Orris root extract, composition and method of skin application

Abstract

An orris root extract is disclosed. The orris root extract is obtained by selective extraction from orris root material and is selectively enriched in (A) a phytochemical melanogenesis stimulator or (B) a phytochemical melanogenesis inhibitor. The phytochemical melanogenesis stimulator (A) contains germanisum B and the phytochemical melanogenesis inhibitor (B) contains iriflorental and / or iripalidal. A method of preparing an orris root extract composition is also provided and includes selectively extracting orris root material to yield at least one orris root extract. A functional composition containing the orris root extract is also provided. The functional composition is adapted for administration to a subject by topical application and demonstrates activity related to skin pigmentation.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to and all benefits of U.S. Provisional Application No. 63 / 197,132, filed June 4, 2021, the contents of which are incorporated herein by reference in their entirety.

[0002] FIELD OF THEINVENTION FIELD OF THE DISCLOSURE The present disclosure relates generally to functional compositions, and more particularly to orris root extract compositions, useful for altering skin pigmentation, and methods relating thereto. [Background technology]

[0003] 2. Description of Related Art Skin pigmentation varies widely in the human population due to the presence of a chemically inert pigment called melanin. Melanin is produced deep inside the skin and deposited in a mosaic pattern at the surface of the skin, where both the amount and distribution of melanin are responsible for the variation in skin color. Functionally, melanin is essential for the defense of the skin against ultraviolet (UV) radiation. Specifically, UV-induced generation of reactive oxygen species (ROS) is well known and has been linked to DNA damage and dermal matrix degradation, which can lead to skin aging or even skin cancer in some cases.

[0004] Although melanin is important to provide a self-defense mechanism against such harmful environmental factors, there has also been much research into regulating melanin synthesis and transport to improve the aesthetic problems caused by hyper- or hypo-pigmentation of the skin. Regulation of melanin synthesis (i.e., melanogenesis) is highly complex, and it has become an important strategy in the beauty industry worldwide leading to the development of products that alleviate undesirable skin pigmentation conditions. Melanogenesis occurs in intracellular vesicles called melanosomes that are purified within melanocytes in the skin. It is believed that more than 250 genes are known that are involved in the cascades involved in melanogenesis, along with various proteins and cofactors. For example, microphthalmia-associated transcription factor (MITF), a melanocyte-specific transcription factor known to be the master regulator of melanogenesis, is controlled by many cascades of signaling pathways, such as α-MSH / MClR, Wnt / b-catenin, and SCF / c-Kit (ERK signaling pathway). MITF upregulates tyrosinase (TYR) expression, with TYR being established as the rate-limiting enzyme in melanogenesis, where it has been reported to control the process of tyrosine oxidation and polymerization by TYR-related proteins 1 and 2.

[0005] Commercial interest in skin pigmentation has led to a market in the cosmetics industry for both skin lightening and darkening products. Skin darkening is often desirable to improve appearance or provide a more uniform skin tone. Tanning is the more commonly used process in which skin darkening is increased through exposure to UV radiation from sunlight. However, prolonged exposure to UV light can result in accelerated signs of skin aging and increased risk of skin cancer, as previously explained. Thus, the ability to produce a darker skin tone without incurring photo-damage has led to the development of cosmetics and "self-tanning" applications. As such, DHA (dihydroxyacetone)-based products or temporary bronzers have been developed as topical tanners applied to the skin to produce a tanned appearance without contributing to the pigmentation of the underlying skin. Alternative approaches such as stimulating inner skin pigmentation by targeting the melanogenesis pathway are also undertaken using synthetic or natural substances. For example, the synthetic α-MSH analog afamelanotide induces melanogenesis via activation of the α-MSH / MClR pathway. A number of salt-inducible kinase (SIK) inhibitors have also been shown to stimulate melanogenesis by amplifying its target TRPM1 independent of MITF expression and α-MSH / MClR activation. Synthetic agents such as forskolin and isobutylmethylxanthine (IBMX) have been shown to modulate adenylyl cyclase and phosphodiesterase, respectively, and induce downstream of the α-MSH / MClR pathway, resulting in increased melanin biosynthesis. Many pigment-enhancing agents have been isolated from numerous plant sources, such as Glycyrrhiza glabra, Vigna angularis, and citrus plants, which induce melanogenesis by stimulating the expression of melanogenic proteins and pathways in both in vitro and in vivo systems.

[0006] Skin whitening products are commercially available for cosmetics aimed at obtaining a lighter skin complexion, as well as for the treatment of hyperpigmentation disorders such as melasma, dark spots, and solar lentigines. Since skin pigmentation is determined primarily by the content of melanin in melanosomes and the distribution of melanosomes in keratinocytes, downregulation of melanogenesis and melanosome transfer to keratinocytes is often considered to be the primary target of skin whitening agents. Since the establishment of TYR as the rate-limiting enzyme of melanogenesis, it has become the most prominent and successful target of melanogenesis inhibitors, leading to the use of hydroquinone, L-ascorbic acid, kojic acid, arbutin, azelaic acid, ellagic acid, tranexamic acid, and resorcinol derivatives as skin whitening agents. Other routes for skin whitening are also being pursued. For example, α-viniferin and diacetyl caffeic acid cyclohexyl ester (DACE) are known to reduce melanin levels by targeting the α-MSH / MClR pathway without directly affecting TYR activity. In addition, since the transfer of mature melanosomes to keratinocytes is another important factor in skin pigmentation, melanosome transfer inhibitors, such as protease-activated receptor 2 (PAR-2) inhibitors, niacinamide, and cytidine, have been studied and have been shown to have skin whitening effects without affecting melanin synthesis. Summary of the Invention

[0007] Quick summary An orris root extract ("extract") is provided. The extract is obtained from orris root and is selectively enriched in (A) a phytochemical melanogenesis stimulator or (B) a phytochemical melanogenesis inhibitor. In some embodiments, the phytochemical melanogenesis stimulator (A) contains germanaism B. In these or other embodiments, the phytochemical melanogenesis inhibitor (B) contains iriflorental and / or iripalidal.

[0008] Methods of preparing the extracts ("Preparation Methods") are also provided. The methods include drying orris root material to produce dried orris root raw material, and selectively extracting the dried orris root raw material with a matched solvent system to produce an orris root extract selectively enriched in the phytochemical melanogenesis stimulator (A) or the phytochemical melanogenesis inhibitor (B). In some embodiments, the extraction includes a two-step hydroethanolic extraction to produce a first and a second extract, the first extract enriched in the phytochemical melanogenesis stimulator (A) and the second extract enriched in the phytochemical melanogenesis inhibitor (B).

[0009] Also provided is a topical composition containing the extract, which may be utilized in personal care or other products to induce a skin and / or hair darkening (e.g., tanning) or whitening effect in a subject after application.

[0010] These and other objects, advantages, and features of the present invention will be more fully understood and appreciated with reference to the present description of the embodiments and drawings.

[0011] Before the embodiments of the present invention are described in detail, it should be understood that the present invention is not limited to the operational details or construction details and arrangement of components set forth in the following description or illustrated in the drawings. The present invention may be implemented in various other embodiments and practiced or carried out in alternative ways not expressly disclosed herein. It should also be understood that the phraseology and terminology used herein are for the purpose of description and are not to be regarded as limiting. The use of "comprises" and "contains" and variations thereof means the inclusion of the items listed thereafter and their equivalents, as well as additional items and their equivalents. Furthermore, enumerations may be used to describe various embodiments. Unless expressly stated otherwise, the use of enumerations should not be construed as limiting the present invention to any particular order or number of components. The use of enumerations should not be construed as excluding from the scope of the present invention any additional steps or components that may be combined with or with the listed steps or components. [Brief description of the drawings]

[0012] BRIEF DESCRIPTION OF THE DRAWINGS [Figure 1] FIG. 1 provides the chemical structures of phytochemicals extracted from orris root material. [Diagram 2] FIG. 2 shows the results of bioassay-guided fractionation (BDF) by LC-MS. [Diagram 3] FIG. 3 provides the results of a B16 pigmentation assay showing the effect of purified Germanium B and Illifloidal on melanin production. [Figure 4] FIG. 4 provides the results of a skin equivalent melanoderm assay showing the effect of select orris root extracts on melanin production. [Diagram 5] FIG. 5 shows a flow chart of one embodiment of a method for preparing an orris root extract. [Figure 6] FIG. 6 shows a flow chart of another embodiment of a method for preparing an orris root extract. [Figure 7] FIG. 7 shows a flow chart of a further embodiment of a method for preparing an orris root extract. [Figure 8] FIG. 8 shows a flow chart of one embodiment of a method for preparing orris root extract by supercritical fluid extraction (SCFE) with CO2. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] Detailed Description of the Invention The present disclosure provides an orris root extract ("extract"), as well as functional compositions and methods for preparing each thereof. Generally, the extract contains one or more botanical compounds that have been found to modify skin pigmentation and / or appearance. Specifically, it is believed that certain botanical compounds in the extract, as described below, act on the melanogenesis pathway and affect melanin production, which in turn may affect the visual lightness / darkening of skin and / or hair appearance. Thus, the extract may be utilized in topical compositions adapted for skin and / or hair lightening or darkening (e.g., tanning).

[0014] As will be appreciated from the description herein, in various embodiments, the extract is prepared in a selective process ("preparation method") utilizing an inventive extraction with two different solvent systems used sequentially on the same raw material, which provides a unique route to obtain two different extracts with very different - and contrasting - biological / practical effects through selective enrichment of melanogenesis stimulants and depletion of melanogenesis inhibitors, or vice versa. This preparation method thus provides improved resource economy by producing two different functional components from one starting material. Furthermore, this preparation method, as well as the extract prepared thereby, provides the first use of the phytochemical melanogenesis stimulant germanisum B to affect the melanogenesis effect of the composition, and the orris root extract is believed to reveal a skin darkening effect when applied to a subject. Thus, in contrast to conventional orris root extracts known and utilized for ironic compositions and contents, it should be understood that the present embodiment is unique in its use of germanisum B and the relative proportions of germanisum B to the particular iridal extract to accommodate the skin darkening or lightening properties of the novel orris root extract.

[0015] extract The term "extract" as used herein in the context of extracts, functional compositions, and related embodiments should be understood in its ordinary and customary sense, i.e., as a substance obtained by extraction of a material using a solvent system or an equivalent process. Examples of extraction processes (i.e., "extractions") include warm solvent extraction, supercritical fluid extraction (SFE), such as fractional supercritical fluid extraction (FSFE), and the like, which are described in further detail below. In the same context, the term "orris root" is used herein to generally refer to certain parts of plants of the Iridaceae family, including Iris germanica L. (i.e. "bearded iris"), Iris florentina L. (i.e. "Florentine iris" or "Glaive lily"), and Iris pallida L. ("Dalmatian iris" or "sweet iris"), with the term "orris root" including the lower part(s) of the plant naturally occurring below ground, in the ground, and / or sometimes above ground. In this sense, it is understood that orris root extract may be prepared from any part of the relevant plant, including the rhizome, root, stem, rhizome, etc., which will be readily understood by those skilled in the art in view of the following description. Typically, the extract is obtained from the rhizome of the iris plant (i.e., rhizoma iridis) via extraction techniques that are described in further detail below.

[0016] In view of the foregoing, it will be understood that the term "orris root extract" as used herein generally refers to material obtained by extraction of orris root material (i.e., material that includes or consists of the root portion of the iris plant). As understood herein, a "root" is any part of a plant that is typically mostly underground. This definition includes rhizomes. However, it will be understood that the material in the extract of this embodiment encompasses forms that are more specifically described as "isolates," "distillates," "concentrates," and the like. Thus, while the term "extract" has a specific meaning with respect to a particular product, in the context of the present disclosure, it should be understood that the terms "orris root extract" and corresponding references to "the extract" should be interpreted broadly in light of the following description and examples.

[0017] plant compounds The extract contains or consists essentially of one or more plant compounds obtained or otherwise derived from orris root material. As will be appreciated by those skilled in the art, plant compounds, which may also be generally referred to as "phytochemicals", are chemical entities found or derived from plants and thus represent a diverse group of substances that vary widely in terms of structure, shape, and bioactivity in non-plant organisms. For example, certain plant compounds may be classified as macromolecules, polymeric molecules, low molecular weight molecules, or small molecules. Many plant compounds are not bioactive with respect to certain biological processes, for example because they are indigestible, have poor bioavailability, and / or are otherwise resistant or inactive with respect to certain biological targets. However, other plant compounds are bioactive and thus are utilized in functional compositions, as further detailed below. Several specific classifications of plant compounds are also known in the art and are based on certain characteristics or properties, such as plant toxins (i.e., plant compounds that are toxic to humans and / or other species), antinutrients (i.e., plant compounds that interfere with the absorption of nutrients in the host), etc. Because of such diverse activities and associated actions, and as further detailed below, particular plant compounds, or defined groups of plant compounds, in the present extracts may be advantageously used in a variety of ways that may not be practical, effective, or even possible depending on the orris root material from which they were obtained (i.e., extracted).

[0018] As will be apparent in light of the further description and examples herein, generally, plant compounds that may be present in the extract include terpenes, terpenoids, flavonoids, phenols, glycosides, and alkaloids, and derivatives thereof. Three specific plant compounds, Germanium B, Iripallidal, and Iriplorental, are shown in Figure 1 and are then described below.

[0019] Germanium B In certain embodiments, the extract contains (A) a phytochemical melanogenesis stimulator. In such embodiments, the extract typically exhibits a skin-darkening effect and may therefore be utilized as a component of a skin-darkening composition, such as the topical compositions described below. It will be understood that the term "stimulate" in this context is not limiting and may include promotion of melanogenesis, inhibition of competing / regulatory pathways, or both. In this sense, the term "melanogenesis stimulator" is used descriptively to refer to the general effect of melanogenesis and / or skin pigmentation involving melanin, but may be used more specifically with respect to a particular biological pathway, when indicated.

[0020] Typically, the phytochemical melanogenesis stimulator (A) contains, consists essentially of, or is Germanium nisum B (CAS#123648-56-6; also known as "irisolone 4'-O-β-D-glucoside" and "niglysine 4'-O-β-D-glucoside"). As demonstrated in the Examples below, Germanium nisum B is effective in increasing pigmentation via its effect(s) on melanin-related biological pathways.

[0021] Iridal In certain embodiments, the extract contains (B) a phytochemical melanogenesis inhibitor. In such embodiments, the extract typically exhibits a skin-whitening effect and may therefore be utilized as a component of a skin whitening composition, such as the topical compositions described below. It will be understood that the term "inhibit" in this context is not limiting and may include direct inhibition of melanogenesis, promotion of competing / regulatory pathways, or both. In this sense, the term "melanogenesis inhibitor melanogenesis stimulator" is used descriptively to refer to the general effect of reducing melanogenesis and / or skin pigmentation involving melanin, but may also be used more specifically with respect to a particular biological pathway, when indicated.

[0022] Typically, the phytochemical melanogenesis inhibitor (B) comprises one or more irone precursors known as "iridals." Examples of such iridals include the bicycloiridals iriparidal and iriflorental. In certain embodiments, the phytochemical melanogenesis inhibitor (B) consists essentially of, or alternatively is, iriparidal and / or iriflorental.

[0023] Selective enrichment It will be understood that the phytochemical melanogenesis influencing substances (A) and (B) (e.g., as exemplified by Germanium B, and the iridal species iripalidal and iriflorental, respectively) have opposing activities in the context of melanogenesis. Thus, as further explained and exemplified below, the present extract contains a predominant amount of one of these phytochemical melanogenesis influencing substances. Specifically, in certain embodiments, the present extract is selectively enriched in the phytochemical melanogenesis stimulator (A). In some such embodiments, the present extract is selectively depleted in the phytochemical melanogenesis inhibitor (B). In other embodiments, the present extract is selectively enriched in the phytochemical melanogenesis inhibitor (B). In some such other embodiments, the present extract is selectively depleted in the phytochemical melanogenesis stimulator (A). The terms "enriched" and "depleted" in this context may be understood with respect to the orris root material from which the present extract is obtained. Stated differently, the extract may be "enriched" with respect to phytochemical (A) by containing a higher proportion of phytochemical (A) than orris root material, a lower proportion of compounds other than phytochemical (A) as compared to orris root material, or both. The same is true for enrichment or depletion with respect to phytochemical (B), the proportion may also refer to the relative amount and / or overall concentration of this phytochemical in the orris root material. In this manner, the extract contains a predominant amount of the desired melanogenesis-influencing substance (i.e., phytochemical (A) or (B)) and thus may reveal biological effects / activities not possible with raw orris root material, or even with extracts containing phytochemicals (A) and (B) in proportions similar to those found in such orris root material.

[0024] Other plant compounds The extract may be enriched in one or more desired plant compounds, i.e., other than phytochemicals (A) or (B), relative to the concentration of such plant compounds in the orris root material. In addition, the extract may contain lower concentrations of undesirable materials, including certain plant compounds (e.g., certain terpenes, alkaloids, waxes, acids, etc.), relative to the orris root material. For example, in some embodiments, the extract is substantially free or free of iliflorentin.

[0025] Extract Form The form of the extract is not particularly limited and will be selected by the skilled artisan based on, for example, the particular techniques and materials used in the preparation method as described below. In general, the extract may be a direct extract, such as a solvent-based composition obtained from a solvent-based extraction process, or a processed form, such as an extract (e.g., prepared by solvent removal and / or additional processing / formulation steps). In this manner, the extract may be further defined or otherwise characterized as an oil or essential oil, a tincture, a concentrate, an isolate, a distillate, or the like, or a combination thereof, based on the particular techniques utilized in the preparation method. Such characterization may be based on colloquial or common usage of these terms, on art-specific usage of these terms, or both, for example, in this context "tincture" generally refers to a solvent extract of plant material, a solution of such an extract, and / or a solution of low volatility substances obtained from such extraction. Similarly, the terms "concentrate" and "essential oil" may both be used in the context of the extract to refer to a substance obtained by extraction of plant material using a solvent, followed by removal, or substantial removal, of the solvent. In certain cases, the extract may be defined or otherwise characterized based on regulatory definitions. For example, in certain embodiments, the extract may be prepared from cleaned rhizomes that are substantially free of other plant material, and fall within the bounds of regulatory guidelines for orris root extracts.

[0026] It will be understood that certain forms of the extracts, such as those introduced herein, may overlap with each other in terms of production methods, state-specific properties, intermediate forms, etc. For example, a tincture prepared by hot solvent extraction of orris root material may be concentrated or distilled to prepare a concentrate or essential oil. In certain embodiments, the extracts are prepared by one or more post-extraction processes, which may be characterized as purification processes. In the context of extracts, such purification processes may be utilized to remove or reduce substances from the composition to be purified or to remove desired substances (i.e., the extract) from a mixture of substances obtained from orris root material. Examples of substances that may be removed include waxes, pigments, oils, terpenes, alkaloids, and even parts of the plant biomass that are not soluble in the solvent system utilized in the extraction process. Examples of purification techniques that may be utilized thus include distillation, concentration, filtration, chromatography, fractionation, isolation, secondary extraction, and the like, as well as combinations thereof. In this manner, it will be appreciated that the extract may be selectively enriched with certain plant compounds, including the phytochemical melanogenesis stimulator (A), the phytochemical melanogenesis inhibitor (B), as well as other phytochemicals present in the orris root material. Similarly, the extract may contain lower concentrations of any such phytochemicals that are undesirable in a particular formulation of the desired final composition.

