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Correction: Tumor-targeting, enzyme-activated nanoparticles for simultaneous cancer diagnosis and photodynamic therapy
Huaxia
Shi
a,
Wucheng
Sun
a,
Changbing
Liu
a,
Guiying
Gu
b,
Bo
Ma
b,
Weili
Si
c,
Nina
Fu
a,
Qi
Zhang
*b,
Wei
Huang
*ac and
Xiaochen
Dong
*c
aKey Laboratory for Organic Electronics & Information Displays (KLOEID), Nanjing University of Posts and Telecommunications, Nanjing 210023, China
bSchool of Pharmaceutical Science, Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing 211816, China. E-mail: zhangqi@njtech.edu.cn
cKey Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), NanjingTech University (NanjingTech), 30 South Puzhu Road, Nanjing 211816, China. E-mail: iamxcdong@njtech.edu.cn; iamwhuang@njtech.edu.cn
First published on 20th June 2023
Abstract
Correction for ‘Tumor-targeting, enzyme-activated nanoparticles for simultaneous cancer diagnosis and photodynamic therapy’ by Huaxia Shi et al., J. Mater. Chem. B, 2016, 4, 113–120, https://doi.org/10.1039/C5TB02041G.
The authors regret that due to a figure compilation error, the representative tumor image on day 7 for the DBHA-NPs without light group was incorrect in Fig. 6b. The corrected version of Fig. 6 is provided below.
 | ||
| Fig. 6 (a) Comparison of cell viabilities by MTT assay (λ > 600 nm). (b) The relationship between tumor volume and treatment time for the DBHA-NPs in the HCT-116 mouse model tumor cells via tail vein injection. Twenty-four mice were randomly assigned into four groups (6 mice per group), including saline with light, HA with light, DBHA-NPs without light and DBHA-NPs with light. (c) Typical photographs of tumor-bearing mice treated at different times. Note, *p < 0.05, **p < 0.01. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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