Abstract

Knowledge of the interactions between nanomaterials and large-size mammalian cells, including cellular uptake, intracellular localization and translocation, has greatly advanced nanomedicine and nanotoxicology. Imaging techniques that can locate nanomaterials within the structures of intact large-size cells at nanoscale resolution play crucial roles in acquiring this knowledge. Here, the quantitative imaging of intracellular nanomaterials in three dimensions was performed by combining dual-energy contrast X-ray microscopy and an iterative tomographic algorithm termed equally sloped tomography (EST). Macrophages with a size of ∼20 µm that had been exposed to the potential antitumour agent [Gd@C82(OH)22]n were investigated. Large numbers of nanoparticles (NPs) aggregated within the cell and were mainly located in phagosomes. No NPs were observed in the nucleus. Imaging of the nanomedicine within whole cells advanced the understanding of the high-efficiency antitumour activity and the low toxicity of this agent. This imaging technique can be used to probe nanomaterials within intact large-size cells at nanometre resolution uniformly in three dimensions and may greatly benefit the fields of nanomedicine and nanotoxicology.

Highlights

  • Dual-energy contrast X-ray microscopy is based on the abrupt change in the absorption when the energy of the incident X-rays changes from just below the absorption edge of a specific element to above it

  • The observed differences in images collected at two energies reflect the locations of element-specific nanomaterials. This method can simultaneously image the ultrastructures of cells and intracellular nanomaterials and, can be used to investigate the interactions between nanomaterials and biological systems

  • We applied dual-energy contrast X-ray microscopy to explore the intracellular localization of nanomaterials in whole large-size mammalian cells

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Summary

Introduction

We applied dual-energy contrast X-ray microscopy to explore the intracellular localization of nanomaterials in whole large-size mammalian cells. To explore the interactions between nanomaterials and cells, dual-energy X-ray microscopy is a promising choice and can achieve quantitative nondestructive three-dimensional (3D) imaging of both cellular structures and nanomaterials at nanometer resolution simultaneously.

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Conclusion

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