CA2701378C

CA2701378C - Seaweed-derived cosmetic compositions

Info

Publication number: CA2701378C
Application number: CA2701378A
Authority: CA
Inventors: Gina Athwal
Original assignee: SKINERGISTICS CLINICAL SKIN SOLUTIONS Inc
Current assignee: SKINERGISTICS CLINICAL SKIN SOLUTIONS Inc
Priority date: 2010-04-22
Filing date: 2010-04-22
Publication date: 2022-11-01
Anticipated expiration: 2030-04-22
Also published as: CA2701378A1; CA3129790A1

Abstract

A cosmetic composition is disclosed for applying to skin. The composition includes a liquid and dispersed in the liquid: an amount or form of fucoidan, an amount or form of beta glucan; and an amount of a marine extract. When the cosmetic composition is applied to the skin, the appearance of the skin is improved.

Description

SEAWEED-DERIVED COSMETIC COMPOSITIONS
BACKGROUND OF THE INVENTION
1. Field of Invention The present invention relates generally to a cosmetic composition and more particularly to a cosmetic composition containing seaweed for application to skin to improve the appearance of the skin.

2. Description of Related Art The skin is one of the largest organs in the body. Skin is comprised of three main layers: the epidermis, the dermis and subcutaneous layers. At the outermost part of the epidermis, a layer of dead cells forms what is known as a stratum comeum layer. The dermis is the middle layer of skin and is comprised of arrangements of collagen fibres, which surround many specialized cells and structures. The innermost layer of the skin is the subcutaneous layer, often called the sub-dermis. The subcutaneous layer is comprised largely of fat and connective tissue and houses larger blood vessels and nerves. Elastin may be found in all layers of the skin, but is most prominent in the dermis layer.
The condition and appearance of the skin is a major concern to most people.
Enhancing the appearance of the skin is of significant interest for many people. The appearance of the skin can be affected by many sources including environmental conditions such as sun exposure, building heating and air conditioning, and air pollution can accelerate deterioration of the condition and appearance of skin.
Additionally, certain diseases can affect the appearance of the skin. Deterioration of the appearance of the skin may include, but is not limited to, wrinkles, loss of firmness and elasticity of the skin, age spots, discolorations, and dryness. In addition, individual factors such as diet, stress, age and genetics may affect the appearance of the skin.
Various compositions and methods for manipulating the appearance of the skin have been reported. For example, international patent application, published under number WO/2004/100889, describes anti-ageing agents, including 3,3' -thiodipropionic acid or derivatives thereof for improving the aesthetic appearance of skin.
Another method of manipulating the quality of the skin is cosmetic surgery. It has been reported that seaweed extracts can be incorporated in compositions for use on the skin (see, for e.g., United States patent application 2004/0219124).
SUMMARY OF THE INVENTION
In accordance with one aspect of the invention there is provided a cosmetic composition for applying to skin. The composition includes a liquid, and dispersed in the liquid an amount of fucoidan, an amount of beta glucan, and an amount of a marine extract, wherein the cosmetic composition improves the appearance of the skin to which the composition is applied.
The composition may further include water as the liquid. The composition may further include the liquid being a glycolic acid-salicylic acid solution. The composition may further include the liquid being water and a glycolic acid-salicylic acid solution. The composition may further include the marine extract being any one or more of a green seaweed, a brown seaweed, an exopolysaccharide, or an algae. The composition may further include the marine extract being Ulva lactuta, Alteromonas maclodeii, Astaxanthin, or EckIonia cava.
In another aspect of the invention, the composition may include an amount of tourmaline. In another aspect of the invention, the composition may include an amount of volcanic obsidian. In another aspect of the invention, the composition may include an amount of Aloe barbadensis. In another aspect of the invention, the composition may include an amount of hydrolyzed pearl nacre. In another aspect of the invention, the composition may include an amount of chitosan. In another aspect of the invention, the composition may include an amount of a phospholipid.
In accordance with another aspect of the invention, the composition may include an amount of glyceryl stearate. In another aspect of the invention, the composition may include an amount of stearic acid. In another aspect of the invention, the composition may include an amount of cetearyl alcohol. In another aspect of the invention, the composition may include an amount of ceteareth 20. In another aspect of the invention, the composition may include an amount of isopropyl palmitate. In another aspect of the invention, the composition may include an amount of ascorbyl polypeptide. In another aspect of the invention, the composition may include an amount of tocotrienol.
In another aspect of the invention, the composition may include an amount of tocopheryl acetate. In

-3-another aspect of the invention, the composition may include an amount of ergocalciferol.
In another aspect of the invention, the composition may include an amount of niacinamide.
In another aspect of the invention, the composition may include an amount of ferulic acid.
In another aspect of the invention, the composition may include an amount of Camellia sinensis. In another aspect of the invention, the composition may include an amount of Centella asiatica. In another aspect of the invention, the composition may include an amount of Chamomile matricaria. In another aspect of the invention, the composition may include an amount of Echinacea augustifolia.
In accordance with another aspect of the invention, the composition may include an amount of Ginko biloba. In another aspect of the invention, the composition may include an amount of butylene glycol. In another aspect of the invention, the composition may include an amount of phenoxyethanol. In another aspect of the invention, the composition may include an amount of caprylyl glycol. In another aspect of the invention, the composition may include an amount of sorbic acid. In another aspect of the invention, the composition may include an amount of peg8/SMDI copolymer. In another aspect of the invention, the composition may include an amount of superoxide dismutase liposomes.
In another aspect of the invention, the composition may include an amount of N-acetyl carnitine. In another aspect of the invention, the composition may include an amount of alpha lipoic acid. In another aspect of the invention, the composition may include an amount ofl-arginine.
In accordance with another aspect of the invention, the composition may include an amount of Glycine sofa. In another aspect of the invention, the composition may include an amount of Rumex crispis. In another aspect of the invention, the composition may include an amount of Vitis vinifera. In another aspect of the invention, the composition may include an amount of hinokitiol. In another aspect of the invention, the composition may include an amount of retinol. In another aspect of the invention, the composition may include an amount of Panax ginseng. In another aspect of the invention, the composition may include an amount of allantoin. In another aspect of the invention, the composition may include an amount of kaolin. In another aspect of the invention, the composition may include an amount of bentonite. hi another aspect of the invention, the composition may include an amount of Undaria pinnatifida. In another aspect of the invention, the composition may include an amount of diatomite silica. In another aspect

-4-of the invention, the composition may include an amount of n-acetyl glucosamine. In another aspect of the invention, the composition may include an amount of phytoplankton.
In another aspect of the invention, the composition may include an amount of a member of the Skeletonema. In another aspect of the invention, the composition may include an amount of a member of the Thalassiosira. In another aspect of the invention, the composition may include an amount of a member of the Chaetoceros. In another aspect of the invention, the composition may include an amount of Fucus vesiculosus. In another aspect of the invention, the composition may include an amount of sodium pCA.
In another aspect of the invention, the composition may include an amount of magnesium ascorbyl phosphate. In another aspect of the invention, the composition may include an amount of epigallocatechin (EGCG). In another aspect of the invention, the composition may include an amount of ellagic acid. In another aspect of the invention, the composition may include an amount of sodium citrate. In another aspect of the invention, the composition may include an amount of tetrasodium EDTA. In another aspect of the invention, the composition may include an amount of an emollient. In another aspect of the invention, the composition may include an amount of a sunscreen. The sunscreen may be an organic sunscreen. The sunscreen may be an inorganic sunscreen. In another aspect of the invention, the composition may include an amount of a silicone surfactant. The silicone surfactant may be cyclomethicone or dimethicone copolyol.
In another aspect of the invention, the composition may include an amount of a preservative. The preservative may be methylisothiazolinone, cetylsyredinium chloride, silver, benzyl pCA, or polyaminopropyl biguamide. In another aspect of the invention, the composition may include an amount of an aqueous botanical antioxidant. The aqueous botanical antioxidant may be hydroxytyrosol, rutin, silymarin, turmeric, genistein, apple, green coffee, quercetin, or rosemary. In another aspect of the invention, the composition may include an amount of a humectant. The humectant may be a glycerol, a sorbitol, or a polyol. In another aspect of the invention, the composition may include an amount of a thickener. The thickener may be a cosmetic gum. The cosmetic gum may be alginic acid, xanthan gum, cellulose gum, hydroxtethyl cellulose, dextrin, agar, guar gum, phycocolloid, ghatti gum, cellulose ester, modified potato starch, or pectin.
In another aspect of the invention, the composition may include an amount of an oligomer.
The oligomer may be iso-olefin, isodecane, hydrogenated polybutene, hydrogenated

