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636 results about "Bone tissue engineering" patented technology

Calcium phosphate/collagen composite biologic ceramic material and preparation method thereof

The invention relates to a CaP (Calcium Phosphate)/collagen composite biologic ceramic material and a preparation method thereof. The composite biologic ceramic is prepared by adopting a porous calcium phosphate ceramic as the substrate and I-type collage as the toughening reinforcing phase in a vacuum negative pressure pouring and crosslinking mode. The process is as follows: firstly, preparing the first type through porous calcium phosphate ceramic, wherein the porosity is 60-95%; dipping the porous calcium phosphate ceramic into a collagen solution of which the concentration is 5-20mg/ml; and vacuuming to 0-10Pa at normal temperature and pouring, keeping the pressure for 1-3 hours and carrying out ultrasonic oscillation. The vacuum negative pressure pouring process can be repeated according to demands. The calcium phosphate ceramic poured with the collagen is frozen and dried to prepare the composite biologic ceramic after being subjected to crosslinking. The prepared biologic ceramic has good biocompatibility and biological activity, and at the same time has a mechanical strength better than that of a pure calcium phosphate ceramic material, so that the biologic ceramic can be used as artificial bones and bone tissue engineering bracket materials, and has wide clinical application prospects in orthopedics.
Owner:SICHUAN UNIV

Degradable open porous magnesium and magnesium alloy biomaterial and preparation method thereof

ActiveCN104232972ANo residueUniform distribution throughoutProsthesisPorosityPressure casting
The invention discloses a degradable open porous magnesium and magnesium alloy biomaterial and a preparation method thereof. The magnesium and magnesium alloy biomaterial is in a completely open structure, the hole shape and size are controllable, holes are communicated by virtue of communicating holes, and the number and size of the communicating holes in hole walls are controllable; the holes are uniformly distributed and the porosity is adjustable. The preparation method comprises the following steps: sintering sodium chloride crystal particles to obtain an open porous sodium chloride prefabricated structure; pouring molten magnesium or magnesium alloy into a mould cavity with a sodium chloride prefabricated body, and performing seepage pressure casting; and removing magnesium or magnesium alloy block outer skin with the sodium chloride prefabricated body, washing with alkali, and filtering to remove sodium chloride to obtain the degradable open porous magnesium and magnesium alloy biomaterial. The preparation process is simple, convenient to perform and pollution-free; the prepared open porous structure is provided with the communicated and uniformly distributed holes, is controllable in hole shape and size, relatively high in porosity and strength, free of pore former residues and pore closing phenomenon and adjustable in degradation rate, and can serve as a new-generation degradable bone tissue engineering scaffold.
Owner:SHANGHAI INNOVATON MEDICAL TECH CO LTD

Bone tissue repair ink, composition and bracket, and preparation methods thereof as well as kit

The invention relates to the field of bone tissue engineering, in particular to bone tissue repair ink, a bone tissue repair composition and a bone tissue repair bracket, and preparation methods thereof as well as a kit. The bone tissue repair ink and a bioactive carrier wrapping cells are used as raw materials, and the bone tissue repair bracket is printed according to a preset three-dimensionalstructure by adopting a biological printer. Meanwhile, living cell printing is realized by adopting the bone tissue repair ink and the bioactive carrier as the raw materials. The cells are uniformly distributed on a bracket model formed by the bone tissue repair ink and difficultly slide down to the bottom of the bracket, so that the problem that the expression of some characteristic proteins of the cells is easily lost in the prior art is effectively solved. The growth of the cells on the bracket is facilitated. A human body bone cell growth environment is better simulated, the cell proliferation, the directional differentiation and the specific protein expression are promoted, the extension and the migration of the cells in the bone tissue bracket and the cell junction establishment arefacilitated, and an organic construction body is formed.
Owner:REGENOVO BIOTECH

Bionics design bone-line porous bone product and preparation method and purpose thereof

The invention relates to a bionics design bone-line porous bone product and a preparation method and a purpose thereof, and belongs to the field of biomedical materials. The bionics design bone-line porous bone product is of a body-centered three-dimensional lattice micropore space structure, the atom positions of a unit body of the micropore space structure are filled by geometries, each geometry is a sphere casing or a sphere body, and is crossed with the surrounding sphere casings or the sphere bodies, and a through circular hole is formed in each crossing part. The bionics design bone-line porous bone product has the advantages that by utilizing a three-dimensional printing quick forming manufacturing technique, the excessive cutting waste is avoided, the utilization rate of material is high, and the processing is rapid; the bone-line porous bone nails, bars and plates prepared by the bionics design bone-line porous bone product are used for the human body hard tissue defect repair, bone tissue engineering stents, and bearing part bone tissue wound repair and reconstruction, the good structure integrity and shape customizing capability are realized, various shapes can be processed according to the patient bone tissue defect repair requirements, and the personalized medical requirements of the patient are met.
Owner:成都百年贝雅医疗科技有限公司

