JP2633964B2 - Anti-caries agent - Google Patents

Anti-caries agent

Info

Publication number
JP2633964B2
JP2633964B2 JP25796189A JP25796189A JP2633964B2 JP 2633964 B2 JP2633964 B2 JP 2633964B2 JP 25796189 A JP25796189 A JP 25796189A JP 25796189 A JP25796189 A JP 25796189A JP 2633964 B2 JP2633964 B2 JP 2633964B2
Authority
JP
Japan
Prior art keywords
caries
mutans
genistein
caries agent
isoflavone
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
JP25796189A
Other languages
Japanese (ja)
Other versions
JPH03120209A (en
Inventor
勝 松浦
明雄 小幡
則夫 志村
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.)
KITSUKOOMAN KK
Original Assignee
KITSUKOOMAN 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 KITSUKOOMAN KK filed Critical KITSUKOOMAN KK
Priority to JP25796189A priority Critical patent/JP2633964B2/en
Publication of JPH03120209A publication Critical patent/JPH03120209A/en
Application granted granted Critical
Publication of JP2633964B2 publication Critical patent/JP2633964B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、う蝕予防を目的とした抗う蝕剤に関するも
のである。
Description: TECHNICAL FIELD The present invention relates to an anti-caries agent for preventing caries.

〔従来の技術及び課題〕[Conventional technology and problems]

う蝕(むし歯)には多くの人が悩まされており、厚生
省の歯科疾患実態調査によると我が国の約90%もの人が
う蝕に罹患しており、その治療に要する費用は膨大なも
のとなっている。
Many people are suffering from caries (cavities), and according to a survey of dental diseases by the Ministry of Health and Welfare, about 90% of Japan suffers from dental caries, and the cost of treatment is enormous. Has become.

う蝕はストレプトコッカス・ミュータンス(Storepto
ccocus mutans)を主とする口腔連鎖球菌により惹起さ
れる。すなわちS.mutansの特異的な歯面への吸着能とシ
ュークロースの存在による不溶性グルカン生成を介して
の強固なプラーク(歯垢)形成能及び酸生成能によって
う蝕が生じる。
Caries are Streptococcus mutans (Storepto
ccocus mutans) caused by oral streptococci. That is, caries are generated due to the ability of S. mutans to specifically adsorb to the tooth surface and the ability to form strong plaque (plaque) and the ability to generate acid through the formation of insoluble glucan due to the presence of sucrose.

従ってう蝕の予防にはS.mutansを減らすこと(抗菌)
が最も重要であり、かつ効果的である。
Therefore, reducing S.mutans to prevent caries (antibacterial)
Is most important and effective.

この為には抗菌あるいは殺菌作用のある薬剤を投与し
該菌を駆逐する方法があり、またブラシでの歯磨きによ
り物理的に歯垢を取り除くと共に該菌の成育の元となる
栄養源を除去する方法がとられる。
For this purpose, there is a method in which an agent having an antibacterial or bactericidal action is administered to eliminate the bacteria, and plaque is physically removed by brushing the teeth, and a nutrient source which is a source of the growth of the bacteria is removed. The method is taken.

しかしながら薬剤の投与は副作用の危険が指摘されて
おり、またブラシでの除去は不完全となりがちである。
However, administration of the drug has been pointed out as a risk of side effects, and removal with a brush tends to be incomplete.

この様な観点から安全性の高いう蝕予防剤の開発が望
まれているところであり、その一つとして各種薬草中に
含まれるケンフェロール、ケルセチン、ミリセチン、ラ
ムノシトリンを有効成分とする歯苔形成抑制剤も開発さ
れている。(特公昭63−10133号) しかしながら、これらの物質は薬草中に含有されるも
のであり、大量に入手するには多くの困難が予想され
る。
From this point of view, the development of highly safe caries preventive agents has been desired. One of them is the suppression of dental plaque formation using kaempferol, quercetin, myricetin, and rhamnocitrin contained in various herbs as active ingredients. Agents have also been developed. However, these substances are contained in medicinal herbs, and many difficulties are expected to be obtained in large quantities.

一方、大豆中のサポニン及びイソフラボンを代表とす
る配糖体及びその非糖区分(アグリコン)は各種生理作
用、例えば、抗酸化、抗溶血作用あるいは抗カビ作用等
を有することが知られているが、これらの生理作用は配
糖体あるいはアグリコンに共通するものであり、例えば
ゲニステイン及びダイゼインは共にカビの増殖を阻害す
ることが報告されている。
On the other hand, it is known that glycosides represented by saponins and isoflavones in soybeans and their non-sugar fractions (aglycones) have various physiological actions, for example, antioxidant, antihemolytic or antifungal actions. These physiological actions are common to glycosides or aglycones. For example, it has been reported that both genistein and daidzein inhibit mold growth.

