Impedance-based cellular assay technologies: recent advances, future promise

被引:61
作者
McGuinness, Ryan [1 ]
机构
[1] MDS Analyt Technol, Drug Discovery, Sunnyvale, CA 94089 USA
关键词
D O I
10.1016/j.coph.2007.08.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cell-based assays are continuing to grow in importance in the drug discovery workflow. Their early introduction holds the promise of limiting attrition in the later, more costly phases of the process. This article reviews recent advances in the development of impedance technologies for label-free cell-based assays. These systems are capable of monitoring endogenous receptor activation, and thus generate more physiologically relevant measures of pharmacological endpoints. Primary cells can be investigated as well, thus producing disease relevant information. Label-free assays significantly decrease assay development efforts and avoid many complications inherent in recombinant readout systems. Impedance-based systems have great potential to advance the utility of cell-based assays as they are applied to drug discovery and pharmacology.
引用
收藏
页码:535 / 540
页数:6
相关论文
共 31 条
[1]   Dynamic and label-free cell-based assays using the real-time cell electronic sensing system [J].
Atienza, Josephine M. ;
Yu, Naichen ;
Kirstein, Shelli L. ;
Xi, Biao ;
Wang, Xiaobo ;
Xu, Xiao ;
Abassi, Yama A. .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2006, 4 (05) :597-607
[2]   Cellular dielectric spectroscopy: A powerful new approach to label-free cellular analysis [J].
Ciambrone, GJ ;
Liu, VF ;
Lin, DC ;
McGuinness, RP ;
Leung, GK ;
Pitchford, S .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (06) :467-480
[3]  
COMELIO D, 2007, ANN ONCOL
[4]   Comparative analysis of P2Y4 and P2Y6 receptor architecture in native and transfected neuronal systems [J].
D'Ambrosi, Nadia ;
Iafrate, Monia ;
Saba, Elena ;
Rosa, Patrizia ;
Volonte, Cinzia .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2007, 1768 (06) :1592-1599
[5]   A bivalent ligand (KDAN-18) containing δ-antagonist and k-agonist pharmacophores bridges δ2 and k1 opioid receptor phenotypes [J].
Daniels, DJ ;
Kulkarni, A ;
Xie, ZH ;
Bhushan, RG ;
Portoghese, PS .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (06) :1713-1716
[6]  
FOSTER KR, 1989, CRIT REV BIOMED ENG, V17, P25
[7]   Distinct β-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation [J].
Gesty-Palmer, D ;
Chen, MY ;
Reiter, E ;
Ahn, S ;
Nelson, CD ;
Wang, ST ;
Eckhardt, AE ;
Cowan, CL ;
Spurney, RF ;
Luttrell, LM ;
Lefkowitz, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (16) :10856-10864
[8]   Dielectric behaviour of gap junction connected cells: a microscopic approach [J].
Gheorghiu, E ;
Balut, C ;
Gheorghiu, M .
PHYSICS IN MEDICINE AND BIOLOGY, 2002, 47 (02) :341-348
[9]   A MORPHOLOGICAL BIOSENSOR FOR MAMMALIAN-CELLS [J].
GIAEVER, I ;
KEESE, CR .
NATURE, 1993, 366 (6455) :591-592
[10]   Dynamic detection of natural killer cell-mediated cytotoxicity and cell adhesion by electrical impedance measurements [J].
Glamann, Joakim ;
Hansen, Anker Jon .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2006, 4 (05) :555-563