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Approaches to High Throughput Toxicity Screening
 
 
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Approaches to High Throughput Toxicity Screening [Hardcover]

C. K. Atterwill (Editor), P. Goldfarb (Editor), W Purcell (Editor)

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Book Description

0748407529 978-0748407521 December 16, 1999 1
The toxicology of safety testing of new pharmaceutical medicines using in vitro cell culture systems as animal alternatives in an important new science. The recent application of molecular biology (or toxicogenomics) to toxicity testing has enabled more accurate prediction of safety using in vitro systems and high throughput screening systems. These screening systems can be automated to provide fast, cost-effective and more ethical approaches to toxicity screening. Toxicogenomics is the study of organ and cellular responses to toxicity in terms of cellular stress gene induction. This family of genes (or stress gene `fingerprints') may in future allow accurate prediction of human hazard at low doses of compounds using human cell-bases systems. The recent development of gene expression microarrays (GEMs) in-situ based assays for stress gene induction using gene-probes (e.g. scintillation proximity assays and reporter gene technology) and organotypic culture systems (e.g. liver and brain spenoids) has and will enable automation and miniturisation of toxicogenomic-based high throughput screens in toxicology and drug metabolism. This book takes an integrated approach to in vitro toxicology and ADME screening using these new technologies and discusses how they might be applied to the pre-clinical safety assessment and `lead optimisation' of new pharmaceutical products in drug discovery. Edited and written by leading authorities in the field, this practical and comprehensive volume will be valuable reading for postgraduate and professional toxicologists and pre-clinical scientists in academia, contract testing organisations and the chemical and pharmaceutical industries.

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Inside This Book (learn more)
First Sentence:
The search for new medicines is one of the central themes in a board disciplinary approach to tackling human disease. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
throughput toxicity screens, maximum fold induction, throughput toxicity screening, basal cytotoxicity, ranking compounds, toxic outcomes, streptavidin beads, unique nucleotides, toxicity endpoints, microtitre plates, human cytochrome, vitro toxicology, selective cytotoxicity, human liver microsomes, molecular toxicology, high throughput screening, stress genes, assay volume, high throughput screens, drug development process, apoptotic cells, screening operation, heterologous expression systems, probe sets, chinese hamster cells
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Journal of Biological Chemistry, Biomolecular Screening, Methods Enzymol, Arch Biochem Biophys, Cancer Research, Biol Chem, New York, San Diego, Drug Metab Dispos, Pharmacol Exp Ther, Biochem Pharmacol, Biochemical Pharmacology, Drug Dis, Environmental Health Perspectives, Experimental Cell Research, Fold Induction Fold Ind, Mol Pharmacol, Nucleic Acids Res, Toxicologic Pathology
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