AU2017264375B2 - A cosmetic composition - Google Patents

A cosmetic composition Download PDF

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AU2017264375B2
AU2017264375B2 AU2017264375A AU2017264375A AU2017264375B2 AU 2017264375 B2 AU2017264375 B2 AU 2017264375B2 AU 2017264375 A AU2017264375 A AU 2017264375A AU 2017264375 A AU2017264375 A AU 2017264375A AU 2017264375 B2 AU2017264375 B2 AU 2017264375B2
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composition
polymer
film forming
hydrophobically modified
modified silica
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AU2017264375A1 (en
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Naresh Dhirajlal Ghatlia
Yan Wu
Qiqing Zhang
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Unilever Global IP Ltd
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    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25Silicon; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/064Water-in-oil emulsions, e.g. Water-in-silicone emulsions
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/29Titanium; Compounds thereof
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/896Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q13/00Formulations or additives for perfume preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants

Abstract

The present invention relates to cosmetic compositions formulated at low pH like those comprising antiperspirant actives for providing long lasting perfume impact to the skin surface. It is achieved by including perfumery molecule and a film forming polymer in a base emulsion comprising hydrophobically modified silica, aminofunctional silicone and water.

Description

A COSMETIC COMPOSITION
Field of the invention
The present invention is in the field of cosmetic compositions, in particular compositions comprising antiperspirant actives. The present invention more particularly relates to providing enhanced and long lasting perfumery impact to the skin surface in addition to the anti-perspirancy benefits.
Background of the invention
The present invention relates to cosmetic compositions, which are formulated at low pH in the range of 2 to 6. One class of such compositions are those that contain antiperspirant actives. These actives are added to compositions to reduce perspiration on application to the surface of the body, particularly to the underarm regions of the human body. Antiperspirant actives are typically astringent metal salts such as aluminium or zirconium salts. Such salts are incorporated in compositions at low pH in the range of 2 to 6. It has been found that in addition to looking for good anti-perspirancy benefits especially in the underarm region, consumers also seek to have enhanced and long lasting perfume impact from such surfaces. Usually these benefits are delivered through what are known as deodourant compositions. Yet, there is a need to provide compositions that in addition to anti-perspirancy also deliver enhanced positive odour impact, after the composition is applied to the skin.
The present inventors have now developed a composition in which such low pH antiperspirant actives can be incorporated along with perfumery molecules and these can be delivered in a composition comprising an emulsion comprising hydrophobically modified silica, amino-functionalised silicone and water by the incorporation of a film forming polymer of select classes.
The present applicants have disclosed mild emulsions comprising hydrophobically modified silica, amino-functionalised silicone and water which has been published as WO2013064367. In other co-pending applications, they have disclosed various other
2017264375 20 May 2019 uses of this emulsion. But so far it has not been disclosed that this emulsion can be used to incorporate low pH actives like anti-perspirancy actives along with perfumery compounds which at this low pH exhibit enhanced and long lasting positive odour impact through incorporation of film forming polymers.
It is thus an object of the present invention to provide for a low pH cosmetic composition where the perfumery impact is delivered over a long period of time.
Summary of the invention
According to the first aspect of the present invention there is provided a cosmetic composition comprising an emulsion comprising (i) hydrophobically modified silica;
(ii) amino functionalized silicone; and (iii) water;
the cosmetic composition further comprising (iv) a perfumery molecule;
(v) a film forming polymer selected from an acrylate polymer, a methacrylate polymer, a urethane polymer, aliphatic polyurethane resin, silicone resin, polyquaternium or co-polymers thereof;
wherein the pH of the composition at 25 °C is from 2 to 6.
It is particularly preferred that the pH of the composition is from 2 to 4.
According to another aspect of the present invention there is provided a method of 25 delivering long lasting perfumery impact from a cosmetic composition comprising the step of topically applying to the skin the composition of the first aspect.
According to another aspect there is provided a cosmetic composition for delivering low pH compositions to the axilla of an individual for anti-perspirancy and deodourancy 30 benefits comprising an emulsion comprising hydrophobically modified silica; amino functionalized silicone; and water; the cosmetic composition further comprising a perfumery molecule; a film forming polymer selected from an acrylate polymer, a methacrylate polymer, a urethane polymer, aliphatic polyurethane resin, silicone resin,
2017264375 20 May 2019
2A polyquaternium or co-polymers thereof wherein the film forming polymer is distinct from water soluble polymers like cross-linked polyacrylic acid polymers sold as Carbopol®; wherein the pH of the composition at 25 °C is from 2 to 6 and wherein said composition further comprises an antiperspirant skin care active selected from aluminium chlorohydrate, aluminum-zirconium tetrachlorohydrex glycine complex, aluminumzirconium octachlorohydrex glycine complex, aluminum-zirconium pentachlorohydrate, aluminum sesquichlorohydrate or mixtures thereof.
