NZ614244B2 - Composition comprising banyan tree, lotus, and clover serum fractions (aging) - Google Patents

Abstract

Disclosed are anti-ageing compositions comprising banyan tree (Ficus Benghalensis), lotus (Nelumbo Nucifera), and clover (Trifolium Pratense) serum fractions. Further disclosed are methods of improving the appearance of aging skin comprises the step of applying a composition having an effective amount of banyan tree serum fraction, lotus serum fraction, and clover serum fraction to a sign of aging on a skin surface, wherein the composition is applied for a period of time sufficient to improve the appearance of the aging skin wherein claudin-1 and aquaporin-3 are upregulated and the moisture and barrier function of human epidermis is increased. nt of banyan tree serum fraction, lotus serum fraction, and clover serum fraction to a sign of aging on a skin surface, wherein the composition is applied for a period of time sufficient to improve the appearance of the aging skin wherein claudin-1 and aquaporin-3 are upregulated and the moisture and barrier function of human epidermis is increased.

Description

PCT/U82012/025910 COMPOSITION COMPRISING BANYAN TREE, LOTUS, AND CLOVER SERUM FRACTIONS (AGING) FIELD OF THE INVENTION The t ion relates to compositions comprising banyan tree, lotus, and clover serum fractions. The present invention also relates to methods for ing the appearance of aging mammalian skin using a composition comprising banyan tree, lotus, and clover serum fractions.

BACKGROUND OF THE INVENTION The epidermis, the outermost layer of the skin, comprises a ar continuum of four layers: the stratum corneum, the granular layer, the s layer, and the basal layer. Each cellular layer in the epidermis represents various stages along a process in which basal epidermal keratinocytes undergo a continuous cycle of proliferation, differentiation, and apoptosis, moving upward from the basal layer to finally yield corneocytes. These corneocytes form the cornified layer known as the stratum comeum.

Basal keratinocytes reside at the lower portion of the epidermis. These mitotically active cells undergo a proliferative cycle to generate er cells that are physically dislocated upward into the spinous and granular layers and undergo the process of differentiation into corneocytes. On passing through the spinous and granular layers, the cells undergo morphological changes that render them flatter in structure as they lose their cellular viability, undergo alternate keratin expression profiles, and transform into cellular ts. On average, a younger-aged epidermis turns over in about one month, shedding the older cells and ing them with newer ones, but this process can increase to over forty days in older skin.

The stratum corneum’s comeocytes remain connected to one other via proteins and lipids, creating a protective barrier between the organism and its outside environment. This y ted epidermal permeability barrier ons as a physical and selective barrier against chemical and biological insults. Important ons of this barrier include attenuation of the penetration of free radicals and prevention of penetration of harmful radiation, including UV ion, into deeper layers. The stratum corneum also acts as a permeability barrier and functions to prevent loss of body moisture to the outside environment. Dysfunction of this r can lead to chronic skin conditions, es, and in extreme cases can even en the viability of the organism.

Skin aging is a multifactorial process driven by both intrinsic (chronological aging) and extrinsic (environmental) factors, ing ultraviolet (UV) exposure, environmental toxins, pollutants, and smoking. It is well known in the art that the ability of the stratum corneum to cyclically generate new layers of skin diminishes with age so that the m corneum turnover rate is substantially reduced in aged skin, with the cornified layer ng lly thinner. This results in a reduction in the functioning capacity of the barrier so that harmful stimuli penetrate the stratum corneum more easily, leading to UV-damage, for example, of the underlying dermal layers, degradation of collagen and elastin, and eventually manifests in appearance as wrinkling and skin atrophy. ng of the stratum corneum by the sum of intrinsic and extrinsic aging factors increases the e appearance of fine lines and wrinkles. Further, the barrier suffers from an age-related increase in permeability to free radicals and a reduction in the amount of lipid in the intercellular matrix, decreasing barrier capacity to diffiise toxins from deeper layers. Recovery capacity of the barrier to environmental insult is also substantially d with age.

Thus, the skin’s barrier function is key to the skin’s ability to regenerate and protect itself from the appearance of aging skin. Accordingly, it would be desirable to provide compositions and methods of treatment that can improve the skin’s barrier function and also improve the appearance of aging skin.

SUMMARY OF THE INVENTION The present invention relates to compositions comprising banyan tree, lotus, and clover serum fractions and mixtures and/or combinations thereof. In one ment, the t invention provides use of a serum fraction blend in formulating topically applied skin compositions, said blend comprising banyan tree serum fraction, lotus serum fraction and clover serum fraction to increase the moisture and barrier function of human epidermis, as evidenced by the statistically significant up— regulation of claudin-l and aquaporin-3 in said human epidermis.

Also provided in another aspect is a process to increase the moisture and barrier on of human epidermis, as evidenced by the statistically significant up-regulation of claudin-l and aquaporin-3 in said human epidermis, by topically applying a skin care composition comprising a blend of banyan tree serum fraction, lotus serum fraction and clover serum fraction.

A method of improving the appearance of aging skin comprising the step of applying a first composition comprising an effective amount of banyan tree serum fraction, lotus serum fraction, and clover serum fraction blend to an area of aging skin, wherein the ition is applied for a period of time ent to improve the ance of the aging skin. In certain embodiments the composition also comprises a dermatologically acceptable carrier.

PCT/U82012/025910 In some embodiments the area of aging skin is aging facial skin. In particular embodiments, ing the appearance of aging skin comprises improving the appearance of wrinkles, fine lines, coarse deep lines, crevices, bumps, large pores; thickening of keratinous tissue (e.g., building the mis and/or dermis and/or sub-dermal layers of the skin); increasing the convolution of the dermal-epidermal border (also known as the rete ridges); skin ning; preventing loss of skin elasticity, for example, due to loss, damage and/or inactivation of functional skin elastin, resulting in such conditions as elastosis, sagging, loss of skin recoil from deformation; change in coloration to the skin, for example, under-eye circles, blotchiness (e.g., uneven red coloration due to, for example, rosacea), sallowness, discoloration caused by hyperpigmentation, etc.; and combinations thereof.

