DESCRIPTION
A COSMETIC PRODUCT AND METHOD OF APPLYING A MASCARA COMPOSITION
TECHNICAL FIELD
The present invention relates to a cosmetic product including a mascara composition and an eyelash heating device, whereby the mascara composition is applied to the eyelashes by fluidizing the mascara composition via heat generated by the eyelash heating device. The product provides improved performance of a mascara composition, while also being safe for the general consumer to use. The present invention further relates to a method of applying a mascara composition to the eyelashes.
BACKGROUND ART
Mascara products are used to enhance the beauty of a person's eyes by coating the eyelashes to primarily thicken, lengthen, color, and define the individual eyelashes. For the last 60 years, mascara products have been provided in the form of mascara applicators having an applicator brush attached to a handle, the applicator brush portion dipped in a package, such as a tube, containing a liquid to semi-solid mascara composition. Mascara compositions typically take the form of emulsions or dispersions of waxes and pigments in water or other volatile carriers. Mascara composition and delivery systems are limited by emulsion or solution chemistry and film forming technologies that are applied wet and then dried to create a film of mascara that sets and holds the
eyelashes.
These mascara compositions which are liquid to semi-solid have a low viscosity profile and low yield point, such that they are inherently prone to smearing and smudging after application to the eyelashes. The solid components dispersed in the composition, such as waxes, may also be difficult to apply, as clumping and globbing may occur due to lack of film smoothness of the solid components.
From another aspect, solvents and carriers of the composition that do not evaporate in timely manner may also provide smearing and smudging after application to the eyelashes. The so-called waterproof mascaras intend to solve such problem by employing volatile hydrocarbon solvents. While such volatile hydrocarbon solvents provide wear benefits, the application and beauty benefits may be compromised. Further, the volatile hydrocarbon solvents may cause odor and safety concerns.
One solution for providing a mascara composition having improved application and improved wearability, is to provide the composition solid, wherein the composition is heated prior to application to the eyelashes, for softening, and/or smoothing the composition upon application. Such heating would also benefit in shortening the evaporation time required after application. The solid film provided on the eyelashes after application would have a much higher yield point than films made by conventional mascara compositions, thereby being less prone to smearing and smudging. Based on the foregoing, there is a need for a mascara product which can apply a solid mascara composition to the eyelashes in a safe and effective manner.
Meanwhile, there have been proposed in the art eyelash curling devices,
such as WO 99/22782 including a applicator brush and heater combination. However, the applicator brush is designed to curl the eyelashes by application of heat, while applying the mascara composition of liquid or semi-liquid condition fetched from a container. Due to the absence of the idea and structure for heating and fluidizing the solid mascara composition, the applicator brush is practically impossible to use in combination with the mascara composition proposed by the present invention. There is a need of providing a dedicated heating device which takes the full benefit of the mascara composition to apply the fluidized composition successfully and uniformly to the eyelashes.
None of the existing art provides all of the advantages and benefits of the present invention.
DISCLOSURE OF THE INVENTION
The present cosmetic product comprises a mascara composition and an eyelash heating device, whereby the mascara composition is applied to the eyelashes by softening the mascara composition via heat, the applied mascara composition forms a solid film on the eyelashes, which film has improved wearability. The product provides improved performance of a mascara composition, while also being safe for the general consumer to use.
The mascara composition is solid at room temperature, however is softened at elevated temperature, so it may be applied to the eyelashes. The eyelash heating device comprises a heater for providing enough heat to the mascara composition, yet safe for application to the eyelashes, even in accidental situations where the user inadvertently touches the device with the eyelids or eyeballs. The eyelash heating device comprises an applicator for receiving,
heating (softening), and applying the mascara composition.
Once the softened mascara composition is applied to the eyelashes, the mascara composition is quickly cooled and thus solidified by the atmosphere. The mascara composition thus applied to the eyelashes provide a firm film covering the eyelashes, which is not softened at body temperature, and thus provides enhanced wearability.
In particular, the mascara composition of the present invention fulfills the above performances by incorporation of a solid hydrophobic component which gives a unique rhelogical profile to the composition. The rheological profile of the composition is defined in terms of a needle penetration as measured according to ASTM (American Society for Testing and Material) Test Method D5, a yield stress, and a viscosity. The mascara composition of the present is prepared to have the needle penetration of from about 1 to about 40, the yield stress of at least about 1500 Pa at 25 °C, and the viscosity of between about 1 mPas and about 10,000,000 mPas at 100 0C. The mascara composition with the above rheological profile can be therefore applied to the eyelashes by being softened via heat and is then solidified on the eyelashes to provide a firm film on the eyelashes.
