Patent Grant
7368486
The invention concerns abrasion-resistant dental materials and their use for making artificial teeth and/or their enamel or cutting area.
Dental materials with a host of different types of fillers are already established.
The production and composition of a tooth material is described e.g. in U.S. Pat. No. 6,063,830 (Shofu, Kyoto; A). It comprises a combination of silanated silicic acid (SiO2) finely dispersed in urethane dimethacrylate with meth-/acrylate monomers and PMMA copolymers. An amount of 10-70% SiO2 is claimed, relative to the urethane dimethacrylate used. A high abrasion resistance while, at the same time, increased strength is also documented there.
A tooth material that contains an inorganic filler material is known from EP0962215 A2 (GC Dental Corp.; B). In addition to different monomers and crosslinked and non-crosslinked polymers, an inorganic-organic filler complex (1) is contained. Optionally, a second inorganic filler (2) can be contained. For producing the filler complex (1), inorganic filler materials are dissolved and polymerized into meth/acrylate-based monomers. Then, the polymer is broken down by ball milling and used as a ground powder. The fillers (2) can be a variety of glasses known in the dental industry, wherein attention is drawn to the issue of insufficient plaque resistance and silanation is suggested as a remedy.
DE2462271 A1 (Ivoclar, Schaan; C) concerns a material for making dental shaped bodies, including artificial teeth. Silicium dioxide and aluminum oxide are used as filler material in particle sizes of 5-700 nm and an amount of 10-90%. Optionally, the fillers can be silanated.
U.S. Pat. No. 5,548,001 (D1) and U.S. Pat. No. 4,389,507 (D2) (Heraeus Kulzer and/or Bayer AG) concern the production of pearl polymers with inorganic filler components. D1 refers several times to production with crosslinking monomers, whereas D2 describes the possibilities for producing inorganically fortified polymer pearls in general. No possible applications or areas of applications are mentioned.
U.S. Pat. No. 4,617,327 (D3) concerns fillers with an inorganic core, a vinyl silane layer and a second methacrylate polymer layer and the use thereof for making bridges, teeth or fillings with high mechanical strength and great resistance to wear (column 4, pages 19, 20). The fillers are processed together with BisGMA and TEGDMA as well as pigments into artificial teeth, for example.
Tooth material is described in EP0677286 B1 (Heraeus Kulzer; E) that contains barium aluminum silicate glass and microfine silicium dioxide as inorganic fillers. The mixture is made there by adding the silanated fillers to a matrix made from a variety of meth-/acrylates.
In summary, the following commonalities came from prior art:
Relevant features of individual documents are:
The compositions known from prior art have considerable drawbacks. Some of those are:
Therefore, the goal of the present invention is to at least partially eliminate these drawbacks and, in particular, to achieve the following improvements:
The task is solved by dental materials of the following composition:
In the tests performed, contrary to what was expected, it turned out that considerably better product characteristics can be attained with a properly balanced ratio of components in the presence of a specially-designed polymer preliminary stage. This preliminary stage is a methacrylate-based pearl polymer, in which inorganic dental glass is polymerized as filler.
Preferred are dental materials, essentially containing:
The components of the mixture are explained in more detail as appropriate below: Component (a), (b)-falling under consideration as monofunctional or crosslinked (meth)acrylates are:
Monofunctional or polyfunctional (meth)acrylates, which can be used alone or in mixtures. Examples of such compounds to consider are methylmethacrylate, isobutylmethacrylate, cyclohexylmethacrylate, triethylene glycoldimethacrylate, diethylene glycoldimethacrylate, tetraethylene glycoldimethacrylate, ethylene glycoldimethacrylate, polyethylene glycoldimethacrylate, butandiol dimethacrylate, hexandiol methacrylate, decandiol dimethacrylate, dodecandiol dimethacrylate, bisphenol-A-dimethacrylate, trimethylolpropane trimethacrylate, ethoxylated bisphenol-A-dimethacrylate, but also bis-GMA (2,2-bis-4-(3-methacryloxy-2-hydroxypropyl)-phenylpropane) as well as the reaction products from isocyanates, in particular di- and/or triisocyanates and methacrylates that contain OH-groups, and the appropriate acrylates of all the above compounds. Examples of reaction products of isocyanates are the transformation products of I mol hexamethylene diisocyanate with 2 mol 2-hydroxyethylmethacrylate, of 1 mol (tri(6-isocyanatohexyl)biuret with 3 mol hydroxy ethylmethacrylate and of 1 mol trimethylhexamethylene diisocyanate with 2 mol hydroxyethylmethacrylate, which are also called urethane dimethacrylates. Suitable monomers are the monomers themselves respectively, polymerizable prepolymers made from them as well as mixtures thereof.
