Ramírez-Cando Lenin Javier, De Simone Uliana, Coccini Teresa
J Nanosci Nanotechnol. 2017 Jan;17(1):203-11. doi: 10.1166/jnn.2017.13046.
Several studies suggest that Iron Oxide nanoparticles may arrive to central nervous system independently of the route of administration. Actually, evidences indicate that the presence iron oxide nanoparticles into nervous system are linked to several neurodegenerative diseases. In this regard, our goal was to assess in vitro PolyVinylPirrolidone coated Iron Oxide nanoparticles, diameter of 20 nm, neuro-toxicity and their mechanism of action, which was fixed over the human neuronal cell line SH-SY5Y. Inducted biological effects were evaluated after 4–48 hours at crescents doses 1–100 μg/mL using the following endpoints: (i) Membrane integrity: Nanoparticles have produced no effect over cellular membrane for every dose and time evaluated; (ii) Mitochondrial activity: Starting at 10 μg/mL with a decrease of cellular vitality of 35%, and a maximum decrease of 45% at highest dose (100 μg/mL); (iii) Cellular morphology: Cells have evidenced no alteration after 48 hours of exposure; (iv) Cellular uptake: Dose-time dependent accumulation has observed: blue spots have been found at 10 μg/mL and over. Concluding, mitochondria are apparently the target: considering that the toxic effect produced by PolyVinylPirrolidone coated Iron Oxide nanoparticles after 48 hours of exposure in a dose-time dependent manner was evident.
多项研究表明,氧化铁纳米颗粒可能会独立于给药途径进入中枢神经系统。实际上,有证据表明,神经系统中氧化铁纳米颗粒的存在与多种神经退行性疾病有关。在这方面,我们的目标是评估体外直径为20 nm的聚乙烯吡咯烷酮包覆的氧化铁纳米颗粒的神经毒性及其作用机制,该纳米颗粒作用于人类神经母细胞瘤细胞系SH-SY5Y。在4至48小时内,使用以下指标评估递增剂量(1至100 μg/mL)下诱导的生物学效应:(i)膜完整性:在评估的每个剂量和时间下,纳米颗粒对细胞膜均无影响;(ii)线粒体活性:从10 μg/mL开始,细胞活力下降35%,在最高剂量(100 μg/mL)下最大下降45%;(iii)细胞形态:暴露48小时后细胞未出现改变;(iv)细胞摄取:观察到剂量-时间依赖性积累:在10 μg/mL及以上剂量发现蓝色斑点。结论是,线粒体显然是靶点:考虑到聚乙烯吡咯烷酮包覆的氧化铁纳米颗粒在暴露48小时后以剂量-时间依赖性方式产生的毒性作用是明显的。