Liu H C, Yao C H, Sun J S, Lee C J, Huang C W, Lin F H
Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan, Republic of China.
Artif Organs. 2001 Aug;25(8):644-54. doi: 10.1046/j.1525-1594.2001.025008644.x.
The cytotoxicity of the synthetic bone substitute composed of tricalcium phosphate and glutaraldehyde crosslinked gelatin (GTG) were evaluated by osteoblast cell culture. In a previous study, the GTG composites were soaked in distilled water for 1, 2, 4, 7, 14, 28, and 42 days, and then the solutions (or extracts) were cocultured with osteoblasts to evaluate the cytotoxicity of GTG composites by alive cell counting. In this study, the extracts were cocultured with the osteoblasts; thereafter, the concentration of transforming growth factor-beta (TGF-beta1) and prostaglandin E2 (PGE2) in the medium was analyzed to strictly reflect the biological effects of GTG composites on the growth of osteoblasts. In order to investigate the osteoconductive potential of the GTG composites on new bone formation in a relative short term, a model of neonatal rat calvarial organ culture was designed prior to animal experiments. Three experimental materials of 4, 8, and 12% GTG composites were evaluated by fetal rat calvarial organ culture for their ability for bone regeneration. Deproteinized bovine and porcine cancellous bone matrixes were used as the controlled materials. All the organ culture units were maintained in cultured medium for 5 weeks. Following the culture period, the morphology of tissue was observed under an optical microscope, and the quantitative evaluation of the new generation bone was determined by using a semiautomatic histomorphometeric method. Except in the initial 4 days, the concentration of TGF-beta1 of 4% and 8% GTG composites was higher than that of the blank group for all the other experimental time periods. The PGE2 concentration for 4% and 8% GTG composites was lower than that of the blank group. It revealed that the 4% and 8% GTG composites would not lead to inflammation and would promote osteoblast growth. The morphology and activity of the osteoblasts were not transformed or changed by the 2 GTG composites. For the 12% GTG composite, the performance of the in vitro condition was inferior to the blank group and the other 2 GTG composites. Although the concentration of TGF-beta1 and PGE2 was gradually back to normal after 14 days, the morphology of the osteoblasts was abnormal with features such as contracted cytoplast structures. The osteoblast was damaged perhaps in the initial stage. We suggested that the 4% and 8% GTG composites should be soaked in distilled water at least for 4 days before medical applications. The 12% GTG composite and the composites with a concentration of glutaraldehyde solution higher than 12% were not recommended as a medical prostheses in any condition. The fetal rat calvaria culture also showed the same results with the analysis of TGF-beta1 and PGE2. From the study, we could predict the results of animal experiments in the future.
通过成骨细胞培养评估了由磷酸三钙和戊二醛交联明胶(GTG)组成的合成骨替代物的细胞毒性。在先前的一项研究中,将GTG复合材料在蒸馏水中浸泡1、2、4、7、14、28和42天,然后将溶液(或提取物)与成骨细胞共培养,通过活细胞计数评估GTG复合材料的细胞毒性。在本研究中,将提取物与成骨细胞共培养;此后,分析培养基中转化生长因子-β(TGF-β1)和前列腺素E2(PGE2)的浓度,以严格反映GTG复合材料对成骨细胞生长的生物学效应。为了在相对短期内研究GTG复合材料对新骨形成的骨传导潜力,在动物实验之前设计了新生大鼠颅骨器官培养模型。通过胎鼠颅骨器官培养评估了4%、8%和12% GTG复合材料这三种实验材料的骨再生能力。将脱蛋白的牛和猪松质骨基质用作对照材料。所有器官培养单位在培养基中维持5周。培养期结束后,在光学显微镜下观察组织形态,并使用半自动组织形态计量学方法对新一代骨进行定量评估。除了最初的4天,在所有其他实验时间段,4%和8% GTG复合材料的TGF-β1浓度均高于空白组。4%和8% GTG复合材料的PGE2浓度低于空白组。这表明4%和8% GTG复合材料不会引发炎症,并且会促进成骨细胞生长。这两种GTG复合材料不会使成骨细胞的形态和活性发生转化或改变。对于12% GTG复合材料,其体外性能不如空白组和其他两种GTG复合材料。尽管14天后TGF-β1和PGE2的浓度逐渐恢复正常,但成骨细胞的形态异常,具有细胞质结构收缩等特征。成骨细胞可能在初始阶段就受到了损伤。我们建议4%和8% GTG复合材料在医学应用前应至少在蒸馏水中浸泡4天。不建议在任何情况下将12% GTG复合材料以及戊二醛溶液浓度高于12%的复合材料用作医用假体。胎鼠颅骨培养对TGF-β1和PGE2的分析也显示了相同的结果。从该研究中,我们可以预测未来动物实验的结果。