MX2007003096A - Cosmetic or dermatologic compositions containing microspheres. - Google Patents
Cosmetic or dermatologic compositions containing microspheres.Info
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- MX2007003096A MX2007003096A MX2007003096A MX2007003096A MX2007003096A MX 2007003096 A MX2007003096 A MX 2007003096A MX 2007003096 A MX2007003096 A MX 2007003096A MX 2007003096 A MX2007003096 A MX 2007003096A MX 2007003096 A MX2007003096 A MX 2007003096A
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- 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
- A61K8/8164—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 carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0204—Specific forms not provided for by any of groups A61K8/0208 - A61K8/14
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- 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
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- 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
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; 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
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
The invention relates to cosmetic or dermatologic compositions comprising a microsphere and a film forming component.
Description
COSMETIC OR DERMATOLOGICAL COMPOSITIONS CONTAINING MICROSPHERES
FIELD OF THE INVENTION The present invention relates generally to cosmetic or dermatological compositions comprising a microsphere and a film-forming component. These compositions have improved cosmetic or dermatological properties and characteristics, such as, for example, increase in the length and / or volume of eyelashes, improvement in the retention of the shape or curl of the hair / eyelashes, opportunity that the hair or eyelashes are Form the original style without reapplying a styling composition of the hair or eyelashes and / or heat, or increasing the properties of transfer resistance, waterproofing and / or prolonged durability.
Background of the Invention Fixation of keratin materials such as hair and eyelashes in place is an important element in styling, and this generally comprises either fixing a shape that has already been styled, or forming and fixing simultaneous of the keratin material. While stylization compositions currently on the market are generally effective in retaining the REF material: 180579
Keratin in a desired shape or configuration, many are not designed to allow the style to be subsequently modified to a desired shape or to re-form the original style without re-applying a stylization and / or heat composition. Additionally, under various stress classes, the styles resulting from the use of conventional products have a tendency to take an undesirable permanent decoration, which can not be easily modified. U.S. Patent No. 6,548,051 and U.S. Patent Application Publication Nos. 2002/0059941 and 2006/0024255 address these drawbacks of the traditional stylizing composition by providing re-formable styling compositions of the hair. While there have been pioneering advances in hair styling products through the introduction of re-formable hair care systems, further improvement remains desirable. They are still respectable, if there are no high goals, additional advances in the adjustment of the degree of adhesion and in the improvement of the overall appearance, sensation and maneuverability of the hair. Accordingly, one aspect of the present invention is a care and / or make-up composition and / or treatment for keratin materials such as hair, eyelashes, skin, lips and nails which it is capable of coping with.
overcoming at least some of the problems generally associated with cosmetic or dermatological compositions, such as, for example, not allowing the reforming ability, poor resistance to transfer or adhesion, poor retention characteristics, etc.
Brief Description of the Invention The present invention relates to cosmetic or dermatological compositions comprising a microsphere and a film-forming component. The present invention relates to cosmetic or dermatological compositions that are free of, essentially free of, or substantially free of, non-adhesive particles comprising a microsphere and a film-forming component. The present invention also relates to compositions for eyelashes such as mascara, layers and bases comprising a microsphere and a film-forming component. The present invention also relates to hair compositions such as sprays, creams, styling gels, leave-on conditioners, shampoos, conditioners, permanent waving compositions, hair care products, hair treatment products, and hair care products. stylization of
hair comprising a microsphere and a film-forming component. The present invention also relates to compositions for skin or lips such as foundation, lipstick, liquid pencil color, layers or bases comprising a microsphere and a film-forming component. The present invention also relates to methods for improving the performance properties of compositions for keratin materials such as for example, resistance to transfer, prolonged durability and / or waterproofing, which comprises combining in a cosmetic or dermatological composition a microsphere and a film-forming component. The present invention also relates to methods for increasing the volume, strength and / or length of the eyelashes or hair, which comprises applying to the eyelashes or hair an effective amount in increasing the volume, strength and / or length of eyelashes or hair of a composition comprising a microsphere and a film-forming component. The present invention also relates to methods for styling a keratin material such as hair or eyelashes which comprises applying an effective amount to the keratin material to the stylization of the keratin material.
and a composition comprising a microsphere and a film-forming component. The present invention also relates to methods for re-styling, re-forming or repeatedly fixing a keratin material such as hair or eyelashes which comprises initially applying to the keratin material an effective amount in the styling of the keratin material of a composition comprising a microsphere and a film-forming component, and subsequently re-styling, re-forming or repeatedly fixing the keratin material without re-applying the composition to the keratin material. The present invention also relates to methods for retaining the shape or curl of a keratin material such as hair or eyelashes comprising applying to the keratin material an effective amount in retaining the shape or curl of a composition comprising a microsphere and a film-forming component. The present invention further relates to methods for applying keratin materials such as eyelashes, nails, skin or lips comprising applying an effective amount in eyelash, nail, skin or lip makeup of a composition comprising a microsphere and a forming component. from film, to eyelashes, nails, skin or lips in need of this makeup.
The present invention also relates to methods for treating or caring for keratin materials keratin materials such as eyelashes, nails, hair, skin or lips when applying the compositions of the present invention to the eyelashes, nails, hair, skin or lips in a enough to treat and / or care for the lashes, nails, hair, skin or lips. The present invention further relates to methods for improving the appearance of keratin materials such as eyelashes, nails, hair, skin or lips by applying compositions of the present invention to the eyelashes, nails, hair, skin or lips in a sufficient amount. to improve the appearance of eyelashes, nails, hair, skin or lips. In certain embodiments, the present invention facilitates the delivery of at least one desirable property such as, without limitation, reduced tactile tack, luster, gloss, silky feel or appearance to keratin materials. In a particularly preferred embodiment, the present invention provides formulations that facilitate the imparting of at least one desirable property to keratin materials such as hair and eyelashes such as, without limitation, reduced tactile tack, luster, gloss, silky feel and / or appearance , while maintaining substantially the fixability and capacity
of re-formation of keratin materials. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only, and are not restrictive of the invention.
