JPS6254502B2 - - Google Patents

Info

Publication number
JPS6254502B2
JPS6254502B2 JP53111172A JP11117278A JPS6254502B2 JP S6254502 B2 JPS6254502 B2 JP S6254502B2 JP 53111172 A JP53111172 A JP 53111172A JP 11117278 A JP11117278 A JP 11117278A JP S6254502 B2 JPS6254502 B2 JP S6254502B2
Authority
JP
Japan
Prior art keywords
denture
adhesive
fixing adhesive
present
denture fixing
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
Application number
JP53111172A
Other languages
Japanese (ja)
Other versions
JPS5538143A (en
Inventor
Hiroshi Ninomya
Hiroshi Takai
Wataru Tanaka
Junichi Takeda
Tokio Hashimoto
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.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku 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 Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP11117278A priority Critical patent/JPS5538143A/en
Publication of JPS5538143A publication Critical patent/JPS5538143A/en
Publication of JPS6254502B2 publication Critical patent/JPS6254502B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Dental Preparations (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は床義歯固定粘着剤に関する。 従来、歯肉表面に対する床義歯の安定性が悪い
場合、会話、食事などの際に床義歯が移動した
り、著しい場合には脱落したりして、日常生活を
不快ならしめるのみではなく、口腔粘膜損傷もし
ばしば生じていた。 このため腫瘍、奇形、外傷などによる顎欠損の
ある場合、欠損歯が多くかつ残存歯の骨髄が不良
な場合、咀嚼等に関して悪習慣のある場合など多
くの場合に床義歯固定粘着剤が広く望まれてい
た。 床義歯固定粘着剤は唾液と接触したとき、ただ
ちに湿潤し、義歯床を歯肉表面に粘着させること
により床義歯の安定な維持を長時間保持すると共
に、特に顎補綴床義歯の場合には応力緩衝性を有
するゲルを形成して両者間の接触による歯肉表面
の各種の障害を阻止できるものであることが望ま
しい。なお、ゲルの形成は、床義歯と歯肉表面の
間で真空シールが生ずることにもなるので、より
両者の密着性を高める効果がある。 以上に述べた性能を満足する床義歯の固定粘着
剤としてこれ迄に多くの材料の適用が試みられて
来たが、満足できるものを見出すに至つていな
い。すなわち、グアーガム、ザンサンガム、トラ
ガカントゴム、アラビアゴム、アルギン酸ナトリ
ウムなどの天然ガム類やメチルセルローズ、ヒド
ロオキシメチルセルローズ、カルボキシメチルセ
ルローズなどの半合成高分子が主に検討されて来
たが、これらはいずれも粘着力が弱く、又、その
持続時間が短かいため床義歯固定粘着剤としては
不適当であつた。 又、エチレンオキサイドのホモ重合体であるポ
リエチレンオキシドを使つた総義歯固定剤が特開
昭47−44895に開示されているが、このものの粘
着性は未だ十分でなく、さらにその持続時間も短
く、又生成したゲルの安定性も十分でない。 以上の状況のもとに、本発明者らは床義歯固定
粘着剤としての性能を実用的観点から備える物質
について鋭意検討した結果ポリアクリル酸金属塩
の粉末を用いると粘着性が高く、その持続時間も
長く、又、安定した弾性ゲルを形成することを見
出し本発明を完成した。 本発明で用いられるポリアクリル酸金属塩は平
均分子量が300万〜1000万のアルカリ金属塩、ア
ルカリ土類金属塩及び3価の金属塩であるが好ま
しくは平均分子量500万〜800万のポリアクリル酸
のアルカリ金属塩類、及び存在するカルボキシル
基の全モル数の約40%以下がアルカリ土類、又は
3価の金属、60%以上がアルカリ金属で置換され
た塩類である。 又ポリアクリル酸アルカリ金属塩の粉末の粒度
は100メツシユより微細なものが好ましい。 本発明を実施するには、ポリアクリル酸金属塩
の粉末のみを単独で用いても十分であるが、矯味
矯臭剤としてメントールなどを添加してもよく、
さらに流動促進剤としてポリアクリル酸金属塩に
0.01〜5%の割合で乾燥澱粉、タルク、ステアリ
ン酸の金属塩類、無水ケイ酸、高級脂肪酸の微粉
末などを、又粘着性の増強剤として0.01〜10%の
アルギン酸ナトリウム、メチルセルロースなどを
添加してもよい。 又、本発明の床義歯固定粘着剤にフラジオマイ
シンなどの抗生物質、キシロカイン等の局所麻酔
剤、硼砂などの収歛剤、ブレオマイシンなどの制
ガン剤などを適宜に配合して歯槽膿漏や歯莖周辺
の癌や口内炎などの治療目的にも使用することが
できる。 本発明の床義歯固定粘着剤を使用するには水な
どで湿らせた義歯床に適量を表面にふりかけ、そ
れをそつと歯莖にセツトし、2〜3分軽くかみ合
わせればよい。 なお、ポリアクリル酸の金属塩類の中で、ポリ
アクリル酸ナトリウムは、食品添加物公定書と化
粧品原料基準にも収載されて居る安全性の確認さ
れた物質である。 次に本発明の床義歯固定粘着剤の優れた性能を
実験例により具体的に説明する。 実験例 1 本発明の床義歯固定粘着剤の粘着力の測定。 (1) 試料の調製 表1に示される処方に基づいて試料を調製し
た、試料No.1〜13が本発明の試料でありNo.14〜
22が対照試料である。 (2) 実験方法 第1図に示した装置によつて測定を行なつ
た。すなわち37℃の流水を環流できる恒温セル
Dの底部に水で湿らせた牛の床皮片Aを固定
し、その上に500mgの床義歯固定粘着剤を2cm2
の面積で円形状に付着せしめB、その上に、不
