JPH08239304A - Antibacterial agent - Google Patents

Antibacterial agent

Info

Publication number
JPH08239304A
JPH08239304A JP7066649A JP6664995A JPH08239304A JP H08239304 A JPH08239304 A JP H08239304A JP 7066649 A JP7066649 A JP 7066649A JP 6664995 A JP6664995 A JP 6664995A JP H08239304 A JPH08239304 A JP H08239304A
Authority
JP
Japan
Prior art keywords
fungicide
biguanide
antibacterial agent
agent
compound
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.)
Pending
Application number
JP7066649A
Other languages
Japanese (ja)
Inventor
Tomomasa Tsuchibuchi
智正 土渕
Ryuichi Murayama
隆一 村山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP7066649A priority Critical patent/JPH08239304A/en
Publication of JPH08239304A publication Critical patent/JPH08239304A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE: To obtain a biguanide-based antibacterial agent absolutely free from fungi in the agent and capable of preventing the secondary contamination of a food factory, etc., with fungus by adding a fungicide to a biguanide-based antibacterial agent. CONSTITUTION: This biguanide-based antibacterial agent contains a fungicide (especially preferably a halogen-containing nitrogen-sulfur compound or an isothiazoline compound). The biguanide-based antibacterial agent is chlorhexidine (for pharmaceutical use), polyhexamethylene biguanidine hydrochloride (for food factory), etc., and the agent exhibits antibacterial power against Gram-positive bacteria and Gram-negative bacteria at a low concentration. The content of the biguanide compound in the agent is 2-50%. Sufficient effect can be attained by adding the fungicide to the biguanide-based antibacterial agent in an amount of 50-5,000ppm for a halogen-containing nitrogen compound and 10-1,000ppm for an isothiazoline compound. There is no contamination of the antibacterial agent with fungi and the secondary contamination of a food factory, etc., caused by the contamination of the antibacterial agent can be prevented by the use of the antibacterial agent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はビグアナイド系殺菌剤に
殺カビ剤を配合し,カビによる2次汚染をなくした殺菌
剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a fungicide containing a biguanide fungicide and a fungicide which eliminates secondary contamination by fungi.

【0002】[0002]

【従来の技術】ビグアナイド系殺菌剤は毒性が低く,グ
ラム陽性・陰性菌に強い抗菌力を示すことから食品工場
で広く利用されている。
BACKGROUND OF THE INVENTION Biguanide fungicides are widely used in food factories because they have low toxicity and show strong antibacterial activity against Gram-positive / negative bacteria.

【0003】[0003]

【発明が解決しようとする課題】通常,殺菌剤は殺カビ
効果も有しているため,殺菌成分が高濃度(例えば1%
以上)に存在する殺菌剤自体がカビで汚染されることは
常識的には考えられず,従って,従来から,殺菌剤に更
に殺カビ剤を添加することは全く必要ないと考えられて
いた。ところが,本発明者らはビグアナイド系殺菌剤に
ついては,殺菌剤自身がある種のカビに汚染されるこ
と,従ってその使用により食品工場をカビにより2次汚
染する可能性のあることを初めて見出した。
Generally, since the bactericide also has a fungicidal effect, the bactericidal component has a high concentration (for example, 1%).
It is not common knowledge that the fungicide present in (1) above is contaminated with mold, and therefore it has been conventionally considered that it is not necessary to add a fungicide to the fungicide at all. However, the present inventors have found for the first time that with regard to the biguanide fungicides, the fungicides themselves are contaminated by certain molds, and therefore their use may cause secondary contamination of food factories. .

【0004】[0004]

【課題を解決するための手段】そこで,本発明者らが種
々検討した結果,ビグアナイド系殺菌剤に殺カビ剤を添
加混合することにより,殺菌剤中のカビは皆無となり,
食品工場でカビの2次汚染が無い殺菌剤を得ることが出
来ることを見出した。
[Means for Solving the Problems] Therefore, as a result of various investigations by the present inventors, by adding and mixing a fungicide to a biguanide fungicide, there is no mold in the fungicide,
It has been found that it is possible to obtain a fungicide without secondary contamination of mold in a food factory.

【0005】即ち,本発明は,殺カビ剤を含有すること
を特徴とするビグアナイド系殺菌剤に関する。従来,ビ
グアナイド系殺菌剤にも殺カビ作用があることは知られ
ており,この殺菌剤自体がカビに汚染されることは常識
的に考えられず,ビグアナイド系殺菌剤に殺カビ剤の添
加が必要であるということは,全く予想外なことであ
る。
That is, the present invention relates to a biguanide fungicide containing a fungicide. Conventionally, it is known that a biguanide fungicide also has a fungicidal action, and it is not common sense that the fungicide itself is contaminated by mold. Therefore, it is necessary to add a fungicide to the biguanide fungicide. The need is entirely unexpected.

