WO2017173241A1 - Sanitizer composition with probiotic/prebiotic active ingredient - Google Patents

Sanitizer composition with probiotic/prebiotic active ingredient Download PDF

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Publication number
WO2017173241A1
WO2017173241A1 PCT/US2017/025324 US2017025324W WO2017173241A1 WO 2017173241 A1 WO2017173241 A1 WO 2017173241A1 US 2017025324 W US2017025324 W US 2017025324W WO 2017173241 A1 WO2017173241 A1 WO 2017173241A1
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WO
WIPO (PCT)
Prior art keywords
composition
topical
probiotic
active ingredient
skin
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PCT/US2017/025324
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English (en)
French (fr)
Inventor
Sarah GANTZ
Amanda Copeland
Carrie Anne Zapka
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Go-Jo Industries Inc
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Go-Jo Industries Inc
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Application filed by Go-Jo Industries Inc filed Critical Go-Jo Industries Inc
Priority to AU2017240069A priority Critical patent/AU2017240069B2/en
Priority to EP17716757.4A priority patent/EP3436041B1/en
Priority to CA3018866A priority patent/CA3018866C/en
Priority to JP2018550566A priority patent/JP2019510036A/ja
Publication of WO2017173241A1 publication Critical patent/WO2017173241A1/en
Anticipated expiration legal-status Critical
Priority to JP2022119617A priority patent/JP7512329B2/ja
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A61K35/741—Probiotics
    • A61K35/742—Spore-forming bacteria, e.g. Bacillus coagulans, Bacillus subtilis, clostridium or Lactobacillus sporogenes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/02—Local antiseptics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents

Definitions

  • the skin is the human body's largest organ, colonized by a diverse range of microorganisms, the majority of which are harmless or even beneficial to their host. These microorganisms often provide vital functions that the human genome has not yet evolved to perform. In this way, the skin constantly regulates a balance between host-human and microorganism. Disruptions in this delicate balance, on either side, can result in serious skin disorders or infections.
  • Pathogens on the skin are known to cause illness and may be easily transmitted from one person to another. Some pathogens stick strongly to skin. Typically, when pathogens stick to skin, they are more difficult to remove or kill using traditional approaches to skin cleaning and disinfection such as washing with soap or using a waterless sanitizer. Pathogens that are stuck to skin are more dangerous because they remain on the skin longer. The longer the pathogen is on the skin, the more the chance that they will either cause infections on the person with them or be shared with other people.
  • Probiotics are being used to control microbes on skin in new ways that do not require the use of antimicrobials.
  • Probiotics are live or inactivated microorganisms that, when either present as part of the normal microbiota or when administered in adequate amounts, confer a health or cosmetic benefit on the host. Benefits from probiotics can be from the microbial components directly or can come from the byproducts of bacterial growth.
  • a topical composition for restoring skin's natural balance of bacteria includes about 0.02 wt. % to 10.0 wt. % of an active ingredient that is one or more of a probiotic, a probiotic derivative, and a prebiotic.
  • the topical composition also includes at least 40.0 wt. % of one or more Ci -6 alcohols, with the balance of the composition comprising water.
  • the application of the topical composition reduces pathogen binding on the surface by an amount that is statistically significant compared to an otherwise identical topical composition without the active ingredient.
  • the active ingredient is a probiotic or probiotic derived ingredient, which can be selected from a strain of one or more the following families: Actinomycetaceae, Corynebacteriaceae, Nocardiaceae, Intrasporangiaceae, Micrococcaceae, Propionibacteriacea, Bacteroidaceae, Porphyromonadaceae, Flavobacteriaceae, Sphingobacteriaceae, Bacillaceae, Exiguobacteraceae, Gemellaceae, Planococcaceae, Staphlococcaceae, Carnobacteriaceae, Aeorcoccaceae, Lactobacillaceae, Acidaminacoccaceae, Clostridiaceae, Lachnospiraceae, Peptostreptococcaceae, Veillonellaceae, Caulobactereaceae, Acetobacteraceae, Rhodobacteriaceae, Bradyrh
  • the active ingredient is a probiotic or probiotic derived ingredient, which can be selected from a strain of one or more the following: Lactobacillus, strains and derivatives of Clostridia, strains and derivatives of Bifidobacterium, strains and derivatives of Saccharomyces, strains and derivatives of Lactococcus, strains and derivatives of Pedicoccus, strains and derivatives of Enter ococcus, strains and derivatives of Escherichia, strains and derivatives of Alcaligenes, strains and derivatives of Corynebacterium, strains and derivatives of Bacillus, and strains and derivatives of Propionibacterium .
  • a probiotic or probiotic derived ingredient which can be selected from a strain of one or more the following: Lactobacillus, strains and derivatives of Clostridia, strains and derivatives of Bifidobacterium, strains and derivatives of Saccharomyces, strains and derivatives of Lactococcus,
  • the topical composition also contains up to about 20.0 wt. % of a humectant selected from the group consisting of propylene glycol, hexylene glycol, 1,4-dihydroxyhexane, 1,2,6-hexanetriol, sorbitol, butyl ene glycol, caprylyl glycol, propanediols, such as methyl propane diol, dipropylene glycol, triethylene glycol, glycerin (glycerol), polyethylene glycols, ethoxydiglycol, polyethylene sorbitol, and combinations thereof.
  • a humectant selected from the group consisting of propylene glycol, hexylene glycol, 1,4-dihydroxyhexane, 1,2,6-hexanetriol, sorbitol, butyl ene glycol, caprylyl glycol, propanediols, such as methyl propane diol, dipropylene glycol, triethylene glycol
  • the topical composition also contains up to 10.0 wt. % of a moisturizing ester, selected from the group consisting of selected from the group consisting of cetyl myristate, cetyl myristoleate, and other cetyl esters, diisopropyl sebacate, isopropyl myristate, and combinations thereof.
  • a moisturizing ester selected from the group consisting of selected from the group consisting of cetyl myristate, cetyl myristoleate, and other cetyl esters, diisopropyl sebacate, isopropyl myristate, and combinations thereof.
  • a skin treatment method for reducing pathogen binding on skin, nails, or any other epithelial cell includes applying a topical composition to a skin surface, wherein the topical composition includes about 0.02 wt. % to about 10.0 wt. % of an active ingredient.
  • the active ingredient may be one or more of a probiotic, a probiotic derivative, or a prebiotic.
