Patent Application
20090285768
A composition for and method of covalent modification of surface properties of a substrate, comprising an active material having functional groups capable of covalent attachment to a substrate in the presence of an acid or a base, a photocatalyst capable of generating an acid or a base upon exposure to light, and a vehicle.
Materials may be characterized in terms of bulk properties and surface properties. The overall properties of a material are controlled in significant part by the surface properties and the bulk properties of the material. The surface properties of a material are largely controlled by the surface chemistry and surface structure of the material. The bulk properties of a material are largely controlled by the bulk chemistry and bulk structure of the material. It is sometimes desirable to modify the surface chemistry and/or surface structure of a material in order to produce certain surface properties. In addition, it is sometimes desirable to modify the bulk chemistry and/or bulk structure of a material in order to produce certain bulk properties.
Surface modifications generally fall into two categories: (1) chemically or physically altering the atoms, compounds, or molecules in the existing surface (e.g., treatment, etching, chemical modification), or (2) over-coating the existing surface with a material having a different composition and/or structure (e.g., coating, grafting, thin film deposition). The particular method of surface modification used in a given application may often be controlled, at least in part, by the material to be modified and the applications for which the material is to be used. Bulk modifications involve analogous considerations.
In various contexts, it may be desirable to modify the surface of a material by forming a covalent bond between functional groups on the material surface and complementary functional groups in an active material. It may be particularly desirable to covalently modify the surface of certain materials with active materials in order to modify the surface properties of the materials.
In various contexts, it may also be desirable to modify the surface of a material by locally forming an active material on the material surface by reacting one or more active components to create covalent bonds between the one or more active components. An active material including active components covalently bound together may remain localized to the material surface by chemical or physical phenomena such as, for example, adsorption, absorption, electrostatic interaction, frictional interaction, steric interaction, and/or size exclusion effects. In various contexts, it may additionally be desirable to modify the bulk of a material by forming active material in a similar manner within the bulk of the material.
Materials suitable for surface and/or bulk modification include, for example, physiological materials such as hair, skin, nails, teeth, and gums. Modification of surface and/or bulk properties may also be useful for non-physiological materials such as, for example, fabric, paper, wood, plastic, glass, tile, stone, concrete, brick, other ceramics, coated or painted metal surfaces, coated glass, polymeric films, and composites.
Hair and skin are physiological materials of particular interest in terms of surface and/or bulk modification. Hair and skin are exposed to a variety of chemical and physical environments. For example, common hair care practices often include one or more of washing, blow drying, brushing, coloring, perming, relaxing, styling, and the like. These activities repeatedly expose hair to mechanical and chemical factors that may result in the loss of the natural luster and texture that characterizes healthy hair. Moreover, environmental factors may add to these effects and substantially contribute to weathered or damaged hair. Skin also suffers from surface damage as a result of similar mechanical, chemical and environmental factors. Acute damage to the surface of hair and skin may build over time, resulting in chronic damage.
Hair is naturally protected from mechanical, chemical, and environmental mediated damage by the fiber cuticle surface membrane (“FCSM”). The FCSM comprises the outermost surface layer of hair fibers and includes protein and lipid components. The FCSM functions as a highly resistant, hydrophobic, surface-protective barrier to mechanical, chemical and environmental factors that would otherwise substantially contribute to hair damage. The FCSM comprises a surface lipid mono-layer, sometimes referred to as the F-layer, covalently bound to an underlying layer of heavily cross-linked keratinous protein, sometimes referred to as the epicuticle. The F-layer comprises predominately fatty acids such as 18-methyl-eicosanoic acid (“18-MEA”) bound to the epicuticle through thioester linkages formed between the thiol groups on the cysteine residues in the keratin and other proteins in the epicuticle and the carboxyl group on the 18-MEA or other fatty acid. The F-layer gives hair fibers a hydrophobic surface, which in part facilitates the shiny luster, silky texture and smoothness of healthy hair.
Skin is naturally protected from mechanical, chemical, and environmental mediated damage by the stratum corneum. The stratum corneum is the outermost layer of epidermis. The stratum corneum comprises lipid-depleted keratinous cells embedded in a lipid-rich interstitium comprising keratin, fatty acids and ceramides. The fatty acids, ceramides and other lipid components of the stratum corneum are thought to be covalently attached to the proteinaceous components through ester and thioester linkages in a manner similar to the covalent attachment of the F-layer to the epicuticle in hair. The stratum corneum functions to prevent percutaneous moisture loss, regulate percutaneous absorption, and provide a physiologic barrier to protect the lower layers of the epidermis.
Despite differences in microstructure, the F-layer and the stratum corneum both possess similar protective functions for hair and skin respectively. However, mechanical, chemical and environmental factors may result in loss of at least a portion of the F-layer and the stratum corneum. For example, during permanent hair coloring, the combinations of hydrogen peroxide, ammonia and high pH may remove at least a portion of the protective F-layer, allowing for additional oxidation of the underlying hair surface, which may cause irreversible physiochemical changes in the hair fibers. Repeated colorings may cause the F-layer to completely disappear from the surface of hair fibers. As a result, the previously hydrophobic hair fiber surfaces may become hydrophilic because the keratinous epicuticle is exposed to the surface when the F-layer is lost. The natural protective and lubricating properties of the hair fiber surface are consequently diminished, and hair may feel dry, rough, frizzy, become difficult to brush and/or detangle, appear duller and less colorful, possess increased levels of static, and become substantially more susceptible to additional damage due to other mechanical, chemical and environmental factors.
The stratum corneum is similarly susceptible to damage mediated by mechanical, chemical and environmental factors. For example, during the winter months in relatively cold climates, lower humidity levels, low temperatures, and high winds may contribute to xerosis (dry skin), characterized, for example, by redness, itchiness and/or flaking. Damaged skin is substantially more susceptible to further damage, which may transform an acute problem to a chronic condition.
Damage to the surface portions of these materials may lead to damage to the underlying bulk portions of the materials. This may ultimately result in substantial, and perhaps irreparable, damage to these materials. A variety of mechanical, chemical and environmental factors may contribute (solely or collectively) to hair and/or skin damage. For example, excessive exposure to sunlight, exposure to chlorine in pool water (and to a lesser extent in the water provided by municipal supply), exposure to other forms of water pollution, exposure to various forms of air pollution, frictional interactions between hair fibers, and frictional interaction between hair fibers or skin and other surfaces may contribute to hair and skin damage.
A variety of approaches and products are available for treating hair and skin in order to compensate for the loss of the F-layer and the stratum corneum respectively, as well as underlying bulk damage. For example, leave-on and rinse-off hair conditioners attempt to compensate for F-layer loss by depositing various actives on the surfaces of hair fibers. Conditioners may include a variety of types of actives, for example, emollients, humectants, reconstructors (e.g., hydrolyzed proteins or peptides and free amino acids intended to penetrate the hair and strengthen its bulk structure through crosslinking), pH regulators, detanglers, thermal protectors (e.g., heat-absorbing polymers), glossers (e.g., silicones such as dimethicone or cyclomethicone), essential oils and fatty acids (e.g., as sebum substitutes), surfactants (e.g., moieties having hydrophobic and cationic functionality), and/or lubricants (e.g., panthenol). In addition, hair conditioners may include sequestrants/chelators, antistatic agents, rheology modifiers, emulsifiers, feel agents, fillers and/or preservatives. In an analogous manner, skin moisturizers attempt to compensate for stratum corneum loss by depositing various actives on the surface of the epidermis. Other varieties of skin protectants and healers deposit actives that are absorbed into the lower layers of the skin to protect and/or repair bulk damage.
Hair conditioners and skin moisturizers function by depositing hydrophobic actives (e.g., petrolatum, dimethylsiloxanes, fatty alcohols, fatty acids, and/or hydrophobic quaternary ammonium salts) on the surface of hair fibers or skin. The actives are deposited in their active state and adhere to the surfaces through physical or physiochemical means such as, for example, absorption, adsorption, hydrogen bonding, ionic bonding, other electrostatic interaction, and/or other transient non-covalent association. Consequently, as a result of the transient non-covalent association with the hair fiber or skin surfaces, these compositions may have a substantially limited active life because they may be substantially removed from hair or skin surfaces due to interactions such as washing, rinsing, or other mechanical, chemical, or environmental interactions during normal daily activities.
Accordingly, there exists a need for compositions and methods to compensate for F-layer and stratum corneum loss from hair fibers and skin, respectively, that provides a more durable conditioning and protective benefit. Covalent modification of the surface properties of damaged hair and skin is one example of such an approach. There is also a need to protect, repair, and/or strengthen these materials. Modification of the surface of a material by locally forming an active material on the material surface by reacting one or more active components to create covalent bonds between the one or more active components and modification the bulk of a material by forming active material in a similar manner within the bulk of the material are promising approaches.
Various non-physiological materials may also benefit from covalent modification of their surface properties. For example, cotton-based fabrics are naturally hydrophilic. It may be desirable to modify the surface properties of cotton-based fabrics by covalently attaching a hydrophobic active material. In this manner, the water-repellency of cotton-based fabrics may be increased. Moreover, the surface and/or bulk properties of cotton-based fabrics may be modified by locally forming an active material on the surface of fabric fibers by reacting one or more active components to create covalent bonds between the one or more active components and by locally forming active material within the bulk of the fabric. Additional fabrics that are also amenable to surface and/or bulk modification include polyester, polycotton, silk, cellulosic-derived materials (e.g., rayon), and wool, for example.
It may also be useful to covalently modify various additional materials such as, for example, fabric, paper, wood, plastic, glass, tile, stone, concrete, brick, other ceramics, coated or painted metal surfaces, coated glass, polymeric films, and composites. For example, when water is placed in contact with glass, droplets may form that tend to adhere to the glass surface. Accordingly, it may be desirable to modify the surface properties of glass materials by covalently attaching a hydrophobic active material. In this manner, the water-repellency of glass may be increased resulting in improved water removal capability. Alternatively, covalent attachment of hydrophilic active material may create a water sheeting effect that reduces droplet formation and fogging.
Ceramic tile may also benefit from surface modification by covalent attachment of a hydrophobic active material, for example. Cleaned and dried ceramic tiles may exhibit water spotting, particularly in areas where the water has increased levels of dissolved minerals. Attachment of a hydrophobic active material, for example, may decrease the drying time of ceramic tiles and reduce water spotting.
Accordingly, there exists a need for compositions and methods for the modification of the surface and/or bulk properties of various materials in addition to physiological materials.
A personal care composition comprising an active material having one or more functional groups capable of covalent attachment in the presence of an acid or a base to one or more complementary functional groups; a photocatalyst capable of generating an acid or a base upon exposure to light; and a physiological acceptable vehicle for dispersing or dissolving the active material and the photocatalyst for application of the composition to a substrate; and wherein the vehicle is a physiological acceptable vehicle and the substrate is selected from the group consisting of hair, skin, nail, teeth and combinations thereof.
A method for treating a substrate comprising applying at least one active material to the substrate, the active material having one or more functional groups, and the substrate having one or more complementary functional groups; applying to the substrate at least one photocatalyst capable of generating an acid or base on exposure to light; and exposing the photocatalyst and the at least one active material to light for forming covalent attachments between the one or more functional groups of the at least one active material and a reagent selected from the group consisting of a second active material, a substrate and a combination thereof.
Various embodiments described herein may be understood by reference to the following description, taken with the accompanying drawings as follows.
