JP2004113332A - Dental alginate impression material for dentistries - Google Patents

Dental alginate impression material for dentistries Download PDF

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Publication number
JP2004113332A
JP2004113332A JP2002278728A JP2002278728A JP2004113332A JP 2004113332 A JP2004113332 A JP 2004113332A JP 2002278728 A JP2002278728 A JP 2002278728A JP 2002278728 A JP2002278728 A JP 2002278728A JP 2004113332 A JP2004113332 A JP 2004113332A
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impression material
alginate impression
dental alginate
weight
dental
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JP2002278728A
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JP4159839B2 (en
Inventor
Takashi Kanbara
蒲原 敬
Nobutaka Watanabe
渡邉 信孝
Makiko Takeo
竹尾 万紀子
Hiroki Naito
内藤 裕樹
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GC Corp
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GC Corp
GC Dental Industiral Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a dental alginate impression material that solves inconvenience in terms of the kneadability and storage stability of a dental alginate impression material used for collecting the impressions of an oral cavity in a dentistry, can be uniformly mixed in a short time because powder does not easily coagulate when the dental alginate impression material powder and water are mixed and kneaded into a uniform paste, less strongly resists during kneading, and has a good storage stability before use. <P>SOLUTION: This dental alginate impression material is made by adding a 0.05 to 10 w.t.% nonreactive organopolysiloxane and a 0.01 to 10 w.t.% nonionic surface active agent to the dental alginate impression material including an alginate, a gelation reaction agent, a gelation regulator and a filler. <P>COPYRIGHT: (C)2004,JPO

Description

【0001】
【産業上の利用分野】
本発明は、歯科において口腔内の印象採得を行うために用いる歯科用アルギン酸塩印象材に関するものである。更に詳細には、粉末状の歯科用アルギン酸塩印象材と水とを混合・練和し、均一なペーストにする際に粉末同士が凝集し難く、短時間に均一に混合でき、練和時の抵抗が小さく、しかも使用前の保存安定性が良好な歯科用アルギン酸塩印象材に関するものである。
【0002】
【従来の技術】
歯科において補綴物作製の際に口腔内の印象を採得する印象材としては、歯科用アルギン酸塩印象材が広く用いられている。この歯科用アルギン酸塩印象材は、通常、アルギン酸塩,ゲル化反応剤,ゲル化調整剤及び充填材を含む粉末状であり、使用時に水と練和することによりゲル状に変化し硬化する。この際、最も練和の操作性が高く且つ硬化後に高い諸性能が得られるように歯科用アルギン酸塩印象材の粉末の量及び練和に必要とされる水の量がそれぞれの歯科用アルギン酸塩印象材について規定されている。
【0003】
