Synthesis of Fluorescence/MRI Dual Targeted Imaging Theranostics Reagent

被引:2
|
作者
Chen Qing-Tao [1 ]
Shi Xiang-Dong [1 ]
Liang Wei-Wei [1 ]
Jiang Li-Ying [2 ]
Fang Shao-Ming [1 ]
Chen Feng-Hua [1 ]
机构
[1] Zhengzhou Univ Light Ind, Coll Mat & Chem Engn, Zhengzhou 450002, Peoples R China
[2] Zhengzhou Univ Light Ind, Coll Elect & Informat Engn, Zhengzhou 450002, Peoples R China
关键词
graphene quantum dots; fluorescence; magnetic resonance imaging; nanoparticles; theranostics; GRAPHENE QUANTUM DOTS; CONTRAST AGENTS; IN-VITRO; MRI; RELAXIVITY;
D O I
10.11862/CJIC.2021.181
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Poly (ethylene glycol diamine) (NH2-PEG-NH2) modified graphene quantum dots (GODs) were conjugated with diethylenetriaminepentaacetic acid (DTPA) via an amide bond. Then the product further coordinated with Gd3+ ions, followed by the subsequent linkage of folic acid (FA) to form FA/GODs-Gd(DTPA). Next, an anticancer drug, doxorubicin ( DOX), was loaded on the surface of FA/GODs-Gd(DTPA) to obtain the final fluorescence/MRI dual targeted imaging diagnostic reagents (FA/GODs-Gd(DTPA)/DOX) for lung cancer cells. The sample was characterized by transmission electron microscopy, UV-Vis absorption spectroscopy, fluorescence spectroscopy, laser confocal microscopy, and so on. Compared with normal HLF cells, the results of MRI, confocal laser scanning microscopy and MTT showed that the prepared FA/GODs-Gd(DTPA)/DOX could be targeted to detect lung cancer H460 cells, in which folate receptor was highly expressed, and also displayed significant anti-tumor activity.
引用
收藏
页码:1555 / 1562
页数:8
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