[0027] Preparation method As previously introduced, the present preparation methods produce an extract from orris root material. Typically, the orris root material includes or is the rhizome of the iris plant. However, it will be appreciated that other parts or materials from the iris plant (e.g., hairy roots, stems, leaves, etc.) may also be utilized in the present preparation methods. Such other materials may be combined with the orris root material prior to or simultaneously with pre-extraction treatment of the orris root material, the extraction process itself, or post-extraction treatment. Generally, the orris root material utilized in the present preparation methods may be prepared, purchased, or otherwise obtained.

[0028] In some embodiments, the preparation method includes preparing the orris root material for extraction (i.e., pre-extraction processing). In such embodiments, techniques that may be utilized include cutting, grinding, soaking, blending, sifting, grinding, drying, desiccating, and the like, as well as combinations thereof (e.g., by sequential use). In certain embodiments, chemical processes (e.g., initiated by heating, acidification, oxidation, etc.) may be used to modify one or more substances in the orris root material to enhance or alter the effectiveness of a subsequent extraction step. Similarly, various purification techniques (e.g., screening, filtration, chromatography, etc.) may be utilized prior to and / or following individual steps or sequences in conjunction with such processes.

[0029] Pre-extraction treatment For example, in certain embodiments, preparation of the orris root material for extraction includes harvesting an iris plant and isolating the rhizomes from the harvested iris plant (e.g., by removing therefrom the root hairs and / or other parts of the iris plant). In other embodiments, the harvested iris plant is used in the extraction process whole or partially whole, i.e., without removing therefrom the root hairs or certain plant parts. In various embodiments, preparation of the orris root material also includes washing the harvested iris plant and / or rhizomes isolated therefrom, e.g., to remove dirt and debris, prior to further processing. In some such embodiments, washing may include cleaning the iris plant material, e.g., by soaking the rhizomes and / or other harvested plant parts in a sterilized and / or cleaned solution.

[0030] In some embodiments, the preparation of the orris root material includes a drying process to provide an orris root material with a particular moisture content prior to the extraction step. For example, in certain embodiments, the preparation method includes drying the washed rhizomes by exposure to the air and temperature of the environment (i.e., air drying). However, in some embodiments, an oven or other such drying device may be utilized to forcibly remove or transport moisture from the plant material. For example, in some embodiments, the preparation of the orris root material includes oven drying the rhizomes to a moisture content of less than 15% by weight, for example 5-15, or 6-12, or 8-10% by weight, based on the weight of the orris root material. In such embodiments, the orris root material may be resized to aid in the drying or other processing steps. For example, in certain embodiments, the preparation of the orris root material includes grinding the dried rhizomes and preparing a powder therefrom. In such embodiments, the orris root powder may be used directly in the extraction process. Alternatively, the orris root powder may be processed for medium to long term storage, for example by freezing.

[0031] It will be appreciated that variations in the pre-extraction processing of the orris root material may be utilized without departing from the scope of the present embodiment. Alternative size optimization steps, such as chopping, dicing, cubing, etc., may be used in addition to or instead of the grinding described above to prepare orris root material in various shapes, e.g., differing in homogeneity, average particle size, surface area, etc. Such characteristics may be modified depending on the size / scale of the processing and / or extraction being performed, as will be understood by those skilled in the art. For example, harvested orris root material may be coarsely chopped (e.g., by chopping) to aid in washing / soaking / drying / etc., and the final dried product further ground or milled to produce orris root powder for extraction. Alternatively, such coarsely chopped forms may be directly dried and extracted.

[0032] extraction As previously introduced, the present preparation method involves a selective extraction process in which two different solvent systems are sequentially utilized on the same raw material (i.e., orris root material) resulting in two different orris root extracts. Specifically, a first extraction is utilized to prepare a first extract and an extracted raw material from the orris root material, and a second extraction is utilized to prepare a second extract from the extracted raw material. This sequence of extractions, as well as the specific features of the first and second extractions, are further described below.

[0033] Generally, the present preparation methods utilize a solvent-based extraction process. In other words, the extraction steps of the present preparation methods are carried out using solvent-based extraction techniques known in the art. Thus, the specific techniques utilized in each extraction are not particularly limited and may be adjusted and / or replaced by alternative extraction techniques suitable for preparing the extracts described herein. That said, it will be appreciated that certain limitations also apply to the conditions utilized during extraction, as well as the pre-extraction processing steps described above. For example, steam distillation of orris root material has been found to oxidize iridal, resulting in various aroma phytochemicals, such as irones. While such irones may sometimes be desirable in extracts or final products containing them, such oxidation may deplete the amount of iridal available for extraction and therefore may be avoided in certain embodiments. In certain embodiments, the present preparation methods are carried out under conditions selected to reduce or minimize the oxidation or chemical / thermal degradation of the target phytochemicals (e.g., germanisum B, iridal, etc.) extracted from the orris root material.

[0034] Extraction Solvent The solvent system utilized in the extraction step will be selected to dissolve or suspend the desired plant compounds present in the orris root material and will therefore be selected based on the solubility of the various plant compounds therein. In general, solvents suitable for use in the extraction step of the present preparation method include aqueous and / or water-compatible solvents. Examples of such solvents, or components of suitable solvent systems, generally include water (e.g., purified water, deionized water, etc.); certain organic solvents, such as alcohols (especially lower alcohols, e.g., methanol, ethanol, etc.), glycols (e.g., propylene glycol, pentylene glycol, butylene glycol, and glycerol (glycerin)), aliphatic alcohols (e.g., lanolin, etc.); mixtures of water and organic solvents (e.g., water and alcohol), and mixtures of organic solvents, such as alcohol and glycerol (optionally with water); and the like, as well as derivatives, modifications, and combinations thereof. Other organic solvents that may be utilized in addition to the aforementioned include acetone, tetrahydrofuran, ethyl acetate, chloroform, methylene chloride, diethyl ether, and hexane. Other solvent types may also be utilized. For example, in certain embodiments, supercritical CO2 is utilized in the extraction of orris root material. In some embodiments, supercritical CO2 is utilized along with an optional ethanol co-solvent, as shown in FIG.

[0035] Notwithstanding the above, it will be appreciated that the solvent(s) selected for use in the present preparation methods must be capable of retaining the desired plant compounds from the orris root material. As will be further understood from the additional description herein, the solvent(s) utilized will also determine the relative concentrations of the phytochemical melanogenesis stimulator (A) and / or phytochemical melanogenesis inhibitor (B) obtained from the orris root material. Thus, certain solvents may not be broadly applicable. For example, in certain embodiments, a pure water extraction (i.e., using only water) may not sufficiently extract the desired plant compounds from the orris root material to prepare an extract suitable for use in the functional compositions described herein. More specifically, the desired plant compounds are typically not polar enough to be isolated from the orris root material by water alone, but may instead require a non-polar solvent used together with water for successful extraction.

[0036] Since the desired plant compounds differ from one another in terms of polarity, the preparation method typically utilizes different solvent systems to selectively prepare extracts enriched in the phytochemical melanogenesis stimulator (A) or the phytochemical melanogenesis inhibitor (B). As previously introduced, the preparation method typically utilizes sequential extractions, each with a different solvent system, to prepare two separate extracts from the orris root material. An exemplary embodiment is illustrated by the preparation method flow diagrams shown in Figures 5-8.

[0037] In some embodiments, the preparation method utilizes a hydroethanolic solvent system for the extraction step. More specifically, in such embodiments, the extraction solvent comprises a mixture of ethanol (EtOH) and water (HO).

[0038] First Extraction As previously introduced, in a general embodiment, the preparation method includes subjecting orris root material to a first extraction to produce a first extract and a raw material extracted therefrom. Typically, the first extraction utilizes a hydroethanolic solvent system, such as a solvent system containing, or consisting essentially of, a mixture of ethanol (EtOH) and water (HO). For example, in some embodiments, the first extraction utilizes a hydroethanolic solvent system containing ethanol and water in a relative ratio of greater than 0% to 50% ethanol in water, such as 5-40, or 10-35, or 10-20% ethanol in water. In a specific embodiment, the first extraction solvent is a hydroethanolic solvent system containing ethanol and water in a ratio of about 15:85 (EtOH:HO). It will be appreciated that these exemplary ranges are examples of hydroethanolic solvent systems that may be utilized, and that alternative ranges may be selected based on the particular solvents in any given solvent system and the desired extract to be prepared. However, the first solvent system is generally selected to be more polar than the second extract, i.e., to extract the more polar components from the orris root material. More specifically, in certain embodiments, the first extract contains a phytochemical melanogenesis stimulator (A), exemplified by germanisum B, which is more difficult to extract based on its increased polarity than the phytochemical melanogenesis inhibitor (B), exemplified by the iridal species iriflorental and iripalidal. Thus, the first extract is typically enriched in terms of its content of the phytochemical melanogenesis stimulator (A) and depleted in terms of its content of the phytochemical melanogenesis inhibitor (B) compared to the orris root material utilized in the present preparation method.

[0039] Any suitable technique can be utilized for the first extraction to obtain a first extract therefrom. Typically, the first extraction involves heating and agitating a mixture of the first extraction solvent and the orris root material. For example, in some embodiments, the first extraction involves combining the first extraction solvent and the orris root material together to produce a first extraction mixture, and then agitating (e.g., via stirring, etc.) the first extraction mixture to facilitate the extraction process. In these or other embodiments, the first extraction further involves heating the first extraction mixture.

[0040] It should be appreciated that if heating is utilized, a conservative temperature is typically utilized to avoid undesirable oxidation and / or chemical or thermal degradation of the desired plant compounds in the extracted orris root material, as well as to protect the extracted plant compounds once solubilized in the mobile phase of the extraction. Thus, the temperature of the first extraction is typically tied to an upper limit by the reflux temperature of the solvent system utilized. However, a temperature suitable for rupturing, compromising, or destroying the plant cell walls of the orris root material will typically be utilized to increase the efficiency of the extraction. Similarly, the viscosity of the soluble components of the first extraction mixture will also be considered when selecting an appropriate temperature, since reducing the viscosity of the desired phytochemicals will generally increase their diffusion and, consequently, extraction capacity. In a specific embodiment, the temperature of the first extraction is maintained within a range of above room temperature to 70° C., for example, 30-65, alternatively, 40-65, alternatively, 50-65, alternatively, about 60° C.

[0041] The mixture of first extraction solvent and orris root material may be selected to control the relative ratio of solvent to orris root material therein. For example, in certain embodiments, the first extraction is carried out at a ratio of approximately 10:1 parts by weight of solvent to orris root material. It will be appreciated that ratios outside this range may also be utilized. However, if the mixture is too concentrated (e.g., less than 6-8:1 parts by weight of solvent to orris root material), reduced yields will be obtained, and if the mixture is too dilute, such that an excessive amount of the required solvent is utilized, waste products will be produced. That said, in some embodiments, excess, or gross excess, solvent may be utilized.

[0042] This first extraction may be carried out for any period of time suitable for extraction of the desired plant compound(s) from the orris root material. For example, in some embodiments, the first extraction involves agitating a mixture of the orris root material and the hydroethanolic solvent within the foregoing temperature ranges for a period of from 30 minutes to 4 hours, such as from 1 to 3 hours, or about 2 hours. Of course, longer periods of time may be utilized if the orris root material is not processed prior to the first extraction, if the scale of the first extraction is relatively large, if the temperature is maintained at the lower end of the preferred range, if a lower ratio of first extraction solvent is utilized, etc.

[0043] It will be appreciated that this first extraction prepares a mixture containing the extracted / intermediate orris root material (e.g., solids) and the solvent system utilized in the first extraction, which also contains the extracted plant compounds. Typically, the first extraction process includes a filtration step or similar technique to separate the phases of this mixture, thereby producing a first extract (i.e., filtrate) and the extracted orris root raw material (i.e., filtrate). In certain embodiments, the first extraction process of the present preparation method includes cooling and filtering the first extraction mixture, for example through a mesh, to separate and separately obtain the first extract and the extracted orris root raw material.

[0044] As introduced above, this first extract generally contains the phytochemical melanogenesis stimulator (A), exemplified by Germanium germanisum B. Thus, once obtained, the first extract may be used directly in the formulation of a functional composition, such as that described below for skin darkening applications, or may alternatively be subjected to a post-extraction treatment to produce a final first extract composition. For example, in some embodiments, the filtrate obtained after the first extraction and post-extraction filtration is concentrated to remove all or a portion of the extraction solvent therefrom, and produces the first extract as a concentrate. The particular concentration process is not particularly limited, and the final amount of solvent / solids in the first extract may be independently selected, for example, based on their desired end use. For example, in certain embodiments, the first extract is concentrated to reach a final solids content of 15-25%, for example about 20%, of the total solids. Of course, the final concentration of the phytochemical melanogenesis stimulator (A) (e.g., Germanium B) may vary and can be readily determined by one of skill in the art through a myriad of known analytical techniques, such as those illustrated in the Examples herein. In certain embodiments, the first extract, in the form of a concentrate, is lyophilized and ground to obtain the first extract as a powder (e.g., as shown in Figures 6 and 7).

[0045] Second Extraction The extracted / intermediate orris root raw material resulting from the first extraction may be further extracted with a second extraction solvent system, i.e., in a second extraction step of the present preparation method. Importantly, it will be appreciated that based on the differential extraction utilized between the first and second extractions, the extracted orris root raw material will generally be depleted in terms of the content of the phytochemical melanogenesis stimulator (A) therein, such that the second extract will also contain a significantly reduced amount of that plant compound compared to the orris root material used in the first extraction. Conversely, the second extract will typically be enriched in terms of the content of the phytochemical melanogenesis inhibitor (B) as well as depleted in terms of the content of the phytochemical melanogenesis stimulator (A) compared to the orris root material utilized in the present preparation method. In this manner, the present preparation method utilizes sequential extractions to prepare two separate extracts from a single raw material, each extract containing plant compounds with different melanogenesis-related activities.

[0046] The preparation methods may include one or more processing steps between these extractions to prepare or condition the orris root material for a second extraction. For example, in certain embodiments, the extracted / intermediate orris root material is obtained as a cake from a filtration step following the first extraction, and the preparation methods include washing or suspending the cake (e.g., with 5-15 parts, or 10 parts water) and filtering the suspension to remove the washing solvent and yield the extracted / intermediate orris root as the raw material for the second extraction. Illustrative examples of some of such steps are shown in the processes depicted in Figures 5-7.

[0047] With respect to the second extraction, the above discussion of techniques and solvents associated with the first extraction are generally equally applicable. However, the second extraction solvent is typically less polar than the first extraction solvent due to the different polarity of the desired plant compound(s) to be extracted (i.e., the phytochemical melanogenesis inhibitor (B)). For example, in some embodiments, the second extraction utilizes a hydroethanolic solvent system containing ethanol and water in relative ratios of 50-100% ethanol in water, e.g., 60-80, or 65-75, or 70-75% ethanol in water. In a specific embodiment, the second extraction solvent is a hydroethanolic solvent system containing ethanol and water in a ratio of about 70:30 (EtOH:H2O). It will be appreciated that these exemplary ranges are illustrative of the hydroethanolic solvent system utilized, and that alternative ranges may be selected based on the particular solvent in any given solvent system, and the desired extract to be prepared. However, the second solvent system is generally selected to be less polar than the first extract, i.e., to extract less polar components from the orris root material as compared to the first extract. More specifically, in certain embodiments, the second extract contains a phytochemical melanogenesis inhibitor (B), exemplified by the iridal species iriflorental and iripalidal. Thus, the second extract is typically enriched in content of the phytochemical melanogenesis inhibitor (B) and depleted in content of the phytochemical melanogenesis stimulator (A) as compared to the orris root material utilized in the present preparation method.

[0048] In certain embodiments, this second extraction is carried out with a ratio of approximately 10:1 parts by weight of solvent to extracted / intermediate orris root material. It will be appreciated that ratios outside this range may also be utilized. However, as with the first extraction, reduced yields may be obtained if the mixture is too concentrated (e.g., less than 6-8:1 parts by weight of solvent to extracted / intermediate orris root material), as well as waste products may be generated if the mixture is too dilute, such that an excess of the required amount of solvent is utilized and subsequently removed. That said, in some embodiments, an excess, or total excess, of second extraction solvent may be utilized.

[0049] The temperature of the second extraction is typically maintained within the range of from above room temperature to 70° C. for the reasons explained above with respect to the first extraction. Thus, in some embodiments, a temperature of 30-65, alternatively 40-65, alternatively 50-65, alternatively about 60° C. is utilized.

[0050] This second extraction may be carried out for any period of time suitable to extract the desired plant compound(s) from the extracted / intermediate orris root material. For example, in some embodiments, the second extraction involves agitating a mixture of the extracted / intermediate orris root material and the second hydroalcoholic solvent within the foregoing temperature ranges for a period of from 30 minutes to 4 hours, such as from 1 to 3 hours, or about 2 hours. Of course, longer periods of time may also be utilized.

[0051] It will be appreciated that this second extraction prepares a mixture containing the spent orris root material and the solvent system utilized in the second extraction, which also contains the extracted plant compounds. Typically, the second extraction process includes a filtration step or similar technique to separate the phases of this mixture, thereby producing a second extract (i.e., filtrate) and the spent / extracted orris root material (i.e., filtrate). In certain embodiments, the second extraction process of the present preparation method includes cooling and filtering the second extraction mixture, for example through a mesh and / or a screw press, to separate and separately obtain the second extract and the spent / extracted orris root material.

[0052] As introduced above, this second extract generally contains the phytochemical melanogenesis inhibitor (B), exemplified by the iridal species iriflorental and iripalidal. Thus, once obtained, the second extract may be used directly in the formulation of a functional composition, such as those described below for skin whitening applications, or may alternatively be subjected to a post-extraction treatment to produce a final second extract composition. For example, in some embodiments, the filtrate obtained after the second extraction and post-extraction filtration is concentrated to remove all or a portion of the second extraction solvent therefrom, and produces the second extract as a concentrate. This particular concentration process is not particularly limited, and the final amount of solvent / solids in the second extract may be independently selected, for example, based on their desired end use. For example, in certain embodiments, the second extract is concentrated to reach a final solids content in the range of 25-35%, for example about 30%, of the total solids. Of course, the final concentration of the phytochemical melanogenesis inhibitor (B) (e.g., iriflorental and / or iripalidal) may vary and can be readily determined by one of skill in the art through a myriad of known analytical techniques, such as those illustrated in the Examples herein. In certain embodiments, the second extract, in the form of a concentrate, is lyophilized and ground to obtain the second extract as a powder.

[0053] In some embodiments, the first and / or second extract and / or concentrate of the first and / or second extract may be sterilized, for example, by pasteurization or other heat / cool protocols. One such embodiment is depicted in FIG. 5. In certain embodiments, the first and / or second extract is sterilized after the extract is concentrated. Similarly, additives such as carriers (e.g., isononyl isononanoate) and preservatives (e.g., phenoxyethanol) may be added to the first and / or second extract during preparation.

[0054] Generally, both the first and second extracts contain germanisum B. However, the differential extraction provided herein in the present method of preparation embodiment provides a first extract enriched in germanisum B and depleted in iridal, which retains antagonist activity. Similarly, the second extract is generally enriched in iriflorent and / or iripallidal, and depleted in germanisum B.

[0055] In certain embodiments, the first and second extracts may also contain at least one cosmetically acceptable carrier.In specific embodiments, the cosmetically acceptable carrier is not natural.In other words, this carrier is not a natural product in these specific embodiments.In other embodiments, this carrier can be selected from commonly used carriers understood in the art and used in conventional amounts.