While the specification concludes with claims which particularly point out and distinctly claim the present invention; it is believed that the present invention will be better understood from the following description of various non-limiting embodiments.
It is to be understood that certain descriptions of various embodiments have been simplified to illustrate only those elements and/or features that are relevant to a clear understanding of the present invention, while eliminating, for purposes of clarity, other elements and/or features. Those of ordinary skill in the art, upon considering the present description of the various non-limiting embodiments of the present invention, will recognize that other elements and/or features may be desirable in order to implement the present invention. However, because such other elements and/or features may be readily ascertained by one of ordinary skill upon considering the present description of various embodiments of the invention, and are not necessary for a complete understanding of the present invention, a discussion of such elements and/or features is not provided herein. As such, it is to be understood that the description set forth herein is merely exemplary to the present invention and is not intended to limit the scope of the claims.
Other than in the examples herein, or unless otherwise expressly specified, all of the numerical ranges, amounts, values, and percentages, such as those for amounts of materials, elemental contents, times and temperatures of reaction, ratios of amounts, and others, in the specification and attached claims may be read as if prefaced by the word “about,” even though the term “about” may not expressly appear with the value, amount, or range. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains error necessarily resulting from the deviation found in its underlying respective testing measurements. Furthermore, when numerical ranges are set forth herein, these ranges are inclusive of the recited range end points (i.e., end points may be used). Also, it should be understood that any numerical range recited herein is intended to include all sub-ranges subsumed therein. For example, a range of “1 to 10” is intended to include all sub-ranges between (and including) the recited minimum value of 1 and the recited maximum value of 10, that is, having a minimum value equal to or greater than 1 and a maximum value equal to or less than 10.
All patents, publications, or other disclosure material referenced herein are incorporated by reference in their entirety. Any patent, publication, or other disclosure material, in whole or in part, that is incorporated by reference herein is incorporated herein only to the extent that the incorporated material does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
The articles “a,” “an,” and “the” are used herein to refer to one or more than one (i.e., to at least one) of the grammatical objects of the article. By way of example, “a component” means one or more components, and thus, possibly, more than one component is contemplated and may be employed or used.
All percentages, parts and ratios are based upon the total weight of the compositions of the present invention, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore, do not include solvents or by-products that may be included in commercially available materials, unless otherwise specified.
As used herein, the term “functional group” means an atom or group of associated atoms that, at least in part, defines the structure and determines the properties of a particular family of chemical compounds. A functional group may be a region on or in a molecule or material that is a site of specific chemical reactivity compared to other regions of the molecule or material. Functional groups generally have characteristic properties and may control, in part, the reactivity of a molecule as a whole. Functional groups include, but are not limited to, hydroxyl groups, thiol groups, carbonyl groups, carboxyl groups, sulfonate groups, sulfide groups, ether groups, halogen atoms, amino groups, cyano groups, nitro groups, and the like. Compounds that are generally classified (structurally and/or functionally) according to functional groups include, but are not limited to, alkanes, alkenes, alkynes, aromatic compounds, halides, alcohols, ethers, esters, amines, imines, imides, carboxylic acids, amides, acid halides, acid anhydrides, nitriles, ketones, aldehydes, carbonates, peroxides, hydroperoxides, carbohydrates, acetals, epoxides, sulfonic acids, sulfonate esters, sulfides, sulfoxides, thioethers, thiocyanates, disulfides, phosphonic acids, phosphate esters, phosphines, azides, azo compounds, nitro compounds, nitrates, nitriles, nitrites, nitroso compounds, thiols, cyanates, and isocyanates, for example.
The terms “active material”, “active component”, “active compound”, and combinations and modifications of these terms, as used herein means substances to be applied to a substrate to modify the surface and/or bulk properties of the substrate material. These terms may be used interchangeably. Substrate surface properties may include, for example, surface hydrophobicity/hydrophilicity, oleophobicity/oleophilicity, color, optical properties, absorptivity, adsorptivity, bonding capability, brightness, dullness, frictional resistance, stain resistance, surface texture, odor, washability, wettability, elasticity, plasticity, and rigidity. Substrate bulk properties may include, for example, tensile strength, rigidity, absorptivity, elasticity, plasticity, and biological activity.
Active materials may include compounds having one or more functional groups capable of covalent attachment in the presence of an acid or a base to one or more complementary functional groups present at the surface or in the bulk of a substrate. Active materials may also include compounds capable of forming covalent bonds between molecules in the presence of an acid or a base, for example, monomers capable of acid or base catalyzed polymerization. A “cosmetically active material” is an active material suitable for use in a personal care product without undue toxicity, incompatibility, instability, allergic response, and the like.
The term “monomer” as used herein means a compound that may be covalently bonded to other monomers (that may have the same or different chemical structures) to form a polymer or copolymer. The term “polymer” (and “copolymer”) as used herein means a compound comprising a plurality of monomers. Accordingly, as used herein the term polymer includes dimers, trimers, oligomers, and the like.
As used herein, the terms “modify”, “modification”, “functionalize” or “functionalization”, with regard to a substrate, refers to (1) covalently attaching an active component to the substrate surface, (2) covalently attaching an active component to the substrate in the bulk of the substrate material, (3) forming covalent bonds between two or more active components (which may be the same or different chemical moieties) where the resultant secondary active material localizes to the substrate surface, and/or (4) forming covalent bonds between two or more actives (which may be the same or different chemical moieties) where the actives are present within the bulk of the substrate.
The term “suitable for application to human hair” and “suitable for application to human skin” as used herein means that the compositions or components thereof so described are suitable for use in contact with human hair and the scalp and skin without undue toxicity, incompatibility, instability, allergic response, and the like.
The term “shampoo” as used herein means a composition for cleaning hair or skin, including scalp, face, and body. Accordingly, the term “shampoo” includes, but is not limited to, the conventional understanding of a hair shampoo, a body wash, a face wash, or other surface washing composition, for example. In addition, the term “shampoo” includes compositions for use on humans and/or animals.
The term “conditioner” as used herein means a composition for treating hair or skin, including scalp, face, and body, in order to provide protection to hair or skin from mechanical, chemical, and/or environmental factors that contribute to damaged or weathered hair or skin, and/or to alleviate the characteristics of such damage. Accordingly, the term “conditioner” includes, but is not limited to, the conventional understanding of a hair conditioner (leave-in and/or rinse-out), a skin lotion, or a facial moisturizer, for example. In addition, the term “conditioner” includes compositions for use on humans and/or animals.
The term “personal care product” as used herein means a product such as, for example, lipstick, mascara, rouge, foundation, blush, eyeliner, lipliner, lip gloss, other cosmetics, facial powder, body powder, sunscreen, sun block, nail polish, mousse, hair spray, styling gel, nail conditioner, bath gel, shower gel, body wash, face wash, shampoo, hair conditioner (leave-in or rinse-out), cream rinse, hair dye, hair coloring product, hair shine product, hair serum, hair anti-frizz product, hair split-end repair product, lip balm, skin conditioner, cold cream, moisturizer, body spray, soap, body scrub, exfoliant, astringent, scruffing lotion, depilatory, permanent waving solution, antidandruff formulation, antiperspirant composition, deodorant, shaving product, pre-shaving product, after shaving product, cleanser, skin gel, rinse, toothpaste, mouthwash, or oral care strips.
The term “consumer care product” as used herein means a product such as, for example, soft surface cleaner, a hard surface cleaner, a glass cleaner, a ceramic tile cleaner, a toilet bowl cleaner, a wood cleaner, a multi-surface cleaner, a surface disinfectant, a dishwashing composition, a laundry detergent, a fabric conditioner, a fabric dye, a surface protectant, a surface disinfectant, motor vehicle surface treatment, and the like. Consumer care products may be in the form of liquids, gels, suspensions, powders, and the like. Consumer care products may also be for household or home care use as well as for professional, commercial and/or industrial use.
One object of the compositions and methods described herein is to provide for the modification of the surface and/or bulk properties of a substrate by covalently attaching an active material to the surface of the substrate. Another object of the compositions and methods described herein to provide for the modification of the surface and/or bulk properties of a substrate by treating the substrate with an active compound capable of reacting with itself to form covalent bonds between two or more molecules of the active compound thereby forming a secondary active material. It is still another object of the compositions and methods described herein to provide for the functionalization of the surface of a substrate by covalently attaching active material to the surface of the substrate. In order to achieve effective treatment, it is occasionally desirable to initially attach onto a substrate a material that contains multiple similar functional groups in its molecule, followed by another step of attaching another material/benefit agent by reacting with the initially attached material. This is especially useful if the substrate contains only limited density of functional groups that are able to react with a benefit agent towards a chemical bond. For Example, initial attachment of malic acid (2-hydroxy-1,4-dibutanoic acid) onto a substrate increases the reactivity of the substrate by a factor of two towards subsequent attachment of an active. It is yet another object of the compositions and methods described herein to provide for such modification/functionalization in a manner that is readily amenable to health and safety regulations, and which may be readily implemented in a personal care product and/or a consumer care product space.
The various embodiments relate, in general, to compositions and methods for treating a substrate. As used herein, the term “substrate” means any material for which it is useful to treat the surface and/or bulk with the compositions and methods described herein, including, but not limited to, physiological materials such as, for example, hair fibers, skin, nails, gums, and teeth. Substrate may also mean non-physiological materials such as, for example, fabric, paper, wood, plastic, glass, tile, stone, concrete, brick, other ceramics, coated or painted metal surfaces, coated glass, polymeric films, and composites. Substrates may also include surfaces that have been previously modified such as, for example, coated surfaces (e.g., varnished or painted) or laminated surfaces. The terms “substrate” and “material” may be used interchangeably in the context of substances to be modified by the compositions and methods described herein.
In various embodiments, the compositions described herein include an active component that can modify a substrate in the presence of an acid or a base, a photocatalyst capable of generating an acid or a base upon exposure to light, and a suitable vehicle, which may optionally be a physiological acceptable vehicle. In various embodiments, the compositions described herein may also include one or more optional components, including surfactants, emulsifiers, oxidants, reductants, pH regulators, emollients, humectants, proteins, peptides, amino acids, additive polymers, glossers, essential oils and/or fatty acids, lubricants, sequestrants/chelators, antistatic agents, rheology modifiers, feel agents, fillers, preservatives, perfumes, other functional components, or combinations thereof.
In various embodiments, the methods described herein include treating a substrate by forming one or more covalent bonds between an active component and/or the substrate, where the covalent bond is formed in the presence of an acid or base generated by a photocatalyst upon exposure to light. In various embodiments, the methods described herein include treating a substrate by forming one or more covalent bonds between two or more active component molecules, where the covalent bond is formed in the presence of an acid or base generated by a photocatalyst upon exposure to light and the active material localizes to the surface and/or bulk of the substrate. As used herein, the term “molecule” means a sufficiently stable group of at least two atoms in a definite arrangement held together by chemical bonds. Accordingly, the term molecule includes, but is not limited to, neutral molecular compounds, polyatomic ions, radical species, biomolecules, monomers, dimers, trimers, oligomers, polymers, and the like.
In various embodiments, the methods described herein include treating a substrate by preparing and covalently bonding a compound to the substrate, or forming covalent bonds between compounds on the substrate surface or in the substrate bulk, in situ, by providing a substrate, providing one or more reagents, providing a photocatalyst, and exposing the photocatalyst to light in the presence of the substrate and the one or more reagents, where the photocatalyst generates an acid or a base, the acid or the base catalyzes reaction between the one or more reagents and/or reaction between the one or more reagents and the substrate, and where the reaction(s) forms covalent bonds. In various embodiments, the methods described herein include providing a system including a substrate, an active component that can modify a substrate in the presence of an acid or a base, and a photocatalyst capable of generating an acid or a base upon exposure to light, and exposing the system to light.
