WO2004000983A1 - A hand cleansing agent comprising polystyrene sulfonate salts - Google Patents

A hand cleansing agent comprising polystyrene sulfonate salts Download PDF

Info

Publication number
WO2004000983A1
WO2004000983A1 PCT/KR2003/001193 KR0301193W WO2004000983A1 WO 2004000983 A1 WO2004000983 A1 WO 2004000983A1 KR 0301193 W KR0301193 W KR 0301193W WO 2004000983 A1 WO2004000983 A1 WO 2004000983A1
Authority
WO
WIPO (PCT)
Prior art keywords
hand cleaner
weight
hand
polystyrene sulfonate
sulfonate salts
Prior art date
Application number
PCT/KR2003/001193
Other languages
French (fr)
Inventor
Moon-Sig Kang
Gyou-Jin Cho
Original Assignee
Paru Co., Ltd.
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
Application filed by Paru Co., Ltd. filed Critical Paru Co., Ltd.
Priority to AU2003240033A priority Critical patent/AU2003240033A1/en
Publication of WO2004000983A1 publication Critical patent/WO2004000983A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/34Organic compounds containing sulfur
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/378(Co)polymerised monomers containing sulfur, e.g. sulfonate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8105Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • A61K8/8117Homopolymers or copolymers of aromatic olefines, e.g. polystyrene; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/26Organic compounds containing oxygen
    • C11D7/261Alcohols; Phenols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/32Organic compounds containing nitrogen
    • C11D7/3218Alkanolamines or alkanolimines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/32Organic compounds containing nitrogen
    • C11D7/329Carbohydrate or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/40Products in which the composition is not well defined

