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Reduction of polyethylenimine-coated iron oxide nanoparticles induced autophagy and cytotoxicity by lactosylation
Author(s) -
Jiuju Du,
Wencheng Zhu,
Li Yang,
Changqiang Wu,
Bingbing Lin,
Jun Wu,
Rongrong Jin,
Taipeng Shen,
Hua Ai
Publication year - 2016
Publication title -
regenerative biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.166
H-Index - 25
ISSN - 2056-3426
DOI - 10.1093/rb/rbw023
Subject(s) - polyethylenimine , chemistry , amphiphile , cytotoxicity , viability assay , surface modification , nanotechnology , nanoparticle , iron oxide nanoparticles , autophagy , biophysics , cell , combinatorial chemistry , iron oxide , biochemistry , organic chemistry , materials science , polymer , in vitro , apoptosis , transfection , biology , copolymer , gene
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 (C12-PEI2K) 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.

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