JPH11302122A - Separating material for dental use - Google Patents

Separating material for dental use

Info

Publication number
JPH11302122A
JPH11302122A JP10108306A JP10830698A JPH11302122A JP H11302122 A JPH11302122 A JP H11302122A JP 10108306 A JP10108306 A JP 10108306A JP 10830698 A JP10830698 A JP 10830698A JP H11302122 A JPH11302122 A JP H11302122A
Authority
JP
Japan
Prior art keywords
cavity
water
separating
separating material
weight
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.)
Granted
Application number
JP10108306A
Other languages
Japanese (ja)
Other versions
JP4232214B2 (en
Inventor
Ihei So
維平 曽
Tsuyoshi Baba
剛志 馬場
Akisato Shimozono
明里 下園
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.)
Sun Medical Co Ltd
Original Assignee
Sun Medical 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 Sun Medical Co Ltd filed Critical Sun Medical Co Ltd
Priority to JP10830698A priority Critical patent/JP4232214B2/en
Publication of JPH11302122A publication Critical patent/JPH11302122A/en
Application granted granted Critical
Publication of JP4232214B2 publication Critical patent/JP4232214B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Dental Preparations (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a separating material for dental use capable of preventing the adhesion of a resin used as an adhesive, a restorative agent, etc., in the dental treatment to a contact surface of a dentin surface, a prosthesis surface, a mucous membrane surface in an oral cavity, etc., and easily separating both and good in operating efficiency such as coating or removal. SOLUTION: This separating material contains (A) 15-95 pts.wt. of a water-soluble or a water-dispersible hydroxyl group-containing compound having at least two hydroxyl groups in the molecule and <=15 deg.C solidifying point, e.g. ethylene glycol and (B) 5-85 pts.wt. of a water-soluble or a water-dispersible hydroxyl group-containing compound having at least two hydroxyl groups in the molecule and >=30 deg.C solidifying point, e.g. polyethylene glycol [the sum total of ingredients (A) and (B) is 100 pts.wt.].

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は歯科治療用の分離材
に関し、詳しくは、接着材や修復用材等として用いられ
るレジンと、歯質表面、補綴物表面、口腔粘膜表面など
の接触面との固着を防ぐために用いられる歯科用分離材
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a separating material for dental treatment, and more particularly, to a resin used as an adhesive or a restorative material and a contact surface such as a tooth surface, a prosthetic surface, or an oral mucosal surface. The present invention relates to a dental separation material used to prevent sticking.

【0002】[0002]

【従来の技術】歯科治療では、治療修復物を歯質または
修復物に接着させるために、種々のレジンからなる接着
材が使用されている。この場合、修復物の接着修復にお
いて、溢出した余剰接着材が接着を必要としない歯質表
面、補綴物表面、口腔粘膜表面、または歯肉縁下などに
粘着して硬化することがしばしばある。不必要に粘着、
硬化した接着材を除去するには多大な労力を要するほ
か、歯肉縁下に粘着、硬化した接着材が除去不完全な場
合には歯肉炎を引き起こす可能性がある。
2. Description of the Related Art In dental treatment, an adhesive made of various resins is used to adhere a restoration to a tooth or a restoration. In this case, in the adhesive restoration of the restoration, the excess adhesive that has overflowed often adheres to the surface of the tooth, the surface of the prosthesis, the surface of the oral mucosa, the surface of the gingiva, or the like that does not require adhesion, and hardens. Unnecessarily sticky,
Removal of the hardened adhesive requires a great deal of effort, and can cause gingivitis if the hardened adhesive is incompletely removed beneath the gingiva.

【0003】また、これまでに深い齲蝕窩洞の修復には
通常間接法が用いられている。この方法は、齲蝕窩洞を
形成し、修復物作製ための印象を採取した後、仮封材で
窩洞を暫間的に覆い、修復物ができた後に改めて仮封材
を除去し修復物を装着する。ところが、この方法では数
回の来院が必要のほか、開放した象牙質が細菌感染され
やすい懸念がある。このため、窩洞を形成直後にその場
で未硬化のレジンを充填し、紫外線の露光により硬化し
た修復物を作製し、装着する直接修復方法が望ましい
が、この場合、硬化レジンである修復物を取り出し、窩
洞内の表面を表面処理すると共に接着材を塗布する操作
が必要であるので、窩洞壁と硬化した修復物を確実に分
離することが可能な分離材が不可欠である。
[0003] Conventionally, an indirect method has been used for repairing deep carious cavities. In this method, a cavity is formed, an impression for preparing a restoration is taken, the cavity is temporarily covered with a temporary sealing material, and after the restoration is completed, the temporary sealing material is removed again and the restoration is attached. I do. However, this method requires several visits, and there is a concern that open dentin is susceptible to bacterial infection. For this reason, it is desirable to use a direct repair method in which an uncured resin is filled in place immediately after the cavity is formed, and a cured product that is cured by exposure to ultraviolet light is prepared and mounted. Since it is necessary to take out, surface-treat the surface in the cavity, and apply an adhesive, a separating material capable of reliably separating the cavity wall from the cured restoration is indispensable.