Definitions

  • the present invention relates to a hand cleaner containing polystyrene sulfonate salts.
  • the infection of the human body, particularly the skin, with microbes, and the contamination of foods with microorganisms, are mainly mediated by contact with other persons contaminated with organisms, as well as environmental factors, contaminated food itself, and raw materials of foods.
  • the cleaning and sterilization of hand are more important than everything else.
  • Korean patent laid-open publication No. 2000-64060 discloses a volatile hand cleaner containing ethanol and PCMX (p-chloro-m-xylenol) as antibacterial and ger icidal components.
  • Korean patent laid-open publication No. 2000-64060 discloses a volatile hand cleaner containing ethanol and PCMX (p-chloro-m-xylenol) as antibacterial and ger icidal components.
  • 2001-44514 discloses a gel-type hand cleaner containing ethanol, triclosan and
  • Korean patent laid-open publication No. 2001-110625 discloses a lotion-type hand cleaner prepared by uniformly mixing ethanol, isopropyl alcohol, benzalkonium chloride and a moisturizer, etc.
  • Such hand cleaners can maintain their antibacterial and germicidal activities by alcohol, tnclosan and PCMX, but upon long-term application, shows skin irritation and has a high possibility of causing inflammation and the like.
  • an object of the present invention is to provide a hand cleaner, which has excellent antibacterial and germicidal activities and is harmless to the human body even upon long-term application.
  • the present invention provides a hand cleaner containing polystyrene sulfonate salts.
  • the hand cleaner according to the present invention contains polystyrene sulfonate salts at the amount of 0.03-0.05% by weight relative to the hand cleaner.
  • the hand cleaner according to the present invention comprises ethanol, isopropyl alcohol, carbomer, distilled water and polystyrene sulfonate salts.
  • the hand cleaner according to the present invention comprises 60-80% by weight of ethanol, 1.3-3.0% by weight of isopropyl alcohol, 0.2-0.6% by weight of carbomer, 16-35% by weight of distilled water and 0.03-0.05%o by weight of polystyrene sulfonate salts.
  • ethanol 1.3-3.0% by weight of isopropyl alcohol
  • carbomer 1.3-3.0% by weight of carbomer
  • 16-35% by weight of distilled water 0.03-0.05%o by weight of polystyrene sulfonate salts.
  • polystyrene sulfonate salts acts as an antibacterial agent of immobilizing and killing bacteria.
  • Polystyrene sulfonate salts which is used in the present invention, is prepared as described below with reference to a method described in POLYMER
  • polystyrene is added to methylene chloride and refluxed. When the polymer is dissolved, it is reacted with sulfuric acid and acetic anhydride. At the end of the reaction, the solution is dropped in distilled water to give a polymer, which is then dried in a vacuum oven. The dried material is dissolved in ethanol, filtered, added with sodium hydrogen carbonate, filtered, and then dried to give polystyrene sulfonate salts.
  • the content of polystyrene sulfonate salts in the hand cleaner according to the present invention is preferably 0.03-0.05% by weight, and most preferably 0.047% by weight.
  • ethanol has germicidal and evaporating actions.
  • the ethanol content in the hand cleaner where ethanol has the most excellent germicidal activity is 60-80% by weight.
  • ethanol content is less than 60% by weight or more than 80% by weight, ethanol will have little or no sterilizing powder or germicidal effect.
  • isopropyl alcohol is used for the purpose of supplementing or reinforcing the germicidal action of ethanol.
  • the content of isopropyl alcohol in the hand cleaner according to the present invention is 1.3-3.0%) by weight. If isopropyl alcohol is used at an amount larger than 3.0%> by weight, the resulting hand cleaner will give persons some rejection due to a specific odor of isopropyl alcohol, but there will be no significant change in physical properties of the hand cleaner.
  • carbomer is a gelling agent and includes carbomers 938, 940 and 941, etc.
  • Carbomer 940 is most preferable for use in the present invention. Due to a difference in molecular weight of such carbomers, the viscosity of the hand cleaner will vary even when the carbomers are used at the same amount. Even when carbomer 941 is used at increased amount, the viscosity of the hand cleaner will not be increased. Generally, the higher the amount of carbomer, the viscosity of the hand cleaner is increased, and the lower the amount of carbomer, the viscosity of the hand cleaner is reduced.
  • the preferred content of carbomer in the hand cleaner of the present invention is 0.2-0.6% by weight.
  • distilled water plays the greatest role in gelling of carbomer.
  • the preferred content of distilled water in the hand cleaner of the present invention is 16-35% by weight. If distilled water is used at an amount larger than 35 > by weight, the concentration of the gel will be reduced, whereas if it is used at an amount lower than 16%> by weight, the concentration of the gel will be increased.
  • the viscosity of the resulting gel can be controlled by adjusting the amounts of distilled water and carbomer.