Generally, covalent attachment of active components on substrates such as hair and skin, for example, often proves difficult to achieve. This is especially true in the presence of water, which may rapidly degrade reactive moieties before substrate functionalization occurs. Moreover, aqueous media are known to chemically facilitate hydrolysis and oxidation reactions that may compete against covalent attachment of active components to substrates. This may pose particular problems, for example, in personal care products where water is often used as a physiologically acceptable vehicle. Consumer care products also often use water in a variety of capacities, most notably as a solvent.
In addition, substrates such as, for example, hair, skin, fabric, glass and ceramic may not contain particularly reactive chemical functional groups on the surface that would readily react with active components to form covalent bonds. This relatively low substrate surface reactivity may result in a reaction system that is outside the practical time frame of an apply-and-rinse environment (e.g., shampooing and conditioning hair, washing skin, laundering fabrics, or cleaning hard surfaces). Furthermore, strict regulatory requirements concerning product safety and environmental protection increase the challenge of providing compositions and methods for treating a substrate such as, for example, hair, skin, fabric, glass or ceramic, through covalent attachment of active components.
However, the various embodiments of the compositions and methods described herein are directed toward a photocatalyst technology that allows the use of light to promote a reaction such as, for example, the covalent attachment of an active component to a substrate or formation of covalent bonds between two or more active components in situ on the surface or in the bulk of a substrate material. The various embodiments may be used, for example, to promote the covalent attachment of long-chain alkyl groups to damaged hydrophilic hair and/or skin in order to replenish and/or fortify the normally hydrophobic character of these substrates. In addition, the various embodiments may be used, for example, to promote the covalent attachment of active materials to fabrics or hard surfaces. Furthermore, the various embodiments may be used, for example, to locally polymerize monomers on the surface and/or in the bulk of substrate materials in order to modify the surface and/or bulk properties of a material.
In various embodiments, covalent attachment may yield a variety of substantial benefits to individuals that possess damaged hair and/or skin. For example, hair conditioning benefits may include, among others, improved feel, lower friction, easier combing/brushing, reduced dryness, increased smoothness, decreased frizziness, increased shine, decreased levels of static, and improved protection against damage due to other mechanical, chemical and environmental factors. Skin conditioning benefits may include, among others, decreased dryness, decreased redness, decreased itchiness, decreased flaking, and improved texture and smoothness. At least some of these benefits may be imparted by increased or targeted deposition of actives resulting from the surface modification via covalent attachment. The benefits imparted by the compositions and methods described herein are potentially more durable because a non-labile covalent bond is employed, which is generally stronger and more stable relative to the absorption, adsorption, hydrogen bonding, ionic bonding, other electrostatic interactions, and/or other transient non-covalent associations employed in prior conditioners to deposit or apply active components onto hair and/or skin. This may substantially reduce the frequency of application and reapplication encountered with prior conditioners.
Various embodiments of the compositions and methods described herein provide for the covalent attachment of active components to substrates, which may be described as an approach toward repairing and/or fortifying the hair F-layer or skin stratum corneum for example. In the context of hair, and not to be bound or otherwise limited by theory, the F-layer of virgin hair may be stripped from the hair fiber by processes mediated by various mechanical, chemical, and/or environmental factors as illustrated in
The anionic sulfonate groups on the cysteine residues at the surface of the epicuticle render the surface of any damaged hair fibers hydrophilic, which may result in the undesirable properties of damaged hair. Moreover, it has been observed that the more hydrophilic (and consequently the more damaged) the hair fibers, the lower the deposition of prior hydrophobic conditioning actives (such as, for example, dimethylsiloxanes, fatty alcohols and acids, and quaternary amines) by non-covalent interactions and associations. Accordingly, the compositions and methods described herein provide an attractive approach for treating such damaged substrates.
In various embodiments, the active components may be one or more monomers capable of polymerizing in the presence of acid or base. The hair fibers are treated with a composition comprising photocatalyst and monomer, which at least partially penetrates the fiber. Upon exposure to light, the photocatalyst is activated thereby generating acid or base, which catalyzes the polymerization of the monomer, thereby forming a polymer in situ, which may optionally attach to the hair fiber by way of covalent bonds formed between the thiol groups and the polymer.
In other embodiments (not shown), the polymer does not covalently attach to the hair fiber. For example, the polymer formed in situ may be physically immobilized on the surface of the hair fiber or within pores in the hair fiber. The polymer formed in situ may also be associated with the hair fiber by a physical and/or chemical interaction such as, for example, adsorption, absorption, electrostatic interaction, frictional interaction, steric interaction, and/or size exclusion effects with the surface and/or bulk of the substrate.
In various embodiments, the monomer may be styrene or a styrene derivative such as, for example, α-methyl styrene. The monomer may also comprise mixtures of different monomers such that the in situ polymerization (on the surface and/or in the bulk of the substrate) produces copolymer.
In various embodiments of the compositions and methods described herein, the photocatalyst may be a photoacid that deprotonates upon exposure to light. The proton (which may be solvated, e.g., in the form of a hydronium ion) may catalyze the formation of a covalent bond through an esterification reaction or a thioesterification reaction, for example. In various embodiments of the compositions and methods described herein, the photocatalyst may be a photobase that generates hydroxide anion upon exposure to light. The hydroxide anion may catalyze the formation of a covalent bond through an esterification reaction or thioesterification reaction, for example. In various embodiments, the mechanism of action of a photoacid or photobase is not limited to an Arrhenius-type or Bronsted-Lowry type acid or base system, but rather may also include a Lewis-type acid or base that is catalytically activated upon exposure to light. The compositions and methods described herein are not limited in this context.
Esterification reactions are generally reversible. In relatively neutral media, such as water, the reversible esterification reaction may not thermodynamically favor the formation of the ester bond and water, as opposed to the reverse reaction of hydrolysis of the ester bond to respective hydroxyl and carboxyl containing moieties. Thioesterification systems generally behave in an analogous manner. Thus, the formation of covalent bonds between active components and substrates in prior systems, for example in prior conditioners, was impracticable in the context of treating substrates such as, for example, hair or skin.
In addition, acid or base catalysis of esterification or thioesterification reactions are generally impracticable in the context of personal care products because it is difficult to generate sufficient acid or base concentration at the surface or within the bulk of the substrate without having relatively high or relatively low pH. The use of products having relatively high or relatively low pH is generally inappropriate because such acidic and caustic substances may be physiologically unacceptable.
The compositions and methods described herein overcome these limitations. The use of a photocatalyst allows for the co-localization of the catalyst and an active component at a substrate surface or within the bulk of the substrate material. The photocatalyst however is not activated until it is exposed to light. Photoacid catalysts, for example, exhibit a decrease in pKa upon exposure to light of suitable wavelength. Photobase catalysts, for example, may exhibit an increase in pKb upon exposure to light of a suitable wavelength. The respective increase in acid or base strength upon exposure to light results in a localized increase in proton or hydroxide concentration at the substrate surface which facilitates rapid esterification or thioesterification, for example. Moreover, because the proton or hydroxide concentration is localized at the substrate surface for a short period of time (before diffusing into the surrounding medium), bulk pH may be essentially unaffected by the photocatalytic reaction and may remain close to neutral, given the quantity of the photocatalyst used. This is advantageous for physiological applications such as, for example, in personal care products and in various consumer care product applications. In addition, the transient localized nature of the acidic or basic catalysis also contributes to the stability of the covalent bond formed during the process in cases where the covalent bond is sensitive to high or low pH.
Therefore, photocatalysis of the reactions forming ester and/or thioester covalent bonds between active components and substrates in the various embodiments of the compositions and methods described herein provides for an efficient, controllable, stable and physiologically acceptable approach to substrate treatment such as, for example, F-layer and stratum corneum repair and/or fortification in hair and skin respectively.
The secondary active material formed according to the photocatalyzed acid or base mechanism described herein may localize to the surface and/or bulk of the substrate material. In various embodiments, the localization may be a result of covalent attachment of the secondary active material to the substrate material. In other embodiments, the localization may be a result of non-covalent chemical or physical interactions between the secondary active material and the surface and/or bulk of the substrate material. For example,
In various embodiments the secondary active material formed according to the photocatalyzed acid or base mechanism described herein may localize on the surface of a substrate and/or in the bulk of the substrate due to changes in the properties of the active material after the formation of covalent bonds between two or more active material molecules. For example, where the active material comprises a monomer/polymer system, the active material may be polymerized and/or crosslinked on the surface of a substrate. The polymerization and/or crosslinking may change the solubility of the active material in the reaction medium, which may facilitate the deposition of the secondary active material onto the substrate surface. In this manner, a surface layer of secondary active material may form on the substrate surface thereby modifying the surface properties. This may result in the encapsulation of constituent fibers in fibrous substrates such as, for example, hair and fabrics. In various embodiments (not shown in
The compositions and methods described herein facilitate in situ and localized modification of material properties in a controlled manner. The active components are covalently altered (e.g., by the formation of covalent bonds between active components to form a secondary active material and/or between active components and a substrate material) in a photoacid or photobase reaction system.
The substrate to be modified may be treated by spraying, soaking, spreading, coating, rinsing, or any other suitable means of introducing the composition onto the surface of the substrate or into the bulk of the substrate material. In various embodiments, it is important to ensure the entire surface of the substrate is wetted by reagent solution in order to ensure sufficient modification of the substrate surface and/or bulk. If the active material is at least partially insoluble in the vehicle, it is important to maximize contact between the active and the substrate by, for example, minimizing the drop size or particle size of the active in the vehicle. In various embodiments, it may be desired to introduce reagent solution onto only a single portion or multiple portions of a substrate surface. In other embodiments, it may be desired to irradiate only a single portion or multiple portions of a substrate surface with light of a wavelength suitable to activate the photocatalyst. The covalent modification only occurs on those areas of the substrate surface (and underlying bulk) that are both in contact with a reagent solution and irradiated with light of a wavelength suitable to activate the photocatalyst. This allows for control of the location and extent of the surface and/or bulk modification.
The acid or base photocatalytic covalent modification/functionalization mechanisms described herein may also be reversible. For example, substrate surfaces covalently modified or functionalized through esterification and/or thioesterification reactions may be contacted with an acidic aqueous surfactant solution. Alternatively, an alkaline surfactant solution may be employed. These solutions may facilitate the hydrolytic cleavage of the ester and/or thioester bonds attaching the active components to the substrate, thereby removing the active components.
This removability is limited to active component-substrate bonds that are reversible under the appropriate conditions. For example, in the case of photoacid-catalyzed esterification, the ester bond is formed when the reagent and the catalyst are present in the vicinity of the substrate and exposed to the appropriate light. The high concentration of protons at the moment of irradiation results in ester bond formation that remains intact because the generated protons diffuse rapidly into the bulk of the medium. The low content of the photoacid allows for subsequent stable and near-neutral pH of the bulk aqueous solution. Under these conditions the ester bond is hydrolyzed at a very slow rate. However, treatment with significantly lower (or significantly higher) pH aqueous solutions will more readily break the ester bonds resulting in the original unmodified substrate surface.
