But they indicated a dose-dependent decrease of the mitochondrial enzyme activity (MTT assay) after 24 h of exposure, similar to the results seen before in other published studies [16, 17, 113] www.selleckchem.com/products/anlotinib-al3818.html and detected a dose‒ and time‒dependent increase of intracellular ROS [114]. ROS induction was also observed by exposure to carbon black [115]. Some doubt on the evaluation of MTT toxicity assays were expressed by Wörle-Knirsch et al. [116] because they demonstrated that MTT formazan interacts with CNT interfering

with the basic principle of the assay. The authors strongly suggest verifying cytotoxicity data with an independent test system as we did by using different test systems. A key finding in our study was that ROS generation in three cell lines (RTL-W1, T47Dluc, and H295R) went up in 45 min even in a low dose of incubation group (3.13 mg/L), which was 1.2 times higher

than in the controls. Chen et al. [114] assumed that ROS generation came out much earlier than other phenotypes selleck products including oxidative stress and cytotoxicity. This might be the reason why other studies in which ROS was measured after more than 4 h exposure to CNT showed inconsistent results [50, 117–119]. Several studies [112, 120] concluded that cytotoxicity can be attributed to oxidative stress. Interestingly, no cytotoxic effect was found in this study in three different MWCNT-treated cells, although generation of ROS was observed in all cell lines used. Similar experiments to determine the ROS generation in RTL-W1 cells were performed using multilayer graphene flakes (synthesized by thermal reduction of graphitic oxide at the Federal Institute for Materials and Research and Testing

BAM, Berlin) as non-nanomaterial (data not shown). Thereby, same increases of ROS generation were observed up to concentrations of 12.5 mg/L. Whereas, 1.5 times lower increases could be observed for both 25 and 50 mg/L compared to the MWCNT treatment. This lead us to the conclusion that the impurities of metal catalysts (cobalt) are not responsible for the increased production of ROS and such effects may be due to the nanostructure of these materials. Our findings are in accordance with other studies where intracellular Etofibrate ROS generation could be determined by using pristine graphene-treated murine RAW 264.7 macrophages [121], few-layer graphene (3 to 5 layers)-treated PC12 cells [122], and graphene oxide-treated human lung epithelial cells [123] in a time- and dose-dependent manner. However, Creighton et al. [124] showed that graphene-based materials have significant potential to interfere with in vitro toxicity testing methods, such as the H2DCF-DA assay, through optical and adsorptive effects at toxicologically relevant doses (less than 10 to 100 mg/L). They could also show that the GSK2399872A price removal of the nanomaterial by washing can remove optical interferences.