TW201836619A - Disinfectant composition - Google Patents

Disinfectant composition Download PDF

Info

Publication number
TW201836619A
TW201836619A TW107108380A TW107108380A TW201836619A TW 201836619 A TW201836619 A TW 201836619A TW 107108380 A TW107108380 A TW 107108380A TW 107108380 A TW107108380 A TW 107108380A TW 201836619 A TW201836619 A TW 201836619A
Authority
TW
Taiwan
Prior art keywords
chondroitin sulfate
composition
weight
disinfecting
surfactant
Prior art date
Application number
TW107108380A
Other languages
Chinese (zh)
Other versions
TWI771388B (en
Inventor
山田耕太郎
櫻井英知
柴田知佳
稲見浩之
Original Assignee
日商志瑞亞新藥工業股份有限公司
日商大阪製藥股份有限公司
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 日商志瑞亞新藥工業股份有限公司, 日商大阪製藥股份有限公司 filed Critical 日商志瑞亞新藥工業股份有限公司
Publication of TW201836619A publication Critical patent/TW201836619A/en
Application granted granted Critical
Publication of TWI771388B publication Critical patent/TWI771388B/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/737Sulfated polysaccharides, e.g. chondroitin sulfate, dermatan sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/02Local antiseptics
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

To provide a disinfectant composition belonging to the category of disinfectants to be used for sterilizing fingers, etc., said disinfectant composition containing chondroitin sulfate or a chondroitin sulfate salt as a moisturizing agent and thus having an improved moisturizing effect, being capable of preventing chapped hand skin causing bacterial or viral invasion and infection, and ensuring the uniform dispersion of the chondroitin sulfate or chondroitin sulfate salt in the composition. A disinfectant composition characterized by comprising 20-60 wt% of a lower alcohol having 1-3 carbon atoms, 40-65 wt% of water and 0.006-1 wt% of chondroitin sulfate or a chondroitin sulfate salt; a disinfectant composition comprising an oily component, a thickener and a surfactant and having a viscosity of 50-300 Pa.s at 25 DEG C; etc.

Description

消毒用組成物Disinfecting composition

本發明係關於屬於使用在手指等之殺菌等之消毒劑,保濕性及性狀優異之消毒用組成物。The present invention relates to a disinfecting composition which is excellent in moisturizing properties and properties, and is a disinfectant which is used for disinfection of a finger or the like.

以往,乙醇、異丙醇等碳數1~3之低級醇藉由細菌之細胞膜或病毒之外膜的破壞或酵素等之蛋白質的凝固而對於細菌或病毒具有消毒作用為一般所知悉,廣泛使用摻合該等低級醇之消毒劑。然而,一般而言於摻合乙醇、異丙醇等之低級醇之消毒劑,例如在為了消毒手指而使用時,有引起使用者之手粗糙等的問題。手粗糙係指去除角質層與皮脂膜而角質層不足,失去皮膚隔離機能的狀態,此狀態可說是藉由從隔離缺陷部侵入細菌或病毒而變容易感染。由此等來看,依然期望即使摻合低級醇,仍可防止手粗糙亦即皮膚隔離機能的缺陷之保濕性優異之消毒劑。Conventionally, a lower alcohol having 1 to 3 carbon atoms such as ethanol or isopropyl alcohol is generally known to be sterilized by bacteria or viruses by the destruction of a bacterial cell membrane or a membrane other than a virus, or a protein such as an enzyme. A disinfectant that blends the lower alcohols. However, in general, a disinfectant which incorporates a lower alcohol such as ethanol or isopropyl alcohol, for example, when used for disinfecting a finger, causes problems such as roughness of a user's hand. Rough hand refers to a state in which the stratum corneum and the sebaceous membrane are removed and the stratum corneum is insufficient, and the skin is isolated from the function of the skin. This state can be said to be easily infected by invading bacteria or viruses from the isolated defect portion. From this point of view, it is still desired to prevent the hand roughness, that is, the disinfectant which is excellent in moisture retention of the defect of the skin barrier function even if the lower alcohol is blended.

例如,專利文獻1中揭示有一種消毒劑,其係含有羧基乙烯基聚合物、天然多糖類等、脂肪酸酯及低級醇,其低級醇的摻合比例為20~50重量%。藉由摻合黏性劑之羧基乙烯基聚合物,由於在手指摩擦時產生因手指的鹽類導致聚合物成分在手指上析出(樹脂化)即所謂鱗片狀渣屑,為了防止此事而將摻合天然多糖類或其衍生物作為特徵。 [先前技術文獻] [專利文獻]For example, Patent Document 1 discloses a disinfectant containing a carboxyvinyl polymer, a natural polysaccharide, or the like, a fatty acid ester, and a lower alcohol, and the blending ratio of the lower alcohol is 20 to 50% by weight. In order to prevent this, the carboxyvinyl polymer blended with the adhesive will cause the polymer component to precipitate on the finger (resinized) due to the salt of the finger when rubbed by the finger. A natural polysaccharide or a derivative thereof is blended as a feature. [Prior Technical Literature] [Patent Literature]

[專利文獻1]日本特開平10-130173號公報[Patent Document 1] Japanese Patent Laid-Open No. Hei 10-130173

[發明欲解決之課題][Questions to be solved by the invention]

然而,於專利文獻1之實施例所記載之組成物,存在保濕性尚未充分的課題。However, the composition described in the examples of Patent Document 1 has a problem that the moisture retention property is not sufficient.

又,於專利文獻1所記載之發明,雖披露使用硫酸軟骨素鈉作為天然多糖類,但實際上摻合硫酸軟骨素鈉時,有因組成物其他成分的平衡導致不溶解等無法均勻存在於組成物中之問題。Further, in the invention described in Patent Document 1, although sodium chondroitin sulfate is used as a natural polysaccharide, when sodium chondroitin sulfate is actually blended, it may not be uniformly dissolved due to the balance of other components of the composition. The problem in the composition.

因此,於本發明,提供一種屬於使用在手指等之殺菌等之消毒劑,藉由摻合軟骨素硫酸或軟骨素硫酸鹽作為保濕劑,提昇保濕性,邊防止細菌或病毒的侵入及成為感染原因之手粗糙,邊使軟骨素硫酸或軟骨素硫酸鹽均勻存在於組成物中之消毒用組成物作為目的。 [用以解決課題之手段]Therefore, in the present invention, a disinfectant which is used for sterilization of a finger or the like is provided, and by mixing chondroitin sulfate or chondroitin sulfate as a moisturizing agent, moisturizing property is enhanced, and invasion of bacteria or virus is prevented and infection is caused. The cause of the hand is rough, and the purpose is to make the composition for disinfection in which the chondroitin sulfate or chondroitin sulfate is uniformly present in the composition. [Means to solve the problem]

[1]亦即,本發明係一種消毒用組成物,其特徵為含有碳數1~3之低級醇20~60重量%、水40~65重量%、軟骨素硫酸或軟骨素硫酸鹽0.006~1重量%。[1] That is, the present invention is a disinfecting composition characterized by containing 20 to 60% by weight of a lower alcohol having 1 to 3 carbon atoms, 40 to 65% by weight of water, chondroitin sulfuric acid or chondroitin sulfate 0.006 to ~ 1% by weight.

