JPS6032602B2 - Treatment for livestock skin mycosis - Google Patents

Treatment for livestock skin mycosis

Info

Publication number
JPS6032602B2
JPS6032602B2 JP51085957A JP8595776A JPS6032602B2 JP S6032602 B2 JPS6032602 B2 JP S6032602B2 JP 51085957 A JP51085957 A JP 51085957A JP 8595776 A JP8595776 A JP 8595776A JP S6032602 B2 JPS6032602 B2 JP S6032602B2
Authority
JP
Japan
Prior art keywords
skin
livestock
bpmc
mycosis
treatment
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.)
Expired
Application number
JP51085957A
Other languages
Japanese (ja)
Other versions
JPS5312424A (en
Inventor
一郎 田中
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.)
Eisai Co Ltd
Original Assignee
Eisai 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 Eisai Co Ltd filed Critical Eisai Co Ltd
Priority to JP51085957A priority Critical patent/JPS6032602B2/en
Publication of JPS5312424A publication Critical patent/JPS5312424A/en
Publication of JPS6032602B2 publication Critical patent/JPS6032602B2/en
Expired legal-status Critical Current

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Memory System Of A Hierarchy Structure (AREA)

Description

【発明の詳細な説明】 本発明は家畜の皮膚真菌症治療剤に関するものである。[Detailed description of the invention] The present invention relates to a therapeutic agent for skin mycosis in livestock.

更に詳述すれば2ーセカンダリーブチルフェニル−N−
メチルカーバメート(以下BPMCと略称する)を有効
成分とする家畜の外用皮膚真菌症治療剤に関するもので
ある。家畜の皮膚真菌症は皮膚糸状菌の感染によりおこ
る皮膚病で、皮膚のケラチン化した組織に病変をおこし
、病変部は円心性に広がって円形になるゆえをもって輪
鷹と命名され、牛、馬、豚、羊、山羊等の家畜に観察さ
れる。
More specifically, 2-secondary butylphenyl-N-
The present invention relates to a therapeutic agent for external skin mycosis of domestic animals, which contains methyl carbamate (hereinafter abbreviated as BPMC) as an active ingredient. Dermatomycosis of livestock is a skin disease caused by infection with dermatophytes, and it causes lesions on the keratinized tissue of the skin.The lesions spread concentrically and become circular, hence the name ring hawk. , observed in livestock such as pigs, sheep, and goats.

皮膚真菌症に確患した家畜は、その症状である患部の蓬
感、疾病感、灼熱感等による苛立ち、不眠等が原因して
摂食性が悪くなり、栄養障害により、発育、肥育、搾乳
量の低下をみることとなる。また、他の有害細菌による
二次感染の危険もあり、他方、家畜としての商品価値を
大きく低下させる原因ともなる。近年、土地利用の合理
化により、濃密牧畜が促進され、家畜個体の接触性が高
くなり、家畜間の感染性が一層高まっている。
Livestock infected with skin mycosis have poor eating habits due to symptoms such as a dull feeling in the affected area, a feeling of illness, irritation due to burning sensation, insomnia, etc., and malnutrition, resulting in decreased growth, fattening, and milk production. We will see a decline in In addition, there is a risk of secondary infection by other harmful bacteria, which also causes a significant decrease in the commercial value of livestock. In recent years, rationalization of land use has promoted intensive grazing, which has increased contact between individual livestock and further increased the risk of infection between livestock.

さらに、これら真菌の人体に対する感染性も高いために
、この家畜の真菌感染症は畜産業にたずさわる者にとっ
ても大きな問題となっている。
Furthermore, since these fungi are highly infectious to the human body, these fungal infections of livestock are also a major problem for those involved in the livestock industry.

皮膚真菌症の病原体は皮膚真菌(糸状菌)で、菌体は菌
糸と胞子からなる。菌糸はもっぱら痴皮および表皮内に
あり、芽胞は被毛に付着し、また毛幹内に入る。真菌に
はきわめて種類が多くト分類もまちまちであるが、大別
すると次のa.小胞子菌(micro−sporon)
b.白鷹菌(mchophyPn)およびc.黄鷹菌(
achorion)の3種であり、通常は、これらの菌
種の単独または混合感染の形をとる。
The pathogen of dermatomycosis is a skin fungus (filamentous fungus), and the fungal body consists of hyphae and spores. The hyphae are found exclusively within the epidermis and epidermis, and the spores attach to the hair coat and also enter the hair shaft. There are many types of fungi and different classifications, but they can be broadly classified into the following types: a. micro-sporon
b. mchophyPn and c. yellow hawk fungus (
achorion) and usually takes the form of single or mixed infections of these bacterial species.

