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Polymerizable composition and dental material

a polymerizable composition and dental material technology, applied in the field of polymerizable composition and dental material, can solve the problems of easy loss, difficulty in supporting teeth, loose teeth, etc., and achieve the effects of good adhesive properties to tooth structure, bone, metals, and good viscosity and forming properties

Inactive Publication Date: 2015-05-07
KURARAY NORITAKE DENTAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0023]The polymerizable composition of the present invention has both good viscosity and forming property at the same time before curing and thus has excellent handling property. Further, it exhibits good adhesive properties to tooth structure, bones, and metals. Furthermore, a cured product of the polymerizable composition has excellent flexibility, transparency, and color stability. Accordingly, the polymerizable composition of the present invention can be applied suitably to biological tissues (such as teeth and bones, particularly teeth). As specific applications, the polymerizable composition of the present invention is optimally used as a temporary cement for implant use and a mobile tooth-fixing material, and also is suitably used as a dental cement and a dental composite resin.

Problems solved by technology

Meanwhile, the growth of periodontal disease causes gingival recession also due to aging, etc., making it difficult to support teeth sufficiently.
As a result, the teeth become loose and lost easily.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

reference example 1

Production of the Acrylic Block Copolymer (a)-1

[0111](1) A three-way stopcock was attached to a 1 liter three-necked flask, the inside of which was degassed and substituted by nitrogen. Thereafter, 390 g of toluene, 1.4 ml of N,N′,N′,N″,N″-pentamethyl diethylene triamine, and 18 ml of a toluene solution containing 11 mmol of isobutylbis(2,6-di-t-butyl-4-methylphenoxy)aluminum was added thereto at room temperature, and 1.7 ml of a mixed solution of cyclohexane and n-hexane containing 2.2 mmol of sec-butyl lithium was further added thereto. 14 ml of methyl methacrylate was added thereto, which was allowed to react at room temperature for 1 hour. 1 g of the reaction solution at that time was collected as Sample 1. Subsequently, the internal temperature of the polymerization solution was cooled to −15° C., and 120 ml of n-butyl acrylate was added dropwise thereto over 6 hours. After completion of addition, 1 g of the reaction solution was collected as Sample 2. Subsequently, 14 ml of me...

reference example 2

Production of the Acrylic Block Copolymer (a)-2

[0113](1) A three-way stopcock was attached to a 1 liter three-necked flask, the inside of which was degassed and substituted by nitrogen. Thereafter, 390 g of toluene, 1.4 ml of N,N′,N′,N″,N″-pentamethyl diethylene triamine, and 18 ml of a toluene solution containing 11 mmol of isobutylbis(2,6-di-t-butyl-4-methylphenoxy)aluminum was added thereto at room temperature, and 1.7 ml of a mixed solution of cyclohexane and n-hexane containing 2.2 mmol of sec-butyl lithium was further added thereto. 35 ml of methyl methacrylate was added thereto, which was allowed to react at room temperature for 1 hour. 1 g of the reaction solution at that time was collected as Sample 1. Subsequently, the internal temperature of the polymerization solution was cooled to −15° C., and 75 ml of n-butyl acrylate was added dropwise thereto over 5 hours. After completion of addition, 1 g of the reaction solution was collected as Sample 2. Subsequently, 35 ml of met...

reference example 3

Production of the Acrylic Block Copolymer (a)-3

[0115](1) A three-way stopcock was attached to a 1 liter three-necked flask, the inside of which was degassed and substituted by nitrogen. Thereafter, 390 g of toluene, 0.95 ml of N,N′,N′,N″,N″-pentamethyl diethylene triamine, and 12 ml of a toluene solution containing 11 mmol of isobutylbis(2,6-di-t-butyl-4-methylphenoxy)aluminum was added thereto at room temperature, and 1.1 ml of a mixed solution of cyclohexane and n-hexane containing 2.2 mmol of sec-butyl lithium was further added thereto. 5 ml of methyl methacrylate was added thereto, which was allowed to react at room temperature for 1 hour. 1 g of the reaction solution at that time was collected as Sample 1. Subsequently, the internal temperature of the polymerization solution was cooled to −15° C., and 97 ml of n-butyl acrylate was added dropwise thereto over 5 hours. After completion of addition, 1 g of methanol was added to this reaction solution to stop the polymerization. Th...

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Abstract

The present invention provides a polymerizable composition that is suitably used as a temporary cement for implant use and a mobile tooth-fixing material. The present invention is a polymerizable composition that includes an acrylic block copolymer (a) having at least one polymer block A that mainly contains a (meth)acrylic acid ester unit and that functions as a hard segment and at least one polymer block B that mainly contains an acrylic acid ester unit and that functions as a soft segment, a polymerizable monomer (b), and a polymerization initiator (c).

Description

TECHNICAL FIELD[0001]The present invention relates to a polymerizable composition that is suitable for application to biological tissues, particularly suitable as a temporary cement for implant use and a mobile tooth-fixing material, and relates to a dental material using the polymerizable composition.BACKGROUND ART[0002]Adhesive materials or filling materials are used for restorative treatment of teeth, bones, etc. Polymerizable compositions containing a polymerizable monomer, a polymerization initiator, a filler, etc., are generally used as such adhesive materials or filling materials. Polymerizable compositions for restorative treatment of teeth, bones, etc., can be roughly classified into two types depending on the hardness after curing. One type is a soft material, a cured product of which is flexible, to be used as an adhesive material, a shock absorber, etc., with respect to biological tissues, such as a temporary sealing material, a rebase for denture base, and an artificial...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K6/083C08G81/02
CPCC08G81/021A61K6/083C08F265/06C08F287/00A61K6/62A61K6/30A61K6/887C08L33/08C08L33/10C08L53/00
Inventor SUZUKI, KENJI
Owner KURARAY NORITAKE DENTAL