In response to the problems identified in the background, the present invention may take other forms. Further forms of the t invention will be appreciated in the detailed description that follows.

BRIEF DESCRIPTION OF THE DRAWINGS It is believed that the present invention will be better understood from the following description taken in conjunction with the accompanying gs. The nced drawings are not to be construed as limiting the scope of the present invention.

Fig. 1 is a bar graph g the up—regulation of aquaporin-3 (AQP3) and claudin—l when banyan tree, clover, and lotus serum fractions are evaluated separately and as a blend in a keratinocyte assay.

DETAILED DESCRIPTION OF THE INVENTION All percentages and ratios used herein are by weight of the total ition and all measurements made are at 25°C, unless otherwise designated. All numeric ranges are inclusive of narrower ranges; delineated upper and lower range limits are hangeable to create further ranges not explicitly delineated.

The itions of the present invention can comprise, t essentially of, or consist of, the essential components as well as optional ingredients described herein. As used herein, “consisting essentially of” means that the composition or component may include additional ingredients, but only if the additional ingredients do not materially alter the basic and novel characteristics of the claimed itions or methods.

The term “apply” or “application” as used in reference to a composition, means to apply or spread the itions of the present invention onto a human skin surface such as the epidermis.

The term “dermatologically acceptable” as used herein means that the compositions or components described are suitable for use in contact with human skin tissue without undue toxicity, incompatibility, instability, allergic response, and the like.

The term “effective amount” as used herein means an amount of a compound or composition sufficient to significantly induce a positive appearance and/or feel benefit, but low enough to avoid serious side effects (i.e., to provide a reasonable benefit to risk ratio, within the scope of sound judgment of the skilled artisan). As used herein, tive amount” in relation to the banyan tree, lotus, and clover blend means an amount of the three materials in combination sufficient to significantly induce a positive appearance and/or feel , but low enough to avoid serious side effects (i.e., to provide a reasonable benefit to risk ratio, within the scope of sound judgment of the skilled artisan).

The term “post-inflammatory hyperpigmentation” as used herein refers to an acute to c increase in pigmentation as a response to a transient inflammatory event. Post- inflammatory hyperpigmentation is ularly prevalent in, but not limited to, dark skin subjects. Post-inflammatory igmentation typically subsides once the ent inflammatory event dissipates. Examples of transient inflammatory events include, but are not limited to, acne lesions, ingrown hairs, scratches, insect bites, surfactant damage, and short-term UV exposure.

The term “hyperpigmented spot” as used herein refers to a defined area of skin wherein the pigmentation is greater than that of an adjacent area of skin due to localized and c or systemic overproduction of melanin. Hyperpigmented spots typically are between about 2 mm and about 10 mm in diameter but smaller or larger spots are possible.

Hyperpigmented spots can include one or more of age spots, sun spots, solar lentigos, hypo- melanotic lesions, freckles, and a spots.

The term “age spots” as used herein refers to a aging spot wherein the pigmentation is due to localized and chronic overproduction of melanin caused by intrinsic or sic aging factors.

The term “skin tone agent” as used herein refers to an agent that regulates melanin production signals, synthesis of melanin, systemic transfer of melanin between the cyte and the keratinocyte, and/or n degradation. Skin tone agents can improve WO 15947 PCT/U82012/025910 the appearance of uneven skin tone by acting as a lightening or pigmentation reduction cosmetic agent.

The term “skin tone” as used herein refers to the overall appearance of n in the skin caused by the systemic, rather than transient, synthesis of melanin. Skin tone is typically characterized over a larger area of the skin. The area ideally may be than 100 m2, but larger areas are envisioned such as the entirety of the facial skin or any of the facial skin surfaces.

Skin tone can be measured by image analysis. For example, overall lightness can be measured by L"< coordinate in L*a*b* color space (International Commission on Illumination). Chromophore mapping such as melanin mapping and melanin concentration may be used as an indicator of overall skin tone. Mean melanin may be calculated from the phore map data. Additionally, skin tone evenness can be determined by n evenness which also may be calculated from the Chromophore map data. Suitable Chromophore mapping techniques are discussed in the example below.

The term “facial skin surface” as used herein refers to one or more of ad, periorbital, cheek, perioral, chin, and nose skin surfaces.

“Skin care s,” or “actives,” as used herein, means compounds that, when applied to the skin, provide a benefit or ement to the skin.

“Improving the appearance of aging skin” means ing a visually and/or tactilely perceptible positive , or benefit, in skin appearance and/or feel. As used herein, “improving the appearance of aging skin” also includes preventing or ng the appearance of aging skin. Benefits that may be provided include, but are not limited to, one or more of the following: Reducing the appearance of wrinkles and coarse deep lines, fine lines, crevices, bumps, and large pores; thickening of keratinous tissue (e.g., building the epidermis and/or dermis and/or sub-dermal layers of the skin); increasing the convolution of the dermal-epidermal border (also known as the rete ridges); skin lightening; preventing loss of skin elasticity, for example, due to loss, damage and/or inactivation of fianctional skin elastin, resulting in such conditions as elastosis, sagging, loss of skin recoil from deformation; change in coloration to the skin, for e, under—eye circles, blotchiness (e.g., uneven red coloration due to, for e, rosacea), sallowness, discoloration caused by hyperpigmentation, etc.