家畜の皮膚真菌症の治療方法としては、紫外線・X線照
射等の理学的療法やL角質溶解剤(サリチル酸、クリサ
ロビン等)、不飽和脂肪酸(ウンデシレン酸等)、抗生
物質(グリセオフラビン、バリオチン等)の薬物療法が
行われているが箸効はない。
Treatment methods for skin mycosis in livestock include physical therapy such as ultraviolet rays and etc.), but it has no effect.

近年、有機隣系薬剤の1種である2,2,2ートリクロ
ル−1一オキシェチルホスホン酸ジメチル(一般名トリ
クロルホン)を有効成分とする製剤が家畜の皮膚真菌症
治療剤として使用されているが、効果の点および薬物の
安定性、毒性等の点で未だ解決されない問題が残されて
いる。
In recent years, preparations containing dimethyl 2,2,2-trichlor-1-oxyethylphosphonate (generic name trichlorfon), which is a type of organic compound, have been used as a treatment for skin mycosis in livestock. However, there are still unresolved problems in terms of efficacy, drug stability, toxicity, etc.

本発明者は、上記の如く、牧畜家に多大の経済的被害を
与え、ひいては畜産業界に大きな打撃を与えているこれ
ら家畜の皮膚真菌症に対し、更に治療に有効な化合物を
探索した結果、BPMCの使用が所期の目的を達成し、
家畜の皮膚真菌症に対し、予想外の効果があることを見
出した。
As mentioned above, the present inventors have searched for compounds that are more effective in treating skin mycosis in livestock, which causes great economic damage to livestock farmers and is also a major blow to the livestock industry. The use of BPMC achieves the intended purpose,
It was discovered that it has an unexpected effect on skin mycosis in livestock.

従って本発明の目的は、家畜の皮膚真菌症に対して、新
規で有効な治療剤を提供することにある。本発明に使用
する化合物BPMC(化学名:2ーセカンダリーブチル
フエニルーNーメチルカーバメート)は次の化学式(1
)で表わされるカーバメィト系薬剤の1種であり、融点
3〆○で僅かな芳香を有し、アセトン、トルェン、キシ
レン等には可溶であり、水には殆ど溶けない。
Therefore, an object of the present invention is to provide a new and effective therapeutic agent for skin mycosis in livestock. The compound BPMC (chemical name: 2-sec-butyl phenyl-N-methyl carbamate) used in the present invention has the following chemical formula (1
It is a type of carbamate drug represented by ), has a melting point of 3〆○, has a slight aroma, is soluble in acetone, toluene, xylene, etc., and is almost insoluble in water.

毒性に関しては、BPMCの毒性は極めて低く、安全性
が高い。
Regarding toxicity, BPMC has extremely low toxicity and is highly safe.

即ち、雄性マウスによる急性毒性(LD則経口)は34
0のo/k9で、雄性ラットでは410の夕/k9であ
り、マウスによる経皮毒性(LD5o)は4,200の
9/k9である。BPMCの家畜の皮膚真菌に対する抗
菌性式験(ィンビトロ)の概要およびその結果は次の如
くである。
That is, the acute toxicity (LD rule oral) for male mice is 34
It has an o/k9 of 0, an o/k9 of 410 in male rats, and a dermal toxicity (LD5o) of 4,200 in mice. The outline and results of the antibacterial test (in vitro) of BPMC against livestock skin fungi are as follows.

なお比較化合物としてトリクロルホンを設定した。抗皮
膚真菌試験 〔1〕 試験化合物 BPMC トリクロルホン 〔2〕 供試皮膚真菌 TrichophれonVermCOS山mTrich
ophれonmbてmmMicrospommgyPS
eum Microsporumlangeronll〔3〕
試験方法Official Methods of A
nal$is of AOAC(1973王)F皿ぎc
idaITesK51の方法に従って行った。
Note that trichlorfon was set as a comparative compound. Anti-skin fungal test [1] Test compound BPMC Trichlorfon [2] Test skin fungus Trichoph onVermCOS YamamTrich
ophreonmbetemmMicrospommgyPS
eum Microsporumlangeronll [3]
Test method Official Methods of A
nal$is of AOAC (1973 King) F Saragi c
It was carried out according to the method of idaITesK51.

■ 供試皮膚真菌々株をポテトデキストローズ寒天スラ
ント培地に純培養する。
■ Purely culture the test skin fungus strain on potato dextrose agar slant medium.

