A61K6/30

MEDICAL DEVICE, METHOD FOR PRODUCING MEDICAL DEVICE, AND MEDICAL DEVICE PRODUCING APPARATUS
20170258556 · 2017-09-14 ·

Provided is a medical device including a porous portion and a dense portion, wherein an arithmetic average roughness of a surface of the porous portion is 2.0 μm or greater but 20 μm or less, and wherein an arithmetic average roughness of a surface of the dense portion is less than 2.0 μm.

Dental implant unit

A dental implant unit includes a layer of synthetically created titanium dioxide. The dental implant unit has one end for connection and a lateral surface covering the implant unit except for the end for connection. The lateral surface includes a layer of synthetically created titanium dioxide while the end for connection is free from synthetically created titanium dioxide. Also, a method produces a whitened implantable dental unit. The method includes thermal oxidation of a dental implant unit that includes titanium.

Allyl disulfide-containing addition-fragmentation oligomers

A Addition-fragmentation oligomers containing allylic disulfide groups are described. The oligomers may be added to polymerizable compositions to provide labile crosslinks that can cleave and reform during the polymerization process.

Allyl disulfide-containing addition-fragmentation oligomers

A Addition-fragmentation oligomers containing allylic disulfide groups are described. The oligomers may be added to polymerizable compositions to provide labile crosslinks that can cleave and reform during the polymerization process.

Compositions and methods for dental applications involving zinc-oxide cements

Described are compositions and methods for the removal of zinc-oxide eugenol-based temporary cements or root canal filling materials from a variety of surfaces including surfaces inside the oral cavity, such as teeth, as well as surfaces of objects located outside of the oral cavity, such as instruments and prostheses. In certain compositions, the resin-dentin bond between permanent cements and collagen-containing surfaces can be increased. The compositions are non-toxic, can be used inside the oral cavity, and do not require special disposal procedures.

BIOACTIVE COATED GUTTA-PERCHA AS ROOT CANAL FILLING MATTER

The present invention relates to the deposition of a micro-crystalline hydroxyapatite and tricalcium phosphate coating onto gutta-percha cones, to be used as dental composite for root canal filling. The method proposed for coating involves the surface pretreatment of gutta-percha cones with sodium hydroxide; immersion of gutta-percha cones in simulated body fluid, which contains calcium and phosphate ions; and replacing consumed simulated body fluid after an interval of time, at physiological pH and temperature. The nucleation process results in the biomimetic deposition of a thin and uniform layer of calcium phosphates and hydroxyapatite. Improved characteristics such as in sealing ability, bonding strength, and ability to form hermetic seal, therefore allows the dental composite produced, to be used appropriately as filling matter in root canal treatments.

BIOACTIVE COATED GUTTA-PERCHA AS ROOT CANAL FILLING MATTER

The present invention relates to the deposition of a micro-crystalline hydroxyapatite and tricalcium phosphate coating onto gutta-percha cones, to be used as dental composite for root canal filling. The method proposed for coating involves the surface pretreatment of gutta-percha cones with sodium hydroxide; immersion of gutta-percha cones in simulated body fluid, which contains calcium and phosphate ions; and replacing consumed simulated body fluid after an interval of time, at physiological pH and temperature. The nucleation process results in the biomimetic deposition of a thin and uniform layer of calcium phosphates and hydroxyapatite. Improved characteristics such as in sealing ability, bonding strength, and ability to form hermetic seal, therefore allows the dental composite produced, to be used appropriately as filling matter in root canal treatments.

ANTIMICROBIAL ADHESIVE COMPOSITION WITH COPPER NANOPARTICLES FOR DENTURES

The present invention concerns a new antimicrobial denture adhesive composition useful to be used for fixing dentures, which includes copper nanoparticles (CuNPs) that provides antimicrobial properties against dental pathogens such as Candida albicans, Streptococcus mutans, Staphylococcus aureus and Aggregatibacter actinomycetemcomitans. Surprisingly, the composition for a denture adhesive comprising copper nanoparticles (CuNPs) not only shown excellent antimicrobial properties, but also improved adhesive properties in comparison with other denture adhesives existing currently in the marked, which do not contain said CuNPs.

ANTIMICROBIAL ADHESIVE COMPOSITION WITH COPPER NANOPARTICLES FOR DENTURES

The present invention concerns a new antimicrobial denture adhesive composition useful to be used for fixing dentures, which includes copper nanoparticles (CuNPs) that provides antimicrobial properties against dental pathogens such as Candida albicans, Streptococcus mutans, Staphylococcus aureus and Aggregatibacter actinomycetemcomitans. Surprisingly, the composition for a denture adhesive comprising copper nanoparticles (CuNPs) not only shown excellent antimicrobial properties, but also improved adhesive properties in comparison with other denture adhesives existing currently in the marked, which do not contain said CuNPs.

(METH)ACRYLATE, MONOMER COMPOSITION, MOLDED BODY, COMPOSITION FOR DENTAL MATERIAL, AND DENTAL MATERIAL
20210403632 · 2021-12-30 · ·

A (meth)acrylate includes a compound (X) having a structure formed by a reaction of an epoxy compound (A) containing an epoxy group and a tertiary carbon atom or a quaternary carbon atom, a (meth)acrylic acid (B), and an iso(thio)cyanate compound (C) having two or more iso(thio)cyanate groups.