-5-polydecene, polycaprolactone, fibronectin or polyethylene glycol. In another aspect of the invention, the composition may include an amount or combination of an amino acid. The amino acid may be present in its natural form. The amino acid may be a synethetic amino acid.
In another aspect of the invention, the composition may include an amount of a mineral and its salt. The mineral may be calcium, magnesium, manganese, or zinc. In another aspect of the invention, the composition may include an amount of a base. The base may be a soluble plant butter, a soluble plant wax, an anhydrous plant based cholesterol base, a phycocolloid gel base, a prepared polyethylene glycol ointment base, or a prepared carbomer gel base. In another aspect of the invention, the composition may include an amount of a marine component. The marine component may be an Enteromorpha species, a Porphyra species, a Chrondus species, a Laminares species, a kelp species or a FucaIs species. In another aspect of the invention, the composition may include an amount of an anti-inflammatory agent. The anti-inflammatory agent may be Glycyrrhiza glabria, Boswellia serrate, Curcuma longa, turmeric, Arnica montana, silymarin, water melon, calendula, eidelweiss, or ginger. In another aspect of the invention, the composition may include an amount of a surfactant. The surfactant may be amphoteric. The surfactant may be cocomidopropyl betaine. The surfactant may be non-ionic. The surfactant may be cocoglucoside or coco polyglucose. The surfactant may be cationic. The surfactant may be lauryl dimoniumhydrolysed collagen.
In another aspect of the invention, the composition may include an amount of a percutaneous penetration enhancer. The percutaneous penetration enhancer may be polyethylene glycol or oleic acid. In another aspect of the invention, the composition may include an amount of a preservative enhancer. The preservative enhancer may be ethylhexyl glycerin, benzethonym chloride, or a hydantoin/PCB blend. In another aspect of the invention, the composition may include an amount of a vasodilator. The vasodilator may be adenosine triphosphate or liposomal 1 arginine. In another aspect of the invention, the composition may include an amount of a vasoconstrictor. The vasoconstrictor may be sea buckthorn, milk thistle, or marshmallow root. In another aspect of the invention, the composition may include an amount of a whitening agent. In another aspect of the invention, the composition may include an amount of a tyrosinase inhibitor.
The tyrosinase inhibitor may be selected from the Glycyrrhiza species. The tyrosinase

- 6 -inhibitor may be a favnoid, a polyphenol, an isoflavon, or a coumarin. In another aspect of the invention, the composition may include an amount of octadecnedioic acid. In another aspect of the invention, the composition may include an amount of chalcones.
In another aspect of the invention the composition may be absorbed by human skin. In another aspect of the invention the composition may be homogeneous.
Various embodiments of the invention relate to a cosmetic composition for applying to skin, the composition comprising: from about 1.5 wt.% to about 5.5 wt.% of a seaweed complex consisting essentially of Ulva lactuca, Alteromonas macleodii and Astaxanthin in a ratio of about

7:1.5:1.5 by weight; 0.15 wt.% tourmaline; 0.05 wt.% volcanic obsidian; from about 8 wt.% to about 12 wt.% of a 1:1 B-glucan:fucoidan ratio by weight mixture, said B-glucan consisting of a 1:1 ratio by weight of yeast B- glucan and fungi B - glucan; 10 wt.% of aqueous Aloe barbadensis leaf extract; 1.5 wt.% hydrolyzed pearl nacre; 1.0 wt.% chitosan; 10 wt.%
phospholipids; 3 wt.%
glyceryl stearate; 3 wt.% stearic acid; 3 wt.% cetearyl alcohol; 3 wt.%
ceteareth 20; 3 wt.%
isopropyl palmitate; 6 wt.% of a 3:1:1:1:1 ratio by weight mixture of ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, and niacinamide; 1.5 wt.% of a 1:1:1:1:1 ratio by weight mixture of an aqueous extract of Camellia sinensis, Centella asiatica, Matricaria chamomilla, Echinacea angustifolia, and Ginkgo biloba; 2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer; 8 wt.% of aqueous superoxide dismutase liposomes; 20.8 wt.% purified water; and 10 wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with ammonium hydroxide, ammonium glycolate or sodium lactate.
Various embodiments of the invention relate to a cosmetic composition for applying to skin, the composition comprising: from about 3.5 wt.% to about 5.5 wt.% of a seaweed complex consisting essentially of Ecklonia cava, Alteromonas macleodii and Astaxanthin in a ratio of about 7:1.5:1.5 by weight; 0.15 wt.% tourmaline; 0.05 wt.% volcanic obsidian; from about 8 wt.% to about 10 wt.% of a 1:1 B- glucan:fucoidan ratio by weight mixture, said B -glucan consisting of a 1:1 ratio by weight of yeast B - glucan and fungi B- glucan; 10 wt.% of aqueous Aloe barbadensis leaf extract; 1.5 wt.% hydrolyzed pearl nacre; 1.0 wt.% chitosan; 10 wt.%
phospholipids; 4 wt.%
glyceryl stearate; 4 wt.% stearic acid; 4 wt.% cetearyl alcohol; 4 wt.%
ceteareth 20; 4 wt.%
Date Recue/Date Received 2021-09-02 - 6a -isopropyl palmitate; 6 wt.% of a 3:1.5:1.5:0.5 ratio by weight mixture of tocotrienol, tocopheryl acetate, niacinamide, and retinal; 2.5 wt.% of a 1:1:1:1:1:1 ratio by weight mixture of the aqueous extracts of Vitis vinifera, Matricaria chamomilla, Echinacea angustifolia, Panax ginseng, Glycine soja, and allantoin; 2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer; 8 wt. %
of aqueous superoxide dismutase liposomes; 14.8 wt.% purified water; and 10 wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with ammonium hydroxide, ammonium glycolate or sodium lactate.
Various embodiments of the invention relate to a cosmetic composition for applying to skin, the composition comprising: 5.5 wt.% of a seaweed complex consisting essentially of Undaria pinnatifida and Astaxanthin in a ratio of about 7:5 by weight; 0.15 wt.% tourmaline; 0.05 wt.% volcanic obsidian; 8 wt.% of a 1:1 B - glucan:fucoidan ratio by weight mixture, said B -glucan consisting of a 1:1 ratio by weight of yeast B - glucan and fungi B -glucan; 10 wt.% of aqueous Aloe barbadensis leaf extract; 1.5 wt.% hydrolyzed pearl nacre; 1.0 wt.% chitosan; 10 wt.% phospholipids; 4 wt.% glyceryl stearate; 4 wt.% stearic acid; 4 wt.%
cetearyl alcohol; 4 wt.%
ceteareth 20; 4 wt.% isopropyl palmitate; 6 wt.% of a 3:1.5:1.5:0.5 ratio by weight mixture of tocotrienol, tocopheryl acetate, niacinamide, and crithmum maritimum; 2.5 wt.%
of a 1:1:1:1:1:1 ratio by weight mixture of an aqueous extract of Vitis vinifera, Matricaria chamomilla, Echinacea angustifolia, Panax ginseng, Glycine soja, and allantoin; 2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer; 8 wt.% of aqueous superoxide dismutase liposomes; 14.8 wt.% purified water; and 10 wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with ammonium hydroxide, ammonium glycolate or sodium lactate.
Various embodiments of the invention relate to a cosmetic composition for applying to skin, the composition comprising: from 4 wt.% to 10 wt.% of a seaweed complex consisting essentially of Ulva lactuca, Alteromonas macleodii and Astaxanthin in a ratio of about 7:1.5:1.5 by weight; 0.15 wt.% tourmaline; 0.05 wt.% volcanic obsidian; from 10 wt.% to 16 wt.% of a 1:1 B- glucan:fucoidan ratio by weight mixture, said B - glucan consisting of a 1:1 ratio by weight of yeast B - glucan and fungi B - glucan; 12 wt.% of aqueous Aloe barbadensis leaf extract; 0.9 wt.%
hydrolyzed pearl nacre; 0.6 wt.% chitosan; 3.5 wt.% of a 1.5:1.5:0.5 ratio by weight mixture of N-acetyl camitine, a-lipoic acid, and L-arginine; 6.4 wt.% phospholipids; 1.6 wt.% sodium Date Recue/Date Received 2021-09-02 - 6b -hyaluronate; 3 wt.% glyceryl stearate; 3 wt.% stearic acid; 3 wt.% cetearyl alcohol; 3 wt.%
ceteareth 20; 3 wt.% isopropyl palmitate; 5 wt.% of a 3:1:0.5:0.5:0.5:0.5 ratio by weight mixture of ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, ferulic acid, and niacinamide; 2 wt.% of a 1:1:1:1 ratio by weight mixture of Glycine soja, Rumex crispis, Vitis vinifera, and hinokitiol; 2.5 wt.% of a 1:1:1:1:1 ratio by weight mixture of the aqueous extracts of Camellia sinensis, Centella asiatica, Matricaria chamomilla, Echinacea angustifolia, and Ginkgo biloba; 3.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer; 8 wt.%
of aqueous superoxide dismutase liposomes; and 18.8 wt.% purified water.
Other aspects and features of the present invention will become apparent to those ordinarily skilled in the art upon review of the following description of specific embodiments of the invention.
DETAILED DESCRIPTION
Any terms not directly defined herein shall be understood to have the meanings commonly associated with them as understood within the art of the invention. Certain terms are discussed below, or elsewhere in the specification, to provide additional guidance to the practitioner in describing the compositions, devices, methods and the like of embodiments of the invention, and how to make or use them. It will be appreciated that the same thing may be said in more than one way. Consequently, alternative language and synonyms may be used for any one or more of the terms discussed herein. No significance is to be placed upon whether or not a term is elaborated or discussed herein. Some synonyms or substitutable methods, materials and the like are provided.
Recital of one or a few synonyms or equivalents does not exclude use of other synonyms or equivalents, unless it is explicitly stated. Use of examples in the specification, including examples of terms, is for illustrative purposes only and does not limit the scope and meaning of the embodiments of the invention herein.
In accordance with one aspect of the invention there is provided a cosmetic composition for applying to skin. The composition is comprised of a liquid and dispersed in the liquid is an amount or form of fucoidan, an amount or form of beta glucan, and an amount of a marine extract.
When applied to the skin, the cosmetic composition improves the appearance of the skin. Improved appearance of the skin may be associated with any one of the following but is not limited to the Date Recue/Date Received 2021-09-02 - 6c -following: decreased skin wrinkles, increased skin smoothness, decreased roughness of the skin, increased luminosity of the skin, increased clarity of the skin, increased firmness of the skin, increased tautness of the skin, decreased irritation of the skin, decreased skin-associated inflammation, improved skin Date Recue/Date Received 2021-09-02 tone, improved hydration of the skin, decreased dryness of the skin, improvements in skin discoloration, and decreased breakouts of skin conditions such as acne.
Optionally, the liquid may be water, and can include but is not limited to distilled water. Optionally, the liquid may be a glycolic acid-salicylic acid solution.
Further, and optionally, the liquid may be a combination of water, including but not limited to distilled water, and a glycolic acid-salicylic acid solution. Optionally, the marine extract used in the combination may include one or more of a green seaweed, a brown seaweed, an exopolysaccharide, or an algae. A green seaweed may include but is not limited to the Ulva genus and particularly Ulva lactuta. A brown seaweed may include but is not limited to laminariales, which is commonly known as kelp, and fucals. A brown seaweed may include Ecklonia cava. An expolysaccharide is understood to be a high-molecular-weight polymer of sugar residues. Algae may include but are not limited to members of the following groups: Archaeplastida, Rhizaria, Excavata, Excavata, Chromista, and Alveolata. Optionally, the composition may include a marine extract selected from any one or more of the following: Ulva lactuta, Alteromonas maclodeii, Astaxanthin, or Ecklonia cava.
Optionally, the composition may include an amount of tourmaline. Optionally, the composition may include an amount of volcanic obsidian. The composition may include an amount of Aloe barbadensis. The composition may further include an amount of hydrolyzed pearl nacre. Optionally, the composition may include an amount of chitosan.
Optionally, the composition may include an amount of a phospholipid. A
phospholipid is understood as being any of a variety of phosphorous-containing lipids that are composed mainly of fatty acids, a phosphate group, and a simple organic molecule.
Optionally, the composition may include an amount of glyceryl stearate. Optionally, the composition may include an amount of stearic acid. Optionally, the composition may include an amount of cetearyl alcohol.
Further, the composition may include an amount of ceteareth 20. The composition may also include an amount of isopropyl palmitate. Optionally, the composition may include an amount of one or more of the following: ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, niacinamide, or ferulic acid.
Optionally, the composition may include an amount of Camellia sinensis. Further, the composition may include an amount of one or more of the following: Centella asiatica, Chamomile

