Literature DB >> 20017577

The use of computer models in pharmaceutical safety evaluation.

Scott Boyer1.   

Abstract

With the ever increasing volume of data available to scientists in drug discovery and development, the opportunity to leverage an increasing amount of these data in the assessment of drug safety is clear. The challenge in an environment of increasing data volume is in the structuring and the analysis of these data, such that decisions can be made without excluding information or overstating their meaning. Informatics and modelling play a crucial role in addressing this challenge in two basic ways: a) the data are structured and analysed in a transparent and objective way; and b) new experiments are designed with the model as part of the design process, much like modern experimental physics. Enhancing the use and impact of informatics and modelling on drug discovery is not simply a matter of increasing processor speed and memory capacity. The transformation of raw data to usable, and useful, information is a scientific, technical and, perhaps most importantly, cultural challenge within drug discovery. This review will highlight some of the history, current approaches and promising future directions in this rapidly expanding area. 2009 FRAME.

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Year:  2009        PMID: 20017577     DOI: 10.1177/026119290903700505

Source DB:  PubMed          Journal:  Altern Lab Anim        ISSN: 0261-1929            Impact factor:   1.303


  2 in total

Review 1.  In silico toxicology models and databases as FDA Critical Path Initiative toolkits.

Authors:  Luis G Valerio
Journal:  Hum Genomics       Date:  2011-03       Impact factor: 4.639

2.  Large-scale prediction and testing of drug activity on side-effect targets.

Authors:  Eugen Lounkine; Michael J Keiser; Steven Whitebread; Dmitri Mikhailov; Jacques Hamon; Jeremy L Jenkins; Paul Lavan; Eckhard Weber; Allison K Doak; Serge Côté; Brian K Shoichet; Laszlo Urban
Journal:  Nature       Date:  2012-06-10       Impact factor: 49.962

  2 in total

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