[0056] Amount of phytochemical melanogenesis stimulator In general, a particular phytochemical extracted from the orris root material may be present in the first or second extract at any suitable concentration, which may be selected or otherwise determined based on the requirements of a particular end application. In some embodiments, for example, each extract contains the relative plant compound (e.g., phytochemical (A) or (B)) in an amount of at least 0.1%, alternatively at least 1, alternatively at least 2, alternatively at least 5, alternatively at least 10, alternatively at least 15, alternatively at least 20, alternatively at least 25, alternatively at least 30, alternatively at least 35, alternatively at least 40, alternatively at least 50, alternatively at least 55, alternatively at least 60, alternatively at least 65, alternatively at least 70, alternatively at least 75, alternatively at least 80, alternatively at least 85, alternatively at least 90, alternatively at least 95, alternatively at least 98% by weight, based on the total weight of the extract. In some embodiments, the plant compound fractions are selected at one of the same % values, but compared on a weight / volume or volume / volume basis to the extract as a whole. In addition to the embodiments described above, it should be appreciated that the extract can be combined or otherwise supplemented with one or more additional compounds, for example, for the purpose of enriching the composition of the extract with respect to those compound or compounds in particular.

[0057] Although described herein with respect to the contemplated two-step extraction process, it should be appreciated that the present preparation methodology required is not utilized to obtain two final extracts for further use, but instead may be utilized to selectively prepare orris root extracts with relative amounts of plant compounds that stimulate and inhibit melanogenesis that are suitable for use as effective agents for modifying skin pigmentation. Thus, the prepared extract is tailored based on the ratio of plant compounds extracted, such that the present preparation methodology provides improved control over the functionality of the extract(s) prepared thereby.

[0058] functional composition As previously introduced, functional compositions containing the extract are also provided. More specifically, as will be appreciated from this disclosure, the functional compositions may be formulated to prepare various consumer compositions (i.e., personal care products in the form of topical compositions) suitable for administration to a subject, for example to provide one or more components of the extract thereto. In this context, the terms "administer", "administering" or "administration" are used herein in their broadest sense to refer to any method of delivering the functional compositions described herein to a subject.

[0059] The subject is typically an animal, such as a mammal (i.e., a vertebrate of the class Mammalia, such as dogs, cats, goats, sheep, pigs, cows, horses, donkeys, camels, and the like). Additional mammals specifically contemplated herein include semi-domesticated mammals, and mammals that are conventionally bred in cages. Of course, the term mammal also encompasses humans (which may be referred to as "people" and / or "individual(s)"). When describing humans, the term "adult" is typically used herein to refer to a human who has reached a state of sexual maturity. In contrast, the terms "child" and "juvenile" are used herein to refer to a human who has not yet reached a state of sexual maturity. Typically, the term "child" refers to a human subject between birth and about 10 years of age (i.e., a child), and the term "juvenile" refers to a human subject who is greater than about 10 years of age and has not yet completed the adolescent stage. Of course, the terms child, juvenile, adult, and infant are all encompassed by the term human, which is itself a subcategory of mammal, which is a subcategory of animal as defined herein. The subject may be a particular subset or population of the types described above. For example, in certain embodiments, the subject may be characterized as an elderly person (i.e., at least 60 years old, alternatively at least 65 years old, alternatively at least 70 years old, alternatively at least 75 years old), an athlete, a bald man, a new mom, a student, a person with acne-prone skin, a teenager, a late teen, or a child under 13 years old, etc. However, in certain embodiments, the subject is simply an adult who is attempting to obtain a change in his / her skin pigmentation.

[0060] As introduced above, the functional composition is generally adapted to provide one or more components (e.g., extracts) of the composition to a subject to achieve a specific effect. More specifically, the component(s) of the extract may be utilized to mediate a specific therapeutic and / or preventative effect, such that the functional composition containing the same may be used to treat or ameliorate a condition in a subject through mediation of melanogenesis. Thus, it will be generally understood that the functional composition contains an effective amount of the extract (i.e., formulated to provide an effective or therapeutically effective amount of the phytochemical melanogenesis stimulator (A) or phytochemical melanogenesis inhibitor (B) to a subject). The term "therapeutically effective amount" as used herein refers to its meaning as generally accepted in the art. Specifically, the term generally refers to an amount of the functional composition that will induce a desired and / or required biological response (e.g., skin lightening / darkening) in a subject. For example, if a given treatment / application is considered to be effective if there is at least about a 25% reduction in a measurable parameter associated with a disease or disorder, then a therapeutically effective amount of a drug for treating that disease or disorder is that amount required to act to reduce that parameter by at least about 25%.

[0061] As used herein, the terms "treatment" or "treating" may be used interchangeably and refer to an approach to obtain beneficial or desired results, including, but not limited to, therapeutic benefit and / or prophylactic benefit. Therapeutic benefit can mean eradication or amelioration of the underlying disorder being treated. Similarly, therapeutic benefit can be achieved by eradication or amelioration of one or more physiological symptoms associated with the underlying disorder, such that an improvement is observed in a subject, who may still be afflicted with the underlying disorder. Prophylactic effects include delaying, preventing, or eliminating the onset of a disease or condition, delaying or eliminating the onset of symptoms of a disease or condition, slowing, halting, or reversing the progression of a disease or condition, or any combination thereof. With respect to prophylactic benefit, subjects at risk of developing a particular disease or who report one or more physiological symptoms of a disease may be treated, even if a diagnosis of the disease has not yet been made.

[0062] Generally, the functional compositions can be used to improve conditions such as those mentioned above by delivering bioactive plant compounds to a subject (i.e., mediating, inducing, or inhibiting melanogenesis in a subject).

[0063] In view of the foregoing, it will be appreciated that the functional compositions may be used to improve conditions affecting the skin health (e.g., melanogenesis / pigmentation) of a subject. More specifically, the functional compositions may be formulated as topical compositions, e.g., for topical administration to a subject. Thus, in certain embodiments, the functional compositions are formulated based on a specific biological activity that may be achieved specifically via topical application and / or transdermal delivery methods. Typically, the functional compositions are formulated to modulate human skin and / or hair pigmentation, e.g., to darken or lighten the appearance of skin, via stimulation or inhibition of melanogenesis.

[0064] In some embodiments, the functional composition contains the extract in an amount of at least 0.01-99.9% by weight, alternatively 0.1-90% by weight, alternatively 0.5-80% by weight, alternatively 1-50% by weight, alternatively 1.5-35% by weight, or alternatively 2-20% by weight. In a specific embodiment, the functional composition contains the extract in an amount of about 2% by weight.

[0065] Typically, the functional composition is formulated as a topical composition (i.e., a personal care product). For example, the extract may be formulated with an acceptable carrier to prepare a topical composition. The choice of carrier will also be selected in consideration of the desired end use or application of the topical composition. For example, the topical composition may be formulated as a cream, gel, powder, paste, or pourable liquid, depending, for example, on the desired route of application to the subject / consumer. These and other embodiments will be understood in view of the following description.

[0066] The functional composition may contain additional components in addition to the orris root extract(s). For example, the composition may contain one or more carriers (e.g., pharma- ceutically acceptable carriers, diluents, solvents, excipients, etc.), such as any of those described below or elsewhere herein. In some embodiments, however, the functional composition consists essentially of an orris root extract, or a combination of orris root extracts as specified above. In these or other embodiments, the functional composition consists of, or consists essentially of, the extract, optionally the botanical compounds obtained by this extraction, and optionally a carrier vehicle.

[0067] In certain embodiments, for example, the functional composition includes a carrier (i.e., a carrier vehicle). Suitable carrier vehicles and components include water (e.g., purified water, deionized water, etc.); organic solvents, such as alcohols (especially lower alcohols that can easily evaporate from the skin, such as ethanol), glycols (e.g., propylene glycol, pentylene glycol, butylene glycol, and glycerol (glycerin)), fatty alcohols (e.g., lanolin), etc.; mixtures of water and organic solvents (e.g., water and alcohol), and mixtures of alcohols and organic solvents (optionally with water), such as glycerol; lipid-based substances, such as fatty acids, acylglycerols (including oils, such as mineral oil, and fats and oils of natural or synthetic origin), phosphoglycerides, triglycerides, sulphides, glycer ... The carrier vehicle may include, for example, glyceryl esters ... In other embodiments, the carrier can be selected from any conventional carrier understood in the art and used in conventional amounts.

[0068] Topical Compositions As previously introduced, the functional composition is typically formulated as a topical composition. In general, the topical composition contains an extract (e.g., the first or second extract) and one or more other components, which may generally be selected from carriers, coactives, additives, excipients, etc. The topical composition can generally be formulated to provide the extract to a part of a subject via direct application (e.g., topically to a surface such as the skin, mucous membrane, etc.). Thus, the topical composition is optionally formulated or otherwise adapted for topical administration to a mammal (e.g., a human). For example, in various embodiments, the topical composition can be formulated to be administered to the skin of a human.

[0069] In certain embodiments, the topical composition contains the extract in an amount of at least 0.001-20%, alternatively 0.01-15%, alternatively 0.1-10%, alternatively 0.5-5%, alternatively 1-3%, or alternatively 1.5-2.5% by weight. In some specific embodiments, the topical composition contains the extract in an amount of about 2% by weight.

[0070] Certain embodiments of the topical composition that vary in terms of formulation and / or form are described below. However, as previously introduced, the topical composition is not particularly limited in terms of substance and / or form, and may contain any number of components / ingredients in addition to the extract, such as other active agents and / or additives described herein. Similarly, the specific additives, carriers, adjuvants, fillers, etc. present in or combined with the topical composition may also vary. Generally, the components of the topical composition will be selected individually or collectively based on the intended use of the topical composition (e.g., as a skin lightening or darkening composition). Furthermore, the amount of any particular component will be selected individually, such as based on the desired final form (e.g., cream vs. spray, etc.). However, as will be appreciated by one of skill in the art in light of the description and examples herein, specific components will typically be selected to maximize the effectiveness of the extracts, for example, by avoiding components that inhibit and / or prevent the transport of those components (e.g., phytochemicals (A) / (B) that affect melanogenesis) to the skin surface, and instead, as desired, by selecting a carrier vehicle that facilitates transport of the plant compounds to or through the skin surface.

[0071] The topical composition may comprise any form for topical application, including powder, spray, ointment, paste, cream, lotion, gel, solution, and the like, and combinations thereof. In other words, the physical form of the topical composition is not particularly limited. Rather, the topical composition may be formulated as a liquid, dry powder, suspension, dispersion, emulsion (e.g., oil-in-water, water-in-oil, water-in-silicone, etc.), gel, paste, etc., and combinations thereof. It will be appreciated that the topical composition may thus be provided in the form of a gel, cream, aerosol spray, foam, liquid, mousse, pomade, powder, solid, or ointment. In some embodiments, the topical composition is provided as an aqueous solution, dispersion, or emulsion.

[0072] As described above, the topical composition may be utilized to improve the skin condition of a subject and / or to provide a skin-related health benefit to the subject. Thus, in certain embodiments, the topical composition may contain, in addition to the extract, an active agent that may provide the same, similar, or different benefit as the extract. For example, in various embodiments, the topical composition may contain, in addition to the extract, a plurality of active agents, each of which may be selected independently (e.g., based on the desired properties of the active agent, such as the benefit to be provided to the subject through application of the topical composition). Such active agents may include tanning agents, whitening agents, and the like, as well as pharmaceuticals, nutraceuticals, anesthetics, counterirritants, chondroprotective agents, and the like, which are exemplified by those listed herein.

[0073] In some embodiments, the topical composition can contain additives specifically selected for use in formulating and / or using the topical composition, such as a pharma- ceutically / medically acceptable carrier, a functional additive, a formulation additive, or a combination of such additives, selected based on, for example, the desired form of the topical composition, the use of the topical composition, etc.

[0074] In some embodiments, the topical composition contains a medicament acceptable carrier.The medicament acceptable carrier can be a non-toxic carrier, a physiologically acceptable carrier, etc.The medicament acceptable carrier can be in the form of emulsion, paste, cream, lotion, gel, jelly, ointment, oil, aerosol, powder, solvent, liposome, micelle, peptide (e.g., albumin), synthetic polymer (e.g., polyethylene glycol), natural polymer (e.g., hyaluronic acid, dextran, chitosan), n-dimensional material (e.g., where n=0, 1, 2, 3), such as 0-dimensional nanomaterial (e.g., quantum dot, nanoparticle, etc.), l-dimensional nanomaterial (e.g., nanotube, nanorod, etc.), 2-dimensional nanomaterial (e.g., quantum well, film, etc.), 3-dimensional material such as matrix (e.g., polymer matrix such as polyethylene glycol (PEG)), etc. The medicamentically acceptable carrier may provide timed release, modulate the pharmacokinetic properties (e.g., absorption, distribution, metabolism, excretion) of the extract or its plant compounds, and modulate the pharmacodynamic properties (e.g., concentration at the site of action, effect produced, etc.) of such orris root plant compounds. For example, the medicamentically acceptable carrier may be an active carrier that promotes the transport of germanisum B, iriflorent, and / or iripallidal across the skin. Examples of such active carriers are described below. In specific embodiments, the medicamentically acceptable carrier is not natural. In other words, the carrier is not a natural product in these specific embodiments. In other embodiments, the carrier is selected from conventional carriers understood in the art and can be used in conventional doses.

[0075] The carrier can optionally be selected to be generally compatible with the individual components of the topical composition, and to enhance or not significantly interfere with the application of the extract, or at least the active plant compounds thereof, to the surface of the subject's skin, and, optionally, to enhance or not interfere with the transport of other components of the topical composition to or through the skin. General examples of suitable carriers include those that aid and / or promote the transport of the various components of the topical composition through the skin. Specific examples of carriers include water (e.g., deionized water), oils and / or waxes (e.g., mineral oil, synthetic oil, natural oil, such as jojoba oil, castor oil, and the like, and waxes formed therefrom), alcohols (e.g., monols, diols, and polyols, such as ethanol, isopropanol, butanediol, 1,2,6-hexanetriol, and the like, glycols, such as ethylene glycol, propylene glycol, and the like), polyoxyalkylenes and / or polyoxyalkylene esters (e.g., polyethylene glycol, polypropylene glycol, mixed Polyalkylene glycols, polyethylene glycol-8 stearate, etc.), fatty acid esters (e.g., alkyl stearates, alkyl oleates, alkyl linoleates, isopropyl palmitate, etc.), organic polymers (e.g., polyacrylamides), organic solvents (e.g., dimethylsulfoxide, dimethylformamide, dimethylacetamide, methylsulfonylmethane), and the like, as well as derivatives, modifications, and combinations thereof, as well as any of the other carriers described herein, such as the applicable vehicles and / or vehicle components described above.

[0076] In some embodiments, the topical composition contains an active carrier. The active carrier is adapted to enhance the bioavailability of the active components of the topical composition (e.g., germanisum B, iriflorent, and / or iripalidal). For example, the active carrier typically aids in the penetration of the active components of the topical composition through the pores of the skin. The active carrier also retains good skin moisturizing activity and reduces the particle size of the emulsion, which helps to achieve better stability of the topical composition. In some embodiments, the active carrier improves the aesthetic appeal of the topical composition. In some embodiments, the active carrier works synergistically with additives in the topical composition, such as preservatives. In some embodiments, the active carrier improves the water resistance of the topical composition and enhances the ability of the extract to be incorporated, for example, into a sunscreen formulation. In some embodiments, the active carrier promotes skin repair and reconstruction, acts as an anti-wrinkle agent, exerts broad spectrum antimicrobial activity, and the like. In some embodiments, the active carrier possesses good solvent and solubility properties.

[0077] Non-limiting examples of active carriers and components useful for preparing them include aqueous and organic solvents, such as alcohols such as ethanol, propanediol, butylene glycol, isopropanol, glycerin, and mixtures thereof. In some embodiments, the active carrier may include pentylene glycol, ethoxydiglycol, cyclohexane 1,4-dicarboxylate bis-ethoxydiglycol, dipalmitoyl hydroxyproline, potassium palmitoyl hydrolyzed wheat protein, glyceryl stearate, cetearyl alcohol, potassium lauroyl wheat amino acid, palm glyceride, capryloyl glycine, potassium palmitoyl hydrolyzed oat protein, behenyl alcohol, palm glyceride, sodium stearoyl glutamate, sucrose palmitate, polyglyceryl-3 sorbitylinseedate, or combinations thereof. In some embodiments, the active carrier contains pentylene glycol, ethoxydiglycol, bis-ethoxydiglycol cyclohexane 1,4-dicarboxylate, dipalmitoyl hydroxyproline, potassium palmitoyl hydrolyzed wheat protein, glyceryl stearate, cetearyl alcohol, potassium lauroyl wheat amino acids, palm glycerides, caproyl glycine, potassium palmitoyl hydrolyzed oat protein, behenyl alcohol, palm glycerides, sodium stearoyl glutamate, sucrose palmitate, polyglyceryl-3 sorbity linseedate, or combinations thereof. According to some embodiments, the anti-inflammatory agent may include alpha-bisabolol, allantoin, sea whip extract, chamomile extract (matricaria) extract, tocopheryl acetate, tea leaf extract, turmeric root extract, oat kernel extract, magnolia bark extract, vitis vinifera (grape) seed extract, cananga (ginger) root extract, dipotassium glycyrrhizinate, or mixtures thereof. In some embodiments, the collagen synthesis enhancer may include methyl glucoside phosphate, inula chrysum flower / leaf extract, collagen prepeptide (e.g., gp-hyp type tripeptide), madecassoside, asiaticoside, or combinations thereof.The anti-wrinkle agent may include Echinacea purpurea extract, ticholic acid, resveratrol, trifluoroacetyl tripeptide-2, or combinations thereof. The keratinocyte growth factor stimulator may include swertiamarin extract in purified form (at least 95% pure) or concentrated.

[0078] Other common examples of carrier vehicles include water (e.g., purified water, deionized water, etc.); organic solvents, such as alcohols, glycols (such as propylene glycol, pentylene glycol, butylene glycol, and glycerol / glycerin), fatty alcohols (such as lanolin), etc.; mixtures of water and organic solvents (such as water and alcohols), and mixtures of alcohols and organic solvents (optionally with water) such as glycerol; lipid-based materials, such as fatty acids, acylglycerols (including oils such as mineral oil, and fats and oils of natural or synthetic origin), phosphoglycerides, triglycerides, sphingolipids, and waxes; protein-based silicone-based materials (both non-volatile and volatile), such as cyclomethicone, dimethiconol, and dimethicone copolyol; hydrocarbon-based materials, such as petrolatum, hydrogenated polyisobutene, and squalane; emollient esters (such as diisobutyl adipate and diisobutyl caprylate), thickeners (acrylates (carbomer), acrylamide, acrylic taurate, hydroxyethyl cellulose, methylcellulose, xanthan gum, pectin, and the like), and the like, as well as derivatives, modifications, and combinations thereof.

[0079] In certain embodiments, the topical composition may contain functional additives. The functional additives are not limited and may contain, and may be, any compound or composition selected to provide functional features or impart functionality to the topical composition. Examples of such functional additives include antioxidants (e.g., alkylated hydroxytoluene, alkylated hydroxyanisole, propyl gallate, etc.), colorants, moisturizers and emollients (e.g., sunflower oil, jojoba oil, isopropyl palmitate, etc.), fragrances (e.g., natural fragrances, e.g., rosemary oil, synthetic fragrances, etc.), cooling agents (e.g., peppermint oil), preservatives (e.g., antimicrobial and antifungal agents, e.g., propylene glycol, methylparaben, propylparaben, diazodilinyl urea, etc.), and the like, as well as derivatives, modifications, and combinations thereof. Many such additives are specified below, but additional options are illustrated in the examples herein.