-8-matricaria, Echinacea augustifolia, or Ginko biloba. Optionally, the composition may include an amount of one or more of the following: butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, peg8/SMDI copolymer, superoxide dismutase liposomes, N-acetyl carnitine, alpha lipoic acid, or 1-arginine.
Further, the composition may include an amount of one or more of the following:
Glycine sofa, Rumex crispis, Vitis vinffera, hinokitiol, retinol, Panax ginseng, allantoin, kaolin, bentonite, Undaria pinnatifida, diatomite silica, or n-acetyl glucosamine. The composition may further include an amount of a phytoplankton species. The composition may include an amount of a member of the Skeletonema. The composition may include an amount of a member of the Thalassiosira. The composition may include an amount of a member of the Chaetoceros.
Further, the composition may include an amount of Fucus vesiculosus. The composition may include an amount of one or more of the following: sodium pCA, magnesium ascorbyl phosphate, epigallocatechin (EGCG), ellagic acid, sodium citrate, or tetrasodium EDTA. The composition may include an amount of an emollient. An emollient is understood as being a material used for the prevention or relief of dryness, as well as for the protection of the skin.
The composition may include an amount of a sunscreen. The sunscreen may be an organic sunscreen. According to an embodiment of the invention, the composition may include from approximately 0.1 to approximately 10%, and preferably from approximately 1 to approximately 5% by weight of an organic sunscreen material. The sunscreen may be an inorganic sunscreen. According to an embodiment of the invention, the composition may include an inorganic sunscreen such as titanium dioxide or zinc oxide, having an average particle size of from 1 to 300 nm, or iron oxide, having an average particle size of from 1 to 300 nm, or silica, having an average particle size of from 1 to 100 nm.
The composition may include an amount of a silicone surfactant, which may include but is not limited to cyclomethicone or dimethicone copolyol. The composition may include an amount of a preservative. Examples of a preservative include but are not limited to methylisothiazolinone, cetylsyredinium chloride, silver, benzyl pCA, or polyaminopropyl biguamide.
Further, the composition may include an amount of an aqueous botanical antioxidant. Examples of an aqueous botanical antioxidant include, but are not limited to:

-9-hydroxytyrosol, rutin, silymarin, turmeric, genistein, apple, green coffee, quercetin, or rosemary. Further, the composition may include an amount of a humectant. The humectant may be a glycerol, a sorbitol, or a polyol. The humectant chosen is not limited to the foregoing list of humectants.
The composition may include an amount of a thickener, including but not limited to, a cosmetic gum. The cosmetic gum may include, but is not limited to, alginic acid, xanthan gum, cellulose gum, hydroxtethyl cellulose, dextrin, agar, guar gum, phycocolloid, ghatti gum, cellulose ester, modified potato starch, or pectin.
Further, the composition may include an amount of an oligomer, including but not limited to, an oligomer of iso-olefin, isodecane, hydrogenated polybutene, hydrogenated polydecene, polycaprolactone, fibronectin or polyethylene glycol. An oligomer is understood as representing a few of the aforementioned monomeric units.
The composition may include an amount of an amino acid. The composition may include a combination of amino acids, for example, a peptide comprised of amino acids.
The amino acid may be in its natural form or it may be a synthetic amino acid.
An amino acid may be described as, for example, polar, non-polar, acidic, basic, aromatic or neutral.
A polar amino acid is an amino acid that may interact with water by hydrogen bonding at biological or near-neutral pH. The polarity of an amino acid is an indicator of the degree of hydrogen bonding at biological or near-neutral pH. Examples of polar amino acids include serine, praline, threonine, cysteine, asparagine, glutamine, lysine, histidine, arginine, aspartate, tyrosine and glutamate. Examples of non-polar amino acids include glycine, alanine, valine leucine, isoleucine, methionine, phenylalanine, and tryptophan.
Acidic amino acids have a net negative charge at a neutral pH. Examples of acidic amino acids include aspartate and glutamate. Basic amino acids have a net positive charge at a neutral pH. Examples of basic amino acids include arginine, lysine and histidine.
Aromatic amino acids are generally nonpolar, and may participate in hydrophobic interactions. Examples of aromatic amino acids include phenylalanine, tyrosine and tryptophan. Tyrosine may also participate in hydrogen bonding through the hydroxyl group on the aromatic side chain. Neutral, aliphatic amino acids are generally nonpolar and hydrophobic. Examples of neutral amino acids include alanine, valine, leucine, isoleucine and methionine. An amino acid may be described by more than one descriptive category. Amino acids sharing a common descriptive category may be substitutable for each other in a peptide.
An amino acid residue may be generally represented by a one-letter or three-letter designation, corresponding to the trivial name of the amino acid, in accordance with the following Table A.
Amino acids comprising the peptides described herein will be understood to be in the L- or D- configuration.
Amino acids described herein, may be modified by methylation, amidation, acetylation or substitution with other chemical groups which may change the circulating half-life of the peptide without adversely affecting their biological activity. Additionally, a disulfide linkage may be present or absent in the peptides of the invention.
Nonstandard amino acids may occur in nature, and may or may not be genetically encoded.
Examples of genetically encoded nonstandard amino acids include selenocysteine, sometimes incorporated into some proteins at a UGA codon, which may normally be a stop codon, or pyrrolysine, sometimes incorporated into some proteins at a UAG codon, which may normally be a stop codon. Some nonstandard amino acids that are not genetically encoded may result from modification of standard amino acids already incorporated in a peptide, or may be metabolic intermediates or precursors, for example.
Examples of nonstandard amino acids include 4-hydroxyproline, 5-hydroxylysine, methyllysine, gamma-carboxyglutamate, desmosine, selenocysteine, ornithine, citrulline, lanthionine, 1-aminocyclopropane-1 -carboxylic acid, gamma-aminobutyric acid, camitine, sarcosine, or N-formylmethionine. Synthetic variants of standard and non-standard amino acids are also known and may include chemically derivatized amino acids, amino acids labeled for identification or tracking, or amino acids with a variety of side groups on the alpha carbon. Examples of such side groups are known in the art and may include aliphatic, single aromatic, polycyclic aromatic, heterocyclic, heteronuclear, amino, alkylarnino, carboxyl, carboxamide, carboxyl ester, guanidine, amidine, hydroxyl, alkoxy, mercapto-, alkyhnercapto-, or other heteroatom-containing side chains. Other synthetic amino acids may include alpha-amino acids, non-alpha Table A. Nomenclature and abbreviations of the 20 standard L-amino acids commonly found in naturally occurring peptides Full name Three-letter abbreviation One-letter abbreviation Alanine Ala A
Cysteine Cys Aspartic add Asp Glutamic acid Glu Phenylalanine Phe Glycine Gly Histidine His Isoleucine Ile Lysine Lys Leucine Leu Methionine Met Asparagine Asp Proline Pro Glutamine Gin Arginine Arg Serine Ser Threonine Thr Valine Val V
Tryptophan Trp Tyrosine Tyr amino acids such as beta-amino acids, des-carboxy or des-amino acids.
Synthetic variants of amino acids may be synthesized using general methods known in the art, or may be purchased from commercial suppliers, for example RSP Amino Acids LLC (Shirley, MA).
Additionally, the composition may include an amount of a mineral and its salt.
The mineral may be calcium, magnesium, manganese, or zinc. The mineral chosen is not limited to the aforementioned minerals. The composition may include an amount of a base, including but not limited to, a soluble plant butter, a soluble plant wax, an anhydrous plant based cholesterol base, a phycocolloid gel base, a prepared polyethylene glycol ointment base, or a prepared carbomer gel base. The composition may include an amount of a marine component including, but not limited to, any one or more of the following: an Enteromorpha species, a Porphyra species, a Chrondus species, a Laminares species, a kelp species or a Fucals species. The marine component or seaweed utilized in the composition can be selected from the group consisting of brown algae, red algae and green algae. Further the marine component or seaweed utilized in the composition can be selected by pre-determining the content of any one of the following in the marine component: natural amino acids, fatty acids and their glycosyl derivatives, sterols, natural antimicrobials, ursolic acid, or mono / polysaccharides. Methods for analyzing the above are known in the art and include but are not limited to the techniques disclosed in Sanchez-Machado et at. (2004) Biomedical Chromatography 18(3):183-90.
Further, the composition may include an amount of an anti-inflammatory agent.
The anti-inflammatory agent may include, but is not limited to, any one or more of the following: Glycyrrhiza glabria, Boswellia serrate, Curcuma longa, turmeric, Arnica montana, silymarin, water melon, calendula, eidelweiss, or ginger.
The composition may include an amount of a surfactant. The surfactant may be amphoteric. They surfactant may be, but is not limited to, cocomidopropyl betaine. The surfactant may be non-ionic. The surfactant may be, but is not limited to, cocoglucoside or coco polyglucose. The surfactant may be cationic. The surfactant may be, but is not limited to, lauryl dimoniumhydrolysed collagen.
The composition may include an amount of a percutaneous penetration enhancer including, but not limited to, any one or more of the following: polyethylene glycol or oleic acid. The composition may include an amount of a preservative enhancer including, but not limited to, any one or more of the following: ethylhexyl glycerin, benzethonym chloride, or a hydantoin/PCB blend. Further, the composition may include an amount of a vasodilator including, but not limited to, any one of the following: adenosine triphosphate or liposomal I arginine.
Further, the composition may include an amount of a vasoconstrictor including, but not limited to, any one or more of the following: sea buckthorn, milk thistle, or marshmallow root. Additionally, the composition may include an amount of a whitening agent. The composition may include an amount of a tyrosinase inhibitor including, but not limited to, an inhibitor selected from the Glycyrrhiza species. The tyrosinase inhibitor may include, but is not limited to, a favnoid, a polyphenol, an isoflavon, or a coumarin.
Further, the composition may include an amount of octadecnedioic acid or chalcones or a combination thereof.
Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be readily apparent to those of skill in the art in light of teachings of this invention that changes and modification may be made thereto without departing from the spirit or scope of the invention.
EXAMPLES
Example 1. Composition with acidified fucoidan, beta glucan, and ascorbyl polypeptide In accordance with an embodiment of the present invention, a composition is described having the components shown in Table 1 below. The methodology employed in producing the composition using the amounts described in Table 1 below is generally as follows.
Method Sequence No. 1 In a first mixture, neutralized glycolic and salicyclic acid solution (source:

Spectrum Chemical; Gardena, California) was heated in a stainless steel container to approximately 85 degrees Celsius. The seaweed complex consisting of Ulva lactuta, Alteromonas maclodeii, and astaxanthin (source: Unipex Innovations, Mississauga, Ontario) was added to the heated glycolic acid mixture. The combined mixture was mixed for approximately 45 to 60 minutes.

Table 1. Components of an embodiment of the Invention Sequence No. Component Amount (70 by weight) Glycolic acid-salicylic acid solution (ratio: 8:1) 10 (neutralized with ammonium hydroxide; ammonium glycolate, sodium lactate can also be added to obtain a preferable pH of -4) Seaweed complex containing Ulva lactuta, 5.5 Alteromonas maclodeii and Astaxanthin (ratio:
7:1.5:1.5) Distilled Water 20.8 Tourmaline (0.15%) and volcanic obsidian (0.05%) 0.2 Beta glucan (yeast and specified medicinal fungi 8 extract combined in a 1:1 ratio) and fucoidan complex (beta glucan and fucoidan are present in a 1:1 ratio) Aqueous Aloe barbadensis extract 10 Hydrolyzed pearl nacre (1.5%) and chitosan (0.5%) 2.5 Phospholipids 10 Glyceryl stearate, stearic acid, cetearyl alcohol, 15 ceteareth 20, isopropyl palmitate complex (each of these products is added at an equal amount) Ascorbyl polypeptide, toc,otrienol, tocopheryl 6 acetate, ergocalciferol, niacinamide complex (ratio of these products: 3:1:1:1:1:1) Aqueous extract of Camellia sinensis, ConteIla 1.5 asiatica, Chamomile matricaria, Echinacea augustifolia, Ginko biloba (each of these products is added at an equal amount) Complex of butylene glycol, phenoxyethanol, 2.5 caprylyl glycol, sorbic acid, peg8/SMDI copolymer (these products are added at the following ratio: 1.5:
0.5: 0.25 : 0.25 : 0.25) lii Aqueous superoxide dismutase liposomes 8 A polarized water was developed by adding tourmaline and obsidian (source:
Soliance; Paris, France) to the distilled water. The beta glucan (source:
Biothera; Eagen, Minnesota) and fucoidan (source: Marinova; Cambridge, Tasmania, Australia) complex was dissolved in one-third of the polarized water. The dissolved beta glucan-fucoidan complex was added to the glycolic acid mixture (previously described above) and the entire solution was maintained at approximately 85 degrees Celsius for approximately 30 minutes. While maintaining mixing of the mixture, aqueous Aloe barbedensis leaf extract (source: Tri K Industries; Northvale, New Jersey) was added and the entire mixture was allowed to cool for approximately 30 minutes. Thereafter, hydrolyzed pearl nacre (source:
Active Concepts; Lincolnton, North Carolina) and chitosan (source: Alfa Chem;
Kings Point, New York) were added to the cooled mixture. The entire mixture was allowed to cool to approximately 30 degrees Celsius. Thereafter, phospholipids (source:
Arch Personal Care; Norwalk, Connecticut) were added to the cooled mixture.
Method Sequence No. 2 In a further mixture, glyceryl stearate, stearic acid, cetearyl alcohol, ceteareth 20, and isopropyl palmitate complex (source: Hallstar Corp.; Chicago, Illinois) were heated to 75 degrees Celsius in a 200 kg stainless steel vat. The mixture was mixed by continuous stirring for approximately 60 minutes.
Separately, the remaining two-thirds of polarized water (as described above) was used to dissolve the ascorbyl polypeptide-tocotrienol complex (source: Arch Personal Care). The ascorbyl polypeptide-tocotrienol complex was allowed to dissolve in the polarized water for approximately one hour. Thereafter, aqueous extracts of Camellia sinensis, Centella asiatica, Chamomile matricaria, Echinacea augustifolia, and Ginko biloba (source: Active Organics; Louisville, Texas) were added to the ascorbyl polypeptide ¨ tocotrienol complex.
Method Sequence No. 3 In a further mixture, butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and peg8/SMDI copolymer were added at the ratio described above to make a complex (source: International Specialty Products; Mississauga, Ontario). Thereafter, this complex was added to the glyceryl stearate complex mixture described above, the glyceryl stearate complex having been maintained at approximately 75 degrees Celsius.
Thereafter, the ascorbyl polypeptide-tocotrienol complex, which had previously been mixed with the aqueous extracts described above, was added and agitation of the mixture continued at approximately 75 degrees Celsius. Thereafter, the entire mixture was cooled down to approximately 30 degrees Celsius.
Thereafter, the mixture developed from Method Sequence No. 1 was added to the mixture. The mixture was allowed to cool down to approximately 20 degrees Celsius and liposomal superoxide dismutase (source: Arch Personal Care) was added. The mixture developed in Example 1 is a homogenous mixture.
In a modification to the above, the seaweed complex can be present as 1.5% of the formulation instead of 5.5% as described in Table 1. Further, the beta glucan and fucoidan complex can be present as 12% of the formulation instead of 8% as described in Table 1.
Testing efficacy of Example 1 To test the efficacy of the mixture described in Example 1, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that following application of the mixture described in Example 1, the human subjects exhibited improved appearance of their skin.
Serving as an example, JT, a female under the age of 30 years of age, used the formulation defined in Example 1. Prior to using the formulation of Example 1, JT had exhibited sensitive skin and a tendency to have acne breakouts. JT also described numerous fine lines being visible in her forehead region. On day 0, JT began using an amount approximately equivalent to the size of a quarter and used approximately that amount each morning on her skin. After one week, JT described her skin as being brighter and with an improved complexion. After two weeks, JT described that the fine lines on her skin were blurred. After one month, JT described that her skin had less breakouts and was very smooth. JT identified at least the following attributes as being associated with the formulation defined in Example 1: increased smoothness and brightness of the skin, decreased lines on JT's forehead, and decreased breakouts of acne. Further, JT
identified the formulation of Example 1 as being associated with decreased dryness of the skin.
It was determined that the formulation/mixture of Example 1 was absorbed by human skin.

