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WO2002028179A1 - Compositions de neutralisation d'allergenes - Google Patents

Compositions de neutralisation d'allergenes Download PDF

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Publication number
WO2002028179A1
WO2002028179A1 PCT/US2000/027018 US0027018W WO0228179A1 WO 2002028179 A1 WO2002028179 A1 WO 2002028179A1 US 0027018 W US0027018 W US 0027018W WO 0228179 A1 WO0228179 A1 WO 0228179A1
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WO
WIPO (PCT)
Prior art keywords
allergen
composition
allergen neutralization
acid
compositions
Prior art date
Application number
PCT/US2000/027018
Other languages
English (en)
Inventor
Abul Khaer Mohamad Quamrul Hasan
Mark Hsiang-Kuen Mao
Ryoko Kobayashi
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to AU2000277428A priority Critical patent/AU2000277428A1/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to EP00967195A priority patent/EP1322154A1/fr
Priority to JP2002531816A priority patent/JP2004510841A/ja
Priority to CA002425068A priority patent/CA2425068A1/fr
Priority to CN00819937.XA priority patent/CN1454053A/zh
Priority to PCT/US2000/027018 priority patent/WO2002028179A1/fr
Priority to CNA008199388A priority patent/CN1469709A/zh
Priority to CA002357828A priority patent/CA2357828A1/fr
Priority to CA002357839A priority patent/CA2357839A1/fr
Priority to ARP010104587A priority patent/AR030814A1/es
Priority to AU77324/01A priority patent/AU7732401A/en
Publication of WO2002028179A1 publication Critical patent/WO2002028179A1/fr
Priority to US10/397,732 priority patent/US20030203035A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
    • A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
    • A61L2/186—Peroxide solutions
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
    • A01N25/10—Macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
    • A61L2/22—Phase substances, e.g. smokes, aerosols or sprayed or atomised substances
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
    • A61L2202/20—Targets to be treated
    • A61L2202/26—Textiles, e.g. towels, beds, cloths