Detailed Description of the Invention As used herein, the term "at least one" means one or more and thus includes individual components as well as mixtures / combinations. "Cosmetically acceptable medium" means a medium that is compatible with any keratin material, such as skin, hair, nails, eyelashes, eyebrows, lips and any other area of the body or facial skin. "Transfer resistance" as used herein refers to the quality exhibited by the compositions that are not easily removed by contact with another material, such as, for example, a lens, a cloth article or the skin, for example, when you eat or drink. Transfer resistance can be evaluated by any method known in the art for the evaluation thereof. For example, resistance to the transfer of a composition can be evaluated by a "kiss" test. The "kiss" test may include the application of the composition to human lips followed by the "kissing" a
material, for example, a sheet of paper, after the expiration of a certain amount of time after the application, such as 2 minutes after the application. Similarly, the transfer resistance of a composition can be evaluated by the amount of product transferred from a user to any other substrate, such as the transfer from the neck of an individual to a collar after the expiration of a certain amount of time. time after the application. The amount of compositions transferred to the substrate (e.g., collar or paper) can then be evaluated and compared. For example, a composition may be resistant to transfer, if a majority of the product is left on the user, for example, lips, neck, etc. Additionally, the amount transferred can be compared to that transferred by other compositions, such as commercially available compositions. The compositions of "prolonged durability" as used herein, refers to compositions where at least one chosen property of consistency, texture and color remains the same as at the time of application, as seen by the naked eye, after a period of time. prolonged time, such as, for example, 1 hour, 2 hours, and additionally such as 8 hours. The properties of prolonged durability can be evaluated by any method known in the art for
evaluate these properties. For example, prolonged durability can be evaluated by a test comprising the application of a composition to human skin (including the lips) and the evaluation of the consistency, texture and color of the composition after a prolonged period of time. For example, the consistency, texture and color of a lip composition can be evaluated immediately after application and these characteristics can then be re-evaluated and compared after an individual has used the lip composition for a certain amount of time. Additionally, these characteristics can be evaluated with respect to other compositions, such as commercially available compositions. "Impermeability" as used herein refers to the ability to repel water and permanence with respect to water. The waterproofing properties can be evaluated by any method in the art to evaluate these properties. For example, a mascara composition can be applied to false eyelashes, which can then be placed in water for a certain amount of time, such as, for example, 20 minutes. At the expiration of the pre-determined amount of time, false eyelashes can be removed from the water and passed over a
material, such as, for example, a sheet of paper. The extent of the residue left in the material can then be evaluated and compared with other compositions, such as, for example, commercially available compositions. Similarly, for example, a composition can be applied to the skin, and the skin can be immersed in water for a certain amount of time. The amount of composition that remains on the skin after the pre-determined amount of time can then be evaluated and compared. For example, a composition can be waterproof if the majority of the product is left on the user, for example, on the eyelashes, skin, etc. "Stickiness" as used herein refers to the measurement of the maximum tensile force, Fmax, required as long as the two surfaces are separated. Depending on the contemplated application and the formulation being designed, the desirable value for Fmax may vary · In some embodiments, the substantially non-tacky compositions have an Fmax of less than about 4 Newton (N), less than about 1 N, less of about 0.5 N, less than about 0.3 N, less than about 0.2 N or less than 0.1 N. A person skilled in the art can determine the Fmax of the composition
for example when determining the maximum tensile force, measured with a LLOYD type LR5K extensiometer, necessary to detach two surfaces. For example, two surfaces A and B of 38 mm2, which are solid, rigid, inert and non-absorbent, are mounted on movable mounts, which faces each other. Surfaces can move either by moving closer or farther away from each other, or one can move surface A independently of surface B or vice versa. Prior to insertion into the extensiometer, the surface A is coated with the composition to be measured, which can be dissolved in a solvent such as aqueous, hydroalcoholic, hydrocarbon, silicone and alcoholic solvents in a concentration of about 10 to about 30%, preferably 20%, the surface A is coated in a thickness of 1 to 10 thousandths of an inch (0.0254 to 0.254 mi), preferably 0.0254 mi (1 thousandth of an inch), and the surface is dried for 24 hours. hours at room temperature, for example 22 to 25 ° C, at a relative humidity of about 50%. Once inserted into the extensiometer, the surface A is subjected for 20 seconds to a compression force of 3 N against the surface B and then subjected for 30 seconds to the tensile force at a speed of 20 mm / minute. The amount of force, Fmax, necessary to obtain the initial separation is then signaled. An average Fmax is determined
carrying out the process with multiple pairs, preferably at least six pairs, of the surface A and the surface B. The term "re-formable" means to provide a hair style (fixability) and / or retention that can be re-stored or modify without additional material or that heat is applied. This does not mean that additional product and / or heat can be applied. It may be desirable to add additional heat and / or styling compositions in terms of speed, ease of use, if the hair becomes too wet or soiled, if it is combed in excess, if it is brushed or handled, washed, or when the hair it's going to re-stylize dramatically. At least some of the compositions according to the invention must be re-formable, as judged by a professional hair stylist of ordinary skill, for at least 4 hours and up to 24 hours or more after the initial application. Preferably and only as an example, in order to restore or modify the style of the hair in case of "fall" or loss of fixation (disorder), no new materials are required, such as water or any form of fixing agent or heat . Other terms that can be synonymous with deformable include relocatable, removable, re-stylizable, rearrangeable and removable. The term "reformable" also means providing a hair style that can retain
or maintaining a desired shape or configuration until water, heat, time and / or physical contact destroy the desired shape or configuration. The cosmetic compositions and methods of the present invention may comprise, consist of, or consist essentially of the essential materials and limitations of the invention described herein, as well as any additional or optional ingredients, components or limitations described herein or any other useful ingredient found in personal care compositions proposed for application to keratin materials. The composition of the present invention can be in any form. For example, it can be a paste, a solid or a cream. The composition of the invention can be transparent or clear, including for example, a composition without pigments. The composition can also be a molded or cast composition such as a bar or a disc. The composition in one embodiment is a solid such as a molded bar or a poured disk. The compositions of the present invention may be in the form of a lip composition such as a lipstick or liquid lip color, a foundation, a mascara product, a hair gel, a hair cream, or a hair spray (aerosol or non-aerosol).
As defined herein, stability is tested by placing the composition in a controlled environment chamber for 8 weeks at 25 ° C. In this test, the physical condition of the sample is inspected as it is placed in the chamber. The sample is then inspected again at 24 hours, 3 days, 1 week, 2 weeks, 4 weeks and 8 weeks. At each inspection, the sample is examined for compositional abnormalities such as phase separation if the composition is in the form of an emulsion. Stability is further tested by repeating the 8-week test at 40 ° C, 37 ° C, 45 ° C, 50 ° C and / or under freeze-thaw conditions. A composition is considered unstable if in any of these tests an abnormality is observed that impedes the functioning of the composition. The skilled person will easily recognize an abnormality that prevents the operation of a composition based on the proposed application.
