Dental composite materials and method of manufacture thereof
View Patent ↗A dental composite material that comprises a polyhedral oligomeric silsesquioxane is disclosed. The dental composite material is useful for a variety of dental materials, treatments, and restorative functions including crown and bridge materials, fillings, adhesives, sealants, luting agents or cements, denture base materials, orthodontic materials and sealants, and other dental restorative materials.
1. A dental restorative composition comprising:
a polymerizable, ethylenically unsaturated dental restorative resin composition;
a filler composition comprising a modified polyhedral oligomeric silsesquioxane filler; and
a curing system.
2. The composition of claim 1 , wherein the resin composition comprises an acrylate or methacrylate resin.
3. The composition of claim 2 , wherein the resin composition further comprises 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, ethylene glycol methacrylate, diethylene glycol methacrylate, tri(ethylene glycol) dimethacrylate, tetra(ethylene glycol) dimethacrylate, butanedioldimethacrylate, dodecanedioldimethacrylate, 1,6-hexanedioldimethacrylate, or a mixture comprising at least one of the foregoing methacrylate monomers.
4. The composition of claim 1 , wherein the resin composition comprises polyurethane dimethacrylate, diurethane dimethacrylate, polycarbonate dimethacrylate, ethoxylated bisphenol A dimethacrylate, 2,2′-bis [4-(3-methacryloxy-2-hydroxy propoxy)-phenyl]-propane, or a mixture comprising at least one of the foregoing resins.
5. The composition of claim 1 , wherein the modified polyhedral oligomeric silsesquioxane filler comprises at least one functional group reactive with the resin composition.
6. The composition of claim 5 , wherein the reactive group comprises halide, alcohol, amine, isocyanate, acid, acid chloride, silanol, silane, acryl, methacryl, olefin, epoxy, or a mixture comprising at least one of the foregoing reactive groups.
7. The composition of claim 5 , wherein the reactive group comprises an acryl or methacryl.
8. The composition of claim 5 , wherein the reactive group comprises an alkoxysilane, a styrene, an olefin, an epoxy, a chlorosilane, an amine, an alcohol, a phenol, a phosphine, a norbornenyls, a nitrile, an isocyanate, a halide, an ester, or a mixture comprising at least one of the foregoing reactive groups.
9. The composition of claim 1 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; and Y is an organic group comprising an epoxy functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising an epoxy functional group; and
a (meth)acrylic acid, or a hydroxy (meth)acrylate of the formula
wherein q and r are independently integers from 1 to 6; G is a substituted or unsubstituted C 1 –C 33 alkyl, substituted or unsubstituted aryl group, or (C 1 –C 6 ) alkyl-oxy-(C 1 –C 6 ) alkyl; and R 1 is hydrogen or methyl, wherein the substitution is linear or branched, saturated or unsaturated C 1 –C 12 alkyl; C 1 –C 12 alkoxy; cyclic C 3 –C 7 alkyl; halogens; ester groups; ether groups; amide groups; aryl; or a combination comprising at least one of the foregoing substitutions.
10. The composition of claim 1 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; and
a compound comprising both (meth)acrylate functionality and epoxy functionality.
11. The composition of claim 1 , wherein the composition further comprises a polyhedral oligomeric silsesquioxane filler.
12. The composition of claim 1 , wherein the filler composition further comprises fumed silica, colloidal silica, aluminosilicate glass, fluoroaluminosilicate glass, silica, quartz, strontium silicate, strontium borosilicate, lithium silicate, lithium alumina silicate, amorphous silica, ammoniated or deammoniated calcium phosphate, alumina, zirconia, tin oxide, titania, or a mixture comprising at least one of the foregoing fillers.
13. A method for the production of a dental restoration, comprising applying the composition of claim 1 to a site on a tooth to be restored; and curing the composition.
14. The method of claim 13 , wherein the resin composition comprises an acrylate or methacrylate resin.
15. The method of claim 13 , wherein the resin composition comprises polyurethane dimethacrylate, diurethane dimethacrylate, polycarbonate dimethacrylate, ethoxylated bisphenol A dimethacrylate, 2,2′-bis [4-(3-methacryloxy-2-hydroxy propoxy)-phenyl]-propane, or a mixture comprising at least one of the foregoing resins.
16. The method of claim 15 , wherein the resin composition further comprises 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, ethylene glycol methacrylate, diethylene glycol methacrylate, tri(ethylene glycol) dimethacrylate, tetra(ethylene glycol) dimethacrylate, butanedioldimethacrylate, dodecanedioldimethacrylate, 1,6-hexanedioldimethacrylate, or a mixture comprising at least one of the foregoing methacrylate monomers.
17. The method of claim 13 , wherein the modified polyhedral oligomeric silsesquioxane filler comprises at least one functional group reactive with the resin composition.
