JP6109683B2 - Foam antibacterial composition - Google Patents
Foam antibacterial composition Download PDFInfo
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- JP6109683B2 JP6109683B2 JP2013172885A JP2013172885A JP6109683B2 JP 6109683 B2 JP6109683 B2 JP 6109683B2 JP 2013172885 A JP2013172885 A JP 2013172885A JP 2013172885 A JP2013172885 A JP 2013172885A JP 6109683 B2 JP6109683 B2 JP 6109683B2
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- foam
- antibacterial
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- antibacterial composition
- toilet paper
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- 239000000203 mixture Substances 0.000 title claims description 45
- 230000000844 anti-bacterial effect Effects 0.000 title claims description 40
- 239000006260 foam Substances 0.000 title description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- 229920001661 Chitosan Polymers 0.000 claims description 15
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 14
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 4
- XIWFQDBQMCDYJT-UHFFFAOYSA-M benzyl-dimethyl-tridecylazanium;chloride Chemical group [Cl-].CCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 XIWFQDBQMCDYJT-UHFFFAOYSA-M 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 241000282320 Panthera leo Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000003242 anti bacterial agent Substances 0.000 description 3
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical group [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- -1 sucrose modified ethanol Chemical class 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 229940028444 muse Drugs 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- GMVPRGQOIOIIMI-DWKJAMRDSA-N prostaglandin E1 Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(O)=O GMVPRGQOIOIIMI-DWKJAMRDSA-N 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010058667 Oral toxicity Diseases 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 229920002385 Sodium hyaluronate Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- 229960001950 benzethonium chloride Drugs 0.000 description 1
- OCBHHZMJRVXXQK-UHFFFAOYSA-M benzyl-dimethyl-tetradecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 OCBHHZMJRVXXQK-UHFFFAOYSA-M 0.000 description 1
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000000850 deacetylating effect Effects 0.000 description 1
- 230000006196 deacetylation Effects 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 229960002442 glucosamine Drugs 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、洋式トイレの便座表面やトイレ壁面等の抗菌を目的に表面を清拭するための泡状抗菌性組成物に関する。 The present invention relates to a foamy antibacterial composition for wiping the surface of a Western-style toilet such as a toilet seat surface and a toilet wall surface for antibacterial purposes.
最近は他人が使用した洋式トイレの便座をそのまま使用することに抵抗がある人が増え、使用前に便座を清拭するのが当たり前になってきた。そのためのクリーナが各種知られている(特許文献1及び2参照)。
これらのクリーナの使用方法は、まず抗菌剤をトイレットペーパーに塗布し、便座等を清拭し、使用したトイレットペーパーはトイレに流して廃棄する。しかし、トイレットペーパーは水に溶解するため、クリーナはトイレットペーパーを容易に溶解させないように、例えばアルコール濃度を10質量%以上にする等の工夫がなされている(特許文献1参照)。
また、便座クリーナとして、キトサンと第四級アンモニウム塩を含有する組成物(特許文献2参照)が知られているが、これを使用しても十分に便座の菌を除去できないことが判明した。そのために除菌剤の濃度を高くしようとしたが、最近肌が敏感の人が増加し、人によっては肌に赤みがでる場合もあり、抗菌剤を多くすることもできなかった。そこで、簡単にトイレットペーパーを使って便座の除菌ができるクリーナの要望が高くなっている。
Recently, the number of people who are reluctant to use the toilet seat of a Western-style toilet used by others has increased, and it has become natural to wipe the toilet seat before use. Various cleaners for this purpose are known (see Patent Documents 1 and 2).
In order to use these cleaners, first, an antibacterial agent is applied to toilet paper, the toilet seat and the like are wiped off, and the used toilet paper is poured into the toilet and discarded. However, since toilet paper dissolves in water, the cleaner has been devised, for example, to increase the alcohol concentration to 10% by mass or more so that the toilet paper is not easily dissolved (see Patent Document 1).
Moreover, although the composition (refer patent document 2) containing chitosan and a quaternary ammonium salt is known as a toilet seat cleaner, even if it used, it turned out that the bacteria of a toilet seat cannot fully be removed. For this reason, attempts were made to increase the concentration of the disinfectant, but recently, the number of people with sensitive skin has increased, and some people have redness on their skin, and it has not been possible to increase the amount of antibacterial agents. Therefore, there is a growing demand for cleaners that can easily sterilize toilet seats using toilet paper.
