JPH01261325A - Emulsifier for suppressing formation of bacterial plaque - Google Patents

Emulsifier for suppressing formation of bacterial plaque

Info

Publication number
JPH01261325A
JPH01261325A JP8979188A JP8979188A JPH01261325A JP H01261325 A JPH01261325 A JP H01261325A JP 8979188 A JP8979188 A JP 8979188A JP 8979188 A JP8979188 A JP 8979188A JP H01261325 A JPH01261325 A JP H01261325A
Authority
JP
Japan
Prior art keywords
fatty acid
polyglycerin
emulsifier
ester
bacterial plaque
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
Application number
JP8979188A
Other languages
Japanese (ja)
Other versions
JPH0672090B2 (en
Inventor
Masatsugu Yamashita
政続 山下
Masato Murata
村田 昌人
Noriaki Kadota
門田 則昭
Yoshiro Toda
戸田 義郎
Nagataka Yamazaki
山崎 長孝
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 Kagaku KK
Original Assignee
Taiyo Kagaku KK
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 Kagaku KK filed Critical Taiyo Kagaku KK
Priority to JP63089791A priority Critical patent/JPH0672090B2/en
Publication of JPH01261325A publication Critical patent/JPH01261325A/en
Publication of JPH0672090B2 publication Critical patent/JPH0672090B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

PURPOSE:To obtain a bacterial plaque formation-suppressing emulsifier capable of suppressing formation of bacterial plaque and preventing dental caries or progress of the dental caries and having high safeness. CONSTITUTION:Polyglycerin ester of 8-16C fatty acid is contained as ingredient. The above-mentioned ingredient is mono-, di-, tri-, tetra- or penta- fatty acid ester of polyglycerin having >=2 polymerization degree, preferably mono- or di-fatty acid ester and is used alone or as mixture thereof. The ingredient is obtained by esterification reaction of polyglycerin with fatty acid in the presence or absence of a solvent. The aimed composition is added at an amount of 0.01-10wt.% to an agent for oral cavity or food.

Description

【発明の詳細な説明】 本発明は新規な歯垢形成抑制乳化剤に関する。[Detailed description of the invention] The present invention relates to a novel plaque formation inhibiting emulsifier.

詳しくは、安全性の高い炭素数8〜16を有する脂肪酸
のポリグリセリンエステルからなる歯垢形成抑制乳化剤
に関し歯面における歯垢の形成を抑制し虫歯を予防又は
その進行を阻止するために有効な歯垢形成抑制乳化剤を
提供するものである。
Specifically, regarding a highly safe dental plaque formation-inhibiting emulsifier made of a polyglycerin ester of a fatty acid having 8 to 16 carbon atoms, it is effective for inhibiting the formation of dental plaque on tooth surfaces and preventing or inhibiting the progression of dental caries. The present invention provides an emulsifier that inhibits plaque formation.

〔産業上の利用分野〕[Industrial application field]

虫歯は現代の食生活において重要な問題となっている。 Tooth decay has become an important problem in modern diets.

この虫歯という現象は、口腔連鎖球菌であるストレプト
コッカス・ミュータンスが食物に含有される砂糖を基質
として粘着性の多糖体を生成し、この多糖体によって菌
体が歯の平滑面に付着し歯の破壊が始まると言われてい
る。
This phenomenon of tooth decay is caused by the oral streptococcus Streptococcus mutans producing sticky polysaccharides using sugars contained in food as a substrate, and these polysaccharides allow bacterial cells to adhere to the smooth surfaces of teeth, resulting in tooth decay. It is said that destruction will begin.

本発明の歯垢形成抑制乳化剤は皮膚、粘膜に対する刺激
性が極めて弱く、歯垢形成の抑制や虫歯を予防及びその
進行を阻止するのに特に有用である。
The plaque formation-inhibiting emulsifier of the present invention has extremely weak irritation to the skin and mucous membranes, and is particularly useful for inhibiting dental plaque formation and preventing and inhibiting the progression of dental caries.

