A61K6/06

METHOD FOR CREATING A MINERAL TRIOXIDE AGGREGATE MATERIAL WITH IMPROVED BIOLOGICAL EFFECTS
20190021958 · 2019-01-24 · ·

A dental device is improved in its ability to produce hydroxyl apatite by having a layer of mineral trioxide aggregate (MTA) deposited thereon. A tile of MTA is prepared, heat treated and sintered to produce a micronized tile of MTA that can then be deposited by physical vapor depositions, hot isostatic pressing, molding or other conventional technique.

Dental Materials Based On Low-Viscosity Radically Polymerizable Monomers With A High Refractive Index
20190015301 · 2019-01-17 ·

Radically polymerizable, difunctional phenylene sulfide according to Formula I

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in which X, Y independently of each other in each case are absent or are O or NR.sup.6, R.sup.1, R.sup.2 independently of each other in each case are H, a linear or branched C.sub.1 to C.sub.10 alkyl radical, OR.sup.7, SR.sup.8, Cl or Br, R.sup.3 is absent or is a C.sub.1-C.sub.10 alkylene radical which can be interrupted by O or S, R.sup.4 is absent or is a C.sub.1-C.sub.10 alkylene radical which can be interrupted by O or S, wherein R.sup.3 and R.sup.4 cannot be absent at the same time, R.sup.5 is H or a C.sub.1-C.sub.5 alkyl radical, R.sup.6, R.sup.7, R.sup.8 independently of each other in each case are H or a linear or branched C.sub.1 to C.sub.10 alkyl radical, a, b, c, d independently of each other in each case are 0 or 1 and e is 1 or 2.

Polymer Materials With Silane-Based Transfer Reagents

Radically polymerizable silane according to the general formula I

##STR00001##

in which R.sup.1 is a linear or branched aliphatic C.sub.1-C.sub.9-alkyl radical, phenyl or alkylated phenyl radical, R.sup.2, R.sup.3 independently of each other in each case are absent or are a linear or branched aliphatic C.sub.1-C.sub.20-alkylene radical, which can be interrupted by S or O atoms, R.sup.4, R.sup.5, R.sup.6 independently of each other in each case are Cl, OCH.sub.3, OC.sub.2H.sub.5, CH.sub.3 or C.sub.2H.sub.5, X is CH.sub.2 or O, Y is absent, or is O or NR, wherein R is H or a C.sub.1-5-alkyl radical, and Z is absent, or is O, NR, COO, CONR, OCOO, OCONR, or NRCONR, wherein R is H or a C.sub.1-5-alkyl radical and wherein the radicals R.sup.2 and R.sup.3 cannot be absent at the same time and Z is absent if R.sup.2 or R.sup.3 is absent, polycondensates based thereon and fillers surface-modified therewith.

DENTAL COMPOSITION AND METHOD OF DIRECT PULP CAPPING

A method of direct pulp capping of a tooth including administering a dental composition comprising betamethasone and gentamicin onto an exposed pulp of a tooth, and covering the dental composition present on the tooth with a glass ionomer cement. The dental composition is administered in an amount effective to form a calcification over the exposed pulp. A dental composition having betamethasone, gentamicin, and optionally including a Portland cement. The dental composition is administered to an exposed pulp of a tooth to form a calcification over the exposed pulp.

Injectable, Biodegradable Bone Cements And Methods Of Making And Using Same

Compositions of, methods of making, and methods of using alkaline earth phosphate bone cements are disclosed.

Single paste type hydraulic dental filling composition
10154945 · 2018-12-18 · ·

According to one aspect of the present disclosure, there is provided a single paste type hydraulic dental filling composition. The single paste type hydraulic dental filling composition includes hydraulic cement, non-aqueous liquid having hygroscopic properties, and a radiopaque material.

OBTURATION COMPOSITION

A dental composition comprising pre-reacted particulate mineral trioxide aggregate (MTA) dispersed in a hydrogel wherein the content of MTA in the composition is in the range of 20 to 50 percent by weight based on the total weight of the composition.

FLOWABLE COMPOSITION

A dental composition comprising a pre-reacted particulate mineral trioxide aggregate (MTA) dispersed in a polymer matrix wherein the content of MTA in the composition is in the range of 20 to 50 percent by weight based on the total weight of the composition.

Monolithic bodies of sintered chemically bonded ceramic (CBC) biomaterial prepared ex vivo for implantation, preparation and use thereof
10117964 · 2018-11-06 · ·

The present invention generally relates to the use of pre-formed bodies of Chemically Bonded Ceramics (CBCs) biomaterial for implantation purposes wherein the bodies are prepared ex vivo allowing process parameters to be optimized for desired long term properties of the resulting CBC biomaterial. More particularly, the pre-formed CBC material bodies of the present invention are sintered. The pre-formed body of CBC material is machined to the desired geometry and then implanted using a CBC cementation paste for fixation of the body to tissue. The invention also relates to a method of preparing pre-formed bodies of CBC biomaterial for implantation purposes, methods of preparing an implant thereof having desired geometry, and a method of implantation of the implant, as well as a kit for use in the method of implantation.

RESIN BLOCK AND PROCESS FOR PRODUCING THE SAME
20180303587 · 2018-10-25 ·

A resin block that can be favorably used for obtaining dental prosthetics through the milling work, containing very little voids, having excellent property for being cut, exhibiting excellent appearance and mechanical strength, and without permitting the formation of defective products. The resin block contains a thermoplastic resin having a fluidizing temperature in a range of 310 to 500 C. and inorganic particles in an amount of 30 to 150 parts by mass per 100 parts by mass of said thermoplastic resin. The inorganic particles are at least one kind of inorganic oxide particles selected from the group consisting of silica particles, silica composite particles of silica and other metal oxides, titania particles, and titania composite particles of titania and other metal oxides. The resin block has a thick portion of a thickness of at least not less than 5 mm, and does not contain any void whose length is not less than 1.0 mm.