Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS5835966B2 - Oral composition - Google Patents
[go: Go Back, main page]

JPS5835966B2 - Oral composition - Google Patents

Oral composition

Info

Publication number
JPS5835966B2
JPS5835966B2 JP14177778A JP14177778A JPS5835966B2 JP S5835966 B2 JPS5835966 B2 JP S5835966B2 JP 14177778 A JP14177778 A JP 14177778A JP 14177778 A JP14177778 A JP 14177778A JP S5835966 B2 JPS5835966 B2 JP S5835966B2
Authority
JP
Japan
Prior art keywords
composition
dextranase
alanine
acyl
item
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
JP14177778A
Other languages
Japanese (ja)
Other versions
JPS5569505A (en
Inventor
洋一 山本
景 菊地
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.)
SANSUTAA KK
Original Assignee
SANSUTAA 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 SANSUTAA KK filed Critical SANSUTAA KK
Priority to JP14177778A priority Critical patent/JPS5835966B2/en
Publication of JPS5569505A publication Critical patent/JPS5569505A/en
Publication of JPS5835966B2 publication Critical patent/JPS5835966B2/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • 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

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)
  • Oral & Maxillofacial Surgery (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】 本発明は口腔組成物、さらに詳しくは、歯垢の歯牙への
付着を抑制し、かつ、歯牙に付着した歯垢を分解、除去
する効力を有する口腔組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oral composition, and more particularly to an oral composition that has the effect of suppressing the adhesion of dental plaque to teeth, and decomposing and removing dental plaque adhering to teeth.

一般に、歯垢は種々の細菌群、細菌の代謝産物、唾液成
分などからなる歯牙付着物で、歯垢中で口腔内細菌が産
生ずる酸や蛋白質分解酵素が虫歯や歯槽膿漏の一原因と
されている。
In general, dental plaque is a dental deposit made up of various bacterial groups, bacterial metabolites, saliva components, etc., and the acids and proteolytic enzymes produced by oral bacteria in plaque are a cause of tooth decay and alveolar pyorrhea. has been done.

そこで、虫歯や歯槽膿漏の予防、治療には歯垢の歯牙へ
の付着抑制および歯牙に付着した歯垢の除去が非常に有
効な手段となる。
Therefore, suppressing the adhesion of dental plaque to teeth and removing dental plaque adhering to teeth are very effective means for preventing and treating dental caries and alveolar pyorrhea.

従来、かかる目的のため、歯垢の構成成分であるデキス
トランを、デキストラン分解酵素、デキストラナーゼを
用いて分解、溶解させる試みがなされているが、未だ充
分満足するものは見当らない。
Conventionally, attempts have been made to decompose and dissolve dextran, which is a component of dental plaque, using dextran-degrading enzymes and dextranases for this purpose, but none have yet been found to be fully satisfactory.

本発明者らはデキストラナーゼについて種々研究を重ね
る間に、特定のN−アシル−β−アラニン塩がデキスト
ラナーゼを賦活化する作用を有することを知り、これを
デキストラナーゼと共存させると歯垢の歯牙への付着抑
制および歯牙に付着した歯垢の除去が効率よく行なえる
ことを見出し、本発明を宗族するにいたった。
While carrying out various studies on dextranase, the present inventors learned that a specific N-acyl-β-alanine salt has the effect of activating dextranase, and when it is allowed to coexist with dextranase. It was discovered that the adhesion of dental plaque to teeth can be suppressed and that dental plaque adhering to teeth can be efficiently removed, and the present invention was established.

