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. 2020 Jan 31;18:25. doi: 10.1186/s12951-020-0583-y

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© The Author(s) 2020

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. 7 — The effect of intravenous free OA and OA-loaded nanocarriers on LPS-induced lung injury in mice. a The lung histology (H&E staining) of LPS-challenged mice treated by free OA and OA-loaded nanocarriers. b The immunohistochemistry (MPO antibody staining) of LPS-challenged mice treated by free OA and OA-loaded nanocarriers. c The immunohistochemistry (Ly6G antibody staining) of LPS-challenged mice treated by free OA and OA-loaded nanocarriers. d MPO expression. e TNF-αexpression. f IL-1β expression. g IL-6 expression. h CXCL-2 expression. All data represent mean ± SEM (n = 6). *p < 0.05, **p < 0.01, ***p < 0.001 as compared to LPS-treated group without OA intervention