25qoで10〜20日間(菌株によって発育速度が異
なる)培養後、2〜5℃で保存する。
After culturing at 25qo for 10 to 20 days (growth rate varies depending on the strain), store at 2 to 5°C.

■ 使用直前に袷所より菌株を取出し、胞子生食液を作
り、冷所(2〜500)にに保存する。
■ Immediately before use, remove the bacterial strain from the sleeve, make a spore saline solution, and store it in a cool place (2-500℃).

■ 試験化合物を蒸留水を用いて最高濃度1%とし、各
1M音希釈液を作る。(最終濃度1%、0.1%、0.
01%および0.001%の4段階濃度の希釈液を調製
する)■ ■で調製した試験化合物の各濃度の希釈液1
の上に■で調製した各菌株の胞子生食液0.1の‘をよ
く蝿拝しながら加え、感作開始とし、開始15分後、6
0分後、2御特間後および4報時間後に各々の溶液より
1ェーゼを取り、これを生食水で1〜2回洗い、脳心臓
浸出寒天平板に接種し、2500で15日間培養後、判
定する。
■ Make 1M sonic dilutions of each test compound using distilled water to a maximum concentration of 1%. (Final concentration 1%, 0.1%, 0.
Prepare dilution solutions with four concentrations of 0.01% and 0.001%) ■ Dilution solution 1 of each concentration of the test compound prepared in ■
Add 0.1% of the spore saline solution of each strain prepared in ① to the top of the sensitization, stirring carefully. 15 minutes after the start, 6
After 0 minutes, 2 hours, and 4 hours, remove 1ase from each solution, wash it once or twice with saline, inoculate it on a brain heart infusion agar plate, and culture it at 2500℃ for 15 days. judge.

〔4〕結果 試験結果は次表の如くである。[4] Results The test results are shown in the table below.

表は供試皮膚真菌々株毎に、機に感作時間15分、6び
分、2岬時間および4斑時間をとり、縦に試験化合物の
濃度を示した。
The table shows the sensitization time of 15 minutes, 6 minutes, 2 days and 4 days for each skin fungus strain tested, and the concentration of the test compound is shown vertically.

効果の判定において−:抗菌作用あり土:抗菌作用の影
響が認められる (菌の発育は著しく認められているか、死滅しつつある
In determining effectiveness -: Antibacterial effect Soil: Antibacterial effect is observed (bacterial growth is significant or is dying out.

)十:抗菌作用なし とする。) 10: No antibacterial effect shall be.

{l) Trichophyton VetruC0S
um(ii1 Trichophyton rubr
um(iiD MiCrOSp。
{l) Trichophyton VetruC0S
um(ii1 Trichophyton rubr
um(iiD MiCrOSp.

rum gypSeumこの試験結果より明らかなよう
に、BPMCの家畜の皮膚真菌に対する抗菌性は優れた
ものであり、その作用はトリクロルホンよりも強力であ
る。次に、BPMCを皮膚真菌症に感染している牛の治
療に用いた例を示すことにより、BPMCの治療効果を
示す。
As is clear from the results of this test, BPMC has excellent antibacterial properties against skin fungi of livestock, and its action is stronger than that of trichlorfon. Next, the therapeutic effect of BPMC will be demonstrated by showing an example in which BPMC was used to treat a cow infected with a skin mycosis.

なお、比較化合物としてトリクロルホンを設定した。牛
の皮膚真菌症治療〔1〕 試験化合物 BPMC トリクロルホン BPMCは濃度1%および0.1%の流動パラフィン溶
液とした。
Note that trichlorfon was set as a comparative compound. Treatment of Bovine Skin Mycosis [1] Test Compound BPMC Trichlorfone BPMC was prepared as a liquid paraffin solution with a concentration of 1% and 0.1%.

トリクロルホンは少量のエタノールで溶解したのち、流
動パラフィンを加えて濃度1%およびo.1%溶液とし
た。
After dissolving trichlorfon in a small amount of ethanol, liquid paraffin was added to give a concentration of 1% and o. It was made into a 1% solution.

〔2〕 対象動物 ホルスタイン種牛、雄 約3カ月齢 比較的症状が重く、梶患初期と判断されるもの8頭を選
出し、試験薬剤各濃度につき2頭を使用した。
[2] Target Animals Eight male Holstein cows, approximately 3 months old, with relatively severe symptoms, and considered to be in the early stages of pharyngeal disease were selected, and 2 were used for each concentration of the test drug.

〔3〕 治療方法 〔1〕で調製した試験化合物の各濃度の溶液を1週間々
隔で3回患部に塗布し、最終塗布1週間後の患部の状態
を観察した。
[3] The solution of each concentration of the test compound prepared in treatment method [1] was applied to the affected area three times at one-week intervals, and the condition of the affected area was observed one week after the final application.

