Xubo
Zhao
and
Peng
Liu
*
State Key Laboratory of Applied Organic Chemistry and Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China. E-mail: pliu@lzu.edu.cn; Fax: +86 0931 8912582; Tel: +86 0931 8912582
First published on 6th February 2015
Correction for ‘Biocompatible graphene oxide as a folate receptor-targeting drug delivery system for the controlled release of anti-cancer drugs’ by Xubo Zhao et al., RSC Adv., 2014, 4, 24232–24239.
The description of the determination of the cytotoxicity was incorrect. The WST-1 (4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate) assay was used for cell toxicity studies in KB cells, rather than the MTT assay in HepG2 cells. For the WST-1 assay, the cells were seeded into 96-well plates at densities of 1 × 105 cells per well for 24 h, and washed. Then, CG-PEG-FA nanocarriers at different concentrations, drug-loaded CG-PEG-FA and CG-PEG nanocarriers, and DOX were added to the cells and incubated for 24 h. Thereafter, direct detection at 450 nm was processed for the WST-1 assay to determine the cell viability.
These corrections do not influence any descriptions or conclusions in the article.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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