【0004】このように、接着材が不必要な部分に接着
材が粘着し、その後硬化した硬化物を分離し得る分離
材、さらには齲蝕窩洞の修復を直接法で行う場合に不可
欠である窩洞壁と硬化した修復物を確実に分離する分離
材が望まれている。勿論、分離材の操作性は良好である
ことが望ましい。
[0004] As described above, the adhesive adheres to a portion where the adhesive is unnecessary, and a separating material capable of separating the cured product after curing, and a cavity which is indispensable when the carious cavity is repaired by a direct method. There is a need for a separator that reliably separates the wall and the cured restoration. Of course, it is desirable that the operability of the separating material is good.

【0005】特公昭63−37082号公報には、平均
分子量150〜420のポリエチレングリコール100
重量部と平均分子量1800〜20000のポリエチレ
ングリコール20〜200重量部をペースト状に混合し
てなる、歯科用レジン修復材の表面硬化を完全ならしめ
るための表面被覆剤が記載されている。しかしながら、
該公報には、上記表面被覆剤が空気中の酸素により重合
阻害を受けやすい重合硬化型歯科用修復材と酸素を遮断
するために用いられることが記載されているのみであ
り、上記のような分離材に用いることは開示も示唆もさ
れていない。
[0005] JP-B-63-37082 discloses polyethylene glycol 100 having an average molecular weight of 150 to 420.
A surface coating agent for completely leveling the surface of a dental resin restorative, which is obtained by mixing paste parts of 20 parts by weight and 20 to 200 parts by weight of polyethylene glycol having an average molecular weight of 1,800 to 20,000 is described. However,
The publication only describes that the surface coating is used to block oxygen with a polymerization-curable dental restorative material that is susceptible to polymerization inhibition by oxygen in the air. It is neither disclosed nor suggested for use as a separating material.

【0006】[0006]

【発明が解決しようとする課題】本発明の課題は、歯科
治療において、接着材や修復用材などとして用いられて
いるレジンと、歯質表面、補綴物表面、口腔粘膜表面な
どの接触面との固着を防止して、両者を容易に分離し得
るとともに、塗布、除去などの操作性が良好な歯科用分
離材を提供することである。本発明の他の課題は、直接
修復方法における窩洞から該窩洞に充填した未硬化の硬
化性レジンの硬化物である修復物を確実に分離すること
ができる歯科用分離材を提供することである。
An object of the present invention is to provide a resin used as an adhesive or restorative material in dental treatment with a contact surface such as a tooth surface, a prosthetic surface or an oral mucosa surface. An object of the present invention is to provide a dental separation material which can prevent sticking and can be easily separated from each other, and has good operability such as application and removal. Another object of the present invention is to provide a dental separation material capable of reliably separating a restoration, which is a cured product of an uncured curable resin filled in the cavity, from the cavity in the direct restoration method. .

【0007】[0007]

【課題を解決するための手段】本発明は、次の歯科用分
離材である。 (1)(A)分子内に少なくとも2個の水酸基を有し、
凝固点が15℃以下であって、水溶性または水分散性で
ある水酸基含有化合物15〜95重量部、および(B)
分子内に少なくとも2個の水酸基を有し、凝固点が30
℃以上であって、水溶性または水分散性である水酸基含
有化合物5〜85重量部(ここで、(A)と(B)の合
計は100重量部である)を含有することを特徴とする
歯科用分離材。 (2)(B)化合物がポリエチレングリコールであるこ
とを特徴とする上記(1)に記載の歯科用分離材。 (3)齲蝕歯牙に窩洞を形成した後、窩洞表面に分離材
を塗布し、その後硬化性レジンを充填、硬化し、窩洞か
らレジン硬化体を取り出し、窩洞表面を前処理して接着
材で硬化したレジン硬化体を窩洞に接着することからな
る齲蝕歯牙の窩洞修復方法にあって、未硬化の硬化性レ
ジンを充填する前の窩洞表面に塗布される分離材として
使用される上記(1)または(2)に記載の歯科用分離
材。
The present invention relates to the following dental separating material. (1) (A) having at least two hydroxyl groups in the molecule,
(B) a water-soluble or water-dispersible hydroxyl-containing compound having a freezing point of 15 ° C. or lower and 15 to 95 parts by weight;
It has at least two hydroxyl groups in the molecule and has a freezing point of 30
C. or higher and contains 5 to 85 parts by weight of a water-soluble or water-dispersible hydroxyl group-containing compound (here, the total of (A) and (B) is 100 parts by weight). Dental separation material. (2) The dental separation material according to the above (1), wherein the compound (B) is polyethylene glycol. (3) After forming a cavity in the carious tooth, apply a separating material to the cavity surface, then fill and cure the curable resin, take out the cured resin from the cavity, pre-treat the cavity surface and cure with adhesive (1) or a method for repairing a cavity of a carious tooth, which comprises bonding the cured resin body to a cavity, wherein the resin is used as a separating material applied to the cavity surface before filling with an uncured curable resin. The dental separating material according to (2).