“Signs of skin aging,” as used herein, include but are not limited to, all outward y and tactilely perceptible manifestations, as well as any macro— or microeffects, due to skin aging. These signs may result from processes which include, but are not limited to, the PCT/U82012/025910 development of textural discontinuities such as wrinkles and coarse deep wrinkles, fine lines, skin lines, crevices, bumps, large pores, unevenness or roughness; loss of skin elasticity; discoloration (including undereye circles); blotchiness; sallowness; hyperpigmented skin regions such as age spots and freckles; keratoses; abnormal entiation; eratinization; sis; collagen breakdown, and other histological changes in the stratum corneum, dermis, epidermis, vascular system (e.g., telangiectasia or spider vessels), and underlying tissues (e.g., fat and/or muscle), especially those proximate to the skin.

“Hyperpigmentation,” as used herein, refers to an area of skin wherein the pigmentation is greater than that of an adjacent area of skin (e.g., a pigment spot, an age spot, and the like).

“Desquamation, exfoliation, and/or turnover,” as used herein, mean the removal of the upper layers of the stratum corneum (comprising the horny layers).

“Sallowness,” as used herein means the pale color, yellow color or the like ion of skin that occurs as a result of a loss of, damage to, tions to, and/or abnormalities in skin components such that they become colored (e.g., yellow in color) due to processes such as protein glycation and accumulation of lipofuscin or in the decrease in peripheral blood flow that typically anies skin aging.

As used herein, “exogenous solven ” means any solvent that is not ntly present in the plant material, but is placed in contact with the plant material for the e of separating (e.g., extracting) compounds from the plant material.

I. Compositions The present invention s to various compositions and, more specifically, to compositions for ation to a skin surface. The compositions may be in a wide variety of product forms that include, but are not limited to, solutions, suspensions, s, creams, gels, toners, sticks, pencil, sprays, aerosols, nts, cleansing liquid washes and solid bars, shampoos and hair conditioners, pastes, foams, powders, mousses, shaving creams, wipes, strips, patches, electrically-powered patches, wound dressing and adhesive bandages, hydrogels, film-forming products, facial and skin masks (with and without insoluble sheet), make-up such as foundations, eye liners, and eye s, and the like. The composition form may follow from the particular dermatologically acceptable carrier chosen, if present in the composition.

PCT/U82012/025910 A. Serum Fractions Compositions of the present invention comprise effective amounts of banyan tree serum fraction, lotus serum fraction, and clover serum fraction.

Banyan tree, lotus, and clover serum fractions consist essentially of the flower, leaf, and stem serum ons obtained from Ficus Benghalensis, Nelumbo Nucz’fera, and Trz'folz'um Pratense, respectively. Preferred serum fractions herein are produced by Akzo Nobel Surface Chemistry LLC of Ossining, New York, USA, under the trade names Ficus Bengalensis Enriched Serum FractionTM (TNCI Name: Ficus Indica Flower/Leaf/Stem Juice), Lotus Enriched Serum FractionTM (INCI Name: Nelumbo Nucz’fem /Leaf/Stem Juice), and Red Clover Enriched Serum FractionTM (INCI Name: Trz'folz'um Pratense (Clover) Flower/Leaf/Stem Juice).

In some embodiments, the ition may comprise banyan tree serum fraction in an amount of from 0.001% to 15%, alternatively from 0.002% to 10%, alternately from 0.025% to 10%, in other embodiments from 0.05% to 10%, in others from 0.05% to 5%, and in others from 0.1% to 5%, by weight of the total ition. The composition may comprise lotus serum on in an amount of from 0.001% to 15%, alternatively from 0.002% to 10%, alternatively from 0.01% to 15%, alternately from 0.025% to 10%, in other embodiments from 0.05% to 10%, in others from 0.05% to 5%, and in others from 0.1% to %, by weight of the total composition. The ition may comprise clover serum fraction in an amount of from 0.001% to 15%, alternatively from 0.002% to 10%, alternatively from 0.01% to 15%, alternately from 0.025% to 10%, in other embodiments from 0.05% to 10%, in others from 0.05% to 5%, and in others from 0.1% to 5%, by weight of the total composition.

The method for making a serum fraction comprises the steps of: (a) separating cell juice from clean, fresh, un—wilted plant matter to obtain fresh cell juice, wherein no ous liquid is added prior or during said separating; (b) filtering said fresh cell juice to obtain fiber-free cell juice; and (c) fractionating said fiber-free cell juice to obtain the serum fraction for use herein. Suitable serum fraction preparation methods are set forth in US.

Patent No. 7,442,391, “Bioactive Botanical Cosmetic Compositions and Processes for their tion,” to Koganov, and in co-pending US. Provisional Application Serial No. 61/381,748, filed 10 September 2010 by Swanson et al., the disclosures of which are hereby incorporated by reference herein.

The resulting serum fractions have superior bioactivity versus traditionally prepared plant extracts. Unlike traditional extracts, the serum fraction is prepared from fresh plant cell juice that has been ically separated from the rest of the fresh plant material.

Importantly, no exogenous solvent (e.g., water, hexane, acetone, ethanol) is added during the juice separation process. The ing cell juice contains the full spectrum of compounds found in fresh plant , thus the resulting serum fractions contain a much broader range of active compounds than do traditional plant extracts, which contain only the narrow range of compounds that can be separated with a particular solvent.

Furthermore, using fresh plants maintains the integrity of the ive components inherently present in the fresh plant matter. Traditional plant ts are not prepared from fresh plant matter, but rather from dried plant material, which has undergone degradation due to dehydration. During dehydration, the cell walls are compromised, causing the ation of nds through mechanisms such as hydrolysis, oxidation, polymerization, Maillard reactions, and isomerization. When the dried leaves are extracted, the resulting extract thus contains these ation products that were not originally present in the fresh plant matter.

Accordingly, the composition of the resulting dry leaf extract greatly differs from that of fresh juice and the resulting serum on.

