摘要
BACKGROUND：In previous studies of skull defects and regeneration, bone morphogenetic protein as an inductor and nanohydroxyapatite as a scaffold have been cocultured with osteoblasts. OBJECTIVE： To verify the characteristics of the new skull regenerated material after compound soft regenerated skull material implantation. DESIGN, TIME AND SETTING： The self-control and inter-group control animal experiment was performed at the Sun Yat-sen University, China from February to July 2007. MATERIALS： Twenty-four healthy adult dogs of both genders weighing 15–20 kg were used in this study. Nanohydroxyapatite as a scaffold was cocultured with osteoblasts. Using demineralized canine bone matrix as a carrier, recombinant human bone morphogenetic protein-2 was employed to prepare compound soft regenerated skull material. Self-designed compound soft regenerated skull material was implanted in models of skull defects. METHODS： Animals were randomly assigned into two groups, Group A （n = 16） and Group B （n = 8）. Bilateral 2.5-cm-diameter full-thickness parietal skull defects were made in all animals. In Group A, the right side was reconstructed with calcium alginate gel, osteoblasts, and nanometer bone meal composite; the left side was reconstructed with calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 composite. In Group B, the right side was kept as a simple skull defect, and the left side was reconstructed with calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 composite. MAIN OUTCOME MEASURES： Bone regeneration and histopathological changes at the site of the skull defect were observed with an optical microscope and a scanning electron microscope after surgery. The ability to form bone was measured by alizarin red S staining. In vitro cultured osteoblasts were observed for morphology. RESULTS： One month following surgery, newly formed bone trabeculae mostly covered the broken ends of the fractured bone and grew towards the defect regions. Two months after surgery, many disordered bone islands had formed. Three months after surgery, mature bone, medullary cavities and a large number of new bones were detected in the defect regions. Six months after surgery, the left defect was mostly repaired, with a high bone density compared with the right side in Groups A and B. The right defect was mostly repaired in Group A, but only a small fraction of the right defects was repaired in Group B. CONCLUSION： A composite of calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 can metabolize by itself, gradually ossify and form new bone.
BACKGROUND：In previous studies of skull defects and regeneration, bone morphogenetic protein as an inductor and nanohydroxyapatite as a scaffold have been cocultured with osteoblasts. OBJECTIVE： To verify the characteristics of the new skull regenerated material after compound soft regenerated skull material implantation. DESIGN, TIME AND SETTING： The self-control and inter-group control animal experiment was performed at the Sun Yat-sen University, China from February to July 2007. MATERIALS： Twenty-four healthy adult dogs of both genders weighing 15–20 kg were used in this study. Nanohydroxyapatite as a scaffold was cocultured with osteoblasts. Using demineralized canine bone matrix as a carrier, recombinant human bone morphogenetic protein-2 was employed to prepare compound soft regenerated skull material. Self-designed compound soft regenerated skull material was implanted in models of skull defects. METHODS： Animals were randomly assigned into two groups, Group A （n = 16） and Group B （n = 8）. Bilateral 2.5-cm-diameter full-thickness parietal skull defects were made in all animals. In Group A, the right side was reconstructed with calcium alginate gel, osteoblasts, and nanometer bone meal composite; the left side was reconstructed with calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 composite. In Group B, the right side was kept as a simple skull defect, and the left side was reconstructed with calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 composite. MAIN OUTCOME MEASURES： Bone regeneration and histopathological changes at the site of the skull defect were observed with an optical microscope and a scanning electron microscope after surgery. The ability to form bone was measured by alizarin red S staining. In vitro cultured osteoblasts were observed for morphology. RESULTS： One month following surgery, newly formed bone trabeculae mostly covered the broken ends of the fractured bone and grew towards the defect regions. Two months after surgery, many disordered bone islands had formed. Three months after surgery, mature bone, medullary cavities and a large number of new bones were detected in the defect regions. Six months after surgery, the left defect was mostly repaired, with a high bone density compared with the right side in Groups A and B. The right defect was mostly repaired in Group A, but only a small fraction of the right defects was repaired in Group B. CONCLUSION： A composite of calcium alginate gel, osteoblasts, nanometer bone meal and recombinant human bone morphogenetic protein-2 can metabolize by itself, gradually ossify and form new bone.
基金
the Science and Technology Foundation of Technology Department of Guangdong Province, No. 2007B031003001
the Science Research Foundation of Technology Bureau of Guangzhou City, No. 2006CBG0091
