JPS60197622A - Bacteriocidic composition - Google Patents

Bacteriocidic composition

Info

Publication number
JPS60197622A
JPS60197622A JP5392184A JP5392184A JPS60197622A JP S60197622 A JPS60197622 A JP S60197622A JP 5392184 A JP5392184 A JP 5392184A JP 5392184 A JP5392184 A JP 5392184A JP S60197622 A JPS60197622 A JP S60197622A
Authority
JP
Japan
Prior art keywords
compound
composition
silver salt
sodium laurylsulfate
bactericidal
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
JP5392184A
Other languages
Japanese (ja)
Inventor
Ryuichi Kawahara
川原 隆一
Hideaki Matsuda
松田 秀明
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.)
SSP Co Ltd
Original Assignee
SSP 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 SSP Co Ltd filed Critical SSP Co Ltd
Priority to JP5392184A priority Critical patent/JPS60197622A/en
Publication of JPS60197622A publication Critical patent/JPS60197622A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:A bacteriocidal composition that is obtained by adding sodium laurylsulfate as a surface active agent to a silver salt of sulfa drug, thus markedly increasing the bactericidal effect of the sulfa drug which has been used as a bactericidal or bacteriostatic agent. CONSTITUTION:The objective composition is obtained by adding sodium laurylsulfate to a silver salt of sulfa drugs such as compounds of formulas I and II. The amount of the sodium laurylsulfate is 0.01-1% based on the composition and 6.5-20,000 at a weight ratio. When the drug is not heat-treated, the addition of more than 0.01% of sodium laurylsulfate increases the bactericidal effect 8- 250 times.

Description

【発明の詳細な説明】 本発明は、殺菌−剤組放物に関し、更に詳細にはスルフ
ァ剤銀塩とラウリル硫酸ナトリウムを含有する殺菌剤組
成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a disinfectant composition, and more particularly to a disinfectant composition containing a sulfur drug silver salt and sodium lauryl sulfate.

本発明者らは、抗生物質とともに殺菌剤、静菌剤として
広く用いられているスルファ剤について、更にその薬効
を向上すべく種々研究をおこなっていたところ、スルフ
ァ剤の銀塩に界面活性剤の6性も曳くなることを見出し
、本発明を完成した。
The present inventors were conducting various studies to further improve the efficacy of sulfa drugs, which are widely used as bactericidal and bacteriostatic agents along with antibiotics. The present invention was completed based on the discovery that the same effect can be applied to sexes.

したがって本発明は、スルファ剤銀塩とラウリル硫酸ナ
トリウムを含有する殺菌剤組成物を提供するものである
Accordingly, the present invention provides a disinfectant composition containing a sulfonate silver salt and sodium lauryl sulfate.

本発明で用いられるスルファ剤銀塩としては、例えば次
の式で示されるものが挙げられる。
Examples of the sulfur agent silver salt used in the present invention include those represented by the following formula.

化合物1゜ 化合物2゜ 化合物3゜ 化合物4゜ 化合物5゜ 化合物6゜ 化合物7・ 化合物8、 化合物9・ Aヌ 化合物10゜ 化合物11゜ 化合物12゜ 化合物13゜ 化合物14゜ 化合物15゜ 化合物16゜ 化合物17゜ 化合物18゜ 化合物19゜ 化合物20゜ 化合物21゜ 化合物22゜ 化合物23゜ 化合物24゜ 化合物25゜ 化合物26゜ 化合物27゜ 化合物29゜ 化合物30゜ 化合物31゜ 化合物32゜ 化合物33゜ 化合物34゜ 化合物35゜ 化合物36゜ 化合物37゜ 化合物38゜ 化合物39゜ 化合物40゜ これら銀塩は、常法に従い、例えばスルファ剤ナトリウ
ム塩に硝酸銀を滴下することによシ調製される。
Compound 1゜Compound 2゜Compound 3゜Compound 4゜Compound 5゜Compound 6゜Compound 7, Compound 8, Compound 9, Compound 10゜Compound 11゜Compound 12゜Compound 13゜Compound 14゜Compound 15゜Compound 16゜Compound 17° Compound 18° Compound 19° Compound 20° Compound 21° Compound 22° Compound 23° Compound 24° Compound 25° Compound 26° Compound 27° Compound 29° Compound 30° Compound 31° Compound 32° Compound 33° Compound 34 Compound 35° Compound 36° Compound 37° Compound 38° Compound 39° Compound 40° These silver salts are prepared by a conventional method, for example, by dropping silver nitrate onto the sodium salt of the sulfa drug.

