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. 2023 Oct 31;27:107. doi: 10.1186/s40824-023-00446-y

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© The Author(s) 2023

Open Access This 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. 4 — Observation of wound closure and histological analysis of wound tissues via. (A) Representative images of full-thickness skin wounds as administered by four different patch groups (AS, AES, AC, and AEC) at 0, 2, 4, 7, and 14 day post-treatment. Scale bar is 8 mm. (B) quantitative measurement of wound closure rate (%) for up to 14 days. (C) Representative images of regenerated wound tissues for each patch group on day 7 and 14 as stained by H&E. Red arrows indicate the wound edges. Scale bar is 2 mm. Statistically significant difference (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001)