[0080] For example, in certain embodiments, the topical composition can contain moisturizing agent.Suitable examples of moisturizing agents include hydroxy acids (e.g., lactic acid) and their salts, glycerol, propylene glycol, pentylene glycol, butylene glycol, sodium salt of pyrrolidone carboxylic acid (i.e., sodium PCA), sodium hyaluronate, polyethylene glycol (PEG) (e.g., Carbowax PEG200, Carbowax PEG400, Carbowax PEG800, etc.), and the like, and their derivatives, modifications, and combinations.In these or other embodiments, the topical composition contains emollient and / or moisturizing agent. Examples of suitable emollients or moisturizers include cetyl palmitate, glycerol (i.e., glycerin), polypropylene glycol-15 stearyl ether (i.e., PPG-15 stearyl ether), lanolin and its derivatives (such as, for example, lanolin alcohol), cholesterol, petrolatum, isostearyl neopentanoate, octyl stearate, mineral oil, isocetyl stearate, myristyl myristate, octyldodecanol, octyl palmitate (e.g., 2-ethylhexyl palmitate), dimethicone, phenyl trimethicone, cyclomethicone, C benzoate, and the like. 12 -C 15 Alkyl, dimethiconol, propylene glycol, pentylene glycol, Theobroma grandiflorum seed butter, shea butter, ceramides (e.g., ceramide 2, ceramide 3, etc.), hydroxypropyl bispalmitamide MEA, hydroxypropyl bislauramide MEA, hydroxypropyl bisisostearamide MEA, 1,3-bis-(N-2-(hydroxyethyl)stearoylamino)-2-hydroxypropane, bis-hydroxyethyl tocopheryl succinoylamido hydroxypropane, urea, aloe, allantoin, glycyrrhizic acid, dicaprylate / dicaprate, and the like, as well as derivatives, modifications, and combinations thereof.

[0081] In certain embodiments, the topical composition can contain a preservative.Suitable examples of preservatives include urea (e.g., imidazolidinyl urea, diazolinyl urea, etc.), phenoxyethanol, sodium methylparaben, methylparaben, ethylparaben, propylparaben, potassium sorbate, sodium benzoate, sorbic acid, benzoic acid, formaldehyde, citric acid, sodium citrate, chlorine dioxide, quaternary ammonium preservative compounds (e.g., benzalkonium chloride, benzethonium chloride, cetrimide, dequalinium chloride, cetylpyridinium chloride, etc.), mercury preservatives (e.g., phenylmercuric nitrate, phenylmercuric acetate, thimerosal, etc.), piroctone olamine, Vitis vinifera seed oil, alcohol preservatives (e.g., chlorobutanol, dichlorobenzyl alcohol, phenylethyl alcohol, benzyl alcohol, etc.), and the like, and their derivatives, modifications, and combinations. In these or other embodiments, the topical composition contains an antioxidant. Examples of suitable antioxidants include ascorbic acid and their esters, sodium bisulfite, butylated hydroxytoluene, butylated hydroxyanisole, tocopherols (e.g., α-tocopherol), tocopheryl acetate, sodium ascorbate / ascorbic acid, ascorbyl palmitate, ascorbyl glucoside, propyl gallate, chelating antioxidants (e.g., ethylenediaminetetraacetic acid (EDTA), disodium EDTA, etc.), citric acid, sodium citrate, and the like, as well as derivatives, modifications, and combinations thereof.

[0082] In certain embodiments, the topical composition may contain a formulation additive. The formulation additive is not limited and may include, or may be, any compound or composition selected to impart physical characteristics to the topical composition. Examples of such formulation additives include emulsifiers (e.g., isoparaffin, e.g., C 13 -C 14The formulation additives include surfactants (e.g., isoparaffin, etc.), surfactants (e.g., laureth-7, polymers such as polyacrylamide and polyalkylene glycols, etc.), buffers, excipients, propellants, and the like, and combinations thereof. Typically, the formulation additives are selected based on the desired form of the topical composition. For example, in some embodiments, the topical composition is formulated as an ointment, paste, cream, and / or gel, and contains excipients exemplified by animal and vegetable fats, oils, waxes, paraffins, starches, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonite, silicic acid, talc, zinc oxide, and the like, and derivatives, modifications, and combinations thereof. In certain embodiments, the topical composition is formulated as a powder and / or spray, and contains excipients exemplified by lactose, talc, silicic acid, aluminum hydroxide, calcium silicate, polyamide powder, and the like, and derivatives, modifications, and combinations thereof. In certain embodiments, the topical compositions are formulated as sprays and propellants, such as volatile organic compounds exemplified by halogenated hydrocarbons (e.g., hydrocarbons substituted with chlorine, fluorine, or both) and low molecular weight unsubstituted hydrocarbons (e.g., butane, propane, etc.). Generally, the topical compositions contain formulation additives, if present, in an amount of 1 to 50, alternatively 1 to 20 weight percent, based on the total weight of the topical composition.

[0083] In certain embodiments, the topical composition may contain lipophilic solubilizer.Some examples of lipophilic solubilizer include non-comedogenic esters, such as adipates (e.g., diisobutyl adipate), caprylates, isononanoates (e.g., isononyl neopentanoate), ethoxylated triglycerides, and the like, and their modifications, derivatives, and combinations.Other examples of lipophilic solubilizer generally include cetyl esters, polyethylene glycol cetyl esters, hydrogenated polyisobutene, argan oil, soybean oil, chemical UV filters / boosters (e.g., octinosalate, octinoxate, butyloctyl salicylate, etc.), and the like, and their modifications, derivatives, and combinations.

[0084] In some embodiments, the topical composition can contain free radical stabilizer.Examples of free radical stabilizer generally include lipophilic antioxidants, such as tocotrienols, carotenoids (e.g., tocopherol, tocopherol acetate, retinyl palmitate, tetrahexyl ascorbate, lutein, natural oils rich in unsaturated fatty acids such as docosahexaenoic acid, etc.), and the like, and their modifications, derivatives, and combinations.

[0085] In certain embodiments, the topical composition can contain a surfactant. Examples of suitable surfactants include ionic (e.g., anionic, zwitterionic, etc.) and non-ionic surfactants. Some specific examples of such surfactants include polysorbates (e.g., polyoxyethylene (20) sorbitan monolaurate (i.e., polysorbate 20), polyoxyethylene (20) sorbitan monopalmitate (i.e., polysorbate 40), polyoxyethylene (20) sorbitan monostearate (i.e., polysorbate 60), polyoxyethylene (20) sorbitan monooleate (i.e., polysorbate 80), and the like), vegetable sorbitan stearates, steareth-10 and other octadecyl polyoxyethylene ethers, sodium dodecyl sulfate (e.g., sodium lauryl sulfate), lauryl dimethylamine oxide, cetyltrimethylammonium bromide (CTAB), polyethoxylated alcohols, polyoxyethylene sorbitan, octoxynol, N,N-dimethyldodecylamine-N-oxide, hexadecyltrimethylammonium bromide (HTAB), Polyoxyl 10 lauryl ether, bile salts (e.g., sodium deoxycholate, sodium cholate, etc.), polyoxyl castor oil, nonylphenol ethoxylate, cyclodextrin, lecithin, dimethicone copolyol, lauramide diethanolamine, cocamide diethanolamine, cocamide monoethanolamine, betaine (e.g., oleyl betaine, cocamidopropyl betaine, etc.), cocamidopropyl phosphatidyl PG- Dimonium chloride, dicetyl phosphate (dihexadecyl phosphate), ceteareth-10 phosphate, polyglyceryl-2 triisostearate, cetyl PEG / PPG-1 / 1 dimethicone (ethoxylated or organo-modified silicones for W-in-Si emulsions, glyceryl stearate, glyceryl dilaurate, lecithin, unsaturated lecithins, etc.), methylbenzethonium chloride, and the like, as well as modifications, derivatives, and combinations thereof.

[0086] In some embodiments, the topical composition can contain an emulsifier, which can be the same as or different from surfactant.Examples of such emulsifiers include behentrimonium methosulfate-cetearyl alcohol, nonionic emulsifiers (e.g. emulsifying wax), polyoxyethylene oleyl ether, polyethylene glycol stearate (i.e. PEG-40 stearate, PEG-100 stearate, etc.), cetostearic alcohol (e.g. cetearyl alcohol), ceteareth-12, ceteareth-20, ceteareth-30, ceteareth alcohol, glyceryl stearate, steareth-2 and steareth-20, cationic emulsifiers (e.g. stearamidopropyl dimethylamine, behentrimonium methosulfate, etc.), and the like, and their modifications, derivatives, and combinations.

[0087] In certain embodiments, the topical composition can contain a viscosity adjusting agent (e.g., a thickening or thinning agent, which may be referred to as a viscosity modifier).Examples of such agents generally include protective colloids, non-ionic gums such as hydroxyethylcellulose, xanthan gum, and sclerotium gum, magnesium aluminum silicate, silica, microcrystalline wax, beeswax, paraffin, cetyl palmitate, and the like, as well as modifications, derivatives, and combinations thereof.

[0088] In certain embodiments, the topical compositions may contain one or more additional components, which may include or be selected from skin protectants, adsorbents, analgesics, emollients, moisturizers, hydrating agents, buffering agents, sustained release materials, solubilizers, skin-penetrating agents, skin soothing agents, deodorants, antiperspirants, sunscreening agents, sunless tanning agents, vitamins, hair conditioning agents, anti-irritants, anti-aging agents, abrasives, absorbents, anticaking agents, antistatic agents, astringents (e.g., witch hazel, alcohol, chamomile extracts, etc.), binders / excipients, buffering agents, chelating agents, film formers, conditioning agents, opacifying agents, lipids, pH adjusting agents (e.g., citric acid, sodium hydroxide, sodium monohydrogen phosphate, sodium dihydrogen phosphate, etc.), and the like, as well as modifications, derivatives, and combinations thereof. Specific examples of such additional components are exemplified in U.S. Patent Publication No. 2018 / 0110722A1, the disclosure of which regarding components of topical compositions is incorporated herein by reference.

[0089] In some embodiments, the topical composition contains one or more additional components selected from thickeners, emulsion stabilizers, emulsifiers, emollients, conditioners, humectants, moisturizers, preservatives, antioxidants, pH adjusters, surfactants, fragrances, etc. In some such embodiments, the topical composition may further comprise at least one additional cosmetic agent, such as vitamins, sunscreens, anti-aging agents, anti-wrinkle agents, antioxidants, anti-redness agents, moisturizers, exfoliants, or combinations thereof. Examples of suitable antioxidant additives include Olea europaea (olive) fruit extract, Terminaria ferruginosa (cacadu plum) fruit extract, soy isoflavones, and Jagran nigra (walnut) seed extract. In some embodiments, the antioxidant may also act as an anti-wrinkle agent.

[0090] In these or other embodiments, the topical composition contains a hydrating agent. In such embodiments, the hydrating agent may be selected from compounds known to penetrate the skin and absorb / retain water (e.g., sodium hyaluronate) and compounds useful for promoting water transport and / or hydrating compounds to or through the skin (e.g., liposomes). For example, in some embodiments, the topical composition contains liposomes, such as those formed from or otherwise containing omega fatty acids (e.g., omega 3, 6, and / or 9 fatty acids). Other hydrating agents may also be utilized, such as those known or otherwise sold under the name Aquacel, which represents a blend of water, glycerin, Citrus vulgaris (watermelon) fruit extract, Pyraus malus (apple) fruit extract, Lens esculenta (lentil) fruit extract, sodium pyrrolidone carboxylate (PCA), and sodium lactate, and Lubragel (e.g., oil-free), which represents a blend of glycerin and glyceryl acrylate / acrylic acid copolymer and PVM / MA copolymer.

[0091] In some embodiments, the topical composition contains an oil-regulating agent, such as zinc (PCA), white willow bark extract, witch hazel extract, hexamethylene diisocyanate (HDI) / trimethylol hexyllactone crosspolymer, silica, or a combination thereof. In these or other embodiments, the topical composition contains an exfoliant, such as oat extract, sugar or sugar derivative, or a combination thereof. In these or other embodiments, the topical composition contains an anti-irritant, where the anti-irritant contains glycyrrhizinate, an astringent (e.g. witch hazel extract); or a combination thereof. In these or other embodiments, the topical composition contains one or more cosmetic additives, such as acerola cherry extract, biosaccharide gum, fragrance, glycerin, butylene glycol, disodium EDTA, polyoxyethylene ether of cetyl and / or stearyl alcohol, or any combination thereof.

[0092] The topical composition can optionally include a topical moisturizer (e.g., a skin protectant). Any suitable topical skin protectant can be utilized, provided that the skin is effectively protected or moisturized and the skin protectant remains stable in the formulation. Suitable skin protectants include, for example, aloe, lanolin, glycerin, calamine, vitamin E, vitamin E acetate, vitamin C, allantoin, aluminum hydroxide gel, bismuth subnitrate, boric acid, calamine, cocoa butter, dimethicone, glycerin, kaolin, live yeast cell derivatives, petrolatum, pyridoxine hydrochloride, shark liver oil, sodium bicarbonate, sulfur, tannic acid, topical starch, trolamine, white petrolatum, zinc acetate, zinc carbonate, zinc oxide, zinc sulfate, shea butter, and any combination thereof.

[0093] As used herein, calamine is a pink powder of zinc oxide and a skin protectant containing about 98% zinc oxide and about 0.5% iron oxide; aloe is the dried latex of the leaves of Curacao aloe (Aloe barbadensis miller, Aloe vera linnaeus) or Cape aloe (Aloe ferox miller and hybrids) of the lily family; vitamin E is 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12- Vitamin E acetate is 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol acetate; and lanolin is an oil-like secretion of the sebaceous glands of sheep that is deposited on wool fibers (i.e., a complex mixture of esters and polyesters of 33 high molecular weight alcohols and 36 fatty acids). In one embodiment, the topical moisturizer can be aloe and vitamin E.

[0094] Aloe is commercially available as Aloe vera gel from Terry Laboratories, Melbourne, Fla. Aloe vera gel is commercially available as Aloe vera gel 40X (a 20.0% by weight solution in water), Aloe vera gel 1X (a 0.5% by weight solution in water), Aloe vera gel (a 5.0% by weight solution in water), or as solid Aloe vera. Solid Aloe vera can be dissolved in a carrier, such as water, to the desired concentration. In addition, commercially available forms of Aloe vera are optionally available as decolorized Aloe vera.

[0095] Any suitable amount of topical moisturizer can be used, provided that the suitable amount of topical moisturizer or skin protectant effectively protects or moisturizes skin, and the effective amount of skin protectant remains stable in the formulation for an extended period of time.The suitable and effective amount of topical moisturizer can depend in part on the specific moisturizer or moisturizers present in the formulation.In a specific embodiment, the nature and amount of the topical moisturizer is selected so that it is generally recognized as safe (GRAS) for topical use.

[0096] The topical composition can optionally include one or more polyhydric alcohols. Suitable polyhydric alcohols include, for example, ethylene glycol, propylene glycol, triethylene glycol, tetraethylene glycol, sorbitol, or any combination thereof. Specifically, the polyhydric alcohol can include propylene glycol. Any suitable amount of polyhydric alcohol can be utilized. For example, when present in the topical composition, the polyhydric alcohol can be present at up to about 35% by weight of the topical composition, up to about 15% by weight of the topical composition, or up to about 5% by weight of the topical composition. In one embodiment, the polyhydric alcohol can be present at about 0.5% to about 5.0% by weight of the topical composition.

[0097] The topical composition may optionally include water, such as deionized water (DI). Any suitable amount of water may be utilized, provided that the amount of water maintains the adhesive properties of the adhesive as well as maintains the appropriate stability of the topical composition. For example, deionized water may be present in up to about 50% by weight of the topical composition, up to about 40.0% by weight of the formulation, or up to about 30.0% by weight of the topical composition. In one embodiment, deionized water may be present in up to about 20.0% by weight of the topical composition. In one embodiment, deionized water may be present in up to about 10.0% by weight of the topical composition. In one embodiment, deionized water may be present in about 5.0% to about 15.0% by weight of the topical composition.

[0098] Personal Care Ingredients / Compositions In some embodiments, the topical composition is formulated for use as a personal care composition and further contains a personal care ingredient.Examples of personal care compositions include antiperspirants and deodorants, skin care creams, skin care lotions, moisturizers, facial treatments (e.g., acne or wrinkle removers), personal and facial cleansers, bath oils, perfumes, colognes, sachets, sunscreens, pre-shave and after-shave lotions, shaving soaps and foams, shampoos, conditioners, hair dyes, hair straighteners, hair sprays, mousses, hair gels, permanents, depilatories, cuticle coats, makeup products, color cosmetics, foundations, concealers, blushers, lipsticks, eyeliners, mascaras, oil removers, color cosmetics removers, and medicated creams, pastes or sprays (e.g., anti-acne products, dental hygiene products, antibiotics, healing agents, etc.).

[0099] The specific personal care ingredient or mixture of specific personal care ingredients may be selected based on the type of personal care composition for which the composition is to be formulated. In these embodiments, the personal care ingredient may be a liquid, a solid, an encapsulated liquid, etc. Various examples of personal care ingredients are described below. Any of these combinations of personal care ingredients, or two or more different personal care ingredients, may be utilized as the personal care ingredient. For clarity and consistency, "personal care ingredient" encompasses embodiments in which the composition includes not one, or two or more personal care ingredients.

[0100] In specific embodiments, the personal care ingredient is an antiperspirant and / or deodorant (AP / DEO) agent. In these embodiments, the composition may be referred to as an antiperspirant and / or deodorant (AP / DEO) composition. Examples of antiperspirant and deodorant agents include aluminum chloride, aluminum zirconium tetrachlorohydrex GLY, aluminum zirconium tetrachlorohydrex PEG, aluminum chlorohydrex, aluminum zirconium tetrachlorohydrex PG, aluminum chlorohydrex PEG, aluminum zirconium trichlorohydrate, aluminum chlorohydrex PG, aluminum zirconium trichlorohydrex GLY, hexachlorophene, benzalkonium chloride, aluminum sesquichlorohydrate, sodium bicarbonate, aluminum sesquichlorohydrex PEG, chlorophyllin copper complex, triclosan, aluminum zirconium octachlorohydrate, zinc ricinoleate, and mixtures thereof.

[0101] In certain embodiments, the personal care ingredient comprises skin care ingredient.When utilized to prepare the composition, the skin care ingredient is typically selected from aqueous phase stabilizer, cosmetic biocide, conditioning agent (which can be silicone, cationic, hydrophobic, etc.), emollient, moisturizer, colorant, dye, ultraviolet (UV) absorber, sunscreen, antioxidant, fragrance, antimicrobial, antibacterial, antifungal, anti-aging active, anti-acne agent, skin-whitening agent, pigment, preservative, pH adjuster, electrolyte, chelating agent, plant extract, botanical extract, sebum absorber, sebum control agent, vitamin, wax, surfactant, detergent, emulsifier, thickener, propellant, skin protectant, film-forming polymer, light scattering agent, and combinations thereof. In some of these embodiments, the composition is referred to as a skin care composition, a cosmetic composition, a sunscreen, a shower gel, a soap, a hydrogel, a cream, a lotion, a balm, a foundation, a lipstick, an eyeliner, a cuticle coat, a blusher, etc. Various types of such skin care ingredients are set forth below, along with similar and alternative types known to those of skill in the art.