Microsphere According to the present invention, compositions comprising at least one microsphere are provided. Preferably, the microspheres have adhesive properties and / or are not film forming agents. More preferably, the microspheres have adhesive properties and are not film forming agents. The
Suitable microspheres include, but are not limited to, Tac Gel microspheres (available from API) such as, for example, those found in the commercial products Gel Tac Gel Tac 100 A, Gel Tac 100 B, Gel Tac 100 C, Gel Tac 100 K and Tac 205 D Gel, as well as those microspheres described in United States Patent Application Publication Nos. 2006/0024255 and 2002/0041858, the complete contents of both of which are incorporated herein by reference. The microspheres of the present invention are preferably prepared by suspension polymerization of one or more free radical polymerizable monomers in the presence of surfactants, polymerization initiators and / or suspension stabilizers. More preferably, the microspheres are prepared by suspension polymerization of acrylic monomers in the presence of a polymerization initiator. Suitable methods for preparing the microspheres are described in U.S. Patent Number 3,691,140, U.S. Patent Number 4,166,152, U.S. Patent Number 4,495,318, U.S. Patent Number 4,598,112, U.S. Patent Number 4,786,696 , United States Patent Number 4,839,416, United States Patent Number 4,968,562, United States Patent Number 5,045,569, Patent of US Pat.
United States Number 5,571,617, United States Patent Number 5,409,977, United States Patent Number 5,656,705, United States Patent Number 5,719,247 and / or United States Patent Application Publication Number 2003/0109630, the complete contents of which are incorporated in this way as a reference. Preferably, monomers should be chosen to produce microspheres having a glass transition temperature (Tg) below -20 ° C. This choice of monomers provides the microspheres with improved adhesive properties. According to preferred embodiments, the microspheres are prepared by homo- or co-polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, acrylamides, acrylonitriles, pyrrolidones, vinyl esters, and mixtures thereof. same. For example, monomers that can be used to prepare the microspheres include, but are not limited to, alkyl acrylates such as butyl acrylate, ethyl acrylate, methyl acrylate, and 2-ethylhexylacrylate, alkyl methacrylates such as methacrylate, methyl and butyl methacrylate, polar comonomers such as acrylic acid, methacrylic acid, hydroxyethyl acrylate, hydroxypropyl acrylate, N-tertiary octylacrylamide, acrylonitrile, arrylamide, l-vinyl-2-
pyrrolidone, sodium vinyl sulfonate, vinyl esters such as vinyl acetate, vinyl propionate, vinyl neodecanoate, vinyl stearate and vinyl pivalate. Crosslinking monomers such as, for example, butanediol diacrylate and hexanediol diacrylate can also be used. Other useful monomers and combinations thereof that can be used in the practice of the invention will be apparent to the person skilled in the art. Polymerization initiators useful in the polymerization of microspheres include, but are not limited to, dialkyl peroxides such as lauroyl peroxide (Laurox from Akzo Novel), diacyl peroxides such as dibenzoyl peroxide (Lucidol A75 from Elf Atochem), peroxyesters such as t-amyl-peroxypivalate (Lupersol 554-M50 from Elf Atochem), t-butyl-peroctoate (Luperox 26 from Elf Atochem and Trigonox 21 from Akzo Chemicals), azo compounds such as 2, 2'-azobis (isobutyronitrile) (VAZO 64) and 2, 2'-azobis (2-methylbutanonitrile) (VAZO 67), and .2, 2'-azobiñ (2,4-dimethylpentanenitrile) (VAZO 52), all from DuPont. Other initiators and combinations thereof that can be used in the practice of the invention will be apparent to one skilled in the art. According to particularly preferred embodiments of the present invention, 2-ethylhexyl acrylate (monomer) and t-butylperoctoate (as initiator) are used for
preparing the microspheres as described in U.S. Patent Application Publication No. 2003/0109630, the entire contents of which are hereby incorporated by reference. The microspheres of the present invention can be of widely varied forms such as spheres, spheroids, platelets, and irregularly shaped particles. The size of the microspheres is usually described in terms of their length and / or width. In the context of the present invention, "length" of the microsphere is proposed to mean the maximum possible distance to be measured by appropriate microscopy techniques, between two opposite points of the microsphere. The "width" of the microsphere is proposed to mean the minimum possible distance to be measured by appropriate microscopy techniques, between two opposite points of the microsphere. In one embodiment, the microspheres have a length to width ratio of greater than or equal to about 1: 1. In another embodiment, the microspheres have an average length of from about 1 to about 1000 microns, preferably from 1 to less than 30 microns, preferably from 30 to 1000 microns, preferably from 30 to 100 microns, and so more preferably from about 30 to about 50 microns. The
The average length of the microspheres can be measured by the following methods: optical microscopy, sieving, sedimentation, radiant diffusion, absorption, Coulter principle, laser light diffraction, X-ray, and perceptual zone method, which are described by Clyde Orr , "Size Measurement of Particles", in Kirk-Othmer Encyclopedia of Chemical Technology, vol. 21, pp. 106-131 (3rd ed. 1983) and by Ferry Alien, "Analyze et Characterization, Technique de I'ingenieur" in Etudes de Structure-Granulometrie, vol. 12, pp. 1040-9 to 1040-26 (1996). In one embodiment, optical microscopy is used to determine the average length of the microsphere. Preferably, the microspheres are present in an amount ranging from about 0.5% to about 40% by weight of the total weight of the composition, more preferably from about 1% to about 30% of the total weight of the composition, more preferably from about 2% to about 20% of the total weight of the composition, and more preferably from about 3% to about 15%, including all ranges and sub-ranges therebetween.