すなわち、本発明は、酵素賊活化剤としてNココイル−
N−メチル−β−アラニン塩、N−ラウロイル−N−メ
チル−β−アラニン塩およびN−ミリストイル−N−メ
チル−β−アラニン塩からなる群から選ばれる1種また
は2種以上のNアシル−β−アラニン塩を配合したデキ
ストラナーゼ配合口腔組成物を提供するもので、本発明
の口腔組成物は歯垢の歯牙への付着抑制および歯牙に付
着した歯垢の除去を効率よ(行ない、虫歯や歯槽膿漏の
予防にきわめて優れた効果を発揮する。
That is, the present invention uses N cocoyl- as an enzyme activator.
One or more N-acyl- selected from the group consisting of N-methyl-β-alanine salt, N-lauroyl-N-methyl-β-alanine salt, and N-myristoyl-N-methyl-β-alanine salt. The purpose of the present invention is to provide a dextranase-containing oral composition containing β-alanine salt. It is extremely effective in preventing cavities and alveolar pyorrhea.

つぎに、これらのN−アシル−β−アラニン塩のデキス
トラナーゼ賊活化作用を試験した結果を示す。
Next, the results of testing the dextranase activation activity of these N-acyl-β-alanine salts are shown.

試験1 デキストラナーゼ17V(10’O万単位/す)を0.
2M酢酸緩衡液(1)H5,5) 100mlに溶解し
、この酵素溶液1 mlずつにつぎの第1表に示す各種
の化合物を添加し、40℃で10分間加温した。
Test 1 Dextranase 17V (100,000 units/su) was added at 0.
The enzyme solution was dissolved in 100 ml of 2M acetic acid buffer (1) H5,5), and various compounds shown in Table 1 below were added to each 1 ml portion of this enzyme solution, followed by heating at 40° C. for 10 minutes.

ついで、各溶液に0.5%デキストラン(シグマ社製、
分子量200万)溶液1rrLlずつを加え、40℃で
10分間反応させた後、遊離した還元糖をノモギネルソ
ン法で定量した。
Next, 0.5% dextran (manufactured by Sigma,
After adding 1rrLl of a solution (molecular weight: 2 million) and reacting at 40°C for 10 minutes, the liberated reducing sugars were quantified by the Nomogyinelson method.

同様に化合物を添加しない場合の還元糖を測定し、化合
物添加区の無添加区に対する還元糖量の増加率(%)を
賦活化率とした。
Reducing sugar was measured in the same manner when no compound was added, and the increase rate (%) in the amount of reducing sugar in the compound-added area relative to the non-additive area was defined as the activation rate.

なお、対照としては熱失活させた酵素溶液を用いた。Note that a heat-inactivated enzyme solution was used as a control.

結果をっぎの第1表に示す。示さないか、あるいは逆に
活性を低下させるが、該N−アシル−β−アラニン塩は
、ことに比較的低濃度で特異的にデキストラナーゼを賦
活化する。
The results are shown in Table 1 below. The N-acyl-β-alanine salt specifically activates dextranase, especially at relatively low concentrations, although it does not show or on the contrary reduces its activity.

試験2 アラカシめ、フレーンハートインフユージョン培地で3
7℃、18時間培養したストレプトコッカス・ミュータ
ンス(S tr 、 mutans )を、つぎの第2
表に示す酵素および/またはN−ラウロイルN−メチル
−β−アラニンナトリウムを溶解した5%ショ糖加〜・
−トインフユージョン培地5rr11入りの試験官に搗
種し、この試験官を85°の角度に傾斜させて保持して
37℃で18時間培養した。
Test 2 Arakashi female, 3 with Frayn heart infusion medium
Streptococcus mutans (S tr , mutans) cultured at 7°C for 18 hours was cultured in the following second step.
5% sucrose containing dissolved enzymes and/or sodium N-lauroyl N-methyl-β-alanine shown in the table.
- The seeds were placed in a test tube containing 5rr11 of infusion medium, and the test tube was held at an angle of 85° and cultured at 37° C. for 18 hours.

培養後、培地を捨て、試験官を生理食塩水で洗浄し、つ
いで、0.5N水酸化ナトリウム溶液5酢を加えて管壁
に付着した菌体を均一に懸濁させ、その濁度(550m
μの透過率)を測定した。
After culturing, the medium is discarded, the test tube is washed with physiological saline, and then 0.5N sodium hydroxide solution and 5 vinegar are added to uniformly suspend the bacterial cells attached to the tube wall, and the turbidity (550 m
μ transmittance) was measured.

