Abstract

Biomedical application of engineered nanoparticles (NPs) is a growing area of research and development. Uncertainty remains as to the mode of action of many NP types and TEM is a tool capable of addressing this if used in conjunction with standard cellular response assays. We will demonstrate imaging of thin sections of fixed, plastic embedded cells by analytical TEM to identify: superparamagnetic iron oxide NP translocation into cell compartments such as endosomes; amorphous silica NP penetration through a cell membrane without membrane encapsulation and zinc oxide NP degradation in cell compartments. We will then discuss how the in vitro cellular responses to a dose of NPs exposed to cell lines can be correlated to the internalized dose per cell section noting however that quantification of the latter requires random sampling procedures or correlation to higher throughout techniques to measure a population of whole cells. Similarly, analytical TEM measures of NP degradation within intracellular compartments will require a more appropriate sample preparation such as cryo-fixation.

Highlights

  • Engineered nano-particles (NPs) have been the focus of much recent research with a particular emphasis on application in the field of medicine as imaging probes for cells and tissues, for drug delivery and as sensors of target molecules [1,2,3]

  • The key challenges for this work are representative sample preparation and suitable control of the electron fluence applied during imaging and, more importantly, spectroscopic analysis such that the particle structure remains unaltered during investigation [6]

  • Dextran coated superparamagnetic iron oxide NPs are used as MRI contrast enhancement agents partial oxidation of these particles has been shown to dramatically alter cellular internalization, with the more oxidised form exhibiting the most uptake and inducing significant DNA damage [7]

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Summary

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Measuring in vitro cellular uptake of nanoparticles by transmission electron microscopy This content has been downloaded from IOPscience. Please scroll down to see the full text. Ser. 522 012058 (http://iopscience.iop.org/1742-6596/522/1/012058) View the table of contents for this issue, or go to the journal homepage for more. Download details: IP Address: 129.11.132.214 This content was downloaded on 18/06/2014 at 11:09 Please note that terms and conditions apply

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