Film Forming Component According to the present invention, there are provided
compositions comprising a film-forming component. The film-forming component comprises at least one film-forming agent, perhaps two, three or more film-forming agents. In a preferred embodiment, a film-forming agent is present. In another preferred embodiment, two film-forming agents are present. Any substance capable of forming a film in application to keratin materials and having a glass transition temperature (Tg) can be used as a film-forming agent according to the present invention. Although not wishing to be bound by any particular theory, it is believed that the film-forming component according to the present invention provides a matrix-like environment in or around the keratin materials, and that this environment allows the microspheres to remain in or around the keratin materials and impart their characteristics in the keratin materials for a prolonged period of time. Thus, according to preferred embodiments of the present invention, sufficient film-forming component is present in the compositions of the invention to improve and / or lengthen the effect of the microspheres in the keratin materials to which the materials have been applied. compositions It is also believed that the film-forming component improves the
cosmetic effects of compositions containing microspheres. For example, the film-forming component of the present invention reduces the tackiness of the compositions containing microspheres of the present invention. According to preferred embodiments, the film-forming component comprises at least two film-forming agents. In these embodiments, the at least two film-forming agents are preferably chosen to create an environment that enhances and / or lengthens the effect of the microspheres in the keratin materials to which the compositions of the present invention have been applied. , and what improves the cosmetic properties of the compositions of the present invention. According to this embodiment, the at least two film-forming agents have substantially different vitreous transition temperatures (Tg). For example, the Tg's of the two film-forming agents differ by at least about 20 ° C, 30 ° C, 40 ° C, 50 ° C, 60 ° C, 70 ° C, 80 ° C, 90 ° C, including all the intervals and sub-intervals between these. More preferably, a film-forming agent has a Tg below about -20 ° C and the other film-forming agent has a Tg above about 0 ° C. According to this other modality, one of the
Film-forming agents possess a glass transition temperature (Tg) that is greater than 0 ° C, while the other film-forming agent has a Tg that is less than 0 ° C. Examples of Tg for film-forming agents above 0 ° C include, without limitation, 10 ° C, 20 ° C, 30 ° C, 40 ° C, 50 ° C, 60 ° C, 70 ° C. , 80 ° C, 90 ° C, including all the intervals and sub-intervals between them. Examples of Tg for film-forming agents below 0 ° C include, without limitation, -10 ° C, -20 ° C, -30 ° C, -40 ° C, -50 ° C, -60 ° C. C, -70 ° C, -80 ° C, -90 ° C, including all the intervals and sub-intervals between them. According to other preferred embodiments, the film-forming component comprises at least one film-forming agent. In a particularly preferred embodiment, the Tg of a film-forming agent is less than 0 ° C. Examples of Tg for film-forming agents below 0 ° C include, without limitation, -10 ° C, -20 ° C, -30 ° C, -40 ° C, -50 ° C, -60 ° C. C, -70 ° C, -80 ° C, -90 ° C, including all the intervals and sub-intervals between them. In these embodiments, at least one film-forming agent is preferably chosen to create an environment that enhances and / or lengthens the effect of the microspheres in the keratin materials to which the compositions of the present invention have been applied,
and / or improving the cosmetic properties of the compositions of the present invention. Suitable film-forming agents for use in accordance with the present invention include, without limitation, polyorganosiloxane-containing polymers such as polysilicon-polyamides or polysilicon-polyurethanes; silicone resins (preferably MK or MQ resins), silicone / (meth) acrylate copolymers, acrylates / dimethicone copolymers, liquid siloxy silicates and silicone-esters such as those described in U.S. Patent No. 5,334 , 737, the description of which is thus incorporated by reference, silicone polymers comprising a chosen structure of vinyl polymers, metacrylic polymers, and acrylic polymers and at least one chain chosen from pendant siloxane groups and pendant fluorochemical groups, such as those described in U.S. Patent Nos. 5,209,924 and 4,972,037, and in WO 01/32737, the descriptions of which are hereby incorporated by reference in their entirety, a copolymer selected from vinyl-graft copolymers. silicone such as those polymers described in U.S. Patent No. 5,468,477, the full disclosure of which is incorporated in this way as a reference. The film-forming agents suitable for
use in accordance with the present invention is also described in United States Patent Application Publication No. 2004/0170586, the entire contents of which are hereby incorporated by reference. According to particularly preferred embodiments, at least one of the film-forming agents is a polymer prepared by polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, and mixtures thereof. According to more preferred embodiments, both film-forming agents are polymers prepared by polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid and mixtures thereof. Suitable examples of these film-forming agents include, but are not limited to, acrylic or vinyl-acrylic polymers, emulsion polymerized, water based which are pressure sensitive adhesives, ethylene-vinyl acetate emulsions. , polyurethane dispersions and natural rubber latex. Specific examples include, without limitation, Carbotac 26222 (BF Goodrich), Nacrylic 78-6408 (National Starch and Chemical), Rhoplex N580 (Rohm and Haas), Acronal NV 146CR (BASF), Acronal NV 155CR (BASF) ), Acronal NV 189CR (BASF), Acronal NV 162CR (BASF), Acronal NN 171CR
(BASF), Acronal NA 182CR (BASF), NACRYLIC CP3600 (National Starch), NACRYLIC CP2550 (National Starch), NACRYLIC CP3650 (National Starch), Luphen D259U (BASF), DUROSET C-325 (National Starch), RESYN 1025 ( National Starch), and DUROSET E-200 (National Starch). According to more preferred embodiments, the film-forming agents are compatible / miscible with the microspheres, and are compatible / miscible with each other if more than one is present. According to preferred embodiments, the film-forming component is present in the composition in an amount ranging from 0.3% to 50% by weight relative to the total weight of the composition. Preferably, the film-forming component is present in an amount ranging from 1.0 to 40% by weight relative to the total weight of the composition, more preferably from 2% to 30%. One skilled in the art will recognize that these weight percentages are based on dry weight of the film-forming agents, and that the film-forming agents of the present invention can be commercially available from suppliers in the form of a diluted solution. The amounts of the film-forming agent described herein therefore reflect the weight percent of the active material. According to preferred modalities, where are
present two film-forming agents, the ratio of the first film-forming agent to the second film-forming agent is between about 1:10 to 20: 1, about 1:10 to 10: 1, about 1: 5 to 5: 1, including all the intervals and sub-intervals between these. In accordance with the present invention, microspheres and the film-forming component can be added to the composition during the preparation simultaneously or separately. According to particularly preferred embodiments of the present invention, the microspheres and the film-forming component are added simultaneously, more preferably in the form of a composition containing microspheres and a suitable film-forming component such as the compositions described in the publication of patent application number 2003/0109630, the complete contents of which are incorporated in this way as reference. Suitable examples of compositions containing microspheres and a suitable film-forming component are Multi-Lok 38-454A (National Starch).
