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Correction to: Binding affinity screening of polyphenolic compounds in Stachys affinis extract (SAE) for their potential antioxidant and anti-inflammatory effects (Scientific Reports, (2024), 14, 1, (18095), 10.1038/s41598-024-68880-z)open access

Authors
Kim, Hun HwanJeong, Se HyoPark, Min YeongBhosale, Pritam BhangwanAbusaliya, AbuyaseerLee, Sang JoonHeo, Jeong DooKim, Hyun WookSeong, Je KyungKim, Dong IlPark, Kwang IlKim, Gon Sup
Issue Date
Dec-2025
Publisher
Nature Publishing Group
Citation
Scientific Reports, v.15, no.1
Indexed
SCIE
SCOPUS
Journal Title
Scientific Reports
Volume
15
Number
1
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/77314
DOI
10.1038/s41598-025-87356-2
ISSN
2045-2322
2045-2322
Abstract
Correction to: Scientific Reportshttps://doi.org/10.1038/s41598-024-68880-z, published online 05 August 2024 The original version of this Article contained an error in Figure 3 panel A, where the x-axis was presented as ‘SAE (µg/mL)’ instead of ‘SAE (ng/mL)’. The original Figure 3 and the accompanying legend appear below. (Figure presented.) Cytotoxicity effect of SAE on RAW264.7 cells and the inhibition of inflammatory marker in LPS inflammation-induced RAW264.7 cells. RAW264.7 cells were pretreated without or with LPS (1 µg/mL) for 1 h at 37 °C. Following that, cells were treated with SAE (0, 10, 25, 50, 75, 100, 250 ng/mL) for 24 h at 37 °C. (A) Cytotoxicity effect of SAE on without LPS induced RAW264.7 cells. (B) SAE on LPS induced cell viability in RAW264.7 cells. The RAW264.7 cells were treated with SAE (25, and 50 ng/mL) at indicated concentration for 24 h. COX2 and iNOS levels were quantified. (C) The relative area of COX2 and (D) the relative area of iNOS. Results from three independent experiments were expressed as mean ± standard error of the mean (SEM) compared with control. ###p < 0.001 versus untreated group; *p < 0.05 **p < 0.01, ***p < 0.001 versus LPS treated group. The original Article has been corrected. © The Author(s) 2025.
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