JP2566676B2 - Dental composition - Google Patents

Dental composition

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Publication number
JP2566676B2
JP2566676B2 JP2286640A JP28664090A JP2566676B2 JP 2566676 B2 JP2566676 B2 JP 2566676B2 JP 2286640 A JP2286640 A JP 2286640A JP 28664090 A JP28664090 A JP 28664090A JP 2566676 B2 JP2566676 B2 JP 2566676B2
Authority
JP
Japan
Prior art keywords
weight
aqueous solution
alkali metal
hypochlorite
aluminum oxide
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
JP2286640A
Other languages
Japanese (ja)
Other versions
JPH03279330A (en
Inventor
聰明 柏田
光伸 河島
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.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
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Filing date
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Publication of JPH03279330A publication Critical patent/JPH03279330A/en
Application granted granted Critical
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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、歯科医療分野において象牙質または根管内
の清掃・消毒剤として用いられる歯科用組成物に関す
る。
TECHNICAL FIELD The present invention relates to a dental composition used as a cleaning / disinfecting agent for dentin or root canals in the field of dentistry.

(従来の技術) 歯科治療においてカリエスを研削除去した象牙質面お
よび根管内の清掃・消毒に次亜塩素酸ナトリウム水溶液
が用いられている。
(Prior Art) A sodium hypochlorite aqueous solution is used for cleaning and disinfecting the dentin surface and root canal from which caries have been ground and removed in dental treatment.

(発明が解決しようとする課題) しかしながら、従来用いられている次亜塩素酸ナトリ
ウム水溶液は粘性が低いため、目的とする場所のみに限
定的に塗布することが困難であった。すなわち、次亜塩
素酸ナトリウム水溶液を歯面のある部位に塗布しても、
目的の部位の周囲まで液が広がってしまい、従って清掃
・消毒に必要な量がその部位で確保されなくなったり、
あるいは流れ出した該水溶液が口膣内軟組織を侵すとい
う不都合があった。
(Problems to be Solved by the Invention) However, since the conventionally used sodium hypochlorite aqueous solution has a low viscosity, it was difficult to apply the solution only to a desired place. That is, even if the sodium hypochlorite aqueous solution is applied to a part of the tooth surface,
The liquid spreads around the target area, so the amount required for cleaning and disinfection cannot be secured in that area,
Alternatively, there is the inconvenience that the flowing out aqueous solution attacks the soft tissue in the vagina of the mouth.

また、次亜塩素酸ナトリウムの清掃・消毒効果がその
酸化作用によるものであることに着眼して検討を行った
ところ、同様の作用を有する類縁元素の金属塩を用いて
も同じ清掃・消毒効果が得られることが明らかとなり、
次亜塩素酸塩としてはナトリウム塩に限定する必要がな
いことを確認した。
In addition, we conducted a study focusing on the fact that the cleaning / disinfecting effect of sodium hypochlorite is due to its oxidative effect, and found that the same cleaning / disinfecting effect can be obtained by using metal salts of related elements that have similar effects. It became clear that
It was confirmed that the hypochlorite need not be limited to the sodium salt.

従って、本発明の目的は必要とされる部位のみに限定
的に塗布することが可能な次亜塩素酸アルカリ金属塩製
剤を提供することにある。
Therefore, an object of the present invention is to provide an alkali metal hypochlorite preparation which can be applied only to a required site in a limited manner.

(課題を解決するための手段) ところで前記課題を解決するには次亜塩素酸アルカリ
金属塩水溶液に増粘剤を加えればよいが、実際に検討し
てみると水溶性有機ポリマーやコロイド状シリカなどの
代表的増粘剤は次亜塩素酸アルカリ金属塩水溶液の強ア
ルカリ性、かつ強力な酸化性に耐えられなかったり、次
亜塩素酸アルカリ金属塩の分解を促進したりするため実
用性に欠けることがわかった。そこで、これらの条件を
満たす増粘剤を見い出すべく、特に無機化合物について
鋭意検討を重ね、その結果、酸化アルミニウム微粒子が
増粘効果、貯蔵安定性の点で優れていることを見いだし
本発明の完成に至った。
(Means for Solving the Problems) By the way, in order to solve the above problems, a thickener may be added to an aqueous solution of an alkali metal hypochlorite, but when actually examined, a water-soluble organic polymer or colloidal silica is used. Typical thickeners such as are not practical because they cannot withstand the strong alkaline and strong oxidizing properties of the aqueous solution of alkali metal hypochlorite or accelerate the decomposition of alkali metal hypochlorite. I understand. Therefore, in order to find a thickener satisfying these conditions, in particular, intensive studies were carried out on inorganic compounds, and as a result, aluminum oxide fine particles were found to be excellent in thickening effect and storage stability, and the present invention was completed. Came to.

すなわち、本発明は次亜塩素酸アルカリ金属塩、水お
よびBET比表面積10m2/g以上の酸化アルミニウム微粒子
を主成分とし、かつ50センチポイズ以上の粘度を有する
ことを特徴とする歯科用組成物である。
That is, the present invention is a dental composition characterized by having an alkali metal hypochlorite, water and BET specific surface area of 10 m 2 / g or more of aluminum oxide fine particles as a main component, and having a viscosity of 50 centipoise or more. is there.

本発明の組成物は次亜塩素酸アルカリ金属塩を水溶液
とし、その中に酸化アルミニウム微粒子を均一に分散さ
せることにより調製される。本発明で用いられる次亜塩
素酸アルカリ金属塩としてはリチウム塩、ナトリウム
塩、カリウム塩、およびセシウム塩が挙げられ、なかで
も安定性の点でナトリウム塩、カリウム塩が好適であ
る。象牙質および根管内の清掃・消毒効果は次亜塩素酸
アルカリ金属塩水溶液中の次亜塩素酸アルカリ金属塩濃
度に一義的に依存し、本発明として好適な濃度は0.1〜2
0重量%である。なお、従来、殺菌消毒、漂白などの目
的で用いられている次亜塩素酸アルカリ金属塩水溶液に
は、安定剤として水酸化ナトリウムに代表される水酸化
アルカリが加えられている。本発明における次亜塩素酸
アルカリ金属塩の水溶液にも従来と同様に安定剤として
水酸化ナトリウムなどの水酸化アルカリが1〜20重量%
加えられることが好ましい。
The composition of the present invention is prepared by using an alkali metal hypochlorite salt as an aqueous solution and uniformly dispersing aluminum oxide fine particles therein. Examples of the alkali metal hypochlorite used in the present invention include lithium salt, sodium salt, potassium salt, and cesium salt. Among them, sodium salt and potassium salt are preferable from the viewpoint of stability. The cleaning / disinfecting effect on the dentin and the root canal is uniquely dependent on the concentration of alkali metal hypochlorite in the aqueous solution of alkali metal hypochlorite, and the preferred concentration of the present invention is 0.1 to 2
It is 0% by weight. Incidentally, alkali hydroxide represented by sodium hydroxide is added as a stabilizer to an aqueous solution of alkali metal hypochlorite which has been conventionally used for the purpose of sterilization and bleaching. The aqueous solution of the alkali metal hypochlorite in the present invention also contains 1 to 20% by weight of alkali hydroxide such as sodium hydroxide as a stabilizer as in the conventional case.
It is preferably added.

本発明で用いられる酸化アルミニウム微粒子は次亜塩
素酸アルカリ金属塩水溶液の増粘剤としてBET比表面積1
0m2/g以上のものが用いられる。この酸化アルミニウム
微粒子の形状は本発明の効果に影響を及ぼすものではな
く、粒状、針状、繊維状、あるいは板状等、いずれの形
状のものが用いられても構わない。従って本発明におけ
る「微粒子」なる用語は、上記の形状を総括したものと
して用いられる。
The aluminum oxide fine particles used in the present invention have a BET specific surface area of 1 as a thickener for an aqueous solution of alkali metal hypochlorite.
Those of 0 m 2 / g or more are used. The shape of the aluminum oxide fine particles does not affect the effect of the present invention, and any shape such as granular, needle-like, fibrous or plate-like may be used. Therefore, the term "fine particles" in the present invention is used as a general term for the above shapes.

次亜塩素酸アルカリ金属塩水溶液の増粘剤として酸化
アルミニウム微粒子を必要とする理由は、増粘剤の条件
である、増粘剤が次亜塩素酸アルカリ金属塩の分解を促
進しない点と、増粘剤が次亜塩素酸アルカリ金属塩水溶
液の酸化作用及び強アルカリ性に対して安定である点の
二点を同時に満足するためである。
The reason why the aluminum oxide fine particles are required as a thickener for the alkali metal hypochlorite aqueous solution is a condition of the thickener, that the thickener does not accelerate the decomposition of the alkali metal hypochlorite salt, This is because the thickener simultaneously satisfies the two points that it is stable against the oxidizing action of the alkali metal hypochlorite aqueous solution and strong alkalinity.

従来、水溶液の増粘剤としては、水溶性有機ポリマ
ー、あるいはコロイド状シリカを用いるのが一般的であ
る。例えば、歯科治療において歯面酸処理剤として用い
られているリン酸、クエン酸等の酸水溶液は、ポリビニ
ルアルコール、ポリビニルピロリドン、ポリエチレング
リコール、カルボキシルメチルセルロースナトリウム塩
等の水溶性有機ポリマーや、コロイド状シリカで増粘さ
れている。
Conventionally, a water-soluble organic polymer or colloidal silica is generally used as a thickener for an aqueous solution. For example, an aqueous acid solution of phosphoric acid, citric acid, etc., which is used as a tooth surface acid treating agent in dental treatment, is a water-soluble organic polymer such as polyvinyl alcohol, polyvinylpyrrolidone, polyethylene glycol, carboxymethyl cellulose sodium salt, or colloidal silica. Is thickened with.

次亜塩素酸アルカリ金属塩水溶液を上述と同様に水溶
性有機ポリマーで増粘したところ、調製直後では粘度の
上昇が見られるものの、次亜塩素酸アルカリ金属塩水溶
液の酸化作用あるいは強アルカリ性によってポリマーが
変性、分解し、その粘度を維持することはできなかっ
た。
When an aqueous solution of an alkali metal hypochlorite was thickened with a water-soluble organic polymer in the same manner as described above, a viscosity increase was observed immediately after the preparation, but the polymer was formed by the oxidizing action or strong alkalinity of the aqueous solution of the alkali metal hypochlorite. Was denatured and decomposed, and its viscosity could not be maintained.

一方、シリカ、酸化アルミニウムをはじめ、アルカリ
性水溶液に耐性のある無機微粒子を次亜塩素酸アルカリ
金属塩水溶液の増粘剤として用いることについても数多
くの実験を行ったが、酸化アルミニウム微粒子以外の無
機微粒子はいずれも次亜塩素酸アルカリ金属塩の分解を
促進することがわかった。即ち、予想外の知見ながら、
次亜塩素酸アルカリ金属塩水溶液の増粘剤として用いる
ことができるのは酸化アルミニウムのみに限定されるこ
とが明らかとなったわけである。
On the other hand, many experiments were conducted using silica, aluminum oxide, and other inorganic fine particles resistant to an alkaline aqueous solution as a thickener for an aqueous alkali metal hypochlorite solution. Were found to accelerate the decomposition of alkali metal hypochlorite. That is, despite unexpected findings,
It has been clarified that only aluminum oxide can be used as a thickener for an aqueous solution of alkali metal hypochlorite.

かかる理由で選ばれた酸化アルミニウム微粒子を次亜
塩素酸アルカリ金属塩水溶液に加えペースト状とするこ
とで、本発明の目的は達せられるわけであるが、該組成
物を鉛直面に付与しても自重で流れ落ちないのは該組成
物の粘度が50センチポイズ以上の場合である。従って、
次亜塩素酸アルカリ金属塩水溶液に対する酸化アルミニ
ウム微粒子の添加量は、組成物の粘度が50センチポイズ
以上、より好ましくは100センチポイズ以上になるよう
に選ばれる。酸化アルミニウム微粒子の添加量と組成物
の粘度との関係は酸化アルミニウムの比表面積の大きさ
も関わるため一概には言えないが、50センチポイズ以上
の組成物は、例えばBET比表面積100m2/gの酸化アルミニ
ウム微粒子を次亜塩素酸アルカリ金属塩水溶液100重量
部に対し12重量部加える(152センチポイズ)、あるい
はBET比表面積14m2/gの酸化アルミニウム微粒子を100重
量部加える(50センチポイズ)ことで得られる。BET比
表面積10m2/g未満の酸化アルミニウム微粒子では増粘効
果が著しく劣るうえに、酸化アルミニウム微粒子の沈降
が極めて生じ易いため、実用的な組成物を得ることがで
きない。例えばBET比表面積6m2/gの酸化アルミニウム微
粒子を次亜塩素酸アルカリ金属塩水溶液100重量部に対
し100重量部加えても50センチポイズ以上にはならな
い。更に添加量を増せば必然的に粘度の高い組成物を得
ることはできるが、この組成物は静置しておくと短時間
のうちに層分離を生じてしまう。また、酸化アルミニウ
ムの添加量を増すと相対的に次亜塩素酸アルカリ金属塩
の含有量が低下するため、該組成物の本来の目的である
歯牙の清掃・消毒の効果が低下してしまうおそれがあ
る。従って、酸化アルミニウム微粒子としては、そのBE
T比表面積が10m2/g以上、より好ましくは50m2/g以上の
ものが用いられる。
By adding aluminum oxide fine particles selected for such a reason to an aqueous solution of an alkali metal hypochlorite to form a paste, the object of the present invention can be achieved, even if the composition is applied to a vertical surface. It does not run off under its own weight when the viscosity of the composition is 50 centipoise or more. Therefore,
The addition amount of the aluminum oxide fine particles to the aqueous solution of alkali metal hypochlorite is selected so that the viscosity of the composition is 50 centipoise or more, more preferably 100 centipoise or more. The relationship between the added amount of aluminum oxide fine particles and the viscosity of the composition cannot be generally stated because the size of the specific surface area of aluminum oxide is also involved, but a composition of 50 centipoise or more, for example, BET specific surface area of 100 m 2 / g oxidation Obtained by adding 12 parts by weight of aluminum fine particles to 100 parts by weight of an aqueous solution of alkali metal hypochlorite (152 centipoise), or by adding 100 parts by weight of aluminum oxide fine particles having a BET specific surface area of 14 m 2 / g (50 centipoise). . Aluminum oxide fine particles having a BET specific surface area of less than 10 m 2 / g are extremely inferior in the thickening effect, and the precipitation of the aluminum oxide fine particles is very likely to occur, so that a practical composition cannot be obtained. For example, even if 100 parts by weight of aluminum oxide fine particles having a BET specific surface area of 6 m 2 / g is added to 100 parts by weight of an aqueous solution of an alkali metal hypochlorite solution, it does not exceed 50 centipoise. If the amount of addition is further increased, a composition with high viscosity can be obtained inevitably, but if this composition is left to stand, layer separation will occur in a short time. Moreover, since the content of the alkali metal hypochlorite is relatively decreased when the added amount of aluminum oxide is increased, the effect of cleaning and disinfecting the teeth, which is the original purpose of the composition, may be reduced. There is. Therefore, as the aluminum oxide fine particles, the BE
A T specific surface area of 10 m 2 / g or more, more preferably 50 m 2 / g or more is used.

このように、次亜塩素酸アルカリ金属塩水溶液の増粘
剤にはBET比表面積10m2/g以上の酸化アルミニウム微粒
子が選ばれ、これを粘度が50センチポイズ以上になるよ
う添加することで流動性が抑えれた次亜塩素酸アルカリ
金属塩製剤を得ることができ、本発明の目的を達成する
ことができる。
As described above, aluminum oxide fine particles having a BET specific surface area of 10 m 2 / g or more are selected as a thickener for an aqueous solution of an alkali metal hypochlorite salt, and the fluidity is obtained by adding it so that the viscosity becomes 50 centipoise or more. It is possible to obtain an alkali metal hypochlorous acid salt formulation in which the amount is suppressed, and the object of the present invention can be achieved.

