WO2010014328A2 - Compositions et procédés pour boucler des fibres kératiniques - Google Patents

Compositions et procédés pour boucler des fibres kératiniques Download PDF

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Publication number
WO2010014328A2
WO2010014328A2 PCT/US2009/049057 US2009049057W WO2010014328A2 WO 2010014328 A2 WO2010014328 A2 WO 2010014328A2 US 2009049057 W US2009049057 W US 2009049057W WO 2010014328 A2 WO2010014328 A2 WO 2010014328A2
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WIPO (PCT)
Prior art keywords
liquid
contractile
curl
agent
curling
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PCT/US2009/049057
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English (en)
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WO2010014328A3 (fr
Inventor
Phillip Cummins
Jean Harry Xavier
John R. Castro
Christina Fthenakis
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Elc Management Llc
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Publication of WO2010014328A2 publication Critical patent/WO2010014328A2/fr
Publication of WO2010014328A3 publication Critical patent/WO2010014328A3/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • A61K8/8117—Homopolymers or copolymers of aromatic olefines, e.g. polystyrene; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara

Definitions

  • the invention is in the field of methods for curling keratinous fibers such as eyelashes or hair and related products and packages.
  • the eyelashes are heated and bent into a curled shape. Bending the lashes is usually done with a tool designed for the purposes (i.e. an eyelash curler), but may be done with a finger or even a spoon.
  • the heat may be supplied by the eyelash curler or some other source.
  • the curling effect is the result of a rearrangement of hydrogen bonds in the hair fiber structure.
  • the curl will only last for a relatively brief period of time, after the eyelash curler is removed, unless a curl retention agent is employed.
  • This method may give better results than curling with a mascara brush alone, as described above.
  • heating the lashes may damage them, especially if done repeatedly, day after day.
  • a separate heating device is needed and the process takes longer than simply brushing the eye lashes, because it is a two step process, first curling, then applying a curl retention agent.
  • a curl retention method may also be employed when curling other keratinous fibers. For example, using hair spray to hold a curl in head hair or wax to hold a curl in a moustache. Like the mascara, the hair spray or wax do not impart the curl; they merely hold the curl in place after a mechanical force has been used to induce a curl.
  • US2004/0151685 discloses curl retention methods comprising applying to the keratinous material a retention effective amount of a transglutaminase enzyme.
  • the curl retention agent i.e. mascara, hairspray, wax, transglutaminase
  • the curl retention agent is applied liberally, to all sides of hair fibers. No intentional effort is made to consistently apply a curl retention agent unevenly, on one or more sides of each hair fiber.
  • Consistently apply we mean that more curl retention agent is applied to the same side of each adjacent fiber and significantly less or none is applied to the opposite side of each adjacent fiber.
  • Hair Perming Another method of curling keratinous fibers is to "perm" the fibers.
  • hair is treated with a reducing agent to open up the disulfide bonds in the hair, then bent into a curled shape, and then treated with an oxidizing agent to reform new disulfide bonds.
  • the hair fibers remain curled until they grow out.
  • This is unlike the curl retention methods above, which provide a relatively brief effect, typically no more than one day.
  • lashes mechanically curled and held in place by mascara
  • permanent eyelash curling persists even after swimming, showering, crying or sweating.
  • the drawback of this method is the use of certain reactive agents in close proximity to the eye, the relatively complicated and long process needed to achieve a simple aesthetic effect.
  • US2004/0151685 also states that transglutaminase can be used to enhance or impart curl, perhaps by forming covalent crosslinks between lysine and glutamine, two of the more common amino acids in hair.
  • the present invention curls hair without forming covalent crosslinks between lysine and glutamine, and without altering the natural covalent bond structures in the hair. This a benefit, since such alterations may have short or long term negative side-effects on the health of the hair.
  • US2004/0151685 does not disclose the methods described herein, specifically, methods of applying a curl-imparting composition to only one side of the hair fibers.
  • a main object of the invention to provide compositions that impart curl to keratinous fibers, safely and effectively.
  • Another main object of the invention is to provide compositions that impart curl to eyelashes, the compositions being safe for use in the eye area.
  • Another main object of the invention is to provide safe and effective, one-step methods of curling keratinous fibers, that do not involve oxidation and reduction of protein bonds.
  • a further object of the invention to provide a consumer package that comprises a composition, applicator and instructions for curling keratinous fibers.