Detailed description of the invention
These and other aspects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. For the avoidance of doubt, any feature of one aspect of the present invention may be utilized in any other aspect of the invention. The word “comprising” is
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PCT/EP2017/059591 intended to mean “including” but not necessarily “consisting of” or “composed of.” In other words, the listed steps or options need not be exhaustive. It is noted that the examples given in the description below are intended to clarify the invention and are not intended to limit the invention to those examples per se. Similarly, all percentages are weight/weight percentages unless otherwise indicated. Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description and claims indicating amounts of material or conditions of reaction, physical properties of materials and/or use are to be understood as modified by the word “about”. Numerical ranges expressed in the format from x to y are understood to include x and y. When for a specific feature multiple preferred ranges are described in the format from x to y, it is understood that all ranges combining the different endpoints are also contemplated.
By “A Cosmetic Composition” as used herein, is meant to include a composition for topical application to the skin of mammals, especially humans. Such a composition is preferably of the leave-on type. By a leave-on composition is meant a composition that is applied to the desired skin surface and left on for a period of time (say from one minute to 24 hours) after which it may be wiped or rinsed off with water, usually during the regular course of personal washing. The composition may also be formulated into a product which is applied to a human body for improving the appearance, cleansing, odor control or general aesthetics. The composition of the present invention can be in the form of a liquid, lotion, cream, foam, scrub, gel or stick form and may be delivered through a rollon device or using a propellant containing aerosol can. It is especially useful for delivering low pH compositions to the axilla of an individual for anti-perspirancy and deodourancy benefits. “Skin” as used herein is meant to include skin on any part of the body (e.g., neck, chest, back, arms, underarms, hands, legs, buttocks and scalp) especially the underarms.
The cosmetic composition of the invention is delivered through an emulsion comprising hydrophobically modified silica, amino functionalized silicone; and water. The cosmetic composition further comprises a perfumery molecule, a film forming polymer selected from an acrylate polymer, a methacrylate polymer, a urethane polymer, aliphatic
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PCT/EP2017/059591 polyurethane resin, silicone resin, polyquaternium or co-polymers thereof. The pH of the composition at 25°C is from 2 to 6. The pH is preferably from 2 to 4.
Hydrophobicallv Modified silica
The only limitation with respect to the type of hydrophobically modified silica that may be used in this invention is that the same is suitable for use in an antiperspirant composition by consumers at a pH from 2 to 6.
In a preferred embodiment, the hydrophobically modified silica comprises at least one of the following groups:
- O - Si (CH3)3 ch3 *--Si----0--*
CH3 (I) (II)
---O---- Si----R
--------(III) in which R is a C4 to Cw alkyl group.
or
Figure AU2017264375B2_D0001
The hydrophobically modified silica most preferably comprises (IV)
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PCT/EP2017/059591
Figure AU2017264375B2_D0002
wherein R is a C4 to Cw alkyl group, more preferably a CsHw alkyl group.
Such silicas are described in US 7 282 236 and made commercially available from suppliers like Evonik Degussa GmbH under the names Aerosil R805, R972, R202, R812, R104, R816 and R711. Preferably, the silica particles comprise the group represented by formula III. More preferably, the silica particles comprise octylsilane (sold under the name Aerosil R805, Aerosil R974, Aerosil R202, Aerosil R805, Aerosil R812from Evonik; HDK H113L, HDK H15, HDK H20, HDK H30 for Wacker.
The hydrophobically modified silica according to the present invention can be of different sizes and shapes. Particle size, as used herein, refers to particle diameter unless otherwise stated. Diameter is meant to mean the largest measurable distance on a particle in the event a well-defined sphere is not generated. Particle size can be measured, for example, by dynamic light scattering (DLS) or transmission electron microscope (TEM). The volume average primary particle size of hydrophobically modified silica is often from 1 nm to 100 nm, more preferably from 5 nm to 70 nm, most preferably from 5 nm to 20 nm, including all ranges subsumed therein.
Typically, the antiperspirant composition of the present invention comprises from 0.05 to 20% by weight of the hydrophobically modified silica, more preferably from 0.05 to 15%, further more preferably from 0.1 to 10%, most preferably from 0.2 to 5% based on the total weight of the antiperspirant composition and including all ranges subsumed therein.
