JPH05908A - Mildew proofing agent - Google Patents
Mildew proofing agentInfo
- Publication number
- JPH05908A JPH05908A JP18040491A JP18040491A JPH05908A JP H05908 A JPH05908 A JP H05908A JP 18040491 A JP18040491 A JP 18040491A JP 18040491 A JP18040491 A JP 18040491A JP H05908 A JPH05908 A JP H05908A
- Authority
- JP
- Japan
- Prior art keywords
- lactic acid
- mildew
- agent
- mildew proofing
- proofing agent
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は防カビ剤に関する。本発
明の防カビ剤は、一般家庭、公衆施設、産業機器などの
湿度の高い箇所に多発するカビを防止および除去するた
めの製剤に関する。FIELD OF THE INVENTION The present invention relates to an antifungal agent. The antifungal agent of the present invention relates to a preparation for preventing and removing mold which frequently occurs in places with high humidity such as general households, public facilities, and industrial equipment.
【0002】[0002]
【従来の技術および課題】近年、暖房設備の完備、室内
の気密化に伴い、家庭、事務所、学校などの室内におけ
るカビの発生が増加している。カビの発生は、美観上、
保健衛生上も好ましくない。カビを防止するには、風通
しをよくして乾燥に保ち清潔にすることが必要である。
しかしながら、湿度の高い浴室やトイレ、洗面所、ある
いは冷蔵庫、オーブン、ミキサーなどの電子機器、畳、
カーペットなどは、カビが発生しやすい。さらに撹拌
機、混練機、充填機、地下ケーブル、医療機器などの様
々な機器にもカビが発生し、汚れ、不衛生、感染、漏電
などの障害をもたらす。また、最近は乾燥条件下にあっ
ても生育する好乾性カビの存在も多数報告され、カビ発
生によるアレルギー性諸症状の発症例も非常に多い。2. Description of the Related Art In recent years, with the completion of heating facilities and the airtightness of rooms, the occurrence of mold in rooms such as homes, offices and schools has been increasing. The appearance of mold is aesthetically
It is not good for hygiene. To prevent mold, it is necessary to keep it well-ventilated, dry and clean.
However, humid bathrooms and toilets, washrooms, or electronic devices such as refrigerators, ovens, mixers, tatami mats,
Molds easily occur on carpets and the like. In addition, various devices such as stirrers, kneaders, filling machines, underground cables, medical equipment, etc. will be moldy, causing damages such as dirt, unsanitary conditions, infection, and electric leakage. In addition, recently, a large number of psychrophilic molds that grow even under dry conditions have been reported, and there are very many cases of allergic symptoms caused by mold development.
【0003】従来、このようなカビの除去および防止す
る市販の薬剤として、次亜塩素酸塩を用いた強アルカリ
性溶液や、塩酸を用いた強酸性溶液が市販されている。
このような薬剤はいずれもカビ除去に一定の効果を示す
が、強アルカリ(pH12以上)や強酸(pH3以下)であ
るため非常に危険であり、皮膚に付着した場合はやけ
ど、皮の剥離、失明などの危険性がある。また、塩素系
の防カビ剤は悪臭が強く、鼻、のどに炎症を起こし、眼
に対する刺激も強く、充分な換気を行いながら作業する
ことが必要である。また、このような物理化学的作用の
強い防カビ剤を常用すると慢性的な呼吸障害を生じかね
ない。本発明の目的は、優れた防カビ作用を有し、しか
も人体に対し危険性のない防カビ剤を提供するものであ
る。Conventionally, a strong alkaline solution using hypochlorite and a strong acidic solution using hydrochloric acid are commercially available as commercially available agents for removing and preventing such molds.
All of these agents have a certain effect on mold removal, but they are very dangerous because they are strong alkali (pH 12 or more) or strong acid (pH 3 or less) .If they adhere to the skin, burns, peeling of skin, There is a risk of blindness. In addition, chlorine-based antifungal agents have a strong odor, cause inflammation of the nose and throat, and have a strong irritation to the eyes. Therefore, it is necessary to work with adequate ventilation. Moreover, chronic use of such an antifungal agent having a strong physicochemical action may cause a chronic respiratory disorder. An object of the present invention is to provide an antifungal agent which has an excellent antifungal effect and is not dangerous to the human body.
