Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

106results about How to "Avoid stress shielding" patented technology

Bone grafts

Spinal spacers 20 are provided for fusion of a motion segment. The spacers include a load bearing member 21 having a wall 22 sized for engagement within a space between adjacent vertebrae to maintain the space and an effective amount of an osteogenic composition to stimulate osteoinduction. The osteogenic composition includes a substantially pure osteogenic factor in, a pharmaceutically acceptable carrier. In one embodiment the load bearing member includes a bone graft impregnated in an osteogenic composition. In another embodiment, the osteogenic composition 30 is packed within a chamber 25 defined in the graft. Any suitable configuration of a bone graft is contemplated, including bone dowels, D-shaped spacers and cortical rings. A spinal spacer 300 for engagement between vertebrae is also provided which includes a body 301 formed of a bone composition. The body 301 includes a first end 311, an opposite second 315 end, a superior face 335 defining a superior vertebral engaging surface 337 and an inferior face 338 defining an inferior vertebral engaging surface 340. At least one of the vertebral engaging surfaces defines a set of migration resistance grooves 350. Each of the grooves 350 includes a first face 355 defining an angle of no more than about 90 degrees relative to the engaging surface 340 and a second opposing sloped face 360. The first and second faces 355, 360 define an arcuate pocket 370 therebetween for trapping vertebral bone to resist migration of the spacer 300. In one embodiment, the grooves 350 are arranged in series in that all of the second faces 360 slope in the same direction.
Owner:MEDTRONIC SOFAMOR DANEK

Bone grafts

Spinal spacers 20 are provided for fusion of a motion segment. The spacers include a load bearing member 21 having a wall 22 sized for engagement within a space between adjacent vertebrae to maintain the space and an effective amount of an osteogenic composition to stimulate osteoinduction. The osteogenic composition includes a substantially pure osteogenic factor in, a pharmaceutically acceptable carrier. In one embodiment the load bearing member includes a bone graft impregnated in an osteogenic composition. In another embodiment, the osteogenic composition 30 is packed within a chamber 25 defined in the graft. Any suitable configuration of a bone graft is contemplated, including bone dowels, D-shaped spacers and cortical rings. A spinal spacer 300 for engagement between vertebrae is also provided which includes a body 301 formed of a bone composition. The body 301 includes a first end 311, an opposite second 315 end, a superior face 335 defining a superior vertebral engaging surface 337 and an inferior face 338 defining an inferior vertebral engaging surface 340. At least one of the vertebral engaging surfaces defines a set of migration resistance grooves 350. Each of the grooves 350 includes a first face 355 defining an angle of no more than about 90 degrees relative to the engaging surface 340 and a second opposing sloped face 360. The first and second faces 355, 360 define an arcuate pocket 370 therebetween for trapping vertebral bone to resist migration of the spacer 300. In one embodiment, the grooves 350 are arranged in series in that all of the second faces 360 slope in the same direction.
Owner:RAY III EDDIE F +4

Medical titanium/magnesium composite material and preparation method thereof

InactiveCN103599560AAvoid stress shieldingGood for bone conductionSurgeryProsthesisPorosityTitanium alloy
The invention discloses a medical titanium/magnesium composite material which comprises a porous skeleton, wherein the porous skeleton is prepared from medical-grade titanium wires or titanium alloy wires and prepared into a preset shape and a preset porosity by using a conventional winding or knitting machine, the porous skeleton is filled with three-dimensional through pores with different porosities capable of meeting various bone implantation requirements, then a medical magnesium or magnesium alloy melt is infiltrated in the pores of the porous skeleton by pressureless infiltration or negative-pressure suction casting, and after the porous skeleton is cooled, a medical titanium/magnesium composite material is formed. The composite material disclosed by the invention is reasonable in structure and excellent in mechanical properties; in the early stage of body implantation, the mechanical properties of the composite material can be matched with bones well, thereby avoiding stress shielding; after the composite material is implanted, with the degradation of magnesium, a porous structure of an implant is constantly restored, so that bone conduction is facilitated, and the requirements of most of bone filling, bone repair and bone transplantation applications can be met, therefore, the composite material is applicable to bone implanting operations with relatively high strength requirements.
Owner:SHANGHAI JIAO TONG UNIV