  • the hand cleaner of the present invention can contain a curing accelerator, a skin moisturizer and a nutrient.
  • the curing accelerator serves to accelerator curing and at the same time to neutralize the carboxylic group of acrylic acid in carbomer.
  • Preferred examples of the curing accelerator, which is used in the present invention include amine compounds, such as diisopropanolamine, aminomethylpropanol, aminomethylpropanediol, triethanolamine and the like. Among such substances, diisopropanolamine is most preferably used.
  • the curing accelerator has some connection with the amount of carbomer, and the preferred content of the curing accelerator in the hand cleaner of the present invention is 0.2-1.7%) by weight.
  • the resulting hand cleaner will tend to have acidity due to a reduction in pH, whereas it is used at an amount larger than 1.7%» by weight, the resulting hand cleaner will have basicity and thus will be slick upon application on hand.
  • the skin moisturizer If the skin moisturizer is used at reduced amount, alcohol will be volatilized from hands after the application of the hand cleaner on hands, so that hands will somewhat roughen. On the other hand, if the skin moisturizer is used at excessive amount, some moisture will remain on hands after the application of the hand cleaner on hands, thereby causing sticky feeling on hands.
  • the skin moisturizer which is used in the present invention, include isopropyl myristate, propylene glycol, silicon derivatives, aloe vera, sorbitol, and a mixture thereof.
  • the preferred content of the skin moisturizer in the hand cleaner of the present invention is 0.5-4.0% by weight.
  • the nutrient used in the present invention consists of oligosaccharide and chitosan.
  • the preferred content of the nutrient in the hand cleaner of the present invention is 0.001-0.01%) by weight.
  • the hand cleaner formulation of the present invention is prepared according to the conventional method, and can be prepared in form of a gel, lotion, cream, or mineral oil-type formulation by addition of components, such as an antioxidant, perfume, a softening agent, an antimicrobial agent and the like.
  • the hand cleaner of the present invention can be prepared in form of various products, such as portable products, desk products, wall products, and body washers.
  • FIG. 1 shows bacterial colony count after culturing a bacterial sample, which was taken from hand before washing the hand;
  • FIG. 2 shows bacterial colony count after culturing a bacterial sample, which was taken from hand just after washing the hand with water and soap and toweling the washed hand;
  • FIG. 3 shows bacterial colony count after culturing a bacterial sample, which was taken from hand after cleaning the hand with a cleaner prepared in Comparative Example 1;
  • FIG. 3 shows bacterial colony count after culturing a bacterial sample, which was taken from hand after cleaning the hand with a hand cleaner prepared in Example 1. Best Mode for Carrying Out the Invention
  • a beaker was charged with 61.61 of ethanol, 0.05g of perfume, 24.33g of distilled water, 0.5g of glycerin and 0.047g of polystyrene sulfonate salts, followed by stirring at 25 °C and 3,000 rpm for 1 minute.
  • 0.5g of propylene glycol, 1.5g of isopropyl alcohol, 0.5g of isopropyl myristate, 0.004g of oligosaccharide and 0.004g of chitosan were added, and stirred for about 1 minute while adding 0.2g of diisopropanolamine. After all the components were completely dissolved, 0.22g of a pigment and 0.3g of carbomer were added, and stirred at 3,000 rpm for about 30 minutes, thereby producing a hand cleaner gel.
  • Hand cleaner gels each having a composition shown in Table 1 below were prepared in the same method as described in Example 1.
  • Cotton swabs were prepared and sterilized at 121 °C under 1 atm for 20 minutes. With the sterilized cotton swabs, bacteria were taken from hands washed according to the following conditions (l)-(4). The taken bacteria were transferred to the solid medium, and cultured overnight at 85%> humidity and 28 °C temperature. In this case, the above operation was carried out in a sterilized room such that the cotton swabs were not exposed to other bacteria.
  • the sample according to the present invention and the sample according to Comparative Examples were applied on hands, and then a change in the skin was examined by sensory evaluation.
  • 60 volunteers were divided into three groups each consisting of 20 volunteers, in which the three groups consist of a group where a hand cleaner is not used; a group where the hand cleaner of the present invention is used; and a group where the hand cleaners according to Comparative Examples are used.
  • the hand cleaners were applied on the volunteers for 20 days three times a day, and then a change in the skin was observed.
  • the hand cleaner of the present invention has excellent germicidal and antibacterial activities and is harmless to the skin.
  • the hand cleaner of the present invention has excellent germicidal and antibacterial activities, and harmless to the skin even upon long-term application.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Dermatology (AREA)
  • Detergent Compositions (AREA)
  • Cosmetics (AREA)