同様に、酵素および該化合物無添加対照についても濁度
を測定し、対照の濁度を100とした場合の酵素および
/または該化合物添加区の濁度の比率を算出した。
Similarly, the turbidity was also measured for a control without the addition of the enzyme and the compound, and the ratio of the turbidity of the turbidity in the area to which the enzyme and/or the compound had been added was calculated when the turbidity of the control was set as 100.

結果を第2表に示す。試験官壁に付着した菌体は歯垢と
同様なものと考えられ、濁度の比率の低いものほど歯垢
の分解、除去効果が強い。
The results are shown in Table 2. The bacterial cells attached to the tester wall are thought to be similar to dental plaque, and the lower the turbidity ratio, the stronger the plaque decomposition and removal effect.

第2表から明らかなごとく、デキストラナーゼと該N−
アシル−β−アラニン塩を併用することによりデキスト
ラナーゼが賦活され、歯垢の分解が著しく促進される。
As is clear from Table 2, dextranase and the N-
By using acyl-β-alanine salt in combination, dextranase is activated and decomposition of dental plaque is significantly promoted.

かくして、本発明の口腔組成物には必須の活性成分とし
てデキストラナーゼと該特定のN−アシル−β−アラニ
ン塩を配合する。
Thus, the oral composition of the present invention contains dextranase and the specific N-acyl-β-alanine salt as essential active ingredients.

用いるデキストラナーゼとしては通常のものでよく、F
りえば、ペニシリウム(Penicillium )属
、アスペルギル、;< (Aspergillus )
属1.フェルティシリウム(Vertici lliu
m )属、スピカリア(5picaria )属、スト
レプトマイセス(S treptomyces )属な
どの微生物を通常の栄養源あるいはこれにテキストラン
を添加した培地で培養し、その上澄を塩析法、吸着法、
溶媒分画法などで分別して得られる。
The dextranase used may be any ordinary one, such as F
Lie, Penicillium genus, Aspergillus, ;< (Aspergillus)
Genus 1. Verticillium (Verticillium)
Microorganisms such as the genus M), the genus Spicaria, and the genus Streptomyces are cultured in a medium supplemented with a normal nutrient source or Textlan, and the supernatant is subjected to salting-out method, adsorption method,
Obtained by fractionation using solvent fractionation methods.

該酵素を産生ずる微生物の種類によって若干性質が変化
するが、般に、至適pHは酸性側にあり、いずれもデキ
ストランをエンド型、エキソ型に分解し、還元糖を遊離
させて、粘度を低下させる作用を有する。
Although the properties vary slightly depending on the type of microorganism that produces the enzyme, the optimum pH is generally on the acidic side, and both degrade dextran into endo-type and exo-type, liberate reducing sugars, and reduce viscosity. It has the effect of reducing

該N−アシル−β−アラニン塩としては、そのナトリウ
ム、カリウムのようなアルカリ金属塩、アルカリ土類金
属塩、アンモニウム塩などの塩が用いられる。
As the N-acyl-β-alanine salt, salts such as alkali metal salts such as sodium and potassium salts, alkaline earth metal salts, and ammonium salts are used.

これらは、単独でも、あるいは2種以上混合して用いて
もよい。
These may be used alone or in combination of two or more.

デキストラナーゼおよび該N−アシル−β−アラニン塩
の配合割合は、所望の効果に応じて適宜選択できるが、
効力や安定性などの点から、組成物全量に対してデキス
トラナーゼを1.0〜20重量%(5000〜100万
単位/lとして)、Nアシル−β−アラニン塩をo、o
ooi〜1.0重量%とすることが好ましい。
The blending ratio of dextranase and the N-acyl-β-alanine salt can be selected as appropriate depending on the desired effect;
From the viewpoint of efficacy and stability, 1.0 to 20% by weight of dextranase (as 5000 to 1 million units/l) based on the total amount of the composition, and o and o of N-acyl-β-alanine salts were added.
It is preferable to set it as ooi - 1.0 weight%.