The removal of the covalently-attached active can also be achieved by treatment of the modified or functionalized substrate with a composition including a photocatalyst (photoacid or photobase). This allows for improved control over the timing of the removal of the active component from the substrate. This can be achieved if the photocatalyst is chosen so that it is unaffected by ambient light but can generate acid or base species under light of a specific wavelength provided by an appropriate device.
Each of the various components of the compositions and associated methods described herein, as well as preferred and optional components, are described in detail.
The active component or active material may be any chemical moiety that is capable of modifying/functionalizing a substrate in the presence of acid or base. Non-limiting examples of active materials include, but are not limited to, hydroxyl- or carboxyl-containing long-chain alkyl (straight- or branched-chain) moieties. In various embodiments, the active material may be one or more of a fatty acid, a fatty alcohol, a fatty amine, an aminosilicone, a polyvinyl alcohol, a polyvinyl alcohol-polyvinyl pyrrolidone copolymer, a polycaprolactone, an optical brightener, a humectant, a silanol, a dimethylsilicone functionalized with one or more of primary, secondary, carboxyl or hydroxyl functional groups.
In various embodiments, the active material preferably includes a substantial hydrophobic portion. However, in other embodiments, the active material may be hydrophilic. In various embodiments, the active material is one or more of a dye or other coloring agent or a perfume. In one embodiment the active component may be a perfume, that contains in its chemical structure a primary or secondary hydroxyl group, and/or an amine group, or a carboxyl group.
In various embodiments, the active material includes at least two active compounds capable of covalent attachment to a substrate in the presence of an acid or a base upon reaction between the at least two active compounds. In various embodiments, the active material forms secondary compounds, such as, for example, dimers, oligomers, polymers and combinations thereof, and, optionally, the secondary material has functional groups capable of covalent attachment to the substrate.
Non-limiting examples of additional active materials may include one or more of glycerin, stearyl alcohol, lauric acid, direct dye 243, ethylene carbonate, poly(acrylic acid), ethyl oxazoline, poly(vinyl pyrrolidone-co-acrylic acid), butane tetracarboxylic acid, citric acid, and poly(styrene sulfonate-co-acrylic acid).
The active material may be present in the compositions and methods described herein in an amount from 0.01 percent to 80 percent by weight relative to the total weight of the composition.
The photocatalyst may be any acid, base (or conjugate thereof) having a pKa (or pKb) value that decreases (or increases) upon exposure to light. The light may be light of any suitable wavelength to result in the respective decrease or increase in pKa or pKb. For example the light may be ambient light, sunlight, incandescent light, fluorescent light, LED light, laser light, and the like. The light may fall within any classification along the electromagnetic spectrum, such as, for example, visible light, near or far ultraviolet light, or near or far infrared light. It will be readily apparent to one of ordinary skill in the art that the appropriate wavelength or wavelengths of light will be dependant upon the identities of the one or more photocatalysts employed.
In addition, the suitable light may be provided from any source capable of illuminating the substrate surface. For example, ambient sunlight, incandescent light, fluorescent light, and the like may provide light of suitable wavelength. Accordingly, the light may be provided by conventional sources such as lamps and portable or battery-powered lights. In addition, specific devices may be developed or adapted for use with the compositions and method described herein. For example, a hair brush configured to incorporate LEDs that provide light of a suitable wavelength may be used to covalently modify the surface of hair fibers. In various embodiments, a laser may be used to provide precise targeting of the covalent modification of substrate surfaces, for example.
In various embodiments, the photocatalyst is a photoacid such as, for example, an aromatic hydroxy compound, a sulfonated pyrene compound, an onium salt, a diazomethane derivative, a bissulfone derivative, a disulfuno derivative, a nitrobenzyl sulfonate derivate, a sulfonic acid ester derivative, a sulfonic acid ester of an N-hydroxyimide, or combinations thereof.
Photoacid catalysts may include, for example, hydroxy-substituted aromatics such as, for example, 8-hydroxyquinoline, 8-hydroxyquinoline sulfate, 8-quinolinol-1-oxide, 5-hydroxyquinoline, 6-hydroxyquinoline, 7-hydroxyquinoline, 5-iodo-7-sulfo-8-hydroxyquinoline, 5-fluoro-8-hydroxyquinoline, 5-fluoro-7-chloro-8-hydroxyquinoline, 5-fluoro-7-bromo-8-hydroxyquinoline, 5-fluoro-7-iodo-8-hydroxyquinoline, 7-fluoro-8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline, 5,7-dichloro-8-hydroxyquinoline, 5-chloro-7-brono-8-hydroxyquinoline, 5-chloro-7-iodo-8-hydroxyquinoline, 7-chloro-8-hydroxyquinoline, 5-bromo-8-hydroxyquinoline, 5-bromo-7-chloro-8-hydroxyquinoline, 5,7-dibromo-8-hydroxyquinoline, 5-bromo-7-iodo-8-hydroxyquinoline, 7-bromo-8-hydroxyquinoline, 5-iodo-8-hydroxyquinoline, 5-iodo-7-chloro-8-hydroxyquinoline, 5,7-diiodo-8-hydroxyquinoline, 7-iodo-8-hydroxyquinoline, 5-sulfonic acid-8-hydroxyquinoline, 7-sulfonic acid-8-hydroxyquinoline, 5-sulfonic acid-7-iodo-8-hydroxyquinoline, 5-thiocyano-8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline, 5-bromo-8-hydroxyquinoline, 5,7-dibromo-8-hydroxyquinoline, 5-iodo-8-hydroxyquinoline, 5,7-diiodo-8-hydroxyquinoline, 7-azaindole, 7-cyano-2-naphthol, 8-cyano-2-naphthol, 5-cyano-2-naphthol, 1-hydroxy-3,6,8-pyrenetrisulfonic acid, Trans-3-hydroxystilbene, 2-hydroxymethylphenol, or Pelargonidin.
Photoacid catalysts may include onium salts such as, for example, bis(4-tert-butylphenyl)iodonium perfluoro-1-butanesulfonate, diphenyliodonium perfluoro-1-butanesulfonate, diphenyliodonium-9,10-dimethoxyanthracene-2-sulfonate, diphenyliodonium hexafluorophosphate, diphenyliodonium nitrate, diphenyliodonium p-toluenesulfonate, diphenyliodonium triflate, (4-methylphenyl)diphenylsulfonium triflate, (4-methylthiophenyl)methyl phenyl sulfonium triflate, 2-naphthyl diphenylsulfonium triflate, (4-phenoxyphenyl)diphenylsulfonium triflate, (4-phenylthiophenyl)diphenylsulfonium triflate, thiobis(triphenyl sulfonium hexafluorophosphate), triarylsulfonium hexafluoroantimonate, triarylsulfonium hexafluorophosphate salt, triphenylsulfonium perfluoro-1-butanesulfonate, triphenylsulfonium triflate, tris(4-tert-butylphenyl)sulfonium perfluoro-1-butanesulfonate, tris(4-tert-butylphenyl)sulfonium triflate, bis(4-tert-butylphenyl)iodonium p-toluenesulfonate, bis(4-tert-butylphenyl)iodonium triflate, (4-bromophenyl)diphenylsulfonium triflate, (tert-butoxycarbonylmethoxynaphthyl)diphenylsulfonium triflate, (tert-butoxycarbonylmethoxyphenyl)diphenylsulfonium triflate, (4-tert-butylphenyl)diphenylsulfonium triflate, (4-chlorophenyl)diphenylsulfonium triflate, (4-fluorophenyl)diphenylsulfonium triflate, [4-[2-hydroxytetradecyl)oxy]phenyl]phenyliodonium hexafluoroantimonate, (4-iodophenyl)diphenylsulfonium triflate, (4-methoxyphenyl)diphenylsulfonium triflate, diphenyliodo hexafluorophosphate, diphenyliodo hexafluoroarsenate, diphenyliodo hexafluoroantimonate, diphenyl p-methoxyphenyl triflate, diphenyl p-toluenyl triflate, diphenyl p-isobutylphenyl triflate, diphenyl p-t-butylphenyl triflate, triphenylsulfonium hexafluorophosphate, triphenylsulfonium hexafluoroarsenate, triphenylsulfonium hexafluoroantimonate, triphenylsulfonium triflate, dibutylnaphthyl sulfonium triflate, diphenyliodonium trifluoromethanesulfonate, (p-tert-butoxyphenyl)phenyliodonium trifluoromethanesulfonate, diphenyliodonium p-toluenesulfonate, (p-tert-butoxyphenyl)phenyliodonium p-toluenesulfonate, triphenylsulfonium trifluoromethanesulfonate, (p-tert-butoxyphenyl)diphenylsulfonium trifluoromethanesulfonate, bis(p-tert-butoxyphenyl)phenylsulfonium trifluoromethanesulfonate, tris(p-tert-butoxyphenyl)-sulfonium trifluoromethanesulfonate, triphenylsulfonium p-toluenesulfonate, (p-tert-butoxyphenyl)diphenylsulfonium p-toluenesulfonate, bis(p-tert-butoxyphenyl)phenylsulfonium p-toluenesulfonate, tris(p-tert-butoxyphenyl)sulfonium p-toluenesulfonate, triphenylsulfonium nonafluorobutanesulfonate, triphenylsulfonium butanesulfonate, trimethyl-sulfonium trifluoromethanesulfonate, trimethylsulfonium p-toluenesulfonate, cyclohexylmethyl(2-oxocyclohexyl)-sulfonium trifluoromethanesulfonate, cyclohexylmethyl(2oxocyclohexyl) sulfonium p-toluenesulfonate, dimethylphenyl-sulfonium trifluoromethanesulfonate, dimethylphenyl-sulfonium p-toluenesulfonate, dicyclohexylphenylsulfonium trifluoromethanesulfonate, dicyclohexylphenylsulfonium p-toluenesulfonate, trinaphthylsulfonium trifluoromethane-sulfonate, cyclohexylmethyl(2-oxocyclohexyl)sulfonium trifluoromethanesulfonate, (2-norbornyl)methyl(2-oxocyclo-hexyl)sulfonium trifluoromethanesulfonate, ethylenebis-[methyl(2-oxocyclopentyl)sulfonium trifluoromethane-sulfonate], or 1,2′-naphthylcarbonylmethyltetrahydrothiophenium triflate.
Photoacid catalysts may include diazomethane derivatives such as, for example, bis(benzenesulfonyl)-diazomethane, bis(p-toluenesulfonyl)diazomethane, bis(xylenesulfonyl)diazomethane, bis(cyclohexylsulfonyl)-diazomethane, bis(cyclopentylsulfonyl) diazomethane, bis(n-butylsulfonyl)diazomethane, bis(isobutylsulfonyl)-diazomethane, bis(sec-butylsulfonyl)diazomethane, bis(n-propylsulfonyl) diazomethane, bis(isopropylsulfonyl)-diazomethane, bis(tert-butylsulfonyl) diazomethane, bis(n-amylsulfonyl)diazomethane, bis(isoamylsulfonyl)-diazomethane, bis(sec-amylsulfonyl)diazomethane, bis(tert-amylsulfonyl) diazomethane, 1 -cyclohexylsulfonyl-1-(tert-butylsulfonyl)diazomethane, 1-cyclohexylsulfonyl-1-(tert-amylsulfonyl)diazomethane, or 1-tert-amylsulfonyl-1-(tert-butylsulfonyl)diazomethane.
