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. 2020 Sep 21;7(21):2002002. doi: 10.1002/advs.202002002

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© 2020 The Authors. Published by Wiley‐VCH GmbH

This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Construction of HepG2 cells and HUVECs‐laden PLGA PMs, respectively. A) The dynamic culture method for culture of PLGA PMs laden with cells. The dynamic culture was carried out at 37 °C and 110 rpm. B) CLSM images showing the adhesion of HepG2 cells cultured with the PLGA PMs in the dynamic culture method for various time periods (6 h and 1 d). C) CLSM images showing the cytoskeleton of HepG2 cells on the PLGA PMs skeleton after 3 d. D) Graphical representations showing adhesion and initial proliferation of the HepG2 cells (6, 24, and 48 h). E) CLSM images showing adhesion of HUVECs dynamic cultured with the PLGA PMs for various time periods (6 h and 1 d). F) Graphical representations showing adhesion and initial proliferation of HUVECs (6, 24, and 48 h). G) CLSM images showing the endothelial‐specific junction protein of HUVECs on the PLGA PMs skeleton after 3 d. :::P < 0.001 and ::::P < 0.0001.