本発明は、洋式トイレの便座等の広い面積の抗菌を目的として、清拭によってトイレットペーパーが崩壊せず、また、最小限の第四級アンモニウム塩で抗菌作用を醸し出すことができる抗菌性組成物の提供を課題とする。 The present invention is an antibacterial composition capable of producing antibacterial action with a minimum amount of quaternary ammonium salt without the toilet paper being disintegrated by wiping for the purpose of antibacterial purposes over a wide area such as a toilet seat of a Western-style toilet The issue is to provide
本発明者らは、抗菌性組成物の形状を泡状にすることで、便座等の表面に均一に塗布することが可能となり、そのためキトサン被覆膜を均一に形成できることを見出し、それにより最小限の第四級アンモニウム塩の濃度で抗菌作用を最大限発揮できることを見出した。さらに泡状にするには、キトサン、第四級アンモニウム塩、及びアルコール類を含有する組成物にすること、前記アルコール類の含有量を特定の量とすればよいことを見出し、本発明を完成するに至った。
すなわち、本発明は、下記(A)、(B)及び(C)を含有することを特徴とする泡状抗菌性組成物に関する。
(A)キトサン
(B)0.001〜0.10質量%の第四級アンモニウム塩
(C)10〜30質量%のアルコール類
さらに、前記アルコール類の含有量が15〜25質量%であることが好ましく、前記第四級アンモニウム塩が塩化ベンザルコニウムであることが好ましく、前記アルコール類がエタノールであることが好ましい。
The inventors of the present invention have found that the antibacterial composition can be formed into a foam shape so that the antibacterial composition can be uniformly applied to the surface of a toilet seat and the like, so that a chitosan coating film can be formed uniformly. It was found that the antibacterial action can be exerted to the maximum with the concentration of the limited quaternary ammonium salt. In order to make it more foamy, it was found that a composition containing chitosan, a quaternary ammonium salt, and alcohols, and that the content of the alcohols should be a specific amount, and the present invention was completed. It came to do.
That is, this invention relates to the foamy antibacterial composition characterized by containing the following (A), (B), and (C).
(A) Chitosan (B) 0.001 to 0.10% by mass of quaternary ammonium salt (C) 10 to 30% by mass of alcohol Further, the content of the alcohol is 15 to 25% by mass The quaternary ammonium salt is preferably benzalkonium chloride, and the alcohol is preferably ethanol.
本発明はトイレットペーパー上に形成される泡状抗菌性組成物であり、便座等を清拭してもトイレットペーパーが崩壊することがなく、また、長時間、泡状態を維持できるので広い面積でも十分に清拭でき、最小限の抗菌剤で十分な抗菌作用を発揮することができる。 The present invention is a foam-like antibacterial composition formed on toilet paper, and toilet paper does not collapse even if the toilet seat is wiped off. It can be wiped off sufficiently and can exhibit a sufficient antibacterial effect with a minimum of antibacterial agents.
本発明は抗菌性組成物を泡状に形成した泡状組成物であり、抗菌性組成物を泡状に形成する工程も含有する。
泡状に形成する工程は、泡状に形成する容器を用いて行なうことが好ましいが、どのような容器を用いても良く、泡状の形状を形成することができればよい。
The present invention is a foam composition in which the antibacterial composition is formed into a foam, and includes a step of forming the antibacterial composition into a foam.
The step of forming in a foam shape is preferably performed using a container formed in a foam shape, but any container may be used as long as it can form a foam shape.
(抗菌性組成物)
本発明の抗菌性組成物は、
(A)キトサン
(B)第四級アンモニウム塩
(C)アルコール類
を含有する。
(Antimicrobial composition)
The antibacterial composition of the present invention is
(A) Chitosan (B) quaternary ammonium salt (C) contains alcohols.
キトサンは、カニ、エビ等の甲殻、昆虫類の外皮その他のキチン質源を細粉し、希塩酸で処理して炭酸カルシウムを除き、アルカリ濃溶液で処理してタンパク質その他の夾雑物を除いて得られるキチンを、高温下、高濃度アルカリにより脱アセチル化して得られる白色無定形粉末の、グルコサミンからなる塩基性多糖類である。キトサンは、それ自体生体高分子であるため、全く経口毒性を示さず、且つ皮膚を刺激する恐れがない。 Chitosan is obtained by crushing crab, shrimp shells, insect shells and other chitinous sources, treating with dilute hydrochloric acid to remove calcium carbonate, and treating with alkaline concentrated solution to remove proteins and other contaminants. It is a basic polysaccharide composed of glucosamine, which is a white amorphous powder obtained by deacetylating chitin obtained under high temperature with high concentration alkali. Chitosan is a biopolymer itself, so it does not show any oral toxicity and has no fear of irritating the skin.
