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JPH0717499B2 - Caries fungus growth inhibitor - Google Patents
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JPH0717499B2 - Caries fungus growth inhibitor - Google Patents

Caries fungus growth inhibitor

Info

Publication number
JPH0717499B2
JPH0717499B2 JP61171683A JP17168386A JPH0717499B2 JP H0717499 B2 JPH0717499 B2 JP H0717499B2 JP 61171683 A JP61171683 A JP 61171683A JP 17168386 A JP17168386 A JP 17168386A JP H0717499 B2 JPH0717499 B2 JP H0717499B2
Authority
JP
Japan
Prior art keywords
caries
growth inhibitor
formation
growth
fungus growth
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 - Lifetime
Application number
JP61171683A
Other languages
Japanese (ja)
Other versions
JPS6330409A (en
Inventor
英昭 宮脇
出 湯本
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.)
Taiyo Corp
Original Assignee
Taiyo Corp
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 Taiyo Corp filed Critical Taiyo Corp
Priority to JP61171683A priority Critical patent/JPH0717499B2/en
Publication of JPS6330409A publication Critical patent/JPS6330409A/en
Publication of JPH0717499B2 publication Critical patent/JPH0717499B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Confectionery (AREA)
  • Furan Compounds (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は虫歯(う蝕)の形成に大きく関与しているスト
レプトコッカス・ミュータンス(Strepto-coccus mutan
s)に代表される口腔内細菌に対して優れた抗菌活性を
示し、且つ口腔内微生物が関与するグリカン形成を阻止
しうる、う蝕菌生育阻害剤に関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to Strepto-coccus mutan, which is greatly involved in the formation of caries (caries).
The present invention relates to a cariogenic growth inhibitor which has excellent antibacterial activity against oral bacteria represented by s) and can prevent glycan formation involving oral microorganisms.

〈従来の技術〉 従来、口腔内細菌の生育を阻害する薬剤としてはクロル
ヘキシジン、アレキシジン等の殺菌剤及びペニシリン、
テトラサイクリン等の抗生物質等の使用が知られている
他、多くの合成品、天然品が報告されている。
<Prior art> Conventionally, as agents that inhibit the growth of oral bacteria, chlorhexidine, fungicides such as alexidine and penicillin,
The use of antibiotics such as tetracycline is known, and many synthetic and natural products have been reported.

〈発明が解決しようとする問題点〉 しかしながら、これら公知の口腔内細菌の生育阻害剤は
投与方法、投与量によっては人体に対する安全性に問題
があったり、安定性に問題があったり、安定性が確認さ
れているものは抗菌性が低かったり、また投与した際、
不快な臭いがするなどの欠点があった。
<Problems to be Solved by the Invention> However, these known growth inhibitory agents for oral bacteria have a safety problem for human body, a stability problem, and a stability depending on the administration method and dose. Is confirmed to have low antibacterial properties, or when administered,
There were drawbacks such as an unpleasant odor.

〈発明の目的〉 本発明の目的は、虫歯菌であるストレプトコッカス・ミ
ュータンス菌の生育阻害に非常に有効で、且つ歯垢の原
因となるデキストラン(グルカン)形成抑制にも有効で
あっても快い芳香を有するう蝕菌生育阻害剤を提供する
ことにある。
<Object of the Invention> The object of the present invention is very effective in inhibiting the growth of Streptococcus mutans, which is a dental caries, and is also pleasing even in suppressing dextran (glucan) formation that causes plaque. It is intended to provide a caries fungus growth inhibitor having an aroma.

〈問題点を解決するための手段〉 本発明によれば、トランス−ピノカルベオール、パラ−
イソプロピルシクロヘキサノール、カンホレニックアル
デヒド、γ−デカラクトン及びγ−ウンデカラクトンか
ら成る群から選ばれた少くとも一種を有効成分として含
有する、う蝕菌生育阻害剤が提供される。
<Means for Solving Problems> According to the present invention, trans-pinocarbeol, para-
There is provided a caries growth inhibitor containing at least one selected from the group consisting of isopropylcyclohexanol, campholenic aldehyde, γ-decalactone and γ-undecalactone as an active ingredient.

以下本発明につき更に詳細に説明する。The present invention will be described in more detail below.