Amino Functionalized Silicone
The cosmetic composition of this invention comprises an amino functionalized silicone. By “amino functionalized silicone” is meant a silicone containing at least one primary, secondary or tertiary amine group, or a quaternary ammonium group.
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The primary, secondary, tertiary and/or quaternary amine groups may either form part of the main polymer chain or more preferably be carried by a side or pendant group carried by the polymeric backbone. Such polymers are described, for example, in US 4 185 087.
In a preferred embodiment, the amino functionalized silicone has the general formula: R1 R2 R1
Figure AU2017264375B2_D0003
NR (C(R)2)x
N(r)2 (V) where:
each R is independently H, OH, OCH3 or C1-4 alkyl;
each R1 is independently OR, or a C1-4 alkyl;
each R2 is independently OR, or a C1-4 alkyl; and each x is independently an integer from 1 to 4 and each y is greater than zero and independently an integer to yield a polymer having a molecular weight from 500 to 1 million, and preferably, from 750 to 25,000, and most preferably from 1,000 to 15,000.
Other amino functionalized silicone suitable to use includes silicone cationic polymers represented by the formula:
R2aZ3.a-Si(OSiZ2)n-(OSiZbR22.b)m-O-SiZ3.a-R2a (VI) where:
Z is hydrogen, phenyl, OH or a C1-C10 alkyl group;
each a is independently an integer from 0 to 3;
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PCT/EP2017/059591 b is an integer from 0 to 1; and m and n are integers whereby the sum of n+m ranges from 1 to 3,500, and preferably from 10 to 160;
each R2 is independently a monovalent radical of formula -CqH2qL where each q is independently a number from 2 to 10 and L is an amine or a quaternized amine represented by one of the following groups:
-NR3-CH2-CH2-N(R3)2
-N(R3)2
-N®(R3)3A-N(R3)-CH2-CH2-N+R3(H)2A-, where:
each R3 is independently hydrogen, phenyl, benzyl or a Ci to Ci2 alkyl; and each A- is independently fluoride, chloride, bromide or iodide anion.
Still other amino functionalized silicone suitable for use includes those having the formula:
(R4)3—Si
Figure AU2017264375B2_D0004
where:
each R4 is independently a Ci to C2o alkyl or C2 to C2o alkenyl; R5 is a divalent Ci-Cw group;
A' is as previously defined;
r is an integer from 2 to 20; and s is an integer from 15 to 75.
Preferably, the amino functionalized silicone has the INCI designation amodimethicone.
More preferably, the amodimethicone is represented by formula (V) and made commercially available, for example, as DC 8500 by Dow Corning. It is also within the
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PCT/EP2017/059591 scope of this invention for the amino functionalized silicone to comprise trimethylsilylamodimethicone represented by formula (VI).
Typically, the cosmetic composition of the present invention comprises amino functionalized silicone in an amount from 0.01 to 25%, more preferably from 0.03 to 15%, more preferably still from 0.05 to 10%, most preferably from 0.1 to 5% by total weight of the composition and including all ranges subsumed therein.
Preferably the weight ratio of hydrophobically modified silica to amino functionalized silicone is from 10:1 to 1:3, more preferably from 5:1 to 1:3 and most preferably from 2:1 to 1:2..
Typically, the cosmetic composition of the invention comprises an emulsion. Generally the water content is from 10 to 80%, more preferably from 15 to 70%, most preferably from 20 to 60% based on the total weight of the cosmetic composition and including all ranges subsumed therein.
Perfumery molecule
The cosmetic composition of the invention comprises a perfumery molecule which may be included in the composition as a fragrance.
The term fragrance is defined as a mixture of odoriferous components, optionally mixed with a suitable solvent diluent or carrier, which is employed to impart a desired odor. A perfumery molecule or a group of perfumery molecules formulated as a perfume is generally incorporated in most personal care compositions. Any perfumery molecule which is cosmetically acceptable may be included in the composition of the invention.
Fragrance components and mixtures thereof may be obtained from natural products such as essential oils, absolutes, resinoids, resins and concretes, as well as synthetic products such as hydrocarbons, alcohols, aldehydes, ketones, ethers, carboxylic acids, esters, acetals, ketals, nitriles and the like, including saturated and unsaturated compounds, aliphatic, carbocyclic and heterocyclic compounds.
