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. 2018 Nov 15;20(11):305. doi: 10.1007/s11051-018-4406-0

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© The Author(s) 2018

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 9 — Flow cytometry dot plot showing the cytotoxicity profile of primary lymphocytes—PBMC—(upper panels) or Jurkat tumor cells (lower panels), cultured with the indicated NPs. Cells (at least 10,000) were electronically gated according to their size/granularity distribution. Histograms corresponding to three Live/dead™ cell staining (dead cells) experiments are shown for each Np. Within each histogram, different experiments for each NP are shown in different colors, with the control sample with no NP shown in black. According to a one-way ANOVA analysis (XLSTAT® Excell®), only PBMC cultured in the presence of Au-GSH showed a significant increase in cell dead when compared to cells cultured in the absence of NPs (p < 0.002)