【0008】本発明に用いられる水分散性の化合物の
「水分散性」は、90重量%の水に10重量%の(A)
または(B)化合物を分散し、室温で30分間の静置で
分層しないことを意味する。また、本発明に用いられる
水溶性化合物の「水溶性」は、水に対する溶解度が5重
量%以上であることを意味する。
The "water dispersibility" of the water-dispersible compound used in the present invention is as follows: 90% by weight of water and 10% by weight of (A)
Alternatively, it means that the compound (B) is dispersed and the layers are not separated by standing at room temperature for 30 minutes. The “water solubility” of the water-soluble compound used in the present invention means that the solubility in water is 5% by weight or more.

【0009】本発明に用いられる(A)水酸基含有化合
物は分子内に少なくとも2個の水酸基を有し、その凝固
点は15℃以下、好ましくは10℃以下である。そして
(A)水酸基含有化合物は水分散性または水溶性であ
る。(A)水酸基含有化合物が水溶性の場合、水に対す
る溶解度は、50重量%以上であることが好ましく、水
と任意の割合で溶解することが最も好ましい。このよう
な(A)水酸基含有化合物として、例えばエチレングリ
コール、プロピレングリコール、ブタンジオールなどの
グリコール類;グリセリン、1、2、4−ブタントリオ
ール、エリスリトールなどの多価アルコール;分子量5
00以下のポリエチレングリコール、および分子量20
00以下のポリプロピレングリコールなどを好ましく挙
げることができる。なかでも、グリセリンおよび分子量
400以下のポリエチレングリコールが特に好ましい。
これら(A)水酸基含有化合物は、1種単独であるいは
2種以上を組み合わせて用いることができる。
The hydroxyl group-containing compound (A) used in the present invention has at least two hydroxyl groups in the molecule and has a freezing point of 15 ° C. or lower, preferably 10 ° C. or lower. And (A) the hydroxyl group-containing compound is water-dispersible or water-soluble. When the hydroxyl group-containing compound (A) is water-soluble, the solubility in water is preferably 50% by weight or more, and most preferably dissolved in water at an arbitrary ratio. Examples of such (A) hydroxyl group-containing compounds include glycols such as ethylene glycol, propylene glycol and butanediol; polyhydric alcohols such as glycerin, 1,2,4-butanetriol and erythritol;
Polyethylene glycol of not more than 00, and molecular weight of 20
Preferable examples include polypropylene glycol of 00 or less. Among them, glycerin and polyethylene glycol having a molecular weight of 400 or less are particularly preferred.
These (A) hydroxyl group-containing compounds can be used alone or in combination of two or more.

【0010】本発明に用いられる(B)水酸基含有化合
物は分子内に少なくとも2個の水酸基を有し、その凝固
点は30℃以上、好ましくは35℃以上、より好ましく
は40℃以上である。そして(B)水酸基含有化合物は
水分散性または水溶性である。(B)水酸基含有化合物
が水溶性の場合、水に対する溶解度は、50重量%以上
であることが好ましく、水と任意の割合で溶解すること
が最も好ましい。このような(B)水酸基含有化合物と
して、例えば平均分子量1000〜70000のポリエ
チレングリコール、室温で固体のポリプロピレングリコ
ールやポリビニルアルコールなどを例示できる。なかで
も、平均分子量1300〜50000のポリエチレング
リコールなどが好ましい。これら(B)水酸基含有化合
物は、1種単独であるいは2種以上を組み合わせて用い
ることができる。
The hydroxyl group-containing compound (B) used in the present invention has at least two hydroxyl groups in the molecule, and has a freezing point of 30 ° C. or higher, preferably 35 ° C. or higher, more preferably 40 ° C. or higher. And (B) the hydroxyl group-containing compound is water-dispersible or water-soluble. When the hydroxyl group-containing compound (B) is water-soluble, the solubility in water is preferably 50% by weight or more, and most preferably dissolved in water at an arbitrary ratio. Examples of (B) the hydroxyl group-containing compound include polyethylene glycol having an average molecular weight of 1,000 to 70,000, and polypropylene glycol and polyvinyl alcohol which are solid at room temperature. Among them, polyethylene glycol having an average molecular weight of 1300 to 50,000 is preferred. These (B) hydroxyl group-containing compounds can be used alone or in combination of two or more.