動工業製レオメーターに連絡した、先端にステ
ンレス製の円板を付属したスピンドルCをかぶ
せて、スピンドルCに約1Kg/cm2の圧力を2分
間加え、図1のAとCをBで十分粘着せしめ
る。次に37℃の流水の環流を開始し、2分後に
レオメーターの支持台Eを5cm/分の速度で上
昇せしめ、スピンドルCが牛の床皮Aより剥離
するに要する力、すなわち床義歯固定粘着剤の
粘着力(g/cm2)を測定した。 (3) 結果 各試料の粘着力を表1に示す。
The present invention relates to a denture fixing adhesive. Conventionally, if the stability of the denture against the gingival surface is poor, the denture may move during conversation, eating, etc., or in severe cases may fall off, which not only makes daily life uncomfortable, but also damages the oral mucosa. Damage was also common. For this reason, denture fixing adhesives are widely desired in many cases, such as when there is a jaw defect due to a tumor, malformation, or trauma, when there are many missing teeth and the bone marrow of the remaining teeth is poor, or when there are bad chewing habits. It was rare. When the denture fixing adhesive comes into contact with saliva, it immediately becomes wet, and by adhering the denture base to the gingival surface, it maintains the stability of the denture for a long time, and also provides stress buffering, especially in the case of jaw prosthetic dentures. It is desirable that the gel forms a gel that has properties and can prevent various damage to the gingival surface due to contact between the two. Note that the formation of the gel also creates a vacuum seal between the denture and the gingival surface, which has the effect of further increasing the adhesion between the two. Many materials have been tried so far to be used as fixing adhesives for dentures that satisfy the above-mentioned performance, but none have been found to be satisfactory. Specifically, natural gums such as guar gum, xanthan gum, gum tragacanth, gum arabic, and sodium alginate, and semisynthetic polymers such as methylcellulose, hydroxymethylcellulose, and carboxymethylcellulose have been mainly investigated, but none of these Due to its weak adhesive strength and short duration, it was unsuitable as a denture fixing adhesive. Furthermore, a complete denture fixative using polyethylene oxide, which is a homopolymer of ethylene oxide, is disclosed in JP-A-47-44895, but the adhesiveness of this agent is still insufficient and its duration is short. Furthermore, the stability of the produced gel is also insufficient. Under the above circumstances, the present inventors conducted intensive studies on materials that have the performance as a denture fixing adhesive from a practical point of view, and found that the use of polyacrylic acid metal salt powder has high adhesiveness and long-lasting properties. The present invention was completed by discovering that a stable elastic gel can be formed over a long period of time. The polyacrylic acid metal salts used in the present invention are alkali metal salts, alkaline earth metal salts, and trivalent metal salts with an average molecular weight of 3 million to 10 million, but preferably polyacrylic acid salts with an average molecular weight