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. 2022 Jun 28;13:3727. doi: 10.1038/s41467-022-31338-9

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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. 6 — a Confocal imaging of live/dead stained HaCaT cell cultured for 7 days (scale bar, 100 µm). The sample group of a soaking method for UCDEs: Acetone (Ac), Hydrochloric acid (HCl), Nitric acid (NA), and gold flakes. b Relative fluorescence intensity of cells cultured for 7 days is presented as average and standard error of means (*p < 0.05 TTEST).