〔課題を解決するための手段〕[Means for solving the problem]

本発明者等は大豆から得られるイソフラボン配糖体あ
るいはアグリコンの入手容易性、安全性に着目し、検討
を進めたところ、アグリコンの中でもゲニステインのみ
がS.mutansの増殖抑制に効果があり、ダイゼインにはそ
の効果が見られないという知見を得た。
The present inventors have focused on the availability and safety of isoflavone glycosides or aglycone obtained from soybeans and studied the safety, and among the aglycones, only genistein was effective in suppressing the growth of S. mutans, and daidzein Did not show that effect.

前述の如く大豆中のアグリコンあるいはその配糖体の
生理作用の多くは共通するものであるが、S.mutansの増
殖抑制効果はゲニステインのみにしか見ることができな
い特異的なものであり、この様な知見は本発明者等によ
って初めて明らかにされたものである。
As mentioned above, many of the physiological actions of aglycone or its glycosides in soybeans are common, but the growth inhibitory effect of S. mutans is specific, which can be seen only in genistein, and Such findings were first clarified by the present inventors.

本発明はこの様な知見に基づいて完成されたものであ
り、以下に本発明を具体的に説明する。
The present invention has been completed based on such knowledge, and the present invention will be specifically described below.

ゲニステインは植物体、例えば大豆から抽出して得ら
れるものであり、具体的には特開昭62−126186号に開示
された方法、あるいはこの方法で得られたイソフラボン
配糖体を、酵素ないし酸で加水分解したアグリコンを樹
脂に吸着させたのちゲニステインを選択的に溶出させた
り、アグリコン混合物を乾燥させた後エーテル抽出する
ことによって得ることができる。
Genistein is obtained by extracting from a plant, for example, soybean. Specifically, the method disclosed in JP-A-62-126186, or an isoflavone glycoside obtained by this method is used as an enzyme or acid. After the aglycone hydrolyzed in step (1) is adsorbed on the resin, the genistein is selectively eluted, or the aglycone mixture is dried and then extracted with ether.

また本発明者等が先に特許出願した特願昭63−83135
号に開示した方法によっても得ることができる。
In addition, Japanese Patent Application No. 63-83135, filed by the present inventors earlier,
Can also be obtained by the method disclosed in the above item.

更には、脱皮大豆をpH8〜11、50〜60℃の温水に浸漬
し、イソフラボン配糖体を抽出し、これを酵素ないし酸
で加水分解した分解物あるいは豆乳を限外濾過膜により
濾過して得られるイソフラボン含有区分や、分離大豆蛋
白製造過程で得られる非蛋白区分中のイソフラボン含有
区分を、酸ないし酵素で加水分解した分解物をそのまま
あるいは濃縮したものでも良い。
Furthermore, the dehulled soybeans are immersed in warm water of pH 8-11, 50-60 ° C. to extract isoflavone glycosides, and the hydrolyzate or soymilk hydrolyzed with an enzyme or acid is filtered through an ultrafiltration membrane. The isoflavone-containing fraction obtained, or the isoflavone-containing fraction in the non-protein fraction obtained in the process of producing isolated soybean protein, may be hydrolyzed with an acid or an enzyme as it is or may be concentrated.

この様にして得られるゲニステインはそのままの形で
口腔内に適用してもよく、あるいは他の口腔剤、例えば
歯磨剤、うがい剤、チューインガム、トローチ等に混合
しても良い。
The genistein thus obtained may be applied as it is to the oral cavity, or may be mixed with other oral preparations such as dentifrice, gargle, chewing gum, troche and the like.

以下に実施例を示す。 Examples will be described below.

〔実施例〕〔Example〕

S.mutansの増殖抑制効果について以下の実験を行なっ
た。
The following experiments were performed on the growth inhibitory effect of S. mutans.

ディフコ・ラボラトリー社のブレイン・ハート・イン
ヒュージョン(Brain heart infusion)の液体培地(3.
7%)およびこれにシュークロースを10%添加した培地
に第1表に示すイソフラボン配糖体及びアグリコンを20
0P.P.M.添加したのち120℃、15分間の殺菌処理をし、こ
れ等の培地にS.mutans(IFO 13955)を102ケ/mlになる
様に添加し、37℃で24時間培養したところ、第1表に示
す結果を得た。
Liquid medium of Brain heart infusion from Difco Laboratory (3.
7%) and 10% sucrose to this medium were added with 20% isoflavone glycoside and aglycone as shown in Table 1.
0P.PM 120 ℃ after addition, the sterilization treatment for 15 minutes, where it like adding medium S.mutans the (IFO 13955) of the As of 10 2 pcs / ml, were cultured for 24 hours at 37 ° C. The results shown in Table 1 were obtained.

