Preclinical Drug Metabolism in the Age of High-Throughput Screening: An Industrial Perspective |
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Authors: | Rodrigues A. David |
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Affiliation: | (1) Drug Metabolism (Preclinical), Merck Research Laboratories, Sumneytown Pike, P.O. Box 4, WP26A 2044, West Point, Pennsylvania, 19486-0004 |
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Abstract: | With the advent of genomics, combinatorial paradigms and high-throughput screen (HTS)-based pharmacological testing, the number of compounds flowing through the discovery pipeline is likely to escalate. At the same time, with increased knowledge of the human drug-metabolizing enzymes and the availability of in vitro absorption-metabolism (AM) models, Preclinical Drug Metabolism is poised to meet the challenges of HTS. In order to be successful, however, a rational HTS strategy (vs. serendipitous HTS) has to be employed. Such a strategy is based on automation, validation and integration of in vitroAM models and database management (AVID). A generalized strategy for rational (AVID-based) HTS in Preclinical Drug Metabolism is described briefly. |
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Keywords: | high-throughput in vitro models in vitro-in vivo correlations metabolism absorption drug discovery screening |
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