of 5 million to 8 million. Alkali metal salts of acids and salts in which about 40% or less of the total number of moles of carboxyl groups present are substituted with alkaline earth or trivalent metals, and 60% or more are substituted with alkali metals. The particle size of the alkali metal salt polyacrylate powder is preferably finer than 100 mesh. In carrying out the present invention, it is sufficient to use only the powder of polyacrylic acid metal salt alone, but menthol or the like may be added as a flavoring agent.
Furthermore, polyacrylic acid metal salts are used as glidants.
Dry starch, talc, metal salts of stearic acid, silicic anhydride, fine powder of higher fatty acids, etc. are added at a ratio of 0.01 to 5%, and sodium alginate, methyl cellulose, etc. are added at a ratio of 0.01 to 10% as adhesive enhancers. It's okay. In addition, antibiotics such as fradiomycin, local anesthetics such as xylocaine, astringents such as borax, anticancer agents such as bleomycin, etc. may be appropriately blended with the denture fixing adhesive of the present invention to treat alveolar pyorrhea and surrounding areas. It can also be used for therapeutic purposes such as cancer and stomatitis. To use the denture fixing adhesive of the present invention, sprinkle an appropriate amount on the surface of a denture base moistened with water, gently set it on the tooth pad, and lightly bite it for 2 to 3 minutes. Among the metal salts of polyacrylic acid, sodium polyacrylate is a substance whose safety has been confirmed and is listed in the Japan Food Additives Standard and the Cosmetic Raw Materials Standards. Next, the excellent performance of the denture fixing adhesive of the present invention will be specifically explained using experimental examples. Experimental Example 1 Measurement of the adhesive strength of the denture fixing adhesive of the present invention. (1) Preparation of samples Samples Nos. 1 to 13 were prepared based on the recipe shown in Table 1, and Nos. 14 to 13 were the samples of the present invention.
22 is the control sample. (2) Experimental method Measurements were carried out using the apparatus shown in Figure 1. That is, a piece of cow skin A moistened with water was fixed to the bottom of a thermostatic cell D that could circulate running water at 37°C, and 2 cm 2 of 500 mg of denture fixing adhesive was placed on top of it.
Place the spindle C connected to a Fudo Kogyo rheometer with a stainless steel disc on the tip, and apply a pressure of about 1 kg/cm 2 to the spindle C. Add for 2 minutes to fully adhere A and C in Figure 1 with B. Next, reflux of running water at 37°C is started, and after 2 minutes, the support base E of the rheometer is raised at a speed of 5 cm/min, and the force required to separate the spindle C from the cow's skin A, i.e., fixing the denture. The adhesive force (g/cm 2 ) of the adhesive was measured. (3) Results Table 1 shows the adhesive strength of each sample.

