Buacheen P.Karinchai J.Kammasit N.Temviriyanukul P.Butkinaree C.Watthana S.Wongnoppavich A.Imsumran A.Pitchakarn P.Mahidol University2025-12-142025-12-142025-12-01Scientific Reports Vol.15 No.1 (2025)https://repository.li.mahidol.ac.th/handle/123456789/113509Correction to: Scientific Reportshttps://doi.org/10.1038/s41598-023-30227-5, published online 20 February 2023 The original version of this Article contained an error in Figure 1, panel B, where the images representing the “BPA” and “BBP” groups were swapped. The original Figure 1 and accompanying legend appear below. (Figure presented.) Cytotoxicity of BBP and BPA on 3T3-L1 adipocyte during adipocyte differentiation tested by SRB assay (A), BBP and BPA induced lipid accumulation in adipocyte (B). Lipid droplet staining using Oil red O dye and the level of lipid accumulation obtained by spectrophotometry of the dye dissolved, Cytotoxicity of ABE (C) and Kin (D) in the absence or presence of BBP or BPA investigated by SRB assay. The data indicated as mean ± SD of three independent experiments **p < 0.01 and ***p < 0.001, compared to differentiation control (B). In addition, in Figure 2, the image for the “BBP (50 μM)” group in panel A and that for “BPA (50 μM)” group in panel C were incorrect. The original Figure 2 and accompanying legend appear below. (Figure presented.) The effect of ABE or Kin on obesogen-induced lipid accumulation in 3T3-L1 cells determined by Oil-red-O staining assay. Intracellular lipid droplet (A), and the level of lipid accumulation (B) of ABE- or Kin-treated cells in the presence of BBP (50 µM). Intracellular lipid droplet (C), and the level of lipid accumulation (D) of ABE- or Kin-treated cells in the presence of BPA (50 µM). The data indicated as mean ± SD of three independent experiments *p < 0.05 and ***p < 0.001, compared to obesogen-treated control. The original Article has been corrected.MultidisciplinaryErratumSCOPUS10.1038/s41598-025-30577-22-s2.0-1050238956732045232241339734