Bonding agent used between oral implant and upper prosthesis

Abstract

The invention relates to a bonding agent used between an oral implant and an upper prosthesis, which comprises a powder agent and a liquid agent. In the powder agent, ultrafine fully vulcanized powder rubber or plastic shock resistant modifier MBS or processing modifier ACR is prepared by respectively mixing organic resin, padding, a reducing agent and other auxiliary components or blending powder prepared from zinc oxide, magnesium oxide, calcium fluoride, tin fluoride and aluminum oxide (trace). The liquid agent comprises a resin substrate, an adhesive monomer, a thinning agent, an oxidizing agent, a polymerization inhibitor or polyacrylic acid, and the balance water, wherein the mass fraction of polyacrylic is 30%-48%. The using process comprises the following steps: weighing the powder and the liquid according to the proportion of 1:1, uniformly mixing the powder and the liquid into paste, and curing the paste for 3-5 minutes under the condition of room temperature.

Description

technical field

[0001] The invention relates to an adhesive used between an oral cavity implant and an upper restorative body, and is particularly suitable for bonding an oral dental implant and its upper restorative body such as a porcelain crown, a porcelain fixed bridge, and the like. Background technique

[0002] The artificial tooth root implant and the alveolar bone tissue in oral implant restoration treatment are osseointegrated. In order to reduce the traumatic impact of mastication force on the alveolar bone tissue during mastication, the artificial tooth root implant should have bone tissue matching mechanical properties. Studies have shown that reducing the elastic modulus of denture implants is more conducive to transferring the load to the surrounding bone tissue in the form of compressive stress, which is conducive to maintaining the stability of the interface and improving the biomechanical compatibility of the implant. . At present, the vast majority of imp...

Examples

Embodiment 1

[0012] Embodiment 1: An adhesive used between an oral implant and an upper prosthesis, which consists of powder and liquid respectively. The powder includes 7 grams of ultrafine fully vulcanized powdered acrylate rubber with a particle size of 50-150 nanometers 10 grams of polymethyl methacrylate and polyhydroxyethyl methacrylate and their modified products; 80 grams of glass powder with a particle size of 3 to 150 microns and activated surface treatment; N, N--dimethyl It is formed by mixing 3 grams of toluidine / sodium p-toluene sulfinate (1:4). The liquid preparation consists of 42 grams of triethylene glycol dimethacrylate, 30 grams of acrylate monomer prepolymer monomer, 26 grams of glycidyl methacrylate, 1.97 grams of benzoyl peroxide, 2,6 --Di-tert-butyl-p-cresol 0.03 g mixed.

Embodiment 2

[0013] Embodiment 2: An adhesive used between an oral implant and an upper prosthesis, which is composed of a powder and a liquid respectively. The powder includes a plastic impact modifier MBS with a particle size of 200-300 nanometers or a processing modification. 6 grams of agent ACR; 11 grams of polymethyl methacrylate and polyhydroxyethyl methacrylate and their modified products; 80 grams of glass powder with a particle size of 3 to 150 microns and activated surface treatment; N, N- -Dimethyl-p-toluidine / sodium p-toluenesulfinate (1:4) mixed with 3 grams. The liquid preparation consists of 42 grams of triethylene glycol dimethacrylate, 30 grams of acrylate monomer prepolymer monomer, 26 grams of glycidyl methacrylate, and 1.97 grams of benzoyl peroxide; 2,6 --Di-tert-butyl-p-cresol 0.03 g mixed.

Embodiment 3

[0014] Embodiment 3: An adhesive used between the oral implant and the upper prosthesis, which consists of powder and liquid respectively. The powder includes 5 grams of ultrafine fully vulcanized powdered acrylate rubber with a particle size of 50-150 nanometers , mixed with 95 grams of powder made of zinc oxide 90% to 95% (mass fraction), magnesium oxide 5% to 10% (mass fraction), calcium fluoride, stannous fluoride, aluminum oxide (trace amount) . The liquid preparation is 30%-48% (mass fraction) of polyacrylic acid and the balance of water.

technical field

[0001] The invention relates to an adhesive used between an oral cavity implant and an upper restorative body, and is particularly suitable for bonding an oral dental implant and its upper restorative body such as a porcelain crown, a porcelain fixed bridge, and the like. Background technique

[0002] The artificial tooth root implant and the alveolar bone tissue in oral implant restoration treatment are osseointegrated. In order to reduce the traumatic impact of mastication force on the alveolar bone tissue during mastication, the artificial tooth root implant should have bone tissue matching mechanical properties. Studies have shown that reducing the elastic modulus of denture implants is more conducive to transferring the load to the surrounding bone tissue in the form of compressive stress, which is conducive to maintaining the stability of the interface and improving the biomechanical compatibility of the implant. . At present, the vast majority of imp...

Examples

Embodiment 1

[0012] Embodiment 1: An adhesive used between an oral implant and an upper prosthesis, which consists of powder and liquid respectively. The powder includes 7 grams of ultrafine fully vulcanized powdered acrylate rubber with a particle size of 50-150 nanometers 10 grams of polymethyl methacrylate and polyhydroxyethyl methacrylate and their modified products; 80 grams of glass powder with a particle size of 3 to 150 microns and activated surface treatment; N, N--dimethyl It is formed by mixing 3 grams of toluidine / sodium p-toluene sulfinate (1:4). The liquid preparation consists of 42 grams of triethylene glycol dimethacrylate, 30 grams of acrylate monomer prepolymer monomer, 26 grams of glycidyl methacrylate, 1.97 grams of benzoyl peroxide, 2,6 --Di-tert-butyl-p-cresol 0.03 g mixed.

Embodiment 2

[0013] Embodiment 2: An adhesive used between an oral implant and an upper prosthesis, which is composed of a powder and a liquid respectively. The powder includes a plastic impact modifier MBS with a particle size of 200-300 nanometers or a processing modification. 6 grams of agent ACR; 11 grams of polymethyl methacrylate and polyhydroxyethyl methacrylate and their modified products; 80 grams of glass powder with a particle size of 3 to 150 microns and activated surface treatment; N, N- -Dimethyl-p-toluidine / sodium p-toluenesulfinate (1:4) mixed with 3 grams. The liquid preparation consists of 42 grams of triethylene glycol dimethacrylate, 30 grams of acrylate monomer prepolymer monomer, 26 grams of glycidyl methacrylate, and 1.97 grams of benzoyl peroxide; 2,6 --Di-tert-butyl-p-cresol 0.03 g mixed.

Embodiment 3

[0014] Embodiment 3: An adhesive used between the oral implant and the upper prosthesis, which consists of powder and liquid respectively. The powder includes 5 grams of ultrafine fully vulcanized powdered acrylate rubber with a particle size of 50-150 nanometers , mixed with 95 grams of powder made of zinc oxide 90% to 95% (mass fraction), magnesium oxide 5% to 10% (mass fraction), calcium fluoride, stannous fluoride, aluminum oxide (trace amount) . The liquid preparation is 30%-48% (mass fraction) of polyacrylic acid and the balance of water.