Preparation method of porous implant filled with O-intersecting lines units

InactiveCN105559947AThe preparation method is reliable and feasibleGreat potentialJoint implantsFemoral headsSand blastingPorous implant
The invention provides a preparation method of a porous implant filled with O-intersecting lines units. The preparation method comprises the following steps: drawing a three-dimensional model of the O-intersecting lines units, controlling the bore diameter, wall thickness and porosity of the three-dimensional model according to the given specific dimension so as to generate a unit structure cell body, carrying out array copying operation on the unit structure cell body, thus obtaining a space porous network body, introducing in a femoral three-dimensional surface model, scaling the model to reach the proportion actually needed, carrying out cutting and Boolean operation on the porous network body and the femoral three-dimensional surface, thus obtaining a porous main body part, drawing the femoral steam end and a bolt positioning hole part by utilizing three-dimensional modeling, combing the porous main body part to enable the porous main body part to form a single-output porous implant body, saving the single-output porous implant body into an output format file and transmitting the file to layering software, adding with a bottom surface support, printing the porous implant body by adopting a 3D printer, clearing a substrate plate, taking out the porous implant, carrying out sand blasting treatment on the porous implant, and packaging the porous implant. With the adoption of the preparation method, units which are regular and uniform and having no closure can be generated, and the stressing uniformity is guaranteed.
Owner:GUANGZHOU INST OF ADVANCED TECH CHINESE ACAD OF SCI

Porous implant filled with O-intersecting lines units

InactiveCN105496611AThe preparation method is reliable and feasibleGreat potentialJoint implantsTissue regenerationBone structureTissue fluid
A porous implant filled with O-intersecting lines units is mainly oriented to femoral stems and comprises a femoral stem end, a porous main body part and a screw positioning hole part, wherein the femoral stem end is used for positioning the porous implant, the screw positioning hole part is used for fixing the implant and a host, the porous main body part is a three-dimensional through porous network entity mainly formed by being filled with the O-intersecting lines units, the porous network entity comprises hollowed-out entities formed by scanning of O-intersecting lines unit cylinders penetrating through and crossing with one another in space, the hollowed-out entities are formed by pairwise perpendicular and linearly stacked O-intersecting lines unit cylinder surfaces, and the porous network entity has the pore diameter ranging from 400 mu m to 1,000 mu m, the unit wall thickness ranging from 80 mu m to 120 mu m and the porosity ranging from 55% to 85%. Thus, a porous network structure formed by stacking of the hollowed-out entities is close to a bone structure, has the high porosity, the high communication ratio and the larger surface contact area, is suitable for new bone ingrowth and circulation of nutrition tissue liquids and has the considerable clinical medical prospect.
Owner:GUANGZHOU INST OF ADVANCED TECH CHINESE ACAD OF SCI

Preparation method of titanium foams for cancellous bone

The invention relates to a preparation method of titanium foams for cancellous bone. The preparation method comprises the following steps of: (1) mixing raw materials, namely selecting a primary mixture which is obtained by uniformly mixing titanium powder and a pore forming agent in a grinding body, wherein the mass part ratio of the titanium powder to the pore forming agent is (42.8-48.2):(52.8-58.2); (2) carrying out one-direction pressing on the primary mixture by adopting a universal material testing machine to prepare a green pressing body, wherein the one-direction pressure is 200-250MPa, and the pressure holding time is 1 minute; and (3) putting the green pressing body into a vacuum carbon tube furnace, sintering the green pressing body for 2 hours at 1200-1300 DEG C in an argon protective atmosphere to ensure that the pore forming agent is removed, and finally cooling along with the furnace to obtain the titanium foams. According to the titanium foams prepared by using the preparation method, the Young modulus is matched with that of the cancellous bone of the human body, therefore the stress shielding phenomenon is effectively avoided, and an implant can be permanently fixed; and meanwhile, the titanium foams can be prevented from being oxidized as far as possible by adopting the argon protective atmosphere.
Owner:CHONGQING UNIV