Example 2. Composition with non-acidified fucoidan and beta glucan In accordance with a further embodiment of the present invention, a composition is described having the components shown in Table 2. The methodology employed in producing the composition using the amounts described in Table 2 is generally as follows.
Method Sequence No. 1 In a first mixture, a polarized water was developed by adding tourmaline and obsidian (source: Soliance) to the distilled water. The seaweed complex consisting of Ulva lactuta, Astaxanthin, Alteromonas maclodeii (source: Unipex Innovations;
Quebec City, Quebec) was dissolved into one half of the polarized water. The mixture was maintained at approximately 85 degrees Celsius. While maintaining the temperature, the mixture was stirred for approximately 45 minutes to 60 minutes. Thereafter, beta gluean (source: Biothera) and fucoidan (source: Marinova) complex were dissolved in the seaweed complex-distilled water mixture. This mixture was maintained at approximately 85 degrees Celsius and the mixture was stirred for at least approximately 30 minutes.
Thereafter, while maintaining the mixing of the mixture, the aqueous Aloe barbedensis leaf extract (source: Tri K Industries) was added and the entire mixture was allowed to cool for approximately 30 minutes.
Therafter, hydrolyzed pearl nacre (source: Rita Corp.; Crystal Lake, Illinois) and chitosan (source: Alfa Chem), acetyl glucosomine (source: Alfa Chem), n-acetyl carnatine (source: Alfa Chem), alpha lipoic acid (source: Alfa Chem), and 1-arginine (source: Alfa Chem) were added to the cooled mixture. The cooled mixture was further cooled to approximately 30 degrees Celsius. Thereafter, phospholipids (source: Arch Personal Care) and sodium hyaluronate (source: Tri-K Industries) were added to the mixture.

Table 2. Components of an embodiment of the invention Sequence No. Component Amount elk by welaht) Distilled water 18.8 Tourmaline (0.15%) and volcanic obsidian (0.05%) 0.2 Seaweed complex containing Ulva lactuta, 10 Astaxanthin, Alteromonas maclodeii (ratio of these products: 7:1.5:1.5) Beta glucan (yeast and specified medicinal fungi 10 extract combined in a 1:1 ratio) and fucoidan complex (beta glucan and fucoidan are present in a 1:1 ratio) Aqueous Aloe barbedensis leaf extract 12 Hydrolyzed pearl nacre and chitosan (ratio of these 1.5 products: 1.5:1) N-acetyl carnitine, alpha lipoic acid, and I-arginine 3.5 (ratio of these products: 1.5:1.5:0.5) Phospholipids and sodium hyaluronate (ratio of these 8 products: 4:1) II Glyceryl stearate, stearic acid, cetearyl alcohol, 15 ceteareth 20, isopropyl palmitate complex (each of these products is added at an equal amount) II Ascorbyl polypeptide, tocotrienol, tocopheryl acetate, 5 ergocalciferol, ferulic acid, niacinamide complex (ratio of these products: 3:1:0.5:0.5:0.5:0.5) Glycine sofa, Rumex crispis, Vitis vinifera, hinokitiol 2 (beta thujaplicin) (each of these products is added at an equal amount) II Aqueous extract of Camellia sinensis, CenteHa 2.5 asiatica, Chamomile matricaria, Echinacea augustifolia, Ginko biloba (each of these products is added at an equal amount) Ill Complex of butylene glycol, phenoxyethanol, caprylyl 3.5 glycol, sorbic acid, peg8/SMDI copolymer (ratio of these products: 1.5:.05:0.25:0.25:0.25) Ill Aqueous superoxide dismutase liposomes 8 Method Sequence No. 2 In a second mixture, glyceryl stearate, stearic acid, cetearyl alcohol, ceteareth 20, isopropyl palmitate complex (all from source: Hallstar Corp.) were heated to 75 degrees Celsius in a 200 kg. stainless steel vat. The mixture was mixed by continuous stirring for approximately 60 minutes.
Separately, ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, ferulic acid, and niacinamide (all from source: Arch Personal Care) were dissolved into the second half of the polarized water (as described above) over a period of approximately one hour. Thereafter, Glycine sofa, Rumex crispis, Vitis vinifera, and hinokitiol (beta thujaplicin) (all from source: Active Organics); and aqueous extracts of Camellia sinensis, Centella asiatica, Chamomile matricaria, Echinacea augustifolia, and Ginko biloba (all from source: Active Organics) were added to the ascorbyl polypeptide-tocotrienol mixture.
Method Sequence No. 3 Butylene glycol, phenoxyethanol, eapryly1 glycol, sorbic acid and peg8/SMDI
copolymer (all from source: International Specialty Products) were combined to form a complex.
Thereafter, the complex was added to the glyceryl stearate mixture described above, while the glyceryl stearate mixture was maintained at approximately 75 degrees Celsius.
Thereafter, the ascorbyl polypeptide-tocotrienol mixture described above was added and agitation of the mixture continued at approximately 75 degrees Celsius. The entire mixture was then cooled to approximately 30 degrees Celsius. Thereafter, the mixture developed above in Method Sequence No. 1 was added. Thereafter, the mixture was allowed to cool to approximately 20 degrees Celsius and liposomal superoxide dismutase (source: Arch Personal Care) was added. The mixture developed in Example 2 is a homogenous mixture.
In a modification to the above, the seaweed complex can be present as 4% of the formulation instead of 10% as described in Table 2. Further, the beta glucan and fucoidan complex can be present as 16% of the formulation instead of 10% as described in Table 2.