[2]而且,如前述[1]所記載之消毒用組成物,其係含有油脂成分、增黏劑及界面活性劑,且在25℃之黏度為50~300Pa・s。[2] The composition for disinfection according to the above [1], which comprises a fat or oil component, a tackifier, and a surfactant, and has a viscosity at 25 ° C of 50 to 300 Pa·s.

[3]而且,如前述[1]或前述[2]所記載之消毒用組成物,其中,前述增黏劑係選自羧基乙烯基聚合物、纖維素衍生物中之至少一個。[3] The disinfecting composition according to the above [1], wherein the tackifier is at least one selected from the group consisting of a carboxyvinyl polymer and a cellulose derivative.

[4]而且,如前述[1]至前述[3]中任一項所記載之消毒用組成物,其中,前述界面活性劑係含有聚氧乙烯烷基醚及多元醇之脂肪酸酯。[4] The disinfecting composition according to any one of the above [1], wherein the surfactant comprises a polyoxyethylene alkyl ether and a fatty acid ester of a polyhydric alcohol.

[5]而且,如前述[1]至前述[4]中任一項所記載之消毒用組成物,其係含有選自苄索氯銨(benzethonium chloride)、氯化苯甲烴銨(benzalkonium chloride)、葡萄糖酸氯己定(chlorhexidine gluconate)、普維酮碘、異丙基甲基酚、氯二甲酚中之至少一個的消毒成分。 [發明的效果][5] The disinfecting composition according to any one of the above [1], wherein the composition for disinfection is selected from benzethonium chloride or benzalkonium chloride. And a disinfecting component of at least one of chlorhexidine gluconate, povidone iodine, isopropylmethylphenol, and chloroxylenol. [Effects of the Invention]

根據本發明,屬於使用在手指等之殺菌等之消毒劑,可藉由摻合軟骨素硫酸或軟骨素硫酸鹽作為保濕劑,提昇保濕性,邊防止細菌或病毒的侵入及成為感染原因之手粗糙,邊使軟骨素硫酸或軟骨素硫酸鹽均勻存在於組成物中。According to the present invention, it is a disinfectant which is used for sterilization of a finger or the like, and can be used as a moisturizing agent by blending chondroitin sulfate or chondroitin sulfate to enhance moisturization while preventing invasion of bacteria or viruses and becoming a cause of infection. Rough, while allowing chondroitin sulfate or chondroitin sulfate to be uniformly present in the composition.

以下,針對有關本發明之消毒用組成物的實施形態進行詳細說明。尚,有表示在說明中的範圍之標示時,係含有上限與下限者。Hereinafter, embodiments of the disinfecting composition of the present invention will be described in detail. In addition, when there is a sign indicating the range in the description, the upper limit and the lower limit are included.

在本發明之碳數1~3之低級醇係甲醇、乙醇、異丙醇等之碳數為1個至3個的醇。藉由使用該低級醇,可藉由細菌之細胞膜或病毒之外膜的破壞或酵素等之蛋白質的凝固使細菌或病毒死滅,可預防因該等細菌或病毒導致之疾病等對人體之不良影響。The lower alcohol having 1 to 3 carbon atoms of the present invention is an alcohol having 1 to 3 carbon atoms such as methanol, ethanol or isopropyl alcohol. By using the lower alcohol, the bacteria or the virus can be killed by the destruction of the membrane of the bacteria or the membrane of the virus or the coagulation of proteins such as enzymes, thereby preventing the adverse effects on the human body caused by the diseases caused by the bacteria or viruses. .

作為在碳數1~3之低級醇的消毒用組成物之含有比例,較佳為20~60重量%。其含有比例超過60重量%時,軟骨素硫酸或軟骨素硫酸鹽無法均勻溶解或分散。又,其含有比例未滿20重量%時,無法充分消毒細菌或病毒,為了表示所期望之效果有必要添加其他殺菌成分等。The content ratio of the disinfecting composition of the lower alcohol having 1 to 3 carbon atoms is preferably 20 to 60% by weight. When the content exceeds 60% by weight, chondroitin sulfate or chondroitin sulfate cannot be uniformly dissolved or dispersed. Moreover, when the content ratio is less than 20% by weight, the bacteria or the virus cannot be sufficiently disinfected, and it is necessary to add another sterilizing component or the like in order to express the desired effect.

在本發明之軟骨素硫酸或軟骨素硫酸鹽,係於將由D-葡萄糖酸及N-乙醯基-D-半乳胺糖所構成之2糖作為構成單元之糖鏈鍵結硫酸之化合物或其硫酸之氫被鈉、鉀等取代之鹽,作為保濕劑摻合。藉由摻合軟骨素硫酸或軟骨素硫酸鹽,使得在消毒用組成物之保濕性,尤其是在經過時間時之保濕性變佳。The chondroitin sulfate or chondroitin sulfate of the present invention is a compound of a sugar chain-bonded sulfuric acid which comprises a sugar composed of D-gluconic acid and N-ethinyl-D-galactosamine as a constituent unit or A salt whose hydrogen sulfate is replaced by sodium, potassium or the like is blended as a humectant. By blending chondroitin sulfate or chondroitin sulfate, the moisturizing property of the composition for disinfection, especially the moisturizing property at the elapsed time, is improved.

作為在軟骨素硫酸或軟骨素硫酸鹽之消毒用組成物之含有比例,較佳為0.006~1重量%。其含有比例為上述範圍時,可在消毒用組成物均勻溶解或分散,進而可持續保濕性,可防止使用者之手粗糙等。The content ratio of the composition for disinfection of chondroitin sulfate or chondroitin sulfate is preferably 0.006 to 1% by weight. When the content ratio is in the above range, the composition for disinfection can be uniformly dissolved or dispersed, and the moisturizing property can be maintained, and the hand of the user can be prevented from being rough.

在本發明之油脂分於20℃~25℃之常溫為液體或固形之油脂。如有必要可進行摻合。藉由乳化油脂分來使用消毒用組成物時,可藉由其油脂分擴散至手指等之皮膚而抑制從皮膚揮發水分,來防止手粗糙等。作為油脂分,天然物、合成物皆可使用,且作為天然物亦可使用源自植物、源自動物之任一種油脂。The fat or oil of the present invention is a liquid or solid fat at a normal temperature of 20 ° C to 25 ° C. Blending can be carried out if necessary. When the composition for disinfection is used by emulsification of fats and oils, it is possible to prevent moisture from volatilizing from the skin by diffusing the oil to the skin of a finger or the like, thereby preventing hand roughness and the like. As the fats and oils, natural products and synthetic materials can be used, and as the natural product, any of the oils derived from plants and animals can be used.

