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. 2021 Sep 8;19:270. doi: 10.1186/s12951-021-01007-y

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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 — The dual biological activities of osteogenesis and angiogenesis of ACP nanoparticles. a The effect of Ade and ACP nanoparticles on the cell viability. (Left) Proliferation of hBMSCs; (Right) proliferation of EA.hy926 cells. b The effect of Ade and ACP nanoparticles on the osteogenic differentiation of hBMSCs. c Representative photographs showing the effects of ACP nanoparticles on the migration of EA.hy926 cells. d Representative photographs showing the effects of ACP nanoparticles on the tube formation of EA.hy926 cells. e Quantitative analysis of the migration of EA.hy926 cells. f Quantitative analysis of the tube formation of EA.hy926 cells (*comparison between Ade and the blank control, #comparison between Ade and ACP nanoparticles, p < 0.05)