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Correction: Tobramycin-mediated self-assembly of DNA nanostructures for targeted treatment of Pseudomonas aeruginosa-infected lung inflammation
Yuhang
Xu
a,
Qian
Liu
ab,
Bin
Wang
ac,
Quan
Li
a,
Yue
Chen
a,
Yao
Yang
a,
Zhihao
Zhu
a,
Daohui
Gong
a,
Chuan
Zhang
*d,
Guansong
Wang
*ac and
Hang
Qian
*ac
aInstitute of Respiratory Diseases, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China. E-mail: hqian@tmmu.edu.cn; wanggs@tmmu.edu.cn
bLaboratory of Pharmacy and Chemistry, and Laboratory of Tissue and Cell Biology, Lab Teaching & Management Center, Chongqing Medical University, Chongqing, 400016, China
cChongqing Key Laboratory of Precision Medicine and Prevention of Major Respiratory Diseases, Chongqing 400037, China
dSchool of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China
First published on 29th October 2024
Abstract
Correction for ‘Tobramycin-mediated self-assembly of DNA nanostructures for targeted treatment of Pseudomonas aeruginosa-infected lung inflammation’ by Yuhang Xu et al., Biomater. Sci., 2024, 12, 2331–2340, https://doi.org/10.1039/D3BM02121A.
The authors regret that an incorrect version of Fig. 3 was included in the original article. The correct version of Fig. 3 is presented below. The authors note that the correction does not change the conclusions of the paper.
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| Fig. 3 In vitro antibacterial evaluation of the NTTob-Mal. (A) CLSM imaging of PA after incubation with NTTob-Mal. Staphylococcus aureus (SA) and NTTob-Mal group, PA and NTTob group served as control entities. The concentration of Tob was 200 μg mL−1, and that of maleimide was 100 μg mL−1. NTTob-Mal and NTTob were labeled with Cy3 dye, and DAPI was used for bacterial staining. Scale: 10 μm. (B) Antibacterial activity was determined by the plate meter methodology. PA was exposed to Tob/NTTob/NTTob-Mal for 1 h, and the samples were impregnated on agarose plates and propagated at 37 °C for 24 h. NTMg was used as the control group. | ||
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