【0004】[0004]
【課題を解決するための手段】本発明は乳酸を含有する
防カビ剤を提供するものである。本発明の防カビ剤は基
材の表面に付着させることによってカビ発生を防止する
ことができる。本発明で用いられる乳酸はD−乳酸、L
−乳酸、D,L−乳酸のいずれかであってもよい。特に
醗酵法で得られたL−乳酸は人体で代謝され安全性が高
く好ましい。かかる乳酸を防カビ剤として使用するは、
乳酸を水溶液として使用するのが好ましい。かかる乳酸
水溶液の濃度は、0.1〜50%、好ましくは1〜10
%である。濃度がこの範囲より低いと充分な防カビ効果
が表れない。また、濃度がこの範囲より高いと価格も高
くなり、かつ排水を汚す恐れがある。乳酸水溶液を調製
するには、水中に所定量の乳酸粉末を投入し撹拌するの
がよい。また、90%乳酸醗酵液を水で希釈してもよ
い。乳酸の溶解は1〜30℃にて行うのが好ましい。The present invention provides a fungicide containing lactic acid. The fungicide of the present invention can prevent the generation of mold by adhering it to the surface of a substrate. Lactic acid used in the present invention is D-lactic acid, L
It may be either lactic acid or D, L-lactic acid. In particular, L-lactic acid obtained by the fermentation method is preferable because it is metabolized by the human body and is highly safe. The use of such lactic acid as a fungicide,
Preference is given to using lactic acid as an aqueous solution. The concentration of the aqueous lactic acid solution is 0.1 to 50%, preferably 1 to 10%.
%. If the concentration is lower than this range, sufficient antifungal effect cannot be obtained. Further, if the concentration is higher than this range, the price becomes high and the wastewater may be polluted. To prepare the aqueous lactic acid solution, it is preferable to add a predetermined amount of lactic acid powder to water and stir it. Alternatively, the 90% lactic acid fermentation liquid may be diluted with water. It is preferable to dissolve lactic acid at 1 to 30 ° C.
【0005】乳酸は酢酸についで解離定数の小さい有機
酸であって、pHが低くても従来の防カビ剤のような皮
膚への影響はない。特に、光学活性体のL−乳酸は輸液
にも使用され体内代謝される生体安全性の高い酸であ
り、蒸気圧が低く悪臭がない。この醗酵L−乳酸の殺カ
ビ試験の結果を表1に示す。Lactic acid is an organic acid having a small dissociation constant next to acetic acid, and even if the pH is low, it does not affect the skin like conventional fungicides. In particular, L-lactic acid, which is an optically active substance, is a highly biosafe acid that is also used for infusion and is metabolized in the body, and has a low vapor pressure and no bad odor. The results of the fungicidal test of this fermented L-lactic acid are shown in Table 1.
【0006】(試験方法)90%L−乳酸を所定濃度
(50%、10%)に希釈した後、1N−NaOHでp
H調整(pH1、pH3およびpH7)して、表1〜3
に示す所定の濃度のL−乳酸水溶液を各3本ずつ調製
し、各々内径26mmの試験管に18mlずつ用意した。予
め調製した各試験カビPenicilium funiculousum、Clado
spoliumcladosporioides、Aureobacidium pullulamsの
胞子懸濁液(105〜106個/ml)をそれぞれの試験管
に2mlずついれた。この試験管を20℃の恒温槽に入
れ、時々撹拌して3時間及び24時間目に1.0mlを無
菌的に取り出して0.005%エロゾルOT滅菌水で1
0倍希釈列を作った。作用原液及び各々の希釈段階から
0.1mlずつ2枚のブドウ糖ペプトン寒天培地にコンラ
ージ棒で塗布した。培地を27℃にて7日間培養し、発
生したカビの集落数を数えた。結果を表1〜3に示す。(Test method) After 90% L-lactic acid was diluted to a predetermined concentration (50%, 10%), p was added with 1N-NaOH.
H-adjusted (pH 1, pH 3 and pH 7), Tables 1-3
Three L-lactic acid aqueous solutions each having a predetermined concentration shown in (3) were prepared, and 18 ml each was prepared in a test tube having an inner diameter of 26 mm. Pre-prepared test mold Penicillium funiculousum, Clado
A spore suspension (10 5 to 10 6 cells / ml) of spolium cladosporioides and Aureobacidium pullulams was placed in each test tube in an amount of 2 ml. This test tube was put in a constant temperature bath at 20 ° C., stirred occasionally, and 1.0 ml was taken out aseptically at 3 hours and 24 hours, and it was diluted with 0.005% aerosol OT sterilized water to 1 ml.
A 0-fold dilution series was made. Two stocks of peptone agar, 0.1 ml each from the stock solution of action and each dilution step, were spread with a Conradi stick. The medium was cultured at 27 ° C. for 7 days, and the number of mold colonies generated was counted. The results are shown in Tables 1-3.