一般的に虫歯(う蝕)形成の原因としては歯質(Teet
h)と基質(Substrate)とミュータンス菌(St.mutan
s)とを挙げることができ、この3つの要因が同時に存
在するとき、虫歯(う蝕)が発生するとされている。虫
歯(う蝕)形成のメカニズムは、例えば糖類の中で砂糖
を基質(Substrate)とした場合、この砂糖がミュータ
ンス菌(St.mutans)の産出するグルコシルトランスフ
ェラーゼ(酵素)によって水に不溶性で粘着性のデキス
トラン(グルカン)に変化し、歯質(Teeth)の表面に
歯垢を形成する。この歯垢の中では嫌気状態となり乳酸
菌等により醗酵が進み乳酸が生成してpHが低下し、この
乳酸が歯のエナメル質を脱灰し虫歯(う蝕)を形成する
とされている。
Generally, the cause of caries formation is Teeth
h), substrate (Substrate) and mutans (St.mutan)
s), and when these three factors are present at the same time, it is said that caries occur. The mechanism of caries formation is that when sugar is used as a substrate (Substrate) among sugars, this sugar is insoluble in water due to glucosyltransferase (enzyme) produced by St. mutans. It changes into sexual dextran (glucan) and forms plaque on the surface of teeth (Teeth). It is said that the dental plaque becomes anaerobic and fermentation progresses due to lactic acid bacteria to produce lactic acid, which lowers the pH, and this lactic acid decalcifies tooth enamel to form caries (caries).

従って、ストレプトコッカス・ミュータンス(St.mutan
s)に代表される口腔内細菌の増殖を抑え歯垢の形成を
阻止することは虫歯(う蝕)の形成を予防する有効な方
法である。
Therefore, Streptococcus mutans (St.mutan
Suppressing the growth of oral bacteria represented by s) and inhibiting the formation of dental plaque is an effective method for preventing the formation of caries.

本発明者等は歯垢の原因となるデキストラン(グルカ
ン)の形成に大きく関与している虫歯菌であるストレプ
トコッカス・ミュータンス菌の生育を阻害する物質を探
索した結果、トランス−ピノカルベオール、パラ−イソ
プロピルシクロヘキサノール、カンホレニックアルデヒ
ド、γ−デカラクトン及びγ−ウンデカラクトンから成
る群から選ばれた化合物の1種若しくは2種以上が非常
に有効であることが判明した。これらの化合物は既に人
体に安全であることが確認されている公知香料物質であ
るが、この様に口腔内で快い芳香を漂わせる香料物質が
ストレプトコッカス・ミュータンス菌の育成を有効に阻
害し得ることはこれまで全く知られていない。
The present inventors have searched for a substance that inhibits the growth of Streptococcus mutans, which is a caries fungus that is largely involved in the formation of dextran (glucan) that causes dental plaque, and results in trans-pinocarbeol and para. It has been found that one or more compounds selected from the group consisting of: isopropylcyclohexanol, camphorenic aldehyde, γ-decalactone and γ-undecalactone are very effective. These compounds are known perfume substances that have already been confirmed to be safe for the human body, but such perfume substances that have a pleasant aroma in the oral cavity can effectively inhibit the growth of Streptococcus mutans. This has never been known.

本発明のう蝕菌生育阻害剤の投与形態としては口腔中で
比較的滞留時間の長い錠菓、チューインガム、キャンデ
ー及びトローチ等に配合させることによりその効果が期
待できるほか、界面活性剤による抗菌活性の低下も殆ど
無いので歯磨及びマウスウォッシュ等の口腔清浄剤に配
合しても使用できる。その配合量は対象製品の形態、種
類等によって必ずしも一様でないが通常用いられる口腔
用組成物中0.005〜10重量%、好ましくは0.05〜5重量
%配合するのが一般的であり、この配合にて有効にう蝕
防止効果を発現する。
As the administration form of the caries growth inhibitor of the present invention, its effect can be expected by adding it to tablet confectionery, chewing gum, candy, troche, etc., which has a relatively long residence time in the oral cavity, and antibacterial activity by a surfactant. Since there is almost no decrease in the amount, it can be used even when blended with an oral cleaning agent such as toothpaste or mouthwash. The blending amount is not necessarily uniform depending on the form, kind, etc. of the target product, but it is generally 0.005 to 10% by weight, preferably 0.05 to 5% by weight in a commonly used oral composition. Effectively develops a caries prevention effect.

〈発明の効果〉 本発明のう蝕菌生育阻害剤は快い芳香を有し、しかもう
蝕菌の生育を有効に阻害するのでその利用価値は高いも
のである。
<Effect of the Invention> The caries bacterium growth inhibitor of the present invention has a pleasant fragrance, and since it effectively inhibits the growth of caries bacterium, its utility value is high.

〈実施例〉 以下に本発明につき抗菌活性効果を実施例により詳細に
説明する。
<Example> Hereinafter, the antibacterial activity effect of the present invention will be described in detail with reference to Examples.