  • the topical composition also includes at least 40.0 wt. % of one or more Ci -6 alcohols, with the balance of the composition comprising water.
  • the application of the topical composition reduces pathogen binding on skin, nails, or other epithelial cell by a statistically significant amount, as compared to an otherwise identical composition without the active ingredient.
  • a skin treatment composition comprises about 0.02 wt. % to 10.0 wt. % of an active ingredient comprising one or more of a probiotic, a probiotic derivative, and a prebiotic, about 40.0 wt. % to about 95 wt. % of one or more Ci -6 alcohols, about 0.01 wt. % to about 10.0 wt. % of an emollient, and about 0.01 wt. % to about 5.0 wt. % of a viscosity modifier, with the balance up to 100 wt. % being water.
  • a topical composition for restoring skin's natural balance of bacteria is provided.
  • “Restoring skin's natural balance” means helping to change the ratio of transient pathogens to resident microbes (i.e., restores the "good” bacteria and reduces the amount of transient pathogens)
  • the topical composition comprises about 0.02 wt. % to 10.0 wt. % of an active ingredient comprising one or more of a probiotic, a probiotic derivative, or prebiotic, about 40.0 wt. % to about 95.0 wt. % of one or more Ci -6 alcohols, about 0.01 wt. % to about 5.0 wt. % of a foaming agent, and about 0.01 wt. % to about 10.0 wt. % of a humectant, with the balance up to 100 wt.% being water.
  • Figure 1 graphically illustrates the relative Interleukin 8 expression in topical compositions containing 1.0 wt. % BonicelTM compared to a control.
  • Figure 2 graphically illustrates the Involiucrin expression in compositions containing 1.0 wt. % BonicelTM compared to a control.
  • Figure 3 graphically illustrates the DSC3 expression in compositions containing 0.1 wt. % BonicelTM compared to a control.
  • Figure 4 graphically illustrates the HBD-2 expression in compositions containing 0.1 wt. % BonicelTM and 1.0 wt. % BonicelTM compared to a control.
  • Figure 5 graphically illustrates the HBD-2 expression in compositions containing 0.1 wt. % BonicelTM and 1.0 wt. % BonicelTM that have been in contact with ethanol compared to a control.
  • Figure 6 graphically illustrates the response of Staphylococcus aureus adhesion and invasion potential when treated with a probiotic Bacillus ferment.
  • Figure 7 graphically illustrates the affinity of a 1.0% BonicelTM sanitizer to kill more transient bacteria than resident bacteria.
  • microorganism refers to a tiny organism, such as a virus, protozoan, fungus, or bacterium that can only be seen under a microscope.
  • the collection of microorganisms that live in an environment makes up a microbiota.
  • human skin microbiota is all of the microbes on skin or a hospital microbiota would include all of the microbes in a hospital building.
  • microbiome is used when referring to the entire habitat, including the microbiota as well as their genomes and the surrounding environment of the microbiota.
  • topical composition means a composition suitable for application directly to a surface, such as the surface of a human or animal body, including skin, and/or other surfaces, such as hair and nails.
  • test composition vs. a control that does not contain the active ingredient.
  • the analysis is completed using 1) a T-test (a statistical examination of two population means) when only comparing one test article vs. one control); or 2) an analysis of variance (ANOVA) test when comparing two or more test articles vs. controls.
  • T-test a statistical examination of two population means
  • ANOVA analysis of variance
  • the general inventive concepts relate to a topical composition that contains an active ingredient that includes one or more of a probiotic, a probiotic-derived ingredient, and a prebiotic or prebiotic-derived ingredient.
  • the active ingredient helps to restore skin's natural balance of bacteria.
  • the topical composition disclosed herein prevents pathogens from adhering to a surface, such as human skin or any inanimate surface. Such adherence prevention includes not only impeding the binding of a pathogen, but also promoting detachment of any already bound pathogen, and otherwise limiting the presence of such pathogens on a surface.
  • probiotic and probiotic-derived ingredients include strains and derivates of the following families: Actinomycetaceae, Corynebacteriaceae, Nocardiaceae, Intrasporangiaceae, Micrococcaceae, Propionib acted acea, Bacteroidaceae, Porphyromonadaceae, Flavobacteriaceae, Sphingobacteriaceae, Bacillaceae, Exiguobacteraceae, Gemellaceae, Planococcaceae, Staphlococcaceae, Carnobacteriaceae, Aeorcoccaceae, Lactobacillaceae, Acidaminacoccaceae, Clostridiaceae, Lachnospiraceae, Peptostreptococcaceae, Veillonellaceae, Caulobactereaceae, Acetobacteraceae, Rhodobacteriaceae, Bradyrhizobiaceae, Brucellaceae, S
  • the active ingredient is a probiotic or probiotic derived ingredient, which can be selected from a strain of one or more the following: Lactobacillus, strains and derivatives of Clostridia, strains and derivatives of Bifidobacterium, strains and derivatives of Saccharomyces, strains and derivatives of Lactococcus, strains and derivatives of Pedicoccus, strains and derivatives of Enterococcus, strains and derivatives of Escherichia, strains and derivatives of Alcahgenes, strains and derivatives of Corynebacterium, strains and derivatives of Bacillus, and strains and derivatives of Propionibacterium.
  • a probiotic or probiotic derived ingredient which can be selected from a strain of one or more the following: Lactobacillus, strains and derivatives of Clostridia, strains and derivatives of Bifidobacterium, strains and derivatives of Saccharomyces, strains and derivatives of Lactococcus, strain
  • the probiotic or probiotic derived ingredient is a ferment of Bacillus coagulans.
  • Bacillus is a genus of Gram-positive, rod-shaped bacteria of the phylum Fimicutes. Bacillus can be either aerobic or, under certain conditions, anaerobic and produces endospores. Bacillus exhibits a wide range of physiologic properties that allows it to thrive in a number of different habitats— most Bacillus strains are resistant to heat, cold, radiation, and disinfectants.
  • a Bacillus ferment (INCI name) is sold under the trade name BonicelTM by Ganeden Biotech, Inc.
  • BonicelTM is produced though a fermentation process which ensures the formulation includes the maximum amounts of enzymes, bateriocins, and L+ Lactic acid.