【0007】 (試験結果) 表1 Peniciliun funiculousum に対する殺カビ試験 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 作 用 時 間 試 料 試料濃度 3時間 24時間 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 3.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 7.0 50%(原液) 2.2×105 3.6×104 10% 4.5×105 3.0×105 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 対 照 滅菌蒸留水 4.5×105 3.8×105 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━(Test Results) Table 1 Fungicidal test for Peniciliun funiculousum ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ ━ Working time Samples Sample concentration 3 hours 24 hours ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50% (stock solution) <10 <10 10% <10 <10 ───────────────────────────────── ──── pH 3.0 50% (stock solution) <10 <10 10% <10 <10 ──────────────────────────── ───────── pH 7.0 50% (stock solution) 2.2 × 10Five 3.6 x 10Four 10% 4.5 x 10Five 3.0 x 10Five ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Sterilized distilled water 4.5 × 10Five 3.8 x 10Five ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━
【0008】 表2 Cladosporium cladosporioides に対する殺カビ試験 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 作 用 時 間 試 料 試料濃度 3時間 24時間 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 3.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 7.0 50%(原液) 2.0×104 2.0×104 10% 2.4×104 2.3×104 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 対 照 滅菌蒸留水 2.1×104 2.2×104 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━Table 2 Fungicidal test against Cladosporium cladosporioides ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Interval Sample concentration 3 hours 24 hours ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50 % (Stock solution) <10 <10 10% <10 <10 ───────────────────────────────────── pH 3.0 50% (stock solution) <10 <10 10% <10 <10 ──────────────────────────────── ───── pH 7.0 50% (stock solution) 2.0 × 10Four 2.0 x 10Four 10% 2.4 x 10Four 2.3 x 10Four ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Counter sterilized distilled water 2.1 × 10Four 2.2 x 10Four ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━
【0009】 表3 Aureobacidium pullulans に対する殺カビ試験 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 作 用 時 間 試 料 試料濃度 3時間 24時間 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 3.0 50%(原液) <10 <10 10% <10 <10 ──────────────────────────────────── pH 7.0 50%(原液) 2.7×103 1.2×10 10% 1.8×105 1.2×105 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ 対 照 滅菌蒸留水 3.0×105 3.4×105 ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━Table 3 Fungicidal test against Aureobacidium pullulans ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Interval Sample concentration 3 hours 24 hours ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ pH 1.0 50 % (Stock solution) <10 <10 10% <10 <10 ───────────────────────────────────── pH 3.0 50% (stock solution) <10 <10 10% <10 <10 ──────────────────────────────── ───── pH 7.0 50% (stock solution) 2.7 × 103 1.2 × 10 10% 1.8 × 10Five 1.2 x 10Five ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Counter sterilized distilled water 3.0 × 10Five 3.4 x 10Five ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━
【0010】表1〜3に示すごとく、乳酸濃度10%以
下の場合もL−乳酸の殺カビ性はpH3以下で顕著であ
る。L−乳酸は解離定数が低く家庭用、業務用の防カビ
剤として使用するにあたってはpHを低くし低濃度の乳
酸液とするのが価格的に好ましい。このように、光学活
性の乳酸、特に醗酵法で得られたL−乳酸の抗菌、抗カ
ビ作用は非常に高い。これは未解離乳酸が、カビ細胞内
に入り代謝系をくずしてカビを死滅させるか、乳酸菌自
身が抗菌作用を有する物質を産生していると思われる。As shown in Tables 1 to 3, even when the lactic acid concentration is 10% or less, the fungicidal property of L-lactic acid is remarkable at pH 3 or less. When L-lactic acid has a low dissociation constant and is used as a mildewproofing agent for households and businesses, it is preferable in terms of cost to lower the pH and use a low-concentration lactic acid solution. As described above, the optically active lactic acid, particularly L-lactic acid obtained by the fermentation method has a very high antibacterial and antifungal activity. This seems to be because undissociated lactic acid enters mold cells and destroys the metabolic system to kill mold, or lactic acid bacteria themselves produce substances having an antibacterial action.
【0011】本発明防カビ剤の代表的な組成としては、
L−乳酸1〜10%、界面活性剤0〜5%、漂白剤0〜
5%でpH1〜2の水溶液が挙げられる。また、他の防
カビ剤の組成としてはL−乳酸1〜10%、アルコール
55%以下からなるpH1〜2の水溶液が挙げられる。
この防カビ剤は主としてカビが発生していない所に使用
される。アルコールによる殺菌作用も加わりアルコール
蒸発後はL−乳酸の防カビ性が発揮される。The typical composition of the antifungal agent of the present invention is as follows:
L-lactic acid 1-10%, surfactant 0-5%, bleach 0-
An aqueous solution having a pH of 1 to 2 at 5% can be mentioned. Examples of the composition of the other fungicide include an aqueous solution of L-lactic acid 1 to 10% and alcohol 55% or less at a pH of 1 to 2.