B. Skin Tone Agent In some embodiments, it may be desirable to include a skin tone agent in the composition. The skin tone agents can be included to further improve overall skin tone.

When present, the compositions of the present invention n up to about 50%, 40%, 30%, %, 10%, 5%, or 3%, by weight of the composition, of the skin tone agent. When present, the itions of the present invention contain at least about 0.001%, 0.01%, 0.1%, 0.2%, 0.5%, or 1%, by weight of the composition, of the skin tone agent. Suitable ranges include any combination of the lower and upper limits including suitable ranges from about 0.1% to about 50%; from about 0.2% to about 20%; or from about 1% to about 10%, by weight of the composition, of the skin tone agent. The amounts listed herein are only to be used as a guide, as the optimum amount of the skin tone agent will depend on the specific active selected since their potency does vary erably.

Suitable skin tone agents include, but are not limited to, sugar amines, vitamin B3 compounds, arbutin, rbutin, l,3-dihydroxy—4-alkylbenzene such as hexylresorcinol, sucrose dilaurante, bakuchoil (4-[(1E, SS)—3~ethenyl-3,7-dimethyl ~ 1,6 octadienyl] phenol or 2012/025910 monterpene phenol), pyrenoine (available from h , France), panicum miliaceum seed extract, arlatone dioic acid, cinnamic acid, ferulic acid, achromaxyl, methyl nicotinamide, oil soluble licorice extract, folic acid, undecylenic acid (i.e., undecenoic acid), zinc undecylenate, thiamine (Vitamin B1) and its hloride, tophan, helianthus annuus ower) and vitis Vinifera ) leaf extract, carnosine (i.e., dragosine), methyl gentisate, 1,2-hexandiol and l,2-0ctandiol (i.e., combination sold as Symdiol 68 by Symrise AG, Germany), inositol, decylenoylphenylalanine (e.g., sold under the tradename Sepiwhite by , France), kojic acid, hexamidine compounds, salicylic acid, and retinoids including retinol and retinyl propionate.

In certain ments, the additional skin tone agent is selected from vitamin B3 compounds, sugar amines, hexamidine compounds, salicylic acid, hydroxy—4~ alkylbenzene such as hexylresorcinol, and retinoids. As used herein, "vitamin B3 compound" means a compound having the formula: wherein R is - CONH2 (i.e., niacinamide), — COOH (i.e., nicotinic acid) or - CHzOH (i.e., nicotinyl alcohol); derivatives thereof; and salts of any of the foregoing. As used herein, “sugar amine” includes isomers and tautomers of such and its salts (e.g., HCl salt) and its derivatives. Examples of sugar amines include glucosamine, N—acetyl glucosamine, mannosamine, N—acetyl mannosamine, galactosamine, N—acetyl galactosamine, their s (e. g., stereoisomers), and their salts (e.g, HCl salt). As used herein, "hexaminide compound” means a compound having the formula: NH\>C@“Om(CH2)6—O@C/NH HZN \ 1/ 2 R \R2 wherein R1 and R2 are optional or are organic acids (e.g., sulfonic acids, etc). In one embodiment, hexamidine compound is hexamidine diisethionate.

W0 2012f115947 C. Anti-Inflammatory Agents Hyperpigmentation may result from skin inflammation. Transient inflammatory events ring hyperpigmentation and, more specifically, post-inflammatory hyperpigmentation include, but are not limited to, acne lesions, n hairs, scratches, insect bites, surfactant , allergens, and term UV exposure. Inflammation induced hyperpigmentation including post-inflammatory hyperpigmentation may be managed by incorporating into the compositions of the present invention an nflammatory agent.

When present, the compositions of the t invention contain up to about 20%, 10%, 5%, 3%, or 1% by weight of the composition, of the anti—inflarnrnatory agent. When present, the compositions of the present invention contain at least about , 0.01%, 0.1%, 0.2%, 0.3%, 0.5%, or 1%, by weight of the composition, of the anti-inflammatory agent. Suitable ranges include any combination of the lower and upper limits. Suitable anti-inflammatory agents include, but are not limited to nonsteroidal anti—inflammatory agents (NSAIDS including but not limited to ibuprofen, naproxen, flufenamic acid, etofenamate, aspirin, mefenamic acid, meclofenamic acid, piroxicam and felbinac), glycyrrhizic acid (also known as glycyrrhizin, glycyrrhixinic acid, and glycyrrhetinic acid glycoside) and salts such as dipotassium glycyrrhizate, glycyrrhetenic acid, licorice extracts, lol (e.g., alpha bisabolol), manjistha (extracted from plants in the genus Rubia, particularly Rubia cordifolia), and guggal (extracted from plants in the genus Commiphora, particularly Commiphora mukul), kola extract, chamomile, Clover t (e.g., red clover extract), and sea whip extract (extracts from plant in the order Gorgonacea), derivatives of any of the foregoing, and mixtures thereof.

D. Sunscreen Actives The compositions of the subject invention may comprise one or more sunscreen actives (or sunscreen agents) and/or ultraviolet light absorbers. Herein, “sunscreen active” collectively includes, sunscreen actives, sunscreen agents, and/or ultraviolet light absorbers.

Sunscreen actives e both sunscreen agents and physical sunblocks. een actives may be c or inorganic. Examples of le sunscreen actives are disclosed in Personal Care Product Council's ational Cosmetic ient Dictionary and Handbook, Thirteenth Edition, as “sunscreen agents.” Particularly suitable sunscreen actives are 2- ethylhexyl-p-methoxycinnamate (commercially available as PARSOLTM MCX), 4,4’-t-butyl methoxydibenzoyl—methane rcially available as PARSOLTM 1789), 2-hydroxy WO 15947 PCT/U52012/025910 methoxybenzophenone, octyldimethyl-p-aminobenzoic acid, digalloyltrioleate, 2,2— dihydroxymethoxybenzophenone, ethyl—4-(bis(hydroxypropyl))aminobenzoate, 2— ethylhexyl-Z-cyano-3,3-diphenylacrylate, 2-ethylhexy1—salicylate, glyceryl-p-aminobenzoate, 3,3,5-tri-methylcyclohexylsalicylate, menthyl anthranilate, p-dimethyl-aminobenzoic acid or aminobenzoate, 2-ethylhexyl-p-dimethyl-amino—benzoate, 2—phenylbenzimidazolesulfonic acid, imethylaminophenyl)sulfonicbenzoxazoic acid, octocrylene, zinc oxide, benzylidene camphor and derivatives f, titanium dioxide, and mixtures thereof.