【0011】本発明において、(A)水酸基含有化合物
および(B)水酸基含有化合物の凝固点は、JIS K
0065によって測定された値である。また平均分子量
は、JIS K 0070の中和滴定法による水酸基価か
ら求めた値である。
In the present invention, the freezing points of (A) the hydroxyl group-containing compound and (B) the hydroxyl group-containing compound are determined according to JIS K
0065. The average molecular weight is a value determined from a hydroxyl value by a neutralization titration method according to JIS K0070.

【0012】両水酸基含有化合物の配合比は、(A)、
(B)両化合物の合計を100重量部として、(A)水酸
基含有化合物が15〜95重量部、好ましくは25〜9
0重量部、化合物(B)が5〜85重量部、好ましくは
10〜75である。化合物(A)、(B)の配合が上記
範囲であることにより、分離材の流動性が大きくなっ
て、塗布表面から垂れ、期待の分離効果が損なわれるこ
とがなく、また分離材が固くなって、塗布などの操作性
が悪くなることがない。
The compounding ratio of the both hydroxyl group-containing compounds is (A)
(B) 15 to 95 parts by weight, preferably 25 to 9 parts by weight of (A) a hydroxyl group-containing compound, with the total of both compounds being 100 parts by weight.
0 parts by weight, 5 to 85 parts by weight, preferably 10 to 75 parts by weight of the compound (B). When the compounding ratio of the compounds (A) and (B) is in the above range, the fluidity of the separating material is increased, and the separating material does not sag from the application surface, and the expected separating effect is not impaired, and the separating material becomes hard. As a result, the operability such as coating is not deteriorated.

【0013】歯科修復において、接着材から粘着を防ぐ
表面は種々の形状をしている。そのため、分離材は通常
の使用温度条件下で流動性が少ないことと稠度の変化が
少ないことが望まれる。本発明の分離材では、特定の異
なる凝固点を有する2種類の水酸基含有化合物、すなわ
ち室温で液体の化合物と、室温で固体の化合物とが配合
されているので、通常の使用環境(15℃〜30℃)で
は流動性のないペースト状であり、稠度変化が少なく、
また水洗により容易に除去できる長所を有している。稠
度は、JIS T 6602により測定(測定温度23
℃)した値で、好ましくは10〜70、より好ましくは
15〜65である。
In dental restorations, the surface that prevents sticking from the adhesive has various shapes. Therefore, it is desired that the separating material has low fluidity under normal operating temperature conditions and a small change in consistency. In the separation material of the present invention, two kinds of hydroxyl group-containing compounds having specific different freezing points, that is, a compound which is liquid at room temperature and a compound which is solid at room temperature, are blended, so that the compound can be used in a normal use environment (15 ° C. to 30 ° C.). ℃) is a paste without fluidity, little change in consistency,
It also has the advantage that it can be easily removed by washing with water. The consistency is measured according to JIS T6602 (measurement temperature 23
C), preferably 10 to 70, more preferably 15 to 65.

【0014】本発明の特定な凝固点を有する2種類の多
価水酸基含有化合物を適切な配合比により用途に応じた
形態の分離材の調製が可能である。例えば、歯質表面、
補綴物表面、口腔粘膜表面、歯肉縁下などへの接着材の
粘着が生じた際、その硬化物を容易に分離、除去するた
めには、これら表面に塗布する分離材は、高稠度で塗布
しやすいことが好ましい。この場合、化合物(A)の凝
固点が15℃以下にある水酸基含有化合物を、(A)お
よび(B)の水酸基含有化合物の合計量を100重量部
とした場合、好ましくは80〜95重量部、より好まし
くは85〜90重量部、化合物(B)の凝固点が30℃
以上にある水酸基含有化合物を、好ましくは20〜5重
量部、より好ましくは15〜10重量部の割合で配合す
ることにより、高稠度の柔らかいペースト状の分離材得
られる。
According to the present invention, it is possible to prepare a separation material in a form suitable for the intended use by appropriately mixing two kinds of polyvalent hydroxyl group-containing compounds having a specific freezing point. For example, tooth surface,
When the adhesive adheres to the prosthesis surface, oral mucosa surface, subgingival margin, etc., in order to easily separate and remove the cured product, the separating material applied to these surfaces should be applied with high consistency Preferably, it is easy. In this case, the hydroxyl group-containing compound having a freezing point of the compound (A) of 15 ° C. or lower is preferably 80 to 95 parts by weight, when the total amount of the hydroxyl group-containing compounds (A) and (B) is 100 parts by weight, More preferably, the solidification point of the compound (B) is 30 ° C.
By mixing the above-mentioned hydroxyl group-containing compound in a proportion of preferably 20 to 5 parts by weight, more preferably 15 to 10 parts by weight, a soft paste-like separating material having high consistency can be obtained.