Testing efficacy of Example 2 To test the efficacy of the mixture described in Example 2, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that the mixture described in Example 2 improved the appearance of the skin of human subjects.
Serving as an example, MJ, a female over the age of 40 years of age, used the formulation defined in Example 2. Prior to using the formulation of Example 2, MJ had exhibited under-eye skin that was puffy, sensitive and quite dry. On day 0, MJ
began using an amount approximately equivalent to the size of a dime and used approximately that amount each morning and night on her skin. After one week, MJ described her under-eye skin as being less puffy. After two weeks, MJ again described her under-eye skin as being less puffy. After one month, MJ described her under-eye skin as bein tighter looking and having fewer small wrinldes such that the skin appeared to be smoother in appearance. MJ identified at least the following attributes as being associated with the formulation defined in Example 2: decreased skin wrinldes; improvement in skin tone;
increased skin firmness; and increased skin hydration.
It was determined that the formulation/mixture of Example 2 was absorbed by human skin.
Example 3. Composition with acidified fucoidan, beta glucan and retinol In accordance with a further embodiment of the present invention, a composition is described having the components shown in Table 3. The methodology employed in producing the composition using the amounts described in Table 3 is generally as follows.
Method Sequence No. 1 In a first mixture, neutralized glycolic and salicylic acid solution (source:
Dupont or Spectrum Chemical) was heated in a stainless steel container to approximately 85 degrees Celsius. The seaweed complex consisting of Table 3. Components of an embodiment of the invention Sequence No. Component Amount (%
by weight) Glycolic and salicylic acids (ratio: 8:1) (neutralized 10 with ammonium hydroxide; ammonium glycolate, and sodium lactate can also be added to obtain a preferable pH of ¨4) Seaweed complex containing Eckionia cava, 5.5 Alteromonas maclodeii and Astaxanthin [ratio:
7:1.5:1.5]
Distilled water 14.8 Tourmaline (0.15%) and volcanic obsidian (0.5%) 0.2 Beta glucan (yeast and specified medicinal fungi 8 extract combined in a 1:1 ratio) in a 1:1 ratio with fucoidan complex Aqueous Aloe barbedensis leaf extract 10 Hydrolyzed pearl nacre (1.5%) and chitosan (1.0%) 2.5 Phospholipids 10 Glyceryl stearate, stearic acid, cetearyl alcohol, 20 ceteareth 20, isopropyl palmitate (each of these products is added at an equal amount) Tocotrienol, tocopheryl acetate, niacinamide, retinol 6 complex (ratio of these products: 3:1.5:1.5:0.5) Aqueous extract of Vitis vinifera, Chamomile 2.5 matricaria, Echinacea augustifolia, Panax ginseng, Glycine sofa, allantoin (each of these products is added at an equal amount) Ill Complex of butylene glycol, phenoxyethanol, 2.5 caprylyl glycol, sorbic acid, peg8/SMDI copolymer (ratio of these products: 1.5:0.5:0.25:0.25:0.25) Ill Aqueous superoxide dismutase liposomes 8 EckIonia cava, Alteromonas maclodeii, and Astaxanthin (source: Unipex Innovations) was added to the heated glycolic acid mixture. The combined mixture was mixed for approximately 45 to 60 minutes.
Polarized water was developed by adding tourmaline and obsidian (source:
Soliance) to the distilled water. The beta glucan and fucoidan complex (source: Active Concepts, Marinova) was dissolved in one-third of the polarized water. The dissolved beta glucan - fucoidan complex was added to the glycolic acid mixture (previously described above) and the entire solution continued to be stirred while the temperature was maintained at approximately 85 degrees Celsius for approximately 30 minutes.
While maintaining mixing of the mixture, aqueous Aloe barbedensis leaf extract (source: Tri K
Industries) was added and the entire mixture was allowed to cool for 30 minutes.
Thereafter, hydrolyzed pearl nacre (source: Rita Corp.) and chitosan (source:
Alfa Chem) were added to the cooled mixture. The entire mixture was allowed to cool to approximately 30 degrees Celsius. Thereafter, phospholipids (source: Arch Personal Care) were added to the cooled mixture.
Method Sequence No. 2 In a further mixture, glyceryl stearate, stearic acid, cetearyl alcohol, ceteareth 20, and isopropyl palmitate complex (source: Hallstar Corp.) were heated to 75 degrees Celsius in a 200 kg. stainless steel vat. The mixture was mixed by continuous stirring for 60 minutes.
Separately, the remaining two-thirds of polarized water (as described above) was used to dissolve the tocotrienol - retinol complex (source: Arch Personal Care). The tocotrienol - retinol complex was allowed to dissolve in the polarized water for one hour.
Thereafter, aqueous extracts of Vitis vinifera, Chamomile matricaria, Echinacea augustifolia, Panax ginseng, Glycine sofa, and allantoin (source: Active Organics) were added to the tocotrienol - retinol complex.
Method Sequence No. 3 In a further mixture, butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and peg8/SMDI copolymer were combined to make a complex (source: International Specialty Products). Thereafter, this complex was added to the glyceryl stearate complex mixture described above, the glyceryl stearate complex having been maintained at 75 degrees Celsius. Thereafter, the aseorbyl polypeptide-tocotrienol complex, which had previously been mixed with the aqueous extracts described above, was added and agitation of the mixture continued at approximately 75 degrees Celsius. Thereafter, the entire mixture was cooled down to approximately 30 degrees Celsius.
Thereafter, the mixture developed from Method Sequence No. 1 was added to the mixture. The mixture was allowed to cool down to approximately 20 degrees Celsius and liposomal superoxide dismutase (source: Arch Personal Care) was added. The mixture developed in Example 3 is a homogenous mixture.
In a modification to the above, the seaweed complex can be present as 3.5% of the formulation instead of 5.5% as described in Table 3. Further, the beta glucan and fucoidan complex can be present as 10% of the formulation instead of 8% as described in Table 3.
Testing efficacy of Example 3 To test the efficacy of the mixture described in Example 3, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that the mixture described in Example 3 improved the appearance of the skin of human subjects.
Serving as an example, CO, a female between the age of 30-40 years of age, used the formulation defined in Example 3. Prior to using the formulation of Example 3, CO
had exhibited oily skin that was prone to acne breakouts. Further, CO
described that her skin was rough, and that skin pores were visible. Further, CO described that her skin showed an appearance of acne scarring. On day 0, CO began using an amount approximately equivalent to the size of a dime and used approximately that amount each night on her skin. After one week, CO described her skin as having faded acne scarring.
After two weeks, CO described that her skin appeared to be more radiant and glowing in appearance. After one month, CO described her skin as being firmer and that the acne breakouts had stopped. CO identified at least the following attributes as being associated with the formulation defined in Example 3: decreased skin wrinkles;
improvement in skin tone; increased skin firmness; and increased skin hydration.
It was determined that the formulation/mixture of Example 3 was absorbed by human skin.

Example 4. Composition with acidified fucoidan and beta glucan In accordance with a further embodiment of the present invention, a composition is described having the components shown in Table 4.
Table 4. Components of an embodiment of the invention Sequence No. Component Amount Pk by weiaht) Aqueous Aloe barbedensis leaf extract 45 Distilled water 40.8 Tourmaline, volcanic obsidian 0.2 Glycolic and salicylic acids (ratio 8:1) (neutralized 6 with ammonium hydroxide; ammonium glycolate, and sodium lactate can also be added to obtain a preferable pH of -4) Fucoidan, beta glucan, Ulva lactuta (ratio: 5:5:1.5) 4 II Aqueous extract of Came/ha sinensis, Centella 1.5 asiatica, Chamomile matricaria, Echinacea augustifolia, Ginko biloba (these extracts are present in equal amounts) Ill Complex of butylene glycol, allantoin, 2.5 phenoxyethanol, caprylyl glycol, sorbic acid (ratio:
1.5:0.5:0.25:0.25:0.25) The methodology employed in producing the composition using the amounts described in Table 4 is generally as follows.
Tourmaline and volcanic obsidian (source: Soliance) were dissolved into distilled water. Ulva lactuta, fucoidan (source: Marinova), beta glucan (source: Arch Personal Care) were added to above polarized water and mixture was heated to approximately 80 degrees Celsius and stirred for approximately 40 minutes.
Neutralized glycolic acid, as disclosed herein, was added to the above mixture, and stirred at approximately 80 degrees Celsius for approximately another 30 minutes.
Thereafter, Aloe barbedensis leaf extract (source: Tri-K) and aqueous extract of Camellia sinensis, Centella asiatica, Chamomile matricaria, Echinacea augustifolia, and Ginko biloba (source: Active Organics) as detailed in the corresponding Table, were added and the entire mixture was stirred for approximately another 10 minutes.
At this stage any of a variety of surfactants can be incorporated to constitute an effective cleansing composition focusing on the above key ingredients.
Thereafter, butylene glycol, allantoin, phenoxyethanol, caprylyl glycol, sorbic acid (source: International Specialty Products) were added and the entire mixture was stirred for approximately another 10 minutes. The entire mixture was then cooled to room temperature. The mixture developed in Example 4 is a homogenous mixture.
Testing efficacy of Example 4 To test the efficacy of the mixture described in Example 4, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that the mixture described in Example 4 improved the appearance of the skin of human subjects.
Serving as an example, MT, a male under the age of 30 used the formulation defined in Example 4. Prior to using the formulation of Example 4, MT had exhibited slightly acned skin that included a small amount of wrinkling. On day 0, MT
began applying the formulation defined in Example 4 to his skin using a cotton pad soaked in the formulation defined in Example 4. After one week, MT described his skin as appearing clearer with a less dull appearance. After two weeks, MT described his skin as having less breakouts of acne. After one month, MT described his skin as appearing brighter, clearer, and tighter. MT identified at least the following attributes as being associated with the formulation defined in Example 4: increased skin firmness; improved skin tone, and smoother and brighter skin appearance.
It was determined that the formulation/mixture of Example 4 was absorbed by human skin.
Example 5. Composition with acklUied fucoidan In accordance with a further embodiment of the present invention, a composition is described having the components shown in Table 5.