  • compositions comprising materials with certain wetting and contractile properties, as defined herein, are capable of imparting a long lasting curl to keratinous fibers, such as eyelashes, head hair, moustaches, etc. There is no need to first curl the hair with a mechanical force supplied by a user, and then apply a curl retention agent.
  • the composition does the work of curling after it is applied to the hair.
  • the compositions are unique in that they are designed to be applied to one side of the hair fibers, only. To the extent that the compositions are applied to both sides of the hair fibers, the curling effect is diminished or lost. Therefore, the invention is also directed to a novel method for curling hair fibers.
  • the method comprises applying a useful contractile agent consistently, but unevenly to adjacent hair fibers. The amount of useful contractile agent applied and the degree of uneven application must be sufficient to curl hair fibers. Curling may be followed by applying a makeup color composition to the hair fibers, but this is not required.
  • Figure 1 is a plot of percent eyelash curling verses concentration of Flexan® II.
  • Figure 2 is a plot of percent eyelash curling verses ratio of Flexan® II to Antara® 430, at several total concentrations.
  • Figure 3a is a photograph of untreated eyelashes.
  • Figure 3b is an eyelash treated with mascara alone.
  • Figures 3c-3g show eyelashes treated with a composition according to the present invention.
  • Figure 3 c is a low curl application.
  • Figure 3d is a medium curl application.
  • Figure 3e is a high curl application.
  • Figure 3f is an extreme or excessive curl application.
  • Figure 3g shows that mascara may be easily applied after the lashes have been curled according to the present invention.
  • Figures 4 illustrates application of a liquid contractile agent composition to the upper surface of the upper eyelashes, with a beaded applicator.
  • the present invention makes use of materials that we call useful contractile agents.
  • useful contractile agents we focus on a preferred form of contractile agents that we call “liquid contractile agents”, but the principles of the invention may be extended to contractile agents that fall outside the realm of liquid contractile agents.
  • critical parameters include: wetability, contractile strength, application amount, drying time, wet and dry adhesion and internal structure.
  • Methods of the invention also consider the number of passes through the hair to complete an application and the need for uneven coating of the hair.
  • Packages of the invention also consider the type of applicator and how much liquid contractile agent it can deliver.
  • liquid contractile agent the term “liquid” refers to a material that continually deforms (flows) under an applied shear stress. This may include liquids in the conventional sense, as well as other materials, such as gels. It may include materials that are in a liquid phase at room temperature or that can be maintained in liquid phase by the application of heat.
  • the term “liquid” also allows for the presence of solid materials in the liquid, as a dispersion or solution. The need for flowability under applied shear, is to allow the contractile agent to be spread with an applicator, over a portion of the hair fiber surface.
  • liquid contractile agent Although the liquid contractile agent is applied as a liquid, it dries when exposed to the open air. Therefore, in the phrase "liquid contractile agent”, the term “contractile” implies that the material shrinks as it dries, when no shear is being applied.
  • liquid contractile agent the term “agent” may be a single material having the requisite properties, as described herein, or it may be a composite material, wherein one or more individual components do not have the requisite properties, but the composite does have the requisite properties, as described herein.
  • the term “comprise” means that a collection of objects is not necessarily limited to the items explicitly recited, and may include items not explicitly recited.
  • Liquid Contractile Agent Must Provide Suitable Wetting "Wetting” is a measure of the ability of the liquid to maintain contact with a substrate.
  • the degree of wetting of the substrate by the liquid is manifested in the shape of the liquid as it rests on the surface of the substrate.
  • a liquid contacts a substrate, such as the surface of a solid or the surface of a thin polymer film
  • intermolecular interactions arise between the liquid and the substrate.
  • These intermolecular interactions between the liquid and the substrate are adhesive forces that tend to pull the liquid into a less spherical, more spread out shape.
  • Working against the adhesive forces are cohesive forces within the liquid, which tend to minimize contact with the substrate by drawing the liquid into a more spherical shape.
  • a drop of water on a substrate surface may be spread out well beyond where it normally spreads from adhesion and cohesion alone. But once the pressure is removed, the water may retreat in an attempt to revert to a more drop-like state.
  • Another way to think about contact angles is that a larger contact angle between two materials means that the two materials are dissimilar in hydrophilicity/hydrophobicity. A smaller contact angle means that two materials are similar in this hydrophilicity/hydrophobicity.
  • liquid contractile agents useful in the present invention it is important to distinguish between two different contact angles.
