A prototypic microfluidic platform generating stepwise concentration gradients for real-time study of cell apoptosis

被引:29
作者
Dai, Wen [1 ,2 ]
Zheng, Yizhe [1 ]
Luo, Kathy Qian [3 ]
Wu, Hongkai [1 ,2 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, NSNT Program, Kowloon, Hong Kong, Peoples R China
[3] Nanyang Technol Univ, Sch Chem & Biomed Engn, Div Bioengn, Singapore 637457, Singapore
来源
BIOMICROFLUIDICS | 2010年 / 4卷 / 02期
关键词
HL60; CELLS; DEVICE; ACTIVATION; MICROCHIP; CHEMOTAXIS; INHIBITOR; VIABILITY; DYNAMICS; DOCKING; SYSTEMS;
D O I
10.1063/1.3398319
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work describes the development of a prototypic microfluidic platform for the generation of stepwise concentration gradients of drugs. A sensitive apoptotic analysis method is integrated into this microfluidic system for studying apoptosis of HeLa cells under the influence of anticancer drug, etoposide, with various concentrations in parallel; it measures the yellow fluorescent protein/cyan fluorescent protein fluorescence resonance energy transfer (FRET) signal that responds to the activation of caspase-3, an indicator of cell apoptosis. Sets of microfluidic valves on the chip generate stepwise concentration gradient of etoposide in various cell-culture microchambers. The FRET signals from multiple chambers are simultaneously monitored under a fluorescent microscope for long-time observation and the on-chip results are compared with those from 96-well plate study and the methylthiazolyldiphenyl-tetrazolium bromide (MTT) assay. The microfluidic platform shows several advantages including high-throughput capacity, low drug consumption, and high sensitivity. (C) 2010 American Institute of Physics. [doi:10.1063/1.3398319]
引用
收藏
页数:14
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