  • Additional probiotic or probiotic derived ingredients may include Qi601 from Quorum Innovations, Repair Complex CLRTM, EcoSkin® from Solabia Group, Leucidal® Liquid SF from Active Micro Technologies, ProSynergenTM from Lonza, ProBioBalance CLRTM from CLR, Yogurtene® Balance from Lonza, BiodynesTM from Lonza, Bifidobacterium Longum Lysate,
  • prebiotic ingredients include oligosaccharides, alpha and beta-glucan oligosaccharides, galactooligosaccharides, xylooligosaccharide, lactulose, inulin, ginseng, black current extract, sugar-beet extract, aloe extract, almond extract, tea extract, garlic extract, bark extract, chicory extract, corn extract, nerolidol extract, bisabolol extract, farnesol, xylitol, and pectin.
  • Additional prebiotic ingredients may include EmulGoldTM Fibre by Kerry Ingredients, Genu® Explorer Pectin by CP Kelco, Orafti® from Beneo, VitaFiberTM from BioNeutra, Konjac Glucomannan Hydrolysates, and Oat Beta Glucan from VegeTech.
  • the active ingredient also functions to simulate the production of anti-microbial peptides (AMPs) and thereby increase the overall concentration of AMPs on the surface of the skin.
  • AMPs comprise a wide range of natural and synthetic peptides that are made of oligopeptides containing a varying number of amino acids.
  • AMPs may be produced by a host, or by the skin microbiota itself.
  • AMPs are essential components of host defense against infections present in all domains of life.
  • AMPs are produced by all complex organisms and have diverse and intricate antimicrobial activities. As a whole, these peptides demonstrate a broad range of antiviral and antibacterial activities through an array of modes of action.
  • AMPs have been found to kill Gram-negative and Gram-positive bacteria, certain viruses, parasites and fungi. Some research suggests that they can also enhance the internal immunity of complex organisms against a broad range of bacteria and viruses.
  • vertebrates evolved an adaptive immune system based on specific recognition of antigens. Increasing evidence suggests that AMPs released in response to an invasion of microbial can activate adaptive immunity by attracting antigen-presenting dendritic cells to the invasion site.
  • the skin naturally produces AMPs, but the levels each produce are not sufficient to produce the desired effect of long lasting germ defense and innate immunity on the skin.
  • the active ingredient of the subject invention has been found to help increase the concentration of AMPs at levels significantly higher than the skin alone.
  • the active ingredient helps to restore the microbial balance of bacteria on the skin.
  • a human's skin microbiota includes resident skin microorganisms that are continuously present on the skin.
  • the resident skin microorganisms are usually non-pathogenic and either commensals (not harmful to their host) or mutualistic (offer a benefit).
  • Resident skin microorganisms are adapted to survive on skin and they eat, reproduce, and excrete, which has an effect on the skin.
  • certain transient skin microorganisms may attempt to colonize the skin, which could upset a healthy microbiome.
  • Such transient skin microorganisms may include pathogens, such as pathogenic bacteria, yeasts, viruses, and molds.
  • the particular makeup of a human's microbiome may be different than the make-up of another human's.
  • a resident skin microorganism on one person may be a transient on another.
  • the topical composition may comprise up to about 10.0 weight percent (wt. %) of the active ingredient, or up to about 8.0 wt. %, or up to about 5.0 wt. %, or up to about 3.0 wt. %, or up to about 2.0 wt. % of the active ingredient, based upon the total weight of the composition.
  • the topical composition may comprise at least about 0.001 wt. % active ingredient, or at least about 0.005 wt. %, or at least about 0.01 wt. %, or at least about 0.05 wt.%, or at least about 0.1 wt.%, or at least about 0.5 wt. %, or at least about 1.0 wt. % of the active ingredient, based upon the total weight of the topical composition.
  • the topical composition comprises about 0.005 to about 10.0 wt. % of the active ingredient, or from about 0.01 to about 5.0 wt. % of the active ingredient, or from about 0.05 to about 2.0 wt. % of the active ingredient, based upon the total weight of the topical composition. In one exemplary embodiment, the topical composition comprises about 0.08 to about 0.2 wt. % of the active ingredient.
  • the topical composition is used for application to the skin and may be in the form of a skin cleanser, skin sanitizer, skin protectant, a wipe, a salve, foam, and a gel.
  • the topical composition may be applied to the skin before, during, or after skin cleaning. In some exemplary embodiments, the topical composition is applied after skin cleaning.
  • the topical composition is an alcohol based sanitizer, comprising one or more alcohols.
  • Alcohol has antimicrobial properties and has the ability to kill many forms of bacteria, fungi, and viruses.
  • the alcohol is a Ci -6 alcohol, i.e. an alcohol containing 1 to 6 carbon atoms.
  • Such alcohols may be referred to as lower alkanols. Examples of lower alkanols include, but are not limited to, methanol, ethanol, propanol, butanol, pentanol, hexanol, and isomers and mixtures thereof.
  • the alcohol may be either pure alcohol or denatured alcohol.
  • the alcohol comprises ethanol, propanol, or butanol, or isomers or mixtures thereof. In one or more exemplary embodiments, the alcohol comprises isopropanol. In other exemplary embodiments, the alcohol comprises ethanol. In one or more exemplary embodiments, the topical composition comprises a mixture of alcohols. In one or more exemplary embodiments, the topical composition comprises a mixture of ethanol and isopropanol. In one or more exemplary embodiments, the topical composition comprises a mixture of isopropanol and n-propanol. In one exemplary embodiment, the topical composition comprises ethanol.
  • the topical composition may comprise at least about 1.0 wt. % Ci -6 alcohol, based upon the total weight of the composition.
  • the topical composition comprises at least about 2.0 wt. % Ci -6 alcohol, in another embodiment, the topical composition comprises at least about 10.0 wt. % Ci -6 alcohol, in another embodiment, the topical composition comprises at least about 20.0 wt. % Ci -6 alcohol, in another embodiment, the topical composition comprises at least about 40.0 wt. % Ci -6 alcohol, in another embodiment, the topical composition comprises at least about 50.0 wt. % Ci -6 alcohol, in another embodiment, the topical composition comprises at least about 60.0 wt.
  • the topical composition comprises at least about 65.0 wt. % Ci -6 alcohol, in yet another embodiment, the topical composition comprises at least about 70.0 wt. % Ci -6 alcohol, and in still yet another embodiment, the topical composition comprises at least about 80.0 wt. % Ci -6 alcohol, based upon the total weight of composition. In other embodiments, the topical composition comprises from about 70.0 to about 95.0 wt. % Ci -6 alcohol. In one exemplary embodiment, the topical composition comprises from about 71.0 to about 80.0 wt. % Ci -6 alcohol. More or less alcohol may be required in certain instances, depending particularly on other ingredients and/or the amounts thereof employed in the topical composition.
