Metabolizing enzyme toxicology assay chip (MetaChip) for high-throughput microscale toxicity analyses

被引:127
作者
Lee, MY
Park, CB
Dordick, JS [1 ]
Clark, DS
机构
[1] Rensselaer Polytech Inst, Dept Biol & Chem Engn, Troy, NY 12180 USA
[2] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
关键词
in situ drug metabolism; in vitro cytotoxicity; P450; sol-gel encapsulation;
D O I
10.1073/pnas.0406755102
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
The clinical progression of new chemical entities to pharmaceuticals remains hindered by the relatively slow pace of technology development in toxicology and clinical safety evaluation, particularly in vitro approaches, that can be used in the preclinical and early clinical phases of drug development. To alleviate this bottleneck, we have developed a metabolizing enzyme toxicology assay chip (MetaChip) that combines high-throughput P450 catalysis with cell-based screening on a microscale platform. The MetaChip concept is demonstrated by using sol-gel encapsulated P450s to activate the prodrug cyclophosphamide, which is the major constituent of the anticancer drug Cytoxan, as well as other compounds that are activated, by P450 metabolism. The MetaChip provides a high-throughput microscale alternative to currently used in vitro methods for human metabolism and toxicology screening based on liver slices, cultured human hepatocytes, purified microsomal preparations, or isolated and purified P450s. This technology creates opportunities for rapid and inexpensive assessment of ADME/Tox (absorption, distribution, metabolism, excretion/toxicology) at very early phases of drug development, thereby enabling unsuitable candidates to be eliminated from consideration much earlier in the drug discovery process.
引用
收藏
页码:983 / 987
页数:5
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