Method for preparing nano hydroxyapatite/polylactic acid composite microspheres

The invention discloses a method for preparing nano hydroxyapatite/polylactic acid composite microspheres, which uses nano hydroxyapatite (n-HA) and polylactic acid (PLA) as raw materials and adopts an ultrasonic blending composite process and an emulsification-solvent evaporation method to prepare the microspheres of a nano hydroxyapatite/polylactic acid composite material. The preparation method comprises the following steps: nano-crystallizing hydroxyapatite, proportionally preparing complex liquid, performing ultrasonic dissolving and blending, emulsifying the mixture into small liquid drops, reducing pressure to volatilize a solvent, performing refrigeration and filtration, performing washing, and performing freeze-drying to obtain the composite microspheres. Compared with like products, the composite microspheres have the characteristics that the method has simple and easy operation, the size of the microspheres is easy to control, and the prepared microspheres have large surface holes and specific area, and good mechanical property. The prepared nano hydroxyapatite/polylactic acid composite microspheres are mainly applied to microsphere bonding type brackets in bone tissue engineering and cell micro-carriers in cell engineering, and can be applied to conveying medicaments and bioactive molecules.
Owner:CHONGQING UNIV OF ARTS & SCI

Preparation methods of mineralized hydrogel and biomimetic mineralized bone repair material

The invention discloses preparation methods of mineralized hydrogel and a biomimetic mineralized bone repair material. The mineralized hydrogel is prepared by using a photoactivated biomacromoleculesand a photoactivated phosphatase as raw materials; hydrogel is formed by initiating cross-linking by means of light irradiation or initiating polymerization cross-linking by means of a radical initiator; when the hydrogel is put into mineralized liquid, phosphatase can promote the uniform deposition of phosphate in the gel, so that the uniformly mineralized hydrogel is obtained. Phosphoprotein-like molecules are added during the preparation of the hydrogel; the phosphoprotein-like molecules can promote the uniform deposition of phosphate along a molecular network of biomacromolecules, so thatthe high-strength mineralized hydrogel can be obtained. When the phosphoprotein-like molecules and cells are added during the preparation of the hydrogel, the in-situ loading of the cells can be realized, and the enzyme in a process of bone physiological mineralization can be simulated so as to promote a phosphate mineralization process, so that the biomimetic mineralized bone repair material withhigh strength can be obtained, and the personalized customization of the bionic mineralized bone repair material can be realized; therefore, the preparation methods have a broad application prospectin the field of bone tissue engineering.
Owner:SICHUAN UNIV

Degradable open-cell porous zinc/zinc alloy biomaterial and preparation method thereof

ActiveCN104258458ANo residueUniform distribution throughoutProsthesisPorosityBone tissue engineering
The invention discloses a degradable open-cell porous zinc / zinc alloy biomaterial and a preparation method thereof. The degradable open-cell porous zinc / zinc alloy biomaterial is of a completely open-cell structure, wherein the hole pattern and the size are controllable, holes are communicated by use of communicating holes, and the number and the size of the communicating holes in the hole walls are controllable; the biomaterial is even in overall hole distribution and adjustable in porosity. The preparation method of the biomaterial comprises the following steps that sodium chloride crystal particles are sintered to obtain an open-cell porous sodium chloride prefabricated structure; a zinc or zinc alloy melt is poured into a die cavity in which a sodium chloride prefabricated body is put and pressure seepage casting is performed; the outer skin of a zinc or zinc alloy block containing the sodium chloride prefabricated body is removed, and then alkali wash is performed and the sodium chloride is performed to obtain the degradable open-cell porous zinc / zinc alloy biomaterial. The preparation method of the degradable open-cell porous zinc / zinc alloy biomaterial is simple in process, convenient to operate and pollution-free; the obtained open-cell porous structure has the advantages that the holes are communicated with each other and distributed evenly, the appearance and size of the holes are controllable, the porosity and the strength are relatively high, no hole forming agent is left and hole closure is prevented, and meanwhile, the degradation rate is adjustable; as a result, the biomaterial can be used as a new generation degradable bone tissue engineering stent.
Owner:SHANGHAI JIAO TONG UNIV

Preparation method of antibacterial biological activity ceramic coating with magnetic responsiveness

The invention discloses a preparation method of an antibacterial biological activity ceramic coating with magnetic responsiveness, and belongs to the technical field of biological materials. The preparation method is combined with a layer-by-layer self-assembly technology by using ultrahigh adhesiveness of polydopamine so as to construct a coating of a multilayer film structure on the surface of a base material coated with a polydopamine film. A single layer film is prepared by coating polydopamine functionalized magnetic particle dispersion liquid, polydopamine functionalized antibacterial particle dispersion liquid or polydopamine functionalized biological activity ceramic particle dispersion liquid. The coating prepared through the preparation method has good biocompatibility, biological activity and antibacterial property, the coating can respond to an external magnetic field, and the effect of the external magnetic field can strengthen the osteoinductivity of the coating; the preparation method disclosed by the invention can effectively control the composition, thickness and shape of the coating according to actual requirements; the problems that the binding force between films formed by multilayer inorganic particles in the coating and the binding force between the coating and the base material are not strong are solved. The method has significant research value and clinical significance in bone tissue engineering.
Owner:SOUTHWEST JIAOTONG UNIV
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