  • the topical composition includes water in an amount quantum sufficit (q.s.).
  • the topical composition comprises at least about 1.0 wt. % water, in another embodiment the topical composition comprises at least about 10.0 wt. % water, in another embodiment, the topical composition comprises at least about 20.0 wt. % water, in another embodiment, the topical composition comprises at least about 30.0 wt. % water, in another embodiment, the topical composition comprises at least about 40.0 wt. % water, in another embodiment, the topical composition comprises at least about 50.0 wt. % water, and in yet another embodiment, the topical composition comprises at least about 60.0 wt.
  • the topical composition comprises at least about 70.0 wt. % water. In other embodiments, the topical composition comprises from about 20.0 wt. % to about 30.0 wt. % water. In one exemplary embodiment, the topical composition comprises from about 20.0 to about 24.0 wt. % water. More or less water may be required in certain instances, depending particularly on other ingredients and/or the amounts thereof employed in the topical composition.
  • the topical composition includes one or more humectants.
  • humectants include propylene glycol, hexylene glycol, 1,4- dihydroxyhexane, 1,2,6-hexanetriol, sorbitol, butyl ene glycol, caprylyl glycol, propanediols, such as methyl propane diol, dipropylene glycol, triethylene glycol, glycerin (glycerol), polyethylene glycols, ethoxydiglycol, polyethylene sorbitol, and combinations thereof.
  • humectants include glycolic acid, glycolate salts, lactate salts, urea, hydroxyethyl urea, alpha- hydroxy acids, such as lactic acid, sodium pyrrolidone carboxylic acid, hyaluronic acid, chitin, and the like.
  • the humecant is a mixture of caprylyl glycol and glycerin.
  • polyethylene glycol humectants examples include PEG-4, PEG-6, PEG-7, PEG-8, PEG-9, PEG-10, PEG-12, PEG-14, PEG-16, PEG-18, PEG-20, PEG-32, PEG-33, PEG-40, PEG- 45, PEG-55, PEG-60, PEG-75, PEG-80, PEG-90, PEG-100, PEG-135, PEG-150, PEG-180, PEG-200, PEG-220, PEG-240, and PEG-800.
  • the humectant may be included in the topical composition in an amount up to about 20.0 wt. %, or up to about 15.0 wt. %, or up to about 12.0 wt. %, or up to about 10.0 wt. %, or up to about 8.0 wt. % or up to about 8.0 wt. %, or up to about 3.0 wt. %.
  • the humectant is included in an amount from about 0.001 wt. %, or from about 0.01 wt. %, or from about 0.05 wt. %, or from about 0.1 wt. %, or from about 0.5 wt.
  • the humectant is included in an amount from about 0.4 to about 3.0 wt. %, based upon the total weight of the composition.
  • the humectant is included in an amount from about 0.005 to about 10.0 wt. %, or from about 0.01 to about 5.0 wt. %, based upon the total weight of the composition. In one exemplary embodiment the humectant is included in an amount from about 0.1 to about 4.0 wt. %.
  • the topical composition may further comprise one or more conditioning or moisturizing esters.
  • conditioning or moisturizing esters include cetyl myristate, cetyl myristoleate, and other cetyl esters, diisopropyl sebacate, and isopropyl myristate.
  • the ester may be present in an amount of up to about 10.0 wt. %, or up to about 8.0 wt. %, or up to about 5.0 wt. %, or up to about 3.0 wt. %, or up to about 2.0 wt. %, or up to about 1.0 wt. %, based on the total weight of the composition.
  • the moisturizing ester is present in an amount from about 0.001 wt. %, or from about 0.005 wt. %, or from about 0.01 wt. %, or from about 0.05 wt. %, or from about 0.1 wt. %, or from about 0.25 wt. %, or from about 0.5 wt. %, or from about 1.0 wt. %, based on the total weight of the topical composition.
  • the moisturizing ester is present in an amount between 0.01 to 0.30 wt. %, based upon the total weight of the composition.
  • the moisturizing ester is present in an amount between 0.05 wt.
  • the topical composition may include one or more emulsifying agents.
  • emulsifying agents include stearyl alcohol, sorbitan oleate trideceth-2, poloxamers, and PEG/PPG-20/6 dimethicone.
  • the emulsifying agent is present in an amount of up to about 10.0 wt. %, based upon the total weight of the topical composition.
  • the emulsifying agent is present in an amount of from about 0.1 to about 5.0 wt. %, or from about 0.5 to about 2.0 wt. %, based upon the total weight of the topical composition.
  • the topical composition includes one or more skin- conditioners or emollients.
  • suitable skin conditioners and emollients include aloe, vitamin E, vitamin E acetate (tocopheryl acetate), Vitamin B 3 (niacinamide), C 6- io alkane diols, lactic acid, and urea.
  • the skin-conditioner can be included in the topical composition in an amount from about 0.0001 to about 1.0 wt. %, in other embodiments, from about 0.0005 to about 0.01 wt. %, based upon the total weight of the composition.
  • the miscellaneous skin conditioner is present in an amount from about 0.1 to about 0.5 wt. %, based upon the total weight of the composition.
  • the topical composition further includes a carrier component, such as a base cleaner.
  • the topical composition may further comprise one or more deposition enhancers.
  • a suitable deposition enhancer works unidirectionally and will allow ingredients within the composition to penetrate deeper into the stratum corneum whilst preventing the loss of materials from the skin.
  • the deposition enhancer provides a cosmetically acceptable skin feel to the formulation.
  • the deposition enhancers include one or more of surfactants, bile salts and derivatives thereof, chelating agents, and sulphoxides.
  • Some examples of acceptable deposition enhancers include dimethyl sulphoxides (DMSO), DMA, DMF, l-dodecylazacycloheptan-2-one (azone), pyrrolidones such as 2- Pyrrolidone (2P) and N- Methyl -2- Pyrrolidone (NMP), long-chain fatty acids such as oleic acid and fatty acids with a saturated alkyl chain length of about Cio-Co, essential oils, terpenes, terpenoids, oxazolidinones such as 4-decyloxazolidin-2-one, sodium lauryl sulfate (SLS), sodium laureate, polysorbates, sodium glyacolate, sodium deoxycholate, caprylic acid, EDTA, phospholipids, C 12 . 15 Alkyl Benzoate, pentylene glycol, ethoxydiglycol, polysorbate- polyethylenesorbitan-monolaurate
  • the deposition enhancer is a quaternary ammonium compound such as polyquaternium-6, -7, -10, -22, -37, -39, -74 or -101.