【表】【table】

【表】 この表からNo.1〜13の本発明の床義歯固定粘着
剤の粘着力はNo.14〜22の対照試料のそれより優
れていることがわかる。 実験例 2 床義歯固定粘着剤の湿潤ゲルの応力緩衝性(粘
弾性)の測定 (1) 試料の調製 表2に示された処方の試料500mgをガラス平
板上に約3mmの厚さにセツトし、次いで水1.2
mlを添加して24時間静置し、試料とした。試料
No.1〜4が本発明の試料あり、No.5〜7が対照
試料である。 (2) 試験方法 第2図に示した装置によつて測定を行つた。
すなわち、レオメーターの支持台Eを2mm/秒
の速度で、湿潤ゲルの表面Iに向けて移動さ
せ、棒状スピンドルGをゲルの表面IにPx1
圧力で圧迫させながらさらに移動を続け、針状
スピンドルFの先端がゲルの表面Iに接触した
時点でレオメーターの支持台Eの移動が自動的
に停止する(第3図の状態)ようにセツトした
装置を用いた。 第3図の状態で停止した円板端子Hの先端に
は、ゲルの粘弾性に基づく反撥力Px2がかか
る。このPx2の値が高い程ゲルの粘弾性が高い
ことになる。 このようにして各試料の37℃における粘弾性
を測定した。 (3) 結果 床義歯固定粘着剤の湿潤ゲルの粘弾性に基づ
くPx2を表2に示す。
[Table] From this table, it can be seen that the adhesive strength of the denture fixing adhesives of the present invention No. 1 to 13 is superior to that of the control samples No. 14 to 22. Experimental example 2 Measurement of stress buffering properties (viscoelasticity) of wet gel of denture fixing adhesive (1) Sample preparation 500 mg of the sample with the formulation shown in Table 2 was set on a glass flat plate to a thickness of about 3 mm. , then water 1.2
ml was added and left to stand for 24 hours, and used as a sample. sample
Nos. 1 to 4 are samples of the present invention, and Nos. 5 to 7 are control samples. (2) Test method Measurements were performed using the apparatus shown in Figure 2.
That is, the support E of the rheometer is moved at a speed of 2 mm/sec toward the surface I of the wet gel, and the movement is continued while the rod-shaped spindle G is pressed against the surface I of the gel with a pressure of Px 1 . An apparatus was used, which was set so that the movement of the support base E of the rheometer was automatically stopped when the tip of the shaped spindle F came into contact with the surface I of the gel (the state shown in FIG. 3). A repulsive force Px 2 based on the viscoelasticity of the gel is applied to the tip of the disc terminal H that is stopped in the state shown in FIG. The higher the value of Px 2 , the higher the viscoelasticity of the gel. In this way, the viscoelasticity of each sample at 37°C was measured. (3) Results Table 2 shows Px 2 based on the viscoelasticity of the wet gel of the denture fixing adhesive.

【表】【table】

【表】 表2から本発明の試料No.1〜4のPx2は対照
試料No.5〜7のそれより30%以上高い。つまり
本発明の床義歯固定粘着剤は公知のそれより粘
弾性が高いので、歯肉と義歯の間の接触応力緩
衝性が高く、そのため、両者間の接触による歯
肉表面の各種の障害を阻止でき、非常に使いや
すい。 実験例 3 床義歯固定粘着剤の粘着持続試験 (1) 試料の調製 表2の処方の試料を用いた。 (2) 試験方法 床義歯使用者5名が各試料の固定粘着剤を夕
食後使用し、その効果の持続時間を測定した。 (3) 結果 床義歯の粘着持続時間を表3に示す。
[Table] From Table 2, the Px 2 of samples Nos. 1 to 4 of the present invention are higher than those of control samples Nos. 5 to 7 by more than 30%. In other words, the denture fixing adhesive of the present invention has higher viscoelasticity than known ones, so it has high contact stress buffering properties between the gingiva and denture, and therefore can prevent various damage to the gingival surface due to contact between the two. Very easy to use. Experimental Example 3 Adhesion duration test of denture fixing adhesive (1) Sample preparation Samples with the formulations shown in Table 2 were used. (2) Test method Five denture users used each sample of fixing adhesive after dinner, and measured the duration of its effect. (3) Results Table 3 shows the adhesion duration of the dentures.