本発明に用いられるキトサンは、その重量平均分子量が数千〜数十万のものであるが、殺菌効果からすると低分子量の方が望ましい。また、脱アセチル化度に関しては50%以上、水溶性及び静菌効果を考慮すると80%以上が好ましい。 The chitosan used in the present invention has a weight average molecular weight of several thousands to several hundreds of thousands, but a low molecular weight is desirable from the viewpoint of bactericidal effect. Further, the degree of deacetylation is preferably 50% or more and 80% or more in consideration of water solubility and bacteriostatic effect.
そして、遊離のキトサン自体は水に溶けないことから、無機酸又は有機酸で処理して水に可溶であるキトサン塩として用いてもよいし、また塩酸、リン酸などの無機酸や酢酸、乳酸、クエン酸、グルコン酸等の有機酸などに溶解して用いてもよい。好ましくは、酢酸を用いる。
キトサンの含有量は、特に制限はないが、0.01〜5質量%が好ましい。
And since free chitosan itself is not soluble in water, it may be used as a chitosan salt which is treated with an inorganic acid or an organic acid and is soluble in water, or an inorganic acid such as hydrochloric acid or phosphoric acid, acetic acid, It may be dissolved in an organic acid such as lactic acid, citric acid or gluconic acid. Preferably acetic acid is used.
Although there is no restriction | limiting in particular in content of chitosan, 0.01-5 mass% is preferable.
本発明の第四級アンモニウム塩は、一般に、グラム陽性細菌等に対し強い静菌作用を有し、水溶性で腐食性がなく、通常の濃度では無色無臭であり、その毒性が低いことが知られている。本発明に用いられる第四級アンモニウム塩としては、塩化ベンザルコニウム、塩化ベンゼトニウム、塩化セチルピリジニウム、塩化ジメチルアンモニウム、塩化テトラデシルジメチルベンジルアンモニウム等を例示することができるが、塩化ベンザルコニウムが乾燥効果の点で特に望ましい。
第四級アンモニウム塩の含有量は好ましくは、0.001〜0.10質量%であり、さらに好ましくは、0.009〜0.05質量%である。0.001質量%未満では抗菌作用の効果を期待できない。
The quaternary ammonium salts of the present invention generally have a strong bacteriostatic action against Gram-positive bacteria, etc., are water-soluble and non-corrosive, are colorless and odorless at normal concentrations, and have low toxicity. It has been. Examples of the quaternary ammonium salt used in the present invention include benzalkonium chloride, benzethonium chloride, cetylpyridinium chloride, dimethylammonium chloride, tetradecyldimethylbenzylammonium chloride, and the like. It is particularly desirable in terms of effect.
The content of the quaternary ammonium salt is preferably 0.001 to 0.10% by mass, and more preferably 0.009 to 0.05% by mass. If it is less than 0.001% by mass, an antibacterial effect cannot be expected.
アルコール類としては、エタノール、イソプロパノール、八アセチル化蔗糖変性エタノール等を例示することができる。
アルコール類の含有量は好ましくは、10〜30質量%であり、さらに好ましくは、15〜25質量%であり、さらに好ましくは18〜22質量%である。
溶媒としては、通常、水が用いられる。
Examples of alcohols include ethanol, isopropanol, octaacetylated sucrose modified ethanol and the like.
The alcohol content is preferably 10 to 30% by mass, more preferably 15 to 25% by mass, and still more preferably 18 to 22% by mass.
As the solvent, water is usually used.
また、必要に応じて、グリセリン、プロピレングリコール、プチレングリコール、ヒドロキシエチルセルロース、ヒマシ油、ヒアルロン酸ナトリウム、ピコリドンカルボン酸ナトリウム、植物ガム(アラビアガム等)等の保水剤、界面活性剤、芳香剤、消臭剤、pH調整剤、その他の添加剤を併用することができる。 If necessary, water retaining agents such as glycerin, propylene glycol, butylene glycol, hydroxyethyl cellulose, castor oil, sodium hyaluronate, sodium picolidone carboxylate, vegetable gum (such as gum arabic), surfactants, fragrances , Deodorants, pH adjusters, and other additives can be used in combination.
