N-Doped graphene quantum dot@mesoporous silica nanoparticles modified with hyaluronic acid for fluorescent imaging of tumor cells and drug delivery

被引:48
作者
Gui, Wenying [1 ]
Zhang, Jinrui [2 ]
Chen, Xueqian [1 ]
Yu, Dahai [2 ]
Ma, Qiang [1 ]
机构
[1] Jilin Univ, Dept Analyt Chem, Coll Chem, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Coll Iife Sci, Minist Educ, Key Lab Mol Enzymol & Engn, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Doxorubicin; CD-44; Photoluminescence; Forster resonance energy transfer; HeLa; Nanoparticles; Nanocarrier; Fluorescence quenching; Target recognition; Drugs loading; N; P-DOPED CARBON DOTS; SURFACE FUNCTIONALIZATION; RELEASE; SYSTEM; PHOTOLUMINESCENCE; FRET; GQDS; PROBE;
D O I
10.1007/s00604-017-2598-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The authors describe new bifunctional mesoporous silica nanoparticles (NPs) for specific targeting of tumor cells and for intracellular delivery of the cancer drug doxorubicin (DOX). Mesoporous silica nanoparticles (MSNPs) were coated with blue fluorescent N-graphene quantum dots, loaded with the drug DOX, and finally coated with hyaluronic acid (HA). Cellular uptake of the NPs with an architecture of the type HA-DOX-GQD@MSNPs enabled imaging of human cervical carcinoma (HeLa) cells via fluorescence microscopy. The cytotoxicity of the nanoparticles on HeLa cells was also assessed. The results suggest that the NPs are higher cytotoxicity effect and exert in living cell imaging ability. Compared to the majority of other drug nanocarrier systems, the one described here enables simultaneous DOX release and fluorescent monitoring.
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页数:8
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