“…Following oral administration, Cr(III) was reported to be very poorly absorbed via the gastrointestinal tract (0.4 to 2.8 %) in both rats and humans (Conn et al, 1932;Visek et al, 1953;Donaldson and Barreras, 1966;Doisy et al, 1971;Henderson et al, 1979;Anderson et al, 1983;Aitio et al, 1984;Anderson and Kozlovsky, 1985;Polansky et al, 1993;Gargas et al, 1994;Olin et al, 1994;Gammelgaard et al, 1999;ATSDR, 2012;Febel et al, 2001;Garcia et al, 2001).…”