JP2009292762A - Curable composition for dental use - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a curable composition for dental use, curing a polymerizable monomer by reacting an oxidant with a reducing agent, excellent in bonding property, also having a suitable practical operable time and further having the small changes of them toward the change of acidity of the composition caused by the change of paste-mixing ratios. <P>SOLUTION: This separate package type curable composition for dental use consisting of a first paste (A) and a second paste (B) is provided with that the both of the pastes contain a polymerizable monomer (a) without having an acidic group, any one of the pastes contains further an acid group-containing polymerizable monomer (b), and further either one of the pastes contains hydroperoxide (c) and another one contains a specific substituted cyclic thiourea compound (d) respectively. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a dental curable composition. More specifically, the present invention relates to a dental curable composition having excellent adhesiveness and an appropriate operation time.

  A curable composition comprising a polymerizable monomer and a radical polymerization initiator is widely used in various applications such as paints, printing materials, adhesives, model materials, and sealing materials. Among these, in the field of dentistry, those using (meth) acrylate polymerizable monomers as polymerizable monomers are put to practical use in dental cements, dental adhesives, composite resins, dental room temperature polymerization resins, etc. Has been.

  As the radical polymerization initiator, a combination of an oxidizing agent and a reducing agent is generally used. By mixing these, a so-called redox reaction occurs, radicals are generated, a polymerization reaction is started, and curing proceeds.

  Specific examples include a combination in which the oxidizing agent is benzoyl peroxide and the reducing agent is an amine compound. However, benzoyl peroxide has poor thermal stability because of its low thermal stability, and handling properties such as refrigeration are essential. In addition, since amine compounds are easily changed to colored substances due to chemical changes, they have the disadvantages that they are difficult to use where aesthetics are required, such as dental use, due to their ease of coloring. ing.

  In addition, since the redox reaction of benzoyl peroxide and an amine compound has a slow reaction rate, when such a combination is used, the curing rate (polymerization reaction rate) is slow in the curable composition, and the adhesiveness is low in the adhesive. Etc. becomes a problem.

Then, the combination of a hydroperoxide and a thiourea compound is disclosed as a radical polymerization initiator which solves the said subject (refer patent documents 1 and 2). Since hydroperoxide has higher thermal stability than benzoyl peroxide and the like, it can be stored for a long time even at room temperature. In addition, since thiourea compounds are not easily colored like amine compounds, there are few restrictions on their use.
US2003 / 0134933 JP 2007-56020 A

  However, although the combination of hydroperoxide and thiourea compound has the above-mentioned merit, the following problems can be mentioned. That is, when unsubstituted thiourea, N-allylthiourea, trimethylthiourea, acetylthiourea, etc. as described in Patent Documents 1 and 2 are used as the thiourea compound, it is more acidic than the combination of benzoyl peroxide and amine compound. The activity of the redox reaction is increased under the conditions, but the activity is still not sufficient. Therefore, when a combination of hydroperoxide and the thiourea compound is used, there is a problem that the curing rate of the curable composition and the adhesive strength of the adhesive are not yet satisfactory.

  In addition, in order to increase the reliability of dental materials, especially dental cement, it is desired that the adhesive strength to the tooth material and the dental restoration material is excellent. It is more desirable that the adhesive strength is excellent. In addition, in dental cement, in addition to excellent adhesive strength, practically, the operation time (the time from the start of mixing each paste containing an oxidizing agent and a reducing agent to the start of curing, ie, the paste After mixing, it is desired that the time during which the paste can be bonded to dentin or the like is appropriate, and it is necessary to be able to satisfy both of these characteristics.

  Therefore, as a method for solving the problems of the curing speed and the adhesive strength when the thiourea compound is used, a method of increasing the reaction rate of the redox reaction by increasing the concentration of the reducing agent and oxidizing agent to be used can be considered. However, there are cases where the solubility is limited, and the storage stability of the paste may be significantly deteriorated, and it is difficult to adjust to a desired speed.

