Centro de Investigación Científica de Yucatán A.C., México.
J Biomater Appl. 2013 Jul;28(1):38-48. doi: 10.1177/0885328212436706.
Nanocomposites were prepared with segmented polyurethanes and Cloisite 30B by either solution mixing or in situ polymerization and characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis and X-ray diffraction. Cytotoxicity and genotoxicity were assessed with lymphocytes while cell viability was measured by the methyl tetrazolium assay using fibroblasts. It was found that in situ polymerization rendered exfoliated nanocomposites with higher glass transition temperature, tensile modulus and thermal stability compared to nanocomposites obtained by solution mixing. The mitotic index of lymphocytes was significantly reduced at high clay concentrations (6 wt% and 10 wt%), while fibroblast viability improved in the presence of extract obtained after days 2 and 7.
采用溶液混合或原位聚合的方法制备了由嵌段聚氨酯和 Cloisite 30B 组成的纳米复合材料,并通过傅里叶变换红外光谱、差示扫描量热法、热重分析和 X 射线衍射进行了表征。采用淋巴细胞评估细胞毒性和遗传毒性,采用甲基噻唑基四唑比色法评估成纤维细胞的细胞活力。结果发现,与溶液混合法制备的纳米复合材料相比,原位聚合法制备的纳米复合材料具有更高的玻璃化转变温度、拉伸模量和热稳定性,呈现出插层结构。在高粘土浓度(6wt%和 10wt%)下,淋巴细胞的有丝分裂指数显著降低,而在第 2 天和第 7 天提取后存在的提取物中,成纤维细胞活力提高。