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. 2023 May 13;23:435. doi: 10.1186/s12885-023-10928-w

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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. 7 — Migration Studies. The wound healing method determined the effect of GemHCl and 4NSG-SLN on PPCL-192 and PPCL-46 cell migration (a) images of GemHCl and 4NSG-SLN treated PPCL-192 and PPCL-46 cells at 5 µM concentration towards the scratch wound. NIH ImageJ software quantified and analyzed the average number of (b) PPCL-192 and (c) PPCL-46 migrated cells. Wound closures were captured at 10X magnification using the Nikon Eclipse Ti inverted fluorescent microscope. The plots are of the means ± SD, n = 3. Significance (GemHCl and 4NSG-SLN ***p < 0.0001) was determined by t-test