“…Similarly, particle overload in the lung has been implicated in ROS production. In culture, human blood-derived monocytes release ROS, consistent with in vivo monocyte infiltration and subsequent inflammation in the lung as a result of particle overloading [104, 105]. Furthermore , in vitro culture of alveolar macrophages with oil fly ash (OFA), TiO 2 , and SiO 2 shows strong induction of ROS production along with high cytotoxicity, suggesting a direct correlation between ROS production and cytotoxicity [91].…”