Preferred crosslinking monomers are e.g. 2.2-bis-4-(3-methacryloxy-2-hydroxypropyl)-phenyl propane) (bis-GMA), i.e. the transformation product of glycidyl methacrylate and bisphenol-A (containing OH-groups), and 7,7,9-trimethyl-4,13-dioxo-3,14-dioxa-5,12-diazahexadecan-1,16-diyl-dimethacrylate (UDMA), i.e. the urethane dimethacrylate from 2 mol 2-hydroxyethylmethacrylate (HEMA) and 1 mol 2-2,4-trimethylhexamethylene diisocyanate (containing urethane groups). Furthermore, transformation products of glycidyl methacrylate with other bisphenols, like e.g. bisphenol-B (2,2′-bis-(4-hydroxyphenyl)-butane), bisphenol-F (2,2′-methylene diphenol) or 4,4′-dihydroxydiphenyl, as well as transformation products of 2 mol HEMA or 2-hydroxypropyl(meth)acrylate with, in particular, 1 mol, known diisocyanates, such as e.g. hexamethylene diisocyanate, m-xylylene diisocyanate or toluylene diisocyanate are preferred as crosslinking monomers. (Crosslinking meth-/acrylates are by nature compounds with 2 or more methacrylate groups in the monomer.)
(d)—pearl polymers, partially crosslinked, can be PMMA, 2-hydroxyethyl methacrylate-methylmethacrylate copolymer, styrene-maleic acid anhydride copolymer, acrylic polymer, or acrylic acid-maleic acid copolymer. PMMA-pearl polymers are preferred. (f)—The inorganically fortified pearl polymer used as a filler can be one of those described above in D1, D2 and D3. The following composition has preference:
Preferably used as monofunctional monomers should be those that have flexibilizing properties. Those include alkylmeth-/acrylates like ethyl-MA, butyl-MA, ethyl-hexyl-MA, methylacrylate.
Suitable as silanated glass are all the glasses used in the dental sector, e.g. like quartz glass or barium-aluminum silicate glass. The average particle size should be <4 μm since, with larger particles, the abrasion properties (tearing out) and the surface quality suffer. Fillers below 100 nm that are too small do not demonstrate significantly higher abrasion values compared to known materials.
The fillers are produced by means of traditional suspension polymerization. Here, the monomer is predispersed in a water-based phase by adding soap. The inorganic filler is added and integrated into the monomer droplets.
The reaction is induced and the droplets are hardened to pearl polymers by heating the mixture. Benefits of this filler:
(g)—The initiators well known to an expert in the field that are suitable for thermal polymerizaton can be considered as initiators. When selecting the initiator, generally the propensity for polymerization of the monomer and the polymerization conditions are taken into consideration. If something like a methacrylate is polymerized at a high temperature, one uses e.g. an organic peroxide like benzoyl peroxide (“BPO”), di-tert-butyl peroxides or cumolhydroperoxide or an azo compound like 2,2-min-azobisisobutyronitrile or 1,1-min-azo-bis(cyclohexane-1-carbonitrile) is used. For polymerization at room temperature, one purposefully selects redox initiators, like e.g. benzoyl peroxide/dimethylaniline-cumolhydroperoxide/thiourea, ascorbinic acid/Cu salt and organic sulfinic acid (or salt thereof)/amines/peroxides or even tributylborane, e.g. benzoyl peroxide with an aromatic-tertiary amine or tributylborane or tributylborane-partial oxide (TBBO).