[0102] Examples of emollients include volatile or non-volatile silicone oils; silicone resins, such as polypropylsilsesquioxane and phenyltrimethicone; silicone elastomers, such as dimethicone crosspolymers; alkylmethylsiloxanes, such as C 30-45 Alkylmethicones, etc.; volatile or non-volatile hydrocarbon compounds, such as squalene, paraffin oil, petrolatum oil and naphthalene oil; hydrogenated or partially hydrogenated polyisobutenes; isoeicosane; squalane; isoparaffin; isododecane; isodecane or isohexadecane; branched C8-C 16esters; isohexyl neopentanoate; ester oils such as isononyl isononanoate, cetostearyl octanoate, isopropyl myristate, palmitate derivatives (e.g. dextrin palmitate), stearic acid derivatives, diisostearyl malate, isostearyl isostearate, and the heptanoic, octanoic, decanoic or ricinoleic esters of alcohols or polyhydric alcohols, or mixtures thereof; hydrocarbon oils of vegetable origin, such as wheat germ, sunflower, grapeseed, bean sprout, shea, avocado, olive, soybean, sweet almond, palm, rapeseed, cottonseed, hazelnut, macadamia, jojoba, black currant, evening primrose; or caprylic / capric triglycerides; higher fatty acids such as oleic acid, linoleic acid or linolenic acid, and mixtures thereof.

[0103] Examples of waxes include hydrocarbon waxes, such as beeswax, lanolin wax, rice wax, carnauba wax, candelilla wax, microcrystalline wax, paraffin, ozokerite, polyethylene wax, synthetic waxes, ceresin, lanolin, lanolin derivatives, cocoa butter, shellac wax, rice bran wax, kapok wax, sugar cane wax, montan wax, spermaceti wax, bayberry wax, silicone waxes (e.g. polymethylsiloxane alkyl, alkoxy and / or esters, C 30-45 alkyldimethylsilylpolypropylsilsesquioxane), stearyl dimethicone, alkylmethylsiloxanes containing long chain alkyl groups in the alkylmethylsiloxy unit, and mixtures thereof.

[0104] Examples of humectants include low molecular weight aliphatic diols, such as propylene glycol and butylene glycol; polyols, such as glycerin and sorbitol; and polyoxyethylene polymers, such as polyethylene glycol 200; hyaluronic acid and its derivatives, and mixtures thereof.

[0105] Examples of thickening agents include acrylamide copolymers, acrylic acid copolymers and their salts (e.g., sodium polyacrylate, etc.), xanthan gum and derivatives, cellulose gums and cellulose derivatives (e.g., methylcellulose, methylhydroxypropylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, polypropylhydroxyethylcellulose, etc.), starch and starch derivatives (e.g., hydroxyethylamylose and starch amylase, etc.), polyoxyethylene, carbomers, alginates (e.g., sodium alginate, etc. ), gum arabic, cassia gum, locust bean gum, scleroglucan gum, gellan gum, rhamsan gum, karaya gum, carrageenan gum, guar gum and guar gum derivatives, cocamide derivatives (including cocamidopropyl betaine and cocamide MIPA), alkyl alcohols (such as cetearyl alcohol, stearyl alcohol, and other fatty alcohols), gelatin, PEG-derivatives, saccharides (such as fructose, glucose, and the like) and saccharide derivatives (such as PEG-120 methyl glucose diolate), and mixtures thereof.

[0106] Examples of aqueous phase stabilizers include electrolytes (e.g., alkali metal and alkaline earth metal salts, particularly the chlorides, borates, citrates, and sulfates of sodium, potassium, calcium, and magnesium, as well as aluminum chlorohydrate, and polyelectrolytes, particularly hyaluronic acid and sodium hyaluronate), polyols (glycerin, propylene glycol, butylene glycol, and sorbitol), alcohols, such as ethyl alcohol, and hydrocolloids, and mixtures thereof.

[0107] Examples of pH adjusters include any water-soluble acid, such as carboxylic or mineral acids, such as hydrochloric acid, sulfuric acid, and phosphoric acid, monocarboxylic acids, such as acetic acid and lactic acid, and polycarboxylic acids, such as succinic acid, adipic acid, citric acid, and mixtures thereof.

[0108] Examples of preservatives and cosmetic biocides include paraben derivatives (e.g., methylparaben, propylparaben, etc.), hydantoin derivatives, chlorhexidine and its derivatives, imidazolidinyl urea, diazolinyl urea, phenoxyethanol, silver derivatives, salicylic acid ester derivatives, triclosan, ciclopirox olamine, hexamidine, oxyquinoline and its derivatives, povidone iodine, zinc salts and derivatives, such as zinc pyrithione, methylchloroisothiazolinone, methylisothiazolinone, and mixtures thereof.

[0109] Examples of sebum absorbents or sebum control agents include silica silylate, silica dimethylsilylate, dimethicone / vinyl dimethicone crosspolymer, polymethyl methacrylate, crosslinked methyl methacrylate, aluminum starch octenyl succinate, and mixtures thereof.

[0110] Examples of pigments and colorants include surface-treated or untreated iron oxides, surface-treated or untreated titanium dioxide, surface-treated or untreated mica, silver oxide, silicates, chromium oxide, carotenoids, carbon black, ultramarines, chlorophyllin derivatives, and yellow ochre. Examples of organic pigments include the D&C and FD&C designated blue, brown, green, orange, red, yellow, aromatic types including azo, indigoid, triphenylmethane, anthraquinone, and xanthine dyes, and mixtures thereof. Surface treatments include those based on lecithin, silicones, silanes, fluorine compounds, and mixtures thereof.

[0111] Examples of silicone conditioning agents include silicone oils such as dimethicone; silicone gums such as dimethiconol; silicone resins such as trimethylsiloxysilicate, polypropylsilsesquioxane, and the like; silicone elastomers; alkylmethylsiloxanes; organically modified silicone oils such as amodimethicone, aminopropylphenyltrimethicone, phenyltrimethicone, trimethylpentaphenyltrisiloxane, silicone quaternium-16 / glycidoxydimethicone crosspolymer, silicone quaternium-16, and the like; saccharide-functional siloxanes; carbinol-functional siloxanes; silicone polyethers; siloxane copolymers (divinyldimethicone / dimethicone copolymers); acrylate or acryl-functional siloxanes; and mixtures or emulsions thereof.

[0112] Examples of cationic conditioning agents include guar derivatives, such as hydroxypropyltrimethylammonium derivatives of guar gum; cationic cellulose derivatives, cationic starch derivatives; quaternary nitrogen derivatives of cellulose ethers; homopolymers of dimethyldiallylammonium chloride; copolymers of acrylamide and dimethyldiallylammonium chloride; homopolymers or copolymers derived from acrylic or methacrylic acid containing cationic nitrogen functional groups attached to the polymer by ester or amide bonds; polyquaternary ammonium salts of hydroxyethylcellulose reacted with aliphatic alkyldimethylammonium substituted epoxides; N,N'-bis-(2,3-epoxypropyl)-piperazine or polycondensation products of piperazine-bis-acrylamide and piperazine; and copolymers of vinylpyrrolidone and acrylic acid esters with quaternary nitrogen functionality. Specific materials include various polyquats, such as polyquaternium-7, polyquaternium-8, polyquaternium-10, polyquaternium-11, and polyquaternium-23. Other categories of conditioners include cationic surfactants, such as cetyltrimethylammonium chloride, cetyltrimethylammonium bromide, stearyltrimethylammonium chloride, and mixtures thereof. In some instances, cationic conditioning agents are also hydrophobically modified, such as hydrophobically modified quaternized hydroxyethyl cellulose polymers; cationic hydrophobically modified galactomannan ethers; and mixtures thereof.

[0113] Examples of hydrophobic conditioning agents include guar derivatives; galactomannan gum derivatives; cellulose derivatives; and mixtures thereof.

[0114] UV absorbers and sunscreens, as known in the art, include those that absorb ultraviolet light between 290-320 nanometers (UV-B region) and those that absorb ultraviolet light in the range of 320-400 nanometers (UV-A region), as well as blue light absorbers.

[0115] Some examples of sunscreens include aminobenzoic acid, cinoxate, diethanolamine methoxycinnamate, digalloyl trioleate, dioxybenzone, ethyl 4-[bis(hydroxypropyl)]aminobenzoate, glyceryl aminobenzoate, homosalate, lawsone in combination with dihydroxyacetone, menthyl anthranilate, octocrylene, ethylhexyl methoxycinnamate (or octyl methoxycinnamate), octyl salicylate (or ethylhexyl salicylate), oxybenzone, padimate O, phenylbenzimidazole sulfonic acid, red petrolatum, sulisobenzone, titanium dioxide, trolamine salicylate, and mixtures thereof.

[0116] Some examples of UV absorbers are Acetaminosalol, Allatoin PABA, Benzalphthalide, Benzophenone, Benzophenone 1-12,3-benzylidene camphor, benzylidene camphor hydrolyzed collagen sulfonamide, benzylidene camphor sulfonic acid, benzyl salicylate, bornelone, bumetrizole, butyl methoxydibenzoylmethane, butyl PABA, ceria / silica, ceria / silica talc, cinoxate, DEA-methoxycinnamate, dibenzoxazole naphthalene, di-t-butyl hydroxybenzylidene camphor, digalloyl trioleate, methyl diisopropyl cinnamate, dimethyl PABA ethyl cetearyldimonium tosylate, dioctyl butamido triazone, diphenyl carbomethoxyacetoxy naphthopyran, bisethylphenyl thiaminotriazine stilbene disulfonate disodium, distyryl biphenyl triaminotriazine stilbene disulfonate disodium, di Disodium Styrylbiphenyl Disulfonate, Drometrizole, Drometrizole Trisiloxane, Ethyl Dihydroxypropyl PABA, Ethyl Diisopropyl Cinnamate, Ethyl Methoxycinnamate, Ethyl PABA, Ethyl Urocanate, Etocrylene Ferulate, Glyceryl Dimethoxycinnamate Octanoate, Glyceryl PABA, Glycol Salicylate, Homosalate, Isoamyl p-Methoxycinnamate, Isopropyl Benzyl Salicylate, Isopropyl Dibenzoylmethane, Isopropyl Methoxycinnamate, Octyl Methoxycinnamate, Methyl Anthranilate, Methyl Salicylate, 4-Methylbenzylidene, Camphor, Octocrylene, Octrizole, Octyl Dimethyl PABA, Ethylhexyl Methoxycinnamate, Octyl Salicylate, Octyl Triazone, PABA, PEG-25 PABA, Pentyl Dimethyl PABA, Phenyl Benzimidazole Sulfonic Acid, Polyacrylamidomethyl Benzylidene Camphor, Potassium Methoxycinnamate, Potassium Phenyl Benzimidazole Sulfonate, Red Petrolatum, Sodium Phenyl Benzimidazole Sulfonate, Sodium Urocanate, TEA-Phenyl Benzimidazole Sulfonate, TEA Salicylate, Terephthalylidene Dicandicamphor Sulfonic Acid, Titanium Dioxide, Tri-PABA Panthenol, Urocanic Acid, VA / Crotonic Acid / Methacryloxybenzophenone-1 Copolymer, and mixtures thereof.

[0117] Examples of skin protectants include allantoin, aluminum acetate, aluminum hydroxide, aluminum sulfate, calamine, cocoa butter, cod liver oil, colloidal oatmeal, dimethicone, glycerin, kaolin, lanolin, mineral oil, petrolatum, shark liver oil, sodium bicarbonate, talc, witch hazel, zinc acetate, zinc carbonate, zinc oxide, and mixtures thereof.

[0118] Examples of dyes are 1-acetoxy-2-methylnaphthalene; acid dyes; 5-amino-4-chloro-o-cresol; 5-amino-2,6-dimethoxy-3-hydroxypyridine; 3-amino-2,6-dimethylphenol; 2-amino-5-ethylphenol HCl; 5-amino-4-fluoro-2-methylphenol sulfate; 2-amino-4-hydroxyethylaminoanisole; 2-amino-4-hydroxyethylaminoanisole sulfate; 2-amino-5-nitrophenol; 4-amino-2-nitrophenol; 4- Amino-3-nitrophenol;2-Amino-4-nitrophenol sulfate;m-Aminophenol HCl;p-Aminophenol HCl;m-Aminophenol;o-Aminophenol;4,6-Bis(2-hydroxyethoxy)-m-phenylenediamine HCl;2,6-Bis(2-hydroxyethoxy)-3,5-pyridinediamine HCl;2-Chloro-6-ethylamino-4-nitrophenol;2-Chloro-5-nitro-N-hydroxyethyl p-phenylenediamine;2-Chloro-p-phenylenediamine; 3,4-Diaminobenzoic acid;4,5-Diamino-1-((4-chlorophenyl)methyl)-1H-pyrazole-sulfate;2,3-Diaminodihydropyrazolopyrazolone dimethosulfonate;2,6-Diaminopyridine;2,6-Diamino-3-((pyridin-3-yl)azo)pyridine;Dihydroxyindole;Dihydroxyindoline;N,N-Dimethyl-p-phenylenediamine;2,6-Dimethyl-p-phenylenediamine;N,N-Dimethyl-p-phenylenediamine sulfate;Direct dyes;4-Ethoxy-m-fu Phenylenediamine sulfate;3-Ethylamino-p-cresol sulfate;N-Ethyl-3-nitro PABA;Gluconamidopropylaminopropyl dimethicone;Haematoxylon brassiletto tree extract;HC dye;Lawsonia inermis (henna) extract;Hydroxyethyl-3,4-methylenedioxyaniline HCl;Hydroxyethyl-2-nitro-p-toluidine;Hydroxyethyl-p-phenylenediamine sulfate;2-Hydroxyethyl picramate;Hydroxypyridinone;Hydroxysuccinimidyl C 21 -C 22Isoalkyl acidate;Isatin;Isatis tinctoria leaf powder;2-Methoxymethyl-p-phenylenediamine sulfate;2-Methoxy-p-phenylenediamine sulfate;6-Methoxy-2,3-pyridinediamine HCl;4-Methylbenzyl 4,5-diaminopyrazole sulfate;2,2'-Methylenebis 4-aminophenol;2,2'-Methylenebis-4-aminophenol HCl;3,4-Methylenedioxyaniline;2-Methylresorcinol;Methylrosanilinium chloride;1,5-Naphthalenediol;1,7-Naphthalenediol;3-Nitro-p-cresol;2-Nitro-5-glyceryl methylaniline;4-Nitroguaiacol;3-Nitro-p-hydroxyethylaminophenol;2-Nitro-N-hydroxyethyl-p-anisidine;Nitrophenol;4-Nitrophenyl Aminoethylurea;4-nitro-o-phenylenediamine dihydrochloride;2-nitro-p-phenylenediamine dihydrochloride;4-nitro-o-phenylenediamine HCl;4-nitro-m-phenylenediamine;4-nitro-o-phenylenediamine;2-nitro-p-phenylenediamine;4-nitro-m-phenylenediamine sulfate;4-nitro-o-phenylenediamine sulfate;2-nitro-p-phenylenediamine sulfate;6-nitro-2,5-pyridinediamine;6-nitro-o-toluidine;PEG-3 Contains: 2,2'-di-p-phenylenediamine;p-phenylenediamine HCl;p-phenylenediamine sulfate;phenylmethylpyrazolone;N-phenyl-p-phenylenediamine HCl;Blue Dye 15:1;Violet Dye 23;Yellow Dye 13;Pyrocatechol;Pyrogallol;Resorcinol;Sodium picramate;Sodium sulfanilate;Solvent Yellow 85;Solvent Yellow 172;Tetraaminopyrimidine sulfate;Tetrabromophenol Blue;2,5,6-triamino-4-pyrimidinol sulfate;1,2,4-trihydroxybenzene.

[0119] Examples of fragrances include ketone fragrances and aldehyde fragrances. Examples of ketone fragrances are bucconoxime, isojasmone, methyl beta naphthyl ketone, musk indanone, tonalide / musk plus, alpha-damascone, beta-damascone, delta-damascone, iso-damascone, damaskenone, damarose, methyl dihydrojasmonate, menthone, carvone, camphor, fenchone, alpha-ionone, beta-ionone, gamma-methyl so-called ionone, fleuramone, dihydrojasmone, cis-jasmone, iso-E-super, methyl cedrenyl ketone or methyl cedrylone, acetophenone, methyl acetophenone, para-methoxy-acetophenone, methyl beta-naphthyl ketone, benzyl acetone, benzophenone, para-hydroxy-phenyl-butanone, celery ketone or libuscone, 6-isopropyl decahydro-2-naphthone, dimethyl octenone, frescomente, 4-( 1-ethoxyvinyl)-3,3,5,5,-tetramethyl-cyclohexanone, methyl-heptenone, 2-(2-(4-methyl-3-cyclohexen-1-yl)propyl)-cyclopentanone, 1-(p-menthen-6(2)-yl)-1-propanone, 4-(4-hydroxy-3-methoxyphenyl)-2-butanone, 2-acetyl-3,3-dimethyl-norbornane, 6,7-dihydro-1,1,2,3,3- These include pentamethyl-4(5H)-indanone, 4-damascol, dalcinyl or cassion, gerson, hexylone, isocyclime E, methyl-cyclocitron, methyl-lavender-ketone, oribone, para-tertiary-butyl-cyclohexanone, verdon, delphon, muscone, neobutenone, plicatone, veloutone, 2,4,4,7-tetramethyl-oct-6-en-3-one, and tetramelane. The fragrance may be derived from or extracted from the flowers, seeds, leaves, and / or roots of plants, seaweed, etc. The fragrance may be extracted from animals, for example from glands, and may be musk or sperm whale oil. The fragrance may also be synthetically produced, for example menthol, acetate, vanilla, etc.

[0120] In a specific embodiment, the ketone scent is selected for its characteristic odor from alpha damascone, delta damascone, isodamascone, carvone, gamma-methyl-ionone, iso-E-super, 2,4,4,7-tetramethyl-oct-6-en-3-one, benzylacetone, beta damascone, damaskenone, methyl-dihydrojasmonate, methyl-cedrylone, and mixtures thereof.