The mascara composition may be prepared in the form of an oil mixture in which the solid hydrophobic component forms an oil phase. The composition may be alternatively in the form of a water-in-oil emulsion additionally including water and an emulsifier.
Further, the composition may be added with a pigment and/or a film forming polymer for enhanced aesthetic appeal and wearability.
The device of the present invention is specifically designed to give a
structure that is configured to soften the mascara composition and to hold the softened mascara composition for applying it to the eyelashes uniformly. The device includes an applicator equipped with a heater for softening the mascara composition, and a comb arranged along the length of the applicator. The comb is arranged along the length of the applicator to be coated with the softened mascara composition. Whereby the softened mascara composition can be successfully delivered to the eyelashes from the entire length of the comb, leaving the solid mascara film on the eyelashes.
These and other features, aspects, and advantages of the present invention will become evident to those skilled in the art from a reading of the present disclosure with the appended claims.
BRIEF DESCRIPTION OF THE DRAWINGS
While the specification concludes with claims particularly pointing out and distinctly claiming the invention, it is believed that the present invention will be better understood from the following description of preferred, nonlimiting embodiments and representations taken in conjunction with the accompanying drawings in which:
FIG. 1 is a perspective view of an eyelash heating device in accordance with a preferred embodiment of the present invention; FIG. 2 is a top view of the eyelash heating device; FIG. 3 is front view of the device; FIG. 4 is a sectional view of the device;
FIG. 5 is a perspective view of an applicator utilized in the device; FIG. 6 is a top view of the applicator;
FIG. 7 is a sectional view of the applicator;
FIG. 8 is a sectional view of the applicator illustrating how a mascara composition is loaded to the applicator; and
FIGS. 9 to 11 are views explaining how to apply the mascara composition while curling the eyelashes with the use of the device.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
While the description concludes with claims particularly pointing out and distinctly claiming the invention, it is believed that the present invention will be better understood from the following description.
A product in accordance with the present invention is a combination of a mascara composition and an eyelash heating device. Heating Device
Now referring to FIGS. 1 to 4, the eyelash heating device of the present invention is explained in detail. The device includes an elongated hand grip 10 carrying at its one longitudinal end an applicator 20 for applying a softened or fluidized mascara composition to user's eyelashes. The applicator 20 is elongated to have a length generally aligned with a length of the grip 10, and includes a heat radiator 40 and a center comb 30 configured to comb the eyelashes. The heat radiator 40 is provided to heat the mascara composition for softening the composition after it is loaded to the applicator 20 on one hand, and to heat the eyelashes for curling on the other hand. The heat radiator 40 as well as the comb 30 are both arranged to extend over the substantially the full length of the applicator 20.
As shown in FIG. 7, the applicator 20 has a base 22 made of a dielectric
plastic material that carries an electric heater 50 as a heat source for the heat radiator 40, in addition to the center comb 30 and the heat radiator 40. The electric heater 50 is composed of a resister coil 52 wound around a U-shaped core 54 of dielectric material to give two parallel rows running in the length of the applicator 20. The coil 52 is electrically connected to a voltage source, i.e., a battery 12 accommodated within the grip 10 through a switch so as to be energized by manipulating a switch handle 14 on the side of the grip 10.
The heat radiator 40 is shaped from a single metal sheet, for example, a stainless steel to have two parallel rows of continuous heating strip 42 which are joined at the tip of the applicator 20, forming a U-shaped horizontal configuration in match with the heater 50. The rows of the heating strip 42 are exposed on the surface of the applicator 20 to extend along the length of the applicator 20 so as to be capable of being held in direct contact with the eyelashes for curling the eyelashes. Also, the rows of the continuous heating strip 42 define a loading site where the solid mascara composition is loaded on the heat radiator 40. Thus, the mascara composition can be supplied along the entire length of the heating strip 42, i.e., the applicator 20, for example, by squeezing it out of a tube 70 containing the solid mascara composition while moving a point of supply along the length of the applicator 20, as shown in FIG. 8. Alternatively, the solid mascara composition may be prepared in the form of a stick dimensioned to extend the length of the heating strip 42. Since the heating strip 42 extends continuously over the length of the applicator 20, the mascara composition can be supplied over the entire length of the applicator 20, irrespective of the manner of loading the mascara composition.