  • the deposition enhancer may be included in the topical composition in an amount from about 0.005 wt. % to about 10.0 wt. %, in other embodiments, from about 0.01 wt. % to about 5.0 wt. %, and in other embodiments, from about 0.05 wt. % to about 3.0 wt. %, based upon the total weight of the composition.
  • the deposition enhancer comprises a hydroxy-terminated polyurethane compound chosen from polyolprepolymer-2, polyolprepolymer-14, and polyolprepolymer-15.
  • Polyolprepolymer-2 is sometimes referred to as PPG-12/SMDI copolymer.
  • the polyurethane compound may be present in the topical composition in an amount from about 0.005 wt. % to about 5.0 wt. %, in other embodiments, from about 0.01 wt. % to about 3.0 wt. %, and in other embodiments, from about 0.05 wt. % to about 1.0 wt. %, based upon the total weight of the composition.
  • the topical composition may further comprise one or more anti-irritants.
  • Anti-irritants reduce signs of inflammation on the skin such as swelling, tenderness, pain, itching, or redness.
  • anti-irritants include Aloe Vera, allantoin, anion-cation complexes, aryloxypropionates, azulene, carboxymethyl cellulose, cetyl alcohol, diethyl phthalate, Emcol E607, ethanolamine, glycogen, lanolin, N-(2-Hydroxylthyl) Palmitamide, N-Lauroyl Sarcosinates, Maypon 4C, mineral oils, miranols, Myristyl lactate, polypropylene glycol, polyvinyl pyrrolidone (PVP), tertiary amine oxides, thiodioglycolic acid, and zirconia.
  • the anti-irritant is avenanthrmides (avena sativa (oat), kernel oil, and glycerin) and niacinamide.
  • the anti-irritant may be included in the topical composition in an amount up to about 10.0 wt. %, in other embodiments, from about 0.005 wt. % to about 3.0 wt. %, and in other embodiments, from about 0.01 wt. % to about 1.0 wt. %, based upon the total weight of the composition.
  • the topical composition may further comprise a fragrance.
  • Any scent may be used in the topical composition including, but not limited to, any scent classification on a standard fragrance chart, such as floral, oriental, woody, and fresh.
  • Exemplary scents include cinnamon, clove, lavender, peppermint, rosemary, thyme, thieves, lemon, citrus, coconut, apricot, plum, watermelon, ginger and combinations thereof.
  • the fragrance can be included in the topical composition in an amount from about 0.005 wt. % to about 5.0 wt. %, in other embodiments, from about 0.01 wt. % to about 3.0 wt. %, and in other embodiments, from about 0.05 wt. % to about 1.0 wt. %, based upon the total weight of the composition.
  • the fragrance can be any made of any perfume, essential oil, aroma compounds, fixatives, terpenes, solvents, and the like.
  • the essential oils may include, for example, one or more of Limonene, Citrus Aurantium Dulcis (Orange) Peel Oil, Eucalyptus Globulus Leaf Oil, Citrus Grandis (Grapefruit) Peel Oil, Linalool, Litsea Cubeba Fruit Oil, Lavandula Hybrida Oil, Abies Sibirica Oil, Mentha Citrata Leaf Extract, Coriandrum Sativum (Coriander) Fruit Oil, Piper Nigrum (Pepper) Fruit Oil, and Canarium Luzonicum Gum Nonvolatiles.
  • Limonene Citrus Aurantium Dulcis (Orange) Peel Oil
  • Eucalyptus Globulus Leaf Oil Citrus Grandis (Grapefruit) Peel Oil
  • Linalool Litsea Cubeba Fruit Oil
  • Lavandula Hybrida Oil Abies Sibirica Oil
  • Mentha Citrata Leaf Extract Coriandrum Sativum (Coriander) Fruit Oil
  • the topical composition may further comprise a wide range of optional ingredients that do not deleteriously affect the composition's ability to stimulate AMP concentration on the surface and that do not deleteriously affect the composition's ability to restore the microbial balance on the surface.
  • Examples of these functional classes include: abrasives, anti-acne agents, anticaking agents, antioxidants, binders, biological additives, bulking agents, chelating agents, chemical additives; colorants, cosmetic astringents, cosmetic biocides, denaturants, drug astringents, emulsifiers, external analgesics, film formers, fragrance components, opacifying agents, plasticizers, preservatives (sometimes referred to as antimicrobials), propellants, reducing agents, skin bleaching agents, skin-conditioning agents (emollient, miscellaneous, and occlusive), skin protectants, solvents, surfactants, foam boosters, hydrotropes, solubilizing agents, suspending agents (nonsurfactant), sunscreen agents, ultraviolet light absorbers, detackifiers, and viscosity increasing agents (aqueous and nonaqueous).
  • Examples of other functional classes of materials useful herein that are well known to one of ordinary skill in the art include solubilizing agents
  • the topical compositions exhibit a pH in the range of from about 2.5 to about 12.0, or a pH in the range of from about 3.5 to about 8, or in the range of from about 4.0 and about 7.5.
  • a pH adjusting agent or constituent may be used to provide and/or maintain the pH of a composition.
  • Exemplary pH adjusting agents include, but are not limited to, organic acids, such as citric acid, lactic acid, formic acid, acetic acid, proponic acid, butyric acid, caproic acid, oxalic acid, maleic acid, benzoic acid, carbonic acid, and the like.
  • composition of the present invention is not particularly limited.
  • topical compositions of the present invention may be formulated as a foamable composition, a thickened gel composition, a sprayable liquid, a rinse, or may be applied to a wipe.
  • the topical composition of the present invention may be in the form of a thickened gel, with the inclusion of one or more thickeners and optionally one or more stabilizers.
  • thickeners and stabilizers include hydroxyethyl cellulose hydroxypropyl cellulose, methyl cellulose, carboxymethyl cellulose, and ammonium acryloyldimethyltaurate/VP copolymer.
  • the thickener or stabilizer may be present in an amount of up to about 10.0 wt. %, or in an amount of from about 0.1 to about 5.0 wt. %, or from about 0.2 to about 1.0 wt.