しかし、従来の歯科用アルギン酸塩印象材の練和操作は、抵抗が大きく粉末の凝集も生じ易いため、特に熟練していない術者にとっては難しい作業であった。この練和し難いということは、練和物内により多くの練和不良の歯科用アルギン酸塩印象材が残存してしまい硬化後の物性が充分でないことは勿論、未練和物が存在しないように練和すると所定時間内に練和操作が終了せず硬化後の物性に悪影響を与えてしまったりする。特に症例に合わせて術者が水と粉の量を調整して練和する場合に先の問題が顕著となり、設計時の硬化後の性能が発揮できないという問題となる。
【0004】
また、現在使用されている歯科用アルギン酸塩印象材は、保存によって吸湿することによりゲル化時間や練和されたペーストの流動性が変化し易く、保存により品質の安定した練和物が得られ難く、その結果、採得した印象も常に再現性がないという不都合が生じていた。
【0005】
【発明が解決しようとする課題】
本発明は、前記した従来の歯科用アルギン酸塩印象材の練和性,保存安定性に対する不都合を解消し、歯科用アルギン酸塩印象材の粉末と水とを練和する際に粉末が凝集し難く、練和抵抗が小さく、しかも保存安定性に優れた歯科用アルギン酸塩印象材を提供することを課題とする。
【0006】
【問題を解決するための手段】
本発明者らは前記課題を解決すべく鋭意検討を重ねた結果、歯科用アルギン酸塩印象材の粉末の凝集を低下させ且つ練和抵抗を小さくするためには、従来の歯科用アルギン酸塩印象材に非反応性のオルガノポリシロキサン及び非イオン界面活性剤をそれぞれ所定量添加すると効果があることを究明し、またそれと同時に、非反応性のオルガノポリシロキサンを添加することが歯科用アルギン酸塩印象材の保存性も飛躍的に向上させることも究明して本発明を完成したのである。
【0007】
即ち、本発明に係る歯科用アルギン酸塩印象材は、アルギン酸塩,ゲル化反応剤,ゲル化調整剤及び充填材を含む歯科用アルギン酸塩印象材に、非反応性のオルガノポリシロキサンが0.05〜10重量%及び非イオン界面活性剤が0.01〜10重量%添加されていることを特徴とする歯科用アルギン酸塩印象材である。
【0008】
本発明に係る歯科用アルギン酸塩印象材は、従来から用いられているアルギン酸塩,ゲル化反応剤,ゲル化調整剤及び充填材を含む歯科用アルギン酸塩印象材に非反応性のオルガノポリシロキサン及び非イオン界面活性剤をそれぞれ所定量添加することでも得ることができる。
【0009】
従来の歯科用アルギン酸塩印象材とは、アルギン酸塩として、アルギン酸のナトリウム,カリウム,アンモニウム,トリエタノールアミンなどの各塩のような水に可溶な塩の1種以上が通常歯科用アルギン酸塩印象材中に約10〜20重量%含有されており、ゲル化反応剤として2価以上の難溶性の金属塩、好適には硫酸カルシウムの二水塩や半水塩が含有されており、ゲル化調整剤としてナトリウム又はカリウムの各種リン酸塩,ケイ酸塩,炭酸塩,フッ化物などの1種以上が使用されており、また充填材としてケイソウ土,無水ケイ酸,タルク,炭酸カルシウム,パーライトなどの1種以上の粉末が使用されている歯科用アルギン酸塩印象材を示す。
【0010】
本発明に係る歯科用アルギン酸塩印象材に用いる非反応性のオルガノポリシロキサンは、従来の歯科用アルギン酸塩印象材に課題解決のために加える成分の1つである。この非反応性のオルガノポリシロキサンは直鎖状の非反応性のオイルであり、その分子内にケイ素原子に直結した有機基を有する。しかし、この非反応性のオルガノポリシロキサンは他の成分やオルガノポリシロキサン同士が反応しないことにより効果を発揮するため、含まれる有機基は、例えば、メチル基,エチル基などのアルキル基、フェニル基,メチルフェニル基,高級脂肪酸,メチルスチリル,ポリエーテルなど非反応性の置換基であることが必要である。
【0011】
この非反応性のオルガノポリシロキサンは、歯科用アルギン酸塩印象材の粉末粒子の凝集を著しく低下させる効果があり、後述する非イオン系界面活性剤と共に用いることにより水と練和する際に抵抗を少なくして容易に練和することを可能とする。更に、この非反応性のオルガノポリシロキサンは、保存中にアルギン酸塩の吸湿を低減させる効果もあるため、歯科用アルギン酸塩印象材の保存安定性を向上させる効果を持つ。この非反応性のオルガノポリシロキサンは、歯科用アルギン酸塩印象材中に0.05〜10重量%含有される。0.05重量%未満であると歯科用アルギン酸塩印象材の粉末の凝集を防止する効果及び保存安定性が充分ではなく、10重量%を超えると歯科用アルギン酸塩印象材の粉末の撥水作用が大きくなりすぎて水と練和する際の粉末への水の浸透が著しく低下して練和し難くなる。
【0012】
本発明においては非イオン界面活性剤を非反応性のオルガノポリシロキサンと共に添加する。この非イオン界面活性剤は、非反応性のオルガノポリシロキサンと共に用いることにより歯科用アルギン酸塩印象材の粉末粒子が凝集することを防ぐと共に練和時の抵抗を低減することを可能とする。非イオン界面活性剤としては、例えば、ポリオキシエチレンアルキルエーテル,ポリオキシエチレンアルキルフェニルエーテル,ポリオキシエチレンポリオキシエチレンブロックコポリマーのようなエーテル型、グリセリンエステルのポリオキシエチレンエーテル,ソルビタンエステルのポリオキシエチレンエーテルのようなエーテルエステル型、ポリエチレングリコール脂肪酸エステルのようなエステル型、ポリオキシエチレン脂肪酸アミドのような含窒素型の非イオン界面活性剤を例示できる。この非イオン界面活性剤は、歯科用アルギン酸塩印象材中に0.01〜10重量%含有される。0.01重量%未満であると歯科用アルギン酸塩印象材の粉末が凝集し易くなり練和抵抗も大きくなる。また、10重量%を超えると保存安定性が低下してしまうばかりでなく、印象採得した後に石こうを注入して作製した模型の表面性状が悪化してしまう。
