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131 results about "Nonunion" patented technology

Nonunion is permanent failure of healing following a broken bone unless intervention (such as surgery) is performed. A fracture with nonunion generally forms a structural resemblance to a fibrous joint, and is therefore often called a "false joint" or pseudoarthrosis (the Greek stem "pseudo-" means false and "arthrosis" means joint). The diagnosis is generally made when there is no healing between two sets of medical imaging such as X-ray or CT scan. This is generally after 6–8 months.

System and Method of Up-Regulating Bone Morphogenetic Proteins (Bmp) Gene Expression in Bone Cells Via the Application of Fields Generated by Specific and Selective Electric and Electromagnetic Signals

InactiveUS20070299472A1High expressionBiocideElectrotherapyHuman DNA sequencingBone Morphogenetic Protein Gene
Methods and devices are described for the regulation of bone morphogenetic protein gene expression in bone cells via the application of fields generated by specific and selective electric and electromagnetic signals in the treatment of diseased or injured bone. By gene expression is meant the up-regulation or down-regulation of the process whereby specific portions (genes) of the human genome (DNA) are transcribed into mRNA and subsequently translated into protein. Methods and devices are provided for the targeted treatment of injured or diseased bone tissue that include generating specific and selective electric and electromagnetic signals that generate fields optimized for increase of bone morphogenetic protein gene expression and exposing bone to the fields generated by specific and selective signals so as to regulate bone morphogenetic protein gene expression in such bone tissue. The resulting methods and devices are useful for the targeted treatment of bone fractures, fractures at risk, delayed unions, nonunion of fractures, bone defects, spine fusions, osteonecrosis or avascular necrosis, as an adjunct to other therapies in the treatment of one or all of the above, and in the treatment of osteoporosis.
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA

Regulation of transforming growth factor-beta (TGF-beta) gene expression in living cells via the application of specific and selective electric and electromagnetic fields

Methods and devices are described for the regulation of Transforming Growth actor (TGF)-β1, β2, and / or β3 protein gene expression in bone cells and other tissues via the capacitive coupling or inductive coupling of specific and selective electric fields to the bone cells or other tissues, where the specific and selective electric fields are generated by application of specific and selective electric and electromagnetic signals to electrodes or one or more coils or other field generating device disposed with respect to the bone cells or other tissues so as to facilitate the treatment of diseased or injured bone and other tissues. By gene expression is meant the up-regulation or down-regulation of the process whereby specific portions (genes) of the human genome (DNA) are transcribed into mRNA and subsequently translated into protein. Methods and devices are provided for the targeted treatment of injured or diseased bone and other tissue that include generating specific and selective electric and electromagnetic signals that generate fields in the target tissue optimized for increase of TGF-β1, β2, and / or β3 protein gene expression and exposing bone and other tissue to the fields generated by specific and selective signals so as to regulate TGF-β1, β2, and / or β3 protein gene expression in such tissue. The resulting methods and devices are useful for the targeted treatment of bone fractures, fractures at risk, delayed unions, nonunion of fractures, bone defects, spine fusions, osteonecrosis or avascular necrosis, as an adjunct to other therapies in the treatment of one or all of the above, in the treatment of osteoporosis, and in other conditions in which TGF-β1, β2, and / or β3 protein may be implicated.
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA

Regulation of transforming growth factor-beta (TGF-beta) gene expression in living cells via the application of specific and selective electric and electromagnetic fields

Methods and devices are described for the regulation of Transforming Growth actor (TGF)-β1, β2, and/or β3 protein gene expression in bone cells and other tissues via the capacitive coupling or inductive coupling of specific and selective electric fields to the bone cells or other tissues, where the specific and selective electric fields are generated by application of specific and selective electric and electromagnetic signals to electrodes or one or more coils or other field generating device disposed with respect to the bone cells or other tissues so as to facilitate the treatment of diseased or injured bone and other tissues. By gene expression is meant the up-regulation or down-regulation of the process whereby specific portions (genes) of the human genome (DNA) are transcribed into mRNA and subsequently translated into protein. Methods and devices are provided for the targeted treatment of injured or diseased bone and other tissue that include generating specific and selective electric and electromagnetic signals that generate fields in the target tissue optimized for increase of TGF-β1, β2, and/or β3 protein gene expression and exposing bone and other tissue to the fields generated by specific and selective signals so as to regulate TGF-β1, β2, and/or β3 protein gene expression in such tissue. The resulting methods and devices are useful for the targeted treatment of bone fractures, fractures at risk, delayed unions, nonunion of fractures, bone defects, spine fusions, osteonecrosis or avascular necrosis, as an adjunct to other therapies in the treatment of one or all of the above, in the treatment of osteoporosis, and in other conditions in which TGF-β1, β2, and/or β3 protein may be implicated
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA

External fixation rack elasticity device

The invention discloses a resilient device of an external fixator in the clinical application of orthopaedics. The resilient device consists of a cylinder, a sliding axle in the cylinder, a flexible apparatus, a sliding nail body and a sliding axle stopper. An anti-spin rivet, a pressure regulation rivet, a pressure regulation nut, a tightening jack bolt, a hollow screw on the cylinder wall and a pressurization hole are arranged in the radial direction on the cylinder wall, wherein, the sliding axle stopper can be provided with a stop jack bolt in the radial direction on the cylinder wall, or a stop nut or a stop fixture block can be arranged on the sliding axle; the cylinder wall can be designed to have equal inner diameters at the upper and lower parts or have the inner diameter of the upper part at the corresponding position of the sliding axle larger than that of the lower part; the flexible device can be made into a flexible capsule or a spring; and the sliding nail body is connected with the cylinder in a sliding manner. The resilient device can match with external fixators of different shapes and structures to form external flexible fixators. When a limb with a fracture suffers axial pressure, the external flexible fixator can have a slight axial movement so that an interaction force can be generated due to the slight movement at the end of fracture so as to stimulate callus to grow at the end of fracture. The resilient device can avoid osteoporosis due to stress shielding of the external fixator, quicken the fracture healing, increase the strength of healed bone and effectively prevent delayed fracture healing or nonunion.
Owner:河南科科生物科技有限公司

Formula of paste for removing slough and promoting growth of tissue regeneration

In order to overcome symptoms of wound infection, short healing time, relapse and infection, easy incrustation to form scar proliferation and nonunion of wound for long treatment in conventional treatment of traumas as well as allergy to antigen of diabetics and nonunion of wounds of fragile patients, the invention provides a formula of paste for removing slough and promoting growth of tissue regeneration. The formula comprises the following traditional Chinese medicines in parts by weight: 18-22 parts of frankincense, 18-22 parts of myrrh, 13-17 parts of elephant hide, 13-17 parts of lithospermum, 18-22 parts of angelica sinensis, 23-28 parts of astragalus membranaceus, 13-18 parts of muskone, 22-27 parts of propolis, 13-17 parts of salviae miltiorrhizae and 13-17 parts of golden cypress. The forming state of the medicine is a paste or powder. The paste provided by the invention can regenerate severed fingers and heal malignant traumas and infection of soft tissues for long treatment while heals non-pathogenic traumas and pathogenic traumas as well as sport injuries. The patients do not use antibiotics which cause dysfunction of the body. The using method is simple and convenient, and no pains are generated during secondary wet treatment, so that pains of the patients are reduced, and the treatment cost and time are shortened.
Owner:魏春战

Preparation method of immortalized human cartilage endplate stem cell line and use of immortalized human cartilage endplate stem cell line

InactiveCN103865877AStrong osteogenic differentiation abilityLow priceMicroorganism based processesFermentationBone tissue engineeringStem cell line
The invention belongs to the technical field of cell engineering, and particularly relates to a preparation method of an immortalized human cartilage endplate stem cell line and use of the immortalized human cartilage endplate stem cell line. The invention aims to solve the technical problem of providing an effective preparation method for constructing the immortalized human cartilage endplate stem cell line. The technical scheme is as follows: the preparation method for constructing the immortalized human cartilage endplate stem cell line by adopting the lentiviral transfection technology comprises the following steps: a, constructing a SV40T antigen virus vector; b, carrying out gene transfection of a human endplate stem cell on SV40T antigen; and c, passaging and sieving to obtain the immortalized human cartilage endplate stem cell line. The invention further provides the use of the immortalized human cartilage endplate stem cell line prepared by the method in preparation of bone tissue engineering materials. The immortalized human cartilage endplate stem cell line provided by the invention can be applied to preparation of a tissue-engineered bone and clinically provides a seed cell of the bone tissue engineering low in price and strong in osteogenic capability for the patients with a series of long bone defects and bone nonunion.
Owner:THE SECOND AFFILIATED HOSPITAL ARMY MEDICAL UNIV