本発明の殺菌剤組成物は、公知の方法によってクリーム
剤、軟膏剤、全開、殺菌発泡錠等の剤型とすることがで
き、その用量は、通7常のスルファ剤を用いる殺菌剤に
準じて定められる。
The bactericidal composition of the present invention can be made into a cream, ointment, sterile effervescent tablet, etc. by a known method, and the dosage is generally the same as that of a bactericidal agent using a conventional sulfa drug. It is determined by

本発明の殺菌剤組成物を調製するには、組成中にラウリ
ル硫酸ナトリウムを0.0011以上、スルファ剤銀塩
1に対し重量比で0.001以上配合すれば良い。就中
、特に好ましいラウリル硫酸ナトリウムの配合量は、組
成中0.01〜1%、スルファ剤銀塩1に対し、電量比
で6.5〜20000である。
In order to prepare the disinfectant composition of the present invention, sodium lauryl sulfate may be blended in the composition in a weight ratio of 0.0011 or more, or 0.001 or more per 1 of sulfur agent silver salt. Among these, a particularly preferred amount of sodium lauryl sulfate is 0.01 to 1% in the composition, and a coulometric ratio of 6.5 to 20,000 per 1 of sulfur agent silver salt.

次に本発明の殺菌剤組成物についてその殺菌作用を試験
した結果を示す。
Next, the results of testing the bactericidal action of the bactericidal composition of the present invention will be shown.

〔殺菌作用試験〕[Bactericidal action test]

試験例1 ラウリル硫酸ナトリウムを滅菌水で溶解し、100w/
#LIf’、2QIv/a/、2#l/+117.0,
24/m及び0.92M97−の溶液を作る。これらを
各5−づつそれぞれ異なる試験管に分注し、これに更に
それぞれの濃度に滅菌水で溶解又は懸濁した前記化合物
■溶液5dを加えて各種濃度の組成物試料液を調整する
。この各試料液を37℃恒温槽中に約3時間保持した後
、これに予め37℃で20〜24時間培養したニジエリ
シア・コリ0−1、シュードモナス・アエルギノーザI
FO13736及びスタヒロコツカス・アウレウスAT
CC65389それぞれの培養液1wLlを加え、1時
間後この液の1白金耳を普通ブイヨン培養基に接種し、
接種48時間後の菌の発育の有無を観察した。又熱安定
性を見る為120℃−20分間高圧滅菌した各試料液に
ついても同様の試験を行なった。
Test Example 1 Sodium lauryl sulfate was dissolved in sterile water and 100w/
#LIf', 2QIv/a/, 2#l/+117.0,
Make a solution of 24/m and 0.92M97-. Amounts of each of these are dispensed into different test tubes, and a solution 5d of the compound (1) dissolved or suspended in sterilized water at each concentration is added to prepare composition sample solutions of various concentrations. After keeping each sample solution in a 37°C constant temperature bath for about 3 hours, it was added to N. coli 0-1 and Pseudomonas aeruginosa I, which had been previously cultured at 37°C for 20 to 24 hours.
FO13736 and Stahylococcus aureus AT
Add 1wLl of each culture solution of CC65389, and after 1 hour, inoculate one platinum loopful of this solution into a normal bouillon culture medium.
The presence or absence of bacterial growth was observed 48 hours after inoculation. Further, in order to examine thermal stability, the same test was conducted for each sample solution that had been autoclaved at 120° C. for 20 minutes.

この結果を第1表に示す。The results are shown in Table 1.

第 l 表 試験例2 ラウリル硫酸ナトリウムを滅菌水で溶解し2ダ/−の溶
液を作る。これらを各5−づつそれぞわ異なる試験管に
分注し、これに更にそれぞれのE度に滅菌水で溶解又は
懸濁したスルファ剤銀塩氾液5dを加え、各濃度の組成
物試料液を調製しに以下試験例1と同様にしてスタヒ゛
ロコツカス・JタレウスATCC65389に対するM
LC値を演定した。この結革を第2表に示す。
Table l Test Example 2 Dissolve sodium lauryl sulfate in sterile water to make a 2 da/- solution. Dispense 5 ml of these into different test tubes, add 5 d of sulfa drug silver salt solution dissolved or suspended in sterile water to each E degree, and add composition sample solution of each concentration. M against Staphylococcus J. thalaeus ATCC65389 was prepared in the same manner as in Test Example 1.
LC values were determined. The results are shown in Table 2.

