Nishimori H, Kondoh M, Isoda K, Tsunoda S, Tsutsumi Y, Yagi K
Laboratory of Bio-Functional Molecular Chemistry, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.
Pharmazie. 2009 Jun;64(6):395-7.
In the pharmaceutical industry, nano-size materials are designed as drug carriers and diagnosis probes. Interactions between nano-size materials and chemicals need investigating. Here, we investigated whether nano-size materials affect chemical-induced toxicity using silica particles, which have been widely used in cosmetics and drug delivery and have diameters of 70 (SP70), 300 (SP300) and 1000 (SP1000) nm, a popular anti-tumor agent, cisplatin, and a widely used herbicide, paraquat. Mice were treated with either cisplatin (100 micromol/kg, intraperitoneally) or paraquat (50 mg/kg, intraperitoneally), with or without intravenous silica particle administration. All treatments were non-lethal and did not show severe toxicity, except for injection with both cisplatin and SP70, which were lethal. When mice received with paraquat and/or the silica particles, synergistic enhanced toxicity was observed in both paraquat- and SP70-treated mice. These synergic effects were not observed with either Si300 or 1000 treatment. Our findings suggest that further evaluation on the interaction between nano-size materials and chemicals is critical for the pharmaceutical application of nanotechnology.
在制药行业,纳米尺寸材料被设计用作药物载体和诊断探针。纳米尺寸材料与化学物质之间的相互作用需要进行研究。在此,我们使用二氧化硅颗粒研究了纳米尺寸材料是否会影响化学物质诱导的毒性,二氧化硅颗粒已广泛应用于化妆品和药物递送,其直径分别为70(SP70)、300(SP300)和1000(SP1000)纳米,一种常用的抗肿瘤药物顺铂,以及一种广泛使用的除草剂百草枯。给小鼠腹腔注射顺铂(100微摩尔/千克)或百草枯(50毫克/千克),同时或不同时静脉注射二氧化硅颗粒。除了同时注射顺铂和SP70导致小鼠死亡外,所有处理均无致死性且未表现出严重毒性。当小鼠接受百草枯和/或二氧化硅颗粒处理时,在百草枯和SP70处理的小鼠中均观察到协同增强的毒性。而Si300或1000处理未观察到这些协同效应。我们的研究结果表明,进一步评估纳米尺寸材料与化学物质之间的相互作用对于纳米技术在制药领域的应用至关重要。