18. The method of claim 17 , wherein the reactive group comprises halide, alcohol, amine, isocyanate, acid, acid chloride, silanol, silane, acryl, methacryl, olefin, epoxy, or a mixture comprising at least one of the foregoing reactive groups.
19. The method of claim 17 , wherein the reactive group comprises an acryl or methacryl.
20. The method of claim 17 , wherein the reactive group comprises an alkoxysilane, a styrene, an olefin, an epoxy, a chlorosilane, an amine, an alcohol, a phenol, a phosphine, a norbornenyls, a nitrile, an isocyanate, a halide, an ester, or a mixture comprising at least one of the foregoing reactive groups.
21. The method of claim 13 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; D is SiO; Y is an organic group comprising an epoxy functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising an epoxy functional group; and
a (meth)acrylic acid, or a hydroxy (meth)acrylate of the formula
wherein q and r are independently integers from 1 to 6; G is a substituted or unsubstituted C 1 –C 33 alkyl, substituted or unsubstituted aryl group, or (C 1 –C 6 ) alkyl-oxy-(C 1 –C 6 ) alkyl; and R 1 is hydrogen or methyl, wherein the substitution is linear or branched, saturated or unsaturated C 1 –C 12 alkyl; C 1 –C 12 alkoxy; cyclic C 3 –C 7 alkyl; halogens; ester groups; ether groups; amide groups; aryl; or a combination comprising at least one of the foregoing substitutions.
22. The method of claim 13 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; D is SiO; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; and
a compound comprising both (meth)acrylate functionality and epoxy functionality.
23. The method of claim 13 , wherein the composition further comprises a polyhedral oligomeric silsesquioxane filler.
24. The method of claim 13 , wherein the filler composition further comprises fumed silica, colloidal silica, aluminosilicate glass, fluoroaluminosilicate glass, silica, quartz, strontium silicate, strontium borosilicate, lithium silicate, lithium alumina silicate, amorphous silica, ammoniated or deammoniated calcium phosphate, alumina, zirconia, tin oxide, titania, or a mixture comprising at least one of the foregoing fillers.
25. A dental restoration, comprising the cured composition of claim 1 .
26. The restoration of claim 25 , wherein the resin composition comprises an acrylate or methacrylate resin.
27. The restoration of claim 25 , wherein the resin composition comprises polyurethane dimethacrylate, diurethane dimethacrylate, polycarbonate dimethacrylate, ethoxylated bisphenol A dimethacrylate, 2,2′-bis [4-(3-methacryloxy-2-hydroxy propoxy)-phenyl]-propane, or a mixture comprising at least one of the foregoing resins.
28. The restoration of claim 27 , wherein the resin composition further comprises 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, ethylene glycol methacrylate, diethylene glycol methacrylate, tri(ethylene glycol) dimethacrylate, tetra(ethylene glycol) dimethacrylate, butanedioldimethacrylate, dodecanedioldimethacrylate, 1,6-hexanedioldimethacrylate, or a mixture comprising at least one of the foregoing methacrylate monomers.
29. The restoration of claim 25 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; D is SiO; and Y is an organic group comprising an epoxy functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising an epoxy functional group; and
a (meth)acrylic acid, or a hydroxy (meth)acrylate of the formula
wherein q and r are independently integers from 1 to 6; G is a substituted or unsubstituted C 1 –C 33 alkyl, substituted or unsubstituted aryl group, or (C 1 –C 6 ) alkyl-oxy-(C 1 –C 6 ) alkyl; and R 1 is hydrogen or methyl, wherein the substitution is linear or branched, saturated or unsaturated C 1 –C 12 alkyl; C 1 –C 12 alkoxy; cyclic C 3 –C 7 alkyl; halogens; ester groups; ether groups; amide groups; aryl; or a combination comprising at least one of the foregoing substitutions.
30. The restoration of claim 25 , wherein the modified polyhedral oligomeric silsesquioxane filler is the reaction product of
a polyhedral oligomeric silsesquioxane monomer according to the formula R 7 T 4 D 3 (OY) 3 , wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; T is SiO 1.5 ; D is SiO; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; or
a polyhedral oligomeric silsesquioxane monomer according to the formula R n-m T n Y m wherein R is C 1 –C 24 straight, branched, or cyclic alkyl, C 1 –C 24 aromatic, alkylaryl, or arylalkyl, wherein the alkyl or aromatic is optionally substituted with C 1 –C 6 alkyl, halo, C 1 –C 6 alkoxy, C 1 –C 6 perhaloalkyl, or a combination comprising at least one of the foregoing substitutions; n is 6, 8, 10, or 12; m is 1 to n; T is SiO 1.5 ; and Y is an organic group comprising a hydroxy functional group, a phenol functional group, or a carboxyl functional group; and
a compound comprising both (meth)acrylate functionality and epoxy functionality.