Abstract:
PURPOSE: A method for differentiating adipose stem cells to adipocytes using heparin-binding domain(HBD) is provided to induce cell adhesion and to effectively obtain a large amount of adipocytes. CONSTITUTION: A culture container is fixed on a heparin-binding domain(HBD) with an adhesion activity of adipose stem cells. The HBD is fixed in a recombinant protein form with a polypeptide linker by physical absorption. The polypeptide linker is maltose-binding protein(MBP), hydrophobin, or hydrophobic cell penetrating peptides(CPPs). The recombinant protein has an amino acid sequence of sequence number 2.
Abstract:
PURPOSE: A cell colony-hydrogel-polymer supporting complex for a cartilage regeneration, and a cartilage regeneration composition containing thereof are provided to induce the regeneration of a cartilage while maintaining a constant form similar to a natural cartilage. CONSTITUTION: A cell colony-hydrogel-polymer supporting complex for a cartilage regeneration includes a cell colony uniformly dispersed inside a hydrogel matrix. The cell colony-hydrogel complex is dipped in the surface of a polymer supporting body and inserted into a pore to fill the pore. A producing method of the cell colony-hydrogel-polymer supporting complex comprises the following steps: forming the cell colony out of a cell capable of differentiating into a cartilage cell; forming the cell colony-hydrogel complex; and inserting the cell colony-hydrogel complex into a pore after inoculating the colony on the polymer supporting body.
Abstract:
PURPOSE: A fixation of physiologically active polypeptide with a maltose binding protein(MBP) is provided to maintain biologically activity of the polypeptide and fix the peptide on the hydrophobic surface. CONSTITUTION: A fixation of physiologically polypeptide comprises: a step of fusing the physiologically active polypeptide at carboxy terminal of maltose binding protein(MBP) to obtain a fusion protein; and a step of fixing the fusion protein on a hydrophobic surface by physical adsorption between amino terminal and the hydrophobic surface.
Abstract:
A manufacturing method of a tube type porous scaffold of a double-film structure for artificial blood vessel is provided to have excellent interconnectivity between air bubbles, mechanical stability, transfection and breeding efficiency and to prevent fistula blood at the hypertension state. A manufacturing method of a tube type porous scaffold of a double-film structure for artificial blood vessel comprises steps of: dissolving biodegradable polymer in organic solvent and mixing porogen and manufacturing a polymer/porogen mixed solution; coating a cylindrical shaft with polymer/porogen mixed solution and forming an inner film of a porous coating layer; dissolving the biodegradable polymer in the organic solvent and manufacturing a biodegradable polymer gel; dipping the cylindrical shaft forming the inner film of the porous coating layer, rotating it, falling and radiating the biodegradable polymer gel, winding fiber of a gel state to the inner film of the porous coating layer and forming an outer film of a polymeric fiber layer; separating porosity scaffold of the double-film structure formed in a shaft and removing the organic solvent and the porogen.
Abstract:
Provided is a porous osteochondral composite scaffold with layer structure which has features of bioactivation and mechanical strength suitable to regenerate cartilage and bone simultaneously and method for manufacturing the same. The porous osteochondral composite scaffold comprises: a porous bone regeneration layer which includes biocompatable high molecule and bioactivation ceramic; a porous cartilage regeneration layer which includes biocompatable elastic high molocule. The method for manufacturing a porous osteochondral composite scaffold comprises the steps of: mixing biocompatable high molecule, bioactivation ceramic and lacuna-forming material; press-forming the mixed material from the first step in a mold; bonding the obtained material from the second step by heating to form a porous bone regeneration layer; forming composite material by press-forming gelled mixed material for forming cartilage which dissolves in solution with biocompatable high molecule and lacuna-forming material on one surface of the regenerated layer from the third step; removing solution and lacuna-forming material in the composite material from the fourth step.
Abstract:
A method of preparing porous polymer is provided to improve a cell seeding efficiency by a uniform size of a gap and excellent interconnectedness between gaps, and to prepare simply porous polymer scaffold appropriate for a tissue engineering by an excellent mechanical strength. The method comprises the steps of: manufacturing polymer solution by melting biocompatible polymers in organic solvents; forming polymer gel from non-solvent solutions by spinning the polymer solution obtained in the pre-step to non-solvent stirred by a rotating shaft; forming porous polymer scaffold by making the polymer gel formed in the pre-step wound on the rotating shaft; and removing the organic solvents by drying the porous polymer scaffold obtained in the pre-step.