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Suitable characteristics of fragrances can include one or more of lavender, violet, rose, jasmin, pine, woody, floral, fruity, lemon, lime, apple, peach, raspberry, strawberry, banana, plum, apricot, vanilla, pear, eucalyptus, aromatic, aldehydic, tutti frutti, oriental, sweet, amber, Paola, Muguet, Citronella (lime), and the like. Typical fragrance components which may be are one or more of: 2-methoxy naphthalene; allyl cyclohexane propionate; alpha-citronellal; alpha-ionone; alpha- santalol; alphaterpineol; ambrettolide; amyl benzoate; amyl cinnamate; amyl cinnamic aldehyde; aurantiol; benzaldehyde; benzophenone; benzyl acetate; benzyl salicylate; betacaryophyllene; beta-methyl naphthyl ketone; cadinene; cavacrol; cedrol; cedryl acetate; cedryl formate; cinnamyl cinnamate; cis-jasmone; coumarin; cyclamen aldehyde; cyclohexyl salicylate; d-limonene; delta-nonalactone; delta-undecalactone; dihydro isojasmonate; dihydro mycenol; dimethyl acetal; diphenyl methane; diphenyl oxide; dodecalactone; ethyl methyl phenyl glycidate; ethyl undecylenate; ethylene brassylate; eugenol; exaltolide; galaxolide; gamma-n-methyl ionone; gamma-undecalactone; geranial; geranyl acetate; geranyl anthranilate; geranyl phenyl acetate; hexadecanolide; hexenyl salicylate; hexyl cinnamic aldehyde; hexyl salicylate; hydroxycitronellal; indole; iso E super; iso-amyl salicylate; iso-bornyl acetate; iso-butyl quinoline; iso- eugenol; laevo-carvone; lilial (p-t-bucinal); linalool; linalyl acetate; linalyl benzoate; methyl cinnamate; methyl dihydrojasmonate; methyl-N-methyl anthranilate; musk indanone; musk ketone; musk tibetine; myristicin; nerol; oxahexadecanolide-10; oxahexadecanolide-11 ; para-cymene; para-tert-butyl cyclohexyl acetate;; patchouli alcohol; phantolide; phenyl ethyl alcohol; phenyl ethyl benzoate; phenyl heptanol; phenylhexanol; phexylethylphenylacetate; thibetolide; vanillin; vertenex; vetiveryl acetate; yara-yara; and ylangene.
Suitable solvents, diluents or carriers for perfumes as mentioned above are, for example, ethanol, isopropanol, diethylene glycol monoethyl ether, dipropyl glycol, triethyl citrate and the like.
Highly preferred fragrance components used in cosmetic compositions are cyclic and acyclic terpenes and terpenoids. These materials are based upon isoprene repeating
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PCT/EP2017/059591 units. Examples include alpha and beta pinene, myrcene, geranyl alcohol and acetate, camphene, dl-limonene, alpha and beta phellandrene, tricyclene, terpinolene, allocimmane, geraniol, nerol, linanool, dihydrolinanool, citral, ionone, methyl ionone, citronellol, citronellal, alpha terpineol, beta terpineol, alpha fenchol, borneol, isoborneol, camphor, terpinen- 1-ol, terpin-4-ol, dihydroterpineol, methyl chavicol, anethole, 1 ,4and 1 ,8-cineole, geranyl nitrile, isobornyl acetate, linalyl acetate, caryophyllene, alpha cedrene, guaiol, patchouli alcohol, alpha and beta santalol and mixtures thereof. As per the present invention, the perfumery molecule is preferably selected from a compound having an aldehyde, an alcohol, or an ester functional group or combinations thereof. Amounts of the fragrance may range from 0.0001 to 5%, usually from 0.001 to 1.5%, more usually from 0.5 to 0.8% by weight of the personal care composition.
The cosmetic composition of the invention comprises a film forming polymer selected from an acrylate polymer, a methacrylate polymer, a urethane polymer, aliphatic polyurethane resin, silicone resin, polyquaternium or co-polymers thereof.
“Film-forming polymer” as used herein refers to a polymer which is capable of forming a cohesive and continuous covering over the hair and/or skin when applied to the surface. Contact angle, as used herein, means the angle at which a water/vapor interface meets a solid surface at a temperature of 25°C. Such an angle may be measured with a goniometer or other water droplet shape analysis systems with water droplet of 5 pl and at 25°C. The requirement for film-forming polymer, as per the present invention is that the film-forming polymer is suitable to be employed in cosmetic composition. The filmforming polymer, for use in the present invention, preferably has a contact angle of at least 85°. The film forming polymer is generally water insoluble and is distinct from water soluble polymers like cross-linked polyacrylic acid polymers sold as Carbopol which are commonly used in cosmetic product as thickeners. The skilled person knows what is meant by the water-insolubility of a polymer. Preferably, the solubility of the polymer in water at 25 °C is less than 1 wt%, more preferably less than 0.5 wt%, even more preferably less than 0.1 wt% and most preferably less than 0.01 wt%. Especially preferred film forming polymers are acrylate co-polymer, silicone resin and a urethaneacrylic co-polymer. Commercially available film forming polymers which may be used in
WO 2017/194292
PCT/EP2017/059591 the present invention are KOBO-50N, KOBO-HPRC, KOBO-5400 available from Kobo; Dow-UPU-1 from Dow, lnduchem-U6, lnduchem-U15, lnduchem-U1946 from Induchem; PIB 1000 from Evonik and MQ-1640 from Dow Corning. The film forming polymer is preferably included in 0.5-10%, more preferably 0.5 to 8%, even further more preferably 1-6%, most preferably 2-6% by weight of the composition.