【0015】このような高稠度の分離材は、所定の箇所
に接着材を塗布する前に、予め、歯質表面、補綴物表
面、口腔粘膜表面、歯肉縁下などの接着を必要としない
部分に0.005〜0.05g/cm2程度の塗布量で
塗布される。このような塗布処理を行うことにより、上
記箇所に接着材が粘着し、硬化しても、硬化物は、例え
ば歯科用探針などで容易に分離、除去することができ
る。
[0015] Such a high-consistency separating material is used before applying an adhesive to a predetermined portion, and in advance, a portion that does not require adhesion, such as a tooth surface, a prosthetic surface, an oral mucosal surface, or a subgingival margin. Is applied at a coating amount of about 0.005 to 0.05 g / cm 2 . By performing such a coating treatment, even if the adhesive sticks to the above-mentioned portion and is cured, the cured product can be easily separated and removed with, for example, a dental probe.

【0016】また前述した直接修復法で、分離材に低稠
度と耐圧性を必要とする場合には、(A)および(B)の
水酸基含有化合物の合計量を100重量部として、凝固
点が15℃以下である(A)水酸基含有化合物を好まし
くは40〜15重量部、より好ましくは30〜20重量
部、凝固点が30℃以上である(B)水酸基含有化合物
を好ましくは60〜85重量部、より好ましくは70〜
80重量部の割合で配合することにより、低稠度が硬く
て耐圧性を有するペースト状分離材が得られる。
In the above-mentioned direct repair method, when the separation material requires low consistency and pressure resistance, the solidification point is set to 15 with the total amount of the hydroxyl group-containing compounds (A) and (B) being 100 parts by weight. (A) a hydroxyl group-containing compound having a freezing point of at most 40 to 15 parts by weight, more preferably 30 to 20 parts by weight; More preferably 70 to
By blending at a ratio of 80 parts by weight, a paste-like separating material having low hardness and high pressure resistance can be obtained.

【0017】このような低稠度の硬いペースト状分離材
を用いて、齲蝕歯牙を直接法により治療する場合、次の
ような方法で行われる。即ち、齲蝕歯牙に窩洞を形成し
た後、窩洞表面に本発明の分離材を塗布する。塗布量
は、0.002〜0.01g/cm2程度とする。その
後、窩洞内に硬化性レジンを充填し、紫外線などの活性
光線の露光により硬化する。次に窩洞から、修復物であ
るレジン硬化体を取り出す。このとき、窩洞表面が予め
本発明の歯科用分離材で塗布されているので、容易に窩
洞から取り出すことができる。次に修復物が取り出され
た窩洞の表面を前処理し、接着材を塗布した後、修復物
を窩洞にはめ込み接着することにより齲蝕歯牙の窩洞が
修復される。この接着の際、接着を要しない部分に分離
材を塗布して分離を容易にできることは前記と同様であ
る。
When a caries tooth is directly treated using such a low-consistency hard paste-like separating material, the following method is used. That is, after the cavity is formed in the carious tooth, the separating material of the present invention is applied to the cavity surface. The application amount is about 0.002 to 0.01 g / cm 2 . Thereafter, the cavity is filled with a curable resin and cured by exposure to actinic rays such as ultraviolet rays. Next, the resin cured body as a restoration is taken out from the cavity. At this time, since the cavity surface is previously coated with the dental separation material of the present invention, the cavity can be easily removed from the cavity. Next, the surface of the cavity from which the restoration has been removed is pre-treated, an adhesive is applied, and the restoration is fitted into the cavity and adhered to restore the cavity of the carious tooth. At the time of this bonding, the separation can be easily performed by applying a separating material to a portion that does not require bonding, as described above.

【0018】また、本発明の歯科用分離材は水溶性また
は水分散性であるので、塗布後不要となったときは、水
洗して容易に口腔内から除去することができる。
Further, since the dental separation material of the present invention is water-soluble or water-dispersible, it can be easily removed from the oral cavity by washing with water when it becomes unnecessary after application.

【0019】本発明の分離材は、上記の2種類の水酸基
含有化合物を必須成分とするが、本発明の目的を損なわ
ない限り、他の添加材を加えることもできる。添加材と
しては、公知の顔料、染料などの着色剤、水、アルコー
ルなどの水混和性溶剤、水溶性高分子、シリカ微粒子な
どの無機粒子が列挙できる。
The separating material of the present invention contains the above two kinds of hydroxyl group-containing compounds as essential components, but other additives can be added as long as the object of the present invention is not impaired. Examples of the additive include known colorants such as pigments and dyes, water-miscible solvents such as water and alcohol, water-soluble polymers, and inorganic particles such as silica fine particles.

