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. 2021 Oct 15;19:322. doi: 10.1186/s12951-021-01062-5

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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. 7 — Preparation of A54 peptide-coated micelles and drug delivery of ginsenoside CK to HepG2 and Huh-7 cells. A Fabrication and mechanism of APD-CK micelles. B Synthetic procedures of A54-PEG-DA-OCMC polymer. C TEM image and AFM image of micelles indicating the spherical morphology of APD-CK. D, E The effect of micelles on the expression of p53, caspase 6, caspase 9, caspase 3 and PARP apoptosis protein in HepG2 cells. APD A54 peptide, DA deoxycholic acid, OCMC O-arboxymethyl chitosan. Reprinted with the permission from Ref [108].

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