“…Based on work published in the 1970′s and 1980′s [11] , [12] , [17] , there were concerns from regulatory bodies that the standard Ames test, using rat liver S9 and applying the plate incorporation protocol, is not sensitive enough to detect the mutagenic potential especially for nitrosamines with low molecular weight such as nitroso-dimethylamine (NDMA) [9] . Analysis of these publications showed that many of the reported Ames tests have limitations, such as e.g., uncommon strains, few strains or low concentrations.…”