  • This contact angle is a measure of the hydrophobicity or hydrophilicity of the liquid contractile agent. The smaller (larger) the contact angle between the water and the liquid contractile agent, the more hydrophilic (hydrophobic) is the liquid contractile agent.
  • a simply preferred and useful liquid contractile agent is one that, after being spread on the hair fibers by an applicator, may spread out a little further, but only to a degree that the contractile agent is still able to impart a noticeable or cosmetically acceptable curl to the fibers.
  • the adhesive forces of the liquid contractile agent form a significant bond with the hair fiber, but the cohesive forces do not allow the liquid contractile agent to spread much further.
  • a more preferred and useful contractile agent is one that, after being spread on a hair fiber by an applicator, does not spread out any further, and retreats only to a degree that the contractile agent is still able to impart a noticeable and cosmetically acceptable curl to the hair fibers. By not spreading any further, the liquid contractile agent does not migrate to portions of the hair fiber where it should not go. By not retreating, or only retreating a small amount, we can be sure that the liquid contractile agent is forming a significant bond with the hair fiber.
  • liquid contractile agent in the context of wetting, is one that, after being spread on a hair fiber by an applicator, remains in place, not spreading any further, nor retreating.
  • suitable wetting we mean that a liquid contractile agent is one of preferred, more preferred, or most preferred, as just described.
  • a simple wetting test may be conducted. 1 ml of a liquid contractile agent is spread on a 10 cm x 10 cm glass plate using a 2 mil (thousandths of an inch) standard draw down bar, forming a film. The film is allowed to dry for 15-30 minutes. Using a Sony CCD camera model SSC-DC 5OA or similar device, acquire a digital image of the intersection of the air- liquid interface with the liquid-glass interface. The contact angle between the film and glass plate may then be measured through the use of digital image software, which are well known in the art and widely available. Because the glass plate is hydrophobic, a larger contact angle would imply that the liquid contractile agent is more hydrophilic.
  • a smaller contact angle implies a more hydrophilic liquid contractile agent.
  • the tests described here are merely examples, and other suitable tests may substituted for these.
  • the contact angle of a test sample is known, that angle may be compared to the contact angle of one or more standard liquid contractile agents, known to be useful for the present invention.
  • a similar contact angle implies that the test sample may perform similarly to the standard liquid contractile agent, as least as far as wetting is concerned.
  • suitable wetting of keratinous fibers is just one necessary characteristic of a useful liquid contractile agent.
  • a liquid contractile agent that displays preferred wetting, yet has little strength to curl hair fibers is not useful in the present invention.
  • Suitable curling implies that the liquid contractile agent has produced a desired visible effect in the shape of the hair fibers to which the agent was applied. In the beauty field, suitable curling implies that an improvement in aesthetic appeal of the eye lashes or head hair or moustache etc., has been achieved.
  • the radius of a curl should not be too large or too small. If the radius is too large, the curling effect may not be sufficiently dramatic. If the radius of the curl is too small, the effect may be a weird, unnatural appearance (see figure 3f). That which is too little radius or too much radius are subject to some individual interpretation. However, there are accepted
  • Curl 50-70% as High Curl and above 70% as Extreme Curl.
  • curls above 90% are possible. It is even possible to make the fibers curl back on themselves (100% curl or more), but from a commercial beauty standpoint, such extreme curl may not be useful. Although, such extreme curls may find uses in fields outside of the beauty industry, such as in the performing arts.
  • a useful liquid contractile agent is one that is able to provide suitable curling when applied to hair fibers according to the methods of this invention.
  • Two main factors to consider are the strength of the liquid contractile agent and the amount of contractile agent applied.
  • the contractile agents of the present invention do all the work of curling. It is not necessary to apply a mechanical force to the hair fibers before a composition of the invention is applied. This means that application of too much contractile agent can result in too much curling. Also, application of too little liquid contractile agent can result in too little curling, although this may be correctable by applying more contractile agent.
  • the degree of curling depends on the strength of the contractile agent and the amount of contractile agent applied.
  • a main focus of the present invention is curling eyelashes, although the principles of the invention readily adapt to moustaches, beards, hair of the head, etc. While it is difficult to control how much product a consumer may apply to her eye lashes, a sense of this may be gotten from experience in the field of eye lash makeup. For example, to apply mascara to the eye lashes, a woman may dip a brush into mascara and draw the brush through a wiper, as is well known in the art. She may then draw the loaded brush over each eye lash from about one to about ten or twenty times.