〔従来の技術〕[Conventional technology]

虫歯を肪止するためには、歯垢形成を抑制することが望
まれ、そのために種々の方法が行われている0例えば、
ストレプトコッカス・ミュータンスに対して殺菌又は静
菌作用を有する薬物を投与し、口腔内からストレプトコ
ッカス・ミュータンスを駆逐する方法がある。しかしこ
れらの薬物は口腔内及び腸内の細菌叢を乱すと共に、そ
の副作用に伴う危険があり、広く使用されるには至って
いない。
In order to prevent tooth decay, it is desirable to suppress plaque formation, and various methods have been used for this purpose, such as:
There is a method for expelling Streptococcus mutans from the oral cavity by administering a drug that has a bactericidal or bacteriostatic effect on Streptococcus mutans. However, these drugs have not been widely used because they disturb the bacterial flora in the oral cavity and intestines, and there are risks associated with their side effects.

次に機械的方法で歯垢を取り除く方法がある。The next method is to remove plaque mechanically.

すなわちハブラシを用いる物理的清掃であり、各人の清
掃技術の良否の差が激しく完全に歯垢を除去することは
非常に困難である。
That is, it is a physical cleaning using a toothbrush, and it is extremely difficult to completely remove dental plaque because the cleaning techniques of each person vary greatly.

[発明が解決しようとする問題点〕 このようなことから、ストレプトコッカス・ミニータン
スに対して殺菌又は静菌作用を有しており、口腔内及び
腸内の細菌叢を乱すことがなく、人体に対して副作用の
少ない歯垢形成抑制物質が望まれていた。
[Problems to be solved by the invention] For these reasons, it has a bactericidal or bacteriostatic effect against Streptococcus minitans, does not disturb the bacterial flora in the oral cavity and intestines, and is not harmful to the human body. In contrast, there has been a desire for a substance that inhibits plaque formation with fewer side effects.

〔問題を解決するための手段〕[Means to solve the problem]

本発明者らは歯垢形成を抑制し、虫歯を予防又はその進
行を阻止する方法を開発する目的で鋭意研究を行った結
果、炭素数8〜16を有する脂肪酸のポリグリセリンエ
ステルが歯垢の形成を抑制することを見い出し本発明を
完成した。
The present inventors conducted extensive research with the aim of developing a method to inhibit dental plaque formation and prevent or halt the progression of dental caries. As a result, polyglycerin esters of fatty acids having 8 to 16 carbon atoms were found to inhibit dental plaque formation. The present invention was completed based on the discovery that the formation can be suppressed.

すなわち本発明は、安全性が高く、食品添加物に認可さ
れている炭素数8〜16を有する脂肪酸のポリグリセリ
ンエステルからなる歯垢形成抑制乳化剤である。
That is, the present invention is a plaque formation-inhibiting emulsifier made of a polyglycerin ester of a fatty acid having 8 to 16 carbon atoms, which is highly safe and approved as a food additive.

本発明に用いられる炭素数8〜16を膚する脂肪酸ポリ
グリセリンエステルは、重合度が2以上のポリグリセリ
ンの脂肪酸エステルである。ポリグリセリン脂肪酸エス
テルに用いられる脂肪酸はカプリル酸、カプリン酸、ラ
ウリン酸、ミリスチン酸、パルミチン酸等の炭素数8〜
16の飽和又は不飽和の直鎖脂肪酸であり、これらの脂
肪酸は単独又はその混合物でもよい。
The fatty acid polyglycerin ester having 8 to 16 carbon atoms used in the present invention is a fatty acid ester of polyglycerin having a degree of polymerization of 2 or more. Fatty acids used in polyglycerin fatty acid esters have 8 or more carbon atoms, such as caprylic acid, capric acid, lauric acid, myristic acid, and palmitic acid.
16 saturated or unsaturated straight chain fatty acids, these fatty acids may be used alone or in mixtures thereof.

炭素数7以下の脂肪酸及び炭素数17以上の脂肪酸のポ
リグリセリンエステルは、歯垢形成を抑制する効果がほ
とんどなく、実用的ではない。
Polyglycerol esters of fatty acids having 7 or less carbon atoms and fatty acids having 17 or more carbon atoms have almost no effect on inhibiting dental plaque formation and are not practical.

本発明に用いられる炭素数8〜16を有する脂肪酸のポ
リグリセリンエステルのポリグリセリンは重合度が2以
上である0重合度が2未満のポリグリセリン脂肪酸エス
テルは刺激味、苦味が強く又、加水分解が起こりやすく
実用的でない。
The polyglycerin ester of a fatty acid having 8 to 16 carbon atoms used in the present invention has a degree of polymerization of 2 or more. Polyglycerin fatty acid esters with a degree of polymerization of less than 2 have a strong pungent taste and bitter taste, and can be hydrolyzed. is likely to occur and is not practical.

