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Research Article

Cellular uptake and intracellular fate of engineered nanoparticles: A review on the application of imaging techniques

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Pages 381-392 | Received 04 Feb 2010, Accepted 19 Jul 2010, Published online: 16 Sep 2010
 

Abstract

The use of imaging tools to probe nanoparticle-cell interactions will be crucial to elucidating the mechanisms of nanoparticle-induced toxicity. Of particular interest are mechanisms associated with cell penetration, translocation and subsequent accumulation inside the cell, or in cellular compartments. The objective of the present paper is to review imaging techniques that have been previously used in order to assess such interactions, and new techniques with the potential to be useful in this area. In order to identify the most suitable techniques, they were evaluated and matched against a list of evaluation criteria. We conclude that limitations exist with all of the techniques and the ultimate choice will thus depend on the needs of end users, and their particular application. The state-of-the-art techniques appear to have the least limitations, despite the fact that they are not so well established and still far from being routine. For example, super-resolution microscopy techniques appear to have many advantages for understanding the details of the interactions between nanoparticles and cells. Future research should concentrate on further developing or improving such novel techniques, to include the development of standardized methods and appropriate reference materials.

Acknowledgements

This work is financed under P5 (Bio-nanoparticle) project, a DIUS (Department for Innovation, Universities & Skills) NMS (National Measurement System) chemical and biological metrology supported programme. The authors would like to thank Drs Anna Hills, Adrian Horgan, Neil Harrison and Mr Baptiste Lamarre for helpful comments and encouragement.

Declaration of interest : The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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