  • the thickener or stabilizer may be present in an amount of up to about 15.0 wt. %, or from about 0.05 to about 5.0 wt. %, or from about 0.1 to about 1.0 wt. %, based upon the total weight of the composition.
  • the topical composition may be thickened with polyacrylate thickeners such as those conventionally available and/or known in the art.
  • polyacrylate thickeners include carbomers, acrylates/C 10-30 alkyl acrylate cross- polymers, copolymers of acrylic acid and alkyl (C5 -C 10) acrylate, copolymers of acrylic acid and maleic anhydride, and mixtures thereof.
  • the gel composition includes an effective amount of a polymeric thickener to adjust the viscosity of the gel to a viscosity range of from about 1000 to about 65,000 centipoise.
  • the viscosity of the gel is from about 5000 to about 35,000, and in another embodiment, the viscosity is from about 10,000 to about 25,000.
  • the viscosity is measured by a Brookfield RV Viscometer using RV and/or LV Spindles at 22 °C +/- 3 °C.
  • the effective amount of thickener will vary depending upon a number of factors, including the amount of alcohol and other ingredients in the gel composition.
  • an effective amount of thickener is at least about 0.01 wt. %, based upon the total weight of the gel composition.
  • the effective amount is at least about 0.02 wt. %, or at least about 0.05 wt. %, or at least about 0.1 wt. %.
  • the effective amount of thickener is at least about 0.5 wt. %, or at least about 0.75 wt. %, based upon the total weight of the gel.
  • the compositions according to the present invention comprise up to about 10.0 wt. % of the total composition of a polymeric thickener.
  • the amount of thickener is from about 0.01 to about 1.0 wt. %, or from about 0.02 to about 0.4 wt. %, or from about 0.05 to about 0.3 wt. %, based upon the total weight of the antimicrobial gel.
  • the amount of thickener may be from about 0.1 to about 10.0 wt. %, or from about 0.5% to about 5.0 wt. %, or from about 0.75 to about 2.0 wt. %, based upon the total weight of the antimicrobial gel.
  • the gel composition may further comprise a neutralizer.
  • neutralizing agents include amines, alkanolamines, alkanolamides, inorganic bases, amino acids, including salts, esters and acyl derivatives thereof.
  • Exemplary neutralizing agents include triethanolamine, sodium hydroxide, monoethanolamine and dimethyl stearylamine.
  • neutralizing agents are also known, such as HO(C m H 2m ) 2 H, where m has the value of from 2 to 3, and aminom ethyl propanol, aminom ethyl propanediol, and ethoxylated amines, such as PEG-25 cocamine, polyoxyethylene (5) cocamine (PEG-5 cocamine), polyoxyethylene (25) cocamine (PEG-25 cocamine), polyoxyethylene (5) octadecylamine (PEG-5 stearamine), polyoxyethylene (25) octadecylamine (PEG-25 stearamine), polyoxyethylene (5) tallowamine (PEG-5 tallowamine), polyoxyethylene (15) oleylamine (PEG-15 oleylamine), polyethylene (5) soyamine (PEG-5 soyamine), and polyoxyethylene (25) soyamine (PEG-15 soyamine).
  • PEG-25 cocamine polyoxyethylene (5) cocamine
  • PEG-5 cocamine
  • the neutralizing agent includes at least one of sodium hydroxide or sodium hydroxide precursors. Solutions of sodium hydroxide in water are non-limiting examples of neutralizers containing sodium hydroxide.
  • the neutralizer is employed in an effective amount to neutralize a portion of the carboxyl groups of the thickening agent, and produce the desired pH range.
  • the pH of unneutralized thickening agent dispersed in water is generally acidic.
  • the pH of Carbopol ® polymer dispersions is approximately in the range of 2.5 to 3.5, depending upon the polymer concentration.
  • An effective amount of neutralizer, when added to the thickener dispersion, adjusts the pH to a desired range of about 4.1 to 4.8, or of about 4.2 to 4.6.
  • the amount of neutralizer necessary to effect this pH range will vary depending upon factors such as the type of thickening agent, the amount of thickening agent, etc. However, in general, amounts less than 1.0 wt. % and ranging from about 0.001 to about 0.3 wt. % of the neutralizing agent are considered sufficient and effective.
  • the topical composition is formulated as a foamable composition.
  • One or more foam agents may optionally be included in the foamable composition.
  • the foam agent comprises a non-ionic foam agent such as decyl glucoside or an amphoteric foam agent such as cocamidopropylbetaine.
  • the amount of nonionic or amphoteric foam agent is from about 0.5 to about 3.5 wt. %, in other embodiments from about 1.0 to about 3.0 wt. %, based upon the total weight of the topical composition.
  • the amount of decyl glucoside or cocamidopropylbetaine is from about 0.5 to about 3.5 wt. %, in other embodiments from about 1.0 to about 3.0 wt. %, based upon the total weight of the topical composition.
  • the foaming agents include one or more of silicone glycol and fluorosurfactants.
  • Silicone glycols may be generally characterized by containing one or more Si-O-Si linkages in the polymer backbone.
  • Silicone glycols include organopolysiloxane dimethicone polyols, silicone carbinol fluids, silicone polyethers, alkylmethyl siloxanes, amodimethicones, trisiloxane ethoxylates, dimethiconols, quaternized silicone glycols, polysilicones, silicone crosspolymers, and silicone waxes.
  • silicone glycols include dimethicone PEG-7 undecylenate, PEG- 10 dimethicone, PEG-8 dimethicone, PEG- 12 dimethicone, perfluorononyl ethyl carboxydecal PEG 10, PEG-20/PPG-23 dimethicone, PEG- 11 methyl ether dimethicone, bis-PEG/PPG-20/20 dimethicone, silicone quats, PEG-9 dimethicone, PPG- 12 dimethicone, fluoro PEG-8 dimethicone, PEG-23/PPG-6 dimethicone, PEG-20/PPG-23 dimethicone, PEG 17 dimethicone, PEG-5/PPG-3 methicone, bis-PEG-18 methyl ether dimethyl silane, bis-PEG-20 dimethicone, PEG/PPG-20/15 dimethicone copolyol and sulfosuccinate blends
  • the amount of silicone glycol foam agent is not particularly limited, so long as an effective amount to produce foaming is present.
  • the effective amount to produce foaming may vary, depending upon the amount of alcohol and other ingredients that are present.
  • the composition includes at least about 0.002 wt. % of silicone glycol foam agent, based upon the total weight of the composition.