  As dental materials, curable compositions such as self-adhesive, so-called self-adhesive cement, or composite resin are in practical use. These materials include an acidic substance, from the viewpoint of increasing the adhesive strength by increasing the affinity between the curable composition and the adherend by decalcifying, that is, partially dissolving the apatite component of the tooth. Alternatively, an acidic group-containing polymerizable monomer is contained and the acidity is high. Usually, the redox reaction of hydroperoxide and a thiourea compound varies greatly in reaction rate depending on the acidity of the reaction system. Therefore, since the curing rate of a curable composition containing such a compound varies depending on the acidity of the composition, when the mixing ratio of the two pastes is different at the time of paste mixing, the operable time varies, and the adhesive strength There is also a complicated aspect that it is easy to fluctuate.

  An object of the present invention is to provide a composition that cures a polymerizable monomer by reacting an oxidizing agent and a reducing agent, has excellent adhesiveness, and has a reasonable practical operation time. It is an object of the present invention to provide a dental curable composition in which those variations are small relative to variations in the acidity of the composition due to variations.

  As a result of continual research to solve the above-mentioned problems, the present inventors contain an acidic group-containing polymerizable monomer as a polymerizable monomer, and hydroperoxide as an oxidant that is a polymerization initiator. In a dental curable composition, it discovered that said subject could be solved by using the substituted cyclic thiourea compound which has a specific structure as a reducing agent which is a polymerization initiator, and came to complete this invention.

  That is, the present invention relates to a packaged dental curable composition comprising a first paste (A) and a second paste (B), in which none of the pastes has an acidic group. And any one of the pastes further contains an acidic group-containing polymerizable monomer (b), and any one of the pastes further comprises a hydroperoxide (c). ), The other is the formula (I):

(In the formula, R represents an alkylene group having 2 to 5 carbon atoms or a chain group having 2 to 5 atoms containing any of N, O, and S).
And a packaged dental curable composition each containing a substituted cyclic thiourea compound (d).

  The dental curable composition of the present invention can achieve both high adhesiveness and an appropriate operation time, and further, the reaction activity variation between the oxidizing agent and the reducing agent is small with respect to the variation in the acidity of the composition. Therefore, it has an excellent effect that the fluctuation of these characteristics is small with respect to the fluctuation of the paste mixing ratio.

  The present invention relates to a packaged dental curable composition comprising a first paste (A) and a second paste (B), wherein none of the pastes has a polymerizable monomer ( a), and one of the pastes further contains an acidic group-containing polymerizable monomer (b), and one of the pastes further contains hydroperoxide (c) and the other is substituted cyclic. A packaged dental curable composition containing a thiourea compound (d), which is characterized in that the substituted cyclic thiourea compound (d) is a compound having a specific structure.

  The substituted cyclic thiourea compound used in the present invention has the formula (I):

(In the formula, R represents an alkylene group having 2 to 5 carbon atoms, or a chain group having 2 to 5 atoms containing any of N, O, and S).
It has the structure represented by these. Since the substituted cyclic thiourea compound having such a structure has a planar structure, the reaction activity with hydroperoxide can be increased, and as a result, high adhesiveness and appropriate operation time can be achieved. Can be compatible.

  In addition, since the substituted cyclic thiourea compound having the above structure has a planar structure in the same manner as in the neutral condition even under the acidic condition, the acidity of the composition, that is, the contained acidic substance or The fluctuation in the reaction activity between the hydroperoxide and the substituted cyclic thiourea compound becomes small with respect to the presence or absence of the acidic group-containing polymerizable monomer or the fluctuation in the content. As a result, the operable time of the resulting composition (the time from the start of mixing of the paste containing the oxidizing agent and the reducing agent to the start of curing, that is, after mixing the paste, It is presumed that the fluctuation of the operable time due to the fluctuation of the paste mixing ratio in the time during which the bonding operation can be performed becomes small, and further the fluctuation of the adhesive strength also becomes small.

  Furthermore, since the activity of the redox reaction between the hydroperoxide and the substituted cyclic thiourea compound is high, an excellent effect that the content of the polymerization initiator in the composition can be reduced is also obtained.

  Each of the first paste (A) and the second paste (B) in the present invention contains a polymerizable monomer (a) having no acidic group, and any one of the pastes. One further contains an acidic group-containing polymerizable monomer (b), and one of the pastes further contains a hydroperoxide (c), and the other contains the substituted cyclic thiourea compound (d). .