第1表に示す結果から明らかなように、ゲニステイン
はS.mutansの増殖を抑制する特異な効果を有する。それ
故、ゲニステインは抗う蝕剤の有効成分として利用でき
るものである。
As is clear from the results shown in Table 1, genistein has a unique effect of suppressing the growth of S. mutans. Therefore, genistein can be used as an active ingredient of an anti-cariogenic agent.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ゲニステインを有効成分とする抗う蝕剤。An anti-cariogenic agent comprising genistein as an active ingredient.
JP25796189A 1989-10-04 1989-10-04 Anti-caries agent Expired - Lifetime JP2633964B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25796189A JP2633964B2 (en) 1989-10-04 1989-10-04 Anti-caries agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25796189A JP2633964B2 (en) 1989-10-04 1989-10-04 Anti-caries agent

Publications (2)

Publication Number Publication Date
JPH03120209A JPH03120209A (en) 1991-05-22
JP2633964B2 true JP2633964B2 (en) 1997-07-23

Family

ID=17313616

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25796189A Expired - Lifetime JP2633964B2 (en) 1989-10-04 1989-10-04 Anti-caries agent

Country Status (1)

Country Link
JP (1) JP2633964B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4672096B2 (en) * 1999-09-14 2011-04-20 日本ゼトック株式会社 Anti-caries agent and oral composition containing the same
JP2001089385A (en) * 1999-09-22 2001-04-03 Kobayashi Pharmaceut Co Ltd Anti-dental caries agent
CN101715445B (en) 2007-06-21 2012-01-25 J-制油株式会社 Method for producing glycoside aglycone

Also Published As

Publication number Publication date
JPH03120209A (en) 1991-05-22

Similar Documents

Publication Publication Date Title
JP4903131B2 (en) Use of a compound comprising D-mannoheptulose and / or perseitol for the treatment and prevention of innate immune modulatory diseases
KR101354923B1 (en) Oral hygiene composition using an extract of curcuma longa and an extract eriobotrya japonica
KR101955468B1 (en) Preparing method for toothpaste composition comprising natural extracts
KR101704589B1 (en) Composition comprising extracts of Magnolia flower and Magnolia officinlis for preventing or treating periodentitis as an active ingredient
KR930000059B1 (en) Dental composition
JPWO2003099304A1 (en) Anti-periodontal disease bacteria composition, anti-periodontal disease food and drink containing the anti-periodontal disease bacteria composition, and oral cleanser
WO2004026273A1 (en) Composition for oral use
JP2633964B2 (en) Anti-caries agent
JPH08143442A (en) Skin external preparation and its production
JP2004067634A5 (en)
KR19980013946A (en) Oral composition of liquid type
KR100431170B1 (en) Compositions for Dental Clinic Comprising Extracts of Plant
KR0138244B1 (en) Dentifrice compositions
JPH0881380A (en) Anti-periodontitis agent and anti-periodontitis food containing high-molecular weight polyphenol as active component
KR101660467B1 (en) Oral composition containing fermentative extract of lycii fructus as active ingredient
KR101916377B1 (en) Composition for teeth whitening and preparation method therefor
KR101826229B1 (en) A Composition comprising extracts, fractions or isolated compounds of Magnolia flower for preventing and treating of periodentitis as an active ingredient
KR102328978B1 (en) An oral composition for improvement of periodontal disease comprising natural complex extracts
JP2005035907A (en) Anti-periodontal disease medicine
US9295627B2 (en) Mouthwash composition for preventing and/or treating periodontal diseases
JP4633399B2 (en) Glucosyltransferase inhibitor
KR102132873B1 (en) Composition for the prevention or treating of oral diseases comprising extract of indigo, Lindera Root, Madder Root and Psoraleae Semen
JP3281716B2 (en) Glucosyltransferase inhibitors, oral preparations and foods and drinks
KR0149483B1 (en) Antiplague compositions
RU2822421C1 (en) Composition of active dental base for oral care products, stimulating restorative and reparative processes in oral cavity tissues, and composition for oral hygiene based thereon (versions)

Legal Events

Date Code Title Description
FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090425

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090425

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 13

Free format text: PAYMENT UNTIL: 20100425

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 13

Free format text: PAYMENT UNTIL: 20100425