Journal
FOOD AND CHEMICAL TOXICOLOGY
Volume 46, Issue 6, Pages 2261-2266Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2008.03.004
Keywords
accelerator mass spectrometry; aluminum; atomic absorption spectrometry; basic sodium aluminum phosphate; food additive; oral bioavailability
Categories
Funding
- NIEHS NIH HHS [R01 ES11305, R01 ES011305-03, R01 ES011305] Funding Source: Medline
- NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R01ES011305] Funding Source: NIH RePORTER
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Oral aluminum (Al) bioravailability from drinking water has been previously estimated, but there is little information on Al bioavailability from foods. It was suggested that oral Al bioavailability from drinking water is much greater than from foods. The objective was to further test this hypothesis. Oral Al bioavailability was determined in the rat from basic [(26)Al]-sodium aluminum phosphate (basic SALP) in a process cheese. Consumption of similar to 1 g cheese containing 1.5% or 3% basic SALP resulted in oral Al bioravailability (F) of similar to 0.1% and 0.3%, respectively, and time to maximum serum (26)Al concentration (T(max)) of 8-9 h. These Al bioavailability results were intermediate to previously reported results from drinking water (F similar to 0.3%) and acidic-SALP incorporated into a biscuit (F similar to 0.1%), using the same methods. Considering the similar oral bioravailability of Al from food vs. water, and their contribution to the typical human's daily Al intake (similar to 95% and 1.5%, respectively), these results suggest food contributes much more Al to systemic circulation, and potential Al body burden, than does drinking water. These results do not support the hypothesis that drinking water provides a disproportionate contribution to total Al absorbed from the gastrointestinal tract. (C) 2008 Elsevier Ltd. All rights reserved.
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