Pressure-adjustable combined-type outer fixing support and pressure-adjustable fixing arm

The invention relates to a pressure-adjustable combined-type outer fixing support for clinical orthopedic application. Combining forms of the pressure-adjustable combined-type outer fixing support include a single arm type, a semi-ring type and a ring type, fixing clamping blocks include knitting needle clamping blocks and knitting rod clamping blocks, a pressure-adjustable fixing arm is composed of an adjusting shaft, a sliding fit thread sleeve, an elastic device, a connecting nut, a fastening nut and a fixing rod, the sliding fit thread sleeve is radially provided with a limiting pin, a limiting jack screw, a pressure adjusting pin, an outer ferrule, an inner ferrule, a pressure adjusting nut and a pressure adjusting pin hole, the adjusting shaft is in sliding fit with the sliding fit thread sleeve, the connecting nut is in threaded connection with the sliding fit thread sleeve and the fastening nut, the fastening nut and a pipe clamping pin are in relatively fixed fit, the elastic device is composed of a spring or an elastic capsule, a pressure sensor, a sliding base, a pressure sensor connecting device and a pressure displayer and can be provided with a piezometer or not. The pressure-adjustable combined-type outer fixing support can transmit stress to enable stress to be generated at a fracture end, stress shielding can be avoided, and delayed fracture healing and fracture disunion are prevented.
Owner:河南科科生物科技有限公司

Fracture external fixing frame with adjustable axial pressure among bone blocks

The invention relates to a fracture external fixing frame and particularly relates to a fracture external fixing frame with an adjustable axial pressure among bone blocks, belonging to external fixation instruments for fracture treatment. According to the fracture external fixing frame, the problem that the space among fractured blocks usually cannot be properly pressurized when fracture is steadily fixed by virtue of an existing fixing instrument is solved. The fracture external fixing frame is characterized in that a frame rod is segmented, and one or two ends of each segment is / are providedwith plugs or interfaces; spring devices (including one or more of metal springs, gas springs and elastic matter pads) are arranged in the plugs or the interfaces and are spliced to form connecting devices for adjusting the axial pressure among the bone blocks, and the frame rod segments can form an integrated combined frame rod by the connecting devices. By adjusting the elastic forces of the whole spring devices, the action forces of the connecting devices on two frame rod segments on two sides in the long-axis direction are changed, and therefore, the axial pressure among the bone blocks is adjusted. The fracture external fixing frame is applied to fracture fixation, and when the fracture is steadily fixed, excessive stress shielding can be avoided, and the axial pressure among the bone blocks can be flexibly quantized, adjusted and controlled into a proper level required by fracture healing, so that fracture healing is promoted.
Owner:王培林

Multilayer bionic joint based on curved surface 3D printing and preparation method thereof

PendingCN112076009ATo achieve the effect of integrationAids in healingJoint implantsTomographyPorous tantalumBones joints
The invention discloses a bionic bone joint based on curved surface 3D printing and a preparation method thereof. The multilayer bionic joint is formed by an inner layer, a middle layer and an outer layer which are in close contact in sequence, wherein the inner layer is a porous tantalum metal support, the middle layer is a solid biological ceramic support, the outer layer is a solid gelatin/ sodium alginate composite hydrogel support, the inner layer, the middle layer and the outer layer are all of an arc-shaped shell structure, the radian of the arc-shaped shell is 120-240 degrees, and a cell loading cavity formed by continuous or discontinuous edges formed by protruding outwards from the surface of the outer layer and grooves formed between the edges is formed in the surface of the outer layer. The multilayer bionic joint is large in arc surface radian and suitable for repairing large-area osteochondral joint defects, and the repairing area can be larger than 1/2 of the area of thewhole joint. Cells are inoculated into the cell loading cavity, so that the adhesion rate of the cells is increased, and the problem that the surface of the outer layer of the bionic joint is smooth,so that the inoculated cells are not prone to adhesion is solved.
Owner:AFFILIATED ZHONGSHAN HOSPITAL OF DALIAN UNIV +1
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products