Photoacid catalysts may include glyoxime derivatives such as, for example, bis-o-(p-toluene-sulfonyl)-α-dimethylglyoxime, bis-o-(p-toluenesulfonyl)-α-diphenylglyoxime, bis-o-(p-toluenesulfonyl)-α-dicyclohexyl-glyoxime, bis-o-(p-toluenesulfonyl)-2,3-pentanedione-glyoxime, bis-o-(p-toluenesulfonyl)-2-methyl-3,4-pentane-dioneglyoxime, bis-o-(n-butanesulfonyl)-α-dimethylglyoxime, bis-o-(n-butanesulfonyl)-α-diphenylglyoxime, bis-o-(n-butanesulfonyl)-α-dicyclohexylglyoxime, bis-o-(n-butane-sulfonyl)-2,3-pentanedioneglyoxime, bis-o-(n-butane-sulfonyl)-2-methyl-3,4-pentanedioneglyoxime, bis-o-(methanesulfonyl)-α-dimethylglyoxime, bis-o-(trifluoro-methanesulfonyl)-α-dimethylglyoxime, bis-o-(1,1,1 -trifluoroethanesulfonyl)-α-dimethylglyoxime, bis-o-(tert-butanesulfonyl)-α-dimethylglyoxime, bis-o-(perfluorooctanesulfonyl)-α-dimethylglyoxime, bis-o-(cyclohexane-sulfonyl)-α-dimethylglyoxime, bis-o-(benzenesulfonyl)-α-dimethylglyoxime, bis-o-(p-fluorobenzenesulfonyl)-α-dimethylglyoxime, bis-o-(p-tert-butylbenzenesulfonyl)-α-dimethylglyoxime, bis-o-(xylenesulfonyl)-α-dimethyl-glyoxime, or bis-o-(camphorsulfonyl)-α-dimethylglyoxime.
Photoacid catalysts may include bissulfone derivatives such as, for example, bisnaphthylsulfonylmethane, bistrifluoromethylsulfonylmethane, Bismethylsulfonylmethane, bisethylsulfonylmethane, bispropylsulfonylmethane, bisisopropylsulfonylmethane, bis-p-toluenesulfonylmethane, bisbenzenesulfonylmethane, 2-cyclohexyl-carbonyl-2-(p-toluenesulfonyl)propane (β-ketosulfone derivative), 2-isopropyl-carbonyl-2-(p-toluenesulfonyl) propane (β-ketosulfone derivative).
Photoacid catalysts may include disulfono derivatives such as, for example, diphenyl disulfone or dicyclohexyl disulfone.
Photoacid catalysts may include nitrobenzyl sulfonate derivatives such as, for example, 2,6-dinitrobenzyl p-toluenesulfonate or 2,4-dinitrobenzyl p-toluenesulfonate.
Photoacid catalysts may include sulfonic acid ester derivatives such as, for example, 1,2,3-tris(methanesulfonyloxy) benzene, 1,2,3-tris(trifluoro-methanesulfonyloxy)benzene, or 1,2,3-tris(p-toluenesulfonyloxy)benzene.
Photoacid catalysts may include sulfonic acid esters of N-hydroxyimides such as, for example, N-hydroxysuccinimide methanesulfonate, N-hydroxysuccinimide trifluoromethanesulfonate, N-hydroxysuccinimide ethanesulfonate, N-hydroxysuccinimide 1-propanesulfonate, N-hydroxysuccinimide 2-propanesulfonate, N-hydroxysuccinimide 1-pentanesulfonate, N-hydroxysuccinimide 1-octanesulfonate, N-hydroxysuccinimide p-toluenesulfonate, N-hydroxysuccinimide p-methoxybenzenesulfonate, N-hydroxysuccinimide 2-chloroethanesulfonate, N-hydroxysuccinimide benzenesulfonate, N-hydroxysuccinimide 2,4,6-trimethyl-benzenesulfonate, N-hydroxysuccinimide 1-naphthalenesulfonate, N-hydroxysuccinimide 2-naphthalenesulfonate, N-hydroxy-2-phenylsuccinimide methanesulfonate, N-hydroxymaleimide methanesulfonate, N-hydroxymaleimide ethane-sulfonate, N-hydroxy-2-phenylmaleimide methanesulfonate, N-hydroxyglutarimide methanesulfonate, N-hydroxyglutarimide benzenesulfonate, N-hydroxyphthalimide methanesulfonate, N-hydroxyphthalimide benzenesulfonate, N-hydroxyphthalimide trifluoromethanesulfonate, N-hydroxyphthalimide p-toluenesulfonate, N-hydroxynaphthalimide methanesulfonate, N-hydroxynaphthalimide benzenesulfonate, N-hydroxy-5-norbornene-2,3-dicarboxyimide methanesulfonate, N-hydroxy-5-norbornene-2,3-dicarboxyimide trifluoromethanesulfonate, N-hydroxy-5-norbornene-2,3-dicarboxyimide p-toluenesulfonate, N-hydroxynaphthalimide triflate, N-hydroxy-5-norbornene-2,3-dicarboximide perfluoro-1-butanesulfonate.
In certain embodiments, the photocatalyst is 8-hydroxyquinoline, which may act as a photoacid catalyst in lower pH solutions or as a photobase catalyst in higher pH solutions. In certain other embodiments, the photocatalyst is 8-hydroxy-1,3,6-pyrentrisulfonic acid trisodium salt (D&C Green 8). In various embodiments, the photocatalyst is a photobase. Photobase catalysts may include derivatives of trityl alcohols such as, for example, Malachite green. Photobase catalysts may also include acridine derivatives such as, for example, 9-hydroxy-10-methyl-9-phenyl-9,10-dihydroacridine. Photobase catalysts may also include photoactive carbamate-containing compounds.
The photocatalyst may be present in the compositions and methods described herein in an amount from 0.00050 percent to 30 percent by weight relative to the total weight of the composition. Generally, there is a preferred concentration of the photocatalyst. The preferred concentration of photocatalyst depends, in part, on a variety of factors including, for example, the chemical structure of the catalyst, the reaction medium, the reaction type, and the substrate.
The compositions described herein generally include a vehicle suitable for dispersing or dissolving the active material, the photocatalyst, and any other components to facilitate application of the composition onto the substrate surface or into the bulk portions of the substrate. The vehicle may comprise one or more of a solvent, an emulsifier, a surfactant, or other dispersant. The vehicle may also be a physiologically acceptable vehicle. The properties of a suitable vehicle are dependant, at least in part, on the properties of the other components of the composition and the substrate to be modified.
A suitable vehicle operates to disperse or dissolve the active material, the photocatalyst, and any other components, and to facilitate application of the composition onto the substrate surface. A suitable vehicle facilitates sufficient contact between the active material and the substrate. In various embodiments, a physiologically acceptable vehicle may be any carrier, solvent, or solvent-containing composition that is suitable for application to physiological tissues such as human hair and human skin, for example. In various embodiments, a physiologically acceptable vehicle is a cosmetically or dermatologically acceptable carrier.
A suitable vehicle may be a solvent. In personal and consumer care product applications, for example, water is a useful solvent. In various embodiments, the compositions described herein may include water in an amount from 1% to 98% by weight relative to the total weight of the composition. Water is also a physiologically acceptable vehicle. Additional solvent or solvent-containing physiologically acceptable vehicles include, but are not limited to, hydroxyl-containing liquids (e.g., alcohols), silicones, oils, hydrocarbons, glycols, ammonium lauryl sulfate, sodium lauryl sulfate, and combinations thereof. In certain embodiments, for example, where the active material is at least partially insoluble in water, other solvents, dispersants, or emulsifiers may be used as physiologically acceptable vehicles, alone or in combination with each other and/or with water.
A suitable vehicle is therefore generally used to dilute and/or emulsify the components forming the compositions described herein. A suitable vehicle may dissolve a component (true solution or micellar solution) or a component may be dispersed throughout the vehicle (suspension, dispersion or emulsion). The vehicle of suspension, dispersion or emulsion is typically the continuous phase thereof. That is, other components of the suspension, dispersion or emulsion are distributed on a molecular level or as discrete or agglomerated particles throughout the vehicle. The preparation of such emulsions or dispersions of the active in these cases may be highly important. Small particles contribute to an intimate contact between the active, the substrate and the photoacid catalyst, increasing the reaction rate. For example, in the case of hair surface modification using fatty alcohol and 8-hydroxyquinoline in a water medium, an emulsion that contains very small particles (for example, less than 500 nanometers or more preferably less than 200 nanometers) may be substantially more effective in providing a durable hydrophobic surface than an emulsion containing larger particles (for example, see the data in
It will be readily apparent to one of ordinary skill in the art that the appropriate vehicle(s) are dependent upon the specific active material(s), photocatalyst(s), and other optional component(s) used in the compositions described herein.
The compositions and methods described herein may optionally include a variety of components. For example, in various embodiments, the compositions and methods described herein may include surfactants, emulsifiers, oxidants, reductants, pH regulators, emollients, humectants, proteins, peptides, amino acids, additive polymers, glossers, oils and/or fatty acids, lubricants, sequestrants/chelators, antistatic agents, rheology modifiers, feel agents, fillers, dyes, preservatives, perfumes, other functional components, or combinations thereof. Particular optional components may be found in the CTFA International Cosmetic Ingredient Dictionary, Tenth Edition, 2004; and in McCutcheon, Detergents and Emulsifiers, North American Edition (1986). It will be readily apparent to one of ordinary skill in the art that the particular optional components utilized will be dependant, at least in part, upon the specific applications for the compositions and methods.
In various embodiments, the compositions and methods described herein include an oxidizing agent (oxidant). An oxidant may be added, for example, to render a substrate surface more amenable to photocatalytic covalent modification/functionalization in accordance with the various embodiments described herein. An oxidant may be present in an amount form 0.00050% to 25% by weight relative to the total weight of the composition. Suitable oxidants include, for example, one or more of hydrogen peroxide, urea peroxide, melamine peroxide, percarbonates, alkali metal bromates, perborates, bromates, hypochlorites, chlorites, perchlorates, iodates, periodates, permanganates and persulfates. In certain embodiments, the oxidant is hydrogen peroxide.
The identity of the reaction system, the quantities and concentrations of reagents utilized, and the reaction conditions are all dependent, at least in part, upon the substrate to be modified, the active material utilized, and the manner in which the active material is to be associated with the substrate. These considerations are readily determinable by one of ordinary skill in the art in practice of the compositions and methods described herein.
The following examples are intended to more clearly illustrate aspects of the compositions and methods described herein, but are not intended to limit the scope thereof.
A solution of 94.0 grams of deionized water and 2.0 grams of sodium lauryl sulfate is produced in a 200-ml metal beaker. The solution is maintained at a temperature of 80-90° C. 4.0 g of a melt of stearyl alcohol (at 85° C.) is added drop-wise to the solution under high shear mixing (using a Silverson® L4RT homogenizer at 6000 rpm) over 15-20 minutes forming a mixture. The mixture is continuously mixed at 80-90° C. under high shear for 2 hours. The mixture is then allowed to cool at a rate of 0.5° C. per minute to 25° C. under high shear mixing. The pH of the mixture is adjusted to approximately 5.5-6.0 using dilute hydrochloric acid solution or dilute sodium hydroxide. The resulting micro-emulsion contains stearyl alcohol with an average particle size of approximately 150 nanometers that is phase-stable over at least six months. Particle size measurements are performed with a Horiba laser scattering particle size distribution analyzer (Model LA-910).