Dyeing Agents According to the present invention, the compositions may optionally comprise at least one coloring agent. Suitable coloring agents include
enunciatively and without limitation pigments (both goniochromatic and monochromatic), dyes, such as liposoluble dyes, pearlescent pigments, and pearlescent agents. Typically, when the composition contains colorants, it is a coloring composition such as mascara, lipstick or foundation. Alternatively, when the composition does not contain colorants, it is a clear or transparent composition that can be used as a base (or layer) before (or after) the application of a coloring composition to keratin materials. However, it is possible that the layers or bases may contain colorants. Representative liposoluble dyes that can be used according to the present invention include Sudan red, DC 17 red, DC 6 green, β-carotene, soybean oil, Sudan coffee, DC 11 yellow, DC 2 violet, DC 5 orange, achiote and quinoline yellow. The fat-soluble dyes, when present, generally have a concentration that varies up to 20% by weight of the total weight of the composition, such as from 0.0001% to 6%. The pearlescent pigments that can be used according to the present invention can be chosen from white pearlescent pigments such as titanium-coated mica or bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica.
with ferric blue or chromium oxide, titanium mica with an organic pigment chosen from those mentioned above, and pearlescent pigments based on bismuth oxychloride. The pearlescent pigments, if present, are present in the composition in a concentration ranging up to 50% by weight of the total weight of the composition, such as from 0.1% to 20%, preferably from 0.1% to 15%. The pigments, which can be used according to the present invention, can be chosen from white, colored, inorganic, organic, polymeric, non-polymeric, coated and uncoated pigments. They may be monochromatic or goniochromatic (e.g., a multilayer interference structure) such as those described in U.S. Patent No. 6,451,294, the entire disclosure of which is incorporated herein by reference. Representative examples of mineral pigments include titanium dioxide, optionally surface treated, zirconium oxide, zinc oxide, cerium oxide, iron oxide, chromium oxide, manganese violet, ultramarine blue, chromium hydrate, and blue ferric. Representative examples of organic pigments include carbon black, D & C, and lacquers based on cochineal carmine, barium, strontium, calcium, and aluminum. If present, the pigments may be present in the composition in a concentration that varies
up to 50% by weight of the total weight of the composition, such as from 0.5% to 40%, and additionally such as from 2% to 30%. In the case of certain products, the pigments, including pearlescent pigments, may represent, for example, up to 50% by weight of the composition. According to particular aspects of the present invention, the compositions may be in the form of an emulsion. Suitable emulsion forms include, without limitation, oil in water emulsion, water in oil emulsion, oil in water and oil emulsion, water in oil and water emulsion, and nanoemulsions (emulsions whose oil globules are a very fine particle size, that is, they have an average size in number of less than about 100 nanometers (nm)). The emulsions contain at least one oil phase and at least one aqueous phase. Generally speaking, the emulsions contain surfactant-like materials or surfactant-like materials that provide stability to the emulsions and inhibit phase separation of the emulsions.
Additional ingredients The compositions of the present invention can also comprise any additive usually used in the field under consideration. For example, dispersants, antioxidants, essential oils, agents can be added
preservatives, fragrances, liposoluble polymers that can be dispersed in the medium, fillers, neutralizing agents, cosmetic and dermatological active agents such as, for example, emollients, humectants, vitamins, anti-wrinkle agents, essential fatty acids, sunscreens and mixtures thereof. A non-exhaustive listing of these ingredients can be found in U.S. Patent Application Publication No. 2004/0170586, the entire contents of which are incorporated herein by reference. Additional examples of suitable additional components can be found in the other references that have been incorporated by reference in this application, including, without limitation, requests from which this request claims priority. Even further examples of these additional ingredients can be found in the International Cosmetic Ingredient Dictionary and Handbook (9-th edition 2002). One skilled in the art will take care to select the optional additional additives and / or the amounts thereof such that the advantageous properties of the composition according to the invention are not, or are not substantially, adversely affected by the contemplated addition. . These substances can be selected in a
varied by the person skilled in the art in order to prepare a composition having the desired properties, for example, consistency or texture. These additives may be present in the composition in a proportion of 0% to 99% (such as from 0.01% to 90%) relative to the total weight of the composition and additionally such as from 0.1% to 50% (if present) . Needless to say, the composition of the invention must be cosmetically or dermatologically acceptable, that is, it must contain a non-toxic, physiologically acceptable medium and must be capable of being applied to the eyelashes of human beings. For the purposes of the invention, the term "cosmetically acceptable" means a composition of appearance, odor, sensation and / or pleasant taste. In particular, with respect to compositions for application to hair and / or eyelashes, additional optional ingredients include but are not limited to those ingredients set forth in U.S. Patent No. 6,548,051 and U.S. Patent Application Publication Numbers. 2002/0059941 and 2006/0024255, the complete contents of which are incorporated in this way as reference. Examples of these additional ingredients include, but are not limited to, adhesive particles, non-adhesive particles, fixing polymers, and propellants (for
aerosol compositions). However, in a particularly preferred embodiment of the invention, there is provided a cosmetic or dermatological composition that is free of, essentially free of, or substantially free of, non-adhesive particles. By "free of non-adhesive particles", it is meant that no non-adhesive particles are present in the composition. By "essentially free of non-adhesive particles", it is meant that less than 0.01% of non-adhesive particles are present in the composition. By "substantially free of non-adhesive particles", it is meant that less than 0.03% of non-adhesive particles are present in the composition. As used herein, a "non-adhesive" particle is a particle that is not coated with an adhesive as described in U.S. Patent No. 6,548,051, U.S. Patent Application Publication Number 2002/0059941 and U.S. Patent Application Publication Number 2006/0024255. More specifically, a non-adhesive particle is a discrete substrate which is not an adhesive and is not coated with an adhesive coating in whole or in part, and does not comprise an adhesive such as a core or cover material when it is in a structure of core / cover. Specific examples of additional ingredients include oils, particularly if the