[0121] In a specific embodiment, the aldehyde fragrance is selected for its characteristic odor from the following: adoxal; anisic aldehyde; simal; ethyl vanillin; furohydral; helional; heliotropin; hydroxycitronellal; coavone; lauric aldehyde; lyral; methylnonylacetaldehyde; PT bucinal; phenylacetaldehyde; undecylenic aldehyde; vanillin; 2,6,10-trimethyl-9-undecenal, 3-dodecan-1-al, α-n-amylcinnamaldehyde, 4-methoxybenzaldehyde, benzaldehyde, 3-(4-tert-butylphenyl)-propanal, 2-methyl-3-(para-methyl ... 2-methyl-4-(2,6,6-trimethyl-2(1)-cyclohexen-1-yl)butanal, 3-phenyl-2-propenal, cis- / trans-3,7-dimethyl-2,6-octadien-1-al, 3,7-dimethyl-6-octen-1-al, [(3,7-dimethyl-6-octenyl)oxy]acetaldehyde, 4-isopropylbenzaldehyde, 1,2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde, 2,4-dimethyl-3-cyclohexene-1-carboxaldehyde, 2-methyl-3-(isopropylphenyl)propanal, 1-decanal;Decyl aldehyde, 2,6-dimethyl-5-heptenal, 4-(tricyclo[5.2.1.0(2,6)]-decylidene-8)-butanal, octahydro-4,7-methano-1H-indene carboxaldehyde, 3-ethoxy-4-hydroxybenzaldehyde, para-ethyl-α,α-dimethylhydrocinnamaldehyde, α-methyl-3,4-(methylenedioxy)-hydrocinnamaldehyde, 3,4-methylenedioxybenzaldehyde, α-n-hexyl Ruscinnamaldehyde, m-cymene-7-carboxaldehyde, α-methylphenylacetaldehyde, 7-hydroxy-3,7-dimethyloctanal, undecenal, 2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 4-(3)(4-methyl-3-pentenyl)-3-cyclohexene-carboxaldehyde, 1-dodecanal, 2,4-dimethylcyclohexene-3-carboxaldehyde, 4-(4-hydroxy-4-methylpentenyl)-3-cyclohexene-carboxaldehyde 1-methyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde, 7-methoxy-3,7-dimethyloctan-1-al, 2-methylundecanal, 2-methyldecanal, 1-nonanal, 1-octanal, 2,6,10-trimethyl-5,9-undecadienal, 2-methyl-3-(4-tertbutyl)propanal, dihydrocinnamaldehyde, 1-methyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde, 5 or 6-methoxy-10-hexahydro-4,7-methanoindan-1 or 2-carboxaldehyde, 3,7-dimethyloctan-1-al, 1-undecanal, 10-undecen-1-al, 4-hydroxy-3-methoxybenzaldehyde, 1-methyl-3-(4-methylpentyl)-3-cyclohexenecarboxaldehyde, 7-hydroxy-3,7-dimethyl-octanal, trans-4-decenal, 2,6-nonadienal, p-tolylacetaldehyde;4-Methylphenylacetaldehyde, 2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal, ortho-methoxycinnamaldehyde, 3,5,6-trimethyl-3-cyclohexenecarboxaldehyde, 3,7-dimethyl-2-methylene-6-octenal, phenoxyacetaldehyde, 5,9-dimethyl-4,8-deca-dienal, paeonialdehyde (6,10-dimethyl-3-oxa-5,9-undeca-dien-1-al), hexahydro-4,7-methanoindan-1-carboxaldehyde, 2-methyloctanal, α-methyl-4-(1-methyl (ethylethyl)benzeneacetaldehyde, 6,6-dimethyl-2-norpinen-2-propionaldehyde, p-methylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propen-1-aldehyde, 3,5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propyl-bicyclo[2.2.1]-hept-5-ene-2-carbaldehyde, 9-decenal, 3-methyl-5-phenyl-1-pentanal, methylnonylacetaldehyde, hexanal, trans-2-hexanal, 1-p-menthene-q-carboxaldehyde, and mixtures thereof;

[0122] Examples of antioxidants include acetylcysteine, arbutin, ascorbic acid, ascorbic acid polypeptide, ascorbyl dipalmirate, ascorbyl methylsilanol pectin, ascorbyl palmitate, ascorbyl stearate, BHA, p-hydroxyanisole, BHT, t-butylhydroquinone, caffeic acid, tea oil, chitosan ascorbate, chitosan glycolate, chitosan salicylate, chlorogenic acid, cysteine, cysteine ​​HCl, decyl mercaptomethylimidazole, erythorbic acid, diamylhydroquinone, di-t-butylhydroquinone. , Dicetyl thiodipropionate, Dicyclopentadiene / t-butyl cresol copolymer, Digalloyl trioleate, Dilauryl thiodipropionate, Dimyristyl thiodipropionate, Dioleyl tocopheryl methylsilanol, Isoquercitrin, Diosmin, Disodium ascorbyl sulfate, Disodium rutinyl disulfate, Distearyl thiodipropionate, Ditridecyl thiodipropionate, Dodecyl gallate, Ethyl ferulate, Ferulic acid, Hydroquinone, Hydroxylamine HCl, Hydroxylamine sulfate, Isooctyl Ruthioglycolate, Kojic Acid, Madecacoside, Magnesium Ascorbate, Magnesium Ascorbyl Phosphate, Melatonin, Methoxy PEG7 Rutinyl Succinate, Methylene Dit-Butylcresol, Methylsilanol Ascorbate, Nordihydroguaiaretic Acid, Octyl Gallate, Phenylthioglycolic Acid, Phloroglucinol, Potassium Ascorbyl Tocopheryl Phosphate, Thiodiglycolamide, Potassium Sulfite, Propyl Gallate, Rosmarinic Acid, Rutin, Sodium Ascorbate, Sodium Ascorbyl / Cholesteryl Phosphate, Sodium Bisulfite, Sodium Erythorbate, Sodium Metabisulfite, Sodium Sulfite, Sodium Thioglycolate, Sorbityl Furfural, Tea Tree (Melaleuca Aftemifolia) Oil, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Tetrahydrodiferuloylmethane, Tocopheryl Linoleate / Oleate, Thiodiglycol, Tocopheryl Succinate, Thiodiglycolic Acid, Thioglycolic Acid, Thiolactic Acid, Thiosalicylic Acid, Thiotaurine, Retinol, Tocophereth 5, Tocophereth 10, Tocophereth 12,Tocophereth 18, Tocophereth 50, Tocopherol, Tocophersolan, Tocopheryl Linoleate, Tocopheryl Nicotinate, Tocoquinone, Otrylbiguanide, Tris(nonylphenyl)phosphite, Ubiquinone, Zinc Dibutyldithiocarbamate, and mixtures thereof.

[0123] Examples of propellant gases include carbon dioxide, nitrogen, nitrous oxide, volatile hydrocarbons such as butane, isobutane, or propane, and chlorinated or fluorinated hydrocarbons such as dichlorodifluoromethane and dichlorotetrafluoroethane, or dimethyl ether; and mixtures thereof.

[0124] In specific embodiments, the functional composition is a sunscreen. In these embodiments, the personal care ingredient contains the sunscreen. The sunscreen may be, for example, a sunscreen additive, an SPF booster, a light stabilizer, a film-forming polymer, etc. The sunscreen may also or alternatively be utilized in sunless tanning applications. Specific examples of sunscreens are set forth above.

[0125] In other embodiments, the personal care ingredient contains a hair care ingredient. In these embodiments, the composition may be referred to as a hair care composition. When utilized to prepare the functional composition, the hair care ingredient is typically selected from conditioning agents (which may be silicone, cationic, hydrophobic, etc.), colorants, dyes, ultraviolet (UV) absorbers, preservatives, plant extracts, fatty alcohols, vitamins, fragrances, antidandruff agents, color care additives, pearlising agents, pH adjusters, electrolytes, chelating agents, styling agents, ceramides, amino acid derivatives, suspending agents, surfactants, detergents, emulsifiers, thickeners, oxidizing agents, reducing agents, film-forming polymers, and combinations thereof. In some of these hair care embodiments, the composition may be referred to as a shampoo, rinse-off conditioner, leave-in conditioner, gel, pomade, serum, spray, coloring product, or mascara. Many examples of these hair care ingredients are set forth above as suitable personal care ingredients.

[0126] Examples of oxidizing agents are ammonium persulfate, calcium peroxide, hydrogen peroxide, magnesium peroxide, melamine peroxide, potassium bromate, potassium caronate, potassium chlorate, potassium persulfate, sodium bromate, sodium carbonate peroxide, sodium chlorate, sodium iodate, sodium perborate, sodium persulfate, strontium dioxide, strontium peroxide, urea peroxide, zinc peroxide, and mixtures thereof. Examples of reducing agents are ammonium bisulfite, ammonium sulfite, ammonium thioglycolate, ammonium thiolactate, cysteine ​​HCl, cysteine, cysteine ​​HCl, ethanolamine thioglycolate, glutathione, glyceryl thioglycolate, glyceryl thiopropionate, hydroquinone, p-hydroxyanisole, isooctyl thioglycolate, magnesium thioglycolate, mercaptopropionic acid, potassium metabisulfite, potassium sulfite, potassium thioglycolate, sodium bisulfite, sodium hydrosulfite, sodium hydroxymethanesulfonate, sodium metabisulfite, sodium sulfite, sodium thioglycolate, strontium thioglycolate, superoxide dismutase, thioglycerin, thioglycolic acid, thiolactic acid, thiosalicylic acid, zinc formaldehyde sulfoxylate, and mixtures thereof.

[0127] Examples of anti-dandruff agents include pyridinethione salts, selenium compounds such as selenium disulfide, and soluble anti-dandruff agents, and mixtures thereof.

[0128] In certain embodiments, the personal care ingredient contains a film-forming polymer, which may be utilized as a personal care ingredient, regardless of whether the functional composition is utilized for skin care, hair care, etc. As used herein, "film-forming polymer" refers to a polymer or oligomer that is capable of forming a film on a substrate, either by itself or, optionally, in the presence of a film-forming agent. The film-forming polymer may form a film upon application of curing conditions, such as, for example, application of heat, exposure to atmospheric conditions, etc. Alternatively, the film-forming polymer may form a film upon evaporation of any carrier vehicle in which the film-forming polymer may be optionally treated. The film-forming polymer may undergo a reaction, for example, the film-forming polymer may become crosslinked or otherwise include additional bonds in forming the film. However, the film-forming polymer may form a film in the absence of such a reaction. The film-forming polymer may be a gelling agent. The film-forming polymer is of particular advantage when the functional composition is formulated as a sunscreen, although the personal care ingredient may contain a film-forming polymer to form other functional compositions as well.

[0129] Personal Care Actives In various embodiments, the personal care ingredient may include or be referred to as a personal care active, a health care active, or a combination thereof (collectively "active" or "actives"). As used herein, "personal care active" refers to any compound or mixture of compounds known in the art as an additive in personal care formulations, typically to provide cosmetic and / or aesthetic benefits. "Health care active" refers to any compound or mixture of compounds known in the art to provide a pharmaceutical or medical benefit. Thus, "health care active" includes substances considered to be active ingredients or active drug ingredients as commonly used and prescribed by the Food and Drug Administration (FDA) of the U.S. Department of Health and Human Services, as contained in Title 21, Chapter I, Parts 200-299 and 300-499 of the Code of Federal Regulations (CFR). Specific personal care actives and health care actives are described below. These personal care actives and health care actives may constitute the personal care ingredients, regardless of whether the personal care ingredients are used to form, for example, AP / DEO compositions, skin care compositions, hair care compositions, nail care compositions, and / or dental care compositions. For example, in various embodiments, the same personal care ingredients may be used to form either hair care compositions or skin care compositions. As will be understood in the art, at least some of the personal care actives described below are the types of specific personal care ingredients introduced above with respect to skin care compositions, hair care compositions, nail care compositions, and dental care compositions, respectively. For example, numerous types of plant or vegetable extracts are described below, which are illustrative of the examples of plant extracts identified above as suitable personal care ingredients. The active ingredients or actives described below may constitute the personal care ingredients of the topical composition or may be used in combination therewith.

[0130] Personal care active ingredients useful for use in the present topical compositions include vitamins and vitamin derivatives, including "pro-vitamins." Vitamins useful herein include vitamin A1, retinol and its derivatives (e.g., the C2-C3 of retinol, 18 Retinol esters, trans-retinol, 1,3-cis-retinol, 11-cis-retinol, 9-cis-retinol, and 3,4-didehydro-retinol, and trans retinoic acid (i.e., retinoids), vitamin B1, vitamin B2, provitamin B5, panthenol, vitamin B6, vitamin B12, niacin, vitamin C and its derivatives, vitamin E, tocopherol, vitamin E esters, folic acid, biotin, pantothenic acid, and mixtures thereof. Other suitable vitamins and International Cosmetic Ingredients Nomenclature (INCI) names for vitamins suitable for use in the topical composition include ascorbyl dipalmitate, ascorbyl methylsilanol pectin, ascorbyl palmitate, ascorbyl stearate, ascorbyl glucoside, sodium ascorbyl phosphate, sodium ascorbate, disodium ascorbyl sulfate, potassium (ascorbyl / tocopheryl) phosphate, retinyl acetate, retinyl palmitate, retinyl propionate, alpha-tocopherol, tocophersolan, tocopheryl acetate, tocopheryl linoleate, tocopheryl nicotinate, and tocopheryl succinate, and combinations thereof.

[0131] The personal care active can be a protein, such as an enzyme. Enzymes include commercially available types, improved, recombinant, wild-type, variants not found in nature, and mixtures thereof. For example, suitable enzymes include hydrolases, cutinases, oxidases, transferases, reductases, hemicellulases, esterases, isomerases, pectinases, lactases, peroxidases, laccases, catalases, and mixtures thereof. Hydrolases include proteases (bacterial, fungal, acid, neutral, or alkaline), amylases (alpha or beta), lipases, mannanases, cellulases, collagenases, lysozymes, superoxide dismutases, catalases, and mixtures thereof. Proteases include trypsin, chymotrypsin, pepsin, pancreatin and other mammalian enzymes; papain, bromelain and other herbal enzymes; subtilisin, epidermin, nisin, naringinase (L-rhamnosidase), urokinase and other bacterial enzymes. Lipases include triacyl-glycerol lipase, monoacyl-glycerol lipase, lipoprotein lipases such as steapsin, elepsin, pepsin, other mammalian, herbal and bacterial lipases, and purified versions.

[0132] Co-Active Examples of other actives suitable for use in the topical compositions are described below. One or more of these actives may be used either alone or in combination with the actives and / or additives described herein.

[0133] The topical composition may include an antiparasitic agent. Examples of antiparasitic agents include hexachlorobenzene, carbamates, natural pyrethroids, permethrin, allethrin, malathion, piperonyl butoxide, and combinations thereof.

[0134] The topical composition may also include antimicrobial agents, also referred to as germicides. Examples of antimicrobial agents include phenols, including cresols and resorcinol. Such compositions may be used to treat skin infections. Examples of very common skin infections include acne, which is associated with p. acnes, as well as the invasion of the sebaceous glands by Staphylococcus aureus or Pseudomonas. Examples of useful anti-acne actives include keratolytic agents, such as salicylic acid (o-hydroxybenzoic acid), derivatives of salicylic acid such as 5-octanoyl salicylic acid, and resorcinol; retinoids, such as retinoic acid and its derivatives (e.g., cis and trans); sulfur-containing D and L amino acids and their derivatives and salts, particularly their N-acetyl derivatives, a preferred example of which is N-acetyl-L-cysteine; lipoic acid; antibiotics and antimicrobials, such as benzoyl peroxide, octopirox. , tetracycline, 2,4,4'-trichloro-2'-hydroxydiphenyl ether, 3,4,4'-trichlorovanillide, azelaic acid and its derivatives, phenoxyethanol, phenoxypropanol, phenoxyisopropanol, ethyl acetate, clindamycin and meclocycline; sebostats such as flavonoids; and bile salts such as susimnol sulfate and its derivatives, deoxycholate and cholate; parachlorometaxenol; and combinations thereof.

[0135] In general, phenol at concentrations of 0.2, 1.0, and 1.3% by weight is bacteriostatic, bactericidal, and fungicidal, respectively. Some phenol derivatives are more potent than phenol itself, the most important of which are the halogenated phenols and bis-phenols, alkyl-substituted phenols, and resorcinol. Hydrophobic antimicrobial agents include triclosan, triclocarban, eucalyptol, menthol, methyl salicylate, thymol, and combinations thereof.

[0136] The topical composition may contain an antifungal agent.Examples of antifungal agents include azoles, diazoles, triazoles, miconazole, fluconazole, ketoconazole, clotrimazole, itraconazole, griseofulvin, ciclopirox, amorolfine, terbinafine, amphotericin B, potassium iodide, flucytosine (5FC) and combinations thereof.U.S. Patent No. 4,352,808 discloses 3-aralkyloxy-2,3-dihydro-2-(1H-imidazolylmethyl)benzo[b]thiophene compounds with antifungal and antibacterial activity, and this patent is incorporated herein by reference.

[0137] The topical composition may include a steroidal anti-inflammatory agent. Examples of steroidal anti-inflammatory agents include corticosteroids such as hydrocortisone, hydroxyltriamcinolone, alpha methyldexamethasone, dexamethasone phosphate, beclomethasone dipropionate, clobetasol valerate, desonide, desoxymethasone, desoxycorticosterone acetate, dexamethasone, dichlorisone, diflorasone diacetate, diflucortolone valerate, fluadrenolone, fluclarolone acetonide, fludrocortisone, flumethasone pivalate, flucinolone acetonide, fluocinonide, flucortine butyl ester, fluocortolone, fluprednidene (fluprednylidene (prednylidene)) acetate, flurandrenolone, halcinonide, hydrocortisone acetate, hydrocortisone butyrate, methylproline ... Includes rednisolone, triamcinolone acetonide, cortisone, cortodoxone, flucetonide, fludrocortisone, difluorosone diacetate, fluradrenaline acetonide, medrysone, amc, amcinafal, amcinafide, betamethasone and its ester balance, chloroprednisolone, chloroprednisolone acetate, clocortelone, clescinolone, dichlorisone, difluprednate, flucloronide, flunisolide, fluoromethalone, fluperolone, fluprednisolone, hydrocortisone valerate, hydrocortisone cyclopentylpropionate, hydrocortamate, meprednisone, paramethasone, prednisolone, prednisone, beclomethasone dipropionate, betamethasone dipropionate, triamcinolone, and combinations thereof.

[0138] Currently available topical antihistamine preparations include 1% and 2% diphenhydramine (Benadryl® and Caladryl®), 5% doxepin (Zonalon®) cream, filaramine maleate, chlorpheniramine and tripelennamine, phenothiazines, promethazine hydrochloride (Phenergan®) and dimethindene maleate. These drugs, as well as additional antihistamines, may also be included in the composition. In addition, "natural" anti-inflammatory drugs may be useful. For example, candelilla wax, alpha bisabolol, aloe vera, manjistha (extracted from plants of the genus Rubia, particularly from madder), and guggal (extracted from plants of the genus Commiphora, particularly from Commiphora mukul) may be used as actives in the topical composition.

[0139] The topical composition may include a nonsteroidal anti-inflammatory drug (NSAID). Examples of NSAIDs include the following NSAID categories: propionic acid derivatives; acetic acid derivatives; fenamic acid derivatives; biphenyl carboxylic acid derivatives; and oxicams. Such NSAIDs are described in U.S. Patent No. 4,985,459, which is incorporated herein by reference. Further examples include acetylsalicylic acid, ibuprofen, naproxen, benoxaprofen, flurbiprofen, fenoprofen, fenbufen, ketoprofen, indoprofen, pirprofen, carprofen, oxaprozin, pranoprofen, muniloprofen, tioxaprofen, suprofen, aluminoprofen, tiaprofenic acid, fluprofen, bucloxic acid, and combinations thereof.

[0140] The topical composition may include an antioxidant / radical scavenger. Examples of antioxidants include ascorbic acid (vitamin C) and its salts, tocopherol (vitamin E) and its derivatives, such as tocopherol sorbate, other esters of tocopherol, butylated hydroxybenzoic acid and its salts, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (commercially available under the trade name Trolox®), gallic acid and its alkyl esters, especially propyl gallate, uric acid and its salts and alkyl esters, sorbic acid and its salts, ascorbyl esters of fatty acids, amines (e.g., N,N-diethylhydroxylamine, amino-guanidine), sulfhydryl compounds (e.g., glutathione), and dihydroxyfumaric acid and its salts, as well as EDTA, BHT, and the like, and combinations thereof may be used.