以下余白 第 2 表 上記結果から明らかな如く、加熱処理をしない場合には
ラウリル硫酸ナトリウム0.Ol−以上添加する事によ
シスルファ剤銀塩の殺菌効果は1〜64倍に向上し、ま
た、加熱処理した場合はラウリル硫酸ナトリウム0.0
01S以上添加する事によりスルファ剤銀塩の殺菌効果
は8〜250倍に向上する。
Table 2: Table 2 As is clear from the above results, sodium lauryl sulfate is 0.5% when no heat treatment is performed. The bactericidal effect of cisulfur agent silver salt is improved by 1 to 64 times by adding more than 100 ml of sodium lauryl sulfate.
By adding 01S or more, the bactericidal effect of the sulfur agent silver salt is improved by 8 to 250 times.

次に参考例及び実施例を挙げ本発明を説明する。Next, the present invention will be described with reference to reference examples and examples.

参考例1 スルファメタシン2.78y−を20−の水に懸濁し、
水酸化ナトリウム0.40Fを201+11の水に溶か
したものを滴下する。5〜30分攪拌し不溶部を濾過す
る。P液に硝酸銀1.70y−を20+111の水に溶
かしたものを滴下し、ついで水4017を加え30分〜
1時間攪拌する。析出する結晶を水、エタノール、エー
テルで順次洗浄し、風乾するとスルファメタシン銀塩(
化合物5)3.27F(収率85チ)が得られる。融点
300℃以上。
Reference Example 1 2.78y- of sulfamethacin was suspended in 20-y water,
Drop a solution of 0.40F sodium hydroxide dissolved in 201+11 water. Stir for 5 to 30 minutes and filter the insoluble portion. Add 1.70y- of silver nitrate dissolved in 20+111 water to the P solution, then add 4017 of water for 30 minutes.
Stir for 1 hour. The precipitated crystals were washed sequentially with water, ethanol, and ether, and air-dried to form sulfamethacine silver salt (
Compound 5) 3.27F (yield: 85%) is obtained. Melting point 300℃ or higher.

参考例2 スルファメラジンナトリウム塩2.86fを20−の水
に溶解し、不溶部を一過する。f液に、硫酸銀1.70
f−を26mtの水に溶解した溶液を滴下し、ついで水
4011jを加え30分〜1時間攪拌する。析出する結
晶を水、エタノール、エーテルで順次洗浄し、風乾する
とスルファメタシン銀塩(化合物4)3.275!−(
収率88チ)が得られる。
Reference Example 2 2.86f of sulfamerazine sodium salt is dissolved in 20-ml water, and the insoluble portion is passed through. Silver sulfate 1.70 in f solution
A solution of f- dissolved in 26 mt of water is added dropwise, then water 4011j is added and stirred for 30 minutes to 1 hour. The precipitated crystals were sequentially washed with water, ethanol, and ether, and air-dried to yield sulfamethacine silver salt (compound 4) at 3.275%! −(
A yield of 88 h) is obtained.

融点272〜275℃(分解)。Melting point 272-275°C (decomposition).

実施例1(親水軟膏) 常法に従い、下記成分・分量の親水軟膏100?を製し
た。
Example 1 (Hydrophilic ointment) Hydrophilic ointment 100? was manufactured.

スルファベンズアミド銀 11 ラウリル硫酸ナトリウム 1.5を 白色ワセリン 14y− ステアリルアルコール 22? プロピレングリコール 15y− イングロパノールエステル 8? 精製水をもって全量100?とする。Sulfabenzamide silver 11 Sodium lauryl sulfate 1.5 White Vaseline 14y- Stearyl alcohol 22? Propylene glycol 15y- Inglopanol ester 8? Total amount is 100 with purified water? shall be.

実施例2(マクロゴール軟膏) 、常法に従い下記成分・分量のマクロゴール軟膏100
g−を製した。
Example 2 (Macrogol ointment) Macrogol ointment 100 with the following ingredients and amounts according to the usual method
g- was produced.

スルファベンズアミド銀 l? ラウリル硫酸ナトリウム ILt グロビレングリコール IO? マクロゴール4000 44t マクロゴール400 44) 実施例3(殺菌発泡錠) 常法に従い、下記成分・分量の錠剤1個を製した。Sulfabenzamide silver l? Sodium lauryl sulfate ILt Globylene glycol IO? macro goal 4000 44t Macrogoal 400 44) Example 3 (sterilized effervescent tablet) One tablet having the following ingredients and quantities was prepared according to a conventional method.