なお、デキストラナーゼ1単位とは、デキストランを分
解してグルコース換算で1μグ/分の還元糖を遊離させ
る酵素量を意味する。
Note that 1 unit of dextranase means the amount of enzyme that decomposes dextran and releases 1 μg/min of reducing sugar in terms of glucose.

本発明の口腔組成物は常法に従って、練歯磨、粉歯磨、
液状歯磨などの歯磨類、マウスウォッシュなどの口腔洗
浄剤、義歯洗浄剤、トローチなどの剤形とすることがで
きる。
The oral composition of the present invention can be prepared using conventional methods such as toothpaste, powdered toothpaste,
It can be in the form of dentifrices such as liquid toothpaste, oral cleansers such as mouthwash, denture cleansers, troches, and the like.

他の配合成分は通常これらに配合されるものでよく、例
えば、歯磨の場合、グリセリン、ソルビトールなどの湿
潤剤、第ニリン酸カルシウム、炭酸カルシウム、無水ケ
イ酸、水酸化アルミニウム、ピロリン酸カルシウム、不
溶性メタリン酸ナトリウムなどの研磨剤、ラウリル硫酸
ナトリウム、アシルサルコシンナトリウム、ショ糖脂肪
酸エステルなどの発泡剤、カルボキシメチルセルロース
ナトリウム、カラギーナン、アルギン酸ナトリウム、ベ
ントナイトなどの粘結剤、甘味料、香料や、その他モノ
フルオロリン酸ナトリウム、殺菌剤、抗炎症剤などが配
合される。
Other ingredients may be those that are normally added to these, for example, in the case of toothpaste, wetting agents such as glycerin and sorbitol, calcium diphosphate, calcium carbonate, silicic anhydride, aluminum hydroxide, calcium pyrophosphate, and insoluble metaphosphoric acid. Abrasives such as sodium, blowing agents such as sodium lauryl sulfate, sodium acylsarcosinate, and sucrose fatty acid esters, binders such as sodium carboxymethyl cellulose, carrageenan, sodium alginate, and bentonite, sweeteners, flavoring agents, and other monofluorophosphates. Contains sodium, bactericides, anti-inflammatory agents, etc.

つぎに実施例を挙げて本発明をさらに詳しく説明する。Next, the present invention will be explained in more detail with reference to Examples.

実施例 1 つぎの処方に従い、常法によって練歯練を得た。Example 1 A toothpaste was obtained by a conventional method according to the following recipe.

実施列 2 つぎの処方に従い、 シュを得た。Actual row 2 According to the following prescription, I got Shu.

常法によってマウスウオツ 成 分 重量% サッカリンナトリウム 0.05 エタノール 25.0 グリセリン 5.0 ポリオキシエチレン硬化ヒマシ 油 2.0 香 料 1.0 デキストラナーゼ(50万単 位/2) 1、O N−ラウロイル−N−メチル β−アラニンナトリウム 0.0 水 ioo%に調整 実施列 3 つぎの処方に従い、常法によってトローチ2得た。Mouthwatch by conventional method Growth minutes weight% saccharin sodium 0.05 ethanol 25.0 glycerin 5.0 Polyoxyethylene hardened castor oil 2.0 Incense fee 1.0 Dextranase (500,000 units) rank/2) 1, O N-lauroyl-N-methyl β-alanine sodium 0.0 water Adjust to ioo% Implementation row 3 Troche 2 was obtained by a conventional method according to the following recipe.