Definitions

  • the present invention relates to aqueous allergen neutralizing compositions that control allergen containing dust particles while not leaving behind a sticky film on household surfaces. These compositions do not stain fabric materials and are effective for suppressing allergen compounds.
  • the present compositions are particularly effective against the allergens associated with house dust mites and other common allergens such as cat dander, pollen and the like.
  • Allergic reactions can be initiated in many ways, but one of the most common ways is by the inhalation of airborne allergens. Another common way to ingest allergens is when they come in direct contact with a moist surface on the body where they stick and react with the surrounding body tissue. This can happen, for example, when a person lays down in bed and allergen containing dust that lay on the pillow or bed coverings contacts and is absorbed into the person's eyes. This typically results in an allergic reaction as the allergens are gradually absorbed into the mucous around the eye.
  • allergens are protein based molecules, and these protein allergens can originate from many sources. It has been known for some time that one of the most common sources of allergens in a house is from dust mites. Of course, as is the case with all allergens, only certain people are allergic to dust mite allergens. But this group of people can be quite large in many areas, especially in hot humid areas. For example, in the south eastern United States of America, where it is both hot and humid for much of the year, the incidence of house dust mite allergies in the general population can be as high as 25%. House dust mites thrive in plush carpets, overstuffed upholstery, cushy bed comforters and the like. Medical professionals who specialize in the treatment of allergies often recommend the removal of these items from the homes of people who suffer from dust mite allergies. For many reasons, this is often an impractical and unworkable solution to the problem of dust mite allergies.
  • miticides Another common method for removing mite allergens from a house is the use of miticides to kill the mites. But, unfortunately, the proteins that cause allergic reactions can be found in the mite corpses and also the residual mite feces. Thus, killing the mites does not solve the problem. And because some miticides can be relatively harsh chemicals, some consumers are reluctant to use these chemicals throughout their home on a regular basis.
  • allergen neutralization sprays typically use a tannin, or other related polyphenols, as the active component.
  • tannins and related chemicals are notorious for their strong tendency in forming color. Thus, these chemicals cannot be sprayed onto fabrics without a substantial risk of staining the fabric material.
  • the materials used to "cover” or encase allergen containing materials tend to be generally undesirable. Specifically, these materials typically “stick” to dust and other airborne particles making them too heavy to remain aloft. Unfortunately, both the spray and the covered particles become “sticky” resulting in fabric surfaces that feel sticky. This is especially undesirable for bed covers and pillows because they come into direct contact with the consumer's skin. Moreover, it is well known that spraying a fabric with a sticky material results in attracting more dust and other airborne particles to the surface of the material. Ultimately, the surface becomes dirty much quicker than would normally occur.
  • the spray products should be sprayable and compatible with a wide variety of fabric materials. That is, the spray products should not stain or otherwise damage common household fabrics that are used in making draperies, bed covers, carpeting, rugs, clothing, furniture covers and others. Moreover, these materials should create no additional health or environmental problems. For example, the spray products should not have a noxious smell nor should they be toxic to humans and household pets.
  • allergen neutralization products that leave the surfaces on which they are sprayed with a smooth, non-sticky feel. That is, the spray should be effective against allergens without causing the displeasing side effect of leaving household surfaces with a sticky feeling.
  • the present invention comprises an allergen neutralization composition that retains at least about 30%, preferably at least about 35%, and more preferably at least about 40% of dust particles as measured by the Dust Control Test, and the composition has an average MIU value of less than about 3.4, preferably less than about 3.2, more preferably less than about 3.0 as measured by the Friction Coefficient Analysis method, hi a preferred aspect of this invention the composition yields a ⁇ E value of less than about 3.5, preferably, less than about 3.0, and more preferably less than about 1.0 as measured by Fabric Color Evaluation method.
  • the compositions herein are preferably used on inanimate objects and are sprayable.
  • the allergen neutralization compositions comprise allergen denaturing compounds selected from the group consisting of an effective amount of an allergy neutralizing metal ion, polyphenol compounds, hydrogen peroxide, salicylic acid, citric acid, lactic acid, glycolic acid, ascorbic acid, gallic acid, gluconic acids, and mixtures thereof, a solvent, and preferably a wetting agent.
  • allergen denaturing compounds selected from the group consisting of an effective amount of an allergy neutralizing metal ion, polyphenol compounds, hydrogen peroxide, salicylic acid, citric acid, lactic acid, glycolic acid, ascorbic acid, gallic acid, gluconic acids, and mixtures thereof, a solvent, and preferably a wetting agent.
  • the optional metal ions are preferably selected from the group consisting of ions of zinc, stannous, stannic, magnesium, calcium, manganese, titanium, iron, copper, nickel, and mixtures thereof, hi one aspect of this invention the metal ion is present in the composition at about 0.01% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.2% to about 8%, by weight, of the allergen neutralization composition.
  • the solvent for the allergen neutralization compositions of the present invention preferably comprises water, and more preferably the solvent comprises from about 0.01% to about 20%, by weight of the allergen neutralization composition, of a volatile lower alcohol. Even more preferably, the allergen neutralization compositions are essentially free of complexing agents. By "essentially free of it is meant the allergen neutralization composition contains less than about 0.5%, preferably less than about 0.1%, and even more preferably less than 0.01%, by weight, of complexing agents.
  • the allergen neutralization compositions of the present invention provide superior performance in reducing a consumer's allergy symptoms. These compositions operate on the principle of neutralizing allergenic proteins by controlling the dust particles that contain the allergenic proteins.
  • allergenic proteins include, for example, proteins associated with common house dust mites, cat dander and others.
  • the proteins can be neutralized chemically by denaturing, as well as being physically disabled by dust control methods. In either event, the proteins that cause allergic reactions in humans are neutralized or kept from entering the human body, as opposed to simply killing the mites.
  • compositions of the present invention in addition to providing improved efficacy, are compatible with a wide variety of household surfaces where house dust mites, and their feces and corpses might reside. Moreover, the compositions of the present invention leave surfaces feeling smooth and non-sticky. This provides a substantial benefit because many known allergen neutralization compositions are known to leave a sticky film on fabrics and hard surfaces. As can be appreciated, a product that is effective against allergen containing compounds will not be received favorably by consumers if it leaves a sticky film on the surfaces that it is used. Thus, the present compositions provide many unexpected and superior benefits over known allergen neutralizing compositions.
  • allergen neutralization is intended to include both chemical denaturing and physical covering of the allergen containing protein.
  • the compositions of this invention may neutralize allergens by chemically denaturing them, physically covering them, or both. More specifically, by chemical denaturing, it is meant that the chemical structure of an allergen containing protein is altered such that it no longer gives rise to allergic reactions in humans. While not wanting to be bound by any one theory, it is believed that the metal ions of the present compositions, and the optional allergen denaturing compounds, bind with the protein molecule in a way that prevents further reaction with a human. This is only one example of many potential chemical denaturing mechanisms. Ultimately, the allergic reaction is not initiated.
  • an allergen protein must be solubilized or dispersed by the human body to initiate an allergic reaction. This can occur when the protein contacts body fluids such as sweat on the skin, mucous in the eyes and nasal cavities, or saliva in the mouth. It is believed that if the protein is covered in a composition that does not readily solubilize or disperse in bodily fluids, the protein will not be available to initiate the allergic reaction.
  • the particles may be too heavy to become airborne. Because many allergens are inhaled, the simple act of "grounding" the allergen containing particles can significantly decrease the symptoms experienced by an allergy sufferer.
  • One method of relieving allergy symptoms is to control "dust" particles that may contain allergenic protein molecules.
  • "Dust” as used herein refers to any particulate matter that might be found in an enclosed space that might be occupied by one or more humans.
  • the particulate matter can be as small as one or more allergenic protein molecules or it can comprise larger particles, for example, dust mites, their fecal matter and their corpses.
  • Houses and the rooms within a house, cars, hotel rooms, train cars, airline cabins, are among the many places that allergen containing dust might be found. By immobilizing a portion of the dust, the allergenic proteins are unavailable to cause allergic reactions in humans. By this method, dust control can reduce allergic reactions in humans.
  • the allergen neutralization compositions of this invention are sprayed onto common household surfaces where allergen containing dust might be found. A portion of the dust is then immobilized, but a portion of the allergenic proteins may be neutralized as well.
  • the dust particles are generally immobilized by film forming polymers that do not leave a sticky film on fabrics.
  • the ability for a composition to control dust can be measured and quantified by the "Dust Control Test” given in Example I.
  • Stickyness can be measured and quantified by the "Friction Coefficient Analysis” given below in Example LT.
