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Metabolizing enzyme toxicology assay chip (MetaChip) for high-throughput microscale toxicity analyses
Open accessAbstract
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 bottle-neck, 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.
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Cited by
Adaptation of High-Throughput Screening in Drug Discovery—Toxicological Screening Tests
Szymański, P., Markowicz, M., & Mikiciuk-Olasik, E. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms13010427 · Cited by 454
Fernandes, T. G., Diogo, M. M., Clark, D. S., Dordick, J. S., & Cabral, J. M. S. (2009) · Trends in Biotechnology · doi:10.1016/j.tibtech.2009.02.009 · Cited by 285
Self-citationMicroengineered Liver Tissues for Drug Testing
Khetani, S. R., Berger, D. R., Ballinger, K. R., Davidson, M. D., Lin, C., & Ware, B. R. (2015) · SLAS Technology · doi:10.1177/2211068214566939 · Cited by 116
“More recent research has focused on creating miniaturized arrays of spotted enzymes in gels to make the screening process higher throughput.(16) However, cell-free microsomes and other purified enzymatic systems lack the dynamic gene expression and cellular machinery required to be useful for drug toxicity and drug ef…”
Advances in cell‐based biosensors using three‐dimensional cell‐encapsulating hydrogels
Zhou, L., Huang, G., Wang, S., Wu, J., Lee, W. G., Chen, Y., Xu, F., & Lu, T. (2011) · Biotechnology Journal · doi:10.1002/biot.201100098 · Cited by 17
Metadata
- Authors
- Lee, M.-Y., Park, C. B., Dordick, J. S., & Clark, D. S.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2005-01-18
- Volume
- 102
- Issue
- 4
- Pages
- 983-987
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2065137641
- Cited by
- 163
- References
- 0
- FWCI
- 12.29
- Type
- journal article
- Language
- en
- Open access
- green
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- Lee, M.-Y., Park, C. B., Dordick, J. S., & Clark, D. S. (2005). Metabolizing enzyme toxicology assay chip (MetaChip) for high-throughput microscale toxicity analyses. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0406755102
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