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Humanization active forging bone and preparation method thereof

A calcined bone, humanized technology, applied in medical science, prosthesis, etc., to achieve moderate degradation speed, convenient clinical operation, and favorable effects of adhesion and growth

Active Publication Date: 2012-08-29
SHAANXI RUISHENG BIOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The patent uses a collagen coating, which is difficult to form a firm bond with the material; and after calcining bone composite cells, it is difficult to apply clinically due to the immunogenicity of the cells; at the same time, it is difficult to prefabricate irregular bone defects into the desired shape , these deficiencies limit the practical application of this material

Method used

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  • Humanization active forging bone and preparation method thereof
  • Humanization active forging bone and preparation method thereof
  • Humanization active forging bone and preparation method thereof

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] 2. Calcination: Put the dried bone fragments into a corundum crucible and calcinate in a muffle furnace; raise the temperature to 800°C, continue calcination at a constant temperature for 4 hours, lower the temperature in the furnace to room temperature, and take out the calcined bone;

[0024] 3. Surface treatment: After the calcined bone is mechanically crushed, the calcined bone particles with a particle size of 100-200 μm are selected with a sieve, placed in 2 mmol / ml RGD polypeptide solution, soaked for 1 hour after negative pressure suction; Sterilize after drying.

[0025] 4. Preparation of bone marrow mesenchymal stem cell culture medium: its components include by volume percentage: commercial minimum essential culture medium DMEM 67.5%, commercial culture medium F12 22.5%, fetal bovine serum 10%, insulin 50ng / ml, hydrogenated can Pine 500ng / ml, adenine 0.05mM, basic fibroblast growth factor 4ng / ml, transferrin 8μg / ml, vitamin C 40μg / ml.

[0026] 5. Cell planti...

Embodiment 2

[0031] 2. Calcination: put the dried bone fragments into a corundum crucible, and calcinate in a muffle furnace; raise the temperature to 600°C, continue to calcine at a constant temperature for 3 hours, lower the temperature in the furnace to room temperature, and then raise the temperature to 1000°C, and keep the temperature constant Calcined for 3 hours and lowered to room temperature, the calcined bone was taken out, mechanically pulverized, and bone particles with a particle size of 1-2 mm were sorted out with a sieve.

[0032] 3. Surface treatment: In order to make the planting cells easier to attach, place the calcined bone particles in 2 mg / ml collagen solution for negative pressure suction, soak for 1 hour; then vacuum dry and then sterilize.

[0033] 4. Preparation of osteoblast culture medium: its components include by volume percentage: commercial minimum essential culture medium DMEM 67.5%, commercial culture medium F12 22.5%, fetal bovine serum 5%, insulin 10ng / ml...

Embodiment 3

[0039] 2. Calcination: put the dried bone fragments into a corundum crucible, and calcinate in a muffle furnace; heat up to 700°C, and calcine at a constant temperature for 4 hours, then lower the temperature in the furnace to room temperature, and then heat up to 1100°C, and calcine at a constant temperature After 3 hours, it was lowered to room temperature, and the calcined bone was taken out, crushed mechanically, and then separated into bone particles with a particle size of 4-5 mm by a sieve.

[0040] 3. Surface treatment: In order to make it easier for the planting cells to attach, the calcined bone particles are placed in 2 mmol / ml RGD polypeptide solution and vacuum-suctioned, soaked for 1 hour; then dried at room temperature and then sterilized.

[0041] 4. Preparation of bone marrow mesenchymal stem cell culture medium: its components include by volume percentage: commercial minimum essential culture medium DMEM 67.5%, commercial culture medium F12 22.5%, fetal bovine...

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Abstract

The invention discloses a humanization active forging bone and a preparation method thereof. The humanization active forging bone has main components of hydroxyapatite crystal, natural animal cancellous bones, particles of which the particle size is between 0.1 and 5 millimeters and having three-dimensional netlike porous structures, and a coating of which the pore-size distribution is between 50and 600 microns and the surface is compounded with extracellular matrix synthesized and excreted by human cells. The forging bone not only has a similar structure with a human bone and is advantageousfor cell ingrowth, formation of new bones, and bone structure reconstruction at a transplantation position, but also can be firmly combined with the coating of which the surface is coated with the extracellular matrix synthesized and excreted by the human cells and cell growth factors, promotes the attached growth of in vivo osteoblasts, and accelerates the formation of the new bones; and simultaneously, the forging bone has the advantages of molding randomly and not causing immunological rejection reactions, and can satisfy treatment needs of clinical bone defect and nonunion.

Description

technical field [0001] The invention belongs to the technical field of tissue engineering biomaterials, and in particular relates to a humanized active calcined bone and a preparation method thereof. Background technique [0002] Bone transplantation is one of the main methods for treating bone defects. Usually autologous bone transplantation has the best effect, but due to the limited source of autologous bone, it will increase the patient's pain and surgical complications. However, artificially synthesized bone substitute materials (such as bioceramics, calcium phosphate bone cement, polymer polymers, and metal materials, etc.) have more complicated manufacturing processes, higher requirements for the production process, and may contain harmful factors that endanger the health of patients. Some are difficult to absorb and replace after being implanted in the body, hindering the reconstruction and repair of bone tissue. An ideal bone graft material should have an internal...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61L27/36A61L27/56A61L27/54A61L27/58A61L27/40A61L27/12
Inventor 王爱军
Owner SHAANXI RUISHENG BIOTECH