3D cell-based biosensor for cell viability and drug assessment by 3D electric cell/matrigel-substrate impedance sensing

被引:84
|
作者
Pan, Yuxiang [1 ,2 ]
Hu, Ning [1 ]
Wei, Xinwei [1 ]
Gong, Lin [3 ]
Zhang, Bin [1 ]
Wan, Hao [1 ]
Wang, Ping [1 ,2 ]
机构
[1] Zhejiang Univ, Biosensor Natl Special Lab, Key Lab Biomed Engn, Educ Minist,Dept Biomed Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Chinese Acad Sci, State Key Lab Transducer Technol, Shanghai 200050, Peoples R China
[3] Zhejiang Univ, Sch Med, Hangzhou 310058, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
3D cell-based biosensors; 3D electric cell/matrigel-substrate impedance sensing; 3D cell viability; Anti-cancer drug screening in vitro; 3-DIMENSIONAL CULTURE; SYSTEMS; GAP;
D O I
10.1016/j.bios.2018.09.046
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Preclinical efficacy and toxicity assessment of drug candidates plays a significant role in drug discovery and development. Traditional planar cell culture is a common way to perform the preclinical drug test, but it is difficult to correctly predict the drug efficacy and toxicity due to the simple two-dimensional (2D) extracellular microenvironment. Compared to the planar cell culture, three-dimensional (3D) cell culture system can better mimic the complex extracellular microenvironment where cells reside in the 3D tissues/organs in vivo. However, the conventional imaging techniques are difficult to achieve the dynamic and label-free monitoring of cellular behavior in thick sample by 3D cell culture. Here, 3D electric cell/matrigel-substrate impedance sensing (3D-ECMIS) is developed for real-time and non-invasive monitoring of 3D cell viability and drug susceptibility. In this study, human hepatoma cells (HepG2) are encapsulated in the matrigel scaffold and cultured in a 3D ECMIS chip which involves a pair of vertical golden electrodes on the opposite sidewalls of the culture chamber for the in-situ impedance measurement. Moreover, a portable multichannel system is developed to monitor the 3D cell/matrigel construct. The number of 3D-cultured cells was inversely proportional to the impedance magnitude of the entire cell/matrigel construct. Furthermore, anti-cancer drug screening will be conducted on the 3D-cultured cells when the cell proliferation reaches to a plateau phase. To validate the performance of 3D-ECMIS for the cell viability and drug susceptibility, the cell live/dead staining are utilized to confirm the results of drug susceptibility by this 3D-cell-based biosensor system. It is demonstrated that the 3D cell-based biosensor and 3D-ECMIS system will be a promising platform to improve the accuracy of cell-based anti-cancer drug screening in vitro.
引用
收藏
页码:344 / 351
页数:8
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