本発明の炭素数8〜16を有する脂肪酸のポリグリセリ
ン脂肪酸エステルは重合度が2以上のポリグリセリンの
モノ、ジ、トリ、テトラ、ペンタの脂肪酸エステルであ
り中でも、モノ、ジの脂肪酸エステルが望ましく、これ
らは単独又はその混合物で用いられることができる。
The polyglycerin fatty acid ester of a fatty acid having 8 to 16 carbon atoms of the present invention is a mono-, di-, tri-, tetra-, or penta-fatty acid ester of polyglycerin having a degree of polymerization of 2 or more, and among these, mono- and di-fatty acid esters are preferable. , these can be used alone or in mixtures thereof.

本発明の炭素数8〜16を有する脂肪酸のポリグリセリ
ン脂肪酸エステルは、溶媒存在下、又は無溶媒の下で、
ポリグリセリンと脂肪酸のエステル化反応によって得ら
れる。このエステル化反応は一般のエステル化触媒の存
在下、又は無触媒下反応温度150°C〜280℃、窒
素等の不活性ガスを吹き込みながら生成する水を除去す
ることによって行われる。
The polyglycerol fatty acid ester of a fatty acid having 8 to 16 carbon atoms of the present invention can be prepared in the presence of a solvent or in the absence of a solvent.
Obtained by the esterification reaction of polyglycerin and fatty acids. This esterification reaction is carried out in the presence of a general esterification catalyst or without a catalyst at a reaction temperature of 150 DEG C. to 280 DEG C. and by removing produced water while blowing inert gas such as nitrogen.

本発明に用いられる炭素数8〜16を有する脂肪酸のポ
リグリセリンエステルは口腔用剤又は食品に対して0.
01%〜10%(重量部)添加する。0.01%以下の
添加量では本発明の効果がなく、10%以上の添加量で
、はポリグリセリン脂肪酸エステルが口腔用剤又は食品
において苦味が強く感じられ、更に経済的にも高価にな
り舅ましくない、     。
The polyglycerin ester of a fatty acid having 8 to 16 carbon atoms used in the present invention is 0.0% for oral preparations or foods.
01% to 10% (parts by weight) is added. If the amount added is less than 0.01%, the effect of the present invention will not be achieved, and if the amount added is more than 10%, the polyglycerin fatty acid ester will taste strongly bitter in oral preparations or foods, and will also become economically expensive. Not my father-in-law.

本発明の歯垢形成抑制乳化剤は11、水溶液形、態の口
腔内スプレー、うがい剤、水歯みがき1口腔用清掃剤等
に配合することができる。固体状形態としては、うがい
用錠剤、舌下錠、トローチ等の錠剤等があげられる。 
      。
The plaque formation-inhibiting emulsifier of the present invention can be incorporated into oral sprays, gargles, water toothpastes, oral cleaning agents, etc. in the form of an aqueous solution. Examples of the solid form include tablets such as gargling tablets, sublingual tablets, and troches.
.

又、本発明の歯垢形成抑制乳化剤は、チューインガム、
キャンデイ−、ジュース、プリン、コーヒー飲料、ココ
ア飲料、紅茶飲料、しるこ、スーブ、カレー、チョコレ
ート、クツキー、ケーキ。
Further, the plaque formation inhibiting emulsifier of the present invention can be used in chewing gum,
Candy, juice, pudding, coffee drinks, cocoa drinks, tea drinks, shiruko, soup, curry, chocolate, kutsky, cake.

パン、アイスクリーム、氷菓子、砂糖菓子、甘味料等に
配合すると2とができる。
When added to bread, ice cream, frozen confectionery, sugar confectionery, sweeteners, etc., 2 can be obtained.

〔作用〕[Effect]

本発明の歯垢形成抑制乳化剤は、非常に親水性が強<H
LB値が大きい界面活性剤であるためにストレプトコッ
カス・ミュータンスの増殖を抑制し、又殺菌する作用を
有するものと推定される。
The plaque formation inhibiting emulsifier of the present invention has very strong hydrophilicity <H
Since it is a surfactant with a large LB value, it is presumed to have the effect of inhibiting the growth of Streptococcus mutans and also sterilizing it.

又、ストレブトコ・ンカス・ミュータンスによって生成
する多糖体の歯の平滑面への付着も肪止するものと推定
きれる。
It can also be assumed that the adhesion of polysaccharides produced by Strebutococcus mutans to the smooth surfaces of teeth also causes fat retention.