【0013】
本発明に係る歯科用アルギン酸塩印象材は、本発明の特性を失わない範囲で各種の無機あるいは有機の着色剤,流動パラフィン,ポリプロピレングリコール等の液状成分,各種消毒剤,香料等を含有しても良いのは勿論である。
【0014】
【実施例】
次に本発明について実施例を挙げ詳細に説明するが、本発明はこれ等に限定されるものではない。
【0015】
<実施例1>
アルギン酸塩として、
アルギン酸ナトリウム           13重量%
ゲル化反応剤として、
硫酸カルシウム二水塩           13重量%
ゲル化調整剤として、
ピロリン酸ナトリウム            1重量%
弗化チタン酸カリウム            1重量%
充填材として、
ケイソウ土                70重量%
非反応性のオルガノポリシロキサンとして、
メチルフェニルポリシロキサン        1重量%
非イオン界面活性剤として、
モノオレイン酸ポリオキシエチレンソルビタン 1重量%
の各成分をブレンダー中で充分に混合して歯科用アルギン酸塩印象材の粉末を得た。
【0016】
前記歯科用アルギン酸塩印象材の粉末17gと水40ccとを計量し、歯科用ラバーカップにてスパチュラを用いて同一人が均等な条件で練和を開始し、粉末の凝集であるダマを目視にて観察し、このダマが消失するまでの時間を測定した。また、この練和時の抵抗を後述する比較例1でもある市販の歯科用アルギン酸塩印象材(製品名:アローマファインDFIII,ジーシー社製)と比較して官能的に評価し、このアローマファインDFIIIより明らかに練和抵抗が小さいものを「良」とし、同等又は高いものを「不良」とした。保存安定性の試験は、歯科用アルギン酸塩印象材の粉末1kgをアルミパックに入れ、60℃,湿度100%の環境下に1週間放置し、JIST6505に従いゲル化時間を測定し、保存試験開始前のゲル化時間と比較した。結果を表1に示す。
【0017】
<実施例2>
アルギン酸塩として、
アルギン酸ナトリウム          14重量%
ゲル化反応剤として、
硫酸カルシウム二水塩          15重量%
ゲル化調整剤として、
ピロリン酸ナトリウム           1重量%
弗化チタン酸カリウム           1重量%
充填材として、
ケイソウ土               54重量%
非反応性のオルガノポリシロキサンとして、
メチルスチリル変性ポリシロキサン     8重量%
非イオン界面活性剤として、
ポリオキシエチレンノニルフェニルエーテル 7重量%
の各成分をブレンダー中で充分に混合して、歯科用アルギン酸塩印象材の粉末を得た。実施例1と同様の試験を行い結果を表1に示す。
【0018】
<実施例3>
アルギン酸塩として、
アルギン酸ナトリウム          13重量%
ゲル化反応剤として、
硫酸カルシウム二水塩          14重量%
ゲル化調整剤として、
弗化チタン酸カリウム           1重量%
ピロリン酸ナトリウム           1重量%
充填材として、
ケイソウ土              70.7重量%
非反応性のオルガノポリシロキサンとして、
ジメチルポリシロキサン         0.2重量%
非イオン界面活性剤として、
ポリオキシエチレンアルキルエーテル   0.1重量%
の各成分をブレンダー中で充分に混合して、歯科用アルギン酸塩印象材の粉末を得た。実施例1と同様の試験を行い結果を表1に示す。
【0019】
<実施例4>
アルギン酸塩として、
アルギン酸ナトリウム          14重量%
ゲル化反応剤として、
硫酸カルシウム二水塩          15重量%
ゲル化調整剤として、
ピロリン酸ナトリウム           1重量%
弗化チタン酸カリウム           1重量%
充填材として、
ケイソウ土              64.5重量%
非反応性のオルガノポリシロキサンとして、
メチルフェニルポリシロキサン       3重量%
非イオン界面活性剤として、
ポリオキシエチレンアルキルエーテル    1重量%
その他の成分として、
流動パラフィン             0.5重量%
の各成分をブレンダー中で充分に混合して、歯科用アルギン酸塩印象材の粉末を得た。実施例1と同様の試験を行い結果を表1に示す。
【0020】
<比較例1>
市販の歯科用アルギン酸塩印象材(製品名:アローマファインDFIII,ジーシー社製)を用いメーカー指定の粉末と水の比にて計量・練和し、実施例と同様の試験を行った。結果を表1に示す。
【0021】
<比較例2>
アルギン酸塩として、
アルギン酸ナトリウム          15重量%
ゲル化反応剤として、
硫酸カルシウム二水塩          15重量%
ゲル化調整剤として、
ピロリン酸ナトリウム           1重量%
弗化チタン酸カリウム           1重量%
充填材として、
ケイソウ土               68重量%
の各成分をブレンダー中で充分に混合して、歯科用アルギン酸塩印象材の粉末を得た。実施例1と同様の試験を行い結果を表1に示す。
【0022】
【表1】

Figure 2004113332
【0023】
