JPH0338514A - Mouth-washing agent for inhibiting bacterial plaque on teeth - Google Patents
Mouth-washing agent for inhibiting bacterial plaque on teethInfo
- Publication number
- JPH0338514A JPH0338514A JP17136089A JP17136089A JPH0338514A JP H0338514 A JPH0338514 A JP H0338514A JP 17136089 A JP17136089 A JP 17136089A JP 17136089 A JP17136089 A JP 17136089A JP H0338514 A JPH0338514 A JP H0338514A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- mouth
- formula
- mouthwash
- teeth
- 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
Links
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 5
- 238000005406 washing Methods 0.000 title abstract 3
- 230000001580 bacterial effect Effects 0.000 title abstract 2
- -1 fatty acid esters Chemical class 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 8
- 239000000178 monomer Substances 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 5
- 229930195729 fatty acid Natural products 0.000 claims abstract description 5
- 239000000194 fatty acid Substances 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 150000003626 triacylglycerols Chemical class 0.000 claims abstract description 4
- 229920001214 Polysorbate 60 Polymers 0.000 claims abstract description 3
- 239000002324 mouth wash Substances 0.000 claims description 15
- 229940051866 mouthwash Drugs 0.000 claims description 13
- 208000002064 Dental Plaque Diseases 0.000 claims description 8
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 208000002925 dental caries Diseases 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- 229920006243 acrylic copolymer Polymers 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 239000004094 surface-active agent Substances 0.000 abstract 2
- 208000010266 Aggressive Periodontitis Diseases 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000002352 surface water Substances 0.000 abstract 1
- 239000011324 bead Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 241000894006 Bacteria Species 0.000 description 7
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 7
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 238000007796 conventional method Methods 0.000 description 5
- 238000001179 sorption measurement Methods 0.000 description 5
- 241000194019 Streptococcus mutans Species 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 210000003296 saliva Anatomy 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 208000028169 periodontal disease Diseases 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- 208000006558 Dental Calculus Diseases 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 208000005888 Periodontal Pocket Diseases 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002158 endotoxin Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002359 Tetronic® Polymers 0.000 description 1
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003239 periodontal effect Effects 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229950008882 polysorbate Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 229940085605 saccharin sodium Drugs 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940075560 sodium lauryl sulfoacetate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- OVYTZAASVAZITK-UHFFFAOYSA-M sodium;ethanol;hydroxide Chemical compound [OH-].[Na+].CCO OVYTZAASVAZITK-UHFFFAOYSA-M 0.000 description 1
- 239000008279 sol Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
り哀とへ靴韮條狂
本発明は、口腔内細菌、すなわち歯垢の歯牙への付着を
抑制する効果を有し、う蝕予防効果および歯周病の予防
・治療効果をもつ歯垢付着抑制洗口剤に関する。[Detailed Description of the Invention] The present invention has the effect of suppressing the adhesion of oral bacteria, that is, dental plaque, to the teeth, and has the effect of preventing caries and preventing periodontal disease. This invention relates to a mouthwash that suppresses plaque adhesion and has a therapeutic effect.
従来の技術および課題
う蝕や歯周病は歯垢が原因で発症することが明らかにさ
れており、う蝕は歯垢中のストレブトコツカス・ミュー
タンスなどのある種の細菌が、食物中の糖を代謝して生
じる酸が歯牙のエナメル質を脱灰することにより引き起
こされる。また、歯垢中のある細菌は、歯肉を刺激4−
る酵素と内毒素とを分泌し、歯肉に炎症を引き起こす。Conventional techniques and challenges It has been revealed that dental caries and periodontal disease are caused by dental plaque. It is caused by the acid produced by metabolizing the sugars in the tooth that demineralizes tooth enamel. Also, some bacteria in plaque can irritate the gums.
secretes enzymes and endotoxins that cause inflammation of the gums.
そして、歯肉は、出血をおこし弾性を失い、ついには歯
牙から単離して、歯周ポケットを生じる。この歯周ポケ
ットは嫌気性菌の住処となり、それらの菌の産生ずる酵
素や内毒素などにより、歯周組織が破壊されて、歯周病
が引き起こされる。The gums then bleed, lose elasticity, and eventually separate from the teeth, creating periodontal pockets. This periodontal pocket becomes a home for anaerobic bacteria, and the enzymes and endotoxins produced by these bacteria destroy the periodontal tissue and cause periodontal disease.
そのため、かかる発症を防止する目的で、歯垢の歯牙へ
の付着を抑制する方法が数多く提案(特開昭60−16
9423号、特開昭63−8325号など)されている
が、いずれも完全には満足できるものではない。Therefore, in order to prevent such onset, many methods have been proposed to suppress the adhesion of dental plaque to teeth (Japanese Patent Laid-Open No. 60-16
No. 9423, Japanese Unexamined Patent Publication No. 63-8325, etc.), but none of them are completely satisfactory.
本発明の目的は、歯垢(口腔内細菌)の歯牙への付着抑
制効果に優れた新規な洗口剤を提供することである。An object of the present invention is to provide a novel mouthwash that is excellent in suppressing the adhesion of dental plaque (oral bacteria) to teeth.
課題を解決するための手段
本発明者らは、今回、歯垢の歯牙への付着のモデル系で
ある唾液で覆われたヒドロキシアパタイトビーズへのス
トレプトコソカス・ミュータンスの付着が特定のアクリ
ル系共重合体と特定の非イオン界面活性剤を配合した洗
口剤によって、効果的に抑制され、歯垢付着抑制洗口剤
として有用であることを見出し、本発明を完成するに至
った。Means for Solving the Problems The present inventors have now demonstrated that the adhesion of Streptococcus mutans to saliva-covered hydroxyapatite beads, which is a model system for the adhesion of dental plaque to teeth, is observed in a specific acrylic-based system. The present inventors have discovered that a mouthwash containing a copolymer and a specific nonionic surfactant effectively suppresses plaque adhesion and is useful as a mouthwash for suppressing plaque adhesion, and has completed the present invention.
すなわち、本発明は、
必須成分として、
(a)式:
[式中、R8、R2、R5は水素またはメチル基、j3
よびR4、R6は炭素数t−tSのアルキル基を色味す
る。ただし、R1とR5、R4とR6とは同時に同じ基
にはならない。]
で示されるモノマーを共重合させてなる共重合体。That is, the present invention provides the following essential components: (a) Formula: [wherein R8, R2, R5 are hydrogen or methyl groups, j3
and R4 and R6 represent an alkyl group having a carbon number of t-tS. However, R1 and R5 and R4 and R6 cannot be the same group at the same time. ] A copolymer obtained by copolymerizing the monomers shown below.
(b)ポリオキシエチレンオキシ脂肪酸トリグリセライ
ド誘導体、ポリオキシエチレンソルビタン脂肪酸エステ
ルおよびブロックポリマー型からなる群より選ばれる1
種または2種以上の非イオン界面活性剤および
(c)水
を配合したことを特徴とする歯垢付着抑制洗口剤を提供
する・ものである。(b) 1 selected from the group consisting of polyoxyethylene oxyfatty acid triglyceride derivatives, polyoxyethylene sorbitan fatty acid esters, and block polymer types;
The present invention provides a dental plaque adhesion inhibiting mouth rinse characterized by containing one or more nonionic surfactants and (c) water.
なお、ポリアクリル酸とメタアクリル酸3−ヒドロキノ
プロピルとの共重合体などを配合して、歯石を形成する
カルシウムイオンをキレートすることにより、歯石形成
を抑制する口腔組成物が知られているが(特開昭61−
165317号)、本発明とは用いる共重合体の種類お
よび適用目的が異なり、全く別異なものである。Note that oral compositions are known that suppress tartar formation by blending a copolymer of polyacrylic acid and 3-hydroquinopropyl methacrylate to chelate calcium ions that form tartar. (Unexamined Japanese Patent Publication No. 1983-
No. 165317) is completely different from the present invention in the type of copolymer used and the purpose of application.
本発明で用いる共重合体は、前記式[1]のモノマー、
式[11]のモノマーおよび式[In]のモノマーとを
共重合させて得られるもので、重量平均分子量として、
好ましくは約10,000〜約200゜000、さらに
好ましくは約50.000〜10o、o o oである
。これらは商品名プラスサイズL−53D、同L−53
P(互応化学社製)として入手可能である。The copolymer used in the present invention includes the monomer of the formula [1],
It is obtained by copolymerizing the monomer of formula [11] and the monomer of formula [In], and has a weight average molecular weight of
Preferably about 10,000 to about 200°000, more preferably about 50,000 to 10°, o o o. These are product names: Plus Size L-53D, Plus Size L-53
It is available as P (manufactured by Gooh Kagaku Co., Ltd.).
本発明の洗口剤に用いる、共重合体の配合量は、一般に
約0.001重量%〜約10.0重量%、好ましくは約
0.05重量%〜約8.0重屯%、さらに好ましくは約
0.1重量%〜約50重量%である。配合量が0.00
1重量%より少ないと、歯垢付着抑制効果が十分ではな
く、一方、100重量%より多くなると、粘度が高くな
りすぎ使用に適さなくなる。The amount of the copolymer used in the mouthwash of the present invention is generally about 0.001% to about 10.0% by weight, preferably about 0.05% to about 8.0% by weight, and Preferably from about 0.1% to about 50% by weight. The blending amount is 0.00
If it is less than 1% by weight, the effect of inhibiting plaque adhesion will not be sufficient, while if it is more than 100% by weight, the viscosity will become too high and it will not be suitable for use.
また、本発明で用いる非イオン界面活性剤としては、
(1)ポリオキシエチレンオキシ脂肪酸トリグリセライ
ド誘導体、例えば、ポリオキシエチレン硬化ヒマシ油誘
導体、ポリオキシエチレンヒマシ油誘導体など、
(2)ポリオキンエチレンソルヒタン脂肪酸エステル、
例えば、ボリオキノエチレンソルヒタンモノオレエート
、ポリオキンエヂレンソルヒタンモノステアレエート、
ポリオキソエヂレンソルヒクンモノパルミテートなど、
(3)ブロックポリマー型、例えば、プルロニック、テ
トロニックなどが挙げられる。In addition, the nonionic surfactants used in the present invention include (1) polyoxyethylene oxyfatty acid triglyceride derivatives, such as polyoxyethylene hydrogenated castor oil derivatives, polyoxyethylene castor oil derivatives, etc., (2) polyoxyethylene sol tan fatty acid ester,
For example, borioquinoethylene solhitan monooleate, polyoquinoethylene solhitan monostearate,
(3) Block polymer types, such as pluronic, tetronic, etc., such as polyoxoethylene solhikun monopalmitate.
かかる非イオン界面活性剤は単独でも、2F+1以上を
併用してもよい。Such nonionic surfactants may be used alone or in combination with 2F+1 or more.
本発明の洗口剤に用いる非イオン界面活性剤の配合量は
、一般に約0.05重量%〜約150重量%、好ましく
は約0.1重量%〜約5.0重量%、さらに好ましくは
約045重量%〜約【、5盾量%である。配合量が0.
05重項%より少ないと、歯垢付着抑制効果が十分では
なく、一方、150重量%より多くなると、粘度が高く
なりすぎ使用に適さなくなる。The amount of nonionic surfactant used in the mouthwash of the present invention is generally about 0.05% to about 150% by weight, preferably about 0.1% to about 5.0% by weight, and more preferably about 0.1% to about 5.0% by weight. From about 0.45% to about 5% by weight. The blending amount is 0.
If it is less than 0.5 doublet%, the effect of suppressing plaque adhesion will not be sufficient, while if it is more than 150% by weight, the viscosity will become too high and it will not be suitable for use.
本発明の洗口剤は常法により、製造することかでき、他
の成分としては、特に限定するものではなく、通常、用
いられる成分のいずれもが配合できる。例えば、ポリエ
チレングリコール、ソルヒトール、グリセリン、プロピ
レングリコールなとの湿潤剤、ラウリル硫酸ナトリウム
、ドデシルベンゼンスルホン酸ナトリウム、水素添加コ
コナソツ脂肪酸モノグリセリド硫酸ナトリウム、ラウリ
ルスルホ酢酸ナトリウム、N−アシルグルタミン酸塩な
どの発泡剤、香料、甘味剤、防腐剤などが適宜配合でき
る。The mouthwash of the present invention can be produced by a conventional method, and other ingredients are not particularly limited, and any commonly used ingredients can be blended. For example, wetting agents such as polyethylene glycol, sorbitol, glycerin, propylene glycol, blowing agents such as sodium lauryl sulfate, sodium dodecylbenzenesulfonate, sodium hydrogenated coconut fatty acid monoglyceride sulfate, sodium laurylsulfoacetate, N-acylglutamate, Flavoring agents, sweeteners, preservatives, etc. can be added as appropriate.
実施例
次に実験例、実施例むよび比較例を挙げて、本発明をさ
らに詳しく説明する。EXAMPLES Next, the present invention will be explained in more detail with reference to experimental examples, working examples, and comparative examples.
実験例
唾液被覆ヒドロキシアパタイト(HAP)ビーズ上への
ストレプトコッカス・ミュータンス6715の吸着に及
ぼす効果
(1)20xyのHAPピーズをヒトの唾液(血肢型0
)0.5zQとともに室温にて1時間インキュベートし
た。該ビーズを0.05M KC(2,1mMKtt*
po、、lsM CaCQzおよび1mM MgC12
tからなるpH6、0の緩衝液INRで2回洗浄した。Experimental Example Effect on the adsorption of Streptococcus mutans 6715 onto saliva-coated hydroxyapatite (HAP) beads (1) 20xy HAP beads were added to human saliva (blood limb type 0).
) Incubated with 0.5zQ for 1 hour at room temperature. The beads were mixed with 0.05M KC (2,1mM Ktt*
po, lsM CaCQz and 1mM MgC12
The cells were washed twice with INR, a pH 6.0 buffer consisting of T.
(この緩衝液は、唾肢無機威分に似せtこものである)
。(This buffer is an imitation of salivary inorganic fluid.)
.
次いで、室温にて、該ビーズをpH7,0のポリマー溶
液(試料溶液) 0 、5 z(lとともに1時間イン
キュベートし、上記緩衝液1x(lで2回洗浄した。The beads were then incubated for 1 hour at room temperature with a pH 7.0 polymer solution (sample solution) 0,5 z (l) and washed twice with the above buffer 1x (l).
次に、前記緩衝/fL0 、5 村中に[3H]チミジ
ン標識バクテリア(ストレプトコッカス・ミュータンス
)を5.0X10’個含む懸濁液を該ビーズに添加し、
室温にて1時間インキュベートした。前記緩衝液1zQ
で3回洗浄し、ビーズをバイアルに移し、液体ノンヂレ
ーノヨンカウンターを用いて放射能を計測した。一方、
既知の[3H]標識細胞の割合を同じ方法で計数し、バ
クテリア数の検量線を作成した。Next, a suspension containing 5.0 x 10' [3H]thymidine-labeled bacteria (Streptococcus mutans) in the buffer/fL0, 5 cells was added to the beads,
Incubated for 1 hour at room temperature. The buffer solution 1zQ
The beads were washed three times with water, the beads were transferred to a vial, and the radioactivity was counted using a liquid non-deletion counter. on the other hand,
The percentage of known [3H]-labeled cells was counted using the same method, and a standard curve for the number of bacteria was created.
用いた試料溶液は第1表の唾戒被覆HAPの処理の欄に
示す。The sample solutions used are shown in the column of treatment of saliva coated HAP in Table 1.
第1表に示すごとく、0.1%該アクリル系共重合体と
特定の非イオン界面活性剤の水溶液は、バクテリアの唾
液被覆HAPへの吸着を著しく抑制したことが確認され
た。As shown in Table 1, it was confirmed that an aqueous solution of 0.1% of the acrylic copolymer and a specific nonionic surfactant significantly inhibited the adsorption of bacteria to saliva-coated HAP.
実施例1〜8および比較例1〜6
第2表に示す処方に従い、常法により洗口剤を製造し、
実験例におけると同様にHAPビーズ上へのストレプト
コッカス・ミュータンス6715の吸着に及ぼす効果を
調べた。結果を第2表に示す。Examples 1 to 8 and Comparative Examples 1 to 6 Mouthwashes were manufactured by a conventional method according to the formulations shown in Table 2,
As in the experimental example, the effect on the adsorption of Streptococcus mutans 6715 onto HAP beads was investigated. The results are shown in Table 2.
なお、第2表中、粘度、総合評価は次の基準で判定した
。In Table 2, the viscosity and overall evaluation were determined based on the following criteria.
粘度(官能による) ○:良好 ×:高すぎて使用に適さない。Viscosity (according to organoleptic) ○: Good ×: Too expensive to be used.
総合評価
○:吸着に及ぼす効果の相対比率が50%以下で、粘度
が○のもの。Overall evaluation ○: The relative ratio of the effect on adsorption is 50% or less and the viscosity is ○.
×:吸着に及ぼす効果の相対比率が50%より大きいか
、粘度が×のもの。×: The relative ratio of the effect on adsorption is greater than 50%, or the viscosity is ×.
実施例9 次の処方に従い、 た。Example 9 According to the following prescription, Ta.
常法により洗口剤を製造し 成分 グリセリン ポリオキシエチレン硬化 ヒマシ油(60E、O,) エタノール 水酸化ナトリウム サッカリンナトリウム プラスサイズ[、−53P バラオキシ安息香酸メチル 香料 精製水 実施例1O 次の処方に従い、 た。Manufacture mouthwash using conventional methods component glycerin polyoxyethylene hardening Castor oil (60E, O,) ethanol Sodium hydroxide saccharin sodium Plus size [, -53P Methyl roseoxybenzoate fragrance purified water Example 1O According to the following prescription, Ta.
常法により洗口剤を製造し
成分
グリセリン
配合量(%)
0
1.5
0
0.2
2
+、0
0.5
0.5
残部
配合量(%)
ソ
ルビットポ
リソルベート
エタノール 5水酸化ナト
リウム 0.002プラスサイズ
L−53D 0.01安息香酸ナトリ
ウム 05香料
0.5精製水
残部発明の効果
本発明によれば、歯垢の歯牙への付着を有効に抑制する
洗口剤が得られる。A mouthwash was manufactured using a conventional method. Ingredients: Glycerin content (%) 0 1.5 0 0.2 2 +, 0 0.5 0.5 Remaining content (%) Sorbitol polysorbate ethanol 5 Sodium hydroxide 0.002 Plus Size L-53D 0.01 Sodium Benzoate 05 Fragrance
0.5 purified water
Remaining Effects of the Invention According to the present invention, a mouthwash that effectively suppresses the adhesion of dental plaque to teeth can be obtained.
Claims (3)
学式、表等があります▼[II] ▲数式、化学式、表等があります▼[III] [式中、R_1、R_2、R_3は水素またはメチル基
、およびR_4、R_5は炭素数1〜18のアルキル基
を意味する。ただし、R_2とR_3、R_4とR_5
とは同時に同じ基にはならない。] で示されるモノマーを共重合させてなる共重合体。 (b)ポリオキシエチレンオキシ脂肪酸トリグリセライ
ド誘導体、ポリオキシエチレンソルビタン脂肪酸エステ
ルおよびブロックポリマー型からなる群より選ばれる1
種または2種以上の非イオン界面活性剤 (c)水 を配合したことを特徴とする歯垢付着抑制洗口剤。(1) As essential components, (a) Formulas: ▲There are mathematical formulas, chemical formulas, tables, etc.▼[I]▲There are mathematical formulas, chemical formulas, tables, etc.▼[II]▲There are mathematical formulas, chemical formulas, tables, etc.▼[III [In the formula, R_1, R_2, and R_3 represent hydrogen or a methyl group, and R_4 and R_5 represent an alkyl group having 1 to 18 carbon atoms. However, R_2 and R_3, R_4 and R_5
and cannot be based on the same base at the same time. ] A copolymer obtained by copolymerizing the monomers shown below. (b) 1 selected from the group consisting of polyoxyethylene oxyfatty acid triglyceride derivatives, polyoxyethylene sorbitan fatty acid esters, and block polymer types;
A mouthwash for inhibiting dental plaque adhesion, characterized in that it contains one or more nonionic surfactants (c) and water.
,000である請求項(1)の洗口剤。(2) The average molecular weight of the copolymer is 10,000 to 200
.,000. The mouthwash of claim (1).
求項(1)または請求項(2)の洗口剤。(3) The mouthwash of claim (1) or claim (2), which contains 0.001 to 10% by weight of the copolymer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17136089A JPH0338514A (en) | 1989-07-03 | 1989-07-03 | Mouth-washing agent for inhibiting bacterial plaque on teeth |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17136089A JPH0338514A (en) | 1989-07-03 | 1989-07-03 | Mouth-washing agent for inhibiting bacterial plaque on teeth |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0338514A true JPH0338514A (en) | 1991-02-19 |
Family
ID=15921743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17136089A Pending JPH0338514A (en) | 1989-07-03 | 1989-07-03 | Mouth-washing agent for inhibiting bacterial plaque on teeth |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0338514A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0338512A (en) * | 1989-07-03 | 1991-02-19 | Sunstar Inc | Mouth-washing agent for inhibiting bacterial plaque on teeth |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5540646A (en) * | 1978-09-18 | 1980-03-22 | Lion Corp | Composition for oral cavity |
| JPS60501314A (en) * | 1983-05-13 | 1985-08-15 | ブリティッシュ・テクノロジー・グループ・リミテッド | Prevention of unwanted adsorption on surfaces |
| JPS6333321A (en) * | 1986-02-10 | 1988-02-13 | ザ、プロクタ−、エンド、ギヤンブル、カンパニ− | Oral composition |
| JPH024708A (en) * | 1988-03-18 | 1990-01-09 | Colgate Palmolive Co | Anti-tartar oral composition |
| JPH0338512A (en) * | 1989-07-03 | 1991-02-19 | Sunstar Inc | Mouth-washing agent for inhibiting bacterial plaque on teeth |
-
1989
- 1989-07-03 JP JP17136089A patent/JPH0338514A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5540646A (en) * | 1978-09-18 | 1980-03-22 | Lion Corp | Composition for oral cavity |
| JPS60501314A (en) * | 1983-05-13 | 1985-08-15 | ブリティッシュ・テクノロジー・グループ・リミテッド | Prevention of unwanted adsorption on surfaces |
| JPS6333321A (en) * | 1986-02-10 | 1988-02-13 | ザ、プロクタ−、エンド、ギヤンブル、カンパニ− | Oral composition |
| JPH024708A (en) * | 1988-03-18 | 1990-01-09 | Colgate Palmolive Co | Anti-tartar oral composition |
| JPH0338512A (en) * | 1989-07-03 | 1991-02-19 | Sunstar Inc | Mouth-washing agent for inhibiting bacterial plaque on teeth |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0338512A (en) * | 1989-07-03 | 1991-02-19 | Sunstar Inc | Mouth-washing agent for inhibiting bacterial plaque on teeth |
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