次に本発明を試験例によって説明する。Next, the present invention will be explained using test examples.

試験例1 プレインハートインフュージョンブイヨン培地(Di 
f’co社)にデカグリセリンモノミリスチン酸エステ
ル(サンソフトNo、Q−148太陽化学(ロ)製)を
100pprn、300ppm、500ppm、700
ppmになるように添加し試験管3本に5m1分注し試
験用培地とした。
Test Example 1 Plain Heart Infusion Broth Medium (Di
100 pprn, 300 ppm, 500 ppm, 700 ppm of decaglycerin monomyristic acid ester (Sunsoft No., Q-148 manufactured by Taiyo Kagaku (Ro))
It was added at a concentration of ppm and 5 ml was dispensed into three test tubes to prepare a test medium.

この試験培地にあらかじめプレインハートインフュージ
ョンブイヨン培地で調製したストレプトコッカス・ミュ
ータンスM7814B菌液を初発菌数1.2X10”/
mlとなるように加え37°Cで培養し1日、2日、3
日ごとに菌数をプレインハートインフュージョンブイヨ
ン寒天培地で測定した。
Into this test medium, a Streptococcus mutans M7814B bacterial solution prepared in advance with Plain Heart Infusion Broth Medium was added to the initial bacterial count of 1.2 x 10"/
ml and cultured at 37°C for 1, 2, and 3 days.
Bacterial counts were determined every day on plain heart infusion broth agar medium.

比較例1 試験例1において、デカグリセリンモノミリスチン酸エ
ステルを添加しない以外は、全く同じにして菌数を測定
した。その結果を表1に示した。
Comparative Example 1 The number of bacteria was measured in exactly the same manner as in Test Example 1, except that decaglycerol monomyristate was not added. The results are shown in Table 1.

表1.ストレプトコッカス・ミュータンスに対する抗菌
作用(菌数/mj2) 試験例2 下記の処方に従ってうがい剤を調製した。
Table 1. Antibacterial action against Streptococcus mutans (number of bacteria/mj2) Test Example 2 A gargle was prepared according to the following recipe.

デカグリセリンモノミリスチン : 1.5 部酸エス
テル(サンソフトNo、Q−14S太陽化学■製) グリセリン         : 9.0 部青色3号
0.4%溶液     :  0.01部ペパーミント
オイル      : 0.5 部メントール    
     二′0.5  部エタノール       
   : 3.0 部蒸留水            
:85.49部試験例3 下記の処方に従って、コーヒーゼリーを調製した。
Decaglycerin monomyristin: 1.5 parts Acid ester (Sunsoft No., Q-14S Taiyo Kagaku ■) Glycerin: 9.0 parts Blue No. 3 0.4% solution: 0.01 parts Peppermint oil: 0.5 parts menthol
2'0.5 parts ethanol
: 3.0 parts distilled water
: 85.49 parts Test Example 3 Coffee jelly was prepared according to the following recipe.

グラニユー糖          12.0 部ブドウ
糖           8.0 部サンカラNo、5
40       0.75部(カラギナン製剤、太陽
化学■製) コーヒー粉末           2.0 部ブラン
デイ−0,3部 デカグリセリンモノミリスチン酸  0.07部エステ
ル (サンソフトNo、Q−143,太陽化学■製)水  
                 76.88部[本
発明の効果〕 本発明の炭素数8〜16を有する脂肪酸のポリグリセリ
ンエステルからなる歯垢形成抑制乳化剤は試験例の結果
から明らかなように、ストレプトフッカス・ミュータン
スの増殖を抑制し、又、死滅させてしまう、そのためス
トレプトコッカス・ミュータンスによる多糖体が生成さ
れに<<、歯垢の形成が抑制される。
Granulated sugar 12.0 parts Glucose 8.0 parts Sankara No. 5
40 0.75 parts (Carrageenan formulation, manufactured by Taiyo Kagaku ■) Coffee powder 2.0 parts Brandy - 0.3 parts Decaglycerin Monomyristic acid 0.07 parts Ester (Sunsoft No., Q-143, manufactured by Taiyo Kagaku ■) water
76.88 parts [Effects of the present invention] As is clear from the results of the test examples, the plaque formation-inhibiting emulsifier comprising a polyglycerin ester of a fatty acid having 8 to 16 carbon atoms according to the present invention has an effect on Streptofuccus mutans. It inhibits the proliferation and also kills Streptococcus mutans, thereby inhibiting the production of polysaccharides by Streptococcus mutans and inhibiting the formation of dental plaque.