  • the composition includes at least about 0.01 wt. % of silicone glycol foam agent, based upon the total weight of the composition.
  • the composition includes at least about 0.05 wt. % of silicone glycol foam agent, based upon the total weight of the composition.
  • the foam agent is present in an amount of from about 0.002 to about 4.0 wt. %, or in an amount of from about 0.01 to about 2.0 wt. %, based upon the total weight of the composition. It is envisioned that higher amounts may also be effective to produce foam. All such weights as they pertain to listed ingredients are based on the active level, and therefore, do not include carriers or by-products that may be included in commercially available materials, unless otherwise specified.
  • foam agent it may be desirable to use higher amounts of foam agent.
  • the foaming composition of the present invention includes a cleansing or sanitizing product that is applied to a surface and then rinsed off
  • higher amounts of foam agent may be employed.
  • the amount of foam agent is present in amounts up to about 35.0 wt. %, based upon the total weight of the composition.
  • the topical composition of the present invention may be formulated as an aerosol or non-aerosol foamable composition.
  • the topical composition is dispensed from an unpressurized or low-pressure dispenser which mixes the composition with air.
  • the viscosity of the non-aerosol foamable composition is less than about 100 mPas, in one embodiment less than about 50 mPas, and in another embodiment less than about 25 mPas.
  • composition of the present invention may be employed in any type of dispenser typically used for gel products, for example pump dispensers.
  • Pump dispensers may be affixed to bottles or other free-standing containers. Pump dispensers may be incorporated into wall-mounted dispensers. Pump dispensers may be activated manually by hand or foot pump, or may be automatically activated.
  • Useful dispensers include those available from GOJO Industries under the designations NXT® and TFXTM as well as traditional bag-in-box dispensers. Examples of dispensers are described in U. S. Pat. Nos. 5,265,772, 5,944,227, 6,877,642, 7,028,861, 7,61 1,030, and 7,621,426, all of which are incorporated herein by reference.
  • the dispenser includes an outlet such as a nozzle, through which the composition is dispensed.
  • the topical composition is used in dispensers that employ foaming pumps, which combine ambient air or an inert gas and the composition in a mixing chamber and pass the mixture through a mesh screen.
  • the topical composition is integrated into wipe composition.
  • Wipe compositions in accordance with this invention include at least one alcohol, a Ci-io alkanediol enhancer, and are applied to a wipe substrate.
  • the wipe composition is alcohol-free.
  • the wipe may comprise a laminate formed by spunbonding/meltblowing/spunbonding (SMS).
  • SMS spunbonding/meltblowing/spunbonding
  • an SMS material contains a meltblown web sandwiched between two exteriors spunbond webs. SMS materials are further described in U. S. Pat. Nos. 4,041,203, 5, 169,706, 5,464,688, and 4,766,029, and are commercially available, for example from Kimberly-Clark Corporation under marks such as Spunguard 7 and Evolution 7.
  • the SMS laminate may be treated or untreated.
  • the topical composition decreases the concentration of IL-8, a chmokine and proinflammatory cytokine.
  • IL-8 is an important mediator of the immune reaction in the innate immune system response.
  • IL-8 over-expressed is a biomarker of skin irritation.
  • IL-8 is associated with inflammation and plays a role in colorectal cancer.
  • a topical composition comprising up to about 10.0 wt. % of the active ingredient in water is able to reduce the relative concentration of IL-8 by at least about 50%, or at least about 70 %, or at least about 78% as compared to an otherwise identical control composition without the active ingredient.
  • a topical composition comprising up to about 10.0 wt. % of an active ingredient in ethanol is able to reduce the relative concentration of IL-8 by at least about 15%, or at least about 25%, or at least about 30%), as compared to an otherwise identical control composition without the active ingredient.
  • the topical composition increases the expression of Involucrin.
  • Involucrin is a protein component of human skin and is encoded in humans by the IVL gene.
  • a topical composition comprising up to about 10.0 wt. % of an active ingredient is able to increase the relative Involucrin concentration by at least 50%), or at least 70%, or at least 90% or at least 100% as compared to an otherwise identical composition not including the active ingredient.
  • the topical composition increases the expression of DCS3.
  • DSC3 is a calcium-dependent glycoprotein that is found in human epithelial cells and functions as adhesives within the cell.
  • a topical composition comprising up to about 10.0 wt. % of an active ingredient is able to increase the relative DCS3 concentration by at least about 25%, or at least 35%, or at least 50%, or at least 57%, as compared to an otherwise identical composition not including the active ingredient.
  • the topical composition increases the presence of AMPs on the skin, such as, for example, human beta defensin (HBD) 1, HBD-2, and HBD-3 as well as LL37.
  • HBD human beta defensin
  • a topical composition comprising up to about 10.0 wt. % of an active ingredient increases the concentration of HBD-2.
  • HBD-2 is a low molecular weight AMP produced by epithelia cells and is encoded by the DEFB4 gene. It exhibits potent antimicrobial activity against Gram-negative bacteria and Candida. HBD-2 plays an important role in the innate and adaptive immune system of both vertebrates and invertebrates. In humans it provides direct bactericidal action and Toll-like receptor activation.
  • a topical composition comprising up to about 10.0 wt.
  • % of an active ingredient in water is able to increase the relative concentration of HBD-2 by at least about 25%, or at least about 35%, or at least about 45%, or at least about 55%, or at least about 65%), or at least about 75%, or at least about 90%, or at least about 100%, or at least about 125%), or at least 140%, as compared to an otherwise identical control composition without the active ingredient.
  • Topical compositions with BonicelTM were tested for their ability to decrease concentration of Interleukin 8 (IL-8 or CXCL8) which is a chemokine and proinflammatory cytokine produced by macrophages and other cell types such as epithelial cells.
  • IL-8 is secreted from keratinocytes in skin in response to inflammatory stimuli.
  • Control A human dermal keratinocytes were left untreated. No irritation is expected, and therefore Control A provides a baseline (set as 0).
  • Control B IL-8 is induced in human dermal keratinocytes by applying a surfactant mixture that is a combination of sodium laureth sulfate and polyquaternium-10 (set as 100%). Samples of BonicelTM in both a water composition and ethanol composition were tested for their ability to alter IL-8 expression. For all other samples, the human dermal keratinocytes are co-treated with the surfactant mixture and a composition containing indicated concentration of BonicelTM. Decreased IL-8 expression reflects an ingredient's anti -irritation activity.
