JPS61183203A - Composition for etching - Google Patents

Composition for etching

Info

Publication number
JPS61183203A
JPS61183203A JP60024231A JP2423185A JPS61183203A JP S61183203 A JPS61183203 A JP S61183203A JP 60024231 A JP60024231 A JP 60024231A JP 2423185 A JP2423185 A JP 2423185A JP S61183203 A JPS61183203 A JP S61183203A
Authority
JP
Japan
Prior art keywords
etching
etching agent
salt
metal complex
alkali metal
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
Application number
JP60024231A
Other languages
Japanese (ja)
Inventor
Norio Nakabayashi
宣男 中林
Hitomi Shimizu
ひとみ 清水
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.)
Teikoku Chemical Industry Co Ltd
Original Assignee
Teikoku Chemical Industry Co Ltd
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 Teikoku Chemical Industry Co Ltd filed Critical Teikoku Chemical Industry Co Ltd
Priority to JP60024231A priority Critical patent/JPS61183203A/en
Publication of JPS61183203A publication Critical patent/JPS61183203A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an etching agent free from adverse effect to the dental pulp and having comparable adhesive strength, by combining ethy lenediaminetetraacetic acid or its alkali metal salt with its metal complex salt and using the mixture as the etching agent suitable for the etching of dentine. CONSTITUTION:The objective etching agent for especially dentine is produced by compounding (A) ethylenediaminetetraacetic acid or its alkali metal salt (preferably an aqueous solution of 0.1-0.5mol % concentration) and (B) a metal complex salt of ethylenediaminetetraacetic acid (preferably an aqueous solution of 0.1-0.5mol % concentration) at a molar ratio of preferably 1:0.2-20. The etching agent is suitable for the etching of dental enamel. EFFECT:The rate of decalcification is low, and the damage to teeth can be minimized.

Description

【発明の詳細な説明】 (イ)産業上の利用分野 この発明は、ムシ歯予防を目的とした処置をするときに
行われる歯牙の表面処理、あるいは、ムシ歯その他の理
由で欠損を生じた歯牙の修復に際し行われる歯牙の表面
処理に適した前処理剤組成物を提供するにある。従つ、
で、歯科医療分野で利用される。
[Detailed description of the invention] (a) Industrial application field This invention is applicable to surface treatment of teeth performed when performing treatment for the purpose of preventing dental caries, or to teeth that are damaged due to caries or other reasons. An object of the present invention is to provide a pretreatment agent composition suitable for tooth surface treatment performed during tooth restoration. obey,
and is used in the dental medical field.

(ロ)従来の技術 湿潤状態にある口腔内で、欠損を生じた歯牙を修復する
とき、歯牙と接着性組成物とを接着によって、よシ強固
にくつつけるため、被着面を前処即することが行われて
いる。この前処卯によって、歯牙表面にi細な凹凸構造
をつくり、接着面積を拡げるとともに機械的な嵌合や投
錨効、果を求めることができる。
(b) Conventional technology When restoring a defective tooth in the moist oral cavity, in order to firmly attach the tooth and adhesive composition by adhesion, the adhesion surface is pretreated. things are being done. Through this pretreatment, it is possible to create a fine uneven structure on the tooth surface, expand the bonding area, and obtain mechanical fitting and anchoring effects.

ここにおいて採られている前処理方法に、酸エツチング
法がある。使用されるものとしては、リン酸、塩酸など
の無機酸、ギ酸、クエン酸、乳酸などの有機酸があげら
れている。
The pretreatment method employed here is an acid etching method. Examples of what can be used include inorganic acids such as phosphoric acid and hydrochloric acid, and organic acids such as formic acid, citric acid and lactic acid.

これら1佳いずれも歯面の脱灰に関与すると考えられて
いる。脱灰能、接着性向」二においてリン酸が最もすぐ
れており、多用されている。
All of these are thought to be involved in demineralization of the tooth surface. Phosphoric acid has the best demineralization ability and adhesion properties, and is widely used.

しかしながら、リン酸を代表とする酸エツチング法は、
エナメル質に対する接着強度を著るしく増強することに
は寄与したけれども、象牙質への接着については末だ探
索の段階であって、今後の研究に俟だなければならない
状況にあるといえる。
However, acid etching methods, typically using phosphoric acid,
Although it has contributed to significantly increasing the strength of adhesion to enamel, its adhesion to dentin is still in the exploration stage and requires further research.