Not wishing to be bound by theory, the inventors believe the oil in water emulsion formed by the combination of the hydrophobic silica and the amino functionalized silicone with water in combination with the acidic condition in water continuous phase will prevent the film forming polymer to form a film directly on the skin surface. Rather, it is believed that the film forming can be better dispersed in the silicone oil which can be stable in the very acidic condition. Thus, the film forming polymer in the silicone oil phase can form a better film on the skin surface ensuring that the fragrance molecules are held for a longer time even at very acidic conditions and ensure enhanced resistance to rinsing with water.
Antiperspirant Skin Care Active
The cosmetic composition of the invention works in the pH range of 2 to 6. Typically the benefits of the present invention can be utilized when the composition comprises an antiperspirant skin care active which are generally acidic substances. Typically, the antiperspirant actives which could be used herein are astringent active salts including aluminium, zirconium and mixed aluminium/zirconium salts. Such salts include both inorganic salts and salts with organic anions and complexes. Preferably, the antiperspirant actives are aluminium, zirconium and aluminium/zirconium halides and halohydrate salts, such as chlorohydrates and activated aluminium chlorohydrates.
Aluminium halohydrates are usually defined by the general formula Al2(OH)xQy*wH2O in which Q represents chlorine, bromine or iodine, x is variable from 2 to 5 and x+y=6 while WH2O represents a variable amount of hydration.
Zirconium actives can usually be represented by the empirical general formula: ZrO(OH)2n-nzBz-wH20 in which z is a variable in the range of from 0.9 to 2.0 so that the value 2n-nz is zero or positive, n is the valency of B, and B is selected from the group consisting of chloride, other halide, sulfamate, sulfate and mixtures thereof. Possible
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PCT/EP2017/059591 hydration to a variable extent is represented by whkO. In one embodiment B represents chloride and the variable z lies in the range from 1.5 to 1.87. In practice, such zirconium salts are usually not employed by themselves, but as a component of a combined aluminium and zirconium-based antiperspirant.
The above aluminium and zirconium salts may have coordinated and/or bound water in various quantities and/or may be present as polymeric species, mixtures or complexes. In particular, zirconium hydroxy salts often represent a range of salts having various amounts of the hydroxy group. Aluminium zirconium chlorohydrate may be particularly preferred.
Antiperspirant complexes based on the above-mentioned astringent aluminium and/or zirconium salts can be employed. The complex often employs a compound with a carboxylate group, and advantageously this is an amino acid. Examples of suitable amino acids include dl-tryptophan, dl-3-phenylalanine, dl-valine, dl-methionine and βalanine, and preferably glycine which has the formula CH2(NH2)COOH.
It is highly desirable to employ complexes of a combination of aluminium halohydrates and zirconium chlorohydrates together with amino acids such as glycine, examples of which are disclosed in U.S. Pat. No. 3,792,068 (Luedders et al).
Certain of those Al/Zr complexes are commonly called AZG in the literature. AZG actives generally contain aluminium, zirconium and chloride with an Al/Zr ratio in a range from 2 to 10, especially 2 to 6, an AI/CI ratio from 2.1 to 0.9 and a variable amount of glycine. Actives of this type are available from suppliers that include Summit Reheis. In one preferred embodiment the active is enhanced activity or activated aluminium/zirconium halohydrate, in particular, activated aluminium-zirconium tetrachlorohydrex glycine (AAZG).
Other actives which may be utilized include astringent titanium salts, for example those described in GB 2299506A.
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The antiperspirant skin care active is preferably selected from aluminium chlorohydrate, aluminum-zirconium tetrachlorohydrex glycine complex, aluminum-zirconium octachlorohydrex glycine complex, aluminum-zirconium pentachlorohydrate, aluminum sesquichlorohydrate or mixtures thereof. More preferred antiperspirant actives are aluminum-zirconium tetrachlorohydrex glycine complex, aluminum-zirconium octachlorohydrex glycine complex, aluminum-zirconium pentachlorohydrate, aluminum sesquichlorohydrate or mixtures thereof. Most preferred is aluminum sesquichlorohydrate.
