Dual-Color Fluorescence Imaging of Magnetic Nanoparticles in Live Cancer Cells Using Conjugated Polymer Probes

被引:34
|
作者
Sun, Minjie [1 ,2 ,3 ]
Sun, Bin [2 ,3 ]
Liu, Yun [2 ,3 ]
Shen, Qun-Dong [2 ,3 ]
Jiang, Shaojun [4 ]
机构
[1] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Dept Polymer Sci & Engn, Nanjing 210023, Jiangsu, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Key Lab High Performance Polymer Mat & Technol,MO, Nanjing 210023, Jiangsu, Peoples R China
[4] Jinling Hosp, Dept Pathol & Lab Electron Microscopy, Nanjing 210002, Jiangsu, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
IRON-OXIDE NANOPARTICLES; CARBON NANOTUBES; POLYELECTROLYTE; DESIGN; NANOMATERIALS; RECOGNITION; DIAGNOSIS; TRACKING; BACTERIA; DELIVERY;
D O I
10.1038/srep22368
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rapid growth in biological applications of nanomaterials brings about pressing needs for exploring nanomaterial-cell interactions. Cationic blue-emissive and anionic green-emissive conjugated polymers are applied as dual-color fluorescence probes to the surface of negatively charged magnetic nanoparticles through sequentially electrostatic adsorption. These conjugated polymers have large extinction coefficients and high fluorescence quantum yield (82% for PFN and 62% for ThPFS). Thereby, one can visualize trace amount (2.7 mu g/mL) of fluorescence-labeled nanoparticles within cancer cells by confocal laser scanning microscopy. Fluorescence labeling by the conjugated polymers is also validated for quantitative determination of the internalized nanoparticles in each individual cell by flow cytometry analysis. Extensive overlap of blue and green fluorescence signals in the cytoplasm indicates that both conjugated polymer probes tightly bind to the surface of the nanoparticles during cellular internalization. The highly charged and fluorescence-labeled nanoparticles non-specifically bind to the cell membranes, followed by cellular uptake through endocytosis. The nanoparticles form aggregates inside endosomes, which yields a punctuated staining pattern. Cellular internalization of the nanoparticles is dependent on the dosage and time. Uptake efficiency can be enhanced three-fold by application of an external magnetic field. The nanoparticles are low cytotoxicity and suitable for simultaneously noninvasive fluorescence and magnetic resonance imaging application.
引用
收藏
页数:12
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