Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Processes of preparing a desired or intentional composition...
Reexamination Certificate
2001-03-20
2003-03-18
Yoon, Tae H. (Department: 1714)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Processes of preparing a desired or intentional composition...
C523S120000, C524S533000, C433S034000, C433S048000
Reexamination Certificate
active
06534562
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a tough denture fabricated of injectable polymethyl-methacrylate (PMMA) and a method for producing the same. The denture in this invention includes a portion of or a whole artificial tooth, and an artificial tooth base.
2. Description of the Related Art
Present dentures employed clinically, which are known are heat-polymerized type PMMA, injection-type polysulfone (PS) and polycarbonate (PC) resins. The heat-polymerized type PMMA is fabricated of a mixture of methyl-methacrylate (MMA) monomer liquid and PMMA prepolymer powder by mixing and heat-polymerizing in a denture-shaped mold. However, there are several product drawbacks in this method, namely, unstable shape caused by high shrinkage of polymer during polymerization, poor mechanical properties such as impact resistance and toxicity to a living organism that is pointed out to cause an allergy by dissolving a lot of monomer residue after polymerization.
Because of the above drawbacks, PS and PC are employed as injectable denture materials instead of the heat-polymerized type PMMA. However, PS shows poor impact resistance and PC shows toxicity and environmental pollution of bis-phenol A remaining as monomer residue, and poor adhesion to mending material of PMMA that is difficult to improve.
Although it is desirous in the dental field to invent and apply a novel denture that shows excellent mechanical properties including impact resistance and has little monomer residue, however there is still not a PUMA denture which meets the above conditions.
An object of the invention is to provide an excellent denture fabricated of PMMA and a method for the production thereof, having little monomer residue including the bis-phenol A, dissolved in one's mouth, and showing excellent mechanical properties including impact resistance.
SUMMARY OF THE INVENTION
The present invention provides a tough denture and a method for the production thereof, which comprises solid PMMA as a main component, being added to polar elastomer selected from the group of polyacrylate rubber copolymer, methylmethacrylate-alkylacrylate-styrene terpolymer, and fluororubber, and is fabricated in a process of being mixed and injected into a denture mold.
The term “toughness” in the present denture means that tensile and Izod impact strengths are more than 75.0 MPa and 1.62 kg·cm/cm
2
, and bending strain at 5.0 kgf is less than 3.00 mm. Furthermore, elution volume from monomer residue after PMMA polymerization is less than 3% in the invented denture.
DETAILED DESCRIPTION OF THE INVENTION
PMMA of the present invention which is possibly employed is not only pure syndiotactic PMMA used in general industry, but also a blend of syndiotactic and atactic PMMAs in order to improve mechanical and thermal properties by forming a stereo complex.
The higher the tacticity of the PMMA blend composed of both syndiotactic and atactic PMMAs, the better. The tacticity is preferably more than 60%, more preferably more than 80%. The blend ratio of both PMMAs is preferable in a range of 40-60% to 60-40% in order to form a stereo complex, in spite of the fact that the ratio is freely changed. A weight-average molecular weight of PMMA for the invented denture, in both phases, is preferably in a range of 100 to 300 thousand, more preferably in a range of 120 to 250 thousand. A PMMA denture having the weight-average molecular weight of less than 100 thousand shows poor mechanical properties in spite of the fact that it easily injects. Therefore, PMMA having a weight-average molecular weight of more than 100 thousand is preferable.
Although PMMA of a high weight-average molecular weight is preferable in view of mechanical properties, however a uniform-shaped denture is difficult to fabricate from PMMA having a weight-average molecular weight of more than 300 thousand, because it shows poor fluid properties and is therefore poor for injecting as a result of high melt viscosity.
PMMA of present invention is added to polar elastomer selected from a group of polyacrylate rubber copolymer, methylmethacrylate-alkylacrylate-styrene terpolymer, and fluororubber in order to improve the mechanical properties, namely toughness. This process can be applied to not only pure syndiotactic PMMA, but also to a blend of syndiotactic and atactic PMMAs in order to form a stereo complex.