Preferably, the antiperspirant active comprises water soluble calcium salt, such as calcium chloride. It is particularly preferred that the antiperspirant active comprises water soluble calcium salt. Further preferably the antiperspirant active comprises an amino acid, such as glycine. It is especially preferred that the antiperspirant active is heated with the water soluble calcium salt and preferably amino acid prior to or during formulation of the antiperspirant composition. In this way, the antiperspirant active may become ‘activated’, that is to say, have higher antiperspirant efficacy.
When calcium-containing/activated antiperspirant actives are employed, it is preferred that the molar ratio of calcium to aluminium is at least 1:20, more preferably at least 1:15 and most preferably at least 1:10. In combination with each of these preferences, when an amino acid such as glycine is also included, it is preferred that the molar ratio of amino acid to aluminium is at least 1:20 and more preferably at least 1:10.
When calcium-containing/activated antiperspirant actives are employed, particularly at any of the preferred molar ratios of calcium to aluminium referred to in the above paragraph and especially at any of both the preferred molar ratios of calcium to aluminium and the preferred molar ratios of amino acid to aluminium referred to in the above paragraph, it is preferred that the antiperspirant active comprises an aluminium sesquichlorohydrate salt of formula AI2OH4.4CI1.6 to AI2OH4.9CI1.1 and more preferably of formula AI2OH4.7CI1.3 to AI2OH4.9CI1.1. Such actives are particularly suited to use in the compositions of the present invention.
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Typically, the composition comprises antiperspirant active in an amount from 0.1 to 40%, more preferably from 1 to 30%, most preferably from 5 to 20% by total weight of the antiperspirant composition and including all ranges subsumed therein.
Typically, the antiperspirant active is dissolved in the water present in the composition giving an aqueous solution of the antiperspirant active.
It is also possible to provide enhanced skin lightening for an extended period of time by incorporating an optical particle, preferably a whitening particle, in the cosmetic composition of the invention. The optical particle is preferably one of a polymer bead or an inorganic particle with a refractive index higher than 1.8. When a polymer bead is included, it is preferably a hollow sphere. Suitable hollow spheres are those made of a styrene/ acrylate co-polymer, polyurethane, or polyethylene most preferably a styrene/ acrylate co-polymer. Polymer beads which may be included in the composition of the invention preferably have a particle size in the range of 80 to 700 nm. Commercially available hollow sphere polymer beads which may be used in the composition of the invention are Sunspheres™ (from Dow Chemicals). Alternatively and preferably the optical particles are inorganic particles with a refractive index higher than 1.8, preferably higher than 2.0, more preferably higher than 2.5. Preferred inorganic particles as per the invention are titanium dioxide, zinc oxide, boron nitride, iron oxide, mica, mica coated with titanium dioxide or mixtures thereof, more preferred being titanium dioxide, zinc oxide, boron nitride or mixtures thereof. Most preferred inorganic particle is titanium dioxide. The optical particles for inclusion in the composition of the invention preferably have a mean particle size from 15 nm to 30 micron, preferably 15 nm to 1 micron, more preferably 80 to 400 nm. Commercially available titanium dioxide are available as Korons1171 from Korons and KowetTiO 203975 from Sensient, MT700Z from Tayca; and JTTO MS-7 from KOBO. The optical particle is preferably included in 0.1 to 20%, more preferably 0.2 to 10%, further more preferably 0.5 to 8% by weight of the composition.
Preferably the composition is substantially free of surfactants. Substantially free of, as used herein, means less than 1.5%, and preferably less than 1.0%, and more preferably less than 0.75% and more preferably still less than 0.5%, and even more preferably less
WO 2017/194292
PCT/EP2017/059591 than 0.1% and most preferably from 0.0 to 0.01% by weight, based on total weight of the cosmetic composition, including all ranges subsumed therein.
The composition of the present invention can comprise a wide range of other optional components. The CTFA Personal care Ingredient Handbook, Second Edition, 1992, which is incorporated by reference herein in its entirety, describes a wide variety of nonlimiting personal care and pharmaceutical ingredients commonly used in the skin care industry, which are suitable for use in the compositions of the present invention. Examples include: antioxidants, binders, biological additives, buffering agents, colorants, optical particles, thickeners, polymers, astringents, conditioners, exfoliating agents, pH adjusters, preservatives, natural extracts, essential oils, skin sensates, skin soothing agents, and skin healing agents.
The cosmetic compositions of the present invention when comprising anti-perspirant actives are particularly suitable for dispensing from cosmetic roll-on dispensers that involve a container with a roll-on ball on a dispensing end.