  • a preferred and useful liquid contractile agent of the present invention is one that is able to impart a suitable curl to the eyelashes, when an applicator loaded with the liquid contractile agent is drawn over each lash, at least ten to no more than twenty times.
  • a more preferred and useful contractile agent is one that is able to impart a suitable curl to the eye lashes when the loaded applicator is drawn over each lash at least five to no more than ten times.
  • a most preferred and ideal contractile agent is one that is able to impart a suitable curl to the eyelashes when the loaded applicator is drawn over each lash no more than five times.
  • the number of passes through the lashes will depend on how much product a given applicator can retrieve from the product reservoir, but it is well within the ability of a person of ordinary skill in the art, to choose a suitable combination of contractile agent and applicator, after he or she has been made familiar with the various critical parameters as identified, herein.
  • Suitable drying means several things.
  • a liquid contractile agent dries in no more than about fifteen minutes; (2) as it dries, the liquid contractile agent contracts, and remains adhered to the hair fibers as it contracts; (3) after it is dry, the liquid contractile agent continues to adhere to the hair fibers, and has enough internal structure to hold the shape of the hair fibers.
  • useful liquid contractile agents dry in about ten to about fifteen minutes.
  • Preferred liquid contractile agents dry in five or about five minutes to ten minutes. More preferred liquid contractile agents dry in two or about two minutes to five minutes. The most preferred liquid contractile agents dry in one or about one to two minutes.
  • suitable drying means that a liquid contractile agent of the present invention should not dry so fast that a user does not have time to thoroughly apply the agent to her lashes. About one minute may be enough time to thoroughly apply the agent to the lashes. If consumer testing or other information suggests that more time is needed, then a person of skill in the art can adjust the dry time of the liquid contractile agent accordingly. In terms of wet adhesion, the adhesion between the a hair fiber and the liquid contractile agent must be sufficient to withstand the forces of contraction within the liquid the contractile agent.
  • a liquid contractile agent In terms of contraction, a liquid contractile agent must exert a force strong enough to bend the hair fibers to which it adheres. The reshaping of the hair fiber is mechanical, but all of the work is done by the liquid contractile agent.
  • the contraction may occur along one or more principle axes, or it may occur more generally, along all directions (i.e. isotropically).
  • the liquid contractile agent must contract along the direction of the length of the hair fibers, so that the free end of the fibers are pulled toward the insertion point of the fibers. More preferably, the liquid contractile agent contracts much more along the direction of the length of the hair fibers, than in any other direction.
  • a curl is preferable for a curl to remain in the hair for at least eight hours after application. More preferably, the curl is able to remain in the hair for at least sixteen hours after application. Most preferably, the curl is able to remain in the hair for as long as the dried contractile agent is on the hair.
  • the degree of curl retention depends largely on the internal molecular structure of the dried liquid contractile agent. Gravity and forces within the hair, may tend to undo the curl. To counteract those forces, the liquid contractile agent must be able to hold its molecular arrangement. Thus, the more internal structure in the dried liquid contractile agent, the longer a curl will remain in the hair.
  • Identification of agents that that have the necessary contractile strength for use in the methods and products of the invention may be ascertained by performing a simple contractile test as follows. Using a 2 mil draw down bar, 1 ml of a test liquid contractile agent is applied to a 5 cm x 20 cm piece of standard white paper, to form a film.
  • the paper may be, for example, the type used in photocopier machines (for example, International Paper Hammermill® Copy
  • the film is allowed to dry for 15-30 minutes.
  • the degree of curling of the paper sample indicates the contractile ability of the agent. For example, if the dried film does not curl the paper, the agent may not have sufficient contractile properties. If the paper curls, the agent may be suitable. The degree of curling is directly proportional to the curling effectiveness of the agent. The direction(s) of curl may also be noted. Once the degree and direction of paper curling is known, that curled paper may be compared to the paper curling test results of one or more standard liquid contractile agents, known to be useful for the present invention. A similar degree of paper curl implies that the test sample may perform similarly to the standard liquid contractile agent, as least as far as curling is concerned.
  • test described here is merely an example, and other suitable tests may substituted for this one.
  • a similar test may be performed on hair samples.
  • percent curl can be measured as described above.
  • suitable curling of keratinous fibers is just one necessary characteristic of a useful liquid contractile agent.
  • a suitable liquid contractile agent of the present invention is one that, after it is dry, has sufficient internal structure to retain a curl for a desired amount of time.
