Visual and high-throughput detection of cancer cells using a graphene oxide-based FRET aptasensing microfluidic chip

被引:76
作者
Cao, Lili [1 ]
Cheng, Liwei [1 ]
Zhang, Zhengyong [1 ]
Wang, Yi [1 ]
Zhang, Xianxia [1 ]
Chen, Hui [1 ]
Liu, Baohong [1 ]
Zhang, Song [1 ]
Kong, Jilie [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
CIRCULATING TUMOR-CELLS; PLATFORM;
D O I
10.1039/c2lc40564d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rapid and efficient measurement of cancer cells is a major challenge in early cancer diagnosis. In the present study, a miniature multiplex chip was created for in situ detection of cancer cells by implementing a novel graphene oxide (GO)-based Forster resonance energy transfer (FRET) biosensor strategy, i.e. assaying the cell-induced fluorescence recovery from the dye-labeled aptamer/graphene oxide complex. Fluorescence intensity measurement and image analyses demonstrated that this microfluidic biosensing method exhibited rapid, selective and sensitive fluorescence responses to the quantities of the target cancer cells, CCRF-CEM cells. Seven different cancer cell samples can be measured at the same time in such a microfluidic chip. The linear response for target CCRF-CEM cells in a concentration range from 2.5 x 10(1) to 2.5 x 10(4) cells mL(-1) was obtained, with a detection limit about 25 cells mL(-1), which is about ten times lower than those of normal biosensors. The novel fluorescence biosensing microfluidic chip supplies a rapid, visible and high-throughput approach for early cancer diagnosis with high sensitivity and specificity.
引用
收藏
页码:4864 / 4869
页数:6
相关论文
共 32 条
[1]   Evaluation of natural compounds for telomeric DNA interaction using FRET thermal melting analysis [J].
Abachi, Farzane ;
Noureini, Sakineh Kazemi .
CLINICAL BIOCHEMISTRY, 2011, 44 (13) :S257-S257
[2]  
Baker BR, 2006, J AM CHEM SOC, V128, P3138, DOI 10.1021/ja056957p
[3]   Graphene Fluorescence Resonance Energy Transfer Aptasensor for the Thrombin Detection [J].
Chang, Haixin ;
Tang, Longhua ;
Wang, Ying ;
Jiang, Jianhui ;
Li, Jinghong .
ANALYTICAL CHEMISTRY, 2010, 82 (06) :2341-2346
[4]   Microfluidic approaches for cancer cell detection, characterization, and separation [J].
Chen, Jian ;
Li, Jason ;
Sun, Yu .
LAB ON A CHIP, 2012, 12 (10) :1753-1767
[5]   Relative contributions of enzyme cytochemistry and flow cytometric immunophenotyping to the evaluation of acute myeloid leukemias with a monocytic component and of flow cytometric immunophenotyping to the evaluation of absolute monocytoses [J].
Dunphy, CH ;
Orton, SO ;
Mantell, J .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 122 (06) :865-874
[6]   A portable and integrated nucleic acid amplification microfluidic chip for identifying bacteria [J].
Fang, Xueen ;
Chen, Hui ;
Xu, Lingjia ;
Jiang, Xingyu ;
Wu, Wenjuan ;
Kong, Jilie .
LAB ON A CHIP, 2012, 12 (08) :1495-1499
[7]   Fluorescent conjugated polymer-based FRET technique for detection of DNA methylation of cancer cells [J].
Feng, Fude ;
Liu, Libing ;
Wang, Shu .
NATURE PROTOCOLS, 2010, 5 (07) :1255-1264
[8]   Molecular detection and characterisation of circulating tumour cells and micrometastases in solid tumours [J].
Ghossein, RA ;
Bhattacharya, S .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (13) :1681-1694
[9]   Electronic transport properties of individual chemically reduced graphene oxide sheets [J].
Gomez-Navarro, Cristina ;
Weitz, R. Thomas ;
Bittner, Alexander M. ;
Scolari, Matteo ;
Mews, Alf ;
Burghard, Marko ;
Kern, Klaus .
NANO LETTERS, 2007, 7 (11) :3499-3503
[10]   Point of Care Diagnostics: Status and Future [J].
Gubala, Vladimir ;
Harris, Leanne F. ;
Ricco, Antonio J. ;
Tan, Ming X. ;
Williams, David E. .
ANALYTICAL CHEMISTRY, 2012, 84 (02) :487-515