122 results about "Bone particle" patented technology

A load-bearing osteoimplant, methods of making the osteoimplant and method for repairing hard tissue such as bone and teeth employing the osteoimplant are provided. The osteoimplant comprises a shaped, coherent mass of bone particles which may exhibit osteogenic properties. In addition, the osteoimplant may possess one or more optional components which modify its mechanical and/or bioactive properties, e.g., binders, fillers, reinforcing components, etc.

A load-bearing osteoimplant which comprises a shaped, coherent aggregate of bone particles.

An osteoimplant comprising an expandable, biocompatible material. The expandable material may be demineralized bone particles such as demineralized cancelous chips or demineralized cortical fibers or may be another material such as a polymer. The osteoimplant has a first state and a second expanded state. The osteoimplant may be used with another device or on its own. The osteoimplant may be inserted into a device such as an intervertebral body fusion device in the compressed state. The osteoimplant may be rehydrated to expand to an increased size, for example as far as permitted by the confines of the intervertebral body fusion device and spinal endplates, thereby aiding in greater vertebral endplate contact and conformity in spinal surgery.

Biological-based polyurethanes and methods of making the same. The polyurethanes are formed by reacting a biodegradable polyisocyanate (such as lysine diisocyanate) with an optionally hydroxylated biomolecule to form polyurethane. The polymers formed may be combined with ceramic and/or bone particles to form a composite, which may be used as an osteoimplant.

An osteogenic composition is prepared by a process including the steps of subjecting demineralized bone to an extraction medium to produce an insoluble extraction product and a soluble extraction product, separating the insoluble extraction product and the soluble extraction product, drying the soluble extraction product to remove all or substantially all of the moisture in the soluble extraction product, and combining the dried soluble extraction product of step c) with demineralized bone particles. Preferably, the process does not involve heating.

Methods for increasing osteoinductivity and/or surface area of bone material are provided. The methods include providing bone material and dehydrating the bone material with a solvent at its critical point. A useful solvent for critical point dehydrating is carbon dioxide. Critical point dehydration resulting in increased osteoinductivity and/or surface area can be applied to many types of bone material including bone particles, bone chips, bone fibers, bone matrices, both demineralized and non-demineralized. An implantable composition having an enhanced osteoinductivity and/or osteoconductivity is also provided. The implantable composition contains demineralized bone matrix dried at critical point of carbon dioxide. Critical point dried fibers of a demineralized bone matrix have a BET value from about 40 m²/gm to about 100 m²/gm, a value that is 100 times higher than corresponding vacuum dried or lyophilized DBM fibers.

An osteoimplant is made up of a coherent aggregate of elongate bone particles.

The present invention relates to a method for making bone particles from bone of a variety of sizes and a workpiece forming and holding device for use with the method. The workpiece forming device includes a base and a base frame attached to the surface of the base. An apparatus for forming a solidified mass of bone and immobilization medium is also provided which includes the workpiece forming device and a detachable former member enclosing the base frame. Bone is immersed in an immobilization medium within such workpiece forming device, which is solidified to form a solidified mass of bone and immobilization medium and then subdivided to provide particles of bone in association to with immobilization medium. The immobilization medium may be optionally removed to leave bone particles suitable for use in orthopedic applications including implants.

The invention relates to an artificial knee joint bone fusion prosthesis. The artificial knee joint bone fusion prosthesis comprises a femur condyle prosthesis, a tibia platform prosthesis and a joint pad, wherein the femur condyle prosthesis comprises a joint surface, a condyle combination surface, a intercondylar combination surface, a positioning body, a femur intramedullary stem and a femur intramedullary extending stem; the tibia platform prosthesis comprises a platform body, a tibia combination surface, a wing plate or a positioning body, a tibia intramedullary stem and a tibia intramedullary extending stem; the femur intramedullary stem, the femur intramedullary extending stem, the tibia intramedullary stem and the tibia intramedullary extending stem are hollow, the surfaces of the intramedullary stems and the extending stems have porous or mesh structure so as to ensure that the hollow parts in the stem body can be communicated with the external part; when in use, autograft or allograft crushed bone particles are filled in the hollow parts of the intramedullary stems and the intramedullary extending stems, and after the external bone tissue fuses and grows together with the crushed bone particles filled in the intramedullary stems, the overall elastic modulus can be very close to that of the human bone, thus reaching the aim of effectively preventing the loose between the artificial knee joint bone fusion prosthesis and the sclerotin for long time.