In one embodiment, the composition may comprise from about 1% to about 20%, and alternatively from about 2% to about 10% by weight of the composition, of the een active. Exact s will vary depending upon the chosen een active and the desired Sun Protection Factor (SPF), which is within the knowledge of one of skilled in the art.

E. Optional Components The compositions of the present invention may contain a variety of other ingredients provided that they do not unacceptably alter the benefits of the invention. When present, compositions of the present invention may contain from about 0.0001% to about 50%; from about 0.001% to about 20%; or, alternately, from about 0.01% to about 10%, by weight of the composition, of the optional ents. The amounts listed herein are only to be used as a guide, as the optimum amount of the al components used in a composition will depend on the specific active selected since their potency does vary considerably. Hence, the amount of some optional components useful in the present invention may be outside the ranges listed The optional components, when incorporated into the composition, should be suitable for use in contact with human skin tissue without undue toxicity, incompatibility, instability, allergic response, and the like. The compositions of the present invention may e optional components such as anti-acne actives, desquamation actives, anti-cellulite agents, chelating agents, flavonoids, tanning active, non-vitamin antioxidants and radical scavengers, hair growth regulators, anti-wrinkle actives, anti~atrophy actives, minerals, phytosterols and/or plant es, N-acyl amino acid compounds, antimicrobial or antifungal actives, and other useful skin care actives, which are described in further detail in US. application publication No. US2006/0275237Al and U82004/0175347A1, the disclosures of which are hereby incorporated by nce herein.

WO 15947 PCT/U82012/025910 The Personal Care Product Council's International Cosmetic Ingredient Dictionary and Handbook, Thirteenth Edition, describes a wide y of non-limiting cosmetic and pharmaceutical ients commonly used in the skin care industry, which are suitable optional components for use in the compositions of the present invention. Examples of these ingredient classes include: abrasives, absorbents, aesthetic components such as fragrances, pigments, colorings/colorants, essential oils, anti—caking agents, antifoaming agents, antimicrobials, binders, biological additives, buffering agents, bulking agents, chelating agents, al additives, colorants, cosmetic astringents, cosmetic es, denaturants, drug astringents, emollients, external analgesics, film formers or als, opacifying agents, pI—I adjusters, preservatives, propellants, reducing agents, sequestrants, skin cooling agents, skin protectants, thickeners viscosity modifiers, ns, and ations thereof.

F. Dermatologically Acceptable Carrier The compositions of the present invention may also comprise a dermatologically acceptable carrier (which may be referred to as er”) for the ition. The phrase "dermatologically acceptable carrier", as used , means that the carrier is suitable for topical application to the keratinous tissue, has good aesthetic properties, is compatible with the actives in the composition, and will not cause any unreasonable safety or toxicity concerns. In one embodiment, the carrier is present at a level of from about 50% to about 99%, about 60% to about 98%, about 70% to about 98%, or, atively, from about 80% to about 95%, by weight of the ition.

The carrier can be in a wide variety of forms. Non-limiting examples include simple solutions (e.g., aqueous, organic solvent, or oil based), emulsions, and solid forms (e.g, gels, sticks, e solids, or amorphous materials). In certain embodiments, the dermatologically acceptable carrier is in the form of an emulsion. Emulsion may be generally classified as having a continuous aqueous phase (e.g, oil-in-water and water-in-oil- in—water) or a continuous oil phase (e.g., water-in—oil and oil—in-water—in-oil). The oil phase of the present invention may comprise silicone oils, non-silicone oils such as hydrocarbon oils, , ethers, and the like, and mixtures thereof.

The aqueous phase typically comprises water. However, in other embodiments, the aqueous phase may comprise components other than water, including but not limited to water-soluble moisturizing agents, conditioning agents, anti—microbials, humectants and/or other soluble skin care actives. In one embodiment, the non-water component of the -12..

W0 20121115947 composition comprises a humectant such as glycerin and/or other polyols. However, it should be recognized that the composition may be substantially (226., less than 1% water) or fully anhydrous.

A suitable carrier is ed to yield a desired product form. Furthermore, the solubility or dispersibility of the components (e.g., extracts, sunscreen active, additional components) may dictate the form and character of the carrier. In one embodiment, an oil—in- water or water-in-oil emulsion is red.

Emulsions may r comprise an emulsifier. The composition may comprise any suitable percentage of emulsifier to sufficiently emulsify the carrier. Suitable weight ranges include from about 0.1% to about 10% or about 0.2% to about 5% of an emulsifier, based on the weight of the composition. fiers may be nonionic, c or cationic. Suitable emulsifiers are disclosed in, for example, US. Patent 3,755,560, US. Patent 4,421,769, and McCutcheon's Detergents and Emulsifiers, North American Edition, pages 317-324 , the disclosures of which are hereby incorporated by reference herein. Suitable emulsions may have a wide range of Viscosities, ing on the desired product form.

The carrier may further comprise a thickening agent as are well known in the art to provide compositions having a suitable ity and rheological character.