A cosmetic composition of the invention preferably has a viscosity at 25 °C of from 1000 to 200000 cps, preferably 3000 to 60000 cps. The above viscosity is as measured using the following procedure.
DV-II+ PRO Digital Viscometer (from Brookfield Ltd) was used to measure the viscosities of the samples at a consistent shear rate of 10 rpm. The values were measured after one minute at a temperature of 25 °C were used.
The invention further provides for a method of delivering long lasting perfumery impact from a cosmetic composition comprising the step of topically applying to the skin the composition of the invention. The skin surface may thereafter be rinsed with water 10 minutes to 24 hours after the step of applying the composition.
The invention will now be demonstrated with the help of the following non-limiting examples.
WO 2017/194292
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Examples
The following antiperspirant base composition as per the invention (BASE 1) was prepared
Ingredients, wt% Chemical name/details Wt%
Silica Aerosil R805 Hydrophobic silica 1.00
Dow Corning 8500 Amino silicone 0.9
DC-245 Cyclopentasiloxane 18.10
ACH 50% solution of aluminium chlorohydrate 30.00
Sunflower seed oil Sunflower seed oil 4.00
Glycerol Glycerol 4.00
Water Water To 100
Example A-E, 1-3:
Various compositions were prepared using BASE 1 as shown in table 1 below. The 10 compositions were tested for perfumery impact 0, 7, and 24 hours after application of the composition on a vitro skin substrate using the following protocol.
milligram of sample was applied on to 9 cm2 area of bio-skin (from IMS testing Group) evenly by rubbing it for 20 seconds. The samples was left at ambient temperature (25 15 °C) for 24 hours. The samples were measured for perfume impact at various time points and the % of perfume relative to that at 0 time is shown in Table 1 for at 0, 7 and 24 hours. The % of perfume remaining on the sample was extracted using 10 ml acetone under ultrasonication for 5 minutes. The perfumery molecule was quantified by GC-MS.
WO 2017/194292
PCT/EP2017/059591
Table 1
Ingredients A 1 B 2 C 3
Perfumery molecule Hexyl cinnamic aldehyde Hexyl cinnamic aldehyde Bangalol Bangalol Octano I Octanol
Perfumery molecule, wt% 6.7 6.7 6.7 6.7 6.7 6.7
MQ1640, wt% - 1.00 - 1.00 - 1.00
BASE 1, wt% To 100 To 100 To 100 To 100 To 100 To 100
% perfume residue, 0 hr 100 100 100 100 100 100
% perfume residue, 7 hr 67.0 ±5.0 77.8±6.4 24.1±2.8 30.7 ±2.6 27.9±2.0 39.2 ±2.6
% perfume residue, 24 hr 33.1± 1.6 44.3 ± 3.8 3.8 ±0.4 7.2± 0.8 24.1±1.0 34.6±3.1
MQ1640 is a film forming polymer of the silicone resin class sourced from Dow Corning.
The data in Table 1 indicates that the perfume impact for compositions of the invention having the film forming polymer (Examples 1 to 3) provides for enhanced perfume impact at 7 and 24 hours compared to compositions without film forming polymer (Examples A to C).
WO 2017/194292
PCT/EP2017/059591
Examples 4, D to F
The following conventional base composition (BASE 2) was prepared:
Ingredients, wt% Chemical name/details Wt%
Brij 78 Steareth 20 0.6
Brij 72 Steareth 2 2.6
ACH 50% solution of aluminium chlorohydrate 30.00
Sunflower seed oil Sunflower seed oil 4.00
Glycerol Glycerol 4.00
Water Water To 100
Various compositions were prepared using BASE 1 or BASE 2 as shown in table 2 below using bioskin samples similar to the Examples 1 to 3.
Table 2
Ingredients D 4 E F
Perfume, wt% 1.00 1.00 1.00 1.00
MQ1640, wt% - 1.00 - 1.00
BASE BASE1 BASE 1 BASE 2 BASE 2
BASE, wt% To 100 To 100 To 100 To 100
The compositions were tested for perfumery impact after the end of a certain number of 10 hours by a panel of 10 people to give an opinion as to the sample where the perfume impact was better.
The compositions D and 4 were compared for perfumery impact by a panel of 10 persons at the end of 48 hours of storage who graded the samples to give an opinion as to which sample had a higher perfume impact. The data is summarized in Table 3 below:
2017264375 20 May 2019
Table-3
Opinion Sample No. of persons
Higher perfume impact 4 7
Higher perfume impact D 0
uncertain 3
The data in Table 3 above indicates that seven out of ten people preferred the composition as per the invention for perfume impact while three were uncertain.
