Corrigendum to “Non-invasive tracking of hydrogel degradation using upconversion nanoparticles” [Acta Biomater. 55 (2017) 410–419]

Corrigendum to “Non-invasive tracking of hydrogel degradation using upconversion nanoparticles” [Acta Biomater. 55 (2017) 410–419]

Acta Biomaterialia 59 (2017) 361 Contents lists available at ScienceDirect Acta Biomaterialia journal homepage: www.elsevier.com/locate/actabiomat ...

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Acta Biomaterialia 59 (2017) 361

Contents lists available at ScienceDirect

Acta Biomaterialia journal homepage: www.elsevier.com/locate/actabiomat

Corrigendum

Corrigendum to ‘‘Non-invasive tracking of hydrogel degradation using upconversion nanoparticles” [Acta Biomater. 55 (2017) 410–419] Yuqing Dong a,b,c,1, Guorui Jin b,c,1, Changchun Ji b,c, Rongyan He b,c, Min Lin b,c, Xin Zhao e, Ang Li d, Tian Jian Lu b,c, Feng Xu b,c,⇑ a

State Key Laboratory for Mechanical Behavior of Materials, School of Materials Science and Engineering, Xi’an Jiaotong University, Xi’an 710049, PR China The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi’an Jiaotong University, Xi’an 710049, PR China Bioinspired Engineering and Biomechanics Center (BEBC), Xi’an Jiaotong University, Xi’an 710049, PR China d Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi’an Jiaotong University, Xi’an 710049, PR China e The Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hung Hom, Hong Kong Special Administrative Region b c

The authors regret to state that an error was made in Fig. 5J. Mainly, the GelMA-treated group was mislabelled as the control group in the liver columns. The mean values for the control and the GelMA treated-groups are 0.874 and 0.872, respectively. Below please find the corrected Fig. 5. The authors apologise for any inconvenience caused.

Fig. 5. In vivo safety study of UCNPs. The H&E staining of heart (A), lung (C), liver (E) and kidney (G) tissues from rats implanted with UNCP-labeled GelMA hydrogel implantation for 7 days, and heart (B), lung, (D) liver (F) and kidney (H) tissues obtained from rats without hydrogel implantation, respectively. (I) Western blot analysis of active cleaved caspase 12 in lung, liver, spleen, kidney and heart tissues obtained from rats with UNCP-labeled GelMA hydrogel implantation as compared to the control group without implantation. (J) WB bands were normalized to b-actin.

DOI of original article: http://dx.doi.org/10.1016/j.actbio.2017.04.016

⇑ Corresponding author at State Key Laboratory for Mechanical Behavior of Materials, School of Materials Science and Engineering, Xi’an Jiaotong University, Xi’an 710049, PR China. 1

E-mail address: [email protected] (F. Xu). Authors contributed equally.

http://dx.doi.org/10.1016/j.actbio.2017.07.015 1742-7061/Ó 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.