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. 2021 Aug 4;19:229. doi: 10.1186/s12951-021-00978-2

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 9 — In vivo toxicity assessment of PLT@Ag-MOF-Vanc. a Schematic diagram of in vivo toxicity experimental design. b Mice weight changes after injecting with normal saline, Ag-MOF, vancomycin, Ag-MOF-Vanc, and PLT@ Ag-MOF-Vanc during 1 week. c CBC and serum indexes in mice at 1 week after intravenous injection of corresponding drugs. d Histological images of heart, liver, spleen, lung, and kidney samples from mice at 1 week after intravenous injection of corresponding drugs. Scale bar: 100 μm. Control: mice treated with normal saline. Data are indicated as mean ± SD (n = 5). Ns = no significance