(泡状に形成する容器)
泡状に形成する容器は、泡状になればどのような形状、材質、形態である容器であってもよいが、抗菌性組成物を格納する部分、泡を形成するための排出口、前記格納された抗菌性組成物を前記排出口まで誘導する手段を有した方がよく、さらに一体型容器であっても、個別の機能を有する部品の組み合せであってもよい。
前記抗菌性組成物を格納する部分は、前記泡状に形成する容器と固着して一体型でもよく、単独に分離できる構造でもよい。分離できる構造であれば、分離することで前記抗菌性組成物を格納しやすく、また、前記格納部分ごと交換することで前記抗菌性組成物を容器に供給することができる。
前記泡を形成するための排出口は、前記泡状に形成する容器と固着してもよく、分離できる構造でもよい。前記排出口は、液状の抗菌性組成物と空気等の気体とを効率的に混合して泡を形成する。
前記格納された抗菌性組成物を前記排出口まで誘導する手段は、トリガータイプスプレーのトリガーの部分のように手動で誘導する装置であってもよく、電気等で駆動するポンプで誘導してもよい。電気等で駆動するポンプの場合は、スイッチを押すことで駆動させてもよく、光センサー等を用いて、手をかざした時に駆動させてもよい。
(Container that forms foam)
The container to be formed in a foam shape may be a container having any shape, material, or form as long as it is foamed, but a part for storing an antibacterial composition, a discharge port for forming foam, It is better to have means for guiding the stored antibacterial composition to the outlet, and it may be an integrated container or a combination of parts having individual functions.
The part for storing the antibacterial composition may be integrated with the container formed in the foam shape, or may be a structure that can be separated independently. If it is the structure which can be isolate | separated, it will be easy to store the said antibacterial composition by isolate | separating, and the said antibacterial composition can be supplied to a container by replacing | exchanging the said storage part whole.
The discharge port for forming the foam may be fixed to the container formed in the foam shape or may have a structure capable of being separated. The discharge port efficiently mixes a liquid antibacterial composition and a gas such as air to form bubbles.
The means for guiding the stored antibacterial composition to the discharge port may be a device that manually guides, such as a trigger part of a trigger type spray, or may be guided by a pump driven by electricity or the like. Good. In the case of a pump driven by electricity or the like, the pump may be driven by pressing a switch, or may be driven when a hand is held up using an optical sensor or the like.
(泡状に形成する工程)
本発明は長時間泡の状態を維持することができるため、塗布すると共に泡を形成させてもよく、あらかじめ泡を作成してから塗布してもよい。したがって、本発明の泡状クリーナを作成する工程は、泡にすることができる方法であれば特に制限されず、例えば、前記容器を用いて泡を形成してもよく、ビーカー等の容器に抗菌性組成物を入れ、泡立て器等の道具を用いて、手動や電動で泡を形成してもよく、振動させても良く、振っても良い。
(Process of forming foam)
Since this invention can maintain a foam state for a long time, it may apply | coat and form a foam, and may apply | coat after creating a bubble previously. Therefore, the step of creating the foam cleaner of the present invention is not particularly limited as long as it is a method capable of forming a foam. For example, the container may be used to form foam, and the container such as a beaker may be antibacterial. The composition may be put in, and bubbles may be formed manually or electrically using a tool such as a whisk, or may be vibrated or shaken.
