Zhang Guihua, Shinohara Naohide, Kano Hirokazu, Senoh Hideki, Suzuki Masaaki, Sasaki Takeshi, Fukushima Shoji, Gamo Masashi
National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, 305-8569, Japan.
Japan Bioassay Research Center, Hadano, Kanagawa, 257-0015, Japan.
J Appl Toxicol. 2016 Oct;36(10):1268-75. doi: 10.1002/jat.3287. Epub 2016 Feb 16.
Uneven pulmonary nanoparticle (NP) distribution has been described when using single-dose intratracheal administration tests. Multiple-dose intratracheal administrations with small quantities of NPs are expected to improve the unevenness of each dose. The differences in local pulmonary NP distribution (called microdistribution) between single- and multiple-dose administrations may cause differential pulmonary responses; however, this has not been evaluated. Here, we quantitatively evaluated the pulmonary microdistribution (per mesh: 100 μm × 100 μm) of TiO2 in lung sections from rats following one, two, three, or four doses of TiO2 NPs at a same total dosage of 10 mg kg(-1) using X-ray fluorescence microscopy. The results indicate that: (i) multiple-dose administrations show lower variations in TiO2 content (ng mesh(-1) ) for sections of each lobe; (ii) TiO2 appears to be deposited more in the right caudal and accessory lobes located downstream of the administration direction of NP suspensions, and less so in the right middle lobes, irrespective of the number of doses; (iii) there are not prominent differences in the pattern of pulmonary TiO2 microdistribution between rats following single and multiple doses of TiO2 NPs. Additionally, the estimation of pulmonary TiO2 deposition for multiple-dose administrations imply that every dose of TiO2 would be randomly deposited only in part of the fixed 30-50% of lung areas. The evidence suggests that multiple-dose administrations do not offer remarkable advantages over single-dose administration on the pulmonary NP microdistribution, although multiple-dose administrations may reduce variations in the TiO2 content for each lung lobe. Copyright © 2016 John Wiley & Sons, Ltd.
在使用单剂量气管内给药试验时,已观察到肺部纳米颗粒(NP)分布不均。预计使用少量NP进行多剂量气管内给药可改善各剂量的不均一性。单剂量和多剂量给药之间局部肺部NP分布的差异(称为微观分布)可能会导致不同的肺部反应;然而,这一点尚未得到评估。在此,我们使用X射线荧光显微镜,对总剂量为10 mg kg(-1)的TiO2纳米颗粒进行一、二、三或四次剂量给药后,大鼠肺切片中TiO2的肺部微观分布(每网格:100μm×100μm)进行了定量评估。结果表明:(i)多剂量给药时,每个肺叶切片中TiO2含量(ng网格(-1))的变化较小;(ii)无论给药剂量如何,TiO2似乎在NP悬浮液给药方向下游的右尾叶和副叶中沉积较多,而在右中叶中沉积较少;(iii)单剂量和多剂量TiO2纳米颗粒给药的大鼠之间,肺部TiO2微观分布模式没有显著差异。此外,对多剂量给药的肺部TiO2沉积估计表明,每剂TiO2仅会随机沉积在固定的30-50%的肺区域中。有证据表明,尽管多剂量给药可能会减少每个肺叶中TiO2含量的变化,但在肺部NP微观分布方面,多剂量给药并不比单剂量给药具有显著优势。版权所有© 2016 John Wiley & Sons, Ltd.