Sun Minjie, Sun Bin, Liu Yun, Shen Qun-Dong, Jiang Shaojun
Department of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, China.
Department of Polymer Science &Engineering and Key Laboratory of High Performance Polymer Materials &Technology of MOE, Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry &Chemical Engineering, Nanjing University, Nanjing 210023, China.
Sci Rep. 2016 Mar 2;6:22368. doi: 10.1038/srep22368.
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 μg/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.
纳米材料在生物应用中的快速发展引发了对探索纳米材料与细胞相互作用的迫切需求。通过依次静电吸附,将阳离子蓝色发光和阴离子绿色发光共轭聚合物作为双色荧光探针应用于带负电荷的磁性纳米颗粒表面。这些共轭聚合物具有大的消光系数和高荧光量子产率(PFN为82%,ThPFS为62%)。因此,通过共聚焦激光扫描显微镜可以在癌细胞内可视化痕量(2.7μg/mL)的荧光标记纳米颗粒。通过流式细胞术分析,共轭聚合物的荧光标记也被验证用于定量测定每个细胞内内化的纳米颗粒。细胞质中蓝色和绿色荧光信号的广泛重叠表明,在细胞内化过程中,两种共轭聚合物探针都紧密结合在纳米颗粒表面。高电荷且荧光标记的纳米颗粒非特异性地结合到细胞膜上,随后通过内吞作用被细胞摄取。纳米颗粒在内体中形成聚集体,产生点状染色模式。纳米颗粒的细胞内化取决于剂量和时间。通过施加外部磁场,摄取效率可提高三倍。这些纳米颗粒具有低细胞毒性,适用于同时进行无创荧光和磁共振成像应用。