Further development and update of EFSA's Chemical Hazards Database
In: EFSA supporting publications, Band 12, Heft 7
ISSN: 2397-8325
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In: EFSA supporting publications, Band 12, Heft 7
ISSN: 2397-8325
In: EFSA supporting publications, Band 14, Heft 4
ISSN: 2397-8325
In: EFSA supporting publications, Band 15, Heft 7
ISSN: 2397-8325
In: EFSA supporting publications, Band 15, Heft 6
ISSN: 2397-8325
In: EFSA supporting publications, Band 17, Heft 3
ISSN: 2397-8325
The European Union's ban on animal testing for cosmetic ingredients and products has generated a strong momentum for the development of in silico and in vitro alternative methods. One of the focus of the COSMOS project was ab initio prediction of kinetics and toxic effects through multiscale pharmacokinetic modeling and in vitro data integration. In our experience, mathematical or computer modeling and in vitro experiments are complementary. We present here a summary of the main models and results obtained within the framework of the project on these topics. A first section presents our work at the organelle and cellular level. We then go toward modeling cell levels effects (monitored continuously), multiscale physiologically based pharmacokinetic and effect models, and route to route extrapolation. We follow with a short presentation of the automated KNIME workflows developed for dissemination and easy use of the models. We end with a discussion of two challenges to the field: our limited ability to deal with massive data and complex computations.
BASE
The European Union's ban on animal testing for cosmetic ingredients and products has generated a strong momentum for the development of in silico and in vitro alternative methods. One of the focus of the COSMOS project was ab initio prediction of kinetics and toxic effects through multiscale pharmacokinetic modeling and in vitro data integration. In our experience, mathematical or computer modeling and in vitro experiments are complementary. We present here a summary of the main models and results obtained within the framework of the project on these topics. A first section presents our work at the organelle and cellular level. We then go toward modeling cell levels effects (monitored continuously), multiscale physiologically based pharmacokinetic and effect models, and route to route extrapolation. We follow with a short presentation of the automated KNIME workflows developed for dissemination and easy use of the models. We end with a discussion of two challenges to the field: our limited ability to deal with massive data and complex computations.
BASE
In: EFSA supporting publications, Band 18, Heft 3
ISSN: 2397-8325