なお、該組成物の付与を識別しやすくするために酸化
鉄等の無機系顔料を微量加え着色してもさしつかえな
い。
In addition, in order to make it easy to identify the application of the composition, a small amount of an inorganic pigment such as iron oxide may be added and colored.

(発明の効果) 本発明の歯科組成物は増粘剤の添加により流動性が抑
えられた次亜塩素酸アルカリ金属塩製剤であり、象牙質
または根管内を清掃する際に塗布部分の外に流出して例
えば、口膣内軟組織を侵すなどのトラブル発生を抑止す
る効果がある。さらに本組成物は象牙質および根管内の
清掃・消毒のみならず、歯科用修復材料の表面を清掃す
るに当たっても、流動して広がらないという取り扱い性
の良さが大きな利点である。
(Effects of the Invention) The dental composition of the present invention is an alkali metal hypochlorite preparation whose fluidity is suppressed by the addition of a thickener, and is applied to the outside of the applied portion when cleaning the dentin or the root canal. It has the effect of suppressing the occurrence of troubles such as invading the soft tissue in the vagina of the mouth. Further, the composition has a great advantage not only in cleaning and disinfecting the dentin and the root canal but also in the handling property that it does not spread and spread even when cleaning the surface of the dental restorative material.

以下に実施例をあげて本発明を更に詳細に説明する
が、本発明はかかる実施例に限定されるものではない。
Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the examples.

(実施例) 実施例1、2および比較例1〜6 10重量%次亜塩素酸ナトリウム水溶液100重量部と粒
状、BET比表面積100m2/gの酸化アルミニウム10重量部か
らなる組成物、および10重量%次亜塩素酸ナトリウム水
溶液100重量部と粒状、BET比表面積10m2/gの酸化アルミ
ニウム100重量部からなる組成物を調製し37℃で4日間
保存した。保存前後の次亜塩素酸ナトリウムの量変化を
滴定法にて定量して保存後の次亜塩素酸ナトリウムの残
存率を算出し、それぞれ実施例1および2とした。その
結果を表1に示した。
(Examples) Examples 1 and 2 and Comparative Examples 1 to 6 Compositions comprising 100 parts by weight of 10% by weight sodium hypochlorite aqueous solution, 10 parts by weight of aluminum oxide having a granular and BET specific surface area of 100 m 2 / g, and 10 A composition comprising 100 parts by weight of an aqueous solution of sodium hypochlorite in a weight ratio of 100 parts by weight, 100 parts by weight of aluminum oxide having a BET specific surface area of 10 m 2 / g was prepared and stored at 37 ° C. for 4 days. Changes in the amount of sodium hypochlorite before and after storage were quantified by a titration method to calculate the residual ratio of sodium hypochlorite after storage, which were taken as Examples 1 and 2, respectively. The results are shown in Table 1.

10重量%次亜塩素酸ナトリウム水溶液100重量部に、
シリカ(BET比表面積380m2/g)、二酸化チタン(BET比
表面積50m2/g)、ケイ酸マグネシウム(BET比表面積3m2
/g)、炭酸バリウム(BET比表面積5m2/g)、または二酸
化ジルコニウム(BET比表面積50m2/g)を10重量部加え
た組成物を調製し、実施例1、2と同様に37℃で4日間
保存して次亜塩素酸ナトリウムの残存率を求め、それぞ
れ比較例1〜5とし結果を表1に示した。10重量%次亜
塩素酸ナトリウム水溶液のみを、実施例1、2と同様に
37℃で4日間保存して次亜塩素酸ナトリウムの残存率を
求め、比較例6とし結果を表1に示した。
To 100 parts by weight of 10% by weight sodium hypochlorite aqueous solution,
Silica (BET specific surface area 380 m 2 / g), titanium dioxide (BET specific surface area 50 m 2 / g), magnesium silicate (BET specific surface area 3 m 2
/ g), barium carbonate (BET specific surface area 5 m 2 / g), or zirconium dioxide (BET specific surface area 50 m 2 / g) was added to 10 parts by weight to prepare a composition at 37 ° C. as in Examples 1 and 2. After storage for 4 days, the residual rate of sodium hypochlorite was determined, and the results are shown in Table 1 as Comparative Examples 1 to 5, respectively. A 10% by weight aqueous solution of sodium hypochlorite alone was used as in Examples 1 and 2.
It was stored at 37 ° C. for 4 days and the residual rate of sodium hypochlorite was determined. The result is Comparative Example 6 and the results are shown in Table 1.

