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. 2022 Jun 7;13:3149. doi: 10.1038/s41467-022-30713-w

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© The Author(s) 2022

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a Schematic illustration of the PDT treatment regimen. b Photographs of tumor tissues extracted from the mice that received a set of treatments at 21 days including PBS, PW, CW, UCNPs-DI, PW + ICG, CW + ICG, PW + UCNPs-I, CW + UCNPs-I, PW + UCNPs-DI, and CW + UCNPs-DI. Relative tumor volume growth curve (c), mice body weight (d), and tumor weight (e) of the mice treated with different treatments. f SOSG immunofluorescence sections treated in series of groups. Scale bar, 100 μm. g H&E staining of tumor slices for treatments. Scale bar, 100 μm. All quantitative data in (c–e) are expressed as mean ± SD (n = 6, biologically independent mice). P values were calculated by Student’s two-sided t-test (^nsP > 0.05).