“…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.…”