  • Film forming polymers suitable for use in the present invention include, water- soluble polymers selected from the group consisting of starch, polyvinyl alcohols, Methyl Cellulose (“MC”), and its derivatives, polyacrylic acids, polyethylene glycols with molecular weight higher than 5000, polyethylene, polypropylene glycol with molecular weight higher than 8000, Cosmetic Toiletry Fragrances Association (“CTFA”) polyquaternium compounds 1 through 14, polyvinyl pyrrolidone (“PNP”), and mixtures thereof.
  • water- soluble polymers selected from the group consisting of starch, polyvinyl alcohols, Methyl Cellulose (“MC”), and its derivatives, polyacrylic acids, polyethylene glycols with molecular weight higher than 5000, polyethylene, polypropylene glycol with molecular weight higher than 8000, Cosmetic Toiletry Fragrances Association (“CTFA”) polyquaternium compounds 1 through 14, polyvinyl pyrrolidone (“PNP”), and mixtures thereof.
  • Certain preferred film forming polymers are selected from the group consisting of hydroxy-propyl starch, Daisel MC 1310, Kuraray poly vinyl alcohol (“PNA”) 205, ⁇ -Polyvinyl-2- pyrrolidone, and mixtures thereof.
  • the film forming polymers are present in the composition at about 0.01% to about 20%, preferably from about 0.05% to about 15%, more preferably from about 0.1% to about 12%, by weight, of the allergen neutralization composition.
  • An optional component of the present invention is an allergen neuralizing metal ion, that is preferably supplied as a metallic salt.
  • the metallic salts are selected from the group consisting of Zinc, Stannous, Stannic, Magnesium, Calcium, Manganese, Titanium, Iron, Manganese, Copper, Nickel, and mixtures thereof.
  • Stannic also known as tin4 + , is less preferred than stannous due primarily to solubility problems with stannic at low pH. But those skilled in the art will be able to formulate suitable compositions with either substance.
  • the preferred metal ions are zinc and stannous as these generally show high efficacy, with few detrimental environmental issues.
  • Highly-ionized and soluble metal salts such as zinc chloride, provide the best source of metal ions. While certain cations yield superior solubility, all cations are acceptable for the metal salts of the present invention. For example, all halides, sulfates, etc.
  • the metallic salts are water- soluble zinc salts, stannous salts or mixtures thereof, and especially ZnCi2 and SnCi2.
  • metallic salts When metallic salts are added to the composition of the present invention they are typically present at a level of from about 0.01% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.2% to about 8% by weight of the usage composition.
  • the pH of the solution is adjusted to less than about 7, more preferably less than about 6, most preferably, less than about 5, in order to keep the solution clear.
  • allergen denaturing compounds While the metal ions discussed above perform an allergen denaturing function, additional allergen denaturing compounds may optionally be incorporated in the present compositions. These allergen denaturing compounds are preferably selected from the group consisting of polyphenol compounds, hydrogen peroxide, salicylic acid, citric acid, lactic acid, glycolic acid, ascorbic acid, gallic acid, gluconic acids, and mixtures thereof. Other alkyl acids are appropriate for use herein. When allergen denaturing compounds are incorporated into the compositions of this invention, it is preferred that low molecular weight alcohols, for example, ethanol, methanol, propanol or isopropanol, are used in the solvent.
  • low molecular weight alcohols for example, ethanol, methanol, propanol or isopropanol
  • the solvent is discussed in greater detail below, but the use of low molecular weight alcohols in this context is to ensure solubility and stability of the allergen denaturing compounds in the composition. Low molecular weight alcohols are especially preferred when the concentration of the allergen denaturing compound exceeds 10% by weight of the allergen neutralization composition.
  • the polyphenol compounds include tannins, catechins, gallic acid and the like. These include either a natural or a synthetic substance such as, but not limited to, tannic acid or a synthetic tanning agent. Synthetic tannins/tannic acids generally fall into three chemical groups: 1) the so called auxiliary tans which are generally strong simple organic acids; 2) combination tans which are general sulphonic acids of complex phenolic materials; and, 3) exchange or replacement tans which are weakly acidic polymeric derivatives containing a large number of phenolic groups.
  • Suitable tanning agents may be selected from cresol sulphonic acid ammounium salt (Neosyn RW), melamine formaldehyde sulphonate (Parnel A), a poly phenolic formaldehyde sulphonate (Suparex L) or a multiphenol formaldehyde sulphonate (Basyntan WL) as sold commercially for leather tanning or treatment.
  • cresol sulphonic acid ammounium salt Neosyn RW
  • melamine formaldehyde sulphonate Parnel A
  • Purarex L poly phenolic formaldehyde sulphonate
  • Basyntan WL multiphenol formaldehyde sulphonate
  • Other similar synthetic materials capable of reaction with protein (tanning action) may also prove effective when appropriately formulated.
  • More recently formaldehyde reaction products of condensates and polymers of urea and melamine and mixtures thereof have been introduced for
  • Naturally derived tannic acids and polyphenolics are also desirable for the present invention.
  • the ones that do not develop color rapidly with air are most preferred.
  • a most preferred tannin source is the kaki extract supplied as Pancil by Ririsu Scientific Industry of Osaka, Japan. This tannin is described in Japan Patent Application No 1991-3-61457; the entire disclosure of this Japan Patent Application is incorporated herein by reference.
  • the allergen denaturing compositions are typically present at a level of from about 0.01% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.2% to about 8% by weight of the usage composition.
  • the solvent for the allergen neutralization compositions of the present invention preferably comprises water, and more preferably the solvent comprises a volatile lower alcohol.
  • the water that is used can be distilled, deionized, or tap water. Water not only serves as the liquid carrier for the metal ions and other ingredients, it also facilitates the complexation reaction between the metal ion, the optional allergen denaturing compositions and the allergenic protein. Not to be bound by theory, it is believed that water solubilizes the allergenic protein allowing it to react with the metal ions, allergen denaturing compounds or both.
  • Low molecular weight alcohols with relatively low boiling points, as compared to water, such as methanol, ethanol, propanol and butanol, are preferred optional ingredients for improving the drying speed of the present compositions.
  • the aqueous based compositions of this invention are sprayed on a solid surface, the surface necessarily becomes wet. Consumers, in general, do not like having wet counter tops, furniture, bedding and other common surfaces. Thus, for consumer acceptance, it is preferred that the compositions herein dry quickly after being applied to a surface.
  • the addition of a low molecular weight alcohol substantially improves the drying time of the present compositions.
  • alcohol is added to the composition of the present invention at a level of from about 0.01% to about 20%, by weight of the composition, preferably from about 0.05% to about 10%, more preferably from about 0.1% to about 5.0%, by weight of the composition. It is understood that specialty products, for example, concentrated or refill solutions, solutions for industrial use, and the like, may contain higher levels of alcohol. In these products the alcohol can be present at levels of from greater than 20% to about 70%.
  • the solvent is preferably present in the allergen neutralization composition at a concentration of from 1% to 98%, preferably from about 3% to about 95%, and more preferably from about 5% to about 90%, by weight of the composition.
  • compositions of the present invention include a wetting agent such as a surfactant or the like.
  • the wetting agent is fully compatible with the metal ions and the optional allergen denaturing compounds and other optional ingredients.
  • the compatible wetting agent reduces surface tension of the composition of the present invention such that when the composition is sprayed on a surface the composition spreads evenly over the surface, and wets the surface better. This allows the maximum amount of the active ingredients to contact the surface where the allergens may be present.
  • Preferred wetting agents for use in the present allergen neutralization compositions have an HLB of greater than about 8, and do not foam excessively. Excessive foaming can be determined by placing 300 ppm of the wetting agent in 100ml of distilled water in a 1000 ml stoppered graduated cylinder. The cylinder is shaken by inverting it 50 times. The cylinder should then be left to settle for 5 minutes. The resulting foam height after the settling period should be less than 50 ml.
  • Non-limiting examples of wetting agents suitable for use herein include fatty alcohol ethloxylates, fatty alcohol ethoxylate-propoxylate, sulfates of alcohols or ethxoylated fatty alcohols, sorbitan monoesters, amine oxides, ethoxylated fatty acid esters, alkyl ether phosphates, alkyl polyglycosides, fatty acid glucosamides, alkyl phenol ethoxylates, alkyl phenol ethoxylated sulfates, paraffin sulfonates, fatty alcohols sulfates, alkyl phenyl sulfonates, linear alkyl benzene sulfonates, alkyl dimethyl betaines, alkyl dimethyl hydroxy propyl sultaines, alkyoxylated polydimethyl siloxanes, alkyl dimethyl amine oxides having alkyl chains with 6-18 carbons, and mixtures
  • One preferred cationic surfactant suitable for use as a wetting agent in the present invention is Coco K3, which is a mono dodecanoate or tetradecanoate ester of methyl triethanol ammonium chloride. Typical levels of wetting agents for use in the present compositions are from about
  • Nonlimiting examples of compatible nonionic surfactants include block copolymers of ethylene oxide and propylene oxide.
  • Suitable block polyoxyethylene- polyoxypropylene polymeric surfactants include those based on ethylene glycol, propylene glycol, glycerol, trimethylolpropane and ethylenediamine as the initial reactive hydrogen compound.
  • Polymeric compounds made from a sequential ethoxylation and propoxylation of initial compounds with a single reactive hydrogen atom, such as C12-I8 aliphatic alcohols are not generally compatible with the cyclodextrin.
  • Certain of the block polymer surfactant compounds designated Pluronic® and Tetronic® by the BASF- Wyandotte Corp., Wyandotte, Michigan, are readily available. Examples of Pluronic® and Tetronic® surfactants are given below.
  • Typical examples of cyclodextrin-compatible Pluronic surfactants are:
  • Tetronic Surfactants have the general formula:
  • Tetronic surfactants are:
  • Reverse Pluronic surfactants are: Reverse Pluronic surfactants:
  • Nonionic wetting agents includes polyalkyleneoxide polysiloxanes having a dimethyl polysiloxane hydrophobic moiety and one or more hydrophilic polyalkylene side chains.
  • surfactants are the Silwet® surfactants which are available OSi Specialties, Inc., Danbury, Connecticut, and have the general formula:
  • a + b are from about 1 to about 50, preferably from about 3 to about 30, more preferably from about 10 to about 25, and Rl is mainly one or more random poly(ethyleneoxide/propyleneoxide) copolymer groups having the general formula:
  • n 3 or 4, preferably 3; total c (for all polyalkyleneoxy side groups) has a value of from 1 to about 100, preferably from about 6 to about 100; total d is from 0 to about 14, preferably from 0 to about 3; and more preferably d is 0; total c+d has a value of from about 5 to about 150, preferably from about 9 to about 100 and each R ⁇ is the same or different and is selected from the group consisting of hydrogen, an alkyl having 1 to 4 carbon atoms, and an acetyl group, preferably hydrogen and methyl group.
  • Representative Silwet surfactants are as follows.
  • the molecular weight of the polyalkyleneoxy group (Ri is less than or equal to about 10,000.
  • the molecular weight of the polyalkyleneoxy group is less than or equal to about 8,000, and most preferably ranges from about 300 to about 5,000.
  • the values of c and d can be those numbers which provide molecular weights within these ranges.
  • the number of ethyleneoxy units (-C2H4O) in the polyether chain (R 1 ) must be sufficient to render the polyalkyleneoxide polysiloxane water dispersible or water soluble. If propyleneoxy groups are present in the polyalkylenoxy chain, they can be distributed randomly in the chain or exist as blocks.
  • Preferred Silwet surfactants are L- 7600, L-7602, L-7604, L-7605, L-7657, and mixtures thereof. Besides surface activity, polyalkyleneoxide polysiloxane surfactants can also provide other benefits, such as antistatic benefits, lubricity and softness to fabrics.
  • polyalkyleneoxide polysiloxanes of the present invention can be prepared according to the procedure set forth in U.S. Pat. No. 3,299,112, incorporated herein by reference.
  • polyalkyleneoxide polysiloxanes of the surfactant blend of the present invention are readily prepared by an addition reaction between a hydrosiloxane (i.e., a siloxane containing silicon-bonded hydrogen) and an alkenyl ether (e.g., a vinyl, allyl, or methallyl ether) of an alkoxy or hydroxy end-blocked polyalkylene oxide).
  • a hydrosiloxane i.e., a siloxane containing silicon-bonded hydrogen
  • an alkenyl ether e.g., a vinyl, allyl, or methallyl ether
  • reaction conditions employed in addition reactions of this type are well known in the art and in general involve heating the reactants (e.g., at a temperature of from about 85° C. to 110° C.) in the presence of a platinum catalyst (e.g., chloroplatinic acid) and a solvent (e.g., toluene).
  • a platinum catalyst e.g., chloroplatinic acid
  • a solvent e.g., toluene
  • Nonlimiting examples of compatible anionic surfactants are the alkyldiphenyl oxide disulfonate, having the general formula:
  • R is an alkyl group.
  • examples of this type of surfactants are available from the Dow Chemical Company under the trade name Dowfax® wherein R is a linear or branched Cg-Ci ⁇ alkyl group.
  • An example of these cyclodextrin-compatible anionic surfactant is Dowfax 3B2 with R being approximately a linear Ci Q group.
  • These anionic surfactants are preferably not used when the composition contains a cationic material so as to minimize the interaction with the cationic actives, since the effect of both surfactant and active are diminished.
  • Miticides can be optionally added to the compositions of the present invention to kill mites.
  • mites corpses are allergenic so killing the mites does not necessarily reduce the level of allergens. But dead mites cannot breed, so killing a portion of the mites can help to control the mite population.
  • Miticides acceptable for use in the present invention include compounds known under the common names as resuethrin, phenothrin, permethrin, allethrins, tetramethrin, furamethrin, cypermethrin, decamethrin, phenvalerate, phenpropathrin, terallethrin, empenthrin and pyrethrin.
  • Additional miticides include pyrethroid compounds such as 1- ethynyl-2-methyl-2-pentenyl-2,2-dimethyl-3-3-(2,2-dichlorovinyl)-cyclopropane-l- carboxylate, 1 -ethynyl-2-methynyl-2-pentenyl-2,2,3 ,3 -tetramethylcyclopropane- 1 - carboxylate, ⁇ -cyano-3-phenoxybenzyl-2,2-dimethyl-3-(2,2,3-tribromethyl)- cyclopropane-1-carboxylate; organic phosphorus compounds such as sumithion, fenthion, tetrachlorvinphos, diazinon and DDNP; and carbamate compounds such as those sold under the trademarks Baygon and Sevin.
  • pyrethroid compounds such as 1- ethynyl-2-methyl-2-pentenyl-2,2-dimethyl-3-3-(2,2-dichloro
  • one or more optional miticides are added to the composition of the present invention they are typically present at a level of from about 0.01% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.2% to about 8% by weight of the usage composition.
  • the allergen neutralization compositions can optionally include ingredients to prevent color formation either in the product or on the fabrics and articles on which it is sprayed. As mentioned above, some of the allergen denaturing compounds, especially the preferred tannins, are known to discolor fabric materials.
  • the optional color stabilization ingredients are intended to reduce or eliminate the discoloration problem. When used, the color stabilization ingredient will be present at a concentration of from about 0.1 % to about 25%, preferably from about 0.2% to about 15% and more preferably from about 1% to about 10%), by weight of the allergen neutralization composition.
  • Preferred chemicals include glycolic acid and its salts, lactic acid and its salts, gluconic acid and its salts, pyruvic acid and its salts, glucaric acid and its salts, ascorbic acid and its salts, hydroxy benzoic acids and the salts, aspartic acid and its salts, hydroxyglutamic acid and its salts, hydroxyphathalic acids and the salts, malic acid and its salts, and mixtures thereof.
  • Soluble detergent builders can also be included for color stabilization. Included among the soluble polycarboxylate builders are a variety of categories of useful materials. One important category of polycarboxylate builders encompasses the ether polycarboxylates, including oxydisuccinate, as disclosed in Berg, U.S.
  • Suitable ether polycarboxylates also include cyclic compounds, particularly alicyclic compounds, such as those described in U.S. 3,923,679; 3,835,163; 4,158,635; 4,120,874 and 4,102,903.
  • ether hydroxypolycarboxylates copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6- trisulphonic acid, and carboxymethyloxysuccinic acid
  • polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid
  • polycarboxylates such as mellitic acid, pyromellitic, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof.
  • Citrate builders e.g., citric acid and soluble salts thereof (particularly sodium salt), are polycarboxylate builders of particular importance due to their availability from renewable resources and their biodegradability. Oxydisuccinates are also especially useful in such compositions and combinations.
  • Other suitable polycarboxylates are disclosed in U.S 4,144,226 and in U.S. 3,308,067. See also U.S. 3,723,322.
  • succinic acid builders include the C5-C20 a lkyl an d alkenyl succinic acids and salts thereof.
  • a particularly preferred compound of this type is dodecenylsuccinic acid.
  • succinate builders include: laurylsuccinate, myristylsuccinate, palmitylsuccinate, 2-dodecenylsuccinate (preferred), 2-pentadecenylsuccinate, and the like. Laurylsuccinates are the preferred builders of this group, and are described in EP 0,200,263.
  • Fatty acids e.g., C12-C1 g monocarboxylic acids such as oleic acid and/or its salts
  • C12-C1 g monocarboxylic acids such as oleic acid and/or its salts
  • the aforesaid builders especially citrate and/or the succinate builders, to provide additional builder activity.
  • Such use of fatty acids will generally result in a diminution of foaming, which should be taken into account by the formulator.
  • phosphorus-based builders can be used, the various alkali metal phosphates such as the well-known sodium tripolyphosphates, sodium pyrophosphate and sodium orthophosphate can be used.
  • Phosphonate builders such as ethane- l-hydroxy-l,l-diphosphonate and other known phosphonates (see, for example, U.S. Patents 3,159,581; 3,213,030; 3,422,021; 3,400,148 and 3,422,137) can also be used.
  • the allergen neutralization compositions of the present invention can also optionally include a perfume to provide a pleasing scent to the spray product.
  • the perfume should not be designed to be overwhelming or to be used as an odor masking ingredient.
  • Perfumes are typically added at low levels, e.g., from about 0% to about 0.5%, preferably from about 0.003% to about 0.3%, more preferably from about 0.005% to about 0.2%, by weight of the usage composition. Perfume can also be added as a more intense odor in product and on surfaces.
  • the perfume is hydrophilic and is composed predominantly of ingredients selected from two groups of ingredients, namely, (a) hydrophilic ingredients having a ClogP of less than about 3.5, more preferably less than about 3.0, and (b) ingredients having significant low detection threshold, and mixtures thereof.
  • at least about 50%, preferably at least about 60%, more preferably at least about 70%, and most preferably at least about 80% by weight of the perfume is composed of perfume ingredients of the above groups (a) and (b).
  • Suitable perfume ingredients can be found in US Patent No. 5,670,475, which issued to Trinh et al. On September 23, 1997. The entire disclosure of the Trinh patent is incorporated herein by reference.
  • compositions of the present invention can optionally contain ingredients including, solution phase stabilizers, chelating agents, antistatic agents, colorants, especially bluing agents, antioxidants, and mixtures thereof.
  • the total level of optional ingredients is low, preferably less than about 8.0%, more preferably less than about 5.0%, and even more preferably less than about 3.0%, by weight of the usage composition.
  • Solution phase stabilizers include, alkali metal salts, for example, NaCl, CaCl2, MgCb., KC1, KSO4, and they are added to modify viscosity as well as to stabilize the solution. These optional ingredients exclude the other ingredients specifically mentioned hereinbefore.
  • Colorant Colorants and dyes can be optionally added to the present compositions for visual appeal and performance impression. When colorants are used, they are used at extremely low levels to avoid fabric staining.
  • Preferred colorants for use in the present compositions are highly water-soluble dyes, e.g., Liquitint® dyes available from Milliken Chemical Co.
  • Non-limiting examples of suitable dyes are, Liquitint Blue HP®, Liquitint Blue 65®, Liquitint Patent Blue®, Liquitint Royal Blue®, Liquitint Experimental Yellow 8949-43®, Liquitint Green HMC®, Liquitint Yellow II®, and mixtures thereof, preferably Liquitint Blue HP®, Liquitint Blue 65®, Liquitint Patent Blue®, Liquitint Royal Blue®, Liquitint Experimental Yellow 8949-43®, and mixtures thereof, preferably Liquitint Blue HP®, Liquitint Blue 65®, Liquitint Patent Blue®, Liquitint Royal Blue®, Liquitint Experimental Yellow 8949-43®, and mixtures thereof.