The compositions E and F were tested for perfumery impact by a panel of 10 persons at the end of 72 hours of storage who graded the samples to give an opinion as to which sample had a higher perfume impact. The data is summarized in Table 4 below:
Table - 4
Opinion Sample No. of persons
Higher perfume impact E 6
Higher perfume impact F 2
uncertain 2
The data in Table 4 above indicates that inclusion of film forming polymer in a conventional base (BASE 2) does not provide enhanced perfume impact.
The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as, an acknowledgement or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.

Claims (14)

  1. The claims defining the invention are as follows:
    1. A cosmetic composition for delivering low pH compositions to the axilla of an individual for anti-perspirancy and deodourancy benefits comprising an emulsion comprising (i) hydrophobically modified silica;
    (ii) amino functionalized silicone; and (Hi) water;
    the cosmetic composition further comprising (iv) a perfumery molecule;
    (v) a film forming polymer selected from an acrylate polymer, a methacrylate polymer, a urethane polymer, aliphatic polyurethane resin, silicone resin, polyquaternium or co-polymers thereof wherein the film forming polymer is distinct from water soluble polymers like cross-linked polyacrylic acid polymers sold as Carbopol®;
    wherein the pH of the composition at 25 °C is from 2 to 6 and wherein said composition further comprises an antiperspirant skin care active selected from aluminium chlorohydrate, aluminum-zirconium tetrachlorohydrex glycine complex, aluminum-zirconium octachlorohydrex glycine complex, aluminumzirconium pentachlorohydrate, aluminum sesquichlorohydrate or mixtures thereof.
  2. 2. A composition as claimed in claim 1 wherein the pH is from 2 to 4.
  3. 3. A composition as claimed in any one of the preceding claims wherein the hydrophobically modified silica comprises \
    O—Si---R oz wherein R is a C4 to Cw alkyl group, or CsHv alkyl group.
    2017264375 20 May 2019
  4. 4. A composition as claimed in any one of the preceding claims wherein the hydrophobically modified silica has a primary particle size from 1 nm to 100 nm, or from 5 nm to 70 nm.
  5. 5. A composition as claimed in any one of the preceding claims wherein the hydrophobically modified silica is present in 0.05 to 20 % by weight of the total composition.
  6. 6. A composition as claimed in any one of the preceding claims wherein the aminofunctionalised silicone is amodimethicone.
  7. 7. A composition as claimed in any one of the preceding claims comprising amino functionalized silicone from 0.01 to 25% by weight of the total composition.
  8. 8. A composition as claimed in any one of preceding claims wherein the weight ratio of hydrophobically modified silica to amino functionalized silicone is from 10:1 to 1:3.
  9. 9. A composition as claimed in any one of the preceding claims wherein the perfumery molecule is selected from a compound having an aldehyde, an alcohol, or an ester functional group or combinations thereof.
  10. 10. A composition as claimed in any one of the preceding claims where in the film forming polymer is an acrylate co-polymer, silicone resin, or a urethane-acrylic co-polymer.
  11. 11. A composition as claimed in any one of the preceding claims where in the film forming polymer is present in 0.5 to 10% by weight of the composition.
  12. 12. A composition as claimed in any one of the preceding claims comprising 0.1 to 40% anti-perspirant active by weight of the composition.
  13. 13. A method of delivering long lasting perfumery impact from a cosmetic composition comprising the step of topically applying to the skin the composition as claimed in any one of the preceding claims.
    2017264375 20 May 2019
  14. 14. A method as claimed in claim 13 wherein the skin is rinsed with water 10 minutes to
    24 hours after the step of applying the composition.
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WO2018237218A1 (en) 2017-06-23 2018-12-27 The Procter & Gamble Company Composition and method for improving the appearance of skin
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WO2020094489A1 (en) * 2018-11-08 2020-05-14 Unilever Plc Antiperspirant compositions comprising fragrance
WO2020094490A1 (en) * 2018-11-08 2020-05-14 Unilever Plc Antiperspirant compositions and methods
CN115843238A (en) 2020-06-01 2023-03-24 宝洁公司 Method for improving penetration of vitamin b3 compounds into the skin
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US4185087A (en) 1977-12-28 1980-01-22 Union Carbide Corporation Hair conditioning compositions containing dialkylamino hydroxy organosilicon compounds and their derivatives
GB2299506B (en) 1995-04-03 1999-04-14 Unilever Plc Antiperspirant actives and compositions
GB2357497A (en) 1999-12-22 2001-06-27 Degussa Hydrophobic silica
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