表1から明らかなように、本発明に係る歯科用アルギン酸塩印象材は、粉末と水とを練和する際にダマが練和早期に消失し、練和抵抗も市販品である比較例1よりも小さいので非常に練和し易いことが確認できた。また、保存性においても、60℃,湿度100%,1週間という環境下においてゲル化時間の遅延は生じないか、ごく僅かな時間しか生じないことから保存安定性は良好であることが判った。
【0024】
【発明の効果】
以上に詳述した如く、本発明に係る歯科用アルギン酸塩印象材は、歯科用アルギン酸塩印象材の粉末と水とを混合・練和しペーストにする際に、粉末同士が凝集し難く、短時間に均一に混合でき、更に練和時の抵抗が小さく練和し易い。更に、歯科用アルギン酸塩印象材としての保存安定性が良好であるため経時変化によるゲル化時間のばらつき・遅延をも防止することが可能な歯科用アルギン酸塩印象材であり、歯科医療に貢献する価値の大なるものである。[0001]
[Industrial applications]
The present invention relates to a dental alginate impression material used for obtaining an oral impression in dentistry. More specifically, the powdered dental alginate impression material and water are mixed and kneaded, and when a uniform paste is formed, the powders are unlikely to agglomerate and can be uniformly mixed in a short time. The present invention relates to a dental alginate impression material having low resistance and good storage stability before use.
[0002]
[Prior art]
Alginate impression materials for dental use are widely used as impression materials for obtaining an impression in the oral cavity when a prosthesis is made in dentistry. This dental alginate impression material is usually in the form of a powder containing an alginate, a gelling agent, a gelling agent and a filler, and changes into a gel state and hardens when mixed with water at the time of use. At this time, the amount of the powder of the dental alginate impression material and the amount of water required for the kneading are adjusted to the respective dental alginate so as to obtain the highest operability in kneading and high performance after curing. It is specified for impression materials.
[0003]
However, the kneading operation of a conventional dental alginate impression material is a difficult operation, especially for an unskilled operator, because of the high resistance and the tendency of powder agglomeration to occur. This difficulty in kneading means that a lot of poorly kneaded dental alginate impression material remains in the kneaded material and the physical properties after curing are not sufficient, and of course, there is no unmixed material. When kneading, the kneading operation is not completed within a predetermined time, which may adversely affect the physical properties after curing. In particular, when the surgeon adjusts the amounts of water and powder according to the case and kneads them, the above problem becomes remarkable, and the performance after curing at the time of design cannot be exhibited.