II. Methods of Treatment Various methods of ent, application, regulation, or improvement may utilize the aforementioned compositions. Identification of a region of aging skin may occur on any skin surface of the body. Skin surfaces of the most concern tend to be those not typically covered by clothing such as facial skin surfaces, hand and arm skin surfaces, foot and leg skin surfaces, and neck and chest skin surfaces (e.g., décolletage). In particular, identification of the region of aging skin may be on a facial skin surface including the forehead, perioral, chin, periorbital, nose, and/or cheek skin surfaces.

The method may comprise the step of applying the ition to the usly fied area of aging skin, or an area where one seeks to prevent the appearance of aging skin. Many regimens exist for the application of the composition. The composition may be applied at least once a day, twice a day, or on a more nt daily basis, during a treatment period. When applied twice daily, the first and second applications are separated by at least 1 to about 12 hours. lly, the composition may be applied in the morning and/or in the evening before bed.

PCT/U82012/025910 The treatment period is ideally of sufficient time to provide an improvement in the appearance of aging skin. The treatment period may be at least about 1 week, and in some embodiments the treatment period may last about 4 weeks or about 8 weeks. In certain embodiments, the treatment period will extend over multiple months (i.e., 3-12 months) or multiple years. In one embodiment the composition is applied at least once a day during a treatment period of at least about 4 weeks or at least about 8 weeks. In one embodiment the composition is applied twice a day during a treatment period of at least about 4 weeks or 8 weeks.

The step of applying the composition may be accomplished by localized application.

In reference to ation of the ition, the terms ized”, “local”, or “locally” mean that the ition is delivered to the targeted area (such as age spots) while minimizing delivery to skin surface not requiring treatment. The composition may be applied and lightly massaged into area of aging skin. The form of the composition or the dermatologically acceptable carrier should be ed to facilitate localized application.

While certain ments of the present invention contemplate applying a composition locally to an area, it will be appreciated that compositions of the t invention can be applied more generally or broadly to one or more skin surfaces.

In some embodiments, the composition may be red by a variety of applicators appropriate for localized and general application. Such applicators can include droppers, applicator wands, cotton swabs, or any other suitable device. Other suitable applicators include SH-0127 pen applicator ble from Shya Hsin Plastic Works, Inc., Taiwan and either the Xpress Tip or liquid filled swab available from SwabPlus, Inc., China. The applicator may be configured to easily apply the composition to age spots having an approximate er between about 2 mm and about 10 mm and allowing for a dosed amount of the composition of between about 1 to about 50 uL/cm2 or between about I to about SuL/cmz. In another embodiment, the ition is applied to the one or more aging spots and more generally to one or more facial skin surfaces contemporaneously (z'.e., over a period of less than 30 s or, more typically, less than 5 minutes).

While some methods described herein contemplate applying the compositions of the t invention with an applicator, it will be appreciated that applicators are not required and the compositions of the present invention can also be applied directly by using one’s finger or in other conventional manners.

PCT/U82012/025910 In one embodiment, the method comprises the steps of applying a first composition comprising an effective amount of banyan tree serum fraction, lotus serum fraction, and clover serum fraction to a skin surface and of applying a second composition to the skin surface, before or after the first composition. The first and second compositions may be any compositions described ; however, the second composition may optionally se an effective amount of the serum ons present in the first ition. The second composition may comprise one or more tone agents, sunscreen actives, nflammatory agents, or optional components. The first composition may be generally or locally applied, While the second composition may be lly or locally applied to the skin surface ing the aging skin to which the first composition is applied. In certain embodiments, the skin surface is facial skin surface which include one or more of the forehead, perioral, chin, periorbital, nose, and cheek skin surfaces. In another embodiment, the first and second itions are applied contemporaneously to at least the cheek, forehead, and chin/perioral skin surfaces. For general application to a skin surface and, particularly a facial skin surface, the closed amount of the first or second composition may be between about 1 to about 50 uL/cm2 per application (i.e., per single application to the skin surfaces).

Suitable methods may comprise any one or more of the entioned steps. All of the aforementioned steps are applicable to application, treatment, regulation, and/or improvement of aging skin appearance. One suitable method of improving the appearance of aging skin includes the step of topically applying a composition comprising an effective amount of banyan tree serum fraction, lotus serum fraction, and clover serum fraction blend to the aging skin surface, wherein the composition is applied for a period of time sufficient for the serum fraction blend to improve the ance of the aging skin.

III. Mechanisms ofAction The stratum corneum is a tightly regulated epidermal permeability barrier and functions as a physical and selective barrier t chemical and biological s, as well as acts as a permeability barrier to prevent loss of body moisture to the outside environment.

The m corneum’s cells control these barriers by regulating the movement of water, ions, and proteins across them. Flow of ions and molecules between cells, often referred to as the paracellular permeability pathway, is regulated by tight junctions. (Koval, Michael.

Claudins — Key Pieces in the Tight Junction Puzzle. Cell ication and Adhesion. 13:127—138, 2006.) Tight ons are sites of cell-cell contact composed of a number of transmembrane and peripheral proteins, assembled into a complex tethered to the cytoskeleton. Of these transmembrane proteins, those identified as “Claudins” are the major determinant of cellular permeability. Claudins serve several roles in maintaining barrier on. Claudins are a major component of the strands that constitute the permeability barrier to limit diffusion of ns and other macromolecules between cells, and they also form specific paracellular channels that regulate ion diffusion between cells. n-l mutations have been associated with several types of ichthyosis (a family of skin disorders causing dry, ned, scaly, or flaky skin), and a study has shown that the epidermal barrier function of claudin-l deficient mice is so compromised that their cells are unable to hold water, causing the skin to dry up and leading to death within a day. (M. Furuse, et al. The Journal of Cell Biology, 156 (No. 6): 1099-1111, 2002) Aquaporin-3 (AQP3) is a membrane transporter of water and glycerol expressed in the basal layer of epidermal keratinocytes. Aged human skin has been shown to experience decreased AQP3 expression, which also correlates to a reduced stratum corneum water content and elasticity compared with young, undamaged skin. In studies involving AQP3- knockout mice, reduced AQP3-dependent glycerol transport in AQP3-deficiient epidermis has been show to be sible for dehydrated, inelastic skin. (“Aquaporin—3 functions as a glycerol transporter in mammalian skin,” hikuma M, Biol Cell. 2005 Jul;97(7):479- 86.); (”Roles of Aquaporin-3 in the mis”, Hara—Chikuma, M., J Invest Dermatol. 2008 Sep;128(9):2145-51. Epub 2008 Jun 12); (“Glycerol replacement corrects ive skin hydration, elasticity, and barrier function in aqaporin-3—deficient mice,” Hara M., Proc Natl Acad Sci U S A. 2003 Jun (12):7360-5. Epub 2003 May 27).