[0141] The topical composition may include an antibiotic. Examples of antibiotics may include chloramphenicol, tetracycline, synthetic and semi-synthetic penicillins, β-lactams, quinolones, fluoroquinolones, macrolide antibiotics, peptide antibiotics, cyclosporines, erythromycin, clindamycin, and combinations thereof.

[0142] The topical composition may include a local anesthetic. Examples of local anesthetics include benzocaine, lidocaine, bupivacaine, chloroprocaine, dibucaine, etidocaine, mepivacaine, tetracaine, dyclonine, hexylcaine, procaine, cocaine, ketamine, pramoxine, phenol, pharma- ceutically acceptable salts thereof, and combinations thereof.

[0143] The topical composition may include an antiviral drug. Examples of antiviral drugs include specific proteins, polypeptides, peptides, fusion proteins, antibodies, nucleic acid molecules, organic molecules, inorganic molecules, and small molecules that inhibit or reduce the binding of the virus to its receptor, the internalization of the virus into the cell, the replication of the virus, or the release of the virus from the cell. In particular, antiviral drugs include nucleoside analogs (e.g., zidovudine, acyclovir, acyclovir prodrugs, famciclovir, gangciclovir, vidarabine, idoxuridine, trifluridine, and ribavirin), n-docosanol foscarnet, amantadine, rimantadine, saquinavir, indinavir, ritonavir, idoxuridine, alpha-interferon and other interferons, AZT, and combinations thereof.

[0144] Additional examples of actives include analgesics and antihypertensives. Analgesics are known in the art and are colloquially referred to as painkillers. Analgesics may be selected from known analgesics, and specific examples include paracetamol (acetaminophen), morphine, codeine, heroin, methadone, thebaine, opailin, buprenorphine, morphinan, benzomorphan, acetaminophen, butorphanol, diflunisal, fenoprofen, fentanyl, fentanyl citrate, hydrocodone, aspirin, sodium salicylate, ibuprofen, oxymorphone, pentaxin, naproxen, nalbuphine, mefenamic acid, meperidine and dihydroergotamine, nonsteroidal anti-inflammatory drugs such as salicylates, and opioid drugs such as morphine and oxycodone. Antihypertensives are known in the art for treating or lowering hypertension, i.e. high blood pressure. The antihypertensive agent may be selected from any known antihypertensive agent, specific examples of which include diuretics, adrenergic receptor antagonists (eg, beta-blockers), benzodiazepines, calcium channel blockers, renin inhibitors, and the like.

[0145] A representative anesthetic antagonist is haloxone. Illustrative antitussives include diphenhydramine, guaifenesin, hydromorphone, ephedrine, phenylpropanolamine, theophylline, codeine, noscapine, levopropoxyphene, carbetapentane, chlophedianol, and benzonatate.

[0146] Illustrative sedatives include chloral hydrate, butabarbital, alprazolam, amobarbital, chlordiazepoxide, diazepam, mephobarbital, secobarbital, diphenhydramine, etinamate, flurazepam, halazepam, haloperidol, prochlorperazine, oxazepam, and talbutal.

[0147] Examples of cardiac agonists include quinidine, propranolol, nifedipine, procaine, dobutamine, digitoxin, phenyloin, sodium nitroprusside, nitroglycerin, verapamil HCl, digoxin, nicardipine HCl, and isosorbide dinitrate.

[0148] Antiemetics are exemplified by thiethylperazine, metoclopramide, cyclizine, meclizine, prochlorperazine, doxylamine succinate, promethazine, triflupromazine, and hydroxyzine.

[0149] A representative dopamine receptor agonist is bromocriptine mesylate. Illustrative amino acid, peptide and protein hormones are thyroxine, growth hormone (GH), interstitial cell stimulating hormone (ICSH), follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), adrenocorticotropic hormone (ACTH), gonadotropin releasing hormone (GnRH), vasopressin and their active decomposition products, such as leuprolide acetate. Some products may have a sufficiently high molecular weight that absorption through the stratum corneum or mucous membranes is difficult. Thus, in some embodiments, only hormones with a molecular weight and configuration that allows passage through the skin are utilized. Examples of hormones include estradiol, diethylstilbestrol, conjugated estrogens, estrone, norethindrone, medroxyprogesterone, progesterone, norgestrel, testosterone, methyltestosterone, and fluoxymesterone.

[0150] In certain embodiments, the topical composition contains a combination of the extract and an additional active substance.In such embodiments, the functional composition may be homogenous or mixed as a single composition, or may be adapted as a kit, comprising a first component containing the extract and a second component containing an additional active substance.The components of the kit may be administered together or separately (e.g., sequentially, in any order).

[0151] Additional Components In addition to the components described above (i.e., compositions / extracts, pharma- ceutically acceptable additives, etc.), the topical composition may contain any number of ingredients / components. For example, in some embodiments, the topical composition contains an additive component, which may include one or more additives.

[0152] Examples of additives suitable for use in the additive component include amino acids, peptides, proteins, lipids, vitamins, carbohydrates, nucleic acids, minerals, nutrients, antioxidants, probiotic bacterial strains, lipophilic substances, extracts, concentrates, oils, gums, and combinations thereof.In certain embodiments, the additive component includes flavorings, dyes, flow improvers, preservatives, fillers, binders, dispersants, solubilizers, supplemental nutrients, excipients, buffers, lubricants, sweeteners, humectants, or any combination thereof.Specific examples of suitable additives include vitamin A, vitamin D, calcium, methylcellulose, lecithin, lysolecithin, and long chain aliphatic alcohols.In certain embodiments, the additive component includes a carrier, such as a consumable carrier, a nutritional carrier, and / or a pharmaceutical carrier, or a mixture thereof.

[0153] In certain embodiments, the additive components of the topical composition include one or more of the following: excipients, such as diluents and binders; granulating agents; glidants (or flow aids); fillers; lubricants; stabilizers; bulking agents; anti-caking agents; coating agents; disintegrants; fragrances; natural or artificial sweeteners; flavorings; and colors; alcohols, such as ethanol, propyl alcohol, and benzyl alcohol; glycerin; glyceryl triacetate; mineral oil; water; silicones, such as silicone oil; silicon dioxide; waxes, such as carnauba wax and beeswax; fatty esters and fatty alcohols; carob; corn syrup, such as hydrolyzed corn syrup solids; celluloses, such as methylcellulose, hydroxypropylmethylcellulose, carboxymethylcellulose, microcrystalline cellulose, and powdered cellulose; fructose; maltodextrins. phosphorus and maltol, such as natural maltol; sorbitol; preservatives, such as p-hydrobenzoic acid esters; potassium sorbate; sodium benzoate; flow agents; stearates, such as calcium stearate, magnesium stearate, and sodium magnesium stearate; calcium hydrogen phosphate; vegetable oils, such as hydrogenated vegetable oils; antioxidants, such as ascorbic acid or tocopherol; starches, such as corn starch and potato starch; glycols and polyglycols; moisturizers; emollients; emulsifiers; surfactants; oils; extracts; skin protectants; disinfectants; preservatives; drugs and active pharmaceutical ingredients; analgesic compounds; anti-neuralgia compounds; antioxidants; blood circulation enhancers; antidepressant compounds; anti-anxiety compounds; anti-stress compounds; colorants; fillers; solvents; vehicles; carriers; other types of additives known to those skilled in the art; and combinations thereof.

[0154] It is recognized that each additive may be utilized in the topical composition in any amount, which is typically selected based on the type of additive, the formulation of the topical composition, the desired end use of the topical composition, and the like. It is also recognized that certain additives may be classified under different terms in the art, and may have similar, overlapping, or different functions with additives having different classifications. In certain embodiments, each additive is present in the functional composition in an amount of 0 to 75% by weight based on the total weight of the composition, such as 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, or 75% by weight based on the total weight of the composition, or within a range defined by any two of such values.

[0155] The topical composition may be presented in unit dosage form, such as in a pack (e.g., metal or plastic foil, blister pack, etc.) or dispenser device that contains one or more unit doses of the composition. The pack or dispenser device may be accompanied by instructions for administration. Useful dosage forms may be prepared by methods and techniques that will be well understood by those skilled in the art, and may include the use of additional ingredients to create bulk or dosage forms, such as those described below. Illustrative dosage amounts, administration frequencies, and methods of administration are discussed herein, but these are merely illustrative, and it should be understood that the dosage, administration frequency, and administration mode may vary according to the age, weight, condition, and response of the individual subject, consumer, or patient, as well as the specific formulation of the topical composition.

[0156] As will be understood in light of the following description, the topical composition may be administered in any form, daily, several times a day, or in any suitable regimen as needed to achieve desired outcome. In the treatment method using the topical composition, the frequency of administration may depend on several factors, including the desired level of prevention or improvement. In general, an exemplary regimen includes administering the topical composition to the subject once or twice a day, including, for example, administering in the morning and / or in the evening. The amount of the topical composition administered to the subject during each administration (i.e., dosage) may depend on several factors, including the level of desired outcome, and the specific topical composition used, the number of doses administered, etc.

[0157] Generally, the topical composition is administered in a therapeutically or prophylactically effective amount, which refers to the amount (i.e., quantity) of the composition (e.g., the topical composition of the present embodiment) required to achieve a particular therapeutic and / or prophylactic effect, for example, in the treatment of a subject (e.g., by improving its condition), as introduced above. Similarly, the term "physiologically effective amount" as used herein refers to the amount of the composition (e.g., the topical composition of the present embodiment) required to achieve a desired physiological effect. Such an effective amount is typically measured and / or expressed in terms of the amount of the topical composition over time (e.g., g / day, mg / day, etc.), but may also incorporate the subject's body weight (e.g., kg), as expressed by the unit g / kg / day. Typically, the topical composition is administered in an amount effective to provide the extract (i.e., those plant compounds) to the subject. In certain embodiments, the topical composition is administered in an amount effective to improve the condition of the subject. In these or other embodiments, the functional composition is administered in an amount effective to improve at least two conditions of the subject, including any of those described herein.

[0158] Activity amount / concentration The topical composition may contain any amount of extract in any form as described herein, which will typically be limited by the nature of the specific plant compound content therein (e.g., germanisum B or iriflorental and / or iripallidal). In particular, daily exposure limits are specified by numerous regulatory / governmental agencies and are periodically reviewed and updated based on an increased understanding of the biological effects of such compounds. Thus, the specific amount and limit of any given plant compound present in the topical composition may be changed (i.e., a stronger content is prohibited by law or regulation) regardless of efficacy.

[0159] It will be appreciated that in addition to the forms of the topical composition described above, the composition may be formulated for delivery / administration to (or through) the dermis to a subject. In such embodiments, the topical composition may be prepared in a form for use in, on, with and / or as an ointment, patch (i.e., transdermal patch), intradermal implant, subdermal implant, or transdermal implant. As used herein, "dermal delivery" or "dermal administration" refers to a route of administration in which a pharmaceutical dosage form is taken up into or through the dermis (i.e., the layer of skin between the epidermis (together forming the skin) and the subcutaneous tissue). Transdermal patches are typically provided as medicated adhesive patches that are placed on the skin to deliver a specific dosage of the phytochemical melanogenesis stimulator or inhibitor (A / B) through the skin and into the bloodstream of a subject. Such patches are known in the art and may be utilized with the functional composition in general to provide a therapeutic route of administration to a subject.

[0160] The various forms of the topical compositions will be best understood in view of the following illustrative compositions. Such compositions may be tailored for specific application and / or dosing regimens, which will be readily understood by one of ordinary skill in the art.

[0161] The personal care composition can be used by any method, such as through application to the human body (e.g., skin or hair) by hand or with an applicator (e.g., brush or sprayer). In some embodiments, the personal care composition may be intended to be removed after such application, such as by washing, wiping, stripping, and the like, or a combination thereof.

[0162] Methods of improving (e.g., treating, preventing) a condition with the topical composition ("methods of treatment") are also provided. The methods of treatment include administering to a subject the topical composition in an amount effective to elicit a biological response from the subject. In certain embodiments, the methods of treatment include topically administering to a subject the topical composition, e.g., in the form of a personal care product. EXAMPLES

[0163] The following examples, illustrating embodiments of the present disclosure, are intended to illustrate, but not limit, the present invention. Unless otherwise noted, all reactions were carried out under atmosphere, and all solvents, substrates, and reagents were purchased or otherwise obtained from various commercial suppliers and utilized as received. All components are mixed or combined according to conventional combination routes.

[0164] Iris Plant Growth Authentication: Iris florentina L. specimens were obtained from a commercial nursery (Companion Plants, Athens, Ohio) and grown in Grant County, Washington State using organic farming practices.

[0165] Verification of phytomorphological characteristics was performed using benchmarks provided by the American Iris Society to help confirm the authenticity of specimens as Iris florentina L. HPTLC phytochemical profiles of extracts obtained from several specimens were also tested by a certified laboratory (Alkemist Labs, Costa Mesa, CA) and found to match the profile of Iris germanica.

[0166] Further testing using a universal plant DNA test (DNA Species Identification SOP AT-SP-278-7, NSF Authentechnologies, Petaluma, CA) confirmed that the specimens were consistent with Iris florentina and Iris germanica.

[0167] Because the phytochemical profile and DNA testing did not conclusively distinguish I. florentina from I. germanica, further comparative validation using whole genome sequencing was performed. Chloroplast DNA sequences were used for the placement of single nucleotide polymorphisms (SNPs) for several different I. germanica cultivars and I. florentina specimens. Twenty-one positions were initially identified in an algorithmic search, and eleven were confirmed by observation. Primers were developed for five of these sequences and used for DNA testing. Three of these SNPs successfully distinguished I. florentina specimens from other I. germanica varieties tested.

[0168] Rhizome cleaning process: Rhizomes were dug from the field with root hairs still attached. Rhizomes and roots were washed in 5 gallon buckets with drinking water from the Columbia River provided by the Irrigation District Company (Ephrata, WA). After washing, root hairs were removed using hand clippers. Rhizomes were sliced ​​by hand with a kitchen knife into 2-5 mm slices until most of the rhizome was removed from the plant.

[0169] Process ranges tested for solvent extraction: Extraction Solvent Range: Various extraction conditions were evaluated and assessed based on extraction yield.

[0170] The primary extractions were tested over a range of 0-30% ethanol in water. At 0% EtOH (100% water), very little Germanium was extracted with the primary extract and also resulted in less iriflorentals in the secondary extract. At 30% ethanol in the primary extract (70% water), a high amount of Germanium B was extracted in the primary extract, but iriflorentals were reduced in the secondary extract. A primary extraction using 15:85 EtOH / H2O was determined to be best for the skin-lightening extract. A primary extraction using 30:70 EtOH / H2O was determined to be best for the skin-darkening extract. The best balance was also determined to be a 15:85 EtOH / H2O solvent system, which removed measurable amounts of Germanium B in the primary extract while producing the greatest concentration of iriflorentals in the secondary extract.

[0171] Secondary extractions were tested over a range of 70-84% ethanol in water. All extractions yielded similar results, therefore 70% (i.e., 70:30 EtOH / H2O) was economically selected.

[0172] Mixing times of the second extract + ININ: 20, 40, and 60 minutes were tested with similar results for marker levels. 30 minutes was chosen as the midpoint for further analysis.

[0173] Extraction time, temperature, and raw material / solvent ratio: Times ranging from 60 to 120 minutes, temperatures ranging from 100 to 140°F, and raw material:solvent ratios ranging from 1:8 to 1:10 were evaluated.

[0174] Slightly more material was extracted at a 1:10 ratio for 120 minutes and these parameters were selected for further work. Note that as the temperature decreases, the yield from the extraction decreases, therefore 140°F was utilized.

[0175] The addition of a water wash of the raw materials between the first and second extracts (Method #3 in Table 1 below) reduced the concentration of germanism and increased the concentration of iriflorent, with the downside of reduced yield for the second extract (a skin lightening ingredient). Method #1 provided a good balance of effective skin lightening with favorable yields.

[0176] The first extract removes very little irriflourental but has a similar concentration of germanisum B. See column 3 of Table 1 below. This shows that it helps to reduce the concentration of germanisum B in the second extract, allowing for the whitening activity of the second extract and the darkening activity of the first extract. [Table 1]

[0177] The variations in the extraction methods utilized to prepare these extracts are illustrated in the flow diagrams in Figures 5-7.

[0178] CO 2 Process ranges tested for Supercritical Fluid Extraction (SCFE) by: The temperature was always 55°C, the range tested was 80-200 bar, extraction times were 15-60 min, with and without 20% ethanol as co-solvent, packed vs. unpacked columns.

[0179] The best results (based on 3D tissue models) were obtained with an unpacked column at 200 bar for 60 min and either CO2 alone, or with 20% ethanol co-solvent, and an unpacked column at 100-200 bar. Similar results were obtained at lower pressures by using ethanol as a co-solvent with CO2.

[0180] The SCFE-based process utilized to prepare the extract is illustrated in the flow diagram of FIG.

[0181] LC and LCMS Reagents: Water, acetonitrile, and isopropanol were Optima LC-MS grade from Fisher Scientific. Formic acid was LC-MS grade from Sigma-Aldrich. Mobile phase solvents were prepared as 0.1% formic acid in water (solvent A) or acetonitrile (solvent B). DMSO was HPLC grade from Fisher Scientific. Germanium B and Iriflorentinum reference standards were isolated from extracts of Iris florentina L. rhizomes by the Center for Natural Products Research at the University of Mississippi and structures were confirmed by 1H and 13C NMR and high-resolution mass spectrometry.

[0182] Instrumentation: Liquid chromatography-mass spectrometry (LC-MS) and bioassay-guided fractionation (BDF) were performed using a Waters Synapt G2 instrument equipped with an Acquity H-class UPLC. The effluent from the column was directed to a photodiode array detector (PDA) and subsequently to the electrospray (ES) ionization source of the mass spectrometer. UV data were acquired from 200-800 nm with 1.2 nm resolution and a sampling rate of 5 scans / s. Mass spectral data were collected from m / z 50-1200 at 0.25 scans / s with a resolution of 20,000 (FWHM) in both positive and negative ion modes. Within each run, alternating low-energy (4V) and high-energy (20V) collision-induced dissociation scans were collected using argon as the collision gas (MSe mode). Leucine-enkephalin was used as the lock mass for accurate mass analysis.

[0183] LC-MS Analysis. Sample extracts were prepared in DMSO at 10 mg / mL and sonicated for 20 minutes to solubilize. Process samples were diluted 1:10 in isopropanol. All samples were filtered through a 0.2 μm Whatman Anotop 25 syringe filter into an autosampler vial for assay. The column was a Waters Acquity HSS T3, 1.8 μm, 2.1×100 mm, and the column oven was maintained at 40° C. The solvent program was linearly ramped as follows: 90% A / 10% B at 0 h, 100% B at 6 min, 100% B held until 8 min, then 90% A / 10% B at 8.01 min, and 90% A / 10% B held until 10 min. A flow rate of 0.4 mL / min and an injection volume of 2 μL were used. Tentative identification of the compounds was based on the accurate masses determined for the protonated (or deprotonated) molecules and by comparison with an online mass spectral database. The identified compounds are shown in Table 2 below. [Table 2]

[0184] Bioassay-guided fractionation (BDF) Sample extracts were prepared at 50 mg / mL in DMSO and sonicated for 20 min. Sample solutions were then filtered through 0.2 μm Whatman Anotop 25 syringe filters into autosampler vials for assay. The LC-MS system was modified to incorporate a 10:1 splitter placed between the UV detector and the MS ion source. The majority of the LC effluent was directed to a Waters Fraction Collector II equipped with a 96-deep well plate (96 wells / run), into which fractions were collected at 20 s / well intervals for the first 32 min of each run. The LC column was an XBridge Shield RP18, 5 μm, 4.6×250 mm, maintained at ambient temperature (22° C.). The solvent program was linearly ramped as follows: 95% A / 5% B at 0 h, 100% B at 30 min, held at 100% B until 32 min, then 95% A / 5% B at 32.1 min, and held at 95% A / 5% B until 36 min. A flow rate of 0.8 mL / min and an injection volume of 10 μL / injection (0.5 mg solids / injection) were used. The effluent of four consecutive LC runs was collected per plate (2 mg solids / plate). Plates were then dried under nitrogen at 40° C. to remove acetonitrile, and residual water was removed by lyophilization. Plates were stored at −80° C. until assayed for pigmentation reaction.