This fungicide is mainly used in places where no mold is generated. The bactericidal action of alcohol is also added, and the fungicidal property of L-lactic acid is exhibited after the evaporation of alcohol.
【0012】これらの組成物はスプレー、エアゾール、
液状等の形態として容器に充填して用いる。使用にあた
っては防カビ剤をカビの発生の可能性のある壁、装置、
器具などの対象物に塗布する。既にカビの発生した部分
については塗布後軽くスポンジ等で洗い落とせばカビを
除去することができる。また、L−乳酸を他の溶剤およ
び成形品に混入して用いても同様の効果を生ずる。カビ
を除去した後、時々対象物に塗布することにより防カビ
効果が保持される。These compositions are sprays, aerosols,
It is used by filling it in a container in a liquid form or the like. Before use, use a fungicide on walls, devices, or
Apply to objects such as appliances. Molds can be removed by lightly washing them with a sponge or the like after application on the part where mold has already occurred. Further, the same effect can be obtained by using L-lactic acid mixed with other solvents and molded articles. After removing the mold, it is sometimes applied to the object to maintain the antifungal effect.
【0013】本発明の防カビ剤には、乳酸のほか非イオ
ン系界面活性剤などの適宜の界面活性剤、H2O2などの
漂白剤などを加えてもよい。In addition to lactic acid, an appropriate surface active agent such as a nonionic surface active agent and a bleaching agent such as H 2 O 2 may be added to the fungicide of the present invention.
【0014】[0014]
【実施例】つぎに本発明を実施例にもとづきさらに具体
的に説明する。L−乳酸5重量部、H2O22重量部、界
面活性剤3重量部および水90重量部を混合し防カビ剤
を調整した。pHは1.6であった。この防カビ剤を浴
室のメジに塗布したところ約3ケ月間カビ発生は認めら
れなかった。EXAMPLES Next, the present invention will be described more specifically based on examples. 5 parts by weight of L-lactic acid, 2 parts by weight of H 2 O 2 , 3 parts by weight of a surfactant and 90 parts by weight of water were mixed to prepare an antifungal agent. The pH was 1.6. When this fungicide was applied to a bathroom image, no mold was found for about 3 months.
【0015】[0015]
【発明の効果】本発明の防カビ剤は人体に対する安全性
が高くかつ優れた防カビ効果が得られる。EFFECT OF THE INVENTION The antifungal agent of the present invention is highly safe to the human body and has an excellent antifungal effect.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3180404A JPH0739325B2 (en) | 1991-06-24 | 1991-06-24 | Antifungal agent for home |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3180404A JPH0739325B2 (en) | 1991-06-24 | 1991-06-24 | Antifungal agent for home |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05908A true JPH05908A (en) | 1993-01-08 |
JPH0739325B2 JPH0739325B2 (en) | 1995-05-01 |
Family
ID=16082656
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3180404A Expired - Fee Related JPH0739325B2 (en) | 1991-06-24 | 1991-06-24 | Antifungal agent for home |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0739325B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006106673A1 (en) * | 2005-03-31 | 2006-10-12 | Calpis Co., Ltd. | Growth inhibitor for thermotolerant acidophilic bacterium, method for inhibition of growth of the bacterium, and method for production of acidic beverage |
JP2008515911A (en) * | 2004-10-08 | 2008-05-15 | メディクエスト セラピューティックス インク | Organogel preparation for treatment |
US20120269751A1 (en) * | 2009-11-11 | 2012-10-25 | Medner Holding Bv | Composition for topical application, uses thereof, applicator device and kit of parts |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5122825A (en) * | 1974-08-21 | 1976-02-23 | Rikagaku Kenkyusho | Kankitsuruino kajitsuno chozobyogaibojozai |
-
1991
- 1991-06-24 JP JP3180404A patent/JPH0739325B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5122825A (en) * | 1974-08-21 | 1976-02-23 | Rikagaku Kenkyusho | Kankitsuruino kajitsuno chozobyogaibojozai |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008515911A (en) * | 2004-10-08 | 2008-05-15 | メディクエスト セラピューティックス インク | Organogel preparation for treatment |
WO2006106673A1 (en) * | 2005-03-31 | 2006-10-12 | Calpis Co., Ltd. | Growth inhibitor for thermotolerant acidophilic bacterium, method for inhibition of growth of the bacterium, and method for production of acidic beverage |
JP4988560B2 (en) * | 2005-03-31 | 2012-08-01 | カルピス株式会社 | Method for producing acidic beverage |
US20120269751A1 (en) * | 2009-11-11 | 2012-10-25 | Medner Holding Bv | Composition for topical application, uses thereof, applicator device and kit of parts |
Also Published As
Publication number | Publication date |
---|---|
JPH0739325B2 (en) | 1995-05-01 |
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