【0020】本発明の分離材で分離の対象となるレジン
としては、上記の接着材および補修用材が代表的である
が、本発明の分離材は他の目的で使用されるレジンとそ
の接触面との分離にも適用することができる。
As the resin to be separated by the separation material of the present invention, the above-mentioned adhesives and repair materials are typical, but the separation material of the present invention is a resin used for other purposes and a contact surface thereof. Can also be applied to separation from

【0021】[0021]

【発明の効果】本発明の歯科用分離材は、歯科治療に良
好な操作性と分離能を有し、接着材や補修用材などとし
て用いられるレジンと、歯質表面などの接触面との固着
を防止することができる。従って、例えば治療修復物を
歯質に接着させるために用いられる接着材が、接着材を
必要としない歯質表面、補綴物表面、口腔粘膜表面、お
よび硬化したレジン表面などに粘着しても、予め歯質表
面に本発明の歯科用分離材を塗布しておけば、硬化した
接着材を歯科用探針などにより容易に分離することがで
きる。また齲蝕歯牙の窩洞修復方法を直接法で行う際、
窩洞を形成した後、窩洞壁に予め本発明の分離材を塗布
することにより、窩洞内で硬化した修復材を窩洞壁から
確実に分離することができるので、齲蝕歯牙の窩洞修復
方法を直接法で容易に行なうことができる。
Industrial Applicability The dental separation material of the present invention has good operability and separation ability for dental treatment, and adheres a resin used as an adhesive or a repair material to a contact surface such as a tooth surface. Can be prevented. Thus, for example, even if the adhesive used to adhere the therapeutic restoration to the dentin adheres to the dentin surface, prosthesis surface, oral mucosal surface, and cured resin surface that do not require the adhesive, If the dental separating material of the present invention is applied to the tooth surface in advance, the cured adhesive can be easily separated with a dental probe or the like. In addition, when performing the cavity repair method of carious teeth by the direct method,
After the cavity is formed, the restoration material of the present invention is applied to the cavity wall in advance, so that the restoration material hardened in the cavity can be reliably separated from the cavity wall. Can be easily performed.

【0022】[0022]

【発明の実施の形態】以下、本発明を実施例によりさら
に具体的に説明するが、本発明は以下の実施例に限定さ
れることはない。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to the following examples.

【0023】実施例1(本発明の分離材1〜4の製造) 分離材1の製造 グリセリン(凝固点約0℃)30gとポリエチレングリ
コール(PEG)1540(凝固点40〜50℃、数平
均分子量1540)70gをガラス容器に入れ、70℃
まで加熱して溶液を得た。この溶液を室温まで放冷し、
白色の硬いペースト状物(分離材1)を得た。分離材1の
稠度をJIS T 6602の稠度測定方法(測定温度2
3℃)で測定したところ、15であった。垂直状態に設
置した牛歯歯頚部に分離材1を約0.002〜0.01g
/cm2に塗布し1分間放置した後、塗布部からの垂れ
具合を温度37℃で観測したところ、塗布した位置から
の垂れが観測されなかった。
Example 1 (Production of Separating Materials 1 to 4 of the Present Invention) Production of Separating Material 1 30 g of glycerin (coagulation point of about 0 ° C.) and polyethylene glycol (PEG) 1540 (coagulation point of 40 to 50 ° C., number average molecular weight 1540) 70 g in a glass container,
Until a solution was obtained. Allow the solution to cool to room temperature,
A white hard paste (separation material 1) was obtained. The consistency of the separation material 1 was measured by the method of measuring the consistency according to JIS T6602 (measurement temperature 2
3 ° C.). Approximately 0.002 to 0.01 g of separation material 1 is placed on the cervical portion of the bovine tooth placed vertically.
/ Cm 2 and allowed to stand for 1 minute. When the degree of sagging from the applied part was observed at a temperature of 37 ° C., no sagging from the applied position was observed.

【0024】分離材2〜4の製造 表1に示される化合物とその配合比で分離材1の製造方
法と同様にして分離材2〜4を製造した。分離材2〜4
の稠度は表1に示す通りであり、分離材1と同様にして
垂れ具合を観測したところ、垂れは観測されなかった。
Production of Separating Materials 2 to 4 Separating materials 2 to 4 were produced in the same manner as in the production method of the separating material 1 with the compounds shown in Table 1 and the compounding ratio thereof. Separation material 2-4
Is as shown in Table 1. When the degree of sagging was observed in the same manner as in the case of the separation material 1, no sagging was observed.