Culture method for composition of periosteal biological scaffold and allogenic seed cells

The invention discloses a culture method for the composition of a periosteal biological scaffold and allogenic seed cells. The culture method comprises the following steps: the non-immunogenic periosteal biological scaffold and the seed periosteal cells are prepared; the non-immunogenic periosteal biological scaffold is sealed after low-temperature drying; after gamma-ray disinfection of the non-immunogenic periosteal biological scaffold, the seed periosteal cells, with the concentration of 1*106 per milliliter, are dripped on the surface of the disinfected scaffold; a culture medium is added after the periosteal cells gradually permeate into the non-immunogenic periosteal biological scaffold together with a suspension, the medium change is carried out every 2 to 3 days, and the in-vitro composite culture lasts for one week. The periosteal biological scaffold obtained through the method has the characteristics of complete removal of immunogenic cells, as well as good preservation of the structure and major components of extracellular matrix; effective composition of the allogenic periosteal cells and the biological scaffold can be achieved, so that a biological composite scaffold material can be provided for tissue engineering researches on bone defects and bone nonunion.
Owner:THE FIRST AFFILIATED HOSPITAL OF WENZHOU MEDICAL UNIV

External fixation rack elasticity device

The invention discloses a resilient device of an external fixator in the clinical application of orthopaedics. The resilient device consists of a cylinder, a sliding axle in the cylinder, a flexible apparatus, a sliding nail body and a sliding axle stopper. An anti-spin rivet, a pressure regulation rivet, a pressure regulation nut, a tightening jack bolt, a hollow screw on the cylinder wall and apressurization hole are arranged in the radial direction on the cylinder wall, wherein, the sliding axle stopper can be provided with a stop jack bolt in the radial direction on the cylinder wall, ora stop nut or a stop fixture block can be arranged on the sliding axle; the cylinder wall can be designed to have equal inner diameters at the upper and lower parts or have the inner diameter of the upper part at the corresponding position of the sliding axle larger than that of the lower part; the flexible device can be made into a flexible capsule or a spring; and the sliding nail body is connected with the cylinder in a sliding manner. The resilient device can match with external fixators of different shapes and structures to form external flexible fixators. When a limb with a fracture suffers axial pressure, the external flexible fixator can have a slight axial movement so that an interaction force can be generated due to the slight movement at the end of fracture so as to stimulate callus to grow at the end of fracture. The resilient device can avoid osteoporosis due to stress shielding of the external fixator, quicken the fracture healing, increase the strength of healed bone and effectively prevent delayed fracture healing or nonunion.
Owner:河南科科生物科技有限公司

Regulation of fibroblastic growth factor-2 (FGF-2) gene expression in living cells with the application of specific and selective electric and electromagnetic fields

Methods and devices are described for the regulation of Fibroblastic Growth Factor-2 mRNA and / or FGF-2 protein in bone cells and other tissues via capacitive coupling or inductive coupling of specific and selective electric and / or electromagnetic fields to the bone cells or other tissues, where the specific and selective fields are generated by application of specific and selective signals to electrodes or one or more coils or other field generating device disposed with respect to the bone cells or other tissues so as to facilitate the treatment of diseased or injured bone and other tissues. By gene expression is meant the up-regulation or down-regulation of the process whereby specific portions (genes) of the human genome (DNA) are transcribed into mRNA and subsequently translated into protein. Methods and devices are provided for the targeted treatment of injured or diseased bone and other tissue that include generating specific and selective signals that generate electric and / or electromagnetic fields in the target tissue optimized for increase of FGF-2 protein gene expression and exposing bone and other tissue to the fields generated by specific and selective signals so as to regulate FGF-2 protein gene expression in such tissue. The resulting methods and devices are useful for the targeted treatment of osteoporosis, osteopenia, osteonecrosis, fresh bone fractures, fractures at risk, nonunion, bone defects, spine fusion, and / or other conditions in which FGF-2 protein has been implicated.
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA
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