The composition is an anhydrous composition or an emulsion. Any oil according to the present invention can be used. The oils can be volatile or non-volatile, based on silicone and / or based on hydrocarbon, etc. Thus, for example, the external oil phase may contain, independently or in combination, volatile silicone oils, non-volatile silicone oils, volatile non-silicone oils and non-volatile non-silicone oils. In one embodiment, the compositions of the present invention are substantially free of silicone oil (ie, they contain less than about 1% silicone oil). In another embodiment, the compositions are substantially free of non-silicone oils (i.e., they contain less than about 1% non-silicone oil). In another embodiment, the compositions are substantially free of non-volatile oils (i.e., they contain less than about 1% of the non-volatile oil). In yet another embodiment, the compositions are substantially free of volatile oils (i.e., they contain less than about 1% volatile oil). According to one embodiment, the oil phase may contain one or more volatile silicone oils. Examples of these volatile silicone oils include linear or cyclic silicone oils that have a
viscosity at room temperature less than or equal to 6cSt and having from 2 to 7 silicon atoms, these silicones which are optionally substituted with alkyl or alkoxy groups of 1 to 10 carbon atoms. Suitable oils that can be used in the invention include octamethyltetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, heptamethyloctyltrisiloxane, hexamethyldisiloxane, decamethyltetrasiloxane, dodecamethylpentasiloxane and mixtures thereof. Other volatile oils that can be used include KF 96A with a viscosity of 6 cSt, a commercial product of Shin Etsu having a flash point of 94 ° C. Preferably, volatile silicone oils have a flash point of at least 40 ° C. Non-limiting examples of volatile silicone oils are listed in Table 1 below. Table 1 Compound Viscosity Point Inflammation (cSt) (° C) Octyltrimethicone 93 1.2
Hexyltrimethicone 79 1.2
Decamethylcyclopentasiloxane 72 4.2
(cyclopentasiloxane or D5)
Octamethylcyclotetrasiloxane 55 2.5
(cycotetradimethylsiloxane or D4) Dcdecamethylcyclohexasiloxane (D6) 93 7 Decamethyltetrasiloxane (L4) 63 1.7
KF-96 A from Shin Etsu 94 6 PDS (polydimethylsiloxane) DC 200 (1.5 56 1.5 cSt) from Dcw Corning PDMS DC 200 (2cSt) from Dow Corning 87 2 PDMS DC 200 (5cSt) from Dow Coming 134 5 PDMS DC 200 ( 3St) from Dow Corning 102 3
Additionally, a volatile linear silicone oil may be employed in the compositions of the present invention. Suitable volatile silicone linear oils include those described in U.S. Patent No. 6,338,839 and WO 03/042221, the contents of which are incorporated herein by reference. In one embodiment, the volatile silicone linear oil is decamethyltetrasiloxane. In another embodiment, the decamethyltetrasiloxane is further combined with another solvent that is more volatile than decamethyltetrasiloxane. The volatility of the solvents / oils can be determined using the evaporation rate as set forth in U.S. Patent No. 6,338,839. Examples of other silicone oils that can be used in the invention include non-volatile linear polydimethylsiloxanes (PDMS), which are liquid at room temperature; polydimethylsiloxanes
comprising alkyl, alkoxy or phenyl groups, which are pendant and / or at the end of a silicone chain, these groups each contain from 2 to 24 carbon atoms; phenylsilicon, for example phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes and 2-phenylethyltrimethylsiloxysilicates. According to other preferred embodiments, the oil phase may contain one or more volatile non-silicone oils and may be selected from volatile hydrocarbon oils, alcohols, volatile esters and volatile ethers. Examples of these volatile non-silicone oils include, but are not limited to, volatile hydrocarbon oils having from 8 to 16 carbon atoms and mixtures thereof and in particular branched Ci to C6 alkanes such as isoalkanes from Q to Ci6. (also known as isoparaffins), isododecane, isodecane, isohexadecane, and for example, oils sold under the trade names of Isopar or Permethyl, the branched esters of Cs to Ci6 such as isohexyl or isodecyl neopentanoate and mixtures thereof. Preferably, volatile non-silicone oils have a flash point of at least 40 ° C.
Table 2 Compound Flash point (° C) Isododecane 43 Isohexadecane 102 Isodecyl-neopentanoate 118 N-butyl propylene glycol 60 ethyl 3-ethoxypropionate 58 Methyl ether of propylene glycol 46 Isopar L (isoparaffin C11-C13) 62 Isopar H (isoparaffin C11-C12) 56
Examples of other non-silicone oils that can be used in the compositions of the present invention include polar oils such as: - vegetable oils based on hydrocarbons with a high content of triglycerides consisting of fatty acid esters of glycerol, fatty acids of which may have varying lengths of chain, these chains that are possibly linear or branched, and saturated or unsaturated; These oils are especially wheat germ oil, corn oil, sunflower oil, kárite butter, castor oil, sweet almond oil, macadam oil, apricot oil, soybean oil,
turnip, cottonseed oil, alfalfa oil, poppy oil, pumpkin oil, sesame oil, zucchini oil, avocado oil, hazelnut oil, grapeseed oil, black currant oil, spring oil, millet oil , barley oil, quinoa oil, olive oil, rye oil, safflower oil, sweet walnut oil, passion flower oil or musk rose oil; or triglycerides of caprylic / capric acid, for example those sold by the company Stearineries Dubois, or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel; synthetic oils or esters of the formula R5COOR6, in which R5 represents a linear or branched higher fatty acid residue containing from 1 to 40 carbon atoms, including and even better from 7 to 19 carbon atoms, and R6 represents a branched hydrocarbon-based chain containing from 1 to 40 carbon atoms, including and even better from 3 to 20 carbon atoms, with R6 + R7 = 10, such as, for example, Purcellin oil (ketostearyl octanoate), isononyl isononanoate, C12 to C15 alkyl benzoate, isopropyl myristate, 2-ethylhexyl palmitate; and octanoates, decanoates or ricinoleates of alcohols or polyalcohols; hydroxylated esters, for example isostearyl lactate or diisostearyl malate; and esters of
pentaerythritol: - synthetic ethers containing from 10 to 40 carbon atoms; - fatty alcohols of Cs to C26 for example oleyl alcohol; and - mixture thereof. Preferably, the oils, if present, represent from about 5% to about 80% by weight of the total weight of the composition, more preferably from about 10% to about 60% of the total weight of the composition, and most preferably from about 15% to about 50%, including all ranges and sub-intervals therebetween. The water, when present, preferably represents from about 1% to about 70% by weight of the total weight of the composition, more preferably from about 5% to about 60% of the total weight of the composition, and so more preferably from about 10% to about 50%, including all ranges and sub-ranges therebetween. According to preferred embodiments, methods are provided to improve the performance properties of compositions for keratin materials such as, for example, transfer resistance,
prolonged durability and / or impermeability, comprising combining in a cosmetic or dermatological composition a microsphere and a film-forming component. The compositions can be applied to the keratin materials as needed, preferably once or twice daily, more preferably once a day and then preferentially allowed to dry before being subjected to contact such as with clothing or other objects. According to particularly preferred embodiments, sufficient microspheres are combined with sufficient film-forming component such that the performance properties of the compositions are greater than the performance properties of the compositions containing any ingredient individually. Thus, according to these particularly preferred embodiments, the compositions for keratin materials contain an effective amount improving the transfer resistance, prolonged durability and / or impermeability of microspheres and / or the film-forming component. According to other preferred embodiments, methods are provided for increasing the volume, strength and / or length of the eyelashes or hair that comprises applying to the eyelashes or hair an effective amount to increase the volume, strength and / or length of the lashes.
eyelashes or hair of a composition comprising a microsphere and a film-forming component. The compositions can be applied to keratin materials as needed, preferably once or twice per day, more preferably once per day and then preferably let dry before submitting to contact such as with clothes or other objects. According to still other embodiments of the present invention, methods are provided for styling a keratin material such as hair or eyelashes which comprises applying to the keratin material an amount effective in styling the keratin material of a composition comprising a microsphere and a film-forming component. In accordance with other embodiments of the present invention, there are provided methods for re-stylizing, reforming or repeatedly fixing a keratin material such as hair or eyelashes comprising initially applying to the keratin material an effective amount in styling the keratin material. of a composition comprising a microsphere and a film-forming component, and subsequently re-styling, reforming or repeatedly fixing the keratin material without reapplying the composition to the keratin material. According to preferred embodiments,
provide methods for retaining the shape or curl of a keratin material such as hair or eyelashes comprising applying to the keratin material an effective amount in retaining the shape or curl of a composition comprising a microsphere and a film-forming component. According to other embodiments of the present invention, methods are provided for machining keratin materials such as eyelashes, nails, skin or lips which comprises applying an effective amount in eyelash, nail, skin or lip makeup of a composition comprising a microsphere and a film-forming component, to the eyelashes, nails, skin or lips in need of this makeup. According to still other embodiments, methods are provided for treating or caring for keratin materials such as eyelashes, nails, hair, skin or lips when applying compositions of the present invention to the eyelashes, nails, hair, skin or lips in a sufficient amount. to treat and / or care for lashes, nails, hair, skin or lips. According to other preferred embodiments, methods are provided for improving the appearance of keratin materials such as eyelashes, nails, hair, skin or lips by applying compositions of the present invention to the eyelashes, nails, hair, skin or lips in a
enough to improve the appearance of eyelashes, nails, hair, skin or lips. According to the above preferred embodiments, the compositions of the present invention are applied topically to keratin materials in an amount sufficient to treat, care for and / or machine the keratin materials, or to improve their appearance. The compositions can be applied to tabs as needed, preferably once or twice daily, more preferably once daily and then preferably allowed to dry before being subjected to contact such as with clothing or other objects. The present invention also contemplates pre-packaged equipment and / or materials suitable for use by the consumer that contain one or more compositions according to the description herein (e.g., equipment containing (1) a mascara; ) a base and / or layer). The packaging and application device for any object of the invention can be chosen and manufactured by persons skilled in the art on the basis of their general knowledge, and adapted according to the nature of the composition to be packaged. In fact, the type of device to be used can be linked in a particular way to the consistency of the composition, in particular to its viscosity; It may also depend on the nature of the
constituents present in the composition, such as the presence of volatile compounds. Unless otherwise indicated, all numbers expressing amounts of ingredients, reaction conditions, and others used in the specification and claims will be understood as being modified in all cases by the term "approximately". Accordingly, unless otherwise indicated, the numerical parameters set forth in the following specification and claims are approximations that may vary depending on the desired properties sought by the present invention. Although approximations are the numerical ranges and the parameters that expose the broad scope of the invention, the numerical values set forth in the specified examples are reported as precisely as possible. However, any numerical value inherently contains certain errors necessarily resulting from the standard deviation found in their respective measurements. The following examples are proposed to illustrate the invention without limiting the scope as a result. The percentages are given on a weight basis. Example 1. Microspheres A. Ingredients that can be used to prepare microspheres by suspension polymerization with free radicals according to the patent application publication
United States number 2003/0109630
B.- Formulation of Multi-Lok 38-454A
Example 2 A.- Preparation of composition (Cream) Ingredient Percentage
Multi-Lok 38-454A 2.35%
Empicol BSD 52 * (surfactant 0.19%
Water DI 91.46%
Propeller A-46 6.00%
* Empicol BSD 52 contains laureth-8-sodium sulfate, sodium laureth sulfate, magnesium laureth-8-sulfate, magnesium laureth sulfate, sodium oleth sulfate, magnesium oleth sulfate. The aqueous phase was prepared by dissolving the surfactant in deionized water under appropriate stirring speed. Then, the polymer (optional - not present in Example A) was added and mixed well. Finally, Multi-Lok 38-454A was added dropwise under continuous stirring. 94 parts of the aforementioned aqueous phase were mixed with 6 parts of propellant A-46 in an aerosol bottle [Lata: Exal PAM 2P 8460 N (50 x 125); Valve: YL31974; Actuator: Mars] B. - Application: 2 g of cream was applied in 1/2 of the head of wet hair, followed by blow-drying. C. - Evaluation: The composition provided good retention and re-training capacity. Example 3 The following compositions were prepared according to the procedures set forth in Example 2.
Formula A
Formula B Ingredient Percentage e
Multi-Lok 38-454A 2.00% (acrylic copolymer) (National Starch) Empicol BSD 52 0.19%
Syntran 5760 1.41%
(styrene / acrylate / ammonium methacrylate copolymer) (Interpolymer; Tg: 19 ° C) Water DI 90.40%
Propellant A-46 6.00% (isobutane / propane)
Formula C Ingredient Percentage e
Multi-Lok 38-454A 2.00% (acrylic copolymer) (National Starch) Empicol BSD 52 0.19%
Copolymer 845 1.41%
(Vinylpyrrolidone / dimethylaminoethylmethacrylate) (ISP; Tg: 175 ° C) Water DI 90.40%
Propeller A-46 6.00%
(isobutane / propane)
Formula D Ingredient Percentage
Multi-Lok 38-454A 2.00% (acrylic copolymer) (National Starch) Empicol BSD 52 0.20%
Aculyn 88 0.75%
(acrylate / steareth-20-methacrylate crosslinked polymer) (ROHM &HAAS; Tg: 24 ° C as supplied, and 54 ° C
when hydrolyzed at pH = 7.0) Water DI 91.05%
Propeller A-46 6.00%
(isobutane / propane)
Formula E Ingredient Percentage
Multi-Lok 38-454A 1.88% (acrylic copolymer) (National Starch) Empicol BSD 52 0.20%
Luviset Clear 0.94%
(vinylpyrrolidone / methacrylamide / N-vinylimidazole copolymer) (BASF, Tg: 219 ° C, dry film, 85 ° C at 52% relative humidity, 51 ° C at 76% relative humidity) DI Water 90.98%
Propeller A-46 6.00%
(isobutane / propane) These compositions were applied to damp hair, followed by blow-drying. Like the composition in Example 2, these compositions provided good retention and re-formation ability. Also, the arrangements provided hair with a smooth, non-sticky feel.
It is noted that in relation to this date, the best method known to the applicant to practice said invention is that which is clear from the present description of the invention.
Claims (23)
- CLAIMS Having described the invention as above, the content of the following claims is claimed as property: 1. Composition, characterized in that it comprises a cosmetically acceptable medium, an adhesive microsphere and a film-forming component.
- 2. Composition in accordance with the claim 1, characterized in that the film-forming component comprises at least two film-forming agents.
- 3. Composition in accordance with the claim 2, characterized in that the Tg of at least two film-forming agents are separated by at least about 20 ° C.
- 4. Composition in accordance with the claim 2, characterized in that the Tg of at least two film-forming agents are separated by at least about 60 ° C.
- Composition according to claim 2, characterized in that the Tg of one of the two film-forming agents is above 25 ° C and the Tg of the other of the two film-forming agents is below 25 ° C.
- 6. Composition according to claim 1, characterized in that the composition comprises from about 0.3% to about 50% of the film-forming component on a dry weight basis with respect to the total weight of the composition.
- 7. Composition in accordance with the claim 1, characterized in that the composition comprises from about 2% to about 30% of the film-forming component on a dry weight basis with respect to the total weight of the composition.
- 8. Composition in accordance with the claim 2, characterized in that the composition of the first film-forming agent to the second film-forming agent is 1:10 to 20: 1.
- Composition according to claim 1, characterized in that the adhesive microsphere is prepared by polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, arrylamides, acrylonitriles, pyrrolidones, vinyl- esters, and mixtures thereof.
- Composition according to claim 1, characterized in that the adhesive microsphere is prepared by polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, and mixtures thereof.
- 11. Composition according to claim 1, characterized in that the adhesive microsphere is prepared by polymerization of ethexyl lacrylate.
- Composition according to claim 2, characterized in that at least one of the film-forming agents is a polymer prepared by polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, and mixtures thereof .
- 13. Composition according to claim 2, characterized in that both film-forming agents are polymers prepared with polymerization of monomers selected from the group consisting of acrylates, methacrylates, acrylic acid, methacrylic acid, and mixtures thereof.
- 14. Composition according to claim 1, characterized in that the composition further comprises at least one sun blocking agent, at least one pigment or mixture thereof.
- 15. Composition according to claim 1, characterized in that the composition is essentially free of non-adhesive particles.
- 16. Composition according to claim 1, characterized in that the microsphere adhesive has an average length of about 30 to about 1000 microns.
- 17. Composition according to claim 1, characterized in that the adhesive microsphere has an average length of about 30 to about 100 microns.
- Method for styling a keratin material, characterized in that it comprises applying to the keratin material an amount effective to stylize the keratin material of a composition comprising a cosmetically acceptable medium, an adhesive microsphere, and a film-forming component.
- 19. Method according to claim 18, characterized in that the keratin material is hair.
- Method according to claim 18, characterized in that the keratin material is a flange.
- 21. Method for retaining the shape or curl of a keratin material, characterized in that it comprises applying to the keratin material an effective amount of shape retention or curl of a composition comprising a cosmetically acceptable medium, an adhesive microsphere and a forming component. movie .
- 22. Method according to claim 21, characterized in that the keratin material is hair.
- 23. Method according to claim 21, characterized in that the keratin material is a flange.
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US11/500,344 US20070224140A1 (en) | 2006-03-21 | 2006-08-08 | Cosmetic or dermatologic compositions containing microspheres |
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FR2946871B1 (en) * | 2009-06-19 | 2013-01-04 | Oreal | PROCESS FOR MAKEING KERATIN FIBERS |
US20110212145A1 (en) * | 2010-03-01 | 2011-09-01 | Honeywell International Inc. | Hair fixatives comprising cross linked starches |
JP6723771B2 (en) * | 2016-03-10 | 2020-07-15 | ジャパンコーティングレジン株式会社 | Acrylic resin emulsion for hairdressing agent and method for producing the same, and hairdressing agent and method for producing the same |
US11033478B2 (en) * | 2017-11-29 | 2021-06-15 | L'oreal | Mascara compositions comprising a polymer having cyclic amide, cyclic amine and acrylamide functionality |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2539247B2 (en) * | 1987-04-21 | 1996-10-02 | 花王株式会社 | Hair cosmetics |
US5053221A (en) * | 1989-11-20 | 1991-10-01 | Maybe Holding Co. | Novel mascara composition having very small particles |
FR2779643B1 (en) * | 1998-06-11 | 2000-08-11 | Oreal | COSMETIC COMPOSITION COMPRISING AT LEAST ONE ADHESIVE POLYMER AND AT LEAST ONE FIXING POLYMER |
FR2798061A1 (en) * | 1999-09-07 | 2001-03-09 | Oreal | COSMETIC COMPOSITION COMPRISING PARTICLE DISPERSIONS OF POLYMERS IN A LIQUID FATTY PHASE |
US6548051B2 (en) * | 2000-08-16 | 2003-04-15 | L′Oreal | Hair styling composition comprising adhesive particles |
US6503521B1 (en) * | 2000-11-22 | 2003-01-07 | L'ORéAL S.A. | Fiber-containing base composition for use with mascara |
US6726917B2 (en) * | 2000-12-18 | 2004-04-27 | L'oreal Sa | Fiber-containing cosmetic composition |
JP2002226328A (en) * | 2001-01-31 | 2002-08-14 | Sanyo Chem Ind Ltd | Hair-treating agent and hair-treating method |
CN1564673A (en) * | 2001-10-03 | 2005-01-12 | 宝洁公司 | Hair styling composition containing particles |
US20030109630A1 (en) * | 2001-10-23 | 2003-06-12 | Smith Dawn E. | Microsphere adhesive formulations |
EP1419759B1 (en) * | 2002-11-18 | 2012-12-26 | Rohm And Haas Company | Durable hold hair styling compositions and method for styling hair |
US20050061349A1 (en) * | 2003-09-19 | 2005-03-24 | L'oreal S.A. | Two-step mascara |
-
2007
- 2007-03-13 CA CA002581521A patent/CA2581521A1/en not_active Abandoned
- 2007-03-15 MX MX2007003096A patent/MX2007003096A/en not_active Application Discontinuation
- 2007-03-20 KR KR1020070027142A patent/KR20070095789A/en not_active Application Discontinuation
- 2007-03-21 BR BRPI0700990-9A patent/BRPI0700990A/en not_active IP Right Cessation
- 2007-03-22 JP JP2007074550A patent/JP2007254469A/en active Pending
Also Published As
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JP2007254469A (en) | 2007-10-04 |
CA2581521A1 (en) | 2007-09-21 |
BRPI0700990A (en) | 2007-11-27 |
KR20070095789A (en) | 2007-10-01 |
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FA | Abandonment or withdrawal |