  • Internal structure is molecular level property.
  • materials with a high degree of crosslinking, and/or a high degree of non-covalent intramolecular forces i.e. ionic bonds, hydrophobic interactions, hydrogen bonds, Van der Waals forces, i.e. "London dispersion forces", and dipole-dipole bonds
  • materials with a high degree of crosslinking, and/or a high degree of non-covalent intramolecular forces i.e. ionic bonds, hydrophobic interactions, hydrogen bonds, Van der Waals forces, i.e. "London dispersion forces", and dipole-dipole bonds
  • Polymers Charge density. Young's Modulus, etc. In general, polymers have good non-specific adhesive affinity to various surfaces.
  • the liquid contractile agent includes a polymer
  • Safety is also an issue, especially when the polymer may be used around the eyes. More on this below.
  • Charge Density Useful polymers have a surface charge density of 1 to 10%, more preferably from about 2 to 8%, as measured by X-ray fluorescence.
  • Preferred polymers are anionic with a rigid hydrophobic backbone, while cationic polymers are less preferred. This is because a many cationic polymers tend to plasticize the medium in which they are dispersed, which means the medium deforms easily and may not support initial curling and/or curl retention, very well.
  • cationic, non-ionic, zwitterionic and amphoteric polymers are not a priori excluded from use in the present invention, but their selection and incorporation into a useful hair curling composition may be more difficult. Ultimately, their suitability is determined by the curling results.
  • Stiffness Human eye lash fibers have an elastic modulus on the order of 4 GPa, say about 1-7
  • preferred polymers have a stiffness characterized by an elastic modulus (or Young's modulus) ranging from about 1 to 12, preferably from 4 to 8, more preferably about 6 GPa, as measured by ASTM test methods D638, D882 or E1875. This amount of stiffness (internal structure) is required to transmit the contracting force that curls the hair fiber and retains the curl for a desired amount of time. Dispersability
  • a suitable polymer may be applied by itself, to the hair fibers (i.e. neat) or they may be dispersed in a solvent.
  • Preferred polymers are dispersible in polar solvents, such as aqueous or aqueous/alcoholic solutions or dispersions.
  • p ⁇ A preferred polymer is one that is stable at the pH of its environment. For example, personal care and cosmetic products often have a pH in the 5-7 range. Thus, for a product of this type, the polymer used should be stable in the 5-7 range. If the polymer is not stable at that pH, then formulating a useful product may be more difficult.
  • the length of time over which the polymer must be stable also depends on the intended use. In the personal care industry, stability often implies that a product does not degrade for at least 6 months, preferably at least 1 year, more preferably at lest 2 years.
  • the viscosity of solution is preferably about 1-3 poise. This viscosity allows spreading the polymer solution over the fibers, but provides enough internal resistance to prevent the polymer solution from migrating to the opposite side of the fiber.
  • liquid contractile agent may adhere directly to the hair fibers, so that when the liquid contractile agent contracts, the hair fibers are bent.
  • some other material in the composition adheres to the hair fibers. In this case, the contraction of the liquid contractile agent in the composition would have to be transmitted to the hair fibers through some additional structure in the composition.
  • Laponite® platelets are about 20 to 50 nm in size, and provide over 700 m 2 per gram of surface area populated by Na + ions. In general, these ions may participate in ion-dipole and ion exchange interactions with a liquid contractile polymer. Other interactions may occur between the polymer and oxygen, silicon, Mg, Li, or OH groups near the surface of the Laponite®. At the same time, Laponite®, has good adhesion to hair fibers and significant internal structure. As a example, a water base composition of the Flexan® and Laponite®, effectively and safely curls the eyelashes. One side of the Laponite® platelets adhere to the
  • the present invention makes use of materials that we call contractile agents or liquid contractile agents.
  • critical parameters that define what is a useful contractile agent. These critical parameters include: wetability, contractile strength, contractile direction, application amount, drying time, wet and dry adhesion, internal structure, safety concerns.
  • charge density and Young's modulus For polymers, we discussed charge density and Young's modulus. Working ranges of some of these parameters were also disclosed. While it may be possible to devise a battery of tests that conclusively categorize a material as a useful or non-useful liquid contractile agent, that approach is likely to be overkill and not commercially feasible.
  • a hair curling composition according to the present invention must contain at least one useful contractile agent.
  • a material having the properties described, herein, in the working ranges described, herein, is a useful contractile agent, specifically, a liquid contractile agent.