成 分 重量% アラビアガム 6.0 グルコース 72.0 香 料 1.0 デキスト 位/グ) ラナーゼ(50万単 0.1 N−ラウロイル−N−メチル β−アラニンナトリウム 1.0 水 00%に調整Growth minutes weight% gum arabic 6.0 glucose 72.0 Incense fee 1.0 Dexto place/g) Lanase (500,000 units) 0.1 N-lauroyl-N-methyl β-alanine sodium 1.0 water Adjust to 00%

Claims (1)

【特許請求の範囲】 1 デキストラナーゼ配合口腔組成物において、N−コ
コイル−N−メチル−β−アラニン塩、N−ラウロイル
−N−メチル−β−アラニン塩およびN−ミリストイル
−N−メチル−β−アラニン塩からなる群から選ばれる
1種または2種以上のN−アシル−β−アラニン塩を配
合したことを特徴とする口腔組成物。 2 組成物全量に対してデキストラナーゼを1.0〜2
0重量%(5000〜1oo万単位/グとして)、該N
−アシル−β−アラニン塩を0.0001〜i、o重量
%配合した前記第1項の組成物。 3 歯磨の剤形である前記第1項または第2項の組成物
。 4 口腔洗浄剤の剤形である前記第1項または第2項の
組成物。 5 義歯洗浄剤の剤形である前記第1項または第2項の
組成物。 6 トローチの剤形である前記第1項または第2項の組
成物。
[Scope of Claims] 1. In a dextranase-containing oral composition, N-cocoyl-N-methyl-β-alanine salt, N-lauroyl-N-methyl-β-alanine salt, and N-myristoyl-N-methyl- An oral composition comprising one or more N-acyl-β-alanine salts selected from the group consisting of β-alanine salts. 2. Add 1.0 to 2 dextranase based on the total amount of the composition.
0% by weight (as 5000-100,000 units/g), the N
- The composition according to item 1 above, which contains 0.0001 to i,0% by weight of acyl-β-alanine salt. 3. The composition of item 1 or 2 above, which is in the form of a toothpaste. 4. The composition of item 1 or 2 above, which is in the form of a mouthwash. 5. The composition of item 1 or 2 above, which is in the form of a denture cleaning agent. 6. The composition of item 1 or 2 above, which is in the form of a troche.
JP14177778A 1978-11-16 1978-11-16 Oral composition Expired JPS5835966B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14177778A JPS5835966B2 (en) 1978-11-16 1978-11-16 Oral composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14177778A JPS5835966B2 (en) 1978-11-16 1978-11-16 Oral composition

Publications (2)

Publication Number Publication Date
JPS5569505A JPS5569505A (en) 1980-05-26
JPS5835966B2 true JPS5835966B2 (en) 1983-08-05

Family

ID=15299918

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14177778A Expired JPS5835966B2 (en) 1978-11-16 1978-11-16 Oral composition

Country Status (1)

Country Link
JP (1) JPS5835966B2 (en)

Also Published As

Publication number Publication date
JPS5569505A (en) 1980-05-26

Similar Documents

Publication Publication Date Title
US4150113A (en) Enzymatic dentifrices
DE2152620C3 (en) Mutanase, process for its production and its use
US4096241A (en) Tooth preparations
US4438093A (en) Oral composition containing dextranase and α-1,3 glucanase and a method for preventing and suppressing oral diseases using the same
JP2005008579A (en) Coaggregation inhibitor of oral bacteria
JPS5811924B2 (en) Oral composition
JP3336688B2 (en) Oral composition
JPS5835966B2 (en) Oral composition
US4107291A (en) Compositions for cleaning teeth and oral cavity
JP2999791B2 (en) Method for enhancing glucosyltransferase inhibitory activity
JPS5811927B2 (en) Oral composition
JPH0363215A (en) Bacterial plaque decomposition composition
JPH10298049A (en) Dental plaque inhibitor and oral composition
JPS643165B2 (en)
JP2736794B2 (en) Plaque formation inhibitor
US3733399A (en) Oral compositions containing an enzyme
JPS5936882B2 (en) Oral composition
JPS60501311A (en) Composition for oral dental treatment
JPH0136802B2 (en)
US2554465A (en) Mucous liquefying preparation
JP2546263B2 (en) Bad breath remover
JP4709735B2 (en) Coaggregation inhibitor of oral bacteria
JPH03218308A (en) Oral composition
JP2949896B2 (en) Oral composition
CA1042805A (en) Enzyme containing oral hygiene compositions