TW201836619A - 消毒用組成物 - Google Patents
消毒用組成物 Download PDFInfo
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- 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
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- TW
- Taiwan
- Prior art keywords
- weight
- chondroitin sulfate
- composition
- disinfecting
- disinfection
- Prior art date
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Abstract
本發明的課題為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。 本發明的解決手段可藉由下述消毒用組成物等解決,該消毒用組成物係將含有碳數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%作為特徵,及含有油脂成分、增黏劑及界面活性劑,在25℃之黏度為50~300Pa・s。
Description
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。
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。
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]
[專利文獻1]日本特開平10-130173號公報
[發明欲解決之課題]
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。
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。
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]
[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%。
[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。
[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。
[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。
[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]
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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%。
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。
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。
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。
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]
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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
[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。
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。
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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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。
[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
[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。
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。
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。
[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。
[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。
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。
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。
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%。
- 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。
- 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。
- 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。
- 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。
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| CN (1) | CN110545825A (zh) |
| TW (1) | TWI771388B (zh) |
| WO (1) | WO2018173917A1 (zh) |
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|---|---|---|---|---|
| KR102202917B1 (ko) | 2020-07-24 | 2021-01-14 | (주)뉴젠사이언스 | 살균효과를 갖는 소독용 조성물 및 그 제조 방법 |
| KR102229800B1 (ko) | 2020-07-24 | 2021-03-19 | (주)뉴젠사이언스 | 효소성분을 함유하는 소독용 조성물 및 그 제조 방법 |
| KR102229814B1 (ko) | 2020-07-24 | 2021-03-19 | (주)뉴젠사이언스 | 살균효과를 갖는 소독 티슈 및 그 제조 방법 |
| JPWO2022071587A1 (zh) * | 2020-10-02 | 2022-04-07 | ||
| KR102345209B1 (ko) * | 2021-09-08 | 2022-01-03 | 김인희 | 살바이러스, 살균 효과 및 피부 보습 효과가 탁월한 소독제 조성물 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06128125A (ja) * | 1992-10-14 | 1994-05-10 | Kose Corp | 養毛料 |
| EP0833606B1 (en) * | 1995-06-22 | 2003-10-01 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
| JPH09110680A (ja) * | 1995-10-19 | 1997-04-28 | Yuutoku Yakuhin Kogyo Kk | 皮膚炎治療貼付剤 |
| JPH10130173A (ja) * | 1996-10-28 | 1998-05-19 | Japan Medic Kk | 速乾性消毒剤 |
| US6582711B1 (en) * | 1997-01-09 | 2003-06-24 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
| JPH10324624A (ja) * | 1997-05-23 | 1998-12-08 | Kao Corp | 殺菌消毒剤組成物 |
| CA2568888C (en) * | 2004-06-03 | 2012-12-18 | James Steven Brown | Sanitizing composition and method of preparation |
| JP2008024701A (ja) * | 2006-06-21 | 2008-02-07 | Rohto Pharmaceut Co Ltd | アルギン酸又はその塩を含有するソフトコンタクトレンズ用組成物 |
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2017
- 2017-03-22 JP JP2017055369A patent/JP6830629B2/ja active Active
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2018
- 2018-03-13 TW TW107108380A patent/TWI771388B/zh active
- 2018-03-15 KR KR1020197030005A patent/KR20190126135A/ko not_active Ceased
- 2018-03-15 KR KR1020237019184A patent/KR102748384B1/ko active Active
- 2018-03-15 CN CN201880019987.8A patent/CN110545825A/zh active Pending
- 2018-03-15 WO PCT/JP2018/010226 patent/WO2018173917A1/ja not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| TWI771388B (zh) | 2022-07-21 |
| KR20230086819A (ko) | 2023-06-15 |
| KR20190126135A (ko) | 2019-11-08 |
| JP2018158890A (ja) | 2018-10-11 |
| CN110545825A (zh) | 2019-12-06 |
| KR102748384B1 (ko) | 2024-12-30 |
| JP6830629B2 (ja) | 2021-02-17 |
| WO2018173917A1 (ja) | 2018-09-27 |
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