The blend of banyan tree, clover, and lotus serum fractions resulted in positive increases in moisture and barrier function, as evidenced by the statistically significant up- regulation of claudin—l and rin-3 (“AQP3”) in Example 3 below.

In Example 2, the blend’s effect on nine different genes associated with aging skin was ted. These nine genes, and their associated functions, are described in Table l of Example 2. The fold-increase / decrease in expression, versus control, was determined for the aging-related genes at two ent concentration levels. In both cases, as shown in Tables 2a and 2b, the blend effected a positive fold increase in all nine genes, indicating the desirable up—regulation of that gene, and thus a positive anti—aging benefit.

PCT/U82012/025910 EXAMPLES Example 1 — afl Compositions Table 1 sets forth non-limiting examples of the compositions of the present invention.

The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention, as many ions thereof are possible without departing from the spirit and scope of the invention, which would be recognized by one of ordinary skill in the art. In the es, all concentrations are listed as weight percent, unless ise specified and may exclude minor als such as diluents, filler, and so forth.

The listed formulations, therefore, comprise the listed components and any minor materials associated with such components. As is nt to one of ordinary skill in the art, the ion of these minor materials will vary depending on the physical and chemical characteristics of the particular ingredients selected to make the present invention as described herein.

All examples may be used to treat or improve the appearance of one or more signs of aging. The present invention may further relate to a regimen involving the localized treatment for one or more aging signs by a first composition (e. g., Examples A or B) and a more broad or general facial skin treatment by a second composition (e.g., Examples C or D), which can be applied before or after the localized treatment to improve a particular sign of aging (e.g., across the entire face).

Table l Exemplary Compositions Comonent/%b wt.

Ficus Benghalensis (Banyan Tree) Flower/Leaf/Stem Juice Nelumbo Nucifera (Lotus) Flower/LeaflStem Juice (manufactured b (**) Trifolium Pratense (Clover) Flower/Leaf/Stem Juice (**) “mm-mu —-m_‘m--m_-m SepiwhiteTM (Undecylenoyl- phenylalanine, neutralized) (available from SEPPIC Com onent / % by wt Sepigel 305TM crylamide + Cl3—l4 2'00 2'00 isoparaffin + laureth-7) (available from SEPPIC) Inn—n —m--m_mm_m —mm_.m--m_-m_ IRE-M“— -m-m-m— _-m--m-—-m_ Butylene Glycol (CAS No. '50 5'50 5'50 5'50 Eifmlde‘wm DC 1503 Flu1dTM (avallable 2.50 2.50 250 250 from DowCormn) LubraJ el OilTM (available 144 1.44 1.44 1.44 from Sederma) Phenonip XBTM (available ligf’oin‘henWSN“ Tospearl 2000TM (Polymethylsils esquioxane) (CAS No. 68554—70—1) (available from GE Silicones/Momentive) DL-Alpha Tocopheryl Acetate (CAS No. 7695—91~ 0.50 0.50 0.50 0.50 Prodew 400TM (available 0.50 0.50 0.50 0.50 from A‘inomoto) Pemulen TR-ZTM (Acrylates/C10—30 Alkyl te Crosspolymer) (available from Noveon) Polysorbate 20 (CAS No.

Sodium Metabisulfite (CAS Sodium Hydroxide (CAS No. 3-2)(50% 0.17 0.17 0.17 0.17 solution b wei_ht in water Disodium EDTA (CAS No.

Com onent / % b Wt.

Xanthan Gum (CAS No.

Sodium Hyaluronate (CAS TOTAL (% W welgh‘ 0f 100.00 100.00 100.00 100.00 total com n) ** Manufactured by Akzo Nobel e Chemistry LLC of Ossining, New York, USA.

The compositions of the present invention are generally prepared by conventional methods such as are known in the art of making topical itions. Such methods typically involve mixing of the ingredients in one or more steps to a relatively uniform state, with or without heating, cooling, ation of vacuum, and the like. Typically, emulsions are prepared by first mixing the aqueous phase materials separately from the fatty phase materials and then combining the two phases as appropriate to yield the desired continuous phase. The compositions are preferably prepared such as to optimize stability (physical stability, chemical stability, tability) and/or delivery of the active als. This optimization may include appropriate pH (e.g., less than 7), exclusion of materials that can complex with the active agent and thus negatively impact stability or delivery (e.g., exclusion of contaminating iron), use of approaches to prevent complex formation (e.g., appropriate dispersing agents or dual tment ing), use of appropriate photostability approaches (e.g., incorporation of sunscreen/sunblock, use of opaque packaging), etc.

Example 2 — Ex Vivo Tissue Analysis Individual banyan tree, lotus, and clover serum fractions, as well as their blend, were evaluated at two different concentrations according to the method described herein. The fold- increase / decrease in expression, versus control, was determined for the aging-related genes set forth in Table 2, below. A positive fold se tes the desirable up-regulation of that gene, and thus a positive anti-aging benefit.