The rows of the heating strip 42 are spaced in a width direction of the
applicator 20 to define therebetween a trough 44 which runs over the length of the applicator 20 for holding the softened mascara composition, as shown in FIG. 8. In detail, the metal sheet is bent to form a U-shaped vertical section, as shown in FIG. 7, composed of a rounded top defining the heating strip 42 and legs 43 depending from opposite sides of the rounded top. It is within a space left between the legs of the U-shaped vertical section that the electric heater 50 is received in contact with or in closely adjacent relation to the heat radiator 40 for thermal conduction to the heating strip 42 and the trough 44. Thus, the whole applicator 20 can be made into a low-profile structure, yet providing a large heating capacity. The heat radiator 40 thus configured is assembled to the base 22 with the bottom of the trough 44 seated on top of the base 22. The center comb 30 is held at the width center of the applicator 20 with its root 32 received within the bottom of the trough 44 in such a manner as to project comb teeth 34 above the heating strip 42. It is noted that the root 32 does not interfere the continuity of the trough 44 along its length so that the softened mascara composition is held over the length of the trough 44. Thus, once the mascara composition is supplied over the length of the heating strip 42 and is heated thereat, the softened composition can spread into the trough 44, thereby coating the root of the center comb 30. With this result, the softened composition is allowed to climb-up to the comb 30 by the action of a surface tension to be ready for being delivered to the eyelashes as the comb 30 combs the eyelashes. For smooth flow of the softened composition into the trough 44, the heating strip 42 is inclined or rounded down to the trough 44. Some of the softened composition remains on the heating strip 42 to be delivered directly to the eyelashes when the eyelashes come into contact with the heating strip 42.
Also included in the applicator 20 are arrays of side comb 60 arranged along the opposite width ends of the applicator 20 in a closely adjacent relation to the rows of the heating strip 42. The side comb 60 is integrated in one unit which is secured to the base 22 by engagement of hooks 63 into side grooves 23 of the base 22. The side comb 60 has its top end bent over a portion of the adjacent heating strip 42 for smoothing the eyelashes in combination with the center comb 30. The root of the side comb 60 shields the opposite sides of the heat radiator 40 against the contact with the user's face around the eyes.
In operation, the applicator 20 is firstly placed in a position with the comb 30 just below the eyelashes, as shown in FIG. 9. Then, the applicator 20 is raised and twisted to some extent for smoothing the eyelashes with the center comb 30 carrying the softened mascara composition, as shown in FIG. 10, thereby applying the fluidizing mascara composition to the eyelashes, while lifting the eyelashes. In this condition, the heating strip 40 comes into contact with the eyelashes for heating and curling the eyelashes. As soon as the applicator 20 is moved away from the eyelashes, as shown in FIG. 11 * the softened mascara composition is cooled quickly to give a firm film of the solidified mascara composition on the eyelashes. Thus, the above single operation can give the effect of forming the mascara film as well as curling the eyelashes. When the eyelashes are first coming into contact with the heating strip 42, the side comb 60 smoothes the eyelashes in advance of the center comb 30 to ensure uniform application of the mascara composition to the previously smoothed eyelashes. Also when the eyelashes are leaving from the heating strip 42, the side comb 60 comes to again smooth the wetted eyelashes for assuring a stylish mascara treated finish.
The heater 50 is controlled to heat the heating strip 42 to a temperature of about 50 °C to 100 0C for softening the mascara composition. At the elevated temperature, the softened mascara composition exhibits a viscosity of between about 1 mPas and about 10,000,000 mPas, sufficient for coating the eyelashes, but being kept from flowing out of the applicator 20 for assuring a safe application of the mascara composition. Mascara Composition
All percentages, parts and ratios are based upon the total weight of the compositions of the present invention, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore do not include carriers or by-products that may be included in commercially available materials.
All ingredients such as actives and other ingredients useful herein may be categorized or described by their cosmetic and/or therapeutic benefit or their postulated mode of action. However, it is to be understood that the active and other ingredients useful herein can, in some instances, provide more than one cosmetic and/or therapeutic benefit or operate via more than one mode of action. Therefore, classifications herein are made for the sake of convenience and are not intended to limit an ingredient to the particularly stated application or applications listed.
The mascara composition of the present invention is solid at room temperature, namely 25QC, and is softened with elevated temperature such that it can be applied to the eyelashes. By "solid" herein for describing the mascara composition, what is meant is that the composition has a certain hardness to retain its structure, and also that the composition is stable against stress or shear.
The present composition has a needle penetration, as measured according to the American Standard prescribed by the American Society for Testing and Materials (ASTM) Test Method D5, of from about 1 to about 40, and a yield stress of no less than about 1500 Pa, both measurements at 25 SC, preferably at 35QC.
