Inducing cells to disperse nickel nanowires via integrin-mediated responses

被引:25
作者
Sharma, Anirudh [1 ]
Orlowski, Gregory M. [2 ]
Zhu, Yuechen [3 ]
Shore, Daniel [1 ]
Kim, Seung Yeon [1 ]
DiVito, Michael D. [3 ]
Hubel, Allison [3 ]
Stadler, Bethanie J. H. [1 ]
机构
[1] Univ Minnesota, Elect & Comp Engn, Minneapolis, MN 55455 USA
[2] UMass Med Sch, Worcester, MA 01545 USA
[3] Univ Minnesota, Mech Engn, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
magnetic nanowires; nickel; RGD; integrin; internalization; cell proliferation; MAGNETIC NANOWIRES; DRUG-DELIVERY; MULTIFUNCTIONAL NANORODS; SURFACE MODIFICATION; TUMOR-CELLS; IN-VITRO; NANOPARTICLE; RGD; CANCER; SEPARATION;
D O I
10.1088/0957-4484/26/13/135102
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We present non-cytotoxic, magnetic, Arg-Gly-Asp (RGD)-functionalized nickel nanowires (RGD-nanowires) that trigger specific cellular responses via integrin transmembrane receptors, resulting in dispersal of the nanowires. Time-lapse fluorescence and phase contrast microscopy showed that dispersal of 3 mu m long nanowire increased by a factor of 1.54 with functionalization by RGD, compared to polyethylene glycol (PEG), through integrin-specific binding, internalization and proliferation in osteosarcoma cells. Further, a 35.5% increase in cell density was observed in the presence of RGD-nanowires, compared to an increase of only 15.6% with PEG-nanowires. These results promise to advance applications of magnetic nanoparticles in drug delivery, hyperthermia, and cell separation where uniformity and high efficiency in cell targeting is desirable.
引用
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页数:12
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