A bone-repairing agent excellent in workability and applicability to clinical surgical techniques and having a drastically enhanced bone formation rate, obtained by including an elastin hydrolysate in a complex of DNA and at least one selected from the group consisting of protamine, a protamine derivative, and a protamine hydrolysate can be provided. A medical or dental material for bone formation using this bone-repairing agent can be provided.

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

Cellulose cyanoacrylate is employed to bond two surfaces, fill voids or duplicate the shape of a three-dimensional object, Two surfaces may be bonded by placing a sheet of cellulose material between the surfaces and applying cyanoacrylate glue around the edge of the sheet until saturated and allowing it to cure. Paper toweling may favorably be employed as the cellulose material. A break or fracture in an article can be overlaid with a sheet of cellulose that when saturated with cyanoacrylate glue and temporarily held in place and shaped with a releasable film, the fracture can be corrected. A dry powder comprising highly abrasion-resistant particles can be mixed with the cellulose material to enhance abrasion resistance and to improve long-term color stabilityespecially important for dental cavity treatment. To duplicate the shape of a three-dimensional object, a sheet of releasable film is placed over the object, followed by a sheet of cellulose that is then saturated with cyanoacrylate glue. A sheet of releasable film is then placed over the cellulose and used to hold the cellulose in place and shape it as it hardens.

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

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

The present invention concerns the preparation of chemically modified derivatives of chitosan with acrylic groups and their use in the field of enamel-dentin adhesives. Chitosan derivatives have physical-chemical features (hydrophilicity, presence of electrical charges on the chain) which allow them to interact with the organic part of the demineralized tooth. At the same time, the acrylic groups incorporated in the polymer chain allow the formation of a covalent bond with the restorative material used in the dental field that is typically composed of acrylic resins. By combining the adhesion to the tooth surface and the bond with the restorative material, the chemically modified chitosan described herein is able to increase the lifespan of the dental restoration and can thus find use in the field of adhesives, in particular enamel-dentin adhesives.

A vegetable-based adhesive preparation for mandibular prostheses. The preparation has improved adhesive properties, consistency and stability as a result of a filler containing: 35 to 45 wt. % vegetable oil; 25 to 50 wt % structure-forming stabilizer; 5 to 15 wt % bonding agent; and silicon oxide making up the remainder.

Methods for removing endotoxin from naturally occurring materials, such as polysaccharides (e.g., agarose and/or carrageenan) are described herein. Polysaccharides that are substantially free of endotoxins and uses thereof are also described. The polysaccharide materials can be isolated from microorganisms, multicellular organisms, such as, algae, plants, seaweed, etc. The method involves the use of acidic and basic solutions to hydrolyze the lipid-polysaccharide bond in endotoxins. Cleaving the fatty acid from the polysaccharide reduces the water-solubility of the fatty acid and enables its removal with an organic solvent such as ethanol. The polysaccharide component can also undergo acidic or basic hydrolysis due to the weak glycosidic bond between the sugar rings.