2011520842A (en) 2008-05-16 2009-05-15 Sunscreen agent

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08009080 2008-05-16
EP08009080.6 2008-05-16

Publications (1)

Publication Number Publication Date
WO2009138485A1 true WO2009138485A1 (en) 2009-11-19

Family

ID=40933214

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2009/055902 WO2009138485A1 (en) 2008-05-16 2009-05-15 Sunscreens

Country Status (8)

Country Link
US (1) US20110052516A1 (en)
EP (1) EP2274057A1 (en)
JP (1) JP2011520842A (en)
KR (1) KR20110014148A (en)
CN (1) CN102026683A (en)
AU (1) AU2009248015A1 (en)
BR (1) BRPI0911849A2 (en)
WO (1) WO2009138485A1 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010127987A3 (en) * 2009-05-04 2011-03-31 Dsm Ip Assets B.V. Sunscreens comprising a phosphate ester surfactant
EP2630990A3 (en) * 2012-01-04 2013-09-18 Beiersdorf AG Lightweight, waterproof cosmetic preparation
WO2012062755A3 (en) * 2010-11-11 2013-12-05 Dsm Ip Assets B.V. Cosmetic or dermatological emulsions
WO2014004170A3 (en) * 2012-06-28 2014-09-25 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004171A3 (en) * 2012-06-28 2014-10-02 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004173A3 (en) * 2012-06-28 2014-10-09 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004172A3 (en) * 2012-06-28 2014-10-09 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2016142026A1 (en) * 2015-03-06 2016-09-15 Merck Patent Gmbh Fluorine surfactants in emulsions
WO2016173927A1 (en) * 2015-04-29 2016-11-03 Dsm Ip Assets B.V. Topical sunscreen emulsions
US9592190B2 (en) 2012-06-28 2017-03-14 Johnson & Johnson Consumer Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
JP2021516679A (en) * 2018-03-20 2021-07-08 ディーエスエム アイピー アセッツ ビー.ブイ.Dsm Ip Assets B.V. Topical composition

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2201927A3 (en) 2008-12-29 2013-05-22 Henkel AG & Co. KGaA Sun screen compounds
BR112012031957A2 (en) 2010-06-17 2016-08-23 Galaxy Surfactants Ltd broad spectrum sunscreen composition comprising cinnamidoalkyl amine 2-hydroxy sulfobetaine
EP2934430B1 (en) * 2012-12-19 2019-11-06 L'Oréal Sunscreen compositions having synergistic combination of uv filters
US9132074B2 (en) 2012-12-19 2015-09-15 L'oreal Sunscreen compositions having synergistic combination of UV filters
CN105358123B (en) * 2013-07-08 2018-11-13 帝斯曼知识产权资产管理有限公司 Including UV lightscreening agents, with the UV shielding compositions of the functionalized organopolysiloxane of UV absorbents and porous silica and/or poly methyl methacrylate particle
KR102413187B1 (en) * 2015-03-11 2022-06-27 주식회사 엘지생활건강 UV block cosmetic composition containing anionic surfactant and polymeric surfactant
US9572759B2 (en) 2015-06-25 2017-02-21 L'oreal Sunscreen compositions having synergistic combination of UV filters
US9539194B1 (en) 2015-06-25 2017-01-10 L'oreal Sunscreen compositions having synergistic combination of UV filters
US9539195B1 (en) 2015-06-25 2017-01-10 L'oreal Sunscreen compositions having synergistic combination of UV filters

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01143823A (en) * 1987-11-30 1989-06-06 Kanebo Ltd Anti-sunburn cosmetic
WO2003020233A2 (en) * 2001-08-29 2003-03-13 Beiersdorf Ag Stabilisation of uv-sensitive active ingredients
EP1449516A1 (en) * 2003-02-21 2004-08-25 Beiersdorf AG Cosmetic and dermatological emulsions comprising phosphoric acid esters
US20070264216A1 (en) * 2006-05-11 2007-11-15 Mcentire Edward Enns Water resistant sunscreen formulas with sulfopolyesters and phosphate ester surfactants
WO2009079486A1 (en) * 2007-12-18 2009-06-25 Schering-Plough Healthcare Products, Inc. Enhanced photostability of avobenzone in the presence of zinc oxide using phosphate-based emulsifiers

