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首页> 外文期刊>Journal of toxicology >In Vitro Toxicity Evaluation of Engineered Cadmium-Coated Silica Nanoparticles on Human Pulmonary Cells
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In Vitro Toxicity Evaluation of Engineered Cadmium-Coated Silica Nanoparticles on Human Pulmonary Cells

机译:工程化镉包覆的二氧化硅纳米粒子对人肺细胞的体外毒性评估

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Cytotoxicity of cadmium-containing silica nanoparticles Cd-SiO_2NPs (0.05-100 mug/mL) versus SiO_2NPs and CdCl_2 was evaluated by an in vitro test battery in A549 by assessing (i) mitochondrial function, (ii) membrane integrity/cell morphology, (iii) cell growth/proliferation, (iv) apoptotic pathway, (v) oxidative stress, after short- (24-48 h) and long-term (10 days) exposure. Both Cd-SiO_2NPs and CdCl_2 produced dose-dependent cytotoxic effects: (i) MTT-assay: similar cytotoxicity pattern was observed at both 24 and 48 h, with a more Cd-SiO_2NPs pronounced effect than CdCl_2. Cd-SiO_2NPs induced mortality (about 50%) at 1 mug/mL, CdCl_2 at 25 mug/mL; (ii) calcein-AM/PI staining: decrease in cell viability, noticeable at 25 mug/mL, enhanced markedly at 50 and 100 mug/mL, after 24 h. Cd-SiO_2NPs induced higher mortality than CdCl_2 (25% versus 4%, resp., at 25 mug/mL) with further exacerbation after 48h; (iii) clonogenic assay, exposure for longer period (10 days) compromised the A549 proliferative capacity at very low dose (0.05 mug/mL); (iv) a progressive activation of caspase-3 immunolabelling was detected already at 1 mug/mL; (v) GSH intracellular level was modified by all compounds. In summary, in vitro data demonstrated that both Cd-SiO_2NPs and CdCl_2 affected all investigated endpoints, more markedly after Cd-SiO_2NPs, while SiO_2NPs influenced GSH only.
机译:在A549中通过体外测试电池通过评估(i)线粒体功能,(ii)膜完整性/细胞形态,(a)含镉的二氧化硅纳米颗粒Cd-SiO_2NPs(0.05-100 mug / mL)对SiO_2NPs和CdCl_2的细胞毒性iii)短期(24-48小时)和长期(10天)暴露后,细胞生长/增殖,(iv)细胞凋亡途径,(v)氧化应激。 Cd-SiO_2NPs和CdCl_2均产生剂量依赖性的细胞毒性作用:(i)MTT分析:在24 h和48 h观察到相似的细胞毒性模式,Cd-SiO_2NPs的作用明显大于CdCl_2。 Cd-SiO_2NPs诱导的死亡率为1杯/ mL,约50%; CdCl_2诱导为25杯/ mL。 (ii)钙黄绿素-AM / PI染色:24小时后,细胞活力降低,在25杯/毫升时明显,在50和100杯/毫升时明显增强。 Cd-SiO_2NPs引起的死亡率高于CdCl_2(分别为25%/ mL,分别为25%对4%),并在48小时后进一步加剧。 (iii)克隆形成试验,长时间(10天)暴露会损害极低剂量(0.05杯/毫升)的A549增殖能力; (iv)已经检测到caspase-3免疫标记的进行性激活已达到1杯/毫升; (v)所有化合物均修饰了GSH细胞内水平。总之,体外数据表明,Cd-SiO_2NPs和CdCl_2都影响所有研究终点,在Cd-SiO_2NPs之后更明显,而SiO_2NPs仅影响GSH。

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