PsycEXTRA Dataset 2010
DOI: 10.1037/e573112012-068
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“…Thus, LCIA will likely need to evolve beyond in vivo toxicity data if it is to be applicable for decision support involving new and emerging chemicals. (38) The U.S. National Research Council (NRC) (88) has recommended a transition from in vivo animal testing to in vitro assays (89,90) to address toxicity gaps on the large numbers of chemicals in commerce. For example, data generated under the Tox21 program (a collaboration between the U.S. National Institutes of Health and U.S. EPA) have resulted in information on the bioactivity of thousands of substances.…”
Section: Effectsmentioning
confidence: 99%
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“…Thus, LCIA will likely need to evolve beyond in vivo toxicity data if it is to be applicable for decision support involving new and emerging chemicals. (38) The U.S. National Research Council (NRC) (88) has recommended a transition from in vivo animal testing to in vitro assays (89,90) to address toxicity gaps on the large numbers of chemicals in commerce. For example, data generated under the Tox21 program (a collaboration between the U.S. National Institutes of Health and U.S. EPA) have resulted in information on the bioactivity of thousands of substances.…”
Section: Effectsmentioning
confidence: 99%
“…Instead, in vitro toxicity concentrations can be linked to doses using dosimetry modeling to forward-calculate a resulting blood or target tissue concentration from a given exposure. (89,92) Alternatively, reverse dosimetry can be used to convert a target tissue concentration to an equivalent absorbed dose, which can then be compared with an estimated exposure. (31,55,(93)(94)(95) Other sources of toxicity data include computational (or in silico) models,(96) which do not necessarily require the use of dosimetry modeling and instead may be designed to predict effects based on exposures or absorbed doses.…”
Section: Effectsmentioning
confidence: 99%