Abstract

The present invention relates to a hand cleaner containing polystyrene sulfonate salts. The hand cleaner comprises 60-80% by weight of ethanol, 1.3-3.0% by weight of isopropyl alcohol, 0.2-0.6% by weight of carbomer, 16-35% by weight of distilled water, and 0.03-0.05% by weight of polystyrene sulfonate salts. The hand cleaner of the present invention has excellent germicidal and antibacterial activities, and harmless to the skin even upon long-term application.

Description

A HAND CLEANSING AGENT COMPRISING POLYSTYRENE SULFONATE SALTS
Technical Field
The present invention relates to a hand cleaner containing polystyrene sulfonate salts.
Background Art
The infection of the human body, particularly the skin, with microbes, and the contamination of foods with microorganisms, are mainly mediated by contact with other persons contaminated with organisms, as well as environmental factors, contaminated food itself, and raw materials of foods. Thus, in order to prevent microbial contamination from being spread in persons engaged in the preparation of products sensitive to foods or a living body, the cleaning and sterilization of hand are more important than everything else.
Recently, a hand cleaner containing germicides or antifungals is used to minimize direct or indirect microbial infection through hand. For example, Korean patent laid-open publication No. 2000-64060 discloses a volatile hand cleaner containing ethanol and PCMX (p-chloro-m-xylenol) as antibacterial and ger icidal components. Korean patent laid-open publication No.
2001-44514 discloses a gel-type hand cleaner containing ethanol, triclosan and
PCMX, as antibacterial and germicidal components. Also, Korean patent laid-open publication No. 2001-110625 discloses a lotion-type hand cleaner prepared by uniformly mixing ethanol, isopropyl alcohol, benzalkonium chloride and a moisturizer, etc.
Such hand cleaners can maintain their antibacterial and germicidal activities by alcohol, tnclosan and PCMX, but upon long-term application, shows skin irritation and has a high possibility of causing inflammation and the like.
Thus, there is a need for the development of a hand cleaner, which has excellent antibacterial and germicidal activities, and at the same time, is harmless to the skin even upon long-term application.
Disclosure of Invention
Therefore, an object of the present invention is to provide a hand cleaner, which has excellent antibacterial and germicidal activities and is harmless to the human body even upon long-term application. The present invention provides a hand cleaner containing polystyrene sulfonate salts.
The hand cleaner according to the present invention contains polystyrene sulfonate salts at the amount of 0.03-0.05% by weight relative to the hand cleaner.
The hand cleaner according to the present invention comprises ethanol, isopropyl alcohol, carbomer, distilled water and polystyrene sulfonate salts.
The hand cleaner according to the present invention comprises 60-80% by weight of ethanol, 1.3-3.0% by weight of isopropyl alcohol, 0.2-0.6% by weight of carbomer, 16-35% by weight of distilled water and 0.03-0.05%o by weight of polystyrene sulfonate salts. Hereinafter, the hand cleaner according to the present invention will be described in detail.
Among the components forming the hand cleaner of the present invention, polystyrene sulfonate salts acts as an antibacterial agent of immobilizing and killing bacteria. Polystyrene sulfonate salts, which is used in the present invention, is prepared as described below with reference to a method described in POLYMER
ENGINEERING AND SCIENCE, 37, 1, 1997.
In a method of preparing polystyrene sulfonate salts, polystyrene is added to methylene chloride and refluxed. When the polymer is dissolved, it is reacted with sulfuric acid and acetic anhydride. At the end of the reaction, the solution is dropped in distilled water to give a polymer, which is then dried in a vacuum oven. The dried material is dissolved in ethanol, filtered, added with sodium hydrogen carbonate, filtered, and then dried to give polystyrene sulfonate salts.
The content of polystyrene sulfonate salts in the hand cleaner according to the present invention is preferably 0.03-0.05% by weight, and most preferably 0.047% by weight.
Among the components forming the hand cleaner of the present invention, ethanol has germicidal and evaporating actions. The ethanol content in the hand cleaner where ethanol has the most excellent germicidal activity is 60-80% by weight.
If the ethanol content is less than 60% by weight or more than 80% by weight, ethanol will have little or no sterilizing powder or germicidal effect.