The preparation described in Example-1 is repeated using 1.0 grams of sodium lauryl sulfate instead of 2.0 grams as in Example-1. This modification results is a more opaque emulsion than the micro-emulsion prepared in Example-1. The resulting emulsion contains stearyl alcohol with an average particle size of approximately 1.5 micrometers that is phase-stable over at least two months. Particle size measurements are performed with a Horiba laser scattering particle size distribution analyzer (Model LA-910).
0.0150 g of 8-hydroxyquinoline is added to the micro-emulsion from Example-1 in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
0.0150 g of 8-hydroxyquinoline is added to the emulsion from Example-1A in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the emulsion from Example-1. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-3. The hair switch is treated with the emulsion from Example-IA under the same conditions described in Example-3. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-3. The hair switch is treated with the micro-emulsion from Example-2 under the same conditions described in Example-3. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-3. The hair switch is treated with the emulsion from Example-2A under the same conditions described in Example-3. The procedure is repeated with two more identical hair switches (from the same lot)
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. Under ambient light, 2.0 g of the micro-emulsion from Example-1 is spread onto the hair switch. The spreading process includes addition of small quantities of the micro-emulsion on different spots of the hair surfaces followed by immediate spreading by hand after each addition. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. The hair switch is treated with the micro-emulsion from Example-2 under exactly the same conditions described in Example-5. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. In a dark room, the hair switch is dipped into a beaker containing 100.0 g of the emulsion from Example-1. The hair switch is removed from the beaker after 5 minutes and exposed to a bright light (Aquarium 20W Fluorescent tube AquaRays® Model No F20WT12-AR-FS) for 1 minute. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. The hair switch is treated with the micro-emulsion from Example-2 under exactly the same conditions described in Example-7. The procedure is repeated with two more identical hair switches (from the same lot).
A solution of 94.0 grams of deionized water and 2.0 grams of sodium lauryl sulfate is produced in a 200-ml metal beaker. The solution is maintained at a temperature of 80-90° C. 4.0 g of a melt of stearyl alcohol (at 85° C.) is added drop-wise to the solution under high shear mixing (using a Silverson® L4RT homogenizer at 6000 rpm) over 15-20 minutes forming a mixture. The mixture is continuously mixed at 80-90° C. under high shear for 2 hours. The mixture is then allowed to cool at a rate of 0.5° C. per minute to 25° C. under high shear mixing. The pH of the mixture is adjusted to approximately 5.5-6.0 using dilute hydrochloric acid solution or dilute sodium hydroxide. 0.030 g of hydrogen peroxide (35% solution) are then added to the mixture. The resulting micro-emulsion contains stearyl alcohol with an average particle size of approximately 150 nanometers that is phase-stable over at least six months. Particle size measurements are performed with a Horiba laser scattering particle size distribution analyzer (Model LA-910).
0.0150 g of 8-hydroxyquinoline is added to the micro-emulsion from Example-9 in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
Treatment Containing an Oxidizing Agent and a Preservative System
A prototype stearyl alcohol aqueous emulsion containing hydrogen peroxide, 8-hydroxyquinoline photocatalyst, and a sodium lauryl sulfate vehicle is prepared in a manner analogous to Examples 9 and 10. Additionally, the composition includes a preservative system including three components: 1,2-octanediol; 1,3-dimethylol-5,5-dimethylhydrantoin (DMDMH-Glydant® available from Lonza Inc.); and benzyl alcohol.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. In a dark room, the hair switch is dipped into a beaker containing 100.0 g of the emulsion from Example-9. The hair switch is removed from the beaker after 5 minutes and exposed to a bright light (Aquarium 20W Fluorescent tube AquaRays® Model No F20WT12-AR-FS) for 1 minute. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. The hair switch is treated with the micro-emulsion from Example-10 under exactly the same conditions described in Example-11. The procedure is repeated with two more identical hair switches (from the same lot).
A solution of 94.0 grams of deionized water and 2.0 grams of sodium lauryl sulfate is produced in a 200-ml metal beaker. The solution is maintained at a temperature of 80-90° C. 4.0 g of a melt of lauric acid (at 85° C.) is added drop-wise to the solution under high shear mixing (using a Silverson® L4RT homogenizer at 6000 rpm) over 15-20 minutes forming a mixture. The mixture is continuously mixed at 80-90° C. under high shear for 2 hours. The mixture is then allowed to cool at a rate of 0.5° C. per minute to 25° C. under high shear mixing. The pH of the mixture is adjusted to approximately 6.0 using dilute hydrochloric acid solution or dilute sodium hydroxide. The resulting micro-emulsion contains lauric acid with an average particle size of less than approximately 200 nanometers that is phase-stable over at least six months. Particle size measurements are performed with a Horiba laser scattering particle size distribution analyzer (Model LA-910).
0.0150 g of 8-hydroxyquinoline is added into the micro-emulsion from Example-13 in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed, air dried, treated with a reducing agent, washed, and air dried. In a dark room, the hair switch is dipped into a beaker containing 100.0 g of the emulsion from Example-9. The hair switch is removed after 5 minutes and exposed to a bright light (Aquarium 20 W Fluorescent tube AquaRays® Model No F20WT12-AR-FS) for 1 minute, rinsed with tap water for 60 seconds, and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed, air dried, treated with a reducing agent, washed, and air dried. The hair switch is from the same lot as the hair switches used in Example-15. The hair switch is dipped into a beaker containing the micro-emulsion from Example-14 under exactly the same conditions described in Example-15. The procedure is repeated with two more identical hair switches (from the same lot).
A solution of 94.0 grams of deionized water and 2.0 grams of sodium lauryl sulfate is prrepared in a 200-ml metal beaker. The solution is maintained at a temperature of 80-90° C. 4.0 g of a melt of stearyl alcohol (at 85° C.) is added drop-wise to the solution under high shear mixing (using a Silverson® L4RT homogenizer at 6000 rpm) over 15-20 minutes forming a mixture. The mixture is continuously mixed at 80-90° C. under high shear for 2 hours. The mixture is then allowed to cool at a rate of 0.5° C. per minute to 25° C. under high shear mixing. The pH of the mixture is adjusted to approximately 8.5-9.0 using sodium hydroxide. The resulting micro-emulsion contains stearyl alcohol with an average particle size of approximately 150 nanometers that is phase-stable over at least six months. Particle size measurements are performed with a Horiba laser scattering particle size distribution analyzer (Model LA-910).
0.0150 g of 8-hydroxyquinoline is added into the micro-emulsion from Example-17 in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the emulsion from Example-17. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-19. The hair switch is treated with the micro-emulsion from Example-18 under the same conditions described in Example-19. The procedure is repeated with two more identical hair switches (from the same lot).
In a dark room, 0.0150 g of 8-hydroxyquinoline and 0.03 g of D&C Green 8 (8-hydroxy-1,3,6-pyrenetrisulfonic acid trisodium salt) are added into the micro-emulsion from Example-9 immediately after its preparation. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. In a dark room, the hair switch is dipped into a beaker containing 100.0 g of the emulsion from Example-9. The hair switch is removed from the beaker after 5 minutes and exposed to a bright light (Aquarium 20W Fluorescent tube AquaRays® Model No F20WT12-AR-FS) for 1 minute. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-3. The hair switch is treated with the micro-emulsion from Example-21 under the same conditions described in Example-22. The procedure is repeated with two more identical hair switches (from the same lot).
0.10 g of 6-cyano-2-naphthol is added into the micro-emulsion from Example-1 immediately after its preparation. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-3. In a dark room, the hair switch is dipped into a beaker containing 100.0 g of the emulsion from Example-1. The hair switch is removed from the beaker after 5 minutes and exposed UV light (wavelength between approximately 300 nm and 350 nm) using a brush equipped with light emitting diodes for 1 minute. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 6 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switch used in Example-3. The hair switch is treated with the micro-emulsion from Example-24 under the same conditions described in Example-25. The procedure is repeated with two more identical hair switches (from the same lot).
Two hair fibers randomly extracted from a hair switch are attached on two pairs of anchors (3 cm apart) in such a way that the fibers are 0.20 micrometers apart and parallel to each other under controlled temperature and humidity conditions (approximately 22-25° C. and 20-25% humidity). A 0.20 microliter deionized water droplet (±0.02 microliter) is placed onto the two hair fibers with a micro syringe. A video image of the water droplet is taken from the side using a digital camera/software (Model FTA32). The initial contact angle of the droplet on the hair fiber is measured. A typical determination of a treatment includes averaging of 60 contact angle measurements for three switches, four fiber pairs for each switch, and five places across each fiber pair. The error of the method is approximately 1-2%.
The contact angles of treated hair from Examples 3, 4, 5, 6, 11, 12, 15, 16, 19, 20, 22, 23, 25, 26, B, and C are measured using this method. Benchmark contact angle data of hair of various natures (virgin, mildly oxidized, and bleached) are also measured for comparison. The corresponding results of the measurements are given in Table 1 and
All three hair switches from Example-3 are treated with silicone-containing, rinse-off hair conditioner (Pantene Pro-V® Always Smooth; 0.1 mL of conditioner for 1.0 g of hair) and then rinsed with running tap water for 30 seconds and air dried for at least 5 hours.
All three hair switches from Example-4 are treated with silicone-containing, rinse-off hair conditioner (Pantene Pro-V® Always Smooth; 0.1 mL of conditioner for 1.0 g of hair) and then rinsed with running tap water for 30 seconds and air dried for at least 5 hours.
An evaluation of the hair switches from Example-29 relative to the hair switches from Example-28 is provided in Table 2.
The hair from Example-29 has lower dry friction and mechanical damage than the hair from Example 28. The hair from Example-29 has higher levels of deposited silicones on the hair surface than the hair from Example-28. Combability and shine are also enhanced in the hair from Example-29 relative to the hair from Example-28.
A glycerin solution is prepared by adding 90.0 grams of deionized water 10 grams of glycerin into a 200-ml glass beaker and mixed with a magnetic stirrer for 5 minutes.
0.0150 g of 8-hydroxyquinoline and 0.030 g of hydrogen peroxide (35% solution) are added into the solution from Example-30 in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the solution from Example-30. The treated hair switch is rinsed with tap water for 60 seconds and air dried. The treated hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated 2 times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-32. The hair switch is treated with the prototype moisturizer from Example-31 under exactly the same conditions described in Example-32. The procedure is repeated with two more identical hair switches (from the same lot).
Evaluation of the hair switches from Example-33 shows lower rate of moisture loss compared to hair switches from Example-32 when humidity is decreased from 70% to 20%. When formulations from Examples-32 and 33 are evaluated by consumer panel (via spray devise), it is concluded that formulation from Example-33 contributes to softer hair.
A dye solution is prepared by adding 100 g of deionized water and 0.50 gram of Direct Dye 243 (Red BWS supplied by Aakash Chemicals & Dye-Stuffs, Inc.) into a 200-ml glass beaker. The solution is mixed with a magnetic stirrer for 10 minutes to a dark red solution.
0.0150 g of 8-hydroxyquinoline are added into the solution from Example-34 in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. In a dark room, the hair switch is dipped into a 200-ml glass beaker containing 100 g of the dye solution from Example-34 for 10 minutes. The treated hair switch is then removed from the dye solution, rinsed under running tap water for 60 seconds, and air dried. The dried hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The shampoo washing/rinsing cycle is repeated 3 more times. The color of the hair switch is then measured via Color Computer (Microflash® by Datacolor) and compared to the color of the initial (untreated) hair switch. This difference in color between the treated and untreated switches is expressed as DeltaE. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-36. The hair switch is dipped into the prototype dye solution from Example-35 and treated under exactly the same conditions described in Example-36. The color of the hair switch is then measured via Color Computer (Microflash® by Datacolor) and compared to the color of the initial (untreated) hair switch. This difference in color between the treated and untreated switches is expressed as DeltaE. The procedure is repeated with two more identical hair switches (from the same lot).