  • a hair curling composition may comprise only the useful contractile agent(s), or it may comprise other ingredients in addition to the useful contractile agent(s), so long as those other ingredients do not interfere with the ability of the useful contractile agent(s) to curl keratinous fibers.
  • a hair curling composition of the invention comprises from about 0.1 to 100%, more preferably from about 1-95%, most preferably from about 1 to 90% by weight of the total composition of liquid contractile agent(s).
  • the other ingredients present may include water, polar non-aqueous solvents such as mono-, di-, or polyhydric alcohols, and the like. If present, suggested ranges for the water or polar non-aqueous solvent are from about 0.1 to 99%, preferably from about 0.5 to 75%, more preferably from about 1 to 60% by weight of the total composition.
  • the liquid contractile agent(s) may be dispersions or solutions of useful contractile agents in water or non-aqueous polar solvents.
  • the compositions are aqueous solutions or dispersions of the liquid contractile agent in a cosmetically safe concentrations.
  • Suitable Contractile Agents include natural or synthetic compounds, polymers, mixtures of natural ingredients, and the like, so long as they behave within the critical parameters defined above.
  • the term "natural” means that the agent is naturally occurring, for example, the agent may be found in resins, gums, or extracts from plants. Examples include, but are not limited to various botanical extracts and plant exudates, such as gums or resins.
  • any polymer having the properties of a useful contractile agent, as described herein, may be suitable for use in the invention.
  • the polymers are charged, that is they may be negatively or positively charged such as anionic, cationic, zwitterionic, or amphoteric polymers.
  • the charged polymers are anionic and have a charge density in the range of about 1 to 10%, more preferably from about 2 to 8%, as measured by X-ray fluorescence.
  • the polymers have a preferred elastic modulus (or Young's modulus) of about 6 GPa.
  • the polymers of this embodiment are water soluble or dispersible, and the polymers or polymer solutions are stable at a pH of about 5 to 7. Examples of suitable polymers include, but are not limited to:
  • Styrene/acrylates/ammonium methacrylate copolymer one type being an anionic polymer sold by Interpolymer Corporation under the trademark Syntran® PC5100NP, which comprises about 25% solids in aqueous solution comprising sodium laureth sulfate, Cl 1-15 pareth-7, butylene glycol, phenoxyethanol, potassium sorbate, caprylyl glycol, and water.
  • Vinyl caprolactam/VP/dimethylaminoethylmethacrylate copolymer one type being a nonionic polymer sold by International Specialty Products under the trademark Gaffix® VC-713 which comprises about 35-40% polymer and the remainder ethanol.
  • Sodium polystyrene sulfonate and PVP styrene copolymer one type being a mixture of anionic and nonionic polymers, such as those sold by National Starch Personal Care under the trademark Flexan® II and International Specialty Products under the trademark Antara® 430.
  • Figure 2 shows the effects achievable with Flexan® 11/ Antara® 430. Also useful is the mixture Flexan® 11/ Polectron® 430.
  • Polectron® 430 (from ISP) is a "cleaner" version of Antara® 430 in that the residual monomer level of Polectron® 430 is significantly lower than the residual monomer level of Antara® 430. For this reason, Polectron® 430 may be preferred over Antara® 430, for eye products or anytime that safety is an issue.
  • Another useful liquid contractile agent comprises a combination of Flexan® II and one or more clays. Specifically, Flexan® II with Laponite® clay.
  • Example I is a composition according to the present invention which achieves a high degree of curl.
  • compositions of the present invention 60-70% curling is achievable. Because the preferred compositions are aqueous and the liquid contractile agent is water soluble, the composition may be easily rinsed from the hair. This is especially useful, if too much composition is applied, and the user wants to start over. Another useful feature is that the composition can be applied over a previous, dried application, either hours or even days later.
  • Figure 3a is a photograph of an untreated eyelashes.
  • Figure 3b is an eyelash treated with mascara alone.
  • Figures 3c-3g show eyelashes treated with a composition according to the present invention.
  • Figure 3c is low curl
  • 3d is medium curl
  • 3e is high curl
  • 3f is extreme or excessive curl.
  • Figure 3g shows that mascara may be easily applied after the lashes have been curled according to the present invention. The mascara may add to the curl retention provided by the composition of the present invention, but the mascara is not required.
  • compositions of the present invention could refine compositions of the present invention to suit a particular user or classes of users.
  • Hair varies from person to person and ethic group to ethic group.