Among the components forming the hand cleaner of the present invention, isopropyl alcohol is used for the purpose of supplementing or reinforcing the germicidal action of ethanol. The content of isopropyl alcohol in the hand cleaner according to the present invention is 1.3-3.0%) by weight. If isopropyl alcohol is used at an amount larger than 3.0%> by weight, the resulting hand cleaner will give persons some rejection due to a specific odor of isopropyl alcohol, but there will be no significant change in physical properties of the hand cleaner.
Among the components forming the hand cleaner of the present invention, carbomer is a gelling agent and includes carbomers 938, 940 and 941, etc. Carbomer 940 is most preferable for use in the present invention. Due to a difference in molecular weight of such carbomers, the viscosity of the hand cleaner will vary even when the carbomers are used at the same amount. Even when carbomer 941 is used at increased amount, the viscosity of the hand cleaner will not be increased. Generally, the higher the amount of carbomer, the viscosity of the hand cleaner is increased, and the lower the amount of carbomer, the viscosity of the hand cleaner is reduced. However, when the amount of carbomer is excessively increased as compared to the concentrations of alcohol and distilled water, the gelling time of the hand cleaner will be increased, and also the application of the hand cleaner on the hand will cause sticking and foreign substances. The preferred content of carbomer in the hand cleaner of the present invention is 0.2-0.6% by weight.
Among the components forming the hand cleaner of the present invention, distilled water plays the greatest role in gelling of carbomer. The preferred content of distilled water in the hand cleaner of the present invention is 16-35% by weight. If distilled water is used at an amount larger than 35 > by weight, the concentration of the gel will be reduced, whereas if it is used at an amount lower than 16%> by weight, the concentration of the gel will be increased. The viscosity of the resulting gel can be controlled by adjusting the amounts of distilled water and carbomer.
In addition to the essential components as described above, the hand cleaner of the present invention can contain a curing accelerator, a skin moisturizer and a nutrient.
The curing accelerator serves to accelerator curing and at the same time to neutralize the carboxylic group of acrylic acid in carbomer. Preferred examples of the curing accelerator, which is used in the present invention, include amine compounds, such as diisopropanolamine, aminomethylpropanol, aminomethylpropanediol, triethanolamine and the like. Among such substances, diisopropanolamine is most preferably used. The curing accelerator has some connection with the amount of carbomer, and the preferred content of the curing accelerator in the hand cleaner of the present invention is 0.2-1.7%) by weight. If the curing accelerator is used at an amount lower than 0.2%> by weight, the resulting hand cleaner will tend to have acidity due to a reduction in pH, whereas it is used at an amount larger than 1.7%» by weight, the resulting hand cleaner will have basicity and thus will be slick upon application on hand.
If the skin moisturizer is used at reduced amount, alcohol will be volatilized from hands after the application of the hand cleaner on hands, so that hands will somewhat roughen. On the other hand, if the skin moisturizer is used at excessive amount, some moisture will remain on hands after the application of the hand cleaner on hands, thereby causing sticky feeling on hands. Examples of the skin moisturizer, which is used in the present invention, include isopropyl myristate, propylene glycol, silicon derivatives, aloe vera, sorbitol, and a mixture thereof. The preferred content of the skin moisturizer in the hand cleaner of the present invention is 0.5-4.0% by weight. If the skin moisturizer is used at an amount smaller than 0.5%) by weight, skin moisturization will get worse rapidly, and if it is used at an amount larger than 4.0% by weight, the resulting hand cleaner will be too sticky and thus will give persons a bad feeling upon its application. The nutrient used in the present invention consists of oligosaccharide and chitosan. The preferred content of the nutrient in the hand cleaner of the present invention is 0.001-0.01%) by weight.
The hand cleaner formulation of the present invention is prepared according to the conventional method, and can be prepared in form of a gel, lotion, cream, or mineral oil-type formulation by addition of components, such as an antioxidant, perfume, a softening agent, an antimicrobial agent and the like.
Furthermore, the hand cleaner of the present invention can be prepared in form of various products, such as portable products, desk products, wall products, and body washers.
Brief Description of Drawings
FIG. 1 shows bacterial colony count after culturing a bacterial sample, which was taken from hand before washing the hand;
FIG. 2 shows bacterial colony count after culturing a bacterial sample, which was taken from hand just after washing the hand with water and soap and toweling the washed hand;