[0004]
In addition, the dental alginate impression material currently used tends to change the gelation time and the fluidity of the kneaded paste by absorbing moisture during storage, and a kneaded material of stable quality can be obtained by storage. As a result, there has been a disadvantage that the obtained impression is not always reproducible.
[0005]
[Problems to be solved by the invention]
The present invention eliminates the disadvantages of the conventional dental alginate impression material for kneadability and storage stability described above, and makes it difficult for the powder of the dental alginate impression material to agglomerate when kneaded with water. Another object of the present invention is to provide a dental alginate impression material having low kneading resistance and excellent storage stability.
[0006]
[Means to solve the problem]
The present inventors have conducted intensive studies to solve the above problems, and as a result, in order to reduce the agglomeration of the powder of the dental alginate impression material and to reduce the kneading resistance, a conventional dental alginate impression material was used. It has been found that it is effective to add a predetermined amount of a non-reactive organopolysiloxane and a non-ionic surfactant to each other, and at the same time, adding a non-reactive organopolysiloxane to a dental alginate impression material. The present invention was completed by investigating that the preservability of the product was also dramatically improved.
[0007]
That is, the dental alginate impression material according to the present invention is a dental alginate impression material containing alginate, a gelling agent, a gelling modifier and a filler, and a non-reactive organopolysiloxane containing 0.05%. An alginate impression material for dental use, wherein 10 to 10% by weight of a nonionic surfactant and 0.01 to 10% by weight of a nonionic surfactant are added.
[0008]
The dental alginate impression material according to the present invention comprises an organopolysiloxane which is non-reactive with a dental alginate impression material containing alginate, a gelling agent, a gelling agent and a filler, which are conventionally used. It can also be obtained by adding a predetermined amount of each of the nonionic surfactants.
[0009]
The conventional dental alginate impression material is usually a dental alginate impression material in which at least one kind of water-soluble salt such as sodium, potassium, ammonium and triethanolamine of alginic acid is used as the alginate. It contains about 10 to 20% by weight in the material and contains a sparingly soluble metal salt having a valency of 2 or more, preferably a dihydrate or hemihydrate of calcium sulfate, as a gelling agent. At least one of sodium or potassium phosphates, silicates, carbonates, fluorides and the like is used as a regulator, and diatomaceous earth, silicic anhydride, talc, calcium carbonate, perlite, etc. are used as fillers. 1 shows a dental alginate impression material in which one or more powders of the formula (1) are used.
[0010]
The non-reactive organopolysiloxane used in the dental alginate impression material of the present invention is one of the components added to the conventional dental alginate impression material to solve the problem. This non-reactive organopolysiloxane is a linear non-reactive oil and has an organic group directly bonded to a silicon atom in the molecule. However, since this non-reactive organopolysiloxane exerts its effect by preventing other components or organopolysiloxanes from reacting with each other, the organic groups contained therein include, for example, an alkyl group such as a methyl group and an ethyl group, and a phenyl group. , Methylphenyl group, higher fatty acid, methylstyryl, polyether, etc.
[0011]
This non-reactive organopolysiloxane has an effect of remarkably reducing the agglomeration of powder particles of the dental alginate impression material, and when used together with a nonionic surfactant described later, the resistance to kneading with water is reduced. It is possible to mix easily with less. Furthermore, since this non-reactive organopolysiloxane also has the effect of reducing the moisture absorption of alginate during storage, it has the effect of improving the storage stability of the dental alginate impression material. The non-reactive organopolysiloxane is contained in the dental alginate impression material in an amount of 0.05 to 10% by weight. If it is less than 0.05% by weight, the effect of preventing agglomeration of the powder of the dental alginate impression material and the storage stability are not sufficient. If it exceeds 10% by weight, the water repellency of the powder of the dental alginate impression material is obtained. Becomes too large and the penetration of water into the powder when kneading with water is significantly reduced, making it difficult to knead.
