A method for making a ceramic body comprised of a ceramic material having an inhibitory effect on bacterial growth is provided. A dental prosthesis may be made of a ceramic material that comprises a molybdenum-containing component on a portion of the prosthesis that contacts the gingival surface of a patient. In one method, a porous zirconia ceramic structure is shaped in the form of a dental prosthesis, and then infiltrated with a molybdenum-containing composition, before sintering to densify the ceramic structure.

A method for making a ceramic body comprised of a ceramic material having an inhibitory effect on bacterial growth is provided. A dental prosthesis may be made of a ceramic material that comprises a molybdenum-containing component on a portion of the prosthesis that contacts the gingival surface of a patient. In one method, a porous zirconia ceramic structure is shaped in the form of a dental prosthesis, and then infiltrated with a molybdenum-containing composition, before sintering to densify the ceramic structure.

A method for preparing a slurry for photocuring 3D printing is provided, comprising the steps of: mixing monomer molecules of a thermosensitive hydrogel, a photocuring initiator, a crosslinking agent, a solvent, and a ceramic material to obtain the slurry. a method for manufacturing photocuring 3D printed articles is further provided, comprising using the slurry as a raw material, performing a 3D printing procedure by a photocuring 3D printer to obtain a green compact of a 3D printed article; and coating oil to the green compact of the 3D printed article, followed by heating and sintering the oil-coated article, to obtain the 3D printed article.

Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The pellets may advantageously facilitate sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The pellets may advantageously facilitate sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

A method for producing an implant blank (100), in particular a dental implant blank from a starting body, said implant blank (100) comprising at least one first area, which is a surface area (102), and a second area, which is a core area (101), wherein the surface area (102) has at least one bioactive surface material (502) and extends from at least one first surface (103) in the direction of the core area (101), and the core area (101) has at least one carrier material that can be subjected to mechanical load. The starting body has a porosity for controlling a targeted distribution of the bioactive surface material (502) within the starting body and is loaded with a solution (500) of the bioactive surface material (502) in a first step, which is a loading step. In a second step, which is a distribution control step, the distribution of the bioactive surface material (502) within the starting body is controlled such that the solution (500) has a higher concentration within the surface area (102) than within the core area (101), the control being effected by regulating one or more environmental parameters in a closed environment (200), in particular by regulating the humidity and/or the pressure and/or the temperature.

A method for producing an implant blank (100), in particular a dental implant blank from a starting body, said implant blank (100) comprising at least one first area, which is a surface area (102), and a second area, which is a core area (101), wherein the surface area (102) has at least one bioactive surface material (502) and extends from at least one first surface (103) in the direction of the core area (101), and the core area (101) has at least one carrier material that can be subjected to mechanical load. The starting body has a porosity for controlling a targeted distribution of the bioactive surface material (502) within the starting body and is loaded with a solution (500) of the bioactive surface material (502) in a first step, which is a loading step. In a second step, which is a distribution control step, the distribution of the bioactive surface material (502) within the starting body is controlled such that the solution (500) has a higher concentration within the surface area (102) than within the core area (101), the control being effected by regulating one or more environmental parameters in a closed environment (200), in particular by regulating the humidity and/or the pressure and/or the temperature.

The present disclosure provides a composite material. The composite material includes 20 to 40 weight percent (wt. %) of a polymerizable component; 6 to 40 wt. % of ceramic fibers; and 30 to 70 wt. % of nanoclusters. Each of the ceramic fibers has a diameter and a length, the ceramic fibers having an arithmetic mean diameter of 0.3 micrometers to 5 micrometers, and the length of fifty percent of the ceramic fibers (based on a total number of the ceramic fibers) is at least 10 micrometers and the length of ninety percent of the ceramic fibers is no greater than 500 micrometers. The present disclosure also provides a method of making the composite material. The method includes obtaining components and admixing the components to form a composite material. Further, the present disclosure provides a method of using a composite material including placing a composite material near or on a tooth surface, changing the shape of the composite material near or on a tooth surface, and hardening the composite material. In addition, the present disclosure provides dental products and kits. Hardened composite materials can exhibit high strength.

The present disclosure provides a composite material. The composite material includes 20 to 40 weight percent (wt. %) of a polymerizable component; 6 to 40 wt. % of ceramic fibers; and 30 to 70 wt. % of nanoclusters. Each of the ceramic fibers has a diameter and a length, the ceramic fibers having an arithmetic mean diameter of 0.3 micrometers to 5 micrometers, and the length of fifty percent of the ceramic fibers (based on a total number of the ceramic fibers) is at least 10 micrometers and the length of ninety percent of the ceramic fibers is no greater than 500 micrometers. The present disclosure also provides a method of making the composite material. The method includes obtaining components and admixing the components to form a composite material. Further, the present disclosure provides a method of using a composite material including placing a composite material near or on a tooth surface, changing the shape of the composite material near or on a tooth surface, and hardening the composite material. In addition, the present disclosure provides dental products and kits. Hardened composite materials can exhibit high strength.

A direct filling composite resin restorative featuring a CTE that is similar to dentin and an antimicrobial is disclosed. The exemplary anti-microbial compound is zinc oxide. The CTE of the direct filling composite resin restorative is in the range of 12-15 ppm/° C. The low CTE is achieved by high filler loading of a trimodal distribution of low CTE filler. By maintaining a CTE substantially similar to that of dentin, the “Marginal Percolation” phenomenon is minimized, which decreases the incidence of secondary caries.