FIG. 3 shows bacterial colony count after culturing a bacterial sample, which was taken from hand after cleaning the hand with a cleaner prepared in Comparative Example 1; and
FIG. 3 shows bacterial colony count after culturing a bacterial sample, which was taken from hand after cleaning the hand with a hand cleaner prepared in Example 1. Best Mode for Carrying Out the Invention
The present invention will hereinafter be described in further detail by examples. It should however be borne in mind that the present invention is not limited to or by the examples.
Example 1: Preparation of hand cleaner
A beaker was charged with 61.61 of ethanol, 0.05g of perfume, 24.33g of distilled water, 0.5g of glycerin and 0.047g of polystyrene sulfonate salts, followed by stirring at 25 °C and 3,000 rpm for 1 minute. To the stirred mixture, 0.5g of propylene glycol, 1.5g of isopropyl alcohol, 0.5g of isopropyl myristate, 0.004g of oligosaccharide and 0.004g of chitosan were added, and stirred for about 1 minute while adding 0.2g of diisopropanolamine. After all the components were completely dissolved, 0.22g of a pigment and 0.3g of carbomer were added, and stirred at 3,000 rpm for about 30 minutes, thereby producing a hand cleaner gel. Examples 2-4 and Comparative Examples 1-2
Hand cleaner gels each having a composition shown in Table 1 below were prepared in the same method as described in Example 1.
Table 1:
Figure imgf000009_0001
Test Example 1 : Germicidal effect
In order to examine the germicidal effect of the hand cleaner according to the present invention, a test on the germicidal effect of the hand cleaner was carried out before and after washing hand.
1) Preparation of solid medium (Glucose Yeast Extra Agar (GYEA))
500 ml of distilled water was charged into each of two erlenmeyer flasks. One flask was charged with glucose and yeast, and the other flask was charged with agar. After confirming that all the components were mixed well, the contents of the two flasks ware combined into one flask. In this case, since agar is not completely dissolved, the contents of the flasks were quickly combined when agar was dissolved to some degree. An opening of the flask was closed with a sterilized cap, followed by sterilization at 121 °C under 1 atm for 20 minutes. The sterilized substances was cooled to a tepid degree, and then put in a sterilized petri dish so as to fill a half of the petri dish. The resulting medium was cooled in a sterilized room.
2) Culturing of bacteria
Cotton swabs were prepared and sterilized at 121 °C under 1 atm for 20 minutes. With the sterilized cotton swabs, bacteria were taken from hands washed according to the following conditions (l)-(4). The taken bacteria were transferred to the solid medium, and cultured overnight at 85%> humidity and 28 °C temperature. In this case, the above operation was carried out in a sterilized room such that the cotton swabs were not exposed to other bacteria.
Washing conditions of hands:
(1) no washing;
(2) washing with water and soap and then toweling;
(3) washing with a hand cleaner prepared in Comparative Example 1; and
(4) washing with a hand cleaner prepared in Example 1 of the present invention.
The results of the bacteria-culturing test were shown in Table 2 below and FIGS. 1 to 4.
Table 2:
Figure imgf000010_0001
As shown in Table 2 and FIGS. 1 to 4, it was found that there were no bacteria in the sample taken from the hand washed with the hand cleaner of the present invention.
Test Example 2: Observation of skin irritation
In order to examine if the hand cleaner of the present invention causes skin irritation, the sample according to the present invention and the sample according to Comparative Examples were applied on hands, and then a change in the skin was examined by sensory evaluation.
60 volunteers were divided into three groups each consisting of 20 volunteers, in which the three groups consist of a group where a hand cleaner is not used; a group where the hand cleaner of the present invention is used; and a group where the hand cleaners according to Comparative Examples are used. The hand cleaners were applied on the volunteers for 20 days three times a day, and then a change in the skin was observed.
The observed results showed that the group treated with the hand cleaner of the present invention had little or no skin problem like the group where the hand cleaner was not used. On the other hand, the group treated with the hand cleaners according to Comparative Examples showed skin irritation unlike the group where the hand cleaner was not used.
As a result, it can be found that the hand cleaner of the present invention has excellent germicidal and antibacterial activities and is harmless to the skin.
Industrial Applicability
As described above, the hand cleaner of the present invention has excellent germicidal and antibacterial activities, and harmless to the skin even upon long-term application.