表1より酸化アルミニウムのみが次亜塩素酸ナトリウ
ムの分解反応を促進しないことが明らかである。
It is clear from Table 1 that only aluminum oxide does not accelerate the decomposition reaction of sodium hypochlorite.

実施例3および比較例7〜9 10重量%次亜塩素酸カリウム水溶液100重量部と粒
状、BET比表面積100m2/gの酸化アルミニウム10重量部か
らなる組成物を調製し37℃で4日間保存した。保存前後
の次亜塩素酸カリウムの量変化を滴定法にて定量して保
存後の次亜塩素酸カリウムの残存率を算出し、実施例3
とした。その結果を表2に示した。
Example 3 and Comparative Examples 7 to 9 A composition comprising 100 parts by weight of a 10% by weight potassium hypochlorite aqueous solution, 10 parts by weight of aluminum oxide having a granular and BET specific surface area of 100 m 2 / g was prepared and stored at 37 ° C. for 4 days. did. A change in the amount of potassium hypochlorite before and after storage was quantified by a titration method to calculate the residual ratio of potassium hypochlorite after storage, and Example 3
And The results are shown in Table 2.

10重量%次亜塩素酸カリウム水溶液100重量部に、シ
リカ(BET比表面積380m2/g)、または二酸化チタン(BE
T比表面積50m2/g)を10重量部加えた組成物を調製し、
実施例3と同様に37℃で4日間保存して次亜塩素酸カリ
ウムの残存率を求め、それぞれ比較例7〜8とし結果を
表2に示した。10重量%次亜塩素酸カリウム水溶液のみ
を、実施例3と同様に37℃で4日間保存して次亜塩素酸
カリウムの残存率を求め、比較例9とし結果を表2に示
した。
100 parts by weight of 10% by weight potassium hypochlorite aqueous solution, silica (BET specific surface area 380 m 2 / g), or titanium dioxide (BE
10 parts by weight of T specific surface area 50 m 2 / g) was added to prepare a composition,
It was stored at 37 ° C. for 4 days in the same manner as in Example 3, and the residual ratio of potassium hypochlorite was determined. The results are shown in Table 2 as Comparative Examples 7 to 8, respectively. The 10% by weight potassium hypochlorite aqueous solution alone was stored at 37 ° C. for 4 days in the same manner as in Example 3 to determine the residual rate of potassium hypochlorite. The results are shown in Table 2 as Comparative Example 9.

表2より酸化アルミニウムのみが次亜塩素酸カリウム
の分解反応を促進しないことが明かである。
It is clear from Table 2 that aluminum oxide alone does not accelerate the decomposition reaction of potassium hypochlorite.

実施例4 実施例1で調製した組成物の粘度をE形粘度計(東京
計器)にて測定したところ152センチポイズであった。
この組成物を37℃で4日間保存したが、保存前後で粘度
に変化は見られなかった。
Example 4 The viscosity of the composition prepared in Example 1 was measured with an E-type viscometer (Tokyo Keiki Co., Ltd.) and found to be 152 centipoise.
The composition was stored at 37 ° C. for 4 days, but no change in viscosity was observed before and after storage.