Claims (1)

【特許請求の範囲】[Claims] 炭素数8〜16を有する脂肪酸のポリグリセリンエステ
ルからなる歯垢形成抑制乳化剤
Dental plaque formation-inhibiting emulsifier consisting of polyglycerin ester of fatty acid having 8 to 16 carbon atoms
JP63089791A 1988-04-11 1988-04-11 Streptococcus inhibitor Expired - Lifetime JPH0672090B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63089791A JPH0672090B2 (en) 1988-04-11 1988-04-11 Streptococcus inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63089791A JPH0672090B2 (en) 1988-04-11 1988-04-11 Streptococcus inhibitor

Publications (2)

Publication Number Publication Date
JPH01261325A true JPH01261325A (en) 1989-10-18
JPH0672090B2 JPH0672090B2 (en) 1994-09-14

Family

ID=13980511

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63089791A Expired - Lifetime JPH0672090B2 (en) 1988-04-11 1988-04-11 Streptococcus inhibitor

Country Status (1)

Country Link
JP (1) JPH0672090B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6233694B1 (en) 1997-12-24 2001-05-15 Thomson Licensing S.A. Synchronization device for synchronous dynamic random-access memory
JP2018030786A (en) * 2016-08-22 2018-03-01 ピジョン株式会社 Personal care composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4067997A (en) * 1975-05-21 1978-01-10 Med-Chem Laboratories Synergistic microbecidal composition and method
JPS6360917A (en) * 1986-09-02 1988-03-17 Lion Corp Composition for oral cavity

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4067997A (en) * 1975-05-21 1978-01-10 Med-Chem Laboratories Synergistic microbecidal composition and method
JPS6360917A (en) * 1986-09-02 1988-03-17 Lion Corp Composition for oral cavity

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6233694B1 (en) 1997-12-24 2001-05-15 Thomson Licensing S.A. Synchronization device for synchronous dynamic random-access memory
JP2018030786A (en) * 2016-08-22 2018-03-01 ピジョン株式会社 Personal care composition

Also Published As

Publication number Publication date
JPH0672090B2 (en) 1994-09-14

Similar Documents

Publication Publication Date Title
RU2388457C2 (en) Breath refresher for disinfecting oral cavity and containing magnolia bark extract and surface active substance
FI85212B (en) SAMMANSAETTNING FOER MUNHYGIEN.
DE69312547T2 (en) Process for improving the taste of a spruce extract and product obtained for oral use
RU2398593C2 (en) Fast-release chewing composition with magnolia bark extract
KR19990036418A (en) Coolant composition
WO2005107769A1 (en) Oral flora-improving agent, antibacterial agent and growth promoter
PT94656A (en) PROCESS FOR THE PREPARATION OF ANTI-SEPTIC COMPOSITIONS CONTAINING HEXA-HYDRO-5-PYRIMIDINAMINES AND AN ACTRESSING TENSILE-ACTIVE AGENT
KR100539495B1 (en) Acyl derivatives of glycosy-l-ascorbic acid
JP3241955B2 (en) Oral composition
JPS62503033A (en) Solid oral composition for caries prevention
JP2002020253A (en) Composition for oral use
JP2006316053A (en) Cytotoxicity inhibitor and use thereof
JPS61171423A (en) Drug for alleviating dental caries and periodontosis
KR20150061762A (en) Oral composition having anti-detal caries efficacy
KR102614880B1 (en) Oral composition and growth promoter for oral bacteria
JP3481269B2 (en) Antibacterial composition and antibacterial method
JPH01261325A (en) Emulsifier for suppressing formation of bacterial plaque
JP2003137797A (en) Mastic-containing emulsion
JPH0432047B2 (en)
US20040265247A1 (en) Mouth rinse composition
JPH0639375B2 (en) Anti-caries agent
JP4763441B2 (en) Plaque formation inhibitor and oral composition and food containing the same
JPH0427204B2 (en)
KR102269164B1 (en) Composition for improvement of dental caries and periodontal disease using an extract of seeds of Phaseolus radiatus, etc.
JP3203572B2 (en) Method for improving palatability of pine extract and oral intake obtained by this method