(ハ) 発明が解決しようとする問題点「)11記した
ように、接着という手段で歯牙を修復するとき、あるい
はムシ歯予防をするとき、エナメル質であると象牙質で
あるとを問わず、接着強度を高めるため((エツチング
と称する前処却を施すが、エナメル質部分でのエツチン
グに用いられるエツチング剤を、象牙質にその捷まi箇
月することは、象牙質が有機物に富んだ層であることと
、該層は歯髄に近いためそれへの影響が指摘されている
こと等からみて種々の問題をひき起こす。
(C) Problems to be Solved by the Invention As stated in 11 above, when repairing teeth by adhesive means or preventing cavities, regardless of whether the tooth is enamel or dentin, In order to increase the adhesive strength ((pre-treatment called etching), applying the etching agent used for etching the enamel part to the dentin for a period of one month is important because the dentin is rich in organic matter. This causes various problems because it is a layer, and because the layer is close to the dental pulp, it has been pointed out that it may have an effect on the pulp.

しかしながら、象牙質への接着を強固にするためには、
スメア層の除去を行うことが必要と考えられていて、象
牙質用の前処即剤が既に市販されている。それら市販品
は、クエン酸を主成分とするもの、エチレンジアミン四
1ト酸(E D ’I” A )を主成分とするものな
どである。しかし、クエン酸は、エナメル質の前処却に
も使用されるリン酸に次ぐ強いエツチング剤であるので
歯髄反応が憂慮されている。歯髄に対して安全でしかも
スメア層の除去1/′c効果があるとされているI”:
 D Tハを主成分とする清掃剤は、多少効果の点にお
いて弱いとされているので、本発明者らは、この糸の発
展を考え、好捷しい作用機能を作詩しつつ、弱点とされ
ている効果を高めることに鋭意研究を重ねた結果、本発
明に到ったものである。
However, in order to strengthen the adhesion to dentin,
It is considered necessary to remove the smear layer, and pre-treatment preparations for dentin are already commercially available. These commercially available products include those whose main component is citric acid and those whose main component is ethylenediaminetetratoic acid (ED'I''A).However, citric acid is not suitable for pre-treatment of enamel. Since it is the second strongest etching agent after the commonly used phosphoric acid, there are concerns about pulp reactions.It is safe for the pulp and is said to be effective in removing the smear layer by 1/'c.
Cleaning agents containing D.T. as a main ingredient are said to be somewhat weak in effectiveness, so the inventors of the present invention have thought about the development of this thread, and while writing poems about its favorable functions, we have also tried to overcome its weak points. The present invention was developed as a result of extensive research into improving the effectiveness of the technology.

即ち、EDTA又はそのアルカリ金属塩とその金属錯塩
とを組み合せることによって、象牙質の好rBなエツチ
ング剤となることを見い出した。本発明によって提供さ
れるエツチング剤は、象牙質のエツチング剤として使用
されている10%クエン塩−3%塩化第二鉄(I O−
8)に比べて、歯髄への影響を心配しないで済むし、接
着強度においても遜色のないものである。加えて、単に
象牙質のみならずエナメル層のエツチング剤としても、
多用されているエツチング剤と同等の効果を発揮するこ
とがわかった。
That is, it has been found that by combining EDTA or its alkali metal salt with its metal complex salt, it becomes an etching agent suitable for rB of dentin. The etching agent provided by the present invention is a 10% citric salt-3% ferric chloride (I O-
Compared to 8), there is no need to worry about the effect on the dental pulp, and the adhesive strength is comparable. In addition, it can be used as an etching agent not only for dentin but also for the enamel layer.
It was found to be as effective as the commonly used etching agent.

に) 問題点を解決するための手段 かくて、本発明によって提供される歯牙象牙質のエツチ
ングに適したエツチング剤は、E I) T A又はそ
のアルカリ金属塩と、EDTA金属錯塩とを含む組成物
である。
Therefore, the etching agent suitable for etching tooth dentin provided by the present invention has a composition comprising E I) T A or an alkali metal salt thereof, and an EDTA metal complex salt. It is a thing.