Nlアセチルスルファニルアミド°銀 500Qラウリ
ル硫酸ナトリウム 1000# クエン酸 700ダ 炭酸水重ナトリウム 1000+19 ヒドロキシグロビルセルロース 101vマンニツトを
もって全量を400 (19とする。
Nl acetylsulfanilamide ° Silver 500 Q Sodium lauryl sulfate 1000 # Citric acid 700 Da Bisodium carbonate 1000 + 19 Hydroxyglobil cellulose 101 V Mannitol makes the total amount 400 (19).

以上 手続補正書(自発) 1、 事件の表示 昭和59年 特 許 願第 53921号2、発明の名
称 殺菌剤組成物 3、 補正をする者 事件との関係 出願人 住 所 東京都中央区日本橋浜町2丁目12番4号名 
称 エスエ諷製薬株式金社 代表者泰 道直方 4、代理人 6、 補正の対象 明細書の「発明の詳細な説明」の欄 7、補正の内容 α) 明細書中、第2Jj第4行、 (り 同、第5員第4行、 (3) 同、第6員第6行、 」 ←) 同、第11頁、第12行 「工FO13736及び」とめるを、 「工yo137!16又は」と訂正する。
Written amendment to the above procedure (voluntary) 1. Indication of the case Patent Application No. 53921 filed in 1982 2. Title of the invention: Fungicide composition 3. Relationship with the case by the person making the amendment Applicant's address: Nihonbashihama-cho, Chuo-ku, Tokyo 2-chome 12-4 name
Name: SA Yoshiyaku Co., Ltd. Representative Yasushi Michi Naokata 4, Agent 6 Column 7 of "Detailed Description of the Invention" of the specification to be amended, Contents of the amendment α) In the specification, line 2Jj, line 4, (Ibid., 5th member, line 4, (3) 6th member, line 6, ←) Ibid., page 11, line 12, "Eng. FO13736 and" stop, "Eng. yo137!16 or" I am corrected.

(5) 同、同、第13〜14行 「ムT0065389それぞれの培養液1−」とめる會
、 rATa06538Fの培養液1−」と訂正する。
(5) Identical, same, lines 13-14 are corrected to "Culture solution 1- of each of MuT0065389, culture solution 1- of rATa06538F."

(6) 同、第12員第1表中、最小致死濃度(MI、
O) (μf/Wrt)の右欄、「スタヒ四プツカスー
アウVクス ムTO065389Jとおるを、 「スタヒロコツ力ス・アウレウス ム丁006538P Jと訂正する。
(6) Minimum lethal concentration (MI,
O) In the right column of (μf/Wrt), ``Stahi 4 Putskasuau V Kusum TO065389J Toru is corrected to ``Stahirokotsu Force Aureusum TO006538P J.''

(η 同、第13頁第8行、 rATOc!65389Jとあるを、 「ムT(306538P Jと1正する。(η Same, page 13, line 8, rATOc! It says 65389J, "M T (306538P J and 1 correct.

(8) 同、第163に第1行 rFll[に、硫」とめる金、 rFi[に、硝」と訂正する。(8) Same, line 163 rFll [in, sulfur] gold, rFi [ni, nitsu] is corrected.

Claims (1)

【特許請求の範囲】[Claims] 1、スルファ剤銀塩とラウリル硫酸ナトリウムを含有す
る殺菌剤組成物。
1. A disinfectant composition containing a sulfur agent silver salt and sodium lauryl sulfate.
JP5392184A 1984-03-21 1984-03-21 Bacteriocidic composition Pending JPS60197622A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5392184A JPS60197622A (en) 1984-03-21 1984-03-21 Bacteriocidic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5392184A JPS60197622A (en) 1984-03-21 1984-03-21 Bacteriocidic composition

Publications (1)

Publication Number Publication Date
JPS60197622A true JPS60197622A (en) 1985-10-07

Family

ID=12956178

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5392184A Pending JPS60197622A (en) 1984-03-21 1984-03-21 Bacteriocidic composition

Country Status (1)

Country Link
JP (1) JPS60197622A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01153644A (en) * 1987-12-10 1989-06-15 Meiji Seika Kaisha Ltd Germicidal composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01153644A (en) * 1987-12-10 1989-06-15 Meiji Seika Kaisha Ltd Germicidal composition

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