A particulate bone of defined sizes which has a unique property of direct bone osteoinduction without going through endochondral ossification stage is disclosed. The bone is not subjected to chemical extraction or decalcification. This allows for the retention of all physiologically active components of native bone. The invention hinges on the newly discovered ability of bone particles of defined sizes to exert osteoinduction by a pathway superior to and distinct from demineralized bone matrix and similar preparations.

The invention relates to a second cervical vertebra displacer with a merging structure. The second cervical vertebra displacer comprises an atlas connecting part, a fixed connector and a third cervical vertebra connecting part, wherein the atlas connecting part is fixedly connected with the atlas through a hollow atlas bolt, at least one merging hole is arranged on the bolt body of the hollow atlas bolt, the merging hole is internally provided with bone particles, and a support merging device matched with the shape of the lower surface of the atlas is arranged at the lower part of the atlas connecting part. The second cervical vertebra displacer can integrate a vertebral merging device bolt and a vertebral body, and greatly enhance the connecting performance and the fixation performance of the displacer. The second cervical vertebra displacer has the advantages that the displacer is more reliable, and the length of the displacer can be adjusted as required.

The invention is directed toward an improved formable bone composition for application to a bone defect site to promote new bone growth at the site which comprises a new bone growth inducing compound of demineralized lyophilized allograft bone particles ranging from about 100 to 850 microns. The bone particles are mixed in an excipient carrier combination containing carboxymethylcellulose, sodium hyaluronate, and a sodium phosphate saline buffer, the carboxymethylcellulose component of the carrier ranging from about 5.0 to about 11.0% of the composition and the sodium hyaluronate component of the carrier ranging from about 0.3 to about 0.7% of the composition, the composition having a pH between 6.5-7.5.

The invention provides a bone-repairing hydrogel stent and a preparation method thereof. The bone-repairing hydrogel stent comprises a polymer gel carrier and mineralized nano bone particles. The polymer gel carrier comprises polymer gel and matrix metalloprotease responding peptide chains. The matrix metalloprotease responding peptide chains are directly crosslinked to the polymer gel. The bone-repairing hydrogel stent is prepared by 3D printing under the irradiation of UV rays. Furthermore, the invention also relates to a preparation method of the bone-repairing hydrogel stent. The providedbone-repairing hydrogel stent has the advantages of high porosity and mechanical strength, and can intelligently response to mesenchymal stem cells or bone cell systems, promote tissue growth, and induce bone healing. Moreover, the preparation technology is simple, and once moulding can be realized.

Embodiments of the present inventions comprise composites of bone particles and polyurethane(s), as well as methods of making such composite and uses thereof. Certain embodiments further comprise a growth factor that can be provided in powder form. Growth factors may be bone morphogenic proteins, such as rhBMP-2. A porous composite comprises a plurality of bone particles, polyurethanes with which the bone particles are combined, and at least one growth factor. A composition may be moldable and/or injectable. After implantation or injection, a composition may be set to form a porous composite that provides mechanical strength and supports the in-growth of cells. Inventive composites have the advantage of being able to fill irregularly shape implantation site while at the same time being settable to provide the mechanical strength for most orthopedic applications.

The invention relates to an artificial hip joint bone fusion femoral stem. The femoral stem comprises a head part, a neck part and a stem body, wherein the whole or partial stem body is formed by three-dimensional mesh structure, all mesh units are mutually communicated, holes are arranged in the proper places of the stem body and used to be filled with autograft or allograft crushed bone particles; and after the femoral stem is implanted through the surgical operation, the external bone tissue permeates and grows in the three-dimensional mesh and grows together with the crushed bone particles filled in the holes of the stem body, thus reaching the aim of effectively preventing the loose between the artificial hip joint bone fusion femoral stem prosthesis and the sclerotin for long time.