Table 5. Components of an embodiment of the invention Sequence No. Component Amount (70 by weight) Glycolic and salicylic acids (ratio 8:1) (neutralized 12.8 with ammonium hydroxide; ammonium glycolate, and sodium lactate can also be added to obtain a preferable pH of -4) Tourmaline (0.15%) and volcanic obsidian (0.5%) 0.2 Kaolin and bentonite (ratio of these products: 26 0.6:0.3) Beta glucan (yeast and specified medicinal fungi 10 extract combined in a 1:1 ratio) in a 1:1 ratio with fucoidan complex, Ulva lactuta [5:5:1.5]
Undaria pinnatifida 4 Diatomite silica, n-acetyl glucosamine, hydrolyzed 2.5 pearl nacre, and chitosan (ratio of these products:
1:1:0.25:0.25) Aqueous Aloe barbedensis leaf extract 10 Echinacea augustifolia and Panax ginseng (ratio of 2 these products: 1:1) Stearic acid, cetearyl alcohol, and ceteareth 20 30 complex in equal parts (each of these products is added at an equal amount) III Complex of phenoxyethanol, caprylyl glycol, sorbic 2.5 acid (ratio of these products: 1.5:0.5:0.5) The methodology employed in producing the composition using the amounts described in Table 5 is generally as follows.
Method Sequence No. /
In a first mixture, neutralized glycolic acid (source: Dupont or Spectrum Chemical), salicylic acid (source: Spectrum), tourmaline and volcanic obsidian (source:
SoHance) was heated in a stainless steel container to approximately 85 degrees Celsius.
The seaweed complex consisting of ulva lactuta (source: Unipex Innovations), beta glucan fucoidan complex (source: Biothera, Marinova), and Undaria pinnatifida (source:
Marinova) were added to the heated glycolic acid mixture. The combined mixture was agitated for approximately 30 minutes. Diatomite silica, n-acetyl glucosamine, hydrolyzed pearl nacre (source: Rita Corp.), and chitosan (source: Alfa Chem) were added to the above mixture.
Kaolin and bentonite (source: Xenex Labs; Vancouver, British Columbia] were separately mixed and added to the above mixture. While maintaining mixing of the mixture, aqueous Aloe barbedensis leaf extract (source: Tri K Industries), Echinacea augustifolia, and Panax ginseng (source: Active Organics) were added.
Method Sequence No. 2 Thereafter, and separately, stearic acid, cetearyl alcohol, and ceteareth 20 complex (source: Hallstar Corp.) were heated to approximately 75 degrees C, stirring for approximately 60 minutes.
Method Sequence No. 3 In a further mixture, phenoxyethanol, caprylyl glycol, and sorbic acid (source:
International Specialty Products) were combined to make a complex. Thereafter, this complex was added to the stearic acid complex described above, the stearic complex having been maintained at approximately 75 degrees Celsius. Thereafter, the entire mixture was cooled down to approximately 30 degrees Celsius. Thereafter, the mixture developed from Method Sequence No. 1 (see above) was added to the mixture. The mixture was allowed to cool to approximately 20 degrees Celsius. The mixture developed in Example 5 is a homogenous mixture.

In a modification to the above, the beta glucan complex can be present as 12%
of the formulation instead of 10% as described in Table 5. Further, the Undaria pinnatifida can be present at 2% instead of 4% as described in Table 5.
Testing efficacy of Example 5 To test the efficacy of the mixture described in Example 5, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that the mixture described in Example 5 improved the appearance of the skin of human subjects.
Serving as an example, JT, a female between the age of 30-40, used the formulation defined in Example 5. Prior to using the fotinulation of Example 5, JT had exhibited skin conditions that included acne and rough spots. On day 0, JT
began using an amount approximately equivalent to the size of a quarter and used approximately twice that amount twice a week. After one week, JT described her skin as having fewer breakouts of acne. After two weeks, JT described her skin as being clearer.
After one month, JT described her skin as appearing smoother. JT identified at least the following attributes as being associated with the formulation defined in Example 5:
increased smoothness of the skin, increased luminosity of the skin, increased firmness of the skin, increased tautness of the skin, and less irritation and skin-associated inflammation.
It was determined that the formulation/mixture of Example 5 was absorbed by human skin.
Example 6. Serum composition The methodology employed in producing the non-acidified serum composition using the amounts described in Table 6 is generally as follows.
Method Sequence No. 1 Polarized water was developed by adding tourmaline and obsidian (source:
Soliance) to the distilled water. The seaweed complex consisting of phytoplankton extract (source: Canadian Pacific Phytoplankton), Fucus vesiculosus extract (source:
Xenex), ecklonia cava (source: JP Renew; San Francisco, California) was dissolved into one-half of the distilled water, heated to approximately 85 degrees Celsius.
The combined mixture was then stirred for approximately 45 minutes to 60 minutes. The beta glucan and fucoidan complex (source: Biothera, Marinova) and vegetal astaxanthin (source:
Unipex Innovations) was dissolved in the seaweed complex-distilled water mixture (previously described above). The heated mixture continued to Table 6. Components of an embodiment of the invention SEQUENCE INGREDIENT AMOUNT
Distilled water 40.8 Tourmaline, volcanic obsidian [1 0.2 1 Phytoplankton extract, Fucus vesiculosus extract, 6 EckIonia cava complex [1:1:.5:.5]
Beta glucan (yeast and specified medicinal fungi 8 extract combined in a 1:1 ratio), fucoidan, vegetal astaxanthin complex [5:5:1.5]
Hydrolyzed pearl nacre, chitosan [1:.5] 1.5 1 Phospholipids, sodium pCA [1:.5] 8 II Magnesium ascorbyl phosphate, tocotrienol, 25 niacinamide, tocopheryl acetate, ergocalciferol complex [10:1:.5:.5:.5]
II CameNa sinensis, epigallocatechin (EGCG), ellagic 4 acid, 1-arginine [2:1:.5:.5]
Ill Complex of butylene glycol, phenoxyethanol, caprylyl 3.5 glycol, sorbic acid, peg8/SMDI copolymer [2:1 : .5: .5: .5]
Ill Sodium citrate, tetrasodium EDTA [1:.5] 3 be stirred while the temperature was maintained at approximately 85 degrees Celsius for a minimum of approximately 30 minutes. The entire mixture was allowed to cool to approximately 30 degrees Celsius. Thereafter, hydrolyzed pearl nacre (source:
Active Concepts) and chitosan (source: Alfa Chem) were added to the cooled mixture.
Thereafter, phospholipids (source: Arch Personal Care) and sodium hyaluronate (source: Tri-K
Industries) were added to the cooled mixture.

Method Sequence No. 2:
In a further mixture, a complex comprising magnesium ascorbyl phosphate (source: Optima Specialty; Huntington, Connecticut) with tocotrienol, niacinamide, tocopheryl acetate, ergocalciferol (source: Arch Personal Care) was mixed into the remaining one-half of polarized water and heated to approximately 70 degrees Celsius.
This mixture was allowed to dissolve in the polarized water for one hour.
Thereafter, Camellia sinensis (source: Active Organics), epigallocatechin (EGCG) (source:
DSM
Nutritional Products; Belvedere, New Jersey), ellagic acid (source: DSM), and 1-arginine (source: Alpha Chem) were added to the ascorbyl polypeptide ¨ tocotrienol complex.
Method Sequence No. 3 In a further mixture, butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and peg8/SMDI copolymer (source: International Specialty Products) are combined in the ratio specified in the Table 6 above to make a complex. Thereafter, this complex was added to the magnesium ascorbyl ¨ tocotrienol mixture described above in Method Sequence No. 2, the magnesium ascorbyl ¨ tocotrienol having been maintained at approximately 70 degrees Celsius. Thereafter sodium citrate and tetrasodium EDTA (source: Xenex) was added.
The mixture was then stirred for approximately 15 minutes, while maintaining at approximately 70 degrees Celsius. Thereafter, the entire mixture was cooled down to approximately 30 degrees Celsius. Thereafter, the mixture developed from Method Sequence No. 1 was added to the mixture. The mixture was allowed to cool down to approximately 20 degrees Celsius. The mixture developed in Example 6 is a homogenous mixture.
In a modification to the above, the phytoplankton extract can be present as 2%
of the formulation instead of 6% as described in Table 6. Further, the bet glucan complex can be present at 12% instead of 8% as described in Table 6.
Testing efficacy of Example 6 To test the efficacy of the mixture described in Example 6, the mixture was used by human subjects to determine the effect on the appearance of their skin. The results routinely showed that the mixture described in Example 6 improved the appearance of the skin of human subjects.

