Ra. Yokel et al., Aluminum bioavailability from drinking water is very low and is not appreciably influenced by stomach contents or water hardness, TOXICOLOGY, 161(1-2), 2001, pp. 93-101
The objectives were to estimate aluminum (Al) oral bioavailability under co
nditions that model its consumption in drinking water, and to test the hypo
theses that stomach contents and co-administration of the major components
of hard water affect Al absorption. Rats received intragastric Al-26 in the
absence and presence of food in the stomach and with or without concomitan
t calcium (Ca) and magnesium (Mg) at concentrations found in hard drinking
water. The use of Al-26 enables the study of Al pharmacokinetics at physiol
ogical Al concentrations without interference from Al-27 in the environment
or the subject. Al-27 was intravenously administered throughout the study.
Repeated blood withdrawal enabled determination of oral Al-26 bioavailabil
ity from the area under its serum concentration x time curve compared to se
rum Al-27 concentration in relation to its infusion rate. Oral Al bioavaila
bility averaged 0.28%. The presence of food in the stomach and Ca and Mg in
the water that contained the orally dosed Al-26 appeared to delay but not
significantly alter the extent of Al-26 absorption. The present and publish
ed results suggest oral bioavailability of Al from drinking water is very l
ow, about 0.3%. The present results suggest it is independent of stomach co
ntents and water hardness. (C) 2001 Elsevier Science Ireland Ltd. All right
s reserved.