  • solubilized, water-soluble, antimicrobial preservative can be added to the compositions.
  • solubilized, water-soluble, antimicrobial preservative which is effective for inhibiting or regulating microbial growth in order to increase storage stability of the preferably clear, aqueous allergen neutralization compositions of this invention.
  • a broad spectrum preservative e.g., one that is effective on both bacteria (both gram positive and gram negative) and fungi.
  • a limited spectrum preservative e.g., one that is only effective on a single group of microorganisms, e.g., fungi, can be used in combination with a broad spectrum preservative or other limited spectrum preservatives with complimentary and/or supplementary activity.
  • a mixture of broad spectrum preservatives can also be used, hi some cases where a specific group of microbial contaminants is problematic (such as Gram negatives), aminocarboxylate chelators may be used alone or as potentiators in conjunction with other preservatives.
  • chelators which include, e.g., ethylenediaminetetraacetic acid (EDTA), hydroxyethylenediaminetriacetic acid, diethylenetriaminepentaacetic acid, and other aminocarboxylate chelators, and mixtures thereof, and their salts, and mixtures thereof, can increase preservative effectiveness against Gram-negative bacteria, especially Pseudomonas species.
  • Antimicrobial preservatives useful in the present invention include biocidal compounds, i.e., substances that kill microorganisms, or biostatic compounds, i.e., substances that inhibit and/or regulate the growth of microorganisms.
  • Preferred antimicrobial preservatives are those that are water-soluble and are effective at low levels.
  • Water-soluble preservatives useful in the present invention are those that have a solubility in water of at least about 0.3 g per 100 ml of water, i.e., greater than about 0.3% at room temperature, preferably greater than about 0.5% at room temperature.
  • the water-soluble antimicrobial preservative in the present invention is included at an effective amount.
  • effective amount means a level sufficient to prevent spoilage, or prevent growth of inadvertently added microorganisms, for a specific period of time.
  • the preservative is not being used to kill microorganisms on the surface onto which the composition is deposited in order to eliminate odors produced by microorganisms. Instead, it is preferably being used to prevent spoilage of the allergen neutralization composition in order to increase the shelf- life of the composition.
  • Preferred levels of preservative are from about 0.0001% to about 0.5%, more preferably from about 0.0002% to about 0.2%, most preferably from about 0.0003% to about 0.1%, by weight of the usage composition.
  • the preservative can be any organic preservative material which will not cause damage to fabric appearance, e.g., discoloration, coloration, bleaching.
  • Preferred water- soluble preservatives include organic sulfur compounds, halogenated compounds, cyclic organic nitrogen compounds, low molecular weight aldehydes, quaternary ammonium compounds, dehydroacetic acid, phenyl and phenolic compounds, and mixtures thereof.
  • Anti-Oxidant The compositions of the present invention can optionally comprise anti-oxidants. The level of anti-oxidants can vary widely depending upon the end use • of the composition. When present, the compositions will typically comprise from about 0.01% to about 10%, more typically from about 0.1% to about 5%, by weight, of anti-oxidants.
  • Preferred anti-oxidants herein are selected from the group consisting of D- isoascorbic acid, Dibutyl hydroxy toluene (BHT), dl-alpha-tocophenol, n-dodecyl gallate, styrenated phenol, 4, 4'-butylidene bis (6-ter-butyl-3-methylpheno), 4,4'-thio bis (6-tert- butyl-3-methylphenol), 1,1-bis (4-hydroxyphenyl)cyclohexane, 2,2,thio (diethyl bis 3,3,5- di-t-butyl-4-hydroxyphenyl) propionate, hexane-l,6-diamine, N, N'-bis (-2,2,6,6,- tetramethyl-4-diperidinyl), and mixture therof
  • compositions of the present invention can also be used in an article of manufacture comprising said composition plus a spray dispenser.
  • a spray dispenser When the commercial embodiment of the article of manufacture is used, it is optional, but preferable, to include the preservative.
  • the article of manufacture herein comprises a spray dispenser.
  • the allergen neutralization composition is placed into a spray dispenser in order to be distributed onto fabrics or other surfaces.
  • the spray dispenser is preferably any of the manually activated means for producing a spray of liquid droplets as is known in the art, e.g. trigger-type, pump-type, non-aerosol self-pressurized, and aerosol-type spray means.
  • the spray dispenser herein does not normally include those that will substantially foam the allergen neutralization composition. It has been found that the performance is increased by providing smaller particle droplets.
  • the Sauter mean particle diameter is from about 10 ⁇ m to about 120 ⁇ m, more preferably, from about 20 ⁇ m to about 100 ⁇ m.
  • the spray dispenser can be an aerosol dispenser.
  • An aerosol dispenser comprises a container which can be constructed of any of the conventional materials employed in fabricating aerosol containers.
  • the dispenser must be capable of withstanding internal pressure in the range of from about 20 to about 110 p.s.i.g., more preferably from about 20 to about 70 p.s.i.g.
  • One important requirement concerning the dispenser is that it be provided with a valve member which will permit the allergen neutralization composition contained in the dispenser to be dispensed in the form of a spray of very fine, or finely divided, particles or droplets.
  • the aerosol dispenser utilizes a pressurized sealed container from which the allergen neutralization composition is dispensed through a special actuator/valve assembly under pressure.
  • the aerosol dispenser is pressurized by incorporating therein a gaseous component generally known as a propellant.
  • a gaseous component generally known as a propellant.
  • a propellant e.g., gaseous hydrocarbons such as isobutane, and mixed halogenated hydrocarbons, which are not preferred.
  • Halogenated hydrocarbon propellants such as chlorofluoro hydrocarbons have been alleged to contribute to environmental problems.
  • Preferred propellants are compressed air, nitrogen, inert gases, carbon dioxide, etc.
  • the spray dispenser can be a self-pressurized non-aerosol container having a convoluted liner and an elastomeric sleeve.
  • Said self-pressurized dispenser comprises a liner/sleeve assembly containing a thin, flexible radially expandable convoluted plastic liner of from about 0.010 to about 0.020 inch thick, inside an essentially cylindrical elastomeric sleeve.
  • the liner/sleeve is capable of holding a substantial quantity of odor-absorbing fluid product and of causing said product to be dispensed.
  • FIG. 1 Another type of aerosol spray dispenser is one wherein a barrier separates the odor absorbing composition from the propellant (preferably compressed air or nitrogen), as disclosed in U.S. Pat. No. 4,260,110, issued April 7, 1981, and incorporated herein by reference.
  • a dispenser is available from EP Spray Systems, East Hanover, New Jersey.
  • the spray dispenser is a non-aerosol, manually activated, pump- spray dispenser.
  • Said pump-spray dispenser comprises a container and a pump mechanism which securely screws or snaps onto the container.
  • the container comprises a vessel for containing the aqueous odor-absorbing composition to be dispensed.
  • the pump mechanism comprises a pump chamber of substantially fixed volume, having an opening at the inner end thereof.
  • a pump stem having a piston on the end thereof disposed for reciprocal motion in the pump chamber.
  • the pump stem has a passageway there through with a dispensing outlet at the outer end of the passageway and an axial inlet port located inwardly thereof.
  • the container and the pump mechanism can be constructed of any conventional material employed in fabricating pump-spray dispensers, including, but not limited to: polyethylene; polypropylene; polyethyleneterephthalate; blends of polyethylene, vinyl acetate, and rubber elastomer.
  • a preferred container is made of clear, e.g., polyethylene terephthalate. Other materials can include stainless steel.
  • the spray dispenser is a manually activated trigger-spray dispenser.
  • Said trigger-spray dispenser comprises a container and a trigger both of which can be constructed of any of the conventional material employed in fabricating trigger- spray dispensers, including, but not limited to: polyethylene; polypropylene; polyacetal; polycarbonate; polyethyleneterephthalate; polyvinyl chloride; polystyrene; blends of polyethylene, vinyl acetate, and rubber elastomer. Other materials can include stainless steel and glass.
  • a preferred container is made of clear, e.g. polyethylene terephthalate.
  • the trigger-spray dispenser does not incorporate a propellant gas into the odor-absorbing composition, and preferably it does not include those that will foam the odor-absorbing composition.
  • the trigger-spray dispenser herein is typically one which acts upon a discrete amount of the odor-absorbing composition itself, typically by means of a piston or a collapsing bellows that displaces the composition through a nozzle to create a spray of thin liquid.
  • the trigger-spray dispenser typically comprises a pump chamber having either a piston or bellows which is movable through a limited stroke response to the trigger for varying the volume of said pump chamber. This pump chamber or bellows chamber collects and holds the product for dispensing.
  • the trigger spray dispenser typically has an outlet check valve for blocking communication and flow of fluid through the nozzle and is responsive to the pressure inside the chamber.
  • the trigger As the trigger is compressed, it acts on the fluid in the chamber and the spring, increasing the pressure on the fluid.
  • the bellows spray dispenser As the bellows is compressed, the pressure increases on the fluid.
  • the increase in fluid pressure in either trigger spray dispenser acts to open the top outlet check valve.
  • the top valve allows the product to be forced through the swirl chamber and out the nozzle to form a discharge pattern.
  • An adjustable nozzle cap can be used to vary the pattern of the fluid dispensed.
  • a broad array of trigger sprayers or finger pump sprayers are suitable for use with the compositions of this invention. These are readily available from suppliers such as Calmar, Inc., City of Industry, California; CSI (Continental Sprayers, Inc.), St. Peters, Missouri; Berry Plastics Corp., Evansville, Indiana, a distributor of Guala® sprayers; or Seaquest Dispensing, Cary, Illinois.
  • the preferred trigger sprayers are the blue inserted Guala® sprayer, available from Berry Plastics Corp., or the Calmar TS800-1A® , TS1300®, and TS-800-2®, available from Calmar Inc., because of the fine uniform spray characteristics, spray volume, and pattern size. More preferred are sprayers with precompression features and finer spray characteristics and even distribution, such as Yoshino sprayers from Japan.
