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Correction: An E-selectin targeting and MMP-2-responsive dextran–curcumin polymeric prodrug for targeted therapy of acute kidney injury
Jing-Bo
Hu
ab,
Di
Liu
a,
Jing
Qi
a,
Kong-jun
Lu
a,
Fei-yang
Jin
a,
Xiao-Ying
Ying
a,
Jian
You
a and
Yong-Zhong
Du
*a
aInstitute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, 866 Yuhangtang Road, Hangzhou 310058, China. E-mail: duyongzhong@zju.edu.cn
bInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China
First published on 19th January 2024
Abstract
Correction for ‘An E-selectin targeting and MMP-2-responsive dextran–curcumin polymeric prodrug for targeted therapy of acute kidney injury’ by Jing-Bo Hu et al., Biomater. Sci., 2018, 6, 3397–3409, https://doi.org/10.1039/C8BM00813B.
The authors regret an error in Fig. 3a where the wrong panel was used for Fig. 3a 0.5 h + LPS SA-DEX-CUR. An independent expert has viewed the corrected data and has concluded that it is consistent with the discussions and conclusions presented.
The corrected Fig. 3 is shown below.
 | ||
| Fig. 3 The cellular uptake of SA-DEX-PVGLIG-CUR by HUVECs with or without LPS pretreatment, with SA-DEX-CUR as the control. (A) Representative fluorescence images of HUVECs with or without LPS pretreatment which were incubated with SA-DEX-PVGLIG-CUR or SA-DEX-CUR for 0.5 h, 1 h and 2 h, respectively. Scale bar = 100 μm. (B) The semi-quantitative fluorescence values of (A). (C) The internalization behaviors of SA-DEX-PVGLIG-CUR or SA-DEX-CUR by HUVECs with or without LPS pretreatment were quantitatively determined using flow cytometry. Data are presented as mean ± SD (n = 3), *P < 0.05. | ||
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