(実施形態)
本発明品を充填した泡状に形成する容器を用いて、トイレットペーパーに適量の泡を形成する。適量の泡の量は抗菌したい表面積によって調整する。泡が形成されたトイレットペーパーを、例えば便座表面に付着させて塗り広げる。本発明品を用いると、長時間泡の状態を維持するため、塗り広げている途中で泡が消えることがなく、便座とトイレットペーパーとの抵抗が小さいので滑りやすく、広い範囲に抗菌性組成物を塗布することができる。本発明品を用いない場合では、最初から液状であったり、塗り広げている間に泡が消えるので、強くトイレットペーパーを便座に押し当てなければ塗布できない。しかし、トイレットペーパーを強く押し当てると、トイレットペーパーが破れてしまう。そのため、本発明品を用いないと塗布できないだけでなく、破れたトイレットペーパーが余計なゴミになってしまう。本発明品を用いて塗り広げた抗菌性組成物は、速やかに泡が消泡し、消泡した抗菌性組成物で抗菌することができる。
本発明品にはキトサンが含有されているため、塗布した便座には抗菌性の被覆膜が形成される。そのため、抗菌性を長く持続することもできる。それに対して、液状のキトサン含有組成物を用いると、均一な抗菌性被覆膜が形成できず、抗菌性が低下する。本発明品は、均一な抗菌性被覆膜を形成することができるため、抗菌成分である第四級アンモニウム塩の含有量を少なくすることが出来る。このため、第四級アンモニウム塩によって皮膚に炎症等が発生する可能性を最小限に抑えることができる。
(Embodiment)
An appropriate amount of foam is formed on the toilet paper using a container formed into a foam filled with the product of the present invention. The appropriate amount of foam is adjusted according to the surface area to be antimicrobial. For example, the toilet paper on which the foam is formed is spread on the toilet seat surface. When the product of the present invention is used, since the foam state is maintained for a long time, the foam does not disappear during spreading, the resistance between the toilet seat and the toilet paper is small, and it is slippery and has an antibacterial composition in a wide range. Can be applied. In the case where the product of the present invention is not used, since it is liquid from the beginning or the foam disappears while spreading, it cannot be applied unless the toilet paper is strongly pressed against the toilet seat. However, if the toilet paper is pressed hard, the toilet paper will be torn. Therefore, it cannot be applied unless the product of the present invention is used, and torn toilet paper becomes extra waste. The antibacterial composition spread using the product of the present invention quickly defoams and can be antibacterial with the defoamed antibacterial composition.
Since the product of the present invention contains chitosan, an antibacterial coating film is formed on the applied toilet seat. Therefore, antibacterial properties can be maintained for a long time. On the other hand, when a liquid chitosan-containing composition is used, a uniform antibacterial coating film cannot be formed, and the antibacterial property is lowered. Since the product of the present invention can form a uniform antibacterial coating film, the content of the quaternary ammonium salt that is an antibacterial component can be reduced. For this reason, possibility that inflammation etc. will generate | occur | produce in skin by a quaternary ammonium salt can be suppressed to the minimum.
以下に本発明の実施例を示すが、本発明の技術的範囲はこれらに限定されるものではない。 Examples of the present invention are shown below, but the technical scope of the present invention is not limited thereto.
[実施例1]
第1表の実施例1に記載の組成物を、「キレイペット用除菌できるふきとりフォーム(ライオン株式会社製)」の容器を使用して、泡状組成物0.9gを作成し、トイレットペーパー(ネピアネピネピシングル(登録商標)、王子ネピア株式会社製)にとり、6×9cmのポリプロピレン板に塗り広げた。その後、塗布した板を、常温下、室温で24時間放置し、落下細菌を集めた。板表面にCRスタンプ(株式会社アテクト製)を用いて全面を拭取り、一般生菌数用標準寒天培地(株式会社アテクト製)の表面全体にスポンジ部分を10回押し付けて均一に塗布した。この寒天培地を30℃で2日間培養後、目視でコロニー数を測定した。その結果を第1表に示す。
[Example 1]
Using the container described in Example 1 of Table 1 as a “foaming foam that can be sterilized for clean pets (manufactured by Lion Corporation)”, 0.9 g of a foam composition was prepared, and toilet paper was used. (Nepane Nepinepi Single (registered trademark), manufactured by Oji Napier Co., Ltd.) was applied to a 6 × 9 cm polypropylene plate. Thereafter, the coated plate was allowed to stand at room temperature for 24 hours to collect falling bacteria. The entire surface of the plate was wiped using a CR stamp (manufactured by Actec Co., Ltd.), and the sponge portion was pressed 10 times on the entire surface of the standard agar medium for general viable cell count (manufactured by Actect Co., Ltd.) and applied uniformly. The agar medium was cultured at 30 ° C. for 2 days, and the number of colonies was visually measured. The results are shown in Table 1.
[比較例1]
第1表の実施例1に記載の組成物を、液状のまま0.9gトイレットペーパー(ネピアネピネピシングル(登録商標)、王子ネピア株式会社製)にとり、実施例1と同様の作業を行った。その結果を第1表に示す。
[Comparative Example 1]
The composition described in Example 1 of Table 1 was applied to 0.9 g of toilet paper (Nepane Nepinepi Single (registered trademark), manufactured by Oji Napier Co., Ltd.) in the liquid state, and the same operation as in Example 1 was performed. It was. The results are shown in Table 1.