  As the polymerizable monomer having no acidic group (a), without having an acidic group such as a phosphoric acid group, a pyrophosphoric acid group, a thiophosphoric acid group, a phosphonic acid group, a sulfonic acid group, and a carboxylic acid group, If it is a radically polymerizable monomer which has a polymeric group, there will be no limitation in particular. Preferable examples of such compounds include those having an acryloyl group or a methacryloyl group. In this specification, “(meth) acryl” is a general term for methacryl and acryl.

  Specific examples include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, glycidyl (meth) acrylate, and 2-hydroxyethyl (meth) acrylate as monofunctional ones. (2-hydroxyethyl methacrylate may hereinafter be referred to as HEMA), 3-hydroxypropyl (meth) acrylate, 3-chloro-2-hydroxypropyl (meth) acrylate, etc. are aliphatic bifunctional As ethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, 1,2-bis [3- (meth) acryloyloxy- 2- Droxypropoxy] ethane, 1,6-hexanediol di (meth) acrylate, 1,10-decanediol di (meth) acrylate and the like are aromatic bifunctional ones such as 2,2-bis [4- ( (Meth) acryloyloxypolyethoxyphenyl] propane, 2,2-bis [4- (meth) acryloyloxydiethoxyphenyl]] propane, 2,2-bis [4- (3- (meth) acryloyloxy) -2- Hydroxypropoxyphenyl] propane (2,2-bis [4- (3-methacryloyloxy) -2-hydroxypropoxyphenyl] propane may hereinafter be referred to as Bis-GMA), and the like. For example, pentaerythritol tri (meth) acrylate is a polyfunctional one such as 1,7-di (me ) Acryloyloxy-2,2,6,6-tetra (meth) acryloyloxy-methyl-4-oxa-heptane dipentaerythritol hexa (meth) acrylate. These may be used alone or in combination of two or more. Among these, Bis-GMA, HEMA, neopentylglycol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, 1,10-decanediol di (meth) acrylate are used from the viewpoint of improving adhesive strength. 2,2-bis [4- (meth) acryloyloxydiethoxyphenyl] propane is preferred, and Bis-GMA and HEMA are more preferred.

  The acidic group-containing polymerizable monomer (b) is contained in either one of the first paste (A) and the second paste (B). From the viewpoint of the stability of the paste, the hydropar described later. It is preferably contained in the same paste containing oxide (c).

  The acidic group-containing polymerizable monomer (b) has at least one acidic group such as a phosphoric acid group, a pyrophosphoric acid group, a thiophosphoric acid group, a phosphonic acid group, a sulfonic acid group, and a carboxylic acid group, and , Radical polymerizable monomers having at least one radical polymerizable group (unsaturated group capable of radical polymerization) such as acryloyl group, methacryloyl group, vinyl group and styrene group. The acidic group-containing polymerizable monomer (b) improves the affinity with the adherend and has a decalcifying action on the tooth.

  Examples of phosphoric acid group-containing polymerizable monomers include 2- (meth) acryloyloxyethyl dihydrogen phosphate, 3- (meth) acryloyloxypropyl dihydrogen phosphate, 4- (meth) acryloyloxybutyl dihydrogen phosphate. 5- (meth) acryloyloxypentyl dihydrogen phosphate, 6- (meth) acryloyloxyhexyl dihydrogen phosphate, 7- (meth) acryloyloxyheptyl dihydrogen phosphate, 8- (meth) acryloyloxyoctyl dihydro Genphosphate, 9- (meth) acryloyloxynonyl dihydrogen phosphate, 10- (meth) acryloyloxydecyl dihydrogen phosphate (10-methacryloyloxy) Sildihydrogen phosphate may hereinafter be referred to as MDP), 11- (meth) acryloyloxyundecyl dihydrogen phosphate, 12- (meth) acryloyl oxide decyl dihydrogen phosphate, 16- (meth) Acryloyloxyhexadecyl dihydrogen phosphate, 20- (meth) acryloyloxyecosyl dihydrogen phosphate, bis [2- (meth) acryloyloxyethyl] hydrogen phosphate, bis [4- (meth) acryloyloxybutyl] hydro Gen phosphate, bis [6- (meth) acryloyloxyhexyl] hydrogen phosphate, bis [8- (meth) acryloyloxyoctyl] hydrogen phosphate, bis [9- ( Ta) acryloyloxynonyl] hydrogen phosphate, bis [10- (meth) acryloyloxydecyl] hydrogen phosphate, 1,3-di (meth) acryloyloxypropyl dihydrogen phosphate, 2- (meth) acryloyloxyethylphenyl Hydrogen phosphate, 2- (meth) acryloyloxyethyl-2-bromoethyl hydrogen phosphate, bis [2- (meth) acryloyloxy- (1-hydroxymethyl) ethyl] hydrogen phosphate and acid chlorides thereof, alkali Examples thereof include metal salts and ammonium salts.