The principle of the measurement of the needle penetration according to the ASTM D5 consists of measuring the depth, expressed in tenths of a millimeter, to which a standard needle (weighing 2.5 g and placed in a needle holder weighing 47.5 g, i.e., a total of 50 g) penetrates when placed on the composition for 5 seconds. The principle of the measurement of yield stress consists of measuring oscillation stress sweep for understanding flow behavior and viscoelastic character for fluids and semi-solids as a function of stress, shear rate, or temperature. In the present invention, the yield stress is measured using a TA Instrument Rheometer AR-500 using a 40 mm Al Parallel Plate (Gap: 600 mm) at 1 Hz. At 25 QC, the present composition preferably has no measurable yield point under stress or shear.
The mascara composition changes rheology as it is heated, and finally reaches a point where it is liquid by 100 2C, preferably by 90 2C. By "liquid" herein for describing the mascara composition, what is meant is that the composition has a viscosity of between about 1 mPas and about 10,000,000 mPas. The present mascara composition goes through a transition change in terms of rheology between 25 9C and 100 SC, such that during these temperatures, there is a range of temperature and rheology in which the composition is suitably softened for application to the eyelashes. The softened state of the mascara composition is fluid enough to be applied to the eyelashes with an average number of strokes of an applicator holding the composition,
however, is viscous enough to stay on the applicator upon application, and on the eyelashes after application. When the composition is too thin or watery, the composition is difficult to hold on the applicator, and amount of composition applied to the eyelashes decreases.
The mascara composition is designed to have a rheology profile which gives suitable rheology during the temperature band to which the eyelash heating device is heated. The temperature band may be selected to provide suitable balance of applicability of the mascara composition and eyelash curling/lifting benefit. Typically, the temperature band is between about 509C and about 100QC.
The components for the composition are selected in order to provide the desired rheology profile. The composition comprises at least a solid hydrophobic component for providing the essential physical characteristics of the present invention. The composition may be made solely by the solid hydrophobic component.
The composition may take the phase form of an oil mixture, the oil being mainly made by the wax, or a water-in-oil emulsion. Water-in-oil emulsion forms are suitable for encompassing water-soluble or water-dispersible components. Solid Hydrophobic Component
The present composition comprises a solid hydrophobic component for providing the solid characteristic of the mascara composition. Solid hydrophobic components are typically used at levels from about 25% to about 100% in oil mixture forms, and from about 25% to about 95% in water-in-oil emulsion forms. Suitable solid hydrophobic components include waxes and fats.
Waxes are defined as lower-melting organic mixtures or compounds of high molecular weight, solid at room temperature and generally similar in composition to fats and oils except that they contain no glycerides. Some are hydrocarbons, others are esters of fatty acids and alcohols. Waxes useful in the present invention are selected from the group consisting of animal waxes, vegetable waxes, mineral waxes, synthetic waxes petroleum waxes, ethylenic polymers, hydrocarbon types such as Fischer-Tropsch waxes, silicone waxes, and mixtures thereof wherein the waxes have a melting point between 25°C and 1000C.
The specific waxes useful in the present invention are selected from the group consisting of beeswax, lanolin wax, shellac wax (animal waxes); carnauba, candelilla, bayberry (vegetable waxes); ozokerite, ceresin, (mineral waxes); paraffin, microcrystalline waxes (petroleum waxes); polyethylene, (ethylenic polymers); polyethylene homopolymers (Fischer-Tropsch waxes); C24-45 alkyl methicones (silicone waxes); and mixtures thereof.
Highly preferable commercially available waxes herein include stearyl palmitate by the tradename PURESTER 34, available from Strahl & Pitsch, ceresin by the tradename CERESIN 252 available from Strahl & Pitsch, and paraffin wax by the tradenames PARAFFIN SP-673P, PARAFFIN 206, and PARAFFIN 192 available from Strahl & Pitsch.
Useful herein are fats, namely glyceryl esters of higher fatty acids such as stearic and palmitic. Such esters and their mixtures are solid at room temperature and exhibit crystalline structure. The fats employed according to the invention are selected from the group consisting of fats derived from animals, vegetables, synthetically derived fats, and mixtures thereof wherein said fats
have a melting point from about 55°C to about 100°C. Preferably, the fats are selected from the group consisting of glyceryl monostearate, glyceryl distearate, glyceryl tristearate, palmitate esters of glycerol, C18-36 triglycerides, glyceryl tribehenate, C18-36 acid triglycerides and mixtures thereof.
