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Us Patents
Apparatus For Mixing A Liquid And Dry Powdered Components
Brian Edwards - West Milford NJ Paul Higham - Ringwood NJ Joseph Zitelli - River Edge NJ
Assignee:
Howmedica Osteonics Corp. - Allendale NJ
International Classification:
B01F 1100
US Classification:
366209, 366216, 366218
Abstract:
An apparatus for mixing dry and liquid components is used to form a setting paste. A holder is mounted on the apparatus for reciprocating movement with respect to a base of the apparatus. The movement has an amplitude with components in first and second perpendicular directions. A drive system is operatively connected to the holder for imparting said reciprocating movement to said holder at a predetermined number of cycles per minute. A container having a mass of said dry and liquid components therein is mounted in the holder. The mass, amplitude and cycles per minute of reciprocation being chosen to produce an energy input of at least about 3Ã10 Joules per second per 3 cc of mixture.
Brian Edwards - West Milford NJ Paul Higham - Ringwood NJ Joseph Zitelli - River Edge NJ
Assignee:
Howmedica Osteonics Corp. - Allendale NJ
International Classification:
A61L 2402
US Classification:
106 35, 106646, 501 84, 523116, 623 2362
Abstract:
A kit and a method for making a porous cement which self sets to hydroxyapatite and has an interconnected porosity is produced by mixing a calcium source and a phosphate source with a carbonate source and mixing this powdered component with a liquid component having an acid component. The liquid component comprises water or an aqueous solution containing an acid. The acid and the carbonate react to form carbon dioxide thereby producing an interconnected porosity in the normally solid self-hardening bone cement. The method requires only a relatively low weight percent of the acid and base to be mixed with the liquid and powder cement components.
Calcium Phosphate Composition And Method Of Preparing Same
A method for controlling the formation of a hydroxyapatite bone filler from dry calcium phosphate precursors in an aqueous solution uses coated sodium phosphate powder. The sodium phosphate powder is coated with a water soluble cellulose. Until the cellulose dissolves in the aqueous solution setting of the calcium phosphate cements proceeds slowly but when the exposed sodium phosphate particles start to solubilize in the aqueous solution the setting rate increases.
Brian Edwards - West Milford NJ Paul Higham - Ringwood NJ Joseph Zitelli - River Edge NJ
Assignee:
Howmedica Osteonics Corp. - Allendale NJ
International Classification:
B01F 506
US Classification:
366268, 336130, 336332, 336334
Abstract:
An apparatus and method for mixing a liquid component and a powdered component to form a bone filler has first and second syringes each having a barrel, a plunger and an exit port. The plunger is moveable with the barrel of each syringe along a longitudinal axis of the barrel. An end portion of each plunger extends beyond the end of each barrel when the plunger tip is spaced from the exit port and can be activated to move the plunger tip toward the exit port. A mechanism for mixing the liquid and powdered components is operatively connected to each of the barrels and plungers of the first and second syringes so that the relative sliding movement of first and second parts of the mechanism simultaneously moves the plungers and barrels of the first and second syringes relative to one another to move the combined liquid and powdered components back and forth between the first and second syringe.
A process for applying a coating having a therapeutic agent such as an antibiotic to an implant uses the high surface area of a calcium phosphate coated metal implant as a repository for the therapeutic agent. The implant is coated with one or more layers of calcium phosphate minerals such as hydroxyapatite. After the crystalline layer is applied, which is usually done within an aqueous solution, the implant is dried and packaged. Immediately prior to implantation, the implant is removed from the package and the crystalline layer of calcium phosphate is wetted with an aqueous solution containing the therapeutic agent.
Brian Edwards - West Milford NJ Paul Higham - Ringwood NJ Joseph Zitelli - River Edge NJ
Assignee:
Howmedica Osteonics Corp. - Allendale NJ
International Classification:
A61L 2402
US Classification:
501 84, 501 1, 106 35, 106646, 623 2362
Abstract:
A kit and a method for making a porous cement which self sets to hydroxyapatite and has an interconnected porosity is produced by mixing a calcium source and a phosphate source with a carbonate source and mixing this powdered component with a liquid component having an acid component. The liquid component comprises water or an aqueous solution containing an acid. The acid and the carbonate react to form carbon dioxide thereby producing an interconnected porosity in the normally solid self-hardening bone cement. The method requires only a relatively low weight percent of the acid and base to be mixed with the liquid and powder cement components.
Paul Higham - Ringwood NJ Philip F. Williams - Teaneck NJ John Lapszynski - Oak Ridge NJ Chau Ngo - Secaucus NJ
Assignee:
Howmedica Osteonics Corp. - Allendale NJ
International Classification:
B29C 4500
US Classification:
2643281, 264 26, 264340, 264343, 524916
Abstract:
A high strength hydrogel having a constant swelling pressure upon implantation and thereafter is formed by preparing a hydrogel solution and then injecting the solution into a mold and cause to gel. The molded gel is then washed in a saline solution from about one day to twelve weeks, after which the gel is irradiated for sterilization purposes, dehydrated and packaged. The pre-treatment with the use of a physiologic solution results in an implant which exhibits a constant swelling pressure profile after implantation.
A process for applying a coating having a therapeutic agent such as an antibiotic or a bone morphogenic protein to an implant uses the high surface area of a calcium phosphate coated metal implant as a repository for the therapeutic agent. The implant is coated with one or more layers of calcium phosphate minerals such as hydroxyapatite. After the crystalline layer is applied, which is usually done within an aqueous solution, the implant is dried and packaged. Immediately prior to implantation, the implant is removed from the package and the crystalline layer of calcium phosphate is wetted with an aqueous solution containing the therapeutic agent.
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