Table 2 provides the average results (for three switches) of the color evaluation for treatments of Examples 36 and 37. Treatment of Example-37 results in more effective hair dying (higher DeltaE from the original hair).
Five virgin hair switches A, B, and C (4-g, 20 cm long; from the same batch) are dyed with a permanent oxidative dye (Koleston Perfect Shade Red 77/44; level 3) according to the product instructions. After air drying, the switches are treated with 2.0 grams of the prototype emulsion from Example 2 by spraying, rinsed with water, washed with clarifying shampoo and then thoroughly rinsed again with water and air-dried (as described in Example 3). Switch A is measured for color using color computer Minolta and retained for future comparison. Switch B is washed with Wella Lifetex color protection shampoo (using 0.10 ml of shampoo per gram of hair) and rinsed with water of 37° C. and flow rate of 1.0 gallon per minute for 30 seconds. After rinsing, the switch is squeezed once between fingers to remove excess water and blow-dried on high heat for 3.0 minutes and then measured with a color computer. The shampoo-washing/color measurement procedure is repeated five more times (one washing every day). The same shampoo washing protocol (followed by color measurement) is applied for switch C for 12 days (one each day).
Six virgin hair switches D, E, and F (4-g, 20 cm long; from same batch as in Example I) are dyed with a permanent oxidative dye (Koleston Perfect Shade Red 77/44; level 3) according to the product instructions. After air drying, the switches are treated with 2.0 grams of the emulsion from Example 1 by spraying, rinsed with water, washed with clarifying shampoo and then thoroughly rinsed again with water and air-dried (as described in Example 3). Switch D is measured for color using color computer Minolta and retained for future comparison. Switch E is washed with Wella Lifetex color protection shampoo (using 0.10 ml of shampoo per gram of hair) and rinsed with water of 37° C. and flow rate of 1 gallon per minute for 30 seconds. After rinsing, the switch is squeezed once between fingers to remove excess water and blow-dried on high heat for 3.0 minutes. The shampoo-washing/color measurement procedure is repeated five more times (one washing every day) and then the switch is measured for color with a color computer. The same shampoo washing protocol is applied for switch F for 12 days (one each day) and then measured for color with a color computer.
Six virgin hair switches G, H, and I (4-g, 20 cm long; from same batch as in Example I) are dyed with a permanent oxidative dye (Koleston Perfect Shade Red 77/44; level 3) according to the product instructions. After air drying, the switches are treated with 2.0 grams of water by spraying, rinsed with water, washed with clarifying shampoo and then thoroughly rinsed again with water and air-dried (as described in Example 3). Switch G is measured for color using color computer Minolta and retained for future comparison. Switch H is washed with Wella Lifetex color protection shampoo (using 0.10 ml of shampoo per gram of hair) and rinsed with water of 37° C. and flow rate of 1.0 gallon per minute for 30 seconds. After rinsing, the switch is squeezed once between fingers to remove excess water and blow-dried on high heat for 3.0 minutes and then measured with a color computer. The shampoo-washing/color measurement procedure is repeated five more times (one washing every day) and then the switch is measured for color with a color computer. The same shampoo washing protocol is applied for switch I for 12 days (one each day) and then measured for color with a color computer. The color fade ranking of switches (from higher fading to lower) for the switches washed 12 times is I>F>C (as determined by Delta E versus G, D, and A respectively. The color fade ranking of switches (from higher to lower) for the switches washed 6 times is H>E>B (as determined by Delta E versus G, D, and A respectively. Visual inspection of the hair switches confirms these fading profiles.
A solution of 94.0 grams of deionized water and 2.0 grams of sodium lauryl sulfate is produced in a 200-ml metal beaker. The solution is maintained at a temperature of 80-90° C. Five grams of 2-hydroxyethyl benzene is added over 15 minutes to the solution under high shear mixing (using a Silverson® L4RT homogenizer at 6000 rpm). The mixture is continuously mixed at 80-90° C. under high shear for 2 hours. The mixture is then allowed to cool at a rate of 0.5° C. per minute to 25° C. under high shear mixing. The pH of the mixture is adjusted to approximately 5.5-6.0 using dilute hydrochloric acid solution or dilute sodium hydroxide.
The emulsion form Example IV was separated in two equal portion of 100.0 grams. Into one of them, a quantity of 0.0150 g of 8-hydroxyquinoline is added to the emulsion from Example IV in a dark room. The resulting emulsion is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the emulsion from Example V. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 2 more times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch of the same lot as the switch of Example VI is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the emulsion from Example IV. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 2 more times. The procedure is repeated with two more identical hair switches (from the same lot).
A panel of 10 consumers is requested to evaluate perfume intensity of the hair switches at various times after the preparation (1 day, 1 week, and 1 month) and compared with the perfume intensity of the hair switches from Example VI. At all three times, the perfume intensity of hair switches from Example VI is higher than that of hair switches from Example VII.
Into solution of 199.1 grams of deionized water and 0.30 grams of anionic surfactant Dowfax® 3B2 are added under stirring 0.30 grams of beta-cyclodextrin and 0.30 grams hydroxypropyl beta-cyclodextrin having an average degree of substitution of 3.3. The pH of the mixture is adjusted to approximately 5.5-6.0 using dilute hydrochloric acid solution or dilute sodium hydroxide.
The solution from Example VIII is separated into two equal parts. Into on of the parts, a quantity of 0.0150 g of 8-hydroxyquinoline is added in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is sprayed with the solution from Example VIII under the same conditions described in Example-3. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 4 more times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch from the same lot as the switch of Example X is oxidized with bleach solution, washed and air dried. The hair switch is sprayed with the solution from Example IX under the same conditions described in Example-3. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 4 more times. The procedure is repeated with two more identical hair switches (from the same lot).
All switches from Examples X and XI are evaluated for effectiveness of the treatment in reducing malodor. About 90 microliters of a synthetic body malodor composition is uniformly applied over each hair switch. Each malodor-treated hair switch is then sealed in a plastic bag and allowed to equilibrate overnight at ambient temperature. Qualified odor graders evaluate malodor level of each of the switches. Switches from Examples X are found to have stronger malodor present that switches from Example XI.
A polyvinyl alcohol solution is prepared by adding 4.0 grams of polyvinyl alcohol (Gohsenol® GH-23, available from Nippon Gohsei) to 96.0 grams of deionized water over 10 minutes under stirring at 85° C. until a clear solution develops. The solution is left to cool to room temperature before use.
0.0150 g of 8-hydroxyquinoline and 0.030 g of hydrogen peroxide (35% solution) are added into the solution from Example-38 in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
0.0150 g of 8-hydroxyquinoline are added into the solution from Example-38 in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. Under ambient light, the hair switch is thoroughly sprayed with 2.0 g of the solution from Example-38. The hair switch is rinsed with tap water for 60 seconds and air dried. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed with running tap water for 3.0 minutes, and air dried for at least 5 hours. The washing/rinsing is repeated. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-51. The hair switch is treated with the prototype hair styling primer from Example-50 under exactly the same conditions described in Example 51. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and air dried. The hair switch is from the same lot as the hair switches used in Example-51. The hair switch is treated with the prototype hair styling primer from Example-52A under exactly the same conditions described in Example 51. The procedure is repeated with two more identical hair switches (from the same lot).
Visual and sensory inspection of the switches from Example-51, Example-52, and Example-52A shows that hair switches from Example-52 and Example-52A are smoother and shinier than hair switches from Example-51, especially near the hair tips.
All three hair switches from Example-51 are treated while wet with a styling mousse. The hair switches are combed twice using a large tooth comb and combed once using a small tooth comb. The hair switches are lightly blotted with paper towel and the mousse is added using a syringe (0.25 grams of mousse per gram of hair). The mousse is spread throughout the hair and the hair is massaged with the mousse.
The mousse has the following composition in weight percent: 72.73% water; 2.0% Luviskol® VA 73W (50% PVPNVA copolymer available from BASF); 10.0% Carbowax® 600 (PEG-12 available from Dow); 2.0% cyclopentasiloxane (SF1202 available from Momentive); 2.0% silicone emulsion (50% dimethicone emulsion available from Toray Silicones); 0.45% isosteareth-20; 0.50% benzyl alcohol; 0.2% methyl paraben; 0.12% disodium EDTA; and 10.0% Propellant Aeron® A-70 (propane/isobutene available from Diversified CPC).
The mousse is prepared by mixing all the ingredients, except the propellant, into a uniform mixture using a Silverson® R L4RT homogenizer (5000 rpm) at 48-52° C. The mixture is then cooled to 25° C., filled into an aerosol container, and the aerosol propellant is added.
All three hair switches from Example 52 and Example-52A are treated in exactly the same protocol as described in Example-53.
Hair switches from Examples 53 and 54 are fixated around 0.5 inch Teflon® cylindrical rods and dried. The dried hair switches are removed from the rod. The hair curl possesses an initial length (L0). A small weight is applied to the hair switches and their lengths (L1) are measured. The hair switches are then allowed to relax to a final length (L2). The percent recoveries of the hair switches are calculated as (L1−L2)/(L1−L0). Hair switches from Example-54 have a higher percent recovery than hair switches from Example-53.
The initial rigidity of six individual hair fibers is measured. The fibers are then soaked in a solution of 20% (w/v) ethylene carbonate and 2% (w/v) 6-cyano-2-naphthol in 3:2 methanol hexane for 30 minutes without light exposure at wavelengths <550 nm. After soaking, the hair fibers are exposed to a light source with significant light intensity at the wavelengths absorbed by 6-cyano-2-naphthol (approximately 300 nm-350 nm). After exposure, the hair fibers are rinsed, allowed to dry and the rigidity of the hair measured again. The average rigidity of the six hair fibers shows an increase of 44%. Scanning electron microscopy of the hair fibers shows that the surface of the fibers is unchanged.
The initial rigidity of six individual hair fibers is measured. The fibers are then soaked in a solution of 20% (w/v) poly(acrylic acid) (molecular weight approximately 10,000) and 2% (w/v) 6-cyano-2-naphthol in 3:2 methanol hexane for 30 minutes without light exposure at wavelengths <550 nm. After soaking, the hair fibers are exposed to a light source with significant light intensity at the wavelengths absorbed by 6-cyano-2-naphthol (approximately 300 nm-350 nm). After exposure, the hair fibers are rinsed, allowed to dry, and the rigidity of the hair measured again. The average rigidity of the six hair fibers shows an increased of 56%. Scanning electron microscopy of the hair fibers shows that the surface of the fibers is unchanged.
The initial rigidity of six individual hair fibers is measured. The fibers are then soaked in a solution of 20% (w/v) ethyl oxazoline and 2% (w/v) 6-cyano-2-naphthol in 3:2 methanol hexane for 30 minutes without light exposure at wavelengths <550 nm. After soaking, the hair fibers are exposed to a light source with significant light intensity at the wavelengths absorbed by 6-cyano-2-naphthol (approximately 300 nm-350 nm). After exposure, the hair fibers are rinsed, allowed to dry, and the rigidity of the hair measured again. The average rigidity of the six hair fibers shows an increase of 30%. Scanning electron microscopy of the hair fibers shows that the surface of the fibers is unchanged.
