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Tissue distribution and clearance of intravenously administered titanium dioxide (TiO2) nanoparticles

机译:静脉注射二氧化钛(TiO2)纳米颗粒的组织分布和清除

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The organ-tissue distribution and clearance of Degussa P25 TiO2 nanoparticles were determined after intravenous administration to rats (0.95 mg/kg body weight) using an inductively coupled plasma sector field mass spectrometer. The detection limits of Ti analysis, 0.54 and 1.4 ng/mL for blood and urine and 0.35-2.0 ng/g tissue for several organ tissues, enabled determination of tissue distribution and clearance for organs in which Ti content could not be previously determined due to low concentrations. Blood concentrations of TiO2 were 420 and 19 ng/mL at 5 and 15 min after administration, which were equivalent of only 2.8% and 0.13% of the administration dose, respectively. At 6 h, 94%, 2.0%, 0.17%, 0.023%, 0.014% and 0.026% of administered TiO2 was found in the liver, spleen, lung, kidney, heart and blood, respectively. Liver and spleen TiO2 burden was significantly higher in the administration than control group (p < 0.01) and did not decrease up to 30 days after administration, while TiO2 burden in the lung, kidney, heart and blood decreased over time. A two-step decay model was more suitable than a one-step decay model for the decay curves of pulmonary TiO2 burden but did not improve fitting to the decay curves of kidney TiO2 burden. No translocation to the brain was confirmed at a lower detection limit than was applied in previous studies. Ti content in faeces and urine in the TiO2 administration group did not differ from that in the control group.
机译:使用感应耦合等离子体扇区质谱仪对大鼠静脉内给药(0.95 mg / kg体重)后,测定Degussa P25 TiO2纳米颗粒的器官组织分布和清除率。 Ti分析的检出限为血液和尿液为0.54和1.4 ng / mL,几种器官组织为0.35-2.0 ng / g组织,从而能够确定由于以下原因无法预先确定Ti含量的器官的组织分布和清除率低浓度。给药后5分钟和15分钟,TiO2的血药浓度分别为420和19 ng / mL,分别相当于给药剂量的2.8%和0.13%。在6小时后,分别在肝脏,脾脏,肺,肾,心脏和血液中发现分别有94%,2.0%,0.17%,0.023%,0.014%和0.026%的TiO2被施用。肝和脾中TiO2的负担明显高于对照组(p <0.01),并且在给药后30天没有减少,而肺,肾,心脏和血液中的TiO2的负担随着时间的推移而减少。对于肺部TiO2负荷的衰减曲线,两步衰减模型比单步衰减模型更合适,但并未改善对肾脏TiO2负荷的衰减曲线的拟合。在比以前的研究更低的检出限下,没有确认到大脑易位。 TiO2给药组的粪便和尿液中的Ti含量与对照组无差异。

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