  • the parameters identified herein allow the present invention to be used by anyone.
  • differences in hair fiber structure and hair fiber chemistry between subpopulations i.e. differences in elastic modulus, surface tension, degree of cross linking
  • a critical feature of the invention is the step of applying the composition unevenly over the surface of one or more keratinous fibers so that sufficiently more of the composition is applied to one side of the fiber.
  • sufficiently more we mean that the excess curling composition on one side of a fiber is enough to curl the fiber toward that side, and the amount of curl is visible to the naked eye.
  • one side of the fiber receives at least twice as much curling composition as the opposite side of the fiber. More preferably, one side of the fiber receives at least three times as much curling composition as the opposite side.
  • one side of the fiber receives an effective amount of curling composition, and the opposite side of the fiber receives none.
  • a curling composition of the present invention should not be able to spread so easily, that it flows, via gravity, to the underside of the lashes.
  • a liquid contractile agent is applied to a portion of the keratinous fiber where it is desired to form a concave surface.
  • the contractile agent is applied to the upper surface of the upper eyelashes. This may be unusual for those mascara users who routinely apply mascara only to the undersides of the lashes.
  • Figure 4 shows application of the contractile agent composition to the upper surface of the upper eyelashes using a beaded applicator. While a beaded applicator is depicted in figure 4, any other applicator known to be effective in the hair care field, may be used to apply a composition of the present invention, including but not limited to those set forth in provisional application US61/085,140, herein incorporated by reference, in its entirety.
  • methods of the invention include the step of treating the hair fibers with a color or treatment product, prior to or after, the step of applying a liquid contractile agent.
  • the color product may be any type of mascara that does not interfere with the curling action of the liquid contractile agent.
  • the treatment product may be any product that does not interfere with the curling action of the liquid contractile agent, such as a lengthening or volumizing product.
  • the liquid contractile agent composition is translucent or transparent, to allow the color to show through.
  • the hair fibers are treated with a color or treatment product after the step of applying a liquid contractile agent.
  • the hair fibers are treated with a color or treatment product after the liquid contractile agent has dried on the hair fibers.
  • a user dips a mascara-type applicator into a vial of liquid contractile agent composition; draws the applicator out of the vial, through a wiper; draws the loaded applicator five times, over the top surface of her eyelashes; waits at least two minutes for the applied composition to curl the eyelashes and dry; applies eyeliner in her usual fashion; and applies mascara to the curled eyelash in her usual fashion.
  • Methods of the invention include applying a liquid contractile agent to the same hair fibers, one or more times per day.
  • the hair fibers may be rinsed or cleaned with water alone or with a mild, common cleanser, to remove residual liquid contractile agent from a previous application.
  • a mild, common cleanser is needed.
  • liquid contractile agent may be applied over a previous application of liquid contractile agent.
  • This is convenient for a user who applies a composition to her eyelashes, allows the composition to dry, and then realizes that she wants more curl in her lashes. Without having to clean the lashes, she simply applied another coat of the composition to gain even more curling. This process may be repeated until the used is satisfied with the curl.
  • a package of the invention provides a reservoir for storing and applying the contractile agent composition.
  • One embodiment of the invention is directed to a package for use in curling keratinous fibers containing a composition comprising a contractile agent and an applicator for application of the composition to a portion of the keratinous fibers in an amount sufficient to curl the fibers.
  • a user may quickly gain a feel for how much curling composition to apply, how many strokes are needed, how many times to dip the applicator, etc.
  • some guidance may be provided on a package in which the composition and/or applicator is sold.
  • a package for consumer sales that comprises a liquid contractile agent of the type described herein, and instructions for using the liquid contractile agent according to the methods disclosed herein, is novel and non-obvious over the prior art.
  • a reservoir that holds a curling composition may be a type that requires an applicator to be dipped into it, to retrieve some the composition.
  • it may be the type that is integrally connected to an applicator surface via a flow path from the reservoir to the applicator surface.
  • Various arrangements of these two systems are well known in the art.
  • compositions that curl keratinous fibers when applied to one side of the fibers were unknown. Methods associated with such compositions were also unknown.
  • the benefits achieved with the compositions and methods herein described were not previously achievable by other methods.
  • the main benefit is the ability to impart long lasting curl to keratinous fibers, in one-step, without heating the fibers and without subjecting the fibers to oxidation and reduction of protein bonds.
  • the compositions and methods are safe for use in the eye area.

