Non-blinking, highly luminescent, pH- and heavy-metal-ion-stable organic nanodots for bio-imaging

被引:28
作者
An, Fei-Fei [1 ,2 ]
Ye, Jun [1 ,2 ]
Zhang, Jin-Feng [1 ,2 ]
Yang, Yin-Long [4 ,5 ]
Zheng, Cai-Jun [1 ,2 ]
Zhang, Xiu-Juan [4 ,5 ]
Liu, Zhuang [4 ,5 ]
Lee, Chun-Sing [3 ]
Zhang, Xiao-Hong [1 ,2 ]
机构
[1] Chinese Acad Sci, Nanoorgan Photoelect Lab, Tech Inst Phys & Chem, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Key Lab Photochem Convers & Optoelect Mat, Tech Inst Phys & Chem, Beijing 100190, Peoples R China
[3] City Univ Hong Kong, Dept Phys & Mat Sci, Ctr Super Diamond & Adv Films COSDAF, Hong Kong, Hong Kong, Peoples R China
[4] Soochow Univ, Funct Nano & So Mat Lab FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[5] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
FLUORESCENT BIOLOGICAL LABELS; SEMICONDUCTING POLYMER DOTS; QUANTUM DOTS; SINGLE MOLECULES; IN-VIVO; NANOPARTICLES; NANOCRYSTALS; EMISSION; CANCER; PHOTOLUMINESCENCE;
D O I
10.1039/c3tb20271b
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Heavy-metal-free, organic-small-molecule-based fluorescent nanodots (Sdots, 31-60 nm in diameter) based on 2,7-di(4-(diphenylamino)phenyl-2,1,3-benzothiadiazol-7-yl)-9,9'-spirobifluorene (Spiro-BTA) were prepared through a simple solution process. The Sdots show not only non-blinking and high-brightness fluorescence but also stability in various pH conditions and heavy metal ion solutions. More importantly, Spiro-BTA Sdots demonstrate obviously much higher brightness with very high signal-to-background ratio in Hela cell, compared with common CdSe/ZnS QDs. In addition, they exhibit large Stokes shifts, broad absorption spectra, and low toxicity to living cells which enable their applications as good fluorescence probes for bio-imaging. Further application of Sdots for folate receptor-mediated live-cell endocytosis was demonstrated by non-convalent modification with folic acid linked multidentate ligands.
引用
收藏
页码:3144 / 3151
页数:8
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