【0025】実施例2(分離材5〜8の製造) 分離材5の製造 PEG400(凝固点4〜8℃、数平均分子量400)
85gとPEG4000(凝固点50〜60℃、数平均
分子量4000)15gをガラス容器に入れ、70℃ま
で加熱して溶液を得た。この溶液を室温まで放冷し半透
明白色のやわらかいペースト状の分離材5を得た。分離
材5の稠度をJIS T 6602の稠度測定方法(測定
温度23℃)で測定したところ、36であった。垂直状
態に設置した牛歯歯頚部に当分離材0.005〜0.05
g/cm2を塗布し1分間放置した後、塗布部からの垂
れ具合を温度37℃で観測したところ、塗布した位置か
らの垂れが観測されなかった。
Example 2 (Production of Separating Materials 5 to 8) Production of Separating Material 5 PEG400 (solidification point: 4 to 8 ° C., number average molecular weight: 400)
85 g and 15 g of PEG 4000 (freezing point: 50 to 60 ° C., number average molecular weight: 4000) were placed in a glass container and heated to 70 ° C. to obtain a solution. The solution was allowed to cool to room temperature to obtain a translucent white soft paste-like separating material 5. The consistency of the separation material 5 was measured by the consistency measurement method (measuring temperature 23 ° C.) of JIS T6602, and it was 36. The separation material is 0.005 to 0.05 on the cervical part of the bovine tooth installed vertically.
After applying g / cm 2 and allowed to stand for 1 minute, the degree of sagging from the applied part was observed at a temperature of 37 ° C., and no sagging from the applied position was observed.

【0026】分離材6〜8の製造 表1に示される化合物とその配合比で分離材5の製造方
法と同様にして分離材6〜8を製造した。分離材6〜8
の稠度は表1に示す通りであり、分離材5と同様にして
垂れ具合を観測したところ、垂れは観測されなかった。
Production of Separators 6 to 8 Separators 6 to 8 were produced in the same manner as in the production method of the separator 5 with the compounds shown in Table 1 and the compounding ratio thereof. Separation material 6-8
Is as shown in Table 1. When the degree of sagging was observed in the same manner as in the case of the separation material 5, no sagging was observed.

【0027】[0027]

【表1】 各ポリエチレングリコールの数平均分子量は下記の通り
である。 PEG400 :400 PEG1540:1500 PEG2000:2000 PEG4000:3000
[Table 1] The number average molecular weight of each polyethylene glycol is as follows. PEG400: 400 PEG1540: 1500 PEG2000: 2000 PEG4000: 3000

【0028】実施例3(分離材1〜4の分離能評価) 牛前歯唇面に直径約2〜3mm深さ2mmの窩洞を形成し、
該窩洞内壁を分離材1を綿棒で塗布した後、市販コンポ
ジットレジン「XRV ハーキュライト(KERR社製、
商標)」を充填した。可視光照射器で窩洞に充填したコ
ンポジットレジンを60秒間照射硬化した後、ピンセッ
トで硬化したレジン体簡単に取り出せることを確認し
た。分離材2〜4についても分離材1の確認方法と同様
にして分離性能を評価した。いずれの分離材を使用して
も窩洞からレジン硬化体が簡単に取り出された。
Example 3 (Evaluation of Separation Ability of Separating Materials 1 to 4) A cavity having a diameter of about 2 to 3 mm and a depth of 2 mm was formed on the front labial surface of the bovine.
After applying the separating material 1 to the inner wall of the cavity with a cotton swab, a commercially available composite resin “XRV Herculite (manufactured by KERR,
(Trademark) ". After irradiating and curing the composite resin filled in the cavity with a visible light irradiator for 60 seconds, it was confirmed that the cured resin body could be easily removed with tweezers. Separation materials 2 to 4 were also evaluated for separation performance in the same manner as in the method for confirming separation material 1. Regardless of which separation material was used, the cured resin body was easily removed from the cavity.

【0029】比較例1 分離材の塗布操作だけを省略し、実施例3と同様に牛歯
窩洞に充填硬化させたレジン体が取り出せるかどうかを
評価した処、窩洞からレジン硬化体が取り出されなかっ
た。
Comparative Example 1 The same procedure as in Example 3 was carried out except that only the operation of applying the separation material was omitted, and it was evaluated whether or not the resin body filled and cured in the bovine cavity could be taken out. Was.

【0030】実施例4(分離材5〜8の分離能評価) 牛前歯歯頚部表面および#2000のSiC研磨紙で研
磨したCo−Cr合金表面に分離材5を筆にて塗布し
て、続いて市販接着材スーパーボンド(サンメディカル
社(株)製)の混和泥を塗布し、硬化させた。接着材が硬
化した後、歯科用探針で接着材硬化体が容易に除去でき
るかどうかを評価した。分離材6〜8についても分離材
5の確認方法と同様にして分離性能を評価した。いずれ
の分離材を使用しても接着材硬化体が簡単に除去でき
た。
Example 4 (Evaluation of Separation Ability of Separating Materials 5 to 8) Separating material 5 was applied to the cervical surface of bovine anterior teeth and the surface of Co-Cr alloy polished with # 2000 SiC abrasive paper, followed by brushing. A mixture of commercially available adhesive Super Bond (manufactured by Sun Medical Co., Ltd.) was applied and cured. After the adhesive was cured, it was evaluated whether the cured adhesive could be easily removed with a dental probe. Separation materials 6 to 8 were also evaluated for separation performance in the same manner as in the method for confirming separation material 5. The cured adhesive material could be easily removed using any of the separation materials.