Ex Vivo tissue Method: Skin explants were collected from surgical waste and d with actives in media. Control skin was untreated. After 7 days, punch biopsies were taken for RNA isolation and PCR analysis.

RT-PCR Method: Purified RNA is converted to cDNA using Quanta iScriptTM. 500 ng ofRNA is mixed with iScript and run on a thermocycler according to kit instructions.

One ul of the resulting cDNA is then mixed with Quanta Perfecta MasterTM mix according to ctions and aliquoted across SAbiosciencesTM custom array plate. The plate is then W0 2012/115947 PCT/U82012/025910 sealed and run on the Step-one PlusTM machine from Applied temsTM. The data analysis is performed by uploading raw data into the data is software from SAbiosciencesTM.

Table 2 Reresentative Genes Havin Decreased EXoression with Skin A ' Associated Function Fibrillin-l (FBNI) Structural comonents of microfibrils, which occur in association with elastin ectin—l (FNl) Adhesive ated with wound healin - Collagen 3, a1 (COL3A1) Ma'or colla en ofthe dermis Table 2a Sample Concentration l Up-Down Regulation Fold Chan oe vs. Control Banyan Tree Lotus Serum Serum Combination Fraction Fraction (statistically significant vs. 0.55% 0.1% l -< 0.05 EEK-___— HIE-___— Table 2b Samle Concentration 2 Up-Down Regulation Fold Chan e vs. Control Clover Serum Combination Fraction Lotus (statistically significant vs. 0.01% 0.01% control .< 0.05 Example 3 — Keratinoc e Assa for Claudin l and A P-3 EX ression Keratinocyte Culture: A multiplex mRNA analysis was conducted. RNA was isolated from neonatal human nocytes. Neonatal human keratinocytes (Cascade Biologics # C-OOl-SC) were grown to 40% confluence in 6-well tissue culture plates then treated with compounds for 24 hours (3 replicates per treatment). The treatments ed several concentrations of banyan tree + clover + lotus blends along with individual juices, Additionally, a vehicle control was used.

Several targets were measured with Panomics QuantiGene Plex Assay kit, a multi- analyte quantitative bead—based assay. The fluorescence ity values, measured by a Bio— Rad Bio-Plex 100 instrument, for those samples ng ent RNA are shown for Aquaporin 3 and Claudin 1.

The graph of Figure 1 shows that claudin-l and AQP3 were desirably up—regulated in response to the banyan tree + clover + lotus blend herein.

Example 4 — Method of Treatment A test subject topically applies composition A of Example 1 to the entire face once a day for 8 weeks. As a result, the subject’s facial skin feels and appears to be more hydrated than at week 0, and the subject notices a decrease in the appearance of fine lines and wrinkles.

The ions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values d. 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 nt cited herein, including any cross referenced or d patent or application, is hereby incorporated herein by reference in its entirety unless expressly ed or otherwise limited. The citation of any document is not an ion 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 govern.

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 ations can be made without departing from the range and scope of the invention. It is therefore ed to cover in the appended claims all such s and modifications that are within the scope of this invention.

Claims (11)

WHAT IS CLAIMED IS:

1. Use of a serum fraction blend in ating lly d skin compositions, said blend comprising: a. Banyan tree serum fraction; b. Lotus serum fraction; and c. Clover serum fraction, to increase the moisture and barrier function of human epidermis, as evidenced by the statistically significant up-regulation of n-l and aquaporin—3 in said human epidermis.

2. The use in accordance with claim 1 wherein the serum fraction blend comprises: a. from 0.001% to 15% Banyan tree serum fraction; b. from 0.001% to 15% Lotus serum fraction; and c. from 0.001 % to 15% Clover serum fraction.

3. The use in accordance with claim 1 wherein the serum fraction blend comprises: a. from 0.002% to 10% Banyan tree serum fraction; b. from 0.002% to 10% Lotus serum fraction; and c. from 0.002% to 10% Clover serum fraction.

4. The use in accordance with claim 1 n the serum fraction blend comprises: a. from 0.025% to 10% Banyan tree serum fraction; b. from 0.025% to 10% Lotus serum fraction; and c. from 0.025% to 10% Clover serum fraction.

5. The use in accordance with claim 1 wherein the serum fraction blend comprises: a. from 0.05% to 5% Banyan tree serum fraction; b. from 0.05% to 5% Lotus serum fraction; and c. from 0.05% to 5% Clover serum fraction.

6. A s to increase the moisture and barrier function of human epidermis, as evidenced by the statistically significant up-regulation of claudin-l and aquaporin- 3 in said human epidermis, by topically applying a skin care composition comprising a blend of: a. Banyan tree serum fraction; b. Lotus serum fraction; and c. Clover serum fraction.

A process in accordance with claim 6 wherein the skin care composition comprises a blend of: a. from 0.001% to 15% Banyan tree serum fraction; b. from 0.001% to 15% Lotus serum fraction; and c. from 0.001% to 15% Clover serum fraction.

A process in accordance with claim 6 wherein the skin care composition comprises a blend of: a. from 0.002% to 10% Banyan tree seium fraction; b. from 0.002% to 10% Lotus serum fraction; and c. from 0.002% to 10% Clover serum on.

A process in accordance with claim 6 wherein the skin care composition comprises a blend of: a. from 0.025% to 10% Banyan tree serum fraction; b. from 0.025% to 10% Lotus serum fraction; and c. from 0.025% to 10% Clover serum fraction.

10. A process in accordance with claim 6 wherein the skin care composition ses a blend of: a. from 0.05% to 5% Banyan tree serum fraction; b. from 0.05% to 5% Lotus serum fraction; and c. from 0.05% to 5% Clover serum fraction.

ll. Use in ance with claim 1, substantially as herein described with reference to any one of the Examples f and/or