  Examples of pyrophosphate group-containing polymerizable monomers include bis [2- (meth) acryloyloxyethyl pyrophosphate], bis [4- (meth) acryloyloxybutyl pyrophosphate], and bis [6- (meth) acryloyl pyrophosphate. Oxyhexyl], bis [8- (meth) acryloyloxyoctyl] pyrophosphate, bis [10- (meth) acryloyloxydecyl] pyrophosphate, and acid chlorides, alkali metal salts, and ammonium salts thereof.

  Examples of the thiophosphate group-containing polymerizable monomer include 2- (meth) acryloyloxyethyl dihydrogen thiophosphate, 3- (meth) acryloyloxypropyl dihydrogen thiophosphate, 4- (meth) acryloyloxybutyl dihydro Genthiophosphate, 5- (meth) acryloyloxypentyl dihydrogenthiophosphate, 6- (meth) acryloyloxyheptyl dihydrogenthiophosphate, 7- (meth) acryloyloxyheptyl dihydrogenthiophosphate, 8- (meta ) Acrylyloxyoctyl dihydrogenthiophosphate, 9- (meth) acryloyloxynonyl dihydrogenthiophosphate, 10- (meth) acryloyloxydecyl dihydrogenthio Sulfate, 11- (meth) acryloyloxyundecyl dihydrogen thiophosphate, 12- (meth) acryloyl oxide decyl dihydrogen thiophosphate, 16- (meth) acryloyloxy hexadecyl dihydrogen thiophosphate, 20- (meth) ) Acrylyloxyeicosyl dihydrogenthiophosphate and acid chlorides, alkali metal salts, ammonium salts thereof and the like.

  Examples of the phosphonic acid group polymerizable monomer include 2- (meth) acryloyloxyethylphenyl phosphate, 5- (meth) acryloyloxypentyl-3-phosphonopropionate, 6- (meth) acryloyloxyhexyl-3- Examples thereof include phosphonoacetate, 10- (meth) acryloyloxydecyl-3-phosphonoacetate and acid chlorides, alkali metal salts, ammonium salts and the like thereof.

  Examples of the sulfonic acid group-containing polymerizable monomer include 2- (meth) acrylamide-2-methylpropane sulfonic acid, styrene sulfonic acid, 2-sulfoethyl (meth) acrylate, and alkali metal salts and ammonium salts thereof. It is done.

  Carboxylic acid group-containing polymerizable monomers include those having one carboxyl group in the molecule, (meth) acrylic acid, N- (meth) acryloylglycine, N- (meth) acryloylaspartic acid, N- ( (Meth) acryloyl-5-aminosalicylic acid, O- (meth) acryloyl tyrosine, N- (meth) acryloyl tyrosine, N- (meth) acryloylphenylalanine, N- (meth) acryloyl-p-aminobenzoic acid, N- (meta ) Acryloyl-o-aminobenzoic acid, p-vinylbenzoic acid, 2- (meth) acryloyloxybenzoic acid, 3- (meth) acryloyloxybenzoic acid, 4- (meth) acryloyloxybenzoic acid, N- (meth) Acryloyl-5-aminosalicylic acid, N- (meth) acryloyl-4-aminosalicylic acid and As these acid halides having a plurality of carboxyl groups in the molecule, 2- (meth) acryloyloxyethyl hydrogen succinate, 2- (meth) acryloyloxyethyl hydrogen phthalate, 2- (meth) acryloyl Oxyethyl hydrogenmalate, 6- (meth) acryloyloxyhexane-1,1-dicarboxylic acid, 9- (meth) acryloyloxynonane-1,1-dicarboxylic acid, 10- (meth) acryloyloxydecane-1,1 -Dicarboxylic acid, 11- (meth) acryloyloxyundecane-1,1-dicarboxylic acid, 12- (meth) acryloyl oxide decane-1,1-dicarboxylic acid, 13- (meth) acryloyloxytridecane-1,1- Dicarboxylic acid, 4- (meth) acryloyl Xylethyl trimellitate, 4- (meth) acryloyloxybutyl trimellitate, 4- (meth) acryloyloxyhexyl trimellitate, 4- (meth) acryloyloxydecyl trimellitate, 2- (meth) acryloyloxyethyl -3 ′-(meth) acryloyloxy-2 ′-(3,4-dicarboxybenzoyloxy) propyl succinate and acid anhydrides or acid halides thereof may be mentioned.