(実施例−1) ショ糖2%添加のハートインフュージョンブイヨンの液
体培地に5%−アルコール溶液とした試料化合物を試料
化合物濃度が0.1%(1/1000濃度)となる様に添加し、
これに前培養しておいたストレプトコッカス・ミュータ
ンス(Streptococcus mutans)3125001株を白金耳によ
り接種し、37℃にて24時間培養した。次に培養液を攪拌
し、沈澱物を分散させた後、550nmにおける吸光度(濁
度)を測定し、ミュータンス菌によるグルカン形成量を
チェックした。又、グルカン形成時にミュータンス菌に
よる糖発酵が生起し培地が酸性となることから、培養液
のpHも測定した。
Example 1 A 5% -alcohol solution of a sample compound was added to a liquid medium of a heart infusion broth containing 2% of sucrose so that the concentration of the sample compound was 0.1% (1/1000 concentration),
The pre-cultured Streptococcus mutans 3125001 strain was inoculated with a platinum loop and cultured at 37 ° C. for 24 hours. Next, the culture solution was stirred to disperse the precipitate, and then the absorbance (turbidity) at 550 nm was measured to check the amount of glucan formed by mutans bacteria. The pH of the culture solution was also measured because sugar fermentation by mutans bacteria occurs during glucan formation and the medium becomes acidic.

結果を表1に示す。The results are shown in Table 1.

尚、歯垢形成量は、コントロール(滅菌水)を100%と
した場合の百分率で表わした。
The amount of plaque formation was expressed as a percentage when the control (sterile water) was 100%.

表−1に示される様に、培地のpH低下及びグルカン形成
は見られず、ミュータンス菌の生育を阻止するのに有効
であることが明白である。
As shown in Table 1, no decrease in pH of the medium and glucan formation were observed, which is clearly effective in inhibiting the growth of mutans.

(実施例−2) 実施例−1に於いて培地のpHの低下及びグルカン形成が
全く認められなかった表−1の化合物について、実施例
−1と同じ培地及び同じ方法で、試料化合物を希釈して
抗菌試験を実施し、各々化合物の最低有効阻止濃度を測
定した。最低有効阻止濃度試験の評価は、実施例−1と
同じく培地のpHの変化、及びグルカン形成量で判定し
た。判定の結果、培地のpHの低下及びグルカン形成が全
く認められなったものは抗菌活性があるとし、その試験
試料の最低有効濃度の逆数でもって抗ミュータンス菌活
性値とした。その結果を表−2に示す。
(Example-2) With respect to the compounds of Table-1 in which the decrease of the pH of the medium and the formation of glucan were not observed at all in Example-1, the sample compound was diluted with the same medium and the same method as in Example-1. Then, an antibacterial test was conducted to determine the minimum effective inhibitory concentration of each compound. The evaluation of the lowest effective inhibitory concentration test was carried out by the change in the pH of the medium and the amount of glucan formed, as in Example-1. As a result of the judgment, those in which the pH of the medium was not lowered and glucan formation was not observed at all were considered to have antibacterial activity, and the reciprocal of the lowest effective concentration of the test sample was used as the anti-mutans activity value. The results are shown in Table-2.

表−2より明らかなように、本発明の化合物はいずれも
高活性を示すことが明らかである。
As is clear from Table 2, all the compounds of the present invention show high activity.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A23G 3/30 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display area A23G 3/30

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】トランス−ピノカルベオール、パラ−イソ
プロピルシクロヘキサノール、カンホレニックアルデヒ
ド、γ−デカラクトン及びγ−ウンデカラクトンより成
る群から選ばれた化合物の少なくとも一種を有効成分と
して含有することを特徴とするう蝕菌生育阻害剤。
1. An active ingredient containing at least one compound selected from the group consisting of trans-pinocarbeol, para-isopropylcyclohexanol, camphorenic aldehyde, γ-decalactone and γ-undecalactone. A characteristic inhibitor of caries growth.
JP61171683A 1986-07-23 1986-07-23 Caries fungus growth inhibitor Expired - Lifetime JPH0717499B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61171683A JPH0717499B2 (en) 1986-07-23 1986-07-23 Caries fungus growth inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61171683A JPH0717499B2 (en) 1986-07-23 1986-07-23 Caries fungus growth inhibitor

Publications (2)

Publication Number Publication Date
JPS6330409A JPS6330409A (en) 1988-02-09
JPH0717499B2 true JPH0717499B2 (en) 1995-03-01

Family

ID=15927759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61171683A Expired - Lifetime JPH0717499B2 (en) 1986-07-23 1986-07-23 Caries fungus growth inhibitor

Country Status (1)

Country Link
JP (1) JPH0717499B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012072179A (en) * 2005-08-30 2012-04-12 Kao Corp Biofilm inhibitor
JP5946608B2 (en) * 2011-05-26 2016-07-06 花王株式会社 Autoinducer-2 inhibitor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3920849A (en) * 1974-10-15 1975-11-18 Int Flavors & Fragrances Inc Chewing gum containing flavor composition

Also Published As

Publication number Publication date
JPS6330409A (en) 1988-02-09

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