【0006】本発明におけるビグアナイド系殺菌剤とし
ては,クロルヘキシジン,ポリヘキサメチレンビグアニ
ジン塩酸塩等があり,クロルヘキシジンは毒性が低いた
め,医療用に広く利用され,ポリヘキサメチレンビグア
ニジン塩酸塩は食品工場における機械,器具,容器,工
場環境の殺菌に利用されている公知の物質である。ビグ
アナイド系殺菌剤はグラム陽性菌,グラム陰性菌に対し
低濃度で強い殺菌力を示す。発明者の実験によればポリ
ヘキサメチレンビグアニジン塩酸塩のグラム陽性菌,グ
ラム陰性菌へのMICは数10〜数100ppm,カビ
へのMICは数100〜数1000ppmであった。本
発明のビグアナイド系殺菌剤は,他の殺菌剤,界面活性
剤,食用色素,水等の溶媒等の他の成分を含有すること
ができ,殺菌成分であるクロルヘキシジン,ポリヘキサ
メチレンビグアニジン塩酸塩等のビグアナイド系化合物
の含有量は,殺菌剤中,好ましくは1〜100%,通常
2〜50%である。
As the biguanide fungicides in the present invention, there are chlorhexidine, polyhexamethylene biguanidine hydrochloride and the like. Since chlorhexidine has low toxicity, it is widely used for medical purposes, and polyhexamethylene biguanidine hydrochloride is a food factory. It is a known substance used for sterilization of machinery, equipment, containers, and factory environment. Biguanide fungicides show strong bactericidal activity against gram-positive and gram-negative bacteria at low concentrations. According to experiments conducted by the inventor, the MIC of polyhexamethylene biguanidine hydrochloride for gram-positive bacteria and gram-negative bacteria was several tens to several hundreds ppm, and the MIC for mold was several hundreds to several thousand ppm. The biguanide fungicide of the present invention can contain other fungicides, surfactants, food dyes, other components such as solvents such as water, and the fungicides chlorhexidine and polyhexamethylene biguanidine hydrochloride. The content of biguanide compound such as is preferably 1 to 100%, and usually 2 to 50% in the fungicide.

【0007】本発明における殺カビ剤は公知の物質で良
く特に限定されないが,安全性の高いものが望ましい。
例えば,エタノール,イソプロピルアルコールなどのア
ルコール類,ソルビン酸,デヒドロ酢酸,パラオキシ安
息香酸エステルなどの有機酸類,チアベンダゾール,含
ハロゲン窒素硫黄系化合物,イソチアゾリン系化合物等
があげられるが,含ハロゲン窒素硫黄系化合物,イソチ
アゾリン系化合物が好ましい。
The fungicide in the present invention may be a known substance and is not particularly limited, but one having high safety is desirable.
Examples include alcohols such as ethanol and isopropyl alcohol, organic acids such as sorbic acid, dehydroacetic acid, paraoxybenzoic acid ester, thiabendazole, halogen-containing nitrogen-sulfur compounds, isothiazoline-based compounds, etc. , Isothiazoline compounds are preferred.

【0008】本発明においてビグアナイド系殺菌剤への
殺カビ剤の添加量はビグアナイド系殺菌剤の有効成分
(殺菌成分)濃度と関係無く,殺菌剤中に殺カビ剤をそ
の殺カビ有効濃度となるように添加し充分均一と成るよ
うに混合すればよい。例えば,含ハロゲン窒素硫黄系化
合物は殺菌剤中50ppm以上なら良く,好ましくは5
0〜5000ppmが良く,イソチアゾリン系化合物は
殺菌剤中10ppm以上,好ましくは10〜1000p
pmが良い。本発明の殺菌剤はそのまま用いてもよく,
水で適当に希釈して用いてもよい。
In the present invention, the addition amount of the fungicide to the biguanide fungicide is not related to the concentration of the active ingredient (bactericidal component) of the biguanide fungicide, and the fungicide in the fungicide has the fungicidal effective concentration thereof. And added so that they are sufficiently homogeneous. For example, the halogen-containing nitrogen-sulfur compound in the bactericide may be 50 ppm or more, preferably 5 ppm.
0-5000ppm is good, isothiazoline compounds are 10ppm or more in the bactericide, preferably 10-1000p
pm is good. The bactericide of the present invention may be used as it is,
It may be appropriately diluted with water before use.

【0009】[0009]

【実施例】以下に本発明の実施例を示す。 実施例1 ガラスビーカーにポリヘキサメチレンビグアニジン塩酸
塩20%水溶液を1kgを取り,含ハロゲン窒素硫黄系
化合物(商品名;スラオフ620(武田薬品工業株
製))を500mg添加し,スターラーで30分撹拌混
合し,本発明の殺菌剤Xを得た。
Examples of the present invention will be described below. Example 1 To a glass beaker, 1 kg of a 20% aqueous solution of polyhexamethylene biguanidine hydrochloride was added, and 500 mg of a halogen-containing nitrogen-sulfur compound (trade name; Slaoff 620 (manufactured by Takeda Pharmaceutical Co., Ltd.)) was added, and the mixture was stirred for 30 minutes with a stirrer. The mixture was stirred and mixed to obtain the bactericide X of the present invention.