  The acidic group-containing polymerizable monomer may be used alone or in combination of two or more, but MDP is preferable from the viewpoint of improving the adhesive strength with the tooth.

  The curable composition of the present invention contains an acidic group-containing polymerizable monomer because the reaction activity of the hydroperoxide and the substituted cyclic thiourea compound is not easily affected by variations in the acidity of the composition. The amount is not particularly limited, but from the viewpoints of improved adhesiveness and storage stability of the paste, the total polymerizable monomer is preferably 1 to 40% by weight, more preferably 3 to 35% by weight, and still more preferably. 5 to 30% by weight, more preferably 10 to 25% by weight. In the present specification, “totally polymerizable monomer” and “total amount of polymerizable monomer” refer to all polymerizable monomers having no acidic group contained in the curable composition (a ) And the total weight of all acidic group-containing polymerizable monomers (b).

  Polymerization of these polymerizable monomers can be performed according to a known method using the hydroperoxide (c) and the substituted cyclic thiourea compound (d) contained in each paste.

  Hydroperoxide (c) is contained in one of the first paste (A) and the second paste (B), but from the viewpoint of paste stability, an acidic group-containing polymerizable monomer is used. It is preferable to be contained in the contained paste.

  As the hydroperoxide (c) in the present invention, any known one can be used without any limitation as long as it has one or more hydroperoxide groups (—OOH groups) in the molecule. A hydroperoxide having an —OOH group bonded to a tertiary carbon atom is preferred.

  Specific examples include 1,1,3,3-tetramethylbutyl hydroperoxide, cumene hydroperoxide, t-butyl hydroperoxide, t-amyl hydroperoxide, p-menthane hydroperoxide, p-isopropyl group. Examples thereof include mill hydroperoxide, diisopropylbenzene hydroperoxide, and diisopropylbenzene dihydroperoxide. These may be used alone or in combination of two or more.

  The content of the hydroperoxide is preferably 1.0 to 4.0 parts by weight with respect to 100 parts by weight of the total amount of polymerizable monomers, from the viewpoint of improvement in adhesive strength and paste stability. Preferably it is 1.5-3.8 weight part, More preferably, it is 2.0-3.5 weight part.

  The substituted cyclic thiourea compound (d) is contained in one of the first paste (A) and the second paste (B) that does not contain hydroperoxide.

  As the substituted cyclic thiourea compound (d) in the present invention, any known compound can be used without any limitation as long as it has a structure represented by the above formula (I). For example, ethylenethiourea, trimethylene Thiourea, tetramethylenethiourea, pentamethylenethiourea, tetrahydro-4H-1,3,5-oxadiazine-4-thione, tetrahydro-4H-1,3,5-thiadiazine-4-thione, tetrahydro-1,3 , 5-triazine-2 (1H) -thione and the like. These can be used singly or in appropriate combination of two or more, but ethylenethiourea and trimethylenethiourea are preferred from the viewpoint of improvement in adhesive strength and availability. Furthermore, ethylenethiourea is more preferable from the viewpoint of solubility in the polymerizable monomer.

  The content of the substituted cyclic thiourea compound is 100 parts by weight based on the total amount of the polymerizable monomers from the viewpoint of ensuring an appropriate curing rate and the solubility of the substituted cyclic thiourea compound (d) in the polymerizable monomer. Is preferably 0.2 to 1.0 part by weight, more preferably 0.3 to 0.9 part by weight, and still more preferably 0.4 to 0.8 part by weight.

