期刊
TOXICOLOGY
卷 161, 期 1-2, 页码 93-101出版社
ELSEVIER SCI IRELAND LTD
DOI: 10.1016/S0300-483X(01)00335-3
关键词
aluminum; oral bioavailability; drinking water; gastric contents; water hardness; accelerator mass spectrometry; rat
The objectives were to estimate aluminum (Al) oral bioavailability under conditions that model its consumption in drinking water, and to test the hypotheses 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 concomitant calcium (Ca) and magnesium (Mg) at concentrations found in hard drinking water. The use of Al-26 enables the study of Al pharmacokinetics at physiological 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 bioavailability from the area under its serum concentration x time curve compared to serum Al-27 concentration in relation to its infusion rate. Oral Al bioavailability 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 published results suggest oral bioavailability of Al from drinking water is very low, about 0.3%. The present results suggest it is independent of stomach contents and water hardness. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
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