本発明に使用されるEDTASEDTA−アルカリ金属
塩は、通常、水溶液にして使用される。濃度は殊に特定
される訳でもないが、使い易さからみて0.1〜0.5
モル%のものが良い。EDTAを用いた場合には、水に
溶は難いので、水酸化ナトリウム、水酸化カリウムなど
で中和するとよい。
EDTASEDTA-alkali metal salt used in the present invention is usually used in the form of an aqueous solution. The concentration is not particularly specified, but from the viewpoint of ease of use, it is 0.1 to 0.5.
Mol% is better. When EDTA is used, it is difficult to dissolve in water, so it is best to neutralize it with sodium hydroxide, potassium hydroxide, etc.

次に、EDTA−金属錯塩も、通常、水溶液にして使用
される。濃度は0.1〜0.5モル%のものがよい。
Next, EDTA-metal complex salts are also usually used in the form of aqueous solutions. The concentration is preferably 0.1 to 0.5 mol%.

かくして、EDTA又はそのアルカリ金属塩水溶液と、
E D T A−金属錯塩水溶液とを併せることによっ
て、本発明の目的とする象牙質のエツチングに適したエ
ツチング用組成物が提供される。ここにおいてEDTA
又はそのアルカリ金属塩とEDTA−金属錯塩との割合
は、E I) T A又はそのアルカリ金属塩1モルに
対し、EDTA−金属錯塩05〜20モルとなるように
配合するのがよい。ここにおいて、使用されるEDTA
−金属錯塩は、EDTAアルカリ金属塩、又はEJ)T
Aアンモニウム塩あるいはEDTAと金属錯塩イオンと
から成っている。
Thus, an aqueous solution of EDTA or an alkali metal salt thereof;
By combining it with the EDTA-metal complex salt aqueous solution, an etching composition suitable for etching dentin, which is the object of the present invention, is provided. Here EDTA
Alternatively, the ratio of the alkali metal salt thereof and the EDTA-metal complex salt is preferably blended such that the EDTA-metal complex salt is 05 to 20 moles per mole of E I) TA or its alkali metal salt. Here, the EDTA used
- the metal complex is EDTA alkali metal salt or EJ)T
A: It consists of ammonium salt or EDTA and metal complex salt ions.

O鵠 発明の効果 本発明によって提供される組成物は中性でアリ、これを
象牙質のエツチングに使用すると、10−3にてエツチ
ングしたときに得られる接着性組成物の接着強度と同等
以」二の結果が得られるうえに、】0−3では憂慮され
る歯髄への影響を心配しなくてもよく、その上10−3
やリン酸に比して脱灰量が少なく、歯牙へ与える損傷を
減らせることも、従来技術にくらべ本発明の利点といえ
る。
Effects of the Invention The composition provided by the present invention is neutral, and when used for etching dentin, the adhesive strength is equal to or higher than that of the adhesive composition obtained when etching at 10-3. In addition to obtaining the results of ``2'', there is no need to worry about the effect on the pulp that is a concern with 0-3, and on top of that, 10-3
It can be said that the present invention has an advantage over the prior art in that the amount of demineralization is small compared to phosphoric acid and phosphoric acid, and damage to teeth can be reduced.

本発明によって提供される組成物はエナメル質のエツチ
ング剤として使用しても、治療上充分な接着強度が得ら
れる。又、E l) T A又はそのアルカリ金属塩、
居DTA−金属錯塩単独で使用したときは、比較例から
も判るとおり、決して強い接着強度が得られていないこ
ともflE目に1貞する。
Even when the composition provided by the present invention is used as an etching agent for enamel, sufficient adhesive strength for therapeutic purposes can be obtained. Also, E l) T A or an alkali metal salt thereof,
As can be seen from the comparative example, when the DTA-metal complex salt was used alone, strong adhesive strength was never obtained.

以下本発明を具体的に説明するために実施例を記述する
Examples will be described below to specifically explain the present invention.

実施例1゜ 0、3 モ/L’ 1℃D A、 T−2N aと02
モルのE D T A −F e  Naとを水101
00Oに溶かし、均一な水溶液を得た。得られた溶液で
、エメリペーパー≠600で研削した新鮮な生歯の象牙
質部を60秒間処ill! l、た後、蒸溜水でよく洗
浄し、気絖で表面に付着した水分を除去し、被着面とし
7た。
Example 1゜0, 3 mo/L' 1℃DA, T-2N a and 02
Moles of E D T A -F e Na and water 101
00O to obtain a homogeneous aqueous solution. Using the resulting solution, treat the dentin of a fresh tooth ground with Emery Paper ≠ 600 for 60 seconds! After washing, the surface was thoroughly washed with distilled water, and the moisture adhering to the surface was removed using a sieve, and the surface was used as a surface to be adhered.

