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Biomedical subjects

Xu Lan

Publications and source records attributed to Xu Lan.

4 recordsLinked to original sources

[Bio-derived bone material].

OBJECTIVE: To review researches on bone defect repaired by different kinds of bio-derived bone. METHODS: The recent relevant literatures were extensively investigated. Preparation of bio-derived bone and effect of bone defect repair were reviewed. RESULTS: The allogeneic and xenogeneic bone treated by different physicochemical method were not only the substitution for bone but also the scaffold material co-cultured with seed cells to reconstruct tissue engineered bone. CONCLUSION: The tissue engineered bio-derived bone is a breakthrough for treatment of bone defect.

Animals↗

[Experimental study on repairing segmental bone defect with bio-derived bone preserved by various methods].

OBJECTIVE: To study the difference of repairing segmental bone defect with bio-derived bone preserved by various methods. METHODS: Freeze-dried biomaterials had been stored in two different preservation solutions for three months, while the biomaterials stored for same period were observed as control group. The experimental model of 15 mm radial segmental defect was made in 60 New Zealand white rabbits, which were divided into groups A, B and C according to transplant materials preserved by various methods. Groups A and B were deeply divided into A1 and A2 subgroups, B1 and B2 subgroups according to whether materials were cocultured with osteoblasts. Tissue engineered bone was used to repair bone defects of left limbs in A1 and B1 subgroups, while simple material to repair defects of right limbs in A2 and B2 subgroups. Group C was divided into C1 and C2 subgroups. Freeze-dried material was used to repair bone defects of the left limbs, while defects of the right limbs as blank control group. The samples were harvested and observed by the roentgenographical, histomorphological, biomechanical and computerized graphical analysis at 4, 8 and 16 weeks. RESULTS: All of the defects treated with implants exhibited new bone formation 4, 8 and 16 weeks postoperatively, increasing with time. The radiological, histomorphological and biomechanical evaluation showed that the ability of new bone formation was arranged in 6 subgroups as follows: A1>A2>C1>B1>B2>C2, the difference was significant between them (P<0.001, P<0.05). The ability of new bone formation was strongest and at 16 weeks the defect was bridged with the appearance of marrow cavities in A1 subgroup, the biomechanical properties in implants approached to those of normal bone. CONCLUSION: The choice of proper preservation solution can improve the ability of repairing bone defect.

Animals↗

Culture of osteoblasts on bio-derived bones.

OBJECTIVE: To study the effect of bio-derived bones, as substitutes of autogenous bone grafts and demineralized cadaver bones, on the attachment, spreading and proliferation of isolated osteoblasts. METHODS: Osteoblasts were isolated from the calvaria of a fetal rabbit through sequential collagenase digestion. In the attachment study, the osteoblasts labeled with 3H-leucine were incubated with the bio-derived bone materials in sterile microcentrifugable tubes for 15, 90 and 180 minutes, and 24 hours, respectively. The attached cells were collected and the radioactivity was measured with liquid scintillation spectrometry. In the proliferation study, the osteoblasts were cultured with the bio-derived bone materials for 24 hours and 3H-thymidine was added during the last 2 hours of the incubation. The attached cells were collected and the radioactivity was measured with liquid scintillation spectrometry. Osteoblasts were seeded on the bone graft materials for 60 or 120 minutes, 24 or 48 hours, and 3 or 7 days, then the co-culture was processed for scanning electron microscopy to observe the interaction of osteoblasts and the bio-derived bone materials. RESULTS: Osteoblasts attached to the bio-derived bone materials in a time-dependent manner. There were significantly (P<0.05) more attached cells after 180 minutes than after 15 and 90 minutes of incubations (P<0.05). Osteoblasts were proliferated in a large amount on the surface and in the materials. Osteoblasts seeded onto 100 mg bio-derived bones resulted in significantly (P<0.05) more measurable proliferation than those seeded onto 10 mg bones. Osteoblasts appeared round as they attached to the materials, then flattened and spread over with time passing. CONCLUSIONS: Bio-derived bones can provide a good environment for the attachment and proliferation of osteoblasts.

Animals↗

[Effect of various storage methods on cellular compatibility of bio-derived bone].

OBJECTIVE: To study the effect of various storage methods on cellular compatibility of bio-derived bone. METHODS: Freeze-dried biomaterials had been stored in two different preservation solutions for three months, while the biomaterials stored for the same time were observed as control group. The experiment was divided into groups A, B, C and D according to different storage methods (group A: with materials stored in preservation solution 1; group B: with materials stored in preservation solution 2; group C: with freeze-dried materials; and group D: simple osteoblasts). Osteoblasts at 2 x 10(6)/ml had been cocultured with materials for 1, 3, 5, and 7 days. The cell-material complex was observed under phase microscope and electronic scanning microscope to evaluate the adhesion and growth of osteoblasts; the cell viability and alkaline phosphatase(ALP) activity were measured, and the cell cycle was analysed by flow cytometer. RESULTS: Osteoblasts adhered to materials preserved by different methods, differentiated and proliferated in the hole of materials. The difference of cell viability was not significant between three groups on day 1 and day 3. The cell viability of osteoblasts adhered to three materials was A > C > B group on day 5 and day 7 (P < 0.01, P < 0.05). The ALP activity of osteoblasts adhered to three materials was A > C > B group on day 7 (P < 0.01). The cell cycle of different groups did not change significantly, the abnormal cells were not seen. CONCLUSION: The choice of proper preservation solution can optimize the cellular compatibility of bio-derived bone.

Alkaline Phosphatase↗