【0031】比較例2 分離材を塗布せずに、実施例4と同様に牛前歯歯頚部表
面、および#2000のSiC研磨紙で研磨したCo−
Cr合金表面に、スーパーボンドの混和泥を塗布し、硬
化させた後容易に除去できるかどうかを評価した処、接
着材硬化体が除去できなかった。
Comparative Example 2 Cobalt polished with a # 2000 SiC abrasive paper and the cervical surface of the bovine anterior teeth in the same manner as in Example 4 without applying the separating material.
When the mixed mud of Super Bond was applied to the surface of the Cr alloy and cured to evaluate whether or not it could be easily removed, the cured adhesive could not be removed.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)分子内に少なくとも2個の水酸基
を有し、凝固点が15℃以下であって、水溶性または水
分散性である水酸基含有化合物15〜95重量部、およ
び(B)分子内に少なくとも2個の水酸基を有し、凝固
点が30℃以上であって、水溶性または水分散性である
水酸基含有化合物5〜85重量部(ここで、(A)と
(B)の合計は100重量部である)を含有することを
特徴とする歯科用分離材。
(A) 15 to 95 parts by weight of a water-soluble or water-dispersible hydroxyl-containing compound having at least two hydroxyl groups in a molecule, having a freezing point of 15 ° C. or lower, and (B) 5 to 85 parts by weight of a water-soluble or water-dispersible hydroxyl-containing compound having at least two hydroxyl groups in the molecule, having a freezing point of 30 ° C. or higher (where the total of (A) and (B) Is 100 parts by weight).
【請求項2】 (B)化合物がポリエチレングリコール
であることを特徴とする請求項1に記載の歯科用分離
材。
2. The dental separation material according to claim 1, wherein the compound (B) is polyethylene glycol.
【請求項3】 齲蝕歯牙に窩洞を形成した後、窩洞表面
に分離材を塗布し、その後硬化性レジンを充填、硬化
し、窩洞からレジン硬化体を取り出し、窩洞表面を前処
理して接着材で硬化したレジン硬化体を窩洞に接着する
ことからなる齲蝕歯牙の窩洞修復方法にあって、未硬化
の硬化性レジンを充填する前の窩洞表面に塗布される分
離材として使用される請求項1または2に記載の歯科用
分離材。
3. After forming a cavity in a carious tooth, a separating material is applied to the cavity surface, and then a curable resin is filled and cured, a cured resin body is taken out from the cavity, and the surface of the cavity is pre-treated and an adhesive material is provided. 2. A method for repairing a cavity of a carious tooth, comprising bonding a cured resin body cured by the method to a cavity, wherein the method is used as a separating material applied to the cavity surface before filling with an uncured curable resin. Or the dental separating material according to 2.
JP10830698A 1998-04-17 1998-04-17 Dental separator Expired - Fee Related JP4232214B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10830698A JP4232214B2 (en) 1998-04-17 1998-04-17 Dental separator

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10830698A JP4232214B2 (en) 1998-04-17 1998-04-17 Dental separator

Publications (2)

Publication Number Publication Date
JPH11302122A true JPH11302122A (en) 1999-11-02
JP4232214B2 JP4232214B2 (en) 2009-03-04

Family

ID=14481368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10830698A Expired - Fee Related JP4232214B2 (en) 1998-04-17 1998-04-17 Dental separator

Country Status (1)

Country Link
JP (1) JP4232214B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002029910A (en) * 2000-07-13 2002-01-29 Sun Medical Co Ltd Resin-separating material composition for dentistry
JP2009167207A (en) * 2000-10-12 2009-07-30 Three M Innovative Properties Co Adhesives for use in oral environment having color changing capability
JP2019218297A (en) * 2018-06-20 2019-12-26 株式会社トクヤマデンタル Dental separation material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002029910A (en) * 2000-07-13 2002-01-29 Sun Medical Co Ltd Resin-separating material composition for dentistry
JP2009167207A (en) * 2000-10-12 2009-07-30 Three M Innovative Properties Co Adhesives for use in oral environment having color changing capability
JP2019218297A (en) * 2018-06-20 2019-12-26 株式会社トクヤマデンタル Dental separation material

Also Published As

Publication number Publication date
JP4232214B2 (en) 2009-03-04

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