Evaluation of Toxicity and Neural Uptake In Vitro and In Vivo of Superparamagnetic Iron Oxide Nanoparticles

被引:30
|
作者
Khalid, Muhammad Kamran [1 ]
Asad, Muhammad [1 ]
Henrich-Noack, Petra [2 ]
Sokolov, Maxim [2 ]
Hintz, Werner [1 ]
Grigartzik, Lisa [2 ]
Zhang, Enqi [2 ]
Dityatev, Alexander [3 ,4 ,5 ]
van Wachem, Berend [1 ]
Sabel, Bernhard A. [2 ]
机构
[1] Otto Von Guericke Univ, Chair Mech Proc Engn, Inst Proc Engn, Univ Pl 2, D-39106 Magdeburg, Germany
[2] Otto Von Guericke Univ, Inst Med Psychol, Leipziger Str 44, D-39120 Magdeburg, Germany
[3] German Ctr Neurodegenerat Dis, Leipziger Str 44, D-39120 Magdeburg, Germany
[4] Otto Von Guericke Univ, Fac Med, Leipziger Str 44, D-39120 Magdeburg, Germany
[5] CBBS, D-39106 Magdeburg, Germany
关键词
superparamagnetic iron oxide nanoparticles (SPIO-NPs); drug delivery; in vitro toxicity; cellular uptake; MAGNETIC NANOPARTICLES; CYTOTOXICITY; PRECIPITATION;
D O I
10.3390/ijms19092613
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Superparamagnetic iron oxide nanoparticles (SPIO-NPs) have great potential to be used in different pharmaceutical applications, due to their unique and versatile physical and chemical properties. The aim of this study was to quantify in vitro cytotoxicity of dextran 70,000-coated SPIO-NPs labelled/ unlabelled with rhodamine 123, in C6 glioma cells and primary hippocampal neural cells. In addition, we analyzed the in vitro and in vivo cellular uptake of labelled SPIO-NPs. The nanoparticles, with average size of 10-50 nm and polydispersity index of 0.37, were synthesized using Massart's co-precipitation method. The concentration-dependent cytotoxicity was quantified by using tetrazolium dye 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). Intracellular localization of SPIO-NPs was detected by confocal laser microscopy. In vivo confocal neuroimaging (ICON) was performed on male Wistar rats after intravitreal injection followed by ex vivo retina whole mount analysis. When used for in vitro testing concentrations in the range of diagnostic and therapeutic dosages, SPIO-NPs proved to be non-cytotoxic on C6 glioma cells for up to 24 h incubation time. The hippocampal cell culture also did not show impaired viability at low doses after 24 h incubation. Our results indicate that our dextran-coated SPIO-NPs have the potential for in vivo drug delivery applications.
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页数:14
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