  • Any suitable bottle or container can be used with the trigger sprayer, the preferred bottle is a 17 fl-oz. bottle (about 500 ml) of good ergonomics similar in shape to the Cinch® bottle.
  • It can be made of any materials such as high density polyethylene, polypropylene, polyvinyl chloride, polystyrene, polyethylene terephthalate, glass, or any other material that forms bottles.
  • it is made of high density polyethylene or clear polyethylene terephthalate.
  • a finger pump can be used with canister or cylindrical bottle.
  • the preferred pump for this application is the cylindrical Euromist ⁇ ® from Seaquest Dispensing. More preferred are those with precompression features.
  • the present compositions can be used by distributing, e.g., by placing the allergen neutralizing composition into a dispensing means, preferably a spray dispenser and spraying an effective amount onto the desired surface or article.
  • An effective amount is defined herein as an amount to neutralize at least about 50%, preferably at least about 60%, more preferably at least about 80%, and most preferably at least about 90% of the allergens on the surface or article that is sprayed.
  • the amount of allergen that is neutralized can be measured by the Elisa test defined below.
  • the delivery mechanism should be controlled such that a pool of liquid is not created on the article or surface and so that when dry there is no visual deposit readily discernible. Distribution can be achieved by using a spray device, a roller, a pad, etc.
  • the present invention encompasses the method of spraying an effective amount of allergen neutralizing composition onto household surfaces.
  • household surfaces are selected from the group consisting of countertops, cabinets, walls, floors, bathroom surfaces and kitchen surfaces.
  • the present invention encompasses the method of spraying a mist of an effective amount of allergen neutralizing composition onto fabric and/or fabric articles.
  • the fabric and/or fabric articles include, but are not limited to, clothes, curtains, drapes, upholstered furniture, carpeting, bed linens, bath linens, tablecloths, sleeping bags, tents, car interior, etc.
  • the present invention relates to the method of spraying a mist of an effective amount of allergen neutralizing composition onto cat litter, pet bedding and pet houses.
  • allergen neutralization compositions according to the present invention, and standardized methods for measuring Dust Control, friction, efficacy and fabric coloration of the present compositions.
  • This test method measures and quantifies the amount of dust retained on a fabric surface after treatment with a test composition.
  • the test method is conducted on a 30cm x 30cm swatch of white cotton muslim, 86/14 blend with polyester. On the fabric swatch, spread evenly 2 grams of vacuum cleaner dust that has been sieved through a 37 micron filter. Spray approximately lOg of the test composition on the fabric swatch with a standard sprayer to cover the surface completely.
  • the bottle of test composition should be weighed before and after spraying to insure the delivery of lOg of solution, but it is understood that a small portion of the spray will be lost as "overspray". Weigh the fabric and allow it to dry overnight under controlled humidity and temperature.
  • Preferred allergen neutralization compositions according to the present invention retain more than about 30%, preferably more than about 35%, and even more preferably more than about 40%, by weight, of the starting dust amount.
  • This test measures the "slipperiness" of a fabric sprayed with a test composition.
  • This test is a standardized test well known to the textile industry.
  • the allergen neutralization compositions of the present invention have an average MIU value of less than 3.4, preferably less than 3.2, more preferably less than about 3.0 as measured by the Friction Coefficient Analysis method.
  • Method Spray approximately 3 grams of the test composition onto a 10cm x 10cm fleece swatch (100% polyester). Dry the swatch at room temperature. Measure the friction on the fabric with a KES-SE-STP Friction Tester (available from Kato Tech., Kyoto, Japan) under the conditions described below.
  • Measurement 20 mm while sensor moves 30 mm; three times each for vertically and horizontally
  • the efficacy of an allergen neutralization composition can be determined by the ELISA protocol.
  • Enzyme-linked immunosorbent assay (“ELISA") is a highly sensitive assay technique for detection and measurement of antigens or antibodies in solution.
  • the assay uses enzyme-linked antigens or antibodies to amplify an antigen-antibody reaction.
  • a single enzyme-linked antibody-antigen complex can convert orders of magnitude more of colorless substrate molecules into detectable colored products, thus considerably amplifying the original antigen-antibody reaction.
  • the antigen or antibody is adsorbed onto the surface of the well of a microtiter plate, and all the relevant reactions take place in solution inside the well. While the following protocol will be easily understood by those skilled in the art, for a more detailed explanation please see Konishi, E.
  • At least two samples are prepared.
  • One sample contains only distilled water and samples of one or more allergen neutralization compositions containing the allergen neutralization active, for example ZnC12, tannin, etc.
  • the samples are all treated according to the same protocol, and the distilled water sample is used as the control. All samples are prepared as follows:
  • Each well of a microplate is coated at 4°C overnight with 100 ⁇ l of Der f 2 monoclonal antibody (clone 15E11, from Asahi Breweries., AB-A-4) at a protein concentration of 2 ⁇ g per ml of Phosphate Buffer Saline (PBS), pH 7.4 containing 0.1% sodium azide.
  • PBS Phosphate Buffer Saline
  • the monoclonal antibody is discarded and the plate is incubated with 100 ⁇ l of 1% BSA PBS containing 0.1 % sodium azide for 1 hour.
  • the plate is washed 3 times with PBS containing 0.05% Tween 20 (PBS-T). 100 ⁇ l of an allergen sample is added and incubated for 1 hour at 37°C.
  • the wells are incubated with 100 ⁇ l of o-phenylene diamine at 2.0 mg/ml of 0.1M phosphate buffer (pH 6.2) containing 0.03% H 2 O 2 .
  • the enzyme reaction is terminated by adding 50 ⁇ l of 2 M H 2 SO 4 .
  • the absorbance of the sample is read at 490 run with a cell length of 1 cm.
  • the absorbance reading is directly proportional to the quantity of Der f 2 bound and the values calculated from the respective standard curve (Optical Density, or absorbance range is 0.001 to 3.6).
  • the absorbance reading for the control (water) is considered as 0% allergen neutralization (100% of the Der f 2 remaining) and an absorbance reading of 0 is considered 100% allergen neutralization (0% of the Der f 2 remaining).
  • the absorbance of the active containg sample(s) is then normalized based on these two end points.
  • the allergen neutralization compositions of the present invention neutralize at least about 50%, preferably at least about 60%, more preferably at least about 80% and most preferably at least about 90% of allergen containing proteins as measured by the ELISA test protocol.
  • Table HI illustrates that the "effective amount" of the metal ion will vary depending on the metal and its associated anion.
  • concentration of 1.4% was an arbitrary selection, but one can see that except for FeSO4, all of the metals remove more than 50% of the allergen.
  • the effective amount to remove 50% of allergens for FeSO4 is greater than 1.4%, while the effective amount for the same removal rate for SnCi2 is substantially less than 1.4%.
  • the effective amount will vary based on the desired allergen removal amount. For example, if 80% removal is necessary, then the effective amount of ZnCi2 will be slightly greater than 1.4%, and the effective amount for SnCi2 will be about 1.4%.
  • Those skilled in the art will be able to determine the effective amount for different metal ions with various anions without undue experimentation using the teachings and Examples herein.
  • a standard Hunter Color Meter Analysis is performed on fabrics that are treated with sample allergen neutralization compositions. As was described above, it is desirable that the present compositions do not stain or discolor common household surfaces such as fabrics, for example, bed covers, floor coverings, and curtains, and hard surfaces, for example, counter tops, furniture, doors and walls.
  • a standardized test is given below that tests the propensity for a given sample composition to stain a test fabric. Acceptable performance for this test method will generally mean a composition can be used on household surfaces without fear of substantial discoloration.
  • the allergen neutralization compositions of the present invention yield a ⁇ E value of less than about 3.5, preferably, less than about 3.0, and more preferably less than about 1.0 as measured by Fabric Color Evaluation method.
  • Sample Preparation Spray approximately 15 grams of a sample composition on a 20x20 cm cotton knit (100%) cotton) fabric swatch. Spray approximately 15 grams of distilled water on a similar 20x20 cm fabric swatch. Dry the fabric swatches near a glass-window to expose them to sun light. Leave the swatches near the window for 2-3 days after they have dried. The sun light accelerates the color development.
  • the treated and non-treated fabric swatches are ready for analysis by the method defined below.
  • Instrument The instrument used in this method is a ColorQUEST 45/0 from Hunter
  • L measures lightness and varies from 100 (for perfect white) to zero (for black); "a” measures the intensity of red (plus), gray (zero) and green (minus); “b” measures the intensity of yellow (plus), gray (zero) and blue (minus).
  • ⁇ E is the difference of "L a b” values from the standard. The Hunter Lab total color difference ( ⁇ E) is calculated as follows:
  • ⁇ E ⁇ L + ⁇ a + ⁇ b
  • ⁇ L SMP -L S TD
  • ⁇ a a S MP - a ST D
  • ⁇ b b S MP - DSTD •
  • Two solutions containing Tannic acid and Zinc chloride are prepared and a third solution containing only Zinc chloride is prepared.
  • the concentration of Tannic acid (from Kanto Chemicals, Japan) is 0.025%, 0.05% and 0%, by weight in the three solutions.
  • the concentration of Zinc chloride (from Wako Pure Chemicals, Japan) is 0.5%, by weight in all three samples.
  • the three samples are each split into two pairs of six equal samples.
  • the pH of each solution is adjusted to the desired pH of about 3.6.
  • One sample from each pair is adjusted with l lOmM citrate buffer (citric acid and sodium citrate), and one sample from each pair is adjusted with 0.4mM HCl, as shown in Table rV below.
  • Six sample swatches are prepared according to the method given above using the six different compositions. The colors for each swatch, and a control swatch, are measured and the results are shown in the following Table:
  • Table V contains sample compositions according to the present invention.
  • MC Methyl Cellulose 2
  • CTFA PQ 6 Cosmetic Toiletry Fragrances Association polyquatemium 6 Buffer is HCl, Citric acid, or mixtures of each
  • Diethylene Glycol is used to neutralize the odor associated with ethanol 5
  • Wetting agent is Silwet L-7600 or Coco K3 (a cationic surfactant)

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Abstract

La présente invention concerne des compositions de neutralisation d'allergènes qui retiennent au moins 30 % environ des particules de poussière telles que mesurées par un test de contrôle des poussières et qui possèdent une valeur moyenne de coefficient de frottement (MIU) inférieure à 3,4. Les compositions contiennent de préférence un polymère filmogène destiné à maîtriser la poussière tout en préservant la sensation de toucher lisse sur la surface traitée. Les compositions de neutralisation d'allergènes de l'invention sont destinées à être utilisées sur des objets inanimés et elles peuvent être pulvérisées. Les compositions de l'invention contiennent de préférence des composés qui dénaturent l'allergène comme, par exemple, un ion métallique neutralisateur d'allergie, des composés polyphénols, du peroxyde d'hydrogène, de l'acide salicylique, de l'acide citrique, de l'acide lactique, de l'acide glycolique et des mélanges de ces derniers. En maîtrisant les particules de poussière contenant des protéines allergènes, les compositions de neutralisation des allergènes de l'invention s'avèrent d'une excellente efficacité contre divers allergènes et, en particulier, contre les allergènes associés aux acariens détriticoles et autres allergènes courants tels que les poils de chat, le pollen et analogues.
PCT/US2000/027018 2000-09-29 2000-09-29 Compositions de neutralisation d'allergenes WO2002028179A1 (fr)

