Importance of Having Low-Density Functional Groups for Generating High-Performance Semiconducting Polymer Dots

被引:105
作者
Zhang, Xuanjun [1 ]
Yu, Jiangbo [1 ]
Wu, Changfeng [1 ]
Jin, Yuhui [1 ]
Rang, Yu [1 ]
Ye, Fangmao [1 ]
Chiu, Daniel T. [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
semiconducting polymer; nanoparticles; low-density functionalization; cellular targeting; brightness; ENERGY-TRANSFER; QUANTUM DOTS; NANOPARTICLES; FLUORESCENCE; POLYFLUORENE; ULTRABRIGHT; MULTICOLOR; PHASE; CELLS;
D O I
10.1021/nn301308w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Semiconducting polymers with low-density side-chain carboxylic acid groups were synthesized to form stable, functionalized, and highly fluorescent polymer dots (Pdots). The influence of the molar fraction of hydrophilic side-chains on Pdot properties and performance was systematically investigated. Our results show that the density of side-chain carboxylic acid groups significantly affects Pdot stability, internal structure, fluorescence brightness, and nonspecific binding in cellular labeling. Fluorescence spectroscopy, single-particle imaging, and a dye-doping method were employed to investigate the fluorescence brightness and the internal structure of the Pdots. The results of these experiments indicate that semiconducting polymers with low density of side-chain functional groups can form stable, compact, and highly bright Pdots as compared to those with high density of hydrophilic side-chains. The functionalized polymer dots were conjugated to streptavidin (SA) by carbodiimide-catalyzed coupling and the Pdot-SA probes effectively and specifically labeled the cancer cell-surface marker Her2 in human breast cancer cells. The carboxylate-functionalized polymer could also be covalently modified with small functional molecules to generate Pdot probes for click chemistry-based bio-orthogonal labeling. This study presents a promising approach for further developing functional Pdot probes for biological applications.
引用
收藏
页码:5429 / 5439
页数:11
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