[実施例2]
第2表の実施例2に記載の組成物を「キレイペット用除菌できるふきとりフォーム(ライオン株式会社製)」および「ミューズノータッチ泡ハンドソープ(登録商標、レキッドベンギーザー・ジャパン株式会社製)」の容器を使って、泡状組成物0.9gを作成し、トイレットペーパー(ネピアネピネピシングル(登録商標、王子ネピア株式会社製))にとった。その泡を目視にて観察して、泡の消えるまでの時間を測定した。その結果を第2表に示す。
[Example 2]
The composition described in Example 2 of Table 2 is “Clean wipe form for clean pet use (made by Lion Corporation)” and “Muse no touch foam hand soap (registered trademark, manufactured by Liquid Bengeiser Japan Co., Ltd.) ”Was used to prepare 0.9 g of a foamy composition, which was taken on toilet paper (Nepia Nepinepi Single (registered trademark, manufactured by Oji Napier Co., Ltd.)). The bubbles were observed visually, and the time until the bubbles disappeared was measured. The results are shown in Table 2.
[比較例2〜3]
実施例2に記載の組成物に代えて、比較例2及び比較例3に記載の組成物において、実施例2と同じ評価を行なった。その結果を第2表に示す。
[Comparative Examples 2-3]
Instead of the composition described in Example 2, the same evaluation as in Example 2 was performed on the composition described in Comparative Example 2 and Comparative Example 3. The results are shown in Table 2.
[実施例3〜5]
第3表の実施例3〜5に記載の組成物をそれぞれ、「キレイペット用除菌できるふきとりフォーム(ライオン株式会社製)」及び「ミューズノータッチ泡ハンドソープ(登録商標、レキッドベンギーザー・ジャパン株式会社製)」の容器を使って、泡状組成物0.9gを作成し、トイレットペーパー(ネピアネピネピシングル(登録商標)、王子ネピア株式会社製)にとった。その泡を目視にて観察して、泡が消えるまでの時間を測定した。また、同様の方法で泡状組成物0.9gを付着させたトイレットペーパーで机上60cm幅を3往復して拭き、その後のトイレットペーパーを以下の指針で評価した。その結果を第3表に示す。
拭き取り試験の評価
○:拭いた際に、机上に破れカスがでない
△:拭いた際に、机上に破れカスがでる。
×:拭いた際に、トイレットペーパーが破れる
[Examples 3 to 5]
Each of the compositions described in Examples 3 to 5 in Table 3 is “Clean wipeable foam for clean pet (manufactured by Lion Corporation)” and “Muse No Touch Foam Hand Soap (registered trademark, Liquid Bengeiser Japan). 0.9 g of a foamed composition was prepared using a container of “made by Co., Ltd.” and taken on toilet paper (Nepane Nepinepi Single (registered trademark), produced by Oji Napier Co., Ltd.). The bubbles were observed visually, and the time until the bubbles disappeared was measured. Moreover, the toilet paper which 0.9g of foamy compositions adhered by the same method wiped 60 cm width on a desk 3 times, and evaluated the subsequent toilet paper with the following guidelines. The results are shown in Table 3.
Evaluation of wiping test ○: When wiping, there is no tearing residue on the desk. Δ: When wiping, tearing residue is left on the desk.
×: Toilet paper tears when wiped
[比較例4〜5]
実施例3に記載の組成物に代えて、比較例4〜5に記載の組成物において、実施例3と同じ評価を行なった。その結果を第3表に示す。
[Comparative Examples 4 to 5]
In place of the composition described in Example 3, the same evaluation as in Example 3 was performed on the compositions described in Comparative Examples 4 to 5. The results are shown in Table 3.
第3表の結果から、エタノール濃度が30質量%以下の組成物を用いると泡の持続時間が長く、また、10質量%以上の組成物を用いると、トイレットペーパーの破損が少ないことが判明した。 From the results in Table 3, it was found that the use of a composition having an ethanol concentration of 30% by mass or less resulted in a longer foam duration, and that the use of a composition of 10% by mass or more caused less damage to the toilet paper. .
Claims (4)
(A)キトサン
(B)0.001〜0.10質量%の第四級アンモニウム塩
(C)10〜30質量%のアルコール類 A foamy antibacterial composition for toilets comprising the following (A), (B) and (C).
(A) Chitosan (B) 0.001 to 0.10 mass% quaternary ammonium salt (C) 10 to 30 mass% alcohol
The foamed antibacterial composition for toilets according to any one of claims 1 to 3, wherein the alcohol is ethanol.
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