作為油脂分,例如較佳為流動石蠟、輕質流動石蠟、鯊烷等之烴、棕櫚酸異丙酯、棕櫚酸辛酯、肉荳蔻酸異丙酯、異壬酸異壬酯、由碳數8~碳數22之脂肪酸所構成之中鏈脂肪酸甘油三酯、三(癸醯基・癸酸)甘油基等之酯油、肉荳蔻基醇(碳數14)、鯨蠟醇(碳數16)、硬脂基醇(碳數18)、鯨蠟硬脂基醇(碳數16及18之混合物)、二十二烷基醇(碳數22)、異硬脂基醇(碳數18)、2-己基癸醇(碳數16)、2-辛基十二醇(碳數20)等之飽和一元醇類,或油烯基醇(碳數18)等之不飽和一元醇類等之脂肪族醇、大豆油、紅花油、葡萄籽油、玫瑰果油、葵花油、月見草籽油、棉籽油、芝麻油,小麥胚芽油,杏仁油等,作為不乾性油,較佳為橄欖油、山茶花油、山茶油、蓖麻油、花生油、鱷梨油、澳洲堅果油、榛子油、繡線菊油、荷荷巴油等,作為精油,較佳為桉樹油、薄荷油、羅馬甘菊油等(植物油)。此等之油脂分可僅1種或組合2種以上使用。As the fat and oil component, for example, a hydrocarbon such as flowing paraffin, light flowing paraffin, or squalane, isopropyl palmitate, octyl palmitate, isopropyl myristate, isodecyl isononanoate, and carbon number 8 are preferable. - a fatty acid such as a medium chain fatty acid triglyceride or a tris(decyl/decanoic acid) glyceryl group, a myristyl alcohol (carbon number 14), and a cetyl alcohol (carbon number 16). , stearyl alcohol (carbon number 18), cetearyl alcohol (mixture of carbon numbers 16 and 18), behenyl alcohol (carbon number 22), isostearyl alcohol (carbon number 18), a saturated monohydric alcohol such as 2-hexyl decyl alcohol (carbon number 16) or 2-octyldodecanol (carbon number 20), or an unsaturated monohydric alcohol such as oleyl alcohol (carbon number 18) Alcohol, soybean oil, safflower oil, grape seed oil, rosehip oil, sunflower oil, evening primrose seed oil, cottonseed oil, sesame oil, wheat germ oil, almond oil, etc., as a non-drying oil, preferably olive oil, camellia oil , camellia oil, castor oil, peanut oil, avocado oil, macadamia nut oil, hazelnut oil, meadowfoam oil, jojoba oil, etc., as essential oils, preferably eucalyptus oil, peppermint oil, Roman chamomile Etc. (vegetable oil). These oils and fats may be used alone or in combination of two or more.

作為在油脂分之消毒用組成物的含有比例,較佳為0.5~20重量%,更佳為1.0~10重量%。其含有比例為上述範圍時,可防止使用時使用者之手粗糙等。The content of the composition for disinfection in the oil and fat is preferably 0.5 to 20% by weight, more preferably 1.0 to 10% by weight. When the content ratio is in the above range, it is possible to prevent the user's hand from being rough during use.

在本發明之增黏劑係使消毒用組成物的黏度增加之成分。如有必要可進行摻合。藉由使用增黏劑,可使消毒用組成物的黏度上昇至成為如指定的黏度般之黏度。The tackifier of the present invention is a component which increases the viscosity of the composition for disinfection. Blending can be carried out if necessary. By using a tackifier, the viscosity of the disinfecting composition can be increased to a viscosity as specified.

作為增黏劑,例如較佳為交聯型聚丙烯酸之羧基乙烯基聚合物或羧基甲基纖維素、羥基乙基纖維素、羥基丙基纖維素等之纖維素衍生物、黃原膠、瓜爾豆膠、阿拉伯膠、海藻酸鈉、海藻酸丙二醇、乙基纖維素、聚丙烯酸鈉、環糊精等,其中,更佳為羧基乙烯基聚合物、羧基甲基纖維素。此等之增黏劑可僅1種或組合2種以上使用。As the tackifier, for example, a carboxyvinyl polymer of a crosslinked polyacrylic acid or a cellulose derivative such as carboxymethylcellulose, hydroxyethylcellulose or hydroxypropylcellulose, xanthan gum or melon is preferred. Glycol gum, gum arabic, sodium alginate, propylene glycol alginate, ethyl cellulose, sodium polyacrylate, cyclodextrin, etc., among which, a carboxyvinyl polymer or a carboxymethyl cellulose is more preferred. These tackifiers may be used alone or in combination of two or more.

作為在增黏劑之消毒用組成物之含有比例,較佳為0.1~10重量%,更佳為0.2~7重量%。其含有比例為上述範圍時,可調整成適合使用所期望之黏度。The content of the composition for disinfection in the tackifier is preferably from 0.1 to 10% by weight, more preferably from 0.2 to 7% by weight. When the content ratio is in the above range, it can be adjusted to suit the desired viscosity.

在本發明之界面活性劑,係均勻混合消毒用組成物,用以使乳霜狀的性狀安定之成分。如有必要可進行摻合。藉由使用界面活性劑,可防止消毒用組成物的成分之碳數1~3之低級醇等分離。The surfactant in the present invention is a component which uniformly mixes the disinfecting composition and stabilizes the creamy property. Blending can be carried out if necessary. By using a surfactant, it is possible to prevent the lower alcohol or the like having a carbon number of 1 to 3 from being separated from the components of the disinfecting composition.

作為界面活性劑,例如可列舉陽離子界面活性劑、陰離子系界面活性劑、兩性界面活性劑、非離子界面活性劑。陽離子界面活性劑係於水中解離時成為陽離子之界面活性劑,例如較佳為烷基三甲基銨鹽、烷基二甲基銨鹽、烷基苄基二甲基銨鹽等。其中,烷基較佳為碳數12~22,作為反陰離子,較佳為氯化物離子、氫氧化物離子、溴化物離子等。Examples of the surfactant include a cationic surfactant, an anionic surfactant, an amphoteric surfactant, and a nonionic surfactant. The cationic surfactant is a surfactant which becomes a cation when dissociated in water, and is preferably, for example, an alkyltrimethylammonium salt, an alkyldimethylammonium salt, an alkylbenzyldimethylammonium salt or the like. Among them, the alkyl group is preferably a carbon number of 12 to 22, and as the counter anion, a chloride ion, a hydroxide ion, a bromide ion or the like is preferable.

而且,陰離子界面活性劑係於水中解離時成為陰離子之界面活性劑,例如較佳為脂肪酸鹽、單烷基硫酸鹽、烷基聚氧乙烯硫酸鹽、烷基苯磺酸鹽、單烷基磷酸鹽等。其中烷基較佳為碳數12~22,作為反陽離子,較佳為鈉離子、鉀離子、鈣離子、鎂離子等。Further, the anionic surfactant is an anionic surfactant when dissociated in water, and is preferably, for example, a fatty acid salt, a monoalkyl sulfate, an alkyl polyoxyethylene sulfate, an alkylbenzenesulfonate, or a monoalkyl phosphate. Salt and so on. The alkyl group is preferably a carbon number of 12 to 22, and as a counter cation, a sodium ion, a potassium ion, a calcium ion, a magnesium ion or the like is preferable.

而且,兩性界面活性劑係於分子內一併具有陰離子性部位與陽離子性部位兩方,因應溶液之pH成為陽離子、陰離子、及陽離子與陰離子兩性之界面活性劑,例如較佳為烷基二甲基氧化胺、烷基羧基甜菜鹼等。其中烷基較佳為碳數12~22。Further, the amphoteric surfactant has both an anionic portion and a cationic portion in the molecule, and the pH of the solution becomes a cationic, an anionic, and a cationic and anionic surfactant, for example, an alkyl group. Base amine oxide, alkyl carboxyl betaine, and the like. The alkyl group is preferably a carbon number of 12 to 22.

而且,非離子界面活性劑係具有親水部未離子化之親水性部位的活性劑,例如較佳為聚氧乙烯十六烷基醚或聚氧乙烯硬脂基醚等之聚氧乙烯烷基醚、甘油脂肪酸酯或山梨糖醇脂肪酸酯、蔗糖脂肪酸酯等之多元醇脂肪酸酯、聚氧乙烯加成多元醇之脂肪酸酯、脂肪酸二乙醇醯胺等。上述非離子界面活性劑當中,藉由Griffin之式所算出之HLB更佳為3~17者。於上述非離子界面活性劑具有聚氧乙烯骨架者可適當變更氧乙烯之加成莫耳數。HLB為上述範圍的非離子界面活性劑時,消毒用組成物之保存安定優異,具體而言即使隨著時間經過亦不會引起分離等可保持乳霜狀。又,此等之界面活性劑雖可僅1種或組合2種以上使用,但較佳為組合HLB3~6之界面活性劑與HLB12~17之界面活性劑。Further, the nonionic surfactant is an active agent having a hydrophilic portion which is not ionized in the hydrophilic portion, and is preferably a polyoxyethylene alkyl ether such as polyoxyethylene cetyl ether or polyoxyethylene stearyl ether. A polyhydric alcohol fatty acid ester such as a glycerin fatty acid ester or a sorbitan fatty acid ester or a sucrose fatty acid ester, a fatty acid ester of a polyoxyethylene addition polyhydric alcohol, or a fatty acid diethanolamine. Among the above nonionic surfactants, the HLB calculated by the formula of Griffin is preferably from 3 to 17. When the nonionic surfactant has a polyoxyethylene skeleton, the addition molar number of oxyethylene can be appropriately changed. When the HLB is a nonionic surfactant in the above range, the composition for disinfection is excellent in storage stability, and specifically, it can maintain a creamy state even if it does not separate over time. Further, these surfactants may be used alone or in combination of two or more. However, it is preferred to combine the surfactants of HLB 3 to 6 and the surfactants of HLB 12 to 17.

又,本發明之消毒用組成物中摻合水。作為水,較佳為日本藥典標準之水,例如為自來水、井水等之常水,而且為蒸餾、藉由離子交換膜之離子交換處理、藉由超過濾膜之超過濾處理的任一種,或藉由該等之組合來處理常水之純化水,而且,較佳為藉由加熱等滅菌處理純化水之滅菌純化水等。而且,上述水的摻合比例係去除本發明所使用之乙醇、軟骨素硫酸或軟骨素硫酸鹽的殘餘,又,摻合增黏劑、界面活性劑等時,去除該等之殘餘,較佳為40~65重量%,更佳為42~63重量%。Further, the disinfecting composition of the present invention is blended with water. The water is preferably water of the Japanese Pharmacopoeia standard, for example, normal water such as tap water or well water, and is any one of distillation, ion exchange treatment by an ion exchange membrane, and ultrafiltration treatment by an ultrafiltration membrane. Alternatively, the purified water of the normal water is treated by the combination of the above, and it is preferably a sterilized purified water obtained by sterilizing purified water by heating or the like. Further, the blending ratio of the above water is to remove the residual of the ethanol, chondroitin sulfate or chondroitin sulfate used in the present invention, and when the tackifier, the surfactant, etc. are blended, the residue is removed, preferably. It is 40 to 65 wt%, more preferably 42 to 63 wt%.

又,本發明之消毒用組成物中如有必要可摻合消毒成分。消毒成分係為了消毒於碳數1~3之低級醇無法充分消毒之菌或病毒等而摻合。作為消毒成分,例如較佳為苄索氯銨、氯化苯甲烴銨、葡萄糖酸氯己定、普維酮碘、異丙基甲基酚、氯二甲酚等,更佳為苄索氯銨。又,此等之消毒成分可僅1種或組合2種以上使用。Further, the disinfecting composition of the present invention may be blended with a disinfecting component if necessary. The disinfecting component is blended in order to sterilize bacteria or viruses which are not sufficiently sterilized by the lower alcohols having 1 to 3 carbon atoms. As the disinfecting component, for example, benzethonium chloride, benzalkonium chloride, chlorhexidine gluconate, pravone iodine, isopropylmethylphenol, chloroxylenol, etc., more preferably benzethon chloride Ammonium. Further, these disinfecting components may be used alone or in combination of two or more.

在本發明之消毒用組成物,可藉由摻合增黏劑提昇黏度時,本發明之消毒用組成物的黏度在使用JIS K7117-1所記載之布魯克菲爾德(Brookfield)形旋轉黏度計B型(東機產業股份有限公司製、商品名「TVB-10M」)之計測,25℃條件下較佳為50~300Pa・s,更佳為100~250 Pa・s。消毒用組成物的黏度為此範圍時,即使附著在手指等之皮膚亦不會瞬間脫落,又,塗敷時易於抹開。In the disinfecting composition of the present invention, when the viscosity is increased by blending the tackifier, the viscosity of the disinfecting composition of the present invention is Brookfield-shaped rotational viscometer type B as described in JIS K7117-1. (Measured by Toki Sangyo Co., Ltd., product name "TVB-10M"), it is preferably 50 to 300 Pa·s at 25 ° C, more preferably 100 to 250 Pa·s. When the viscosity of the composition for disinfection is in this range, even if it adheres to the skin of a finger or the like, it does not fall off instantaneously, and it is easy to smear when applied.

本發明之消毒用組成物中可進一步摻合軟骨素硫酸或軟骨素硫酸鹽以外之其他保濕劑。作為其他保濕劑,例如較佳為甘油、聚甘油、丙二醇、1,3-丁二醇、1,2-戊二醇、1,2-己二醇、聚乙二醇、麥芽糖醇、山梨糖醇等之多元醇、玻尿酸鈉、尿素、乳酸鈉、三甲基甘胺酸等。The sterilizing composition of the present invention may further incorporate a humectant other than chondroitin sulfate or chondroitin sulfate. As other humectants, for example, glycerin, polyglycerin, propylene glycol, 1,3-butanediol, 1,2-pentanediol, 1,2-hexanediol, polyethylene glycol, maltitol, sorbose are preferred. Polyol such as alcohol, sodium hyaluronate, urea, sodium lactate, trimethylglycine, and the like.

本發明之消毒用組成物中除了上述成分之外,如有必要亦可摻合生育酚、維生素C、BHT等之抗氧化劑、pH調整劑、緩衝劑、香料、色素等。 [實施例]In addition to the above components, the disinfecting composition of the present invention may be blended with an antioxidant such as tocopherol, vitamin C or BHT, a pH adjuster, a buffer, a perfume, a coloring matter or the like, if necessary. [Examples]

[實施例1]   調整乙醇30重量份、硫酸軟骨素鈉1重量份、殘餘為水之100重量份的組成物,充分混合製作消毒用組成物。[Example 1] A composition for 30 parts by weight of ethanol, 1 part by weight of sodium chondroitin sulfate, and 100 parts by weight of water was adjusted, and thoroughly mixed to prepare a composition for disinfection.

[實施例2]   除了將乙醇定為50重量份之外,其他與實施例1相同,製作消毒用組成物。[Example 2] A disinfecting composition was produced in the same manner as in Example 1 except that the amount of ethanol was changed to 50 parts by weight.

[實施例3]   除了將硫酸軟骨素鈉定為0.01重量份之外,其他與實施例1相同,製作消毒用組成物。[Example 3] A disinfecting composition was prepared in the same manner as in Example 1 except that the sodium chondroitin sulfate was set to 0.01 part by weight.

[比較例1]   除了將乙醇定為10重量份之外,其他與實施例1相同,製作消毒用組成物。[Comparative Example 1] A disinfecting composition was produced in the same manner as in Example 1 except that the amount of ethanol was changed to 10 parts by weight.

[比較例2]   除了將乙醇定為70重量份之外,其他與實施例1相同,製作消毒用組成物。[Comparative Example 2] A disinfecting composition was produced in the same manner as in Example 1 except that the amount of ethanol was changed to 70 parts by weight.

[比較例3]   除了未摻合硫酸軟骨素鈉之外,其他與實施例1相同,製作消毒用組成物。[Comparative Example 3] A disinfecting composition was prepared in the same manner as in Example 1 except that the chondroitin sulfate sodium was not blended.

[外觀性狀]   針對剛製作之消毒用組成物的性狀由目視進行評估時,作為評估基準,將硫酸軟骨素鈉均勻溶解的狀態評估為「○」,將硫酸軟骨素鈉未溶解或產生因硫酸軟骨素鈉導致變模糊(dullness)的狀態評估為「×」,「○」評估為較佳,「×」評估為不佳。[Appearance property] When the properties of the composition for disinfection to be produced were evaluated by visual observation, the state in which the sodium chondroitin sulfate was uniformly dissolved was evaluated as "○", and the sodium chondroitin sulfate was not dissolved or produced by sulfuric acid. The state of durness caused by chondroitin sodium was evaluated as "x", "○" was evaluated as better, and "x" was evaluated as poor.

[保濕性]   評估製作之消毒用組成物的保濕性時,作為評估基準,在專門官能檢查員5名,進行將使用後之保濕感從1點至5點的5階段之官能評估,求出其平均點,針對下述之評估基準進行區分,進行「〇」評估為較佳,「△」評估及「×」評估為不佳之評估。   ○:平均點為4.0以上   △:平均點為2.0以上未滿4.0   ×:平均點未滿2.0[Moisturizing property] When evaluating the moisture retention of the disinfectant composition to be produced, the five-stage functional evaluation of the moisturizing sensation from 1 to 5 points after the use of the special-purpose inspector is performed as the evaluation standard. The average point is to distinguish between the following evaluation criteria. It is better to conduct a "〇" assessment, and the "△" assessment and the "×" assessment are poor assessments. ○: The average point is 4.0 or more. △: The average point is 2.0 or more and less than 4.0 ×: The average point is less than 2.0.

[殺菌效力]   評估製作之消毒用組成物的殺菌效力時,直接接觸檢體與菌液後塗抹在平板培養基,進行菌數之評估。作為評估基準,將相對於對照之菌數,藉由與前述消毒用組成物接觸而死滅之菌數的比例為99.99%以上效力者評估為「○」,將未滿99.99%效力者評估為「×」,「○」評估為較佳,「×」評估為不佳。[Bactericidal effect] When evaluating the bactericidal efficacy of the produced disinfectant composition, the sample and the bacterial liquid were directly contacted, and then applied to a plate medium to evaluate the number of bacteria. As a basis for the evaluation, the number of bacteria killed by contact with the disinfecting composition was 99.99% or more, and the effect was evaluated as "○", and the effect of less than 99.99% was evaluated as "". ×”, “○” is evaluated as better, and “×” is evaluated as poor.

針對實施例1~3、比較例1~3,將關於外觀性狀、保濕性、殺菌效力之結果示於表1。The results of the appearance properties, moisture retention, and sterilization efficacy of Examples 1 to 3 and Comparative Examples 1 to 3 are shown in Table 1.

如表1所示,在摻合乙醇及水之組成物,摻合硫酸軟骨素鈉時,雖保濕性佳,乙醇的摻合量成為70重量份時,硫酸軟骨素鈉無法溶解,乙醇的摻合量為10重量份左右時,殺菌效力不佳。由此等之結果,瞭解到作為消毒用組成物,為了顯示不僅具有均勻溶解硫酸軟骨素鈉之良好的性狀,而且較佳之殺菌效力,乙醇、水及硫酸軟骨素鈉的摻合比例有必要為指定的範圍。As shown in Table 1, when the composition of ethanol and water is blended, when the chondroitin sulfate sodium is blended, although the moisturizing property is good, when the blending amount of ethanol is 70 parts by weight, the sodium chondroitin sulfate cannot be dissolved, and the ethanol is mixed. When the amount is about 10 parts by weight, the sterilization effect is not good. As a result of the above, it has been found that as a composition for disinfection, in order to exhibit not only a good trait of uniformly dissolving sodium chondroitin sulfate but also a good bactericidal effect, it is necessary to mix the ratio of ethanol, water and sodium chondroitin sulfate. The specified range.

[實施例4]   調整乙醇30重量份、保濕劑之硫酸軟骨素鈉(1.0重量份、增黏劑之羧基乙烯基聚合物(和光純藥工業股份有限公司製、商品名:「HIVISWAKO103」)0.4重量份、非離子界面活性劑之聚氧乙烯十六烷基醚(日光化學股份有限公司製、商品名:「NIKKOL BC-15」、HLB:15.5)2重量份、非離子界面活性劑之單硬脂酸甘油(日光化學股份有限公司製、商品名:「NIKKOL MGS-AMV」、HLB:4.0) 2重量份、油脂分之流動石蠟(中央化成股份有限公司製、商品名:「流動石蠟350S」)1重量份、油脂分之肉荳蔻酸異丙酯1重量份、油脂分之硬脂基醇0.5重量份、保濕劑之甘油0.5重量份、二甲基聚矽氧烷(東麗・道康寧股份有限公司製、商品名:「Q7-9120SILICONE FLUID350CST」) 0.2重量份、消毒成分之苄索氯銨0.05重量份、氫氧化鈉0.072重量份、殘餘為水之100重量份的組成物,充分混合製作消毒用組成物。[Example 4] Adjusting 30 parts by weight of ethanol and a humectant sodium chondroitin sulfate (1.0 part by weight, a carboxyvinyl polymer of a tackifier (manufactured by Wako Pure Chemical Industries, Ltd., trade name: "HIVISWAKO103") 0.4 2 parts by weight of a polyoxyethylene cetyl ether (manufactured by Nikko Chemical Co., Ltd., trade name: "NIKKOL BC-15", HLB: 15.5), a nonionic surfactant, and a nonionic surfactant Stearic acid glycerin (manufactured by Nikko Chemical Co., Ltd., trade name: "NIKKOL MGS-AMV", HLB: 4.0) 2 parts by weight, and liquid paraffin (manufactured by Central Chemicals Co., Ltd., trade name: "mobile paraffin 350S" 1) 1 part by weight, 1 part by weight of isopropyl myristate, 0.5 parts by weight of stearyl alcohol, 0.5 parts by weight of humectant, and dimethyl polyoxane (Dolly Dow Corning) Co., Ltd. product name: "Q7-9120SILICONE FLUID350CST") 0.2 parts by weight, 0.05 parts by weight of benzethonium chloride as a disinfecting component, 0.072 parts by weight of sodium hydroxide, and 100 parts by weight of water remaining, thoroughly mixed For disinfection As it was.

[實施例5]   除了將在實施例4乙醇定為50重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為80Pa・s。[Example 5] A disinfecting composition was produced in the same manner as in Example 4 except that the amount of the ethanol in Example 4 was 50 parts by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 80 Pa·s.

[實施例6]   除了將在實施例4硫酸軟骨素鈉定為0.5重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為95Pa・s。[Example 6] A disinfecting composition was prepared in the same manner as in Example 4 except that the sodium chondroitin sulfate of Example 4 was set to 0.5 part by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 95 Pa·s.

[實施例7]   除了將在實施例4硫酸軟骨素鈉定為0.1重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為101Pa・s。[Example 7] A disinfecting composition was prepared in the same manner as in Example 4 except that the sodium chondroitin sulfate of Example 4 was made 0.1 part by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 101 Pa·s.

[實施例8]   除了將在實施例4之硫酸軟骨素鈉定為0.01重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為95Pa・s。[Example 8] A disinfecting composition was prepared in the same manner as in Example 4 except that the sodium chondroitin sulfate of Example 4 was set to 0.01 part by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 95 Pa·s.

[比較例4]   除了取代在實施例4之硫酸軟骨素鈉,改將玻尿酸鈉定為0.01重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為128Pa・s。[Comparative Example 4] A disinfecting composition was prepared in the same manner as in Example 4 except that sodium chondroitin sulfate of Example 4 was replaced with 0.01 parts by weight of sodium hyaluronate. Further, when the viscosity was measured in the same manner as in Example 4, it was 128 Pa·s.

[比較例5]   除了未摻合在實施例4之硫酸軟骨素鈉,將羧基乙烯基聚合物定為0.05重量份、氫氧化鈉定為0.09重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為211Pa・s。[Comparative Example 5] The same procedure as in Example 4 was carried out except that the sodium chondroitin sulfate of Example 4 was not blended, the carboxyvinyl polymer was 0.05 parts by weight, and the sodium hydroxide was determined to be 0.09 parts by weight. Make a disinfectant composition. Further, when the viscosity was measured in the same manner as in Example 4, it was 211 Pa·s.

[比較例6]   除了將在實施例4之乙醇定為40重量份,未摻合硫酸軟骨素鈉,將羧基乙烯基聚合物定為0.05重量份、定為0.09重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為183Pa・s。[Comparative Example 6] Except that the amount of the ethanol in Example 4 was 40 parts by weight, the sodium chondroitin sulfate was not blended, and the carboxyvinyl polymer was set to 0.05 part by weight to 0.09 part by weight. Example 4 was carried out in the same manner to prepare a disinfecting composition. Further, when the viscosity was measured in the same manner as in Example 4, it was 183 Pa·s.

[比較例7]   除了將在實施例4之乙醇定為70重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且,製造後有分離或白濁等,無法與實施例4同樣測定黏度。[Comparative Example 7] A disinfecting composition was produced in the same manner as in Example 4 except that the amount of the ethanol in Example 4 was 70 parts by weight. Further, after the production, separation or white turbidity was observed, and the viscosity could not be measured in the same manner as in Example 4.

[比較例8]   除了將在實施例4硫酸軟骨素鈉定為0.005重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為105Pa・s。[Comparative Example 8] A disinfecting composition was prepared in the same manner as in Example 4 except that the sodium chondroitin sulfate of Example 4 was made 0.005 parts by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 105 Pa·s.

[比較例9]   除了將在實施例4乙醇定為10重量份之外,其他與實施例4同樣進行,製作消毒用組成物。而且與實施例4同樣測定黏度時為185Pa・s。[Comparative Example 9] A disinfecting composition was produced in the same manner as in Example 4 except that the amount of the ethanol in Example 4 was 10 parts by weight. Further, when the viscosity was measured in the same manner as in Example 4, it was 185 Pa·s.

[外觀性狀]   針對將製作之消毒用組成物的性狀藉由目視評估時,作為評估基準,將均勻溶解硫酸軟骨素鈉,亦未觀察到以乳霜狀分離的狀態評估為「○」,雖有變模糊但已溶解硫酸軟骨素鈉,亦未觀察到分離的狀態評估為「△」,已分離未成為均勻的狀態評估為「×」,「○」評估及「△」評估為較佳,「×」評估為不佳。[Appearance property] When the properties of the composition for disinfection to be produced were visually evaluated, the chondroitin sulfate sodium was uniformly dissolved as a criterion for evaluation, and the state in which the cream was separated was not evaluated as "○", although There was ambiguity but dissolved chondroitin sulfate sodium, and no separation was observed as "△". The state in which the separation was not uniform was evaluated as "X", and the "○" evaluation and "△" evaluation were preferable. The "X" assessment is not good.

[保濕性]   評估製作之消毒用組成物的保濕性時,在專門官能檢查員5名,進行將使用後之保濕感從1點至5點的5階段之官能評估,求出其平均點,針對下述之評估基準進行區分,進行「〇」評估為較佳,「△」評估及「×」評估為不佳之評估。   ○:平均點為4.0以上   △:平均點為2.0以上未滿4.0   ×:平均點未滿2.0[Moisturizing property] When evaluating the moisturizing property of the prepared disinfectant composition, five members of the specialized inspector were evaluated for the five-stage functionality of the moisturizing feeling after use from 1 to 5, and the average point was determined. For the following assessment criteria, the "〇" assessment is preferred, and the "△" assessment and the "×" assessment are poor assessments. ○: The average point is 4.0 or more. △: The average point is 2.0 or more and less than 4.0 ×: The average point is less than 2.0.

[殺菌效力]   評估製作之消毒用組成物的殺菌效力時,直接接觸檢體與菌液後塗抹在平板培養基進行培養,進行菌數之評估。作為評估基準,將相對於對照之菌數,藉由與前述消毒用組成物接觸而死滅之菌數的比例為99.99%以上效力者評估為「○」,將未滿99.99%效力者評估為「×」,「○」評估為較佳,「×」評估為不佳。[Bactericidal effect] When the bactericidal efficacy of the produced disinfectant composition is evaluated, the sample and the bacterial liquid are directly contacted, and then applied to a plate medium for cultivation, and the number of bacteria is evaluated. As a basis for the evaluation, the number of bacteria killed by contact with the disinfecting composition was 99.99% or more, and the effect was evaluated as "○", and the effect of less than 99.99% was evaluated as "". ×”, “○” is evaluated as better, and “×” is evaluated as poor.

針對實施例4~8、比較例4~9,將有關黏度、外觀性狀、保濕性、殺菌效力之結果示於表2。The results regarding the viscosity, the appearance property, the moisture retention property, and the sterilization efficacy are shown in Table 2 for Examples 4 to 8 and Comparative Examples 4 to 9.

由表2,瞭解到在乙醇、硫酸軟骨素鈉、增黏劑、界面活性劑、水等之摻合系,藉由將乙醇、硫酸軟骨素鈉、水成為指定的含有比例,於消毒用組成物的製作時安定,可保持乳霜狀的性狀,保濕性及殺菌效力亦佳。如此,藉由含有油脂成分、增黏劑及界面活性劑,且將黏度成為指定的範圍,即使碳數1~3之低級醇被以高比例摻合,亦可形成乳化安定性優異,進而使用時亦可防止手粗糙之保濕性良好之半固形狀有高黏度之消毒用乳化組成物。From Table 2, it is known that a blending system of ethanol, sodium chondroitin sulfate, a tackifier, a surfactant, water, etc., is made into a disinfecting composition by using ethanol, chondroitin sulfate, and water as specified contents. The product is stable during the production, and can maintain the cream-like properties, and has good moisturizing and bactericidal effects. In this way, by containing the oil and fat component, the tackifier, and the surfactant, and the viscosity is within the specified range, even if the lower alcohol having 1 to 3 carbon atoms is blended at a high ratio, the emulsion stability can be excellent and further used. It also prevents the hand-roughness of the semi-solid shape with good moisture retention and high-viscosity emulsified composition for disinfection.

[比較例10]   製作乙醇78重量份、羧基乙烯基聚合物0.4重量份、氫氧化鈉0.072、殘餘為水之消毒用組成物。[Comparative Example 10] A disinfecting composition was prepared by preparing 78 parts by weight of ethanol, 0.4 parts by weight of a carboxyvinyl polymer, and 0.072 of sodium hydroxide.

[比較例11]   製作乙醇54重量份、羧基乙烯基聚合物0.4重量份、氫氧化鈉0.072、殘餘為水之消毒用組成物。[Comparative Example 11] A disinfecting composition was prepared by preparing 54 parts by weight of ethanol, 0.4 parts by weight of a carboxyvinyl polymer, and 0.072 of sodium hydroxide.

對於實施例8、比較例10~11之消毒用組成物,針對水分蒸散量測定。亦即,將該等之消毒用組成物在溫度約25℃、濕度30~40%的環境下,將1次塗佈及連續10次塗佈時之經皮水分蒸散量,1次塗佈後於5分鐘及10分鐘後,連續10次塗佈後於5、10、20、30分鐘後使用Tewameter TM300(Courage+Khazaka公司製)測定。而且,藉由該等之經時後之經皮水分蒸散量、與塗佈前之經皮水分蒸散量的差,算出變化量,評估皮膚之皮膚隔離性。從1次塗佈及連續10次塗佈時,由在10分鐘後之後的經皮水分蒸散量,算出減去塗佈前之經皮水分蒸散量的差之變化量,將此變化量為負者評估為良好。將此等之結果示於表3。The disinfection compositions of Example 8 and Comparative Examples 10 to 11 were measured for the amount of water evapotranspiration. That is, the transdermal moisture evapotranspiration amount of the disinfecting composition at a temperature of about 25 ° C and a humidity of 30 to 40% in one application and 10 consecutive application, after one application After 5 minutes and 10 minutes, the coating was applied 10 times, and after 5, 10, 20, and 30 minutes, it was measured using Tewameter TM300 (Courage+Khazaka Co., Ltd.). Then, the amount of change was calculated from the difference between the transepidermal water evapotranspiration after the passage and the percutaneous water evapotranspiration amount before application, and the skin barrier property of the skin was evaluated. The amount of change in the difference in the amount of percutaneous water evapotranspiration before coating was calculated from the amount of percutaneous water evapotranspiration after 10 minutes from the first application and the ten consecutive coatings, and the amount of change was negative. The assessment is good. The results of these are shown in Table 3.

由表3,瞭解到在實施例8之消毒用組成物,在1次塗佈後及10次塗佈後,10分鐘後之經皮水分蒸散量較塗佈前之經皮水分蒸散量更小,在10分鐘後之經皮水分蒸散量之與初期的經皮水分蒸散量之變化量成為負之數,抑制水分的蒸散,對於皮膚隔離性,與比較例10~11比較為優異。又,藉由皮膚隔離性優異,可預防來自皮膚之細菌或病毒之侵入及感染。From Table 3, it is understood that in the disinfecting composition of Example 8, after one application and after 10 coatings, the transdermal moisture evapotranspiration after 10 minutes is smaller than the percutaneous moisture evapotranspiration before coating. The amount of change in the transdermal moisture evapotranspiration after 10 minutes and the initial transdermal water evapotranspiration amount was negative, and the evapotranspiration of the water was suppressed, and the skin barrier properties were superior to those of Comparative Examples 10 to 11. Moreover, by being excellent in skin barrier properties, invasion and infection of bacteria or viruses from the skin can be prevented.

Claims (5)

一種消毒用組成物,其特徵為含有碳數1~3之低級醇20~60重量%、水40~65重量%、軟骨素硫酸或軟骨素硫酸鹽0.006~1重量%。A disinfecting composition comprising 20 to 60% by weight of a lower alcohol having 1 to 3 carbon atoms, 40 to 65% by weight of water, and 0.006 to 1% by weight of chondroitin sulfate or chondroitin sulfate. 如請求項1之消毒用組成物,其係含有油脂成分、增黏劑及界面活性劑,在25℃之黏度為50~300Pa・s。The disinfecting composition according to claim 1, which comprises a fat or oil component, a tackifier and a surfactant, and has a viscosity at 25 ° C of 50 to 300 Pa·s. 如請求項1或請求項2之消毒用組成物,其中,前述增黏劑係選自羧基乙烯基聚合物、纖維素衍生物中之至少一個。The disinfecting composition according to claim 1 or claim 2, wherein the tackifier is at least one selected from the group consisting of a carboxyvinyl polymer and a cellulose derivative. 如請求項1或請求項2之消毒用組成物,其中,前述界面活性劑係含有聚氧乙烯烷基醚及多元醇之脂肪酸酯。The composition for disinfection according to claim 1 or claim 2, wherein the surfactant comprises a polyoxyethylene alkyl ether and a fatty acid ester of a polyhydric alcohol. 請求項1或請求項2之消毒用組成物,其係含有選自苄索氯銨、氯化苯甲烴銨、葡萄糖酸氯己定(chlorhexidine gluconate)、普維酮碘、異丙基甲基酚、氯二甲酚中之至少一個消毒成分。The disinfectant composition of claim 1 or claim 2, which comprises a benzethonium chloride, benzalkonium chloride, chlorhexidine gluconate, puerone iodine, isopropylmethyl At least one disinfecting component of phenol or chloroxylenol.
TW107108380A 2017-03-22 2018-03-13 composition for disinfection TWI771388B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017-055369 2017-03-22
JP2017055369A JP6830629B2 (en) 2017-03-22 2017-03-22 Disinfectant composition

Publications (2)

Publication Number Publication Date
TW201836619A true TW201836619A (en) 2018-10-16
TWI771388B TWI771388B (en) 2022-07-21

Family

ID=63584392

Family Applications (1)

Application Number Title Priority Date Filing Date
TW107108380A TWI771388B (en) 2017-03-22 2018-03-13 composition for disinfection

Country Status (5)

Country Link
JP (1) JP6830629B2 (en)
KR (2) KR20230086819A (en)
CN (1) CN110545825A (en)
TW (1) TWI771388B (en)
WO (1) WO2018173917A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102229814B1 (en) 2020-07-24 2021-03-19 (주)뉴젠사이언스 Cleaning wipes for sterilization and disinfection and the manufacturing method thereof
KR102229800B1 (en) 2020-07-24 2021-03-19 (주)뉴젠사이언스 Compositions for sterilization and disinfection comprising enzyme and the manufacturing method thereof
KR102202917B1 (en) 2020-07-24 2021-01-14 (주)뉴젠사이언스 Compositions for sterilization and disinfection and the manufacturing method thereof
KR102345209B1 (en) * 2021-09-08 2022-01-03 김인희 Sanitizer composition has excellent anti-viral effect, sterilization effect and skin moisturizing effect

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06128125A (en) * 1992-10-14 1994-05-10 Kose Corp Hair tonic
JPH09110680A (en) * 1995-10-19 1997-04-28 Yuutoku Yakuhin Kogyo Kk Dermatitis-curing strap
JPH10130173A (en) * 1996-10-28 1998-05-19 Japan Medic Kk Quick-drying disinfectant
JPH10324624A (en) * 1997-05-23 1998-12-08 Kao Corp Bactericidal disinfectant composition

Also Published As

Publication number Publication date
CN110545825A (en) 2019-12-06
JP2018158890A (en) 2018-10-11
TWI771388B (en) 2022-07-21
WO2018173917A1 (en) 2018-09-27
KR20230086819A (en) 2023-06-15
KR20190126135A (en) 2019-11-08
JP6830629B2 (en) 2021-02-17

Similar Documents

Publication Publication Date Title
TW201836619A (en) Disinfectant composition
ES2612939T3 (en) High clarity aqueous concentrates of 4-hexylresorcinol
WO2007094332A1 (en) Disinfectant ointment
US20090082472A1 (en) Hand sanitizer and method of preparation
JPH07330505A (en) Antimicrobial composition
JP6125718B2 (en) Deodorant composition and deodorant agent
KR101189344B1 (en) Self-preserving skin care formulation
KR102338256B1 (en) Hand sanitizer composition that contains ionized calcium and has excellent skin moisturizing effect, sterilization effect and viral effect
JP2007284412A (en) Germicidal disinfectant cream
JP2019014765A (en) Antimicrobial compositions and production methods thereof
JP2001081024A (en) Milky oil-in-water type emulsification composition and method for producing the same composition
JP2007217394A (en) Pharmaceutical composition
WO2008061375A1 (en) Antiseptic
ES2616495T3 (en) Composition in gel form for virucidal disinfection of mammalian skin
JP6741433B2 (en) Emulsion composition for disinfection
JP5264829B2 (en) Antiseptic disinfectant and cosmetic composition
JPWO2015064681A1 (en) Composition for external use
JP5507146B2 (en) Water-in-oil emulsified paste pharmaceutical preparation for lips
JP2006083111A (en) Disinfecting composition
JP2011144146A (en) Gel-like bactericide for finger
CN111511346A (en) No-clean liquid bactericidal detergent composition
JP7045750B1 (en) Alcohol-based rubbing-type hand disinfection composition with improved usability
WO2023276203A1 (en) Better-feeling alcohol-based rub-in hand sanitizer composition
JP2023044437A (en) emulsified cosmetic composition
JP2009190986A (en) Transparent gel cosmetic