Highly preferable commercially available fats herein include glyceryl monostearate by the tradename CUTINA GMS-V available from Cognis Cutina. Pigments
The compositions of the present invention may comprise pigments selected from the group consisting of inorganic pigments, organic pigments, and organic lake pigments, pearlescent pigments, and mixtures thereof. The present invention comprises mascara compositions devoid of pigments however, as such compositions may also provide the benefits of the present invention.
When employed, the pigments are present in proportions depending on the color and the intensity of the color that it is intended to produce. When employed, the level of pigments in the composition is from about 3 % to about 25 %, preferably from about 5 % to about 15 %. The pigments may optionally be surface-treated with treatments that include, but are not limited to, silicones, perfluorinated compounds, lecithin, and amino acids.
Inorganic pigments useful in the present invention include those selected from the group consisting of rutile titanium dioxide, anatase titanium dioxide (both coded in the Color Index under the reference Cl 77891); black, yellow and red iron oxides (Cl 77499, 77492 and 77491); bismuth oxychloride (Cl 77163); manganese violet (Cl 77742); ultramarines (Cl 77007); chromium oxide (Cl 77288); chromium hydroxide (Cl 77289); ferric ferrocyanide (Cl 77510); zinc oxide (Cl 77947); and mixtures thereof.
The organic pigments useful in the present invention include carbons black, and the dyes and the analogous lakes selected from the group consisting of D&C Red 6 (Cl 15850); D&C Red 7 (Cl 15850:1); D&C Red 21 (Cl 45380:2); D&C Red 22 (Cl 45380); D&C Red 27 (Cl 45410:1); D&C Red 28 (Cl 45410); D&C Red 30 (Cl 73360); D&C Red 33 (Cl 17200); D&C Red 34 (Cl 15880:1); D&C Red 36 (Cl 12085); D&C Orange 4 (Cl 15510); D&C Orange 5 (Cl 45370:1); D&C Orange 11 (Cl 45425); FD&C Yellow 5 (Cl 19140), FD&C Yellow 6 (Cl 15985); D&C Yellow 10 (Cl 47005); FD&C Green 3 (Cl 42053); D&C Green 5 (Cl 61570); FD&C Blue 1 (Cl 42090); Cochineal Carmine (Cl 75470); Guanine (Cl 75170) and mixtures thereof.
The pearlescent pigments useful in the present invention include those selected from the group consisting of mica (or a similar plate-like substrate) coated with any of the following materials alone or in combination: titanium dioxide, bismuth oxychloride, iron oxides, ferric ferrocyanide, chromium oxide, chromium hydroxide, and any organic pigment of the above-mentioned type and mixtures thereof. Film Forming Polymer
The compositions of the present invention may comprise a film forming polymer, for imparting wear and/or transfer resistant properties. When included, such materials are typically used in an amount of from about 0.5 % to about 20 % preferably from about 0.5% to about 10% by weight of the composition. Preferred polymers form a non-tacky film which is removable with water used with cleansers such as soap. The film forming polymers herein can be hydrophobic or hydrophilic, and can be provided in a lipophilic or aqueous carrier. When polymers provided in aqueous carriers are employed in the composition, a
water-in-oil form is selected. Polymers of hydrophilic nature are also compatible with a water-in-oil form composition.
Examples of suitable film forming polymeric materials include: a) sulfopolyester resins, such as those with tradename AQ sulfopolyester resins, such as AQ29D, AQ35S, AQ38D, AQ38S, AQ48S, and AQ55S available from Eastman Chemicals; b) polyvinylacetate/polyvinyl alcohol polymers, such as tradename Vinex resins available from Air Products, including Vinex 2034, Vinex 2144, and Vinex 2019; c) acrylic resins, including water dispersible acrylic resins available from National Starch under the trade name "Dermacryl", including Dermacryl LT; d) acrylates and their derivative polymers, including acrylates copolymer with tradename Luvimer available from BASF, Avalure series available from Noveon, Daitosol 5000AD available from Daito Kasei Kogyo, ethylene.styrene/acrylates copolymer such as Syntran series available from Interpolymer, acrylates/ammonium methacrylate copolymer with tradename Ultrasol 2075C available from Presperse, octyl acrylates copolymer with tradename Daitotol SJ available from Kobo, acrylates silicone copolymer with tradename Daitotol ASC available from Kobo, AMP-acrylates/allyl methacrylate copolymer with tradename Fixate G100 Polymer available from Noveon, acrylate/dimethicone copolymer with tradename KP545 available from ShinEtsu; e) styrene, such as sodium polystyrene sulfonate with tradename Flexan available from National Starch;
f) urethanes, such as polyurethane-1 polymer with tradename Luviset PUR available from BASF; g) polyvinylpyrrolidones (PVP), including tradenames Luviskol K17, K30 and K90 available from BASF PVP K-30, PVP K-120 available from ISP, tricontanyl PVP with tradename Ganex WP 660 Resin available from ISP, water soluble copolymers of PVP, including PVP/VA S-630 and W-735 and PVP/dimethylaminoethylmethacrylate Copolymers such as Copolymer 845, Copolymer 937, and Styleze CC-10 available from ISP, VP/DAM available from Daiichi Kogyo Seiyaku, PVP/acrylates/lauryl methacrylate copolymer with tradename Styleze 2000 available from ISP; h) high molecular weight silicones such as dimethicone and organic-substituted dimethicones, especially those with viscosities of greater than about 50,000 mPas; i) high molecular weight hydrocarbon polymers with viscosities of greater than about 50,000 mPas such as polybutene, polybutene terephthalate, polydecene, polycyclopentadiene, and similar linear and branched high molecular weight hydrocarbons, including isooctane with tradename Permethyl 97A available from Presperse; j) organosiloxanes, including organosiloxane resins, fluid diorganopolysiloxane polymers and silicone ester waxes.
Also useful herein are latex polymers including copolymer PVP/hexadecane or the copolymer PVP/eicosene marketed by ISP under the tradenames Ganex V-216® and Ganex V-220®, respectively. Ganex V-216® is a PVP/hexadecane copolymer comprising approximately 15-23% of pyrrolidone units with a weight average molecular weight of 7300. Ganex V-220® is a
copolymer PVP/eicosene which comprises approximately 20-28% of pyrrolidone units and a weight average molecular weight of 8600.
Emulsifiers
The compositions of the present invention in emulsion form comprises an emulsifier, which is typically a lipophilic surfactant, preferably by weight of the entire composition at from about 1 % to about 15 %. The lipophilic surfactant herein has an HLB value of less than about 8.
The HLB value is a theoretical index value which describes the hydrophilicity-hydrophobicity balance of a specific compound. Generally, it is recognized that the HLB index ranges from 0 (very hydrophobic) to 40 (very hydrophilic). The HLB value of the lipophilic surfactants may be found in tables and charts known in the art, or may be calculated with the following general equation: HLB = 7 + (hydrophobic group values) + (hydrophilic group values). The HLB and methods for calculating the HLB of a compound are explained in detail in Surfactant Science Series, Vol. 1 : Nonionic Surfactants", pp 606-13, M. J. Schick (Marcel Dekker Inc., New York, 1966).
Without being bound by theory, the species and levels of the lipophilic surfactant herein are believed to provide a stable water-in-oil emulsion in view of the other components of the present invention.
The lipophilic surfactant can be an ester-type surfactant. Ester-type surfactants useful herein include: sorbitan monoisostearate, sorbitan diisostearate, sorbitan sesquiisostearate, sorbitan monooleate, sorbitan dioleate, sorbitan sesquioleate, glyceryl monoisostearate, glyceryl diiostearate, glyceryl sesquiisostearate, glyceryl monooleate, glyceryl dioleate, glyceryl sesquioleate, diglyceryl diisostearate, diglyceryl dioleate, diglycerin monoisostearyl ether,
diglycerin diisostearyl ether, and mixtures thereof.
Commercially available ester-type surfactants are, for example, sorbitan isostearate having a tradename Crill 6 available from Croda, and sorbitan sesquioleate with tradename Arlacel 83 available from Kao Atras.
The lipophilic surfactant can be a silicone-type surfactant. Silicone-type surfactants useful herein are (i), (ii), and (iii) as shown below, and mixtures thereof, (i) dimethicone copolyols having the formulation:
wherein x is an integer from 5 to 100, y is an integer from 1 to 50, a is zero or greater, b is zero or greater, the average sum of a+b being 1-100. (ii) dimethicone copolyols having the formulation:
wherein R is selected from the group consisting of hydrogen, methyl, and combinations thereof, m is an integer from 5 to 100, x is independently zero or greater, y is independently zero or greater, the sum of x+y being 1-100. (iii) branched polyether-polydiorganosiloxane emulsifiers herein having the
formuiation:
O-(C2H4O)e(C3H6O)f-R3 wherein R1 is an alkyl group having from about 1 to about 20 carbons; R2 is
CH3
wherein g is from about 1 to about 5, and h is from about 5 to about 20; R3 is H or an alkyl group having from about 1 to about 5 carbons; e is from about 5 to about 20; f is from about 0 to about 10; a is from about 20 to about 100; b is from about 1 to about 15; c is from about 1 to about 15; and d is from about 1 to about 5.
Commercially available silicone-type surfactants are, for example, dimethicone copolyols DC5225C, BY22-012, BY22-008, SH3746M, SH3771 M, SH3772M, SH3773M, SH3775M, SH3748, SH3749, and DC5200, all available from Dow Corning, and branched polyether-polydiorganosiloxane emulsifiers such as PEG-9 polydimethylsiloxyethyl Dimethicone, having an HLB of about 4 and a molecular weight of about 6,000 having a tradename KF 6028 available from ShinEtsu Chemical. Water
The composition of the present invention in water-in-oil form comprises water in an amount sufficient to provide a discontinuous aqueous phase,
preferably an amount such that water is no more than about 50 %, more preferably from about 10 % to about 40 % of the entire composition. Use of water allows the inclusion of useful components such as film forming polymers which are hydrophilic and/or aqueous carrier-based, hydrophilic conditioning agents, and other water soluble or water dispersible components described below.
In the present invention, deionized water is typically used. Water from natural sources including mineral cations can also be used, depending on the desired characteristic of the product. Hydrophobic Conditioning Agents
The compositions of the present invention may further comprise a hydrophobic conditioning agent. Nonlimiting examples of hydrophobic conditioning agents include those selected from the group consisting of mineral oil, petrolatum, lecithin, hydrogenated lecithin, lanolin, lanolin derivatives, C7-C40 branched chain hydrocarbons, C1-C30 alcohol esters of C1-C30 carboxylic acids, C1-C30 alcohol esters of C2-C30 dicarboxylic acids, monoglycerides of C1-C30 carboxylic acids, diglycerides of C1 -C30 carboxylic acids, triglycerides of C1 -C30 carboxylic acids, ethylene glycol monoesters of C1-C30 carboxylic acids, ethylene glycol diesters of C1-C30 carboxylic acids, propylene glycol monoesters of C1 -C30 carboxylic acids, propylene glycol diesters of C1-C30 carboxylic acids, C1-C30 carboxylic acid monoesters and polyesters of sugars, polydialkylsiloxanes, polydiarylsiloxanes, polyalkarylsiloxanes, cyclomethicones having 3 to 9 silicon atoms, polysiloxane crosspolymers such as vinyl dimethicone crosspolymer available as a dimethicone mixture fluid with tradename KSG series available from ShinEtsu,
vegetable oils, hydrogenated vegetable oils, polypropylene glycol C4-C20 alkyl ethers, di C8-C30 alkyl ethers, and combinations thereof. Hydrophilic Conditioning Agents
The compositions of the present invention may further comprise a hydrophilic conditioning agent. Nonlimiting examples of hydrophilic conditioning agents include those selected from the group consisting of polyhydric alcohols, polypropylene glycols, polyethylene glycols, ureas, pyrolidone carboxylic acids, ethoxylated and/or propoxylated C3-C6 diols and triols, alpha-hydroxy C2-C6 carboxylic acids, ethoxylated and/or propoxylated sugars, polyacrylic acid copolymers, sugars having up to about 12 carbons atoms, sugar alcohols having up to about 12 carbon atoms, and mixtures thereof. Solvents
The compositions of the present invention may contain a volatile or non-volatile solvent that dissolves or uniformly disperses certain components of the present invention. They include, but are not limited to, lower alcohols (such as ethanol, isopropanol), dihydric alcohols such as propylene and butylene glycol, polyols such as glycerin, hydroalcoholic mixtures, hydrocarbons (such as isobutane, hexane, decene, acetone), halogenated hydrocarbons (like Freon), linalool, hydrocarbon esters (such as ethyl acetate, dibutyl phthalate), volatile silicon derivatives, especially siloxanes (such as phenyl pentamethyl disiloxane, phenethyl pentamethyl disiloxane, methoxypropyl heptamethyl cyclotetrasiloxane, chloropropyl pentamethyl disiloxane, hydroxypropyl pentamethyl disiloxane, octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloxane), and mixtures thereof. Additional components
The compositions hereof may further contain additional components such as are conventionally used in topical products, e.g., for providing aesthetic or functional benefit to the composition or skin, such as sensory benefits relating to appearance, smell, or feel, therapeutic benefits, or prophylactic benefits (it is to be understood that the above-described required materials may themselves provide such benefits).
The CTFA Cosmetic Ingredient Handbook, Second Edition (1992) describes a wide variety of nonlimiting cosmetic and pharmaceutical ingredients commonly used in the industry, which are suitable for use in the topical compositions of the present invention. Such other materials may be dissolved or dispersed in the composition, depending on the relative solubilities of the components of the composition.
Examples of suitable topical ingredient classes include: sunscreen actives, anti-cellulite agents, antioxidants, radical scavengers, chelating agents, vitamins and derivatives thereof, abrasives, other oil absorbents, astringents, dyes, essential oils, fragrance, structuring agents, emulsifiers, solubilizing agents, anti-caking agents, antifoaming agents, binders, buffering agents, bulking agents, denaturants, pH adjusters, propellants, reducing agents, sequestrants, cosmetic biocides, and preservatives, such as propylparaben, methyl paraben, phenoxyethanol, benzyl alcohol, and EDTA and its salts. Additional Usages
The cosmetic products herein may also be used for other usages in the personal care field, with necessary modifications to the composition and/or device suitable for the usage. Unlimited examples of such usages include coloring and treatment of eyebrows; treatment, styling, removing, and coloring of
hair; treatment and tattooing of skin, and nail coloring. EXAMPLES
The following examples further describe and demonstrate the preferred embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration, and are not to be construed as limitations of the present invention since many variations thereof are possible without departing from its spirit and scope. Examples C1-C3
Examples C1 and C2 are mascara compositions in the form of oil mixture, and C3 is a mascara composition in the form of a water-in-oil emulsion. Each composition has a needle penetration of between 1 -25 at 35QC, a yield stress of over 1500Pa at 35eC, and has a viscosity of between 1 mPas and 10,000,000 mPas at 903C. The mascara compositions can be suitably applied to the eyelashes when heated to between 50-803C via use of the device described hereinabove. Composition The following components are used at the respective w/w %.
Definition of components:
*1 Glyceryl monostearate-vegetable derived: GMS-V available from Cognis
*2 Stearyl Palmitate: Purester 34 available from Strahl & Pitsch
*3 Ceresine wax: Ceresine Wax SP-252 available from Strahl & Pitsch
*4 Paraffin wax: Paraffin Wax SP-673P available from Strahl & Pitsch
*5 Dimethicone/Vinyl Dimethicone Crosspolymer: KSG 16 available from
Sh in Etsu
*6 Tricontanyl PVP: Ganex WP-660 available from ISP
*7 Sorbitan Sesquioleate: Crill 6 available from Croda
*8 Cl 77499 (iron oxide) and Methicone: Si Black Iron Oxide available from
Daito Kasei
*9 Sodium polystyrene sulfonate: Flexan Il available from National Starch &
Chemical
Method of preparation
Examples C1 -C3 may be made in any suitable method known to one skilled in the art. Preferably, the examples are made by the following methods.
Example C1
1 ) Heat components 1 -4 to 85-90 0C. Being low shear mixing when enough
wax has melted.
2) Once components 1 -4 have completely melted, add components 6 and 8. Continue mixing for about 10 min.
3) Add component 9 to product of Step 2, and disperse for 30 min - 1 hr with a dispersator.
4) Pour the product of Step 3 into molds and allow product to cool and solidify. Example C2
1 ) Heat components 1 -4 to 85-900C. Being low shear mixing when enough wax has melted.
2) Once components 1 -4 has completely melted, add component 5. Continue mixing for about 10 min.
3) Add components 6 and 8 to product of Step 2. Continue mixing for about 10 min.
4) Add component 9 to product of Step 3, and disperse for 30 min - 1 hr with a dispersator.
5) Pour the product of Step 4 into molds and allow product to cool and solidify. Example C3
1) Heat components 1 -4 to 85-900C. Being low shear mixing when enough wax has melted.
2) Separately heat components 10-15 to 85-9O0C and mix with low shear mixing.
3) Once components 1-4 has completely melted, add components 6-8. Continue mixing for about 10 min.
4) Add component 9 to product of Step 3, and disperse for 30 min - 1 hr with a dispersator 2. Homogenize for 30 min - 1 hr by mixing.
5) Add the product of Step 2 to product of Step 4 while mixing with low shear mixing.
6) Further mix product of Step 5 with moderate shear mixing for 15 - 30 min. to effect emulsification.
7) Pour the product of Step 6 into molds and allow product to cool and solidify.
All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.