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Abstract

L’invention concerne des compositions renfermant des matériaux qui présentent certaines propriétés de mouillage et de contractilité, telles que définies dans la description, qui sont capables de conférer une boucle de longue durée à des fibres kératiniques. La composition effectue le travail de bouclage après avoir été appliquée au cheveu. Les compositions ne sont appliquées que sur un côté des fibres capillaires. L’invention concerne également des procédés sûrs et efficaces pour boucler des fibres kératiniques, ainsi qu’un emballage de vente qui renferme une composition, un applicateur et des instructions pour boucler les fibres kératiniques.
PCT/US2009/049057 2008-07-31 2009-06-29 Compositions et procédés pour boucler des fibres kératiniques WO2010014328A2 (fr)

Applications Claiming Priority (2)

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US61/085,140 2008-07-31

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Cited By (10)

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WO2012059402A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour courber des fibres de kératine
WO2012059403A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour recourber des fibres de kératine
WO2012059404A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour courber des fibres de kératine
CN110339096A (zh) * 2019-08-15 2019-10-18 杭州海珠实业有限公司 一种具有粘接功能的眼线产品
WO2020047347A1 (fr) 2018-08-31 2020-03-05 L'oreal Kits pour l'application de compositions cosmétiques
US10835476B2 (en) 2017-11-29 2020-11-17 L'oreal Mascara compositions including vinylpyrrolidone homopolymer and inorganic particulate
US10987298B2 (en) 2018-06-29 2021-04-27 L'oreal Mascara compositions comprising a polymer having cyclic amide, cyclic amine and acrylamide functionality
US11033478B2 (en) 2017-11-29 2021-06-15 L'oreal Mascara compositions comprising a polymer having cyclic amide, cyclic amine and acrylamide functionality
US11065192B2 (en) 2017-11-29 2021-07-20 L'oreal Mascara compositions including vinylpyrrolidone homopolymer and an acrylic film-forming polymer
US11452684B2 (en) 2019-03-29 2022-09-27 L'oreal Mascara compositions and methods

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US5534247A (en) * 1993-03-25 1996-07-09 Maybelline Intermediate Co. Mascara composition
US6482400B1 (en) * 1999-06-30 2002-11-19 L'Oréal S.R. Mascara containing film-forming polymers
US6517823B1 (en) * 2000-01-27 2003-02-11 L'oreal S.A. High gloss mascara
US6534047B1 (en) * 1999-06-30 2003-03-18 L'oreal S.A. Mascara containing film-forming polymers

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US5534247A (en) * 1993-03-25 1996-07-09 Maybelline Intermediate Co. Mascara composition
US6482400B1 (en) * 1999-06-30 2002-11-19 L'Oréal S.R. Mascara containing film-forming polymers
US6534047B1 (en) * 1999-06-30 2003-03-18 L'oreal S.A. Mascara containing film-forming polymers
US6517823B1 (en) * 2000-01-27 2003-02-11 L'oreal S.A. High gloss mascara

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012059402A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour courber des fibres de kératine
WO2012059403A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour recourber des fibres de kératine
WO2012059404A1 (fr) 2010-11-05 2012-05-10 L'oreal Composition cosmétique et procédé pour courber des fibres de kératine
FR2967059A1 (fr) * 2010-11-05 2012-05-11 Oreal Composition cosmetique et procede de recourbement des fibres keratiniques
US10835476B2 (en) 2017-11-29 2020-11-17 L'oreal Mascara compositions including vinylpyrrolidone homopolymer and inorganic particulate
US11033478B2 (en) 2017-11-29 2021-06-15 L'oreal Mascara compositions comprising a polymer having cyclic amide, cyclic amine and acrylamide functionality
US11065192B2 (en) 2017-11-29 2021-07-20 L'oreal Mascara compositions including vinylpyrrolidone homopolymer and an acrylic film-forming polymer
US10987298B2 (en) 2018-06-29 2021-04-27 L'oreal Mascara compositions comprising a polymer having cyclic amide, cyclic amine and acrylamide functionality
WO2020047347A1 (fr) 2018-08-31 2020-03-05 L'oreal Kits pour l'application de compositions cosmétiques
US11452684B2 (en) 2019-03-29 2022-09-27 L'oreal Mascara compositions and methods
CN110339096A (zh) * 2019-08-15 2019-10-18 杭州海珠实业有限公司 一种具有粘接功能的眼线产品

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