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A human in vivo model for the determination of lead bioavailability using stable isotope dilution.

Beverages stored in lead-crystal glass accumulate extraordinary concentrations of lead. We obtained a lead-crystal decanter manufactured with lead from Australia, where the ratio of 206Pb/207Pb is distinctly different from that in the United States. We sought to determine the bioavailability of crys...

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Detalles Bibliográficos
Autores principales: Graziano, J H, Blum, C B, Lolacono, N J, Slavkovich, V, Manton, W I, Pond, S, Moore, M R
Formato: Texto
Lenguaje:English
Publicado: 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1469275/
https://www.ncbi.nlm.nih.gov/pubmed/8820585
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author Graziano, J H
Blum, C B
Lolacono, N J
Slavkovich, V
Manton, W I
Pond, S
Moore, M R
author_facet Graziano, J H
Blum, C B
Lolacono, N J
Slavkovich, V
Manton, W I
Pond, S
Moore, M R
author_sort Graziano, J H
collection PubMed
description Beverages stored in lead-crystal glass accumulate extraordinary concentrations of lead. We obtained a lead-crystal decanter manufactured with lead from Australia, where the ratio of 206Pb/207Pb is distinctly different from that in the United States. We sought to determine the bioavailability of crystal-derived lead, using the technique of stable isotope dilution in blood. We conducted a single-dose, nonrandomized cross-over study in which participants were admitted to the Clinical Research Center twice, 1 week apart. During the first admission, subjects ingested sherry obtained from the original bottle. During the second admission, they ingested sherry that had been stored in the crystal decanter and that had achieved a lead concentration of 14.2 mu mol/l. After ingesting decanter-stored sherry, mean blood lead rose significantly (p = 0.0003) from 0.10 to 0.18 mu mol/l, while mean 206Pb/207Pb fell from 1.202 to 1.137 (p = 0.0001). On average, 70% of the ingested dose of lead was absorbed. We conclude that lead derived from crystal glass is highly bioavailable; repeated ingestions could cause elevated blood lead concentration. The technique of stable isotope dilution lends itself to the study of the bioavailability of lead in other matrices, including soil.
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spelling pubmed-14692752006-06-01 A human in vivo model for the determination of lead bioavailability using stable isotope dilution. Graziano, J H Blum, C B Lolacono, N J Slavkovich, V Manton, W I Pond, S Moore, M R Environ Health Perspect Research Article Beverages stored in lead-crystal glass accumulate extraordinary concentrations of lead. We obtained a lead-crystal decanter manufactured with lead from Australia, where the ratio of 206Pb/207Pb is distinctly different from that in the United States. We sought to determine the bioavailability of crystal-derived lead, using the technique of stable isotope dilution in blood. We conducted a single-dose, nonrandomized cross-over study in which participants were admitted to the Clinical Research Center twice, 1 week apart. During the first admission, subjects ingested sherry obtained from the original bottle. During the second admission, they ingested sherry that had been stored in the crystal decanter and that had achieved a lead concentration of 14.2 mu mol/l. After ingesting decanter-stored sherry, mean blood lead rose significantly (p = 0.0003) from 0.10 to 0.18 mu mol/l, while mean 206Pb/207Pb fell from 1.202 to 1.137 (p = 0.0001). On average, 70% of the ingested dose of lead was absorbed. We conclude that lead derived from crystal glass is highly bioavailable; repeated ingestions could cause elevated blood lead concentration. The technique of stable isotope dilution lends itself to the study of the bioavailability of lead in other matrices, including soil. 1996-02 /pmc/articles/PMC1469275/ /pubmed/8820585 Text en
spellingShingle Research Article
Graziano, J H
Blum, C B
Lolacono, N J
Slavkovich, V
Manton, W I
Pond, S
Moore, M R
A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title_full A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title_fullStr A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title_full_unstemmed A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title_short A human in vivo model for the determination of lead bioavailability using stable isotope dilution.
title_sort human in vivo model for the determination of lead bioavailability using stable isotope dilution.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1469275/
https://www.ncbi.nlm.nih.gov/pubmed/8820585
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