Manganese Doped Fluorescent Paramagnetic Nanocrystals for Dual-Modal Imaging

被引:25
|
作者
Sharma, Vijay Kumar [1 ]
Gokyar, Sayim [1 ]
Kelestemur, Yusuf [1 ]
Erdem, Talha [1 ]
Unal, Emre [1 ]
Demir, Hilmi Volkan [1 ,2 ]
机构
[1] Bilkent Univ, Dept Phys, Dept Elect & Elect Engn, UNAM Inst Mat Sci & Nanotechnol, TR-06800 Ankara, Turkey
[2] Nanyang Technol Univ, Sch Math & Phys Sci, Sch Elect & Elect Engn, Luminous Ctr Excellence Semicond Lighting & Displ, Singapore 639798, Singapore
基金
欧盟第七框架计划;
关键词
QUANTUM DOTS; CONTRAST AGENTS; HIGH RELAXIVITY; ZNS-MN; NANOPARTICLES; MRI; PHOTOLUMINESCENCE;
D O I
10.1002/smll.201401143
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, dual-modal (fluorescence and magnetic resonance) imaging capabilities of water-soluble, low-toxicity, monodisperse Mn-doped ZnSe nanocrystals (NCs) with a size (6.5 nm) below the optimum kidney cutoff limit (10 nm) are reported. Synthesizing Mn-doped ZnSe NCs with varying Mn2+ concentrations, a systematic investigation of the optical properties of these NCs by using photoluminescence (PL) and time resolved fluorescence are demonstrated. The elemental properties of these NCs using X-ray photoelectron spectroscopy and inductive coupled plasma-mass spectroscopy confirming Mn2+ doping is confined to the core of these NCs are also presented. It is observed that with increasing Mn2+ concentration the PL intensity first increases, reaching a maximum at Mn2+ concentration of 3.2 at% (achieving a PL quantum yield (QY) of 37%), after which it starts to decrease. Here, this high-efficiency sample is demonstrated for applications in dual-modal imaging. These NCs are further made water-soluble by ligand exchange using 3-mercaptopropionic acid, preserving their PL QY as high as 18%. At the same time, these NCs exhibit high relaxivity (approximate to 2.95 mM(-1) s(-1)) to obtain MR contrast at 25 degrees C, 3 T. Therefore, the Mn2+ doping in these water-soluble Cd-free NCs are sufficient to produce contrast for both fluorescence and magnetic resonance imaging techniques.
引用
收藏
页码:4961 / 4966
页数:6
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