Tissue Specific Fate of Nanomaterials by Advanced Analytical Imaging Techniques - A Review.

Uschi M Graham, Alan K Dozier, Günter Oberdörster, Robert A Yokel, Ramon Molina, Joseph D Brain, Jayant M Pinto, Jennifer Weuve, David A Bennett

Journal: Chemical research in toxicology 2021;33(5):1145-1162

PMID: 32349469

Abstract

A variety of imaging and analytical methods have been developed to study nanoparticles in cells. Each has its benefits, limitations, and varying degrees of expense and difficulties in implementation. High-resolution analytical scanning transmission electron microscopy (HRSTEM) has the unique ability to image local cellular environments adjacent to a nanoparticle at near atomic resolution and apply analytical tools to these environments such as energy dispersive spectroscopy and electron energy loss spectroscopy. These tools can be used to analyze particle location, translocation and potential reformation, ion dispersion, and in vivo synthesis of second-generation nanoparticles. Such analyses can provide in depth understanding of tissue-particle interactions and effects that are caused by the environmental "invader" nanoparticles. Analytical imaging can also distinguish phases that form due to the transformation of "invader" nanoparticles in contrast to those that are triggered by a response mechanism, including the commonly observed iron biomineralization in the form of ferritin nanoparticles. The analyses can distinguish ion species, crystal phases, and valence of parent nanoparticles and reformed or in vivo synthesized phases throughout the tissue. This article will briefly review the plethora of methods that have been developed over the last 20 years with an emphasis on the state-of-the-art techniques used to image and analyze nanoparticles in cells and highlight the sample preparation necessary for biological thin section observation in a HRSTEM. Specific applications that provide visual and chemical mapping of the local cellular environments surrounding parent nanoparticles and second-generation phases are demonstrated, which will help to identify novel nanoparticle-produced adverse effects and their associated mechanisms.

Address: Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 5555 Ridge Avenue, Cincinnati, Ohio 45213, United States.; Pharmaceutical Sciences, University of Kentucky, 789 South Limestone, Lexington, Kentucky 40506, United States.; School of Medicine and Dentistry, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, New York 14642, United States.; Harvard T.H. Chan School of Public Health, 677 Huntington Ave, Boston, Massachusetts 02115, United States.; Department of Surgery, The University of Chicago Medicine, 5841 S. Maryland Avenue, Chicago, Illinois 60637, United States.; School of Public Health, Department of Epidemiology, Boston University, 715 Albany Street, The Talbot Building, T3E & T4E, Boston, Massachusetts 02118, United States.; Department of Neurological Sciences, Rush University Medical Center, 1725 W. Harrison Street, Suite 1118, Chicago, Illinois 60612, United States.
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