〔4〕結果 溶液塗布患部の痴皮の脱落および発毛の状態を判定基準
とした。
[4] Results The criteria for evaluation were the shedding of the skin and the state of hair growth on the affected area where the solution was applied.

判定基準は次の通りである。The judgment criteria are as follows.

− 痴皮の脱落、発毛は認められず。- No shedding of skin or hair growth was observed.

十 痴皮の脱落は認められたが、発毛は認められなかっ
た。
(10) Shedding of the skin was observed, but no hair growth was observed.

什 痴皮の脱落、発毛が認められた。However, shedding of the skin and hair growth were observed.

川 痴皮の脱落、著しい発毛が認められた。Kawa: Shedding of the skin and significant hair growth were observed.

結果は次表の如くである。(iv) Microspo
rum langeronllこの結果より、BPMC
には優れた治療効果が認められ、その効果はトリクロル
ホンよりも優れたものである。
The results are shown in the table below. (iv) Microspo
rum langeroll From this result, BPMC
It has been shown to have excellent therapeutic effects, and its efficacy is superior to that of trichlorfon.

本発明を実施する場合の剤形としては、粉剤、乳剤、塗
布剤、清拭剤、軟膏剤、パスタ剤、リニメント剤、ロー
ション剤、水和剤、油剤等の外用製剤を挙げる事ができ
る。
Examples of dosage forms for carrying out the present invention include external preparations such as powders, emulsions, liniments, wipes, ointments, pastes, liniments, lotions, wettable powders, and oils.

この場合、製剤化に際しては、通常の製剤学の技術を用
いることができる。次にBPMCを有効成分とする製剤
例を実施例として示す。
In this case, ordinary pharmaceutical techniques can be used for formulation. Next, examples of formulations containing BPMC as an active ingredient will be shown as examples.

実施例1 乳 剤 処方: 常法により乳剤を調製する。Example 1 Emulsion Prescription: An emulsion is prepared by a conventional method.

実施例 2 処方: 常法により粉剤を調製する。Example 2 Prescription: A powder is prepared by a conventional method.

実施例3 水和剤 処方: BPMC 4の重量%
ホワイトカーボン 40 〃ア
ルキルアリールトリエチングリコール6 〃ドデシルベ
ンゼンスルホン酸ソーダ 5 ″ポリビニルアルコール
2 〃常法により水和剤を調製する。
Example 3 Wettable powder formulation: Weight % of BPMC 4
White carbon 40 Alkylaryltriethine glycol 6 Sodium dodecylbenzenesulfonate 5 ″Polyvinyl alcohol
2. Prepare a hydrating powder using a conventional method.

実施例 4 油剤 処方: 常法により油剤を調製する。Example 4 Oil agent Prescription: Prepare an oil solution using a conventional method.

Claims (1)

【特許請求の範囲】 1 2−セカンダリ−ブチルフエニル−N−メチルカー
バメートを有効成分とする家畜の皮膚真菌症治療剤。 2 外用剤である特許請求の範囲第1項記載の家畜の皮
膚真菌症治療剤。
[Scope of Claims] 1. A therapeutic agent for skin mycosis of domestic animals, which contains 2-secondary-butylphenyl-N-methylcarbamate as an active ingredient. 2. The therapeutic agent for skin mycosis in domestic animals according to claim 1, which is an external preparation.
JP51085957A 1976-07-21 1976-07-21 Treatment for livestock skin mycosis Expired JPS6032602B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51085957A JPS6032602B2 (en) 1976-07-21 1976-07-21 Treatment for livestock skin mycosis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51085957A JPS6032602B2 (en) 1976-07-21 1976-07-21 Treatment for livestock skin mycosis

Publications (2)

Publication Number Publication Date
JPS5312424A JPS5312424A (en) 1978-02-03
JPS6032602B2 true JPS6032602B2 (en) 1985-07-29

Family

ID=13873216

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51085957A Expired JPS6032602B2 (en) 1976-07-21 1976-07-21 Treatment for livestock skin mycosis

Country Status (1)

Country Link
JP (1) JPS6032602B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK181988A (en) * 1988-03-30 1989-10-01 Dumex Ltd As THIOCARBAMIC ACID RESIDUES FOR USE AS A THERAPEUTIC AND PREPARATION FOR THE TREATMENT OF ALCOHOL ABUSE

Also Published As

Publication number Publication date
JPS5312424A (en) 1978-02-03

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