An approximately 4 gram virgin hair switch is treated with an ammonium thioglycolate 5% solution (35° C.; pH 9.6) for 10 minutes and thoroughly rinsed with warm water. The hair switch is then soaked for 10 minutes in a 1% aqueous hydrochloric acid solution and thoroughly rinsed with warm water for 10 minutes and air-dried.
A solution comprising α-Methyl Styrene and a photoacid catalyst is produced by adding 90.0 grams of methanol/acetone (1:1), 2.0 grams of 6-cyano-2-naphthol, and 8.0 grams of alpha-methyl styrene into a 200 ml beaker. The ingredients are mixed for 5 minutes to produce a clear solution in a dark room. The solution is then stored in an opaque bottle that does not allow any light exposure of the product.
The hair switch from Example-59 is soaked in 100 ml of the solution from Example-60 in a dark room for 10 minutes. The hair switch is then removed from the beaker and exposed to a light source with substantial light intensity at the wavelengths absorbed by 6-cyano-2-naphthol (approximately 300-350 nm). After exposure, the hair fibers are rinsed and allowed to air dry. The stiffness (determined as resistance to bending) of hair fibers treated with the protocol of Example-61 is 50% higher than untreated hair fibers.
0.0150 g of 8-hydroxyquinoline is added into the solution from Example-30 in a dark room. The resulting solution is placed into and stored in an opaque bottle that does not allow any light exposure of the product.
Panelists are classified into two groups. Under ambient light, the first group of panelists spreads the glycerin solution from Example-30 on the back of a hand and rubs for 30 seconds twice a day (morning and evening for two weeks). Under ambient light, the second group of panelists spreads the prototype moisturizer from Example-62 on the back of a hand and rubs for 30 seconds twice a day (morning and evening for two weeks). The moisture content (skin hydration) of the treated area on the back of a hand is measured using a corneometer.
Measurement of the treated area with a corneometer shows that panelists who use the prototype moisturizer from Example-62 have skin with higher hydration and moisture content than panelists who use the glycerin solution from Example-30.
Under ambient light, panelists spray solution from Example-31 (or solution fom Example-30) on one area of hand dry skin. The spraying is followed by washing with bar soap after 15 minutes from the application. The procedure is repeated 5 times over a period of 5 hours. Visual assessment shows that the solution from Example-31 is more effective in moisturizing skin than the solution from Example-30.
A cotton knit fabric is soaked in a solution of 1% (w/v) poly(acrylic acid) and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelength absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric with and without treatment is then measured under a lkg load. Without treatment the average extension is 1 inch and with treatment the average extension is ¼ inch.
A cotton knit fabric is soaked in a solution of 1% (w/v) poly(vinyl pyrrolidone-co-acrylic acid) and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is then measured under a 1 kg load. Without treatment the average extension of the fabric is ⅞ inch and with treatment the average extension of the fabric is ¼ inch.
A cotton knit fabric is soaked in a solution of 1% (w/v) butane tetracarboxylic acid and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is then measured under a lkg load. Without treatment the average extension of the fabric is 1 inch and with treatment the average extension of the fabric is ⅜ inch.
A cotton knit fabric is soaked in a solution of 1% (w/v) citric acid and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is then measured under a 1 kg load. Without treatment the average extension of the fabric is 1 inch and with treatment the average extension of the fabric is ½ inch.
Denim jeans fabric is soaked in a solution of 1% (w/v) poly(acrylic acid) and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is evaluated using an Instron® Universal Materials Testing Machine. The extension of the treated fabric is found to be 60 % less than the extension of the untreated fabric at a 30 N load.
Faded denim jeans fabric is soaked in a solution of 1% (w/v) poly(acrylic acid) and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is evaluated using an Instron® Universal Materials Testing Machine. The extension of the treated fabric is found to be 50 % less than the extension of the untreated fabric at a 30 N load.
Faded denim jeans fabric is soaked in a solution of 1% (w/v) poly(acrylic acid), 1% ethoxylated poly(dimethylsiloxane) and 100 ppm 8-hydroxyquinoline for 2 minutes. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is evaluated using an Instron® Universal Materials Testing Machine. The extension of the treated fabric is found to be 40% less than the extension of the non-treated fabric at a 30 N load. In addition, the treated fabric has improved surface feel as compared to (1) the untreated fabric and (2) the fabric treated with poly(acrylic acid) alone (Example-70).
Denim jeans fabric is soaked in a solution of 1% (w/v) poly(acrylic acid). During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The fabric is then soaked in a solution of 1% (w/v) dodecanol in 50/50 THF/water and 100 ppm of 8-hydroxyquinoline. During the soaking period the fabric is kept under illumination of >550 nm. The fabric is removed from the solution, excess fluid is removed by squeezing, the fabric is hung up and exposed to ambient light at wavelengths absorbed by 8-hydroxyquinoline (>380 nm) until dry. The fabric is thoroughly rinsed with water and allowed to dry. The extension of the fabric is evaluated using an Instron® Universal Materials Testing Machine. The extension of the treated fabric is found to be 30% less than the extension of the non-treated fabric at a 30 N load. In addition, the treated fabric has improved surface feel as compared to (1) the untreated fabric and (2) the fabric treated with poly(acrylic acid) alone (Example-70).
0.1% Poly(vinylpyrrolidone-co-acrylic acid) (ACP 1001) and 100 ppm of 8-hydroxyquinoline are dissolved in the commercially available Mr. Propre® bathroom cleaner. Black ceramic tiles are then cleaned with the modified Mr. Propre® cleaner and rinsed with water. The tiles are then evaluated for drying time by rinsing the tile with water and measuring the time to dry under ambient conditions. It is found that tiles cleaned with the modified Mr. Propre® have significantly shorter drying times than untreated tiles. It is also found that this reduced drying time lasts through 7 rinses. The reduction in drying time leads to reduced water spotting of the tile.
0.1% Poly(styrene sulfonate-co-acrylic acid) and 100 ppm of 8-hydroxyquinoline are dissolved in the commercially available Mr. Propre® bathroom cleaner. Black ceramic tiles are then cleaned with the modified Mr. Propre® cleaner and rinsed with water. The tiles are then evaluated for water spot formation by rinsing the tile with water and grading the number of water droplets left on the tile at 1 minute after rinsing. It is found that tiles cleaned with the modified Mr. Propre® cleaner have significantly less water drops than untreated tiles. It is also found that this reduction in water drop formation lasts through 7 rinses. The reduction in spotting leads to an improved tile appearance.
0.1% Omnirez® (an ethyl ester of PVM/MA copolymer commercially available from ISP Inc.) and 100 ppm of 8-hydroxyquinoline are dissolved in the commercially available Mr. Propre® bathroom cleaner. Black ceramic tiles are then cleaned with the modified Mr. Propre® cleaner and rinsed with water. The tiles are then soiled using a soap scum solution prepared by dissolving Ivory® soap in 20 gpg hard water. It is found that tiles cleaned with the modified Mr. Propre have substantially reduced soap scum build up on the tile.
0.1% Poly(styrene sulfonate-co-acrylic acid) and 100 ppm of 8-hydroxyquinoline are dissolved in water. The solution is sprayed onto window glass under ambient illumination and the glass is wiped with a paper towel until dry. The glass treated in this manner is found to have a very low water contact angle (<20 degrees). The glass is also observed to exhibit a sheeting effect when rinsed with water. The water sheeting prevents the formation of water droplets on the window glass. The reduction in the formation of water droplets reduces the incidence of streaking and water-mark formation on cleaned glass.
The following base oral care formulation is prepared:
To the base formulation is added 100 ppm of 8-hydroxyquinoline and 1% poly (acrylic acid-co-styrene sulphonate). Brushing teeth with this formulation provides a hydrophilic surface to the tooth which is resistant to microbial deposition and staining as compared to the base formulation.
To the base formulation is added 100 ppm of 8-hydroxyquinoline and 1% poly (vinyl alcohol). Brushing teeth with this formulation provides a hydrophilic surface to the tooth which is resistant to microbial deposition and staining as compared to the base formulation.
To the base formulation is added 100 ppm of 8-hydroxyquinoline and 1% stearic acid. Brushing teeth with this formulation provides a hydrophobic surface to the tooth which is resistant to microbial deposition as compared to the base formulation.
Into 100 g of conditioner with the composition given below, a quantity of 0.0150 g of 8-hydroxyquinoline is added and mixed for 10 minutes at room temperature. The mixture is then placed into an opaque bottle that does not allow any light exposure of the product.
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and rinsed. A quantity of 0.4 ml of conditioner from Example A (containing 8-hydroxyquinoline) is added, massaged into hair for 30 seconds under ambient light, and rinsed with water. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 5 more times. The procedure is repeated with two more identical hair switches (from the same lot).
A 20 cm long (4.0-gram) hair switch is oxidized with bleach solution, washed and rinsed. A quantity of 0.4 ml of conditioner composition Al (not containing 8-hydroxyquinoline) is added, massaged into hair for 30 seconds under ambient light, and rinsed with water. The hair switch is then washed with clarifying shampoo (Pantene Pro-V® Clarifying Shampoo), thoroughly rinsed for 3.0 minutes with running tap water, and air dried for at least 5 hours. The washing/rinsing is repeated 5 more times. The procedure is repeated with two more identical hair switches (from the same lot as Example 82).
Two hair fibers randomly extracted from a hair switch are attached on two pairs of anchors (3 cm apart) in such a way that the fibers are 0.20 micrometers apart and parallel to each other under controlled temperature and humidity conditions (approximately 22-25° C. and 20-25% humidity). A 0.20 microliter deionized water droplet (±0.02 microliter) is placed onto the two hair fibers with a micro syringe. A video image of the water droplet is taken from the side using a digital camera/software (Model FTA32). The initial contact angle of the droplet on the hair fiber is measured. A typical determination of a treatment includes averaging of 60 contact angle measurements for three switches, four fiber pairs for each switch, and five places across each fiber pair. The error of the method is approximately 1-2%.
The contact angles of treated hair from Examples 3, 4, 5, 6, 11, 12, 15, 16, 19, 20, 22, 23, 25, 26, B, and C are measured using this method. Benchmark contact angle data of hair of various natures (virgin, mildly oxidized, and bleached) are also measured for comparison. The corresponding results of the measurements are given in Table 1 and
The various embodiments of the compositions and methods described herein are primarily discussed in connection with hair, skin and fabric substrates. Nevertheless, it is recognized that the invention set forth in the following claims is not limited in application to any particular substrate. The invention set forth in the following claims may be used in connection with any substrate for which it is useful to treat the surface with the compositions and methods described herein as recognizable by one of ordinary skill in the art. Non-limiting examples of such substrates include, for example, fabric, paper, wood, plastic, glass, tile, stone, concrete, brick, other ceramics, and composites.
Although various embodiments have been described herein, many modifications and variations to those embodiments may be implemented by one of ordinary skill in the art upon consideration of the present disclosure. For example, different types of active components and photocatalysts may be employed. Also, where materials are disclosed as suitable substrates (e.g., human or animal hair or skin), other materials may be used (e.g., synthetic hair fibers or skin materials). The foregoing description and following claims are intended to cover all such modification and variations.
The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.”
Every document cited herein, including any cross referenced or related patent or application, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govem.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.
This application claims the benefit of U.S. Provisional Application No. 61/053,831, filed May 16, 2008, which is incorporated by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| 61053831 | May 2008 | US |
