Graphene oxide-based NIR fluorescence probe with aggregation-induced emission property for lectins detection and liver cells targeting

被引:22
|
作者
Jiang, Tao [1 ]
Tan, Haoqi [2 ,3 ]
Sun, Yi [2 ,3 ]
Wang, Jian [1 ]
Hang, Yandi [1 ]
Lu, Niannian [1 ]
Yang, Ji [1 ]
Qu, Xue [2 ,3 ]
Hua, Jianli [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Inst Fine Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
关键词
Fluorescent probe; NIR; Aggregation induced emission; Lectin; Graphene oxide; CANCER-CELLS; IN-VIVO; SURFACE; SENSOR; AIE; H2S;
D O I
10.1016/j.snb.2017.10.163
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Probing lectin-sugar interactions is crucial to understand important biological process as well as develop clinical diagnostics and drug for the disease. Effective tools that target these interactions are thus in great demand. In this paper, two new aggregation-induced emission (AIE)-based glycosyl probes (PT-Man and PT-Gal) have been developed for the detection of lectin-sugar interactions in the near-infrared region (NIR). PT-Man and PT-Gal show significant fluorescence enhancement upon addition of a selective lectin with a relatively low detection limit. The fluorescence increment mechanism is ascribed to the aggregation of the AIE-based glycosyl probes after complexation with the selective lectin, which has been confirmed by the scanning electron microscope (SEM) measurement. Also, in order to further improve the sensitivity and selectivity of the probes, graphene oxide (GO) has been used as a platform to assemble with the two glycosyl probes. To our delight, the PT-Man@GO and PT-Gal@GO composites exhibit better sensitivity and selectivity for probing lectin-sugar interactions. In addition, due to the specific sugar-receptor interactions, the liver cancer cell line that over express the glycoprotein receptor can be specifically targeted by PT-Gal@GO. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 126
页数:12
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