【表】 * 使用者5名の平均値
表3より本発明の試料(No.1〜4)の持続時
間は対照試料(No.5〜7)のそれに比し、5倍
以上と非常に長く、その効果の優れていること
がわかる。 次に本発明の粘着剤の製造法を実施例により説
明する。 実施例 1 平均分子量が約800万のポリアクリル酸ナトリ
ウムの100〜200メツシユの度の粉末を140℃で5
時間乾燥し、密栓瓶に充填する。 実施例 2 実施例1で得たポリアクリル酸ナトリウムの粉
末95部にタルク5部を均一に混合し、密栓瓶に充
填する。 実施例 3 実施例1で得たポリアクリル酸ナトリウムの粉
末98部に硫酸フラジオマイシン2部を均一に混合
して密栓瓶に充填する。 実施例 4 平均分子量約710万のポリアクリル酸ナトリウ
ム50gと塩化ナトリウム58.5gが溶解している水
溶液1を急速に撹拌しながら、これに8.6%の
塩化カルシウム水溶液200mlを徐々に加える。つ
いで生成したカルボキシル基の70%がNa塩、30
%がカルシウム塩であるポリアクリル酸金属塩を
無水メタノールを添加して沈澱せしめ140℃5時
間加熱して乾燥し、200メツシユ以下の粒度に粉
砕し密栓瓶に充填する。 実施例 5 平均分子量が約800万のポリアクリル酸ナトリ
ウムの200メツシユ以下の粉末40部、アルギン酸
ナトリウム10部、蜜蝋40部およびODO(グリ
セリン脂肪酸エステル)10部を十分均一に練合し
軟膏とする。 実施例 6 平均分子量が約500万のポリアクリル酸ナトリ
ウム1.8%、アルギン酸ナトリウム0.2%の均一混
合水溶液を調製し、これを蒸発乾固後、120℃4
時間十分に乾燥し、200メツシユ以下の粉末に粉
砕し密栓瓶に充填する。 実施例 7 平均分子量が約800万のポリアクリル酸ナトリ
ウムの200メツシユ以下の粉末70部、80℃で10時
間十分に乾燥した馬れいしよ澱粉15部、180℃で
6時間十分に乾燥した無水リン酸カルシウム15部
を均一に混合し密栓瓶に充填する。
[Table] * Average value of 5 users From Table 3, the duration of the samples of the present invention (Nos. 1 to 4) is extremely long, more than 5 times that of the control samples (Nos. 5 to 7). , it can be seen that the effect is excellent. Next, the method for producing the adhesive of the present invention will be explained with reference to Examples. Example 1 A powder of 100 to 200 meshes of sodium polyacrylate with an average molecular weight of about 8 million was heated at 140°C for 5 minutes.
Let dry for a while and fill into sealed bottles. Example 2 95 parts of the sodium polyacrylate powder obtained in Example 1 was uniformly mixed with 5 parts of talc, and the mixture was filled into a sealed bottle. Example 3 2 parts of fradiomycin sulfate were uniformly mixed with 98 parts of the sodium polyacrylate powder obtained in Example 1, and the mixture was filled into a sealed bottle. Example 4 While rapidly stirring aqueous solution 1 in which 50 g of sodium polyacrylate having an average molecular weight of about 7.1 million and 58.5 g of sodium chloride are dissolved, 200 ml of an 8.6% calcium chloride aqueous solution is gradually added. Then, 70% of the carboxyl groups generated are Na salts, 30
% of a calcium salt is precipitated by adding anhydrous methanol, dried by heating at 140°C for 5 hours, crushed to a particle size of 200 mesh or less, and filled into a sealed bottle. Example 5 40 parts of powder of 200 mesh or less of sodium polyacrylate with an average molecular weight of about 8 million, 10 parts of sodium alginate, 40 parts of beeswax, and 10 parts of ODO (glycerin fatty acid ester) are thoroughly and uniformly kneaded to make an ointment. . Example 6 A homogeneous mixed aqueous solution of 1.8% sodium polyacrylate and 0.2% sodium alginate with an average molecular weight of about 5 million was prepared, and after evaporating to dryness, it was heated at 120°C 4
Dry for a sufficient amount of time, crush into a powder of 200 mesh or less, and fill in a sealed bottle. Example 7 70 parts of powder of 200 mesh or less of sodium polyacrylate with an average molecular weight of about 8 million, 15 parts of horse starch thoroughly dried at 80°C for 10 hours, and 15 parts of anhydrous calcium phosphate thoroughly dried at 180°C for 6 hours. Mix the parts evenly and fill into a sealed bottle.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は床義歯固定粘着剤の粘着力測定装置で
あり、第2図及び第3図は床義歯固定粘着剤の湿
潤ゲルの粘弾性力Px2の測定装置である。 A…牛の床皮片(3×3cm2)、B…床義歯固定
粘着剤、C…先端に円板(2cm2)を付属したステ
ンレス製スピンドル、D…37℃の流水を環流でき
る恒温セル(容量100ml)、E…不動工業製レオメ
ーターへの連結支持部、F…ステンレス製針状ス
ピンドル、G…先端に円板状の通電端子(H)を有す
る棒状スピンドル、H…円板端子、I…床義歯固
定粘着剤の湿潤ゲルの表面。
FIG. 1 shows an apparatus for measuring the adhesive force of a denture fixing adhesive, and FIGS. 2 and 3 show an apparatus for measuring the viscoelastic force Px 2 of a wet gel of the denture fixing adhesive. A...Cow bedding skin piece (3 x 3cm2 ), B...Denture fixing adhesive, C...Stainless steel spindle with a disc ( 2cm2 ) attached to the tip, D...Thermostatic cell capable of circulating running water at 37°C (capacity 100ml), E...Connection support part to Fudo Kogyo rheometer, F...Stainless steel needle spindle, G...rod-shaped spindle with a disc-shaped current terminal (H) at the tip, H...disc terminal, I... Surface of wet gel of denture fixing adhesive.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリアクリル酸金属塩の粉末を含有すること
を特徴とする床義歯固定粘着剤。
1. A denture fixing adhesive characterized by containing powder of polyacrylic acid metal salt.
JP11117278A 1978-09-09 1978-09-09 Floor false tooth fixing adhesive Granted JPS5538143A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11117278A JPS5538143A (en) 1978-09-09 1978-09-09 Floor false tooth fixing adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11117278A JPS5538143A (en) 1978-09-09 1978-09-09 Floor false tooth fixing adhesive