比較例10 10重量%次亜塩素酸ナトリウム水溶液100重量部に25
重量%ポリビニルアルコール(重合度1700、懸化度98.5
モル%)水溶液を50重量部溶解したところ、調製直後で
は粘度が51センチポイズまで増加したが室温にて1日経
過すると増加した粘性は消失した。
Comparative Example 10 25% by weight of 100 parts by weight of 10% by weight sodium hypochlorite aqueous solution
Weight% polyvinyl alcohol (degree of polymerization 1700, degree of suspension 98.5
When 50 parts by weight of (mol%) aqueous solution was dissolved, the viscosity increased to 51 centipoise immediately after preparation, but the increased viscosity disappeared after 1 day at room temperature.

実施例5〜11および比較例11〜13 10重量%次亜塩素酸ナトリウム水溶液100重量部に表
3に示されるように粒子形状、BET比表面積の異なる酸
化アルミニウムを混合し、9種類の組成物を調製した。
得られた組成物の粘度をE形粘度計(東京計器)にて測
定した。また、人歯大臼歯のエナメル質を研削除去して
露出させた象牙質面(平面)を鉛直線と平行に保持し、
この面に組成物を塗布し、組成物が塗布された状態を保
持するか、あるいは自重で流れ落ちるかを観察した。
Examples 5 to 11 and Comparative Examples 11 to 13 Aluminum oxide having different particle shapes and BET specific surface areas as shown in Table 3 was mixed with 100 parts by weight of a 10% by weight aqueous solution of sodium hypochlorite to prepare 9 kinds of compositions. Was prepared.
The viscosity of the obtained composition was measured with an E-type viscometer (Tokyo Keiki). In addition, the dentin surface (plane) exposed by grinding and removing the enamel of the human molar is held parallel to the vertical line,
The composition was applied to this surface, and it was observed whether the state where the composition was applied was maintained or whether the composition flowed down by its own weight.

粒子の形状にかかわらず、比表面積10m2/g以上のもの
は効果的に増粘することができた。また、粘度50センチ
ポイズ未満の組成物は自重で流れ落ちてしまうことが明
かである。
Regardless of the particle shape, those with a specific surface area of 10 m 2 / g or more could effectively thicken. Also, it is clear that a composition having a viscosity of less than 50 centipoise will run off under its own weight.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】次亜塩素酸アルカリ金属塩、水およびBET
比表面積10m2/g以上の酸化アルミニウム微粒子を主成分
とし、かつ50センチポイズ以上の粘度を有することを特
徴とする歯科用組成物。
1. An alkali metal hypochlorite salt, water and BET.
A dental composition comprising aluminum oxide fine particles having a specific surface area of 10 m 2 / g or more as a main component and a viscosity of 50 centipoise or more.
JP2286640A 1990-03-28 1990-10-23 Dental composition Expired - Lifetime JP2566676B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP8176790 1990-03-28
JP2-81767 1990-03-28

Publications (2)

Publication Number Publication Date
JPH03279330A JPH03279330A (en) 1991-12-10
JP2566676B2 true JP2566676B2 (en) 1996-12-25

Family

ID=13755613

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2286640A Expired - Lifetime JP2566676B2 (en) 1990-03-28 1990-10-23 Dental composition

Country Status (1)

Country Link
JP (1) JP2566676B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE513404C2 (en) * 1999-01-19 2000-09-11 Mediteam Dentalutveckling I Go Preparations for chemical-mechanical dental treatment containing a chlorine compound as an active component
JP2002338447A (en) * 2001-05-15 2002-11-27 Kuraray Co Ltd Dental composition
DE10237317B4 (en) 2002-08-15 2010-04-08 3M Espe Ag Enzyme-containing composition, process for their preparation and their use
WO2006096893A2 (en) * 2005-03-10 2006-09-14 Marx Management Cc Dental barrier composition
ITPI20060007A1 (en) * 2006-01-24 2007-07-25 Italmed Snc Di Galli G & Pacini G DENTAL COMPOSITION FOR CHANNEL TREATMENT
JP6692535B2 (en) * 2018-09-13 2020-05-13 株式会社トクヤマデンタル Tartar removal accelerator for scaling (SC) and / or root planing (RP)

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
医薬品添加物研究会編「実用医薬品添加物」(昭和49年)、化学工業社、P.94〜98 「水酸化アルミニウム」の項

Also Published As

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