Abstract

Superparamagnetic iron oxide (SPIO) nanoparticles are excellent magnetic resonance contrast agents and surface engineering can expand their applications. When covered with amphiphilic alkyl-polyethyleneimine (PEI), the modified SPIO nanoparticles can be used as MRI visible gene/drug delivery carriers and cell tracking probes. However, the positively charged amines of PEI can also cause cytotoxicity and restricts their further applications. In this study, we used lactose to modify amphiphilic low molecular weight polyethylenimine (C 12 -PEI 2K) at different lactosylation degree. It was found that the N-alkyl-PEI-lactobionic acid wrapped SPIO nanocomposites show better cell viability without compromising their labelling efficacy as well as MR imaging capability in RAW 264.7 cells, comparing to the unsubstituted ones. Besides, we found the PEI induced cell autophagy can be reduced via lactose modification, indicating the increased cell viability might rely on down-regulating autophagy. Thus, our findings provide a new approach to overcome the toxicity of PEI wrapped SPIO nanocomposites by lactose modification.

Details

Title
Reduction of polyethylenimine-coated iron oxide nanoparticles induced autophagy and cytotoxicity by lactosylation
Author
Du, Jiuju 1 ; Zhu, Wencheng 2 ; Yang, Li 1 ; Wu, Changqiang 3 ; Lin, Bingbing 1 ; Wu, Jun 1 ; Jin, Rongrong 1 ; Shen, Taipeng 1 ; Ai, Hua 4 

 National Engineering Research Center for Biomaterials 
 National Engineering Research Center for Biomaterials; Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031, P. R. China 
 National Engineering Research Center for Biomaterials; School of Medical Imaging, North Sichuan Medical College, Nanchong, 637000, P.R. China 
 National Engineering Research Center for Biomaterials; Department of Radiology, West China Hospital, Sichuan University, Chengdu, 610065, P.R. China 
Pages
223-229
Publication year
2016
Publication date
Dec 2016
Publisher
Oxford University Press
ISSN
20563418
e-ISSN
20563426
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3171503273
Copyright
© The Author(s) 2016. Published by Oxford University Press. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.