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. 2018 Jul 20;9:2870. doi: 10.1038/s41467-018-05305-2

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — IONP-HN3-DNA rescue cultured cells from DOX toxicity (scale bar = 5 μm). a Rat heart myoblasts H9C2 cultured with DOX (0.05 mg/mL)—myoblasts are killed by adding DOX to culture (DOX, d). b Myoblasts treated with DOX (0.05 mg/mL) and 0.19 g Dowex ion-exchange resin beads—myoblasts are partially rescued ((DOX + Dowex, d). c Myoblasts treated with DOX (0.05 mg/mL) and 0.19 g IONP-HN3-DNA—myoblasts are completely rescued (DOX + IONP-DNA, d). d Cell counts for each experimental condition; error bars = 1 standard deviation (n = 3)