(h)—The pigments that are standard in the dental sector and that are well known to an expert in the field are taken into consideration as pigments.
The following example arrangement has proven favorable:
Production Method
Normal PMMA-based materials are a mix of a colored powder component and a liquid component containing the initiator. Of great importance thereby are proper mix properties, which prevent inhomogenities and porosities from occurring. Then, the paste can be intermediately stored refrigerated,until heat polymerization occurs. When using the composition described above, hardly any changes to the known method are necessary. Traditional coloring and storage of the powder components are possible thanks to the homogeneous miscibility and the not so extreme density differences between PMMA pearls and inorganically filled pearls. Only pyrogenic silicic acid, which is optionally used, is to be dispersed separately into monomer and within the framework of the mixing process.
Use in the Artificial Tooth
In order to achieve an aesthetic of high quality, artificial teeth are made at least 2-layered, but, as a rule, 3-layered (dentin/neck/cutter and/or enamel). The exterior cutting and/or enamel layer is generally exposed to the greatest mechanical strain. High abrasion resistance is inasmuch the most important requirement for this layer. Therefore, the preferred area of use of the material of the invention is within the enamel layer. The layers below that, the dentin layer and the neck layer, usually comprise a purely PMMA-based material, as the most bonding ease to the PMMA prosthesis base is important there.
Consequently the invention also concerns artificial teeth made from the materials of the invention, particularly their cutting area or enamel area.
Metrological Results
1.1 Hardness Measurements
The hardness is determined using a modified Vickers hardness test. In contrast to measuring the dimensions of the indentation after stress is applied, in the Zwick hardness test, the measurement is taken during the application of stress itself. This eliminates accuracy issues when measuring samples with elastic components like plastics.
1.2 Flexural Strength, E-module, Impact Strength
The flexural strength and the E-module were determined with EN ISO 1567 prostheses plastics and impact strength as per DIN 53435.
1.3 Abrasion Tests
The most common methods are the 2-body-abrasion test (OCA-2-body-abrasion) and the 3-body-abrasion test (CFA 3-body-abrasion). Both methods comply with the ISO/PDTR14569/2-Dental materials guidance on testing wear.
A great loss in volume and/or large depth means there is much abrasion. The data clearly shows the higher abrasion resistances of the materials of the invention as compared to the known inorganically filled materials.
At the same, the material hardness is significantly lower and more in the area of the PMMA, which is known to be tough.
Assessment of the Benefits
The benefits gained from using the formula above, particularly also using the fortified pearl polymers are:
| Number | Date | Country | Kind |
|---|---|---|---|
| 103 35 181 | Jul 2003 | DE | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4389507 | Podszun et al. | Jun 1983 | A |
| 4617327 | Podszun et al. | Oct 1986 | A |
| 5219899 | Panster et al. | Jun 1993 | A |
| 5548001 | Podszun et al. | Aug 1996 | A |
| 6063830 | Deguchi et al. | May 2000 | A |
| 6335385 | Gorlich et al. | Jan 2002 | B2 |
| 20010021728 | Gorlich et al. | Sep 2001 | A1 |
| Number | Date | Country |
|---|---|---|
| 2850917 | Jun 1980 | DE |
| 3000213 | Jul 1981 | DE |
| 2462271 | May 1982 | DE |
| 3135113 | Mar 1983 | DE |
| 3316851 | Nov 1984 | DE |
| 2849936 | Dec 1989 | DE |
| 4004678 | Aug 1991 | DE |
| 0677286 | Oct 1995 | EP |
| 0962215 | Dec 1999 | EP |
| 1 230 906 | Aug 2002 | EP |
| Number | Date | Country | |
|---|---|---|---|
| 20050059751 A1 | Mar 2005 | US |