[0012]
In the present invention, a nonionic surfactant is added together with a non-reactive organopolysiloxane. The use of this nonionic surfactant together with a non-reactive organopolysiloxane makes it possible to prevent the powder particles of the dental alginate impression material from agglomerating and to reduce the resistance during kneading. Examples of the nonionic surfactant include ether type such as polyoxyethylene alkyl ether, polyoxyethylene alkyl phenyl ether and polyoxyethylene polyoxyethylene block copolymer, polyoxyethylene ether of glycerin ester and polyoxyethylene of sorbitan ester. Examples thereof include ether ester types such as ethylene ether, ester types such as polyethylene glycol fatty acid esters, and nitrogen-containing nonionic surfactants such as polyoxyethylene fatty acid amide. This nonionic surfactant is contained in the dental alginate impression material in an amount of 0.01 to 10% by weight. If the amount is less than 0.01% by weight, the powder of the dental alginate impression material is likely to aggregate and the kneading resistance is increased. If the content exceeds 10% by weight, not only does storage stability deteriorate, but also the surface properties of a model prepared by injecting gypsum after taking an impression deteriorate.
[0013]
The dental alginate impression material according to the present invention contains various inorganic or organic coloring agents, liquid components such as liquid paraffin, polypropylene glycol, various disinfectants, fragrances, etc. within a range not to lose the characteristics of the present invention. Of course, it is good.
[0014]
【Example】
Next, the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples.
[0015]
<Example 1>
As alginate,
13% by weight of sodium alginate
As a gelling reagent,
13% by weight calcium sulfate dihydrate
As a gelling modifier,
Sodium pyrophosphate 1% by weight
1% by weight of potassium fluorotitanate
As a filler,
Diatomaceous earth 70% by weight
As a non-reactive organopolysiloxane,
1% by weight of methylphenylpolysiloxane
As a nonionic surfactant,
Polyoxyethylene sorbitan monooleate 1% by weight
These components were thoroughly mixed in a blender to obtain a powder of a dental alginate impression material.
[0016]
17 g of the powder of the dental alginate impression material and 40 cc of water are weighed, and the same person starts kneading under a uniform condition using a spatula in a dental rubber cup. And the time until the lumps disappeared was measured. The resistance at the time of kneading was sensually evaluated in comparison with a commercially available dental alginate impression material (product name: Aromafine DFIII, manufactured by GC Corporation) which is also Comparative Example 1 to be described later. More clearly, the one with a low kneading resistance was defined as “good”, and the one with equal or higher kneading resistance was defined as “bad”. For the storage stability test, 1 kg of dental alginate impression material powder was placed in an aluminum pack, left for 1 week in an environment of 60 ° C. and 100% humidity, and the gelation time was measured according to JIST6505. Was compared with the gelation time. Table 1 shows the results.
[0017]
<Example 2>
As alginate,
Sodium alginate 14% by weight
As a gelling reagent,
15% by weight calcium sulfate dihydrate
As a gelling modifier,
Sodium pyrophosphate 1% by weight
1% by weight of potassium fluorotitanate
As a filler,
Diatomaceous earth 54% by weight
As a non-reactive organopolysiloxane,
8% by weight of methylstyryl-modified polysiloxane
As a nonionic surfactant,
7% by weight of polyoxyethylene nonyl phenyl ether
Were thoroughly mixed in a blender to obtain powder of a dental alginate impression material. The same test as in Example 1 was performed, and the results are shown in Table 1.
[0018]
<Example 3>
As alginate,
13% by weight of sodium alginate
As a gelling reagent,
14% by weight calcium sulfate dihydrate
As a gelling modifier,
1% by weight of potassium fluorotitanate
Sodium pyrophosphate 1% by weight
As a filler,
Diatomaceous earth 70.7% by weight
As a non-reactive organopolysiloxane,
Dimethylpolysiloxane 0.2% by weight
As a nonionic surfactant,
0.1% by weight of polyoxyethylene alkyl ether
Were thoroughly mixed in a blender to obtain powder of a dental alginate impression material. The same test as in Example 1 was performed, and the results are shown in Table 1.
