DIT Centre for Radiation and Environmental Science Centre, Focas Research Institute, Dublin Institute of Technology, Kevin Street, Dublin 8, Ireland.
Toxicol Lett. 2010 Oct 5;198(2):134-43. doi: 10.1016/j.toxlet.2010.06.011. Epub 2010 Jun 23.
PNIPAM nanoparticles, with and without a covalently linked fluorescent label, were prepared by a free radical polymerisation technique. The cyto- and genotoxicity of PNIPAM nanoparticles were analysed in two representative mammalian cell lines, SW480, a colon, and HaCaT, a dermal cell line. Physical characterisation in terms of particle size and zeta potential of the PNIPAM nanoparticles was carried out both in aqueous solution and in the appropriate cell culture media. Uptake and co-localisation of fluorescently labelled PNIPAM nanoparticles was monitored in both cell lines using confocal laser scanning microscope. Genotoxicity analysis using the Comet assay was performed in both cell lines to evaluate any DNA damage. It was observed that the PNIPAM nanoparticles were internalized and localised in lysosomes within 24h. No significant cytotoxic response (p<or.05) was observed in either cell line over concentration ranges from 25 to 1000mg/l for all exposure time periods. Furthermore, no significant genotoxic response (p<or.05) was observed in either cell line over concentration ranges from 12.5 to 800mg/l for all exposure time periods. The results suggest that the PNIPAM nanoparticles show excellent biocompatibility in vitro.
聚 N-异丙基丙烯酰胺(PNIPAM)纳米粒子,带有或不带有共价连接的荧光标记,通过自由基聚合技术制备。在两种代表性的哺乳动物细胞系中,即结肠 SW480 细胞和皮肤细胞系 HaCaT 中,分析了 PNIPAM 纳米粒子的细胞毒性和遗传毒性。在水溶液中和适当的细胞培养基中,对 PNIPAM 纳米粒子的粒径和 zeta 电位进行了物理特性分析。使用共焦激光扫描显微镜监测了荧光标记的 PNIPAM 纳米粒子在两种细胞系中的摄取和共定位。使用彗星试验在两种细胞系中进行了遗传毒性分析,以评估任何 DNA 损伤。结果表明,PNIPAM 纳米粒子在 24 小时内被内化并定位于溶酶体中。在所有暴露时间范围内,浓度范围为 25 至 1000mg/L 时,两种细胞系均未观察到明显的细胞毒性反应(p<0.05)。此外,在所有暴露时间范围内,浓度范围为 12.5 至 800mg/L 时,两种细胞系均未观察到明显的遗传毒性反应(p<0.05)。结果表明,PNIPAM 纳米粒子在体外具有优异的生物相容性。