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01143823A (en) * 1987-11-30 1989-06-06 Kanebo Ltd Anti-sunburn cosmetic
WO2003020233A2 (en) * 2001-08-29 2003-03-13 Beiersdorf Ag Stabilisation of uv-sensitive active ingredients
EP1449516A1 (en) * 2003-02-21 2004-08-25 Beiersdorf AG Cosmetic and dermatological emulsions comprising phosphoric acid esters
US20070264216A1 (en) * 2006-05-11 2007-11-15 Mcentire Edward Enns Water resistant sunscreen formulas with sulfopolyesters and phosphate ester surfactants
WO2009079486A1 (en) * 2007-12-18 2009-06-25 Schering-Plough Healthcare Products, Inc. Enhanced photostability of avobenzone in the presence of zinc oxide using phosphate-based emulsifiers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 198928, Derwent World Patents Index; AN 1989-204074, XP002542921 *

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010127987A3 (en) * 2009-05-04 2011-03-31 Dsm Ip Assets B.V. Sunscreens comprising a phosphate ester surfactant
WO2012062755A3 (en) * 2010-11-11 2013-12-05 Dsm Ip Assets B.V. Cosmetic or dermatological emulsions
EP2630990A3 (en) * 2012-01-04 2013-09-18 Beiersdorf AG Lightweight, waterproof cosmetic preparation
WO2014004172A3 (en) * 2012-06-28 2014-10-09 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004171A3 (en) * 2012-06-28 2014-10-02 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004173A3 (en) * 2012-06-28 2014-10-09 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2014004170A3 (en) * 2012-06-28 2014-09-25 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
CN104427966A (en) * 2012-06-28 2015-03-18 强生消费者公司 Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
US9592190B2 (en) 2012-06-28 2017-03-14 Johnson & Johnson Consumer Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2016142026A1 (en) * 2015-03-06 2016-09-15 Merck Patent Gmbh Fluorine surfactants in emulsions
WO2016173927A1 (en) * 2015-04-29 2016-11-03 Dsm Ip Assets B.V. Topical sunscreen emulsions
US10709649B2 (en) 2015-04-29 2020-07-14 Dsm Ip Assets B.V. Topical sunscreen emulsions
JP2021516679A (en) * 2018-03-20 2021-07-08 ディーエスエム アイピー アセッツ ビー.ブイ.Dsm Ip Assets B.V. Topical composition
JP7413637B2 (en) 2018-03-20 2024-01-16 ディーエスエム アイピー アセッツ ビー.ブイ. topical composition
US11992544B2 (en) 2018-03-20 2024-05-28 Dsm Ip Assets B.V. Topical composition

Also Published As

Publication number Publication date
AU2009248015A1 (en) 2009-11-19
EP2274057A1 (en) 2011-01-19
BRPI0911849A2 (en) 2015-10-06
US20110052516A1 (en) 2011-03-03
KR20110014148A (en) 2011-02-10
CN102026683A (en) 2011-04-20
JP2011520842A (en) 2011-07-21

Similar Documents

Publication Publication Date Title
US20110052516A1 (en) Sunscreens
JP5787415B2 (en) 2-Phenyl-1,2,3-benzotriazole for UV absorption
ES2672990T3 (en) Topical compositions
WO2012062755A2 (en) Cosmetic or dermatological emulsions
WO2010127987A2 (en) Sunscreens
KR101639457B1 (en) Cosmetic composition comprising pentasodium (ethylenediamine) tetramethylenephosphonate
US20140219942A1 (en) Sunscreens
EP2276454B1 (en) Sunscreen compositions
EP3442495B1 (en) 10-hydroxystearic acid compositions
US10786453B2 (en) 10-hydroxystearic acid compositions

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980117724.1

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09745817

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2009745817

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2009248015

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2011508934

Country of ref document: JP

ENP Entry into the national phase

Ref document number: 2009248015

Country of ref document: AU

Date of ref document: 20090515

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 20107025209

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: PI0911849

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20101028