Novel vascularized tissue-engineered bone and construction method thereof
A tissue-engineered bone and vascularization technology, used in bone implants, medical science, prostheses, etc., can solve the problem that tissue-engineered bone has an unsatisfactory osteogenesis promotion effect, limited blood supply in the central part of the stent, and vascular pedicle length requirements. It can achieve the effect of increasing the blood supply and nutrition area, safe and effective vascularization, and clinical feasibility.
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Embodiment 1
[0021] Example 1: Method for vascularization of pre-placed vascular loops in tissue engineered bone
[0022] See figure 1 , take a commercial β-TCP stent, prepare it into a cylindrical shape with a bottom diameter of 12 mm and a height of 10 mm, carefully punch out two axial hollow channels with a diameter of 3 mm inside the stent, and round the exit holes at both ends. After disinfection treatment, BMSCs were inoculated and cultured in vitro for 2 weeks. The saphenous artery and vein were separated about 4cm, and the saphenous artery and vein were ligated at the distal end. The BMSCs / β-TCP complex was replaced with serum-free medium 12 hours before implantation to reduce the impact of residual fetal bovine protein as an antigen on the recipient after implantation. The BMSCs / β-TCP cell scaffold complex was placed on the original saphenous arteriovenous vascular bed, and two sutures were reserved to pass through the tunnel of the cell scaffold complex to facilitate postoperat...
Embodiment 2
[0024] Example 2: Method for vascularization of pre-placed vascular bundles in tissue engineered bone
[0025] See figure 2, take a commercial β-TCP scaffold, prepare it into a cylindrical shape with a bottom diameter of 12mm and a height of 10mm, and carefully punch out two axial hollow channels with a diameter of 3mm inside the scaffold. After aseptic treatment, BMSCs are inoculated and cultured in vitro to induce 2 weeks. The saphenous artery and vein were separated about 4cm, and the saphenous artery and vein were ligated at the distal end. The BMSCs / β-TCP complex was replaced with serum-free medium 12 hours before implantation to reduce the impact of residual fetal bovine protein as an antigen on the recipient after implantation. The BMSCs / β-TCP cell scaffold complex was placed on the original saphenous arteriovenous vascular bed, and two sutures were reserved to pass through the tunnel of the cell scaffold complex to facilitate postoperative fixation. Using the uncut...
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