  The curable composition of the present invention comprises a polymerizable monomer (a) having no acidic group, an acidic group-containing polymerizable monomer (b), a hydroperoxide (c), and a substituted cyclic thiourea compound ( In addition to d), known components and additives used for preparing the curable composition may be contained within a range not impairing the effects of the present invention.

  For example, in order to prepare dental materials such as cement and composite resin, inorganic, organic, or organic-inorganic composite fillers are used. The filler is necessary for adjusting the paste properties of the dental material before curing and for increasing the mechanical strength after curing.

  Inorganic fillers include quartz, silica, alumina, silica-titania, silica-titania-barium oxide, silica-zirconia, silica-alumina, lanthanum glass, borosilicate glass, soda glass, barium glass, strontium glass, glass ceramic, alumino Silicate glass, barium boroaluminosilicate glass, strontium boroaluminosilicate glass, fluoroaluminosilicate glass, calcium fluoroaluminosilicate glass, strontium fluoroaluminosilicate glass, barium fluoroaluminosilicate glass, strontium calcium fluoroaluminosilicate glass, or the like is used. These may be used alone or in combination of two or more. The shape of the inorganic filler is not particularly limited, and an amorphous filler and a spherical filler can be appropriately selected and used.

  In order to adjust the fluidity | liquidity of a composition, you may use an inorganic filler after surface-treating with well-known surface treatment agents, such as a silane coupling agent, as needed. Examples of such surface treatment agents include vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri (β-methoxyethoxy) silane, 3-methacryloyloxypropyltrimethoxysilane, and 11-methacryloyloxyundecyltrimethoxysilane. 3-glycidoxypropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-aminopropyltriethoxysilane and the like are used.

  As the surface treatment method, a known method can be used without any particular limitation. For example, the surface treatment agent is spray-added while vigorously stirring the inorganic filler, the inorganic filler and the surface treatment into an appropriate solvent, and the like. After dispersing or dissolving the agent, remove the solvent, or hydrolyze the alkoxy group of the surface treatment agent with an acid catalyst in an aqueous solution to convert it to a silanol group, and adhere to the surface of the inorganic filler in the aqueous solution In any method, heating is usually performed in the range of 50 to 150 ° C. to complete the reaction between the surface of the inorganic filler and the surface treatment agent. It can be carried out.

  Examples of the organic filler include polymethyl methacrylate, polyethyl methacrylate, methyl methacrylate-ethyl methacrylate copolymer, cross-linked polymethyl methacrylate, cross-linked polyethyl methacrylate, polyamide, polyvinyl chloride, polystyrene, and chloroprene. Rubber, nitrile rubber, ethylene-vinyl acetate copolymer, styrene-butadiene copolymer, acrylonitrile-styrene copolymer, acrylonitrile-styrene-butadiene copolymer, and the like are used. These may be used alone or in combination of two or more. The shape of the organic filler is not particularly limited, and the particle size of the filler can be appropriately selected and used.

  The organic-inorganic composite filler is obtained by previously adding a polymerizable monomer to the above-mentioned inorganic filler, forming a paste, polymerizing, and pulverizing. As the organic-inorganic composite filler, for example, a TMPT filler (trimethylolpropane methacrylate and silica filler mixed and polymerized and then pulverized) can be used. The shape of the organic-inorganic filler is not particularly limited, and the particle diameter of the filler can be appropriately selected and used.

  The average particle diameter of the filler is preferably 0.001 to 50 μm, more preferably 0.001 to 10 μm, from the viewpoints of the handleability and mechanical strength of the resulting composition. In the present specification, the average particle diameter of the filler can be measured by any method known to those skilled in the art, and can be easily measured by, for example, a laser diffraction type particle size distribution measuring apparatus described in the following examples.

  The filler is contained in the first paste (A) and / or the second paste (B). Although content is not specifically limited, From a viewpoint of the handleability of the composition obtained, and mechanical strength, Preferably it is 100-600 weight part with respect to 100 weight part of total amounts of a polymerizable monomer, More preferably, it is 130. It is -400 weight part, More preferably, it is 150-300 weight part. If the filler content is 100 parts by weight or more, the mechanical strength of the cured product is good, and if it is 600 parts by weight or less, the fluidity of the dental cement becomes appropriate and sufficient mixing can be performed. And there is no fear that the strength of the cured product will decrease.