Claims

What Is Claimed Is:
1. A hand cleaner containing polystyrene sulfonate salts.
2. The hand cleaner according to Claim 1, wherein polystyrene sulfonate salts is present at the amount of 0.03-0.05% by weight relative to the hand cleaner.
3. A hand cleaner comprising ethanol, isopropyl alcohol, carbomer, distilled water and polystyrene sulfonate salts.
4. The hand cleaner according to Claim 3, which comprises 60-80% by weight of ethanol, 1.3-3.0% by weight of isopropyl alcohol, 0.2-0.6% by weight of carbomer, 16-35% by weight of distilled water, and 0.03-0.05%o by weight of polystyrene sulfonate salts.
5. The hand cleaner according to any one of Claims 1 to 4, which additionally comprises a curing accelerator.
6. The hand cleaner according to Claim 5, wherein the curing accelerator is selected from amine compounds, including diisopropanolamine, aminomethylpropanol, aminomethylpropanediol and triethanolamine.
7. The hand cleaner according to any one of Claims 1 to 4, which additionally comprises a skin moisturizer.
8. The hand cleaner according to Claim 7, wherein the skin moisturizer is one or more selected from isopropyl myristate, propylene glycol, glycerin, silicon derivatives, aloe vera, and sorbitol.
9. The hand cleaner according to any one of Claims 1 to 4, which additionally comprises a nutrient.
10. The hand cleaner according to Claim 9, wherein the nutrient consists of oligosaccharide and chitosan.
11. The hand cleaner according to any one of Claims 1 to 4, which consists of a gel, lotion, cream, and mineral oil-type formulation.
PCT/KR2003/001193 2002-06-20 2003-06-18 A hand cleansing agent comprising polystyrene sulfonate salts WO2004000983A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003240033A AU2003240033A1 (en) 2002-06-20 2003-06-18 A hand cleansing agent comprising polystyrene sulfonate salts

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2002-0034527A KR100503035B1 (en) 2002-06-20 2002-06-20 A hand cleansing agent comprising polystyrene sulfonate salts
KR10-2002-0034527 2002-06-20

Publications (1)

Publication Number Publication Date
WO2004000983A1 true WO2004000983A1 (en) 2003-12-31

Family

ID=29997365

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2003/001193 WO2004000983A1 (en) 2002-06-20 2003-06-18 A hand cleansing agent comprising polystyrene sulfonate salts

Country Status (3)

Country Link
KR (1) KR100503035B1 (en)
AU (1) AU2003240033A1 (en)
WO (1) WO2004000983A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101475879B (en) * 2009-01-19 2011-04-06 广东拉芳日化有限公司 Sterilizing skin-protective hand cleanser
US8795730B2 (en) 2006-01-31 2014-08-05 David John Vachon Compositions and methods for promoting the healing of tissue of multicellular organisms

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102266094B1 (en) 2020-12-01 2021-06-17 (주)다래월드 Eco-friendly detergent composition and detergent comprising the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01125315A (en) * 1987-11-09 1989-05-17 Lion Corp Composition for oral cavity
US20010031714A1 (en) * 1999-12-13 2001-10-18 Thomas Gassenmeier Laundry, dishwashing or cleaning product detergent portions with controlled release of active substance
KR20010110625A (en) * 2000-11-30 2001-12-13 구본길 Germicide with the skin care of lotion type