【0010】実施例2 ガラスビーカーにポリヘキサメチレンビグアニジン塩酸
塩20%水溶液を500g,塩化ベンザルコニウム50
%水溶液を100g,ポリオキシエチレンアルキルエー
テルを100gそしてイソチアゾリン系化合物(商品
名;サンアイバックIT−20BT(三愛石油株製))
を100mg添加し,水を200ml加えスターラーで
30分撹拌混合して本発明の殺菌剤Yを得た。
EXAMPLE 2 500 g of a 20% aqueous solution of polyhexamethylene biguanidine hydrochloride and 50 g of benzalkonium chloride were placed in a glass beaker.
% Aqueous solution 100 g, polyoxyethylene alkyl ether 100 g, and isothiazoline compound (trade name; San-Ivac IT-20BT (manufactured by San-ai Petroleum Co., Ltd.))
Was added to 200 ml of water, and the mixture was stirred and mixed with a stirrer for 30 minutes to obtain a bactericide Y of the present invention.

【0011】実施例3 実施例1及び2の殺菌剤にカビの混入の無いことを次の
実験により確認した。一般的な混入汚染原因カビである
ペシドミセス属のカビを用いて実施例1及び実施例2の
殺菌剤のカビ汚染防止効果を検討した。表1に示した試
験品を濾過滅菌後,ペシドミセスの浮遊液(105 個/
ml)0.5mlを試験品50mlに加え,25℃で1
晩放置し,メンブランフィルターで濾過し,メンブラン
フィルターをポテトデキストロース寒天培地上で25
℃,7日間培養しカビの発育の有無で効果を判定した。
その結果を表1に示した。本発明の殺菌剤にはカビの発
育は認められずカビの混入の無いことが確認された。
Example 3 The following experiment confirmed that the fungicides of Examples 1 and 2 were free of mold. The fungicidal prevention effect of the fungicides of Examples 1 and 2 was examined using molds of the genus Pesidomyces, which is a common mold causing contamination. After the test products shown in Table 1 were sterilized by filtration, the suspension of Pescidomyces (10 5 /
0.5 ml) to 50 ml of the test product, and add 1 at 25 ° C.
Allow to stand overnight, filter through a membrane filter, and put the membrane filter on potato dextrose agar for 25
After culturing at 7 ° C for 7 days, the effect was judged by the presence or absence of mold growth.
The results are shown in Table 1. Mold growth was not recognized in the bactericide of the present invention, and it was confirmed that mold was not mixed.

【0012】[0012]

【表1】表1 試験品 カビ発生の有無 殺菌剤X(実施例1) カビ発生なし 殺菌剤Xから殺カビ剤を除いたもの 大量にカビ発生 殺菌剤Y(実施例2) カビ発生なし 殺菌剤Yから殺カビ剤を除いたもの 大量にカビ発生[Table 1] Table 1 Test product Presence or absence of mold fungicide X (Example 1) No mold occurrence Fungus disinfectant X excluding fungicides Large amount of mold fungicide Y (Example 2) No mold occurrence Sterilization Agent Y excluding fungicides A large amount of mold is generated

【0013】[0013]

【発明の効果】本発明の殺菌剤は殺菌剤自体が,カビに
汚染されることはなく,本発明の殺菌剤を使用すれば,
食品工場等において,殺菌剤自体のコンタミネーション
によるカビの2次汚染を防止することができる。
The fungicide of the present invention does not contaminate the fungicide itself with the fungicide of the present invention.
In food factories, etc., it is possible to prevent secondary contamination of mold due to contamination of the fungicide itself.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】殺カビ剤を含有することを特徴とするビグ
アナイド系殺菌剤。
1. A biguanide fungicide containing a fungicide.
【請求項2】殺カビ剤としてハロゲン化窒素硫黄系化合
物又はイソチアゾリン系化合物を含有する請求項1の殺
菌剤。
2. The fungicide according to claim 1, which contains a nitrogen halide sulfur compound or an isothiazoline compound as a fungicide.
JP7066649A 1995-03-02 1995-03-02 Antibacterial agent Pending JPH08239304A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7066649A JPH08239304A (en) 1995-03-02 1995-03-02 Antibacterial agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7066649A JPH08239304A (en) 1995-03-02 1995-03-02 Antibacterial agent

Publications (1)

Publication Number Publication Date
JPH08239304A true JPH08239304A (en) 1996-09-17

Family

ID=13321967

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7066649A Pending JPH08239304A (en) 1995-03-02 1995-03-02 Antibacterial agent

Country Status (1)

Country Link
JP (1) JPH08239304A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100325124B1 (en) * 1998-11-16 2002-10-12 에스케이케미칼주식회사 Fungicide composition and sterilization method using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100325124B1 (en) * 1998-11-16 2002-10-12 에스케이케미칼주식회사 Fungicide composition and sterilization method using the same

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