  In addition to the above filler, additives such as promoters for promoting various polymerization initiation reactions, polymerization inhibitors such as BHT, stabilizers, antioxidants, dyes, pigments, photopolymerization initiators , Ultraviolet absorbers, organic solvents, thickeners and the like, but are not limited thereto.

  The dental curable composition of the present invention contains a polymerizable monomer (a) in which neither the paste (A) nor the paste (B) has an acidic group, and one of them is an acidic group-containing polymerization. In particular, if one further contains a hydroperoxide (c) and the other contains a substituted cyclic thiourea compound (d) represented by the formula (I) There is no limitation and it can manufacture easily by a method well-known to those skilled in the art.

  The paste of the dental curable composition of the present invention is usually a kneading stick after filling the first paste (A) and the second paste (B) into a double syringe or the like and extruding the kneaded paper at the time of use. Or by attaching a static mixer to the tip of the double syringe, it can be easily mixed in the static mixer.

  The paste of the curable composition of the present invention thus obtained has an excellent effect that the curing rate is moderate and the adhesiveness is high. Accordingly, the time during which the paste of the dental curable composition of the present invention can be bonded to dentin or the like, that is, the operable time of the dental curable composition of the present invention is preferably 1.5. The range is ˜7 minutes.

  The adhesive strength of the dental curable composition of the present invention is preferably 5 MPa or more, more preferably 6 MPa or more from the viewpoint of the reliability of the adhesive, when the adhesive strength is measured by the method described in the examples described later. More preferably, it is 7 MPa or more.

  When the curable composition of the present invention is used as a dental material, the curable composition alone is applied to the adhesive surface and used as a so-called self-adhesive cement. It is also possible to apply and use the curable composition of the present invention after applying another liquid such as.

  EXAMPLES Hereinafter, although this invention is demonstrated based on an Example and a comparative example, this invention is not limited at all by these Examples. The abbreviations used below are as follows.

[Polymerizable monomer having no acidic group (a)]
Bis-GMA: 2,2-bis [4- (3-methacryloyloxy) -2-hydroxypropoxyphenyl] propane HEMA: 2-hydroxyethyl methacrylate

[Acid group-containing polymerizable monomer (b)]
MDP: 10-methacryloyloxydecyl dihydrogen phosphate

[Hydroperoxide (c)]
THP: 1,1,3,3-tetramethylbutyl hydroperoxide

[Substituted cyclic thiourea compound (d)]
EyTU: Ethylenethiourea

[Other reducing agents]
AcTU: Acetylthiourea TMTU: Trimethylthiourea

[Inorganic filler]
The inorganic fillers 1 and 2 are obtained according to the following production method.

Inorganic filler 1: Silane-treated colloidal silica powder 0.3 parts by weight of acetic acid and 3 parts by weight of 3-methacryloyloxypropyltrimethoxysilane are added to 100 parts by weight of distilled water and stirred, and colloidal silica powder (manufactured by Nippon Aerosil Co., Ltd.) is stirred. 5 parts by weight of product code “Aerosil OX50”) was added and stirred for 1 hour. After removing water by freeze-drying, heat treatment was performed at 80 ° C. for 5 hours to obtain a silane-treated colloidal silica powder.

Inorganic filler 2: Silane-treated barium glass powder Barium glass (manufactured by ESTEC, product code “Raysorb E-3000”) was pulverized with a ball mill to obtain barium glass powder. It was 2.5 micrometers when the average particle diameter of the obtained barium glass powder was measured using the laser diffraction type particle size distribution measuring apparatus (Shimadzu Corporation model "SALD-2100"). A surface treatment was performed on 3 parts by weight of 3-methacryloyloxypropyltrimethoxysilane by a conventional method with respect to 100 parts by weight of this barium glass powder to obtain a silane-treated barium glass powder.

