Electrochemical Biochip for Drug Screening At Cellular Level

被引:7
作者
Chen, Yu [1 ]
Cui, Hui-fang [2 ]
Ye, Jian-shan [2 ]
Chong, Ser-choong [1 ]
Lim, Tit-meng [2 ]
Sheu, Fwu-shan [2 ]
Hui, Wing-cheong [1 ]
机构
[1] Inst Microelect, 11 Sci Pk Rd,Sci Pk 2, Singapore 117685, Singapore
[2] Natl Univ Singapore, Dept Sci Biol, Singapore 117543, Singapore
来源
INTERNATIONAL MEMS CONFERENCE 2006 | 2006年 / 34卷
关键词
microelectrode array; cell chip; cell monitoring; in situ; temporal detection; drug screening; non-invasive;
D O I
10.1088/1742-6596/34/1/033
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Drug screening at cellular level has becomes an attractive field of research. Different researchers have tried to record cellular response to drugs by electrical or optical approach using both invasive and non-invasive methods. Silicon-based microelectrode integrated microchips are useful tools for in situ temporal recording of neurotransmitter releasing from neural cells. A microfabricated electrochemical biochip is presented in this paper. Using dopaminergic cells grown on the chip, the dopamine excytosis can be electrochemical amperomatric detected non-invasively from drug incubated dopaminegic cells by the microelectrode integrated on chip. This silicon-based electrochemical chip has been designed with an electrode array located on the cell culture chamber bottom. Each electrode is individually electrical controlled. MN9D and PC12 dopaminergic cell lines have been demonstrated on this chip for drug effects study. This silicon-based electrochemical microchip provides a non-invasive, in situ, temporal detection of dopamine exocytosis from dopaminegic cells, and holds the potential for applications in studying the mechanisms of dopamine exocytosis and drug screening. It is also extendable for other cell culture and drug effects study.
引用
收藏
页码:198 / 203
页数:6
相关论文
共 19 条
[1]   Microfabrication and microfluidics for tissue engineering: state of the art and future opportunities [J].
Andersson, H ;
van den Berg, A .
LAB ON A CHIP, 2004, 4 (02) :98-103
[2]  
CHEN Y, 2006, SPIE INT SOC OPT ENG
[3]  
CHEN Y, 2003, Patent No. 6503847
[4]   IMMORTALIZATION OF EMBRYONIC MESENCEPHALIC DOPAMINERGIC-NEURONS BY SOMATIC-CELL FUSION [J].
CHOI, HK ;
WON, LA ;
KONTUR, PJ ;
HAMMOND, DN ;
FOX, AP ;
WAINER, BH ;
HOFFMANN, PC ;
HELLER, A .
BRAIN RESEARCH, 1991, 552 (01) :67-76
[5]  
CUI HF, 2005, SENSORS A B IN PRESS
[6]  
GREENE LA, 1987, METHOD ENZYMOL, V147, P207
[7]  
HARUYAMA T, 2002, ADV DRUG DELIVERY RE, V1, P1
[8]   A novel high aspect ratio microfluidic design to provide a stable and uniform microenvironment for cell growth in a high throughput mammalian cell culture array [J].
Hung, PJ ;
Lee, PJ ;
Sabounchi, P ;
Aghdam, N ;
Lin, R ;
Lee, LP .
LAB ON A CHIP, 2005, 5 (01) :44-48
[9]   Release of dopamine and ATP from PC12 cells treated with dexamethasone, reserpine and bafilomycin A1 [J].
Kasai, Y ;
Ohta, T ;
Nakazato, Y ;
Ito, S .
JOURNAL OF VETERINARY MEDICAL SCIENCE, 2001, 63 (04) :367-372
[10]   Voltammetric and pharmacological characterization of dopamine release from single exocytotic events at rat pheochromocytoma (PC12) cells [J].
Kozminski, KD ;
Gutman, DA ;
Davila, V ;
Sulzer, D ;
Ewing, AG .
ANALYTICAL CHEMISTRY, 1998, 70 (15) :3123-3130