添加モノマーとしての4− M TII’T’ Aを5
%含ムメチルメタアクリレー1− K TB B −O
を添加し、車積法にて、ポリメチルメタクリレート粉末
とともに、被着面にとり、直径5.00騎のアクl)ル
棒を被着面に垂直に立て、30分分間上、37Cの水中
に1日浸漬したのち、接着強度を測定した。
4-M TII'T'A as added monomer
%-containing methyl methacrylate 1- K TB B -O
was added and placed on the surface to be adhered together with polymethyl methacrylate powder using the car load method, and an acryl rod with a diameter of 5.0 mm was placed perpendicularly to the surface to be adhered, and immersed in water at 37C for 30 minutes. After being immersed for one day, the adhesive strength was measured.

実施例2〜?。Example 2~? .

添加上ツマ−を代えた以外は実施例1と同様にして、接
着強度を測定した。
The adhesive strength was measured in the same manner as in Example 1 except that the additives were changed.

実施例8゜ エツチング剤を代えた以外は実施例1と同様6てして、
接着強度を測定した。
Example 8 Same as Example 1 except that the etching agent was changed.
Adhesive strength was measured.

−7= 実施例9 実施例1において、象牙質をエナメル質に代えた以外は
実施例】と同様にして、接着強度を測定した。
-7= Example 9 The adhesive strength was measured in the same manner as in Example 1 except that dentin was replaced with enamel.

実施例10−12、 実施例9において、添加モノマーヲ代工た以外は実施例
9と同様にして、接着強度を測定した。
In Examples 10-12 and Example 9, adhesive strength was measured in the same manner as in Example 9 except that the added monomer was used instead.

実施例13 実施例9において、エツチング剤を代えた以外は実施例
9と同様にして、接着強度を測定した。
Example 13 The adhesive strength was measured in the same manner as in Example 9 except that the etching agent was changed.

比較例 実施例において、エツチング剤ヲ他のエツチング剤に代
えた以外は実施例と同様にして、接着強度を測定した。
Comparative Example In the example, the adhesive strength was measured in the same manner as in the example except that the etching agent was replaced with another etching agent.

それらの結果を表1に1とめる。The results are listed in Table 1.

ロ) OQつ タ        −一 − 匁 ″″′   安         わ 八   −− へ シー1−1+1 ※+  曽           曽 トc″              ■目   安  
            安 票/−へ       
N− ム  Qw −1−l            4−l
 +l快  躯  − 、p       %、−i χ  式 。         社 Q ■ 1 に  −旧の寸■    →1 − 、、、、−  +l  +l  +l  曽 寸   
     −0」1       Ω■へ0■ト〇  
      − 8門−Hx   F−1[:+:l O°I 冊 櫓           。     6−   
 \ −→−1+1 部  へ                     
  8斬 へ+           a5     
  +nl!l  幹          −−”  
  (Th   IXl 010  Cr)  ++ 
  u’)  (r)  (Th  (’J耶 Q  
イ。、ゎ、4、  ヨ、よ。
B) OQ Tsuta -1 - Momme""' An wa eight -- to Sea 1-1+1 *+ So Soto c" ■Estimated guideline
Cheap vote/-
N- Mu Qw -1-l 4-l
+lKai body -, p %, -i χ expression. CompanyQ ■ 1 -old size■ →1 - ,,,,- +l +l +l Zeng size
-0” 1 Ω■ to 0■ 〇
- 8 Gates - Hx F-1 [:+:l O°I Book Tower. 6-
\ −→−1+1 part
To 8th slash + a5
+nl! l Trunk --”
(Th IXl 010 Cr) ++
u') (r) (Th ('J耶Q
stomach. , wa, 4, yo.