The polyacrylate rubber copolymer is composed of alkyl acryl ester and cross-linkable vinyl monomer. Here, the alkyl acryl ester includes acryl methyl, acryl ethyl, acryl propyl, acryl i-propyl, acryl n-butyl, acryl i-butyl, acryl t-butyl, acryl n-hexyl, acryl octyl, acryl 2-ethylhexyl, and acyl lauryl. Especially, acryl ethyl, acryl n-butyl and acryl 2-ethylhexyl are preferable because those compounds show a low Tg of −22, −54 and −85° C., and then good elasticity.
The cross-linkable vinyl monomer includes 2-chloroethyl-vinyl-ether, acrylonitrile, glycidyl-methacrylate and acryl-glycidyl-ether. The monomer is copolymerized in a range of 5 to 20% with the above alkyl acryl ester.
The alkyl acryl ester of the methylmethacrylate-alkylacrylate-styrene terpolymer includes acryl methyl, acryl ethyl, acryl propyl, acryl i-propyl, acryl n-butyl, acryl i-butyl, acryl t-butyl, acryl n-hexyl, acryl octyl, acryl 2-ethylhexyl, and acryl lauryl, the same as in the case of the copolymer.
The fluororubber includes VDF-HFP, VDF-CTFE, PTFE-P, VDF-PFVE, TFE-PFVE, FVMQ and VNF (referred to in “Plastic Encyclopedia” p. 509, Asakura).
It is possible in Me present invention to employ a wide range of mixture ratio of polar elastomer selected from a group of polyacrylate rubber copolymer, methylmethacrylate-alkylacrylate-styrene terpolymer, and fluororubber, and PMMA. A preferable weight ratio of the elastomer to the PMMA is a range of 2 to 30 wt. %, and a more preferable ratio is a range of 5 to 15 wt. %. This is because a denture having a mixture ratio of less than 2 wt. % or more than 30 wt. % shows relatively poor toughness or obstruction to PMMA properties.
The invented denture fabricated of injectable PMMA is given a tone of similar color to capillary and molds in oral mucous membrane, by adding red, brown or yellowish white dyes, pigment or dyed fibers. Furthermore, it is possible to optionally add inorganic fillers such as calcium oxide, titanium oxide or hydroxyapatite. The dyed fiber includes natural, chemical or synthetic fibers having heat-resistant properties, in which the fibers are preferable to show heat stability at injection temperatures in a range of 200 to 270 ° C., easy dyeability and adhesion with PMMA. It is possible to choose cotton, rayon, polyacrylonitrile, nylon 66, polyimide and PVA as the above fiber.
The denture fabricated by injecting PMMA pellets cohered with red dyed fiber, looks like a tone of similar color to capillary and molds in oral mucous membrane, because red dyed fiber uniformly disperses throughout the molded denture.
A preferable mixture ratio of the red dyed fiber to the PMMA pellet is a range of 0.01 to 10 wt. %, and a more preferable ratio is a range of 0.1 to 0.5 wt. %. Because a denture having a mixture ratio of less than 0.01 wt. % or more than 10 wt. % shows insufficient coloring or obstruction to PMMA properties. A preferable diameter and length of the fiber is a range of 1 to 30 &mgr;m and 0.5 to 3 mm, and the injected denture fabricated of the above fiber looks like a tone of similar appearance to capillary and molds in oral mucous membrane, because of uniformly dispersing and maintaining the fiber shape after injection.
A method for producing the tough denture, is composed of following steps:
step 1: polymerizing the polymethyl-methacrylate;
step 2: mixing polar elastomer selected from a group of polyacrylate rubber copolymer, methylmethacrylate-alkylacrylate-styrene terpolymer, and fluororubber into the polymethylmethacrylate and pelletizing the mixture;
step 3: optionally adding red, brown or yellowish white dyes, pigment or dyed fibers, furthermore, optionally adding inorganic fillers su
Gen Sho-kyu
Kita Toshio
Tsutsumi Sadami
BMG Inc.
Jordan and Hamburg LLP
Yoon Tae H.
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