Publications (2)

Publication Number Publication Date
JPS5538143A JPS5538143A (en) 1980-03-17
JPS6254502B2 true JPS6254502B2 (en) 1987-11-16

Family

ID=14554299

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11117278A Granted JPS5538143A (en) 1978-09-09 1978-09-09 Floor false tooth fixing adhesive

Country Status (1)

Country Link
JP (1) JPS5538143A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4465517A (en) * 1983-08-01 1984-08-14 Hercules Incorporated Denture adhesive composition
CA1263790A (en) * 1983-08-01 1989-12-05 Armand Joseph Desmarais Denture adhesive composition
JPH0340304Y2 (en) * 1984-10-26 1991-08-23

Also Published As

Publication number Publication date
JPS5538143A (en) 1980-03-17

Similar Documents

Publication Publication Date Title
US4767787A (en) Sheet-shape adhesive preparation
JP2821967B2 (en) Composition for relieving and removing tooth hypersensitivity
TWI327474B (en) Kit for preparation of carbon dioxide agent for external use.
JP3179102B2 (en) Denture stabilizing composition with improved retention
JPS62123133A (en) Preparation of dry carrier for controlled long life blended medicine and dry carrier thereby
JPS6185315A (en) Sheet-like preparation
US4842846A (en) Superoxide dismutase composition for periodontal use
EP0563275B1 (en) Denture stabilizing compositions having improved hold
PT93958B (en) METHOD FOR PREPARING A MIXED PARTIAL SALT OF ETHER COPOLYMER (LOWER) VINYL-MALEIC ACID AND OF DENTIFICAL STABILIZING COMPOSITIONS THAT CONTAIN IT
US3511791A (en) Denture adherent preparation
JP3545162B2 (en) Oral composition
US4436720A (en) Granulated treatment-and-prophylactic dental preparation possessing anticarious effect
JPS6254502B2 (en)
PT97174A (en) Process for the preparation of an adhesive composition comprising a polymeric organic adhesive and a polymer substituted with amine
US3868339A (en) Denture adhesive preparation
EP1396252B1 (en) Denture adhesive comprising carboxymethylcellulose and calcium sulfate
JP2002000626A (en) Denture adhesive
JP4746549B2 (en) Denture stabilizing composition
JP3042917B2 (en) Pastes and paste formulations
HU213849B (en) Preparation with improved taste for stabilizing artificial teeth
JPH04317656A (en) Cement composition
JP2016158665A (en) Denture stabilizer
JPH0265865A (en) Medical or dental curable composition
JP2914466B2 (en) Denture stabilizer
JP6009256B2 (en) Denture stabilizer