[0019]
<Example 4>
As alginate,
Sodium alginate 14% by weight
As a gelling reagent,
15% by weight calcium sulfate dihydrate
As a gelling modifier,
Sodium pyrophosphate 1% by weight
1% by weight of potassium fluorotitanate
As a filler,
Diatomaceous earth 64.5% by weight
As a non-reactive organopolysiloxane,
Methylphenyl polysiloxane 3% by weight
As a nonionic surfactant,
1% by weight of polyoxyethylene alkyl ether
As other ingredients,
Liquid paraffin 0.5% by weight
Were thoroughly mixed in a blender to obtain powder of a dental alginate impression material. The same test as in Example 1 was performed, and the results are shown in Table 1.
[0020]
<Comparative Example 1>
A commercially available dental alginate impression material (product name: Aroma Fine DFIII, manufactured by GC Corporation) was weighed and kneaded at a powder / water ratio specified by the manufacturer, and the same test as in the example was performed. Table 1 shows the results.
[0021]
<Comparative Example 2>
As alginate,
Sodium alginate 15% by weight
As a gelling reagent,
15% by weight calcium sulfate dihydrate
As a gelling modifier,
Sodium pyrophosphate 1% by weight
1% by weight of potassium fluorotitanate
As a filler,
Diatomaceous earth 68% by weight
Were thoroughly mixed in a blender to obtain a powder of a dental alginate impression material. The same test as in Example 1 was performed, and the results are shown in Table 1.
[0022]
[Table 1]
Figure 2004113332
[0023]
As is clear from Table 1, in the dental alginate impression material of the present invention, when kneading powder and water, the lumps disappeared at the early stage of kneading, and the kneading resistance was a commercial product. It was confirmed that it was very easy to mix because it was smaller. In addition, regarding the storage stability, under the environment of 60 ° C., 100% humidity and one week, the gelation time did not delay or occurred only for a very short time, indicating that the storage stability was good. .
[0024]
【The invention's effect】
As described in detail above, the dental alginate impression material according to the present invention is such that when powder and water of the dental alginate impression material are mixed and kneaded to form a paste, the powders are less likely to agglomerate and have a short duration. Mixing can be performed uniformly over time, and the resistance during kneading is small and kneading is easy. Furthermore, since the storage stability as a dental alginate impression material is good, it is a dental alginate impression material that can also prevent dispersion and delay of gel time due to aging, and contribute to dental care. It is of great value.

Claims (1)

アルギン酸塩,ゲル化反応剤,ゲル化調整剤及び充填材を含む歯科用アルギン酸塩印象材に、非反応性のオルガノポリシロキサンが0.05〜10重量%及び非イオン界面活性剤が0.01〜10重量%添加されていることを特徴とする歯科用アルギン酸塩印象材。In a dental alginate impression material containing an alginate, a gelling agent, a gelling agent and a filler, 0.05 to 10% by weight of a non-reactive organopolysiloxane and 0.01 of a nonionic surfactant are added. An alginate impression material for dental use, which is added in an amount of from 10 to 10% by weight.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014017360A1 (en) * 2012-07-25 2014-01-30 株式会社トクヤマデンタル Hardening paste and kit for preparing alginate curable composition
JP2015040194A (en) * 2013-08-22 2015-03-02 株式会社トクヤマデンタル Method for preparing alginate hardenability composition
CN114481010A (en) * 2021-12-30 2022-05-13 西安九洲生物材料有限公司 Method for improving surface hardness and mechanical property of metal dental medical instrument

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014017360A1 (en) * 2012-07-25 2014-01-30 株式会社トクヤマデンタル Hardening paste and kit for preparing alginate curable composition
JPWO2014017360A1 (en) * 2012-07-25 2016-07-11 株式会社トクヤマデンタル Hardener paste and alginate curable composition preparation kit
JP2015040194A (en) * 2013-08-22 2015-03-02 株式会社トクヤマデンタル Method for preparing alginate hardenability composition
CN114481010A (en) * 2021-12-30 2022-05-13 西安九洲生物材料有限公司 Method for improving surface hardness and mechanical property of metal dental medical instrument

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