Serving as an example, TK, a female over the age of 40 used the formulation defined in Example 6. Prior to using the formulation of Example 6, TK had exhibited sensitive skin conditions and her skin was sun-damaged. On day 0, TK began using an amount equivalent to the size of a dime of the formulation in Example 6 on a daily basis.
After one week, TK described her skin as appearing more refreshed. After two weeks, TK
described her skin as appearing less irritated or red as compared with before use of the formulation. After one month, TK described her skin as appearing clearer, and more firm with less wrinkle lines. TK identified at least the following attributes as being associated with the formulation defined in Example 6: increased smoothness (diminished appearance of wrinldes); increased luminosity; increased firmness; increased tautness;
and less irritation and skin-associated inflammation.
It was determined that the formulation/mixture of Example 6 was absorbed by human skin.
While specific embodiments of the invention have been described and illustrated, such embodiments should be considered illustrative of the invention only and not as limiting the invention as construed in accordance with the accompanying claims.

Claims

What is claimed is:

1. A cosmetic composition for applying to skin, the composition comprising:
from about 1.5 wt.% to about 5.5 wt.% of a seaweed complex consisting essentially of Ulva lactuca, Alteromonas macleodii and Astaxanthin in a ratio of about 7:1.5:1.5 by weight;
0.15 wt.% tourmaline;
0.05 wt.% volcanic obsidian;
from about 8 wt.% to about 12 wt.% of a 1:1 B-glucan:fucoidan ratio by weight mixture, said B-glucan consisting of a 1:1 ratio by weight of yeast B- glucan and fungi B - glucan;
wt.% of aqueous Aloe barbadensis leaf extract;
1.5 wt.% hydrolyzed pearl nacre;
1.0 wt.% chitosan;
10 wt.% phospholipids;
3 wt.% glyceryl stearate;
3 wt.% stearic acid;
3 wt.% cetearyl alcohol;
3 wt.% ceteareth 20;
3 wt.% isopropyl palmitate;
6 wt.% of a 3:1:1:1:1 ratio by weight mixture of ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, and niacinamide;
1.5 wt.% of a 1:1:1:1:1 ratio by weight mixture of an aqueous extract of Camellia sinensis, Centella asiatica, Matricaria chamomilla, Echinacea angustifolia, and Ginkgo biloba;
2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer;
8 wt.% of aqueous superoxide dismutase liposomes;
20.8 wt.% purified water; and 10 wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with Date Recue/Date Received 2021-09-02 ammonium hydroxide, ammonium glycolate or sodium lactate.

2. The composition of Claim 1, further comprising a sunscreen.

3. The composition of Claim 1 or 2, further comprising a silicone surfactant.

4. The composition of any one of Claims 1-3, further comprising a preservative.

5. The composition of any one of Claims 1-4, further comprising a botanical antioxidant.

6. The composition of any one of Claims 1-5, further comprising an amino acid.

7. The composition of any one of Claims 1-6, further comprising a percutaneous penetration enhancer.

8. A cosmetic composition for applying to skin, the composition comprising:
from about 3.5 wt.% to about 5.5 wt.% of a seaweed complex consisting essentially of Ecklonia cava, Alteromonas macleodii and Astaxanthin in a ratio of about 7:1.5:1.5 by weight;
0.15 wt.% tourmaline;
0.05 wt.% volcanic obsidian;
from about 8 wt.% to about 10 wt.% of a 1:1 B- glucan:fucoidan ratio by weight mixture, said B - glucan consisting of a 1:1 ratio by weight of yeast B -glucan and fungi B- glucan;
wt.% of aqueous Aloe barbadensis leaf extract;
1.5 wt.% hydrolyzed pearl nacre;
1.0 wt.% chitosan;
10 wt.% phospholipids;
4 wt.% glyceryl stearate;
Date Recue/Date Received 2021-09-02 4 wt.% stearic acid;
4 wt.% cetearyl alcohol; 4 wt.% ceteareth 20;
4 wt.% isopropyl palmitate;
6 wt.% of a 3:1.5:1.5:0.5 ratio by weight mixture of tocotrienol, tocopheryl acetate, niacinamide, and retinal;
2.5 wt.% of a 1:1:1:1:1:1 ratio by weight mixture of the aqueous extracts of Vitis vinifera, Matricaria chamomilla, Echinacea angustifoha, Panax ginseng, Glycine soja, and allantoin;
2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer;
8 wt. % of aqueous superoxide dismutase liposomes;
14.8 wt.% purified water; and wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with ammonium hydroxide, ammonium glycolate or sodium lactate.

9. The composition of Claim 8, further comprising a sunscreen.

10. The composition of Claim 8 or 9, further comprising a silicone surfactant.

11. The composition of any one of Claims 8-10, further comprising a preservative.

12. The composition of any one of Claims 8-11, further comprising a botanical antioxidant.

13. The composition of any one of Claims 8-12, further comprising an amino acid.

14. The composition of any one of Claims 8-13, further comprising a percutaneous penetration enhancer.

15. A cosmetic composition for applying to skin, the composition comprising:
Date Recue/Date Received 2021-09-02 5.5 wt.% of a seaweed complex consisting essentially of Undaria pinnatifida and Astaxanthin in a ratio of about 7:5 by weight;
0.15 wt.% tourmaline;
0.05 wt.% volcanic obsidian;
8 wt.% of a 1:1 B - glucan:fucoidan ratio by weight mixture, said B - glucan consisting of a 1:1 ratio by weight of yeast B - glucan and fungi B - glucan;
wt.% of aqueous Aloe barbadensis leaf extract;
1.5 wt.% hydrolyzed pearl nacre;
1.0 wt.% chitosan;
10 wt.% phospholipids;
4 wt.% glyceryl stearate;
4 wt.% stearic acid;
4 wt.% cetearyl alcohol;
4 wt.% ceteareth 20;
4 wt.% isopropyl palmitate;
6 wt.% of a 3: 1.5:1.5:0 .5 ratio by weight mixture of tocotrienol, tocopheryl acetate, niacinamide, and crithmum maritimum;
2.5 wt.% of a 1:1:1:1:1:1 ratio by weight mixture of an aqueous extract of Vitis viniftra, Matricaria chamomilla, Echinacea angustifolia, Panax ginseng, Glycine soja, and allantoin;
2.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer;
8 wt.% of aqueous superoxide dismutase liposomes;
14.8 wt.% purified water; and 10 wt.% of an aqueous glycolic acid-salicylic acid solution neutralized with ammonium hydroxide, ammonium glycolate or sodium lactate.

16. The composition of Claim 15, further comprising a sunscreen.

17. The composition of Claim 15 or 16, further comprising a silicone surfactant.
Date Recue/Date Received 2021-09-02

18. The composition of any one of Claims 15-17, further comprising a preservative.

19. The composition of any one of Claims 15-18, further comprising a botanical antioxidant.

20. The composition of any one of Claims 15-19, further comprising an amino acid.

21. The composition of any one of Claims 15-20, further comprising a percutaneous penetration enhancer.

22. A cosmetic composition for applying to skin, the composition comprising:
from 4 wt.% to 10 wt.% of a seaweed complex consisting essentially of Ulva lactuca, Alteromonas macleodii and Astaxanthin in a ratio of about 7:1.5:1.5 by weight;
0.15 wt.% tourmaline;
0.05 wt.% volcanic obsidian;
from 10 wt.% to 16 wt.% of a 1:1 B- glucan:fucoidan ratio by weight mixture, said B - glucan consisting of a I I ratio by weight of yeast B - glucan and fungi B -glucan;
12 wt.% of aqueous Aloe barbadensis leaf extract;
0.9 wt.% hydrolyzed pearl nacre;
0.6 wt.% chitosan;
3.5 wt.% of a 1.5:1.5:0.5 ratio by weight mixture of N-acetyl camitine, a-lipoic acid, and L-arginine;
6.4 wt.%phospholipids;
1.6 wt.% sodium hyaluronate;
3 wt.% glyceryl stearate;
3 wt.% stearic acid;
3 wt.% cetearyl alcohol;
Date Recue/Date Received 2021-09-02 3 wt.% ceteareth 20;
3 wt.% isopropyl palmitate;
wt.% of a 3:1:0.5:0.5:0.5:0.5 ratio by weight mixture of ascorbyl polypeptide, tocotrienol, tocopheryl acetate, ergocalciferol, ferulic acid, and niacinamide;
2 wt.% of a 1:1:1:1 ratio by weight mixture of Glycine soja, Rumex crispis, Vitis vinifera, and hinokitiol;
2.5 wt.% of a 1:1:1:1:1 ratio by weight mixture of the aqueous extracts of Camellia sinensis, Centella asiatica, Matricaria chamomilla, Echinacea angustifblia, and Ginkgo biloba;
3.5 wt.% of a 1.5:0.5:0.25:0.25:0.25 ratio by weight mixture of butylene glycol, phenoxyethanol, caprylyl glycol, sorbic acid, and PEG8/SMDI copolymer;
8 wt.% of aqueous superoxide dismutase liposomes; and 18.8 wt.% purified water.
Date Recue/Date Received 2021-09-02