[0185] The BDF results are shown in Figure 2, where LC-UV chromatogram A at 260 nm shows the phytochemical peak profile and time-ordered bar graph B (each bar represents fractions from the LC effluent collected for 20 seconds) shows the pigmentation response using the B16 cell culture assay. Increased pigmentation was observed for fractions corresponding to germanisum B (3) and decreased pigmentation was obtained from fractions corresponding to iriflorental (9) and iripallidal (10).

[0186] cell culture Primary cells and cell lines were grown at 37°C in a humidified atmosphere with 5% CO2. B16-F10 (B16) cells obtained from ATCC (Manassas, VA, USA) were cultured in Dulbecco's modified Eagle's medium (DMEM) containing 4.5 g / L glucose, L-glutamine, and sodium pyruvate, supplemented with 10% fetal bovine serum (FBS) and 1% P / S solution, 100x. These cells were subcultured in T75 flasks at confluency not exceeding 70%, respectively, for 3-4 days to maintain normal growth. Experiments were performed between the fourth and sixth passages.

[0187] Human epidermal melanocyte neonatal darkly pigmented (HEMn-DP) cells were obtained from Thermo Fisher Scientific (Waltham, MA, USA) and maintained in 254 medium containing 60 μM calcium and supplemented with 1% human melanocyte growth supplement (Thermo Fisher Scientific) and 1% penicillin-streptomycin (P / S) solution, 100× (Corning, Manassas, VA, USA). Cells were cultured in T75 and T150 flasks and passaged to just before 80% confluence. Experiments were performed between the fourth and sixth passages.

[0188] B16 Melanin Content Assay B16 cells (6000 cells / well) were subcultured in 96-well plates in DMEM medium supplemented with 10% FBS and 1% P / S for 24 h. For treatment, cells were treated with vehicle or test substances for 96 h in 0.2 ml of DMEM-phenol-free medium supplemented with 10% FBS, 1% P / S, 2 mM L-glutamine, and 50 nM α-MSH (Sigma, St. Louis, MO, USA). Cell viability was tested by measuring absorbance at 405 nm and performing MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Relative melanin content was normalized by % cell viability.

[0189] HEMn-DP melanin content assay HEMn-DP cells (300,000 cells / well) were subcultured in growth medium in 6-well plates. After 24 h of incubation, the cells were treated with vehicle control and test substances on days 1 and 4. On day 7, the growth medium was removed and the cells were lysed using lysis buffer (Thermo Fisher Scientific). The lysed cells were centrifuged at 10,000 g for 10 min and the pellet was washed with ethanol:ether (1:1) solution. The pellet was dried and then solubilized in 2N NaOH at 80° C. for 1 h. The extracts were transferred to 96-well plates and the total melanin content was measured at 405 nm on an M5 Spectramax plate reader. Cell viability was determined with PrestoBlue (Thermo Fisher Scientific) according to the manufacturer's protocol.

[0190] The results of this assay are shown in FIG. 3, where PTU is propylthiouracil, a standard melanogenesis inhibitor.

[0191] Maintenance and Treatment of Human Skin Equivalents MelanoDerm™ skin equivalents (Mattek, Ashland, MA) derived from African American skin (MEL-B) were placed in a 37°C incubator with 5% CO2. The tissues were maintained in LLMM medium. Test articles were dissolved at the desired concentrations in vehicle control solution (90% PBS + 5% EtOH + 5% propylene glycol). After 3 hours of incubation, 25 μL of vehicle control and test articles were applied topically to the skin equivalents on days 0, 1, 3, 6, 8, 10, and 13. The tissues were washed with PBS between treatments and replenished with 5 ml of fresh medium every other day. On day 14, the tissues were collected for visual analysis, melanin extraction, and cytotoxicity assays.

[0192] Human skin equivalent cell viability assay Vehicle control and test articles (25 μl) were applied topically to MEL-B on days 0, 1, 3, 6, 8, 10, and 13. Untreated samples were used as negative controls. On day 14, tissues were rinsed with PBS and placed in 24-well plates. A 2 mg / ml solution of MTT was prepared and 0.3 ml of this solution was added to the wells. After 3 hours of incubation, tissues were transferred to 6-well plates containing 3.0 ml of isopropanol. The plates were stored overnight at -20°C and then shaken at room temperature for at least 2 hours. The extract solutions were measured at 570 nm.

[0193] Melanin content assay of human skin equivalents The melanin content in treated MEL-B was determined as previously reported. Briefly, frozen tissues were immersed in 0.38 ml of 1% SDS, 50 μM EDTA, and 10 mM Tris, pH 6.8, and 20 μl of proteinase K was added at 5 mg / ml. Digestion was allowed to proceed overnight at 45° C., an additional 20 μl of proteinase K was added, and incubated for another 4 hours. Then, 40 μl of 500 mM sodium carbonate and 10 μl of 30% H2O2 were added to the homogenates. The samples were incubated at 80° C. for 30 minutes and cooled to room temperature. A chloroform / methanol (2:1) mixture was prepared and 100 μl was added to the samples. After centrifugation at 10,000 g for 30 minutes, the top phase was collected and the optical density was measured at 450 nm. Synthetic melanin (Sigma-Aldrich) was subjected to the same procedure as a control to generate a standard curve.

[0194] The results of this assay are shown in FIG.

[0195] Serum Composition A series of serum formulations for tissue model testing were prepared as shown in Table 3 below. [Table 3]

[0196] Personal Care Products Various examples of topical compositions formulated as personal care products are provided below.

[0197] skin whitening Formulation Example 1: Facial Foam Cleanser A personal care product composition in the form of a facial foam cleanser for skin lightening is prepared using the components and parameters set forth in Table 4 below. [Table 4]

[0198] Formulation Example 2: Facial Softening Lotion / Toner A personal care product composition in the form of a facial softening lotion / toner for skin lightening is prepared using the components and parameters set out in Table 5 below. [Table 5]

[0199] Formulation Example 3: Facial Complex Serum Concentrate A personal care product composition in the form of a facial complex serum concentrate for skin lightening is prepared using the components and parameters set out in Table 6 below. [Table 6]

[0200] Formulation Example 4: Essence concentrate for facial blemishes A personal care product composition in the form of a facial blemish essence concentrate for skin whitening is prepared using the components and parameters shown in Table 7 below. [Table 7]

[0201] Formulation Example 5: Corrector Treatment for Facial Dark Spots A personal care product composition in the form of a facial blemish corrector treatment for skin lightening is prepared using the components and parameters set forth in Table 8 below. [Table 8]

[0202] Formulation Example 6: Facial milky emulsion / moisturizer A personal care product composition in the form of a facial milky emulsion / moisturizer for skin lightening is prepared using the components and parameters set out in Table 9 below. [Table 9]

[0203] Formulation Example 7: Facial moisturizing cream A personal care product composition in the form of a facial moisturizing cream for skin lightening is prepared using the components and parameters set forth in Table 10 below. [Table 10]

[0204] skin darkening Formulation Example 8: Sunless Tanning Spray A personal care product composition in the form of a sunless tanning spray for skin darkening is prepared using the components and parameters set forth in Table 11 below. [Table 11]

[0205] Formulation Example 9: Two-phase self-tanning mousse A personal care product composition in the form of a two-phase self-tanning mousse for skin darkening is prepared using the components and parameters set forth in Table 12 below. [Table 12]

[0206] Formulation Example 10: Sunless Tanning Milky Emulsion A personal care product composition in the form of a sunless tanning milky emulsion for skin darkening is prepared using the components and parameters set forth in Table 13 below. [Table 13]

[0207] Formulation Example 11: Sunless Self-Tanning Lotion A personal care product composition in the form of a sunless self-tanning lotion for skin darkening is prepared using the components and parameters set forth in Table 14 below. [Table 14]

[0208] Formulation Example 12: Smooth Self-Tanning Cream A personal care product composition in the form of a smooth self-tanning cream for skin darkening is prepared using the components and parameters set out in Table 15 below. [Table 15]

[0209] Formulation Example 13: Smoothing after Sunbutter A personal care product composition in the form of a smoothing after sunbutter for skin darkening is prepared using the components and parameters set forth in Table 16 below. [Table 16]

[0210] Formulation Example 14: Serum for age spotsAn Age Spot Serum was prepared using the components and parameters shown in Table 17 below. In the first phase, Part A, purified water was added to a vessel. The Acrylates / C10-30 Alkyl Acrylate Crosspolymer was then sprinkled on the surface of the water. The Acrylates / C10-30 Alkyl Acrylate Crosspolymer powder was then moistened and allowed to settle to the bottom of the vessel to form the Part A mixture. The Part A mixture was then mechanically agitated. The Part A mixture was heated to 75-80° C. and the butylene glycol, hydroxyethyl cellulose, xanthan gum, disodium EDTA, dipotassium glycyrrhizinate, glycerin (and) glyceryl acrylate / acrylic acid copolymer (and) PVM / MA copolymer, hydrogenated lecithin, chlorphenesin, caprylyl glycol, and niacinamide were added to the Part A mixture.

[0211] In the second phase, Part B, 1.5 cst of dimethicone was added to the vessel to form a Part B mixture. The Part B mixture was heated to 75-80° C. and 5 cst of dimethicone, phenoxyethanol, tocopherol acetate, dl-α-tocopherol, polymethylsilsesquioxane, behenyl alcohol (and) polyglyceryl-10 pentastearate (and) sodium stearoyl lactylate, and batyl alcohol were added to the Part B mixture.

[0212] In the third phase, the Part B mixture was added to the Part A mixture while homogenizing on a Silverson mill (3,700 rpm for 4 minutes) to form an anti-age spot serum mixture. The anti-age spot serum mixture was then mixed at 75-80° C. for 10 minutes. The anti-age spot serum mixture was then cooled to 32-50° C. At 50° C., cytidine was added to the anti-age spot serum mixture. Below 40°C, Liposomes w / Ceramides and β-Sitosterol, Water (and) Acetyl Glucosamine (and) Xanthan Gum (and) Chondrus Crispus (Carrageenan) (and) Glucose, Iris Florentina Root Extract, Hydrolyzed Opuntia Ficus-Indica Flower Extract, Fragrance UAK12854 / 00 Petals and Pearls Mod4, and Potassium Hydroxide (45% wt. solution in water) were added to the Age Spot Serum Mixture. The Age Spot Serum Mixture was then mixed for 10 minutes and cooled to 32-35°C.

[0213] In the fourth phase, purified water was added to a vessel and mixed with ascorbyl glucoside, sodium citrate dihydrate, and potassium hydroxide (45% by weight solution in water) to form a Premix A mixture. The Premix A mixture was mixed until homogenous and then added to the anti-age spot serum mixture. [Table 17]

[0214] Formulation Example 15: Age Spot Corrector An age spot corrector was prepared using the components and parameters shown in Table 18 below. In the first phase, Part A, purified water was added to a vessel. The water was then heated to 75-80° C. Glycerin, ethoxydiglycol, citric acid, sodium citrate dihydrate, disodium EDTA, dipotassium glycyrrhizinate, hydrogenated lecithin, chlorphenesin, Sensiva SC50, tranexamic acid, and potassium hydroxide (45% by weight solution in water) were all added to the heated water to form the Part A mixture. The pH was then adjusted to 6.8-7.2 for best activity stability.

[0215] In the second phase, Part B, caprylic / capric triglyceride, squalane, phenoxyethanol, tocopherol acetate, and polymethylsilsesquioxane were all added to a vessel to form a Part B mixture. The Part B mixture was then heated to 75-80° C. Arachidyl alcohol (and) behenyl alcohol (and) arachidyl glucoside, cetearyl alcohol (and) cetearyl glucoside, and sodium acrylate / acryloyldimethyltaurate copolymer (and) isohexadecane (and) polysorbate 80 were then all added to the Part B mixture.

[0216] When both the Part A and Part B mixtures were at .about.80°C, the Part B mixture was slowly added to the Part A mixture on a Silverston mill at 3,700 rpm over a period of 4 minutes to form the age stain collector mixture, which was then added back to the propellant mixture and cooled to 32-50°C.

[0217] In the third phase, purified water, ascorbyl glucoside, sodium citrate dihydrate, and potassium hydroxide (45% by weight solution in water) were all mixed until homogeneous to form the Premix B mixture. When the age spot collector mixture reached a temperature of 50°C, the Premix B mixture was added to the age spot collector mixture. When the temperature of the age spot collector mixture was below 40°C, Iris florentina root extract, fragrance UAK12854 / 00 Petals and Pearls Mod4, and potassium hydroxide (45% by weight solution in water) were added to the age spot collector mixture. The age spot collector mixture was then mixed for 10 minutes and cooled to ~32-35°C. The final age spot collector was measured to have a pH of 6.5-7.5 and a viscosity of ~150,000 cP. [Table 18]

[0218] It should be understood that the appended claims are not limited to the expressions and specific compounds, compositions, or methods described in the detailed description, which may vary among specific embodiments falling within the scope of the appended claims. With respect to any Markush group relied upon herein to describe particular features or aspects of various embodiments, different, special, and / or unexpected results may be obtained from each member of the Markush group independently of all other Markush members. Each member of the Markush group may be relied upon individually or together, and provides appropriate support for specific embodiments within the scope of the appended claims.

[0219] The terms "containing" or "containing" are used herein in their broadest sense, meaning and including the terms "comprising", "including", "consisting essentially of" and "consisting of". The use of "for example", "for example", "such as" and "including" to enumerate specific examples is not limited to only the enumerated examples. Thus, "for example" or "such as" means "for example, but not limited to" or "such as, but not limited to" and includes other similar or equivalent examples. The term "about" as used herein serves to reasonably encompass or account for small variations in numerical values ​​measured by instrumental analysis or as a result of sample handling. Such small variations may be within the order of ±0-25, ±0-10, ±0-5, or ±0-2.5% of the numerical value. Furthermore, the term "about" applies to both numerical values ​​when referring to a range of values. Furthermore, the term "about" may apply to numerical values ​​even if not expressly stated.

[0220] Moreover, any ranges and subranges that are relied upon in describing various embodiments of the invention are understood to be individually and collectively within the scope of the appended claims, and to describe and contemplate all ranges, including integers and / or fractions therein, even if such values ​​are not expressly recited herein. Those skilled in the art will readily appreciate that the recited ranges and subranges fully describe and enable various embodiments of the invention, and that such ranges and subranges may further delineate corresponding ½, ⅓, ¼, ⅕, etc. As merely an example, the range "from 0.1 to 0.9" may further delineate the lower ⅓, i.e., from 0.1 to 0.3, the middle ⅓, i.e., from 0.4 to 0.6, and the upper ⅓, i.e., from 0.7 to 0.9, which are individually and collectively within the scope of the appended claims, and may be individually and / or collectively dependent and / or provide suitable assistance regarding specific embodiments within the scope of the appended claims. In addition, with respect to words limiting or modifying a range, such as "at least," "more than," "less than," "less than," and the like, it should be understood that such words include subranges and / or upper or lower limits. As another example, the range "at least 10" inherently includes the subranges of at least 10 to 35, at least 10 to 25, 25 to 35, etc., and each subrange may be individually and / or collectively dependent upon and provided with appropriate assistance for specific implementations within the scope of the appended claims. Finally, each individual numerical value within a disclosed range may be dependent upon and provided with appropriate assistance for specific implementations within the scope of the appended claims. For example, the range "from 1 to 9" includes various individual integers, such as 3, as well as individual numbers (or fractions) including decimal points, such as 4.1, which may be dependent upon and provided with appropriate assistance for specific implementations within the scope of the appended claims.

Claims

1. An extract obtained from iris root, containing germanaism B, and selectively enriched with (A) a phytochemical melanin formation stimulant or (B) a phytochemical melanin formation inhibitor.

2. The extract according to claim 1, wherein the extract is selectively enriched with the phytochemical melanin formation stimulant (A), and wherein the phytochemical melanin formation stimulant (A) is germanaism B.

3. The extract according to claim 2, containing the phytochemical melanin formation inhibitor (B) in a reduced proportion compared to the iris root from which the extract is obtained.

4. The extract according to claim 1, wherein the extract is enriched with the phytochemical melanin formation inhibitor (B), and wherein the phytochemical melanin formation inhibitor (B) contains (i) iriflorental; (ii) iriparidal; or (iii) both (i) and (ii).

5. The extract according to claim 4, containing the phytochemical melanin formation stimulant (A) in a reduced proportion compared to the iris root from which the extract is obtained.

6. The extract according to any one of claims 1 to 5, substantially free of iriflorentin.

7. A functional composition containing the extract according to claim 1 and a carrier.

8. The functional composition according to claim 7, adapted for topical application or administration to a subject.

9. A topical composition containing the extract according to claim 1.

10. The topical composition according to claim 2 or 3, containing the extract and adapted for skin darkening.

11. The topical composition according to claim 4 or 5, containing the extract and adapted for skin whitening.

12. The method is as follows: A method for preparing an iris root extract, comprising extracting iris root material with a solvent system to yield an iris root extract, wherein the iris root extract contains germanaism B and is selectively enriched with (A) a phytochemical melanin formation stimulant or (B) a phytochemical melanin formation inhibitor.

13. The method according to claim 12, wherein the extract is selectively enriched with the phytochemical melanin formation stimulant (A), and wherein the phytochemical melanin formation stimulant (A) is germanaism B.

14. The method according to claim 12, wherein the orris root extract is concentrated with the phytochemical melanin formation inhibitor (B), and the phytochemical melanin formation inhibitor (B) contains (i) iriflorental; (ii) iriparidal; or (iii) both (i) and (ii).

15. The method according to claim 12, wherein the orris root material is further defined as the rhizome of Iris germanica L., Iris florentina L., and / or Iris pallida.

16. The method according to claim 12, wherein the dried orris root raw material contains a water content of 5 to 15%.

17. The method according to claim 12, wherein the solvent system is further defined as a hydrous ethanol solvent.

18. The extraction includes subjecting the dried orris root raw material to successive first and second aqueous ethanol solvent extractions, where the first aqueous ethanol solvent extraction is carried out using a 15:85 (EtOH / H ２ O) aqueous ethanol solvent system, yielding a first extract and an extracted raw material, and the second aqueous ethanol solvent extraction is carried out on the extracted raw material using a 70:30 (EtOH / H ２ O) aqueous ethanol solvent system, yielding a second extract, the method according to claim 12.

19. The method according to claim 18, wherein the first extract is concentrated with germainism B and depleted of iriflorental and iriparidal of iridals as compared with the orris root material.

20. The method according to claim 18 or 19, wherein the second extract is concentrated with iriflorental and iriparidal of iridals and depleted of germainism B as compared with the orris root material.

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