ど−+1 cyi +1+l (l 41旧 41+1
−I−1→1楔 胃→−1■c’−(ト)−ω  へa
す9ρ豚  −0′″0°0−  “−0− 1<     <  < <  <  <E−n   
  E−1日E→ 日 [し ■]ΣΣ四lff+ ”
  11口くm 閃H″X Σ山内  Σ ΣΣ山Σ 
芝 aフ  in ※ ヤ  1〜2     1   1121.+1寸
 寸寸国寸 寸 8 ”湿温[有] @ め@@警 悠 箭 ゎ。。。  ゎ リρ■の  の ※1) 添加子ツマ−の略号は次のとおりの化合物を表わす。
Do-+1 cyi +1+l (l 41 old 41+1
-I-1→1 wedge stomach→-1■c'-(g)-ω to a
9ρ pig −0′″0°0− “−0− 1<<<<<<<E-n
E-1 day E → day [shi ■]ΣΣ4lff+”
11 mouth flash H″X Σ Yamauchi Σ ΣΣ Yama Σ
Shiba afu in * Ya 1-2 1 1121. +1 dimension Dimension country dimension Dimension 8 "Humidity temperature [Yes] @ Me @ @ Police Yushu ゎ... ゎ Riρ■'s *1) The abbreviation for additives represents the following compounds.

4−MET’A :  4−メタクリロギシエチルトリ
メグツト酸無水物 丁JPPM  :  2−ヒドロキシ−3−フエノキシ
プロビルノタクリラート HNI)M  :  2−ヒドロキシ−3−β−ナフト
ギシプロビルメタクリラ−1・ 3P  : 2−ヒドロキン−3−(p−フェノキシフ
エノキシ)プロピルメタ クリフート 5F  : 2−ヒドロキシ−3−(ペンタフルオロフ
ェノキン)プロピルメタ クリフート 4−MBTA:  4−メタクリロキシブチル1−リメ
リット酸無水物 ※2) エツチング剤の記−号は以下の成分を水100Q ml
にとかした溶液を表わす(但L−1iを除く。)r:o
、3モルのE D ’1.’ A −2N aと0.2
−E#(7)EDTA−B”e    Na f  : 0,8−rニルのE D T A −2N 
aと0.2 モルノTEID ’r A −M g 2
 N JiI :10%クエン酸3%塩化第二鉄水溶液
W :  0.5モzlz(7)’El)TA−2Na
V  : Q、5−r=)vのEDTA−Fe   N
a■ : リン酸
4-MET'A: 4-methacrylogyethyl trimegutic anhydride JPPM: 2-hydroxy-3-phenoxyprobyl notacrylate HNI) M: 2-hydroxy-3-β-naftogycyprovir Methacryla-1/3P: 2-hydroquine-3-(p-phenoxyphenoxy)propyl methacrylate 5F: 2-hydroxy-3-(pentafluorophenoquine)propyl methacrylate 4-MBTA: 4-methacryloxybutyl 1-Limelic acid anhydride *2) The symbol for etching agent is the following ingredients in 100Q ml of water.
Represents a solution dissolved in water (excluding L-1i) r:o
, 3 moles of E D '1. ' A -2N a and 0.2
-E#(7) EDTA-B"e Na f : EDTA-2N of 0,8-r-nyl
a and 0.2 Morno TEID 'r A -M g 2
N JiI: 10% citric acid 3% ferric chloride aqueous solution W: 0.5 mozlz(7)'El)TA-2Na
V: Q, 5-r=)v EDTA-FeN
a■: Phosphoric acid

Claims (1)

【特許請求の範囲】[Claims] エチレンジアミン四酢酸又はそのアルカリ金属塩と、エ
チレンジアミン四酢酸の金属錯塩とを含むエッチング用
組成物。
An etching composition comprising ethylenediaminetetraacetic acid or an alkali metal salt thereof and a metal complex salt of ethylenediaminetetraacetic acid.
JP60024231A 1985-02-08 1985-02-08 Composition for etching Pending JPS61183203A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60024231A JPS61183203A (en) 1985-02-08 1985-02-08 Composition for etching

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60024231A JPS61183203A (en) 1985-02-08 1985-02-08 Composition for etching

Publications (1)

Publication Number Publication Date
JPS61183203A true JPS61183203A (en) 1986-08-15

Family

ID=12132482

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60024231A Pending JPS61183203A (en) 1985-02-08 1985-02-08 Composition for etching

Country Status (1)

Country Link
JP (1) JPS61183203A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009131250A1 (en) 2008-04-25 2009-10-29 サンメディカル株式会社 Easily removable curable composition for dental use

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS3413828Y1 (en) * 1957-06-21 1959-09-03

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS3413828Y1 (en) * 1957-06-21 1959-09-03

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009131250A1 (en) 2008-04-25 2009-10-29 サンメディカル株式会社 Easily removable curable composition for dental use

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