[Polymerization inhibitor]
BHT: 2,6-di-tert-butyl-4-methylphenol

Examples 1-7 and Comparative Examples 1-2 (Preparation of dental cement)
The raw materials shown in Table 1 were mixed at room temperature to prepare paste (A) and paste (B), and the characteristics were examined according to the methods of Test Examples 1 and 2 below. The results are shown in Table 1.

Test example 1 [operation time]
The paste (A) and paste (B) of each example and comparative example were mixed at a weight ratio of 1: 1, and the paste was started to be cured from the time when the paste was mixed in accordance with the measurement method of ISO 4049: 2000. The time until the time when the temperature started to rise (operable time) was measured. In consideration of practical use, it was determined that the operable time was 1.5 to 7 minutes.

Test Example 2 [Adhesive strength]
The lip surface of the bovine mandibular anterior teeth was polished with # 80 silicon carbade paper (manufactured by Nihon Kenshi Co., Ltd.) under running water to obtain a sample in which the flat surface of dentin was exposed. The obtained sample was further polished with # 1000 silicon carbide paper (Nihon Kenshi Co., Ltd.) under running water. After polishing, the surface water was blown dry with air. An adhesive tape having a round hole with a diameter of 3 mm and having a thickness of about 150 μm was attached to the smooth surface after drying to define the adhesion area.

  The cement composition obtained by kneading the paste (A) and paste (B) of each Example and Comparative Example at a weight ratio of 1: 1 was used as one of stainless steel cylindrical rods (diameter 7 mm, length 2.5 cm). Built on the end face (circular cross section), the end face built with the cement composition was placed on the round hole and pressed so that the center of the round hole and the center of the stainless steel cylindrical rod coincided, A stainless steel cylindrical rod was planted perpendicular to the tooth surface.

  After planting, the excess cement composition that appeared around the stainless steel cylindrical rod was removed with an instrument, and the sample was allowed to stand at room temperature for 30 minutes, and then immersed in distilled water. Thereafter, the immersed sample was allowed to stand in a thermostat kept at 37 ° C. for 24 hours to prepare a sample for adhesion test. A total of five samples for adhesion test were prepared.

  The tensile bond strength of the above five adhesion test samples was measured with a universal testing machine (Shimadzu Corporation) with the crosshead speed set to 2 mm / min, and the average of the measured values obtained. The value was taken as the bond strength. In addition, it was judged that adhesiveness was favorable when the adhesive strength was 5 MPa or more.

  From the above results, it can be seen that the curable compositions of the examples are superior in adhesive strength and have a proper operation time compared to the compositions of the comparative examples. Among them, although the amount of reducing agent used is the same, it is clear that Example 1 using ethylenethiourea has higher reaction activity than that of Comparative Example 1 using trimethylthiourea. is there.

  Further, in the curable compositions of Examples 1 and 4 to 7, even when the acidity of the composition is changed, excellent adhesive strength is maintained, and the fluctuation of the operable time is small and an appropriate time. It can be seen that it is kept within range.

  The dental curable composition of the present invention is suitably used as a dental cement, a dental adhesive, a composite resin, a dental room temperature polymerization resin, or the like in the field of dentistry.

Claims (5)

A packaged dental curable composition comprising a first paste (A) and a second paste (B), wherein none of the pastes has an acidic group (a ) And any one of the pastes further contains an acidic group-containing polymerizable monomer (b), and one of the pastes further contains hydroperoxide (c) and the other is a formula (I):

(In the formula, R represents an alkylene group having 2 to 5 carbon atoms, or a chain group having 2 to 5 atoms containing any of N, O, and S).
A packaged dental curable composition, each containing a substituted cyclic thiourea compound (d) represented by the formula:   The composition of Claim 1 whose content of hydroperoxide (c) is 1.0-4.0 weight part with respect to 100 weight part of total amounts of a polymerizable monomer.   The composition of Claim 1 or 2 whose content of a substituted cyclic thiourea compound (d) is 0.2-1.0 weight part with respect to 100 weight part of total amounts of a polymerizable monomer.   The composition according to any one of claims 1 to 3, wherein the content of the acidic group-containing polymerizable monomer (b) is 1 to 40% by weight in the total polymerizable monomers.   The composition according to any one of claims 1 to 4, wherein the substituted cyclic thiourea compound (d) is selected from the group consisting of ethylene thiourea and trimethylene thiourea.