Analytical High-resolution Electron Microscopy Reveals Organ-specific Nanoceria Bioprocessing

被引:18
|
作者
Graham, Uschi M. [1 ,2 ]
Yokel, Robert A. [1 ]
Dozier, Alan K. [2 ]
Drummy, Lawrence [3 ]
Mahalingam, Krishnamurthy [3 ]
Tseng, Michael T. [4 ]
Birch, Eileen [2 ]
Fernback, Joseph [2 ]
机构
[1] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, 1525 Bull Lea Rd,Ste 10, Lexington, KY 40515 USA
[2] NIOSH, Cincinnati, OH 45226 USA
[3] US Air Force Res Lab, Dayton, OH USA
[4] Univ Louisville, Coll Med, Dept Anat Sci & Neurobiol, Louisville, KY 40292 USA
基金
美国国家环境保护局; 美国国家卫生研究院;
关键词
bioprocessing; ions; liver; nanoceria; nanoparticles; spleen; transformation; CERIUM OXIDE NANOPARTICLES; OXIDATIVE STRESS; BIOMEDICAL APPLICATIONS; PROTECT; RATS; MECHANISMS; BIODEGRADATION; BIOPERSISTENCE; NANOMATERIALS; HYPERTENSION;
D O I
10.1177/0192623317737254
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This is the first utilization of advanced analytical electron microscopy methods, including high-resolution transmission electron microscopy, high-angle annular dark field scanning transmission electron microscopy, electron energy loss spectroscopy, and energy-dispersive X-ray spectroscopy mapping to characterize the organ-specific bioprocessing of a relatively inert nanomaterial (nanoceria). Liver and spleen samples from rats given a single intravenous infusion of nanoceria were obtained after prolonged (90 days) in vivo exposure. These advanced analytical electron microscopy methods were applied to elucidate the organ-specific cellular and subcellular fate of nanoceria after its uptake. Nanoceria is bioprocessed differently in the spleen than in the liver.
引用
收藏
页码:47 / 61
页数:15
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