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS649915A (en) * 1987-06-29 1989-01-13 Lion Corp Cosmetic composition
CA2016368A1 (en) * 1989-05-22 1990-11-23 Hiroshi Takasu A cleaning resin composition
US6200937B1 (en) * 1998-06-09 2001-03-13 Neutrogena Corporation Anti-residue shampoo and liquid toiletry production method
JP2000144103A (en) * 1998-11-12 2000-05-26 Soshin Lining Kk Rod like article for friction material and friction material
KR20010044514A (en) * 2001-03-02 2001-06-05 김남원 Hand cleanser containing alcoholic gel and preparation the same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01125315A (en) * 1987-11-09 1989-05-17 Lion Corp Composition for oral cavity
US20010031714A1 (en) * 1999-12-13 2001-10-18 Thomas Gassenmeier Laundry, dishwashing or cleaning product detergent portions with controlled release of active substance
KR20010110625A (en) * 2000-11-30 2001-12-13 구본길 Germicide with the skin care of lotion type

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8795730B2 (en) 2006-01-31 2014-08-05 David John Vachon Compositions and methods for promoting the healing of tissue of multicellular organisms
CN101475879B (en) * 2009-01-19 2011-04-06 广东拉芳日化有限公司 Sterilizing skin-protective hand cleanser

Also Published As

Publication number Publication date
AU2003240033A1 (en) 2004-01-06
KR20030097241A (en) 2003-12-31
KR100503035B1 (en) 2005-07-22

Similar Documents

Publication Publication Date Title
JP5797673B2 (en) Chemically modified polyaminosaccharide with hydrocarbyl sultone compound (A HYDROCARBYL SULTONE COMPOUND)
CN109646361B (en) Composite biological deodorization spray for pets and preparation method thereof
CN1153565C (en) Physically active antimicrobial gel for cosmetic products
CN1232665A (en) Antimicrobial composition
KR20150141938A (en) Process for producing silver-ion antibacterial liquid, silver-ion antibacterial liquid produced by said process, and silver-ion-containing product containing said antibacterial liquid
CN107970488A (en) A kind of chitin quarternary ammonium salt aquagel antiseptic dressing and preparation method thereof
JP2006512304A (en) Skin cleansing composition and method of use
TW201216859A (en) Disinfectant and antiseptic formulation having reduced iodine content
CN111467249A (en) Washing-free antibacterial gel and preparation method thereof
MXPA06015143A (en) Antimicrobial compositions and methods of use thereof.
EP2320915B1 (en) Gentle, non-irritating, non-alcohoholic skin disinfectant
US20220211606A1 (en) Liquid composition for influencing the microbiota on a subject's skin comprising chitosan
CN112587464A (en) Baby mica talcum powder and preparation method thereof
WO2004000983A1 (en) A hand cleansing agent comprising polystyrene sulfonate salts
KR102481754B1 (en) Antibacterial and deodorant composition including galla rhois
CN112999202A (en) Antibacterial and deodorant film-forming spray liquid and preparation method thereof
CN111514175A (en) Wash-free antibacterial spray and preparation method thereof
CN112516068A (en) Application of bacillus subtilis in antibacterial, deodorizing and cleaning products
CN117883350B (en) Hyposensitization has antibacterial effect improved antiperspirant deodorant compositions of (a)
US20230381217A1 (en) Liquid composition for use in the prevention or reduction of skin irritation, allergy and/or an infectious disease
KR100593706B1 (en) W/S type hydrous cosmetic products with no preservatives and their manufacturing methods by using silicon crosspolymer combinations.
RU2286799C1 (en) Method for preventing inflammatory diseases of female genital organs
US2906761A (en) Argentiferous germicidal medium and process for making same
CN117838566A (en) Washing-free disinfection moisturizing gel and preparation method thereof
CN117025296A (en) Essential oil composition and application thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP