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Drug toxicity observed in pre-/non-clinical animal studies sometimes leads to discontinuation of drug candidates. Understanding
the phenomena or backgrounds surrounding toxicological events occurred must be a key element for attrition improvement
in research and development (R&D) of new chemical entities (NCEs), often requiring mechanistic investigations to understand
toxicological mechanism of actions and then to make â??Goâ? or â??No goâ? decisions. In the post-genomic era, a battery of â??Omicsâ?
technologies was introduced and has been rapidly increasing utilization, among which is the prefix of â??toxico-â? added to each omics
technology in toxicology field. Especially, metabolomics in toxicology, which is so-called â??toxicometabolomicsâ?, has been widely
implemented in this area. The objectives are to identify and characterize the metabolites, both endogenous and exogenous, which are
the end products of cellular metabolism and drug metabolism, respectively. Moreover, toxicometabolomics enables to capture the
phenotypic changes in the events, which are generated by enzymatic proteins as resultants of gene expression, at the molecular level;
therefore, smooth translation of the findings can be made into the clinic. The presentation in this session will review the usefulness
of toxicometabolomics technologies which are generally nuclear magnetic resonance (NMR)-based and mass spectrometry (MS)-
based, and other toxic-Omics technologies. Furthermore, today, newly introduced technology, MS imaging (MSI) is considered
applicable in the toxicology field, hence its toxicological usability will be also reviewed.