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Positively charged graphene/Fe3O4/polyethylenimine with enhanced drug loading and cellular uptake for magnetic resonance imaging and magnet-responsive cancer therapy

Enhanced cellular uptake efficiency of nanoparticles is important for their biomedical applications, including photothermal therapy (PTT) for cancer. In this study, a one-pot method was used to construct a positively charged and magnet-responsive nanocomposite comprising reduced graphene oxide ancho...

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Published in:Nano research 2017-07, Vol.10 (7), p.2280-2295
Main Authors: Du, Baoji, Liu, Jianhua, Ding, Guanyu, Han, Xu, Li, Dan, Wang, Erkang, Wang, Jin
Format: Article
Language:English
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Summary:Enhanced cellular uptake efficiency of nanoparticles is important for their biomedical applications, including photothermal therapy (PTT) for cancer. In this study, a one-pot method was used to construct a positively charged and magnet-responsive nanocomposite comprising reduced graphene oxide anchoring iron oxide (RGI) with a polyethylenimine (PEI) modification, to improve the efficiency of cell internalization. The surface charge can be finely tuned using PEIs of different molecular weights. The obtained RGIlsk composite (RGI modified by 1.8 kDa PEI) could load indocyanine green (ICG) at a high mass ratio of 10:3 and ablate cancer cells using low-density laser irradiation because of its positively charged surface. In addition, the hybrids of RGI1.8k and ICG could kill most cancer cells at a laser density of 0.7 W/cm2 in vitro and 0.3 W/cm2 in vivo. At the same time, cell viability could be controlled by converting the external magnetic-field direction because of the enrichment of the magnet-responsive composite in vitro and in vivo. Furthermore, RGIr8k-ICGs could be used as T2-weighted magnetic resonance and infrared thermal imaging agents. Coupled with the magnetic target effect, the imaging signal could be improved significantly. Therefore, RGII~sk-ICGs represent a new highly efficient PTT and imaging agent with great potential for cancer treatment.
ISSN:1998-0124
1998-0000
DOI:10.1007/s12274-016-1418-x