Priority Applications (12)

Application Number Priority Date Filing Date Title
CNA008199388A CN1469709A (zh) 2000-09-29 2000-09-29 变应原中和组合物
EP00967195A EP1322154A1 (fr) 2000-09-29 2000-09-29 Compositions de neutralisation d'allergenes
JP2002531816A JP2004510841A (ja) 2000-09-29 2000-09-29 アレルゲン中和組成物
CA002425068A CA2425068A1 (fr) 2000-09-29 2000-09-29 Compositions de neutralisation d'allergenes
CN00819937.XA CN1454053A (zh) 2000-09-29 2000-09-29 变应原中和组合物
AU2000277428A AU2000277428A1 (en) 2000-09-29 2000-09-29 Allergen neutralization compositions
PCT/US2000/027018 WO2002028179A1 (fr) 2000-09-29 2000-09-29 Compositions de neutralisation d'allergenes
CA002357828A CA2357828A1 (fr) 2000-09-29 2001-09-27 Compositions de neutralisation d'allergenes renfermant du sulfate d'aluminium et un element de protection en etoffe
CA002357839A CA2357839A1 (fr) 2000-09-29 2001-09-27 Compositions de neutralisation d'allergenes qui renferment un sulfate d'aluminium et ne restent pas collantes lors de leur pulverisation
ARP010104587A AR030814A1 (es) 2000-09-29 2001-09-28 Composicion de neutralizacion de alergeno
AU77324/01A AU7732401A (en) 2000-09-29 2001-09-28 Allergen neutralization compositions that contain aluminum sulfate and are not sticky when sprayed
US10/397,732 US20030203035A1 (en) 2000-09-29 2003-03-26 Allergen neutralization compositions

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PCT/US2000/027018 WO2002028179A1 (fr) 2000-09-29 2000-09-29 Compositions de neutralisation d'allergenes

Related Child Applications (1)

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US10/397,732 Continuation US20030203035A1 (en) 2000-09-29 2003-03-26 Allergen neutralization compositions

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WO2002028179A1 true WO2002028179A1 (fr) 2002-04-11

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EP (1) EP1322154A1 (fr)
JP (1) JP2004510841A (fr)
CN (2) CN1454053A (fr)
AR (1) AR030814A1 (fr)
AU (1) AU2000277428A1 (fr)
CA (1) CA2425068A1 (fr)
WO (1) WO2002028179A1 (fr)

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JP2004189761A (ja) * 2002-12-06 2004-07-08 Kao Corp アレルゲン除去剤
JP2005104847A (ja) * 2003-09-26 2005-04-21 Fumakilla Ltd アレルゲン除去剤
WO2005037980A1 (fr) * 2003-10-22 2005-04-28 Kao Corporation Depresseur d'allergene et technique de depression
JP2005145950A (ja) * 2003-10-22 2005-06-09 Kao Corp アレルゲン低減化方法
EP1542535A1 (fr) * 2002-08-28 2005-06-22 KAPITZ, Carl-Heinz Utilisation de proteases pour la decomposition d'allergenes
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US7482385B2 (en) 2002-12-20 2009-01-27 Envirospecialists, Inc. Wetting agent formulations for hydrotropic moisture control of substrates and dispersed phases
US7482386B2 (en) * 2002-12-20 2009-01-27 Envirospecialists, Inc. Hydrotropic additive to water for dust control
US8133991B2 (en) 2002-07-03 2012-03-13 Kao Corporation Allergen inactivating agent
DE102012219954A1 (de) 2012-10-31 2014-04-30 Henkel Ag & Co. Kgaa Polymere zur allergen-repulsiven Ausrüstung
DE102012219948A1 (de) 2012-10-31 2014-04-30 Henkel Ag & Co. Kgaa Polymere zur allergen-adhäsiven Ausrüstung
US10226543B2 (en) * 2005-03-25 2019-03-12 Fumakilla Limited Allergen inactivator
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BR112020001162B1 (pt) * 2017-07-18 2023-11-21 Before Brands, Inc Método para fabricar uma composição alergênica misturada

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Cited By (22)

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Publication number Priority date Publication date Assignee Title
US8133991B2 (en) 2002-07-03 2012-03-13 Kao Corporation Allergen inactivating agent
WO2004005423A1 (fr) * 2002-07-03 2004-01-15 Kao Corporation Inactivateur d'allergenes
EP1728431A1 (fr) * 2002-08-28 2006-12-06 KAPITZ, Carl-Heinz Utilisation de protéases pour la décomposition d'allergenes
EP1733619A1 (fr) * 2002-08-28 2006-12-20 KAPITZ, Carl-Heinz Utilisation d'un agent actif pour la dénaturation de la kératine des poils d'animaux
EP1542535A1 (fr) * 2002-08-28 2005-06-22 KAPITZ, Carl-Heinz Utilisation de proteases pour la decomposition d'allergenes
JP2004189761A (ja) * 2002-12-06 2004-07-08 Kao Corp アレルゲン除去剤
US7482385B2 (en) 2002-12-20 2009-01-27 Envirospecialists, Inc. Wetting agent formulations for hydrotropic moisture control of substrates and dispersed phases
US7482386B2 (en) * 2002-12-20 2009-01-27 Envirospecialists, Inc. Hydrotropic additive to water for dust control
JP2005104847A (ja) * 2003-09-26 2005-04-21 Fumakilla Ltd アレルゲン除去剤
US8658630B2 (en) 2003-10-22 2014-02-25 Kao Corporation Allergen depressant and depression method
WO2005037980A1 (fr) * 2003-10-22 2005-04-28 Kao Corporation Depresseur d'allergene et technique de depression
JP2005145950A (ja) * 2003-10-22 2005-06-09 Kao Corp アレルゲン低減化方法
US10226543B2 (en) * 2005-03-25 2019-03-12 Fumakilla Limited Allergen inactivator
WO2008013444A1 (fr) * 2006-07-27 2008-01-31 Cleandust Bv I.O. Procédé et dispositif pour empêcher la formation de poussière au cours d'un travail de démolition
NL2000161C2 (nl) * 2006-07-27 2008-01-29 Martinus Hogenes Werkwijze en inrichting voor het tegengaan van stofvorming bij destructiewerkzaamheden.
US10252210B2 (en) 2011-05-10 2019-04-09 The Procter & Gamble Company Methods for reducing particulates in the air
DE102012219954A1 (de) 2012-10-31 2014-04-30 Henkel Ag & Co. Kgaa Polymere zur allergen-repulsiven Ausrüstung
DE102012219948A1 (de) 2012-10-31 2014-04-30 Henkel Ag & Co. Kgaa Polymere zur allergen-adhäsiven Ausrüstung
EP2727985A2 (fr) 2012-10-31 2014-05-07 Henkel AG & Co. KGaA Polymères pour équipement répulsif pour les allergènes
EP2727986A2 (fr) 2012-10-31 2014-05-07 Henkel AG & Co. KGaA Polymères pour équipement adhésif pour les allergènes
EP2727986A3 (fr) * 2012-10-31 2017-08-16 Henkel AG & Co. KGaA Polymères pour équipement adhésif pour les allergènes
EP2727985A3 (fr) * 2012-10-31 2017-08-23 Henkel AG & Co. KGaA Polymères pour équipement répulsif pour les allergènes

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EP1322154A1 (fr) 2003-07-02
CA2425068A1 (fr) 2002-04-11
CN1454053A (zh) 2003-11-05
AR030814A1 (es) 2003-09-03
CN1469709A (zh) 2004-01-21
JP2004510841A (ja) 2004-04-08

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