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. 2021 Dec 14;19:421. doi: 10.1186/s12951-021-01172-0

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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. 2 — Analysis of cell proliferation and migration. Viability of a CT-26 cells and b co-cultured cells (ratio of CT-26 to NIH 3T3 cells was 1:2) after incubation with different formulations at different concentrations for 48 h. c Migration experiment after different formulations treatment for 24 h. Scale bar, 100 μm. d Cell migration percentage. e Western blot analysis of FAP and α-SMA expression levels and f quantification data. ^**P < 0.01, ^***P < 0.001