Open Access Article
Yue
Cao
a,
Yan
Li
c,
Yin
Wu
c,
Wenliang
Li
c,
Chunlei
Yu
c,
Yanxin
Huang
b,
Luguo
Sun
*b,
Yongli
Bao
*c and
Yuxin
Li
*a
aNational Engineering Laboratory for Druggable Gene and Protein Screening, Northeast Normal University, Jingyue Street 2555, Changchun 130117, P. R. China. E-mail: liyx486@nenu.edu.cn; Fax: +86-431-89165917; Tel: +86-431-89165917
bInstitute of Genetics and Cytology, Northeast Normal University, Renmin Street 5268, Changchun 130024, P. R. China. E-mail: sunlg388@nenu.edu.cn; Fax: +86-431-89165922; Tel: +86-431-89165922
cSchool of Life Sciences, Northeast Normal University, Renmin Street 5268, Changchun 130024, P. R. China. E-mail: baoyl800@nenu.edu.cn; Fax: +86-431-89165920; Tel: +86-431-89165920
First published on 16th December 2016
Correction for ‘Co-Delivery of angiostatin and curcumin by a biodegradable polymersome for antiangiogenic therapy’ by Yue Cao et al., RSC Adv., 2016, 6, 105442–105448.
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| Fig. 1 (A) 1H NMR spectrum (400 MHz, CDCl3) of mPEG5k–PCL12k; the blank polymersomes were examined using (B) TEM and (C) DLS; (D) the CAC of the polymersomes. | ||
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