  • an assay kit was employed that was obtained from R&D Systems: Human CXCL8/IL-8 Duoset ELISA Kit (DY208). ELISA was performed after overnight treatment using by applying 100 ⁇ /well of culture medium according to the manufactory instruction of the ELISA kit. The results were measured using a colorimeter, absorbance was measured at 450 nanometers (nm) within 30 minutes. Wavelength correction was set to 570 nm.
  • Neonatal Human Epidermal Keratinocytes (NHEK; Life Technology, Grand Island, NY, USA) were cultured with keratinocyte growth medium (KGM, Medium 154: M-154-500 Life Technology with supplements S-001, Life Technologies). Keratinocytes were treated with the sample compositions in a 6-well plate overnight. After washing with cold phosphate-buffered saline (PBS), total RNAs were prepared from each well.
  • qRT-PCR Real-Time Quantitative Reverse Transcription PCR (qRT-PCR) was performed to detect the target genes (Involucrin) expression level using a One-step TaqMan® RT-PCR kit (Life Technologies).
  • Neonatal Human Epidermal Keratinocytes (NHEK; Life Technology, Grand Island, NY, USA) were cultured with keratinocyte growth medium (KGM, Medium 154: M-154-500 Life Technology with supplements S-001, Life Technologies). Keratinocytes were treated with the sample compositions in a 6-well plate overnight. After washing with cold phosphate-buffered saline (PBS), total RNAs were prepared from each well.
  • qRT-PCR Real-Time Quantitative Reverse Transcription PCR (qRT-PCR) was performed to detect the target genes (DSC3) expression level using a One-step TaqMan® RT-PCR kit (Life Technologies).
  • BonicelTM specifically to determine its ability to simulate growth in concentration of human beta-defensin 2 (HBD-2). BonicelTM was tested at concentrations of both 0.1% and 1.0% and in each of dermatological carriers, ethanol and water.
  • Neonatal Human Epidermal Keratinocytes (NHEK; Life Technology, Grand Island, NY, USA) were cultured with keratinocyte growth medium (KGM, Medium 154: M-154-500 Life Technology with supplements S-001, Life Technologies). NHEK were seeded into 96-well plates at a density of 10000 cells in 200 ⁇ medium per well. After 48 hours, the cells were incubated with varying concentrations of each ingredient solution in a culture medium (KGM) overnight (16 hours) at 37 °C, 5% C02 and 95% humidity at four replicates for each concentration. Each of these active ingredients was tested at the different concentration of weight percents based on the weight of the total culture. Each of these compositions was compared to a control culture medium.
  • KGM keratinocyte growth medium
  • HBD-2 was detected using HBD-2 ELISA developing kits (commercially available from Peprotech). ELISA were performed according to the manufactory instructions of each kit by adding 100 ⁇ /well of culture medium after overnight treatment. The substrate of ELISA reaction was using the substrate reagent from R&D Systems (DY999), and the reactions were stopped by adding 50 ⁇ of IN H 2 S0 4 in each well. The results were measured using a colorimeter, absorbance was measured at 450 nanometers (nm) within 30 minutes. Wavelength correction was set to 570 nm. The concentration of each sample was calculated using ELISA standard curve.
  • BonicelTM is able to increase the concentration of HBD-2 both in a composition with water and in a composition that had been in contact with ethanol.
  • Relative increases in HBD-2 concentration of about 44% and about 90% were observed for 0.1% BonicelTM in a composition with water and 1.0% BonicelTM in a composition with water, respectively.
  • Additionally relative increases in HBD-2 concentration of about 125% and about 144%) were observed for 0.1% BonicelTM in a composition that had been in contact with ethanol and 1.0% BonicelTM in a composition that had been in contact with ethanol, respectively.
  • BonicelTM does not lose its ability to increase the concentration of HBD-2 and in fact, the effectiveness of the composition actually increased substantially when combined with the ethanol.
  • the results for BonicelTM in a water composition are depicted in Figure 4 and the results for BoncielTM that had been in contact with ethanol composition are depicted in Figure 5.
  • exemplary topical compositions were investigated for pathogen blocking potential.
  • Methicillin resistant Staphylococcus aureus strain Mu50 ATCC 33591 Escherichia coli strain K12 was tested against the following exemplary topical compounds: DMEM (cell culture medium, control), 100 nM dexamethasone (DEX, control steroidal anti-inflammatory), 0- 5% Ecoskin (a-gluco-oligosaccharide, fructo-oligosaccharide and inactivated Lactobacillus), 0- 5% Bacillus ferment, and 0-5% of a prebiotic blend of inulin and fructo-oligosaccahride.
  • DMEM cell culture medium, control
  • DEX dexamethasone
  • Ecoskin a-gluco-oligosaccharide
  • fructo-oligosaccharide and inactivated Lactobacillus 0- 5% Bacillus ferment
  • Figure 6 illustrates the dose-dependent response of Staphylococcus aureus adhesion and invasion potential.
  • Bacillus ferment had a consistent increase in the dose response. Particularly, 5% Bacillus ferment resulted in the lowest adhesion occurrence overall.

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US10874700B2 (en) 2016-03-31 2020-12-29 Gojo Industries, Inc. Sanitizer composition with probiotic/prebiotic active ingredient
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JP2023513776A (ja) * 2020-02-14 2023-04-03 エルジー ハウスホールド アンド ヘルスケア リミテッド 多糖類、酵母抽出物及びプロバイオティクス特性を有する菌株発酵物を有効成分として含む皮膚改善用化粧料組成物
EP3871653A1 (en) * 2020-02-27 2021-09-01 MicroCen Trans s.r.o A composition containing a vital probiotic culture for human or veterinary use as a deodorant
TR202019406A2 (tr) * 2020-12-01 2022-06-21 Eczacibasi Tueketim Ueruenleri Sanayi Ve Ticaret Anonim Sirketi Ci̇ldi̇n florasi korunarak dezenfekte edi̇lmesi̇ni̇ sağlayan alkol bazli ürün
KR20240069705A (ko) * 2021-06-15 2024-05-20 밴티지 스페셜티 인그리디언츠 인코포레이티드 국소 프로바이오틱 전달 시스템
WO2024117424A1 (ko) * 2022-12-02 2024-06-06 주식회사 엑티브온 맥주효모 추출물 및 1,3-프로판디올을 포함하는 피부의 마이크로바이옴 균형 유지용 화장료 조성물
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