Abstract

BackgroundThere is a huge body of literature data on ZnOnanoparticles (ZnO NPs) toxicity. However, the reported results are seen to be increasingly discrepant, and deep comprehension of the ZnO NPs behaviour in relation to the different experimental conditions is still lacking. A recent literature overview emphasizes the screening of the ZnO NPs toxicity with more than one assay, checking the experimental reproducibility also versus time, which is a key factor for the robustness of the results. In this paper we compared high-throughput real-time measurements through Electric Cell-substrate Impedance-Sensing (ECIS®) with endpoint measurements of multiple independent assays.ResultsECIS-measurements were compared with traditional cytotoxicity tests such as MTT, Neutral red, Trypan blue, and cloning efficiency assays. ECIS could follow the cell behavior continuously and noninvasively for days, so that certain long-term characteristics of cell proliferation under treatment with ZnO NPs were accessible. This was particularly important in the case of pro-mitogenic activity exerted by low-dose ZnO NPs, an effect not revealed by endpoint independent assays. This result opens new worrisome questions about the potential mitogenic activity exerted by ZnO NPs, or more generally by NPs, on transformed cells. Of importance, impedance curve trends (morphology) allowed to discriminate between different cell death mechanisms (apoptosis vs autophagy) in the absence of specific reagents, as confirmed by cell structural and functional studies by high-resolution microscopy. This could be advantageous in terms of costs and time spent. ZnO NPs-exposed A549 cells showed an unusual pattern of actin and tubulin distribution which might trigger mitotic aberrations leading to genomic instability.ConclusionsZnO NPs toxicity can be determined not only by the intrinsic NPs characteristics, but also by the external conditions like the experimental setting, and this could account for discrepant data from different assays. ECIS has the potential to recapitulate the needs required in the evaluation of nanomaterials by contributing to the reliability of cytotoxicity tests. Moreover, it can overcome some false results and discrepancies in the results obtained by endpoint measurements. Finally, we strongly recommend the comparison of cytotoxicity tests (ECIS, MTT, Trypan Blue, Cloning efficiency) with the ultrastructural cell pathology studies.Graphic

Highlights

  • There is a huge body of literature data on ZnOnanoparticles (ZnO NPs) toxicity

  • In our study, we wanted to analytically compare data obtained by high throughput real-time measurements by Electric Cell-substrate Impedance Sensing (ECIS) with those obtained by multiple endpoint measurements: traditional dye-based tests (MTT, neutral red, and trypan blue) that analyze different cellular parameters, and cell proliferation assay

  • Nanoparticle characterization To avoid artefacts due to possible alteration of commercial preparations, Zinc oxide (ZnO) NPs were characterized by Dynamic Light Scattering (DLS), Variable pressure scanning electron microscopy (VP-SEM), and Transmission Electron Microscopy (TEM) before being used for treatments

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Summary

Introduction

There is a huge body of literature data on ZnOnanoparticles (ZnO NPs) toxicity. A recent literature overview emphasizes the screening of the ZnO NPs toxicity with more than one assay, checking the experimental reproducibility versus time, which is a key factor for the robustness of the results. The importance of developing in vitro tests for toxicity evaluation of nanomaterials is emphasized by the setup of standardized and validated protocols by efforts of international bodies [3, 4]. In agreement with the recommendations of ISO/TR 10993–22:2017 Biological evaluation of medical devices — Part 22: Guidance on nanomaterials: “Corroboration of several test results from different methodologies might be required for a scientifically sound interpretation” the main in vitro assays used in nanotoxicology studies are MTT, WST1, LDH assay, trypan blue, and propidium iodide staining [5]. High-precision toxicity tests require a collection of large numbers of data points from multiple experiments (high-throughput test)

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