Three-dimensional cellular microarray for high-throughput toxicology assays

被引:234
|
作者
Lee, Moo-Yeal [1 ,2 ]
Kumar, R. Anand [4 ]
Sukumaran, Sumitra M. [2 ]
Hogg, Michael G. [1 ,2 ]
Clark, Douglas S.
Dordick, Jonathan S. [2 ,3 ]
机构
[1] Solidus Biosci Inc, Troy, NY 12180 USA
[2] Rensselaer Polytech Inst, Dept Chem & Biol Engn, Troy, NY 12180 USA
[3] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
[4] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
关键词
cytochromes P450; in situ drug metabolism; in vitro cytotoxicity; on-chip cell encapsulation;
D O I
10.1073/pnas.0708756105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have developed a miniaturized 3D cell-culture array (the Data Analysis Toxicology Assay Chip or DataChip) for high-throughput toxicity screening of drug candidates and their cytochrome P450-generated metabolites. The DataChip consists of human cells encapsulated in collagen or alginate gels (as small as 20 nl) arrayed on a functionalized glass slide for spatially addressable screening against multiple compounds. A single DataChip containing 1,080 individual cell cultures, used in conjunction with the complementary human P450-containing microarray (the Metabolizing Enzyme Toxicology Assay Chip or MetaChip), simultaneously provided IC50 values for nine compounds and their metabolites from CYP1A2, CYP2D6, and CYP3A4 and a mixture of the three P450s designed to emulate the human liver. Similar responses were obtained with the DataChip and conventional 96-well plate assays, demonstrating that the near 2,000-fold miniaturization does not influence the cytotoxicity response. The DataChip may therefore enable toxicity analyses of drug candidates and their metabolites at throughputs compatible with the availability of compounds at early-stage drug discovery.
引用
收藏
页码:59 / 63
页数:5
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